GB746037A - Production of aqueous silanol dispersions of superior stability - Google Patents

Production of aqueous silanol dispersions of superior stability

Info

Publication number
GB746037A
GB746037A GB7136/53A GB713653A GB746037A GB 746037 A GB746037 A GB 746037A GB 7136/53 A GB7136/53 A GB 7136/53A GB 713653 A GB713653 A GB 713653A GB 746037 A GB746037 A GB 746037A
Authority
GB
United Kingdom
Prior art keywords
silanol
materials
dispersion
aqueous
siliconate
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
GB7136/53A
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 GB746037A publication Critical patent/GB746037A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10Coating
    • C03C25/24Coatings containing organic materials
    • C03C25/40Organo-silicon compounds
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/28Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
    • C03C17/30Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with silicon-containing compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Aftertreatments Of Artificial And Natural Stones (AREA)
  • Paints Or Removers (AREA)

Abstract

Stable aqueous silanol dispersions are prepared by bringing to a pH between 3 and 7 by means of the hydrogen form of a cation exchanger an aqueous solution of a siliconate of an alkali or alkaline earth metal, preferably sodium or potassium. The siliconate should have from 0.5 to 3 hydrocarbon groups per silicon atom, the hydrocarbon groups being saturated or olefinically unsaturated groups having one to five carbon atoms or phenyl, tolyl or benzyl. A long list of hydrolysable silicones from which the siliconates may be prepared is given, including silanes having two or three silicon atoms joined by hydrocarbon groups and silanes having hydrogen attached to silicon. The siliconates may be prepared by hydrolysis in strongly alkaline solution or by solution in alkali of the normal hydrolysis products of the silanes. In addition to halogen, alkoxy, amino, aroxy and acyloxy groups, hydrogen and b -halo-substituted alkyl and b -g -unsaturated groups are specified as hydrolysable radicals. In examples vinyl triethoxy silane, phenyl triethoxysilane, ethyl triethoxysilane and a mixture of butyl triethoxy silane and ethyl orthosilicate are hydrolysed with aqueous caustic soda and ethanol and the products distilled to remove ethanol. In another example vinyl trichlorosilane is added to concentrated hydrochloric acid and the precipitate dissolved in aqueous caustic soda. The resulting siliconate solutions are converted to silanols by diluting to 98 per cent water and passing the solutions through a column containing a cation-exchanger. The resulting solutions are useful for imparting water repellency to various materials.ALSO:Stable aqueous silanol dispersions are prepared by bringing to a pH between 3 and 7 by means of the hydrogen form of a cation exchanger an aqueous solution of a siliconate of an alkali or alkaline earth metal, preferably sodium or potassium. The siliconate should have from 0.5 to 3 hydrocarbon groups per silicon atom, the hydrocarbon groups being saturated or olefinically unsaturated groups having one to five carbon atoms or phenyl, tolyl or benzyl. A long list of hydrolysable silanes from which the siliconate may be prepared is given, including silanes having two or three silicon atoms joined by hydrocarbon groups and silanes having hydrogen attached to silicon. The siliconates may be prepared by hydrolysis in strongly alkaline solution or by solution in alkali of the normal hydrolysis products of the silanes. In addition to halogen, alkoxy, aroxy, amino and acyloxy groups, hydrogen and b -halo-substituted alkyl and b -g -unsaturated groups are specified as hydrolysable radicals. In examples, vinyltriethoxysilane, phenyltriethoxysilane, ethyl triethoxysilane and a mixture of butylttriethoxy silane and ethylorthosilicate are hydrolysed with aqueous caustic soda and ethanol and the products distilled to remove ethanol. In another example vinyl trichlorosilane is added to concentrated hydrochloric acid and the precipitate dissolved in aqueous caustic soda. The resulting siliconate solutions are converted to silanols by diluting to 98 per cent water and passing the solution through a column containing a cation exchanger. The resulting solutions are useful for imparting water repellency to various materials.ALSO:Materials such as magnesium silicate, cellulose, porous ceramic ware, glass (bottles, fibres and cloth), clay, noncarbonaceous masonry, sand, ores (for flotation), wood products, paper, mica, talc (for use as fillers in moulding compounds), asbestos and related materials, are waterproofed by the application at a pH between 3 and 8, of an aqueous dispersion of a silanol (see Group IV(a)). The materials are dipped in the dispersion or the dispersion is applied to the materials, followed by drying, whereupon the silanol condenses to form an insoluble water-repellent silicone. The silanol may be applied in amounts of from 0.001 to 2 per cent by weight of the material.ALSO:Ores (for flotation) are waterproofed by the application, at a pH between 3 and 8, of an aqueous dispersion of a silanol (see Group IV(a)) The materials are dipped in the dispersion or the dispersion is applied to the materials, followed by drying, whereupon the silanol condenses to form an insoluble water-repellent silicone. The silanol may be applied in amounts of from 0,001 to 2 per cent by weight of the material.ALSO:Materials such as mica, asbestos and related materials, are waterproofed by the application, at a pH between 3 and 8, of an aqueous dispersion of a silanol (see Group IV(a)). The materials are dipped in the dispersion or the dispersion is applied to the materials, followed by drying, whereupon the silanol condenses to form an insoluble water-repellent silicone. The silanol may be applied in amounts of from 0.001 to 2 per cent by weight of the material.
GB7136/53A 1952-03-29 1953-03-16 Production of aqueous silanol dispersions of superior stability Expired GB746037A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US746037XA 1952-03-29 1952-03-29

Publications (1)

Publication Number Publication Date
GB746037A true GB746037A (en) 1956-03-07

Family

ID=22120480

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7136/53A Expired GB746037A (en) 1952-03-29 1953-03-16 Production of aqueous silanol dispersions of superior stability

Country Status (1)

Country Link
GB (1) GB746037A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3955985A (en) * 1973-07-16 1976-05-11 Wacker-Chemie Gmbh Stable water repellent compositions
US4985240A (en) * 1990-02-20 1991-01-15 Dow Corning Corporation Odor-free perm
CN111790377A (en) * 2019-12-26 2020-10-20 东北石油大学 Monoatomic catalyst, preparation method and application thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3955985A (en) * 1973-07-16 1976-05-11 Wacker-Chemie Gmbh Stable water repellent compositions
US4985240A (en) * 1990-02-20 1991-01-15 Dow Corning Corporation Odor-free perm
CN111790377A (en) * 2019-12-26 2020-10-20 东北石油大学 Monoatomic catalyst, preparation method and application thereof

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