Microstructured carbonatable calcium silicate clinkers and methods thereof

Patent metadata

Field	Value
Publication number	US-9926235-B2
Application number	US-201615074659-A
Country	US
Kind code	B2
Filing date	Mar 18, 2016
Priority date	Mar 20, 2015
Publication date	Mar 27, 2018
Grant date	Mar 27, 2018

Abstract

The invention provides novel, microstructured clinker and cement materials that are characterized by superior grindability and reactivity. The disclosed clinker and cement materials are based on carbonatable calcium silicate and can be made from widely available, low cost raw materials via a process suitable for large-scale production. The method of the invention is flexible in equipment and processing requirements and is readily adaptable to manufacturing facilities of conventional Portland cement.

First claim

What is claimed is:

1. A non-hydraulic clinker material, comprising
particles of uncarbonatable silica (SiO 2 ), having diameters from about 0.1 μm to about 1,000 μm, dispersed in a matrix comprising at least one carbonatable calcium silicate phase, wherein
the at least one carbonatable calcium silicate phase comprises at least one of wollastonite and pseudowollastonite and at least one of rankinite (Ca 3 Si 2 O 7 ) and belite (Ca 2 SiO 4 ), and
elemental Ca and elemental Si are present in the clinker at an atomic ratio from about 0.8 to about 1.2.

2. The clinker material of claim 1 , further comprising:
an intermediate layer, comprising melilite ((Ca,Na,K) 2 (Al,Mg,Fe)[(Al,Si)SiO 7 ]) and/or an amorphous phase and surrounding the particles of uncarbonatable silica.

3. The clinker material of claim 2 , wherein
the intermediate layer comprises an amorphous phase comprising one or more components selected from Al 2 O 3 , Fe 2 O 3 , MgO, K 2 O and Na 2 O.

4. The clinker material of claim 3 , wherein
the matrix further comprises one or more components selected from Al 2 O 3 , Fe 2 O 3 , MgO, K 2 O and Na 2 O.

5. The clinker material of claim 1 , wherein the clinker is suitable for carbonation with CO 2 at a temperature of about 30° C. to about 90° C. to form CaCO 3 , under an atmosphere of water and CO 2 having a pressure in the range from ambient atmospheric pressure to about 150 psi above ambient and having a CO 2 concentration ranging from about 10% to about 99% for about 1 hour to about 150 hours, with a mass gain of about 10% or more.

6. The clinker material of claim 5 , wherein the clinker is suitable for carbonation with CO 2 at a temperature of about 40° C. to about 80° C. to form CaCO 3 , under an atmosphere of water and CO 2 having a pressure in the range from ambient atmospheric pressure to about 40 psi above ambient and having a CO 2 concentration ranging from about 50% to about 95% for about 10 hour to about 50 hours, with a mass gain of about 10% or more.

7. The clinker material of claim 4 , comprising about 30% or less of metal oxides of Al, Fe and Mg by total oxide mass.

8. A composite material produced by carbonation of a clinker material of claim 1 .

9. A method for making a clinker material of claim 1 , comprising:
mixing one or more precursors to obtain a blended precursor composition wherein elemental Ca and elemental Si are present at an atomic ratio from about 0.8 to about 1.2 and metal oxides of Al, Fe and Mg are present at about 30% or less by mass; and
heating the blended precursor composition to a temperature between about 800° C. and about 1400° C. for a sufficient time to produce the clinker material.

10. The method of claim 9 , wherein metal oxides of Al, Fe and Mg are present at about 10% or less by mass.

11. The method of claim 9 , wherein the precursors are selected from limestone, sand, silts, sandstones, silica-rich clays and diatomaceous earths.

12. The method of claim 9 , wherein the blended precursor composition is heated to a temperature between about 900° C. and about 1,300° C. for a sufficient time to produce the clinker material.

13. The method of claim 9 , wherein the blended precursor composition is heated for a period of about 10 minutes hour to 5 hours.

14. The method of claim 9 , wherein heating the blended precursor composition is conducted under atmospheric pressure.

15. A powdery material produced by grinding the clinker material of claim 1 , wherein the powdery material is characterized by
a mean particle size (d50) of about 8 μm to about 25 μm, with 10% of particles (d10) sized below about 0.1 μm to about 3 μm, and 90% of particles (d90) sized between about 30 μm to about 100 μm; and
a surface at least 10% covered with the at least one carbonatable phase.

16. The powdery material of claim 15 , wherein the particles comprise single-phase particles and multi-phase particles.

Assignees

• Solidia Technologies Inc
• Lafarge Sa

Inventors

• Sahu Sadananda
• Quinn Sean
• Atakan Vahit
• Decristofaro Nicholas
• Meyer Vincent
• Comparet Cédric
• Walenta Günther

Classifications

• C04B2235/80

  Phases present in the sintered or melt-cast ceramic products other than the main phase · CPC title

• C04B2235/5436

  micrometer sized, i.e. from 1 to 100 micron · CPC title

• C04B2235/349

  Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite · CPC title

• C04B2235/3418

  Silicon oxide, silicic acids or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint · CPC title

• C04B2235/3272

  Iron oxides or oxide forming salts thereof, e.g. hematite, magnetite · CPC title