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US4762937A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for preparing linear organopolysiloxanediols

Assignee: Wacker Chemie AG
•
Filing: 1987-08-06
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Granted: 1988-08-09
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Expires: 2007-08-06
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Abstract

Abstract Linear organopolysiloxanediols are prepared by continuously introducing cyclic organopolysiloxanes, water in an amount of at least 14 mols per gram atom of silicon contained in the cyclic organopolysiloxanes used and water-soluble acid into a recirculating reactor and thereafter separating the aqueous phase from the organopolysiloxanediols more or less immediately after the reaction mixture exits from the recirculating reactor.

Inventors

  • 👤 Ralph Ottlinger
  • 👤 Rudolf Reitmeier

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-07 13:36
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/06; C08G77/14; C08G77/16

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 83 words
A method for preparing linear organopolysiloxanediols, which comprises continuously introducing cyclic organopolysiloxanes, water in an amount of at least 14 moles per gram atom of silicon present in the cyclic organopolysiloxanes and a water-soluble acid catalyst selected from the group consisting of Bronsted acids having an acid dissociation constant of at least 6.5·10 -2 at 25° C., Lewis acids and mixtures thereof into a loop reactor while continuously separating the aqueous phase from the organopolysiloxanediols as the reaction mixture exits from the reactor.
Claim 2
Independent Claim 83 words
A method for preparing linear organopolysiloxanediols, which comprises continuously introducing cyclic organopolysiloxanes, water in an amount of at least 14 moles per gram atom of silicon present in the cyclic organopolysiloxanes and a water-soluble acid catalyst selected from the group consisting of Bronsted acids having an acid dissociation constant of at least 6.5·10 -2 at 25° C., Lewis acids and mixtures thereof into a loop reactor while continuously separating the aqueous phase from the organopolysiloxanediols as the reaction mixture exits from the reactor.
Claim 3
Dependent Claim 12 words
The method of claim 1, wherein the water-soluble acid is sulfuric acid.
Claim 4
Dependent Claim 38 words
The method of claim 1, wherein from 0 to 10 percent by weight based on the weight of the cyclic organopolysiloxanes of a silane having Si-bonded halogen is introduced simultaneously with the cyclic organopolysiloxanes into the loop reactor.
Claim 5
Dependent Claim 63 words
The method of claim 1, wherein a co-catalyst is introduced into the loop reactor, in which the co-catalyst is selected from the group having the formulas, NR 2 3 HX, NR 2 4 X, PR 2 3 HX and PR 2 4 X, where R 2 is an alkyl radical having from 1 to 30 carbon atoms and X is an inorganic anion.

References Cited (Backward Citations)

BE658839A Cited
US2758124A Cited
US3309390A Cited
US3449392A Cited
GB1088187A Cited
US3853932A Cited
US3939195A Cited
US4096160A Cited
US4497942A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-08-09 1992-02-08 1992-08-09 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-08-09 1996-02-08 1996-08-09 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1999-08-09 2000-02-08 2000-08-09 $7700.00 Window Closed / Lapsed

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