GB654054A - Improved manufacture of new organo-silicon oxide condensation products - Google Patents

Improved manufacture of new organo-silicon oxide condensation products

Info

Publication number
GB654054A
GB654054A GB8011/47A GB801147A GB654054A GB 654054 A GB654054 A GB 654054A GB 8011/47 A GB8011/47 A GB 8011/47A GB 801147 A GB801147 A GB 801147A GB 654054 A GB654054 A GB 654054A
Authority
GB
United Kingdom
Prior art keywords
dichlorosilane
organo
monochlorosilane
mono
ethyl
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
GB8011/47A
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.)
Dow Silicones Corp
Original Assignee
Dow Corning Corp
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 Dow Corning Corp filed Critical Dow Corning Corp
Publication of GB654054A publication Critical patent/GB654054A/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

Landscapes

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

Abstract

An organosilicon oxide condensation product is prepared by reacting a mono-organo-dihalo-silane, wherein the organic radical is monovalent and contains at least five carbon atoms, with water at a temperature of 5 DEG C. or below. Mono-organo-dihalosilanes with the following substituents are specified in examples: (1) amyl; (3) benzyl; (4) phenyl; (5) naphthyl; (6) p-methyl phenyl; (7) p-chlorophenyl Mixtures of (2) lauryl dichlorosilane and tetra decyl dichlorosilane, and (8) hexadecyl dichlorosilane and octadecyl dichlorosilane are also employed. In each case the appropriate alkyl, aryl or alkaryl magnesium chloride is reacted in equimolecular amount with trichlorosilane at -70 DEG C. The product is then hydrolysed while cooling with an ice and salt bath. The hydrolysis is preferably carried out in the presence of an inert solvent, e.g. an ether, an aliphatic or aromatic hydrocarbon, or a halohydrocarbon, and also of a weak alkali, e.g. sodium acetate or bicarbonate. On treatment with oxidizing agents the hydrogen atoms of the polymers are removed and cross-linking oxygen bridges are formed. The hydrogen attached directly to the silicon atoms may be estimated by treating the products with sodium hydroxide and pyridine, and measuring the hydrogen evolved. The products may be used as coatings (becoming resinous by air oxidation). lubricants, hydrophobing agents, e.g. for glass, ceramics, felt, or asbestos. When liquid, they may be used as damping or hydraulic fluids. The product of (2) above, applied to a wire coated with organo-siloxane enamel increases the abrasion resistance. The Specification as open to inspection under Sect. 91 comprises also the use as starting material of mono-organo-dihalosilanes in which the organo-radical contains at least two carbon atoms, and no limitation of the hydrolysis temperature is made. Examples describe the hydrolysis of (1), (2), (3) ethyl dichlorosilane; (5) dihalogeno-silanes with one of the following substituents, n-propyl, isopropyl, n-butyl, isobutyl. Other mixtures specified as starting material are of ethyl dibromosilane and diphenyl dichlorosilane, phenyl dichlorosilane and diethyl monochlorosilane, dodecyl dichlorosilane and dodecyl - ethyl - monochlorosilane, methyl dichlorosilane, diphenyl monochlorosilane and silicon tetrachloride. The subject-matter of Specification 654,099 is also included. This subject-matter does not appear in the Specification as accepted.
GB8011/47A 1946-03-30 1947-03-24 Improved manufacture of new organo-silicon oxide condensation products Expired GB654054A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US654054XA 1946-03-30 1946-03-30

Publications (1)

Publication Number Publication Date
GB654054A true GB654054A (en) 1951-06-06

Family

ID=22062481

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8011/47A Expired GB654054A (en) 1946-03-30 1947-03-24 Improved manufacture of new organo-silicon oxide condensation products

Country Status (1)

Country Link
GB (1) GB654054A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999014276A1 (en) * 1997-09-16 1999-03-25 Sunsmart, Inc. Hydrophilic materials and their method of preparation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999014276A1 (en) * 1997-09-16 1999-03-25 Sunsmart, Inc. Hydrophilic materials and their method of preparation
US6045650A (en) * 1997-09-16 2000-04-04 Sunsmart, Inc. Hydrophilic materials and their method of preparation

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