The subject matter disclosed herein relates to multilayer film structure. More particularly, to a multilayer film structure having a cohesive layer that bonds to adjacent layers with a force greater than the force to cause cohesive failure within the cohesive layer.
The cohesive layer adheres to dissimilar layers without the need for an intervening tie layer. The adhesion of the cohesive layer to the dissimilar layers is stronger than the opening strength required to cause cohesive failure within the cohesive layer.
The discussion above is merely provided for general background information and is not intended to be used as an aid in determining the scope of the claimed subject matter.
A cohesive sealant layer directly adhered to two adjacent layers. One adjacent layer comprising predominately polyester. The other adjacent layer comprising predominately polyethylene polymers. The cohesive sealant layer being a blend including polyester and at least a compatibilizer such that the cohesive sealant layer has an opening strength of between 0.4 and 3.4 lb-f/in or between 0.9 and 3.0 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample. The cohesive sealant layer having a bond strength to both of the adjacent layers which is greater than the opening strength resulting in in a continuous portion of the cohesive sealant layer remaining adhered to the two adjacent layers when subjected to a force greater than the opening strength
An advantage that may be realized in the practice of some disclosed embodiments of the cohesive sealant layer is that the cohesive failure can be achieved without an intra-layer failure within a structure.
In one exemplary embodiment, a multilayer package is disclosed. The multilayer package comprises a first layer comprising predominately polyester. The package further comprises a second layer comprising predominately polyethylene polymers. A cohesive sealant layer is directly adhered to the first and second layers. The sealant layer comprises between 35-65 wt % polyester; and between 5-65 wt % compatibilizer. The cohesive sealant layer has an opening strength of between 0.4 and 3.4 lb-f/in or between 0.9 and 3.0 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample and the cohesive sealant layer has a bond strength to both of the first and second layer which is greater than the opening strength resulting in in a continuous portion of the cohesive sealant layer remaining adhered to both the first layer and the second layer when subjected to a force greater than the opening strength.
In another exemplary embodiment, the multilayer structure comprises a flexible film comprising an inner layer comprising predominately polyethylene polymers. The structure includes a rigid or semi-rigid insert comprising a layer comprising predominately polyester. The structure further includes a cohesive sealant layer having two sides which are direct adhered to the inner layer of the flexible film on one side and direct adhered to the layer comprising predominately polyester of the rigid or semi-rigid insert on the other side. The cohesive sealant layer comprising between 25-65 wt % polyester; and between 5-65 wt % compatibilizer. The cohesive sealant layer has an opening strength of between 0.4 and 3.4 lb-f/in or between 0.9 and 3.0 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample and the cohesive sealant layer has a bond strength to both of the inner layer of the flexible film and the layer comprising predominately polyester of the rigid or semi-rigid insert which is greater than the opening strength resulting in in a continuous portion of the cohesive sealant layer remaining adhered to both the inner layer of the flexible film and the layer comprising predominately polyester of the rigid or semi-rigid insert when subjected to a force greater than the opening strength.
In another exemplary embodiment, a method of making a multilayer package is disclosed. The method comprises the steps of i) providing a first layer comprising predominately polyester ii) providing a second layer comprising predominately polyethylene polymers iii) providing a multilayer film comprising a cohesive sealant layer and one of the first layer or the second layer; and iv) heat sealing the cohesive sealant layer to the other of the first layer or the second layer that is not part of the multilayer film. The cohesive sealant layer comprises between 35-65 wt % polyester; and 5-65 wt % compatibilizer. The cohesive sealant layer has an opening strength of between 0.4 and 3.4 lb-f/in or between 0.9 and 3.0 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample and the cohesive sealant layer has a bond strength to both of the first and second layer which is greater than the opening strength resulting in in a continuous portion of the cohesive sealant layer remaining adhered to both the first layer and the second layer when subjected to a force greater than the opening strength.
This brief description of the invention is intended only to provide a brief overview of subject matter disclosed herein according to one or more illustrative embodiments, and does not serve as a guide to interpreting the claims or to define or limit the scope of the invention, which is defined only by the appended claims. This brief description is provided to introduce an illustrative selection of concepts in a simplified form that are further described below in the detailed description. This brief description is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used as an aid in determining the scope of the claimed subject matter. The claimed subject matter is not limited to implementations that solve any or all disadvantages noted in the background.
