GB492344A - Improved treatment of ammoniacal solutions of metal salts - Google Patents
Improved treatment of ammoniacal solutions of metal saltsInfo
- Publication number
- GB492344A GB492344A GB7981/37A GB798137A GB492344A GB 492344 A GB492344 A GB 492344A GB 7981/37 A GB7981/37 A GB 7981/37A GB 798137 A GB798137 A GB 798137A GB 492344 A GB492344 A GB 492344A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ammonia
- acid
- copper
- passed
- ammoniacal
- 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
- C22B15/00—Obtaining copper
- C22B15/0063—Hydrometallurgy
-
- 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)
- Removal Of Specific Substances (AREA)
Abstract
Ammoniacal metal salt solutions, after clarification if necessary, are passed through a cation exchanger of acid character whereby the metals in complex solution are absorbed in the form of ammine while the ammonia passes through unabsorbed. Suitable exchangers are coal activated with acid, resins having an acid character, e.g. as described in Specification 450,308, silica gel and hydrogen zeolites. The ammoniacal filtrate may then be re-used as such, if desired after replenishment with ammonia, e.g. in metallurgical leaching. Alternatively, the ammonia may be retained in a subsequent filter charged with an absorbent of feeble acid character, i.e. silica gel, from which the ammonia may be recovered by thermal treatment, e.g. by means of steam. The exchanger charged with metal values may be regenerated by treatment with a suitable acid, the resulting solution containing salts of the metals and ammonium salt equivalent to the ammonia content of the metal ammine. If desired, the ammonium content of the metal ammine can be wholly or partly removed by heat treatment prior to the acid treatment. A selective removal of heavy metals from a solution may be achieved by the use of hydrogen ion exchangers which exert selective absorption. If in the subsequent stage, it is desired to recover also the ammonia present as ammonium salt, the liquid is passed through a hydrogen ion exchanger of strong acid character, e.g. a sulphonated resin, which may be regenerated by treatment with acid with the formation of the corresponding ammonium salt. If it is desired to recover the total ammonia as free ammonia, the filtrate is passed through a hydroxyl ion exchanger, e.g. an amine resin as described in Specification 450,309, the ammonia now present in the free form being finally bound by an absorbent having having a feeble acid character. According to examples: (1) an ammoniacal copper solution is passed first through silica gel in which copper tetramine is absorbed and subsequently recovered by treating the gel with hydrochloric acid and then through further silica gel in which the ammonia is absorbed and recovered by treatment with steam; (2) an ammoniacal solution containing copper, zinc, cobalt and traces of silver obtained by leaching burnt copper pyrites with aqueous ammonia containing ammonium chloride is passed through a condensate of phenol sulphonic acid with formaldehyde, the filtrate after replenishment with ammonia being returned to the leaching step and the absorbent being regenerated as described in example (1); (3) silica gel is shown to be more favourable to the absorption of zinc, and anthracite sulphonated with oleum more favourable to the absorption of copper, when brought into contact with an ammoniacal solution containing both these metals; (4) an ammoniacal solution containing copper and zinc is passed through a battery of filters consisting of a phenol-formaldehyde condensation product containing-o -sulphonic acid groups, the copper being absorbed prior to the zinc.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE492344X | 1936-04-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB492344A true GB492344A (en) | 1938-09-19 |
Family
ID=6544396
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7981/37A Expired GB492344A (en) | 1936-04-04 | 1937-03-18 | Improved treatment of ammoniacal solutions of metal salts |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB492344A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1056825B (en) * | 1956-03-07 | 1959-05-06 | Wolfen Filmfab Veb | Process for the preparation of insoluble nitrogen-containing cation exchange resins |
GB2146316A (en) * | 1983-09-08 | 1985-04-17 | Little Inc A | Precious metals recovery |
-
1937
- 1937-03-18 GB GB7981/37A patent/GB492344A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1056825B (en) * | 1956-03-07 | 1959-05-06 | Wolfen Filmfab Veb | Process for the preparation of insoluble nitrogen-containing cation exchange resins |
GB2146316A (en) * | 1983-09-08 | 1985-04-17 | Little Inc A | Precious metals recovery |
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