Macroporous, perforated films are commonly used for vapor and liquid permeable applications, whereas microporous perforated films are useful for vapor permeable applications, but not liquid permeable applications. Macroporous perforated films are commonly used as components in personal care garments (e.g., diapers and feminine hygiene products). Perforated films are also used in filtering, and acoustic applications.
Macroporous permeable films are commonly made by first producing a continuous film and then subjecting the film to a perforation process. Mechanical perforating devices include intermeshing rollers, die punching, or needlepunching. Films can also be perforated using perforated rollers having thermal zones or lasers that melt perforations into the film. Other techniques for providing the perforations include casting a film on to a porous quench roll that has vacuum on the holes to pull the melt into the hole and produce an aperture, using electrical corona treatment to create perforations by localized energy treatment, and creating perforations is by blending immiscible materials followed by film stretching to create perforations by generation of film voids. It is also known that after quenching polypropylene in to beta phase crystals, upon orientation, the film will become porous.
There exists a need for additional techniques, preferably relatively simple and economical, to make macroporous layers (including films and sheets).
In one aspect, the present disclosure describes a polymeric layer having first and second, generally opposed major surfaces, comprising an array of openings extending between the first and second major surfaces, wherein the openings each have a series of areas through the openings from the first and second major surfaces ranging from minimum to maximum areas, wherein there is a total area and a total open area for each of the first and second major surfaces, wherein the total open area for each of the first and second major surfaces is not greater than 50 (in some embodiments, not greater than 45, 40, 35, 30, 25, 20, 15, 10, 5, 4, 3, 2, 1, 0.75, 0.5, 0.25, or even not greater than 0.1; in some embodiments, in a range from 0.1 to not greater than 50, 0.1 to not greater than 45, 0.1 to not greater than 40, 0.1 to not greater than 35, 0.1 to not greater than 30, 0.1 to not greater than 25, 0.1 to not greater than 20, 0.1 to not greater than 15, 0.1 to not greater than 10, or even 0.1 to not greater than 5) percent of the total area of the respective major surface, and wherein for at least a majority of the openings, the minimum area is not at either major surface. In some embodiments, for at least a majority of the openings, the area of each opening is not greater than 5 (in some embodiments, not greater than 2.5, 2, 1, 0.5, 0.1, 0.05, 0.01, 0.075, or even not greater than 0.005) mm2.
In another aspect, the present disclosure describes a polymeric layer having first and second, generally opposed major surfaces, comprising an array of openings extending between the first and second major surfaces, wherein the openings each have a series of areas through the openings from the first and second major surfaces ranging from minimum to maximum areas, wherein for at least a majority of the openings, the area of each opening is not greater than is 5 (in some embodiments, not greater than 2.5, 2, 1, 0.5, 0.1, 0.05, 0.01, 0.075, or even not greater than 0.005) mm2, and wherein for at least a majority of the openings, the minimum area is not at either major surface.
In another aspect, the present disclosure describes a method of making a polymeric layer described herein, the method comprising at least one of passing through a nip or calendaring netting comprising an array of polymeric strands periodically joined together at bond regions throughout the array.
In another aspect, the present disclosure describes a method of making a polymeric layer having openings therein, the method comprising at least one of passing through a nip or calendaring a netting comprising an array of polymeric strands periodically joined together at bond regions throughout the array, wherein the netting has a thickness up to 2 mm (in some embodiments, up to 1.5 mm, 1 mm, 750 micrometers, 500 micrometers, 250 micrometers, 100 micrometers, 75 micrometers, 50 micrometers, or even up to 25 micrometers; in a range from 10 micrometers to 2 mm, 10 micrometers to 1.5 mm, 10 micrometers to 1 mm, 10 micrometers to 750 micrometers, 10 micrometers to 750 micrometers, 10 micrometers to 500 micrometers, 10 micrometers to 250 micrometers, 10 micrometers to 100 micrometers, 10 micrometers to 75 micrometers, 10 micrometers to 50 micrometers, or even 10 micrometers to 25 micrometers).
