IP Library Granted Patent US 9,550,852
Granted Patent B2
US 9,550,852 · App. 14/437,959 · Granted Jan 24, 2017

Method for producing vinyl ester urethane resins based on dianhydrohexitol compounds and use thereof

Inventors: Michael Leitner (Landsberg, DE); Beate Gnass (Gersthofen, DE)
Assignee: Hilti Aktiengesellschaft
C08F283/008C08F290/067C08G18/10C08G18/3218C08G18/672C08G18/68C08G18/73C08L75/16
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Quick Facts
Patent No.
US 9,550,852
App. No.
14/437,959
Granted
Jan 24, 2017
Kind
B2
Abstract

Disclosed is a method for producing vinyl ester urethane resins, in which a dianhydrohexitol-compound is reacted with a diisocyanate in the presence of a monomeric radically co-polymerizable compound as a solvent and the product is reacted with a hydroxy-substituted (meth)acrylate. As a result, vinyl ester urethane resins based on dianhydrohexitol-compounds and also based on renewable raw materials can be obtained in a simple manner with high yields. The resins are suitable as binding agents in chemical fixing engineering.

Claims (15)

1. A method for producing a vinyl ester urethane resin, comprising the steps of:

(I) reacting a dianhydrohexitol compound with a diisocyanate in a presence of a monomeric radically copolymerizable compound as a solvent to produce a product; and

(II) reacting the product with a hydroxy-substituted (meth)acrylate.

2. The method according to claim 1 , wherein the monomeric radically copolymerizable compound is 1,4-butanedioldi(meth)acrylate, propyleneglycol(meth)acrylate, tetrahydrofuryl(meth)acrylate, or (2,2-dimethyl-1,3-di oxol ane-4-yl)m ethyl (m eth)acryl ate.

3. The method according to claim 1 , wherein at least two moles of diisocyanate are used per mole of the dianhydrohexitol compound.

4. The method according to claim 1 , wherein the dianhydrohexitol compound is isosorbide, isomannite, or isoidide.

5. The method according to claim 1 , wherein the diisocyanate is an aliphatic diisocyanate.

6. The method according to claim 1 , wherein the hydroxy-substituted (meth)acrylate is a hydroxyalkyl(meth)acrylate.

7. The method according to claim 1 , wherein the reaction is continued in step (I) until a residual isocyanate content has dropped to less than 0.2% measured according to DIN EIN 1242.

8. The method according to claim 1 , wherein starting compounds are obtained from chemicals based on renewable raw materials.

9. A vinyl ester urethane resin obtained using the method according to claim 1 .

10. The vinyl ester urethane resin of claim 9 , wherein the vinyl ester urethane resin is a binding agent in radically curable resin mixtures.

11. The vinyl ester urethane resin of claim 9 , wherein the vinyl ester urethane resin is a binding agent in radically curable reaction resin mortar compositions.

12. The vinyl ester urethane resin according to claim 10 wherein the resin mixtures are used for chemical fixing.

13. The vinyl ester urethane resin according to claim 11 wherein the resin mortar compositions are used for chemical fixing.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2016
From: LEITNER, MICHAEL; GNASS, BEATE
To: HILTI AKTIENGESELLSCHAFT
Reel/Frame 039098/0801 →
Priority Claims (1)
DE 10 2012 219 477 · Oct 24, 2012 · national
Continuity (1)
Related Publication 20150299368A1 · Oct 22, 2015