[go: up one dir, main page]

GB975179A - Coating of olefine polymer films - Google Patents

Coating of olefine polymer films

Info

Publication number
GB975179A
GB975179A GB23311/62A GB2331162A GB975179A GB 975179 A GB975179 A GB 975179A GB 23311/62 A GB23311/62 A GB 23311/62A GB 2331162 A GB2331162 A GB 2331162A GB 975179 A GB975179 A GB 975179A
Authority
GB
United Kingdom
Prior art keywords
copolymer
acid
copolymers
coating
weight
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.)
Expired
Application number
GB23311/62A
Inventor
Matthew Clasper
Philip Stephen Byrne
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB23311/62A priority Critical patent/GB975179A/en
Priority to DK288163AA priority patent/DK105384C/en
Priority to ES0289140A priority patent/ES289140A1/en
Publication of GB975179A publication Critical patent/GB975179A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/052Forming heat-sealable coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/042Coating with two or more layers, where at least one layer of a composition contains a polymer binder
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/043Improving the adhesiveness of the coatings per se, e.g. forming primers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/048Forming gas barrier coatings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2427/00Characterised by the use 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 a halogen; Derivatives of such polymers
    • C08J2427/02Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2427/04Characterised by the use 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08J2427/08Homopolymers or copolymers of vinylidene chloride

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)

Abstract

A dispersion, used for coating an olefine e.g. ethylene, polymer film, comprises a carboxylated butadiene copolymer comprising butadiene-1, 3, and 25 to 70% styrene, acrylonitrile, and/or methyl methacrylate, and containing from 0.05 to 13.5%, by weight of the copolymer, of free carboxyl groups, and a thermosetting resin in the uncured or partially cured state. The carboxyl groups may be introduced into the copolymer by inclusion of an ethylenically unsaturated carboxylic acid e.g. acrylic, methacrylic, ethacrylic and other substituted acrylic acids, cinnamic, maleic, fumaric and itaconic acid; or by the hydrolysis of methyl methacrylate when present by inclusion of hydrolysing agents in the polymerisation recipe, or by treating the copolymer with a hydrolysing agent when polymerization is complete. Examples of hydrolysing agents are hydrochloric and sulphuric acid, dichloracetic acid, sodium and potassium hydroxides, quaternary ammonium bases, and primary, secondary and tertiary amines. The thermosetting resin may be phenol-, urea-, or melamine-formaldehyde, epoxy resin, N-alkoxy methyl polyamide resin, cross-linkable or thermosetting acrylic resin such as that made by reacting formaldehyde with acrylamide-styreneethyl acrylate copolymer. The butadiene copolymer is preferably prepared by an aqueous emulsion process. The coated olefine polymer film may be further coated with a dispersion of a thermoplastic polymer which may be a copolymer comprising vinylidene chloride, from 5 to 30%, by weight of the copolymer, of acrylonitrile, vinyl chloride, vinyl acetate and/or low alkyl acrylates, and from 0 to 10%, by weight of copolymer, of an ethylenically unsaturated acid or derivative thereof e.g. vinylidene chloride with from 7.5 to 15% methyl acrylate and 0 to 2.5% maleic acid; polyvinyl acetate, partially hydrolysed polyvinyl acetate, methyl methacrylate-methacrylic acid copolymers, copolyesters of terephthalic acid and another dicarboxylic acid e.g. sebacic acid, with a glycol, copolymers of vinyl acetate with vinyl chloride or ethylene, and copolymers of vinyl chloride with ethylene. The dispersion may be obtained by polymerizing the monomers by an aqueous emulsion process in the presence of an emulsifying agent preferably an anionic emulsifying agent.ALSO:A coated olefine polymer film is produced by applying to the film surface a coating dispersion of a carboxylated butadiene copolymer which comprises butadiene-1,3 and from 25 to 70% by weight of the copolymer, of a comonomer or mixture of comonomers selected from styrene, acrylonitrile, and methyl methacrylate, and containing from 0,05 to 13,5% by weight of the copolymer of free carboxyl groups, and a thermosetting resin in the uncured or partially cured state, and a coating of a thermoplastic polymeric material, the coatings either being applied consecutively and dried between applications, or being applied mixed together with subsequent removal of the dispersing medium, and in either case curing the thermosetting resin. The olefine polymer may be a homopolymer or copolymer of ethylene including low, intermediate and high density polyethylene, and the crystallizable polymers and copolymers of aliphatic alpha-olefines having at least 3 and preferably 3-6 carbon atoms in the molecule, particularly polymers and copolymers of propylene and butene-1 where the polypropylene or polybutene-1 is at least 75% soluble in boiling n-heptane, e.g. isotactic polypropylene or isotactic polybutene-1. The carboxyl groups may be introduced into the copolymer by inclusion of an ethylenically unsaturated carboxylic acid, e.g. acrylic, methacrylic, ethacrylic and other substituted acrylic acids, cinnamic, maleic, fumaric and itaconic acid; or by the hydrolysis of methyl methacrylate when present. The thermosetting resin may be phenol-, urea-, or melamine-formaldehyde, epoxy resin, N-alkoxymethyl polyamide resin, cross-linkable or thermosetting acrylic resin such as that made by reacting formaldehyde with acrylamidestyrene-ethyl acrylate copolymer. The preferred thermoplastic polymers are copolymers comprising vinylidene chloride, from 5 to 30% by weight of copolymer, of acrylonitrile, vinyl chloride, vinyl acetate and/or low alkyl acrylates, and from 0 to 10% by weight of copolymer, of an ethylenically unsaturated acid or derivative thereof, e.g. vinylidene chloride with from 7,5 to 15% methyl acrylate and 0 to 2,5% maleic acid; polyvinyl acetate, partially hydrolysed polyvinyl acetate, methyl methacrylate-methacrylic acid copolymers, copolyesters of terephthalic acid and another dicarboxylic acid, e.g. sebacic acid, with a glycol, copolymers of vinyl acetate with vinyl chloride or ethylene, and copolymers of vinyl chloride with ethylene. The film may be unorientated or orientated in one direction or equally or unequally in both directions, may be subjected to surface oxidizing conditions by chemical or physical means, e.g. treatment with sulphuric acid, hot nitric acid, chromic acid; with halogens under free radical forming conditions; by exposure to ozone; by exposure to high voltage stress accompanied by corona discharge in the presence of oxygen; exposure in the presence of oxygen, particularly at temperatures above 100 DEG C., to ionizing radiations such as ultraviolet, x-, a -, b - or g -radiation; or by exposure to flame. The coatings may be applied as aqueous dispersions by roller coating, reverse roll coating, gravure roller coating, air knife coating or doctor blade coating. The orientated films may be heat set before, during or after the coating treatment.
GB23311/62A 1962-06-18 1962-06-18 Coating of olefine polymer films Expired GB975179A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB23311/62A GB975179A (en) 1962-06-18 1962-06-18 Coating of olefine polymer films
DK288163AA DK105384C (en) 1962-06-18 1963-06-18 Method for improving the resistance of polyolefin films to fats, lubricants and oils and to the penetration of gases and water vapor.
ES0289140A ES289140A1 (en) 1962-06-18 1963-06-18 Procedure for coating the surface of an olefinic polymer film. (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB23311/62A GB975179A (en) 1962-06-18 1962-06-18 Coating of olefine polymer films