So that the manner in which the features of the invention can be understood, a detailed description of the invention may be had by reference to certain embodiments, some of which are illustrated in the accompanying drawings. It is to be noted, however, that the drawings illustrate only certain embodiments of this invention and are therefore not to be considered limiting of its scope, for the scope of the invention encompasses other equally effective embodiments. The drawings are not necessarily to scale, emphasis generally being placed upon illustrating the features of certain embodiments of the invention. In the drawings, like numerals are used to indicate like parts throughout the various views. Thus, for further understanding of the invention, reference can be made to the following detailed description, read in connection with the drawings in which:
As used herein, the term “film” is inclusive of plastic web, regardless of whether it is film or sheet. The film can have a thickness of 0.25 mm or less, or a thickness of from 0.5 to 30 mils, or from 0.5 to 15 mils, or from 1 to 10 mils, or from 1 to 8 mils, or from 1.1 to 7 mils, or from 1.2 to 6 mils, or from 1.3 to 5 mils, or from 1.5 to 4 mils, or from 1.6 to 3.5 mils, or from 1.8 to 3.3 mils, or from 2 to 3 mils, or from 1.5 to 4 mils, or from 0.5 to 1.5 mils, or from 1 to 1.5 mils, or from 0.7 to 1.3 mils, or from 0.8 to 1.2 mils, or from 0.9 to 1.1 mils.
The multi-layer films described herein may comprise at least, and/or at most, any of the following numbers of layers: 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 and 15. As used herein, the term “layer” refers to a discrete film component which is substantially coextensive with the film and has a substantially uniform composition. Where two or more directly adjacent layers have essentially the same composition, then these two or more adjacent layers may be considered a single layer for the purposes of this application. In an embodiment, the multilayer film utilizes microlayers. A microlayer section may include between 10 and 1,000 microlayers in each microlayer section.
The multi-layer films described herein include a cohesive layer that is directly adhered to a first layer on one side and second layer on the other side. The first and second layers being dissimilar compositions. The cohesive layer bonds to the first and second layer with a strength greater than the intra-film cohesive strength of the cohesive layer. The cohesive failure leaves portions of the cohesive layer still adhered to the first and second layer. The films may further include additional layers, for example to add bulk, provide functionality, abuse resistance, printing capability or to act as a tie layer.
As used herein, the phrase “directly adhered” or “directly adhering”, as applied to film layers, is defined as adhesion of the subject film layer to the object film layer, without a tie layer, adhesive, or other layer there between.
As used herein, the term “bond-strength” refers generally to the adhesive force with which two adjacent films, or two adjacent film layers, are connected and, more specifically, to the force with which two films are connected by a heat-weld. Bond-strength can be measured by the force required to separate two films or film layers that are connected, e.g., via a heat-weld, in accordance with ASTM F88.
As used herein, the term “intra-film cohesive strength” refers to the internal force with which a film remains intact, as measured in a direction that is perpendicular to the plane of the film. In a multilayer film, intra-film cohesive strength is provided both by inter-layer adhesion (the adhesive strength between the layers which binds them to one another) and by the intra-layer cohesion of each film layer (i.e., the cohesive strength of each of the film layers). In a monolayer film, intra-film cohesive strength is provided only by the intra-layer cohesion of the layer which constitutes the film.
As used herein, the term “opening strength” refers to the amount of force required to cause intra-film cohesive failure within a layer of a multilayer film measured in accordance to the methods described herein and with ASTM F88.
All compositional percentages used herein are presented on a “by weight” basis, unless designated otherwise.
Turning now to
The pouch 100 includes a first panel 104 and a second panel 106 that are sealed together about the pouch perimeter with one or more perimeter seals. Perimeter seals can be formed using any suitable method, known and used in the art, such as by the use of heat, pressure, adhesive, and/or mechanical closure. In the depicted embodiment, the perimeter seals include a transverse seal 108 and a channel seal 110. The transverse seal 108 extends directly between longitudinal sides of the pouch 100 to seal one end of the pouch 100. The channel seal 110 extends indirectly between longitudinal sides of the pouch 100 to seal the other end of the pouch 100. The channel seal 110 is shaped to form a tip 112 from which the product 102 can be dispensed. The pouch 100 includes a main section 114 and a channel section 116. The main section 114 is generally the portion of the pouch 100 between the transverse seal 108 and the channel seal 110. The channel section 116 is generally the portion of the pouch 100 between the start of the channel seal 110 and the tip 112.
