GB1459841A - Aqueous polymer blends - Google Patents

Aqueous polymer blends

Info

Publication number
GB1459841A
GB1459841A GB1709674A GB1709674A GB1459841A GB 1459841 A GB1459841 A GB 1459841A GB 1709674 A GB1709674 A GB 1709674A GB 1709674 A GB1709674 A GB 1709674A GB 1459841 A GB1459841 A GB 1459841A
Authority
GB
United Kingdom
Prior art keywords
acrylate
prepared
latex
dispersion
gum
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
GB1709674A
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.)
Union Carbide Corp
Original Assignee
Union Carbide Corp
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 Union Carbide Corp filed Critical Union Carbide Corp
Publication of GB1459841A publication Critical patent/GB1459841A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L57/00Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/005Processes for mixing polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/04Condensation polymers of aldehydes or ketones with phenols only
    • C08L61/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions 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 aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/08Copolymers of styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L31/00Compositions 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 acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
    • C08L31/02Homopolymers or copolymers of esters of monocarboxylic acids
    • C08L31/04Homopolymers or copolymers of vinyl acetate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C08L33/08Homopolymers or copolymers of acrylic acid esters

Landscapes

  • 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)
  • Adhesives Or Adhesive Processes (AREA)
  • Paints Or Removers (AREA)

Abstract

1459841 Aqueous polymer blends UNION CARBIDE CORP 29 April 1974 [30 April 1973] 17096/74 Headings C3R and C3P [Also in Division B2] An aqueous mixed dispersion comprises (a) an addition polymer having film forming properties comprising polymer particles dispersed in water in latex form; and (b) a thermosetting resole formed by the alkaline-catalyzed condensation of a phenol and an aldehyde, having a weight average M.Wt. of 300-3000, and comprising solid particles suspended in water, substantially all of which have diameters of less than 60 microns; wherein the addition polymer is a homo- or co-polymer of at least one of vinyl chloride, vinyl acetate, vinyl alcohol, alkyl acrylate, alkyl methacrylate, butadiene, chloroprene, styrene, ethylene, acrylic acid, methacrylic acid, acrylamide, acrylonitrile, itaconic acid, maleic acid, N-methylolacrylamide, gammahydroxypropyl acrylate, betahydroxyethyl acrylate, neopentyl glycol diaacrylate or glycidyl acrylate. The dispersions preferably contain on a solids basis from 3-90% wt. of the phenolic resin and 10-97% wt. of the addition polymer. Suitable phenols include phenol, m-substituted C 1 -C 9 alkyl, alkoxy or halophenols and bisphenols. The phenolic dispersion may be prepared by carrying out the condensation in the presence of a mixture of gum arabic and at least one polysaccharide gum having mannose and galactose units or D- mannuronic acid and L-guluronic acid units. Suitable polymer latices include those of polyvinylchloride, polyvinylacetate, polyacrylates, polybutadiene, polychloroprene, polystryene and numerous copolymers. The addition polymers may contain up to 20% wt. of functional groups which will react with the phenolic resole resin, e.g. carboxyl, alcoholic hydroxyl, e.g. methylol, sulfonamido, amino or amido groups. In the examples aqueous dispersions are prepared from (1) a latex of either polyvinylacetate or a copolymer of styrene, ethyl acrylate, acrylonitrile, N-methylol acrylamide and acrylic acid, and (2) a phenolic dispersion prepared by the alkaline condensation of phenol and HCHO in the presence of gum arabic and either guar gum or a gum comprising galactose units, and are cured by heating. Aqueous dispersions for use as contact adhesives are also prepared from (1) either (i) a latex copolymer (A) of ethyl acrylate, acrylonitrile, acrylic acid and N- methylol acrylamide alone or in admixture with an acrylate latex copolymer (B) of vinyl acetate and isobutyl acrylate, or (ii) an acrylate latex prepared by adding an aqueous dispersion of a copolymer of ethylene and acrylic acid partially neutralized with N,N-dimethylolethanolamine to an acrylate copolymer latex of ethyl acrylate, methyl methacrylate and methacrylic acid and then heating, alone or in admixture with acrylate latex (B), and (2) either a bisphenol A-HCHO resin dispersion (C) prepared in the presence of gum arabic and Jaguar (R.T.M.) gum or the phenol-HCHO resin dispersion described above. Primer compositions comprising the inventive aqueous dispersion are prepared from (i) a latex copolymer of styrene, ethyl acrylate, acrylic acid and optionally neopentyl glycol diacrylate, and (ii) either a bisphenol A-HCHO resin dispersion similar to (C) above or a phenolic dispersion prepared from bisphenol A, t-butylphenol and HCHO in the presence of gum arabic and "Jaguar" gum, and (iii) CH 3 COO(CH 2 CH 2 O) 2 CH 2 CH 3 and optionally TiO 2 pigment, zinc phosphate and a defoamer. The primers are cast on to phosphated steel and cured and then overcoated with a white pigmented thermosetting acrylic resin and rebaked.
GB1709674A 1973-04-30 1974-04-29 Aqueous polymer blends Expired GB1459841A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US35567573A 1973-04-30 1973-04-30

