IP Library › Granted Patent US 12,378,188
Granted Patent B2
US 12,378,188 · App. 17/791,749 · Granted Aug 5, 2025

Waterborne crosslinker composition

Inventors: Gerardus Cornelis Overbeek (Geleen, NL); Patrick Johannes Maria Stals (Geleen, NL); Daan Van Der Zwaag (Geleen, NL); Alfred Jean Paul Bückmann (Geleen, NL); Jan Van Riel (Geleen, NL); Stella Josette Van Dijk (Geleen, NL); Kristel De Vos-Verschuren (Geleen, NL); Hermanus Adrianus Langermans (Geleen, NL)
Assignee: Covestro (Netherlands) B.V.
C07D203/10C07D251/32C07D403/12C07D403/14C07D413/14C07D487/14C08F220/1804C08G18/027C08G18/0823C08G18/0866C08G18/12C08G18/227C08G18/246C08G18/282C08G18/2825C08G18/283C08G18/2865C08G18/2875C08G18/302C08G18/3228C08G18/3231C08G18/3275C08G18/348C08G18/3842C08G18/4291C08G18/44C08G18/4808C08G18/4825C08G18/4854C08G18/4862C08G18/4879C08G18/6692C08G18/6715C08G18/73C08G18/755C08G18/758C08G18/765C08G18/792C08G18/798C08G18/833C08K5/3412C08K5/34924C08K5/34926C08L63/00C09D7/20C09D7/45C09D7/63C09D7/65C09D11/101C09D133/02C09D133/04C09D175/04C09D175/08C09D175/12C08G2150/00
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 12,378,188
App. No.
17/791,749
Granted
Aug 5, 2025
Kind
B2
Abstract

The present invention relates to a multi-aziridine crosslinker composition, including an aqueous dispersion having a pH ranging from 9 to 14 and including a multi-aziridine compound in dispersed form. The multi-aziridine compound has: a. from 2 to 6 of the following structural units A: (A) whereby R1, R2, R3 and R4 are H; m is 1, R′ and R″ are according to (1) or (2): (2) R′=H or an aliphatic hydrocarbon group containing from 1 to 14 carbon atoms, and R″=an alkyl group containing from 1 to 4 carbon atoms, CH2-O—(C═O)—R′″ or CH2-O—R″″, whereby R′″ is an alkyl group containing from 4 to 12 carbon atoms and R″″ is an alkyl group containing from 1 to 14 carbon atoms, (2) R′ and R″ form together a saturated cycloaliphatic hydrocarbon group containing from 5 to 8 carbon atoms.

Claims (38)

1. A multi-aziridine crosslinker composition, wherein the multi-aziridine crosslinker composition is an aqueous dispersion having a pH ranging from 9 to 14 and comprises a multi-aziridine compound in dispersed form, wherein

said multi-aziridine compound has:

a. from 2 to 6 of the following structural units A:

whereby

R 1 , R 2 , R 3 and R 4 are H;

m is 1,

R′ and R″ are according to (1) or (2):

(1) R′=H or an aliphatic hydrocarbon group containing from 1 to 14 carbon atoms, and

R″=an alkyl group containing from 1 to 4 carbon atoms, CH2-O—(C═O)—R′″ or CH2-O—R″″, whereby R′″ is an alkyl group containing from 4 to 12 carbon atoms and R″″ is an alkyl group containing from 1 to 14 carbon atoms,

(2) R′ and R″ form together a saturated cycloaliphatic hydrocarbon group containing from 5 to 8 carbon atoms;

b. one or more linking chains wherein each one of these linking chains links two of the structural units A, whereby a linking chain is the shortest chain of consecutive atoms that links two structural units A; and

c. a molecular weight in the range from 600 to 10000 Daltons, wherein the molecular weight is determined using MALDI-TOF mass spectrometry.

2. The multi-aziridine crosslinker composition according to claim 1 , wherein the linking chains consist of from 4 to 300 atoms and the linking chains are a collection of atoms covalently connected which collection of atoms consists of i) carbon atoms, ii) carbon and nitrogen atoms, or iii) carbon, oxygen and nitrogen atoms.

3. The multi-aziridine crosslinker composition according to claim 1 , wherein the multi-aziridine compound contains 2 or 3 structural units A.

