US5070175A
Expired / Lapsed
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Method for the preparation of an organopolysiloxane containing tetrafunctional siloxane units
Assignee: Shin-Etsu Chemical Co Ltd
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Filing: 1991-05-28
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Granted: 1991-12-03
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Expires: 2011-05-28
Abstract
Abstract An efficient and economically advantageous method is proposed for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units, i.e. Q units, and, typically, monofunctional siloxy units, i.e. M units, and useful as a reinforcing agent in silicone rubbers. The method comprises the steps of: mixing the reactants for providing the Q and M units, such as ethyl orthosilicate and trimethyl methoxy silane, in a desired molar ratio; and heating the mixture at a temperature higher by at least 10° C. than the boiling point of the mixture under normal pressure in a closed vessel in the presence of water and a catalyst such as a sulfonic acid group-containing compound. In addition to the greatly shortened reaction time and remarkably decreased contents of residual alkoxy groups and gelled matter in the product, the method is advantageous also in respect of the absence of the problems caused by the disposal of the waste water as well as the corrosiveness of hydrogen chloride unavoidably produced in the conventional prior art methods.
Inventors
- 👤 Hiroshi Tsumura
- 👤 Kiyoyuki Mutoh
- 👤 Kazushi Satoh
- 👤 Ken-ichi Isobe
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-01 06:59
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/06; C08G77/08
Claims Analysis
Total Claims: 8
Claim 1
Independent Claim
167 words
A method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units which comprises the steps of: (a) mixing an alkyl silicate or a partial hydrolysis product thereof as a first reactant with an organosilane compound represented by the general formula R.sub.a SiX.sub.4-a, in which R is a hydrogen atom or an unsubstituted or substituted monovalent hydrocarbon group, X is an alkoxy group or a hydroxyl group and the subscript a is 1, 2 or 3, or an oligomeric organosiloxane compound consisting of the siloxane units represented by the general unit formula R.sub.b SiO.sub.(4-b)/2, in which R has the same meaning as defined above and the subscript b is 1, 2 or 3, as a second reactant to form a mixture; and (b) heating the mixture, in a pressurizable reaction vessel, in the presence of water and a sulfonic acid group-containing compound or phosphonitrile chloride as a catalyst at a temperature higher by at least 10° C. than the boiling point of the mixture under atmospheric pressure.
Claim 2
Independent Claim
167 words
A method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units which comprises the steps of: (a) mixing an alkyl silicate or a partial hydrolysis product thereof as a first reactant with an organosilane compound represented by the general formula R.sub.a SiX.sub.4-a, in which R is a hydrogen atom or an unsubstituted or substituted monovalent hydrocarbon group, X is an alkoxy group or a hydroxyl group and the subscript a is 1, 2 or 3, or an oligomeric organosiloxane compound consisting of the siloxane units represented by the general unit formula R.sub.b SiO.sub.(4-b)/2, in which R has the same meaning as defined above and the subscript b is 1, 2 or 3, as a second reactant to form a mixture; and (b) heating the mixture, in a pressurizable reaction vessel, in the presence of water and a sulfonic acid group-containing compound or phosphonitrile chloride as a catalyst at a temperature higher by at least 10° C. than the boiling point of the mixture under atmospheric pressure.
Claim 3
Dependent Claim
68 words
The method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units as claimed in claim 1 in which the organosilane compound as the second reactant is selected from the class consisting of trimethyl methoxy silane, trimethyl ethoxy silane, vinyl dimethyl methoxy silane, vinyl dimethyl ethoxy silane, dimethyl methoxy silane, dimethyl ethoxy silane, dimethyl dimethoxy silane, dimethyl diethoxy silane, vinyl methyl dimethoxy silane and vinyl methyl diethoxy silane.
Claim 4
Dependent Claim
45 words
The method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units as claimed in claim 1 in which the oligomeric organosiloxane compound as the second reactant is selected from the class consisting of hexamethyl disiloxane, 1,1,3,3-tetramethyl-1,3-divinyl disiloxane, 1,1,3,3-tetramethyl disiloxane, octamethyl cyclotetrasiloxane and 1,3,5,7-tetramethyl-1,3,5,7-tetravinyl cyclotetrasiloxane.
Claim 5
Dependent Claim
38 words
The method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units as claimed in claim 1 in which the first reactant is selected from the class consisting of methyl orthosilicate, ethyl orthosilicate and partial hydrolysis products thereof.
Claim 6
Dependent Claim
50 words
The method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units as claimed in claim 1 in which the catalyst is a sulfonic acid group-containing compound selected from the class consisting of sulfuric acid, fuming sulfuric acid, methan sulfuric acid, sulfuric anhydride, p-toluene sulfonic acid and trifluoromethane sulfonic acid.
Claim 7
Dependent Claim
45 words
The method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units as claimed in claim 1 in which the amount of the catalyst is in the range from 0.001 to 3% by weight based on the total amount of the first and second reactants.
Claim 8
Dependent Claim
44 words
The method for the preparation of an organopolysiloxane comprising tetrafunctional siloxane units as claimed in claim 1 in which the amount of water is in the range from 0.6 to 1.5 moles per mole of the alkoxy groups in the first and second reactants.
References Cited (Backward Citations)
US4184995A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1994-12-02 | 1995-06-03 | 1995-12-03 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1998-12-02 | 1999-06-03 | 1999-12-03 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2002-12-02 | 2003-06-03 | 2003-12-03 | $7700.00 | Window Closed / Lapsed |