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US4116879A Expired / Lapsed US ⏱️ 0.0 years remaining

Quaternary hydroxyalkyl tertiary amine bases as polyurethane catalysts

Assignee: Air Products and Chemicals Inc
•
Filing: 1976-08-10
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Granted: 1978-09-26
•
Expires: 1996-08-10
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Abstract

Abstract Catalysts having the following formula have been found to have unexpectedly high activity for the production of polyurethane and polyisocyanate resins: <IMAGE> where:

Inventors

  • 👤 Ibrahim S. Bechara
  • 👤 Felix P. Carroll
  • 👤 Rocco L. Mascioli
  • 👤 John R. Panchak

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 09:20
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/18; C08G18/1875; B; B01; B01J; B01J31/00; B01J31/02; B01J31/06; B01J31/08; B01J31/0234; B01J31/0235; B01J31/0239; C08G2115/00; C08G2115/02; Y; Y10; Y10S; Y10S521/00; Y10S521/902; Y10S521/904

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 158 words
A polyurethane catalyst composition for the polymerization of a polyol and an organic polyisocyanate which comprises a mixture of a tertiary amine selected from the group consisting of trimethylamine, triethylamine, tripropylamine, triisobutylamine and mixtures thereof and a quaternary hydroxyalkyl tertiary amine base prepared by reacting substantially stoichiometric amounts of water or a carbinol selected from the group consisting of methanol, ethanol, benzyl alcohol, furfuryl alcohol, allyl alcohol, phenol, octylphenol, nonylphenol, methylphenol, methoxyphenol, ethoxyphenol, 3-diethylamino phenol, naphthol, resorcinol, 1,4-hydroquinone, chlorophenols, chloronaphthols and p,p'-dihydroxydiphenyldimethylmethane; an alkylene oxide selected from the group consisting of propylene oxide, ethylene oxide, 1,2-butylene oxide, 1,2-pentene oxide, styrene oxide, butadiene epoxide, diepoxides prepared from p,p'-dihydroxydiphenyldimethylmethane and epichlorohydrin, an olefin oxide having 9-14 carbon atoms and mixtures thereof; and a tertiary amine selected from the group consisting of trimethylamine, triethylamine, tripropylamine, triisobutylamine and mixtures thereof, wherein the tertiary amine in said composition is present in a catalytic amount of up to 50% by weight of the composition.
Claim 2
Dependent Claim 158 words
A polyurethane catalyst composition for the polymerization of a polyol and an organic polyisocyanate which comprises a mixture of a tertiary amine selected from the group consisting of trimethylamine, triethylamine, tripropylamine, triisobutylamine and mixtures thereof and a quaternary hydroxyalkyl tertiary amine base prepared by reacting substantially stoichiometric amounts of water or a carbinol selected from the group consisting of methanol, ethanol, benzyl alcohol, furfuryl alcohol, allyl alcohol, phenol, octylphenol, nonylphenol, methylphenol, methoxyphenol, ethoxyphenol, 3-diethylamino phenol, naphthol, resorcinol, 1,4-hydroquinone, chlorophenols, chloronaphthols and p,p'-dihydroxydiphenyldimethylmethane; an alkylene oxide selected from the group consisting of propylene oxide, ethylene oxide, 1,2-butylene oxide, 1,2-pentene oxide, styrene oxide, butadiene epoxide, diepoxides prepared from p,p'-dihydroxydiphenyldimethylmethane and epichlorohydrin, an olefin oxide having 9-14 carbon atoms and mixtures thereof; and a tertiary amine selected from the group consisting of trimethylamine, triethylamine, tripropylamine, triisobutylamine and mixtures thereof, wherein the tertiary amine in said composition is present in a catalytic amount of up to 50% by weight of the composition.
Claim 3
Dependent Claim 47 words
The catalyst composition of claim 1 wherein said quaternary hydroxyalkyl tertiary amine base is selected from the group consisting of N,N,N-trimethyl-N,2-hydroxypropyl ammonium phenoxide, N,N,N-triethyl-N,2-hydroxypropyl ammonium phenoxide, N,N,N-tri-n-propyl-N,2-ammonium phenoxide, N,N,N-triisobutyl-N,2-ammonium phenoxide and mixtures thereof and wherein said tertiary amine is trimethylamine, triethylamine, tri-n-propylamine, triisobutylamine and mixtures thereof, respectively.

References Cited (Backward Citations)

US3010963A Cited
US3620987A Cited
US3726816A Cited
US3746709A Cited
US3766103A Cited
US3892687A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-09-25 1982-03-27 1982-09-26 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-09-25 1986-03-27 1986-09-26 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-09-25 1990-03-27 1990-09-26 $7700.00 Window Closed / Lapsed

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