GB746038A - Stable aqueous vinylsilanol dispersions - Google Patents

Stable aqueous vinylsilanol dispersions

Info

Publication number
GB746038A
GB746038A GB7859/53A GB785953A GB746038A GB 746038 A GB746038 A GB 746038A GB 7859/53 A GB7859/53 A GB 7859/53A GB 785953 A GB785953 A GB 785953A GB 746038 A GB746038 A GB 746038A
Authority
GB
United Kingdom
Prior art keywords
dispersion
silanol
siloxanate
vinyl
hydrolysed
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
GB7859/53A
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.)
Libbey Owens Ford Glass Co
Original Assignee
Libbey Owens Ford Glass 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 Libbey Owens Ford Glass Co filed Critical Libbey Owens Ford Glass Co
Publication of GB746038A publication Critical patent/GB746038A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0834Compounds having one or more O-Si linkage
    • C07F7/0838Compounds with one or more Si-O-Si sequences

Abstract

Stable aqueous dispersions of vinyl silanols are prepared by neutralizing to a pH between 3 and 8 an aqueous solution of an alkali or alkaline earth metal salt of a vinylsiloxanate having from 0.05 to 1 vinyl group per silicon atom and from 0.05 to 3 total organic groups per silicon atom, the organic groups, other than vinyl, being mono- or divalent aliphatic hydrocarbon having from one to five carbon atoms, or mono-or divalent aryl groups having six or seven carbon atoms. The siloxanates may be obtained by hydrolysing the corresponding hydrolysable silanes with caustic alkali or by dissolving the corresponding siloxanes in caustic alkali. A long list of suitable silanes and hydrlysable groups is given. Neutralizing must be carried out rapidly to avoid condensation and consequent precipitation of polymers. The dispersions are useful for applying to surfaces and porous materials to impart water resistance. In examples (1) vinyltriethoxysilane is hydrolysed in aqueous caustic soda containing ethanol, the ethanol is distilled off and the siloxanate cooled to 10 DEG C. and neutralized by adding hydrochloric acid with stirring, over a period of 5 minutes. The silanol dispersion is used to waterproof glass fibres, the result being favourably compared with treatment of the fibres with a siloxanate solution followed by acidification on the fibre. (2) The silanol dispersion of example (1) is used to waterproof glass bottles. (3) Vinyltrichlorosilane is hydrolysed in concentrated hydrochloric acid and the precipitate dissolved in caustic soda. The siloxanate is neutralized as in example (1). (4) Ethylvinyldichlorosilane is hydrolysed and the resulting siloxanate neutralized as in example (1).ALSO:Stable aqueous dispersions of vinyl silanols are prepared by neutralizing to a pH between 3 and 8 an aqueous solution of an alkali or alkaline earth metal salt of a vinyl siloxanate having from 0.05 to 1 vinyl groups per silicon atom and from 0.05 to 3 total organic groups per silicon atom, the organic groups other than vinyl, being mono- or di-valent aliphatic hydrocarbon having from one to five carbon atoms or monoor divalent aryl groups having six or seven carbon atoms. The siloxanates may be obtained by hydrolysing the corresponding hydrolysable silanes with caustic alkali or by dissolving the corresponding siloxanes in caustic alkali. A long list of suitable silanes and hydrolysable groups is given. Neutralizing must be carried out rapidly to avoid condensation and consequent precipitation of polymers. The dispersion are useful for applying to surfaces and porous materials to impart water-resistance. In examples (1) vinyltriethoxysilane is hydrolysed in aqueous caustic soda containing ethanol, the ethanol is distilled off and the siloxanate cooled to 10 DEG C. and neutralized by adding hydrochloric acid with stirring, over a period of 5 minutes. The silanol dispersion is used to waterproof glass fibres, the result being favourably compared with treatment of the fibres with a siloxanate solution followed by acidification on the fibre. (2) The silanol dispersion of example (1) is used to waterproof glass bottles. (3) Vinyltrichlorosilane is hydrolysed in concentrated hydrochloric acid and the precipitate dissolved in caustic soda. The siloxanate is neutralized as in example (1). (4) Ethylvinyldichlorosilane is hydrolysed and the resulting siloxanate neutralized as in example (1).ALSO:Materials such as magnesium silicate, cellulose, porous ceramics, glass (bottles, fibres and cloth), non-carbonaceous masonry, sand, ores, wood products, paper clay, talc and mica (for use as mineral fillers in moulding compositions) and asbestos and related materials are made waterproof by the application, at a pH between 3 and 8, of a vinylsilanol aqueous dispersion (see Group IV(a)). The material may be immersed in the dispersion or the dispersion applied to the material, followed by drying, whereupon the silanol condenses to form an insoluble water-repellant silicone. The silanol may be applied in an amount of from 0.001 to 2 per cent by weight of the material.ALSO:Ores for flotation are made waterproof by the application, at a pH between 3 and 8, of a vinylsilanol aqueous dispersion (see Group IV(a)). The material may be immersed in the dispersion or the dispersion applied to the material, followed by drying, whereupon the silanol condenses to form an insoluble water-repellant silicone. The silanol may be applied in an amount of from 0,001 to 2 per cent by weight of the material.ALSO:Materials such as mica and asbestos and related materials are made waterproof by the application, at a pH between 3 and 8, of a vinylsilanol aqueous dispersion (see Group IV(a)). The material may be immersed in the dispersion or the dispersion applied to the material, followed by drying, whereupon the silanol condenses to form an insoluble water-repellent silicone. The silanol may be applied in an amount of from 0.001 to 2 per cent by weight of the material.
GB7859/53A 1952-03-31 1953-03-23 Stable aqueous vinylsilanol dispersions Expired GB746038A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US746038XA 1952-03-31 1952-03-31

Publications (1)

Publication Number Publication Date
GB746038A true GB746038A (en) 1956-03-07

Family

ID=22120481

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7859/53A Expired GB746038A (en) 1952-03-31 1953-03-23 Stable aqueous vinylsilanol dispersions

Country Status (1)

Country Link
GB (1) GB746038A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3278476A (en) * 1961-07-25 1966-10-11 Owens Illinois Glass Co Treatment of glass surfaces with polymers of alkali metal vinyl siliconates
US3451833A (en) * 1964-10-14 1969-06-24 Basf Ag Organosilicon binders
US4985240A (en) * 1990-02-20 1991-01-15 Dow Corning Corporation Odor-free perm

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3278476A (en) * 1961-07-25 1966-10-11 Owens Illinois Glass Co Treatment of glass surfaces with polymers of alkali metal vinyl siliconates
US3451833A (en) * 1964-10-14 1969-06-24 Basf Ag Organosilicon binders
US4985240A (en) * 1990-02-20 1991-01-15 Dow Corning Corporation Odor-free perm

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