US1955326A - Process for the manufacture of chromates and dichromates - Google Patents
Process for the manufacture of chromates and dichromates Download PDFInfo
- Publication number
- US1955326A US1955326A US512506A US51250631A US1955326A US 1955326 A US1955326 A US 1955326A US 512506 A US512506 A US 512506A US 51250631 A US51250631 A US 51250631A US 1955326 A US1955326 A US 1955326A
- Authority
- US
- United States
- Prior art keywords
- chromium
- chromates
- manufacture
- oxidizing
- dichromates
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G37/00—Compounds of chromium
- C01G37/14—Chromates; Bichromates
Definitions
- This invention relates to the manufacture'of chromates and dichromates.
- Chromates are in general manufactured by roasting chromium ores in the presence of alkali in a furnace at a high temperature.
- Such a process is usually effected by heating the finest ground chromium ore in admixture with sodium carbonate and lime in a stream of air to about 1000 C. and converting the extracted monochromate with sulphuric acid into dichromate.
- Another method consists in roasting the ore with a larger quantity of lime at 1200-1300 C. in a cement furnace and treating the calcium chromatelime mixture with sodium bisulphate.
- alkali chromate can be obtained by treating ferrochrome with fused caustic alkali.
- ferrochrome in the presence of alkali carbonate is converted into chromate by heating above 1000 C.
- the oxidation of metallic chromium, its alloys or mixtures containing chromium is effected in a very simple and economic manner.
- the process of the invention is by subjecting these substances to wet alkaline opening up treatment with oxidizing agents in particular oxidizing gases under pressure, whereby according to the quantity of alkali introduced either monochromate or dichromate or a mixture of monochrome and dichromate can be obtained as required. Since in the oxidation to dichromate, monochromate is first formed, it is clear that instead of alkalies also monochromates can be employed all of which are referred to herein as alkaline agents.
- alkaline agent may accordingly, for the purpose of positive definition, state that the term alkaline agent is used herein to designate a substance which behaves with relation to an acid as a base, and may include oxides, hydroxides, carbonates, and dicarbonates, of both alkali metals and alkaline earths as well as monochromates and other substances.
- chromium metal or its alloys or mixtures behave apparently as equivalents provided that they are applied in a suitably finely divided condition which is certainly also necessary in the case of chromium ore.
- chromium ore As a matter of fact it is the cheapest iron chromium alloys i. e. the most rich in carbon, which are easiest pulverized.
- the carbon advantageously the chemically combined carbon, is likewise taken up in the oxidizing process and appears in the form of carbon dioxide. It may therefore be recommended to remove the latter during the process or to bind it chemically in order not to increase the pressure in the apparatus unnecessarily.
- alkaline agents can be employed caustic alkalies, alkali carbonates, bicarbonates, monochromates and also alkaline earth and alkali metal oxides, hydroxides, carbonates, dicarbonates and monochromates or mixtures in which connection it may be remarked that the alkaline earths are less suited to the formation of dichromate.
- alkaline earths are less suited to the formation of dichromate.
- they are employed in aqueous solution or suspension.
- oxygen As oxidizing agents are advantageously employed oxygen, and oxygen containing or oxidizing gases.
- aqueous alkaline chromium suspension For the execution of the process it is suflicient to heat the aqueous alkaline chromium suspension to a suitable temperature and pressure and to force in the oxidizing gas before or during the working process.
- Example 2 kg. of ferrochrome of 68.2% Cr, 8-l0% C are well pulverized and heated in the presence of 100 kg. of caustic soda lye 40% and 900 kg. of water in a stirring autoclave for about 6 hours to 250-300 C. and oxygen or air passed through. After cooling the dichromate lye is separated from residue by filtration and worked up in the known manner.
- Example 3 54.5 parts of chromium powder 95-96% Cr content are heated with 210-220 parts of caustic soda lye 40% and about 200 parts of water in a stirring autoclave with oxygen or air for 4-6 hours under pressure to 150-250 C. After cooling the chromate lye is filtered from the residue of graphite or other impurities and worked up in the customary manner. The yield is practically quantitative.
- Example 4 7.170 kg. of ferrochrome of 72.5% Cr and 6.8% C. are well pulverized and heated with 100 litres of normal caustic soda lye in a stirring autoclave for 4-6 hours at 200-280 C. under pressure with oxygen or air. After cooling the dilute dichromate lye is separated from the residue and worked up.
- Example 5 152.5 parts of ferrochrome of 68.2% Cr and 8.10% C, well pulverized, are heated with 125 parts of calcium oxide (95-98%) or better with an equivalent quantity of slaked lime and about 400 parts of water for about 5-6 hours in the presence of oxygen to 150-250 C. After cooling, together with some chromate in solution, the majority of the chromate is found in the residue together with iron oxide and some graphite.
- the carbon dioxide formed in the oxidation can be removed in a suitable manner. This operation is to be recommended in particular in working with alkali carbonates.
- oxidizing agents which act in the presence of alkalies can be employed for the oxidation in the aqueous phase, as, for example, hydrogen peroxide, ozonized oxygen or air, halogens and the like, ferricyanides and the like, although oxygen or air are more economic.
