High energy return foam compositions having improved abrasion resistance and uses thereof

TECHNICAL FIELD

The present disclosure generally relates to materials, and in particular to materials for the footwear and related industries and uses thereof.

BACKGROUND

Footwear design involves a variety of factors from the aesthetic aspects, to the comfort and feel, to the performance and durability. While footwear design and fashion may be rapidly changing, the demand for increasing performance in the athletic footwear market is unchanging. To balance these demands, footwear designers employ a variety of materials and designs for the various components that make up an article of footwear.

BRIEF DESCRIPTION OF THE DRAWINGS

Further aspects of the present disclosure will be readily appreciated upon review of the detailed description, described below, when taken in conjunction with the accompanying drawings.

FIG. 1 is an elevation view of an article of footwear with a sole component according to an aspect of the invention.

FIG. 2 is an exploded view of the sole component of the article of footwear of FIG. 1.

FIG. 3 is a plan view of the bottom of the sole component of the article of footwear of FIG.

FIG. 4 is a bottom view of an insert for use in a sole component of an article of footwear.

FIG. 5 is a top view of the insert of FIG. 4 inserted in a first portion to form a sole component.

DETAILED DESCRIPTION

New designs and materials for the footwear industry are needed. In particular, there remains a need for improved foam compositions, for example that can be used in the footwear industry to provide improved cushion and energy return when used in a midsole or other component for an article of footwear. However, foam compositions having a high energy return often result in softer foams that can suffer from poor abrasion resistance leading to increased wear, decreasing lifespan of the foam and impacting customer satisfaction. Typical solutions to improve the abrasion loss in foam compositions result in a hardening of the foam, which is undesirable for high energy return foams as the increased hardness is expected to decrease the energy return properties of the foam. There remains a need for improved high energy return foams, e.g. those having improved abrasion resistance while maintaining the softness and the high energy return of the foam.

Foams that are soft and with a high energy return provide desirable performance characteristics for various articles, e.g. as sole components for articles of footwear. For example, polymer foams containing SEBS, EVA, and linking polymer have been found to exhibit high energy return while being a relatively soft foam. On the other hand, silane polymers commonly used in the footwear industry are known for typically being hard and/or typically acting as a crosslinking agent in polymer foam compositions, so the addition of silanes to these compositions typically results in increasing hardness. Applicants have found that, when adding silanes to soft high energy return foam compositions, the resultant foam is softer. The softness of the foam is increased so much in some instances that the amount of crosslinking agent (DCP in the case of the Examples) had to be increased to compensate and increase the crosslinking density of the new foam formulation. This is so that the new foam had the same hardness as the original foam without the silane. By providing foams with higher crosslink densities while still maintaining the softness and energy return properties, the silane-containing foams provided herein can produce dramatic improvements in the abrasion loss (decrease in the abrasion loss of 30%, 50%, or more as compared to the composition without the silane) while maintaining the desirable softness an/or energy return properties.

In various aspects, compositions are provided that can be foamed, i.e. can be used to produce a foam composition. For clarity, compositions that have not been foamed will, in some instances be referred to as “pre-foam” compositions. Foam compositions are also provided, e.g. compositions that have been prepared by foaming a “pre-foam” composition described herein. Articles of footwear, such as athletic shoes, and components thereof are also provided including one or more of the foam compositions. In particular, various aspects of the present disclosure describe sole components for an article of footwear having exceptionally high energy return. The sole components having exceptionally high energy return can be made from foaming a pre-foam composition described herein. Methods of making the compositions and components made therefrom are also provided.

Before the present disclosure is described in greater detail, it is to be understood that this disclosure is not limited to particular aspects described, and as such may, of course, vary. Other systems, methods, features, and advantages of foam compositions and components thereof will be or become apparent to one with skill in the art upon examination of the following drawings and detailed description. It is intended that all such additional systems, methods, features, and advantages be included within this description, be within the scope of the present disclosure, and be protected by the accompanying claims. It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to be limiting. The skilled artisan will recognize many variants and adaptations of the aspects described herein. These variants and adaptations are intended to be included in the teachings of this disclosure and to be encompassed by the claims herein.

Articles of Footwear

In various aspects, articles of footwear are provided. In particular, articles of footwear are provided including one or more components made entirely or partially from a foam mentioned above and described in more detail below. The foams and components made therefrom can have a range of desirable properties for footwear, including softness, durability, and an exceptionally high energy return. The articles of footwear can, in principal, include any article of footwear. In various aspects, the article of footwear can include a shoe, a boot, or a sandal.

The most common articles of footwear are shoes. Shoes can include athletic shoes such as baseball shoes, basketball shoes, soccer shoes, football shoes, running shoes, cross-trainer shoes, cheerleading shoes, golf shoes, and the like. The shoes can, in some aspects, be cleated. An exemplary article of footwear 10 is shown in FIG. 1. While an athletic shoe is exemplified in FIG. 1, it will be readily understood that some of the terminology employed will also apply to other articles of footwear or to other styles of shoe. Footwear 10 includes an upper 12 and a sole component 14 secured to upper 12. Sole component 14 can be secured to upper 12 by adhesive or any other suitable means. As used herein, the sole component 14 can be a monolithic component formed entirely of the foam material as described herein, or a multi-component assembly formed of a plurality of monolithic components, where at least one of the monolithic components is formed entirely of the foam material as described herein. Footwear 10 has a medial, or inner, side 16 and a lateral, or outer, side 18.

The upper, in some aspects, is unformed until the point that it is attached to the sole component. In some aspects, the upper is a lasted upper. A “lasted upper,” as used herein, refers to an upper that is formed into the shoe shape prior to attachment to the sole by one or more mechanical means. The lasted upper can include a heel counter formed to shape the heel of the upper. The lasted upper can include a strobel sock or a strobel board attached to the upper, typically via a strobel stitch.

Sole component 14, which is generally disposed between the foot of the wearer and the ground, provides attenuation of ground reaction forces (i.e., imparting cushioning), traction, and may control foot motions, such as pronation. As with conventional articles of footwear, sole component 14 can include an insole (not shown) located within upper 12. In some aspects, the sole component is an insole or sockliner or is a multi-component assembly including an insole or sockliner, can further include an insole or sockliner located within the upper, where the insole or sockliner is formed entirely or partially of a foam material described herein. Articles of footwear described herein can include an insole or sockliner formed entirely or partially of a foam material described herein.

The most common components of shoes and other footwear can be classified into one of three types of components: upper components, lower components, and grindery components. Upper components refer collectively to all of the components that are stitched or otherwise joined together to form the upper. The materials in the upper generally contribute to characteristics such as breathability, conformability, weight, and suppleness or softness. The lower components refer collectively to all of the components that collectively form the lower. The lower can include, for example, the outsole and midsole. The choice of outsole materials and design will contribute, for instance, to the durability, traction, as well as to the pressure distribution during use. The midsole materials and design contribute to factors such as the cushioning and support. Grindery components include all of the additional components that can be attached to the upper, lower, or both. Grindery components can include, for example, eyelets, toe puffs, shanks, nails, laces, velcro, catches, backers, linings, padding, heel backings, heel foxings, toe caps, etc.

For purposes of general reference, footwear 10 can be divided into three general portions: a forefoot portion 20, a midfoot portion 22, and a heel portion 24. Portions 20, 22, and 24 are not intended to demarcate precise areas of footwear 10. Rather, portions 20, 22, and 24 are intended to represent general areas of footwear 10 that provide a frame of reference during the following discussion.

Unless otherwise stated, or otherwise clear from the context below, directional terms used herein, such as rearwardly, forwardly, top, bottom, inwardly, downwardly, upwardly, etc., refer to directions relative to footwear 10 itself. Footwear is shown in FIG. 1 to be disposed substantially horizontally, as it would be positioned on a horizontal surface when worn by a wearer. However, it is to be appreciated that footwear 10 need not be limited to such an orientation. Thus, in FIG. 1, rearwardly is toward heel portion 24, that is, to the right as seen in FIG. 1. Naturally, forwardly is toward forefoot portion 20, that is, to the left as seen in FIG. 1, and downwardly is toward the bottom of the page as seen in FIG. 1. Top refers to elements toward the top of the page as seen in FIG. 1, while bottom refers to elements toward the bottom of the page as seen in FIG. 1. Inwardly is toward the center of footwear 10, and outwardly is toward the outer peripheral edge of footwear 10.

As can be seen in FIG. 2, sole component 14 consists of a first portion 26 having an upper surface 27 with a recess 28 formed therein. Upper surface 27 is secured to upper 12 with adhesive or other suitable fastening means. A plurality of substantially horizontal ribs 30 is formed on the exterior of first portion 26. In certain aspects, ribs 30 extend from a central portion of forefoot portion 20 on medial side 16 rearwardly along first portion 26, around heel portion 24 and forwardly on lateral side 18 of first portion 26 to a central portion of forefoot portion 20.

First portion 26 provides the external traction surface of sole component 14. In certain aspects it is to be appreciated that a separate outsole component could be secured to the lower surface of first portion 26.

Recess 28 extends from heel portion 24 to forefoot portion 20. In certain aspects, the rear surface 32 of recess 28 is curved to substantially follow the contour of the rear of heel portion 24 and the front surface 34 of recess 28 extends transversely across first portion 26.

An insert 36 is received in recess 28. Insert 36 has a curved rear surface 38 to mate with curved rear surface 32 of recess 28 and a transverse front surface 40 to mate with transverse front surface 34 of recess 28. An upper surface 42 of insert 36 is in contact with and secured to upper 12 with adhesive or other suitable fastening means.

As seen best in FIG. 3, a ground engaging lower surface 44 of first portion 26 includes a plurality of projections 46. Each projection 46 is surrounded by a groove 48. A plurality of transverse slots 50 are formed in lower surface 44, extending between adjacent projections 46. A longitudinal slot 52 extends along lower surface 44 from heel portion 26 to forefoot portion 20.

As illustrated in FIG. 2, insert 36 can provide cushioning or resiliency in the sole component. First portion 26 can provide structure and support for insert 36. In such aspects, first portion 26 can be formed of a material of higher density and/or hardness as compared to insert 36 such as, for example, non-foam materials including rubber and thermoplastic polyurethane, as well as foam materials. In certain aspects, insert 36 can be formed of a foam material as disclosed herein.

FIGS. 4 and 5 show bottom and top views of an insert 60 which can be used in a sole component as described herein. Insert 60 is similar to insert 36, but as illustrated in FIGS. 4 and 5, insert 60 is formed of two types of materials 62 and 64, where at least one of the materials is a foam as disclosed herein. FIG. 4 shows a bottom view of insert 60, while FIG. 5 shows a top view of insert 60 formed of two types of materials 62 and 64, with the insert placed inside a first portion 66 to form a sole component 14. Inserts with more than two types of materials, at least one of which is a foam as disclosed herein, can also be used. In the example illustrated in FIGS. 4 and 5, a portion of a first material 62 can be used in the heel region of the insert, and a portion of a second material 64 can be used in the toe region of the insert. A higher density material can be used to support the heel region, while a lower density material can be used to support the toe region. For example, the density of the first material can be at least 0.02 g/cm³greater than the density of the second material. The shape of the portions of the two materials 62 and 64 of the insert can be any suitable shape. For example, the heel region can be in the shape of a wedge. Inserts formed of two types of materials can be useful in running shoes, as well as in basketball shoes.

While the compositions and foams described herein can be used for making any of a variety of components for an article of footwear, in particular aspects the components include a midsole, an outsole, an insole, a tongue padding, a collar padding, and a combination thereof. In some aspects, the component is a sole component, such as a sole component 14 depicted in FIGS. 1-5, that includes a foam described herein. In some aspects, the component is an insert such as insert 36 or insert 60 depicted in FIGS. 4-5 that includes a foam described herein. The sole components and inserts for sole components can be made partially or entirely of a foam described herein. Any portion of a sole component or an insert for a sole component can be made of a foam described herein. For example, first portion 26 of the sole component (optionally including the ground engaging lower surface 44, such as the plurality of projections 46 and/or the groove 48 surrounding the projections), the entire insert 36, portions 62 or 64 of insert 60, a separate outsole component, or any combination thereof, can include a foam as described herein. The sole components and inserts can be made by foaming a composition provided herein, for example by injection molding or by injection molding followed by compression molding as described herein. The foams and components can demonstrate improved physical properties including one or more of an enhanced energy return, and enhanced split tear, a decreased specific density, or a combination thereof.

Split tear is an important physical property for a foam for a component of an article of footwear or athletic equipment. In some aspects, the foam or component can have a split tear value of about 1.0 kg/cm to 4.5 kg/cm, about 1.6 kg/cm to 4.0 kg/cm, about 2.0 kg/cm to 4.0 kg/cm, about 2.0 kg/cm to 3.5 kg/cm, or about 2.5 kg/cm to 3.5 kg/cm. The split tear can be measured as described in the examples below. In some aspects, the foam or component is compression molded, and the compression molded foam or component can have a split tear of about 0.08 kg/cm to 4.0 kg/cm, about 0.9 kg/cm to 3.0 kg/cm, about 1.0 to 2.0 kg/cm, about 1.0 kg/cm to 1.5 kg/cm, or about 2 kg/cm. In some aspects, the foam or component is injection molded, and the foam or component can have a split tear of about 0.07 kg/cm to 2.0 kg/cm, or about 0.8 kg/cm to 1.5 kg/cm, or about 0.9 to 1.2 kg/cm, about 1.5 kg/cm to 2.2 kg/cm.

The energy return, a measure of the percentage of energy the foam or component returns when compressed, is an important physical property. This is especially true for running and other athletic shoes. In some aspects, the foams and components provided herein have an energy return of about 60% to 90%, about 60% to 85%, about 65% to 85%, or about 70% to 85%. In some aspects, the foam or component is compression molded and can have an energy return of about 60% to 95% (e.g., about 60% to 85%; about 65% to 80%; about 65% to 75%; about 70% to 80%; or about 75% to 80%; about 75% to 85%; about 80% to 95%; or about 85% to 95%). The energy return can be measured as described in the examples below.

The foams and components can be lightweight. In some aspects, the foams and components can have a specific density of about 0.05 to 0.25, about 0.05 to 0.2, about 0.05 to 0.15, about 0.08 to 0.15, about 0.08 to 0.20, about 0.08 to 0.25, or about 0.1 to 0.15. In some aspects the foam or component is compression molded and can have a specific density of about 0.15 to 0.3, about 0.2 to 0.3, or about 0.15 to 0.25.

In some examples, the process for making the foams and components of the various examples described herein further includes compression molding the foam to give a compression molded foam or a compression molded component. In some aspects, compression molding foamed preforms formed from the foam compositions of the present disclosure can produce compression molded foam components having physical properties which make these components particularly advantageous for use in articles of footwear and athletic equipment. For example, the physical properties of these compression molded foam components make them particularly useful for use as cushioning elements, such as midsoles.

In some aspects, the resiliency and/or energy return of the compression molded foam or compression molded component can be significantly greater than the resiliency and/or energy return of the otherwise same foam preform used to make the compression molded foam component. While compression molded foam components formed from preforms foamed using other blowing methods sometimes have greater resiliency and/or energy return than their preforms, an even greater increase in resiliency and/or energy return can be achieved when compression molding foam preforms that were foamed using an impregnation process utilizing a physical blowing agent, as described herein. The resiliency and/or energy return of the compression molded foam component can be at least at least 6 percentage points, or at least 7 percentage points, or at least 8 percentage points, or at least 9 percentage points, or at least 10 percentage points, or at least 12 percentage points greater than the resiliency and/or energy return of the foam preform used to make the compression molded foam component. In particular examples, the resiliency and/or energy return of the compression molded foam component is at least 9 percentage points greater than the resiliency and/or energy return of the foam preform used for make the compression molded foam component.

This greater increase in the resiliency and/or energy return of the compression molded foam component can thus result in components having higher resiliency and/or energy return than would be possible using foam preforms made using other blowing methods. Using the blowing methods described herein, it has been found that it is possible to produce compression molded foam components having higher than usual resiliencies while using materials and methods which are cost-effective for use in consumer goods such as articles of footwear and athletic equipment. The resiliency and/or energy return of the compression molded foam component can be greater than 45%, or greater than 50%, or greater than 55%, or greater than 60%, or greater than 65%. For example, the resiliency and/or energy return of the compression molded foam component can be from 45% to 95%, or from 50% to 90%, or from 55% to 90%, or from 60% to 80%, or from 50% to 85%, or from 55% to 75%, or from 60% to 75%. Compression molded foam components having resiliencies greater than 45%, or 50%, or 55%, or 60%, or 65%, can be particularly advantageous for use in articles of footwear. Additionally or in combination, the resiliency and/or energy return of the foam preform can be less than 75%, or less than 70%, or less than 65%, or less than 60%. For example, the resiliency and/or energy return of the foam preform can be from 40% to 80%, or from 55% to 75%, or from 50% to 70% or from 65% to 80%.

Several methods of measuring resiliency and/or energy return of foams (e.g., foam preforms and foam components) exist in the art. One method of measuring resiliency of foams is based on ASTM D 2632-92, which is a test for solid rubber materials. For use with foams, the test sample is prepared as described in ASTM D2632-92, but uses a sample of foam in place of the sample of solid rubber. This test uses a plunger which is dropped from a height onto a test sample while being guided by a vertical rod. The drop height is divided into 100 equal parts, and the height to which the plunger rebounds is measured using this 100 part scale, to determine the resiliency of the sample. Alternative methods which use a ball of standard weight dropped onto a sample, and which measure the rebound height of the ball to determine the resiliency of the sample can also be used.

The specific gravity of a foam is also an important physical property to consider when using a foam for a component of an article of footwear or athletic equipment. The foams and components of the present disclosure can have a specific gravity of from 0.02 g/cm³to 0.22 g/cm³, or of from 0.03 g/cm³to 0.12 g/cm³, or of from 0.04 g/cm³to 0.10 g/cm³, or from 0.11 g/cm³to 0.12 g/cm³, or from 0.10 g/cm³to 0.12 g/cm³, from 0.15 g/cm³to 0.2 g/cm³; 0.15 g/cm³to 0.30 g/cm³. Alternatively or in addition, the foam preform can have a specific gravity of from 0.01 g/cm³to 0.10 g/cm³, or of from 0.02 g/cm³to 0.08 g/cm³, or of from 0.03 g/cm³to 0.06 g/cm³; 0.08 g/cm³to 0.15 g/cm³; or from 0.10 g/cm³to 0.12 g/cm³. For example, the specific gravity of the compression molded foam component can be from or from 0.15 g/cm³to 0.2 g/cm³, and the specific gravity of the foam preform can be from 0.10 g/cm³to 0.12 g/cm³. The foam or component can be compression molded.

In particular examples, the resiliency and/or energy return of the compression molded foam component can be at least at least 6 percentage points, or at least 7 percentage points, or at least 8 percentage points, or at least 9 percentage points, or at least 10 percentage points, or at least 12 percentage points greater than the resiliency and/or energy return of the foam preform used to make the compression molded foam component when the compression molded foam component has a resiliency and/or energy return greater than 45%, or greater than 50%, or greater than 55%, or greater than 60%, or greater than 65%, and the compression molded foam can have a specific gravity of from 0.02 g/cm³to 0.15 g/cm³, or of from 0.03 g/cm³to 0.12 g/cm³, or of from 0.04 g/cm³to 0.10 g/cm³or from 0.11 g/cm³to 0.12 g/cm³, from 0.15 g/cm³to 0.2 g/cm³; or 0.15 g/cm³to 0.30 g/cm³.

The specific gravity of the foam or component can be determined by testing at least 3 representative samples taken from a foam preform or compression molded foam component (e.g., a 2 inch×2 inch sample or a 1 inch×1 inch sample), or at least 3 entire foam preforms or compression molded foam components. Using a balance with appropriate accuracy for the weight of the sample, the weight of each sample is determined both in air and when the sample is completely submerged in distilled water at a temperature of 22° C.±2° C., after removing any air bubbles adhered to the surface of the foam sample weighing. The specific gravity (S.G.) is then calculated by taking the weight of the sample in water and subtracting that from the weight of the sample in air, and this value is then divided into the weight of the sample in air, where all the weights are weights in grams.

Compression set of a foam is another important physical property for a foam used as a component of an article of footwear or athletic equipment. In accordance with the present disclosure, the compression molded foam or compression molded component can have a compression set of from 40% to 100%. For example, the compression set can be from 45% to 90%, or from 40% to 80%, or from 50% to 75%.

Compression set can be measured by preparing a sample of a standard thickness (e.g., 10 mm) of a foam preform. Components having a thickness less than the standard can be stacked to make a sample having the standard thickness. The sample is loaded into a metal compression plate and compressed to a height of 50% of the original thickness (e.g., 5 mm). The sample is placed in a 50° C. oven on its side for 6 hours. At the end of the 6 hours, the sample is removed from the oven and from the metal compression plate, and allowed to cool for 30 minutes. Once cooled, the thickness of the sample is measured. The percent compression set (C.S.) is calculated by (a) subtracting the final sample thickness from the original sample thickness, and (b) subtracting the 50% compressed thickness from the original sample thickness, (c) dividing (a) by (b), and (d) multiplying the result by 100 to obtain the percent compression set (where all thicknesses are measured in millimeters).

Durometer is another important physical property of a foam or component that is to be used in an article of footwear or athletic equipment. In accordance with the present disclosure, the compression molded foam or component can have a durometer of at least 20 Asker C, or at least 30 Asker C, or at least 40 Asker C, or at least 50 Asker C. For example, the durometer of the compression molded foam or compression molded component can have a durometer of from 20 Asker C to 70 Asker C, or of from 20 Asker C to 40 Asker C, or from 30 Asker C to 35 Asker C, or of from 25 Asker C to 65 Asker C, or of from 30 Asker C to 50 Asker C, or of from 40 Asker C to 70 Asker C, or of from 35 Asker C to 55 Asker C, or from 50 Asker C to 65 Asker C. The foam preform can have a durometer of less than 40 Asker C, or less than 30 Asker C, or less than 20 Asker C. For example, the durometer of the foam preform can be from 15 Asker C to 50 Asker C, or from 20 Asker C to 50 Asker C, or from 20 Asker C to 40 Asker C, or from 20 Asker C to 30 Asker C. The durometer can be measured on a flat area of foam, e.g., at least 6 mm thick using an Asker C durometer.

In particular examples, the resiliency and/or energy return of the compression molded foam component can be at least at least 6 percentage points, or at least 7 percentage points, or at least 8 percentage points, or at least 9 percentage points, or at least 10 percentage points, or at least 12 percentage points greater than the resiliency and/or energy return of the foam preform used to make the compression molded foam component when the compression molded foam component has a resiliency and/or energy return greater than 45%, or greater than 50%, or greater than 55%, or greater than 60%, or greater than 65%, and the compression molded foam component can have a of at least 20 Asker C, or at least 30 Asker C, or at least 40 Asker C, or at least 50 Asker C. In addition, the compression molded foam can have a specific gravity of from 0.02 g/cm³to 0.15 g/cm³, or of from 0.03 g/cm³to 0.12 g/cm³, or of from 0.04 g/cm³to 0.10 g/cm³, or from 0.11 g/cm³to 0.12 g/cm³from 0.15 g/cm³to 0.2 g/cm³; or 0.15 g/cm³to 0.30 g/cm³.

