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AU5417190A - Gas-sealed material - Google Patents

Gas-sealed material

Info

Publication number
AU5417190A
AU5417190A AU54171/90A AU5417190A AU5417190A AU 5417190 A AU5417190 A AU 5417190A AU 54171/90 A AU54171/90 A AU 54171/90A AU 5417190 A AU5417190 A AU 5417190A AU 5417190 A AU5417190 A AU 5417190A
Authority
AU
Australia
Prior art keywords
gas
polyolefin
acid
sealed material
material according
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.)
Withdrawn
Application number
AU54171/90A
Inventor
Christer Bergstrom
Leila Kettunen
Helge Lindstrom
Hanneli Seppanen
Maria Stjernberg
Olli Tuominen
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.)
Neste Oyj
Original Assignee
Neste Oyj
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
Priority claimed from FI891756A external-priority patent/FI86874C/en
Priority claimed from FI891757A external-priority patent/FI86875C/en
Application filed by Neste Oyj filed Critical Neste Oyj
Publication of AU5417190A publication Critical patent/AU5417190A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/02Homopolymers or copolymers of unsaturated alcohols
    • C08L29/04Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/06Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Laminated Bodies (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Glass Compositions (AREA)

Description

1 Gas-sealed material
5 The present invention concerns a gas-sealed material and products containing gas-sealed material. In particular, the invention concerns a gas-sealed material containing polyolefin, polyvinyl alcohol, and polyamide, and products containing the same.
|0 Polyolefins are widely used, for instance, in packaging industry in manufacturing various film products. Advantages of polyolefins are in particular appropriate strength and water resistance properties. Among the drawbacks may be mentioned permeability to certain gases and liquids, concerning particularly oxygen and hydrocarbon dissolvents.
J5 Therefore, the usability of polyolefin films is limited to packaging certain substances, such as foodstuffs, in which minor oxygen perme¬ ability is required.
It is customary to use in packaging industry multiple layer film 20 structures in which materials of different layers are selected for a given purpose. Therefore, such multiple layer structures may contain layers which form a good barrier against gases, such as oxygen, and layers which provide other properties for the product, such as strength properties. In addition, multiple layer structures may 25 contain- other layers which generate, for instance, adhesion between different layers. Products of this kind are, however, expensive to manufacture.
Polyvinyl alcohol is one of such polymers which has a low oxygen 30 permeability property. Said property has most often been utilized in olefin-vinyl alcohol random-mixed polymers and in olefin-vinyl alcohol segment-mixed polymers. It is also known in the art to manufacture products containing polyolefin and polyvinyl alcohol in the form of mixtures, which have a low oxygen permeability and which therefore 35 are exceedingly appropriate for manufacturing e.g. packaging films. In the Finnish patent application No. 87-5772 is disclosed a mixture of polyolefin and polyvinyl alcohol, moreover containing optionally 1 plasticizers. When polyolefin and polyvinyl alcohol are mixed in molten state, a mixture is obtained which is composed of two phases, a continuous phase and a dispersed phase, when the diameter of the particles in the dispersed phase is small enough, totally transparent
5 films are obtained. The mixing is usually carried out in a separate compounding phase prior to the extrusion of the end product.
When the PVA-in the mixture of polyolefin and PVA establishes a continuous phase, a good sealing is provided in the product, for -|0 instance oxygen sealing, and the product is bright and stable, in spite of two phases, both in molten and in solid state, and it is easy to soften by adding plasticizers.
