GB844128A - Siloxane elastomers - Google Patents

Siloxane elastomers

Info

Publication number
GB844128A
GB844128A GB28043/58A GB2804358A GB844128A GB 844128 A GB844128 A GB 844128A GB 28043/58 A GB28043/58 A GB 28043/58A GB 2804358 A GB2804358 A GB 2804358A GB 844128 A GB844128 A GB 844128A
Authority
GB
United Kingdom
Prior art keywords
parts
siloxane
silicate
atoms
compositions
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
GB28043/58A
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.)
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 GB844128A publication Critical patent/GB844128A/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
    • C08G77/14Polysiloxanes containing silicon bound to oxygen-containing 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
    • C08G77/04Polysiloxanes
    • C08G77/14Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/16Polysiloxanes containing silicon bound to oxygen-containing groups to hydroxyl 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
    • C08G77/04Polysiloxanes
    • C08G77/14Polysiloxanes containing silicon bound to oxygen-containing groups
    • C08G77/18Polysiloxanes containing silicon bound to oxygen-containing groups to alkoxy or aryloxy groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0091Complexes with metal-heteroatom-bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/098Metal salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/56Organo-metallic compounds, i.e. organic compounds containing a metal-to-carbon bond
    • C08K5/57Organo-tin compounds
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Sealing Material Composition (AREA)

Abstract

A composition curable at room temperature to an elastomer comprises by weight (1) 100 parts of a siloxane of at least 100cs. viscosity at 25 DEG C., containing Si-bonded OH groups and being composed of units of the formula <FORM:0844128/IV(a)/1> , wherein each R is a monovalent hydrocarbon or halogenated hydrocarbon radical and in which the average value of n in the polymer is from 1,99 to 2,0 inclusive, (2) from 0,2 to 10 parts of a silicate of the formula R14-mSi(OCH2CH2OR11)m, in which each R1 is a monovalent hydrocarbon or halogenated hydrocarbon radical containing less than 7 C atoms, each R11 is a monovalent aliphatic hydrocarbon radical containing less than 6 C atoms and m is 3 or 4, or a partial hydrolysate thereof, and (3) from 0,01 to 10 parts of a catalyst which is a carboxylate of a metal ranging above H in the electromotive series of metals, and in which the acid radical contains less than 16 C atoms. The radicals in siloxane (1) may be alkyl, alkenyl, cycloaliphatic, aryl, aralkyl or alkaryl, and may be halogenated. The silicate (2) may be diluted with conventional orthosilicates or polysilicates in amounts up to 50% by weight based on siloxane (1). The catalysts, many examples of which are given, can be dispersed in the compositions by means of mutual solvents with siloxane or by dispersion on fillers and thereafter milled into the siloxane. Fillers, e.g. cork, wood, flour, cotton linters, CaCO3, TiO2, C black and SiO2 powders, oxidation inhibitors, compression set additives and pigments, may also be added. If the compositions are to be stored prior to use, the carboxylate or the silicate must be stored separately. The compositions cure at room temperature, though, if desired, they may be press-cured at 150 DEG to 250 DEG C. In a typical Example (1) 100 pts. (by weight) of a liquid end-blocked dimethylpolysiloxane containing Si-OH groups was mixed with 30 parts of diatomaceous earth, 0,5 pt. of lead octoate and varying amounts of different silicates, the lead octoate being added as a mixture of 100 parts of a liquid hydroxyl-free dimethylpolysiloxane, 30 parts of diatomaceous earth, 2 parts of ferrous oxide and 31 parts of lead octoate. The silicate (2), in which R1 can be methyl, ethyl, isohexyl, phenyl, vinyl, allyl, butadienyl, cyclopentenyl, cyclohexyl, chloromethyl, 2-bromo 4-, 6-diiodophenyl, 1, 2-difluorovinyl, 3, 4-dichlorocyclopentyl, 2-bromocyclopentene-2, 3-yl or 6-chlorohexyl, and R11 can be methyl, isopropyl, t-butyl, pentyl, vinyl, allyl, methallyl or butadienyl, can be made by reacting a chlorosilane with the corresponding monoethers of ethylene glycol or a mixture thereof to produce HCl and the required silicate. Uses: for electrical insulation, sealing voids and for taking dental impressions. Specifications 687,759, 746,246 and 804,199 are referred to.
GB28043/58A 1957-10-21 1958-09-01 Siloxane elastomers Expired GB844128A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US844128XA 1957-10-21 1957-10-21

