GB987224A - A process for the extraction of gallium - Google Patents
A process for the extraction of galliumInfo
- Publication number
- GB987224A GB987224A GB1222561A GB1222561A GB987224A GB 987224 A GB987224 A GB 987224A GB 1222561 A GB1222561 A GB 1222561A GB 1222561 A GB1222561 A GB 1222561A GB 987224 A GB987224 A GB 987224A
- Authority
- GB
- United Kingdom
- Prior art keywords
- gallium
- amalgam
- sodium
- column
- electropositive
- 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
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B58/00—Obtaining gallium or indium
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Gallium is recovered from an aqueous alkali metal solution poor in gallium by treating the solution countercurrently with a liquid amalgam of a metal more electropositive than gallium, one of the two solutions being divided into droplets to increase the contact area between the two solutions. At periodic intervals the amalgam containing the gallium and a portion of the metal more electropositive than gallium is separated from the reaction mixture and the gallium recovered by distilling off the mercury, or by treating the amalgam with an acid, with water or with dilute NaOH. Gallium may then be separated from the extraction liquors by electrolytic methods. Temperatures from room temperature to 100 DEG C. may be used for the recovery step; the preferred alkali metal more electropositive than gallium is sodium and the amalgam preferably contains 0.2 to 0.3% by weight of sodium. In one method the amalgam is divided into droplets (by causing it to pass down through a perforated plate at the top of a column) which fall through an aqueous solution containing sodium gallate which flows upwardly through the column which is preferably packed, for example with Raschig rings. The amalgam which is preferably periodically replenished with sodium, and the aqueous solution are recycled until the amalgam has absorbed enough gallium to allow economic recovery. According to another embodiment, the vertical cylindrical column is provided with a series of horizontal perforated plates each of which occupies the entire cross-section of the column and each of which is pierced by a vertical overflow tube. The alkaline solution containing the sodium gallate flows upwardly through the column and is divided into fine droplets by the perforations in the plates and the amalgam is introduced on to the uppermost plate. By adjusting the flow rate of the aqueous solution the amalgam is prevented from passing through the perforations in the plates but instead passes through the overflow on to the next plate. After sufficient gallium has been absorbed by the amalgam, the latter is withdrawn from the foot of the column, the gallium recovered and the amalgam regenerated. The invention is applicable to the extraction of gallium from a sodium aluminate solution containing sodium gallate (the solution being obtained by bauxite extraction with NaOH).ALSO:Gallium is recovered from an aqueous alkali metal solution poor in gallium by treating the solution countercurrently with a liquid amalgam of a metal more electropositive than gallium, one of the two solutions being divided into droplets to increase the contact area between the two solutions. At periodic intervals the amalgam containing the gallium and a portion of the metal more electropositive than gallium is separated from the reaction mixture and the gallium recovered by distilling off the mercury, or by treating the amalgam with an acid, with water or with dilute NaOH. Gallium may then be separated from the extraction liquors by electrolytic methods. Temperatures from room temperature to 100 DEG C. may be used for the recovery step; the preferred alkali metal more electropositive than gallium is sodium and the amalgam preferably contains 0.2-0.3 by weight of sodium. In one method the amalgam is divided into droplets (by causing it to pass down through a perforated plate at the top of a column) which fall through an aqueous solution containing sodium gallate which flows upwardly through the column which is preferably packed, for example with Raschig rings. The amalgam which is preferably replenished with sodium, and the aqueous solution are recycled until the amalgam has absorbed enough gallium to allow economic recovery. According to another embodiment, the vertical cylindrical column is provided with a series of horizontal perforated plates each of which occupies the entire cross-section of the column and each of which is pierced by a vertical overflow tube. The alkaline solution containing the sodium gallate flows upwardly through the column and is divided into fine droplets by the perforations in the plates and the amalgam is introduced on to the uppermost plate. By adjusting the flow rate of the aqueous solution the amalgam is prevented from passing through the perforations in the plates but instead passes through the overflow tube on to the next plate. The invention is applicable to the extraction of gallium from a sodium aluminate solution containing sodium gallate (the solution being obtained by bauxite extraction with NaOH).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR823544A FR1261344A (en) | 1960-04-06 | 1960-04-06 | Gallium extraction |
Publications (1)
Publication Number | Publication Date |
---|---|
GB987224A true GB987224A (en) | 1965-03-24 |
Family
ID=8728735
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1222561A Expired GB987224A (en) | 1960-04-06 | 1961-04-05 | A process for the extraction of gallium |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE602210A (en) |
CH (1) | CH414174A (en) |
FR (1) | FR1261344A (en) |
GB (1) | GB987224A (en) |
IT (1) | IT649828A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102976394A (en) * | 2012-12-14 | 2013-03-20 | 中国铝业股份有限公司 | Method for extracting gallium hydroxide from vanadium slag |
-
0
- IT IT649828D patent/IT649828A/it unknown
-
1960
- 1960-04-06 FR FR823544A patent/FR1261344A/en not_active Expired
-
1961
- 1961-04-05 GB GB1222561A patent/GB987224A/en not_active Expired
- 1961-04-05 CH CH397261A patent/CH414174A/en unknown
- 1961-04-05 BE BE602210A patent/BE602210A/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR1261344A (en) | 1961-05-19 |
IT649828A (en) | 1900-01-01 |
CH414174A (en) | 1966-05-31 |
BE602210A (en) | 1961-10-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3653812A (en) | Process for removal of sulfur dioxide from gas streams | |
US4032616A (en) | Process for the production of sodium bicarbonate from diaphram cell liquors | |
US4321410A (en) | Method of stripping unreacted materials in urea synthesis process | |
GB1133230A (en) | Gas or liquid/liquid counter-current extraction process | |
US2837408A (en) | Process and apparatus for the catalytic decomposition of alkali metal amalgams | |
US2029467A (en) | Distillation of ammonia from aqueous ammoniacal brines | |
GB987224A (en) | A process for the extraction of gallium | |
US2732284A (en) | sakowski | |
US2529803A (en) | Photochemical preparation of gamma benzene hexachloride | |
US2938771A (en) | Method of making hyposulfites | |
US3453072A (en) | Method of producing oxide and hydroxide of zinc | |
US3306712A (en) | Extraction of lithium halides from calcium-containing brines in the presence of urea and alcohol-ketone | |
US4061718A (en) | Method for the recovery of ammonia from liquor from the filters of ammonia-soda plants | |
GB159086A (en) | An improved process of producing oxide of aluminium from chloride of aluminium | |
US1401937A (en) | Purification of maleic acid by reducing agents | |
US2995424A (en) | Hydrogen peroxide via tetrahydroanthraquinone | |
US1708287A (en) | Method of recovering iodine | |
US2375977A (en) | Preparation of alumina from clay | |
US2227948A (en) | Production of epichlorhydrin | |
SU843728A3 (en) | Method of producing chlorocyan and hydrogen chloride | |
GB452302A (en) | Improvements in and apparatus for the manufacture of alkaline liquors or salt solutions | |
US3420757A (en) | Mercury cathode electrolysis | |
US2148971A (en) | Process for the recovery of pure, concentrated sulphur dioxide | |
US3197505A (en) | Process for the preparation of cyclohexanoneoxime from the oxidation products of cyclohexane | |
US4808761A (en) | Demethanolization of aqueous CH3 OH/HCl solutions |