Polymeric layers described herein are useful, for example, as components in personal care garments such as diapers and feminine hygiene products. They can also be useful for filtering (including liquid filtering) and acoustic applications.
Referring to
As shown, polymeric netting 24 is extruded vertically, into nip 40. Nip 40 includes backup roll 42, and nip roll 44. In some embodiments, backup roll 42 is a smooth, chrome-plated steel roll and nip roll 44 is a silicone rubber roll. In some embodiments, both backup roll 42 and nip roll 44 are temperature controlled with, for example, internal water flow.
In some embodiments, for example the one depicted here, polymeric netting 24 passes directly into nip 40, and nip 40 is a quench nip. However, this is not considered necessary, and the extrusion of the netting and the entry into the nip need not be immediately sequential.
After passing through nip 40, polymeric netting 24 has been transformed into polymeric layer having openings therein 50. In some embodiments, it may be advantageous to allow polymeric layer 50 to remain wrapped around backup roll 42 for at least a portion of its circumference. Polymeric layer 50 has first major surface 52 on the side towards the viewer, and second major surface 54 on the side opposite from the viewer. Numerous openings 56 pass through polymeric layer 50 from first major surface 52 to second major surface 54. In some embodiments, openings 56 have well-formed, smooth edges 58. Further, in some embodiments, openings 56 taper inwards from both first major surface 52 and second major surface 54 so that opening 56 has a minimum area 60 somewhere in the interior of polymeric layer 50.
These features of openings 56 can be better appreciated in
As mentioned above, diverse types of netting, produced by any of a variety of techniques may be used in connection to make the polymeric layers having openings therein as described herein. However, extruders 22 that were employed to prepare the Examples recited below will be described with more particularity. Referring to
Referring now to
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In some embodiments, it may be desirable to pattern one side or both sides of the layer. This can be achieved, for example, using patterning the surface of one or both of nip roller 44 and backup roller 42. It has been shown in the field of polymeric hook forming that the use of patterned rolls can preferentially move polymer in the cross direction or downweb direction. This concept can be used to shape the hole on one or both sides of the layer.
Exemplary polymeric materials from which the netting can be made includes thermoplastic resins comprising polyolefins (e.g., polypropylene and polyethylene), polyvinyl chloride, polystyrene, nylons, polyesters (e.g., polyethylene terephthalate) and copolymers and blends thereof; elastomeric materials (e.g., ABA block copolymers, polyurethanes, polyolefin elastomers, polyurethane elastomers, metallocene polyolefin elastomers, polyamide elastomers, ethylene vinyl acetate elastomers, and polyester elastomers); adhesives such as acrylate copolymer pressure sensitive adhesives, rubber based adhesives (e.g., those based on natural rubber, polyisobutylene, polybutadiene, butyl rubbers, and styrene block copolymer rubbers), adhesives based on silicone polyureas or silicone polyoxamides, polyurethane type adhesives, and poly(vinyl ethyl ether), and copolymers or blends of these. Other desirable materials include, for example, styrene-acrylonitrile, cellulose acetate butyrate, cellulose acetate propionate, cellulose triacetate, polyether sulfone, polymethyl methacrylate, polyurethane, polyester, polycarbonate, polyvinyl chloride, polystyrene, polyethylene naphthalate, copolymers or blends based on naphthalene dicarboxylic acids, polyolefins, polyimides, mixtures and/or combinations thereof.
In some embodiments, netting used to make polymeric layers described herein include alternating first and second polymeric strands, wherein the second polymeric strands comprise a second, different polymer.
