GB1149935A - Siloxane-acrylate co-polymers, and emulsions thereof - Google Patents

Siloxane-acrylate co-polymers, and emulsions thereof

Info

Publication number
GB1149935A
GB1149935A GB4604366A GB4604366A GB1149935A GB 1149935 A GB1149935 A GB 1149935A GB 4604366 A GB4604366 A GB 4604366A GB 4604366 A GB4604366 A GB 4604366A GB 1149935 A GB1149935 A GB 1149935A
Authority
GB
United Kingdom
Prior art keywords
siloxane
acrylate
methyl
groups
ethyl
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
GB4604366A
Inventor
Robert Nelson Thomas
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.)
Dow Silicones Corp
Original Assignee
Dow Corning 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 Dow Corning Corp filed Critical Dow Corning Corp
Priority to GB4604366A priority Critical patent/GB1149935A/en
Publication of GB1149935A publication Critical patent/GB1149935A/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
    • C08F290/00Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
    • C08F290/08Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated side groups
    • C08F290/14Polymers provided for in subclass C08G
    • C08F290/148Polysiloxanes
    • 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
    • C08F283/122Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes on to saturated polysiloxanes containing hydrolysable groups, e.g. alkoxy-, thio-, hydroxy-
    • 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)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

1,149,935. Siloxane-acrylate copolymers and emulsions thereof. DOW CORNING CORP. 14 Oct., 1966, No. 46043/66. Headings C3G, C3P and C3T. [Also in Division B2] Siloxane-acrylate copolymers comprise 25- 90% by weight of units of an acrylate monomer selected from acrylic or methacrylic acid and esters, nitriles and amides thereof and esters of α-chloroacrylic, α-hydroxymethylacrylic, cyanoacrylic or ethacrylic acid and 10-75% by weight of units of a siloxane consisting of 40- 100 mol per cent of R 2 SiO units and 0-60 mol per cent of RSiO 3 / 2 units wherein each R is a hydrocarbon or substituted hydrocarbon radical. Specified as acrylate components are methyl, ethyl, butyl, amyl, ethylhexyl, cyclohexyl, vinyl, methallyl, benzyl, p-chlorobenzyl, hydroxyethyl, hydroxypropyl and perfluoroethyl esters of acrylic acid, methyl α-chloroacrylate, ethyl α-hydroxymethyl-acrylate, ethyl cyanaoacrylate, methyl or ethyl methacrylate, hydroxyethyl or hydroxypropyl methacrylate, methyl ethacrylate, ethylene glycol diacrylate, glyceryl triacrylate and diethylene glycol dimethacrylate. In the siloxane component(s), R can be alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, alkaryl or aralkyl or a substituted derivative thereof. R is preferably selected from methyl, ethyl, vinyl, allyl, and 3,3,3-trifluoropropyl, and the number of R radicals that are vinylic in the siloxane is preferably such that the ratio of vinylic radicals to Si atoms is from 0À02: 1 1 to 0À3: 1. In examples the following methods of preparing the copolymers are employed: (a) a siloxane containing vinylic groups is prepared in emulsion and then the product is emulsion copolymerized with acrylate monomers; (b) acrylate monomers (including a hydroxyalkyl acrylate) are emulsion copolymerized with nonvinylic silanes which include hydroxy or alkoxy groups; (c) a modification of (b) wherein the acrylate monomers are copolymerized in the presence of a preformed siloxane copolymer containing OH or alkoxy groups and also, in some cases, vinylic groups; (d) acrylate monomers are copolymerized in solution in an organic solvent and the product (containing hydroxyalkyl groups) is reacted with a siloxane or a mixture of silanes containing methoxy groups; (e) acrylate monomers are emulsion copolymerized in the presence of a siloxane containing mercaptopropyl groups (the siloxane being prepared by reacting a preformed siloxane emulsion with HS(CH2) 3 Si(OCH 3 ) 3 in the presence of dodecylbenzenesulphonic acid). In all cases (a) to (e) the acrylates are polymerized with a catalyst selected from potassium or ammonium persulphate, hydrogen peroxide, azodiisobutyronitrile, benzoyl peroxide, t-butyl hydroperoxide and a mixture of cumene hydroperoxide or benzoyl peroxide with t-dodecyl mercaptan. The emulsions and solutions of the acrylatesiloxane copolymers are useful as adhesives and as coating compositions. They can be formulated into paints by inclusion of pigments such as titanium dioxide, mica, calcium carbonate, aluminium silicate, yellow iron oxide and phthalocyanine green, and additional components such as ethylene glycol, polyethylene glycol, methyl cellulose, di(phenyl mercuric)dodecyl succinate, a defoaming agent (e.g. a silicone) and hexamethoxymethylmelamine. Coatings or films containing the copolymers can be cured by heating.
GB4604366A 1966-10-14 1966-10-14 Siloxane-acrylate co-polymers, and emulsions thereof Expired GB1149935A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4604366A GB1149935A (en) 1966-10-14 1966-10-14 Siloxane-acrylate co-polymers, and emulsions thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4604366A GB1149935A (en) 1966-10-14 1966-10-14 Siloxane-acrylate co-polymers, and emulsions thereof

