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US4119585A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing rigid polyurethane foams using latent catalysts

Assignee: Air Products and Chemicals Inc
•
Filing: 1977-05-10
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Granted: 1978-10-10
•
Expires: 1997-05-10
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Abstract

Abstract The combination of a diorganotin sulfide, -polysulfide, -dithiocyanate, bis(thiocyanato diorganotin) sulfide or bis(thiocyanato diorganotin) oxide with a tertiary amine functions as a latent catalyst for rigid polyurethane foams. Latency is not observed using a tertiary amine with other sulfur-containing organotin compounds.

Inventors

  • 👤 James F. Kenney
  • 👤 Kenneth Treadwell

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 14:16
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/161; C08G18/163; C08G18/165; C08G18/22; C08G18/24; C08G18/242

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 333 words
In an improved method for preparing a rigid polyurethane foam by reacting a polyol containing at least two active hydrogen atoms, as determined by the Zerewitinoff method, with a polyfunctional isocyanate, the reaction being conducted in the presence of a blowing agent, a surfactant and a catalyst, the improved which resides in increasing the time interval between the combining of said polyol with said isocyanate and the initiation of said reaction by employing a latent catalyst consisting essentially of a mixture containing 1) a diorganotin compound represented by a formula selected from the group consisting of R 1 R 2 SnS x , R 1 R 2 Sn(SCN) 2 , (R 1 R 2 SnSCN) 2 S x and (R 1 R 2 SnSCN) 2 O and 2) an amine selected from the group consisting of tertiary amines of the formula R 3 R 4 R 5 N wherein R 1 and R 2 are individually selected from the group consisting of alkyl containing from 1 to 20 carbon atoms, cycloalkyl, aryl, aralkyl and alkaryl, R 3 , R 4 and R 5 are individually selected from the group consisting of alkyl containing from 1 to 20 carbon atoms, hydroxyalkyl containing from 2 to 4 carbon atoms, cycloalkyl, aryl, aralkyl and alkaryl, alternatively two of the carbon atoms of the R 3 , R 4 or R 5 groups bonded to the nitrogen atom can be part of the same divalent hydrocarbon group such that the resultant ring contains 5 or 6 atoms one of which is the nitrogen atom and wherein the resultant heterocyclic ring can also contain one additional heteroatom such as oxygen, nitrogen or sulfur; and x is an interger from 1 to 4, and wherein the concentration of said diorganotin compound is from 0.1 to 10 parts by weight per 100 parts of said polyol and the concentration of said tertiary amine or heterocyclic tertiary amine is from 0.1 to 4 parts by weight per 100 parts of polyol.
Claim 2
Dependent Claim 333 words
In an improved method for preparing a rigid polyurethane foam by reacting a polyol containing at least two active hydrogen atoms, as determined by the Zerewitinoff method, with a polyfunctional isocyanate, the reaction being conducted in the presence of a blowing agent, a surfactant and a catalyst, the improved which resides in increasing the time interval between the combining of said polyol with said isocyanate and the initiation of said reaction by employing a latent catalyst consisting essentially of a mixture containing 1) a diorganotin compound represented by a formula selected from the group consisting of R 1 R 2 SnS x , R 1 R 2 Sn(SCN) 2 , (R 1 R 2 SnSCN) 2 S x and (R 1 R 2 SnSCN) 2 O and 2) an amine selected from the group consisting of tertiary amines of the formula R 3 R 4 R 5 N wherein R 1 and R 2 are individually selected from the group consisting of alkyl containing from 1 to 20 carbon atoms, cycloalkyl, aryl, aralkyl and alkaryl, R 3 , R 4 and R 5 are individually selected from the group consisting of alkyl containing from 1 to 20 carbon atoms, hydroxyalkyl containing from 2 to 4 carbon atoms, cycloalkyl, aryl, aralkyl and alkaryl, alternatively two of the carbon atoms of the R 3 , R 4 or R 5 groups bonded to the nitrogen atom can be part of the same divalent hydrocarbon group such that the resultant ring contains 5 or 6 atoms one of which is the nitrogen atom and wherein the resultant heterocyclic ring can also contain one additional heteroatom such as oxygen, nitrogen or sulfur; and x is an interger from 1 to 4, and wherein the concentration of said diorganotin compound is from 0.1 to 10 parts by weight per 100 parts of said polyol and the concentration of said tertiary amine or heterocyclic tertiary amine is from 0.1 to 4 parts by weight per 100 parts of polyol.
Claim 3
Dependent Claim 15 words
An improved method according to claim 1 wherein R 1 and R 2 are alkyl.
Claim 4
Dependent Claim 15 words
An improved method according to claim 2 wherein said diorganotin compound is a dialkyltin sulfide.
Claim 5
Dependent Claim 15 words
An improved method according to claim 2 wherein said diorganotin compound is a dialkyltin dithiocyanate.
Claim 6
Dependent Claim 16 words
An improved method according to claim 2 wherein said diorganotin compound is a bis(thiocyanato dialkyltin) sulfide.
Claim 7
Dependent Claim 16 words
An improved method according to claim 2 wherein said diorganotin compound is a bis(thiocyanato dialkyltin) oxide.
Claim 8
Dependent Claim 15 words
An improved method according to claim 2 wherein R 1 and R 2 are butyl.
Claim 9
Dependent Claim 14 words
An improved method according to claim 1 wherein said diorganotin compound is dibutyltin sulfide.
Claim 10
Dependent Claim 14 words
An improved method according to claim 1 wherein said diorganotin compound is dibutyltin dithiocyanate.
Claim 11
Dependent Claim 15 words
An improved method according to claim 1 wherein said diorganotin compound is bis(thiocyanato dibutyltin) sulfide.
Claim 12
Dependent Claim 15 words
An improved method according to claim 1 wherein said diorganotin compound is bis(thiocyanato dibutyltin) oxide.
Claim 13
Dependent Claim 20 words
An improved method according to claim 1 wherein R 3 and R 4 are alkyl and R 5 is hydroxyalkyl.
Claim 14
Dependent Claim 13 words
An improved method according to claim 1 wherein the tertiary amine is dimethylethanolamine.

References Cited (Backward Citations)

US3092593A Cited
US3095434A Cited
GB1006630A Cited
US3432474A Cited
US3645927A Cited
US3635906A Cited
US3933692A Cited
US3980579A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-10-09 1982-04-10 1982-10-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-10-09 1986-04-10 1986-10-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-10-09 1990-04-10 1990-10-10 $7700.00 Window Closed / Lapsed

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