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US4255569A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the production of isocyanurate polyisocyanates, and products by the process

Assignee: Bayer AG
•
Filing: 1979-05-04
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Granted: 1981-03-10
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Expires: 1999-05-04
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Abstract

Abstract The instant invention is directed to a process for the production of isocyanate polyisocyanates containing at least 50%, by weight, of tris-isocyanatomonoisocyanurates and at most 3%, by weight, of isocyanurate-free diisocyanate. The process comprises catalytically trimerizing the organic diisocyanates free from isocyanurate groups and terminating the trimerization reaction by deactivation of the catalyst after 5 to 40% of the isocyanate groups of the isocyanurate-free diisocyanate have been trimerized. The unreacted isocyanurate-free diisocyanate is then distilled off in the presence of from 1 to 30%, by weight, based on the end product obtained as distillation residue, of an inert liquid distillation aid which boils at a temperature at least 50 DEG C. above the boiling point of the isocyanurate-free diisocyanate. The invention is also directed to the products produced by this process.

Inventors

  • 👤 Hans-Jurgen Muller
  • 👤 Rudolf Hombach
  • 👤 Manfred Dollhausen
  • 👤 Joachim Zirner

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 12:52
CPC Classifications
C; C09; C09J; C09J121/00; C08; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/72; C08G18/77; C08G18/78; C08G18/79; C08G18/791; C08K; C08K5/00; C08K5/16; C08K5/29; C09J175/00

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 152 words
A process for the production of polyisocyanates of isocyanurate structure containing at least 50%, by weight, of tris-isocyanatomonoisocyanurates and at most 3%, by weight, of diisocyanate free from isocyanurate groups comprising: (a) catalytically trimerizing organic diisocyanates free from isocyanurate groups, selected from the group consisting of 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, and 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane and mixtures thereof, (b) terminating the trimerization reaction by deactivation of the catalyst after from 5 to 40% of the isocyanate groups of the isocyanurate-free diisocyanate have been trimerized, and (c) removing the unreacted isocyanurate-free diisocyanate present in the reaction mixture from the reaction mixture by distillation, said distillation being carried out in the presence of from 1, to 30%, by weight, based on the end product obtained as distillation residue, of a liquid distillation aid which is inert under the distillation conditions and which boils at a temperature at least 50° C. above the boiling point of the isocyanurate-free diisocyanate.
Claim 2
Dependent Claim 152 words
A process for the production of polyisocyanates of isocyanurate structure containing at least 50%, by weight, of tris-isocyanatomonoisocyanurates and at most 3%, by weight, of diisocyanate free from isocyanurate groups comprising: (a) catalytically trimerizing organic diisocyanates free from isocyanurate groups, selected from the group consisting of 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, and 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane and mixtures thereof, (b) terminating the trimerization reaction by deactivation of the catalyst after from 5 to 40% of the isocyanate groups of the isocyanurate-free diisocyanate have been trimerized, and (c) removing the unreacted isocyanurate-free diisocyanate present in the reaction mixture from the reaction mixture by distillation, said distillation being carried out in the presence of from 1, to 30%, by weight, based on the end product obtained as distillation residue, of a liquid distillation aid which is inert under the distillation conditions and which boils at a temperature at least 50° C. above the boiling point of the isocyanurate-free diisocyanate.
Claim 3
Dependent Claim 44 words
Polyisocyanates of isocyanurate structure obtained by the partial trimerization of the isocyanate groups of 2,4- and optionally, 2,6,-diisocyanatotoluene, characterized by a content of at least 50%, by weight, of tris-(isocyanatotolyl)-isocyanurate and a content of less than 3%, by weight, of free 2,4- and/or 2,6-diisocyanatotoluene.
Claim 4
Dependent Claim 44 words
Polyisocyanates of isocyanurate structure obtained by the partial trimerization of the isocyanate groups of 2,4- and optionally, 2,6,-diisocyanatotoluene, characterized by a content of at least 50%, by weight, of tris-(isocyanatotolyl)-isocyanurate and a content of less than 3%, by weight, of free 2,4- and/or 2,6-diisocyanatotoluene.
Claim 5
Dependent Claim 41 words
Polyisocyanates of isocyanurate structure obtained by the partial trimerization of the isocyanate groups of 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane, characterized by a content of at least 50%, by weight, of tris-[(1,3,3-trimethyl-5-isocyanatocyclohexyl)-methyl]-isocyanurate and a content of less than 3%, by weight, of free 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane.
Claim 6
Dependent Claim 41 words
Polyisocyanates of isocyanurate structure obtained by the partial trimerization of the isocyanate groups of 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane, characterized by a content of at least 50%, by weight, of tris-[(1,3,3-trimethyl-5-isocyanatocyclohexyl)-methyl]-isocyanurate and a content of less than 3%, by weight, of free 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane.

References Cited (Backward Citations)

US2952665A Cited
US3517002A Cited
US3619338A Cited
US3641024A Cited
US3631000A Cited
US3773695A Cited
US3919218A Cited
US3996223A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-03-09 1984-09-08 1985-03-10 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-03-09 1988-09-08 1989-03-10 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-03-09 1992-09-08 1993-03-10 $7700.00 Window Closed / Lapsed

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