4. The multi-aziridine crosslinker composition according to claim 1 , wherein R′ is H and R″=an alkyl group containing from 1 to 4 carbon atoms, CH2-O—(C═O)—R″ or CH2-O—R″ “, whereby R” is an alkyl group containing from 4 to 12 carbon atoms and R″″ is an alkyl group containing from 1 to 14 carbon atoms.

5. The multi-aziridine crosslinker composition according to claim 1 , wherein the multi-aziridine compound comprises one or more connecting groups wherein each one of these connecting groups connects two of the structural units A, whereby the connecting groups consist of at least one functionality selected from the group consisting of aliphatic hydrocarbon functionality, cycloaliphatic hydrocarbon functionality, aromatic hydrocarbon functionality, isocyanurate functionality, iminooxadiazindione functionality, ether functionality, ester functionality, amide functionality, carbonate functionality, urethane functionality, urea functionality, biuret functionality, allophanate functionality, uretdione functionality and any combination thereof.

6. The multi-aziridine crosslinker composition according to claim 5 wherein the connecting groups consist of at least one aliphatic hydrocarbon functionality and/or at least one cycloaliphatic hydrocarbon functionality, and further optionally an isocyanurate functionality or an iminooxadiazindione functionality.

7. The multi-aziridine crosslinker composition according to claim 5 , wherein the connecting groups consist of at least one aliphatic hydrocarbon functionality and/or at least one cycloaliphatic hydrocarbon functionality, and further an isocyanurate functionality or an iminooxadiazindione functionality.

8. The multi-aziridine crosslinker composition according to claim 1 , wherein the multi-aziridine compound comprises one or more connecting groups wherein each one of these connecting groups connects two of the structural units A, wherein the connecting groups consist of (i) at least two aliphatic hydrocarbon functionality and (ii) an isocyanurate functionality or an iminooxadiazindione functionality and wherein a pendant group is present on a connecting group, whereby the pendant group has the following structural formula:

wherein

n′ is the number of repeat units and is an integer from 1 to 50,

X is O or NH,

R 7 and R 8 are independently H or CH 3 in each repeating unit,

R 9 is an aliphatic hydrocarbon group, and

R 10 is an aliphatic hydrocarbon group containing from 1 to 20 carbon atoms, a cycloaliphatic hydrocarbon group containing from 5 to 20 carbon atoms or an aromatic hydrocarbon group containing from 6 to 20 carbon atoms.

9. The multi-aziridine crosslinker composition according to claim 1 , wherein the number of consecutive C atoms and optionally O atoms between the N atom of the urethane group in a structural unit A and the next N atom which is either present in the linking chain or which is the N atom of the urethane group of another structural unit A is at most 9.

10. The multi-aziridine crosslinker composition according to claim 1 , wherein the multi-aziridine compound is obtained by reacting at least a polyisocyanate with aliphatic reactivity in which all of the isocyanate groups are directly bonded to aliphatic or cycloaliphatic hydrocarbon groups, irrespective of whether aromatic hydrocarbon groups are also present, and a compound B with the following structural formula:

whereby the molar ratio of compound B to polyisocyanate is from 2 to 6.

11. The multi-aziridine crosslinker composition according to claim 1 , wherein the multi-aziridine compound has a molecular weight of from 600 to 5000 Daltons.

12. The multi-aziridine crosslinker composition according to claim 1 , wherein the aqueous dispersion comprises aziridine functional molecules having a molecular weight lower than 580 Daltons in an amount lower than 5 wt. %, on the total weight of the aqueous dispersion, whereby the molecular weight is determined using LC-MS.

13. The multi-aziridine crosslinker composition according to claim 1 , wherein the pH of the aqueous dispersion is at least 9.5.

14. The multi-aziridine crosslinker composition according to claim 1 , wherein the amount of water in the aqueous dispersion is at least 15 wt. % and at most 95 wt. %, on the total weight of the aqueous dispersion.

15. The multi-aziridine crosslinker composition according to claim 1 , wherein the amount of said multi-aziridine compound in the aqueous dispersion is at least 5 wt. % and at most 70 wt. %, on the total weight of the aqueous dispersion.

16. The multi-aziridine crosslinker composition according to claim 1 , wherein the solids content of the aqueous dispersion is at least 5 and at most 70 wt. %.

17. The multi-aziridine crosslinker composition according to claim 1 , wherein the multi-aziridine crosslinker composition comprises particles comprising said multi-aziridine compound, wherein said particles have a scatter intensity based average hydrodynamic diameter from 50 to 500 nanometer.

