IP Library Granted Patent US 6,994,798
Granted Patent B2
US 6,994,798 · App. 10/275,861 · Granted Feb 7, 2006

Phenolate-containing formulation with low freezing point

Assignee: Omya AG
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Quick Facts
Patent No.
US 6,994,798
App. No.
10/275,861
Granted
Feb 7, 2006
Kind
B2
Abstract

The present invention discloses an aqueous phenolates-containing liquid formulation having a solidification point of less than or equal to −10° C. which is characterized by comprising the following components: a) 50–80% by wt. of one or more phenolates; b) 0.1–10% by wt. of at least one crystallization inhibitor; and water and optionally other components forming the balance.

Claims (48)

1. An aqueous, phenolate-containing liquid formulation, comprising:

a) 50–80% by wt. of one or more phenolates;

b) 0.1–10% by wt. of at least one crystallization inhibitor;

c) water; and

d) optionally a balance of at least one other component having a biocidal effect and/or promoting a biocidal effect of said one or more phenolates;

wherein said aqueous, phenolate-containing liquid formulation has a solidification point of less than or equal to −10° C.;

wherein said one or more phenolates are present in a form selected from the group consisting of a potassium salt, a mixture of a potassium salt and a sodium salt, a mixture of a potassium salt and a lithium salt and mixtures thereof.

2. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises as said one or more phenolates a member selected from the group consisting of salts of phenol, phenolates having one or more aliphatic substituents, phenolates having one or more aromatic substituents mixtures of salts of phenol and phenolates having one or more aliphatic substituents, mixtures of salts of phenol and phenolates having one or more aromatic substituents, and mixtures thereof.

3. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises as said one or more phenolates a member selected from the group consisting of o-phenylphenolates, halogenated phenolates, cresol salts, salts of halogenated cresols, resorcinol salts and mixtures thereof.

4. The aqueous, phenolate-containing liquid formulation according to claim 3 , which comprises as the cresol salts a member selected from the group consisting of salts of o-cresol, salts of m-cresol, salts of p-cresol, salts of isopropyl o-cresol, salts of 4-isopropyl m-cresol, halogenated cresols, and

as the resorcinol salts a member selected from the group consisting of salts of 4-n-hexyl resorcinol.

5. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises one or more phenolates in an amount of 50–75% by wt.

6. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises said at least one crystallization inhibitor in an amount of 0.5–5% by wt.

7. The aqueous, phenolate-containing liquid formulation according to claim 1 , said formulation containing as the crystallization inhibitor a member selected from the group consisting of one or more aliphatic glycol compound(s), one or more aliphatic alcohol(s), one or more aromatic alcohol(s), and mixtures thereof.

8. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises a member selected from the group consisting of organometal compounds, quaternary ammonium compounds and mixtures thereof, and/or a member selected from the group consisting of chelating agents, antioxidants and mixtures thereof.

9. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises a member selected from the group consisting of dicocomethylbenzylammonium chloride, tributyl tin benzoate, N-tallow-1,3-diaminopropane and mixtures thereof.

10. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises 0.05–1% by wt. based on the formulation of a member selected from the group consisting of NTA, EDTA, DTPA, 2-phosphono-1,2,4-butanetricarboxylic acid and mixtures thereof.

11. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises

a) 50–80% by wt. of at least one phenolate; and

b) 20–50% by wt. of a solvent system comprising 90–99% by wt. water and 0.1–10.0% by wt. of at least one crystallization inhibitor;

wherein a proportion of 1.0–4.9% by wt. of said formulation may be replaced by additional microbicidal agents and/or at least one component promoting a microbicidal effect of said phenolate or a microbicidal effect of said additional microbicidal agent.

12. The aqueous, phenolate-containing liquid formulation according to claim 1 , wherein said one or more phenolates are dissolved in a solvent system and are neutralized with an excess of 0.03–0.15 mols of at least one alkali hydroxide, based on the amount of phenolates.

13. The aqueous, phenolate-containing liquid formulation according to claim 12 , wherein 1.03–1.15 of alkali hydroxide per mol of phenolate are used for neutralization.

14. The aqueous, phenolate-containing liquid formulation according to claim 1 , wherein the crystallization inhibitors are present in an amount of 1–3% by wt. in a formulation containing 60–70% by wt. of one or more phenolates.

15. The aqueous, phenolate-containing liquid formulation according to claim 1 , comprising:

50–80% by wt. of said one or more phenolates;

0.1–10% by wt. of a crystallization inhibitor selected from the group consisting of one or more aliphatic glycol compound(s), glycerol, one or more aliphatic alcohol(s), one or more aromatic alcohol(s) and mixtures thereof; and

a balance with respect to 100% by wt. comprising alkali in an excess of 0.03–0.15 mol/mol and water.

16. The aqueous, phenolate-containing liquid formulation according to claim 4 , wherein said halogenated cresol is chlorinated cresols.

17. The aqueous, phenolate-containing liquid formation according to claim 1 , which comprises one or more phenolates in an amount of 55–70% by wt.

18. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises one or more phenolates in an amount of 60–70% by wt.

19. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises one or more phenolates in an amount of 62–67% by wt.

20. The aqueous, phenolate-containing liquid formulation according to claim 1 , which comprises the crystallization inhibitors in an amount of 1–3% by wt.

21. The aqueous, phenolate-containing liquid formulation according to claim 7 , wherein said one or more aliphatic glycol compound(s) are a member selected from the group consisting of ethylene glycol, monopropylene glycol, diethylene glycol and mixtures thereof.

22. A method for the preparation of an aqueous, phenolate-containing liquid formulation, according to claim 1 comprising:

placing water and a neutralizing agent in a vessel;

dissolving a phenol compound; and

adding a crystallization inhibitor.

23. The aqueous, phenolate-containing liquid formulation according to claim 7 , wherein said one or more aromatic alcohol(s) are a member selected from the group consisting of benzyl alcohol, 2-phenylethane-1-ol, 3-phenylpropane-1-ol, 1-phenylpropane-2-ol and mixtures thereof.

24. An aqueous suspension or dispersion, comprising: a member selected from the group consisting of minerals, fillers, pigments, natural organic binders, synthetic organic binders, cooling lubricants and mixtures thereof, and

the aqueous, phenolate-containing liquid formulation according to claim 1 .

25. The aqueous suspension or dispersion according to claim 14 , wherein said aqueous, phenolate-containing liquid formulation is present in an amount of 100 g/ton to 2500 g/ton of the suspension or dispersion.

26. A preservative and/or mordant, comprising:

the aqueous, phenolate-containing liquid formulation according to claim 1 .

27. The aqueous, phenolate-containing liquid formulation according to claim 7 , wherein said one or more aliphatic alcohol(s) are a member selected from the group consisting of methanol, ethanol, n-propanol, iso-propanol, isomers of butanol, isomers of pentanol and mixtures thereof.

28. The method according to claim 27 , comprising:

placing the crystallization inhibitor together with the water and the neutralizing agent in a vessel, and afterwards dissolving the phenol compound therein.

29. The method according to claim 27 , wherein a temperature during dissolving is 5–80° C.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2007
From: OMYA AG
To: OMYA DEVELOPMENT AG
Reel/Frame 019943/0214 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2003
From: BURI, MATTHIAS; SCHWARZENTRUBER, PATRICK
To: OMYA AG
Reel/Frame 014149/0954 →
Priority Claims (2)
DE 100 23 458 · May 12, 2000 · national
DE 100 27 588 · Jun 2, 2000 · national
Continuity (1)
Related Publication 20040023939A1 · Feb 5, 2004