- Process for the manufacture of monochromates and dichromates which comprises oxidizing a substance containing chromium in the presence of water and an alkaline agent by means of an oxidizing gas under pressure.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing ferro-chromium in the presence of water and a monochromate of an alkali metal by means of an oxidizing gas under pressure.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing a substance containing chromium in the presence of water and an alkaline agent by means of oxygen under pressure.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing a substance containing chromium in the presence of water and an alkaline agent by means of oxygen under pressure and removing the carbon dioxide produced.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing ferro-chromium in the presence of water and an alkaline agent by means of an oxidizing gas under pressure and removing the carbon dioxide produced.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing a substance containing chromium in the presence of water and an alkaline agent by means of oxygen under pressure and binding chemically the carbon dioxide produced.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing ferro-chromium in the presence of water and an alkaline agent by means of oxidizing gas under pressure and binding chemically the carbon dioxide produced.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing ferro-chromium in the presence of water and an alkaline agent by means of oxygen under pressure and binding chemically the carbon dioxide produced.
- Process for the manufacture of mono-chromates and dichromates which comprises oxidizing ferro-chromium in the presence of water and an alkaline agent by means of oxygen. under pressure and removing the carbon dioxide produced.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
- Compounds Of Iron (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR710771T | 1930-05-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1955326A true US1955326A (en) | 1934-04-17 |
Family
ID=9073021
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US512506A Expired - Lifetime US1955326A (en) | 1930-05-09 | 1931-01-30 | Process for the manufacture of chromates and dichromates |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US1955326A (fr) |
| CH (1) | CH156745A (fr) |
| DE (1) | DE547422C (fr) |
| FR (1) | FR710771A (fr) |
| GB (1) | GB364361A (fr) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430261A (en) * | 1942-01-26 | 1947-11-04 | Marvin J Udy | Production of chromium compounds |
| US2493789A (en) * | 1948-08-14 | 1950-01-10 | Marvin J Udy | Production of chromate |
| US2494215A (en) * | 1949-05-12 | 1950-01-10 | Marvin J Udy | Chromate production |
| US2754173A (en) * | 1956-07-10 | Method of manufacturing chromium | ||
| US3369861A (en) * | 1964-10-09 | 1968-02-20 | Marathon Oil Co | Method for producing ammonium chromate |
| US3393972A (en) * | 1964-06-09 | 1968-07-23 | Marathon Oil Co | Method for preparing ammonium chromate |
| US3403970A (en) * | 1964-06-02 | 1968-10-01 | Union Carbide Corp | Process for preparing chromates |
| WO2012058801A1 (fr) * | 2010-11-02 | 2012-05-10 | 天津派森科技有限责任公司 | Procédé d'oxydation hydrothermale pour la production de dichromate de métal alcalin à partir de ferrochrome présentant une certaine teneur en carbone |
| CN102897838A (zh) * | 2012-11-19 | 2013-01-30 | 四川省安县银河建化(集团)有限公司 | 一步法制备红矾钠的方法 |
-
1930
- 1930-05-09 FR FR710771D patent/FR710771A/fr not_active Expired
- 1930-05-29 DE DE1930547422D patent/DE547422C/de not_active Expired
-
1931
- 1931-01-23 GB GB2343/31A patent/GB364361A/en not_active Expired
- 1931-01-30 US US512506A patent/US1955326A/en not_active Expired - Lifetime
- 1931-03-06 CH CH156745D patent/CH156745A/fr unknown
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2754173A (en) * | 1956-07-10 | Method of manufacturing chromium | ||
| US2430261A (en) * | 1942-01-26 | 1947-11-04 | Marvin J Udy | Production of chromium compounds |
| US2493789A (en) * | 1948-08-14 | 1950-01-10 | Marvin J Udy | Production of chromate |
| US2494215A (en) * | 1949-05-12 | 1950-01-10 | Marvin J Udy | Chromate production |
| US3403970A (en) * | 1964-06-02 | 1968-10-01 | Union Carbide Corp | Process for preparing chromates |
| US3393972A (en) * | 1964-06-09 | 1968-07-23 | Marathon Oil Co | Method for preparing ammonium chromate |
| US3369861A (en) * | 1964-10-09 | 1968-02-20 | Marathon Oil Co | Method for producing ammonium chromate |
| WO2012058801A1 (fr) * | 2010-11-02 | 2012-05-10 | 天津派森科技有限责任公司 | Procédé d'oxydation hydrothermale pour la production de dichromate de métal alcalin à partir de ferrochrome présentant une certaine teneur en carbone |
| GB2501994A (en) * | 2010-11-02 | 2013-11-13 | Tianjin Passion Science And Technology Co Ltd | A hydrothermal oxidation method for production of alkali metal dichromate from carbon ferrochrome |
| US9157133B2 (en) | 2010-11-02 | 2015-10-13 | Tianjin Passion Science And Technology Co., Ltd. | Hydrothermal oxidation method for production of alkali metal dichromate from carbon ferrochrome |
| GB2501994B (en) * | 2010-11-02 | 2018-09-12 | Tianjin Passion Science And Tech Co Ltd | A hydrothermal oxidation method for production of alkali metal dichromate from carbon ferrochrome |
| CN102897838A (zh) * | 2012-11-19 | 2013-01-30 | 四川省安县银河建化(集团)有限公司 | 一步法制备红矾钠的方法 |
| CN102897838B (zh) * | 2012-11-19 | 2014-12-10 | 四川省银河化学股份有限公司 | 一步法制备红矾钠的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CH156745A (fr) | 1932-08-31 |
| DE547422C (de) | 1932-03-23 |
| GB364361A (en) | 1932-01-07 |
| FR710771A (fr) | 1931-08-28 |
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