GB460410A - Improvements in and relating to the treatment of silicate ores - Google Patents
Improvements in and relating to the treatment of silicate oresInfo
- Publication number
- GB460410A GB460410A GB1683836A GB1683836A GB460410A GB 460410 A GB460410 A GB 460410A GB 1683836 A GB1683836 A GB 1683836A GB 1683836 A GB1683836 A GB 1683836A GB 460410 A GB460410 A GB 460410A
- Authority
- GB
- United Kingdom
- Prior art keywords
- barium
- mixture
- silicate
- metazirconate
- zirconium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B33/00—Silicon; Compounds thereof
- C01B33/20—Silicates
- C01B33/26—Aluminium-containing silicates, i.e. silico-aluminates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Silicate ores containing, besides silica, one or more amphoteric metal oxides such as zirconium, titanium, aluminium, iron, or chromium oxide, and more particularly ores of zirconium, thorium, or beryllium are calcined with a barium compound such as barium carbonate in such amount that the silica is converted to dibarium silicate and one or more of the amphoteric metals to the barium salt thereof, fluxing additions or an excess of barium carbonate which would tend to fuse the mixture at the operating temperature of say 1400 DEG C. being avoided. Reaction may be effected in a rotary or tunnel furnace, the ore and barium carbonate being briquetted in the latter case. In the case of zircon, a mixture of dibarium silicate and barium metazirconate is obtained which may be used as a refractory. Or the mixture may be crushed with hot water to form and remove barium hydroxide and leave a mixture of monobarium silicate and barium metazirconate, the latter mixture being treated either with hot sodium or potassium carbonate solution to form and remove sodium or potassium silicate, or first with carbon dioxide to form silicic acid, and then with caustic soda to form and remove sodium silicate. In either case a mixture of barium carbonate and metazirconate remains, which may be calcined at 1400--1500 DEG C. to obtain a refractory consisting of barium orthozirconate, and the latter, if desired, may be reheated with zirconium oxide to obtain a refractory consisting of the metazirconate. The products contain barium titanate and ferrate, and a small amount of lime and magnesia, if these bases are present in the ore. In a modification, the barium carbonate-metazirconate mixture may be treated with hydrochloric acid to obtain a solution of zirconium and barium chlorides, the solution be first treated with ammonia to precipitate zirconium hydroxide which is calcined to the oxide to obtain a refractory containing a little titanium and iron, and then with carbon dioxide to precipitate barium carbonate which may be re-used; or the solution may be added to sulphuric acid, gypsum, or a soluble sulphate to precipitate barium sulphate, and the zirconium then be precipitated by lime.ALSO:Zirconium silicate ore (zircon) is calcined at 1400 DEG C. with a barium compound such as barium carbonate to obtain a refractory comprising a mixture of dibarium silicate and barium metazirconate. The mixture may be crushed with hot water to obtain a mixture of monobarium silicate and barium metazirconate, from which by removing silica as alkali silicate by means of alkali carbonate a mixture of barium carbonate and metazirconate may be obtained. The latter mixture may be calcined at 1400-1500 DEG C. to obtain a refractory consisting of barium orthozirconate, and the latter, if desired, may be reheated with zirconium oxide to obtain a refractory consisting of the metazirconate. The products contain barium titanate and ferrate, and a small amount of lime and magnesia, if these bases are present in the ore.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1683836A GB460410A (en) | 1936-06-17 | 1936-06-17 | Improvements in and relating to the treatment of silicate ores |
ES0143704A ES143704A1 (en) | 1936-06-17 | 1937-06-11 | IMPROVEMENTS IN AND RELATED TO THE TREATMENT OF SILICAO MINERALS AND THEIR LIKES |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1683836A GB460410A (en) | 1936-06-17 | 1936-06-17 | Improvements in and relating to the treatment of silicate ores |
Publications (1)
Publication Number | Publication Date |
---|---|
GB460410A true GB460410A (en) | 1937-01-27 |
Family
ID=10084584
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1683836A Expired GB460410A (en) | 1936-06-17 | 1936-06-17 | Improvements in and relating to the treatment of silicate ores |
Country Status (2)
Country | Link |
---|---|
ES (1) | ES143704A1 (en) |
GB (1) | GB460410A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2743160A (en) * | 1952-01-31 | 1956-04-24 | Wainer Eugene | Preparation of alkali metal double fluorides of zirconium and hafnium |
US2744060A (en) * | 1952-10-09 | 1956-05-01 | Du Pont | Process for separating hafnium tetrachloride from zirconium tetrachloride |
WO2020206892A1 (en) * | 2019-04-08 | 2020-10-15 | 原初科技(北京)有限公司 | System and method for preparing ultrafine silica by leaching silicate ore using hydrogen chloride gas |
CN112591758A (en) * | 2021-01-08 | 2021-04-02 | 景德镇皓旭陶瓷原料有限公司 | Method for efficiently recycling zirconium and silicon in zirconium slag |
CN115667151A (en) * | 2020-05-27 | 2023-01-31 | 松下知识产权经营株式会社 | Barium compound structure and method for producing same |
-
1936
- 1936-06-17 GB GB1683836A patent/GB460410A/en not_active Expired
-
1937
- 1937-06-11 ES ES0143704A patent/ES143704A1/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2743160A (en) * | 1952-01-31 | 1956-04-24 | Wainer Eugene | Preparation of alkali metal double fluorides of zirconium and hafnium |
US2744060A (en) * | 1952-10-09 | 1956-05-01 | Du Pont | Process for separating hafnium tetrachloride from zirconium tetrachloride |
WO2020206892A1 (en) * | 2019-04-08 | 2020-10-15 | 原初科技(北京)有限公司 | System and method for preparing ultrafine silica by leaching silicate ore using hydrogen chloride gas |
US12011702B2 (en) | 2019-04-08 | 2024-06-18 | Yuanchu Technology (Beijing) Co., Ltd. | System and method for preparing ultrafine silica by leaching silicate ore using hydrogen chloride gas |
CN115667151A (en) * | 2020-05-27 | 2023-01-31 | 松下知识产权经营株式会社 | Barium compound structure and method for producing same |
CN115667151B (en) * | 2020-05-27 | 2024-03-12 | 松下知识产权经营株式会社 | Barium compound structure and method for producing same |
CN112591758A (en) * | 2021-01-08 | 2021-04-02 | 景德镇皓旭陶瓷原料有限公司 | Method for efficiently recycling zirconium and silicon in zirconium slag |
Also Published As
Publication number | Publication date |
---|---|
ES143704A1 (en) | 1937-07-16 |
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