In
In
The pouch 100 may be a convenient package for storing the product 102 before the product 102 is dispensed. The pouch 100 may also be convenient for a user to hold while dispensing the product 102 from the pouch 100. The pouch 100 is also capable of being used to hold and dispense products of different viscosities (e.g., viscoelastic substances, Newtonian fluids, and non-Newtonian fluids). The pouch 100 is also capable of being used to hold and dispense products that are uniform (e.g., water, ketchup, etc.) and non-uniform (e.g., tartar sauce, salsa, pickle relish, etc.).
In embodiments, the first and second layers each have a bond-strength to cohesive sealant layer which is greater than the intra-film cohesive strength of cohesive sealant layer. In this manner, cohesive sealant layer delaminates within itself when applying a sufficient force. By causing cohesive failure in this fashion a fluid pathway is formed that allows for the fluid product to exit the package. The fluid contacting both portions of the cohesive sealant layer as traveling through the fluid pathway.
In embodiments, peeling of the film 28 is initiated by grasping and pulling the film 28 in the direction of the arrow. The pulling creates a force upwards, causing the cohesive sealant layer 38′ and 38″ to cohesively fail.
In embodiments, the product 16 is a food product. In embodiments the food product is a meat product.
Cohesive Sealant Layer
The cohesive sealant layer is directly adhered to the first and second layers. The cohesive layer comprises a blend of polymers that allow for good inter-layer bond strength to adjacent layers and a lower intra-film cohesive strength.
Inter-layer bond strength is the amount of force required to separate or delaminate two adjacent film layers by adhesive failure, as measured in accordance with ASTM F88 where the Instron tensile tester crosshead speed is 10 inches per minute, using six, 1-inch wide, representative samples. As used herein, an “adhesive failure” is a failure in which the interfacial forces (e.g., valence forces or interlocking action or both) holding two surfaces together are overcome. A “cohesive failure” is one in which the molecular attractive forces holding together a layer composition are overcome.
The blend of polymers which forms the cohesive sealant layer includes between 2-75 wt %, 35-65 wt %, 40-60 wt % or 45-55 wt % polyester; and between 5-65 wt %, 15-60 wt %, 20-55 wt % or 25-50 wt % of a compatibilizer. Useful polyesters include, but are not limited to polyethylene terephthalate, polyethylene terephthalate copolymers, amorphous polyethylene terephthalate, recycled polyethylene terephthalate, polyethylene terephthalate glycol-modified, crystallizable polyethylene terephthalate. In embodiments, the polyester is selected from polyethylene terephthalate, polyethylene terephthalate glycol-modified or blends thereof.
In embodiments, the cohesive sealant layer further includes between 5-40 wt %, 10-35 wt % or 15-30 wt % of a polyethylene polymer, or blend of polyethylene polymers. Polyethylene polymers as used herein include ethylene/alpha-olefin copolymer, polyethylene homopolymers and polyethylene copolymers.
The polyethylene polymers may be either heterogeneous or homogeneous. As is known in the art, heterogeneous polymers have a relatively wide variation in molecular weight and composition distribution. Heterogeneous polymers may be prepared with, for example, conventional Ziegler Natta catalysts.
Homogeneous polymers are typically prepared using metallocene or other single site-type catalysts. Such single-site catalysts typically have only one type of catalytic site, which is believed to be the basis for the homogeneity of the polymers resulting from the polymerization. Homogeneous polymers are structurally different from heterogeneous polymers in that homogeneous polymers exhibit a relatively even sequencing of comonomers within a chain, a mirroring of sequence distribution in all chains, and a similarity of length of all chains. As a result, homogeneous polymers have relatively narrow molecular weight and composition distributions. Examples of homogeneous polymers include the metallocene-catalyzed linear homogeneous ethylene/alpha-olefin copolymer resins available from the Exxon Chemical Company (Baytown, Tex.) under the EXACT trademark, linear homogeneous ethylene/alpha-olefin copolymer resins available from the Mitsui Petrochemical Corporation under the TAFMER trademark, and long-chain branched, metallocene-catalyzed homogeneous ethylene/alpha-olefin copolymer resins available from the Dow Chemical Company under the AFFINITY trademark.
Homopolymer refers to a polymer resulting from the polymerization of a single monomer, i.e., a polymer consisting essentially of a single type of repeating unit. Copolymer refers to polymers formed by the polymerization reaction of at least two different monomers. For example, the term copolymer also includes terpolymers.
