Method of manufacturing an automatic dishwashing detergent product

Patent metadata

Field	Value
Publication number	US-10689604-B2
Application number	US-201515322068-A
Country	US
Kind code	B2
Filing date	Jul 1, 2015
Priority date	Jul 2, 2014
Publication date	Jun 23, 2020
Grant date	Jun 23, 2020

Abstract

The present invention provides a method of manufacturing an automatic dishwashing detergent product, said product being provided as a discrete dosage unit and comprising a continuous, non-aqueous gel phase, comprising manufacturing said gel phase by a method comprising free radical polymerisation of monomer(s) in a non-aqueous reaction mixture to form a polymeric builder; wherein said reaction mixture comprises: at least one non-ionic surfactant which is an optionally end-capped alcohol alkoxylate; and one or more monomers comprising acrylic acid and optionally one or more further α,β-ethylenically unsaturated acids, wherein no more than 0.1 wt % of the total amount of the monomer(s) are crosslinking monomer(s).

First claim

The invention claimed is:

1. A method of manufacturing an automatic dishwashing detergent product being provided as a discrete dosage unit and comprising a continuous, non-aqueous gel phase comprising manufacturing the gel phase by a method comprising free radical polymerization of one or more monomers in a non-aqueous reaction mixture to form a polymeric builder without an intermediate step of drying the reaction mixture to form a solid comprising the polymeric builder;
wherein the polymeric builder is in a dissolved state in the non-aqueous gel phase,
wherein the reaction mixture comprises:
10 wt % to 50 wt % of a non-ionic surfactant;
10 wt % to 60 wt % of at least one non-water solvent; and
a monomer comprising acrylic acid,
wherein no more than 0.1 wt % of the total amount of the monomer is a crosslinking monomer.

2. The method according to claim 1 , wherein the monomer consists of acrylic acid.

3. The method according to claim 1 , wherein the free radical polymerization is conducted at a temperature in the range of 20 to 90° C.

4. The method according to claim 1 , wherein the free radical polymerization is conducted at a temperature in the range of 40 to 80° C.

5. The method according to claim 1 , wherein the free radical polymerization is conducted in the presence of a chain transfer agent.

6. The method according to claim 1 , wherein the free radical polymerization is conducted in a feed mode of operation, in which at least a portion of the non-ionic surfactant is present in an initial charge, and at least a portion of the monomer and at least one radical initiator is fed to the initial charge.

7. The method according to claim 1 , wherein up to 40 mol % of acid groups in the polymeric builder are in neutralized form.

8. The method according to claim 1 , wherein the gel phase is free of any ionic surfactant.

9. The method according to claim 1 , wherein the reaction further comprises a monomer comprising α,β-ethylenically unsaturated acid; and
wherein no more than 0.1 wt % of the total amount of the monomers are crosslinking monomers.

10. The method according to claim 9 , wherein the non-ionic surfactant comprises an end-capped alcohol alkoxylate.

11. The method according to claim 10 , wherein the alcohol alkoxylate non-ionic surfactant is liquid at 20° C.

12. The method according to claim 9 , wherein the reaction mixture comprises at least 20 wt % in total of the monomers.

13. The method according to claim 9 , wherein the reaction mixture is free of crosslinking monomers.

14. The method according to claim 9 , wherein the reaction mixture comprises:
at least 20 wt % in total of the non-ionic surfactant; and
at least 40 wt % in total of the monomers.

15. The method according to claim 9 , wherein the α,β-ethylenically unsaturated acid is a carboxylic acid selected from the group consisting of methacrylic acid, ethacrylic acid, maleic acid, crotonic acid, itaconic acid, citraconic acid, mesaconic acid, glutaconic acid, aconitic acid, and fumaric acid.

16. The method according to claim 9 , wherein the weight ratio of acrylic acid to α,β-ethylenically unsaturated acid in the reaction mixture is in the range of 100:1 to 1:1.

17. The method according to claim 1 , wherein the non-water solvent is a water-soluble organic solvent selected from the group consisting of alkylene glycol, dialkylene glycol, monopropylene glycol, and dipropylene glycol.

18. The method according to claim 1 , wherein the alcohol alkoxylate non-ionic surfactant is of the formula R1-O-(EO)x(AO)y-R4, in which:
R1 is an alkyl group;
R4 is H or an optionally substituted alkyl group;
x is 1 to 100;
y is 0 to 100;
EO is ethylene oxide; and
each AO, when present, is independently propylene oxide or butylene oxide;
wherein x and y represent the average degrees of respective alkoxylation per molecule; and
wherein the order of EO and AO groups may be varied but the sum of x and y is at least 3.

19. The method according to claim 1 further comprising providing the gel phase in a water-soluble container.

20. The method according to claim 1 further comprising:
providing the gel phase in a compartment of a multi-compartment water-soluble container; and
providing a solid composition in a different compartment of the multi-compartment water-soluble container;
wherein the solid composition comprises a component selected from the group consisting of bleach, enzyme and builder.

Assignees

• Reckitt Benckiser Finish Bv

Inventors

• Roy Pavlinka
• Schmaelzle Claudia
• Rigobert Caroline
• Weber Heike
• Witteler Helmut
• Fuchs Yannick
• Bohn Roland

Classifications

• C08F2/06 Primary

  Organic solvent · CPC title

• C08F2/08

  with the aid of dispersing agents for the polymer · CPC title

• C11D1/72

  Ethers of polyoxyalkylene glycols · CPC title

• C08F2/44

  Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers · CPC title

• C08F220/06

  Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof · CPC title