US1924710A - Process for the manufacture of dichromates - Google Patents
Process for the manufacture of dichromates Download PDFInfo
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- US1924710A US1924710A US512507A US51250731A US1924710A US 1924710 A US1924710 A US 1924710A US 512507 A US512507 A US 512507A US 51250731 A US51250731 A US 51250731A US 1924710 A US1924710 A US 1924710A
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- chromate
- chromium
- alkali
- dichromates
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- 238000000034 method Methods 0.000 title description 34
- 238000004519 manufacturing process Methods 0.000 title description 19
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 36
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 31
- 239000011651 chromium Substances 0.000 description 29
- 229910052804 chromium Inorganic materials 0.000 description 28
- 239000003513 alkali Substances 0.000 description 24
- 230000001590 oxidative effect Effects 0.000 description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 18
- 239000001301 oxygen Substances 0.000 description 18
- 229910052760 oxygen Inorganic materials 0.000 description 18
- 239000007789 gas Substances 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 230000003647 oxidation Effects 0.000 description 13
- 238000007254 oxidation reaction Methods 0.000 description 13
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 10
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 8
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 7
- 235000011941 Tilia x europaea Nutrition 0.000 description 7
- 239000004571 lime Substances 0.000 description 7
- XVOFZWCCFLVFRR-UHFFFAOYSA-N oxochromium Chemical class [Cr]=O XVOFZWCCFLVFRR-UHFFFAOYSA-N 0.000 description 7
- 239000001569 carbon dioxide Substances 0.000 description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 description 6
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 5
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 5
- 229910000423 chromium oxide Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 235000011121 sodium hydroxide Nutrition 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- JHWIEAWILPSRMU-UHFFFAOYSA-N 2-methyl-3-pyrimidin-4-ylpropanoic acid Chemical compound OC(=O)C(C)CC1=CC=NC=N1 JHWIEAWILPSRMU-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- -1 alkali metal chromate Chemical class 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 150000007514 bases Chemical class 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-M bisulphate group Chemical group S([O-])(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 4
- BCFSVSISUGYRMF-UHFFFAOYSA-N calcium;dioxido(dioxo)chromium;dihydrate Chemical compound O.O.[Ca+2].[O-][Cr]([O-])(=O)=O BCFSVSISUGYRMF-UHFFFAOYSA-N 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 229910021653 sulphate ion Inorganic materials 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910000604 Ferrochrome Inorganic materials 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 239000006286 aqueous extract Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- VQWFNAGFNGABOH-UHFFFAOYSA-K chromium(iii) hydroxide Chemical compound [OH-].[OH-].[OH-].[Cr+3] VQWFNAGFNGABOH-UHFFFAOYSA-K 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 241001600451 Chromis Species 0.000 description 1
- 229910000599 Cr alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CFIGYZZVJNJVDQ-LMJOQDENSA-N Indomethacin farnesil Chemical compound CC1=C(CC(=O)OC\C=C(/C)CC\C=C(/C)CCC=C(C)C)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CFIGYZZVJNJVDQ-LMJOQDENSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000788 chromium alloy Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- UJRBOEBOIXOEQK-UHFFFAOYSA-N oxo(oxochromiooxy)chromium hydrate Chemical compound O.O=[Cr]O[Cr]=O UJRBOEBOIXOEQK-UHFFFAOYSA-N 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
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
- Dichromates in particular sodium dichromate, are technically manufactured in such a manner that the alkali chromates obtained by the oxidizing opening up of chromium ore in the presence of alkalies or alkali carbonates are treated withsulphuric acid or also bisulphate, whereby one equivalent of alkali is taken from the neutral chromate and separated in the form of valkali sulphate.
- sodium dichromate is manu-' factured in this manner this causes a quite considerable loss of alkali since sodium sulphate can no longer be passed back into the process.
- As it also always contains small quantitiesoi chromate which render it discoloured the sulphate is mostly a troublesome valueless secondary product and is consigned as waste.
- Another method is that through calcium chromate which is obtained by the oxidizing opening up of chrome ore with lime at very high temperature. In this case the excess of lime must be neutralized and the calcium chromate treated with sodium bisulphate. Accordingly very large quantities of bisulphate are necessary. Now however since the manufacture of nitric acid from ammonia the bisulphate is obtained less and less as a waste product so that the calcium chromate process is greatly endangered.
- alkali chromate obtained in the known manner is treatedin the aqueous phase together with an equivalent quantity of chromium hydroxide, hydrated chromiumi oxide, chromium oxide or also metallic chromium or alloys or mixtures containing chromium at temperatures above 100 C. under pressure with oxygen or gases containing oxygen.