In some embodiments, polymeric materials of nettings used to make polymeric layers described herein comprise a colorant (e.g., pigment and/or dye) for functional (e.g., optical effects) and/or aesthetic purposes (e.g., each has different color/shade). Suitable colorants are those known in the art for use in various polymeric materials. Exemplary colors imparted by the colorant include white, black, red, pink, orange, yellow, green, aqua, purple, and blue. In some embodiments, it is desirable level to have a certain degree of opacity for one or more of the polymeric materials. The amount of colorant(s) to be used in specific embodiments can be readily determined by those skilled in the (e.g., to achieve desired color, tone, opacity, transmissivity, etc.). If desired, the polymeric materials may be formulated to have the same or different colors. When colored strands are of a relatively fine (e.g., less than 50 micrometers) diameter, the appearance of the web may have a shimmer reminiscent of silk.
In some embodiments, the polymeric strands have an average width in a range from 10 micrometers to 500 micrometers (in a range from 10 micrometers to 400 micrometers, or even 10 micrometers to 250 micrometers).
In some embodiments, nettings used to make polymeric layers described herein have a basis weight in a range from 5 g/m2 to 400 g/m2 (in some embodiments, 10 g/m2 to 200 g/m2).
In some embodiments, nettings used to make polymeric layers described herein have a strand pitch in a range from 0.5 mm to 20 mm (in some embodiments, in a range from 0.5 mm to 10 mm).
In some embodiments, strands of netting used to make polymeric layers described herein do not substantially cross over each other (i.e., at least 50 (at least 55, 60, 65, 70, 75, 80, 85, 90, 95, 99, or even 100) percent by number).
In some embodiments, nettings used to make polymeric layers described herein have alternating first and second polymeric strands exhibiting at least one of diamond-shaped or hexagonal-shaped openings.
In some embodiments, polymeric strands of netting used to make polymeric layers described herein have an average width in a range from 10 micrometers to 500 micrometers (in a range from 10 micrometers to 400 micrometers, or even 10 micrometers to 250 micrometers).
In some embodiments, polymeric strands of netting used to make polymeric layers described herein are elastic.
In some embodiments, nettings used to make polymeric layers described herein are made of, or coated with, hydrophilic material to make them absorbent. In some embodiments, nettings described herein are useful as wound absorbants to remove excess exudate from wounds, and in some embodiments, nettings described herein are made of bioresorbable polymers.
Polymeric layers described herein can be made, for example, at least one of passing through a nip or calendaring netting comprising an array of polymeric strands periodically joined together at bond regions throughout the array.
In forming polymeric layers described herein, it has been observed that the temperature of the melt and the temperature of the quench, and the thickness of the melt affect the size of the holes. Higher melt temperature allows more movement of polymer in the nip which tends to create smaller hole sizes. Low temperature quenching has been shown to limit the amount of polymer movement which creates larger hole sizes.
In some embodiments, polymeric layers described herein have a total open area for each of the first and second, generally opposed major surfaces is not greater than 50 (in some embodiments, not greater than 45, 40, 35, 30, 25, 20. 15, 10, 5, 4 3, 2, 1, 0.75, 0.5, 0.25, or even not greater than 0.1) percent of the total area of the respective major surface. In some embodiments. for at least a majority of the openings, the area of each opening is not greater than is 5 (in some embodiments, not greater than 2.5, 2, 1, 0.5, 0.1, 0.05, 0.01, 0.075, or even not greater than 0.005) mm2.
In some embodiments, for polymeric layers described herein have in a range from 50,000 to 6,000,000 (in some embodiments, 100,000 to 6,000,000, 500,000 to, 6,000,000, or even 1,000,000 to 6,000,000) openings/m2.
In some embodiments, for polymeric layers described herein the openings have widths in a range from 5 micrometers to 1 mm (in some embodiments, 10 micrometers to 0.5 mm). In some embodiments, for polymeric layers described herein the openings have lengths in a range from 100 micrometers to 10 mm (in some embodiments, 100 micrometers to 1 mm). In some embodiments, for polymeric layers described herein the openings have a length to width ratio in a range from 1:1 to 100:1, (in some embodiments, 1:1 to 1.9:1, 2:1 to 100:1 2:1 to 75:1, 2:1 to 50:1, 2:1 to 25:1, or even, 2:1 to 10:1).
