GB624361A - Improvements in or relating to organo-silicon compounds - Google Patents

Improvements in or relating to organo-silicon compounds

Info

Publication number
GB624361A
GB624361A GB7307/46A GB730746A GB624361A GB 624361 A GB624361 A GB 624361A GB 7307/46 A GB7307/46 A GB 7307/46A GB 730746 A GB730746 A GB 730746A GB 624361 A GB624361 A GB 624361A
Authority
GB
United Kingdom
Prior art keywords
silicon
methallyl
hydrocarbon group
general formula
silicone
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
GB7307/46A
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.)
Westinghouse Electric International Co
Original Assignee
Westinghouse Electric International 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 Westinghouse Electric International Co filed Critical Westinghouse Electric International Co
Publication of GB624361A publication Critical patent/GB624361A/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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B26/00Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
    • C04B26/30Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Other silicon-containing organic compounds; Boron-organic compounds
    • C04B26/32Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Other silicon-containing organic compounds; Boron-organic compounds containing silicon

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Silicon Polymers (AREA)

Abstract

An allyl silicon resin is prepared by hydrolysing an organo silicon compound of the general formula <FORM:0624361/IV (a)/1> wherein x is a number from 1 to 2, z is from 0 to 2, the sum of x and z not exceeding 3, R represents a hydrocarbon group which will not undergo a vinyl type of polymerization, and Y represents chlorine or an ethoxyl radical, and dehydrating and condensing the resulting silicol to form a silicone. Polymerization through the p unsaturated allyl group may also take place. The dehydration is preferably carried out in the presence of a dehydrating agent, e.g. boric acid esters such as methyl borate, metal halides, the oxides and halides of phosphorus or sulphuric or hydrochloric acid. The methallyl silicones may be added to alkyl or aryl silicones. Interpolymers are obtained by carrying out the above hydrolysis, dehydration and condensation in the presence of one or more saturated organic silicon compounds of the general formula RxSiY4-x, where R is a non-polymerizing hydrocarbon group such as an alkyl, phenyl or alkyphenyl group, and Y is a halide or ethoxy group, or by dehydrating and condensing a mixture of the corresponding silicols or by mixing the corresponding silicones or solutions thereof when they are liquids due to a low degree of polymerization and heating. The condensation may be continued only until a solvent soluble polymer is obtained which may then be dissolved in a volatile liquid carrier such as a hydrocarbon, or may be dispersed in a volatile liquid carrier such as water with the aid of ammonia or a dispersing agent such as a sodium alkyl sulphonate ester, or a hydrolysed polyvinyl ester and a simple alcohol such as ethyl alcohol. Finely-divided inorganic materials may be added to the silicone polymers of interpolymers, e.g. silica flour, bentonite, glass powders, calcium fluoride, ceramic powders, graphite, anthracite, coal, or petroleum coke. In an example, a mixture of methallyl silicon triethoxide, methyl silicon triethoxide and dimethyl silicon diethoxide is hydrolysed with sulphuric acid in the presence of toluene to yield a silicone dissolved in toluene. The Specification mentions that methallyl silicon chlorides and methallyl silicon ethoxides may be polymerized directly to form resinous bodies by heating in the presence of a catalyst, e.g. methallyl silicon triethoxide may be polymerized by heating in the presence of a catalyst such as tertiary butyl perbenzoate. Allyl esters such as allyl phthalate or allyl carbonate may be polymerized in the presence of methallyl silicon ethoxides. Specifications 596,668, 624,363 and 624,364 are referred to.ALSO:Organo silicon compounds of the general formula <FORM:0624361/IV (b)/1> wherein x represents 1 or 2, R represents a saturated hydrocarbon group, z represents 0, 1 or 2, the sum of x and z not exceeding 3 and Y represents chlorine or an ethoxyl radical, are prepared by treating ethyl orthosilicate or silicon tetrachloride with a Grignard reagent to substitute the desired methallyl and saturated hydrocarbon groups for the chlorine or ethoxy groups. The products may be hydrolysed to the corresponding silicols which may then be dehydrated and condensed to form a silicone. The products may also be mixed with organosilicon compounds of the general formula R1nSiY4-n, wherein R1 represents a saturated hydrocarbon group, Y is a halide or ethoxyl radical and n is a number from 1 to 3, hydrolysing the mixture and dehydrating and condensing the resulting silicol. By saturated hydrocarbon group is meant a hydrocarbon group which will not undergo a vinyl type of polymerization, e.g. alkyl or phenyl radicals. In an example, dimethallyl silicon diethoxide and methallyl silicon triethoxide are prepared by means of a Grignard reaction and then by reaction with a further Grignard reagent methyl, phenyl, chlorophenyl, fluorophenyl and other alkylphenyl radicals may be introduced for one or two ethoxyl groups on the silicon atom. Specifications 596,668, 624,363 and 624,364 are referred to.ALSO:Plastic compositions comprise mica flakes or inorganic fibrous materials such as asbestos, cloth or glass fibres bound together with a methallyl silicone as obtained by hydrolising, condensing and dehydrating an organic silicon compound of the general formula <FORM:0624361/V/1> wherein x is a number from 1 to 2, R represents a hydrocarbon group which will not undergo a vinyl type of polymerisation, Z is from 0 to 2. The sum of X and Z not exceeding 3, and Y represents chlorine or an ethoxyl radical, or with a methallyl silicone interpolymer as obtained by carrying out the above hydrolysis, dehydration and condensation in the presence of one or more organic silicon compounds of the general formula R1n-Si-Y (4-n), wherein R is a non-polymerising hydrocarbon radical, N is from 1 to 3 and Y is a holide or an ethoxyl radical. Specifications 596,668, [Group IV], 624,363 and 624,364 are referred to.
GB7307/46A 1945-03-09 1946-03-08 Improvements in or relating to organo-silicon compounds Expired GB624361A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US624361XA 1945-03-09 1945-03-09

