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US3715337A Expired / Lapsed US ⏱️ 0.0 years remaining

Preparation of poly(isocyanurate-urethanes) using trithiocarbonates as catalysts

Assignee: 3M Co
•
Filing: 1971-06-01
•
Granted: 1973-02-06
•
Expires: 1991-06-01
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Abstract

Abstract Polyisocyanates are trimerized, polymerized, or reacted with polyols in the presence of a trithiocarbonate salt catalyst, such as sodium ethyltrithiocarbonate, to produce polyisocyanurates, or poly(isocyanurate-urethanes).

Inventors

  • 👤 M Allen
  • 👤 Dyke G Van

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 20:45
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/22; C08G18/225; C08G18/02; C08G18/022; C08G18/09; C08G18/092; C08G18/18; C08G18/1875; Y; Y10; Y10S; Y10S521/00; Y10S521/902

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 101 words
A method of making poly(isocyanurate-urethanes) comprising mixing polyisocyanate with polyol in the presence of an effective amount of a trithiocarbonate salt polymerization catalyst having the formula(A)n-R-S-CS2 M wherein A is hydroxyl, mercapto or hydrogen, R is a polyvalent saturated aliphatic group, n is an integer equal to p-1, where p is the valence of R, and M is an alkali metal cation or a quaternary ammonium cation wherein the alkyl groups have from 1 to 18 carbon atoms each, each polyol being selected from the group consisting of polyalkylene ether polyols and polyesters and polyester amides containing plural reactive hydroxyl groups.
Claim 2
Independent Claim 101 words
A method of making poly(isocyanurate-urethanes) comprising mixing polyisocyanate with polyol in the presence of an effective amount of a trithiocarbonate salt polymerization catalyst having the formula(A)n-R-S-CS2 M wherein A is hydroxyl, mercapto or hydrogen, R is a polyvalent saturated aliphatic group, n is an integer equal to p-1, where p is the valence of R, and M is an alkali metal cation or a quaternary ammonium cation wherein the alkyl groups have from 1 to 18 carbon atoms each, each polyol being selected from the group consisting of polyalkylene ether polyols and polyesters and polyester amides containing plural reactive hydroxyl groups.
Claim 3
Dependent Claim 18 words
The method of claim 1 wherein R is alkyleneoxy-alkylene or poly(alkyleneoxy)-alkylene, and M is an alkali metal cation.
Claim 4
Dependent Claim 16 words
The method of claim 1 wherein R is propyleneoxy-propylene and M is sodium or potassium cation.
Claim 5
Dependent Claim 18 words
The method of claim 1 wherein said trithiocarbonate salt is used as a solution in polypropylene-ether-glycol or -triol.
Claim 6
Dependent Claim 12 words
The method of claim 1 wherein said trithiocarbonate salt is sodium ethylthiocarbonate.
Claim 7
Dependent Claim 12 words
The method of claim 1 wherein said trithiocarbonate salt is sodium dodecylthiocarbonate.
Claim 8
Dependent Claim 18 words
The method of claim 1 wherein said polyol is dipropylene glycol, polypropylene ether glycol, or polypropylene ether triol.
Claim 9
Dependent Claim 36 words
A solution of 0.1-20 weight percent of the trithio-carbonate salt defined in claim 1 in a polyol selected from the group consisting of polyalkylene ether polyols and polyesters and polyester amides containing plural reactive hydroxyl groups.

References Cited (Backward Citations)

US2844584A Cited
US3179626A Cited
US3324134A Cited
US3381008A Cited
US3607865A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1976-02-06 1976-08-07 1977-02-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1980-02-06 1980-08-07 1981-02-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1984-02-06 1984-08-07 1985-02-06 $7700.00 Window Closed / Lapsed

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