In some embodiments, the openings have at least two pointed ends. In some embodiments, at least some of the openings are elongated with two pointed ends. In some embodiments, at least some of the openings are elongated with two opposed pointed ends. In some embodiments, at least some of the openings are ovals.
In some embodiments, for polymeric layers described herein have a thickness up to 2 mm (in some embodiments, up to 1 mm, 500 micrometers, 250 micrometers, 100 micrometers, 75 micrometers, 50 micrometers, or even up to 25 micrometers; in a range from 10 micrometers to 750 micrometers, 10 micrometers to 750 micrometers, 10 micrometers to 500 micrometers, 10 micrometers to 250 micrometers, 10 micrometers to 100 micrometers, 10 micrometers to 75 micrometers, 10 micrometers to 50 micrometers, or even 10 micrometers to 25 micrometers. In some embodiments, for polymeric layers described herein are sheets having an average thickness in a range from 250 micrometers to 5 mm. In some embodiments, for polymeric layers described herein are films having an average thickness not greater than 5 mm.
In some embodiments, for polymeric layers described herein at least some of the openings have a first side on the first major surface comprising a first polymeric material and a second, opposed side on the first major surface comprising a second, different polymeric material. In some embodiments, at least one of the first or second polymeric materials are thermoplastic (e.g., nylons, polyesters, polyolefins, polyurethanes, elastomers (e.g., styrenic block copolymers), and blends thereof).
In some embodiments, for polymeric layers described herein have a basis weight in a range from 25 g/m2 to 500 g/m2 (in some embodiments, 50 g/m2 to 250 g/m2)
Polymeric layers described herein are useful, for example, for as components in personal care garments such as diapers and feminine hygiene products. They can also be useful for filtering (including liquid filtering) and acoustic applications.
Exemplary Embodiments
1A. A polymeric layer having first and second, generally opposed major surfaces, comprising an array of openings extending between the first and second major surfaces, wherein the openings each have a series of areas through the openings from the first and second major surfaces ranging from minimum to maximum areas, wherein there is a total area and a total open area for each of the first and second major surfaces, wherein the total open area for each of the first and second major surfaces is not greater than 50 (in some embodiments, not greater than 45, 40, 35, 30, 25, 20, 15, 10, 5, 4, 3, 2, 1, 0.75, 0.5, 0.25, or even not greater than 0.1) percent of the total area of the respective major surface, and wherein for at least a majority of the openings, the minimum area is not at either major surface.
2A. The polymeric layer of Embodiment 1A, wherein the total open area for each of the first and second major surfaces is in a range from 0.1 percent to not greater than 50 percent (in some embodiments, in a range from 0.1 percent to not greater than 45 percent, 0.1 percent to not greater than 40 percent, 0.1 percent to not greater than 35 percent, 0.1 percent to not greater than 30 percent, 0.1 percent to not greater than 25 percent, 0.1 percent to not greater than 20 percent, 0.1 percent to not greater than 15 percent, 0.1 percent to not greater than 10 percent, or even 0.1 percent to not greater than 5 percent) of the total area of the respective major surface.
3A. The polymeric layer of Embodiment 1A, wherein the total open area for each of the first and second major surfaces is not greater than 1 percent of the total area of the respective major surface.
4A. The polymeric layer of any preceding Embodiment A, wherein for at least a majority of the openings, the area of each opening is not greater than is 5 (in some embodiments, not greater than 2.5, 2, 1, 0.5, 0.1, 0.05, 0.01, 0.075, or even not greater than 0.005) mm2.
5A. The polymeric layer of any preceding Embodiment A, wherein the openings have at least two pointed ends.
6A. The polymeric layer of any of Embodiments 1A to 4A, wherein at least some of the openings are elongated with two pointed ends.
