US20120263924A1 - Multi-Layer Films And Methods Of Forming Same - Google Patents

Multi-Layer Films And Methods Of Forming Same Download PDF

Info

Publication number
US20120263924A1
US20120263924A1 US13/084,630 US201113084630A US2012263924A1 US 20120263924 A1 US20120263924 A1 US 20120263924A1 US 201113084630 A US201113084630 A US 201113084630A US 2012263924 A1 US2012263924 A1 US 2012263924A1
Authority
US
United States
Prior art keywords
layer
polymer
film
weight
film layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/084,630
Other languages
English (en)
Inventor
Paul Thomas Weisman
Eric Patton Weinberger
Pier-Lorenzo Caruso
Michael Remus
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
Original Assignee
Procter and Gamble Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to US13/084,630 priority Critical patent/US20120263924A1/en
Assigned to PROCTER & GAMBLE COMPANY, THE reassignment PROCTER & GAMBLE COMPANY, THE ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WEINBERGER, ERIC PATTON, WEISMAN, PAUL THOMAS, CARUSO, PIER-LORENZO, REMUS, MICHAEL
Priority to EP12710637.5A priority patent/EP2686162A1/fr
Priority to PCT/US2012/029208 priority patent/WO2012129045A1/fr
Priority to EP12711090.6A priority patent/EP2686166A1/fr
Priority to CN2012800127181A priority patent/CN103429430A/zh
Priority to BR112013023684A priority patent/BR112013023684A2/pt
Priority to CN2012800127069A priority patent/CN103415391A/zh
Priority to BR112013023796A priority patent/BR112013023796A2/pt
Priority to PCT/US2012/029211 priority patent/WO2012129046A1/fr
Priority to PCT/US2012/032955 priority patent/WO2012142057A2/fr
Publication of US20120263924A1 publication Critical patent/US20120263924A1/en
Priority to US13/968,458 priority patent/US9169366B2/en
Priority to US14/863,480 priority patent/US9802393B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D65/00—Wrappers or flexible covers; Packaging materials of special type or form
    • B65D65/38—Packaging materials of special type or form
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/24—All layers being polymeric
    • B32B2250/242—All polymers belonging to those covered by group B32B27/32
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/72—Density
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2439/00—Containers; Receptacles
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
    • Y10T156/10—Methods of surface bonding and/or assembly therefor
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31855—Of addition polymer from unsaturated monomers
    • Y10T428/31909—Next to second addition polymer from unsaturated monomers
    • Y10T428/31913—Monoolefin polymer

