Dispersed calcium carbonate containing material for an improved stability under alkaline conditions

Patent metadata

Field	Value
Publication number	US-9394428-B2
Application number	US-201314381801-A
Country	US
Kind code	B2
Filing date	Mar 26, 2013
Priority date	Mar 30, 2012
Publication date	Jul 19, 2016
Grant date	Jul 19, 2016

Abstract

The present invention relates to a method for preparing an aqueous calcium carbonate containing suspension, a suspension comprising a calcium carbonate containing material obtainable by said method as well as a calcium carbonate containing material obtainable by drying said suspension and to the use of the suspension or calcium carbonate containing material in paper, paper coating, plastic and/or paint applications and to the use of the suspension for stabilizing the rheology of a sodium silicate and/or sodium hydroxide containing coating formulations for paper applications.

First claim

The invention claimed is:

1. A method for preparing an aqueous calcium carbonate containing suspension, comprising the following steps of:
a) providing a calcium carbonate containing material in the form of an aqueous cake or suspension having solids content of at least 45 wt.-%, based on the total weight of the aqueous cake or suspension;
b) providing at least one alkali metal salt of a phosphonic acid in an amount from 0.01 to 5 wt.-%, based on the total dry weight of the calcium carbonate containing material;
c) providing at least one phosphonic acid in an amount from 0.001 to 0.5 wt.-%, based on the total dry weight of the calcium carbonate containing material;
d) contacting the calcium carbonate containing material of step a) with the at least one alkali metal salt of a phosphonic acid of step b) such as to obtain a suspension having a pH from 10 to 14;
e) contacting the suspension of step d) with the at least one phosphonic acid of step c) such as to obtain a suspension having a pH from 8 to 10; and
f) optionally grinding the suspension obtained in step e).

2. The method of claim 1 , wherein the calcium carbonate containing material of step a) is a ground calcium carbonate, a precipitated calcium carbonate, a modified calcium carbonate or a mixture thereof.

3. The method of claim 1 , wherein the cake or suspension of step a) has solids content from 50 to 98 wt.-%, based on the total weight of the aqueous cake or suspension.

4. The method according to 1 , wherein the calcium carbonate containing material of step a) has a weight median particle size d 50 from 1 to 100 μm.

5. The method according to 1 , wherein the calcium carbonate containing material of step a) has a weight median particle size d 50 from 1 to 10 pm.

6. The method according to claim 1 , wherein the alkali metal of the at least one alkali metal salt of a phosphonic acid of step b) is selected from the group consisting of sodium, potassium, lithium and any mixture thereof.

7. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is an alkali metal salt of a diphosphonic acid or an alkali metal salt of a triphosphonic acid.

8. The method according to 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is an alkali metal salt of a diphosphonic acid selected from the group consisting of 1-hydroxyethane 1,1-diphosphonic acid (HEDP), methylene diphosphonic acid (MDP), hydroxymethylene diphosphonic acid (HMDP), hydroxycyclomethylene diphosphonic acid (HCMDP) and 1-hydroxy-3-aminopropane-1,1-diphosphonic acid (APD).

9. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is an alkali metal salt of 1-hydroxyethane 1,1-diphosphonic acid (HEDP).

10. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is an alkali metal salt of a diphosphonic acid selected from group consisting of tetrasodium (1-hydroxyethylidene) bisphosphonate (Na4HEDP), trisodium (1-hydroxyethylidene) bisphosphonate (Na3HEDP), disodium (1-hydroxyethylidene) bisphosphonate (Na2HEDP), tetrapotassium (1-hydroxyethylidene) bisphosphonate (K4HEDP), tripotassium (1-hydroxyethylidene) bisphosphonate (K3HEDP) and dipotassium (1-hydroxyethylidene) bisphosphonate (K2HEDP).

11. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is tetrasodium (1-hydroxyethylidene) bisphosphonate (Na4HEDP).

12. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is in a form of an aqueous solution comprising the at least one alkali metal salt of a phosphonic acid in an amount from 10 to 80 wt.-%, based on the total weight of the solution.

13. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is in a form of an aqueous solution comprising the at least one alkali metal salt of a phosphonic acid in an amount from 20 to 66 wt.-%, based on the total weight of the solution.

14. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is in a form of an aqueous solution comprising the at least one alkali metal salt of a phosphonic acid in an amount from 30 to 50 wt.-%, based on the total weight of the solution.

15. The method according to claim 1 , wherein the at least one phosphonic acid of step c) is a diphosphonic acid or a triphosphonic acid.

16. The method according to claim 1 , wherein the at least one phosphonic acid of step c) is a diphosphonic acid selected from 1-hydroxyethane 1,1-diphosphonic acid (HEDP), methylene diphosphonic acid (MDP), hydroxymethylene diphosphonic acid (HMDP), hydroxy cyclomethylene diphosphonic acid (HCMDP) and 1-hydroxy-3-aminopropane- 1,1-diphosphonic acid (APD).

17. The method according to claim 1 , wherein the at least one phosphonic acid of step c) is 1-hydroxyethane 1,1-diphosphonic acid (HEDP).

18. The method according to claim 1 , wherein the at least one phosphonic acid of step c) is in form of an aqueous solution comprising the at least one phosphonic acid in an amount from 25 to 75 wt.-%, based on the total weight of the solution.

19. The method according to claim 1 , wherein the at least one alkali metal salt of a phosphonic acid of step b) is a sodium salt of 1-hydroxyethane 1,1-diphosphonic acid (Na 4 HEDP) and the at least one phosphonic acid of step c) is 1-hydroxyethane 1,1-diphosphonic acid (HEDP).

20. The method according to claim 1 , wherein step d) is carried out in that the at least one alkali metal salt of a phosphonic acid of step b) is added to the calcium carbonate containing material of step a) in an amount from 0.05 to 2.5 wt.-%, based on the total dry weight of the calcium carbonate containing material.

21. The method according to claim 1 , wherein the suspension obtained in step d) is diluted with water to solids content of from 40 to 90 wt.-%, based on the total weight of the suspension.

22. The method according to 1 , wherein the suspension obtained in step d) has a Brookfield viscosity from 50 to 5000 mPa-s at 23° C.

23. The method according to claim 1 , wherein step e) is carried out in that the at least one phosphonic acid of step c) is added to the suspension obtained in step d) in an amount from 0.01 to 0.5 wt.-%, based on the total dry weight of the calcium carbonate containing material.

24. The method according to claim 1 , wherein the suspension obtained in step e) has a pH from 9 to 10.

25. The method according to claim 1 , wherein the suspension obtained in step e) has a Brookfield viscosity from 10 to 4900 mPa-s at 23° C.

26. The method according to claim 1 , wherein grinding step f) is carried out after step e).

27. The method according to claim 1 , wherein grinding step f) is carried out at a temperature from 10° C. to 110° C.

28. The method according to claim 1 , wherein grinding step f) is carried out at a temperature from 20° C. to 70° C.

29. The method according to claim 1 , wherein grinding step f) is carried out until the fraction of calcium carbonate containing material having a particle size of less than 2 pm is from 50 to 98 wt.-%, based on the total weight of the calcium carbonate containing material.

30. The method according to c

Assignees

• Omya Int Ag

Inventors

• Gane Patrick A C
• Gantenbein Daniel

Classifications

• C01P2006/22

  Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability · CPC title

• D21H17/10

  Phosphorus-containing compounds · CPC title

• C08K5/5317 Primary

  Phosphonic compounds, e.g. R—P(:O)(OR')2 · CPC title

• D21H19/385

  Oxides, hydroxides or carbonates · CPC title

• C08K2003/265

  Calcium, strontium or barium carbonate · CPC title