7A. The polymeric layer of any of Embodiments 1A to 4A, wherein at least some of the openings are elongated with two opposed pointed ends.
8A. The polymeric layer of any of Embodiments 1A to 4A, wherein at least some of the openings are ovals.
9A. The polymeric layer of any preceding Embodiment A having in a range from 50,000 to 6,000,000 (in some embodiments, 100,000 to 6,000,000, 500,000 to, 6,000,000, or even 1,000,000 to 6,000,000) openings/m2.
10A. The polymeric layer of any preceding Embodiment A, wherein the openings have a length and a width, and a ratio of lengths to widths in a range from 2:1 to 100:1 (in some embodiments, 2:1 to 75:1, 2:1 to 50:1, 2:1 to 25:1, or even, 2:1 to 10:1).
11A. The polymeric layer of any of Embodiments 1A to 9A, wherein the openings have a length and a width, and a ratio of lengths to widths in a range from 1:1 to 1.9:1.
12A. The polymeric layer of any preceding Embodiment A, wherein the openings have widths in a range from 5 micrometers to 1 mm (in some embodiments, 10 micrometers to 0.5 mm).
13A. The polymeric layer of any preceding Embodiment A, wherein the openings have lengths in a range from 100 micrometers to 10 mm (in some embodiments, 100 micrometers to 1 mm).
14A. The polymeric layer of any preceding Embodiment A, wherein the layer has a thickness up to 2 mm (in some embodiments, up to 1 mm, 500 micrometers, 250 micrometers, 100 micrometers, 75 micrometers, 50 micrometers, or even up to 25 micrometers; in a range from 10 micrometers to 750 micrometers, 10 micrometers to 750 micrometers, 10 micrometers to 500 micrometers, 10 micrometers to 250 micrometers, 10 micrometers to 100 micrometers, 10 micrometers to 75 micrometers, 10 micrometers to 50 micrometers, or even 10 micrometers to 25 micrometers.
15A. The polymeric layer of any of Embodiments 1A to 13A, wherein the polymeric layer is a sheet having an average thickness in a range from 250 micrometers to 5 mm.
16A. The polymeric layer of any of Embodiments 1A to 13A, wherein the polymeric layer is a film having an average thickness not greater than 5 mm.
17A. The polymeric layer of any preceding Embodiment A, wherein at least some of the openings have a first side on the first major surface comprising a first polymeric material and a second, opposed side on the first major surface comprising a second, different polymeric material.
18A. The polymeric layer of Embodiment 17A, wherein at least one of the first or second polymeric materials are thermoplastic (e.g., nylons, polyesters, polyolefins, polyurethanes, elastomers (e.g., styrenic block copolymers), and blends thereof).
19A. The polymeric layer of any preceding Embodiment A having a basis weight in a range from 25 g/m2 to 500 g/m2 (in some embodiments, 50 g/m2 to 250 g/m2).
20A. The polymeric layer of any preceding Embodiment A comprising at least one of a dye or pigment therein.
21A. The polymeric layer of any preceding Embodiment A, further comprising a layer of adhesive thereon.
22A. A method of making a polymeric layer of any preceding Embodiment A, the method comprising at least one of passing through a nip or calendaring a netting comprising an array of polymeric strands periodically joined together at bond regions throughout the array.
1B. A polymeric layer having first and second, generally opposed major surfaces, comprising an array of openings extending between the first and second major surfaces, wherein the openings each have a series of areas through the openings from the first and second major surfaces ranging from minimum to maximum areas, wherein for at least a majority of the openings, the area of each opening is not greater than is 5 (in some embodiments, not greater than 2.5, 2, 1, 0.5, 0.1, 0.05, 0.01, 0.075, or even not greater than 0.005) mm2, and wherein for at least a majority of the openings, the minimum area is not at either major surface.
2B. The polymeric layer of Embodiment 1B, wherein at least some of the openings have at least two pointed ends.
