GB1096898A - Improvements in or relating to acrylic polymers - Google Patents

Improvements in or relating to acrylic polymers

Info

Publication number
GB1096898A
GB1096898A GB51595/65A GB5159565A GB1096898A GB 1096898 A GB1096898 A GB 1096898A GB 51595/65 A GB51595/65 A GB 51595/65A GB 5159565 A GB5159565 A GB 5159565A GB 1096898 A GB1096898 A GB 1096898A
Authority
GB
United Kingdom
Prior art keywords
catalyst
molar
acrylate
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
GB51595/65A
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
Publication of GB1096898A publication Critical patent/GB1096898A/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
    • C08F220/00Copolymers 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 a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • 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
    • C08F230/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal
    • C08F230/04Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal
    • C08F230/08Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon
    • C08F230/085Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing phosphorus, selenium, tellurium or a metal containing a metal containing silicon the monomer being a polymerisable silane, e.g. (meth)acryloyloxy trialkoxy silanes or vinyl trialkoxysilanes

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)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A copolyme which cures on exposure to moisture to form an elastomer consists of (a) 100 molar parts of <FORM:1096898/C3/1> (b) 1.0 to 8 molar parts of <FORM:1096898/C3/2> (c) 0 to 50 molar parts of CH2=CA2 and (d) 0.5 to 4 molar parts of HSR11 (Si Xy\ Z3- y)z, the molar quantity of (b) being 0.7 to 4 times the molar quantity of (d), wherein R is H or CH3, the majority of R's in (a) being H; R1 is an alkyl radical containing not more than 12 carbon atoms; Q is an alkylene radial; R11 is a mono- or divalent hydrocarbon radical free from aliphatic unsaturation, the adjacent S atom being bonded to an aliphatic carbon atom; X is a hydrolysable atom or group; Z is a monovalent hydrocarbon radical free from aliphatic unsaturation and containing not more than 7 carbon atoms; A is H, Cl or an acetate, phenyl, nitrile or vinyl radical, or least one A being H or Cl; x has an average value of 0 to 1 and y an average value of 1 to 3. Suitable R1, Q R11, X and Z radicals and compounds (a), (b), (c) and (d) are given, e.g. (a) may be ethyl, methyl, n-butyl or decyl acrylate, or methyl or n-butyl methacrylate, or mixtures thereof and (c) may be styrene, acrylonitrile, vinylidene chloride, vinyl chloride, butadiene or vinyl acetate or a mixture of monomers such as of styrene and vinylidene chloride. The polymerization may be carried out using 0.02 to 1 molar part of a free radical forming catalyst e.g. tertiary butyl perbenzoate, dibenzoyl peroxide, N,N1-azobis (isobutyronitrile), dicumyl peroxide, tertiary butyl peracetate, ammonium persulphate, 2,5-dimethyl - 2,5 - dihydroperoxyhexane or bis (2,4-dichlorobenzoyl) peroxide. On exposure to moisture, preferably at above 5 DEG C., the polymers yield infusible elastomers, curing being accelerated by silanol condensation catalysts. Cross-linking agents e.g. ethyl polysilicate and methyltriethoxy-silane may also be added to the copolymers, as can inorganic fillers. In Examples 1 to 3 ethyl acrylate is copolymerized in benzene, using benzoyl peroxide, as catalyst, with (1) vinyl trimethoxysilane (2) <FORM:1096898/C3/3> and (3) <FORM:1096898/C3/4> compound (d) being HS(CH2)3Si(OCH3)3 in each case. In Example 4, ethyl acrylate and acrylonitrile are copolymerized with the (b) monomer used in (2) in the presence of the same (d) compound, using N,N1-azobisisobutyronitrile as catalyst and benzene as solvent. The monomer in Example 5 are n-butyl acrylate, methyl methacrylate and <FORM:1096898/C3/5> (d) being 2-ethylhexyl mecaptan, the catalyst tertiary butyl perbenzoate and the solvent toluene. In Example 6, methyl acrylate, n-propyl methacrylate, vinyl chloride and the compound <FORM:1096898/C3/6> are copolymerized, (d) being 2-phenylpropyl mercaptan, the catalyst tert-butyl peracetate and the solvent cyclohexane. The copolymers of Examples 1 to 4 are cured using a catalyst selected from dibutyl tin dilaurate, tetraisopropyl titanate and Sn Cl4.
GB51595/65A 1964-12-17 1965-12-06 Improvements in or relating to acrylic polymers Expired GB1096898A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41920664A 1964-12-17 1964-12-17