Split tear is another important physical property for a foam or a component used in an article of footwear or athletic equipment. In accordance with the present disclosure, the compression molded foam or component can have a split tear of from 0.08 kg/cm to 4.0 kg/cm, or of from 0.9 kg/cm to 3.0 kg/cm, or of from 1.0 to 2.0 kg/cm, or of from 1.0 kg/cm to 1.5 kg/cm, or of about 2 kg/cm. Alternatively or in addition, the foam preform can have a split tear of from 0.07 kg/cm to 2.0 kg/cm, or of from 0.8 kg/cm to 1.5 kg/cm, or of from 0.9 to 1.2 kg/cm, or from about 1.5 kg/cm to about 2.2 kg/cm.

Split tear for foam preforms and compression molded foam components can be measured using ASTM D3574-95. Although this method is directed to bonded and molded urethane foams, it can be used on any foam material in accordance with the present disclosure. A sample of foam having a thickness of 10 mm±1 mm. If the foam preform or compression molded foam component has an outer skin, the outer skin should not be present on the test sample. A 3 cm long cut is placed in the center of one end of the specimen, and marked in five successive 2 cm portions along the edge of the sample. The sample is tested as described in ASTM D3574-95.

The tear strength of the compression molded foam component can range from 4 kg/cm to 10 kg/cm.

The tensile strength of the foam is another important physical characteristic. The foam or component can have a tensile strength of from 5 kg/cm²to 25 kg/cm², or of from 10 kg/cm²to 23 kg/cm², or of from 15 kg/cm²to 22 kg/cm². The tensile strength can be measured on a die cut sample of the foam in the shape of a dumbbell of a standard size such as a 2.5 cm in width by 11.5 cm in length, with a minimum thickness of 3 to 4 mm. The dumbbell follows the shape described in ASTM D412, die C. The sample is loaded symmetrically into and tested using a long travel extensometer such as the Instron 2603-080 which allows for a minimum of 1000% strain with a gauge length of 25 mm and a resolution of at least 0.1 mm. The tensile value at the failure point of the sample (the point during testing when the load value initially drops) is recorded. The foam or component can be compression molded.

Another physical property to consider when determining whether or not a foam is suitable for use as a component of an article of footwear or athletic equipment is its 300% elongation. The compression molded foam or component can have an elongation of at least 125 kg/cm², or at least 150 kg/cm².

Some examples described herein are directed to a foam article (e.g., articles used to make at least portions of footwear or athletic equipment) made by a process/method comprising: forming a pre-foam composition comprising a polymer comprising styrene repeating units and non-styrenic repeating units; and a C₄-C₁₀₀unsaturated olefin; crosslinking the polymer comprising styrene repeating units and non-styrenic repeating units and the C₄-C₁₀₀unsaturated olefin olefin block copolymer of the pre-foam composition, forming a crosslinked pre-foam composition; and blowing the pre-foam composition, the crosslinked pre-foam composition, or blowing both the pre-foam composition and the crosslinked pre-foam composition, to give a foam article. In some examples, the cross-linking and the blowing can occur substantially simultaneously. In some examples, the process for forming foam articles further comprises injection molding the pre-foam composition, and the crosslinking occurs during the injection molding. In some examples, the crosslinked composition, or both the pre-foam composition and the crosslinked composition are blown in a mold. In some examples, the crosslinking occurs during the injection molding (e.g., the crosslinking occurs substantially in the mold).

In some examples, the foam articles of the various examples described herein can further comprise at least one ethylene vinyl acetate copolymer and/or at least one olefin block copolymer, as each of the terms is defined herein. The component, such as the midsole, can have a variety of beneficial properties.

It has been found that, for many examples, the resiliency and/or energy return (also referred to as energy return) of the compression molded foam article can be significantly greater than the resiliency and/or energy return of the foam article used to make the compression molded foam article. While compression molded foam articles formed using other blowing methods sometimes have greater resiliency and/or energy return than the corresponding foam article, an even greater increase in resiliency and/or energy return can be achieved when compression molding foam articles that were foamed using an impregnation process utilizing a physical blowing agent, as described herein. The resiliency and/or energy return of the compression molded foam article can be at least at least 6 percentage points, or at least 7 percentage points, or at least 8 percentage points, or at least 9 percentage points, or at least 10 percentage points, or at least 12 percentage points greater than the resiliency and/or energy return of the foam article used to make the compression molded foam article. In particular examples, the resiliency and/or energy return of the compression molded foam article is at least 9 percentage points greater than the resiliency and/or energy return of the foam article used for make the compression molded foam article.

This greater increase in the resiliency and/or energy return of the compression molded foam article can thus result in components having higher resiliency and/or energy return than would be possible using foam articles made using other blowing methods. Using the blowing methods described herein, it has been found that it is possible to produce compression molded foam articles having higher than usual resiliencies while using materials and methods which are cost-effective for use in consumer goods such as articles of footwear and athletic equipment. The resiliency and/or energy return of the compression molded foam article can be greater than 45%, or greater than 50%, or greater than 55%, or greater than 60%, or greater than 65%. For example, the resiliency and/or energy return of the compression molded foam article can be from 45% to 95%, or from 50% to 90%, or from 55% to 90%, or from 60% to 80%, or from 50% to 85%, or from 55% to 75%, or from 60% to 75%. Compression molded foam articles having resiliencies greater than 45%, or 50%, or 55%, or 60%, or 65%, can be particularly advantageous for use in articles of footwear. Additionally or in combination, the resiliency and/or energy return of the foam article can be less than 75%, or less than 70%, or less than 65%, or less than 60%. For example, the resiliency and/or energy return of the foam article can be from 40% to 80%, or from 55% to 75%, or from 50% to 70% or from 65% to 80%.

The durability of the foams and foam components is an important parameter, particularly for articles of footwear. Unfortunately, increasing the energy return of the foams often results in softer foams which may have poor abrasion resistance. The compositions provided herein can produce foam compositions having an improved abrasion loss while still maintaining the desirable softness and energy return properties. In some aspects, injection molded and compression molded foam components have a DIN abrasion loss of about 20%, about 15%, about 10%, or less when measured according to the modified DIN procedure in Example 5.

The specific gravity of a foam article is also an important physical property to consider when using a foam for a component of an article of footwear or athletic equipment. The compression molded foam articles of the present disclosure can have a specific gravity of from 0.02 g/cm³to 0.22 g/cm³, or of from 0.03 g/cm³to 0.12 g/cm³, or of from 0.04 g/cm³to 0.10 g/cm³, or from 0.11 g/cm³to 0.12 g/cm³, or from 0.10 g/cm³to 0.12 g/cm³, from 0.15 g/cm³to 0.2 g/cm³; 0.15 g/cm³to 0.30 g/cm³. Alternatively or in addition, the foam article can have a specific gravity of from 0.01 g/cm³to 0.10 g/cm³, or of from 0.02 g/cm³to 0.08 g/cm³, or of from 0.03 g/cm³to 0.06 g/cm³; 0.08 g/cm³to 0.15 g/cm³; or from 0.10 g/cm³to 0.12 g/cm³. For example, the specific gravity of the compression molded foam article can be from or from 0.15 g/cm³to 0.2 g/cm³, and the specific gravity of the foam article can be from 0.10 g/cm³to 0.12 g/cm³.

In particular examples, the resiliency and/or energy return of the compression molded foam article can be at least at least 6 percentage points, or at least 7 percentage points, or at least 8 percentage points, or at least 9 percentage points, or at least 10 percentage points, or at least 12 percentage points greater than the resiliency and/or energy return of the foam article used to make the compression molded foam article when the compression molded foam article has a resiliency and/or energy return greater than 45%, or greater than 50%, or greater than 55%, or greater than 60%, or greater than 65%, and the compression molded foam article can have a specific gravity of from 0.02 g/cm³to 0.15 g/cm³, or of from 0.03 g/cm³to 0.12 g/cm³, or of from 0.04 g/cm³to 0.10 g/cm³, or from 0.11 g/cm³to 0.12 g/cm³from 0.15 g/cm³to 0.2 g/cm³; or 0.15 g/cm³to 0.30 g/cm³.

Compression set of a foam article is another important physical property for a foam used as a component of an article of footwear or athletic equipment. In accordance with the present disclosure, the compression molded foam article can have a compression set of from 40% to 100%. For example, the compression set can be from 45% to 90%, or from 40% to 80%, or from 50% to 75%.

Durometer is another important physical property of a foam article used as an article of footwear or athletic equipment. In accordance with the present disclosure, the compression molded foam article can have a durometer of at least 20 Asker C, or at least 30 Asker C, or at least 40 Asker C, or at least 50 Asker C. For example, the durometer of the compression molded foam article can have a durometer of from 20 Asker C to 70 Asker C, or of from 20 Asker C to 40 Asker C, or from 30 Asker C to 35 Asker C, or of from 25 Asker C to 65 Asker C, or of from 30 Asker C to 50 Asker C, or of from 40 Asker C to 70 Asker C, or of from 35 Asker C to 55 Asker C, or from 50 Asker C to 65 Asker C. The foam article can have a durometer of less than 40 Asker C, or less than 30 Asker C, or less than 20 Asker C. For example, the durometer of the foam preform can be from 15 Asker C to 50 Asker C, or from 20 Asker C to 50 Asker C, or from 20 Asker C to 40 Asker C, or from 20 Asker C to 30 Asker C. The durometer can be measured on a flat area of foam, e.g., at least 6 mm thick using an Asker C durometer.

In particular examples, the resiliency and/or energy return of the compression molded foam article can be at least at least 6 percentage points, or at least 7 percentage points, or at least 8 percentage points, or at least 9 percentage points, or at least 10 percentage points, or at least 12 percentage points greater than the resiliency and/or energy return of the foam article used to make the compression molded foam article when the compression molded foam article has a resiliency and/or energy return greater than 45%, or greater than 50%, or greater than 55%, or greater than 60%, or greater than 65%, and the compression molded foam article can have a of at least 20 Asker C, or at least 30 Asker C, or at least 40 Asker C, or at least 50 Asker C. In addition, the compression molded foam article can have a specific gravity of from 0.02 g/cm³to 0.15 g/cm³, or of from 0.03 g/cm³to 0.12 g/cm³, or of from 0.04 g/cm³to 0.10 g/cm³, or from 0.11 g/cm³to 0.12 g/cm³from 0.15 g/cm³to 0.2 g/cm³; or 0.15 g/cm³to 0.30 g/cm³.

The tear strength of the compression molded foam or article can range from 4 kg/cm to 10 kg/cm. The tensile strength of the foam or article is another important physical characteristic. The compression molded foam article can have a tensile strength of from 5 kg/cm²to 25 kg/cm², or of from 10 kg/cm²to 23 kg/cm², or of from 15 kg/cm²to 22 kg/cm².

Another physical property to consider when determining whether or not a foam article is suitable for use as a component of an article of footwear or athletic equipment is its 300% elongation. The compression molded foam article can have an elongation of at least 125 kg/cm², or at least 150 kg/cm².

Various examples include methods of manufacturing an article of footwear or components for an article of footwear. In some examples, the methods of manufacturing an article of footwear include blowing a composition described herein to give a foam article; compression molding the foam article to make a compression molded component for an article of footwear. The component can be a midsole, and the method can include providing an upper and an outsole for an article of footwear; and combining the compression molded midsole, the upper, and the outsole to make an article of footwear. In some examples, the method of manufacturing the article of footwear includes combining a compression molded foam article, an upper, and an outsole to make an article of footwear.

In some aspects, the present disclosure is directed to a compression molded foam, and to a method of forming compression molded foam for, among other applications, articles of footwear or athletic equipment. In some examples, the method can be a process comprising providing (e.g., preparing) a foam preform and then compression molding the foam preform to form a compression molded foam.

The present inventors have recognized, among other things, that the compression molded foam of the various examples described herein has improved physical characteristics, such as, for example, improved resiliency and/or energy return.

In some examples, one step of the method comprises providing (e.g., preparing or obtaining) a pre-foam composition as disclosed herein. For example, the pre-foam composition can be prepared using any method known in the art, including using a suitable kneader, a suitable single-screw or a suitable twin-screw extruder. An extruder (e.g., single or twin screw) can be used to provide a pre-foam composition. The extruder can have a motor to turn a screw inside the extruder. Screw may be a single screw or twin screws made of individual elements of various sizes and pitches appropriate for mixing or kneading the specific materials used. In some examples, the extruder has a twin screw.

The various components that make up the pre-foam compositions of the various examples described herein (e.g., a polymer comprising styrene repeating units and non-styrenic repeating units; a C₄-C₁₀₀unsaturated olefin; and optionally one or more additional components selected from an ethylene vinyl acetate copolymer; an olefin block copolymer; blowing agent; a crosslinking agent, and any combination thereof) are added into the extruder through a port. In some examples, the pre-foam compositions of the various examples described herein can be at least partially crosslinked at a first crosslinking temperature in, e.g., section of extruder to form a crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition), which, in some examples, may be a thermoplastic crosslinked pre-foam composition. Various other components (e.g., pigments, fillers, and blowing agents) can be added via a port into the extruder and mixed or kneaded with the pre-foam compositions and/or the crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition).

The various components that make up the pre-foam compositions of the various examples described herein may be added as a melt or as appropriately-sized solid particles, for example chips or pellets, that are melted in section as they are mixed or kneaded with, e.g., the crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition).

The contents of the extruder or mixer may be heated to, achieve, among other things, crosslinking of the pre-foam compositions to give a crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition). In other examples, the heating may trigger foaming (i.e., blowing) (e.g., via triggering a chemical blowing agent), thereby converting the crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition) to a foam composition that is sufficiently thermoplastic to be extruded or injected into a mold from the extruder 10. Alternatively, the crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition) can be foamed in the extruder using a physical blowing agent. And, in some examples, a chemical blowing agent can also be present, such that, when there is heating, the heating can trigger the chemical blowing agent.

In some examples, the pre-foam compositions may be added as a melt at a temperature close to or at the crosslinking temperature such that crosslinking can occur, but at a temperature that is sufficiently below the temperature that would trigger blowing. The temperature of the extruder can then be increased to a temperature close to or at the triggering temperature of a chemical blowing agent, thereby giving a foam composition.

The extent to which the pre-foam compositions is crosslinked to give a crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition) can be controlled so that the crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition) remains thermoplastic and can be mixed with various other components (e.g., pigments, fillers, and blowing agents) if necessary. This can be accomplished in various ways, for instance by controlling the amount of time for crosslinking; by controlling the crosslinking temperature; by causing a temperature reduction at a desired point of crosslinking to stop or slow further crosslinking; or by a combination of these. For example, the amount of time for crosslinking can be controlled by controlling screw speed, by locating port 8 closer to or further from port 6, or by a combination of these.

In some examples, as the crosslinking density increases, the crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition) can form phase separated domains, wherein, for example, the styrenic segments of the crosslinked polymer comprising styrene repeating units and non-styrenic repeating units phase separate into predominately styrene-rich domains.

A crosslinked pre-foam composition (e.g., at least partially crosslinked pre-foam composition) or a foam composition, each of which is sufficiently thermoplastic to be extruded or injected into a mold from the extruder, is extruded at an end of the extruded opposite the motor. In some examples, a vacuum port may be used to remove volatiles, for example water, volatile organic liquids that may have been introduced as solvents with some materials, crosslinking reaction by-products or blowing agent by-products. The extrudate may be shaped by being extruded through a die (not shown). For example, the extrudate (e.g., crosslinked pre-foam composition or foam composition) may be extruded in the form of strands that are then pelletized, in the form of a tube, or in the form of a sheet. The pelletization can be conducted using a cooled die. Additionally or alternatively, the pelletization can be performed under water, thus cooling the resulting pellets as they exited the pelletization die.

In some examples, the foam preforms of the various examples described herein are obtained by blowing the pre-foam composition, the crosslinked composition, or both the pre-foam composition and the crosslinked composition by about 150% to about 240% (e.g., from about 150% to about 220%; about 150% to about 200%, about 175% to about 225%, about 180% to about 230% or about 160% to about 240%) in at least one dimension (e.g., the vertical dimension) using a blowing agent.

In some examples, the foam preforms of the various examples described herein are made using a process that involves impregnating a pre-foam composition, a crosslinked pre-foam composition or combinations thereof (e.g., at or above a softening temperature of the pre-foam composition, crosslinked pre-foam composition or combinations thereof) with a physical blowing agent at a first concentration or first pressure.

As used herein, the term “impregnating” generally means dissolving or suspending a physical blowing agent in a pre-foam composition, a crosslinked pre-foam composition or combinations thereof. The impregnated pre-foam composition, crosslinked pre-foam composition or combinations thereof can then be foamed, or can be cooled (when applicable) and re-softened (when applicable) for blowing at a later time.

In some instances, the impregnated pre-foam composition, crosslinked pre-foam composition or combinations thereof is foamed by reducing the concentration or pressure of the physical blowing agent. The reduction in concentration of the physical blowing agent can release additional amounts (e.g., to create a secondary expansion of an originally-formed microcell in the pre-foam composition, crosslinked pre-foam composition or combinations thereof) of the impregnated physical blowing agent from the pre-foam composition, crosslinked pre-foam composition or combinations thereof, to further blow the pre-foam composition, crosslinked pre-foam composition or combinations thereof, forming a foam composition (e.g., a foam composition having a closed-cell structure).

In addition to injection molding, the pre-foam compositions of the present disclosure can be foamed and optionally molded using various processes known in the art. For example, the pre-foam compositions can be used to form slab foam, particulate (e.g., bead) foams of various shapes and sizes, etc. These various forms of foam can then be used in different ways. For example, slab foam can be used directly as a finished foam article, can be shaped (e.g., cut or trimmed) to form a finished foam article, or can be compression molded to form a finished foam article. The foams can be subjected to annealing processes as part of forming the finished foam article. Pellets of the pre-foam compositions can be used to form individual particulate foams, or can be foamed and molded to form unitary molded foam articles composed of individual portions of foam affixed to each other.

The foam compositions of the various examples described herein (e.g., foam preforms) may be further shaped or molded by any of the methods known for forming articles from thermoplastic materials.

Another step of the method for forming compression molded foam includes providing a foam preform that has been foamed using any suitable blowing process (e.g., blowing using a physical and/or chemical blowing agent), and then compression molding the foam preform to form a compression molded foam.

In some examples, the foam preform is prepared by a process comprising (i) softening a pre-foam composition, a crosslinked pre-foam composition or combinations thereof (e.g., by heating at a first temperature at or above a softening temperature of the pre-foam composition, crosslinked pre-foam composition or combinations thereof); (ii) simultaneously or sequentially with the softening (when applicable), contacting the pre-foam composition, crosslinked pre-foam composition or combinations thereof with a first concentration or first pressure of a physical blowing agent sufficient to drive an amount of the physical blowing agent into the pre-foam composition, crosslinked pre-foam composition or combinations thereof; (iii) changing the concentration or pressure (e.g., decreasing the pressure or concentration) of the physical blowing agent to a second concentration or second pressure that is effective to foam the pre-foam composition, crosslinked pre-foam composition or combinations thereof, thereby forming a foam composition (e.g., a foam composition having a closed-cell structure); and, (iv) following the changing, cooling (when applicable) the foam composition to (e.g., cooling to a temperature below the softening temperature of the foam composition), to form a foam preform having an initial height. In some examples, this process is conducted with a composition comprising, consisting essentially of or consisting of a crosslinked pre-foam composition.

In other examples, the foam preform is prepared by (i) contacting (e.g., dissolving or suspending) the pre-foam composition, crosslinked pre-foam composition or combinations thereof with a first concentration of a chemical blowing agent, in some examples, at or above a softening temperature of the pre-foam composition, crosslinked pre-foam composition or combinations thereof; (ii) triggering the chemical blowing agent to foam the pre-foam composition, crosslinked pre-foam composition or combinations thereof, thereby forming a foam composition (e.g., a foam composition having a closed-cell structure); and, (iii) following the triggering, in some examples, cooling the foam composition to, e.g., a temperature below its softening temperature, to form a foam preform having an initial height. In some examples, this process is conducted with a composition comprising, consisting essentially of or consisting of a crosslinked pre-foam composition. In some examples, the “triggering” of the chemical blowing agent is performed by any suitable method, including heating the pre-foam composition, crosslinked pre-foam composition or combinations thereof comprising a concentration of the chemical blowing agent to a temperature sufficient to “trigger” the chemical blowing agent, wherein the concentration of the chemical blowing agent is effective to foam the pre-foam composition, crosslinked pre-foam composition or combinations thereof, thereby forming a foam composition (e.g., a foam composition having a closed-cell structure).

In some examples, the contacting comprises contacting at a pressure of from about 10 MPa to about 100 MPa (e.g., from about 30 MPa to about 100 MPa, about 20 MPa to about 80 MPa, about 30 MPa to about 60 MPa or about 40 MPa to about 70 MPa).

In some examples, whether the foam preform is prepared using a physical or chemical blowing agent, a foamed composition (e.g, in the form of a foam preform) can be compression molded. For example, the foamed composition can be compression molded by placing the foam preform in a compression mold having a height less than the initial height of the foam preform and closing the mold, thereby compressing the foam preform to the height of the mold. Simultaneously or sequentially with the compressing, the foam preform can be heated in the closed compression mold. During the compression molding, the temperature of at least a portion of the foam preform in the closed mold can be raised to a temperature within ±30° C. of the softening temperature of the foam composition. The temperature can be raised by heating the closed mold. Following the raising of the temperature, while the foam preform remains closed in the compression mold, the temperature of at least a portion of the foam preform can be lowered. The temperature can be lowered by cooling the closed mold. The lowering can lower the temperature of at least a portion of the foam preform to a temperature at least 35° C. below the softening temperature of the foamed composition, thereby forming the compression molded foam. Following the cooling, the compression mold can be opened, and the compression molded foam can be removed from the compression mold.

Some examples contemplated herein are directed to compression molded components of articles of footwear or athletic equipment made in accordance with the compositions and processes described herein.

Other examples contemplated herein are directed to methods of manufacturing articles of footwear or athletic equipment. For example, the method can comprise providing a compression molded foam component of an article of footwear in accordance with the present disclosure, and combining the component with a footwear upper and an outsole to form the article of footwear. Similarly, the method can comprise providing a compression molded foam component of an article of athletic equipment in accordance with the present disclosure, and combining the compression molded foam component with other components to form a finished article of athletic equipment.

One method of making a compression molded foam (and compression molded foam articles) described herein comprises forming a foam preform and compression molding the foam preform to make a compression molded foam. In some examples, the foam preforms of the various examples described herein are obtained by blowing the pre-foam composition, the crosslinked composition, or both the pre-foam composition and the crosslinked composition by about 150% to about 240% (e.g., from about 150% to about 220%; about 150% to about 200%, about 175% to about 225%, about 180% to about 230% or about 160% to about 240%) in at least one dimension (e.g., the vertical dimension) using a blowing agent. In some examples, the blown pre-foam composition, the crosslinked composition, or both the pre-foam composition and the crosslinked composition can be compression molded to about 120% to about 200% (e.g., from about 120% to about 180%; about 130% to about 190%; about 150% to about 200%; or about 160% to about 190%) in at least one dimension.

