IP Library Granted Patent US 9,353,005
Granted Patent B2
US 9,353,005 · App. 14/182,405 · Granted May 31, 2016

Process for production of powder redispersible in water and use thereof

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Quick Facts
Patent No.
US 9,353,005
App. No.
14/182,405
Granted
May 31, 2016
Kind
B2
Abstract

The present invention relates to a process for the production of powders redispersible in water comprising an organic component and a water-soluble organic polymeric protective colloid. The organic component is dispersed and stabilized with the protective colloid in water to form a stable dispersion which is dried to form the powder redispersible in water. The organic component comprises abietic acid, sylvic acid, neoabietic acid, levopinaric acid, pimaric acid, isopimaric acid and/or palustric acid and/or their derivatives. The water-soluble organic polymeric protective colloid comprises synthetic protective colloids and naturally and/or synthetically produced biopolymer which can be synthetically modified. The obtained powder reduces efflorescence in hydraulically set systems.

Claims (20)

1. Process for the production of powder redispersible in water, said powder comprising: an organic component, a water-soluble organic polymeric protective colloid and, optionally, one or more further additives,

wherein the organic component contains at least one compound with a cyclic group, the cyclic group being completely or partially saturated and having a melting point of approximately −20 to 250° C. and a molecular weight of about 100 to 10,000, and the organic component further contains a terpeneoid, a resin acid, colophony, terpene resin, terpene-phenol resin and/or their derivatives, and

wherein the water-soluble organic polymeric protective colloid has a content of monocarboxylic acid and dicarboxylic acid as well as their anhydrides of less than 50 mole %, and not consisting of aromatic sulfonic acid condensates, and

said process comprising the steps of:

dispersing the organic component in water to obtain an aqueous dispersion,

stabilizing the aqueous dispersion with the water-soluble organic polymeric protective colloid, wherein the weight ratio of the organic component to the water-soluble organic polymeric protective colloid is 95:5 to 5:95, and

drying the aqueous dispersion by spray drying, freeze drying, and/or fluid bed drying, thereby forming the redispersible powder.

2. The process according to claim 1 characterised in that the solids content of the stabilized dispersion is 10 to 75% by weight and the average particle size of the dispersed particles to 0.05 to 50 μm.

3. The process according to claim 1 wherein further liquid and/or water-soluble additives are added before, during or after formation of the dispersion, and further additives in powder form are added during or after drying.

4. The process according to claim 1 further comprising the step of mixing the obtained redispersible powder with film-forming dispersion powders redispersible in water, redispersible hydrophobing agents in powder form based on silanes, siloxanes, silicones, fatty acids and/or fatty acid esters and/or polysaccharide ethers.

5. The process according to claim 1 wherein the aqueous dispersion is dried jointly with at least one other dispersion based on film-forming polymers and/or silanes, silane esters, siloxanes, silicones, fatty acids and/or fatty acid esters, wherein the dispersions are mixed with each other before drying or sprayed separately and subsequently dried jointly.

6. The process according to claim 5 wherein the aqueous dispersion is stabilised by emulsifiers and the at least one other dispersion comprises an excess of water-soluble organic polymeric protective colloid in water, the water-soluble organic polymeric protective colloid having a content of monocarboxylic and dicarboxylic acids and their anhydrides of less than 50 mole % and not consisting of aromatic sulfonic acid condensates.

7. Powder redispersible in water obtained from the process according to claim 6 .

8. The process according to claim 1 characterised in that the cyclic group of the organic component is a monocyclic, dicyclic, tricyclic, tetracyclic and/or pentacyclic group.

9. The process according to claim 1 characterised in that the organic component is a natural product selected from the group consisting of a monoterpene, sesquiterpene, diterpene, sesterterpene, triterpene, tetraterpene, polyterpene and their derivatives.

10. The process according to claim 1 characterised in that the organic component is at least one compound with at least one carboxyl group, carbonyl group, aldehyde group and/or alcohol group.

11. The process according to claim 1 characterised in that the organic component is abietic acid, sylvic acid, neoabietic acid, levopinaric acid, pimaric acid, isopimaric acid and/or palustric acid and/or their derivatives.

12. The process according to claim 1 characterised in that the organic component is not soluble in acidic to neutral water.

13. The process according to claim 1 characterised in that the water-soluble organic polymeric protective colloid representing a synthetic protective colloid is a modified and/or unmodified polyvinyl alcohol with a degree of hydrolysis of 70 to 100 mole % and a Höppler viscosity, as 4% aqueous solution, of 1 to 50 mPas, measured at 20° C. according to DIN 53015, and/or polyvinyl pyrrolidone.

14. The process according to claim 1 characterised in that the solids content of the dispersion of the organic component stabilised with the water-soluble organic polymeric protective colloid amounts to 25 to 65% by weight and the average particle size of the dispersed particles is 0.1 to 20 μm.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2020
From: NOURYON CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS AG
Reel/Frame 053616/0266 →
CHANGE OF NAME Recorded Aug 27, 2020
From: NOURYON CHEMICALS AG
To: CELANESE SWITZERLAND AG
Reel/Frame 053616/0659 →
CHANGE OF NAME Recorded Aug 26, 2020
From: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: NOURYON CHEMICALS INTERNATIONAL B.V.
Reel/Frame 053606/0566 →
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 →
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 →