Publications (1)

Publication Number Publication Date
GB844128A true GB844128A (en) 1960-08-10

Family

ID=22184811

Family Applications (1)

Application Number Title Priority Date Filing Date
GB28043/58A Expired GB844128A (en) 1957-10-21 1958-09-01 Siloxane elastomers

Country Status (1)

Country Link
GB (1) GB844128A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3350330A (en) * 1964-12-28 1967-10-31 Gen Electric Siloxane-based, non-skid coating composition
US3419508A (en) * 1965-09-17 1968-12-31 Gen Electric Cellulose surfaces and method of treating
US3518325A (en) * 1969-04-01 1970-06-30 Dow Corning Polysiloxane release coatings
US4602078A (en) * 1984-07-26 1986-07-22 Dow Corning, Ltd. Silicone elastomers and adhesion promoter therefor
FR2618329A1 (en) * 1987-07-22 1989-01-27 Dow Corning Sa METHOD FOR MANUFACTURING A RING CAPABLE OF ENSURING RELEASE OF A THERAPEUTIC AGENT, AND RING MADE THEREBY

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3350330A (en) * 1964-12-28 1967-10-31 Gen Electric Siloxane-based, non-skid coating composition
US3419508A (en) * 1965-09-17 1968-12-31 Gen Electric Cellulose surfaces and method of treating
US3518325A (en) * 1969-04-01 1970-06-30 Dow Corning Polysiloxane release coatings
US4602078A (en) * 1984-07-26 1986-07-22 Dow Corning, Ltd. Silicone elastomers and adhesion promoter therefor
FR2618329A1 (en) * 1987-07-22 1989-01-27 Dow Corning Sa METHOD FOR MANUFACTURING A RING CAPABLE OF ENSURING RELEASE OF A THERAPEUTIC AGENT, AND RING MADE THEREBY

Similar Documents

Publication Publication Date Title
US3296161A (en) Curable organopolysiloxane
USRE29760E (en) Polyfunctional alkoxy endblocked polysiloxanes and their cured compositions
US2902467A (en) Siloxane-silicate elastomers
GB971682A (en) Polysiloxane isocyanates
GB953668A (en) High temperature siloxane compositions
GB905364A (en) Silicone compositions
GB618451A (en) Improvements in and relating to methyl silicone elastomers containing si-bonded vinyl radicals
GB844128A (en) Siloxane elastomers
GB1169411A (en) Organopolysiloxane Compositions which Cure to Elastomers at Room Temperature.
GB942064A (en) Curable liquid siloxane compositions
GB1035492A (en) Organopolysiloxane elastomers
CH453711A (en) Process for the production of compositions which cure in the presence of moisture and the use thereof
GB774869A (en) Silicone rubber of improved thermal stability
US3305502A (en) Process for curing diorgano polysiloxanes at room temperature
GB1066550A (en) Process for the manufacture of polyorganosiloxane elastomers
US3269981A (en) Organotrichlorosilane usage
GB804199A (en) Organosiloxane compositions
US3364175A (en) Polydiorganosiloxanes cured with alkoxysilyl carbamates
GB867511A (en) Improvements in siloxane elastomers
GB835790A (en) Improvements in or relating to siloxane elastomers
GB887976A (en) Organo-polysiloxane compositions convertible to elastomers
GB936408A (en) Improvements in or relating to siloxane elastomers
US3303163A (en) Room temperature vulcanizing silicone compositions
GB939572A (en) Improved organosiloxane compositions and elastomers prepared therefrom
US2558560A (en) Method of pbepabation of flexible