Thus for example, if the foaming of the pre-foam composition, the crosslinked composition, or both the pre-foam composition and the crosslinked composition is about 200%, the blown pre-foam composition, the crosslinked composition, or both the pre-foam composition and the crosslinked composition can be compression molded by a net 20% by compression molding to about 180%. In another example, if the pre-foam composition, the crosslinked composition, or both the pre-foam composition and the crosslinked composition is blown into a 20 mm (height)×10 cm (width)×5 cm (depth) slab, and the slab is compression molded in the height direction by 20%, the compression molded slab would have the dimensions 18 mm (height)×10 cm (width)×5 cm (depth). In some examples, the compression molding is substantially maintained.

In some examples, the foam preform is made using a process that involves impregnating a pre-foam composition, a crosslinked pre-foam composition or combinations thereof (e.g., at or above a softening temperature of the pre-foam composition, crosslinked pre-foam composition or combinations thereof) with a physical blowing agent at a first concentration or first pressure. The impregnated pre-foam composition, crosslinked pre-foam composition or combinations thereof can then be foamed, or can be cooled (when applicable) and re-softened (when applicable) for blowing at a later time. In some instances, the impregnated pre-foam composition, crosslinked pre-foam composition or combinations thereof is foamed by reducing the concentration or pressure of the physical blowing agent. The reduction in concentration of the physical blowing agent can release additional amounts of the impregnated physical blowing agent from the pre-foam composition, crosslinked pre-foam composition or combinations thereof, to further blow the pre-foam composition, crosslinked pre-foam composition or combinations thereof, forming a foam composition (e.g., a foam composition having a closed-cell structure).

In some examples, the compression molding process is conducted by heating the foam preform in a closed compression mold. The foam preform is heated to a temperature close to its softening temperature, to allow the foam to retain the shape of the compression mold. For example, the foam preform can be heated to a temperature within ±30° C. of its softening temperature, or within ±20° C. of its softening temperature, or within ±10° C. of its softening temperature, or within ±5° C. of its softening temperature. For example, the foam preform can be heated to a temperature of from about 100° C. to about 250° C., or of from about 140° C. to about 220° C., or of from about 100° C. to about 150° C., or of from about 130° C. to about 150° C.

The material used to form the compression mold can be any material which can withstand the temperatures used during the process, such as machined metals, including aluminum. The compression mold can be made using two pieces, such as a top and a bottom mold. Depending on the shape of the foam component to be molded, a multiple-piece mold may be used in order to more easily release the compression molded foam from the mold.

The compression molding of the foam preform in the compression mold can result in a closed skin forming on the final compression molded foam component. However, care should be taken during the compression molding not to subject the foam preform to conditions such that more than a desired amount of the closed cell structures of the foam collapse. One way to avoid collapsing more than a desired amount of the closed cell structures is to control the temperature of the polymeric composition, for example, by controlling the temperature of the mold. For example, during the compression molding step, the heating of the foam preform in the compression mold can be conducted for time of from 100 seconds to 1,000 seconds, or of from 150 seconds to 700 seconds.

Once the foam preform has been heated in the compression mold at the appropriate temperature for the desired length of time to soften the preform to the desired level, the softened preform is cooled, for example, to a temperature at least 35° C. below its softening temperature, or at least 50° C. below its softening temperature, or at least 80° C. below its softening temperature, to re-solidify the softened foam, thereby forming the compression molded foam. Once cooled, the compression molded foam component is removed from the compression mold. Following the heating, the cooling of the foam preform in the compression mold can be conducted for a time of from 50 to 1,000 seconds, or for a time of from 100 to 400 seconds.

Compositions

In various aspects, compositions are provided that can be foamed, i.e. can be used to form a foam composition. In some aspects, these compositions are referred to as a “pre-foam composition.” The inventors have found that, by adding an effective amount of a silane to the pre-foam compositions, the abrasion resistance of the foams can be improved while maintaining the desired energy return and softness of the foam.

In various aspects, a composition is provided including a first pre-foam composition and a first effective amount of a silane. When the first pre-foam composition is foamed without the silane, it produces a first foam composition having a first energy return, a first hardness, and a first abrasion loss. However, when the composition including the silane is foamed, the first effective amount of the silane is effective to form a second foam composition having a second energy return, a second hardness, and a second abrasion loss. The first effective amount of the silane is effective to improve the abrasion loss while maintaining the desirable softness and/or energy return.

The added silane can produce foams which maintain the desirable energy return. In some aspects, the second energy return is greater than the first energy return. In some aspects, the second energy return is within about 20%, about 15%, about 10%, or about 5% of the first energy return.

The added silane can produce foams which maintain the desirable softness. In some aspects, the second hardness is less than the first hardness. In some aspects, the second hardness is within about 20%, about 15%, about 10%, or about 5% of the first hardness.

The added silane can improve the abrasion loss of the foam. In some aspects, the abrasion loss is measured according to the modified DIN procedure described below. In some aspects, the second abrasion loss is at least 20%, at least 30%, at least 40%, at least 50%, or at least 60% less than the first abrasion loss.

In some aspects, the first effective amount of the silane is about 0.15 parts per hundred resin, about 0.2 parts per hundred resin, about 0.25 parts per hundred resin, about 0.3 parts per hundred resin, or more. In some aspects, the first effective amount of the silane is about 0.15 parts per hundred resin to about 1 parts per hundred resin, about 0.25 parts per hundred resin to about 1 parts per hundred resin, or about 0.25 parts per hundred resin to about 0.75 parts per hundred resin.

The silanes can include an organofunctionalized silane, e.g. a silane having hydrolysable functional groups, ethylenically unsaturated linkage, or both.

In some aspects, the first effective amount of silanes is added to the first pre-foam composition in order to improve the abrasion loss, and then the crosslinking of the foam is increased by adding an increased amount of an oxide or other free-radical initiator to increase the crosslink density of the foam and produce a foam having a hardness within about 15%, within about 10%, or within about 5% of the hardness of the foam without the silanes and free radical initiator. In some aspects, the oxide added is a dicumyl peroxide (Cosmo chem Colink-40). In some aspects, the amount of added oxide is a +5%-15% peroxide increase compared to the amount of peroxide used in the foam composition without the silane (depending on desired hardness shift), for the 0.35 PHR Silane trials, the increase was 11.5%.

In some aspects, the compositions can be used to generate foam compositions that are soft and have a high energy return, but with improved durability and abrasion loss, making them useful for footwear. The compositions can be used to generate foams using any of a variety of methods known in the art. In some aspects, the foams are generated using injection molding or injection molding followed by compression molding techniques. The foamed compositions can include components of articles of footwear as described above, for example a sole component 14 as depicted in FIGS. 1-5.

The compositions described herein, when used to form foams, in some aspects produced foams having surprisingly high energy return/resiliency values. These compositions also, when used to form foams, in some aspects produce foams having high split-tear values. The compositions can, in some aspects, be used to produce foams having other beneficial properties, including additional properties beneficial for use in footwear including as cushioning components. The compositions of the present disclosure can be foamed and/or molded using various methods. In one example, the polymeric compositions can be foamed as part of an injection molding process. Optionally, the injection molded foam can subsequently be compression molded. Compression molding of the injection molded foam can modify the properties of the polymeric foam, such as reducing the compression set of the foam, which can be beneficial for foams used in footwear-related applications. Foams formed from the polymeric compositions of the present disclosure can be used in footwear-related applications without being compression molded.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including a block copolymer including (1) a first block and a third block, each independently including a linear or branched chain aliphatic polymer having a plurality of aromatic groups attached pendantly thereto, (2) a second block located between the first block and the third block and including an aliphatic polymer having a plurality of aliphatic side chains attached thereto, and (3) a plurality of first ethylenically unsaturated groups present on one or more of the first block, second block, and third block. The block copolymer can include about 50% to 95%, about 60% to 90%, or about 60% to 85% of the second blocks by weight based upon the weight of the block copolymer. The compositions can also include an olefinic copolymer having a plurality of first olefinic segments and a plurality of second olefinic segments having a different chemical structure from the first olefinic segments; and one or more linking polymers, each linking polymer having one or more third olefinic segments. The compositions can include an ethylene vinyl acetate (EVA) copolymer.

The block copolymer can include (1) a first block and a third block, each independently including a linear or branched chain aliphatic polymer having a plurality of aromatic groups attached pendantly thereto, (2) a second block located between the first block and the third block and including an aliphatic polymer having a plurality of aliphatic side chains attached thereto, and (3) a plurality of first ethylenically unsaturated groups present on one or more of the first block, second block, and third block. The aromatic groups can be styrenic groups. The aliphatic groups can include one or more substituted or unsubstituted alkyl side chains having 2 to 20, 2 to 18, 2 to 15, 2 to 12, 5 to 12, 5 to 15, 5 to 18, or 5 to 20 carbon atoms.

The olefinic copolymer can have a plurality of first olefinic segments and a plurality of second olefinic segments having a different chemical structure from the first olefinic segments. For example, the olefinic block copolymer can be a copolymer of ethylene and the second alpha-olefin. In some aspects, the second alpha-olefin has 4 to 20, 4 to 18, 4 to 15, 4 to 12, 6 to 12, 6 to 15, 6 to 18, or 6 to 20 carbon atoms. The olefinic block copolymer can have one or more blocks rich in the first alpha-olefin and one or more blocks rich in the second alpha-olefin.

The linking polymers can each, independently, have one or more third olefinic segments. In some aspects, the compositions include a first alpha-olefin linking polymer and a second alpha-olefin linking polymer different from the first alpha-olefin linking polymer. For example, the first alpha-olefin linking polymer and the second alpha-olefin linking polymer can both be copolymers of ethylene and 1-butene, each having a different ratio of ethylene to 1-butene monomer content in the copolymer.

The ethylene vinyl acetate (EVA) copolymer can have a vinyl acetate content of about 5% to 50%, about 5% to 45%, about 5% to 40%, about 10% to 50%, about 10% to 45%, about 10% to 40%, about 15% to 40%, about 15% to 45%, about 15% to 50%, about 20% to 50%, or about 30% to 50% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including a block copolymer having a first block and a third block, each independently comprising a linear or branched chain aliphatic polymer having a plurality of aromatic groups attached pendantly thereto, a second block located between the first block and the third block and comprising an aliphatic polymer having a plurality of aliphatic side chains attached thereto, and a plurality of first ethylenically unsaturated group present on one or more of the first block, second block, and third block; wherein the block copolymer contains about 40% to 95%, about 40% to 90%, about 50% to 90%, about 60% to 90%, or about 65% to 85% of the second blocks by weight based upon the weight of the block copolymer; an olefinic copolymer comprising a plurality of first olefinic segments and a plurality of second olefinic segments having a different chemical structure from the first olefinic segments; one or more linking polymers, each linking polymer comprising one or more third olefinic segments; and an ethylene vinyl-acetate copolymer.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including an A-B-A block copolymer, wherein each of the A blocks comprise styrenic repeat units, the B block is a random copolymer of ethylene and an alpha-olefin having 2 to 12, 2 to 10, 2 to 8, 3 to 8, 3 to 10, 3 to 12, 6 to 12, or 6 to 8 carbon atoms, and wherein the A-B-A-block copolymer comprises about 5% to 50%, about 10% to 50%, about 10% to 40%, or about 15% to 35% of the A blocks by weight based upon the weight of the A-B-A block copolymer; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of ethylene and an alpha-olefin having 2 to 12, 2 to 10, 2 to 8, 3 to 8, 3 to 10, 3 to 12, 6 to 12, or 6 to 8 carbon atoms, and wherein the olefinic block copolymer has one or more blocks rich in the ethylene and one or more blocks rich in the alpha-olefin; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer is a copolymer of ethylene and an alpha-olefin having about 2 to 12, 2 to 10, 2 to 8, 3 to 8, 3 to 10, 3 to 12, 6 to 12, or 6 to 8 carbon atoms, and wherein the alpha-olefin linking polymer has an alpha-olefin monomer content of about 15% to about 40% by weight based upon the weight of the alpha-olefin linking polymer; and an ethylene-vinyl acetate copolymer having a vinyl acetate content of about 5% to 50%, about 5% to 45%, about 5% to 40%, about 10% to 50%, about 10% to 45%, about 10% to 40%, about 15% to 40%, about 15% to 45%, about 15% to 50%, about 20% to 50%, or about 30% to 50% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

In some aspects, each of the A blocks consists essentially of polystyrene. In some aspects, the B block consists essentially of a copolymer of ethylene and octene. In some aspects, the B block consists essentially of a copolymer of ethylene and butadiene.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including a partially hydrogenated thermoplastic elastomeric block copolymer, the partially hydrogenated thermoplastic elastomeric block copolymer comprising one or more A blocks comprising aromatic repeat units, one or more B blocks comprising aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer comprising one or more second ethylenically unsaturated groups; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer comprises one or more aliphatic sidechains; and an ethylene-vinyl acetate copolymer.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including a partially hydrogenated thermoplastic elastomeric block copolymer, the partially hydrogenated thermoplastic elastomeric block copolymer including one or more A blocks comprising aromatic repeat units, one or more B blocks comprising aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer comprising one or more second ethylenically unsaturated groups; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer comprises one or more aliphatic sidechains; and an ethylene-vinyl acetate copolymer.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including one or more partially hydrogenated thermoplastic elastomeric block copolymers, each of the one or more partially hydrogenated thermoplastic elastomeric block copolymers independently comprising one or more aromatic blocks, one or more aliphatic blocks, and one or more first ethylenically unsaturated units; one or more olefinic block copolymers, each of the one or more olefinic block copolymers comprising second ethylenically unsaturated units; one or more alpha-olefin linking copolymers; and one or more ethylene-vinyl acetate copolymers. The partially hydrogenated thermoplastic elastomeric block copolymer can have an A-B block structure or an A-B-A block structure, wherein each of the A blocks comprise one or more aromatic repeat units, and wherein the B block is an aliphatic polymer block comprising the one or more first ethylenically unsaturated units. The partially hydrogenated thermoplastic elastomeric block copolymer can include about 5% to 50%, about 5% to 40%, about 10% to 50%, about 10% to 40%, about 15% to 40%, or about 15% to 35% of the A block by weight based upon the weight of the partially hydrogenated thermoplastic elastomeric block copolymer.

The composition can include about 5 parts by weight to about 30 parts by weight, about 5 parts by weight to about 20 parts by weight, about 5 parts by weight to about 15 parts by weight, about 10 parts by weight to about 20 parts by weight, about 10 parts by weight to about 30 parts by weight, or about 15 parts by weight to about 25 parts by weight of the A-B-A block copolymer or partially hydrogenated thermoplastic elastomeric block copolymer based upon the total weight of the composition.

The composition can include about 5 parts by weight to about 15 parts by weight, about 5 parts by weight to about 10 parts by weight, about 10 parts by weight to about 15 parts by weight, or about 5 parts by weight to about 20 parts by weight of the A-B-A block copolymer or partially hydrogenated thermoplastic elastomeric block copolymer based upon the total weight of the composition.

The composition can include about 5 parts by weight to about 20 parts by weight, about 5 parts by weight to about 15 parts by weight, about 10 parts by weight to about 20 parts by weight, about 10 parts by weight to about 15 parts by weight, about 5 parts by weight to about 10 parts by weight, about 15 parts by weight to about 20 parts by weight, about 5 parts by weight to about 30 parts by weight, about 5 parts by weight to about 20 parts by weight, about 5 parts by weight to about 15 parts by weight, about 10 parts by weight to about 20 parts by weight, about 10 parts by weight to about 30 parts by weight, or about 15 parts by weight to about 25 parts by weight of the olefinic block copolymer by weight based upon the total weight of the composition.

The composition can include about 10 parts by weight to about 50 parts by weight, about 15 parts by weight to about 50 parts by weight, about 10 parts by weight to about 35 parts by weight, about 10 parts by weight to about 20 parts by weight, about 20 parts by weight to about 30 parts by weight, about 30 parts by weight to about 40 parts by weight, about 40 parts by weight to about 50 parts by weight, about 20 parts by weight to about 35 parts by weight, or about 20 parts by weight to about 30 parts by weight of the alpha-olefin linking polymer based upon the total weight of the composition.

The composition can include about 10 parts by weight to about 50 parts by weight, about 10 parts by weight to about 45 parts by weight, about 20 parts by weight to about 45 parts by weight, about 20 parts by weight to about 50 parts by weight, about 20 parts by weight to about 30 parts by weight, about 30 parts by weight to about 40 parts by weight, or about 40 parts by weight to about 50 parts by weight of the ethylene-vinyl acetate copolymer based upon the total weight of the composition.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including an A-B-A block copolymer, wherein each of the A blocks have styrenic repeat units, the B block is a random copolymer of ethylene and a first alpha-olefin having 3 to 8 carbon atoms (e.g. 3, 4, 5, 6, 7, or 8 carbon atoms), and wherein the A-B-A-block copolymer includes about 10% to 50%, about 10% to 40%, about 15% to 40%, or about 15% to 30% of the A blocks by weight based upon an entire weight of the A-B-A block copolymer; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of ethylene and a second alpha-olefin having about 4 to 14, about 6 to 12, or about 6 to 10 carbon atoms, and wherein the olefinic block copolymer has one or more blocks rich in the ethylene and one or more blocks rich in the second alpha-olefin; and an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer is a copolymer of ethylene and a third alpha-olefin having about 2 to 24, about 3 to 24, about 3 to 18, or about 6 to 18 carbon atoms, and wherein the alpha-olefin linking polymer has an alpha-olefin monomer content of about 10% to 50%, about 10% to 40%, about 15% to 40%, or about 15% to 30% by weight based upon an entire weight of the alpha-olefin linking polymer.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including an A-B-A block copolymer, wherein each of the A blocks include repeat units according to the following formula

embedded image

where each occurrence of R¹is independently a hydrogen, halogen, hydroxyl, or a substituted or unsubstituted alkyl group having from 1 to 18, 1 to 15, 1 to 12, 3 to 18, 3 to 15, or 3 to 12 carbon atoms; where each occurrence of R²is independently none or a substituted or unsubstituted alkyl group having from 1 to 15, 1 to 12, 1 to 8, 3 to 8, 3 to 12, or 3 to 15 carbon atoms; wherein the B block is a random copolymer of ethylene and a first alpha-olefin having about 3 to 12, 3 to 10, or 3 to 8 carbon atoms; and wherein the A-B-A-block copolymer includes about 10% to 50%, about 10% to 40%, about 15% to 40%, or about 15% to 30% of the A blocks by weight based upon an entire weight of the A-B-A block copolymer; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of ethylene and a second alpha-olefin having about 4 to 14, about 6 to 12, or about 6 to 10 carbon atoms, and wherein the olefinic block copolymer has one or more blocks rich in the ethylene and one or more blocks rich in the second alpha-olefin; and an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer is a copolymer of ethylene and a third alpha-olefin having bout 2 to 24, about 3 to 24, about 3 to 18, or about 6 to 18 carbon atoms.

embedded image

where each occurrence of R¹is independently a hydrogen, halogen, hydroxyl, or a substituted or unsubstituted alkyl group having from 1 to 18, 1 to 15, 1 to 12, 3 to 18, 3 to 15, 3 to 12, 1 to 8, 3 to 8, 1 to 5, or 3 to 5 carbon atoms; where each occurrence of R²is independently none or a substituted or unsubstituted alkyl group having from 1 to 15, 1 to 12, 1 to 8, 3 to 8, 3 to 12, 3 to 15, 1 to 8, 1 to 5, or 1 to 3 carbon atoms; wherein the B block is a random copolymer of ethylene and a first alpha-olefin having about 3 to 12, 3 to 10, or 3 to 8 carbon atoms; and wherein the A-B-A-block copolymer includes about 10% to 50%, about 10% to 40%, about 15% to 40%, or about 15% to 30% of the A blocks by weight based upon an entire weight of the A-B-A block copolymer; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of ethylene and a second alpha-olefin having about 4 to 14, about 6 to 12, or about 6 to 10 carbon atoms, and wherein the olefinic block copolymer has one or more blocks rich in the ethylene and one or more blocks rich in the second alpha-olefin; and an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer is a copolymer of ethylene and a third alpha-olefin having bout 2 to 24, about 3 to 24, about 3 to 18, or about 6 to 18 carbon atoms.

In some aspects, the alpha-olefin linking polymer has an alpha-olefin monomer content of about 10% to 50%, about 10% to 45%, about 15% to 45%, about 15% to 40%, or about 20% to 40% by weight based upon an entire weight of the alpha-olefin linking polymer.

In some aspects, each of the A blocks include a large amount of polystyrene. For example, each of the A blocks can include at least 80%, 90% or more styrene repeat units based upon the number of repeat units in the A block. In some aspects, each of the A blocks consists essentially of polystyrene.

In some aspects, each of the B blocks includes a random copolymer of ethylene and a first alpha-olefin having 4, 5, 6, 7, or 8 carbon atoms. In some aspects, the B block is essentially a random copolymer of ethylene and octene, or is random copolymer of ethylene and butadiene.

In some aspects there can be more than one alpha-olefin linking polymer present in the composition. For example, in some aspects, the composition incudes a first alpha-olefin linking polymer and a second alpha-olefin linking polymer, wherein the first alpha-olefin linking polymer and the second alpha-olefin linking polymer are copolymers of ethylene and 1-butene, each having a different ratio of ethylene to 1-butene monomer content in the copolymer.

In some aspects, the composition includes about 5 parts by weight to about 15 parts by weight of the A-B-A block copolymer, about 10 parts by weight to about 20 parts by weight of the olefinic block copolymer, and about 25 parts by weight to about 35 parts by weight of the alpha-olefin linking polymers based upon an entire weight of the composition.

In some aspects, the composition includes an ethylene-vinyl acetate copolymer having a vinyl acetate content of about 10% to about 45% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

In various aspects, the composition also includes comprising an ethylene-vinyl acetate copolymer having a vinyl acetate content of about 5% to 55%, about 5% to 50%, about 10% to 50%, about 10% to 45%, or about 15% to 40% by weight based upon the weight of the ethylene-vinyl acetate copolymer. The

The A-B-A block copolymer can be at least partially or fully hydrogenated. In some aspects, the A-B-A block copolymer has a degree of hydrogenation of about 40% to 99%, about 50% to 99%, about 50% to 95%, about 50% to 90%, about 50% to 80%, or about 60% to 80%.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including a partially hydrogenated thermoplastic elastomeric block copolymer, an olefinic block copolymer, and an alpha-olefin linking polymer. The partially hydrogenated thermoplastic elastomeric block copolymer can include one or more A blocks with aromatic repeat units, one or more B blocks with aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units. In some aspects, the aromatic repeat units are styrenic repeat units. The olefinic block copolymer can be a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer includes one or more second ethylenically unsaturated groups. The alpha-olefin linking polymer can include one or more aliphatic sidechains.

In some aspects, the partially hydrogenated thermoplastic elastomeric block copolymer can have an A-B block structure or an A-B-A block structure, wherein the A blocks and B blocks are as described herein. For example, each of the A blocks can independently include one or more aromatic repeat units such as styrene. Each of the B blocks can be an aliphatic polymer block comprising the one or more first ethylenically unsaturated units.

