Aerogel compositions for high temperature applications
US-2024360363-A1 · Oct 31, 2024 · US
US10259752B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10259752-B2 |
| Application number | US-201515314358-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 11, 2015 |
| Priority date | Jun 11, 2014 |
| Publication date | Apr 16, 2019 |
| Grant date | Apr 16, 2019 |
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A method of calcination includes providing a raw material including whitlockite Ca9(Mg,Fe2+)[PO3(OH)|(PO4)6], and/or iron phosphate FePO4, and/or aluminum phosphate AlPO4 and/or fluorapatite Ca5(PO4)3F; providing an alkaline-sulfuric compound as an additive; and calcining a mixture of the raw material with the additive to obtain a product, including a citrate soluble phosphate compound.
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The invention claimed is: 1. A method of calcination, comprising: providing a raw material comprising whitlockite Ca 9 (Mg,Fe 2+ )[PO 3 (OH)|(PO 4 ) 6 ], and/or iron phosphate FePO 4 , and/or aluminium phosphate AlPO 4 and/or fluorapatite Ca 5 (PO 4 ) 3 F; providing an alkaline-sulfuric compound as an additive; providing a carbonaceous reducing agent as a second additive; calcining a mixture of the raw material with the additives comprising reductive activation of the alkaline-sulfuric compound; and obtaining a product, wherein the product comprises a citrate soluble phosphate compound, wherein the carbonaceous reducing agent comprises a phosphorus containing material, selected from a sewage sludge or a biomass. 2. The method according to claim 1 , wherein the citrate soluble phosphate compound comprises CaNaPO 4 . 3. The method according to claim 1 , wherein the calcining proceeds under reducing conditions at a temperature of 800-1100° C. 4. The method according to claim 1 , wherein CaNaPO 4 is a main phosphate phase. 5. The method according to claim 1 , wherein the alkaline-sulfuric compound is selected from a sodium-sulfuric compound or a potassium sulphuric compound. 6. The method according to claim 1 , wherein the raw material contains a silicon, and an amount of the alkaline-sulfuric compound is correlated to a content of a phosphorus in the raw material and a content of the silicon. 7. The method according to claim 1 , wherein providing the alkaline-sulfuric compound is adapted to obtain in the mixture a molar ratio of Na:P of 1.1-1.8, and a molar ratio of Na:Si of 0.2-0.8, corresponding to an amount of 10 to 40 wt. % of the mixture. 8. The method according to claim 5 , wherein a first alkaline-sulfuric compound is at least partly substituted by a second alkaline-sulfuric compound comprising another alkali metal, and/or by an alkali metal carbonate, and/or by an alkali metal hydroxide. 9. The method according to claim 1 , wherein the calcining proceeds under reducing conditions at a temperature of 850-1000° C. 10. The method according to claim 1 , wherein a fraction of the carbonaceous reducing agent comprises a phosphorus containing material and is a dominant mass fraction. 11. The method according to claim 1 , wherein a sewage sludge ash contained in the raw material is completely substituted by a carbonaceous reducing agent comprising phosphorus containing material. 12. A method of calcination, comprising: providing a raw material comprising whitlockite Ca 9 (Mg,Fe 2+ )[PO 3 (OH)|(PO 4 ) 6 ], iron phosphate FePO 4 , aluminium phosphate AlPO 4 , or fluorapatite Ca 5 (PO 4 ) 3 F; providing an alkaline-sulfuric compound as an additive; providing a carbonaceous reducing agent as a second additive; calcining a mixture of the raw material with the additives comprising reductive activation of the alkaline sulfuric compound; obtaining a product, wherein the product comprises a citrate soluble phosphate compound; and controlling an atmosphere with respect to an oxygen concentration during calcining or during a cooling, wherein a content of sulfur in the product substantially corresponds to the content of sulfur in the mixture, wherein the raw material is an ash selected from a sewage sludge ash or a biomass ash. 13. The method according to claim 12 , wherein the content of sulfur is water soluble, at least partly, by mildly oxidizing the product by contact to an oxidizing atmosphere or air at a reduced temperature of 300-700° C. 14. The method according to claim 12 , wherein calcining is carried out at a temperature of 800-1100° C. to obtain a stable operation condition by avoiding a baking of the product. 