Publications (1)

Publication Number Publication Date
GB624361A true GB624361A (en) 1949-06-07

Family

ID=22042465

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7307/46A Expired GB624361A (en) 1945-03-09 1946-03-08 Improvements in or relating to organo-silicon compounds

Country Status (1)

Country Link
GB (1) GB624361A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632755A (en) * 1947-10-02 1953-03-24 Libbey Owens Ford Glass Co Preparation of silicon-containing heteropolymers
DE1005484B (en) * 1952-06-24 1957-04-04 Owens Corning Fiberglass Corp Process for coating mineral fibers, in particular glass fibers
DE1017132B (en) * 1951-04-17 1957-10-10 Owens Corning Fiberglass Corp Process for finishing glass fibers
DE1043270B (en) * 1951-08-17 1958-11-13 Owens Corning Fiberglass Corp Process for sizing glass fibers with synthetic resins

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632755A (en) * 1947-10-02 1953-03-24 Libbey Owens Ford Glass Co Preparation of silicon-containing heteropolymers
DE1017132B (en) * 1951-04-17 1957-10-10 Owens Corning Fiberglass Corp Process for finishing glass fibers
DE1043270B (en) * 1951-08-17 1958-11-13 Owens Corning Fiberglass Corp Process for sizing glass fibers with synthetic resins
DE1005484B (en) * 1952-06-24 1957-04-04 Owens Corning Fiberglass Corp Process for coating mineral fibers, in particular glass fibers

Similar Documents

Publication Publication Date Title
US2587636A (en) Method of making alkali metal salts of organosiloxanols and organosilanetriols
US2567110A (en) Organopolysiloxanes prepared by the reaction of salts of silanols with halosilanes
CN102001671A (en) Method for preparing white carbon black by using silicon tetrachloride
US2698314A (en) Reaction of alkoxy silanes with silane hydrolysis products
GB624361A (en) Improvements in or relating to organo-silicon compounds
US2562953A (en) Organo-silicon copolymers and process of making same
US2481052A (en) Polymerization of organo-siloxanes
GB645103A (en) Improvements in and relating to the preparation of organo-substituted halogenosilanes
GB1357866A (en) Coating composition
US2441320A (en) Organo-siloxanes and methods of making them
GB624364A (en) Improvements in or relating to organo-silicon compounds
US2628246A (en) Method for the preparation of unsaturated silanes
US2652385A (en) Siloxane resins
KR900011806A (en) Silylated addition polymer with pendant ionic component
GB624362A (en) Improvements in or relating to organo-silicon compounds
GB624363A (en) Improvements in or relating to organo-silicon compounds
US2628213A (en) Copolymers, including siliconols and hydrogen bonded to silicon
US3154431A (en) Method of treating a surface with a stable aqueous silanol dispersion
GB668903A (en) Organo-silicon compounds and their manufacture
US2811541A (en) Polymerization of vinyldihydrocarbylsilanes and products thereof
US2888475A (en) Titanated alkoxy silanes
US2873265A (en) Process for preparing copolymers of organo silicon derivatives
GB706719A (en) Improvements in or relating to co-polymeric siloxanes and the application thereof
US2504839A (en) Organo-siloxanes and methods of preparing them
US2462267A (en) Organo-siloxane polymers and methods of preparing them