Precipitated calcium carbonate with improved resistance to structural breakdown

Patent metadata

Field	Value
Publication number	US-11111388-B2
Application number	US-202016862801-A
Country	US
Kind code	B2
Filing date	Apr 30, 2020
Priority date	Jul 31, 2015
Publication date	Sep 7, 2021
Grant date	Sep 7, 2021

Abstract

The present invention is directed to a process for producing precipitated calcium carbonate with improved resistance to structural breakdown, wherein the milk of lime is carbonated in the presence of at least one gas other than carbon dioxide, or the carbonation is carried out in the presence of a static gas bubble comminution unit as well as to precipitated calcium carbonate obtained by such a process.

First claim

The invention claimed is:

1. A process for producing precipitated calcium carbonate comprising the steps of:
a) providing a calcium oxide containing material,
b) providing an aqueous solution,
c) providing a gas comprising carbon dioxide,
d) preparing a milk of lime comprising Ca(OH) 2 by mixing the aqueous solution of step b) with the calcium oxide containing material of step a),
e) carbonating the milk of lime obtained from step d) with the gas of step c) to form an aqueous suspension of precipitated calcium carbonate, wherein:
the carbonation is carried out in the presence of a static gas bubble comminution unit that is located in the milk of lime and the gas of step c) is flushed around and/or through the static gas bubble comminution unit.

2. The process of claim 1 , wherein the gas of step c) further comprises at least one gas other than carbon dioxide and the gas of step c) is introduced at a rate of 0.06 to 5.00 kg gas/h per kg of dry Ca(OH) 2 with the proviso that the carbon dioxide is introduced at a rate of 0.05 to 3.50 kg CO 2 /h per kg of dry Ca(OH) 2 .

3. The process of claim 1 , wherein the aqueous solution of step b) consists of water.

4. The process of claim 1 , wherein the aqueous solution of step b) comprises one or more further additives selected from the group consisting of water soluble polymers, calcium carbonate nanoparticles, water-soluble calcium salts, and slaking additives.

5. The process of claim 1 , wherein the calcium oxide containing material of step a) and the aqueous solution of step b) are mixed in a mass ratio from 1:1 to 1:15.

6. The process of claim 1 , wherein the calcium oxide containing material of step a) and the aqueous solution of step b) are mixed in a mass ratio from 1:4 to 1:12.

7. The process of claim 1 , wherein the gas of step c) comprises between 4 and 99 vol.-% carbon dioxide, based on the total volume of the gas.

8. The process of claim 1 , wherein the gas of step c) comprises between 6 and 40 vol.-% carbon dioxide, based on the total volume of the gas.

9. The process of claim 1 , wherein the gas of step c) comprises between 8 and 25 vol.-% carbon dioxide, based on the total volume of the gas.

10. The process of claim 1 , wherein the gas in step e) is introduced at a rate of 0.06 to 5.00 kg gas/h per kg of dry Ca(OH) 2 , and/or the carbon dioxide is introduced at a rate of 0.05 to 3.50 kg CO 2 /h per kg of dry Ca(OH) 2 .

11. The process of claim 1 , wherein the gas in step e) is introduced at a rate of 0.09 to 4.00 kg gas/h per kg of dry Ca(OH) 2 , and/or the carbon dioxide is introduced at a rate of 0.07 to 2.00 kg CO 2 /h per kg of dry Ca(OH) 2 .

12. The process of claim 1 , wherein the gas in step e) is introduced at a rate of 0.12 to 3.00 kg gas/h per kg of dry Ca(OH) 2 , and/or the carbon dioxide is introduced at a rate of 0.10 to 1.50 kg CO 2 /h per kg of dry Ca(OH) 2 .

13. The process of claim 1 , wherein the precipitated calcium carbonate obtained in step e) has a specific surface area from 2.0 to 80.0 m 2 /g, measured using nitrogen and the BET method according to ISO 9277:1995.

14. The process of claim 1 , wherein the precipitated calcium carbonate obtained in step e) has a specific surface area from 2.5 to 13.0 m 2 /g, measured using nitrogen and the BET method according to ISO 9277:1995.

15. The process of claim 1 , wherein the precipitated calcium carbonate obtained in step e) is in a form of particles having a weight median particle size d 50 of between 1.0 and 9.0 μm.

16. The process of claim 1 , wherein the precipitated calcium carbonate obtained in step e) is in a form of particles having a weight median particle size d 50 of 1.2 and 3.7 μm; and wherein the carbonation is carried out in the absence of agitators and stirrers.

17. The process of claim 1 , wherein the precipitated calcium carbonate obtained in step e) is in a form of particles having a calcitic crystal form.

18. The process of claim 1 , wherein the milk of lime is stirred during step e).

19. The process of claim 1 , further comprising the steps of:
f) separating the precipitated calcium carbonate from the aqueous suspension obtained from step e), and optionally
g) drying the separated precipitated calcium carbonate obtained from step f).

20. The process of claim 19 , wherein step g) takes place.

21. The process of claim 20 , which further comprises a step h) of contacting at least a part of the surface of the precipitated calcium carbonate obtained from step g) with a surface-treatment agent.

Assignees

• Omya Int Ag

Inventors

• Spiegel Holger
• Kreuger Wolfgang
• Skrzypczak Mathieu
• Wenk Joe
• Dalton Michael
• Salonen Aaro
• Maurer Marc
• Gane Patrick A C
• Ridgway Catherine Jean

Classifications

• C01F11/181 Primary

  Preparation of calcium carbonate by carbonation of aqueous solutions and characterised by control of the carbonation conditions · CPC title

• C01P2004/62

  Submicrometer sized, i.e. from 0.1-1 micrometer · CPC title

• C01P2004/61

  Micrometer sized, i.e. from 1-100 micrometer · CPC title

• C01F11/182

  Preparation of calcium carbonate by carbonation of aqueous solutions and characterised by an additive other than CaCO3-seeds · CPC title

• D21H21/18

  Reinforcing agents · CPC title