IP Library Granted Patent US 10,538,597
Granted Patent B2
US 10,538,597 · App. 15/029,006 · Granted Jan 21, 2020

Acylation process

Inventors: Jana Lubkoll (Freiburg, DE); Armin Stein (Kenzingen, DE)
Assignee: Rhodia Acetow GmbH
C08B33/02C08B1/02C08B3/00C08B35/02C09D103/06C09D103/16C09J103/06C09J103/16Y02P20/582
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Quick Facts
Patent No.
US 10,538,597
App. No.
15/029,006
Granted
Jan 21, 2020
Kind
B2
Abstract

The invention concerns a process for the manufacture of an acylated polymer composition comprising amylose and/or amylopectin, comprising a pre-treatment step in the presence of an acid, a salt and a polycarboxylic acid, subsequent acylation and, preferably, a post-treatment step with an acid. The products obtained are useful as additives in inks, varnishes, lacquers, coatings, thickeners, adhesives or binders.

Claims (32)

1. An acylated polymer composition comprising acylated amylose and/or acylated amylopectin, which is made by a process comprising the following steps:

(a) pre-treating a polymer composition comprising amylose and/or amylopectin with an aqueous phase, the aqueous phase comprising at least one salt, at least one polycarboxylic acid, and one additive selected from the group consisting of at least one acid A having a pKa of equal to or less than 4.8 at 25° C. and an enzyme;

(b) reacting the pre-treated polymer composition with an acylating agent to provide an acylated polymer composition comprising acylated amylose and/or acylated amylopectin; and

(c) reacting the acylated polymer composition obtained in step (b) with at least one acid A′ with a pKa of equal to or less than 4.8 at 25° C., in the presence of water.

2. The acylated polymer composition of claim 1 , the acylated polymer composition having a degree of substitution (DS) in the range of from 2.1 to 2.9, and wherein the acylating agent is acetic acid anhydride.

3. An acylated polymer composition comprising acylated amylose and/or acylated amylopectin, which is made by a process comprising the following steps:

(a) pre-treating a polymer composition comprising amylose and/or amylopectin with an aqueous phase comprising at least one salt, at least one polycarboxylic acid, and one additive selected from the group consisting of at least one acid A having a pKa of equal to or less than 4.8 at 25° C. and an enzyme;

(b) reacting the pre-treated polymer composition with an acylating agent to provide an acylated polymer composition comprising acylated amylose and/or acylated amylopectin; and

(c) reacting the acylated polymer composition obtained in step (b) with at least one acid A′ with a pKa of equal to or less than 4.8 at 25° C., in the presence of water,

wherein the viscosity of polymer composition is equal to or greater than 77 mPas (10 w % in Triacetin at 30° C.).

4. A process for manufacturing an acylated polymer composition comprising acylated amylose and/or acylated amylopectin, having a viscosity of equal to or greater than 77 mPas (10 w % in Triacetin at 30° C.), which comprises:

(a) pre-treating a polymer composition comprising amylose and/or amylopectin with an aqueous phase, the aqueous phase comprising at least one salt, at least one polycarboxylic acid, and one additive selected from the group consisting of at least one acid A having a pKa of equal to or less than 4.8 at 25° C. and an enzyme; and

(b) reacting the pre-treated polymer composition with an acylating agent to provide an acylated polymer composition comprising acylated amylose and/or acylated amylopectin.

5. The process according to claim 4 further comprising:

(c) reacting the acylated polymer composition obtained in step (b) with at least one acid A′ with a pKa of equal to or less than 4.8 at 25° C., in the presence of water.

6. The process according claim 5 , wherein the at least one acid A used in step (a) and the at least one acid A′ used in step (c) can be the same or different and are selected from the group consisting of mineral acids, sulfonic acids, and carboxylic acids, all of which are either monoprotic or polyprotic.

7. The process according to claim 6 , wherein the at least one acid A and the at least one acid A′ are the same or different, and are sulfuric acid, amidosulfonic acid, benzene sulfonic acid, or phosphoric acid.

