GB823039A - Improvements in or relating to organosiloxane resins - Google Patents

Improvements in or relating to organosiloxane resins

Info

Publication number
GB823039A
GB823039A GB26853/57A GB2685357A GB823039A GB 823039 A GB823039 A GB 823039A GB 26853/57 A GB26853/57 A GB 26853/57A GB 2685357 A GB2685357 A GB 2685357A GB 823039 A GB823039 A GB 823039A
Authority
GB
United Kingdom
Prior art keywords
mol
per cent
vinyl
radicals
weight
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
GB26853/57A
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.)
Midland Silicones Ltd
Original Assignee
Midland Silicones 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
Application filed by Midland Silicones Ltd filed Critical Midland Silicones Ltd
Publication of GB823039A publication Critical patent/GB823039A/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
    • C08L83/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/04Polysiloxanes
    • C08G77/20Polysiloxanes containing silicon bound to unsaturated aliphatic groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/70Siloxanes defined by use of the MDTQ nomenclature

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Insulating Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A composition comprises (1) from 5 to 95% (by weight) of a copolymer composed of 4.5 to 17 mol. per cent of diphenylsiloxane, 22 to 55 mol. per cent of monophenylsiloxane, 40 to 65 mol. per cent of monomethylsiloxane and up to 38 mol. per cent of phenylmethylsiloxane, and (2) from 95 to 5% of a polysiloxane having a viscosity of at least 500 cs. at 25 DEG C. and an average of at least 1.5 hydrocarbon radicals which are phenyl and vinyl and optionally methyl radicals, per Si atom, the siloxane having a phenyl to Si ratio of at least 0.7:1 and a vinyl to Si ratio of from 0.3:1 to 1:1. The compositions may be cured by incorporating two types of curing catalyst, (1) an organosilanol condensation catalyst, e.g. lead octoate, zinc hexoate, cobalt-naphthenate, indium octoate, triethanolamine, trimethylammonium-butoxide, benzyltrimethyl ammonium 2-ethylhexoate, b -hydroxyethyltrimethylammoniumbutoxide and phenyltrimethylammonium acetate, and (2) an organic peroxide, e.g. dicumyl and di-tertiary butyl peroxides and tertiary butyl perbenzoate, type (1) catalyst being used, e.g., in amount of 0.05 to 10% by weight of siloxane (1) and type (2) in amount of 0.25 to 10% by weight of siloxane (2). Copolymerization is believed to occur by interaction of the vinyl radicals in (2) with the methyl radicals in (1). If desired the compositions may be diluted with up to 50% by weight of a low molecular weight vinyl-containing silicon compound compatible with siloxanes (1) and (2) and having a viscosity of less than 500 cs. at 25 DEG C., the compound having at least 2 Si-bonded vinyl radicals per molecule and the remaining valencies of the Si atom being satisfied with oxygen atoms, and phenyl, methyl, phenylene and methylene radicals, e.g. divinyldiphenyldimethyldisiloxane, tetraphenyldivinyldisiloxane, tetraphenyltetravinylcyclotetrasiloxane, <FORM:0823039/IV (a)/1> and <FORM:0823039/IV (a)/2> where Me, Ph and Vi represent methyl, phenyl and vinyl respectively. The compositions with or without fillers, e.g. glass or asbestos fibres, clay, glass flakes, diatomaceous earth, sand, ferric oxide, titania, zinc oxide and alumina, pigments and oxidation inhibitors, may be moulded and cured. In a typical example, (1), a laminating resin consisted of a mixture of 60% (by wt.) of a copolymer of 10 mol. per cent of diphenylsiloxane, 35 mol. per cent of monophenylsiloxane and 55 mol. per cent of monomethylsiloxane and 40% a phenylvinyl- and phenylmethyl-siloxane copolymer having a viscosity of 1800 cs. at 25 DEG C., to which had been added 0.8% of dicumylperoxide and 0.12% of b -hydroxyethyl trimethyl ammonium 2-ethyl-hexoate, and the resulting mixture was dissolved in toluene. Uses.-For impregnating electrical equipment, forming cast articles, forming structural laminates and for forming hot air conduits. Specifications 755,198, 762,978, 797,979 and 823,040 are referred to.
GB26853/57A 1956-12-19 1957-08-26 Improvements in or relating to organosiloxane resins Expired GB823039A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US823039XA 1956-12-19 1956-12-19

Publications (1)

Publication Number Publication Date
GB823039A true GB823039A (en) 1959-11-04

Family

ID=22170356

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26853/57A Expired GB823039A (en) 1956-12-19 1957-08-26 Improvements in or relating to organosiloxane resins

Country Status (1)

Country Link
GB (1) GB823039A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2428059A1 (en) * 1978-06-05 1980-01-04 Dow Corning SOLVENT-FREE CURABLE POLYORGANOSILOXANE COMPOSITION

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2428059A1 (en) * 1978-06-05 1980-01-04 Dow Corning SOLVENT-FREE CURABLE POLYORGANOSILOXANE COMPOSITION

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