3B. The polymeric layer of either Embodiment 1B or 2B, wherein at least some of the openings are elongated with at least two pointed ends.
4B. The polymeric layer of either Embodiment 1B or 2B, wherein at least some of the openings are elongated with two opposed pointed ends.
5B. The polymeric layer of either Embodiment 1B or 2B, wherein at least some of the openings are oval.
6B The polymeric layer of any preceding Embodiment B having in a range from 50,000 to 6,000,000 (in some embodiments, 100,000 to 6,000,000, 500,000 to, 6,000,000, or even 1,000,000 to 6,000,000) openings/m2.
7B. The polymeric layer of any preceding Embodiment B, wherein the openings have a length and a width, and a ratio of lengths to widths in a range from 2:1 to 100:1 (in some embodiments, 2:1 to 75:1, 2:1 to 50:1, 2:1 to 25:1, or even, 2:1 to 10:1).
8B. The polymeric layer of any of Embodiments 1B to 6B, wherein the openings have a length and a width, and a ratio of lengths to widths in a range from 1:1 to 1.9:1.
9B. The polymeric layer of any preceding Embodiment B, wherein the openings have widths in a range from 5 micrometers to 1 mm (in some embodiments, 10 micrometers to 0.5 mm).
10B. The polymeric layer of any preceding Embodiment B, wherein the openings have lengths in a range from 100 micrometers to 10 mm (in some embodiments, 100 micrometers to 1 mm).
11B. The polymeric layer of any preceding Embodiment B, wherein the layer has a thickness up to 2 mm (in some embodiments, up to 1 mm, 500 micrometers, 250 micrometers, 100 micrometers, 75 micrometers, 50 micrometers, or even up to 25 micrometers; in a range from 10 micrometers to 750 micrometers, 10 micrometers to 750 micrometers, 10 micrometers to 500 micrometers, 10 micrometers to 250 micrometers, 10 micrometers to 100 micrometers, 10 micrometers to 75 micrometers, 10 micrometers to 50 micrometers, or even 10 micrometers to 25 micrometers.
12B. The polymeric layer of any of Embodiments 1B to 10B, wherein the polymeric layer is a sheet having an average thickness in a range from 250 micrometers to 5 mm.
13B. The polymeric layer of any of Embodiments 1B to 10B, wherein the polymeric layer is a film having an average thickness not greater than 5 mm.
14B. The polymeric layer of any preceding Embodiment B, wherein at least some of the openings have a first side on the first major surface comprising a first polymeric material and a second, opposed side on the first major surface comprising a second, different polymeric material.
15B. The polymeric layer of Embodiment 14B, wherein at least one of the first or second polymeric materials are thermoplastic (e.g., nylons, polyesters, polyolefins, polyurethanes, elastomers (e.g., styrenic block copolymers), and blends thereof).
16B. The polymeric layer of any preceding Embodiment B having a basis weight in a range from 25 g/m2 to 500 g/m2 (in some embodiments, 50 g/m2 to 250 g/m2).
17B. The polymeric layer of any preceding Embodiment B comprising at least one of a dye or pigment therein.
18B. The polymeric layer of any preceding Embodiment B, further comprising a layer of adhesive thereon.
19B. A method of making a polymeric layer of any preceding Embodiment B, the method comprising at least one of passing through a nip or calendaring netting comprising an array of polymeric strands periodically joined together at bond regions throughout the array.
1C. A method of making a polymeric layer having openings therein, the method comprising at least one of passing through a nip or calendaring netting comprising an array of polymeric strands periodically joined together at bond regions throughout the array, wherein the netting has a thickness up to 2 mm (in some embodiments, up to 1.5 mm, 1 mm, 750 micrometers, 500 micrometers, 250 micrometers, 100 micrometers, 75 micrometers, 50 micrometers, or even up to 25 micrometers; in a range from 10 micrometers to 2 mm, 10 micrometers to 1.5 mm, 10 micrometers to 1 mm, 10 micrometers to 750 micrometers, 10 micrometers to 750 micrometers, 10 micrometers to 500 micrometers, 10 micrometers to 250 micrometers, 10 micrometers to 100 micrometers, 10 micrometers to 75 micrometers, 10 micrometers to 50 micrometers, or even 10 micrometers to 25 micrometers).
