Thixotropic agent for curable compositions

Patent metadata

Field	Value
Publication number	US-12240960-B2
Application number	US-201917281311-A
Country	US
Kind code	B2
Filing date	Nov 11, 2019
Priority date	Nov 14, 2018
Publication date	Mar 4, 2025
Grant date	Mar 4, 2025

Abstract

A thixotropic agent for increasing the yield point of a curable composition, wherein the thixotropic agent includes (i) at least one urea compound from the reaction of at least one isocyanate with at least one amine and (ii) at least one polyether having blocked hydroxyl groups. The thixotropic agent is preparable in a simple manner and forms a spreadable paste which is firm at room temperature. It is particularly suitable as a constituent of moisture-curing polyurethane or SMP compositions, giving a good increase in the yield point thereof, without adversely affecting storage stability or migration characteristics. It enables phthalate-free adhesives, sealants or coatings that have surprisingly good conveyability coupled with a high yield point, and do not cause any problems with odor or fogging.

First claim

The invention claimed is:

1. A thixotropic agent for increasing the yield point of a curable composition, wherein the thixotropic agent comprises (i) at least one urea compound from the reaction of at least one isocyanate with at least one amine and (ii) at least one polyether having blocked hydroxyl groups which is free of urethane groups.

2. The thixotropic agent as claimed in claim 1 , wherein the at least one urea compound has the formula (I)

where
E is an alkyl or cycloalkyl radical having 1 to 12 carbon atoms, and
Q is a divalent hydrocarbyl radical having 6 to 15 carbon atoms.

3. The thixotropic agent as claimed in claim 1 , wherein the thixotropic agent takes the form of a spreadable paste which is firm at room temperature.

4. The thixotropic agent as claimed in claim 1 , wherein 5% to 25% by weight of urea compounds and 50% to 95% by weight of polyethers having blocked hydroxyl groups are present.

5. The thixotropic agent as claimed in claim 1 , wherein the at least one polyether having blocked hydroxyl groups has a viscosity at 20° C. in the range from 30 to 500 mPa·s, where the viscosity is determined with a cone-plate viscometer having cone diameter 25 mm, cone angle 1°, cone tip-plate distance of 0.05 mm, at a shear rate of 10 s −1 .

6. The thixotropic agent as claimed in claim 1 , wherein the at least one polyether having blocked hydroxyl groups has an average of 1 to 3 blocked hydroxyl groups per molecule.

7. The thixotropic agent as claimed in claim 1 , wherein the blocked hydroxyl groups are selected from the group consisting of acetal, ester, aceto ester and carbonate groups.

8. The thixotropic agent as claimed in claim 1 , wherein 70% to 100% by weight of the repeat units in the at least one polyether having blocked hydroxyl groups consist of 1,2-propyleneoxy groups, and 0% to 30% by weight of the repeat units in the at least one polyether having blocked hydroxyl groups consists of 1,2-ethyleneoxy groups.

9. The thixotropic agent as claimed in claim 1 , wherein the at least one polyether having blocked hydroxyl groups has an average molecular weight M n in the range from 600 to 2,500 g/mol, determined by means of gel permeation chromatography versus polystyrene as standard with tetrahydrofuran as mobile phase, refractive index detector and evaluation from 200 g/mol.

10. The thixotropic agent as claimed in claim 1 , wherein the at least one polyether having blocked hydroxyl groups is derived from at least one hydroxy-functional polyether selected from the group consisting of
alcohol-started, polyoxypropylene monools having an OH number in the range from 25 to 90 mg KOH/g,
polyoxypropylene diols having an OH number in the range from 45 to 155 mg KOH/g and
trimethylolpropane-started, optionally ethylene oxide terminated, polyoxypropylene triols having an average OH functionality in the range from 2.2 to 3 and an OH number in the range from 90 to 230 mg KOH/g.

11. A preparation of the thixotropic agent as claimed in claim 1 , wherein the reaction between the at least one isocyanate and the at least one amine is performed in the at least one polyether having blocked hydroxyl groups.

12. A method comprising applying the thixotropic agent as claimed in claim 1 in a curable composition for increasing the yield point of the curable composition.

13. A curable composition comprising the thixotropic agent as claimed in claim 1 and at least one polymer containing isocyanate and/or silane groups.

14. The curable composition as claimed in claim 13 , wherein it is a one-component moisture-curing composition.

15. An article bonded or sealed or coated with the curable composition as claimed in claim 13 .

Assignees

• Sika Tech Ag

Inventors

• Kramer Andreas
• Burckhardt Urs
• Schlumpf Michael
• Konstanzer Martin

Classifications

• C09K2003/1071

  Thixotropic materials · CPC title

• C09K3/10

  {Materials in mouldable or extrudable form} for sealing or packing joints or covers (filling pastes C09D5/34) · CPC title

• C08K5/06

  Ethers; Acetals; Ketals; Ortho-esters · CPC title

• C07C273/1818

  from -N=C=O and XNR'R" · CPC title

• C08G18/755

  and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate · CPC title