Coatings with wax-modified hyperbranched and flexible hyperbranched polyols

US10689541B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10689541-B2
Application numberUS-201716333779-A
CountryUS
Kind codeB2
Filing dateSep 6, 2017
Priority dateSep 15, 2016
Publication dateJun 23, 2020
Grant dateJun 23, 2020

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Wax-modified hyperbranched polyols and wax-modified flexible hyperbranched polyols are described, as are coating compositions containing these polyols. These polyols provide excellent coatings, especially matte coatings, and allow for the exclusion of silica in coatings.

First claim

Opening claim text (preview).

The invention claimed is: 1. A coating composition comprising a wax-modified flexible hyperbranched polyol, wherein the wax-modified flexible hyperbranched polyol is prepared by a process comprising: (a) reacting a polyol comprising at least three hydroxyl groups with (a′) a C 8 -C 85 linear or branched unsubstituted carboxylic acid and optionally with (a″) an aliphatic dicarboxylic acid having from 6 to 36 carbon atoms or an esterifiable derivative thereof, to form a hydroxyl-functional first intermediate product; (b) reacting the hydroxyl-functional first intermediate product with a cyclic carboxylic acid anhydride to form a carboxylic acid-functional second intermediate product; and (c) reacting the second intermediate product with an epoxide-functional compound having one epoxide group to form the wax modified flexible hyperbranched polyol. 2. The coating composition according to claim 1 , wherein the wax-modified flexible hyperbranched polyol is prepared by a process comprising: (a) reacting a polyol comprising at least three hydroxyl groups with (a′) a C 8 -C 85 linear or branched unsubstituted carboxylic acid and with (a″) an aliphatic dicarboxylic acid having from 6 to 36 carbon atoms or an esterifiable derivative thereof, to form a hydroxyl-functional first intermediate product. 3. The coating composition according to claim 1 , comprising 5% to 60% by weight of the wax-modified flexible hyperbranched polyol based on a total amount of film-forming materials in the coating composition, and comprising no silica. 4. The coating composition according to claim 3 , further comprising at least one of a hydrogen-functional resin and hydrogen-functional polymer. 5. The coating composition according to claim 1 , wherein the wax-modified flexible hyperbranched polyol has the following structure: where n=14-39 and —OC(O)R1R2R3 is a branched C10 monocarboxylic acid residue. 6. The coating composition according to claim 1 , wherein the wax-modified flexible hyperbranched polyol has the following structure: where n=14-39 and —OC(O)R1R2R3 is a branched C10 monocarboxylic acid residue. 7. A method for coating a substrate, comprising applying to the substrate the coating composition of claim 1 to form a coating layer, and curing the coating layer. 8. A coating composition comprising a wax-modified hyperbranched polyol, wherein the wax-modified hyperbranched polyol is prepared by a process comprising: (a) reacting a polyol comprising at least three hydroxyl groups with (a′) a C 8 -C 85 linear or branched unsubstituted carboxylic acid and with (a″) a first chain extender which comprises a plurality of hydroxyl groups and a carboxyl group, to form a first generation branched core; (b) optionally further reacting the first generation branched core with the first chain extender to form a subsequent generation branched core; (c) reacting the first or subsequent generation branched core with at least one compound selected from the group consisting of carboxylic anhydrides and acids to form an ester bridge therewith, thereby forming an intermediate polyester macromolecule; and (d) reacting the intermediate polyester macromolecule with a second chain extender having a terminal or non-terminal epoxide group and a branched hydrocarbon chain, to form the wax-modified hyperbranched polyol. 