ES320560A1 - Improvements in or relating to coated films - Google Patents

Improvements in or relating to coated films

Info

Publication number
ES320560A1
ES320560A1 ES0320560A ES320560A ES320560A1 ES 320560 A1 ES320560 A1 ES 320560A1 ES 0320560 A ES0320560 A ES 0320560A ES 320560 A ES320560 A ES 320560A ES 320560 A1 ES320560 A1 ES 320560A1
Authority
ES
Spain
Prior art keywords
copolymers
acid
films
methyl
vinyl
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
ES0320560A
Other languages
Spanish (es)
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
Publication of ES320560A1 publication Critical patent/ES320560A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/91Polymers modified by chemical after-treatment
    • C08G63/914Polymers modified by chemical after-treatment derived from polycarboxylic acids and polyhydroxy compounds
    • 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
    • C08J7/0427Coating with only one layer of a composition containing 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
    • C08J7/044Forming conductive coatings; Forming coatings having anti-static properties
    • 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
    • C08J7/046Forming abrasion-resistant coatings; Forming surface-hardening 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
    • C08J7/052Forming heat-sealable coatings

Abstract

Synthetic, organic thermoplastic films are coated with an aqueous dispersion of a heat-sealable polymer containing 0.5 to 5.0% by weight of an ionic antistatic agent comprising the metal, ammonium or amine salt of the sulphonated condensation product of formaldehyde and an aromatic hydrocarbon and thereafter dried so that a continuous layer of the heat-sealable coating is deposited on the films. The films may comprise polymers of propylene, ethylene, butene-1, 4-methyl pentene-1, or block copolymers thereof, polyesters such as polyethylene terephthalate, polyamides such as polyhexamethylene adipamide, sebacamide, or polycaprolactam, oxymethylene polymers and copolymers. The polymers or copolymers may be mixed with stabilisers, pigments. The surface of the films may be activated by say corona discharge, ozone treatment or treatment with chemical oxidizing agents such as halogen, potassium permaganate and chromic acid. The films may be oriented in one or both directions with equal or unequal orientation in these directions. The highest degree of orientation may be in the longitudinal direction. The oriented films may be heat set before or after coating. The heat sealable polymer may be: copoymers of vinylidene chloride in major amounts with another mono ethylenically unsaturated compound copolymerisable therewith such as methyl acrylate, ethyl acrylate, methyl methacrylate, methacrylamide, methyl, ethyl vinyl ether, methyl vinyl ketone, acrylonitrile e.g. copolymers containing 80 to 95% vinylidene chloride and up to 20% acrylonitrile, terepolymers of vinylidene chloride with the above monomers in the presence of 0.5 to 5% by weight of an ethylenically unsaturated monocarboxylic acid or polycarboxylic acid or a partial ester of a monoethylenically unsaturated polycarboxylic acid such as acrylic methacrylic, maleic, fumaric, itaconic, aconitic, ciltraconic, mesaconic acid polyvinyl acetate, partially hydrolysed polyvinyl acetate butadiene/acrylonitrile, butadiene/styrene, butadiene/methyl methacrylate, butadiene/methyl methacrylate/styrene copolymers methyl methacrylate methacrylic acid copolymers copolyesters of terephthalic acid and an other dicarboxylic acid with a glycol e.g. those containing up to 4.0 molecular proportions of combined terephthalic acid for one molecular proportion of combined sebacic acid copolymers of vinylidene chloride and vinyl chloride, or with methyl, ethyl acrylate copolymers of vinyl acetate with ethylene, vinyl proprionate copolymers of vinyl chloride with ethylene, vinyl acetate. It is preferred to use the alkali, or alkaline earth metal salt of the sulphonated condensation product as the antistatic agent, the preferred aromatic hydrocarbons being naphthalene and alkyl naphthalenes. Up to 0.5% of other anionic or cationic surface active agents such as the alkali metal salts of sulphated or sulphonated long chain aliphatic alcohols such as the oleyl and cetyl alcohols active agent such as condensation products of ethylene oxide with fatty acids, fatty acid amides, ethylene oxide/propylene oxide copolymers, polyoxyethylated nonyl phenol, polyoxyethylated octyl cresol, polyoxyethylated alkyl alcohols such as the oleyl and cetylal cohols and hydrolysed polyvinyl acetate, may be included in the dispersion. The dispersion may also contain antioxidants, dyes, pigments, lubricants, u.v. light stabilisers, slip agents such as starch, talc, zinc oxide, calcium carbonate, magnesium carbonate, diatomaceous earths, silica, kaolin, titanium dioxide, triferric tetroxide and other inorganic oxides, carbonates, silicates, aluminates, alumino silicates, polypropylene, polyvinyl chloride, antiblocking agents such as natural waxes, paraffin wax, microcrystalline waxes, beeswax, carnauba wax, montan wax and synthetic waxes such as hydrogenated castor oil, chlorinated hydrocarbon waxes, long chain fatty acid amides. The coatings may be applied by say roller coating, spraying, doctor-knife or air-knife coating. In the Examples, the coated films are tested for heat seal strength and blocking values.
ES0320560A 1964-12-10 1965-12-10 Improvements in or relating to coated films Expired ES320560A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB50363/64A GB1065680A (en) 1964-12-10 1964-12-10 Improvements in or relating to coated films

Publications (1)

Publication Number Publication Date
ES320560A1 true ES320560A1 (en) 1966-12-16

Family

ID=10455641

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0320560A Expired ES320560A1 (en) 1964-12-10 1965-12-10 Improvements in or relating to coated films

Country Status (7)

Country Link
BE (1) BE673602A (en)
CH (1) CH438701A (en)
ES (1) ES320560A1 (en)
FR (1) FR1460218A (en)
GB (1) GB1065680A (en)
LU (1) LU50032A1 (en)
NL (1) NL6516086A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2618446B1 (en) * 1987-07-24 1993-03-19 Centre Nat Etd Spatiales IONIZABLE PAINTS USEFUL IN PARTICULAR AS ANTI-LIGHTNING PAINTS
EP0789051B1 (en) * 1996-02-08 2002-10-02 Teijin Limited Adherent polyester film laminate
WO1999023178A1 (en) * 1997-10-31 1999-05-14 Dynamit Nobel Kunststoff Gmbh Electrically conductive covering paint
US20120228182A1 (en) 2011-03-11 2012-09-13 Honeywell International Inc. Heat sealable food packaging films, methods for the production thereof, and food packages comprising heat sealable food packaging films

Also Published As

Publication number Publication date
NL6516086A (en) 1966-06-13
GB1065680A (en) 1967-04-19
LU50032A1 (en) 1966-02-10
CH438701A (en) 1967-06-30
BE673602A (en) 1966-06-10
FR1460218A (en) 1966-11-25

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