IP Library Granted Patent US 7,534,760
Granted Patent B2
US 7,534,760 · App. 11/129,457 · Granted May 19, 2009

Highly alkaline compositions containing a hexyl glycoside as a hydrotrope

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Quick Facts
Patent No.
US 7,534,760
App. No.
11/129,457
Granted
May 19, 2009
Kind
B2
Abstract

The present invention relates to a clear and stable, highly alkaline composition with controlled foaming, containing a high amount of surface active nonionic alkylene oxide adduct and a hexyl glycoside as a hydrotrope. This composition has a very good wetting and cleaning ability and can be used for cleaning of hard surfaces, in a mercerization process and for a cleaning, desizing or scouring process of fibres and fabrics.

Claims (36)

1. A method for improving the solubility of a surface active nonionic alkylene oxide adduct in a highly alkaline composition having a pH above 11, said adduct containing a hydrocarbon group or an acyl group of from 8 to 24 carbon atoms and at least one primary hydroxyl group in the alkoxylated part of the molecule, said method comprising adding a hydrotrope to said highly alkaline composition, said hydrotrope comprising a hexyl glycoside having the formula

C 5 H 13 OG n   (I),

where G is a monosaccharide residue and n is from 1 to 5, wherein the weight ratio between said hexyl glycoside and said surface active nonionic alkylene oxide adduct is from 1:10 to 4:1, and wherein said composition comprises 3-50% of an alkaline complexing agent as an alkaline agent.

2. The method of claim 1 , wherein the adduct has the formula

R(AO) x (C 2 H 4 O) y H  (II),

where R is an alkoxy group R′O— having 8 to 24 carbon atoms or a group R″CONR′″— where R″ is a hydrocarbon group having 7 to 23 carbon atoms, R′″ is hydrogen or the group —(AO) x (C 2 H 4 O) y H, AO is an alkyleneoxy group with 2-4 carbon atoms, x is a number from 0 to 5 and y is a number from 1 to 10.

3. The method of claim 1 wherein the alkaline composition has a pH-value above 13.

4. The method of claim 1 wherein the glycoside is a n-hexyl glycoside.

5. An aqueous alkaline composition having a pH-value above 11 which comprises

a) 3-50% by weight of a an alkaline complexing agent,

b) 0.05-30% by weight of a surface active nonionic alkylene oxide adduct having a hydrocarbon group or an acyl group of from 8 to 24 carbon atoms and having at least one primary hydroxyl group in the alkoxylated part of the molecule,

c) 0.04-30% by weight of a hexyl glycoside,

d) 20-97% by weight of water.

6. The composition of claim 5 wherein the nonionic surfactant is an alkoxylate having the formula

R(AO) x (C 2 H 4 O) y H  (II)

where R is an alkoxy group R′O— having 8 to 24 carbon atoms or a group R″—CONR′″— where R″ is a hydrocarbon group having 7 to 23 carbon atoms, R′″ is hydrogen or the group —(AO) x (C 2 H 4 O) y H, AO is an alkyleneoxy group with 2-4 carbon atoms, x is a number from 0 to 5 and y is a number from 1 to 10.

7. The composition of claim 5 having a pH-value above 13.

8. The composition of claim 5 wherein the hexyl glycoside is n-hexyl glycoside.

9. A method for cleaning hard surfaces which comprises applying to said hard surfaces a cleaning effective amount of the alkaline composition of claim 5 .

10. A method for cleaning, desizing or scouring fibers and fabrics which comprises adding a cleaning, desizing or scouring effective amount of the alkaline composition of claim 5 to said fibers and fabrics.

11. The method of claim 1 wherein said alkylene oxide adduct is obtained by alkoxylation of an alcohol or an amide.

12. The method of claim 2 wherein R′ is 2-ethylhexyl, octyl, decyl, cocoalkyl, lauryl. oleyl, rape seed alkyl, or tallow alkyl.

13. The method of claim 2 wherein R′ is derived from an oxoalcohol, Guerbet alcohol, methyl substituted alcohols or straight alcohols.

14. The method of claim 1 wherein said alkaline complexing agent is inorganic, organic, or a mixture thereof.

15. The method of claim 14 wherein said alkaline complexing agent is an inorganic alkali salt of silicate, phosphate, or a mixture thereof.

16. The method of claim 15 wherein said alkaline complexing agent is sodium tripolyphosphate, sodium orthophosphate, sodium pyrophosphate, sodium phosphate, and the corresponding potassium salts.

17. The method of claim 14 wherein said alkaline complexing agent is an alkaline aminopolyphosphonate, organic phosphate, polycarboxylate, aminocarboxylates, or a mixture thereof.

18. The method of claim 17 wherein said polycarboxylate is a citrate, and said aminocarboxylate is a sodium nitrilotriacetate (Na 3 NTA), sodium ethylenediaminetetraacetate, sodium diethylenetrlaminepenteacatate, sodium 1,3-propylenediaminetetraacetate, sodium hydroxyethylethylenediaminetriacetate, or mixtures thereof.

19. The composition of claim 5 wherein said alkylene oxide adduct is obtained by alkoxylation of an alcohol or an amide.

20. The composition of claim 2 wherein R′ is 2-ethylhexyl, octyl, decyl, cocoalkyl, lauryl, oleyl, rape seed alkyl, or tallow alkyl.

21. The composition of claim 2 wherein R′ is derived from an oxoalcohol, Guerbet alcohol, methyl substituted alcohols or straight alcohols.

22. The composition of claim 5 wherein said alkaline complexing agent is inorganic, organic, or a mixture thereof.

23. The composition of claim 22 wherein said alkaline complexing agent is an inorganic alkali salt of silicate, phosphate, or a mixture thereof.

24. The composition of claim 23 wherein said alkaline complexing agent is sodium tripolyphosphate, sodium orthophosphate, sodium pyrophosphate, sodium phosphate, and the corresponding potassium salts.

25. The method of claim 22 wherein said alkaline complexing agent is an alkaline aminopolyphosphonate, organic phosphate, polycarboxylate, aminocarboxylates, or a mixture thereof.

26. The method of claim 25 wherein said polycarboxylate is a citrate, and said aminocarboxylate is a sodium nitrilotriacetate (Na 3 NTA) sodium ethylenediaminetetraacetate, sodium diethylenetriaminepentaacetate, sodium 1,3-propylenediaminetetraacetate, sodium hydroxyethylethylenediaminetriacetate, or mixtures thereof.

Assignments (2)
SECURITY INTEREST Recorded Oct 1, 2018
From: STARFRUIT US MERGER SUB 1 LLC; STARFRUIT US MERGER SUB 2 LLC; AKZO NOBEL SURFACE CHEMISTRY LLC; AKZO NOBEL CHEMICALS B.V.; AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
To: WILMINGTON TRUST (LONDON) LIMITED, AS COLLATERAL AGENT
Reel/Frame 047231/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 13, 2017
From: AKZO NOBEL N.V.
To: AKZO NOBEL CHEMICALS INTERNATIONAL B.V.
Reel/Frame 044427/0759 →