Definitions

  • the present disclosure generally relates to multi-layer films having a bio-based content of about 10% to about 100% using ASTM D6866-10, method B.
  • the components of multi-layer films are made from polyolefins such as polyethylene and polypropylene. These polymers are derived from olefinic monomers such as ethylene and propylene which are obtained directly from petroleum via cracking and refining processes.
  • a multi-layer film which comprises at least one polymer at least partially derived from renewable resources, where the at least one polymer has specific performance characteristics making the polymer particularly useful in the multi-layer film. Accordingly, it would be desirable to provide a multi-layer polymeric film which comprises lower basis weight reducing the use of petroleum and lowering costs, where the multi-layer polymeric film has improved performance characteristics to satisfy product and/or packaging needs
  • a multi-layer film comprises a first film layer and a second film layer, wherein the multi-layer film has a bio-based content of about 10% to about 100% using ASTM D6866-10, method B.
  • the first film layer has an upper surface and a lower surface.
  • the first film layer is at least partially found from a polymer (A) and a polymer (B).
  • the first film layer comprises from about 75% to about 99% by weight of the polymer (A) and from about 1% to about 25% by weight of the polymer (B).
  • the polymer (A) comprises at least one of a low density polyethylene (LDPE) and a linear low density polyethylene (LLDPE).
  • the polymer (B) comprises a copolymer.
  • the second film layer at least partially overlies one of the upper surface and the lower surface of the first film layer.
  • the second film layer is at least partially formed from the polymer (A), the polymer (B), a polymer (C), and optionally an opacifying agent.
  • the polymer (C) comprises a homo polypropylene (homo-PP).
  • At least one of the polymer (A), the polymer (B) and the polymer (C) is synthetic and is at least partially derived from a renewable resource.
  • a method of forming a multi-layer film comprises processing a first film layer, wherein the first film layer has an upper surface and a lower surface; processing a second film layer and at least partially overlying the second film layer onto one of the upper surface and the lower surface of the first film layer to form a multi-layer film having a bio-based content of about 10% to about 100% using ASTM D6866-10, method B.
  • the first film layer is at least partially formed from a polymer (A) and a polymer (B).
  • the first film layer comprises from about 75% to about 99% by weight of the polymer (A) and from about 1% to about 25% by weight of the polymer (B).
  • the polymer (A) comprises at least one of a low density polyethylene (LDPE) and a linear low density polyethylene (LLDPE).
  • the polymer (B) comprises a copolymer.
  • the second film layer is at least partially formed from the polymer (A), the polymer (B), a polymer (C), and optionally an opacifying agent.
  • the polymer (C) comprises a homo polypropylene (homo-PP). At least one of the polymer (A), the polymer (B) and the polymer (C) is synthetic and is at least partially derived from a renewable resource.
  • a multi-layer film comprises a first film layer, a second film layer, a third film layer and a bio-based content of about 10% to about 100% using ASTM D6866-10, method B.
  • the first film layer has an upper surface and a lower surface.
  • the second film layer at least partially overlies one of the upper surface and the lower surface of the first film layer.
  • the third film layer at least partially overlies the second film layer such that the second film layer forms a core layer.
  • the multi-layer film has a thickness from about 10 microns to about 200 microns, a tensile strength at 10% elongation from about 8 N/mm 2 to about 24 N/mm 2 , and a seal strength from about 0.10 N/mm to about 2.0 N/mm.
  • a multi-layer film comprises from about 40% to about 90% by weight of the polymer (A), from about 5% to about 50% by weight of a polymer (B), from about 1% to about 20% by weight of a polymer (C), and a bio-based content of about 10% to about 100% using ASTM D6866-10, method B.
  • the polymer (A) comprises at least one of a low density polyethylene (LDPE) and a linear low density polyethylene (LLDPE).
  • the polymer (B) is a copolymer.
  • the polymer (C) comprises a homo polypropylene (homo-PP).
  • FIG. 1 is a representative view of a multi-layer film having two layers
  • FIG. 2 is a representative view of a multi-layer film having three layers.
  • “Absorbent article” means devices that absorb and/or contain liquid. Wearable absorbent articles are absorbent articles placed against or in proximity to the body of the wearer to absorb and contain various exudates discharged from the body. Non-limiting examples of wearable absorbent articles include diapers, pant-like or pull-on diapers, training pants, sanitary napkins, tampons, panty liners, incontinence devices, and the like. Additional absorbent articles include wipes and cleaning products.
  • Agricultural product refers to a renewable resource resulting from the cultivation of land (e.g. a crop) or the husbandry of animals (including fish).
  • Bio-based content refers to the amount of carbon from a renewable resource in a material as a percent of the mass of the total organic carbon in the material, as determined by ASTM D6866-10, method B. Note that any carbon from inorganic sources such as calcium carbonate is not included in determining the bio-based content of the material.
  • Communication refers to a medium or means by which information, teachings, or messages are transmitted.
  • Disposed refers to an element being located in a particular place or position.
  • Frm refers to a sheet-like material wherein the length and width of the material far exceed the thickness of the material.
  • “Monomeric compound” refers to an intermediate compound that may be polymerized to yield a polymer.
  • Paper product refers to any formed fibrous structure product, which may, but not necessarily, comprise cellulose fibers.
  • the paper products of the present disclosure include tissue-towel paper products.
  • Petroleum refers to an organic compound derived from petroleum, natural gas, or coal.
  • Crude oil refers to crude oil and its components of paraffinic, cycloparaffinic, and aromatic hydrocarbons. Crude oil may be obtained from tar sands, bitumen fields, and oil shale.
  • Polymer refers to a macromolecule comprising repeat units where the macromolecule has a molecular weight of at least 1000 Daltons.
  • the polymer may be a homopolymer, copolymer, terpoymer etc.
  • the polymer may be produced via fee-radical, condensation, anionic, cationic, Ziegler-Natta, metallocene, or ring-opening mechanisms.
  • the polymer may be linear, branched and/or crosslinked.
  • Polyethylene and “polypropylene” refer to polymers prepared from ethylene and propylene, respectively.
  • the polymer may be a homopolymer, or may contain up to about 10 mol % of repeat units from a co-monomer.
  • “Related environmental message” refers to a message that conveys the benefits or advantages of the multi-layer film comprising a polymer derived from a renewable resource. Such benefits include being more environmentally friendly, having reduced petroleum dependence, being derived from renewable resources, and the like.
  • “Renewable resource” refers to a natural resource that can be replenished within a 100 year time frame.
  • the resource may be replenished naturally, or via agricultural techniques.
  • Renewable resources include plants, animals, fish, bacteria, fungi, and forestry products. They may be naturally occurring, hybrids, or genetically engineered organisms. Natural resources such as crude oil, coal, and peat which take longer than 100 years to form are not considered to be renewable resources.
  • Synthetic polymer refers to a polymer which is produced from at least one monomer by a chemical process. A synthetic polymer is not produced directly by a living organism.
  • tissue-towel paper product refers to products comprising paper tissue or paper towel technology in general, including, but not limited to, conventional felt-pressed or conventional wet-pressed tissue paper, pattern densified tissue paper, starch substrates, and high bulk, uncompacted tissue paper.
  • tissue-towel paper products include toweling, facial tissue, bath tissue, table napkins, and the like.
  • a number of renewable resources contain polymers that are suitable for use in multi-layer films (i.e., the polymer is obtained from the renewable resource without intermediates). Suitable extraction and/or purification steps may be necessary, but no intermediate compound is required.
  • Such polymers derived directly from renewable resources include cellulose (e.g. pulp fibers), starch, chitin, polypeptides, poly(lactic acid), polyhydroxyalkanoates, and the like. These polymers may be subsequently chemically modified to improve end use characteristics (e.g., conversion of cellulose to yield carboxycellulose or conversion of chitin to yield chitosan). However, in such cases, the resulting polymer is a structural analog of the starting polymer.