Publications (1)

Publication Number Publication Date
GB1096898A true GB1096898A (en) 1967-12-29

Family

ID=23661256

Family Applications (1)

Application Number Title Priority Date Filing Date
GB51595/65A Expired GB1096898A (en) 1964-12-17 1965-12-06 Improvements in or relating to acrylic polymers

Country Status (4)

Country Link
AT (1) AT267169B (en)
DE (1) DE1570489A1 (en)
GB (1) GB1096898A (en)
NL (2) NL6516388A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107922444A (en) * 2015-08-27 2018-04-17 株式会社可乐丽 Organo-silicon compound, high-molecular compound, inorganic material and resin combination
EP3611196A4 (en) * 2017-04-10 2020-08-19 Shin-Etsu Chemical Co., Ltd. Polysiloxane monomer and method for producing same

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107922444A (en) * 2015-08-27 2018-04-17 株式会社可乐丽 Organo-silicon compound, high-molecular compound, inorganic material and resin combination
EP3342775A4 (en) * 2015-08-27 2019-03-27 Kuraray Co., Ltd. Organosilicon compound, polymer compound, inorganic material and resin composition
EP3611196A4 (en) * 2017-04-10 2020-08-19 Shin-Etsu Chemical Co., Ltd. Polysiloxane monomer and method for producing same
US11180614B2 (en) 2017-04-10 2021-11-23 Shin-Etsu Chemical Co., Ltd. Polysiloxane monomer and method for preparing the same

Also Published As

Publication number Publication date
DE1570489A1 (en) 1969-08-21
AT267169B (en) 1968-12-10
NL6516388A (en) 1966-06-20
NL127446C (en)

Similar Documents

Publication Publication Date Title
US3453230A (en) Room temperature curable acrylate rubbers
GB1529844A (en) Composition with selected vinyl-idene compounds and process for avoiding scorching of ethylene polymer composition
GB1034753A (en) A process for the production of polymers of conjugated dienes
US3565851A (en) Organopolysiloxane coatings
JPS595227B2 (en) Method of bonding room temperature vulcanized organopolysiloxane compositions to porous non-metallic substrates
US4014851A (en) Polyolefin-filled vinyloranopolysiloxane composition and method of preparation
KR890000584A (en) Hydrocurable compositions
US3694478A (en) Process for grafting organopolysiloxanes
GB906627A (en) Improvements in or relating to treating siliceous materials
GB763634A (en) Improvements in or relating to vinyl ethers
GB944061A (en) Improvements in or relating to organosilicon polymers
US3480584A (en) Organosilicon modified materials
US3655633A (en) Method of silylating organic vinylic polymers
GB1096898A (en) Improvements in or relating to acrylic polymers
KR950702597A (en) TRANSPARENT MOULDING COMPOUNDS OF GLUTARIMIDE-CONTAINING POLYMERS AND STYRENE-ACRYLONITRILE COPOLYMERS
KR940014595A (en) Alkoxysilane Functionalized Acrylic Polymer Composition
JPS5776047A (en) Thermoplastic resin composition
US3525778A (en) Organophosphatostannanes and curable organopolysiloxane compositions containing the same
ES450268A1 (en) Thermoplastic moulding compositions
GB1116728A (en) Improvements in or relating to azidoformates, homopolymers and copolymers thereof and coating compositions containing the same
GB994401A (en) Organosilicon polymers
GB1308459A (en) Siloxane organic block copolymers
US3829527A (en) Room temperature curable organopolysiloxanes
US3477973A (en) Room temperature curing organopolysiloxanes
JPS5462267A (en) Coating composition for polycarbonate resin