GB1169605A - Silicone-Containing Room Temperature Vulcanizing Compositions - Google Patents

Silicone-Containing Room Temperature Vulcanizing Compositions

Info

Publication number
GB1169605A
GB1169605A GB2408167A GB2408167A GB1169605A GB 1169605 A GB1169605 A GB 1169605A GB 2408167 A GB2408167 A GB 2408167A GB 2408167 A GB2408167 A GB 2408167A GB 1169605 A GB1169605 A GB 1169605A
Authority
GB
United Kingdom
Prior art keywords
groups
grafted
vinyl
examples
dibutyltin
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
GB2408167A
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.)
Stauffer Chemical Co
Original Assignee
Stauffer Chemical Co
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 Stauffer Chemical Co filed Critical Stauffer Chemical Co
Publication of GB1169605A publication Critical patent/GB1169605A/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
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/10Block- or graft-copolymers containing polysiloxane sequences
    • 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
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/12Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
    • C08F283/124Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes on to polysiloxanes having carbon-to-carbon double bonds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Silicon Polymers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Graft Or Block Polymers (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

1,169,605. Grafted organopolysiloxanes. STAUFFER CHEMICAL CO. 24 May, 1967 [2 June, 1966], No. 24081/67. Heading C3G. A silicone composition comprises an organopolysiloxane having, as terminal groups attached to the terminal silicon atoms of the siloxane chain, -OH groups or groups which are hydrolyzable to hydroxyl groups in the presence of ambient moisture, and further having a polymeric segment, derived from at least one ethylenically unsaturated monomer, grafted on to the siloxane chain through an organo side group of the chain. When the organopolysiloxane contains -OH groups, the composition is cross-linked by addition of a polyalkoxysilane or polyalkoxysiloxane, e.g. ethyl orthosilicate or decaethyl tetrasilicate, and a catalyst such as dibutyltin dilaurate or dibutyltin butoxychloride. Alternatively, a silane is added to the composition containing -OH groups and the resulting product is hydrolysed by moisture to yield a cross-linked composition. In Examples I to XI, hydroxyterminated polydimethylsiloxane is grafted with styrene and m-butyl methacrylate, vinyl triethoxysilane being present in Examples IX and XI and also n-butyl methacrylate in the latter. The resulting graft polymers are cured with (i) vinyl triacetoxysilane; (ii) methyl triacetoxysilane, in the presence of (a) clay and ground silica; (b) fumed silica and calcium silicate; or (c) fumed silica and ground silica; (iii) partially hydrolysed ethyl silicate and dibutyltin dilaurate; (iv) dibutyltin butoxychloride; or (v) stannous octoate. In Examples XII to XV, an -OH fluid comprising -OH terminated methyl polysiloxane is grafted with vinyl chloride, vinyl acetate, decene-1 or vinyl pyrrolidone. The graft polymers in Examples XII and XIII are cured with ethyl silicate and the said tin dilaurate.
GB2408167A 1966-06-02 1967-05-24 Silicone-Containing Room Temperature Vulcanizing Compositions Expired GB1169605A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US55468366A 1966-06-02 1966-06-02

Publications (1)

Publication Number Publication Date
GB1169605A true GB1169605A (en) 1969-11-05

Family

ID=24214293

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2408167A Expired GB1169605A (en) 1966-06-02 1967-05-24 Silicone-Containing Room Temperature Vulcanizing Compositions

Country Status (7)

Country Link
BR (1) BR6790060D0 (en)
CH (1) CH553836A (en)
DE (1) DE1694973C3 (en)
GB (1) GB1169605A (en)
IL (1) IL27997A (en)
NO (1) NO123245B (en)
SE (1) SE354475B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4797501A (en) * 1986-12-31 1989-01-10 Union Carbide Corporation Silicone-based stabilizers useful in the preparation of improved polyurethane foams

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3030195A1 (en) * 1980-08-09 1982-04-08 Bayer Ag, 5090 Leverkusen CROSSLINKABLE GRAFT POLYMERISAT DISPERSIONS AT ROOM TEMPERATURE
DE3105499A1 (en) * 1981-02-14 1982-09-02 Bayer Ag, 5090 Leverkusen STABLE, ORGANIC MULTI-COMPONENT DISPERSIONS
DE102006059295B4 (en) * 2006-12-11 2009-12-17 Kometra Kunststoff-Modifikatoren Und -Additiv Gmbh Hydrolyzed silane-grafted olefin homo- and (block) copolymers and processes for their preparation
CN102964983B (en) * 2012-12-12 2015-01-07 广州市高士实业有限公司 Silicon hybrid composite coating electronic adhesive and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4797501A (en) * 1986-12-31 1989-01-10 Union Carbide Corporation Silicone-based stabilizers useful in the preparation of improved polyurethane foams

Also Published As

Publication number Publication date
SE354475B (en) 1973-03-12
IL27997A (en) 1971-07-28
BR6790060D0 (en) 1973-01-16
DE1694973A1 (en) 1971-12-30
CH553836A (en) 1974-09-13
NO123245B (en) 1971-10-18
DE1694973C3 (en) 1975-05-07
DE1694973B2 (en) 1974-09-05

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