  • Polymers derived directly from renewable resources (i.e., with no intermediate compounds) and their derivatives are known and these materials are not within the scope of the present disclosure.
  • Synthetic polymers of the present disclosure can be derived from a renewable resource via an indirect route involving one or more intermediate compounds.
  • Suitable intermediate compounds derived from renewable resources include sugars.
  • Suitable sugars include monosaccharides, disaccharides, trisaccharides, and oligosaccharides.
  • Sugars such as sucrose, glucose, fructose, maltose may be readily produced from renewable resources such as sugar cane and sugar beets.
  • Sugars may also be derived (e.g., via enzymatic cleavage) from other agricultural products such as starch or cellulose. For example, glucose may be prepared on a commercial scale by enzymatic hydrolysis of corn starch.
  • Wheat, buckwheat, arracaha, potato, barley, kudzu, cassava, sorghum, sweet potato, yam, arrowroot, sago, and other like starchy fruit, seeds, or tubers are may also be used in the preparation of glucose.
  • Suitable intermediate compounds derived from renewable resources include monofunctional alcohols such as methanol or ethanol and polyfunctional alcohols such as glycerol.
  • Ethanol may be derived from many of the same renewable resources as glucose.
  • cornstarch may be enzymatically hydrolyzed to yield glucose and/or other sugars. The resultant sugars can be converted into ethanol by fermentation.
  • corn is an ideal renewable resource in North America; however, other crops may be substituted.
  • Methanol may be produced from fermentation of biomass.
  • Glycerol is commonly derived via hydrolysis of triglycerides present in natural fats or oils, which may be obtained from renewable resources such as animals or plants.
  • Other intermediate compounds derived from renewable resources include organic acids (e.g., citric acid, lactic acid, alginic acid, amino acids etc.), aldehydes (e.g., acetaldehyde), and esters (e.g., cetyl palmitate, methyl stearate, methyl oleate, etc.).
  • organic acids e.g., citric acid, lactic acid, alginic acid, amino acids etc.
  • aldehydes e.g., acetaldehyde
  • esters e.g., cetyl palmitate, methyl stearate, methyl oleate, etc.
  • Additional intermediate compounds such as methane and carbon monoxide may also be derived from renewable resources by fermentation and/or oxidation processes.
  • Intermediate compounds derived from renewable resources may be converted into polymers (e.g., glycerol to polyglycerol) or they may be converted into other intermediate compounds in a reaction pathway which ultimately leads to a polymer useful in a multi-layer film.
  • An intermediate compound may be capable of producing more than one secondary intermediate compound.
  • a specific intermediate compound may be derived from a number of different precursors, depending upon the reaction pathways utilized.
  • Olefins such as ethylene and propylene may also be derived from renewable resources.
  • methanol derived from fermentation of biomass may be converted to ethylene and or propylene, which are both suitable monomeric compounds, as described in U.S. Pat. Nos. 4,296,266 and 4,083,889.
  • Ethanol derived from fermentation of a renewable resource may be converted into the monomeric compound ethylene via dehydration as described in U.S. Pat. No. 4,423,270.
  • propanol or isopropanol derived from a renewable resource can be dehydrated to yield the monomeric compound of propylene as exemplified in U.S. Pat. No. 5,475,183.
  • Propanol is a major constituent of fusel oil, a by-product formed from certain amino acids when potatoes or grains are fermented to produce ethanol.
  • Charcoal derived from biomass can be used to create syngas (i.e., CO+H 2 ) from which hydrocarbons such as ethane and propane can be prepared (Fischer-Tropsch Process). Ethane and propane can be dehydrogenated to yield the monomeric compounds of ethylene and propylene.
  • syngas i.e., CO+H 2
  • hydrocarbons such as ethane and propane
  • propane can be dehydrogenated to yield the monomeric compounds of ethylene and propylene.
  • Sources of materials to form polymers derived from renewable resources include post-consumer recycled materials.
  • Sources of synthetic post-consumer recycled materials can include plastic bottles, e.g., soda bottles, plastic films, plastic packaging materials, plastic bags and other similar materials which contain synthetic materials which can be recovered.
  • Olefins derived from renewable resources may be polymerized to yield polyolefins.
  • Ethylene and propylene derived from renewable resources may be polymerized under the appropriate conditions to prepare polyethylene and/or polypropylene having desired characteristics for use in multi-layer films.
  • the polyethylene and/or polypropylene may be high density, medium density, low density, or linear-low density.
  • polypropylene can include homo-PP.
  • Polyethylene and/or polypropylene may be produced via free-radical polymerization techniques, or by using Ziegler-Natta (Zn) catalysis or Metallocene catalysts. Examples of such bio-sourced polyethylenes and polypropylenes are described in U.S. Publication Nos.
  • olefins that can be derived from renewable resources include butadiene and isoprene. Examples of such olefins are described in U.S. Publication Nos. 2010/0216958 and 2010/0036173.
  • Such polyolefins being derived from renewable resources can also be reacted to form various copolymers, including for example random block copolymers, such as ethylene-propylene random block copolymers (e.g., BorpactTM BC918CF manufactured by Borealis).
  • random block copolymers such as ethylene-propylene random block copolymers (e.g., BorpactTM BC918CF manufactured by Borealis).
  • Such copolymers and methods of forming same are contemplated and described for example in European Patent No. 2121318.
  • polyolefin derived from a renewable resource may be processed according to methods known in the art into a form suitable for the end use of the polymer.
  • the polyolefin may comprise mixtures or blends with other polymers such as polyolefins derived from petrochemicals.
  • any of the aforementioned synthetic polymers may be formed by using a combination of monomers derived from renewable resources and monomers derived from non-renewable (e.g., petroleum) resources.
  • the copolymer can comprise propylene repeat units derived from a renewable resource and isobutylene repeat units derived from a petroleum source.
  • the invention comprises a multi-layer film 20 having at least two layers (e.g., a first film layer 22 and a second film layer 24 ).
  • the first film layer 22 and the second film layer 24 can be layered adjacent to each other to form the multi-layer film (e.g., FIG. 1 ).
  • a multi-layer film 120 can have at least three layers (e.g., a first film layer 122 , a second film layer 124 and a third film layer 126 ).
  • the second film layer 124 can at least partially overlie at least one of an upper surface 128 or a lower surface 130 of the first film layer 122 .
  • the third film layer 126 can at least partially overlie the second film layer 124 such that the second film layer 124 forms a core layer.
  • multi-layer films may include additional layers (e.g., binding layers, non-permeable layers, etc.).
  • FIGS. 1 and 2 generally illustrate various layer arrangements for multi-layer films, it will be appreciated that such multi-layer films can comprise from about 2 layers to about 1000 layers; in certain embodiments from about 3 layers to about 200 layers; and in certain embodiments from about 5 layers to about 100 layers.
  • the multi-layer films contemplated herein can have a thickness (e.g., caliper) from about 10 microns to about 200 microns; in certain embodiments a thickness from about 20 microns to about 100 microns; and in certain embodiments a thickness from about 40 microns to about 60 microns.
  • a thickness e.g., caliper
  • each of the film layers can have a thickness less than about 100 microns; in certain embodiments less than about 50 microns; and in certain embodiments less than about 10 microns. It will be appreciated that the respective film layers can have substantially the same or different thicknesses.
  • Thickness of the multi-layer films can be evaluated using various techniques, including the methodology set forth in ISO 4593:1993, Plastics—Film and sheeting—Determination of thickness by mechanical scanning.
  • a sample of the multi-layer film comprises about a 1.0 inch diameter (having a basis weight from about 10 gsm to about 50 gsm)
  • section 2.1.2 of ISO 4593:1993 will apply, such that a force applied to the sample shall be 0.1 N to 0.5 N. It will be appreciated that out suitable methods may be available to measure the thickness of the multi-layer film described herein.
  • Each respective layer of the multi-layer film can be formed from a number of the respective synthetic polymers described herein.
  • the selection of polymers used to form the multi-layer film can have an impact on a number of physical parameters, and as such, can provide improved characteristics such as lower basis weights and higher tensile and seal strengths. Examples of commercial multi-layer films with improved characteristics are described in U.S. Patent No. 7,588,706.
