IP Library Granted Patent US 10,899,866
Granted Patent B2
US 10,899,866 · App. 15/744,899 · Granted Jan 26, 2021

Process for producing a ring-opening polymerization product

Inventors: Sophie Putzien (Ampfing, DE); Maximilian Köhler (Trostberg, DE); Heimo Woelfle (Traunstein, DE)
Assignee: Construction Research & Technology GmbH
C08G18/281C08G18/10C08G18/20C08G18/2018C08G18/2063C08G18/246C08G18/48C08G18/4829C08G18/714C08G18/73C08G18/75C08G18/755C08G18/76C08G18/7621C08G18/79C08G18/792C08G18/80C08G18/8061C08G2101/0008
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Quick Facts
Patent No.
US 10,899,866
App. No.
15/744,899
Granted
Jan 26, 2021
Kind
B2
Abstract

The invention relates to a process for producing a ring-opening polymerization product by reacting at least one polyisocyanate and 2-oxo-1,3-dioxolane-4-carboxylic acid and subjecting the reaction product to a temperature within the range of from about 40 to about 150° C. in the presence of a catalytic amount of at least one non-nucleophilic base. The obtained polymerization product may be present as a foam and is suitable as binder, insulation material, sealant or coating and in the production of mattresses or wound pads.

Claims (30)

1. A process for producing a ring-opening polymerization product in the form of an open-cell foam which comprises the steps of:

a) providing a reaction product of at least one polyisocyanate and 2-oxo-1,3-dioxolane-4-carboxylic acid; and

b) subjecting said reaction product to a temperature within the range of from 40 to 150° C. in the presence of a catalytic amount of at least one non-nucleophilic base,

wherein carbon dioxide is cleaved off.

2. The process of claim 1 , wherein the polyisocyanate is selected from an aliphatic isocyanate, an aromatic isocyanate, a cycloaliphatic isocyanate, or a combination thereof, having an —NCO functionality of ≥2.

3. The process of claim 1 , wherein the polyisocyanate is selected from toluylenediisocyanate, isophorondiisocyanate, diphenylmethanediisocyanate, 4,4′-diisocyanato-dicyclohexylmethane, tetramethylenediisocyanate, pentamethylenediisocyanate, hexamethylene-diisocyanate, and mixtures thereof.

4. The process of claim 1 , wherein the polyisocyanate is a polyisocyanate prepolymer which is obtained by reacting a molar excess of a polyisocyanate with a polyol, wherein the polyisocyanate:

i.) is selected from an aliphatic isocyanate, an aromatic isocyanate, a cycloaliphatic isocyanate, or a combination thereof, having an —NCO functionality of ≥2; or

ii.) is selected from toluylenediisocyanate, isophorondiisocyanate, diphenylmethanediisocyanate, 4,4′-diisoyanatodicyclohexylmethane, tetramethylene diisocyanate, pentamethylenediisocyanate, hexamethylenediisocyanate, and mixtures thereof.

5. The process of claim 4 , wherein the polyol has an average OH functionality of 2 to 8.

6. The process of claim 5 , wherein the polyol is a poly-C 2-4 -alkylenoxide having a number average molecular weight Mn in the range of from 400 to 10000.

7. The process of claim 1 , wherein the reaction product of step (a) is obtained by:

(1) reacting the polyisocyanate with an equimolar amount of 2-oxo-1,3-dioxolane-4-carboxylic acid; or by

(2) reacting in a first step a molar excess of the polyisocyanate with 2-oxo-1,3-dioxolane-4-carboxylic acid to obtain an intermediate, and in a second step reacting the intermediate with a polyol, wherein the polyol has an average OH functionality of 2 to 8.

8. The process of claim 7 , wherein the polyol is a poly-C 2-4 -alkylenoxide having a number average molecular weight Mn in the range of from 400 to 10000.

9. The process of claim 1 , wherein the reaction product of step (a) is of formula (I)

wherein R is an x-valent radical derived from said polyisocyanate by formally removing the NCO groups and x is an integer from 2 to 6.

10. The process of claim 1 , wherein step (b) is carried out at a temperature in the range of from 60 to 150° C.

11. The process of claim 1 , wherein the non-nucleophilic base is selected from 1,8-diazabicyclo[5.4.0]undec-7-ene, 1,5-diazobicyclo[4.3.0]non-5-ene, 1,4-diazabicyclo[2.2.2]octane, 2,6-di-tert-butylpyridine, diisopropylethylamine, tetramethylguanidine or mixtures thereof.

12. A process for producing a ring-opening polymerization product in the form of an open-cell foam which comprises the steps of:

a) providing a reaction product of at least one polyisocyanate and 2-oxo-1,3-dioxolane-4-carboxylic acid; and

b) subjecting said reaction product to a temperature within the range of from 40 to 150° C. in the presence of a catalytic amount of at least one non-nucleophilic base,

wherein carbon dioxide is cleaved off;

wherein the reaction product of step (a) is obtained by: (1) reacting the polyisocyanate with an equimolar amount of 2-oxo-1,3-dioxolane-4-carboxylic acid; or by (2) reacting in a first step a molar excess of the polyisocyanate with 2-oxo-1,3-dioxolane-4-carboxylic acid to obtain an intermediate, and in a second step reacting the intermediate with a polyol; and

wherein the polyol has an average OH functionality of 2 to 8; wherein the polyol is a poly-C 2-4 -alkylenoxide having a number average molecular weight Mn in the range of from 400 to 10000.

13. A ring-opening polymerization product in the form of an open-cell foam obtained by the process of claim 1 .

14. The product of claim 13 , wherein the polyisocyanate:

i.) is selected from an aliphatic isocyanate, an aromatic isocyanate, a cycloaliphatic isocyanate, or a combination thereof, having an —NCO functionality of ≥2; or

ii.) is selected from toluylenediisocyanate, isophorondiisocyanate, diphenylmethanediisocyanate, 4,4′-diisocyanatodicyclohexylmethane, tetramethylene diisocyanate, pentamethylenediisocyanate, hexamethylenediisocyanate and mixtures thereof.

15. The product of claim 13 , wherein the non-nucleophilic base is selected from 1,8-diazabicyclo[5.4.0]undec-7-ene, 1,5-diazobicyclo[4.3.0]-non-5-ene, 1,4-diaza bicyclo[2.2.2]octane, 2,6-di-tert-butylpyridine, diisopropylethylamine, tetramethyl guanidine or mixtures thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2023
From: CONSTRUCTION RESEARCH & TECHNOLOGY GMBH
To: SIKA TECHNOLOGY AG
Reel/Frame 064640/0880 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2019
From: PUTZIEN, SOPHIE; KOEHLER, MAXIMILIAN; WOELFLE, HEIMO
To: BASF CONSTRUCTION SOLUTIONS GMBH
Reel/Frame 049113/0598 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2019
From: BASF CONSTRUCTION SOLUTIONS GMBH
To: CONSTRUCTION RESEARCH & TECHNOLOGY GMBH
Reel/Frame 049113/0644 →