Polyethylene homopolymer or copolymer refers to ethylene homopolymer such as low density polyethylene; ethylene/alpha olefin copolymer such as those defined hereinbelow; and other ethylene copolymers such as ethylene/vinyl acetate copolymer; ethylene/alkyl acrylate copolymer; or ethylene/(meth)acrylic acid copolymer.
Ethylene/alpha-olefin copolymer herein refers to copolymers of ethylene with one or more comonomers selected from C4 to C12 alpha-olefins such as butene-1, hexene-1, octene-1, etc. in which the molecules of the copolymers comprise long polymer chains with relatively few side chain branches arising from the alpha-olefin which was reacted with ethylene. This molecular structure is to be contrasted with conventional high pressure low or medium density polyethylenes which are highly branched with respect to ethylene/alpha-olefin copolymers and which high pressure polyethylenes contain both long chain and short chain branches. Ethylene/alpha-olefin copolymers include one or more of the following: 1) high density polyethylene, for example having a density greater than 0.94 g/cm3, 2) medium density polyethylene, for example having a density of from 0.93 to 0.94 g/cm3, 3) linear medium density polyethylene, for example having a density of from 0.926 to 0.94 g g/cm3, 4) low density polyethylene, for example having a density of from 0.915 to 0.939 g/cm3, 5) linear low density polyethylene, for example having a density of from 0.915 to 0.935 g/cm3, 6) very-low or ultra-low density polyethylene, for example having density below 0.915 g/cm3, and homogeneous ethylene/alpha-olefin copolymers. Homogeneous ethylene/alpha-olefin copolymers include those having a density of less than about any of the following: 0.925, 0.922, 0.92, 0.917, 0.915, 0.912, 0.91, 0.907, 0.905, 0.903, 0.90, and 0.86 g/cm3. Unless otherwise indicated, all densities herein are measured according to ASTM D1505.
Useful compatibilizers include in the context of the present disclosure are those generally useful to bind to polyester such as ethylene vinyl acetate, ethylene methyl acrylate, ionomer or ethylene butyl acrylate. It is understood that variants of the previously listed compatibilizers are contemplated, for example, maleic anhydride grafted compatibilizers. In some embodiments, the compatibilizer is ethylene vinyl acetate or ethylene methyl acrylate.
As used herein, the term “ionomer” (Io) refers to the ionized or partially ionized form of a copolymer of ethylene with a copolymerisable ethylenically unsaturated carboxylic acid monomer selected from acrylic acid and methacrylic acid wherein the neutralizing cation can be any suitable metal ion, e.g. an alkali metal ion, a zinc ion, or other multivalent metal ions.
In embodiments the cohesive sealant layer has an opening strength of between 0.4 and 3.4 lb-f/in or between 0.9 and 3.0 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample. In other embodiments the cohesive sealant layer has an opening strength of at least 0.9 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample. In other embodiments the cohesive sealant layer has an opening strength of at not more than 1.6 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample. The cohesive sealant layer has a bond strength to adjacent layers that is greater than the opening strength resulting in in a continuous portion of the cohesive sealant layer remaining bonded to both adjacent layers when subjected to a force greater than the opening strength.
The thickness of the cohesive sealant layer may be selected to provide sufficient material result in a strong seal bond and to provide good peelability, yet not so thick so as to negatively affect the characteristics of the film to an unacceptable level. The cohesive sealant layer may have a thickness of at least any of the following values: 0.3 mils, 0.35 mils, 0.4 mils, 0.45 mils, 0.5 mils, and 0.6 mils. The cohesive sealant layer may have a thickness less than any of the following values: 5 mils, 4 mils, 3 mils, 2 mils, 1 mil, 0.7 mils, 0.5 mils, and 0.3 mils. The thickness of the cohesive sealant layer as a percentage of the total thickness of the film may be less that any of the following values: 50%, 40%, 30%, 25%, 20%, 15%, 10%, and 5%; and may range between any of the forgoing values (e.g., from 10% to 30%).
First Layer
The first layer which is adhered to the cohesive sealant layer is predominately a polyester. The first layer may be a rigid or semi-rigid tray, a rigid or semi-rigid insert a flexible film or a support member such as a tray. In embodiments, the first layer comprises at least 90 wt %, 92 wt %, 94 wt %, 96 wt %, 98 wt %, or greater than 99 wt % of a polyester.