  • the first film layer 22 can include a polymer (A) and a polymer (B).
  • the first film layer 22 can include from about 75% to about 99% by weight of the polymer (A); and in certain embodiments from about 85% to about 95% by weight of the polymer (A).
  • the first film layer 22 can include from about 1% to about 25% by weight of the polymer (B); and in certain embodiments from about 5% to about 10% by weight of the polymer (B).
  • the polymer (A) can include a synthetic polymer as described herein, and in particular, a polyethylene, such as LDPE or LLDPE. Examples of such suitable polyethylenes that can be used to form the first film layer are described in U.S. Pat. No. 7,588,706.
  • the polymer (B) can include a copolymer, such as an ethylene-propylene random block copolymer.
  • the second film layer 24 can include the polymer (A), the polymer (B) and a polymer (C). In one embodiment, the second film layer 24 can include from about 20% to about 90% by weight of the polymer (A); and in certain embodiments from about 30% to about 85% by weight of the polymer (A). In one embodiment, the second film layer 24 can include from about 35% to about 60% by weight of the polymer (B); and in certain embodiments from about 40% to about 50% by weight of the polymer (B). In one embodiment, the second film layer 24 can include from about 1% to about 35% by weight of the polymer (C); and in certain embodiments from about 3% to about 25% by weight of the polymer (C).
  • the second film layer 24 can include from about 40% to about 75% by weight of the polymer (A) and an additive material. In certain embodiments, the second film layer 24 can include from about 25% to about 60% by weight of the polymer (B) and polymer (C).
  • Polymer (C) can include polypropylenes (e.g., homo-PP). Such suitable polypropylenes are described in European Patent No. 2121318.
  • the second film layer 24 can optionally include an opacifying agent (e.g., titanium dioxide, calcium carbonate) which can provide increased opacity to the multi-layer film.
  • each of the polymer (A), polymer (B) and polymer (C) can be synthetic and at least partially derived from a renewable resource.
  • the polymer (B) is present in both the first film layer and the second film layer provided additional advantages.
  • Such advantages include better interfacial interaction between the respective layers, thus providing better adhesion between the film layers, particularly when the polymer (B) is an ethylene-propylene random block copolymer.
  • a multi-layer film can include a 3-layer arrangement wherein a first film layer 122 and a third film layer 126 form the skin layers and a second film layer 124 is formed between the first film layer 122 and the third film layer 126 to form a core layer.
  • the first film layer 122 and the second film layer 124 of FIG. 2 can be similarly formed as the first film layer 22 and the second film layer 24 of FIG. 1 .
  • the third film layer 126 can be the same or different from the first film layer 122 , such that in certain embodiments, the third film layer 126 can include the polymer (A) and polymer (B) as described herein. It will be appreciated that similar film layers could be used to form multi-layer films having more than 3 layers.
  • the 3-layer arrangement as illustrated in FIG. 2 can provide a multi-layer film having from about 40% to about 90% by weight of the polymer (A), from about 5% to about 50% by weight of the polymer (B) and from about 1% to about 20% by weight of the polymer (C).
  • the layers of the multi-layer film can further include additional additives.
  • opacifying agents can be added to one or more of the film layers.
  • Such opacifying agents can include iron oxides, carbon black, aluminum, aluminum oxide, titanium dioxide, talc and combinations thereof. These opacifying agents can comprise about 0.1% to about 5% by weight of the multi-layer film; and in certain embodiments, the opacifying agents can comprise about 0.3% to about 3% of the multi-layer polymeric film. It will be appreciated that other suitable opacifying agents may be employed and in various concentrations. Examples of opacifying agents are described in U.S. Pat. No. 6,653,523.
  • the multi-layer films may comprise other additives, such as other polymers (e.g., a polypropylene, a polyethylene, a ethylene vinyl acetate, a polymethylpentene any combination thereof, or the like), a filler (e.g., glass, talc, calcium carbonate, or the like), a mold release agent, a flame retardant, an electrically conductive agent, an anti-static agent, a pigment, an antioxidant, an impact modifier, a stabilizer (e.g., a UV absorber), wetting agents, dyes, or any combination thereof.
  • other additives such as other polymers (e.g., a polypropylene, a polyethylene, a ethylene vinyl acetate, a polymethylpentene any combination thereof, or the like), a filler (e.g., glass, talc, calcium carbonate, or the like), a mold release agent, a flame retardant, an electrically conductive agent, an anti-static agent, a pigment, an antioxidant,
  • the multi-layer films described herein can have enhanced properties, such as higher tensile and seal strengths.
  • the tensile strength of the multi-layer film measured at 10% elongation can be from about 8 N/mm 2 to about 24 N/mm 2 ; and in certain embodiments from about 10 N/mm 2 to about 15 N/mm 2 .
  • the tensile strength of the multi-layer film measured at break can be from about 20 N/mm 2 to about 60 N/mm 2 ; and in certain embodiments from about 25 N/mm 2 to about 40 N/mm 2 .
  • Such tensile strength measurements are provided in normalized states (e.g., tensile strength was divided by the caliper of the film (e.g., 50 microns)). However, it will be appreciated that tensile strength could also be measured in units N/mm.
  • tensile strength can be measure in a variety of ways, including an evaluation of the tensile strength at either 10% elongation or at break.
  • One standard to apply in measuring tensile strength is the methodology set forth in ISO 527-5:2009, Plastics—Determination of tensile properties.
  • ISO 527-5:2009 a sample of the multi-layer film will need to be prepared. In one embodiment, a sample size of 25.4 mm (or 1 inch) can be prepared. The sample can then be placed under pressure by a clamping mechanism, such that a grip distance of about 50 mm is established. Next, the sample is subject to a testing speed of about 500 mm/min such that sufficient force is placed on the sample to stretch it accordingly.
  • a model can be developed calculating the tensile strength associated with the sample of the multi-layer film.
  • the results of the modeling can then be evaluated pursuant to the parameters set forth in the ISO 527-5:2009 permitting calculation of the tensile strength at both 10% elongation and at break. It will be appreciated that other suitable techniques may be available by which to measure tensile strength of a multi-layer film.
  • the multi-layer films can have a seal strength from about 0.10 N/m to about 2.0 N/m; and in certain embodiments from about 0.20 N/m to about 1.0 N/m.
  • the seal strength can be measured using a variety of techniques, including the methodology set forth in ISO 527-5:2009. To apply the methodology of ISO 527-5:2009, a sample of the multi-layer film will need to be prepared. In one embodiment, a sample size of 25.4 mm (or 1 inch) can be used, wherein the sample includes a seal extending along the mid-region of the sample.
  • the “seal” can include any region where one edge of the multi-layer film has been joined with another edge of the same (or different) multi-layer film.
  • this seal can be formed using a variety of suitable techniques (e.g., heat sealing).
  • the sample can then be placed under pressure by a clamping mechanism, such that a grip distance of about 50 mm is established and the seal is placed between the grip distance.
  • the sample is subject to a testing speed pursuant to ISO 527-5:2009 such that sufficient force is placed on the sample to stretch it accordingly.
  • the seal strength associated with the sample of the multi-layer film can be measured.
  • the results of the modeling can then be evaluated pursuant to the parameters set forth in the ISO 527-5:2009. It will be appreciated that other suitable techniques may be available by which to measure seal strength of a multi-layer film.
  • the present disclosure further relates to a method for making a multi-layer film comprising a synthetic polymer derived from a renewable resource.
  • the method comprises the steps of providing a renewable resource; deriving an intermediate monomer from the renewable resource; polymerizing the intermediate monomer to form a synthetic polymer and incorporating the synthetic polymer into a multi-layer film.
  • the present disclosure further relates to providing one or more of the multi-layer films to a consumer and communicating reduced petrochemical usage to the consumer.
  • the synthetic polymer derived from renewable resources may undergo additional process steps prior to incorporation into the multi-layer film.
  • the present disclosure further relates to a method for making the layered arrangement for a multi-layer film.
  • Multi-layer films can be made by known layering processes typically using a uni-axial cast or planar sheet process or lamination.
