Fast-curing composition containing silane groups

Patent metadata

Field	Value
Publication number	US-10301422-B2
Application number	US-201515519307-A
Country	US
Kind code	B2
Filing date	Nov 23, 2015
Priority date	Nov 24, 2014
Publication date	May 28, 2019
Grant date	May 28, 2019

Abstract

A composition containing two different silane-functional polymers, only one of the two polymers having terminal groups of formula (I). The composition has a surprisingly rapid skin forming time and low viscosity, crosslinks quickly even without the use of EHS-critical catalysts such as organotin compounds or DBU, and cures to a non-sticky material with good strength and elasticity. Also relates to a method for accelerating the curing of a silane-crosslinking composition by adding to it a further silane-functional polymer having terminal groups of formula (I).

First claim

The invention claimed is:

1. A composition comprising
at least one silane-functional polymer P1; and
at least one silane-functional polymer P2 having end groups of the formula (I)

where
R 1a and R 1b are each independently a hydrogen atom or a monovalent hydrocarbyl radical having 1 to 12 carbon atoms, or together are an alkylene radical having 2 to 6 carbon atoms,
R 2 is a hydrogen atom or a monovalent hydrocarbyl radical which has 1 to 12 carbon atoms and optionally contains ether groups, ester groups, nitrile groups, amino groups or silane groups,
R 3 is a linear or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, optionally having aromatic components, and optionally having one or more heteroatoms, especially nitrogen atoms,
R 4 is an alkyl radical having 1 to 8 carbon atoms,
R 5 is an alkyl radical which has 1 to 10 carbon atoms and optionally contains ether groups, and
x is 0, 1 or 2,
where the weight ratio between the silane-functional polymer P1 and the silane-functional polymer P2 is in the range from 99:1 to 10:90, and
where the silane-functional polymer P1 does not have any end groups of the formula (I).

2. The composition as claimed in claim 1 , wherein the silane-functional polymer P1 is a polyether containing silane groups.

3. The composition as claimed in claim 2 , wherein the silane-functional polymer P1 is selected from the group consisting of
polyethers containing silane groups that have been obtained from the reaction of polyethers containing allyl groups with hydrosilanes, optionally with chain extension;
polyethers containing silane groups that have been obtained from the copolymerization of alkylene oxides and epoxysilanes, optionally with chain extension;
polyethers containing silane groups that have been obtained from the reaction of polyether polyols with isocyanatosilanes, optionally with chain extension with diisocyanates; and
polyethers containing silane groups that have been obtained from the reaction of urethane polyethers containing isocyanate groups with aminosilanes or hydroxysilanes or mercaptosilanes.

4. The composition as claimed in claim 3 , wherein the silane-functional polymer P1 is either a polyether containing silane groups that has been obtained from the reaction of polyethers containing allyl groups with hydrosilanes or a polyether containing silane groups that has been obtained from the reaction of polyether polyols with isocyanatosilanes.

5. The composition as claimed in claim 1 , wherein the silane-functional polymer P2 is a polyether and/or polyester and/or polycarbonate containing silane groups.

6. The composition as claimed in claim 1 , wherein R 1a is a methyl radical and R 1b is a hydrogen atom.

7. The composition as claimed in claim 1 , wherein R 1a is a methyl radical, R 1b is a hydrogen atom, R 2 is a hydrogen atom, R 3 is a radical selected from the group consisting of 1,3-propylene, 2-methyl-1,3-propylene, 1,4-butylene, 3-methyl-1,4-butylene and 3,3-dimethyl-1,4-butylene, R 5 is a methyl radical or an ethyl radical and x is 0.

8. The composition as claimed in claim 1 , wherein the weight ratio between the silane-functional polymer P1 and the silane-functional polymer P2 is in the range from 98:2 to 20:80.

9. The composition as claimed in claim 1 , wherein the silane-functional polymer P1 and the silane-functional polymer P2 both contain either exclusively methoxysilane groups or exclusively ethoxysilane groups.

10. The composition as claimed in claim 1 , wherein it comprises at least one further constituent selected from fillers, crosslinkers, plasticizers, solvents, catalysts, adhesion promoters, desiccants, stabilizers, pigments and rheology aids.

11. The composition as claimed in claim 10 , wherein it has a content of silane-functional polymers in the range from 5% to 95% by weight.

12. The composition as claimed in claim 1 , wherein it is free of heavy metal-containing organic compounds.

13. A cured composition obtained from a composition as claimed in claim 1 after it has reacted with moisture.

14. A method comprising applying a composition as claimed in claim 1 as an adhesive or sealant or as a coating.

15. A method of accelerating curing of a moisture-curing composition comprising at least one silane-functional polymer P1, by adding to the composition at least one silane-functional polymer P2 having end groups of the formula (I)

where
R 1a and R 1b are each independently a hydrogen atom or a monovalent hydrocarbyl radical having 1 to 12 carbon atoms, or together are an alkylene radical having 2 to 6 carbon atoms,
R 2 is a hydrogen atom or a monovalent hydrocarbyl radical which has 1 to 12 carbon atoms and optionally contains ether groups, ester groups, nitrile groups, amino groups or silane groups,
R 3 is a linear or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, optionally having aromatic components, and optionally having one or more heteroatoms, especially nitrogen atoms,
R 4 is an alkyl radical having 1 to 8 carbon atoms,
R 5 is an alkyl radical which has 1 to 10 carbon atoms and optionally contains ether groups, and
x is 0, 1 or 2;
where the silane-functional polymer P1 does not have any end groups of the formula (I).

Assignees

• Sika Tech Ag

Inventors

• Kramer Andreas
• Burckhardt Urs

Classifications

• C08G18/4866 Primary

  having a low unsaturation value · CPC title

• C08G18/227

  of antimony, bismuth or arsenic · CPC title

• C08G65/336

  containing silicon · CPC title

• C08G18/289

  containing silicon · CPC title

• C08G18/718

  containing silicon · CPC title