IP Library Granted Patent US 12,509,545
Granted Patent B2
US 12,509,545 · App. 17/426,666 · Granted Dec 30, 2025

Anhydride catalysts for urethane and urethane-urea systems

Inventor: Johnathon A. Cribb (Meriden, CT)
Assignee: Urethane Systems USA LLC
C08G18/168C08G18/10C08G18/4238C08G18/7621
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,509,545
App. No.
17/426,666
Granted
Dec 30, 2025
Kind
B2
Abstract

Polyurethane and polyurethane-urea compositions are prepared by amine cure under catalyzed reaction conditions. The curing reaction is performed with an acid anhydride based curing catalyst which is added to a prepolymer and then subsequently reacted with an amine based curative.

Claims (41)

1 . A polyurethane forming composition, comprising the reaction product of:

i) a diisocyanate,

ii) a polyol,

iii) a latent catalyst,

iv) a chain extender, and

v) optionally one or more additives,

wherein

the diisocyanate and the polyol are reacted to form a prepolymer and the prepolymer is subsequently added with the latent catalyst to form a modified prepolymer and the modified prepolymer is reacted with the chain extender and optionally one or more of the additives,

the prepolymer contains less than 0.5% by weight of unreacted diisocyanate monomer,

the latent catalyst is at least one of maleic anhydride, acetic anhydride, propionic anhydride, isobutyric anhydride, hexanoic anhydride, and benzoic anhydride,

the polyol is at least one of poly(adipate) glycol, poly(hexamethyleneadipate) glycol, poly(ethylene adipate) glycol (PEAG), poly(diethylene adipate) glycol, poly(ethylene/propylene adipate) glycol, poly(trimethylolpropane/hexamethylene adipate) glycol, poly(ethylene/butylene adipate) glycol, poly(butylene adipate) glycol, poly(hexamethylene/neopentyl adipate) glycol, poly(butylene/hexamethylene adipate) glycol (PBHAG), poly(neopentyl adipate) glycol, and mixtures, copolymers and terpolymers thereof, and

the chain extender is at least one of 4,4′-methylene-bis (2-chloroaniline) (MOCA); 4,4,′-methylene-bis(3-chloro-2,6-diethylaniline); diethyl toluene diamine; t-butyl toluene diamine; dimethylthiotoluene diamine; trimethylene glycol di-p-amino-benzoate; methylenedianiline; methylenedianiline-sodium chloride complex; and mixtures thereof.

2 . The polyurethane forming composition according to claim 1 , wherein the latent catalyst is present in an amount of from 0.5 to 2 wt % based on the weight of the prepolymer.

3 . An article comprising the polyurethane forming composition according to claim 1 .

4 . A process for curing a polyurethane forming composition, comprising:

mixing a prepolymer and a latent catalyst, wherein the latent catalyst comprises an anhydride, thereby forming a modified prepolymer,

mixing the modified prepolymer and a chain extender and optionally further additives, whereby a curative mixture is formed, and

reacting the curative mixture,

wherein

the prepolymer is the reaction product of a diisocyanate and a polyol,

the prepolymer contains less than 0.5% by weight of unreacted diisocyanate monomer,

the latent catalyst is at least one of maleic anhydride, acetic anhydride, propionic anhydride, isobutyric anhydride, hexanoic anhydride, and benzoic anhydride,

the polyol is at least one of poly(adipate) glycol, poly(hexamethyleneadipate) glycol, poly(ethylene adipate) glycol (PEAG), poly(diethylene adipate) glycol, poly(ethylene/propylene adipate) glycol, poly(trimethylolpropane/hexamethylene adipate) glycol, poly(ethylene/butylene adipate) glycol, poly(butylene adipate) glycol, poly(hexamethylene/neopentyl adipate) glycol, poly(butylene/hexamethylene adipate) glycol (PBHAG), poly(neopentyl adipate) glycol, and mixtures, copolymers and terpolymers thereof, and

the chain extender is at least one of 4,4′-methylene-bis (2-chloroaniline) (MOCA); 4,4,′-methylene-bis(3-chloro-2,6-diethylaniline); diethyl toluene diamine; t-butyl toluene diamine; dimethylthiotoluene diamine; trimethylene glycol di-p-amino-benzoate; methylenedianiline; methylenedianiline-sodium chloride complex; and mixtures thereof.

5 . The process of claim 4 , wherein the prepolymer comprises the reaction product of toluene diisocyanate (TDI) and at least one polyester polyol, comprising poly(ethylene adipate) glycol (PEAG) and the chain extender comprises 4,4′-methylene bis (o-chloroaniline) (MOCA).

6 . The polyurethane forming composition according to claim 1 , wherein the polyurethane forming composition have a pot life between 5 min to 7 min.