  • Coextruded cast film or sheet structures typically have 2 to 5 layers; however, cast film or sheet structures including hundreds of layers are known.
  • early multi-layer processes and structures are shown in U.S. Pat. No. 3,565,985; U.S. Pat. No. 3,557,265; and U.S. Pat. No. 3,884,606.
  • WO 2008/008875 discloses a related art method of forming multi-layered structures having many, for example fifty to several hundred, alternating layers of film.
  • the film structures can also be made as described in a tenter-frame technique, such as that used for oriented polypropylene.
  • the multi-layer films can be laminated onto another layer(s) in a secondary operation, such as that described in Packaging Foods With Plastics, by Wilmer A. Jenkins and James P. Harrington (1991) or that described in “Coextrusion For Barrier Packaging” by W. J. Schrenk and C. R. Finch, Society of Plastics Engineers RETEC Proceedings, Jun. 15-17 (1981), pp. 211-229, the disclosure of which is incorporated herein by reference. If a monolayer film layer is produced via tubular film (i.e., blown film techniques) or flat die (i.e., cast film) as described by K. R. Osborn and W. A. Jenkins in “Plastic Films, Technology and Packaging Applications” (Technomic Publishing Co., Inc.
  • the film must go through an additional post-extrusion step of adhesive or extrusion lamination to other packaging material layers to form a multi-layer film. If the film is a coextrusion of two or more layers (also described by Osborn and Jenkins), the film may still be laminated to additional layers of packaging materials, depending on the other physical requirements of the final film. “Laminations Vs. Coextrusion” by D. Dumbleton (Converting Magazine (September 1992), also discusses lamination versus coextrusion.
  • the multi-layer films contemplated herein can also go through other post extrusion techniques, such as a biaxial orientation process.
  • a suitable validation technique is through 14 C analysis.
  • a small amount of the carbon dioxide in the atmosphere is radioactive.
  • This 14 C carbon dioxide is created when nitrogen is struck by an ultra-violet light produced neutron, causing the nitrogen to lose a proton and form carbon of molecular weight 14 which is immediately oxidized to carbon dioxide.
  • This radioactive isotope represents a small but measurable fraction of atmospheric carbon.
  • Atmospheric carbon dioxide is cycled by green plants to make organic molecules during photosynthesis. The cycle is completed when the green plants or other forms of life metabolize the organic molecules, thereby producing carbon dioxide which is released back to the atmosphere. Virtually all forms of life on Earth depend on this green plant production of organic molecules to grow and reproduce. Therefore, the 14 C that exists in the atmosphere becomes part of all life forms, and their biological products.
  • fossil fuel based carbon does not have the signature radiocarbon ratio of atmospheric carbon dioxide.
  • the modern reference standard used in radiocarbon dating is a NIST (National Institute of Standards and Technology) standard with a known radiocarbon content equivalent approximately to the year AD 1950.
  • AD 1950 was chosen since it represented a time prior to thermo-nuclear weapons testing which introduced large amounts of excess radiocarbon into the atmosphere with each explosion (termed “bomb carbon”).
  • the AD 1950 reference represents 100 pMC.
  • a biomass content result is derived by assigning 100% equal to 107.5 pMC and 0% equal to 0 pMC. In this regard, a sample measuring 99 pMC will give an equivalent bio-based content value of 92%.
  • a multi-layer film comprises a bio-based content value from about 10% to about 100% using ASTM D6866-10, method B. In another embodiment, a multi-layer film comprises a bio-based content value from about 20% to about 100% using ASTM D6866-10, method B. In yet another embodiment, a multi-layer film comprises a bio-based content value from about 50% to about 100% using ASTM D6866-10, method B.
  • a representative sample of the component must be obtained for testing.
  • a representative portion of the multi-layer film can be ground into particulates less than about 20 mesh using known grinding methods (e.g., Wiley® mill), and a representative sample of suitable mass taken from the randomly mixed particles.
  • the present disclosure relating to multi-layer films derived from renewable resources further provides means for which to communicate an environmental message to a consumer. Such messages could be displayed on the multi-layer films, in such circumstances where the films are used as packaging materials for absorbent articles (e.g., diapers).
  • the related environmental message may convey the benefits or advantages of the multi-layer film comprising a polymer derived from a renewable resource.
  • the related environmental message may identify the multi-layer film as: being environmentally friendly or Earth friendly; having reduced petroleum (or oil) dependence or content; having reduced foreign petroleum (or oil) dependence or content; having reduced petrochemicals or having components that are petrochemical free; and/or being made from renewable resources or having components made from renewable resources.
  • This communication is of importance to consumers that may have an aversion to petrochemical use (e.g., consumers concerned about depletion of natural resources or consumers who find petrochemical based products unnatural or not environmentally friendly) and to consumers that are environmentally conscious. Without such a communication, the benefit of the present disclosure may be lost on some consumers.
  • the communication may be effected in a variety of communication forms. Suitable communication forms include store displays, posters, billboard, computer programs, brochures, package literature, shelf information, videos, advertisements, internet web sites, pictograms, iconography, or any other suitable form of communication. The information could be available at stores, on television, in a computer-accessible form, in advertisements, or any other appropriate venue. Ideally, multiple communication forms may be employed to disseminate the related environmental message.
  • the communication may be written, spoken, or delivered by way of one or more pictures, graphics, or icons.
  • a television or internet based-advertisement may have narration, a voice-over, or other audible conveyance of the related environmental message.
  • the related environmental message may be conveyed in a written form using any of the suitable communication forms listed above.
  • the related environmental message may also include a message of petrochemical equivalence.
  • Many renewable, naturally occurring, or non-petroleum derived polymers are known. However, these polymers often lack the performance characteristics that consumers have come to expect when used in conjunction with multi-layer films. Therefore, a message of petroleum equivalence may be necessary to educate consumers that the polymers derived from renewable resources, as described above, exhibit equivalent or better performance characteristics as compared to petroleum derived polymers.
  • a suitable petrochemical equivalence message can include comparison to multi-layer films that do not have a polymer derived from a renewable resource. For example, a suitable combined message may be, “Packaging for Product Brand A with an environmentally friendly material is just as effective as Packaging for Product Brand B.” This message conveys both the related environmental message and the message of petrochemical equivalence.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Laminated Bodies (AREA)
  • Wrappers (AREA)
US13/084,630 2011-03-18 2011-04-12 Multi-Layer Films And Methods Of Forming Same Abandoned US20120263924A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
US13/084,630 US20120263924A1 (en) 2011-04-12 2011-04-12 Multi-Layer Films And Methods Of Forming Same
PCT/US2012/029211 WO2012129046A1 (fr) 2011-03-18 2012-03-15 Pellicules polymères multicouches renforcées et leurs procédés de fabrication
CN2012800127069A CN103415391A (zh) 2011-03-18 2012-03-15 多层聚合物膜及其形成方法
PCT/US2012/029208 WO2012129045A1 (fr) 2011-03-18 2012-03-15 Pellicules polymères multicouches et leurs procédés de fabrication
EP12711090.6A EP2686166A1 (fr) 2011-03-18 2012-03-15 Pellicules polymères multicouches renforcées et leurs procédés de fabrication
CN2012800127181A CN103429430A (zh) 2011-03-18 2012-03-15 多层聚合物强化膜及其形成方法
BR112013023684A BR112013023684A2 (pt) 2011-03-18 2012-03-15 filmes poliméricos multicamadas e métodos para formação dos mesmos
EP12710637.5A EP2686162A1 (fr) 2011-03-18 2012-03-15 Pellicules polymères multicouches et leurs procédés de fabrication
BR112013023796A BR112013023796A2 (pt) 2011-03-18 2012-03-15 filmes poliméricos multicamadas reforçados e métodos para fabricação dos mesmos
PCT/US2012/032955 WO2012142057A2 (fr) 2011-04-12 2012-04-11 Films multicouches et leurs procédés de fabrication
US13/968,458 US9169366B2 (en) 2011-04-12 2013-08-16 Multi-layer films and methods of forming same
US14/863,480 US9802393B2 (en) 2011-04-12 2015-09-24 Multi-layer films and methods of forming same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US13/084,630 US20120263924A1 (en) 2011-04-12 2011-04-12 Multi-Layer Films And Methods Of Forming Same

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/968,458 Division US9169366B2 (en) 2011-04-12 2013-08-16 Multi-layer films and methods of forming same

Publications (1)

Publication Number Publication Date
US20120263924A1 true US20120263924A1 (en) 2012-10-18

Family

ID=46001793

Family Applications (3)

Application Number Title Priority Date Filing Date
US13/084,630 Abandoned US20120263924A1 (en) 2011-03-18 2011-04-12 Multi-Layer Films And Methods Of Forming Same
US13/968,458 Active 2031-12-27 US9169366B2 (en) 2011-04-12 2013-08-16 Multi-layer films and methods of forming same
US14/863,480 Active 2031-04-13 US9802393B2 (en) 2011-04-12 2015-09-24 Multi-layer films and methods of forming same

Family Applications After (2)

Application Number Title Priority Date Filing Date
US13/968,458 Active 2031-12-27 US9169366B2 (en) 2011-04-12 2013-08-16 Multi-layer films and methods of forming same
US14/863,480 Active 2031-04-13 US9802393B2 (en) 2011-04-12 2015-09-24 Multi-layer films and methods of forming same

Country Status (2)

Country Link
US (3) US20120263924A1 (fr)
WO (1) WO2012142057A2 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20140329103A1 (en) * 2013-05-01 2014-11-06 Avery Dennison Corporation Multilayer film
WO2015054350A1 (fr) 2013-10-11 2015-04-16 The Procter & Gamble Company Pellicules polymères multicouches
US20170095376A1 (en) * 2011-07-29 2017-04-06 Unicharm Corporation Bodily fluid absorbent matrix and method for manufacturing the same

