GB835790A - Improvements in or relating to siloxane elastomers - Google Patents

Improvements in or relating to siloxane elastomers

Info

Publication number
GB835790A
GB835790A GB13392/58A GB1339258A GB835790A GB 835790 A GB835790 A GB 835790A GB 13392/58 A GB13392/58 A GB 13392/58A GB 1339258 A GB1339258 A GB 1339258A GB 835790 A GB835790 A GB 835790A
Authority
GB
United Kingdom
Prior art keywords
silica
viscosity
added
weight
mixture
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
GB13392/58A
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
Societe des Usines Chimiques Rhone Poulenc SA
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 Rhone Poulenc SA, Societe des Usines Chimiques Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB835790A publication Critical patent/GB835790A/en
Expired legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Dental Preparations (AREA)

Abstract

A composition cold vulcanizable to an elastomer comprises a mixture of liquid linear diorganopolysiloxanes having Si-bonded hydrocarbon or halogenated hydrocarbon radicals, a viscosity of 5000 to 500,000 c.s. at 25 DEG C. and containing at least 0.1% by weight of Si-bonded OH groups, and from 0.5 to 10% by weight of the siloxanes of methyltriacetoxysilane. The methyltriacetoxysilane, which may be made by the processes described in Specifications 622,985 and 640,834, may be diluted with octamethylcyclotetrasiloxane, dimethyl diacetoxysilane or inert powders. Fillers, e.g. natural, precipitated, combustion or surface modified silicas, alumina, or oxides of Fe, Zn or Cd, and accelerators, e.g. oxalic or p-aminobenzoic acid, morpholine, ethanolamines, diethylaminoethanol, methyl diethanolamine, o-toluene sulphonamide or urea derivatives, may also be added. Octamethylcyclotetrasiloxane (M.P. 17.5 DEG C.) was heated under nitrogen at 150 DEG C. with aqueous KOH to give an oil, to which, whilst hot, water was added in small fractions to reduce its viscosity, and when cool, the KOH content was neutralized by agitation with a precipitated silica. The resulting liquid was then heated under a current of nitrogen to remove volatiles and leave an oil having a viscosity of 21,000 c.s. at 25 DEG C. and a hydroxy content of 0.15%. In examples this oil was mixed with (1) methyltriacetoxy silane and (2) a combustion silica or a natural silica and oxalic acid; (3) various silicas, ZnO and diethylaminoethanol with or without o-toluene sulphonamide; (4, 5) natural silica and ZNO. In Example (6) the siloxane used was a methylphenyl siloxane. Uses.-For various packings, mouldings (particularly biological mouldings for use in dentistry and as prostheses), production of laminar products, sticking of silicone elastomers, insulating coating of electrical wires and treatment of fabrics.ALSO:A composition cold vulcanizable to an elastomer, for making biological mouldings for use in dentistry and as prostheses, comprises a mixture of liquid linear di-organopolysiloxanes having Si-bonded hydrocarbon or halogenated hydrocarbon radicals, a viscosity of 5000 to 500,000 cs. at 25 DEG C. and containing at least 0.1% by weight of Si-bonded OH groups, and from 0.5 to 10% by weight of the siloxanes of methyltriacetoxysilane (see Group IV (a)). Inert fillers and curing accelerators may also be added. In Example (3) diethylaminoethanol (accelerator) is added to a pasty mixture of a dimethylsiloxane oil containing 0.15% Si -OH groups, combustion silica, natural silica and zinc oxide. This mixture, which is then triturated with methyltriacetoxy silane, thickens rapidly and is moulded for 30 seconds and immediately used for taking dental impressions. Specifications 622,985 and 640,834 are referred to.
GB13392/58A 1957-07-12 1958-04-28 Improvements in or relating to siloxane elastomers Expired GB835790A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR835790X 1957-07-12

Publications (1)

Publication Number Publication Date
GB835790A true GB835790A (en) 1960-05-25

Family

ID=9297790

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13392/58A Expired GB835790A (en) 1957-07-12 1958-04-28 Improvements in or relating to siloxane elastomers

Country Status (1)

Country Link
GB (1) GB835790A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3274145A (en) * 1962-09-04 1966-09-20 Dow Corning Novel siloxane compositions
US4489199A (en) * 1983-08-08 1984-12-18 General Electric Company Room temperature vulcanizable organopolysiloxane compositions
US4517337A (en) * 1984-02-24 1985-05-14 General Electric Company Room temperature vulcanizable organopolysiloxane compositions and method for making
GB2174401A (en) * 1985-03-26 1986-11-05 Gen Electric Self-leveling silicone sealant compositions
US5032660A (en) * 1988-11-04 1991-07-16 Tioxide Group Plc Curable compositions

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3274145A (en) * 1962-09-04 1966-09-20 Dow Corning Novel siloxane compositions
US4489199A (en) * 1983-08-08 1984-12-18 General Electric Company Room temperature vulcanizable organopolysiloxane compositions
US4517337A (en) * 1984-02-24 1985-05-14 General Electric Company Room temperature vulcanizable organopolysiloxane compositions and method for making
GB2174401A (en) * 1985-03-26 1986-11-05 Gen Electric Self-leveling silicone sealant compositions
FR2587351A1 (en) * 1985-03-26 1987-03-20 Gen Electric SILICONE COMPOSITIONS EQUALIZING FOR SEALING AND METHOD FOR THE PRODUCTION THEREOF
GB2174401B (en) * 1985-03-26 1989-12-13 Gen Electric Self-leveling silicone sealant compositions and methods for making same
US5032660A (en) * 1988-11-04 1991-07-16 Tioxide Group Plc Curable compositions

Similar Documents

Publication Publication Date Title
US3847848A (en) Two-part room temperature vulcanizable silicone rubber compositions
US3837878A (en) Process for treating silica fillers
US3884866A (en) High strength organopolysiloxane compositions
US3779987A (en) Process for producing diorganopolysiloxane polymers
GB953668A (en) High temperature siloxane compositions
GB1113576A (en) Finely divided inorganic powders
GB1474096A (en) Vulcanizable systems
GB922828A (en) Process for treating paper with silicones
GB835790A (en) Improvements in or relating to siloxane elastomers
US3919136A (en) Room temperature vulcanizable silicone rubber composition
JPS6215584B2 (en)
US2999077A (en) Method of preparing organopolysiloxane elastomers
US3419516A (en) Deep section cure silicone rubber
GB1035492A (en) Organopolysiloxane elastomers
GB1002452A (en) Vulcanisable organopolysiloxane compositions and vulcanised products obtained therefrom
US3305502A (en) Process for curing diorgano polysiloxanes at room temperature
US3957704A (en) Cross-linking agents for room temperature vulcanizable silicone rubber compositions
US3231527A (en) Curing organopolysiloxanes with a combination of trichloroacetic acid andidibutylxtin
GB936408A (en) Improvements in or relating to siloxane elastomers
GB793594A (en) Vulcanisable compositions
GB844128A (en) Siloxane elastomers
GB890007A (en) Modified rubbery organopolysiloxane putty compositions
KR100197346B1 (en) Silicone rubber having molding release properties
JPH0391564A (en) Room temperature-curable organopolysiloxane composition
GB849069A (en) Organopolysiloxane compositions