In the EP patent publicizing print No. 280455-A discloses oxygen- J5 sealed materials containing polyethylene, a polyolefin containing carboxyl groups, and a third polymer which is incompatible with the polyethylene. Said third polymer may be, as stated in the publication, a polyamide (PA), ethylene-vinyl alcohol copolymer, polyvinyl alcohol (PVA), polyester, or a mixture thereof, although no examples of 0 mixtures, for instance mixtures of polyamide and polyvinyl alcohol is presented. A mixture of polyethylene and PVA is not useful because of its brittleness, neither is the mixture of polyethylene and poly¬ amide useful because of its barrier properties. If, instead, poly¬ ethylene is mixed with PVA and polyamide, the product is both sealed 5 and viscous.
Although polyolefin-PVA-PA mixtures are generally speaking provided with good oxygen sealing properties in dry circumstances, in moist circumstances their oxygen sealing property reduces significantly, 0 so that they are sensitive to moisture. In addition, when mixtures of polyolefins, PVA, and polyamide are mixed in molten state, partial dissolution of PVA and colouring of the product take place. When plasticizers are used, their stability in the mixture is not as good as possible because of which migration of plasticizers take place in 5 the product. One more drawback in conventional PE/PVA/PA mixtures is that the melt index of the product is not low enough. 1 The object of the present invention is a material containing polyolefin, polyvinyl alcohol, and polyamide, in which the moisture sensitivity of the product regarding oxygen sealing is reduced, the lightness of the product has increased, and the need for plasticizers
5 has been eliminated, and, in addition, the strength properties of the films manufactured from the product, such as viscosity, tensile strength, impact tensile strength, and resistance to rupture, have improved.
jO As taught by the invention, it has been surprisingly found that when certain internally plasticized polyvinyl alcohol polymers and amorphous polyamide are mixed in molten state with polyolefins to which carboxyl acid has been copolymerized or grafted, such products are obtained which have a lighter colour and the oxygen sealing gained
"|5 in which is considerably less sensitive to moisture than in using conventional polyvinyl alcohol, and in addition, the strength proper¬ ties of the films manufactured from the product are better than in using unmodified polyolefin, ordinary polyvinyl alcohol, and poly¬ amide.
20
Therefore, the invention concerns a gas-sealed material containing polyolefin, vinyl alcohol polymer, and polyamide. The gas-sealed material of the invention is characterized in that it is produced by mixing in molten state 3 to 60 per cent by weight of polyolefin, and
25 10 to 96 per cent by weight of internally plasticized vinyl alcohol polymer, and 1 to 50 per cent by weight of an amorphous polyamide.
The term 'internally plasticized vinyl alcohol polymer' refers to a vinyl alcohol polymer which contains polyglycol groups (polyether
30 groups) or other groups plasticizing polyvinyl alcohol in the side chains thereof. Said plasticizer groups are connected into a chain by copolymerizing, grafting or by means of reactive compounding. One such internally plasticized polyvinyl alcohol is Vinex polymer (trade name, Air Products and Chemicals Inc.) , in which for comonomer is 5 used an ester of methacrylic acid and of polyethylene glycol.
Said internally plasticized vinyl alcohol polymers may be manu- 1 factured, for instance in the manner as disclosed in the US. patent No. 4,709,999. Said patent presents that the product is provided with good oxygen sealing and that it is appropriate for cast, in¬ jection moulding and extrusion products, and that it is characterized
5 by good water solubility, and therefore, it is particularly well appropriate for manufacturing films which are required to possess water solubility.
The vinyl alcohol polymer used in the polyolefin/polyvinyl alcohol/ -|Q polyamide mixture of the invention is advantageously such in which in the poly(alkyleneoxy)ester derivative for use as a comonomer the alkylene of the alcohol component is an ethylene or propylene, and the acid component is an acrylic acid or methacrylic acid. Said modified vinyl alcohol polymers may be manufactured, for instance, by poly- J5 merizing vinyl acetate monomer and poly(alkyleneoxy)aerylate co¬ monomer, and hydrolyzing the copolymer thus obtained in order to produce an internally plasticized vinyl alcohol polymer.