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11197787B2 (en) 2011-07-08 2021-12-14 The Procter & Gamble Company Absorbent article package with enhanced opening and recloseability
US20150104628A1 (en) * 2013-10-11 2015-04-16 The Procter & Gamble Company Multi-Layer Polymeric Films Containing Energy Dissipating Layers
US20150197679A1 (en) * 2014-01-10 2015-07-16 Empire Technology Development Llc Thermostatic packaging and methods for their preparation and use
US9492332B2 (en) 2014-05-13 2016-11-15 Clopay Plastic Products Company, Inc. Breathable and microporous thin thermoplastic film
AU2015321533B2 (en) 2014-09-24 2019-01-17 The Chemours Company Fc, Llc Materials with enhanced protection of light sensitive entities
KR102704216B1 (ko) 2015-07-10 2024-09-06 베리 글로벌 인코포레이티드 마이크로다공성 통기성 필름 및 마이크로다공성 통기성 필름의 제조 방법
US11472085B2 (en) 2016-02-17 2022-10-18 Berry Plastics Corporation Gas-permeable barrier film and method of making the gas-permeable barrier film
US10576718B2 (en) 2016-07-01 2020-03-03 The Proctor & Gamble Company Heat sealable multilayer packaging film with improved opacity
WO2018081487A1 (fr) 2016-10-28 2018-05-03 The Procter & Gamble Company Emballage d'article absorbant à ouverture et refermeture améliorées
US9827150B1 (en) 2016-11-30 2017-11-28 The Procter & Gamble Company Absorbent article package with enhanced opening and recloseability
WO2018227035A1 (fr) 2017-06-08 2018-12-13 The Procter & Gamble Company Emballage pour des articles absorbants à ouverture et refermeture améliorées
US11433158B2 (en) 2017-12-12 2022-09-06 The Procter & Gamble Company Recycle friendly and sustainable absorbent articles
WO2019213192A1 (fr) * 2018-05-02 2019-11-07 Corning Incorporated Films multi-couches
EP3611111B1 (fr) 2018-08-13 2021-06-23 The Procter & Gamble Company Emballage d'articles absorbants avec ouverture refermable
HUE064686T2 (hu) 2018-08-22 2024-04-28 Procter & Gamble Egyszer használatos nedvszívó termékek
EP3856110A1 (fr) 2018-09-27 2021-08-04 The Procter & Gamble Company Articles absorbants du type culotte
US11707548B2 (en) 2018-10-09 2023-07-25 The Procter & Gamble Company Absorbent article comprising a lotion resistant polymeric filler composition
EP3656697B1 (fr) 2018-11-22 2021-06-30 The Procter & Gamble Company Emballage d'articles absorbants avec ouverture refermable
WO2021212348A1 (fr) 2020-04-22 2021-10-28 The Procter & Gamble Company Articles absorbants ayant des matériaux non tissés avec des fibres naturelles
WO2021236700A1 (fr) 2020-05-22 2021-11-25 The Procter & Gamble Company Articles absorbants munis de ceintures et de recouvrements de ceintures
US20220087881A1 (en) 2020-09-22 2022-03-24 The Procter & Gamble Company Absorbent articles with patterned front ears
JP2024514014A (ja) 2021-04-30 2024-03-27 ザ プロクター アンド ギャンブル カンパニー パッケージ化された吸収性物品
EP4088704A1 (fr) 2021-05-10 2022-11-16 The Procter & Gamble Company Noyau absorbant avec bande(s) non tissée(s) comprenant des fibres superabsorbantes
JP2024520090A (ja) 2021-06-08 2024-05-21 ザ プロクター アンド ギャンブル カンパニー 脆弱接合部を有する腰部パネルを含む吸収性物品
EP4129259A1 (fr) 2021-08-04 2023-02-08 The Procter & Gamble Company Article absorbant avec inhibiteur de l'urée et utilisation de l'article
CN218338615U (zh) 2021-09-22 2023-01-20 宝洁公司 图案化纤维基底
CN118251196A (zh) 2021-11-19 2024-06-25 宝洁公司 带有具有高拉伸区域和低拉伸区域的前腰区和/或后腰区的吸收制品及其制备方法
US20230310229A1 (en) 2022-04-04 2023-10-05 The Procter & Gamble Company Absorbent articles including a waist panel
EP4279049A1 (fr) 2022-05-16 2023-11-22 The Procter & Gamble Company Procédé de fabrication d'un article absorbant et article absorbant
EP4279050A1 (fr) 2022-05-16 2023-11-22 The Procter & Gamble Company Article absorbant
WO2023250479A1 (fr) 2022-06-24 2023-12-28 The Procter & Gamble Company Articles absorbants contenant des compositions d'indication d'humidité et procédés de fabrication
US20240000619A1 (en) 2022-06-30 2024-01-04 The Procter & Gamble Company Absorbent articles and methods and apparatuses for making absorbent articles with frangible pathways
WO2024026286A1 (fr) 2022-07-28 2024-02-01 The Procter & Gamble Company Articles absorbants à éléments de fixation jetables ayant des éléments de fixation de type crochets intégrés
WO2024097529A1 (fr) 2022-11-01 2024-05-10 The Procter & Gamble Company Réseau d'articles absorbants avec stratifiés extensibles liés par ultrasons
US20240148562A1 (en) 2022-11-04 2024-05-09 The Procter & Gamble Company Method and apparatus for bonding elastic parts under tension to an advancing carrier
EP4364708A1 (fr) 2022-11-07 2024-05-08 The Procter & Gamble Company Ensemble d'articles absorbants ayant des éléments d'étanchéité de taille
WO2024159066A1 (fr) 2023-01-27 2024-08-02 The Procter & Gamble Company Articles absorbants avec stratifiés extensibles liés
WO2024159065A1 (fr) 2023-01-27 2024-08-02 The Procter & Gamble Company Articles absorbants avec stratifiés extensibles liés
US20240269012A1 (en) 2023-02-10 2024-08-15 The Procter & Gamble Company Absorbent articles with barrier leg cuffs having a backfolded inner cuff
EP4442232A1 (fr) 2023-04-04 2024-10-09 The Procter & Gamble Company Article absorbant et procédé de fabrication d'un article absorbant

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6596385B1 (en) * 1999-04-19 2003-07-22 Exxonmobil Oil Corporation Oriented multi-layer polymer film
US20040138378A1 (en) * 2000-03-28 2004-07-15 Makoto Takagi Regenerated resin composition

