Alkyd for pigment paste

US12129390B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12129390-B2
Application numberUS-201816772056-A
CountryUS
Kind codeB2
Filing dateDec 17, 2018
Priority dateDec 20, 2017
Publication dateOct 29, 2024
Grant dateOct 29, 2024

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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The embodiments herein provide a solvent borne pigment paste comprising an alkyd, where the alkyd is obtainable by a process including the steps of a. producing an OH-functional alkyd from a non-drying oil or fatty acid, one or more polyols, and a first anhydride; where the non-drying oil or fatty acid has an iodine number ≥115; b. esterification of the OH-functional alkyd with trimellitic anhydride (TMA), where at least 80% of the esterified TMA residues has two free carboxylic groups. In some embodiments, at least 85%, at least 90%, or at least 98% of the esterified TMA residues has two free carboxylic groups.

First claim

Opening claim text (preview).

The invention claimed is: 1. A solvent borne pigment paste comprising an alkyd and one or more iron oxide pigments wherein the alkyd is obtainable by a process comprising the steps of a. producing an OH-functional alkyd from a non-drying oil or a fatty acid, one or more polyols, and a first anhydride; wherein the non-drying oil or fatty acid has an iodine number ≤100 and >15 I 2 /100 g; b. esterification of the OH-functional alkyd with trimellitic anhydride (TMA) at a temperature ≤220° C. to obtain an alkyd with esterified TMA residues, wherein at least 80% of the esterified TMA residues has two free carboxylic groups, wherein an acid value of the alkyd is between 15 and 30 mg KOH/g, and wherein the iodine number is determined according to ISO 3961 and the acid value is determined according to ISO 2114. 2. The pigment paste of claim 1 , wherein esterification of the OH-functional alkyd with trimellitic anhydride (TMA) is at a temperature between 100° C. and 200° C. 3. The pigment paste of claim 1 , wherein an amount of fatty acid with 18 carbon atoms and two double bonds (C18:2) and C18:3 in the non-drying oil or fatty acid is less than 20 wt %. 4. The pigment paste of claim 1 , wherein an amount of fatty acids with less than 16 carbon atoms (<C16) in the non-drying oil or fatty acid is less than 10 wt %; or wherein an amount of fatty acids without unsaturations (C16:0) and fatty acids with 16 carbon atoms and one unsaturation (C16:1) in the non-drying oil or fatty acid is less than 15 wt %. 5. The pigment paste of claim 1 , wherein the amount of fatty acid with 18 carbon atoms and one double bond (C18:1) and isostearic acid in the non-drying oil or fatty acid is ≥40 wt %. 6. The pigment paste of claim 5 , wherein the non-drying oil or fatty acid comprises more than 52 wt % of oleic acid. 7. The pigment paste of claim 1 , wherein the one or more polyols comprise at least one member selected from a group consisting of glycerol and pentaerythritol and wherein the first anhydride comprises at least one member selected from a group consisting of phthalic anhydride and hexahydro-phthalic anhydride. 8. The pigment paste of claim 1 , wherein the alkyd has a Number Average Molecular Weight (Mn) of between 2000 and 3500 Da; or wherein the Weight Average Molecular Weight (Mw) is between 5000 and 10,000 Da; and/or wherein the Mw/Mn ratio is between 1 and 3, and wherein Mn and Mw are measured using Gel Permeation Chromatography using polystyrene standards. 9. The pigment paste of claim 1 , wherein the acid value of the OH-functional alkyd is between 10 and 25 mg KOH/g. 10. The pigment paste of claim 1 , wherein the acid value of the alkyd is between 16 and 25 mg KOH/g. 11. The pigment paste of claim 1 , wherein the pigment paste comprises at least 15 wt % of the alkyd. 12. The pigment paste of claim 1 , wherein the iron oxide pigments are selected from the group consisting of yellow iron oxide, orange iron oxide, red iron oxide, brown iron oxide and black iron oxide, or mixtures thereof. 13. The pigment paste of claim 1 , wherein the iron oxide pigments are transparent iron oxide pigments. 14. A coating comprising the pigment paste of claim 1 . 15. The pigment paste of claim 1 , wherein at least 98% of the esterified TMA residues have two free carboxylic groups. 16. The pigment paste of claim 1 , wherein esterification of the OH-functional alkyd with trimellitic anhydride (TMA) is at a temperature between 100° C. and 180° C. 17. The pigment paste of claim 1 , wherein esterification of the OH-functional alkyd with trimellitic anhydride (TMA) is at a temperature between 100° C. and 150° C. 18. The pigment paste of claim 1 , wherein an amount of fatty acid with 18 carbon atoms and two double bonds (C18:2) and C18:3 in the non-drying oil or fatty acid is less than 5 wt %. 19. The pigment paste of claim 1 , wherein the acid value of the OH-functional alkyd is between 13.5 and 16 mg KOH/g.

Assignees

Inventors

Classifications

  • C08G63/48Primary

    by unsaturated higher fatty oils or their acids; by resin acids · CPC title

  • Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation · CPC title

  • Fillers, pigments or reinforcing additives · CPC title

  • Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation · CPC title

  • Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids · CPC title

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What does patent US12129390B2 cover?
The embodiments herein provide a solvent borne pigment paste comprising an alkyd, where the alkyd is obtainable by a process including the steps of a. producing an OH-functional alkyd from a non-drying oil or fatty acid, one or more polyols, and a first anhydride; where the non-drying oil or fatty acid has an iodine number ≥115; b. esterification of the OH-functional alkyd with trimellitic anhy…
Who is the assignee on this patent?
Akzo Nobel Coatings Int Bv
What technology area does this patent fall under?
Primary CPC classification C08G63/48. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 29 2024 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 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).