GB1513310A - Organopolysiloxanes - Google Patents

Organopolysiloxanes

Info

Publication number
GB1513310A
GB1513310A GB32986/75A GB3298675A GB1513310A GB 1513310 A GB1513310 A GB 1513310A GB 32986/75 A GB32986/75 A GB 32986/75A GB 3298675 A GB3298675 A GB 3298675A GB 1513310 A GB1513310 A GB 1513310A
Authority
GB
United Kingdom
Prior art keywords
fluid
per cent
resulting
phenyl
trimethylsilyl
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
GB32986/75A
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.)
General Electric Co
Original Assignee
General Electric 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 General Electric Co filed Critical General Electric Co
Publication of GB1513310A publication Critical patent/GB1513310A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00Compositions of polycarbonates; Compositions of derivatives of polycarbonates

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)
  • Lubricants (AREA)

Abstract

1513310 Organopolysiloxanes; polycarbonate compositions GENERAL ELECTRIC CO 7 Aug 1975 [16 Sept 1974] 32986/75 Headings C3T and C3R A phenyl-containing organopolysiloxane fluid of the general formula wherein Ph is phenyl, R is hydrogen, trimethylsilyl or a mixture thereof, and wherein x and y have a combined value sufficient to provide a phenyl content of from 7-80 weight per cent is made by the solvent hydrolysis of diphenyldichlorosilane and dimethyldichlorosilane generally in a weight ratio of from 1À5 : 1 to 4 : 1. Suitable solvents are benzene, toluene, xylene, esters and ethers. The mixture of organochloro silanes in an organic solvent is mixed with and agitated in preheated water. The resulting organic layer is separated from the aqueous layer and water removed azeotropically therefrom. The resulting hydrolyzate is saturated with anhydrous ammonia and trimethylchlorosilane added thereto generally in an amount of 9À5-25À5 wt. per cent based on the weight of the hydrolyzate. The resulting organic layer is separated and the water and solvent stripped therefrom to yield an organopolysiloxane fluid (A) of the above formula wherein R is a mixture of H and trimethylsilyl. A fluid in which R is substantially all trimethylsilyl may be obtained by employing a sufficient amount of trimethylchlorosilane in the above hydrolysis reaction. The resulting all trimethylsiloxy-chain stopped fluid may then be equilibrated in the presence of KOH and optionally with the addition of further trimethylsiloxy chain-stopping units. The resulting fluid has a phenyl content of 40-80 wt. per cent and is one wherein x = 3-10 and y = 3-10 in the above formula. Alternatively the above equilibration may be carried out with the addition of octamethylcyclotetrasiloxane and trimethylsiloxy containing units provided by, e.g. linear decamethyltetrasiloxane, resulting in a fluid of viscosity 100-200 cS at 25‹ C. and a phenyl content of 30-48 wt. per cent. In another embodiment organopolysiloxane fluid (A) above is modified by adding thereto octamethylcyclotetrasiloxane in an amount sufficient to lower the phenyl content to 30% wt. and then equilibrating. The organopolysiloxane fluids preferably those in which R is a mixture of hydrogen and trimethylsilyl, the phenyl content is 40-80 wt. per cent and the trimethylsiloxy unit content is 12-21 wt. per cent can be added as mould release agents to polycarbonates generally in an amount of from 0À01 to 2À0 wt. per cent based on the polycarbonate. The preferably polycarbonate is the reaction product of phosgene and 2,2-bis(4-hydroxyphenyl)propane. Other uses of the fluid include mechanical and hydraulic fluids; high temperature grease components and transparent and controlled density greases.
GB32986/75A 1974-09-16 1975-08-07 Organopolysiloxanes Expired GB1513310A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US50600774A 1974-09-16 1974-09-16

Publications (1)

Publication Number Publication Date
GB1513310A true GB1513310A (en) 1978-06-07

Family

ID=24012775

Family Applications (1)

Application Number Title Priority Date Filing Date
GB32986/75A Expired GB1513310A (en) 1974-09-16 1975-08-07 Organopolysiloxanes

Country Status (6)

Country Link
JP (2) JPS604213B2 (en)
CA (1) CA1084519A (en)
DE (1) DE2539569A1 (en)
FR (1) FR2284630A1 (en)
GB (1) GB1513310A (en)
NL (1) NL7510804A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100506914C (en) * 2007-04-09 2009-07-01 杭州师范学院 Smoke-inhibition type halogen-free flame-proof polycarbonate
CN103304818A (en) * 2013-06-26 2013-09-18 江苏大学 Preparation method of methyl phenyl silicone oil

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6216809Y2 (en) * 1979-06-28 1987-04-28
US4289859A (en) * 1980-06-02 1981-09-15 Dow Corning Corporation Non-bleeding transparent silicone additives for plastics
JPH0733474B2 (en) * 1988-03-29 1995-04-12 出光石油化学株式会社 Polycarbonate resin composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100506914C (en) * 2007-04-09 2009-07-01 杭州师范学院 Smoke-inhibition type halogen-free flame-proof polycarbonate
CN103304818A (en) * 2013-06-26 2013-09-18 江苏大学 Preparation method of methyl phenyl silicone oil

Also Published As

Publication number Publication date
DE2539569A1 (en) 1976-04-01
FR2284630A1 (en) 1976-04-09
CA1084519A (en) 1980-08-26
JPS604213B2 (en) 1985-02-02
JPS5155399A (en) 1976-05-15
NL7510804A (en) 1976-03-18
JPS5794020A (en) 1982-06-11
FR2284630B1 (en) 1981-12-31
JPS5939449B2 (en) 1984-09-22

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Legal Events

Date Code Title Description
PS Patent sealed
746 Register noted 'licences of right' (sect. 46/1977)
PCNP Patent ceased through non-payment of renewal fee