Family Cites Families (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3456044A (en) 1965-03-12 1969-07-15 Heinz Erich Pahlke Biaxial orientation
US3557265A (en) 1967-12-29 1971-01-19 Dow Chemical Co Method of extruding laminates
US3565985A (en) 1969-04-10 1971-02-23 Dow Chemical Co Method of preparing multilayer plastic articles
US3884606A (en) 1971-10-01 1975-05-20 Dow Chemical Co Apparatus for multilayer coextrusion of sheet or film
US4083889A (en) 1977-05-26 1978-04-11 Mobil Oil Corporation Process for manufacturing ethylene
DE2928922A1 (de) 1979-07-18 1981-02-12 Hoechst Ag Verfahren zur herstellung niederer olefine aus methanol-wasser-gemischen
US4352849A (en) 1981-03-26 1982-10-05 W. R. Grace & Co. Coextruded, heat-shrinkable, multi-layer, polyolefin packaging film
US4423270A (en) 1981-09-28 1983-12-27 Pearson Donald E Process for catalytic dehydration of ethanol vapor to ethylene
US4865902A (en) 1986-01-17 1989-09-12 E. I. Du Pont De Nemours And Company Multilayered polyolefin high shrinkage, low-shrink force shrink film
CA1324749C (fr) 1987-04-10 1993-11-30 Vincent Wayne Herran Film etirable/retractable souple
US4963419A (en) 1987-05-13 1990-10-16 Viskase Corporation Multilayer film having improved heat sealing characteristics
US4820557A (en) 1987-09-17 1989-04-11 W. R. Grace & Co.-Conn. Thermoplastic packaging film of low I10 /I2
US4952451A (en) 1988-11-17 1990-08-28 W. R. Grace & Co.-Conn. Stretch/shrink film with improved oxygen transmission
ATE141579T1 (de) 1991-02-04 1996-09-15 Mitsui Petrochemical Ind Verfahren zur herstellung von propylene
US5344714A (en) * 1992-11-04 1994-09-06 Mobil Oil Corporation LLDPE composite film free of melt fracture
TW330217B (en) 1994-12-20 1998-04-21 Kimberly Clark Co Low gauge films and film/nonwoven laminates
DE69818635T2 (de) * 1998-03-09 2004-08-05 National Research Development Corp. Kunststoff-Folie
SE512292C2 (sv) 1998-07-02 2000-02-28 Sca Hygiene Prod Ab Användning av ett material innehållande polyeten framställd från förnybar råvara som komponent i ett absorberande alster, och det absorberande alstret
EP1008446A1 (fr) 1998-12-07 2000-06-14 Walk Pak Holding Nv Film composite multicouches et utilisation de ce film
DE19859789C1 (de) 1998-12-23 2000-06-08 M & W Verpackungen Gmbh Recyclingfähige IML-Etikettenfolie
US6333096B1 (en) 1999-12-21 2001-12-25 Montell Technology Company Bv Co-extruded, multilayer packaging film made from propylene polymer material
EP1539489B1 (fr) 2002-09-16 2014-06-04 Dow Global Technologies LLC Films a transparence elevee et a rigidite elevee
GB0314189D0 (en) 2003-06-18 2003-07-23 Borealis Tech Oy Food packaging
EP1508439B1 (fr) 2003-08-16 2008-03-12 Renolit AG Film multicouche pour la fabrication d'étiquettes
US7588706B2 (en) 2004-12-16 2009-09-15 Exxonmobil Chemical Patents Inc. Multi-layer films with improved properties
US20060147663A1 (en) 2004-12-30 2006-07-06 Fina Technology, Inc. Co-extruded film structures of polypropylene impact copolymer with other polymers
US7279206B2 (en) 2005-03-22 2007-10-09 Curwood, Inc. Packaging laminates and articles made therefrom
EP1759833A1 (fr) 2005-08-30 2007-03-07 Borealis Technology Oy Film
JP4605384B2 (ja) 2005-11-07 2011-01-05 オムロン株式会社 可搬型情報処理端末装置
BRPI0618557A2 (pt) 2005-11-14 2011-09-06 Mitsui Chemicals Inc método para produzir e método para produzir continuamente propileno contendo carbono derivado de biomassa, propileno de alta pureza, polìmero ou copolìmero de propileno e artigo
US20070190013A1 (en) * 2006-02-13 2007-08-16 Yeli Zhang Film and film-forming compositions
US20070252276A1 (en) * 2006-04-28 2007-11-01 Ian Lloyd-George Thin film for vertical form fill and seal packaging of flowable materials
BRPI0713178B1 (pt) 2006-07-14 2018-06-12 Dow Global Technologies Inc. Estrutura composta multicamada de película- espuma
BRPI0605173A (pt) 2006-12-05 2008-07-22 Braskem Sa processo de produção de uma ou mais olefinas, olefina, e, polìmero
DE602006009412D1 (de) * 2006-12-21 2009-11-05 Borealis Tech Oy Film
DE602006013673D1 (en) 2006-12-21 2010-05-27 Borealis Tech Oy Film
US20100036173A1 (en) 2007-01-09 2010-02-11 E.I. Du Pont De Nemours And Company Production of butenes and derivatives therefrom from aqueous ethanol
WO2008147836A1 (fr) 2007-05-23 2008-12-04 David Bradin Production de polypropylène à partir de ressources renouvelables
CN101687398A (zh) * 2007-07-03 2010-03-31 纳幕尔杜邦公司 包含生物基材料的多层膜结构
US20100260989A1 (en) * 2007-07-16 2010-10-14 Rkw Se Films for label facestock
WO2009098267A1 (fr) 2008-02-07 2009-08-13 Total Petrochemicals Research Feluy Procédé pour fabriquer des oléfines à partir d'éthanol
US8105680B2 (en) * 2008-04-08 2012-01-31 Exxonmobil Oil Corporation Multi-layer slip film for printing and lamination processes
BRPI0802222B1 (pt) 2008-06-03 2022-01-04 Petróleo Brasileiro S.A. - Petrobras Processo para produzir olefinas leves a partir de uma carga contendo triglicerídeos
FR2939139B1 (fr) 2008-12-03 2012-12-21 Arkema France Composition comprenant du polypropylene et/ou un copolymere du propylene obtenus a partir de matieres renouvelables et utilisations
BRPI1008287A2 (pt) 2009-02-24 2016-03-15 Gevo Inc métodos de preparação de butadieno e isopreno renováveis
CN103459148B (zh) * 2011-04-12 2016-07-13 宝洁公司 衍生自可再生资源的柔性阻隔包装

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6596385B1 (en) * 1999-04-19 2003-07-22 Exxonmobil Oil Corporation Oriented multi-layer polymer film
US20040138378A1 (en) * 2000-03-28 2004-07-15 Makoto Takagi Regenerated resin composition

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170095376A1 (en) * 2011-07-29 2017-04-06 Unicharm Corporation Bodily fluid absorbent matrix and method for manufacturing the same
US20140329103A1 (en) * 2013-05-01 2014-11-06 Avery Dennison Corporation Multilayer film
WO2014179451A1 (fr) * 2013-05-01 2014-11-06 Avery Dennison Corporation Film multicouche
WO2015054350A1 (fr) 2013-10-11 2015-04-16 The Procter & Gamble Company Pellicules polymères multicouches

Also Published As

Publication number Publication date
WO2012142057A2 (fr) 2012-10-18
US20130327476A1 (en) 2013-12-12
WO2012142057A3 (fr) 2012-12-27
US20160009059A1 (en) 2016-01-14
US9169366B2 (en) 2015-10-27
US9802393B2 (en) 2017-10-31

Similar Documents

Publication Publication Date Title
US9802393B2 (en) Multi-layer films and methods of forming same
US20120288692A1 (en) Renewably sourced films and methods of forming same
US8871319B2 (en) Flexible barrier packaging derived from renewable resources
US7943218B2 (en) Environmentally-friendly multi-layer flexible film having barrier properties
US20110274892A1 (en) Biaxially oriented bio-based polyolefin films and laminates
JP6791627B2 (ja) 複層ポリエチレン系シーラントフィルム及びこれを使用したラミネートフィルム
US20120237746A1 (en) Multi-Layer Polymeric Films and Methods of Forming Same
US20080226920A1 (en) Multilayer Elastic Film Structures
WO2014046907A1 (fr) Films thermoplastiques flexibles et articles
CN103085415B (zh) 包装用聚烯烃薄膜及其制备方法
EP2990196A1 (fr) Papier ou carton revetu
US20140329103A1 (en) Multilayer film
EP2828079B1 (fr) Film pour frontal d'étiquette
EP2686162A1 (fr) Pellicules polymères multicouches et leurs procédés de fabrication
US20130333327A1 (en) Sustainable Wipes Products And Methods Of Forming Same
RU189951U1 (ru) Пленка для защиты поверхности
DE102011122211A1 (de) Beschichtetes Papier oder Karton
JP2023528591A (ja) 生分解性ポリエステル及びそれから作られた粘着性包装フィルム
WO2012127121A2 (fr) Film frontal pour étiquette
Memon et al. A development of laminating mulberry paper by biodegradable films
DE102011107965A1 (de) Beschichtetes Papier oder Karton

Legal Events

Date Code Title Description
AS Assignment

Owner name: PROCTER & GAMBLE COMPANY, THE, OHIO

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:WEISMAN, PAUL THOMAS;WEINBERGER, ERIC PATTON;CARUSO, PIER-LORENZO;AND OTHERS;SIGNING DATES FROM 20110414 TO 20110503;REEL/FRAME:026252/0693

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION