GB706719A - Improvements in or relating to co-polymeric siloxanes and the application thereof - Google Patents
Improvements in or relating to co-polymeric siloxanes and the application thereofInfo
- Publication number
- GB706719A GB706719A GB17885/51A GB1788551A GB706719A GB 706719 A GB706719 A GB 706719A GB 17885/51 A GB17885/51 A GB 17885/51A GB 1788551 A GB1788551 A GB 1788551A GB 706719 A GB706719 A GB 706719A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrosol
- silanes
- reacting
- water
- solvents
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular 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)
- Silicon Polymers (AREA)
Abstract
A copolymeric siloxane is made by reacting one or more silanes of the general formula RnSiX4-n and/or one or more polysiloxanes of the formula <FORM:0706719/IV (a)/1> , where R is an alkyl, monocyclic aryl or halogenated monocyclic aryl hydrocarbon radical, X is chlorine or alkoxy and n has a value of 1 to 3, the average degree of substitution of the silanes or polysiloxanes being from 2.1 to 3 R radicals per silicon atom, and at least 50 per cent. of the R radicals being alkyl, with a silica hydrosol in amount such that there is a total of at least 1 mol. of organosilicon compound per mol. of SiO2 in the hydrosol and under such conditions that the reaction mass has a pH of less than 5. The hydrosol may be formed separately or in situ by reacting a chlorosilane with an alkali metal silicate, or separately by neutralising sodium silicate solution with an acid. The desired pH may be attained by addition of hydrochloric, sulphuric, nitric, phosphoric, benzene sulphonic or trichloracetic acid. Reaction of the hydrosol with the organo-silicon compound(s), which may be effected in the presence of water-miscible solvents, e.g. fatty alcohols, dioxane, ketones and carboxylic acids or mixtures of water-soluble and water-insoluble solvents such as toluene, xylene and ether, proceeds rapidly at 30 DEG C. or above, usually with formation of an emulsion which on standing separates into two layers from which the copolymer is separated, purified and dried to yield products varying from viscous oils to thermoplastic resins. Using this procedure in the examples, a silica hydrosol, made by reacting sodium silicate solution with hydrochloric acid or trimethylchlorosilane, was reacted with (1) trimethylchlorosilane, (2) dimethylphenylchlorosilane, (3) hexamethyldisiloxane, (4) trimethylethoxysilane, (5) the hydrolysate of ethyldimethylchlorosilane, (6) hexamethyldisiloxane and cyclic dimethylsiloxane, (7) trimethylchloro- and phenyltrichloro-silanes, (8) stearyltrichlorosilane, and (9) bis-chlorophenyltetramethyldisiloxane. The copolymers are useful for waterproofing applications particularly leather, antiflotation of paint pigments, thickening liquid dimethylsiloxanes or for boot greases. Solutions in solvents e.g. petroleum hydrocarbons, benzene, toluene and xylene are usually employed and may also contain other organosilicon polymers, e.g. liquid dimethylsiloxanes, methylphenylsiloxane resins, liquid methylphenylsiloxanes, stearylsilsesquioxane, butylmethylpolysilane, phenylmethylpolysilane and stearylmethylpolysilane, specific compositions being given in examples 10 to 14.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US706719XA | 1950-09-13 | 1950-09-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB706719A true GB706719A (en) | 1954-04-07 |
Family
ID=22096692
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB17885/51A Expired GB706719A (en) | 1950-09-13 | 1951-07-27 | Improvements in or relating to co-polymeric siloxanes and the application thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB706719A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3816152A (en) * | 1970-02-16 | 1974-06-11 | Du Pont | Coupling agent copolymer dispersions of silicic acids and organofunctional silanes |
FR2598564A1 (en) * | 1986-05-09 | 1987-11-13 | Dow Corning Ltd | Method for sealing a junction or termination of a cable, in particular a mineral-insulated cable |
US4774310A (en) * | 1986-06-28 | 1988-09-27 | Dow Corning, Ltd. | Method for making siloxane resins |
US5109095A (en) * | 1989-03-22 | 1992-04-28 | Dow Corning Limited | Siloxane resins and method for making them |
US5110890A (en) * | 1989-03-22 | 1992-05-05 | Dow Corning Limited | Method of making organisiloxane resins |
CN102161765A (en) * | 2011-01-11 | 2011-08-24 | 广东达美新材料有限公司 | Organic silicon resin and preparation method thereof |
-
1951
- 1951-07-27 GB GB17885/51A patent/GB706719A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3816152A (en) * | 1970-02-16 | 1974-06-11 | Du Pont | Coupling agent copolymer dispersions of silicic acids and organofunctional silanes |
FR2598564A1 (en) * | 1986-05-09 | 1987-11-13 | Dow Corning Ltd | Method for sealing a junction or termination of a cable, in particular a mineral-insulated cable |
US4774310A (en) * | 1986-06-28 | 1988-09-27 | Dow Corning, Ltd. | Method for making siloxane resins |
US5109095A (en) * | 1989-03-22 | 1992-04-28 | Dow Corning Limited | Siloxane resins and method for making them |
US5110890A (en) * | 1989-03-22 | 1992-05-05 | Dow Corning Limited | Method of making organisiloxane resins |
CN102161765A (en) * | 2011-01-11 | 2011-08-24 | 广东达美新材料有限公司 | Organic silicon resin and preparation method thereof |
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