8. The process according to claim 5 , wherein the additive is an enzyme, and wherein acid A′ in step (c) is selected from the group consisting of mineral acids, sulfonic acids and carboxylic acids, all of which are either monoprotic or polyprotic.

9. The process according to claim 8 , wherein the enzyme is an amylase.

10. The process according to claim 5 , wherein the reaction time and reaction temperature of step (c) is selected such that the degree of substitution (DS) of the acylated polymer composition comprising amylose and/or amylopectin is from between 2.0 to 2.9.

11. The process of claim 4 , wherein in step (a) the polymer composition comprising amylose and/or amylopectin is pre-treated at a temperature in a range of from 20° C. to 85° C. during a pre-treatment time in a range of from 1 minutes to 30 minutes.

12. The process according to claim 4 , wherein the at least one polycarboxylic acid has from 2 to 12 carbon atoms, and at least two carboxylic acid groups —COOH.

13. The process according to claim 12 , wherein the polycarboxylic acid is at least one dicarboxylic acid and is selected from the group consisting of oxalic acid, malonic acid and succinic acid, glutaric acid, and adipic acid.

14. The process according to claim 4 , wherein the salt consists of a metal cation species and an inorganic or organic anion species.

15. The process according to claim 14 , wherein the metal cation species is selected from the group consisting of Mg 2+ , K + , Na 2+ , Li + , Cu 2+ , and Ca 2+ , and the anion is selected from the group consisting of sulfate, nitrate, chloride, carbonate, acetate, and malonate.

16. The process according to claim 4 , wherein the acylating agent is selected from the group consisting of carboxylic acids, symmetrical or unsymmetrical carboxylic acid anhydrides, carboxylic acid halides, and carboxylic acid carbonylimidazoles.

17. The process according to claim 16 , the acylated polymer composition having a degree of substitution (DS) in the range of from 2.1 to 2.9, and wherein the carboxylic acid anhydride is acetic acid anhydride.

18. The process according to claim 4 , wherein step (a) is carried out in the presence of a monocarboxylic acid, wherein the monocarboxylic acid corresponds to the carboxylic acid obtained by hydrolysis of the acylating agent.

19. The process according to claim 4 , wherein the polymer composition comprising amylose and/or amylopectin provided in step (a) is selected from the group consisting of chemically modified starches, unmodified starches, and a mixture of chemically modified starches and unmodified starches, and wherein the chemically unmodified starch is selected from the group consisting of maize starch, wheat starch, potato starch, rice starch, pea starch, rye starch, millet starch, and manioc starch, and wherein the chemically modified starch is selected from the group consisting of chemically modified maize starch, chemically modified wheat starch, chemically modified potato starch, chemically modified rice starch, chemically modified pea, chemically modified rye starch, chemically modified millet starch, and chemically modified manioc starch.

20. The process according to claim 19 , wherein the chemically modified starch is selected from the group consisting of crosslinked starches, acylated starches, hydroxyethylated starches, hydroxypropylated starches, methylated starches, oxidized starches, and cationic or anionic starches.

21. The process according to claim 4 , wherein the time and temperature of the pre-treatment are selected such that the viscosity of the final acylated polymer composition comprising amylose and/or amylopectin is equal to or greater than 77 mPas (10 w % in Triacetin at 30° C.).

22. A process of manufacturing inks, varnishes, lacquers, coatings, thickeners, adhesives, or binders comprising the acylated polymer composition according to claim 1 as an ingredient in the process.

Assignments (2)
CHANGE OF NAME Recorded Feb 6, 2018
From: SOLVAY ACETOW GMBH
To: RHODIA ACETOW GMBH
Reel/Frame 045253/0451 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 4, 2016
From: LUBKOLL, JANA; STEIN, ARMIN
To: SOLVAY ACETOW GMBH
Reel/Frame 038455/0181 →
Priority Claims (1)
EP 13188986 · Oct 16, 2013 · regional
Continuity (1)
Related Publication 20160257766A1 · Sep 8, 2016