2C. The method of Embodiment 1C, wherein the polymeric strands do not cross each other.
3C. The method of either Embodiment 1C or 2C, wherein the polymeric layer has a basis weight in a range from 25 g/m2 to 500 g/m2 (in some embodiments, 50 g/m2 to 250 g/m2 or 10 g/m2 to 200 g/m2).
4C. The method of any preceding Embodiment C, wherein the netting has a strand pitch in a range from 0.5 mm to 20 mm (in some embodiments, in a range from 0.5 mm to 10 mm).
5C. The method of any preceding Embodiment C, wherein at least some of the polymeric stands include at least one of a dye or pigment therein.
6C. The method of any preceding Embodiment C, wherein at least some of the polymeric strands of the netting comprise a thermoplastic (e.g., nylons, polyesters, polyolefins, polyurethanes, elastomers (e.g., styrenic block copolymers), and blends thereof).
7C. The method of any preceding Embodiment C, wherein the plurality of strand of the netting include alternating first and second polymeric strands, wherein the second polymeric strands comprise a second, different polymer.
8C. The method of any preceding Embodiment C, wherein the nip or calendar has at least one of at least one raised area or at least two zones of different temperatures.
Advantages and embodiments of this invention are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. All parts and percentages are by weight unless otherwise indicated.
A co-extrusion die as generally depicted in
The inlet fittings on the two end blocks were each connected to a conventional single-screw extruder. A chill roll was positioned adjacent to the distal opening of the co-extrusion die to receive the extruded material. The extruder feeding the first cavity was loaded with thirty-five melt flow index polypropylene pellets (obtained under the trade designation “EXXONMOBIL 3155 PP” from ExxonMobil, Irving Tex.). The extruder feeding the second cavity was also loaded with thirty-five melt flow index polypropylene pellets (“EXXONMOBIL 3155 PP”).
The melt was extruded vertically into an extrusion quench takeaway nip. The quench nip was a smooth temperature controlled chrome plated 20 cm diameter steel roll and an 11 cm diameter silicone rubber roll. The rubber roll was about 60 durometer. Both were temperature controlled with internal water flow. The nip pressure was generated with 2 pressurized air cylinders. The web path wrapped 180 degrees around the chrome steel roll and then to a windup roll. A schematic of the quench process is shown in
Other process conditions are listed below:
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured, and are listed below.
An optical digital photo at 10× of the resulting polymeric layer is shown in
Example 2 was made as described for Example 1, except the quench takeaway speed was 1.5 m/min.
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured, and are listed below.
An optical photograph at 10× of the resulting polymeric layer is shown in
Example 3 was made as described for Example 1, except the quench roll temperature was 24° C.
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured, and are listed below.
An optical photograph at 10× of the resulting polymeric layer is shown in
Example 4 was made the same as Example 2 except the quench roll temperature was 24° C.
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured, and are listed below.
An optical photograph at 10× of the resulting polymeric layer is shown in
Example 5 was made the same as Example 4 except the polymer melt temperature was raised to 260° C.
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured, and are listed below.
An optical photograph at 10× of the resulting polymeric layer is shown in
Example 6 was made the same as Example 5 except the quench takeaway speed was 3.1 m/min.
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured, and are listed below.
An optical photograph at 10× of the resulting polymeric layer is shown in
A co-extrusion die as generally depicted in
The inlet fittings on the two end blocks were each connected to a conventional single-screw extruder. A chill roll was positioned adjacent to the distal opening of the co-extrusion die to receive the extruded material. The extruder feeding the first cavity was loaded with thirty-five melt flow index polypropylene pellets (“EXXONMOBIL 3155 PP”). The extruder feeding the second cavity was also loaded with thirty-five melt flow index polypropylene pellets (“ExxonMobil 3155PP”).