The quantity of the internally plasticized vinyl alcohol polymer in 0 the polyethylene-polyvinyl alcohol-polyamide mixture of the invention may be in the range from 10 to 96 per cent by weight, preferably in the range of from 30 to 60 per cent by weight. In some instances, it may be preferable to substitute part of the internally plasticized vinyl alcohol polymer used in the gas-sealed material for unmodified 5 polyvinyl al øhol if the purpose of the product allows.
The polyolefin in a gas-sealed material of the invention may be based on homopolymers or copolymers of the olefins. Therefore, it may be low density polyethylene (LDPE) , medium density polyethylene 0 (MDPE) or high density polyethylene (HDPE) , polypropylene, or poly- butene. The polyolefin may also be a copolymer of ethylene together with other olefins, such as propylene, butene, hexene and octene. The polyolefin may also be an olefin-ester copolymer, such as ethylene-vinyl acetate copolymer, ethylene-acrylate-ester copolymer, 5 or ethylene-methacrylate ester copolymer, or it may be a thermoplastic olefin-based elastomer, such as EP or EPD rubber. The polyolefin in the process according to the invention may also be a homopolymer or a copolymer of the above-mentioned olefins which has been modified with the aid of carboxylic acid. To such a modified olefin polymer is copolymerized or grafted 0.1 to 10 per cent by weight of carboxylic acid. The carboxylic acid may comprise any unsaturated carboxylic acid or carboxylic acid anhydride which can be grafted or copolymerized in polyolefin. Examples of such acids are, for instance, acrylic acid, methacrylic acid, maleic acid fumaric acid, itaconic acid, crotonic acid, sorbic acid, and anhydrides of the afore-mentioned acids. In grafting or in copolymerizing one or several above acids may be used. The polyolefin grafted or copolymer¬ ized with carboxylic acid may also be a mixture containing a poly¬ olefin modified in the manner described above, and un unmodified polyolefin.
The quantity of the polyolefin in the gas-sealed material of the invention may be in the range 1 to 99 per cent by weight, but preferably in the range from 30 to 60 per cent by weight of the quantity of the entire mixture.
A third component in a gas-sealed material of the invention is amorphous polyamide. For the polyamide is used a polyamide in which the degree of crystallization varies in the range 1 to 10 per cent, advantageously in the range 1 to 5 per cent.
The quantity of amorphous polyamide in a material of the invention may be selected from the range 1 to 50 per cent by weight.
The amorphous polyamide enhances the viscosity and deep-drawing properties of the mixture of polyolefin and polyvinyl alcohol co¬ polymer.
The gas-sealed polyolefin/PVA/PA mixture of the invention can be manufactured mixing the polyolefin component, vinyl alcohol/copolymer component, and polyamide component in a melt mixer simultaneously as a dry mixture, premixed in solid or in molten state, or then various components are added separately. 1 From the polyolefin/PVA/PA mixture of the invention various products may be prepared by combining the mixture with polyolefins, other plastics or other materials, such as fibre-based materials. Multiple layer products may be manufactured by coextrusion, (co)extrusion
5 coating, (co)extrusion lamination, adhesion lamination, or using other techniques, and these production procedures may also be combined.
As products containing a gas-sealed material of the invention e.g. films, moulded-blown bottles and containers, plates, tubes, injection
-|0 moulded vessels, deep-drawn films and plates, liquid packaging card¬ board, etc. may be mentioned. Sealed multiple-layer products are generally used for packaging foodstuffs, when oxygen sealing is desired also in moist circumstances, but the sealing of carbon dioxide or some other gas may be thought of. In addition, fat, chemical and
|5 odour sealing may be desired both in various foodstuff packages and technical products.