The aromatic repeat units can include any of a variety of aromatic units. The aromatic repeat units can include aliphatic backbones having a plurality of aromatic side chains.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including at least one polymer containing styrenic repeating units and non-styrenic repeating units; and at least one C₄-C₁₀₀unsaturated olefin. The styrenic repeat units can include blocks of polystyrene. The polymer containing styrenic repeating units and non-styrenic repeating units can be a block copolymer including blocks of polystyrene and non-styrenic polymeric blocks. In some examples, the polymer can include non-styrenic repeating units selected from the group polyester, poly-C₂-C₈-alkylene units, polyether units, polycarbonate units, polyamide units, polyketone units, polysiloxane units, and any combination thereof. The styrene repeating units and non-styrenic repeating units (e.g., polyester, poly-C₂-C₈-alkylene units, polyether units, polycarbonate units, polyamide units, polyketone units, polysiloxane units, and any combination thereof), can be in any order. Mixtures of two or more polymers including styrenic repeat units and non-styrenic repeat units are also contemplated herein.

As used herein, unless otherwise dictated by context, when two of the same type of components are said to be “different” this means that one has a different chemical composition from the other. For example, the second alpha-olefin being different from the first alpha-olefin means the second alpha-olefin has a chemical formula that is different from the chemical formula of the first alpha-olefin.

In some aspects the silane is added to a first pre-foam composition, the first pre-foam composition including a polymer including styrene repeating units and non-styrenic repeating units, wherein the polymer includes block units of polyester. In some examples, the polymer including styrenic repeating units and non-styrenic repeating units includes poly-C₂-C₈-alkylene units. In some examples, the polymer including styrenic repeating units and non-styrenic repeating units of the various examples described herein includes units of polyethylene. In some examples, the polymer including styrenic repeating units and non-styrenic repeating units of the various examples described herein includes units of polypropylene. In other examples, the polymer including styrenic repeating units and non-styrenic repeating units of the various examples described herein includes units of polybutylene. In still other examples, the polymer including styrene repeating units and non-styrenic repeating units of the various examples described herein includes units of polybutadiene. In yet other examples, the polymer including styrenic repeating units and non-styrenic repeating units of the various examples described herein includes units of polyisoprene. The non-styrenic repeating units of the polymer can include polyethylene, polypropylene, polybutylene, polybutadiene, polyisoprene, or any combination thereof, and can be present in the polymer in any order.

In some examples, when the polymer comprising styrene repeating units and non-styrenic repeating units described herein comprise polyethylene, the polyethylene content of the polymer comprising styrene repeating units and non-styrenic repeating units is from about 50 mol % to about 80 mol % (e.g., from about 50 mol % to about 75 mol %; about 60 mol % to about 80 mol %; about 55 mol % to about 70 mol %; about 65 mol % to about 80 mol %; or about 70 mol % to about 80 mol %).

In some examples the polymer comprising styrene repeating units and non-styrenic repeating units is a PS_q-X¹_n-X²_m-X³_pblock copolymer wherein: PS represents polystyrene; X¹is a poly-C₂-C₈-alkylene; X²is a poly-C₂-C₈-alkylene; X³is polyether, polyester, polycarbonate, polyamide, polyketone or polysiloxane; the subscripts q, n, m, and p represent mole fractions; 1>q>0, n is 0 to 1, m is 0 to 1, and p is 0 to 1, provided that q+n+m+p=1; and the order of the PS, X¹, X², and X³blocks can be random or in the order shown. In some examples, X¹is polyethylene, polypropylene, polybutylene, polybutadiene, or polyisoprene. In other examples, X²is polyethylene, polypropylene, polybutylene, polybutadiene, or polyisoprene.

Some examples of polymers comprising styrene repeating units and non-styrenic repeating units contemplated herein include styrene-butadiene-styrene block copolymers; styrene-polybutylene-styrene block copolymers; styrene-ethylene-butadiene-styrene block copolymers; styrene-ethylene-polybutylene-styrene block copolymers; styrene-isoprene-butadiene-styrene block copolymers; and combinations thereof.

Generally speaking, the block copolymers, such as the A-B-A block copolymer or the polymer comprising styrene repeating units and non-styrenic repeating units described herein, can be at least partially unsaturated (e.g., comprising ethylenic unsaturation). Thus, for example, at least one of the repeating units can comprise ethylenic unsaturation. As used herein, the term “partially unsaturated” (e.g., comprising ethylenic unsaturation) generally means that the polymer can have from about 20 mol % to about 60 mol % unsaturation (e.g., from about 20 mol % to about 50 mol %, about 20 mol % to about 30 mol %; about 25 mol % to about 45 mol %; about 30 mol % to about 50 mol %; about 20 mol % to about 40 mol %; or about 25 mol % to about 40 mol % unsaturation, such as ethylenic unsaturation). But it should be understood that, by virtue of the fact that polymers comprising styrene repeating units comprise phenyl rings, they will be “partially unsaturated.”

Generally speaking, partial unsaturation makes it possible to form covalent crosslinking between, for example, the polymer comprising styrene repeating units and non-styrenic repeating units (intermolecular and intramolecular); the C₄-C₁₀₀unsaturated olefin (intermolecular and intramolecular); and between the polymer comprising styrene repeating units and non-styrenic repeating units and the C₄-C₁₀₀unsaturated olefin.

Generally speaking, the block copolymers, such as the A-B-A block copolymer or the polymer comprising styrene repeating units and non-styrenic repeating units described herein, have a weight average molecular weight (Mw) from about 25,000 g/mol to about 1.5×10⁶g/mol (e.g., from about 250,000 g/mol to about 1.5×10⁶g/mol, about 25,000 g/mol to about 100,000 g/mol; about 50,000 g/mol to about 200,000 g/mol, 75,000 g/mol to about 150,000 g/mol; about 100,000 g/mol to about 300,000 g/mol; about 250,000 g/mol to about 750,000 g/mol; about 300,000 g/mol to about 800,000 g/mol; about 250,000 g/mol to about 650,000 g/mol; about 500,000 g/mol to about 1.5×10⁶g/mol; about 750,000 g/mol to about 1.5×10⁶g/mol; or about 650,000 g/mol to about 1.3×10⁶g/mol).

Some examples of polymers comprising styrene repeating units and non-styrenic repeating units include those available from Kraton Performance Polymers Inc., Houston, TX, such as KRATON® D styrene-butadiene-styrene (SBS) polymer comprising styrene repeating units and non-styrenic repeating units; KRATON® D styrene-isoprene-styrene/styrene-isoprene-butadiene-styrene polymer comprising styrene repeating units and non-styrenic repeating units (SIS)/(SIBS); KRATON® G styrene-ethylene-butadiene-styrene/styrene-ethylene-propylene-styrene (SEBS/SEPS) polymer comprising styrene repeating units and non-styrenic repeating units; and KRATON® FG maleic anhydride-grafted styrene-ethylene-butadiene-styrene (SEBS) polymer comprising styrene repeating units and non-styrenic repeating units. Some examples of polymer comprising styrene repeating units and non-styrenic repeating units also include SEPTON® hydrogenated polymer comprising styrene repeating units and non-styrenic repeating units (e.g., SEPTON® 4055; SEPTON® 8006; SEPTON® 4077; and SEPTON® 4099) available from Kuraray Co., Ltd., Tokyo, Japan. Other examples of polymer comprising styrene repeating units and non-styrenic repeating units include hydrogenated SEBS block copolymers available from Asahi Kasei Chemicals Corporation (e.g., the various grades of TUFTEC® hydrogenated SEBS block copolymers, including TUFTEC® P1083). While not being bound by any specific theory, it is believed that the level of hydrogenation of the polymer comprising styrene repeating units and non-styrenic repeating units, which in some examples influences (e.g., reduces) the level of ethylenic unsaturation of the polymer comprising styrene repeating units and non-styrenic repeating units, can influence the crystallinity and/or rigidity of the polymer comprising styrene repeating units and non-styrenic repeating units. Thus, for example, partially hydrogenated polymer comprising styrene repeating units and non-styrenic repeating units (e.g., those that are about 50 to about 80% hydrogenated) can be less crystalline and more rigid than their non-hydrogenated counterparts (e.g., those that are less than about 50% hydrogenated).

In one aspect, the pre-foam compositions of the various examples described herein can comprise any suitable amount of a polymer comprising styrene repeating units and non-styrenic repeating units. In some examples, the pre-foam compositions comprise from about 5 wt. % to about 50 wt. % (e.g., from about 5 wt. % to about 20 wt. %; about 15 wt. % to about 40 wt. %; about 10 wt. % to about 45 wt. %; about 25 wt. % to about 50 wt. %; or about 20 wt. % to about 45 wt. %) of the polymer comprising styrene repeating units and non-styrenic repeating units. In addition, or alternatively, the polymer comprising styrene repeating units and non-styrenic repeating units comprises a content of styrene repeating units from about 5 mol % to about 50 mol % (e.g., from about 5 mol % to about 20 mol %; about 15 mol % to about 40 mol %; about 10 mol % to about 45 mol %; about 25 mol % to about 50 mol %; or about 20 mol % to about 45 mol %). In addition, or alternatively, the polymer comprising styrene repeating units and non-styrenic repeating units comprises a content of non-styrenic repeating units from about 50 mol % to about 95 mol % (e.g., from about 50 mol % to about 80 mol %, about 60 mol % to about 90 mol %, about 70 mol % to about 95 mol % or about 75 mol % to about 95 mol %). In some instances, the sum of the content of styrene repeating units and the content of non-styrenic repeating units is 100 mol %.

In particular examples, the pre-foam compositions described herein comprise from about 5 parts per hundred of resin (phr) to about 45 phr of the polymer comprising styrene repeating units and non-styrenic repeating units component (i.e., the styrenic copolymer component). The pre-foam compositions can comprise from about 10 phr to about 40 phr of the styrenic copolymer component. The pre-foam compositions can comprise from about 12 phr to about 35 phr of the styrenic copolymer component. The pre-foam compositions can comprise from about 15 phr to about 35 phr of the styrenic copolymer component. The pre-foam compositions can comprise from about 10 phr to about 30 phr of the styrenic copolymer component. The pre-foam compositions can comprise from about 10 phr to about 25 phr of the styrenic copolymer component. The pre-foam compositions can comprise from about 10 phr to about 22 phr of the styrenic copolymer component.

As used herein, the styrenic copolymer component is understood to refer to all the polymers present in the pre-foam composition which individually have both styrene repeating units and non-styrenic repeating units. Thus, the concentration of the styrenic copolymer component in a pre-foam composition refers to the total concentration of each polymer comprising styrene repeating units and non-styrenic repeating units present in the composition. In some pre-foam compositions, the styrenic copolymer component can be formed of only a single polymer comprising styrene repeating units and non-styrenic repeating units. In other pre-foam compositions, the styrenic copolymer component can be by formed of a plurality of polymers each of which has both styrene repeating units and non-styrenic repeating units.

The pre-foam composition described herein also comprises at least one C₄-C₁₀₀unsaturated olefin. The C₄-C₁₀₀unsaturated olefin can be a C₈-C₅₀-unsaturated olefin. The C₄-C₁₀₀unsaturated olefin can be a C₁₂-C₃₀-unsaturated olefin. The C₄-C₁₀₀unsaturated olefin can be a C₁₆-C₁₀₀-unsaturated olefin. The C₄-C₁₀₀unsaturated olefin can be a C₅₀-C₁₀₀-unsaturated olefin. As used herein, the C_x-C_ynomenclature is understood to specify the carbon length of the unsaturated olefin, not the location of unsaturation. Mixtures of two or more C₄-C₁₀₀unsaturated olefins are also contemplated herein. In some examples, a C₄-C₁₀₀unsaturated olefin can be pre-polymer (e.g., a monomer); a linear oligomer; a polymer.

As used herein, the term “unsaturated olefin” is understood to encompass any C₄-C₁₀₀olefin comprising at least one terminal C—C double bond and a total of about 4 to about 100 (e.g., 8 to 50; 12 to 30; 4 to 20; 10 to 50; 30 to 90; 20 to 100; 50 to 75; or 20 to 80) total carbon atoms. Additional carbon-carbon double bonds can be present in the unsaturated olefin. Examples of C₄-C₁₀₀unsaturated olefins include propene, 1-butene, 4-methyl-1-pentene, 1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, and 1-octadecene. In other examples, C₄-C₁₀₀unsaturated olefins can be alkyl- or cycloalkyl-substituted unsaturated olefins. As used herein, the term “unsaturated olefin” is also understood to encompass any 04-0100 olefin comprising a plurality of polymerized units, wherein at least a portion of the polymerized units include at least one terminal C—C double bond and a total of about 4 to about 100 (e.g., 8 to 50; 12 to 30; 4 to 20; 10 to 50; 30 to 90; 20 to 100; 50 to 75; or 20 to 80) total carbon atoms. In other words, the unsaturated olefin can be an unsaturated olefin polymer or copolymer, including unsaturated olefin block copolymers. Additional carbon-carbon double bonds can be present in the unsaturated olefin polymer or copolymer. Examples of unsaturated olefinic copolymers include the TAFMER® unsaturated olefin copolymers available from Mitsui Chemicals America, Inc., Rye Brook, NY (e.g., TAFMER® DF110 and TAFMER® DF605 ethylene/unsaturated olefin copolymers); and ENGAGE® and INFUSE® olefin block copolymers, both available from The Dow Chemical Company, Midland, MI (e.g., INFUSE® 9107 olefin block copolymer).

In some examples, the pre-foam compositions of the various examples described herein can comprise one or more polymers comprising styrene repeating units and non-styrenic repeating units, one or more C₄-C₁₀₀unsaturated olefins, and one or more olefin block copolymers.

In some examples, C₄-C₁₀₀unsaturated olefins can comprise one or more heteroatoms (e.g., —O—, NR¹—, —S(O)_q— (wherein q is an integer from 0 to 2) and combinations thereof). An example of such heteroatom-interrupted C₄-C₁₀₀unsaturated olefins include allyl ether and allyl-terminated polyethylene glycol.

In particular examples, the pre-foam compositions described herein comprise from about 30 phr to about 90 phr of the C₄-C₁₀₀unsaturated olefin component (i.e., the unsaturated olefin component). The pre-foam compositions can comprise from about 35 phr to about 85 phr of the unsaturated olefin component. The pre-foam compositions can comprise from about 40 phr to about 80 phr of the unsaturated olefin component. The pre-foam compositions can comprise from about 45 phr to about 75 phr of the unsaturated olefin component. The pre-foam compositions can comprise from about 40 phr to about 85 phr of the unsaturated olefin component. The pre-foam compositions can comprise from about 45 phr to about 85 phr of the unsaturated olefin component. The pre-foam compositions can comprise from about 43 phr to about 82 phr of the unsaturated olefin component.

As used herein, the unsaturated olefin component is understood to refer to all the C₄-C₁₀₀unsaturated olefins present in the pre-foam composition. Thus, the concentration of the unsaturated olefin component in a pre-foam composition refers to the total concentration of each C₄-C₁₀₀unsaturated olefin present in the composition, including all C₄-C₁₀₀unsaturated olefin monomers, C₄-C₁₀₀unsaturated olefin oligomers, C₄-C₁₀₀unsaturated olefin polymers, and C₄-C₁₀₀unsaturated olefin copolymers. In some pre-foam compositions, the unsaturated olefin component can be formed of only a single C₄-C₁₀₀unsaturated olefin, such as, for example, a single C₄-C₁₀₀unsaturated olefin copolymer. In other pre-foam compositions, the unsaturated olefin component can be formed of a plurality of C₄-C₁₀₀unsaturated olefin, such as, for example, a plurality of C₄-C₁₀₀unsaturated olefin copolymers.

The compositions of the various examples described herein can also comprise at least one ethylene vinyl acetate copolymer, in addition to the polymer comprising styrene repeating units and non-styrenic repeating units; and the C₄-C₁₀₀unsaturated olefin. And, in some instances, the at least one ethylene vinyl acetate copolymer comprises two different ethylene vinyl acetate copolymers.

In some examples, the at least one ethylene vinyl acetate copolymer is a random copolymer. In other examples, the at least one ethylene vinyl acetate copolymer comprises an ethylene content. In still other examples, the at least one ethylene vinyl acetate copolymer is at least partially unsaturated (e.g., comprises ethylenic unsaturation). In some examples, the pre-foam composition comprises about 20 wt. % to about 60 wt. % (e.g., from about 25 wt. % to about 50 wt. %; about 30 wt. % to about 50 wt. %; about 40 wt. % to about 60 wt. %; about 30 wt. % to about 60 wt. %; or about 45 wt. % to about 60 wt. %) of the at least one ethylene vinyl acetate copolymer. A suitable ethylene vinyl acetate copolymer includes EVLAX® 40L-03 ethylene vinyl acetate resin available from E.I. DuPont de Nemours Co., Wilmington, DE. Other suitable ethylene vinyl acetate copolymers include EVATHENE® UE659 and EVATHENE® UE3300 ethylene vinyl acetate copolymers available from USI Corporation, Taiwan, ROC.

In some examples, the pre-foam compositions comprise about 1 to about 10 wt. % of a first ethylene vinyl acetate copolymer and about 5 to about 50 wt. % of a second ethylene vinyl acetate copolymer, wherein the wt. % amounts are relative to the weight of the pre-foam composition.

In one example, when the at least one ethylene vinyl acetate copolymer comprises two different ethylene vinyl acetate copolymers, the at least two different ethylene vinyl acetate copolymers can differ in at least vinyl acetate content. Thus, for example, a first ethylene vinyl acetate copolymer can comprise about 15 to about 40 mol % vinyl acetate (e.g., from about 15 to about 30 mol %; about 25 to about 35 mol %; or about 20 mol % to about 40 mol %) and a second ethylene vinyl acetate copolymer comprises about 15 to about 30 mol % (e.g., from about 15 to about 25 mol %; about 20 mol % to about 30 mol %; or about 15 mol % to about 30 mol %) vinyl acetate.

In particular examples, the pre-foam compositions described herein do not include an ethylene vinyl acetate copolymer (EVA). In other words, the pre-foam compositions described herein can be free of an EVA component.

Alternatively, the pre-foam compositions described herein can comprise from about 5 phr to about 50 phr of the EVA component. The pre-foam compositions can comprise from about 10 phr to about 45 phr of the EVA component. The pre-foam compositions can comprise from about 20 phr to about 45 phr of the EVAcomponent. The pre-foam compositions can comprise from about 25 phr to about 40 phr of the EVA component. The pre-foam compositions can comprise from about 25 phr to about 35 phr of the EVA component. The pre-foam compositions can comprise from about 30 phr to about 37 phr of the EVA component. As used herein, the EVA component is understood to refer to all the ethylene vinyl acetate copolymers present in the pre-foam composition. Thus, the concentration of the EVA component in a pre-foam composition refers to the total concentration of each ethylene vinyl acetate copolymer present in the composition. In some pre-foam compositions, the EVA component can be formed of only a single ethylene vinyl acetate copolymer. In other pre-foam compositions, the EVA component can be formed of a plurality of different ethylene vinyl acetate copolymers.

The compositions of the various examples described herein can also comprise a blowing agent, a free-radical initiator or combinations thereof.

The blowing agent can be any appropriate type of physical blowing agent known in the art including nitrogen, carbon dioxide, hydrocarbons (e.g., propane, pentane, isopentane, and cyclopentane), chlorofluorocarbons, noble gases (e.g., helium (He), neon (Ne), argon (Ar), krypton (Kr), and xenon (Xe)) and/or mixtures thereof. In one example, the blowing agent comprises nitrogen. The blowing agent may be supplied in any flowable physical state such as a gas, a liquid, or a supercritical fluid. According to one example, a blowing agent source provides a blowing agent (e.g., carbon dioxide, nitrogen, and methanol) that is in a supercritical fluid state upon contacting (e.g., injection into) the pre-foam compositions of the various examples described herein, e.g., when the pre-foam compositions are formed in an extruder (e.g., a twin-screw extruder).

Alternatively, the blowing agent can be any appropriate type of chemical blowing agent known in the art including carbonates (e.g., ammonium carbonate and carbonates of alkali metals), azo compounds, diazo compounds, and combinations thereof. Chemical blowing agents include 2,2′-azobis(2-cyanobutane), 2,2′-azobis(methylbutyronitrile), azodicarbonamide, p,p′-oxybis(benzene sulfonyl hydrazide), p-toluene sulfonyl semicarbazide, p-toluene sulfonyl hydrazide, and combinations thereof. In the case of chemical blowing agents, gaseous products (e.g., nitrogen gas) and other by-products are formed by a chemical reaction(s), promoted by the process or by a reacting polymer's exothermic heat. Since the blowing reaction occurs forming low molecular weight compounds acting as the blowing gas, additional exothermic heat may also be released.

In some examples, the compositions described herein may require a temperature (e.g., from heating) of from about 130° C. to about 210° C. (e.g., from about 150° C. to about 190° C. or 165° C. to about 195° C.—such as temperatures to which an extruder and/or a mold might be heated) to “trigger” the chemical blowing agent to “decompose” to produce the gas(es) necessary to transform the pre-foam compositions of the various examples described herein into the foam compositions of the various examples described herein.

Examples of blowing agents include UNICELL brand blowing agents, such as UNICELL-D600 MT, available from Dongjin Semichem Co., Ltd., Seoul, Korea.

In some examples, a combination of physical and chemical blowing agents can be used.

The pre-foam compositions of the various examples described herein can also comprise metal oxides, organic acids, fillers, nucleating agents, and combinations thereof. Examples of metal oxides include zinc oxide, titanium dioxide, and combinations thereof. Examples of organic acids include C₃-C₃₀-alkanoic acids (e.g., C₁₄-C₃₀-alkanoic acids such as fatty acids) such as stearic acid and combinations of two or more C₃-C₃₀-alkanoic acids. Calcium carbonate is an example of a material which can be used both as a filler and as a nucleating agent.

The pre-foam compositions of the various examples described herein can also comprise one or more crosslinking agents. Examples of crosslinking agents include aliphatic unsaturated amides, such as methylenebisacryl- or -methacrylamide or ethylenebisacrylamide; aliphatic esters of polyols or alkoxylated polyols with ethylenically unsaturated acids, such as di(meth)acrylates or tri(meth)acrylates of butanediol or ethylene glycol, polyglycols or trimethylolpropane; di- and triacrylate esters of trimethylolpropane; acrylate and methacrylate esters of glycerol and pentaerythritol; allyl compounds, such as allyl (meth)acrylate, alkoxylated allyl (meth)acrylate, triallyl cyanurate, triallyl isocyanurate, maleic acid diallyl ester, poly-allyl esters, vinyl trimethoxysilane, vinyl triethoxysilane, polysiloxane comprising at least two vinyl groups, tetraallyloxyethane, tetraallyloxyethane, triallylamine, and tetraallylethylenediamine. Mixtures of the crosslinking agents can also be employed.

The pre-foam compositions of the various examples described herein can also comprise one or more free-radical initiators, such as an organic peroxide, a diazo compound (e.g., those described in U.S. Pat. No. 6,303,723, which is incorporated by reference as if fully set forth herein) or combinations of two or more free-radical initiators. Examples of organic peroxides that can be used as free-radical initiators include dicumyl peroxide; n-butyl-4,4-di(t-butylperoxy) valerate; 1,1-di(t-butylperoxy)3,3,5-trimethylcyclohexane; 2,5-dimethyl-2,5-di(t-butylperoxy) hexane; di-t-butyl peroxide; di-t-amyl peroxide; t-butyl peroxide; t-butyl cumyl peroxide; 2,5-dimethyl-2,5-di(t-butylperoxy)hexyne-3; di(2-t-butyl-peroxyisopropyl)benzene; dilauroyl peroxide; dibenzoyl peroxide; t-butyl hydroperoxide; and combinations thereof.

