Carbonatable calcium silicate-based cements and concretes having mineral additives, and methods thereof
US-2018273430-A1 · Sep 27, 2018 · US
US10611690B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10611690-B2 |
| Application number | US-201816194685-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 19, 2018 |
| Priority date | Aug 4, 2014 |
| Publication date | Apr 7, 2020 |
| Grant date | Apr 7, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention provides novel carbonatable calcium silicate compositions and carbonatable calcium silicate phases that are made from widely available, low cost raw materials by a process suitable for large-scale production. The method of the invention is flexible in equipment and production requirements and is readily adaptable to manufacturing facilities of conventional cement. The invention offers an exceptional capability to permanently and safely sequesters CO2.
Opening claim text (preview).
What is claimed is: 1. A carbonatable calcium silicate composition in powder form having 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 above about 35 μm to about 100 μm, wherein the composition comprises: calcium silicate in the form of one or more discrete crystalline calcium silicate phases selected from CS (wollastonite or pseudowollastonite), C3S2(rankinite), and C2S (belite, larnite, bredigite), and calcium silicate in the form of an amorphous calcium silicate phase, wherein the one or more discrete crystalline calcium silicate phases are present at about 30% or more by mass of the total phases; elemental Ca and elemental Si are present in the composition at a molar ratio from about 0.8 to about 1.2; and metal oxides of Al, Fe and Mg are present in the composition at about 30% or less by mass, wherein the composition is carbonatable with CO 2 at a temperature of about 30° C. to about 90° C. to form CaCO 3 with a mass gain of about 10% or more. 2. The carbonatable composition of claim 1 , wherein the ratio of d90:d10 is about 5 to about 1,000. 3. The carbonatable composition of claim 1 , wherein the ratio of d50:d10 is about 2 to about 250. 4. The carbonatable composition of claim 1 , wherein the ratio of d90:d50 is about 2 to about 15. 5. The carbonatable composition of claim 1 , comprising one or more residual SiO 2 and CaO phases. 6. The carbonatable composition of claim 1 , comprising one or more melilite phases having the general formula (Ca,Na,K) 2 [(Mg, Fe 2+ ,Fe 3+ ,Al,Si) 3 O 7 ] or ferrite phases having the general formula Ca 2 (Al,Fe 3+ ) 2 O 5 . 7. The carbonatable composition of claim 1 , wherein the composition comprises calcium silicate phases existing in an amorphous state and calcium silicate phases existing in a crystalline state. 8. The carbonatable composition of claim 1 , wherein the molar ratio of elemental Ca to elemental Si is from about 0.90 to about 1.10. 9. The carbonatable composition of claim 1 , comprising about 25% or less of metal oxides of Al, Fe and Mg by total oxide mass. 10. The carbonatable composition of claim 1 , wherein CS is present at about 10 wt % to about 60 wt %, C3S2 in about 5 wt % to 50 wt %, C2S in about 5 wt % to 60 wt %, and CaO in about 0 wt % to 3 wt %. 11. The carbonatable composition of claim 10 , wherein CS is present at about 20 wt % to about 60 wt %, C3S2 in about 10 wt % to 50 wt %, C2S in about 10 wt % to 50 wt % and CaO in about 0 wt % to 3 wt %. 12. A carbonated material produced from the carbonatable calcium silicate composition of claim 1 via carbonation at a temperature of about 30° C. to about 90° C.
Hydraulic cements not provided for in one of the groups C04B7/02 - C04B7/34 · CPC title
Belite cements, e.g. self-disintegrating cements based on dicalciumsilicate · CPC title
Lime cements or magnesium oxide cements · CPC title
the Ca-silicates being present in the starting mixture · CPC title
Carbon capture and storage [CCS] · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.