Polyesters are polymers obtained by the polycondensation reaction of dicarboxylic acids with dihydroxy alcohols. Suitable dicarboxylic acids are, for instance, terephthalic acid, isophthalic acid, 2,6-naphthalene dicarboxylic acid and the like. Suitable dihydroxy alcohols are for instance ethylene glycol, diethylene glycol, 1,4-butanediol, 1,4-cyclohexanedimethanol and the like. Examples of useful polyesters include poly(ethylene 2,6-naphtalate), poly(ethylene terephthalate), and copolyesters obtained by reacting one or more dicarboxylic acids with one or more dihydroxy alcohols, such as polyethylene terephthalate glycol which is an amorphous co-polyesters of terephthalic acid with ethylene glycol and 1,4-cyclohexanedimethanol.
Useful polyesters include, but are not limited to polyethylene terephthalate, polyethylene terephthalate copolymers, amorphous polyethylene terephthalate, recycled polyethylene terephthalate, polyethylene terephthalate glycol-modified, crystallizable polyethylene terephthalate. In embodiments, the polyester is selected from polyethylene terephthalate, polyethylene terephthalate glycol-modified or blends thereof.
The thickness of the first layer may be selected to provide sufficient rigidity to the film structure or to support a product, but not so thick as to negatively affect the characteristics of the film to an unacceptable level. The first layer may have a thickness of at least any of the following values: 0.3 mils, 0.35 mils, 0.4 mils, 0.45 mils, 0.5 mils, and 0.6 mils. The first layer may have a thickness less than any of the following values: 25 mils, 20 mils, 15 mils, 14 mils, 13 mils, 12 mils, 11 mils, 10 mils, 9 mils, 8 mils, 7 mils, 6 mils, 5 mils, 4 mils, 3 mils, 2 mils, 1 mil, 0.7 mils, 0.5 mils, and 0.3 mils. The thickness of the first layer as a percentage of the total thickness of the film may be less that any of the following values: 80%, 70%, 60%, 50%, 40%, 30%, 25%, 20%, 15%, 10%, and 5%; and may range between any of the forgoing values (e.g., from 10% to 30%).
The first layer may be part of a multilayer structure such as depicted in
Second Layer
The second layer which is adhered to the cohesive sealant layer is predominately a polyethylene polymer. Polyethylene polymers do not seal well to polyester and therefore an intermediate layer is needed to create an effective seal. In embodiments, the second layer is a flexible film or a layer in a multilayer film. In embodiments, the first layer comprises at least 90 wt %, 92 wt %, 94 wt %, 96 wt %, 98 wt %, or over 99 wt % of a polyethylene polymer as described herein.
In embodiments, the polyethylene polymer is a high density polyethylene, medium density polyethylene, linear medium density polyethylene, low density polyethylene, linear low density polyethylene, or very-low or ultra-low density polyethylene.
In embodiments, the second layer is flexible film. The flexible film may be a monolayer or multilayer film so long as an outside layer of the flexible film is predominately a polyethylene polymer as described herein. In an embodiment, the flexible film forms a pouch with the second layer defining the pouch or the inner portion of the pouch.
The second layer may include one or more additives useful in packaging films, such as, antiblocking agents, slip agents, antifog agents, colorants, pigments, dyes, flavorants, antimicrobial agents, meat preservatives, antioxidants, fillers, radiation stabilizers, and antistatic agents. Such additives, and their effective amounts, are known in the art.
The second layer may have a thickness of at least any of the following values: 0.3 mils, 0.35 mils, 0.4 mils, 0.45 mils, 0.5 mils, and 0.6 mils. The second layer may have a thickness less than any of the following values: 5 mils, 4 mils, 3 mils, 2 mils, 1 mil, 0.7 mils, 0.5 mils, and 0.3 mils. The thickness of the second layer as a percentage of the total thickness of the film may be less that any of the following values: 50%, 40%, 30%, 25%, 20%, 15%, 10%, and 5%; and may range between any of the forgoing values (e.g., from 10% to 30%).
Additional Layers of the Film
The multilayer film may include one or more additional layers, such as a tie, core, or bulk layers. A tie layer is an inner film layer having the primary purpose of adhering two layers of a film together.
A core or bulk layer may be an inner film layer having a primary purpose other than as a barrier or tie layer—for example, serving to provide a multilayer film with a desired level of strength, modulus, or optics.