In the following non-limiting examples the manufacturing, properties and application of the polyolefin/vinyl alcohol polymer/polyamide 0 mixture of the invention in sealed one-layer products are described. The oxygen permeability of the films was measured with an OX-TRAN 1000 apparatus (ASTM D 3985). The polyolefins, the vinyl alcohol po¬ lymers and polyamides used in the tests of the examples are presented in the table below. 5
Polyolefins
P01 - IDPE (low density polyethylene) , melt index (MI) 0 1.8 g/10 min (190°C)
P02 - LT.DPE (linear low density polyethylene) , grafted with 0.25 per cent by weight of fumaric acid, melt index 0.5 g/10 min (190°C)
5 1 Polyvinyl alcohol
PVAl - vinyl alcohol copolymer wherein the comonomer is an ester of an methacryl acid and an ester of poly- 5 ethylene glycol
(Vinex 4004, Air Products and Chemicals)
PVA2 -= polyvinyl alcohol, viscosity 4, hydrolysis degree 88%
JO Polvamides
PA1 = amorphous polyamide, degree of crystallization
1-5% PA2 - polyamide 6 J5 PA3 - polyamide 11 PA4 -= polyamide 12
Plasticizer
20 glycerol, degree of purity 99%
Example 1
Polyolefin/PVA/polyamide mixtures of the invention were prepared by 25 mixing polyolefin, polyvinyl alcohol and polyamide, in molten state, with the aid of a Berstorff mixer which was provided with a flat film nozzle. The temperature profile was 130 to 190 to 200 to 210 to 210 to 210 to 220 to 220 to 215 to 215 to 210. The production rate was 10 kilograms per hour.
30
The thicknesses of the obtained films were 150 to 200 μm. The com¬ pounds thereof are presented in the accompanying Table 1 A. The properties of the films are presented in the accompanying Table 1 B. The oxygen permeability values of the films are calculated for 25 μm 35 thickness. The lightness of the films was measured as a so-called yellowness index conforming to the standard ASTM D 1925-70 with the Ultra Scan apparatus of Hunter Lab. TABLE ]L A
Test Polwinvl alcohol Polvolefin Polvamide type % by weight type % by w. type % by w.
1 PVA1 60 POl 30 PA1 10
2 PVA1 60 POl 10 PA1 9 PA2 21
3 PVA1 60 POl 10 PA1 9 PA3 21
4 PVA1 60 POl 10 PA1 9 PA4 21
5 PVA1 60 POl 10 PA1 30
6 PVA2 60 POl 40 - -
Note. In test 6, the quantity of polyvinyl alcohol includes 4.5% glycerol of the PVA quantity.
TABLE 1 B
Test Oxygen permeabil. Yellowness Tensile
(ml/m x24hxbar index, thick- strength
0%RH 90%RH ness μm mach. /trans
(210°C) dir. dir. MPa MPa
1 0.01 2.5 0.75 151 15.0 14.5
2 0.09 1.5 0.75 163 44.8 25.0
3 0.12 1.5 0.75 148 44.0 24.5
4 1.11 1.5 0.75 191 42.5 22.7
5 0.01 3.0 0.85 190 47.8 29.0
6 0.20 10.0 10.9 172 10.0 7.0
Example 2
Polyolefin/PVA/polyamide mixtures of the invention were prepared by mixing polyolefin, polyvinyl alcohol and polyamide, in molten state, with the aid of a Berstorff mixer which was provided with a flat film nozzle. The temperature profile was 130 to 190 to 200 to 210 to 210 to 210 to 220 to 220 to 215 to 210. The production rate was 10 kilograms per hour.
The thicknesses of the obtained films were 140 to 190 μm. The com- pounds thereof are presented in the accompanying Table 2 A. The properties of the films are presented in the accompanying Table 2 B. The oxygen permeability values of the films are calculated for 25 μm thickness. The lightness of the films was measured as a so-called yellowness index conforming to the standard ASTM D 1925-70 with the Ultra Scan apparatus of Hunter Lab.
TABLE 2 A
Test Polyvinyl alcohol Polyolefin Polyamide type % by weight type % by w. type % by w.
1 PVA1 80 P02 10 PA1 10
2 PVA1 70 P02 3 PA1 27
3 PVA1 60 P02 30 PA1 10
4 PVA1 30 P02 20 PA1 50
5 PVA1 10 P02 60 PA1 30
6 PVA1 60 P02 10 PA1 9
PA2 21
7 PVA1 60 P02 10 PA1 9
PA3 21
8 PVA1 60 P02 10 PA1 9
PA4 21
9 PVA2 60 POl 40
10 PVA2 70 P02 30
Note. In tests 9 and 10, the quantity of polyvinyl alcohol includes 4.5% glycerol of the PVA quantity.
TABLE 2 B
Test Oxygen permeabil. Yellowness Tensile fml/m^x24hxbar') index, thick- strength
0%RH 90%RH ness μm mach. /trans dir. dir. MPa MPa
1 0.1 2.9 0.80 142 19.9 18.5
2 0.05 1.9 0.70 171 32.2 25.0
3 0.01 2.5 0.75 166 16.8 15.0
4 1.5 25 0.85 151 42.5 39.7
5 3.6 55 0.85 147 35.0 31.6
6 0.08 1.4 0.75 186 46.8 26.0
7 0.10 1.5 0.75 150 45.2 27.8
8 0.10 1.5 0.75 141 44.5 25.5
9 0.20 10.0 10.9 172 10.0 7.0
10 0.20 9.6 11.5 162 14.0 11.0

