IP Library Granted Patent US 12,187,665
Granted Patent B2
US 12,187,665 · App. 15/970,586 · Granted Jan 7, 2025

Crosslinking component for binder resins

Inventors: Michael Herm (Velbert, DE); Frank-Rainer Boehm (Odenthal, DE); Pascal Meiners (Muenster, DE)
Assignee: AXALTA COATING SYSTEMS IP CO., LLC
C07C269/02B05D3/0254B05D7/14C07C271/06C07C273/1854C07C275/00C09D163/00C09D175/04C08K5/205C08K5/21
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Quick Facts
Patent No.
US 12,187,665
App. No.
15/970,586
Granted
Jan 7, 2025
Kind
B2
Abstract

This invention relates to a crosslinking component for binder resins which is especially suitable to be used together with epoxy-group containing binders and/or (poly)isocyanates such as blocked (poly)isocyanates and which comprises at least two blocked isocyanate groups per molecule of the crosslinking component whereby at least one of the at least two blocked isocyanate groups is a group according to structural unit (I), wherein the ratio of structural units of formula (II), if present, to structural units of formula (I) is 0.40 or below. The cross-linking component may also be self-cross-linkable. The present invention further relates to a coating composition, e.g. a one-component coating composition comprising the crosslinking component and a method of its manufacture.

Claims (14)

1. A coating composition comprising a crosslinking component comprising at least two blocked isocyanate groups per molecule of the crosslinking component whereby at least one of the at least two blocked isocyanate groups is a group according to the following structural unit (I)

with

R 1 being a C 2 to C 10 hydrocarbyl group,

wherein

the ratio of structural units of the following formula (II), if present,

to structural units of formula (I) is 0.20 or below; and

a binder resin comprising epoxy groups, alpha-beta-unsaturated ester groups, (blocked) isocyanates, keto groups, aldehyde groups or mixtures thereof;

where the structural unit (I) forms a free amine by generating a C—C double bond containing compound originating from R 1 and CO 2 during reaction with the resin.

2. The coating composition according to claim 1 wherein the crosslinking component is substantially free of structural units (II).

3. The coating composition according to claim 1 wherein R 1 is a C 2 to C 10 alkyl group.

4. The coating composition according to claim 1 wherein R 1 is a tert-butyl group.

5. The coating composition according to claim 1 wherein the number average molecular weight of the crosslinking component is within the range of 350 g/mol to 5000 g/mol.

6. The coating composition of claim 1 wherein the binder resin is a binder resin comprising epoxy and/or blocked isocyanate groups.

7. The coating composition of claim 1 being a one-component coating composition.

Assignments (2)
SECURITY AGREEMENT Recorded Dec 13, 2018
From: AXALTA COATING SYSTEMS IP CO. LLC
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 047827/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 31, 2018
From: HERM, MICHAEL, DR.; BOEHM, FRANK-RAINER, DR.; MEINERS, PASCAL, DR.
To: AXALTA COATING SYSTEMS IP CO. LLC
Reel/Frame 045957/0254 →
Continuity (1)
Related Publication 20190337890A1 · Nov 7, 2019
References Cited (13)
US 3275587A · Weller · 1966 [cited by examiner]
US 4458056A · Holubka · 1984 [cited by applicant]
US 20080152900A1 · Flosbach · 2008 [cited by applicant]
US 20200339737A1 · Munzinger · 2020 [cited by examiner]
CN 101802042A · 2010 [cited by applicant]
CN 101903480A · 2010 [cited by applicant]
CN 104204018A · 2014 [cited by applicant]
CN 106147565A · 2016 [cited by applicant]
Frisch et al. “Polyurethanes” Comprehensive Polymer Science and Supplements vol. 5, 1989, pp. 413-426. [cited by examiner]
Gedan-Smolka et al. “Thermal deblocking of masked low molecular isocyanates I. Aliphatic isocyanates” Thermochimica Acta 351 (2000) 95-105. [cited by examiner]
Mohapatra et al. “Efficient and selective cleavage of the ter-butoxycarbonyl (Boc) group under basic condition” ARKIVOC, Issue 14, 2005, pp. 20-28. (Year: 2005). [cited by examiner]
J&K Scientific “BOC Protection and Deprotection” accessed on the web at https://www.jk-sci.com/blogs/name-reaction/boc-protection-and-deprotection on May 26, 2022. [cited by examiner]
Yuanqin Zhu, Chemistry of terminated Iso-Azonic Acid, Chemistry and Bonding, Dec. 31, 2004, Issue: No. 3. [cited by applicant]