Improved polyurethane prepolymers having little or no plasticizer and their use in vehicular glass adhesives

Patent metadata

Field	Value
Publication number	US-2016297918-A1
Application number	US-201415022941-A
Country	US
Kind code	A1
Filing date	Nov 24, 2014
Priority date	Dec 9, 2013
Publication date	Oct 13, 2016
Grant date	—

Abstract

An isocyanate terminated prepolymer has been discovered that has sufficiently low glass transition temperature (Tg), necessary rheological properties and mechanical properties that allows for the making of adhesive compositions useful for bonding substrates into larger structures (e.g., windows in vehicles and buildings) with minimal or no plasticizers. The polyether prepolymer comprises a polyisocyanate reaction product of a polyisocyanate having an isocyanate functionality of greater than 2 and a polyether monol having an average molecular weight (Mw) of 1000 to 2000 g/moles and said prepolymer having: (i) a weight molecular weight average (Mw) of about 2000 to about 30,000 g/mole, (ii) a free isocyanate content of 0.8% to 4% by weight of said prepolymer, and (iii) viscosity of 1000 to 50,000 centipoises.

First claim

1 . A method of forming an isocyanate terminated prepolymer comprising:
a. providing, a polyisocyanate having an average isocyanate functionality of greater than 2 to 2.7 b. reacting the polyisocyanate with a monol having an average molecular weight (M w ) of 1000 to 2,000 and a polyol to form the isocyanate prepolymer, the polyol and monol having an overall hydroxyl functionality that is from 1 to 3, and the polyol being comprised of
i. a diol having an average molecular weight (M w ) of 500 to 8,000 grams/mole and
ii. a triol having an average molecular weight (M w ) of 1500 to 4500 grams/mole, wherein, the monol is present in an amount from 40% to 60% of the hydroxyl groups in the polyol and monol, the diol is present in an amount from 5% to 35% of the hydroxyl groups present in the polyol and monol and the triol is present in an amount from 10% to 40% of the hydroxyl groups present in the polyol and monol and the isocyanate index is from 1.1 to 2.2.

2 . The method of claim 1 , wherein the isocyanate functionality is at least 2.2.

3 . The method of claim 1 , wherein the monol has a polyether backbone.

4 . The method of claim 1 , wherein the polyether backbone of the monol is comprised of ethylene oxide and propylene oxide groups.

5 . The method claim 4 , wherein the polyether backbone of the monol is comprised of 20% to 80% of ethylene oxide groups with the remainder being propylene oxide groups.

6 . The method of claim 1 , wherein the reacting of the polyisocyanate and polyol and monol is such that at least a portion of the monol is reacted with the polyisocyanate prior to or simultaneously with the polyol.

7 . The method of claim 6 , wherein the portion of the monol is 10% to 100% by weight of the monol.

8 . The method of claim 7 , wherein the portion of the monol is 15% to 50% by weight of the monol.

9 . The method of claim 8 , wherein the portion of monol not reacted prior to or simultaneously with the diol and triol is reacted subsequently.

10 . The method of claim 1 , wherein the polyisocyanate is comprised of methylene diphenyl diisocyanate and an oligomer of methylene diphenyl diisocyanate.

11 . An isocyanate terminated polyether prepolymer comprising a polyisocyanate reaction product of a polyisocyanate having an isocyanate functionality of greater than 2 and a polyether monol having an average molecular weight (M w ) of 1000 to 2000 g/moles and said prepolymer having: (i) a weight molecular weight average (M w ) of about 2000 to about 30,000 g/mole, (ii) a free isocyanate content of 0.8% to 4% by weight of said prepolymer, and (iii) viscosity of 1000 to 50,000 centipoises.

12 . The prepolymer of claim 11 , wherein the polyisocyanate is comprised of a polymeric isocyanate.

13 . The prepolymer of claim 12 , wherein the polymeric isocyanate is an oligomer of hexamethylene diisocyanate, oligomer of methylene diphenyl diisocyanate or combination thereof.

14 . The prepolymer of claim 11 , wherein the prepolymer has an average molecular weight (M w ) of 2000 to about 28,000 g/mole.

15 . An adhesive composition comprised of the prepolymer of claim 11 , a filler, and an isocyanate catalyst.

16 . The adhesive composition of claim 15 , wherein the filler comprises from 20% to 60% of the weight of the composition.

17 . The adhesive composition of claim 15 , wherein the adhesive composition fails to have a plasticizer.

18 . The adhesive composition of claim 15 , wherein the adhesive composition has a plasticizer and the plasticizer is present in an amount less than or equal to 10% of the adhesive composition by weight.

19 . The adhesive composition of claim 18 , wherein the amount of plasticizer is less than or equal to 5% by weight of the adhesive composition.

20 . The adhesive composition of claim 18 , wherein the adhesive composition fails to have a phthalate plasticizer and the adhesive composition is comprised of an alkyl ester of sulfonic acid.

Assignees

• Dow Global Technologies Llc

Inventors

• Sophiea Daniel P
• Krishnan Bindu
• Grier Laura A
• Young Caitlin E

Classifications

• C09J175/08

  from polyethers · CPC title

• C08G18/4812

  Mixtures of polyetherdiols with polyetherpolyols having at least three hydroxy groups · CPC title

• C08G18/283

  Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds · CPC title

• C08G18/7671

  containing only one alkylene bisphenyl group · CPC title

• C09J11/04

  inorganic · CPC title