Methods and systems for treatment of lime to form vaterite
US-12077447-B2 · Sep 3, 2024 · US
US10294115B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10294115-B2 |
| Application number | US-201515518395-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 20, 2015 |
| Priority date | Oct 24, 2014 |
| Publication date | May 21, 2019 |
| Grant date | May 21, 2019 |
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The present invention is directed to a process for producing an aqueous suspension of precipitated calcium carbonate, wherein a milk of lime is prepared by mixing water, a calcium oxide containing material, and a precipitation enhancer, and subsequently, the milk of lime is carbonated to form an aqueous suspension of precipitated calcium carbonate.
Opening claim text (preview).
The invention claimed is: 1. A process for producing an aqueous suspension of precipitated calcium carbonate having a low portlandite content comprising the steps of: i) providing a calcium oxide containing material having a calcium oxide content of at least 90 wt.-%, ii) providing a precipitation enhancer selected from the group consisting of calcium carbonate nanoparticles, a water-soluble calcium salt, and a mixture thereof, wherein the calcium carbonate nanoparticles have a number based median particle size d 50 of from 30 to 70 nm, and a portlandite content of less than 1 wt.-%, based on the total dry weight of the calcium carbonate nanoparticles, iii) preparing a milk of lime by mixing, in any order, water, the calcium oxide containing material of step i), and the precipitation enhancer of step ii), wherein the precipitation enhancer is included in an amount from 0.01 to 25 wt.-%, based on the total weight of the calcium oxide containing material, and iv) carbonating the milk of lime obtained from step iii) until an aqueous suspension of precipitated calcium carbonate having a portlandite content of less than 1 wt.-%, based on the total dry weight of the precipitated calcium carbonate, is obtained. 2. The process of claim 1 , wherein step iii) comprises the steps of: a1) mixing the calcium oxide containing material of step i) with water, and a2) adding the precipitation enhancer of step ii) to the mixture of step a1). 3. The process of claim 1 , wherein step iii) comprises the steps of: b1) mixing the precipitation enhancer of step ii) with water, and b2) adding the calcium oxide containing material of step i) to the mixture of step b1). 4. The process of claim 1 , wherein the precipitation enhancer is calcium carbonate nanoparticles. 5. The process of claim 1 , wherein the precipitation enhancer is a water-soluble calcium salt. 6. The process of claim 5 , wherein the water-soluble calcium salt is an anhydrous salt or hydrate salt. 7. The process of claim 5 , wherein the water-soluble calcium salt is selected from the group consisting of calcium nitrate, calcium sulfate, calcium acetate, calcium benzoate, calcium bicarbonate, calcium bromate, calcium bromide, calcium chlorate, calcium chloride, calcium iodite, calcium nitrite, calcium perchlorate, calcium permanganate, hydrates thereof, and any mixture thereof. 8. The process of claim 5 , wherein the water-soluble calcium salt is selected from the group consisting of calcium nitrate, calcium sulfate, calcium acetate, calcium benzoate, calcium bicarbonate, calcium bromate, calcium bromide, calcium chlorate, calcium chloride, calcium iodite, calcium nitrite, calcium perchlorate, calcium permanganate, calcium nitrate tetrahydrate, calcium chloride dihydrate, and any mixture thereof. 9. The process of claim 5 , wherein the water-soluble calcium salt is selected from the group consisting of calcium nitrate, calcium nitrate tetra hydrate, calcium chloride, calcium chloride dihydrate, and any mixture thereof. 10. The process of claim 1 , wherein the precipitation enhancer of step ii) is added in an amount from 0.1 to 20 wt.-%, based on the total weight of the calcium oxide containing material. 11. The process of claim 1 , wherein the precipitation enhancer of step ii) is added in an amount from 1 to 15 wt.-%, based on the total weight of the calcium oxide containing material. 12. The process of claim 1 , wherein the precipitation enhancer of step ii) is added in an amount from 5 to 10 wt.-%, based on the total weight of the calcium oxide containing material. 13. The process of claim 1 , wherein a slaking additive is added before, during or after step iii). 14. The process of claim 13 , wherein the slaking additive is selected from the group consisting of an organic acid, an organic acid salt, a sugar alcohol, a monosaccharide, a disaccharide, a polysaccharide, a gluconate, a phosphonate, a lignosulfonate, and any mixture thereof. 15. The process of claim 13 , wherein the slaking additive is added in an amount from 0.01 to 2 wt.-%, based on the total amount of calcium oxide containing material. 16. The process of claim 13 , wherein the slaking additive is added in an amount from 0.05 to 1 wt.-%, based on the total amount of calcium oxide containing material. 17. The process of claim 13 , wherein the slaking additive is added in an amount from 0.06 to 0.8 wt.-%, based on the total amount of calcium oxide containing material. 18. The process of claim 13 , wherein the slaking additive is added in an amount from 0.07 to 0.5 wt.-%, based on the total amount of calcium oxide containing material. 19. The process of claim 1 , wherein the obtained suspension of precipitated calcium carbonate has a solids content of at least 5 wt.-%, based on the total weight of the suspension. 20. The process of claim 1 , wherein the obtained suspension of precipitated calcium carbonate has a solids content of from 10 to 50 wt.-%, based on the total weight of the suspension. 21. The process of claim 1 , wherein the obtained suspension of precipitated calcium carbonate has a solids content of from 12 to 45 wt.-%, based on the total weight of the suspension. 22. The process of claim 1 , wherein the obtained suspension of precipitated calcium carbonate has a solids content of from 14 to 40 wt.-%, based on the total weight of the suspension. 23. The process of claim 1 , wherein the obtained precipitated calcium carbonate has a portlandite content of less than 0.1 wt.-%, based on the total dry weight of the precipitated calcium carbonate. 24. The process of claim 1 , wherein the milk of lime is screened after step iii) and before step iv), with a screen having a sieve size from 100 to 300 μm. 25. A process for producing precipitated calcium carbonate comprising the steps i) to iv) of the process according to claim 1 , and step v) of separating the precipitated calcium carbonate from the aqueous suspension obtained from step iv). 26. The process of claim 25 , wherein the process further comprises step vi) of drying the separated precipitated calcium carbonate obtained from step v), and optionally a step vii) of contacting at least a part of the surface of the precipitated calcium carbonate with a surface-treatment agent. 27. The process of claim 25 , wherein the process further comprises step vi) of drying the separated precipitated calcium carbonate obtained from step v), and a step vii) of contacting at least a part of the surface of the precipitated calcium carbonate with a surface-treatment agent.
Particles with a specific particle size distribution · CPC title
Submicrometer sized, i.e. from 0.1-1 micrometer · CPC title
Preparation of calcium carbonate by carbonation of aqueous solutions and characterised by an additive other than CaCO3-seeds · CPC title
defined by measured X-ray, neutron or electron diffraction data · CPC title
Micrometer sized, i.e. from 1-100 micrometer · CPC title
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