Publications (1)

Publication Number Publication Date
GB1149935A true GB1149935A (en) 1969-04-23

Family

ID=10439609

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4604366A Expired GB1149935A (en) 1966-10-14 1966-10-14 Siloxane-acrylate co-polymers, and emulsions thereof

Country Status (1)

Country Link
GB (1) GB1149935A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0019738A1 (en) * 1979-05-02 1980-12-10 Wacker-Chemie GmbH Use of hydrophilic, reticulated, modified polysiloxanes in form of contact lenses or parts of contact lenses
JPS61106614A (en) * 1984-10-30 1986-05-24 Mitsubishi Rayon Co Ltd Production of impact-resistant resin
EP0541395A1 (en) * 1991-11-07 1993-05-12 Takemoto Yushi Kabushiki Kaisha Coating agents
EP0635526A1 (en) * 1993-07-23 1995-01-25 Rhone-Poulenc Chimie Aqueous dispersions of graft functionalized polysiloxanes, their method of preparation and their use in curable silicone compositions
EP0943634A1 (en) * 1998-03-13 1999-09-22 Shin-Etsu Chemical Co., Ltd. Silicone resin-containing emulsion compositions, their preparation, use and corresponding products
CN115850607A (en) * 2022-10-28 2023-03-28 科顺防水科技股份有限公司 Preparation method of silicone-acrylate latex, silicone-acrylate latex and application
US12110394B2 (en) 2019-06-13 2024-10-08 Dow Global Technologies Llc Aqueous polymer dispersion and process of making the same

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0019738A1 (en) * 1979-05-02 1980-12-10 Wacker-Chemie GmbH Use of hydrophilic, reticulated, modified polysiloxanes in form of contact lenses or parts of contact lenses
JPS61106614A (en) * 1984-10-30 1986-05-24 Mitsubishi Rayon Co Ltd Production of impact-resistant resin
JPH0522724B2 (en) * 1984-10-30 1993-03-30 Mitsubishi Reiyon Kk
EP0541395A1 (en) * 1991-11-07 1993-05-12 Takemoto Yushi Kabushiki Kaisha Coating agents
EP0635526A1 (en) * 1993-07-23 1995-01-25 Rhone-Poulenc Chimie Aqueous dispersions of graft functionalized polysiloxanes, their method of preparation and their use in curable silicone compositions
FR2707991A1 (en) * 1993-07-23 1995-01-27 Rhone Poulenc Chimie Aqueous dispersions of grafted functionalized polyorganosiloxanes, process for their preparation and their use for producing curable silicone compositions
US5618879A (en) * 1993-07-23 1997-04-08 Rhone-Poulenc Chimie Aqueous dispersions of functional graft polyorganosiloxanes and curable silicone compositions comprised thereof
EP0943634A1 (en) * 1998-03-13 1999-09-22 Shin-Etsu Chemical Co., Ltd. Silicone resin-containing emulsion compositions, their preparation, use and corresponding products
US6147156A (en) * 1998-03-13 2000-11-14 Shin-Etsu Chemical Co., Ltd. Silicone resin-containing emulsion composition, making method, and article having cured film of the composition
US12110394B2 (en) 2019-06-13 2024-10-08 Dow Global Technologies Llc Aqueous polymer dispersion and process of making the same
CN115850607A (en) * 2022-10-28 2023-03-28 科顺防水科技股份有限公司 Preparation method of silicone-acrylate latex, silicone-acrylate latex and application

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