The pre-foam compositions of the various examples described herein can be solids or liquids at a temperature of about 25° C.

The pre-foam compositions of the various examples described herein can be crosslinked to form crosslinked pre-foam compositions. The pre-foam compositions can be crosslinked using various methods, including chemical crosslinking methods or crosslinking methods using actinic radiation (e.g., thermal radiation, UV light, electron beam and gamma radiation). Such compositions comprise, in some examples, a polymer comprising styrene repeating units and non-styrenic repeating units, the polymer crosslinked with a C₄-C₁₀₀unsaturated-olefin block copolymer comprising blocks of C₄-C₁₀₀unsaturated-olefin olefin. The crosslinking between the polymer comprising styrene repeating units and non-styrenic repeating units and the C₄-C₁₀₀unsaturated olefin block copolymer can occur directly between the molecules of the polymer comprising styrene repeating units and non-styrenic repeating units and the C₄-C₁₀₀unsaturated olefin block copolymer, for example, without an “external” crosslinking agent such as the one or more crosslinking agents described herein. The crosslinking between the polymer comprising styrene repeating units and non-styrenic repeating units and the C₄-C₁₀₀unsaturated olefin block copolymer can also occur with an “external” crosslinking agent, such as the one or more crosslinking agents described herein.

Those of ordinary skill in the art will also recognize that there can be intramolecular crosslinking occurring between portions of a polymer comprising styrene repeating units and non-styrenic repeating units molecule or portions of a C₄-C₁₀₀unsaturated olefin block copolymer. This crosslinking can occur in the presence or in the absence of an “external” crosslinking agent such as the one or more crosslinking agents described herein.

In some examples, the pre-foam compositions of the various examples described herein can be crosslinked to form crosslinked pre-foam compositions in the presence of a blowing agent (e.g., a chemical blowing agent or a physical blowing agent, as described herein).

In some examples, the crosslinked pre-foam compositions of the various examples described herein can be solids or liquids, but generally are solids (e.g., thermoplastic solids) at a temperature of about 25° C. or higher (e.g., at a temperature of from about 25° C. to about 220° C. and a pressure of from about 500 kPa to about 100 MPa). In some examples, the foam compositions of the various examples described herein are generally are solids (e.g., thermoplastic solids) at a temperature of about 25° C. or higher (e.g., at a temperature of from about 25° C. to about 220° C. and a pressure of from about 500 kPa to about 100 MPa).

In some examples, the crosslinked pre-foam compositions of the various examples described herein can further comprise at least one ethylene vinyl acetate copolymer and/or at least one olefin block copolymer, as each of the terms is defined herein.

Foam compositions are also contemplated herein and are interchangeably called “foam preforms.” As used herein, the term “foam compositions” refers to:

- a crosslinked pre-foam composition that is foamed (e.g., foamed using a blowing agent (physical and/or chemical)) before crosslinking, after crosslinking or substantially simultaneously with crosslinking; or
- combinations of a pre-foam composition and a crosslinked pre-foam composition (e.g., a combination of a pre-foam composition and a crosslinked pre-foam composition, wherein the combination is foamed (e.g., foamed using a blowing agent (physical and/or chemical)) after the combination is formed either after mixing two such compositions or after partially crosslinking the pre-foam composition, such that some crosslinked pre-foam composition is formed in situ).

In some examples, the foam compositions of the various examples described herein can further comprise at least one ethylene vinyl acetate copolymer and/or at least one olefin block copolymer, as each of the terms is defined herein.

Some foam compositions of the various examples described herein (e.g., foam compositions comprising a polymer comprising styrene repeating units and non-styrenic repeating units, crosslinked with a C₄-C₁₀₀unsaturated olefin) can form solid (e.g., thermoplastic) foam materials. These thermoplastic foam materials can be used as “foam preforms” and the foam preforms can subsequently be compression molded. The foam compositions of the present disclosure can have a density of about 0.08 g/cm³to about 0.15 g/cm³(e.g., from about 0.10 g/cm³to about 0.12 g/cm³). In some examples, such foam preforms have an energy return from about 60% to about 85% (e.g., from about 65% to about 80%; about 65% to about 75%; about 70% to about 80%; or about 75% to about 80%).

Some foam compositions of the various examples described herein (e.g., foam preforms) can be compression molded to form compression molded foam. Such compression molded foam can have a density of from about 0.15 g/cm³to about 0.30 g/cm³(e.g., from about 0.15 g/cm³to about 0.2 g/cm³).

Definitions

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly defined herein.

All publications, patents, and patent applications cited in this specification are cited to disclose and describe the methods and/or materials in connection with which the publications are cited. All such publications, patents, and patent applications are herein incorporated by references as if each individual publication or patent were specifically and individually indicated to be incorporated by reference. Such incorporation by reference is expressly limited to the methods and/or materials described in the cited publications, patents, and patent applications and does not extend to any lexicographical definitions from the cited publications, patents, and patent applications. Any lexicographical definition in the publications, patents, and patent applications cited that is not also expressly repeated in the instant specification should not be treated as such and should not be read as defining any terms appearing in the accompanying claims.

Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present disclosure, the preferred methods and materials are now described. Functions or constructions well-known in the art may not be described in detail for brevity and/or clarity. Aspects of the present disclosure will employ, unless otherwise indicated, techniques of nanotechnology, organic chemistry, material science and engineering and the like, which are within the skill of the art. Such techniques are explained fully in the literature.

It should be noted that ratios, concentrations, amounts, and other numerical data can be expressed herein in a range format. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the disclosure, e.g. the phrase “x to y” includes the range from ‘x’ to ‘y’ as well as the range greater than ‘x’ and less than ‘y’. The range can also be expressed as an upper limit, e.g. ‘about x, y, z, or less’ and should be interpreted to include the specific ranges of ‘about x’, ‘about y’, and ‘about z’ as well as the ranges of ‘less than x’, less than y′, and ‘less than z’. Likewise, the phrase ‘about x, y, z, or greater’ should be interpreted to include the specific ranges of ‘about x’, ‘about y’, and ‘about z’ as well as the ranges of ‘greater than x’, greater than y′, and ‘greater than z’. In addition, the phrase “about ‘x’ to ‘y’”, where ‘x’ and ‘y’ are numerical values, includes “about ‘x’ to about ‘y’”. It is to be understood that such a range format is used for convenience and brevity, and thus, should be interpreted in a flexible manner to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. To illustrate, a numerical range of “about 0.1% to 5%” should be interpreted to include not only the explicitly recited values of about 0.1% to about 5%, but also include individual values (e.g., 1%, 2%, 3%, and 4%) and the sub-ranges (e.g., 0.5%, 1.1%, 2.4%, 3.2%, and 4.4%) within the indicated range.

The term “about,” as used herein, can include traditional rounding according to significant figures of the numerical value. In some aspects, the term about is used herein to mean a deviation of 10%, 5%, 2.5%, 1%, 0.5%, 0.1%, 0.01%, or less from the specified value.

The articles “a” and “an,” as used herein, mean one or more when applied to any feature in aspects of the present disclosure described in the specification and claims. The use of “a” and “an” does not limit the meaning to a single feature unless such a limit is specifically stated. The article “the” preceding singular or plural nouns or noun phrases denotes a particular specified feature or particular specified features and may have a singular or plural connotation depending upon the context in which it is used.

As used herein, the term “units” can be used to refer to individual (co)monomer units such that, for example, styrenic repeat units refers to individual styrene (co)monomer units in the polymer. In addition, the term “units” can be used to refer to polymeric block units such that, for example, “styrene repeating units” can also refer to polystyrene blocks; “units of polyethylene” refers to block units of propylethylene; “units of polypropylene” refers to block units of polypropylene; “units of polybutylene” refers to block units of polybutylene, and so on. Such use will be clear from the context.

The present disclosure will be better understood upon reading the following numbered aspects, which should not be confused with the claims. In some instances, each of the numbered aspects below can be combined with one or more additional aspects described elsewhere in the disclosure.

Aspect 1. A composition comprising a first pre-foam composition and a first effective amount of a silane; wherein the first pre-foam composition is capable of being foamed without the silane to form a first foam composition having a first energy return, a first hardness, and a first abrasion loss; wherein, when the composition is foamed, the first effective amount of the silane is effective to form a second foam composition having a second energy return, a second hardness, and a second abrasion loss; wherein the second energy return and the second hardness are such that one or both of (i) the second energy return is within about 20% of the first energy return and (ii) the second hardness is within about 20% of the first hardness; and wherein the second abrasion loss is at least 20% less than the first abrasion loss.

Aspect 2. The composition according to any one of Aspects 1-93, wherein the first effective amount of the silane is about 0.2 parts per hundred resin to about 0.75 parts per hundred resin.

Aspect 3. The composition according to any one of Aspects 1-93, wherein the first effective amount of the silane is effective such that the second energy return is within about 10% or within about 5% of the first energy return.

Aspect 4. The composition according to any one of Aspects 1-93, wherein the first effective amount of the silane is effective such that the second hardness is within about 10% or within about 5% of the first hardness.

Aspect 5. The composition according to any one of Aspects 1-93, wherein the first effective amount of the silane is effective such that the second abrasion loss is at least 30%, at least 40%, at least 50%, or at least 60% less than the first abrasion loss.

Aspect 6. The composition according to any one of Aspects 1-93, wherein the second energy return is about 65%, about 70%, about 75% or more, e.g. about 65% to about 95%, about 70% to about 95%, or about 75% to about 95%.

Aspect 7. The composition according to any one of Aspects 1-93, wherein the second hardness is about 30 Asker C to about 40 Asker C or about 32 Asker C to about 36 Asker C when the second foam composition is an injection molded foam composition.

Aspect 8. The composition according to any one of Aspects 1-93, wherein the second hardness is about 30 Asker C to about 40 Asker C, about 35 Asker C to about 45 Asker C, or about 35 Asker C to about 40 Asker C when the second foam composition is a compression molded foam composition.

Aspect 9. The composition according to any one of Aspects 1-93, wherein the silane comprises an organofunctionalized silane; and optionally wherein the organofunctionalized silane is functionalized with one or both of a hydrolyzable functional group and an ethylenically unsaturated linkage.

Aspect 10. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a composition according to any one of Aspects 17-93.

Aspect 11. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises: a block copolymer comprising a first block and a third block, each independently comprising a linear or branched chain aliphatic polymer having a plurality of aromatic groups attached pendantly thereto, a second block located between the first block and the third block and comprising an aliphatic polymer having a plurality of aliphatic side chains attached thereto, and a plurality of first ethylenically unsaturated group present on one or more of the first block, second block, and third block; wherein the block copolymer comprises about 60% to about 90% of the second blocks by weight based upon the weight of the block copolymer; an olefinic copolymer comprising a plurality of first olefinic segments and a plurality of second olefinic segments having a different chemical structure from the first olefinic segments.

Aspect 12. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises one or more linking polymers, each linking polymer comprising one or more third olefinic segments.

Aspect 13. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises an ethylene-vinyl acetate (EVA) copolymer.

Aspect 14. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises: an A-B-A block copolymer, wherein each of the A blocks comprise styrenic repeat units, the B block is a random copolymer of ethylene and an alpha-olefin having about 3 to 8 carbon atoms, and wherein the A-B-A-block copolymer comprises about 10% to about 40% of the A blocks by weight based upon the weight of the A-B-A block copolymer; and an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of ethylene and an alpha-olefin having about 6 to 12 carbon atoms, and wherein the olefinic block copolymer has one or more blocks rich in the ethylene and one or more blocks rich in the alpha-olefin.

Aspect 15. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer is a copolymer of ethylene and an alpha-olefin having about 3 to 8 carbon atoms, and wherein the alpha-olefin linking polymer has an alpha-olefin monomer content of about 15% to about 40% by weight based upon the weight of the alpha-olefin linking polymer.

Aspect 16. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises an ethylene-vinyl acetate copolymer having a vinyl acetate content of about 10% to about 40% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

Aspect 17. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a block copolymer comprising a first block and a third block, each independently comprising a linear or branched chain aliphatic polymer having a plurality of aromatic groups attached pendantly thereto, a second block located between the first block and the third block and comprising an aliphatic polymer having a plurality of aliphatic side chains attached thereto, and a plurality of first ethylenically unsaturated group present on one or more of the first block, second block, and third block; wherein the block copolymer comprises about 60% to about 90% of the second blocks by weight based upon the weight of the block copolymer; an olefinic copolymer comprising a plurality of first olefinic segments and a plurality of second olefinic segments having a different chemical structure from the first olefinic segments; one or more linking polymers, each linking polymer comprising one or more third olefinic segments; and an ethylene-vinyl acetate (EVA) copolymer.

Aspect 18. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises an A-B-A block copolymer, wherein each of the A blocks comprise styrenic repeat units, the B block is a random copolymer of ethylene and an alpha-olefin having about 3 to 8 carbon atoms, and wherein the A-B-A-block copolymer comprises about 10% to about 40% of the A blocks by weight based upon the weight of the A-B-A block copolymer; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of ethylene and an alpha-olefin having about 6 to 12 carbon atoms, and wherein the olefinic block copolymer has one or more blocks rich in the ethylene and one or more blocks rich in the alpha-olefin; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer is a copolymer of ethylene and an alpha-olefin having about 3 to 8 carbon atoms, and wherein the alpha-olefin linking polymer has an alpha-olefin monomer content of about 15% to about 40% by weight based upon the weight of the alpha-olefin linking polymer; and an ethylene-vinyl acetate copolymer having a vinyl acetate content of about 10% to about 40% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

Aspect 19. The composition according to any one of Aspects 1-93, wherein each of the A blocks consists essentially of polystyrene.

Aspect 20. The composition according to any one of Aspects 1-93, wherein the B block consists essentially of a copolymer of ethylene and octene.

Aspect 21. The composition according to any one of Aspects 1-93, wherein the B block consists essentially of a copolymer of ethylene and butadiene.

Aspect 22. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a first alpha-olefin linking polymer and a second alpha-olefin linking polymer, wherein the first alpha-olefin linking polymer and the second alpha-olefin linking polymer are copolymers of ethylene and 1-butene, each having a different ratio of ethylene to 1-butene monomer content in the copolymer.

Aspect 23. The composition according to any one of Aspects 1-93, wherein the composition comprises about 5 parts by weight to about 15 parts by weight of the A-B-A block copolymer, about 10 parts by weight to about 20 parts by weight of the olefinic block copolymer, about 25 parts by weight to about 35 parts by weight of the alpha-olefin linking polymers, and about 30 parts by weight to about 60 parts by weight of the ethylene-vinyl acetate copolymer based upon the weight of the pre-foam composition.

Aspect 24. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a partially hydrogenated thermoplastic elastomeric block copolymer, the partially hydrogenated thermoplastic elastomeric block copolymer comprising: one or more A blocks comprising aromatic repeat units, one or more B blocks comprising aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer comprising one or more second ethylenically unsaturated groups; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer comprises one or more aliphatic sidechains; and an ethylene-vinyl acetate copolymer.

Aspect 25. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a partially hydrogenated thermoplastic elastomeric block copolymer, the partially hydrogenated thermoplastic elastomeric block copolymer comprising: one or more A blocks comprising aromatic repeat units, one or more B blocks comprising aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer comprising one or more second ethylenically unsaturated groups; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer comprises one or more aliphatic sidechains; and an ethylene-vinyl acetate copolymer.

Aspect 26. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises one or more partially hydrogenated thermoplastic elastomeric block copolymers, each of the one or more partially hydrogenated thermoplastic elastomeric block copolymers independently comprising one or more aromatic blocks, one or more aliphatic blocks, and one or more first ethylenically unsaturated units; one or more olefinic block copolymers, each of the one or more olefinic block copolymers comprising second ethylenically unsaturated units; one or more alpha-olefin linking copolymers; and one or more ethylene-vinyl acetate copolymers.

Aspect 27. The composition according to any one of Aspects 1-93, wherein the partially hydrogenated thermoplastic elastomeric block copolymer comprises an A-B block structure or an A-B-A block structure, wherein each of the A blocks comprise one or more aromatic repeat units, and wherein the B block is an aliphatic polymer block comprising the one or more first ethylenically unsaturated units.

Aspect 28. The composition according to any one of Aspects 1-93, wherein the partially hydrogenated thermoplastic elastomeric block copolymer comprises about 10% to about 40% of the A block by weight based upon the weight of the partially hydrogenated thermoplastic elastomeric block copolymer.

Aspect 29. The composition according to any one of Aspects 1-93, wherein the aromatic repeat units comprises styrenic repeat units.

Aspect 30. The composition according to any one of Aspects 1-93, wherein the aromatic repeat units comprise an aliphatic backbone having a plurality of aromatic side chains.

Aspect 31. The composition according to any one of Aspects 1-93, wherein the aliphatic repeat units comprise one or more substituted or unsubstituted alkyl side chains having about 2 to 18 carbon atoms.

Aspect 32. The composition according to any one of Aspects 1-93, wherein the olefinic block copolymer is a copolymer of ethylene and the second alpha-olefin.

Aspect 33. The composition according to any one of Aspects 1-93, wherein the second alpha-olefin has 6 to 12 carbon atoms.

Aspect 34. The composition according to any one of Aspects 1-93, wherein the olefinic block copolymer has one or more blocks rich in the first alpha-olefin and one or more blocks rich in the second alpha-olefin

Aspect 35. The composition according to any one of Aspects 1-93, wherein the composition comprises about 5 parts by weight to about 20 parts by weight of the A-B-A block copolymer or partially hydrogenated thermoplastic elastomeric block copolymer based upon the total weight of the composition.

Aspect 36. The composition according to any one of Aspects 1-93, wherein the composition comprises about 5 parts by weight to about 10 parts by weight of the A-B-A block copolymer or partially hydrogenated thermoplastic elastomeric block copolymer based upon the total weight of the composition.

Aspect 37. The composition according to any one of Aspects 1-93, wherein the composition comprises about 5 parts by weight to about 20 parts by weight of the olefinic block copolymer by weight based upon the total weight of the composition.

Aspect 38. The composition according to any one of Aspects 1-93, wherein the composition comprises about 10 parts by weight to about 15 parts by weight of the olefinic block copolymer by weight based upon the total weight of the composition.

Aspect 39. The composition according to any one of Aspects 1-93, wherein the composition comprises about 15 parts by weight to about 35 parts by weight of the alpha-olefin linking polymer based upon the total weight of the composition.

Aspect 40. The composition according to any one of Aspects 1-93, wherein the composition comprises about 20 parts by weight to about 30 parts by weight of the alpha-olefin linking polymer based upon the total weight of the composition.

Aspect 41. The composition according to any one of Aspects 1-93, wherein the composition comprises about 20 parts by weight to about 45 parts by weight of the ethylene-vinyl acetate copolymer based upon the total weight of the composition.

Aspect 42. The composition according to any one of Aspects 1-93, wherein the composition comprises about 30 parts by weight to about 40 parts by weight of the ethylene-vinyl acetate copolymer based upon the total weight of the composition.

Aspect 43. The composition according to any one of Aspects 1-93, wherein the composition further comprises one or both of a free-radical initiator and a chemical blowing agent.

Aspect 44. The composition according to any one of Aspects 1-93, wherein the composition further comprises the free-radical initiator, and wherein the free-radical initiator is selected from the group consisting of dicumyl peroxide; n-butyl-4,4-di(t-butylperoxy) valerate; 1,1-di(t-butylperoxy)3,3,5-trimethylcyclohexane; 2,5-dimethyl-2,5-di(t-butylperoxy) hexane; di-t-butyl peroxide; di-t-amyl peroxide; t-butyl peroxide; t-butyl cumyl peroxide; 2,5-dimethyl-2,5-di(t-butylperoxy)hexyne-3; di(2-t-butyl-peroxyisopropyl)benzene; dilauroyl peroxide; dibenzoyl peroxide; t-butyl hydroperoxide; and a combination thereof.

Aspect 45. The composition according to any one of Aspects 1-93, wherein the composition further comprises the free-radical initiator, and wherein the free-radical initiator is selected from the group consisting of a peroxide, a diazo compound, and a combination thereof.

Aspect 46. The composition according to any one of Aspects 1-93, wherein the composition further comprises the chemical blowing agent, wherein the chemical blowing agent is selected from the group consisting of a carbonate, bicarbonate, carboxylic acid, azo compound, isocyanate, persulfate, peroxide, and a combination thereof.

Aspect 47. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a block copolymer comprising a first block and a third block, each independently comprising a linear or branched chain aliphatic polymer having a plurality of aromatic groups attached pendantly thereto, a second block located between the first block and the third block and comprising an aliphatic polymer having a plurality of aliphatic side chains attached thereto, and a plurality of first ethylenically unsaturated group present on one or more of the first block, second block, and third block; wherein the block copolymer comprises about 60% to about 90% of the second blocks by weight based upon the weight of the block copolymer; one or more olefinic copolymers, each of the one or more olefinic copolymers comprising a plurality of first olefinic segments and a plurality of second olefinic segments having a different chemical structure from the first olefinic segments; a first linking polymer which is a copolymer of ethylene and 1-butene; a second linking polymer which is a copolymer of ethylene and 1-butene, wherein each of the first linking polymer and the second linking polymer have a different ratio of ethylene to 1-butene monomer content in the respective copolymers, and an ethylene-vinyl acetate (EVA) copolymer, wherein a sum of a ratio I, II, III, IV, and V is from about 1.00 to about 10.00; wherein the ratio I is a ratio of a total parts by weight of the olefinic copolymers present in the composition to a total parts by weight of the block copolymer present in the composition; wherein the ratio II is a ratio of a total parts by weight of the linking polymers present in the composition to a total parts by weight of the block copolymer present in the composition; wherein the ratio III is ratio of a total parts by weight of the EVA copolymers present in the composition to a total parts by weight of the block copolymer present in the composition; wherein the ratio IV is a ratio of the total parts by weight of the first and second linking polymers present in the composition to a total parts by weight of the one or more olefinic copolymers present in the composition, and wherein the ratio V is a ratio of the total parts by weight of the one or more EVA copolymers present in the composition to a total parts by weight of the one or more olefinic copolymers present in the composition.

Aspect 48. The composition according to any one of Aspects 1-93, wherein the sum of ratio I, II, III, IV, and V is from about 3.50 to about 5.00.

Aspect 49. The composition according to any one of Aspects 1-93, wherein one or both of the first block and the third block consist essentially of polystyrene.

Aspect 50. The composition according to any one of Aspects 1-93, wherein in at least one of the one or more olefinic copolymers, the plurality of first olefinic segments comprises ethylene and the plurality of second olefinic segments comprises a second alpha olefin.

Aspect 51. The composition according to any one of Aspects 1-93, wherein the second alpha-olefin has 6 to 12 carbon atoms.

Aspect 52. The composition according to any one of Aspects 1-93, wherein the ethylene-vinyl acetate copolymer having a vinyl acetate content of about 10% to about 45% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

Aspect 53. The composition according to any one of Aspects 1-93, wherein the first composition further comprises one or both of a free-radical initiator and a chemical blowing agent.

