IP Library Granted Patent US 12,006,412
Granted Patent B2
US 12,006,412 · App. 17/414,134 · Granted Jun 11, 2024

Reaction mixture suitable for manufacturing of foam with reduced aldehyde emission

Inventors: Bao Luan (Shanghai, CN); Zuxia Rong (Shanghai, CN); Yuefan Zhang (Shanghai, CN); Lies Bonami (Aalter, BE); Joris Bosman (Herselt, BE)
Assignee: HUNTSMAN INTERNATIONAL LLC
C08J9/0023C08G18/18C08G18/3275C08G18/4841C08G18/6688C08G18/7671C08J9/125C08K5/132C08K5/1535C08K5/1545C08G2110/0083C08J2203/10C08J2375/12
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Quick Facts
Patent No.
US 12,006,412
App. No.
17/414,134
Granted
Jun 11, 2024
Kind
B2
Abstract

Disclosed is a reaction mixture for the manufacturing of a polyurethane foam, which mixture can be obtained by reacting a polyfunctional isocyanate with an isocyanate-reactive compound, in the presence of a scavenger and at least one catalyst; and curing such reaction mixture enables providing a foam with reduced aldehyde emissions particularly useful in means of transport, such as interior part of cars.

Claims (26)

1. A reaction mixture for the manufacturing of a polyurethane foam, the reaction mixture comprising a polyfunctional isocyanate, an isocyanate-reactive compound, a scavenger and at least one catalyst, wherein the scavenger comprises a compound of the following formula (I):

wherein,

R 1 and R 2 are independently of one another selected from —OR 3 , R 4 or from the group consisting of hydroxy, ether, halogen, carbonyl, carboxyl, isocyanate, nitro and/or amine groups,

R 3 and R 4 are independently of one another selected from a combination of saturated linear, saturated branched, cyclic and/or saturated non-cyclic carbon chains, saturated aliphatic hydrocarbons, araliphatic hydrocarbons, aromatic hydrocarbons and mixtures thereof, optionally interrupted by one or more oxygen atoms, nitrogen atoms and/or sulphur atoms, and optionally comprising any functional group selected from hydroxy, ether, halogen, carboxyl, isocyanate, nitro and/or amine groups,

R 1 and R 2 may be linked to each other essentially forming at least one ring structure.

2. The reaction mixture according to claim 1 , wherein said compound with formula (I) is in an aqueous condition when added to the reaction mixture.

3. The reaction mixture according to claim 1 , wherein said scavenger is added to the reaction mixture at a temperature ranging from 18 to 45° C.

4. The reaction mixture according to claim 1 , wherein R 1 is —OR 3 .

5. The reaction mixture according to claim 1 , wherein said scavenger is made of at least 90 wt % of said compound of formula (I) based on the total weight of said scavenger.

6. The reaction mixture according to claim 1 , wherein R 1 and R 2 are linked to each other to form a 5 to 12 membered ring structure and comprise unsaturations, aromatic rings and/or heteroatoms.

7. The reaction mixture according to claim 1 , wherein said scavenger has a molecular weight of at most 3000 g/mol.

8. The reaction mixture according to claim 1 , wherein the reaction mixture further comprises a blowing agent.

9. The reaction mixture according to claim 1 , wherein the polyfunctional isocyanate is selected from a polymeric methylene diphenyl diisocyanate, a methylene diphenyl diisocyanate isomer mixture, or a mixtures thereof.

10. The reaction mixture according to claim 1 , wherein the isocyanate-reactive compound is a polyfunctional polyol or a polyfunctional amine.

11. A process for the manufacturing of a polyurethane foam, comprising the following steps:

(a) providing a reaction mixture comprising a polyfunctional isocyanate and an isocyanate-reactive compound;

(b) adding a scavenger and at least one catalyst to said reaction mixture, then adding at least one blowing agent to the reaction mixture;

wherein said scavenger comprises a compound of the following formula (I):

wherein,

R 1 and R 2 are independently of one another selected from —OR 3 , R 4 , or from the group consisting of hydroxy, ether, halogen, carbonyl, carboxyl, isocyanate, nitro and/or amine groups,

R 3 and R 4 are independently of one another selected from a combination of saturated linear, saturated branched, cyclic and/or saturated non-cyclic carbon chains, saturated aliphatic hydrocarbons, araliphatic hydrocarbons, aromatic hydrocarbons and mixtures thereof, optionally interrupted by one or more oxygen atoms, nitrogen atoms and/or sulphur atoms, and optionally comprising any functional group selected from hydroxy, ether, halogen, carboxyl, isocyanate, nitro and/or amine groups,

R 1 and R 2 may be linked to each other essentially forming at least one ring structure; and

(c) curing said reaction mixture, which comprises at least the reaction product of said polyisocyanate and said isocyanate-reactive compound in the presence of said scavenger and said at least one catalyst, leading to the formation of a polyurethane foam.

12. The process according to claim 11 , wherein said compound with formula (I) is in an aqueous condition when added to the reaction mixture.

13. The process according to claim 11 , wherein, said reaction mixture has an NCO index in the range of from about 0.6 to about 1.5.

14. The process according to claim 11 , wherein, the NCO index of the reaction mixture is in the range of from about 1.05 to about 10.

Assignments (3)
SECURITY INTEREST Recorded May 4, 2026
From: HUNTSMAN INTERNATIONAL LLC; HUNTSMAN ADVANCED MATERIALS AMERICAS LLC; HUNTSMAN NANOCOMP LLC; HUNTSMAN PETROCHEMICAL LLC
To: CITIBANK N.A.
Reel/Frame 075498/0663 →
PATENT SECURITY AGREEMENT Recorded Mar 10, 2026
From: HUNTSMAN INTERNATIONAL LLC; HUNTSMAN ADVANCED MATERIALS AMERICAS LLC; HUNTSMAN NANOCAMP LLC; HUNTSMAN PETROCHEMICAL LLC
To: CITIBANK, N.A.
Reel/Frame 075106/0238 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2021
From: LUAN, BAO; RONG, ZHUXIA; ZHANG, YUEFAN; BONAMI, LIES; BOSMAN, JORIS
To: HUNTSMAN INTERNATIONAL LLC
Reel/Frame 056549/0902 →