WO1995026268A1 - Composite multicouches souple - Google Patents

Composite multicouches souple Download PDF

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Publication number
WO1995026268A1
WO1995026268A1 PCT/GB1995/000584 GB9500584W WO9526268A1 WO 1995026268 A1 WO1995026268 A1 WO 1995026268A1 GB 9500584 W GB9500584 W GB 9500584W WO 9526268 A1 WO9526268 A1 WO 9526268A1
Authority
WO
WIPO (PCT)
Prior art keywords
layer
polymer
composite
composite according
tie
Prior art date
Application number
PCT/GB1995/000584
Other languages
English (en)
Inventor
John Patrick Grayson
Original Assignee
Bp Chemicals Limited
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 Bp Chemicals Limited filed Critical Bp Chemicals Limited
Priority to AU18992/95A priority Critical patent/AU1899295A/en
Priority to EP95911416A priority patent/EP0700338A1/fr
Publication of WO1995026268A1 publication Critical patent/WO1995026268A1/fr

Links

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
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/306—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising vinyl acetate or vinyl alcohol (co)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
    • 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
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • 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
    • B32B2250/246—All polymers belonging to those covered by groups B32B27/32 and B32B27/30
    • 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
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B32B2307/546—Flexural strength; Flexion stiffness
    • 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
    • B32B2323/00—Polyalkenes
    • B32B2323/04—Polyethylene
    • B32B2323/043—HDPE, i.e. high density polyethylene
    • 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
    • B32B2323/00—Polyalkenes
    • B32B2323/04—Polyethylene
    • B32B2323/046—LDPE, i.e. low density polyethylene
    • 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
    • B32B2323/00—Polyalkenes
    • B32B2323/10—Polypropylene
    • 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
    • B32B2329/00—Polyvinylalcohols, polyvinylethers, polyvinylaldehydes, polyvinylketones or polyvinylketals
    • B32B2329/04—Polyvinylalcohol