Aspect 54. The composition according to any one of Aspects 1-93, wherein the first composition comprises the free-radical initiator, and wherein the free-radical initiator is selected from the group consisting of dicumyl peroxide; n-butyl-4,4-di(t-butylperoxy) valerate; 1,1-di(t-butylperoxy)3,3,5-trimethylcyclohexane; 2,5-dimethyl-2,5-di(t-butylperoxy) hexane; di-t-butyl peroxide; di-t-amyl peroxide; t-butyl peroxide; t-butyl cumyl peroxide; 2,5-dimethyl-2,5-di(tbutylperoxy)hexyne-3; di(2-t-butyl-peroxyisopropyl)benzene; dilauroyl peroxide; dibenzoyl peroxide; t-butyl hydroperoxide; and a combination thereof.

Aspect 55. The composition according to any one of Aspects 1-93, wherein the first composition comprises a chemical blowing agent, and wherein the chemical blowing agent is selected from the group consisting of a carbonate, bicarbonate, carboxylic acid, azo compound, isocyanate, persulfate, peroxide, and a combination thereof.

Aspect 56. The composition according to any one of Aspects 1-93, wherein the ratio I is from about 0.8 to about 2.00.

Aspect 57. The composition according to any one of Aspects 1-93, wherein the ratio II is from about 1.00 to about 3.25.

Aspect 58. The composition according to any one of Aspects 1-93, wherein the ratio III is from about 3.50 to about 5.00.

Aspect 59. The composition according to any one of Aspects 1-93, wherein the ratio IV is from about 3.50 to about 5.00.

Aspect 60. The composition according to any one of Aspects 1-93, wherein the ratio V is from about 2.00 to about 5.00.

Aspect 61. The composition according to any one of Aspects 1-93, wherein a ratio VI of a total parts by weight of the EVA copolymer present in the composition to a total parts by weight of the linking polymers present in the composition is from about 1.00 to about 2.00.

Aspect 62. The composition according to any one of Aspects 1-93, wherein the first pre-foam composition comprises a partially hydrogenated thermoplastic elastomeric block copolymer, the partially hydrogenated thermoplastic elastomeric block copolymer comprising: one or more A blocks comprising aromatic repeat units, one or more B blocks comprising aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer comprising one or more second ethylenically unsaturated groups; an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer comprises one or more aliphatic sidechains; and an ethylene-vinyl acetate copolymer; wherein a sum of a ratio I, II, III, IV, V, and VI is from about 5.0 to about 16.0; wherein the ratio I is a ratio of a total parts by weight of the olefinic block copolymer present in the composition to a total parts by weight of the partially hydrogenated thermoplastic elastomeric block copolymer present in the composition; wherein the ratio II is a ratio of a total parts by weight of the alpha-olefin linking polymers present in the composition to a total parts by weight of the partially hydrogenated thermoplastic elastomeric block copolymer present in the composition; wherein the ratio III is ratio of a total parts by weight of the ethylene-vinyl acetate copolymers present in the composition to a total parts by weight of the partially hydrogenated thermoplastic elastomeric block copolymer present in the composition; wherein the ratio IV is a ratio of the total parts by weight of the alpha-olefin linking polymers present in the composition to a total parts by weight of the olefinic block copolymer present in the composition, wherein the ratio V is a ratio of the total parts by weight of the one or more ethylene-vinyl acetate copolymers present in the composition to a total parts by weight of the olefinic block copolymer present in the composition, and wherein the ratio VI is a ratio of the total parts by weight of the ethylene-vinyl acetate copolymer to a total part is by weight of the alpha-olefin linking polymer.

Aspect 63. The composition according to any one of Aspects 1-93, wherein the sum of ratio I, II, III, IV, V, and VI is from about 14.00 to about 16.00.

Aspect 64. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 5 parts by weight to about 20 parts by weight of the partially hydrogenated thermoplastic elastomeric block copolymer based upon an entire weight of the resin components, wherein the entire weight of the resin components, based upon a total parts by weight of the polymers in the first composition, is about 40 parts by weight to about 86 parts by weight.

Aspect 65. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 5 parts by weight to about 20 parts by weight of the olefinic block copolymer by weight based upon an entire weight of the resin components, wherein the entire weight of the resin components, based upon a total parts by weight of the polymers in the first composition, is about 40 parts by weight to about 86 parts by weight.

Aspect 66. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 15 parts by weight to about 35 parts by weight of the alpha-olefin linking polymer based upon an entire weight of the resin components, wherein the entire weight of the resin components, based upon a total parts by weight of the polymers in the first composition, is about 40 parts by weight to about 86 parts by weight.

Aspect 67. The composition according to any one of Aspects 1-93, wherein the ratio I is from about 0.65 to about 7.00.

Aspect 68. The composition according to any one of Aspects 1-93, wherein the olefinic block copolymer does not comprise a cycloalkyl olefin.

Aspect 69. The composition according to any one of Aspects 1-93, wherein the first composition comprises a first alpha-olefin linking polymer and a second alpha-olefin linking polymer, wherein the first alpha-olefin linking polymer and the second alpha-olefin linking polymer are copolymers of ethylene and 1-butene, each having a different ratio of ethylene to 1-butene monomer content in the copolymer.

Aspect 70. The composition according to any one of Aspects 1-93, wherein the ethylene-vinyl acetate copolymer having a vinyl acetate content of about 10% to about 45% by weight based upon the weight of the ethylene-vinyl acetate copolymer.

Aspect 71. The composition according to any one of Aspects 1-93, wherein the ratio IV is from about 1.00 to 10.00, and wherein the ratio V is from about 2.00 to 10.00.

Aspect 72. The composition according to any one of Aspects 1-93, wherein the ratio V is from about 2.50 to 4.50.

Aspect 73. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 10 parts by weight to about 50 parts by weight of the alpha-olefin linking polymer based upon an entire weight of the resin components, wherein the entire weight of the resin components, based upon a total parts by weight of the polymers in the first composition, is about 40 parts by weight to about 86 parts by weight.

Aspect 74. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 30 parts by weight to about 60 parts by weight of the ethylene-vinyl acetate copolymer based upon an entire weight of the resin components, wherein the entire weight of the resin components, based upon a total parts by weight of the polymers in the first composition, is about 40 parts by weight to about 86 parts by weight.

Aspect 75. The composition according to any one of Aspects 1-93, wherein the first composition comprises a partially hydrogenated thermoplastic elastomeric block copolymer, the partially hydrogenated thermoplastic elastomeric block copolymer comprising: one or more A blocks comprising aromatic repeat units, one or more B blocks comprising aliphatic repeat units, and one or more first ethylenically unsaturated groups present on one or both of the aromatic repeat units and the aliphatic repeat units; an olefinic block copolymer, wherein the olefinic block copolymer is a copolymer of a first alpha-olefin and a second alpha-olefin different from the first alpha-olefin, and wherein the olefinic block copolymer comprises one or more second ethylenically unsaturated groups; and an ethylene-vinyl acetate copolymer; wherein a ratio I is from about 0.65 to about 7.00; wherein the ratio I is a ratio of a total parts by weight of the olefinic block copolymer present in the composition to a total parts by weight of the partially hydrogenated thermoplastic elastomeric block copolymer present in the composition.

Aspect 76. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 5 parts by weight to about 20 parts by weight of the partially hydrogenated thermoplastic elastomeric block copolymer based upon an entire weight of the resin components present in the composition, and wherein the entire weight of the resin components present in the composition comprises about 40 parts by weight to about 86 parts by weight of the entire composition.

Aspect 77. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 5 parts by weight to about 20 parts by weight of the olefinic block copolymer by weight based upon an entire weight of the resin components present in the composition, and wherein the entire weight of the resin components present in the composition comprises about 40 parts by weight to about 86 parts by weight of the entire composition.

Aspect 78. The composition according to any one of Aspects 1-93, wherein the first composition further comprises one or both of a free-radical initiator and a chemical blowing agent.

Aspect 79. The composition according to any one of Aspects 1-93, wherein the ratio I is about 0.65 to 2.00.

Aspect 80. The composition according to any one of Aspects 1-93, wherein the ratio I is about 1.00 to about 3.00.

Aspect 81. The composition according to any one of Aspects 1-93, wherein the olefinic block copolymer does not comprise a cycloalkyl olefin.

Aspect 82. The composition according to any one of Aspects 1-93, wherein the ethylene-vinyl acetate copolymer has a vinyl acetate content of about 10 percent to about 45 percent by weight based upon the weight of the ethylene-vinyl acetate copolymer.

Aspect 83. The composition according to any one of Aspects 1-93, wherein a ratio V is from about 2.50 to 4.50; and wherein the ratio V is a ratio of the total parts by weight of the one or more ethylene-vinyl acetate copolymers present in the composition to a total parts by weight of the olefinic block copolymer present in the composition.

Aspect 84. The composition according to any one of Aspects 1-93, wherein the first composition comprises about 30 parts by weight to about 60 parts by weight of the ethylene-vinyl acetate copolymer based upon an entire weight of the resin components present in the composition, and wherein the entire weight of the resin components present in the composition comprises about 40 parts by weight to about 86 parts by weight of the entire composition.

Aspect 85. The composition according to any one of Aspects 1-93, wherein the component has an energy return of about 70 percent to about 85 percent.

Aspect 86. The composition according to any one of Aspects 1-93, wherein the first composition further comprises an alpha-olefin linking polymer, wherein the alpha-olefin linking polymer comprises one or more aliphatic sidechains.

Aspect 87. The composition according to any one of Aspects 1-93, wherein the alpha-olefin linking polymer is a copolymer of ethylene and an alpha-olefin having about 3 to 8 carbon atoms, and wherein the alpha-olefin linking polymer has an alpha-olefin monomer content of about 15 percent to about 40 percent by weight based upon the weight of the alpha-olefin linking polymer.

Aspect 88. The composition according to any one of Aspects 1-93, wherein each of the aromatic repeat units of the A blocks of the partially hydrogenated thermoplastic elastomeric block copolymer comprise aliphatic backbones having a plurality of aromatic side chains.

Aspect 89. The composition according to any one of Aspects 1-93, wherein the partially hydrogenated thermoplastic elastomeric block copolymer has an elongation at break of greater than 650 percent when measured using ASTM D638.

Aspect 90. The composition according to any one of Aspects 1-93, wherein the partially hydrogenated thermoplastic elastomeric block copolymer is a PS_q-X¹_n-X²_m-X³_pblock copolymer; wherein PS represents polystyrene; X¹is a poly-C₂-C₈-alkylene; X²is a poly-C₂-C₈-alkylene; and X³is polyether, polyester, polycarbonate, polyamide, polyketone or polysiloxane; wherein the subscripts q, n, m, and p represent mole fractions such that 1>q>0, n is 0 to 1, m is 0 to 1, and p is 0 to 1 so long as q+n+m+p=1.

Aspect 91. The composition according to any one of Aspects 1-93, wherein the olefinic block copolymer is a copolymer of ethylene and an alpha-olefin having about 6 to 12 carbon atoms.

Aspect 92. The composition according to any one of Aspects 1-93, wherein the ethylene-vinyl acetate copolymer comprises a first ethylene vinyl acetate copolymer and a second ethylene vinyl acetate copolymer; wherein the first ethylene vinyl acetate copolymer comprises about 15 mole percent to about 40 mole percent vinyl acetate; and wherein the second ethylene vinyl acetate copolymer comprises about 15 mole percent to about 30 mole percent vinyl acetate.

Aspect 93. A partially crosslinked pre-foam composition, comprising a pre-foam composition according to any one of Aspects 1-92 that has been reacted to a degree of crosslinking from about 50% to about 99%.

Aspect 94. A composition comprising a crosslinked reaction product of a composition according to any one of Aspects 1-93.

Aspect 95. A composition made by a process comprising crosslinking and foaming a composition according to any one of Aspects 1-94.

Aspect 96. The composition according to any one of Aspects 95-106, wherein the crosslinking and foaming steps occur at about the same time.

Aspect 97. The composition according to any one of Aspects 95-106, wherein the crosslinking and foaming steps comprise injection molding the pre-foam composition into an injection mold and crosslinking the pre-foam composition in the injection mold.

Aspect 98. The composition according to any one of Aspects 95-106, wherein the injection mold is at a temperature from about 150° C. to about 190° C. during the crosslinking.

Aspect 99. The composition according to any one of Aspects 94-106, wherein the composition is compression molded to produce the foam composition.

Aspect 100. The composition according to any one of Aspects 94-106, wherein the process further comprises annealing the foam article and then compression molding the foam article, reducing it in size by at least 10% in at least one dimension relative to its initial foamed and molded state prior to the compression molding.

Aspect 101. The composition according to any one of Aspects 94-106, wherein the composition comprises a degree of crosslinking from about 50% to about 99%.

Aspect 102. The composition according to any one of Aspects 94-106, wherein the composition has a specific density of about 0.08 to about 0.15.

Aspects 103. The composition according to any one of Aspects 94-106, wherein the composition has an energy return from about 60% to about 85%.

Aspect 104. The composition according to any one of Aspects 94-106, wherein the composition has a split tear of about 1.6 kg/cm to about 4.0 kg/cm.

Aspect 105. The composition according to any one of Aspects 94-106, wherein the composition has a split tear of about 2.5 kg/cm to about 3.5 kg/cm.

Aspect 106. The composition according to any one of Aspects 94-105, wherein the composition has an Asker C hardness of about 40 to 60 C or about 30 to 50 C or about 30 to 40 C.

Aspect 107. A method of making a component for an article of footwear, the method comprising foaming and crosslinking a composition according to any one of Aspects 1-93.

Aspect 108. The method according to any one of Aspects 107-112, wherein the crosslinking and foaming steps occur at about the same time.

Aspect 109. The method according to any one of Aspects 107-112, comprising injection molding the composition into an injection mold to form a foamed composition and crosslinking the foamed composition in the injection mold.

Aspect 110. The method according to any one of Aspects 107-112, wherein the injection mold is at a temperature from about 150° C. to about 190° C. during the crosslinking.

Aspect 111. The method according to any one of Aspects 107-112, wherein the foamed composition is compression molded to produce the component.

Aspect 112. The method according to any one of Aspects 107-112, further comprising annealing the foamed composition and then compression molding the foamed composition, reducing it in size by at least 10% in at least one dimension relative to its initial foamed and molded state prior to compression molding.

Aspect 113. A component for an article of footwear, the component comprising a foam composition according to any one of Aspects 1-96.

Aspect 114. A component for an article of footwear, the component made by a by a process comprising injection molding and crosslinking a composition according to any one of Aspects 1-93.

Aspect 115. The component according to any one of Aspects 113-124, wherein the process further comprises compression molding the crosslinked composition to produce the component.

Aspect 116. The component according to any one of Aspects 113-124, wherein the component is a midsole.

Aspect 117. The component according to any one of Aspects 113-124, wherein the component comprises a degree of crosslinking from about 50% to about 99%.

Aspect 118. The component according to any one of Aspects 113-124, wherein the component has a specific density of about 0.08 to about 0.15.

Aspect 119. The component according to any one of Aspects 113-124, wherein the component has an energy return from about 60% to about 85%.

Aspect 120. The component according to any one of Aspects 113-124, wherein the component has a split tear of about 1.6 kg/cm to about 4.0 kg/cm.

Aspect 121. The component according to any one of Aspects 113-124, wherein the component has a split tear of about 2.5 kg/cm to about 3.5 kg/cm.

Aspect 122. The component according to any one of Aspects 113-124, wherein the component has an Asker C hardness of about 40 to 60 C, about 30 to 50 C, or about 30 to 40 C.

Aspect 123. The component according to any one of Aspects 113-124, wherein the article of footwear is a shoe.

Aspect 124. The component according to any one of Aspects 113-124, wherein the shoe is selected from the group consisting of an athletic shoe, a tennis shoe, a cross-trainer shoe, a children's shoe, a dress shoe, and a casual shoe.

Aspects 125. The component according to any one of Aspects 113-124, wherein the component is part of an article of footwear, apparel or equipment.

Aspect 126. An article of footwear comprising a component according to any one of Aspects 113-125.

Aspect 127. The article of footwear according to Aspect 126, wherein the article of footwear is a shoe, wherein the component is a midsole, and wherein the shoe further comprises a shoe upper and a shoe outsole.

Aspect 128. A method of making an article of footwear, the method comprising affixing a component according to any one of Aspects 113-124 to the article of footwear.

Aspect 129. The method according to any one of Aspects 128-131, wherein the article of footwear is a shoe.

Aspect 130. The method according to any one of Aspects 128-131, wherein the shoe is selected from the group consisting of an athletic shoe, a tennis shoe, a cross-trainer shoe, a children's shoe, a dress shoe, and a casual shoe.

Aspect 131. The method according to any one of Aspects 128-131, wherein the component is a midsole and the method comprises affixing the midsole to one or both of a shoe upper and a shoe outsole.

EXAMPLES

Now having described the aspects of the present disclosure, in general, the following Examples describe some additional aspects of the present disclosure. While aspects of the present disclosure are described in connection with the following examples and the corresponding text and figures, there is no intent to limit aspects of the present disclosure to this description. On the contrary, the intent is to cover all alternatives, modifications, and equivalents included within the spirit and scope of the present disclosure.

Materials

The materials referred to throughout the examples are, unless otherwise indicated, described in Table 1 below. The partially hydrogenated SEBS block copolymers from Asahei Kasei (marketed under the trade name TUFTEC®) all have an elongation at break of greater than 650% when measured using ASTM D638. The P1083 (and the research grade JT-83) have a styrene content of about 20%, while the P5051 has a styrene content of about 47%. The SEBS copolymer from KRATON Polymers (KRATON® G1651E) has a styrene content of about 30%-33%. The ENGAGE® polyolefin elastomers are copolymers of ethylene and octene, while the TAFMER® linking polymers are random copolymers of ethylene and 1-butene. For materials where the supplier is not listed in Table 1 (e.g. stearic acid), these materials are generally available from a variety of suppliers.

TABLE 1

Materials Used In Examples

Trade Name
Ingredient
Description
Supplier

TUFTEC ® P1083
Partially hydrogenated
Aromatic/aliphatic
Asahei Kasei

SEBS block copolymer
copolymer

TUFTEC ® JT-83
Partially hydrogenated
Aromatic/aliphatic
Asahei Kasei

(research grade of
SEBS block copolymer
copolymer

P1083)

TUFTEC ® P5051
Partially hydrogenated
Aromatic/aliphatic
Asahei Kasei

SEBS block copolymer
copolymer

KRATON ® G1651E
partially hydrogenated
Aromatic/aliphatic
KRATON Polymers

SEBS block copolymer
copolymer
Group

INFUSE ™ 9000 OBC
Olefin block copolymer
Olefinic Copolymer
Dow Chemical Co.

INFUSE ™ 9107 OBC
Olefin block copolymer
Olefinic Copolymer
Dow Chemical Co.

INFUSE ™ 9530 OBC
Olefin block copolymer
Olefinic Copolymer
Dow Chemical Co.

ENGAGE ® 8480
Polyolefin elastomer
Olefinic Copolymer
Dow Chemical Co.

ENGAGE ® 8540
Polyolefin elastomer
Olefinic Copolymer
Dow Chemical Co.

ENGAGE ® 8440
Polyolefin elastomer
Olefinic Copolymer
Dow Chemical Co.

TAFMER ® DF-110
Alpha-olefin copolymer
Linking Polymer
Mitsui Elastomers

TAFMER ® DF-605
Alpha-olefin copolymer
Linking Polymer
Mitsui Elastomers

EVA-659
Ethylene vinyl acetate
Ethylene vinyl acetate
USI Corporation

copolymer
(EVA)

EVA-3330
Ethylene vinyl acetate
EVA
USI Corporation

copolymer

ELVAX ® 360
Ethylene vinyl acetate
EVA
DuPont

copolymer

ST/AC
Stearic Acid
Organic acid

ZnO
Zinc oxide
Metal oxide

TiO₂
Titanium Dioxide
Metal oxide

CaCO₃
Calcium Carbonate
Filler/Nucleating Agent

TAC-50GR
Triallyl cyanurate
Crosslinking agent

Color base

Coloring agent

27020
Blue tint
Coloring agent

EVA 1375
Red pigment
Coloring agent

8502
Black pigment
Coloring agent

R929

Coloring agent

UNICELL D600-MT

Blowing agent
Tramaco

(MB-50%)

JTR/TL

Blowing agent
Kumyang

COLINK 101-45GE
2,5-Dimethyl-2,5-
Free-radical initiator

di(tert-butylperoxy)hexane

DCP
Dicumyl peroxide
Free-radical initiator

Example 1: Batch Process of Preparing Compositions Capable of Being Foamed

The pre-foam compositions, compositions prior to being foamed, described in Tables 3 and 4 were prepared. Some of the pre-foam compositions were first compounded using the components shown in Table 2 to form pre-foam base compositions (PFBC) 1 and PFBC 2, according to Example 1. These PFBCs were then used to prepare the foam compositions shown in Tables 3, 4. The properties of the foam compositions are described in Table 5. In some instances, PFC 1 or PFBC 2 were further modified as shown in Tables 3, 4 and 5 by adding additional materials. Other formulations were prepared directly, without first forming a pre-foam base composition.

TABLE 2

Composition of Pre-Foam Base Compositions

Used For Making Pre-Foam Compositions

Pre-Foam
Pre-Foam

Base
Base
Formulations

Composition 1
Composition 2
A, B, C,

(PFBC 1)
(PFBC 2)
and D

TABLE 2
phr in
phr in
phr in

Trade Name
PFBC1
PFBC2
formulation

TUFTEC ® P1083
10.0
16.6
**

TUFTEC ® P5051
0.0
0.0
**

TUFTEC ® JT-83
0.0
0.0
**

KRATON ® D G1651E
0.0
0.0
**

INFUSE ™ OBC9000
0.0
0.0
**

INFUSE ™ OBC9107
15.0
24.9
**

INFUSE ™ OBC9507
0.0
0.0
**

INFUSE ™ OBC9530
0.0
0.0
**

ENGAGE ® 8480
0.0
0.0
**

ENGAGE ® 8540
0.0
0.0
**

ENGAGE ® 8440
0.0
0.0
**

TAFMER ® DF-110
12.0
19.9
**

TAFMER ® DF-605
18.0
29.9
**

EVA-659
40.0
0.0
**

EVA-3330
5.0
0.0
**

ELVAX ® 360
0.0
0.0
**

ELVAX ® 40L-03
0.0
0.0
**

ST/AC
1.0
1.7
0.0

ZnO
0.8
1.4
1.5

TiO₂
0.0
0.0
3.6

CaCO₃
0.0
0.0
5.0

TAC-50GR
0.3
0.5
0.0

Color base
11.0
18.3
0.0

27020
0.0
0.0
0.0

EVA 1375
0.0
0.0
0.0

8502
0.0
0.0
0.0

R929
0.0
0.0
0.1

UNICELL D600-MT
11.5
11.5
0.0

JTR/TL
0.0
0.0
9.8

COLINK 101-45GE
0.0
0.0
0.0

DCP
0.7*
0.7*
0.7

*concentration in formulation

**See Table 2 and 3

The pre-foam compositions were formed using a batch process where the partially hydrogenated SEBS block copolymer and the olefin polymer were combined in a kneader for about 20 minutes. During this time, the kneader temperature was maintained at a temperature of from about 100° C. to about 120° C. In some examples, the ethylene vinyl acetate copolymer (the EVA component of the composition) and/or pigments was added to the mixture the partially hydrogenated SEBS block copolymer and the olefin polymer.

Next, where present, the one or more metal oxide, one or more organic acid, and one or more crosslinking agent were added to the mixture. The combined mixture including the partially hydrogenated SEBS block copolymer and the olefin polymer, as well as (if present) the EVA along with the metal oxide, organic acid, and crosslinking agent were mixed in the kneader for about 20 minutes, while the kneader temperature was held at a temperature of from about 100° C. to about 120° C.

Next, the kneader temperature was lowered to about 90° C. or below. The combined mixture in the kneader was then combined with the blowing agent and a free radical initiator. The kneaded mixture was then subjected to pelletization using a die that is cooled to maintain the temperature at about 90° C. or below.

TABLE 3

Composition of foams

Composition

A
B
C
D
E

Parts by
Parts by
Parts by
Parts by
Parts by

Material
Wt.
Wt.
Wt.
Wt.
Wt.

PFBC 1 (MB1)
0.0
0.0
0.0
0.0
0.0

PFBC 2 (MB2)
0.0
0.0
0.0
0.0
70.0

Kraton G1651E
0.0
0.0
0.0
0.0
0.0

TUFTEC ® P1083
0.0
0.0
0.0
0.0
9.3

TUFTEC ® JT-83
20.0
20.0
20.0
20.0
10.0

TUFTEC ® P5051
0.0
0.0
0.0
0.0
0.0

INFUSE ™ 9000 OBC
0.0
0.0
0.0
0.0
0.0

INFUSE ™ 9107 OBC
0.0
0.0
0.0
0.0
13.9

INFUSE ™ 9530 OBC
0.0
0.0
0.0
20.0
20.0

ENGAGE ® 8440
0.0
0.0
20.0
0.0
0.0

ENGAGE ® 8480
20.0
0.0
0.0
0.0
0.0

ENGAGE ® 8540
0.0
20.0
0.0
0.0
0.0

TAFMER ® DF-110
0.0
0.0
0.0
0.0
11.1

TAFMER ® DF-605
0.0
0.0
0.0
0.0
16.7

EVA-659
0.0
0.0
0.0
0.0
0.0

EVA-3330
0.0
0.0
0.0
0.0
0.0

ELVAX ® 360
60.0
60.0
60.0
60.0
0.0

ZnO

1.0

ST/AC

1.0

TAC-GR50

0.3

D600MT

8.9

DCP

0.0

101-45GE

0.9

Total Parts by Wt.
120.7
120.7
120.7
120.7
112.0

Composition

F
G
H
I
J

Parts by
Parts by
Parts by
Parts by
Parts by

Material
Wt.
Wt.
Wt.
Wt.
Wt.

PFBC 1 (MB1)
0.0
0.0
0.0
0.0
0.0

PFBC 2 (MB2)
90.0
70.0
100.0
50.0
80.0

Kraton G1651E
0.0
0.0
0.0
0.0
0.0

TUFTEC ® P1083
11.9
9.3
13.2
6.6
10.6

TUFTEC ® JT-83
10.0
10.0
0.0
10.0
0.0

TUFTEC ® P5051
0.0
0.0
0.0
20.0
0.0

INFUSE ™ 9000 OBC
0.0
0.0
0.0
0.0
0.0

INFUSE ™ 9107 OBC
17.9
13.9
19.9
9.9
15.9

INFUSE ™ 9530 OBC
0.0
20.0
0.0
20.0
20.0

ENGAGE ® 8440
0.0
0.0
0.0
0.0
0.0

ENGAGE ® 8480
0.0
0.0
0.0
0.0
0.0

ENGAGE ® 8540
0.0
0.0
0.0
0.0
0.0

TAFMER ® DF-110
14.3
11.1
15.9
7.9
12.7

TAFMER ® DF-605
21.5
16.7
23.8
11.9
19.1

EVA-659
0.0
0.0
0.0
0.0
0.0

EVA-3330
0.0
0.0
0.0
0.0
0.0

ELVAX ® 360
0.0
0.0
0.0
0.0
0.0

ZnO
1.0
1.0
1.0
1.0
1.0

ST/AC
1.0
1.0
1.0
1.0
1.0

TAC-GR50
0.2
0.4
0.4
0.3
0.4

D600MT
10.0
8.9
15.2
8.9
4.7

DCP
0.4
0.0
0.0
0.0
0.0

101-45GE
0.9
0.8
0.8
0.9
0.8

Total Parts by Wt.
113.5
112.1
118.4
112.0
107.9

Composition

K
L
M
N
O

Parts by
Parts by
Parts by
Parts by
Parts by

Material
Wt.
Wt.
Wt.
Wt.
Wt.

PFBC 1 (MB1)
0.0
0.0
0.0
0.0
0.0

PFBC 2 (MB2)
60.0
80.0
100.0
100.0
70.0

Kraton G1651E
0.0
0.0
0.0
0.0
0.0

TUFTEC ® P1083
7.9
10.6
13.2
13.2
9.3

TUFTEC ® JT-83
0.0
0.0
0.0
0.0
10.0

TUFTEC ® P5051
0.0
0.0
0.0
0.0
0.0

INFUSE ™ 9000 OBC
0.0
0.0
0.0
0.0
20.0

INFUSE ™ 9107 OBC
11.9
15.9
19.9
19.9
13.9

INFUSE ™ 9530 OBC
40.0
20.0
0.0
0.0
0.0

ENGAGE ® 8440
0.0
0.0
0.0
0.0
0.0

ENGAGE ® 8480
0.0
0.0
0.0
0.0
0.0

ENGAGE ® 8540
0.0
0.0
0.0
0.0
0.0

TAFMER ® DF-110
9.5
12.7
15.9
15.9
11.1

TAFMER ® DF-605
14.3
19.1
23.8
23.8
16.7

EVA-659
0.0
0.0
0.0
0.0
0.0

EVA-3330
0.0
0.0
0.0
0.0
0.0

ELVAX ® 360
0.0
0.0
0.0
0.0
0.0

ZnO
1.0
1.0
1.0
1.0
1.0

ST/AC
1.0
1.0
1.0
1.0
1.0

TAC-GR50
0.4
0.4
0.4
0.4
0.3

D600MT
4.4
8.6
5.0
8.6
8.9

DCP
0.0
0.0
0.0
0.0
0.0

101-45GE
0.8
0.8
0.8
0.8
0.9

Total Parts by Wt.
107.6
111.8
108.2
111.8
112.0

Composition

P
Q
R
S
T

Parts by
Parts by
Parts by
Parts by
Parts by

Material
Wt.
Wt.
Wt.
Wt.
Wt.

PFBC 1 (MB1)
0.0
0.0
0.0
0.0
0.0

PFBC 2 (MB2)
70.0
100.0
60.0
70.0
100.0

Kraton G1651E
0.0
0.0
0.0
0.0
0.0

TUFTEC ® P1083
9.3
13.2
7.9
9.3
13.2

TUFTEC ® JT-83
10.0
0.0
0.0
10.0
0.0

TUFTEC ® P5051
0.0
0.0
0.0
0.0
0.0

INFUSE ™ 9000 OBC
0.0
0.0
0.0
0.0
0.0

INFUSE ™ 9107 OBC
13.9
19.9
11.9
13.9
19.9

INFUSE ™ 9530 OBC
20.0
0.0
40.0
20.0
0.0

ENGAGE ® 8440
0.0
0.0
0.0
0.0
0.0

ENGAGE ® 8480
0.0
0.0
0.0
0.0
0.0

ENGAGE ® 8540
0.0
0.0
0.0
0.0
0.0

TAFMER ® DF-110
11.1
15.9
9.5
11.1
15.9

TAFMER ® DF-605
16.7
23.8
14.3
16.7
23.8

EVA-659
0.0
0.0
0.0
0.0
0.0

EVA-3330
0.0
0.0
0.0
0.0
0.0

ELVAX ® 360
0.0
0.0
0.0
0.0
0.0

ZnO
1.0
1.0
1.0
1.0
1.0

ST/AC
1.0
1.0
1.0
1.0
1.0

TAC-GR50
0.3
0.4
0.4
0.4
0.4

D600MT
8.6
8.8
8.3
8.9
15.2

DCP
0.0
0.0
0.0
0.0
0.0

101-45GE
0.9
0.8
0.8
0.8
0.8

Total Parts by Wt.
111.8
116.5
111.5
112.1
118.4

Composition

U
V′
W′

Parts by
Parts by
Parts by

Material
Wt.
Wt.
Wt.

PFBC 1 (MB1)
100.0
100.0
100.0

PFBC 2 (MB2)
0.0
0.0
0.0

Kraton G1651E
0.0
0.0
0.0

TUFTEC ® P1083
8.0
8.0
8.0

TUFTEC ® JT-83
0.0
0.0
0.0

TUFTEC ® P5051
0.0
0.0
0.0

INFUSE ™ 9000 OBC
0.0
0.0
0.0

INFUSE ™ 9107 OBC
12.0
12.0
12.0

INFUSE ™ 9530 OBC
0.0
0.0
0.0

ENGAGE ® 8440
0.0
0.0
0.0

ENGAGE ® 8480
0.0
0.0
0.0

ENGAGE ® 8540
0.0
0.0
0.0

TAFMER ® DF-110
9.6
9.6
9.6

TAFMER ® DF-605
14.4
14.4
14.4

EVA-659
31.9
31.9
31.9

EVA-3330
4.0
4.0
4.0

ELVAX ® 360
0.0
0.0
0.0

ZnO
1.0
1.0
1.0

ST/AC
1.0
1.0
1.0

TAC-GR50
0.4
1.0
0.6

D600MT
8.8
8.4
7.9

DCP
0.0
0.0
0.0

101-45GE
0.8
0.2
0.6

Total Parts by Wt.
112.0
111.6
111.1

Example 2: Continuous Process of Preparing Pre-Foam Compositions

Pre-foam compositions can be prepared using a continuous process where the styrenic copolymer component and the unsaturated olefin component are pre-mixed in a hopper and fed into a twin-screw extruder. The zone in the twin-screw extruder into which the styrenic copolymer component and the unsaturated olefin component are fed (ZONE 1) is held at a temperature of from about 100° C. to about 120° C. When included in the pre-foam composition, the optional EVA component and/or pigments are pre-mixed with the styrenic copolymer component and the unsaturated olefin component.

Next, one or more metal oxide, one or more organic acid, and one or more crosslinking agent are added to the mixture of polymer and unsaturated olefin The particle size of the metal oxide used was less than 1 micron. The combined mixture of the styrenic copolymer component, the unsaturated olefin component, the optional EVA component, and the metal oxide, organic acid, and crosslinking agent are mixed in ZONE 1 of the twin-screw extruder at a temperature of from about 100° C. to about 120° C. until thoroughly mixed.

The combined mixture of the styrenic copolymer component, the, unsaturated olefin component, the optional EVA component, and the metal oxide, organic acid, and crosslinking agent move to ZONE 2 of the twin-screw extruder, where the temperature is about 90° C. or below. The combined mixture of the styrenic copolymer component, the unsaturated olefin component, the EVA component, and the metal oxide, organic acid, and crosslinking agent are then combined in ZONE 2 with a blowing agent and a free radical initiator.

Next, the mixture of the styrenic copolymer component, the unsaturated olefin component, the optional EVA component, and the metal oxide, organic acid, crosslinking agent, blowing agent, and free radical initiator is then subjected to pelletization using a die that is cooled to maintain the temperature at about 90° C. or below. The pelletization can performed under water, thus cooling the resulting pellets as they exit the pelletization die.

Example 3: Forming Foam Articles from Pre-Foam Compositions

Pellets made according to the batch process described in Examples 1 using the pre-foam composition formulations described in Tables 1-4 were injection molded (IM) into a pre-heated mold where the mold temperature was, from about 170° C. to about 180° C. The mold temperature was above the decomposition temperature of the chemical blowing agent, which decomposed producing gas in the softened composition and foaming it. The mold temperature was also above the initiation temperature of the free-radical initiator, producing a polymerization reaction which crosslinked the unsaturated styrenic copolymer component with the unsaturated olefin component of the composition.

As indicated in Table 5, some of the pre-foam compositions were foamed and injection molded in a single-step process (IM) to produce the finished molded foam article without a compression molding step, while other pre-foam compositions were foamed and molded using a process in which the pre-foam composition was first injection molded to form a molded foam pre-foam, then the molded foam pre-form was annealed, and then the annealed molded foam pre-form was compression molded to produce the finished molded foam article (IM+CM).

For the pre-foam compositions which were injection molded and subsequently compression molded to produce the finished molded foam articles (IM+CM), the injection molded foam preform was taken through an annealing process in which the foam preform was heated to a temperature of about 70° C. to about 80° C. for about 10 to about 15 minutes; then cooled to a temperature of about 60° C. to about 70° C. and held at that temperature for about 10 to about 15 minutes; next the preform was cooled to a temperature of about 50° C. to about 60° C. and held at that temperature for about 10 to about 15 minutes; then cooled to a temperature of about 45° C. to about 55° C. and held at that temperature for about 10 to about 15 minutes. The annealed molded foam preform was then washed with water (about 35° C. to about 40° C.) for about 10 to about 15 minutes and subsequently dried for 24 hours.

The annealed molded foam preform was then placed in a compression mold which is at least 10% smaller at least one dimension relative to its initial foamed, molded and annealed state prior to the compression molding. During the compression molding process, the foam preform is heated to a surface temperature of from about 130° C. to about 150° C. Then the foam preform is cooled to a surface temperature of about 30° C. in about 15 minutes or less (e.g., in about 12 minutes or less) to give a finished compression molded foam article.

While this experiment used the pre-foam compositions only to produce injection molded foam articles (IM) and injection molded and compression molded foam articles (IM+CM) using the processes described above, the pre-foam compositions described herein can be foamed and/or molded using other types of processes known in the art. For example, these pre-foam compositions can be used to form slab foam, particulate (e.g., bead) foams, etc. These forms of foam can then be used in various ways. For example, slab foam can be formed, and then can be used as formed as a final component, or can be compression molded to form a final component. Pellets of the pre-foam compositions can be used to form individual particulate foams, or can be foamed and molded to form molded foam articles.

TABLE 4

Compositions and Component Ratios for Foams

Composition
A
B
C
D
E

Aromatic/Aliphatic Block
20.0
20.0
20.0
20.0
19.3

Copolymer (Parts by Wt.)

Olefinic Copolymer (Parts
20.0
20.0
20.0
20.0
33.9

by Wt.)

Linking Polymer (Parts by
0.0
0.0
0.0
0.0
27.8

Wt.)

EVA Copolymer (Parts by
0.0
0.0
0.0
0.0
0.0

Wt.)

Resin Component (Parts
40.0
40.0
40.0
40.0
81.0

by Wt.)

Component Ratios

I: Olefinic Copolymer
1.00
1.00
1.00
1.00
1.76

(Parts by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

II: Linking Polymer (Parts
0.00
0.00
0.00
0.00
1.44

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

III: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

IV: Linking Polymer (Parts
0.00
0.00
0.00
0.00
0.82

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

V: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

VI: EVA Copolymer (Part
N/A
N/A
N/A
N/A
0.00

by Wt.) to Linking

Polymer (Parts by Wt.)

Sum of Ratios I-V
1.00
1.00
1.00
1.00
3.20

Sum of Ratios I-VI*
N/A
N/A
N/A
N/A
4.02

Composition
F
G
H
I
J

Aromatic/Aliphatic Block
21.9
19.3
13.2
36.6
10.6

Copolymer (Parts by Wt.)

Olefinic Copolymer (Parts
17.9
33.9
19.9
29.9
35.9

by Wt.)

Linking Polymer (Parts by
35.7
27.8
39.7
19.9
31.8

Wt.)

EVA Copolymer (Parts by
0.0
0.0
0.0
0.0
0.0

Wt.)

Resin Component (Parts
75.5
81.0
72.8
86.4
78.2

by Wt.)

Component Ratios

I: Olefinic Copolymer
0.82
1.76
1.50
0.82
3.39

(Parts by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

II: Linking Polymer (Parts
1.63
1.44
3.00
0.54
3.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

III: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

IV: Linking Polymer (Parts
2.00
0.82
2.00
0.66
0.89

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

V: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

VI: EVA Copolymer (Part
0.00
0.00
0.00
0.00
0.00

by Wt.) to Linking

Polymer (Parts by Wt.)

Sum of Ratios I-V
2.45
3.20
4.50
1.36
6.39

Sum of Ratios I-VI*
4.45
4.02
6.50
2.02
7.28

Composition
K
L
M
N
O

Aromatic/Aliphatic Block
7.9
10.6
13.2
13.2
19.3

Copolymer (Parts by Wt.)

Olefinic Copolymer (Parts
51.9
35.9
19.9
19.9
13.9

by Wt.)

Linking Polymer (Parts by
23.8
31.8
39.7
39.7
27.8

Wt.)

EVA Copolymer (Parts by
0.0
0.0
0.0
0.0
0.0

Wt.)

Resin Component (Parts
83.7
78.2
72.8
72.8
61.0

by Wt.)

Component Ratios

I: Olefinic Copolymer
6.54
3.39
1.50
1.50
0.72

(Parts by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

II: Linking Polymer (Parts
3.00
3.00
3.00
3.00
1.44

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

III: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

IV: Linking Polymer (Parts
0.46
0.89
2.00
2.00
2.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

V: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

VI: EVA Copolymer (Part
0.00
0.00
0.00
0.00
0.00

by Wt.) to Linking

Polymer (Parts by Wt.)

Sum of Ratios I-V
9.54
6.39
4.50
4.50
2.16

Sum of Ratios I-VI*
10.00
7.28
6.50
6.50
4.16

Composition
P
Q
R
S
T

Aromatic/Aliphatic Block
19.3
13.2
7.9
19.3
13.2

Copolymer (Parts by Wt.)

Olefinic Copolymer (Parts
33.9
19.9
51.9
33.9
19.9

by Wt.)

Linking Polymer (Parts by
27.8
39.7
23.8
27.8
39.7

Wt.)

EVA Copolymer (Parts by
0.0
0.0
0.0
0.0
0.0

Wt.)

Resin Component (Parts
81.0
72.8
83.7
81.0
72.8

by Wt.)

Component Ratios

I: Olefinic Copolymer
1.76
1.50
6.54
1.76
1.50

(Parts by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

II: Linking Polymer (Parts
1.44
3.00
3.00
1.44
3.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

III: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

IV: Linking Polymer (Parts
0.82
2.00
0.46
0.82
2.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

V: EVA Copolymer (Parts
0.00
0.00
0.00
0.00
0.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

VI: EVA Copolymer (Part
0.00
0.00
0.00
0.00
0.00

by Wt.) to Linking

Polymer (Parts by Wt.)

Sum of Ratios I-V
3.20
4.50
9.54
3.20
4.50

Sum of Ratios I-VI*
4.02
6.50
10.00
4.02
6.50

Composition
U
V′
W′

Aromatic/Aliphatic Block
8.0
8.0
8.0

Copolymer (Parts by Wt.)

Olefinic Copolymer (Parts
12.0
12.0
12.0

by Wt.)

Linking Polymer (Parts by
23.9
23.9
23.9

Wt.)

EVA Copolymer (Parts by
35.9
35.9
35.9

Wt.)

Resin Component (Parts
79.8
79.8
79.8

by Wt.)

Component Ratios

I: Olefinic Copolymer
1.50
1.50
1.50

(Parts by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

II: Linking Polymer (Parts
3.00
3.00
3.00

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

III: EVA Copolymer (Parts
4.50
4.50
4.50

by Wt.) to

Aromatic/Aliphatic Block

Copolymer (Parts by Wt.)

IV: Linking Polymer (Parts
2.00
2.00
2.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

V: EVA Copolymer (Parts
3.00
3.00
3.00

by Wt.) to Olefinic

Copolymer (Parts by Wt.)

VI: EVA Copolymer (Part
1.50
1.50
1.50

by Wt.) to Linking

Polymer (Parts by Wt.)

Sum of Ratios I-V
4.50
4.50
4.50

Sum of Ratios I-VI*
15.50
15.50
15.50

NT: not tested

N/A: not applicable

Example 4: Testing of Foam Articles

Examples of foam articles formed from the formulations described in Tables 3 and 4 were made and tested to determine their physical properties (e.g., specific gravity, hardness, split tear, compression set, and energy return). The results for foam articles for the various formulations are reported in Table 5.

The purpose of this experiment was to identify pre-foam compositions with improved split-tear values as compared to conventional ethylene vinyl acetate (EVA) foam, but which otherwise maintained the physical properties of conventional EVA foam which are beneficial for us as components of articles of footwear. The experimental pre-foam compositions were based on using a styrenic copolymer component, an unsaturated olefin component, and optionally an EVA component. Some of the formulations were used to produce foams which were first injection molded and then annealed and compression molded to produce a final foam component (IM+CM), while other formulations were used to produce foams which were injection molded to produce a final foam component (IM). The target range for the split-tear values was from about 2.5 kg/cm to about 3.0 kg/cm or greater. As a comparison, the split tear value for conventional EVA foam is about 1.7. The target ranges for the other physical properties of the final foam component were: a specific gravity of about 0.1 to about 0.2; an Asker C hardness of about 40 to about 50; a compression set of about 20% to about 35%; and a resilience of at least about 60%. These target ranges were based primarily on the physical properties of conventional EVA foam used as components for article of footwear, which has a specific gravity of from 0.080 to 0.095, an Asker C hardness of 34-38, a compression set of 75%, and an resiliency of about 59.

The test method used to obtain the specific gravity values reported in Table 5 is as follows.

The specific gravity of the foam was be determined by testing 3 representative samples taken from a foam preform or compression molded foam component. Using a balance with appropriate accuracy for the weight of the sample, the weight of each sample was determined both in air and when the sample was completely submerged in distilled water at a temperature of 22° C.±2° C., after removing any air bubbles adhered to the surface of the foam sample before weighing. The specific gravity (S.G.) was then calculated by taking the weight of the sample in water and subtracting that from the weight of the sample in air, and this value was then divided into the weight of the sample in air, where all the weights are weights in grams.

Split Tear Test

The test method used to obtain the split tear values for foam articles as shown in Table 5 is as follows.

Four die-cut, rectangular-shaped samples of slab sheet or molded foam were prepared, each measuring 2.54 cm×15.24 cm×10±1 mm (thickness). If the foam material to be tested had a skin, the material had its skin removed before preparing the four samples. A 3 cm long cut was made in the center from one end of the sample. Then five successive 2 cm portions were marked on the sample.

The crosshead speed of the tensile test apparatus was set at 50 mm/min. Each separated end of the sample was clamped in an upper grip and a lower grip of the test apparatus. The separation was placed in the middle between both grips. Each section of the sample was held in a clamp in such a manner that the original adjacent cut edges formed a straight line joining the centers of the clamps.

As needed, the cut was aided with a sharp knife to keep separating the foam material in the center of the sample. Readings caused by cutting with the knife were discarded. The lowest values for each of the five portions of each sample were recorded in kg/cm. Five values were recorded for each sample and an average of the five values was then obtained and reported. If a portion of a sample included a portion having an air bubble more than 2 mm in diameter, the value for the portion including the air bubble was not included in the average. If more than one portion of a sample was found to include air bubbles having a diameter greater than 2 mm, another sample was then tested.

Durometer Hardness Test

The test used to obtain the hardness values for the foam articles reported in Table 5 is as follows.

For flat foams, the sample was a minimum of 6 mm thick for Asker C durometer testing. If necessary, foam samples were stacked to make up the minimum thickness. Foam samples were large enough to allow all measurements to be performed at a minimum of 12 mm from the edge of the sample and at least 12 mm from any other measurement. Regions tested were flat and parallel with an area at least 6 mm in diameter. For the samples tested in Table 5, standard samples having dimensions of approximately 35 cm×13 cm×1.8 cm, were used, and a minimum of five hardness measurements were taken and tested using a 1 kg head weight.

Compression Set

The test used to obtain the compression set values for foam articles reported in Table 5 is as follows.

A foam sample was compressed between two metal plates to 50% of its original thickness and placed in an oven at 50° C. for 6 hours. The sample was then cooled and the difference between its precompression and post-compression thickness was used as the measure of static compression set.

For the tests reported in Table 5, molded plaques having skin on one side and a thickness of 10 mm were used to obtain the samples. The plaque was then skived to a thickness of 10+/−0.5 mm to remove the skin before cutting the samples. Compression molded foam materials having skin on two sides had the skin skived from one side, so that skin remained on only one side. Five 2.54 cm diameter circles were then machine drilled from the plaque to obtain the samples to be tested.

The compression set testing device consists of two flat steel plates set between the parallel faces of the compression device with compression rings and spacer bars for each set of parallel faces. Four compression rings of the same thickness (4.5 mm or 5.0 mm based on the specimen thickness) were used for each parallel face of the compression device. The percent compression set was calculated using the following equation:

% Set=((Original gauge−final gauge)/(50% Original gauge))×100

The center area of each specimen was marked and used to measure the specimens with the use of an AMES gage with no load on top.

Energy Return Test

The test used to obtain the energy return values for foam articles reported in Table 5 is as follows.

Energy return of the foam articles was determined using ASTM D 2632 92, which uses a vertical rebound apparatus.

TABLE 5

Processing Methods and Properties of Foam Articles

Composition
A
B
C
D
E

Processing Method
2
2
2
2
2

Physical Properties

IM Foam

Specific Gravity
0.1185
0.1166
0.1171
0.1153
0.11

Hardness (Asker C)
32-33
33-34
32-33
28-30
41-42

Split Tear (kg/cm)
1.79-1.75
1.61-1.78
1.58-1.62
1.52-1.56
1.3

Compression Set (%)
72-73
70-71
72-74
70-71
51-53

Energy Return (slab) (%)

NA

IM + CM Foam

Specific Gravity
0.2048
0.2089
0.2021
0.2042
0.16-0.17

Hardness (Asker C)
49-50
50-51
49-50
56-58
53-54

Split Tear (kg/cm)
2.7-2.8
2.6-2.8
2.8-2.9
2.4-2.5
2

Compression Set (%)
43-45
39-40
49-50
38-39
21

Energy Return (slab) (%)
50-51
49-50
53-54
47-48
68

Composition
F
G
H
I
J

Processing Method
2
2
1
2
2

Physical Properties

IM Foam

Specific Gravity
0.09
0.1
0.15
0.11
0.159

Hardness (Asker C)
32-34
34-35
52-53
43-45
50-51

Split Tear (kg/cm)
1.9
2
2.5-2.6
1.6
2.98-3.06

Compression Set (%)
71-72
74-76
35-55
69
49-51

Energy Return (slab) (%)
60
83-89
71
64
64-65

IM + CM Foam

Specific Gravity
0.13-0.14
NT
NA
0.18
NT

Hardness (Asker C)
43-48
NT
NA
55-59
NT

Split Tear (kg/cm)
2.3
NT
NA
2.5-2.6
NT

Compression Set (%)
39-41
NT
NA
21-22
NT

Energy Return (slab) (%)
68
NT
NA
69
NT

Composition
K
L
M
N
O

Processing Method
2
1
2
1
2

Physical Properties

IM Foam

Specific Gravity
0.15
0.17
0.167
0.17
0.13

Hardness (Asker C)
46-48
54-55
52-54
54-55
42-44

Split Tear (kg/cm)
2.73-3.01
2.6-2.7
3.0-3.1
2.7-2.8
2

Compression Set (%)
59-61
26-32
43-46
28-33
71

Energy Return (slab) (%)
67-72
69-70
61-63
69-72
65

IM + CM Foam

Specific Gravity
NT
NA
NT
NA
0.17-0.18

Hardness (Asker C)
NT
NA
NT
NA
54-57

Split Tear (kg/cm)
NT
NA
NT
NA
3.0-3.1

Compression Set (%)
NT
NA
NT
NA
28

Energy Return (slab) (%)
NT
NA
NT
NA
69

Composition
P
Q
R
S
T

Processing Method
2
1
1
1
1

Physical Properties

IM Foam

Specific Gravity
0.11
0.17
0.16
0.15
0.11

Hardness (Asker C)
42-43
54-55
51-52
49-51
33-36

Split Tear (kg/cm)
2
3.4
2.6
2.8-3.0
1.4-1.7

Compression Set (%)
66-72
38-39
37-43
40-50
63-70

Energy Return (slab) (%)
NA
68
71-73
74-76
84-87

IM + CM Foam

Specific Gravity
0.17
NA
NA
NA
NA

Hardness (Asker C)
52-55
NA
NA
NA
NA

Split Tear (kg/cm)
3.1
NA
NA
NA
NA

Compression Set (%)
31-37
NA
NA
NA
NA

Energy Return (slab) (%)
67-70
NA
NA
NA
NA

Composition
U
V′
W′

Processing Method
1
1
1

Physical Properties

IM Foam

Specific Gravity
0.18
0.19
0.19

Hardness (Asker C)
42-45
42-44
43-45

Split Tear (kg/cm)
2.5-2.6
2.6-2.7
2.6

Compression Set (%)
29-33
32-34
31-32

Energy Return (slab) (%)
78-80
80
79-82

IM + CM Foam

Specific Gravity
NA
NA
NA

Hardness (Asker C)
NA
NA
NA

Split Tear (kg/cm)
NA
NA
NA

Compression Set (%)
NA
NA
NA

Energy Return (slab) (%)
NA
NA
NA

NT: not tested

NA: not applicable

1: Pre-foam composition was injection molded to form final foam article

2: Pre-foam composition was injection molded to form foam preform, and then the foam preform was compression molded to form final foam article

Results

Four of the 13 final molded foam articles produced using injection molding and compression molding (IM+CM) had split tear values of greater than 2.5, and 8 of the 11 final molded foam articles produced using just the injection molding process (IM) had split tear values of greater than 2.5. Unexpectedly, 12 of the formulations which produced molded foam articles with the target split tear values also had resiliency values significantly higher than expected. Specifically, formulations H, I, L, N, O, P, Q, R, S, U, V and X had resiliency values ranging from 67% to 82%. However, only 2 pre-foam compositions were found which produced final foam components having all their physical properties in the target ranges (formulations U and X). The resiliency values for these two formulations were found to be over 14 percentage points greater than for conventional EVA foam.

In general, the pre-foam compositions which produced final foam components with unexpectedly high resiliency values included from about 10 parts per hundred of resin (phr) to about 22 phr of the styrenic copolymer component, and from about 45 phr to about 80 phr of the unsaturated olefin component. Some of these pre-form compositions also comprised from about 31 phr to about 36 phr of the EVA component, while others were free of the EVA component. Generally, the pre-foam compositions which produced final foam components with target split tear values and unexpectedly high resiliency values had ratios of the phr of the styrenic copolymer component to the phr of the unsaturated olefin component which ranged from about 0.17 to about 0.30. For the pre-foam compositions including an EVA component, the ratios of the phr of the styrenic copolymer component to the phr of the EVA component ranged from about 0.37 to about 0.70. The ratios of the phr of the unsaturated olefin component to the phr of the EVA component ranged from about 2.2 to about 2.3. For the pre-foam compositions including an EVA component, the sum of all three ratios ranged from about 2.7 to about 3.3.

Example 5

High energy return foam compositions from Examples 1-4 were tested for abrasion loss using a modified DIN procedure. Briefly, samples having a 15 mm diameter×10 mm thickness were die cut from a foam slab of the compositions. The weight was recorded, and the samples were glued to a 15 mm diameter×2 mm thick hard plastic disc. The abrasion loss was tested using a standard DIN Abrasion Tester with standard grit per ASTM D5396. The sandpaper was cleaned, and the load was reduced from 20 N to 5 N, after which a single pass was performed at a rate of about 2 minutes.

The high energy return foam composition was prepared with added silane as described in Table 6. The added silane can be used with any high energy return foam composition described in the above examples.

TABLE 6

High Energy Return Foam Tested With Added Silane

Component
Parts Per Hundred Resin

High Energy Return Foam

SEBS (Ashai Kasei P1083)
10
PHR

Polyolefin (Dos Engage 9107)
15
PHR

Polyalphaolefin#1
12
PHR

(Mitsui Tafmer DF110)

Polyalphaolefin#2
18
PHR

(Mitsui Tafmer D605)

EVA #1 (USI 659)
40
PHR

EVA #2 (USI 3300)
5
PHR

Color MB (Janie Color Works)
11
PHR

TAC (Kettlitz TAC-GR50)
0.3
PHR

ZnO (Atman ZnO-80)
1
PHR

ZnStearate (PT Sumi 1801)
1
PHR

Azodicarbonamide
8.45
PHR

(Dongjing AC-D600MT)

Additives

Dicumyl peroxide
1.45
PHR

(Cosmo chem Colink-40)

Silane (Evermore Evisitant K1201)
0.35 PHR (0 PHR to 0.75 PHR)

The foam from Table 6 was tested with varying amounts of added silane from 0 to 0.75 parts per hundred resin and with added peroxide. The results are presented in Table 7, demonstrating that foams formed with 0.075 phr of added silane already demonstrate a greater than 15% reduction in the DIN abrasion loss with very little change in the hardness of the foam. Greater improvements can be seen with about 0.25 to 0.75 phr added silane, which produces foams with a greater than 40% reduction in the DIN abrasion loss as compared to the reference without added silane (0 PHR Silane). The foams including added silane exhibited a slight softening (decreased hardness) in the compression molded foams with added silane. However, this can be improved by adding additional free-radical initiator such as peroxide to increase the crosslink density. These foams still exhibited improved DIN abrasion loss while maintaining the high energy return.

TABLE 7

Asker C Hardness for injection molded (IP) and compression molded (CMP) foams,

specific gravity, and DIN abrasion loss measured according to the modified DIN

procedure for high energy return foam with varying amounts of added silane.

Modified DIN

IP
CMP
CMP
Average
Average
Average

Hardness
Hardness
Specific
Weight Loss
volume Loss
%

Sample
(Asker C)
(Asker C)
Gravity
(mg)
(mL)
loss

0 PHR Silane
34
44
0.2161
91.92
0.425
−25.81%

0.05 PHR Silane
35
44
0.2146
93.71
0.437
−25.85%

0.075 PHR Silane
34
42
0.2110
78.21
0.371
−21.69%

0.25 PHR Silane
33
38
0.2312
51.66
0.223
−14.47%

0.5 PHR Silane
35
38
0.2395
31.18
0.130
−8.36%

0.75 PHR Silane
32
37
0.1948
32.42
0.166
−8.73%

0.35 PHR w/ PO
34
44
0.2204
35.60
0.162
−10.23%

modification

It should be emphasized that the above-described aspects of the present disclosure are merely possible examples of implementations, and are set forth only for a clear understanding of the principles of the disclosure. Many variations and modifications may be made to the above-described aspects of the disclosure without departing substantially from the spirit and principles of the disclosure. All such modifications and variations are intended to be included herein within the scope of this disclosure.

Number	Name	Date	Kind
4910886	Sullivan et al.	Mar 1990	A
6207754	Yu	Mar 2001	B1
6225366	Raetzsch et al.	May 2001	B1
6303723	Sen et al.	Oct 2001	B1
6391438	Ramesh et al.	May 2002	B1
6555214	Yates	Apr 2003	B1
6599597	Bonk et al.	Jul 2003	B1
RE38993	Reedy	Feb 2006	E
7083849	Albrecht et al.	Aug 2006	B1
7105600	Kitano et al.	Sep 2006	B2
7506459	Grisoni et al.	Mar 2009	B2
7784197	Crane et al.	Aug 2010	B2
7810252	Stone et al.	Oct 2010	B2
7883769	Seth et al.	Feb 2011	B2
7941944	Cagliari	May 2011	B2
8008363	Mori et al.	Aug 2011	B2
8333903	Rolland et al.	Dec 2012	B2
8813392	Maron et al.	Aug 2014	B2
9080051	Peterson et al.	Jul 2015	B2
9260578	Su et al.	Feb 2016	B2
20050187355	Tasaka et al.	Aug 2005	A1
20050275127	Shih	Dec 2005	A1
20060154998	Shiba et al.	Jul 2006	A1
20060211819	Hoenig et al.	Sep 2006	A1
20060213600	Wu et al.	Sep 2006	A1
20060249417	Jones	Nov 2006	A1
20070129454	Su et al.	Jun 2007	A1
20070289162	Liu et al.	Dec 2007	A1
20080075914	Cheng	Mar 2008	A1
20080229623	Ferretti	Sep 2008	A1
20080271340	Grisoni et al.	Nov 2008	A1
20080289289	Wiercinski et al.	Nov 2008	A1
20090247656	Jacob et al.	Oct 2009	A1
20090275690	Weaver et al.	Nov 2009	A1
20100055358	Weaver et al.	Mar 2010	A1
20100099784	Su et al.	Apr 2010	A1
20100126042	Wyon	May 2010	A1
20110178195	Cheng	Jul 2011	A1
20110277351	Scoledes	Nov 2011	A1
20120317845	Vattes	Dec 2012	A1
20130055594	Hochart	Mar 2013	A1
20130101826	Haug et al.	Apr 2013	A1
20140013625	Grott et al.	Jan 2014	A1
20140068965	Vattes et al.	Mar 2014	A1
20140196306	Gill	Jul 2014	A1
20140331519	Campbell et al.	Nov 2014	A1
20150143723	Tateishi et al.	May 2015	A1
20150181975	Otsuka et al.	Jul 2015	A1
20150196085	Westmoreland et al.	Jul 2015	A1
20150225526	Tu et al.	Aug 2015	A1
20150257473	Liu et al.	Sep 2015	A1
20170119094	Vontorcik, Jr. et al.	May 2017	A1
20170215522	Tateishi et al.	Aug 2017	A1
20170267846	Baghdadi	Sep 2017	A1
20180022024	Saito et al.	Jan 2018	A1

Number	Date	Country
PI0701866	Dec 2008	BR
1813025	Aug 2006	CN
102031010	Apr 2011	CN
102171281	Aug 2011	CN
102532677	Jul 2012	CN
103192573	Jul 2013	CN
103205026	Jul 2013	CN
104403192	Mar 2015	CN
104448529	Mar 2015	CN
104910507	Sep 2015	CN
104927182	Sep 2015	CN
106117766	Nov 2016	CN
107108833	Aug 2017	CN
107501713	Dec 2017	CN
1457540	Sep 2004	EP
1880625	Jan 2008	EP
2508922	Oct 2012	EP
2695537	Feb 2014	EP
2818062	Dec 2014	EP
2873339	May 2015	EP
3111794	Jan 2017	EP
3202276	Aug 2017	EP
3244240	Nov 2017	EP
2993757	Jan 2014	FR
2411617	Sep 2005	GB
101904591	Dec 2010	IN
H11253201	Sep 1999	JP
2003073494	Mar 2003	JP
2007195944	Aug 2007	JP
2008109152	May 2008	JP
2012159589	Aug 2012	JP
2013028654	Feb 2013	JP
5719980	May 2015	JP
20060016112	Feb 2006	KR
101472929	Dec 2014	KR
109377	Oct 2011	RU
I257850	Jul 2006	TW
200628089	Aug 2006	TW
M297647	Sep 2006	TW
2002014423	Feb 2002	WO
03095657	Nov 2003	WO
2005000958	Jan 2005	WO
2006099631	Sep 2006	WO
2006102154	Sep 2006	WO
2008083451	Jul 2008	WO
2008152414	Dec 2008	WO
2012065333	May 2012	WO
2012092019	Jul 2012	WO
2013090174	Jun 2013	WO
2013150231	Oct 2013	WO
2017115840	Jul 2017	WO
2017160870	Sep 2017	WO
2017160874	Sep 2017	WO
2017160876	Sep 2017	WO
20180005295	Jan 2018	WO

	Number	Date	Country
Parent	16702207	Dec 2019	US
Child	17938701		US

High energy return foam compositions having improved abrasion resistance and uses thereof

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

Field of Search

CPC

International Classifications

Disclaimer

Abstract

Description

Claims

CROSS-REFERENCE TO RELATED APPLICATIONS

US Referenced Citations (55)

Foreign Referenced Citations (55)

Non-Patent Literature Citations (38)

Related Publications (1)

Provisional Applications (1)

Continuations (1)

Entry
Liu et al., “Structure analysis of ethylene/1-octene copolymers synthesized from living coordination polymerization,” European Polymer Journal 54 (2014), pp. 160-171.
Zhao et al., “Tuning the mechanical properties of weakly phase-separated olefin block copolymer by establishing co-crystallization structure with the aid of linear polyethylene; the dependence on molecular chain length,” CrystEngComm, 2017, 19, pp. 2884-2893.
John 0. Akindoyo, M. D. H. Beg, Suriati Ghazal!, M. R. Islam, Nitthiyah Jeyaratnama and A. R. Yuvarajc: “Polyurethane types, synthesis and applications a review”, RSC Advances, vol. 6, Nov. 24, 2016 (Nov. 24, 2016), pp. 114453-114482, XP002794407, DOI: 10.1039/C6RA14525F.
International Search Report and Written Opinion for PCT/US2017/022350 dated Jul. 18, 2017.
Karsli, G.; Aytac, A. “A study on compatibility of SEBS/EVA blends prepared by different techniques” Publisher: Huthig Verlag GmbH; v 64, n 7-8, p. 15-18, Jul.-Aug. 2011.
Yin, H. et al. “EVA/SEBS blends foaming technology” Publisher: Chengdu University of Science and Technology; Gaofenzi Cailiao Kexue Yu Gongcheng/Polymeric Materials Science and Engineering, v 25, n 8, p. 90-93, Aug. 2009 (Language: Chinese).
International Preliminary Report on Patentability for PCT/US2017/022350 dated Jun. 18, 2018.
Liu, C.; Lin, J. “Preparation of Super Light Foamed EVA” China Plastics, 2004, Issue 2, pp. 60-64.
Hydrogenated Styrenic Block Copolymer Offers Benefits for PSAs. ASI Adhesives and sealants, Mar. 20, 2003.
Kemaloglu, S. et al. “Thermally conductive boron nitride/SEBS/EVA ternary composites: Processing and characterization” Publisher: John Wiley and Sons Inc.; Polymer Composites, v 31, n 8, p. 1398-1408, Aug. 2010.
Larkin, J. B. “Block Copolymer Thermoplastic Rubbers: Their Properties and End Use Applications” SPE, p. 26-37, 1976; Conference: SPE Bicenten Reg Tech Conf, Plast in the Mid-Ohio Val, Nov. 30, 1976-Dec. 1, 1976.
Characterization of Ethylene Vinyl Acetate Copolymers by Dielectric Analysis, TA Instruments, https://www.tainstruments.com/pdf/.
Lippa, N. “Mechanical ageing protocol selection affects macroscopic performance and molecular level properties of ethylene vinyl acetate (EVA) running shoe midsole foam” Publisher: Elsevier Ltd; Conference: 2014 10th Conference of the International Sports Engineering Association; Procedia Engineering, v 72, p. 285-291, Jul. 2014.
Written Opinion of the International Preliminary Examining Authority for PCT/US2017/022359 dated Jan. 25, 2018.
International Preliminary Report on Patentability for PCT/US2017/022359 dated Jun. 14, 2018.
Written Opinion of the International Preliminary Examining Authority for PCT/US2017/022350 dated Jan. 23, 2018.
Data Sheet for Tuftec H1051. Asahi Kasei. 2017.
Data Sheet for Tuftec H1221. Asahi Kasei. 2017.
Hiroyuki, M.A.E. “Relationship of mechanical properties between neat PP/SEBS blends and syntactic pp/sebs foams with polymer microballoons” Publisher: Society of Materials Science Japan; v 57, n 12, p. 1253-1260, Dec. 2008.
Damani, A. G. “Polyblends of polystyrene and high impact polystyrene with styrene ethylene butylene styrene thermoplastic elastomer” University of Massachusetts Lowell, ProQuest Dissertations Publishing; MAI 35/04, p. 1058, Aug. 1997.
Sharudin, R. W. B. et al. “Preparation of microcellular thermoplastic elastomer foams from polystyrene-b-ethylene-butylene-b-polystyrene (SEBS) and their blends with polystyrene” Publisher: John Wiley and Sons Inc. Elastomers; Journal of Applied Polymer Science, v 128, n 4, p. 2245-2254, May 15, 2013.
International Preliminary Report on Patentability for PCT/US2019/035258 dated Jul. 13, 2020.
International Search Report and Written Opinion for PCT/US2017/022359 dated Jul. 18, 2017.
Ulug, E. et al. “Effects of HIPS on the mechanical, thermal and morphological properties of SEBS and SIS type elastomers”. 11th International Conference on the Mechanical Behavior of Materials; Procedia Engineering, v 10, p. 3092-3097, 2011.
Schroeder, P. et al. “Gear lever in hand: Two component concept for private cars” Kunststoffe Plast Europe, v 92, n 3, p. 41-42+122-123, Mar. 2002 (Language: German).
International Search Report and Written Opinion for PCT/US2019/035258 dated Oct. 8, 2019.
Phinyocheep, P. et al. “Influence of compatibilizers on mechanical properties, crystallization, and morphology of polypropylene/scrap rubber dust blends” Journal of Applied Polymer Science, v 86, n 1, p. 148-159, Oct. 3, 2002.
Written Opinion of the International Preliminary Examining Authority for PCT/US2017/022356 dated Jan. 29, 2018.
Wang, Y. et al. “SEBS modified reclaimed rubber microcellular foaming material as the sole of the shoe” Publisher: Chengdu University of Science and Technology; Gaofenzi Cailiao Kexue Yu Gongcheng/Polymeric Materials Science and Engineering, v 26, n 12, p. 148-151, Dec. 2010 (Language: Chinese).
International Search Report for PCT/US/2019/064267 dated Feb. 18, 2020.
International Preliminary Report on Patentability for PCT/US2017/022356 dated Jun. 14, 2018.
Tafmer, Alpha olefin copolymer, DF series, Mitsubishi Chem., 2010.
Data Sheet for Tuftec H1062. Asahi Kasei. 2017.
Data Sheet for Tuftec H1052. Asahi Kasei. 2017.
International Search Report and Written Opinion for PCT/US2017/022356 dated Jul. 18, 2017.
Kuraray “Septon Hybar Thermoplastic Elastomers Technical Information,” 2017.
Maiti, M. “Microcellular foam from ethylene vinyl acetate/polybutadiene rubber (EVA/BR) based thermoplastic elastomers for footwear applications” Industrial and Engineering Chemistry Research, v 51, n 32, p. 10607-10612, Aug. 15, 2012.
Written Opinion of the International Preliminary Examining Authority for PCT/US2019/035258 dated Apr. 30, 2020.