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US4136046A Expired / Lapsed US ⏱️ 0.0 years remaining

Storage-stable precursors for rigid polyurethane foams

Assignee: Air Products and Chemicals Inc
•
Filing: 1976-05-20
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Granted: 1979-01-23
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Expires: 1996-05-20
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Abstract

Abstract Diorganotin compounds wherein at least one of the remaining valences on the tin atom is satisfied by a sulfur atom or a thiocyanate group are unique among diorganotin compounds in that they retain their catalytic activity over extended periods of time in the presence of the precursors or masterbatches conventionally employed to prepare rigid, cellular polyurethanes.

Inventors

  • 👤 Justin L. Hirshman
  • 👤 Kenneth Treadwell

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 12:34
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/22; C08G18/24; C08G18/242

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 108 words
In an improved method for preserving catalytic activity during long term storage of precursors for rigid cellular polyurethanes wherein said precursor comprises a polyol containing at least two active hydrogen atoms, as determined by the Zerewitinoff method, and a catalytically effective amount of an organotin compound as the gel catalyst, the improvement which consists of storing said polyol in the presence of a gel catalyst selected from the group consisting of R 2 Sn(SCN) 2 , [R 2 Sn(SCN)] 2 O, (R 2 SnSCN) 2 S, (R 2 SnX) 2 S and R 2 SnS, wherein R is a monovalent hydrocarbon and X is chlorine, bromine or iodine.
Claim 2
Dependent Claim 108 words
In an improved method for preserving catalytic activity during long term storage of precursors for rigid cellular polyurethanes wherein said precursor comprises a polyol containing at least two active hydrogen atoms, as determined by the Zerewitinoff method, and a catalytically effective amount of an organotin compound as the gel catalyst, the improvement which consists of storing said polyol in the presence of a gel catalyst selected from the group consisting of R 2 Sn(SCN) 2 , [R 2 Sn(SCN)] 2 O, (R 2 SnSCN) 2 S, (R 2 SnX) 2 S and R 2 SnS, wherein R is a monovalent hydrocarbon and X is chlorine, bromine or iodine.
Claim 3
Dependent Claim 18 words
A method according to claim 1 wherein the gel catalyst is a diorganotin sulfide or a diorganotin dithiocyanate.
Claim 4
Dependent Claim 45 words
A method according to claim 1 wherein R is selected from the group consisting of alkyl containing from 1 to 12 carbon atoms, cycloalkyl, phenyl, aralkyl and alkaryl, wherein the alkyl portion of said aralkyl and alkaryl groups contain from 1 to 12 carbon atoms.
Claim 5
Dependent Claim 10 words
A method according to claim 3 wherein R is phenyl.
Claim 6
Dependent Claim 13 words
A method according to claim 3 wherein R is methyl, butyl or octyl.
Claim 7
Dependent Claim 10 words
A method according to claim 5 wherein R is butyl.
Claim 8
Dependent Claim 74 words
A method according to claim 1 wherein the polyol is combined with at least one member of the group consisting of (a) a silicon-containing surfactant in an amount from about 1 to 5 parts by weight per 100 parts of said polyol, and (b) a blowing agent in an amount from about 10 to 50 parts by weight per 100 parts of said polyol, and (c) a catalytically effective amount of a tertiary amine.
Claim 9
Dependent Claim 24 words
A method according to claim 7 wherein said tertiary amine is selected from the group consisting of dimethylcyclohexyl amine, N-ethyl morpholine and triethylene diamine.
Claim 10
Dependent Claim 22 words
A method according to claim 7 wherein said blowing agent is a chlorine-containing hydrocarbon and boils from 35 to about 80° C.
Claim 11
Dependent Claim 15 words
A method according to claim 1 wherein said polyol is a polymer of propylene oxide.
Claim 12
Dependent Claim 28 words
A method according to claim 1 wherein said gel catalyst is present at a concentration of from 0.1 to 10 parts by weight per 100 parts of polyol.

References Cited (Backward Citations)

US3194773A Cited
US3392153A Cited
US3822223A Cited
US3620985A Cited
US3876567A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-01-22 1982-07-24 1983-01-23 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-01-22 1986-07-24 1987-01-23 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-01-22 1990-07-24 1991-01-23 $7700.00 Window Closed / Lapsed

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