GB396717A - Improvements in the manufacture and production of cobalt nitrosocarbonyl - Google Patents
Improvements in the manufacture and production of cobalt nitrosocarbonylInfo
- Publication number
- GB396717A GB396717A GB3691/32A GB369132A GB396717A GB 396717 A GB396717 A GB 396717A GB 3691/32 A GB3691/32 A GB 3691/32A GB 369132 A GB369132 A GB 369132A GB 396717 A GB396717 A GB 396717A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cobalt
- nitric oxide
- carbon monoxide
- metallic
- treated
- 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
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G51/00—Compounds of cobalt
- C01G51/80—Compounds containing cobalt, with or without oxygen or hydrogen, and containing one or more other elements
- C01G51/82—Compounds containing cobalt, with or without oxygen or hydrogen, and containing two or more other elements
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Cobalt nitrosocarbonyl and/or cobalt nitrosyl are obtained by acting with nitric oxide, if necessary together with carbon monoxide, upon metallic cobalt or a material containing cobalt in the metallic state or in a state from which it can be reduced to metallic cobalt by the reducing gases present, such as excess of carbon monoxide. The gas mixture may also contain inert gases such as nitrogen. When cobalt nitrosocarbonyl is being produced the nitric oxide may be wholly or in part replaced by substances supplying it such as nitrates or liquid solutions of nitric oxide. Normal, increased or reduced pressure may be employed with room temperature or elevated temperatures not exceeding 250 DEG C. Ores or waste products containing a small amount of cobalt may be converted into the nitroso compounds; the conversion may be preceded by pretreatment such as roasting, conversion into oxides, loosening in order to increase superficial area or reduction to the metallic state. Substances such as copper which facilitate the production of the nitroso compounds may be added. The nitroso compounds may be burnt, or thermally decomposed in the presence of inert gases, to form cobalt oxide, thermally decomposed in the presence of reducing gases such as hydrogen to form metallic cobalt or treated with strong mineral acids to form cobalt salts. According to examples, (1) a precipitate obtained by adding lime to a solution of cobalt sulphate is reduced with hydrogen at 350 DEG C. and then treated with carbon monoxide containing 1 per cent nitric oxide at 60-70 DEG C. and atmospheric pressure to produce cobalt nitroso carbonyl; (2) cobalt nitrate is evaporated to dryness with lime and the resulting mass is treated with flowing carbon monoxide at 240 DEG C. and 200 atmospheres pressure to produce cobalt nitroso carbonyl; (3) an industrial waste containing calcium sulphate and oxides of iron, copper and cobalt is dried, reduced by hydrogen at 380 DEG C. and treated with carbon monoxide containing 5 per cent nitric oxide at 160-180 DEG C. to produce cobalt nitroso carbonyl; (4) a reduced material prepared as in the preceding example is treated at atmospheric pressure and 150 DEG C. with carbon monoxide containing 10 per cent nitric oxide to produce a mixture of cobalt nitroso carbonyl with cobalt nitrosyl; (5) a reduced material prepared as in example (3) is treated at atmospheric pressure and 150-180 DEG C. with a mixture of nitrogen and nitric oxide to produce cobalt nitrosyl. The Provisional Specifications describe also the employment of nitrogen oxides in general in the process.ALSO:Cobalt nitrosocarbonyl and/or cobalt nitrosyl, obtained by the action of nitric oxide together if necessary with carbon monoxide upon metallic cobalt or materials capable of yielding metallic cobalt, may be thermally decomposed in the presence of reducing gases such as hydrogen to produce metallic cobalt.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3691/32A GB396717A (en) | 1932-02-08 | 1932-02-08 | Improvements in the manufacture and production of cobalt nitrosocarbonyl |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3691/32A GB396717A (en) | 1932-02-08 | 1932-02-08 | Improvements in the manufacture and production of cobalt nitrosocarbonyl |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB396717A true GB396717A (en) | 1933-08-08 |
Family
ID=9763129
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3691/32A Expired GB396717A (en) | 1932-02-08 | 1932-02-08 | Improvements in the manufacture and production of cobalt nitrosocarbonyl |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB396717A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113265548A (en) * | 2021-04-21 | 2021-08-17 | 内蒙古兴安铜锌冶炼有限公司 | Enrichment and recovery method of cobalt in cobalt removal agent cobalt slag |
-
1932
- 1932-02-08 GB GB3691/32A patent/GB396717A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN113265548A (en) * | 2021-04-21 | 2021-08-17 | 内蒙古兴安铜锌冶炼有限公司 | Enrichment and recovery method of cobalt in cobalt removal agent cobalt slag |
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