IP Library Granted Patent US 8,703,874
Granted Patent B2
US 8,703,874 · App. 13/126,698 · Granted Apr 22, 2014

Powder to hydrophobise and its use

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Quick Facts
Patent No.
US 8,703,874
App. No.
13/126,698
Granted
Apr 22, 2014
Kind
B2
Abstract

The present invention relates to the use of a solid comprising at least one organosilane and a carrier material to hydrophobise mortars, wherein the organosilane has the formula R 1 Si(OR′) 3 or R 1 R 2 Si(OR′) 2 wherein R 1 and R 2 are the same or different and are a linear or branched C 1 - to C 4 -alkyl and/or alkenyl group, OR′ is an acetoxy, a C 1 - to C 4 -alkoxy and/or a C 2 - to C 6 -methoxyalkoxy and/or ethoxyalkoxy group, and the carrier material is a solid at room temperature. The amount of cement in the final formulation is zero or less than 5 wt.-%, based on the total weight of the final formulation in the dry and uncured form. Claimed are also a powder comprising the silane and a carrier with the carrier being a water-soluble polymer, dry mortar formulations containing no or less than 5 wt.-% cement, based on the dry weight of the uncured mortar formulation, as well as processes to manufacture the formulations and/or compounds.

Claims (36)

1. A process to hydrophobise a mortar formulation, the process comprising:

mixing a solid with the mortar formulation, the solid comprising at least one organosilane and a carrier material, wherein

a) the organosilane has the formula

R 1 Si(OR′) 3   (I)

or

R 1 R 2 Si(OR′) 2   (II)

wherein R 1 and R 2 are the same or different and are a linear or branched C 1 - to C 4 -alkyl and/or alkenyl group, OR′ is an acetoxy, a C 1 - to C 4 -alkoxy and/or a C 2 - to C 6 -methoxyalkoxy and/or ethoxyalkoxy group, and

b) the carrier material is solid at room temperature, and

wherein the weight ratio of the organosilane to the carrier material is between 70:30 and 1:99; the solid is in the form of a powder, a granulate and/or a flake; and the amount of cement in the final mortar formulation is zero or less than 5 wt.-%, based on the total weight of the final mortar formulation in the dry and uncured form.

2. The process according to claim 1 , wherein the final mortar formulation containing zero or less than 5 wt.-% cement is a gypsum-based or a gypsum-free mortar.

3. The process according to claim 1 , wherein R 1 is selected from the group consisting of methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, i-butyl, t-butyl, vinyl and allyl; and wherein R 2 is selected from the group consisting of methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, i-butyl, t-butyl, vinyl and allyl.

4. The process according to claim 1 , wherein the alkoxy group is selected from the group consisting of methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, sec-butoxy, i-butoxy and t-butoxy.

5. The process according to claim 1 , wherein the carrier material is selected from the group consisting of a water-soluble polymer, a combination of a water-soluble and a water-insoluble polymer, a water-dispersible polymer, an inorganic material, and combinations thereof.

6. The process according to claim 1 , wherein the solid further comprises a catalyst to catalyze the hydrolysis of Si—OR′ bonds to form Si—OH groups and/or to catalyze the condensation of Si—OH groups to form Si—O—Si bonds.

7. The process according to claim 6 , wherein the catalyst is selected from the group consisting of a base, an amine, a metal salt, a metal complex, and combinations thereof; and wherein the catalyst is in the form of a powder, a granulate or a flake.

8. The process powder according to claim 2 , wherein R 1 is selected from the group consisting of methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, i-butyl, t-butyl, vinyl and allyl; and wherein R 2 is selected from the group consisting of methyl, ethyl, n-propyl, i-propyl, n-butyl, sec-butyl, i-butyl, t-butyl, vinyl and allyl.

9. The process according to claim 3 , wherein the alkoxy group is selected from the group consisting of methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, sec-butoxy, i-butoxy and t-butoxy.

10. The process according to claim 3 , wherein the carrier material is selected from the group consisting of a water-soluble polymer, a combination of a water-soluble and a water-insoluble polymer, a water-dispersible polymer, an inorganic material, and combinations thereof.

11. The process according to claim 4 , wherein the solid further comprises a catalyst to catalyze the hydrolysis of Si—OR′ bonds to form Si—OH groups and/or to catalyze the condensation of Si—OH groups to form Si—O—Si bonds.

12. The process according to claim 7 , wherein the metal is a transition metal.

13. A powder comprising at least one organosilane and a carrier material, wherein

c) the organosilane has the formula

R 1 Si(OR′) 3   (I)

or

R 1 R 2 Si(OH) 2   (II)

wherein R 1 and R 2 are the same or different and are a linear or branched C 1 - to C 4 -alkyl and/or alkenyl group, OR′ is an acetoxy, a C 1 - to C 4 -alkoxy and/or a C 2 - to C 6 -methoxyalkoxy and/or ethoxyalkoxy group, and

c) the carrier material is at least one water-soluble polymer which is solid at room temperature, and

wherein the weight ratio of the organosilane to the carrier material is between 70:30 and 1:99.

14. A process to manufacture a dry mortar formulation containing zero or less than 5 wt.-% cement, based on the total weight of the dry and uncured mortar formulation, the process comprising:

dry mixing the mortar components with the powder according to claim 13 .

15. The process according to claim 14 , wherein the powder is mixed with the dry mortar components in such an amount that the amount of organosilane is 1.0 wt.-% or lower, based on the dry weight of the formulation.

16. A dry mortar formulation containing the powder of claim 13 , and zero or less than 5 wt.-% cement, based on the total weight of the dry and uncured mortar formulation.

17. The dry mortar formulation according to claim 16 , wherein the powder is present in such an amount that the amount of organosilane is 1.0 wt.-% or lower, based on the dry weight of the formulation.

18. The process according to claim 14 , wherein the powder is mixed with the dry mortar components in such an amount that the amount of organosilane is 0.2 wt.-% or lower, based on the dry weight of the formulation.

19. The dry mortar formulation according to claim 16 , wherein the powder is present in such an amount that the amount of organosilane is 0.5 wt.-% or lower, based on the dry weight of the formulation.

20. The dry mortar formulation according to claim 16 , wherein the powder is present in such an amount that the amount of organosilane is 0.2 wt.-% or lower, based on the dry weight of the formulation.

Assignments (7)
CHANGE OF NAME Recorded Aug 27, 2020
From: NOURYON CHEMICALS AG
To: CELANESE SWITZERLAND AG
Reel/Frame 053616/0659 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2020
From: NOURYON CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS AG
Reel/Frame 053616/0266 →
RELEASE OF SECURITY INTEREST Recorded Apr 2, 2020
From: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
To: NOURYON CHEMICALS INTERNATIONAL B.V. (FORMERLY KNOWN AS AKZO NOBEL CHEMICALS INTERNATIONAL B.V.); NOURYON SURFACE CHEMISTRY LLC (FORMERLY KNOWN AS AKZO NOBEL SURFACE CHEMISTRY LLC); NOURYON CHEMICALS B.V. (F/K/A AKZO NOBEL CHEMICALS B.V.)
Reel/Frame 052296/0436 →
CHANGE OF NAME Recorded Sep 18, 2019
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 050426/0671 →
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2017
From: AKZO NOBEL N.V.
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 044427/0759 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 28, 2011
From: ABERLE, THOMAS; PUSTOVGAR, ANDREY P; VALLEE, FRANCK; EMMENEGGER, PAUL; SCHAUB, DOMINIQUE
To: AKZO NOBEL N.V.
Reel/Frame 026196/0076 →