Matt powder coatings

US11479690B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11479690-B2
Application numberUS-202117196937-A
CountryUS
Kind codeB2
Filing dateMar 9, 2021
Priority dateJul 25, 2014
Publication dateOct 25, 2022
Grant dateOct 25, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A branched carboxylic acid functional polyester resin P is described herein along with thermosetting powder coating compositions (PCC A) comprising a binder K, the binder K comprising the polyester resin P and a crosslinker X. The invention further relates to a cured PCC A. In addition, processes for making said PCC A and processes for coating an article with said PCC A are described as well as articles having coated thereon the PCC A and an articles having coated and cured thereon the PCC A.

First claim

Opening claim text (preview).

The invention claimed is: 1. A branched carboxylic acid functional polyester resin P, having: (a) a T g of at least 40° C. as measured by Differential Scanning calorimetry (DSC) at a heating rate of 5° C./min; (b) an acid value (AV) of at least 65 and of at most 76.8 mg KOH/g of the polyester resin P; (c) a hydroxyl value of at most 9 mg KOH/g of the polyester resin P; and (d) a functionality of at least 3.5 and at most 5; wherein the polyester resin P is a reaction product of at least the following monomers: i) neopentyl glycol in an amount of at least 19 and at most 38 mol %; ii) ethylene glycol in an amount of at least 8 and at most 21 mol %; iii) a polyol in an amount of at least 0 and at most 2 mol %; iv) isophthalic acid in an amount of at least 0 and at most 2.4 mol %; v) terephthalic acid in an amount of at least 38 and at most 47 mol %; vi) adipic acid in an amount of at least 0.01 and at most 10 mol %; and vii) a polycarboxylic acid, in an amount of at least 6 and at most 10.2 mol %; and wherein the mol % is based on a total amount of monomers i)-vii) forming the polyester resin P being 100 mol %. 2. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the polyol monomer iii) is present in an amount of at least 0 and at most 1.4 mol %. 3. The branched carboxylic acid functional polyester resin P according to claim 2 , wherein the branched carboxylic acid functional polyester resin P has an AV of at least 68 mg KOH/g of the polyester resin P. 4. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the branched carboxylic acid functional polyester resin P has an AV of at least 68 mg KOH/g of the polyester resin P. 5. The branched carboxylic acid functional polyester resin P according to claim 4 , wherein the neopentyl glycol monomer i) is present in an amount of at most 36.5 mol %. 6. The branched carboxylic acid functional polyester resin P according to claim 5 , wherein the polyol monomer iii) is present in an amount of at least 0 and at most 1.4 mol %. 7. The branched carboxylic acid functional polyester resin P according to claim 6 , wherein the hydroxyl value of the polyester resin P is at most 7 mg KOH/g of the polyester resin P. 8. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the neopentyl glycol monomer i) is present in an amount of at most 36.5 mol %. 9. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the polycarboxylic acid monomer (vii) is present in an amount of at least 6.5 mol %. 10. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the hydroxyl value of the polyester resin P is at most 8 mg KOH/g of the polyester resin P. 11. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the hydroxyl value of the polyester resin P is at most 7 mg KOH/g of the polyester resin P. 12. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the hydroxyl value of the polyester resin P is at most 6 mg KOH/g of the polyester resin P. 13. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the hydroxyl value of the polyester resin P is at most 5 mg KOH/g of the polyester resin P. 14. The branched carboxylic acid functional polyester resin P according to claim 1 , wherein the hydroxyl value of the polyester resin P is at least 0.01 and at most 5 mg KOH/g of the polyester resin P. 15. A thermosetting powder coating composition A (PCC A) comprising a binder K in an amount of at least 20 and at most 100 pph of PCC A, wherein the binder K comprises: a crosslinker X in an amount of at least 1 and at most 55 pph of the binder K, wherein the crosslinker X is selected from the group consisting of epoxy compounds, compounds having at least two β-hydroxyalkylamide groups (BHA compounds), and mixtures thereof; and the branched carboxylic acid functional polyester resin P according to claim 1 in an amount of at least 45 and at most 99 pph of the binder K. 16. The thermosetting powder coating composition A (PCC A) according to claim 15 , wherein the crosslinker X is a BHA compound. 17. The thermosetting powder coating composition A (PCC A) according to claim 16 , wherein the amount of the crosslinker X is at least 2 and at most 20 pph of the binder K and wherein the branched carboxylic acid functional polyester resin P is present in an amount of at least 80 and at most 98 pph of the binder K. 18. A cured thermosetting powder coating composition which is obtained upon curing the thermosetting powder coating composition A (PCC A) as defined in claim 17 . 19. The thermosetting powder coating composition A (PCC A) according to claim 16 , wherein the amount of the crosslinker X is at least 2 and at most 20 pph of the binder K, and wherein the branched carboxylic acid functional polyester resin P is present in an amount of at least 80 and at most 98 pph of the binder K and has an AV of at least 68 mg KOH/g of the polyester resin P, and wherein the neopentyl glycol monomer i) of the branched carboxylic acid functional polyester resin P is present in an amount of at most 36.5 mol %; and the polyol monomer iii) of the branched carboxylic acid functional polyester resin P is present in an amount of at least 0 and at most 1.4 mol %. 20. The thermosetting powder coating composition A (PCC A) according to claim 16 , wherein the amount of the crosslinker X is at least 2 and at most 20 pph of the binder K, and wherein the branched carboxylic acid functional polyester resin P is present in an amount of at least 80 and at most 98 pph of the binder K, has an AV of at least 68 mg KOH/g of the polyester resin P and a hydroxyl value which is at most 7 mg KOH/g of the polyester resin P; and wherein the neopentyl glycol monomer i) of the branched carboxylic acid functional polyester resin P is present in an amount of at most 36.5 mol %; and the polyol monomer iii) of the branched carboxylic acid functional polyester resin P is present in an amount of at least 0 and at most 1.4 mol %.

Assignees

Inventors

Classifications

  • Crosslinking or vulcanising agents; including accelerators · CPC title

  • Acids containing aromatic rings · CPC title

  • Polyesters · CPC title

  • Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers · CPC title

  • Dicarboxylic acids and dihydroxy compounds · CPC title

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What does patent US11479690B2 cover?
A branched carboxylic acid functional polyester resin P is described herein along with thermosetting powder coating compositions (PCC A) comprising a binder K, the binder K comprising the polyester resin P and a crosslinker X. The invention further relates to a cured PCC A. In addition, processes for making said PCC A and processes for coating an article with said PCC A are described as well as…
Who is the assignee on this patent?
Covestro Netherlands Bv
What technology area does this patent fall under?
Primary CPC classification C08G63/20. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 11 related publications on this page (citations in our corpus or others sharing the same primary CPC).