9. The coating composition according to claim 8 , wherein the wax-modified hyperbranched polyol is prepared by a process comprising: (b) further reacting the first generation branched core with the first chain extender to form a subsequent generation branched core; (c) reacting the subsequent generation branched core with at least one compound selected from the group consisting of carboxylic anhydrides and acids to form an ester bridge therewith, thereby forming an intermediate polyester macromolecule. 10. The coating composition according to claim 8 , comprising 5% to 60% by weight of the wax-modified hyperbranched polyol based on a total amount of film-forming materials in the coating composition, and comprising no silica. 11. The coating composition according to claim 8 , further comprising at least one of a hydrogen-functional resin and hydrogen-functional polymer. 12. A method for coating a substrate, comprising applying to the substrate the coating composition of claim 8 to form a coating layer, and curing the coating layer. 13. A compound of formula (I), (II), (III), or (IV): E-[OC(O)ACOO-] x -P—(—OC(O)W) n   (I) where: P is a C 3 -C 60 polyol moiety, bonded to x [OC(O)ACOO—] and n-(—OC(O)W) moieties through x+n —OH functionalities; n is 1-2; W is a C 8 -C 60 linear or branched alkane moiety; x is 1-8; A is a C 2 -C 22 substituted or unsubstituted aliphatic, alicyclic or aromatic moiety; and E is hydrogen or R—C(OH), where R is a substituted or unsubstituted C 1 -C 22 aliphatic, alicyclic or aromatic moiety; where: P is a C 3 -C 60 polyol moiety, bonded to x [OCOACOO—] and n-(—OCOW) moieties through x+n —OH functionalities; n is 1-2; W is a C 8 -C 60 linear or branched alkane moiety; x is 1-8; A is a C 2 -C 22 substituted or unsubstituted aliphatic, alicyclic or aromatic moiety; E is hydrogen or R—C(OH), where R is a substituted or unsubstituted C 1 -C 22 aliphatic, alicyclic or aromatic moiety; and B is a substituted or unsubstituted C 4 -C 36 aliphatic, alicyclic or aromatic moiety esterified to P through a P —OH functionality; E-[OC(O)ACOO-] x -L y -P-L y -(—OC(O)W) n   (III) where: P is a C 3 -C 60 polyol moiety, bonded to x [OC(O)ACOO—] and n-(—OC(O)W) moieties through x+n —OH functionalities; n is 1-2; W is a C 8 -C 60 linear or branched alkane moiety; x is 1-8; A is a C 2 -C 22 substituted or unsubstituted aliphatic, alicyclic or aromatic moiety; E is hydrogen or R—C(OH), where R is a substituted or unsubstituted C 1 -C 22 aliphatic, alicyclic or aromatic moiety; and L is a lactone moiety where y is 1-5 where P is a C 3 -C 60 polyol moiety, bonded to x [OC(O)ACOO—] and n-(—OC(O)W) moieties through x+n —OH functionalities; n is 1-2; W is a C 8 -C 60 linear or branched alkane moiety; x is 1-8; A is a C 2 -C 22 substituted or unsubstituted aliphatic, alicyclic or aromatic moiety; E is hydrogen or R—C(OH), where R is a substituted or unsubstituted C 1 -C 22 aliphatic, alicyclic or aromatic moiety; B is a substituted or unsubstituted C 4 -C 36 aliphatic, alicyclic or aromatic moiety esterified to P through a P —OH functionality; and L is a lactone moiety where y is 1-5.

Assignees

Inventors

Classifications

  • After treatment of hyperbranched macromolecules · CPC title

  • C07C69/75Primary

    of acids with a six-membered ring · CPC title

  • Hyperbranched macromolecules · CPC title

  • Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain (based on polyester-amides C09D177/12; based on polyester-imides C09D179/08); Coating compositions based on derivatives of such polymers · CPC title

  • The ring being saturated · CPC title

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What does patent US10689541B2 cover?
Wax-modified hyperbranched polyols and wax-modified flexible hyperbranched polyols are described, as are coating compositions containing these polyols. These polyols provide excellent coatings, especially matte coatings, and allow for the exclusion of silica in coatings.
Who is the assignee on this patent?
Basf Coatings Gmbh
What technology area does this patent fall under?
Primary CPC classification C07C69/75. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 23 2020 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).