Definitions

  • This invention relates to a novel multi-layered composite comprising a plurality of polymer layers and having good flexibility and high fiex-crack resistance.
  • Composites comprising several polymers are well known.
  • tie layers having adhesive properties between the virgin polymers.
  • Such tie layers may comprise grafting of maleic anhydride or acrylate ester polymers on to one surface of a polyolefin film and then applying thereon a further layer of a virgin polymer or a metallic layer in order to produce the desired composite.
  • Such composites have found uses in various industries including the production of protective garments, canning of food products, the so called 'bag-in-box' containers and barrier films for oxygen, gasoline or other industries where toxic or hazardous emissions have to be contained.
  • Such composites have also been used to produce a flexible vapour containment liner (hereafter "VCL”) for a fuel tank system in order to minimise the risk of accidental ignition and to control emissions from such tanks whether eg they be used in automotive vehicles, aircraft or in oil tankers.
  • VCL flexible vapour containment liner
  • Most of these prior art laminates have been made from a layer of a hydrolysate of an ethylene-vinyl acetate copolymer, ie ethylene-vinyl alcohol copolymer (hereafter “EVOH”), sandwiched between layers of a polyolefin which may be polyethylene or polypropylene, optionally using a tie layer in between the polyolefin and the EVOH layers to improve adhesion thereof.
  • EVOH ethylene-vinyl alcohol copolymer
  • the primary problem has been their relatively low flex-crack resistance which causes them to lose their performance integrity. This loss of performance is particularly undesirable if the composite is used for storing liquids, especially consumable
  • the present invention is a multi-layer composite comprising at least one sequence of layers comprising a heterophasic polypropylene (co)polymer layer/tie-layer/EVOH/tie-layer/polyolefin layer characterised in that the heterophasic polypropylene (co)polymer layer comprises a homopolymer of propylene or a co-polymer of propylene with ethylene and/or an alpha-olefin.
  • composite as used herein and throughout the specification is meant a product prepared either by lamination of several layers and/or by coextrusion of a number of components in order to give the desired product.
  • various components are referred to herein as “layers” for convenience, whether or not they have been laminated.
  • EVOH signifies an ethylene-vinyl alcohol copolymer which may be derived by the hydrolysis of an ethylene-vinyl acetate copolymer.
  • the heterophasic polypropylene (co)poiymer layer is suitably that derived by the copolymerisation of propylene with ethylene and/or an alpha olefin which has 2-8 carbon atoms such as eg (iso)butene, and may optionally contain other monomers such as dienes, eg butadiene, 1 ,4-hexadiene, 1 ,5-hexadiene and a mixture of ethylidene norbornene and diene monomers.
  • Such heterophasic polypropylenes are suitably produced by an extended Spheripol® process of Himont which is the so called "catalloy” process and involves the use of a multi-component catalyst system to produce engineering resins and elastomers.
  • the polymers are believed to behave as a polyolefin 'alloy' and hence the process is known as the catalloy process.
  • Such polymers are usually copolymers of propylene/ethylene/butene made by a two-stage polymerisation process as described in the following published references: EP-A-0472 946, EP-A-0 477 662, EP-A-0 483 675 AND EP-A-0489 284. The processes described in these documents are incorporated herein by reference.
  • Films made from such (co)polymers have a thickness of about 10-80 ⁇ m and have a flexural modulus of less than 150, suitably in the range of 20-100.
  • a specific example of such a copolymer is HIFAX® 7029XCP (ex Himont).
  • the olefin copolymer layer may be a blend.
  • 7029XCP (80% wt/wt) can be blended with Himont EP2S12B (20% wt/wt, ex Himont), a random copolymer of polypropylene and polyethylene.
  • the thickness of this layer in the composite is suitably in the range from 10-80 ⁇ m, preferably from 20-40 ⁇ m, eg 30 ⁇ m.
  • heteroophasic polypropylene (co)polymer as used herein and throughout the specification signifies that such a polymer may be a homopolymer or a copolymer of propylene.
  • At least one end layer of the composite is of a heterophasic polypropylene (co)polymer.
  • the olefin polymer layer at the other end (opposite to the heterophasic (co)polymer) of such a composite such olefin polymer may itself be a homo-polymer or co-polymer of ethylene, propylene or mixtures thereof with one another or with other comonomers such as vinyl acetate, acrylic acid, alkyl acrylates and alkyl methacrylates.
  • such olefin polymers may be selected from one or more of a heterophasic polypropylene (co)polymer, a polypropylene homopolymer, a polypropylene copolymer, linear low density polyethylene (hereafter “LLDPE”), low density polyethylene (hereafter “LDPE”), high density polyethylene (hereafter “HDPE”), medium density polyethylene (hereafer “MDPE”), very low density polyethylene (hereafter “VLDPE”), ethylene-vinyl acetate copolymer, ethylene-ethyl acrylate copolymer, ionomers such as eg SURLYN® and IOTEK®, ethylene-acrylic acid copolymer, ethylene- methacrylic acid copolymer, a polycarbonate, a polyamide and any blend thereof.
  • LLDPE linear low density polyethylene
  • LDPE low density polyethylene
  • HDPE high density polyethylene
  • MDPE medium density polyethylene
  • VLDPE
  • a blend of LLDPE containing some octene comonomer and VLDPE is preferred. Particularly preferred is a blend of STAMYLEX® 09016 (ex, DSM, 80% wt/wt) and a conventional LDPE grade LD150BW (ex Exxon, 20% wt/wt).
  • the polyolefin layer suitably has the same thickness as that of the heterophasic polypropylene (co)polymer, ie a range of 10-80 ⁇ m, preferably 20-40 ⁇ m, eg 30 ⁇ m.
  • the tie-layer in the composite is the adhesive layer which binds the polyolefin layer or the polyolefin copolymer layer with the layer of EVOH.
  • the tie-layer may be formed by grafting at least one polymerizable ethylenically unsaturated monomer (hereafter "EUM") which is suitably an ethylenically unsaturated carboxylic acid, ester or anhydride on to a material which is the same as the adjacent polyolefinic end layer to form a graft-copolymer.
  • EUM polymerizable ethylenically unsaturated monomer
  • This enables the tie layer to key in and blend into the polyolefin or heterophasic polypropylene (co)polymer end layer as the case may be when preparing the composite.
  • the tie-layer is a graft copolymer of polypropylene and a polymerizable ethylenically unsaturated monomer.
  • polymerizable ethylenically unsatured monomers include maleic acid (hereafter “MA”), maleic anhydride (hereafter “MAH”), acrylic acid (hereafter “AA”), alkyl acrylate esters (hereafter “AAE”), methacrylic acid (hereafter “MAA”), alkyl methacrylate esters (hereafter “AME”), itaconic acid, citraconic acid, mesaconic acid, 4-methyl cyclohex-4-ene-1 ,2-dicarboxylic acid anhydride, bicyclo (2.2.2)oct-5-ene-2,3-dicarboxylic acid anhydride, 1 ,2,3, 4,5,8, 9, 10-octahydrona
  • maleic anhydride tetrahydrophthalic anhydride and bicyclo(2.2.1 )hept-5-ene-2,3-dicarboxylic acid anhydride are preferred.
  • a typical and preferred example of a tie-layer is the graft copolymer derived from a polyolefin and maleic anhydride and sold as ADMER® grades, especially ADMER® NF 530E and ADMER® AT 851. Conjugated unsaturated esters, in addition to the alkyl acrylates and alkyl methacrylates mentioned above, may also suitably be used for co- grafting.
  • esters include, eg, dialkyl maleates, dialkyl fumarates, dialkyl itaconates, dialkyl mesaconates, dialkyl citraconates, alkyl crotonates, alkyl tiglates wherein the alkyl group aliphatic, cycloaliphatic, alicyclic or an arlkyl group and suitably has 1-12 carbon atoms.
  • Dibutyl maleate, diethyl fumarate and dimethyl itaconate are particularly preferred.
  • These monomers may be used either alone or in combination with the anhydrides listed above and are suitably applied to at least one side of the adjacent polyolefinic layer.
  • Methods of grafting these monomers on to the polyolefin layer or polyolefin copolymer layer are well known in the art. For instance, methods of grafting MAH to the polyolefin layer are described eg in US-A-2973344 and US-A- 3290415.
  • the grafting may be performed in a solvent by placing the monomer in a solvent followed by irradiation as described in US-A-3290415 with peroxides.
  • the grafting may be carried out, eg in the case of polypropylene, by melt mixing with peroxides.
  • the peroxides that may be used include, eg, t-butyl hydroperoxide, p-menthane hydroperoxide, pinane hydroperoxide and cumene hydroperoxide.
  • Other grafting techniques include extrusion grafting and coating the polyolefin surface with a molten monomer followed by irradiation as described eg in US-A-3290415. These methods are incorporated herein by reference to these prior publications.
  • the thickness of the tie layer is suitably in the range from 2-1 O ⁇ m, preferably from 3-6 ⁇ m, eg 5 ⁇ m.
  • the EVOH used is suitably of a grade which contains from 25-50 mol% of ethylene, preferably from 29-44 mol% and even more preferably from 32- 38 mol %.
  • EVOH grades that may be used include inter alia, the so-called EVAL® LCH 101 or EPJ 102B (both ex Kuraray Industries).
  • the thickness of the EVOH layer is suitably in the range from 2-25 ⁇ m, preferably from 4-1 O ⁇ m, eg 6 ⁇ m.
  • the thickness of each of the layers in the composite is suitably in the following range: Polypropylene copolymer : 10-80 ⁇ m, preferably 20-50 ⁇ m eg 30 ⁇ m
  • Each tie layer 2-1 O ⁇ m, preferably 4-6 ⁇ m eg 5 ⁇ m
  • EVOH layer 2-25 ⁇ m, preferably 4-1 O ⁇ m eg 6 ⁇ m
  • Polyolefin blend 10-80 ⁇ m, preferably 20 ⁇ 40 ⁇ m eg 30 ⁇ m
  • the total thickness of the composite is from 35-180 ⁇ m, preferably from 60-1 OO ⁇ m, typically 80 ⁇ m.
  • the composite is produced by co-extrusion, this is suitably carried out within an overall average temperature in the range from 170-260° C.
  • the polyolefin layers ie both the heterophasic polypropylene (co)polymer layer and the olefin blend layer at the opposite end are suitably maintained at 180-220°C, the EVOH layer at 180-220°C, and the tie layer at upto 250°C.
  • the adhesive used to combine such sequences is suitably a polyurethane adhesive.
  • additional examples of such adhesives that may be used include a polyester/polyurethane adhesive or a polyether/polyurethane adhesive.
  • the composite preferably has at least two such sequences and the grades of any of the generic components in each sequence may be same or different.
  • a feature of the composites of the present invention is that they have: a. low permeability to oxygen and other gases; b. good heat sealability for conversion of the composites into bags or other containers; c. a very high degree of flexibility thereby allowing collapse of the bag when the contents thereof are dispensed; and d. excellent flex-crack resistance which enable them to retain performance integrity.
  • EXAMPLE Several types of laminates prepared by co-extrusion of various components (shown below) into a 5-layer tubular blown film using a BARMAG four-component five-layer extruder) were tested for their flex crack resistance and other physical properties.
  • the materials used for preparing the various coextruded films are identified below in Table 1 : TABLE 1
  • VLDPE Very low density polyethylene
  • the films were also subjected to an oxygen transmission test (OTR) and the test was carried out using a Mocon Ox-Tran 100 Twin tester.
  • OTR oxygen transmission test
  • the composite films of the present invention when compared with conventional films, show a. a much better flex-crack resistance (as shown by the Gelbo test); b. a lower stiffness (as shown by the tensile properties and Secant Modulus); and c. a greater resistance to pinholing and therefore reduced OTR.

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  • Laminated Bodies (AREA)

Abstract

L'invention concerne un composite multicouches qui comprend au moins une séquence de couches englogant une couche de (co)polymère de polypropylène hétérophase/une couche de liaison/une couche d'éthylène-copolymère d'alcool vinylique/une couche de liaison/une couche de polyoléfine. Cette séquence se caractérise par le fait que la couche de (co)polymère de polypropylène hétérophase comprend un homopolymère ou un co-polymère de propylène et de l'éthylène et/ou une alpha-oléfine. Ces composites présentent (a) une faible perméabilité à l'oxygène et à d'autres gaz, (b) une bonne aptitude au thermosondage qui permet d'en faire des sacs ou d'autres récipients, (c) un degré de souplesse très élevé qui permet d'aplatir ces sacs quand ils sont vidés, et (d) une excellente résistance aux pliures et aux fissures qui leur permet de garder l'intégralité de leurs qualités.
PCT/GB1995/000584 1994-03-28 1995-03-17 Composite multicouches souple WO1995026268A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU18992/95A AU1899295A (en) 1994-03-28 1995-03-17 Flexible multilayered composite
EP95911416A EP0700338A1 (fr) 1994-03-28 1995-03-17 Composite multicouches souple

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9406106A GB9406106D0 (en) 1994-03-28 1994-03-28 Multi-layered composite
GB9406106.6 1994-03-28

Publications (1)

Publication Number Publication Date
WO1995026268A1 true WO1995026268A1 (fr) 1995-10-05

Family

ID=10752625

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB1995/000584 WO1995026268A1 (fr) 1994-03-28 1995-03-17 Composite multicouches souple

Country Status (4)

Country Link
EP (1) EP0700338A1 (fr)
AU (1) AU1899295A (fr)
GB (1) GB9406106D0 (fr)
WO (1) WO1995026268A1 (fr)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0695629A2 (fr) * 1994-07-12 1996-02-07 Alkor Gmbh Kunststoffe Matériau composite multicouche, procédé pour sa fabrication et son utilisation
DE19542716A1 (de) * 1995-11-16 1997-05-22 Braun Melsungen Ag Polymer-Composit-Schlauchfolie
WO2011045329A1 (fr) 2009-10-16 2011-04-21 Ppg Europe B.V. Sachet pour matière colorante de peinture
US8196373B2 (en) 2006-09-05 2012-06-12 Liqui-Box Corporation Pouch making process including use of liquid packaging films of polyethylene and polypropylene blends
US8252397B2 (en) 2006-04-26 2012-08-28 Liqui-Box Corporation Flex crack resistant low density polyethylene films
US8978346B2 (en) 2010-04-16 2015-03-17 Liqui-Box Corporation Multi-layer, ethylene polymer-based films with high-density polyethylene based stiffening layer
US9283736B2 (en) 2010-04-16 2016-03-15 Liqui-Box Corporation Multi-layer, ethylene polymer-based films with novel polypropylene blend-based stiffening layer
US9533477B2 (en) 2010-04-16 2017-01-03 Liqui-Box Corporation Multi-layer, ethylene polymer-based films with polypropylene-based stiffening layer
US9636895B2 (en) 2006-06-20 2017-05-02 Avery Dennison Corporation Multilayered polymeric film for hot melt adhesive labeling and label stock and label thereof
US9662867B2 (en) 2006-06-14 2017-05-30 Avery Dennison Corporation Conformable and die-cuttable machine direction oriented labelstocks and labels, and process for preparing
US9676532B2 (en) 2012-08-15 2017-06-13 Avery Dennison Corporation Packaging reclosure label for high alcohol content products
US9701445B2 (en) 2013-12-20 2017-07-11 Bemis Company, Inc. Liners for bulk containers
USRE46911E1 (en) 2002-06-26 2018-06-26 Avery Dennison Corporation Machine direction oriented polymeric films and methods of making the same
EP2945799B1 (fr) 2013-01-18 2020-04-22 Sartorius Stedim Fmt Sas Film multicouche comprenant une couche de contact, une couche centrale et une autre extérieure pour la paroi d'un sachet à usage unique
US11459488B2 (en) 2014-06-02 2022-10-04 Avery Dennison Corporation Films with enhanced scuff resistance, clarity, and conformability

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2134446A (en) * 1983-01-31 1984-08-15 Grace W R & Co Pasteurizable, cook-in shrink film
EP0472946A2 (fr) * 1990-08-01 1992-03-04 Montell North America Inc. Composition élastoplastique de polyoléfine
EP0477662A2 (fr) * 1990-09-28 1992-04-01 Himont Incorporated Films de polymères d'oléfines
EP0485847A1 (fr) * 1990-11-16 1992-05-20 W.R. Grace & Co.-Conn. Conteneurs multicouches avec des propriétés de mise en oeuvre à chaud améliorées
EP0561428A1 (fr) * 1986-02-28 1993-09-22 W.R. Grace & Co.-Conn. Film d'emballage barrière d'oxygène

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2134446A (en) * 1983-01-31 1984-08-15 Grace W R & Co Pasteurizable, cook-in shrink film
EP0561428A1 (fr) * 1986-02-28 1993-09-22 W.R. Grace & Co.-Conn. Film d'emballage barrière d'oxygène
EP0472946A2 (fr) * 1990-08-01 1992-03-04 Montell North America Inc. Composition élastoplastique de polyoléfine
EP0477662A2 (fr) * 1990-09-28 1992-04-01 Himont Incorporated Films de polymères d'oléfines
EP0485847A1 (fr) * 1990-11-16 1992-05-20 W.R. Grace & Co.-Conn. Conteneurs multicouches avec des propriétés de mise en oeuvre à chaud améliorées

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0695629A2 (fr) * 1994-07-12 1996-02-07 Alkor Gmbh Kunststoffe Matériau composite multicouche, procédé pour sa fabrication et son utilisation
EP0695629A3 (fr) * 1994-07-12 1996-10-23 Alkor Gmbh Matériau composite multicouche, procédé pour sa fabrication et son utilisation
DE19542716A1 (de) * 1995-11-16 1997-05-22 Braun Melsungen Ag Polymer-Composit-Schlauchfolie
EP0774348A3 (fr) * 1995-11-16 1998-05-20 B. Braun Melsungen Ag Film polymère multicouche tubulaire
USRE46911E1 (en) 2002-06-26 2018-06-26 Avery Dennison Corporation Machine direction oriented polymeric films and methods of making the same
US8252397B2 (en) 2006-04-26 2012-08-28 Liqui-Box Corporation Flex crack resistant low density polyethylene films
US8561379B2 (en) 2006-04-26 2013-10-22 Liqui-Box Corporation Process for making pouches from flex-crack-resistant, LDPE films
US9662867B2 (en) 2006-06-14 2017-05-30 Avery Dennison Corporation Conformable and die-cuttable machine direction oriented labelstocks and labels, and process for preparing
US9636895B2 (en) 2006-06-20 2017-05-02 Avery Dennison Corporation Multilayered polymeric film for hot melt adhesive labeling and label stock and label thereof
US8211533B2 (en) 2006-09-05 2012-07-03 Liqui-Box Corporation Resin blend of ethylene alpha olefin interpolymer and heterogeneous interpolymer for liquid packaging films
US8563102B2 (en) 2006-09-05 2013-10-22 Liqui-Box Corporation Resin blend of ethylene alpha olefin interpolymer and heterogeneous interpolymer for liquid packaging films
US8196373B2 (en) 2006-09-05 2012-06-12 Liqui-Box Corporation Pouch making process including use of liquid packaging films of polyethylene and polypropylene blends
WO2011045329A1 (fr) 2009-10-16 2011-04-21 Ppg Europe B.V. Sachet pour matière colorante de peinture
US8978346B2 (en) 2010-04-16 2015-03-17 Liqui-Box Corporation Multi-layer, ethylene polymer-based films with high-density polyethylene based stiffening layer
US9533477B2 (en) 2010-04-16 2017-01-03 Liqui-Box Corporation Multi-layer, ethylene polymer-based films with polypropylene-based stiffening layer
US9757926B2 (en) 2010-04-16 2017-09-12 Liqui-Box Corporation Multi-layer ethylene polymer-based films with polypropylene-based stiffening layer
US9283736B2 (en) 2010-04-16 2016-03-15 Liqui-Box Corporation Multi-layer, ethylene polymer-based films with novel polypropylene blend-based stiffening layer
US9676532B2 (en) 2012-08-15 2017-06-13 Avery Dennison Corporation Packaging reclosure label for high alcohol content products
EP2945799B1 (fr) 2013-01-18 2020-04-22 Sartorius Stedim Fmt Sas Film multicouche comprenant une couche de contact, une couche centrale et une autre extérieure pour la paroi d'un sachet à usage unique
US9701445B2 (en) 2013-12-20 2017-07-11 Bemis Company, Inc. Liners for bulk containers
US11459488B2 (en) 2014-06-02 2022-10-04 Avery Dennison Corporation Films with enhanced scuff resistance, clarity, and conformability

Also Published As

Publication number Publication date
GB9406106D0 (en) 1994-05-18
AU1899295A (en) 1995-10-17
EP0700338A1 (fr) 1996-03-13

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