Claims (10)

1 Claims
1. A gas-sealed material, containing polyolefin, polyvinyl alcohol, and polyamide, characterized in that said material is prepared by
5 mixing in molten state 3 to 60 per cent by weight of polyolefin, 10 to 96 per cent by weight of internally plasticized vinyl alcohol polymer, and 1 to 50 per cent by weight of amorphous polyamide.
2. Gas-sealed material according to claim 1, characterized in that |0 in the vinyl alcohol polymer chains contain polyglycol groups (poly- ether groups) as side groups.
3. Gas-sealed material according to claim 1 or 2, characterized in that the polyvinyl alcohol is a copolymer in which the comonomer is
"15 an unsaturated poly(alkyleneoxy)ester derivative.
4. Gas-sealed material according to claim 3, characterized in that said alkylene is an ethylene or propylene and that the acid component of said ester is an acrylic acid or methacrylic acid.
20
5. A gas-sealed mixture according to any one of the preceding claims, characterized in that the polyvinyl alcohol contains in a mixture an unmodified polyvinyl alcohol and vinyl alcohol polymer according to claims 2 to 4.
25
6. A gas-sealed material according to any one of the preceding claims, characterized in that the polyolefin is a low density polyethylene (LDPE) , medium density polyethylene (MDPE) or high density poly¬ ethylene (HDPE) , polypropylene or polybutene, or ethylene copolymer 30 with propylene, butene, hexene and octene, or an olefin/ester co¬ polymer, such as ethylene-vinyl-acetate copolymer, ethylene-acrylate ester copolymer or ethylene methacrylate ester copolymer, EP rubber, EPD rubber, or other thermoplastic olefin-based elastomer.
35 7. A gas-sealed material according to any one of the preceding claims, characterized in that the polyolefin is modified by copolymerizing or grafting thereto 0.1 to 10 per cent by weight of carboxyl acid 1 selected from the group of acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, crotonic acid, sorbic acid, and anhydrides of the afore-mentioned acids.
5 8. Gas-sealed material according to any one of the preceding claims, characterized In that the polyolefin is formed from a mixture of an unmodified polyolefin and a polyolefin modified with carboxyl acid.
9. A gas-sealed material according to any one of the preceding claims, |0 characterized in that the degree of crystallization of the polyamide is In the range 1 to 5 per cent.
10. Products containing gas-sealed material according to any one of the preceding claims.
15
0
5
0
5
AU54171/90A 1989-04-13 1990-04-11 Gas-sealed material Withdrawn AU5417190A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FI891756A FI86874C (en) 1989-04-13 1989-04-13 Gas-sealed material containing internally plasticized polyvinyl alcohol
FI891757A FI86875C (en) 1989-04-13 1989-04-13 GASTAETT MATERIAL, SOM INNEHAOLLER INVAENDIGT MJUKGJORD POLYVINYLALCOOL
FI891756 1989-04-13
FI891757 1989-04-13

Publications (1)

Publication Number Publication Date
AU5417190A true AU5417190A (en) 1990-11-05

Family

ID=26158539

Family Applications (1)

Application Number Title Priority Date Filing Date
AU54171/90A Withdrawn AU5417190A (en) 1989-04-13 1990-04-11 Gas-sealed material

Country Status (5)

Country Link
EP (1) EP0423270A1 (en)
JP (1) JPH04500538A (en)
AU (1) AU5417190A (en)
CA (1) CA2032122A1 (en)
WO (1) WO1990012063A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU631205B2 (en) * 1989-04-13 1992-11-19 Neste Oy Gas-sealed material containing polyolefin, polyvinyl alcohol and polyamide

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0483695B1 (en) * 1990-10-29 1996-10-02 Nippon Gohsei Kagaku Kogyo Kabushiki Kaisha Resin composition and use thereof
FI922378A (en) * 1991-06-19 1992-12-20 Chevron Res & Tech POLYMER BEARING OF POLYOLEFIN, POLYAMID OCH EN MODIFIEDAD ETHLENICOPOLYMER
FI922379A (en) * 1991-06-19 1992-12-20 Chevron Res & Tech SYREAVLAEGSNANDE HOMOGENA BLANDNINGAR AV EN MODIFIEDAD POLYOLEFIN, EN OXIDERBAR POLYMER OCH ETT METALLSALT
US5939158A (en) * 1998-03-24 1999-08-17 E.I. Du Pont De Nemours And Company Laminar articles of polyolefin and nylon/polyvinyl alcohol blend and methods related thereto
DE10351563A1 (en) * 2003-11-03 2005-06-02 Kuraray Specialities Europe Gmbh Process for the preparation of polyamide-polyvinyl alcohol moldings

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4575532A (en) * 1984-02-08 1986-03-11 Norchem, Inc. Polyvinyl alcohol alloys and method of making the same
US4708999A (en) * 1985-04-26 1987-11-24 Air Products And Chemicals, Inc. Copolymers of vinyl acetate and poly(alkyleneoxy) acrylates
US4824904A (en) * 1986-03-31 1989-04-25 Kuraray Co., Ltd. Resin compositions, laminates and block copolymers
JPS63182313A (en) * 1987-01-16 1988-07-27 エアー.プロダクツ.アンド.ケミカルス.インコーポレーテッド Vinyl acetate-acrylate base copolymer
GB8704385D0 (en) * 1987-02-25 1987-04-01 Du Pont Canada Injection moulding of articles
NZ225901A (en) * 1987-08-24 1990-04-26 Du Pont Blends of ethylene-vinyl alcohol polymer and a minor amount of amorphous polyamide
US4952628A (en) * 1987-08-24 1990-08-28 E. I. Du Pont De Nemours And Company Barrier blends based on amorphous polyamide and ethylene/vinyl alcohol, unaffected by humidity
US4950513A (en) * 1988-03-17 1990-08-21 E. I. Du Pont De Nemours And Company Laminar articles of a polyolefin and a nylon/polyvinyl alcohol blend

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU631205B2 (en) * 1989-04-13 1992-11-19 Neste Oy Gas-sealed material containing polyolefin, polyvinyl alcohol and polyamide

Also Published As

Publication number Publication date
WO1990012063A1 (en) 1990-10-18
JPH04500538A (en) 1992-01-30
EP0423270A1 (en) 1991-04-24
CA2032122A1 (en) 1990-10-14

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