15. The method according to claim 12 , further comprising: removing a heavy metal, comprising Pb, Cd, and Hg contained in the raw material by vaporization and sublimation of the reduced heavy metal species. 16. The method according to claim 15 , wherein reduction of a heavy metal is achieved by adding 10-20% of a phosphorus containing carbonaceous reducing agent and removing 30-50% of Pb, Cd, and Hg. 17. The method according to claim 15 , wherein reduction of a heavy metal is achieved by adding 25-75% of a phosphorus containing carbonaceous reducing agent and removing 40-70% of Pb, Cd, and Hg. 18. A method of calcination, comprising: providing a raw material comprising whitlockite Ca 9 (Mg,Fe 2+ )[PO 3 (OH)|(PO 4 ) 6 ], iron phosphate FePO 4 , aluminium phosphate AlPO 4 , or fluorapatite Ca 5 (PO 4 ) 3 F; providing an alkaline-sulfuric compound as an additive; providing a carbonaceous reducing agent as a second additive; calcining a mixture of the raw material with the additives comprising reductive activation of the alkaline sulfuric compound; and obtaining a product, wherein the product comprises a citrate soluble phosphate compound, wherein the alkaline-sulfuric compound is selected from a by-product of an industrial process selected from a rayon fiber production, a pulp manufacture, ora paper manufacture, or the alkaline-sulfuric compound is selected from biomass, sludge, refuse derived fuel or waste incineration. 19. A process for obtaining a citrate soluble phosphate compound from a P-containing raw material, the raw material comprising a P-phase selected from whitlockite Ca 9 (Mg,Fe 2+ )[PO 3 (OH)|(PO 4 ) 6 ], iron phosphate FePO 4 , aluminium phosphate AlPO 4 or fluorapatite Ca 5 (PO 4 ) 3 F, the process comprising: determining in the raw material a molar ratio of Na/Si and a molar ratio of Na/P; determining a quantity of a sodium-sulfuric compound based on the determined molar ratio of Na/Si and Na/P; calcining under reducing conditions the raw material together with the determined quantity of the sodium-sulfuric compound to obtain the citrate soluble phosphate compound; wherein the step of determining the quantity of the sodium sulfuric compound comprises: detecting a sodium quantity required to obtain by calcining the raw material the citrate soluble phosphate compound CaNaPO 4 by conversion of the P-phase; and calculating an amount of the sodium-sulfuric compound corresponding to the detected sodium quantity, wherein the sodium-sulfuric compound is selected from Na 2 S, Na 2 SO 3 , or Na 2 SO 4 . 20. The process according to claim 19 , wherein the sodium quantity is detected according to the following formula n Me =x·n P +y·n Si , wherein n Me is the amount of sodium expressed in moles, n P is the amount of phosphorus in the raw material expressed in moles, n Si is the amount of silica in the raw material expressed in moles, whereas x and y are coefficients expressing the consumption of alkali metal in alkali metal consuming reactions during calcining. 21. The process according to claim 20 wherein x is selected from the range of 0.8-1.8; and y is selected from the range of 0.25-0.6, and wherein the citrate solubility is detected with aqueous ammonium citrate and comprises 35-100% of a total P content. 22. The process according to claim 19 , further comprising: controlling an atmosphere with respect to an oxygen concentration during calcining or during a cooling. 23. The process according to claim 22 , wherein the step of controlling is adapted to prevent accumulation of a pyrite type iron-sulfur-compound Fe 7 S 8 ; to prevent complete combustion of the pyrite type iron-sulfur compound Fe 7 S 8 and/or to obtain a water soluble sulfuric compound with sodium sulfate as
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