18. The multi-aziridine crosslinker composition according to claim 1 , wherein the aqueous dispersion comprises a dispersant.

19. A method for crosslinking a carboxylic acid functional polymer dissolved and/or dispersed in an aqueous medium, the method comprising providing the multi-aziridine crosslinking composition according to claim 1 , whereby the carboxylic acid functional polymer contains carboxylic acid groups and/or carboxylate groups and the amounts of aziridinyl groups and of carboxylic acid groups and carboxylate groups are chosen such that the stoichiometric amount of aziridinyl groups on carboxylic acid groups and carboxylate groups is from 0.1 to 2.0.

20. A two-component coating system comprising a first component and a second component each of which is separate and distinct from each other and characterized in that the first component comprises a carboxylic acid functional polymer dissolved and/or dispersed in an aqueous medium, whereby the carboxylic acid functional polymer comprises carboxylic acid groups and/or carboxylate groups and the second component comprises the multi-aziridine crosslinker composition according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2022
From: OVERBEEK, GERARDUS CORNELIS; STALS, PATRICK JOHANNES MARIA; VAN DER ZWAAG, DAAN; BÜCKMANN, ALFRED JEAN PAUL; VAN RIEL, JAN; VAN DIJK, STELLA JOSETTE; DE VOS - VERSCHUREN, KRISTEL; LANGERMANS, HERMANUS ADRIANUS
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 061634/0010 →
Priority Claims (14)
EP 20153253 · Jan 20, 2020 · regional
EP 20153154 · Jan 22, 2020 · regional
EP 20153159 · Jan 22, 2020 · regional
EP 20153239 · Jan 22, 2020 · regional
EP 20153240 · Jan 22, 2020 · regional
EP 20153242 · Jan 22, 2020 · regional
EP 20153245 · Jan 22, 2020 · regional
EP 20153246 · Jan 22, 2020 · regional
EP 20153249 · Jan 22, 2020 · regional
EP 20153250 · Jan 22, 2020 · regional
EP 20153251 · Jan 22, 2020 · regional
EP 20153628 · Jan 24, 2020 · regional
EP 20153630 · Jan 24, 2020 · regional
EP 20187717 · Jul 24, 2020 · regional
Continuity (1)
Related Publication 20230096600A1 · Mar 30, 2023
References Cited (75)
US 3329674A · Bulbenko et al. · 1967 [cited by applicant]
US 3337533A · Ham · 1967 [cited by applicant]
US 3523750A · Tesoro · 1970 [cited by applicant]
US 3560415A · Grögler et al. · 1971 [cited by applicant]
US 3583977A · Uelzmann · 1971 [cited by applicant]
US 3763132A · Meiser · 1973 [cited by applicant]
US 3933936A · Smith et al. · 1976 [cited by applicant]
US 4605698A · Briden · 1986 [cited by applicant]
US 5106993A · Kania · 1992 [cited by applicant]
US 5133997A · Maier et al. · 1992 [cited by applicant]
US 5164467A · Kania · 1992 [cited by applicant]
US 5241001A · Kania et al. · 1993 [cited by applicant]
US 5258481A · Hesselmans et al. · 1993 [cited by applicant]
US 5359005A · Kania et al. · 1994 [cited by applicant]
US 5712331A · Ryang · 1998 [cited by applicant]
US 7294449B1 · Guideman et al. · 2007 [cited by applicant]
US 7396891B2 · Gray et al. · 2008 [cited by applicant]
US 8318855B2 · Schafheutle et al. · 2012 [cited by applicant]
US 11878969B2 · Overbeek · 2024 [cited by examiner]
US 12247008B2 · Stals · 2025 [cited by examiner]
US 20030229176A1 · Trombetta et al. · 2003 [cited by applicant]
US 20060117991A1 · Mayo et al. · 2006 [cited by applicant]
US 20060148980A1 · Tielemans et al. · 2006 [cited by applicant]
US 20070298006A1 · Tomalia et al. · 2007 [cited by applicant]
US 20080114096A1 · Qu et al. · 2008 [cited by applicant]
US 20100227945A1 · Bissinger et al. · 2010 [cited by applicant]
US 20110086180A1 · Tielemans · 2011 [cited by applicant]
US 20150118501A1 · Lu et al. · 2015 [cited by applicant]
US 20170218110A1 · Arzt et al. · 2017 [cited by applicant]
CN 1606574A · 2005 [cited by applicant]
CN 1720223A · 2006 [cited by applicant]
CN 1823110A · 2006 [cited by applicant]
CN 101365688A · 2009 [cited by applicant]
CN 101619164A · 2010 [cited by applicant]
CN 102046688A · 2011 [cited by applicant]
CN 104080861A · 2014 [cited by applicant]
CN 104379618A · 2015 [cited by applicant]
CN 105143297A · 2015 [cited by applicant]
CN 105377918A · 2016 [cited by applicant]
CN 105705598A · 2016 [cited by applicant]
CN 107922762A · 2018 [cited by applicant]
CN 108084870 · 2018 [cited by applicant]
CN 110023354A · 2019 [cited by applicant]
CN 110248977A · 2019 [cited by applicant]
CN 110607120A · 2019 [cited by applicant]
CN 112469755A · 2021 [cited by applicant]
CN 117015566A · 2023 [cited by applicant]
CN 117836343A · 2024 [cited by applicant]
EP 0507407 · 1992 [cited by applicant]
EP 0758662 · 1997 [cited by applicant]
EP 1865014 · 2007 [cited by applicant]
GB 1344725 · 1974 [cited by applicant]
JP 47027971 · 1972 [cited by applicant]
JP 51141860 · 1976 [cited by applicant]
JP 59128291 · 1984 [cited by applicant]
JP 2015505889 · 2015 [cited by applicant]
KR 1020060066442A · 2006 [cited by applicant]
WO 2006115547 · 2006 [cited by applicant]
WO 2008069298A1 · 2008 [cited by applicant]
WO 2013089927 · 2013 [cited by applicant]
WO 2015066868 · 2015 [cited by applicant]
WO 2017216767A1 · 2017 [cited by applicant]
WO 2020020714 · 2020 [cited by applicant]
International Search Report for PCT/EP2021/051383, mailed Apr. 12, 2021, 3 pages. [cited by applicant]
Written Opinion of the ISA for PCT/EP2021/051383, mailed Apr. 12, 2021, 7 pages. [cited by applicant]
Dahlquist et al., “Contact allergy to trimethylolpropane triacrylate (TMPTA) in an aziridine plastic hardener”, Contact Dermatitis, 1983, pp. 122-124, vol. 9. [cited by applicant]
Fei et al., “Properties and Curing Kinetic of Acrylic Resin Cured with Aziridine Crosslinker”, Chinese Journal of Synthetic Chemistry, 2002, pp. 120-125, vol. 10, Issue 2. [cited by applicant]
Haitao et al., “Synthesis and Application of Aziridine Crosslinking Agent in Waterborne Coatings”, Shanghai Coatings, 2013, 7 pages, vol. 51, No. 10. [cited by applicant]
Jiao, “Preparation of Waterborne Polyurethane Based on Renewable Resources and Its Film Properties”, Masteral Dissertation, Dalian University of Technology, 2010, 79 pages. [cited by applicant]
Lee et al., “Preparation and characterization of acrylic pressure-sensitive adhesives based on UV and heat curing systems”, International Journal of Adhesion and Adhesives, 2017, 21 pages. [cited by applicant]
Qingfang et al., “Study on heat resistance of polyurethane-imide/organosilicon modified epoxy coatings”, Synthetic Materials and Applications, 2018, 5 pages, vol. 47, No. 3. [cited by applicant]
Walsh et al., “Polyamine-Functional Sterically Stabilized Latexes for Covalently Cross-Linkable Colloidosomes”, Langmuir, 2010, pp. 18039-18048, vol. 26(23). [cited by applicant]
Wang et al., “Pervaporation Properties to Aromatic/Non-Aromatic Hydrocarbon Mixtures of Cross-Linked Membranes of Copoly(methacrylates) with Pendant Phosphate and Carbamoylphosphonate Groups”, Journal of Membrane Scienc… [cited by applicant]
Yoo et al., “Preparation of Acrylic Copolymers and Crosslinking Agents and Properties as a Film”, Journal of Applied Polymer Science, 2009, pp. 1587-1594, vol. 112. [cited by applicant]
Zilin et al., “Effect of Crosslinking Agent on Waterborne Polyurethane Wet Friction Fixing Agent”, Shandon Chemical Industry, 2019, pp. 1-4, vol. 8, Issue 14. [cited by applicant]