One or more layers of the films may include one or more additives useful in packaging films, such as, antiblocking agents, slip agents, antifog agents, colorants, pigments, dyes, flavorants, antimicrobial agents, meat preservatives, antioxidants, fillers, radiation stabilizers, and antistatic agents. Such additives, and their effective amounts, are known in the art.
One or more of the layers of the films—or at least a portion—may be cross-linked to improve the strength of the film, improve the orientation of the film, and help to avoid burn through during heat seal operations. Cross-linking may be achieved by using chemical additives or by subjecting one or more film layers to one or more energetic radiation treatments-such as ultraviolet, X-ray, gamma ray, beta ray, and high energy electron beam treatment—to induce cross-linking between molecules of the irradiated material. Useful radiation dosages include at least about any of the following: 5, 7, 10, 15, 20, 25, 30, 35, 40, 45, and 50 kGy (kiloGrey). Useful radiation dosages include less than about any of the following: 130, 120, 110, 100, 90, 80, and 70 kGy (kiloGrey). Useful radiation dosages include any of the following ranges: from 5 to 150, from 10 to 130, from 5 to 100, and from 5 to 75 kGy.
All or a portion of one or two surfaces the film may be corona and/or plasma treated to change the surface energy of the film, for example, to increase the ability to print or laminate the film. One type of oxidative surface treatment involves bringing the sealant film into the proximity of an O2- or N2-containing gas (e.g., ambient air) which has been ionized. Exemplary techniques are described in, for example, U.S. Pat. No. 4,120,716 (Bonet) and U.S. Pat. No. 4,879,430 (Hoffman), which are incorporated herein in their entirety by reference. The film may be treated to have a surface energy of at least about 0.034 J/m2, at least about 0.036 J/m2, at least about 0.038 J/m2, and at least about 0.040 J/m2.
The film may each be separately manufactured by thermoplastic film-forming processes known in the art (e.g., tubular or blown-film extrusion, coextrusion, extrusion coating, flat or cast film extrusion). A combination of these processes may also be employed.
The resulting inter-layer bond strength between the cohesive sealant layer and the first and second layers is sufficiently strong to withstand the expected use conditions. For example, the inter-layer bond strength must be greater than the intra-film cohesive strength of the cohesive sealant layer. In embodiments the cohesive sealant layer has an intra-film cohesive strength of not more than 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20% or 10% of the bond strength of the cohesive sealant layer to both of the first and second layer as measured in accordance with ASTM F88 where the Instron tensile tester crosshead speed is 10 inches per minute and a 1-inch wide sample.
The weakest point of any of the inter-layer bond strength between adjacent layers and the intra-layer cohesive strength of the layers is located within the cohesive sealant layer.
In embodiments, the multilayer film is non-oriented. The term “non-oriented: refers to films that had not been subjected to any orientation process, also known as “cast films”.
As used herein the term “orientation process” relates to stretching the coextruded tape or tube in at least one or in two perpendicular directions, typically the longitudinal or machine direction (MD) and the transverse or crosswise direction (TD), at a temperature higher than the highest Tg of the resins making up the film layers and lower than the highest melting point of at least one polymer of the film layers, namely at a temperature where the resins, or at least some of the resins, are not in the molten state.
In embodiments, the multilayer film is a non-oriented, non heat-shrinkable film. Such films have not been oriented by stretching under temperature conditions, as indicated above. Upon subsequent reheating, the non-oriented, non heat-shrinkable film will not or will minimally shrink in seeking to recover its original dimensional state as an oriented, heat-shrinkable film does.
In embodiments, the multilayer film is non heat-shrinkable. As used herein “non heat-shrinkable” refers to a film having a free shrink percentage (as measured by ASTM D 2732, at 95° C.) in both the machine and transverse directions of less than 15%, less than 10% or less than 5%. As used herein, the phrases “heat-shrinkable,” “heat-shrink,” and the like, refer to the tendency of the film to shrink upon the application of heat, i.e., to contract upon being heated, such that the size of the film decreases while the film is in an unrestrained state. As used herein said term refer to films with a free shrink in each of the machine and the transverse directions, as measured by ASTM D 2732, of at least 5% at 95° C.
