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US4985578A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of modified polysiloxanes

Assignee: Dow Silicones Belgium SPRL
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Filing: 1988-10-06
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Granted: 1991-01-15
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Expires: 2008-10-06
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Abstract

Abstract The specification describes a method of preparing a polysiloxane including at least one siloxane unit having a silicon-bonded group --OX in which X is a saturated or unsaturated hydrocarbon group, for example methyl, alkenyl or alkynyl. The method comprises bringing about chemical reaction between a polymer having at least one siloxane unit having a silicon-bonded hydroxyl group and an alcohol of the general formula HOX in presnece of an acidic condensation catalyst of the formula (i) RSO 3 H in which R represents an alkyl, aryl or alkaryl group which may be halogenated at a temperature of less than 50° C. under conditions to cause condensation reaction between hydroxyl groups of the siloxane units and the alcohol. Preferred polymers are polyorganosiloxanes comprising predominantly dimethyl siloxane units especially those prepared by polymerization of a precursor siloxane comprising at least two siloxane units which have a silicon-bonded hydroxyl group in presence of an acidic condensation catalyst of the formula (i). Preferably the group R of the acidic condensation catalyst is an alkyl group having a chain of 6 to 18 carbon atoms or a group R"C 6 H 4 where R' represents an alkyl group having 6 to 18 carbon atoms, for example dodecylbenzenesulphonic acid. Water may be present in the reaction mixture to an extent of not more than 7 moles per mole of acidic condensation catalyst. A basic material, e.g. calcium carbonate or magnesium carbonate may be added to the reaction mixture to neutralize the catalyst. Also disclosed are curable compositions including a polysiloxane made according to the invention.

Inventors

  • 👤 Brian R. Trego

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 22:45
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/38; C08G77/06; C08G77/08; C08G77/14; C08G77/18

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 104 words
A method of preparing a polysiloxane including at least one siloxane unit having a silicon-bonded group --OX which method comprises bringing about chemical reaction between a polymer having at least one siloxane unit having a silicon-bonded hydroxyl group and an alcohol of the general formula HOX, where X represents a hydrocarbon group in presence of an acidic condensation catalyst of the formula (i) RSO 3 H in which R represents an alkyl, aryl or alkaryl group which may be halogenated at a temperature of less than 50° C. under conditions to cause condensation reaction between hydroxyl groups of the siloxane units and the alcohol.
Claim 2
Independent Claim 104 words
A method of preparing a polysiloxane including at least one siloxane unit having a silicon-bonded group --OX which method comprises bringing about chemical reaction between a polymer having at least one siloxane unit having a silicon-bonded hydroxyl group and an alcohol of the general formula HOX, where X represents a hydrocarbon group in presence of an acidic condensation catalyst of the formula (i) RSO 3 H in which R represents an alkyl, aryl or alkaryl group which may be halogenated at a temperature of less than 50° C. under conditions to cause condensation reaction between hydroxyl groups of the siloxane units and the alcohol.
Claim 3
Dependent Claim 17 words
A method according to claim 1 wherein the polymer is a polyorganosiloxane comprising predominantly dimethyl siloxane units.
Claim 4
Dependent Claim 71 words
A method according to claim 1 wherein the polymer including at least one siloxane unit having a silicon-bonded hydroxyl group is a polysiloxane prepared by polymerisation of a precursor siloxane comprising at least two siloxane units which have a silicon-bonded hydroxyl group in presence of an acidic condensation catalyst of the formula (i) and the alcohol HOX is added to the polymerising siloxane when the polysiloxane has a desired molecular size.
Claim 5
Dependent Claim 14 words
A method according to claim 1 wherein X represents an alkenyl or alkynyl group.
Claim 6
Dependent Claim 15 words
A method according to claim 1 wherein the alcohol comprises allyl alcohol or propargyl alcohol.
Claim 7
Dependent Claim 47 words
A method according to claim 1 wherein the group R of the acidic condensation catalyst is an alkyl group having a chain of 6 to 18 carbon atoms or a group R"C 6 H 4 where R" represents an alkyl group having 6 to 18 carbon atoms.
Claim 8
Independent Claim 17 words
A method according to any one of claims 1 to 6 wherein the catalyst comprises dodecylbenzenesulphonic acid.
Claim 9
Dependent Claim 29 words
A method according to claim 1 wherein water is present in the reaction mixture to an extent of not more than 7 moles per mole of acidic condensation catalyst.
Claim 10
Dependent Claim 20 words
A method according to claim 1 wherein a basic material is added to the reaction mixture to neutralise said catalyst.

References Cited (Backward Citations)

US3821114A Cited
US3984449A Cited
GB1541637A Cited
US4209454A Cited
US4298753A Cited
US4609752A Cited
US4658006A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1994-01-14 1994-07-16 1995-01-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1998-01-14 1998-07-16 1999-01-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2002-01-14 2002-07-16 2003-01-15 $7700.00 Window Closed / Lapsed

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