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US4032574A Expired / Lapsed US ⏱️ 0.0 years remaining

Production of polyetherpolyols useful in preparing rigid polyurethane foams

Assignee: Takeda Pharmaceutical Co Ltd
•
Filing: 1975-09-25
•
Granted: 1977-06-28
•
Expires: 1995-09-25
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Abstract

Abstract Polyetherpolyols useful in preparing rigid polyurethane foam excellent in dimensional stability and inflammability. These polyetherpolyols are obtained by reacting alkylene oxide with compounds containing active hydrogen atoms, part or all of which comprise the reaction product obtained by heating the distillation residue secured as a byproduct in the distillation process of a crude polyisocyanate in the presence of (1) water, alcohols and/or amines and (2) hydroxides or oxides of alkali metals or alkaline earth metals and/or monoalkanolamines.

Inventors

  • 👤 Akizo Keshi
  • 👤 Katsuhisa Kodama
  • 👤 Ichiro Takemura
  • 👤 Yoshihiko Tairaka
  • 👤 Kunio Yoshinaga

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 09:24
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/16; C08G18/18; C08G18/1808; C08G18/28; C08G18/40; C08G18/48; C08G65/00; C08G65/02; C08G65/26; C08G65/2618

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 117 words
A method for producing a polyetherpolyol consisting essentially of reacting (A) compounds containing active hydrogen atoms, one third by weight to all of which is a reaction product obtained by reacting the distillation residue obtained in the distillation process of a crude organic diisocyanate produced by phosgenation of the corresponding organic diamine with (1) at least a member selected from the group consisting of water, aliphatic alcohols having 1 to 10 carbon atoms and alkanolamines having 1 to 6 carbon atoms and (2) a monoalkanolamine having 2 to 4 carbon atoms at a temperature ranging from 100° to 250° C. with (B) at least a member selected from the group consisting of ethylene oxide and propylene oxide.
Claim 2
Independent Claim 117 words
A method for producing a polyetherpolyol consisting essentially of reacting (A) compounds containing active hydrogen atoms, one third by weight to all of which is a reaction product obtained by reacting the distillation residue obtained in the distillation process of a crude organic diisocyanate produced by phosgenation of the corresponding organic diamine with (1) at least a member selected from the group consisting of water, aliphatic alcohols having 1 to 10 carbon atoms and alkanolamines having 1 to 6 carbon atoms and (2) a monoalkanolamine having 2 to 4 carbon atoms at a temperature ranging from 100° to 250° C. with (B) at least a member selected from the group consisting of ethylene oxide and propylene oxide.
Claim 3
Dependent Claim 22 words
A method according to claim 1, wherein the distillation residue contains not more than 30 weight % of an organic diisocyanate monomer.
Claim 4
Dependent Claim 19 words
A method according to claim 1, wherein the member (1) is an alkanolamine having 1 to 6 carbon atoms.
Claim 5
Dependent Claim 15 words
A method according to claim 1, wherein the members (1) and (2) are both monoethanolamine.
Claim 6
Dependent Claim 19 words
A method according to claim 1, wherein the distillation residue is one obtained from a crude tolylenediisocyanate or diphenylmethanediisocyanate.
Claim 7
Dependent Claim 18 words
A method according to claim 1, wherein the member (1) is water and the member (2) is monoethanolamine.
Claim 8
Independent Claim 145 words
A method for producing a polyetherpolyol which consists essentially of reacting (A) compounds containing active hydrogen atoms, one third by weight to all of which is a reaction product obtained by reacting the distillation residue obtained in the distillation process of a crude organic diisocyanate produced by phosgenation of the corresponding organic diamine with (1) at least a member selected from the group consisting of water, aliphatic alcohols having 1 to 10 carbon atoms and alkanolamines having 1 to 6 carbon atoms and (2) at least a member selected from the group consisting of the hydroxides and oxides of alkali or alkaline earth metals at a temperature ranging from 50° to 250° C., and then removing the carbonate of alkali or alkaline earth metal from the reaction mixture with (B) at least a member selected from the group consisting of ethylene oxide and propylene oxide.
Claim 9
Independent Claim 145 words
A method for producing a polyetherpolyol which consists essentially of reacting (A) compounds containing active hydrogen atoms, one third by weight to all of which is a reaction product obtained by reacting the distillation residue obtained in the distillation process of a crude organic diisocyanate produced by phosgenation of the corresponding organic diamine with (1) at least a member selected from the group consisting of water, aliphatic alcohols having 1 to 10 carbon atoms and alkanolamines having 1 to 6 carbon atoms and (2) at least a member selected from the group consisting of the hydroxides and oxides of alkali or alkaline earth metals at a temperature ranging from 50° to 250° C., and then removing the carbonate of alkali or alkaline earth metal from the reaction mixture with (B) at least a member selected from the group consisting of ethylene oxide and propylene oxide.
Claim 10
Dependent Claim 28 words
A method according to claim 7, wherein the member (1) is an aliphatic alcohol having 1 to 10 carbon atoms and the member (2) is an alkali hydroxide.
Claim 11
Dependent Claim 19 words
A method according to claim 7, wherein the aliphatic alcohol is methylcellosolve and the alkali hydroxide is sodium hydroxide.
Claim 12
Dependent Claim 11 words
A polyetherpolyol which is obtained by the method of claim 1.

References Cited (Backward Citations)

US3128310A Cited
US2999873A Cited
GB972772A Cited
US3225094A Cited
US3499009A Cited
US3415891A Cited
GB1047116A Cited
GB1047101A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-06-27 1980-12-27 1981-06-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-06-27 1984-12-27 1985-06-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-06-27 1988-12-27 1989-06-28 $7700.00 Window Closed / Lapsed

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