The melt was extruded vertically into an extrusion quench takeaway nip. The quench nip was a smooth temperature controlled chrome plated 20 cm diameter steel roll and an 11 cm diameter silicone rubber roll. The rubber roll was about 60 durometer. Both were temperature controlled with internal water flow. The nip pressure was generated with 2 pressurized air cylinders. The web path wrapped 180 degrees around the chrome steel roll and then to a windup roll. A schematic view of the quench process in shown in
Other process conditions are listed below:
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured and are shown below.
An optical photograph at 10× of the resulting polymeric layer is shown in
A co-extrusion die as generally depicted in
The inlet fittings on the two end blocks were each connected to a conventional single-screw extruder. A chill roll was positioned adjacent to the distal opening of the co-extrusion die to receive the extruded material. The extruder feeding the first cavity was loaded with thirty-five melt flow index polypropylene pellets (“EXXONMOBIL 3155 PP”). The extruder feeding the second cavity was also loaded with thirty-five melt flow index polypropylene pellets (“ExxonMobil 3155PP”).
The melt was extruded vertically into an extrusion quench takeaway nip. The quench nip was a smooth temperature controlled chrome plated 20 cm diameter steel roll and an 11 cm diameter silicone rubber roll. The rubber roll was about 60 durometer. Both were temperature controlled with internal water flow. The nip pressure was generated with 2 pressurized air cylinders. The web path wrapped 180 degrees around the chrome steel roll and then to a windup roll. A schematic view of the quench process in shown in
Other process conditions are listed below:
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured and are shown below.
An optical photograph at 10× of the resulting polymeric layer is shown in
Example 9 was made the same as Example 8 except the quench takeaway speed was 2.4 m/min.
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured and are shown below.
An optical photograph at 10× of the resulting polymeric layer is shown in
A co-extrusion die as generally depicted in
The inlet fittings on the two end blocks were each connected to a conventional single-screw extruder. A chill roll was positioned adjacent to the distal opening of the co-extrusion die to receive the extruded material. The extruder feeding the first cavity was loaded with thirty-five melt flow index polypropylene pellets (“EXXONMOBIL 1024 PP”). The extruder feeding the second cavity was also loaded with thirty-five melt flow index polypropylene pellets (“ExxonMobil 1024 PP”).
The melt was extruded vertically into an extrusion quench takeaway nip. The quench nip was a smooth temperature controlled chrome plated 20 cm diameter steel roll and an 11 cm diameter silicone rubber roll. The rubber roll was About 60 durometer. Both were temperature controlled with internal water flow. The nip pressure was generated with 2 pressurized air cylinders. The web path wrapped 180 degrees around the chrome steel roll and then to a windup roll. A schematic view of the quench process in shown in
Other process conditions are listed below:
Using an optical microscope, the dimensions of the resulting polymeric layer having an array of openings between the major surfaces were measured and are shown below.
An optical photograph at 10× of the resulting polymeric layer is shown in
Foreseeable modifications and alterations of this disclosure will be apparent to those skilled in the art without departing from the scope and spirit of this invention. This invention should not be restricted to the embodiments that are set forth in this application for illustrative purposes.
This application is divisional application of prior Application Ser. No. 14/387,332, filed Sep. 23, 2014, which is a national stage filing under 35 U.S.C. 371 of PCT/US2013/030143, filed Mar. 11, 2013, which claims priority to U.S. Provisional Application No. 61/615,676, filed Mar. 26, 2012, the disclosure of which is incorporated by reference in its/their entirety herein.
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Number | Date | Country | |
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20170001342 A1 | Jan 2017 | US |
Number | Date | Country | |
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61615676 | Mar 2012 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 14387332 | US | |
Child | 15269223 | US |