Publications (1)

Publication Number Publication Date
GB1459841A true GB1459841A (en) 1976-12-31

Family

ID=23398357

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1709674A Expired GB1459841A (en) 1973-04-30 1974-04-29 Aqueous polymer blends

Country Status (6)

Country Link
JP (1) JPS5014746A (en)
AU (1) AU6836174A (en)
DE (1) DE2420771B2 (en)
FR (1) FR2227293A1 (en)
GB (1) GB1459841A (en)
IT (1) IT1010237B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5418262A (en) * 1991-12-09 1995-05-23 Heraeus Kulzer Gmbh Adhesive, waterproof and hydrolysis-resistant bonding layer for metal, ceramic, glass, polymer-plastic bonds and dispersion for producing it
NL1005519C2 (en) * 1997-03-13 1998-09-15 Rockwool Lapinus Bv Binder preparation for mineral wool, and the obtained mineral wool.
WO2011022668A1 (en) * 2009-08-20 2011-02-24 Georgia-Pacific Chemicals Llc Modified binders for making fiberglass products
CN116134056A (en) * 2020-07-20 2023-05-16 巴斯夫欧洲公司 Aqueous polymer latex suitable as film-forming copolymer for binders in aqueous coating compositions

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2661418B1 (en) * 1990-04-25 1992-08-14 Derives Resiniques Terpenique RESIN COMPOSITION EMULSION FOR AQUEOUS ADHESIVES.
CN110776863B (en) * 2019-10-31 2021-08-10 湖南高瑞电源材料有限公司 Special adhesive for modified lithium battery ceramic diaphragm and preparation method and application thereof

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5418262A (en) * 1991-12-09 1995-05-23 Heraeus Kulzer Gmbh Adhesive, waterproof and hydrolysis-resistant bonding layer for metal, ceramic, glass, polymer-plastic bonds and dispersion for producing it
NL1005519C2 (en) * 1997-03-13 1998-09-15 Rockwool Lapinus Bv Binder preparation for mineral wool, and the obtained mineral wool.
WO1998040437A1 (en) * 1997-03-13 1998-09-17 Rockwool Lapinus B.V. Binder preparation for mineral wool and the obtained mineral wool
WO2011022668A1 (en) * 2009-08-20 2011-02-24 Georgia-Pacific Chemicals Llc Modified binders for making fiberglass products
US8193107B2 (en) 2009-08-20 2012-06-05 Georgia-Pacific Chemicals Llc Modified binders for making fiberglass products
US20120208935A1 (en) * 2009-08-20 2012-08-16 Georgia-Pacific Chemicals Llc Modified Binders for Making Fiberglass Products
US8703628B2 (en) 2009-08-20 2014-04-22 Georgia-Pacific Chemcicals LLC Modified binders for making fiberglass products
RU2584200C2 (en) * 2009-08-20 2016-05-20 ДЖОРДЖИЯ-ПЭСИФИК КЕМИКАЛЗ ЭлЭлСи Modified binder to create products from glass fibre
CN116134056A (en) * 2020-07-20 2023-05-16 巴斯夫欧洲公司 Aqueous polymer latex suitable as film-forming copolymer for binders in aqueous coating compositions

Also Published As

Publication number Publication date
FR2227293A1 (en) 1974-11-22
AU6836174A (en) 1975-10-30
DE2420771A1 (en) 1974-11-14
IT1010237B (en) 1977-01-10
DE2420771B2 (en) 1976-09-09
JPS5014746A (en) 1975-02-17

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee