GB1433064A - Thermosettable synthetic addition polymers - Google Patents

Thermosettable synthetic addition polymers

Info

Publication number
GB1433064A
GB1433064A GB469774A GB469774A GB1433064A GB 1433064 A GB1433064 A GB 1433064A GB 469774 A GB469774 A GB 469774A GB 469774 A GB469774 A GB 469774A GB 1433064 A GB1433064 A GB 1433064A
Authority
GB
United Kingdom
Prior art keywords
vinyl
groups
modifier
reactive
monomer
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
GB469774A
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.)
PPG Architectural Coatings Canada Inc
Original Assignee
Canadian 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
Priority claimed from CA176,446A external-priority patent/CA984079A/en
Application filed by Canadian Industries Ltd filed Critical Canadian Industries Ltd
Priority to IT4927474A priority Critical patent/IT1078726B/en
Priority to JP4834974A priority patent/JPS5078636A/ja
Publication of GB1433064A publication Critical patent/GB1433064A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium
    • C08F2/22Emulsion polymerisation
    • C08F2/24Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/26Emulsion polymerisation with the aid of emulsifying agents anionic

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polymerisation Methods In General (AREA)
  • Paints Or Removers (AREA)

Abstract

1433064 Production of thermosetting polymer dispersions CANADIAN INDUSTRIES Ltd 1 Feb 1974 [1 Nov 1973] 04697/74 Heading C3P The process of Specification 1,417,713 for producing a thermosetting aqueous dispersion by polymerizing in water at least one α,#- ethylenically unsaturated main monomer which is very slightly soluble in water, with at least one α,#-ethylenically unsaturated monomer containing a reactive group, in the presence of a surfactant, suspending agent or mixture thereof, and also in the presence of at least one modifier containing a complementary reactive group and which is a plasticizer selected from mono epoxy compounds epoxy resins, melamineformaldehyde resins and ureaformaldehyde resins, is modified by including in the monomer mixture a monomer selected from water soluble salts of vinyl sulphonate and of allyl sulphonate, and sulpho-esters or salts thereof of the formula wherein R is a vinyl or alpha-substituted vinyl group, Q is a divalent hydrocarbon group having its valence bonds on different carbon atoms and M is a hydrogen ion or a cation selected from Na, K, Li, ammonium or substituted ammonium groups NR<SP>1</SP> 4 wherein each R<SP>1</SP> is H, C 1-4 alkyl, or C 1-3 alkanolamine, or where two R<SP>1</SP> groups and the nitrogen atom represent together a morpholine residue, and the remaining R<SP>1</SP> groups are as already defined. A long list of such monomers is given. An example of the monoepoxy plasticizer/modifier is, the reaction product of epichlorohydrin and a C 9-11 mixture of saturated tertiary alpha carbon atom carboxylic acids. Some of the reactive modifier may be replaced by a non-reactive modifier such as a monomeric ester, polymeric ester and polyalkylene glycols. The polymerized dispension may also be mixed with an external cross-linking agent containing at least two complementary reactive groups, and also, if desired, a water soluble resin. Examples of main monomers are styrene, C 1-4 alkyl methacrylates, -acrylates, -itaconates, -maleates, and -fumarates, vinyl esters, and vinyl chloride. Examples of monomers containing reactive groups are acrylic-, methacrylic-, itaconic-, maleic- and fumaric acids, acrylamide and its C 1-4 substituted derivatives, N-alkoxy acrylamides, diacetone acrylamide, maleamic acid, maleamide, fumaramide, N-mono-alkyl/aryl substituted amides, hydroxyethyl methacrylate and hydroxy-propyl methacrylate.
GB469774A 1973-07-13 1974-02-01 Thermosettable synthetic addition polymers Expired GB1433064A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
IT4927474A IT1078726B (en) 1974-02-01 1974-03-15 Stable aq. thermosetting latex coating compsns. - by polymsg. unsatd. monomers in aq. emulsion in the presence of a water sol. ionic monomer
JP4834974A JPS5078636A (en) 1973-07-13 1974-05-01

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CA176,446A CA984079A (en) 1972-07-14 1973-07-13 Thermosettable aqueous dispersions of synthetic addition polymers

Publications (1)

Publication Number Publication Date
GB1433064A true GB1433064A (en) 1976-04-22

Family

ID=4097289

Family Applications (1)

Application Number Title Priority Date Filing Date
GB469774A Expired GB1433064A (en) 1973-07-13 1974-02-01 Thermosettable synthetic addition polymers

Country Status (4)

Country Link
DE (1) DE2427341A1 (en)
FR (1) FR2249897B2 (en)
GB (1) GB1433064A (en)
ZA (1) ZA741496B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4373056A (en) 1980-09-19 1983-02-08 Rohm Gmbh Chemische Fabrik Aqueous artificial resin dispersions free of emulsifying agents
US4522962A (en) * 1980-09-08 1985-06-11 Scm Corporation Epoxy modified emulsion polymers
EP0420097A2 (en) * 1989-09-25 1991-04-03 Union Carbide Chemicals And Plastics Company, Inc. Coreactable powdered compositions
US5207954A (en) * 1989-09-25 1993-05-04 Union Carbide Chemicals & Plastics Technology Corporation Method of making coreactable powdered coatings

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522962A (en) * 1980-09-08 1985-06-11 Scm Corporation Epoxy modified emulsion polymers
US4373056A (en) 1980-09-19 1983-02-08 Rohm Gmbh Chemische Fabrik Aqueous artificial resin dispersions free of emulsifying agents
EP0420097A2 (en) * 1989-09-25 1991-04-03 Union Carbide Chemicals And Plastics Company, Inc. Coreactable powdered compositions
EP0420097A3 (en) * 1989-09-25 1992-04-01 Union Carbide Chemicals And Plastics Company, Inc. Coreactable powdered compositions
US5207954A (en) * 1989-09-25 1993-05-04 Union Carbide Chemicals & Plastics Technology Corporation Method of making coreactable powdered coatings

Also Published As

Publication number Publication date
FR2249897A2 (en) 1975-05-30
ZA741496B (en) 1975-10-29
DE2427341A1 (en) 1975-05-07
FR2249897B2 (en) 1980-03-28

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Legal Events

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