Publications (1)

Publication Number Publication Date
GB975179A true GB975179A (en) 1964-11-11

Family

ID=10193560

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23311/62A Expired GB975179A (en) 1962-06-18 1962-06-18 Coating of olefine polymer films

Country Status (3)

Country Link
DK (1) DK105384C (en)
ES (1) ES289140A1 (en)
GB (1) GB975179A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0396055A3 (en) * 1989-04-28 1991-11-21 Nissan Motor Co., Ltd. Aqueous primer composition for polyolefin resins
EP0828608A4 (en) * 1995-06-02 1998-06-10 Mobil Oil Corp HEAT-WELDABLE FILM
US20140319003A1 (en) * 2013-04-30 2014-10-30 The Procter & Gamble Company Flexible Package

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3380546A1 (en) * 2015-11-27 2018-10-03 Solvay SA Vinylidene chloride polymer composition comprising at least one allyl cinnamate

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0396055A3 (en) * 1989-04-28 1991-11-21 Nissan Motor Co., Ltd. Aqueous primer composition for polyolefin resins
EP0828608A4 (en) * 1995-06-02 1998-06-10 Mobil Oil Corp HEAT-WELDABLE FILM
US20140319003A1 (en) * 2013-04-30 2014-10-30 The Procter & Gamble Company Flexible Package

Also Published As

Publication number Publication date
DK105384C (en) 1966-09-19
ES289140A1 (en) 1965-01-01

Similar Documents

Publication Publication Date Title
US2907675A (en) Process of coating polymeric substrates
US3574657A (en) Polymeric images formed by heat
US3271345A (en) Adhering layers to polyester film
US3798194A (en) Preparation of latexes by direct dispersion of acidic organic polymers into aqueous alkaline media containing certain alkanols
US3677991A (en) Anionic acrylate latexes that possess sensitivity to alkalinity
US3144426A (en) Process for the preparation of aqueous dispersions of graft interpolymer material
US3567486A (en) Heat-sealable film
CA1167989A (en) Rubber slab dip
GB975179A (en) Coating of olefine polymer films
US4293476A (en) Interfacial cross-linking of latex films
US2871213A (en) Aqueous composition comprising rubbery copolymer and condensation product of formaldehyde and methylol-forming compound
US4442257A (en) Low temperature cure latexes
US3697466A (en) Polymer composition
US3585063A (en) Production of coated film
US4592953A (en) Polyester film primed with crosslinked vinyl acetate polymers
GB1571583A (en) Coated film
US3497467A (en) Films,latices and coatings of n-3-oxohydrocarbon - substituted acrylamide polymers
JPS61197603A (en) Method for producing high quality vinyl alcohol copolymer
US4218356A (en) Product of and process for polymerizing an aqueous reaction mixture containing ionizing agent and cosolvent that forms an aqueous dispersion of resinous polyelectrolyte
GB1583343A (en) Coated film assemblies
GB799043A (en) Improvement in vinylic fillers and the reinforcement of elastic and plastic materials therewith
US3492260A (en) Polymerization of crosslinkable polymers
DE2435814A1 (en) PROCESS FOR THE MANUFACTURING OF WATER BASED COATING PREPARATIONS
US3367893A (en) Process for the preparation of activated polyamide modified polymers
JP2916662B2 (en) Method for producing aqueous vinyl resin emulsion