Fluid Dispensing Device
In an embodiment as depicted in
The pouch 200 has a product (not shown) disposed therein. The pouch 200 includes a first panel 204 and a second panel 206 that are sealed together about the pouch perimeter with one or more perimeter seals. While the first panel 204 and second panel 206 are depicted as distinct panels, it is understood that a single film can be used to construct the pouch 200 with a single perimeter seal, end seal, side seal or could be formed from tubing. In the depicted embodiment, the perimeter seals include a channel seal 210. The channel seal 210 is shaped to form a tip 212 from which the product can be dispensed. The tip 212 may be centered as depicted, off set, adjacent to an end of the pouch.
The channel section of the pouch 200 includes a valve 224 with an insert (shown in more detail in
In the first instance shown in
In the second instance shown in
In the third instance shown in
In the fourth instance depicted in
In the fifth instance shown in
In the series of the first to fifth instances shown in
For the product to be dispensed from the pouch 200, the pressure induced in the product by an external force will exceed a threshold that causes the curve in the valve 224 to straighten at least partially. A number of variables impact the ease or difficulty to sufficiently straighten the valve 224. Among those variables are the modulus of the films, the rigidity of the insert, the diameter of the curve of the valve 224, and the thickness of the material of the film(s).
Turning now to
Depicted in
Method
A method of making a multilayer package from the multilayer film is contemplated. In embodiments, the method includes i) providing a first layer comprising predominately polyester ii) providing a second layer comprising predominately polyethylene polymers iii) providing a multilayer film comprising a cohesive sealant layer and one of the first layer or the second layer; and iv) heat sealing the cohesive sealant layer to the other of the first layer or the second layer that is not part of the multilayer film. The cohesive sealant layer comprises between 35-65 wt % polyester; and between any of 5-75 wt % or 10-65 wt % compatibilizer. The cohesive sealant layer has an opening strength of between 0.4 and 3.4 lb-f/in or between 0.9 and 3.0 lb-f/in measured according to ASTM F88 with a crosshead speed of 10 inches per minute, using a 1-inch wide sample and the cohesive sealant layer has a bond strength to both of the first and second layer which is greater than the opening strength resulting in in a continuous portion of the cohesive sealant layer remaining adhered to both the first layer and the second layer when subjected to a force greater than the opening strength.
The following examples are presented for the purpose of further illustrating and explaining the present invention and are not to be taken as limiting in any regard.
In the comparatives and examples below, the following materials were used:
PETG1 is polyethylene terephthalate glycol-modified.
PETG2 is polyethylene terephthalate glycol-modified.
PE1 is a linear low density ethylene/hexene copolymer.
PE2 is a commercially available film having an enhanced sealant layer sold by Sealed Air under the trade name FS5535.
EVA1 is an ethylene/vinyl acetate copolymer having a vinyl acetate content of more than 20%.
EVA2 is an ethylene/vinyl acetate copolymer having a vinyl acetate content of less than 10%
Blends of the materials were mixed and dried prior to cast extrusion to create the films having a thickness of approximately 2 mils as shown in Table 1 below. The films being a two-layer film with one layer being the blend recited in Table 1 and the second layer being a polyethylene terephthalate glycol-modified layer (PETG2). After about 1 week, the films were sealed to PE2 in the following manner. The seal was made along the transverse directions of both the film made from blend and PE2. A seal bar was applied to seal the two films together with a pressure of 50 psi at heat of 320° F. for 0.6 s.
Six samples were prepared for each blend. After at least 24 hours, each sample was pulled in a peel arrangement using an Instron tensile tester with a crosshead speed of 10 inches per minute. The maximum amount of force required to cause a cohesive or adhesive failure either within laminate that was sealed to the support member or in the bond between the laminate and the support member was measured in accordance with ASTM F88. The results were averaged for each set of six sample and are shown in Tables 1 and 2 below.
As seen in Tables 1 and 2 above, films created within the specific range of materials resulted in a good cohesive failure within the layer made from the blend. Blend 2 has a delamination failure as the blend to do not bind well to the PETG2 layer. Blend 9 did not have a good adhesive seal to the PE2 layer and therefore had an adhesive failure before the layer made from the blend could cohesively fail.
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal language of the claims.
This application claims priority to U.S. Provisional Patent Application Ser. No. 63/052,479, filed Jul. 16, 2020 and entitled “Multilayer Structure Having A Cohesive Layer,” the entirety of which is incorporated herein by reference.
Filing Document | Filing Date | Country | Kind |
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PCT/US2021/041234 | 7/12/2021 | WO |
Number | Date | Country | |
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63052479 | Jul 2020 | US |