7 . The polyurethane forming composition according to claim 1 , wherein the polyurethane forming composition reaches a hardness of 80 A at 100° C. in 45 min after a gel point.

8 . The polyurethane forming composition according to claim 1 , wherein the diisocyanate is toluene diisocyanate (TDI).

9 . The polyurethane forming composition according to claim 1 , wherein the polyol is poly(ethylene adipate) glycol (PEAG).

10 . The polyurethane forming composition according to claim 1 , wherein the chain extender is 4,4′-methylene-bis( 2 -chloroaniline) (MOCA).

11 . The polyurethane forming composition according to claim 1 , wherein the latent catalyst is acetic anhydride.

12 . The polyurethane forming composition according to claim 1 , wherein

the diisocyanate is toluene diisocyanate (TDI),

the polyol is poly(ethylene adipate) glycol (PEAG),

the chain extender is 4,4′-methylene-bis(2-chloroaniline) (MOCA), and

the latent catalyst is acetic anhydride.

13 . The polyurethane forming composition according to claim 2 , wherein

the diisocyanate is toluene diisocyanate (TDI),

the polyol is poly(ethylene adipate) glycol (PEAG),

the chain extender is 4,4′-methylene-bis(2-chloroaniline) (MOCA), and

the latent catalyst is acetic anhydride.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2025
From: LANXESS CORPORATION
To: URETHANE SYSTEMS USA LLC
Reel/Frame 071852/0694 →
MERGER Recorded Sep 7, 2021
From: LANXESS SOLUTIONS US INC.
To: LANXESS CORPORATION
Reel/Frame 057400/0471 →
Continuity (2)
Provisional Application 62802971 · Feb 8, 2019
Related Publication 20220106429A1 · Apr 7, 2022
References Cited (37)
US 2620516A · Mueller · 1952 [cited by applicant]
US 3314923A · Muller et al. · 1967 [cited by applicant]
US 3541038A · Nakano et al. · 1970 [cited by applicant]
US 3592789A · Bolton · 1971 [cited by applicant]
US 3708458A · Alberino et al. · 1973 [cited by applicant]
US 4070310A · Schneider et al. · 1978 [cited by applicant]
US 4080318A · Smith et al. · 1978 [cited by applicant]
US 4089822A · Vial · 1978 [cited by applicant]
US 4156065A · Onder et al. · 1979 [cited by applicant]
US 4182825A · Jackle · 1980 [cited by examiner]
US 4268426A · Williams et al. · 1981 [cited by applicant]
US 4404258A · Loewrigkeit · 1983 [cited by applicant]
US 4430454A · Castrantas et al. · 1984 [cited by applicant]
US 4784201A · Palinkas · 1988 [cited by applicant]
US 4832098A · Palinkas · 1989 [cited by applicant]
US 4880847A · Credali et al. · 1989 [cited by applicant]
US 4921029A · Palinkas · 1990 [cited by applicant]
US 4929667A · Ban · 1990 [cited by examiner]
US 4934425A · Gajewski · 1990 [cited by applicant]
US 5605657A · Nybakken · 1997 [cited by applicant]
US 6800667B1 · Kreyenschmidt · 2004 [cited by examiner]
US 20020114955A1 · Lamers et al. · 2002 [cited by applicant]
US 20030065124A1 · Rosenberg · 2003 [cited by applicant]
US 20050261447A1 · Koshiro et al. · 2005 [cited by applicant]
US 20160290091A1 · Takahashi et al. · 2016 [cited by applicant]
US 20170152371A1 · Duan et al. · 2017 [cited by applicant]
US 20190002667A1 · Kobayashi et al. · 2019 [cited by applicant]
US 20220106429A1 · Cribb · 2022 [cited by applicant]
EP 1491579A1 · 2004 [cited by applicant]
RU 2275400 · 2004 [cited by examiner]
Ru-2275400_2004-09-11_English Translation. [cited by examiner]
European Search Report from corresponding European Application No. 19160186, dated Jul. 25, 2019, two pages. [cited by applicant]
European Search Report from corresponding European Application No. 19150956.9, dated Jul. 22, 2019, 2 pages. [cited by applicant]
Restriction Requirement mailed May 10, 2024, in co-pending U.S. Appl. No. 17/428,294, 8 pages. [cited by applicant]
Office Action mailed Nov. 25, 2024, in co-pending U.S. Appl. No. 17/428,294, 28 pages. [cited by applicant]
Office Action mailed May 23, 2025, in co-pending U.S. Appl. No. 17/428,294, 14 pages. [cited by applicant]
Office Action mailed Sep. 17, 2025, in co-pending U.S. Appl. No. 17/428,294, 33 pages. [cited by applicant]