- the content of chromate and if desired also the content offree alkali maybe determined and the addition. of trivalent chromi'um containing oxygen correspondingly ascertained.
- trivalent chromium oxygen compounds also chromium metal or its alloys such as ferrochrome can be added. 7
- the mixture is nowheated in the aqueous phase with gases containing oxygen underpressure to a temperature above 100 C. suitably to 250300 C; whereby the whole of the chromium added is converted into dichromate.
- gases containing oxygen underpressure to a temperature above 100 C. suitably to 250300 C; whereby the whole of the chromium added is converted into dichromate.
- the alkali infree' state or combined under the form of monochromate is thereby entirely utilized and the cost of sulphuric acid or bi'sulphate'is saved.
- the trivalent chromium oxygen compound, in theform of chromium hydroxide, hydrated chromium oxide or chromium oxide can be produced by known processes and it is also in this case quite unnecessary that it should be isolated in the purecondition prior'to the further'working up. If it-is obtained for example by reduction of a chromate frit then after reduction the mass is extracted with water'in' order to removethe alkali'content and the residue is conveyed to the oxidation process. Even if it is possible directly to convert a reduced fritin the presence of an equivalent quantity of.
- the material containing chromium oxide hydrate is separated by filtration and washing from the caustic lye which, after suitable concentration, is again brought back into the process.
- Example 2 300 parts of chrome ore 50 percent CrzOs content, 220 parts of sodium carbonate, parts of 'C. and the pressure adjusted with oxygen to about '100 kg.
- the dichromate solution is separated from the residue, by filtration and worked up in the known manner.
- the carbon dioxide ob tained by oxidation of the carbon content is bound by the lime present.
- the pressure oxidation can also take place with equal success by forcing in air.
- the carbon dioxide is continuously removed with theair rich in nitrogen which is drawn off, and it is to be recommended at the end of the operation to convert the lime into carbonate by forcing in carbon dioxide and to decompose calcium chromate formed.
- the other half is treated at d00-600 C. in the furnace a reducing atmosphere; thereby the alkali chroma-ta is reduced to chromite. If there is in the reducing gases at the same time sufiicient carbon dioxide, then all the alkali and also the lime are converted into carbonate.
- the reduced material after cooling, is extracted with water, filtered, and in the presence of the chromate lye obtained above, heated in an autoclave for 6-8 hours to 280-300" C. and the pressure adjusted with oxygen or to about 100 kgs.
- the sodium dichromate is separated by filtration fromthe residue and worked up in the known manner.
- the alkali obtained in leaching the reduced material passes back into the opening up operation. If the reduction is eirected exclusively with hydrogen, then free caustic soda is obtained.
- Process for the manufacture of dichromates which consists of treating aqueous extract of a frit obtained by an alkaline oxidizing operation of a material containing chromium, together with an equivalent quantity of a substance containing a trivalent chromium oxygen compound in the aqueous solution, at a temperature above 100 C. under pressure, with a gas containing oxygen.
- Process for the manufacture of dichromates which consists of treating aqueous extract of a frit obtained by an alkaline oxidizing operation of a material containing chromium, together with an equivalent quantity of a substance containing metallic chromium in the aqueous solution, at a temperature above 100 C. under pressure, with a gas containing oxygen.
- Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent, neutralizing said basic alkaline earth metal compound and then treating the said chromate frit together with an equivalent quantity of a trivalent chromium oxygen compound in the aqueous solution at a temperature above 100 C., under pressure, with a gas containing oxygen.
- Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent, neutralizing said basic alkaline earth metal compound and then treating the said chromate ulcer together with an equivalent quantity of a substance containing metallic chromium, in the aqueous solution at a temperature above 100 C., under pressure, with a gas containing oxygen.
- Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent, treating the said chromate frit together with an equivalent quantity of a substance containing metallic chromium, in the aqueous solution at a temperature above C., under pressure, with a gas containing oxygen and simultaneously neutralizing said basic alkaline earth metal compound.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Description
Patented Aug. 29, 1933 1,924,710 PROCESS FOR THE MANUFACTURE or DICHROMATES Jules Emile Demant, Cuise-Lamotte, France, as-
signer to Bozel Maletra Societe Industrielle de Produits Chimiques, Paris, France, a corpora tion of France No Drawing. Application January 30', 1931, Serial No. 512,507, and in France'August 14,
14 Claims. (01. 23-56)' This invention relates to the manufacture of dichromates.
Dichromates, in particular sodium dichromate, are technically manufactured in such a manner that the alkali chromates obtained by the oxidizing opening up of chromium ore in the presence of alkalies or alkali carbonates are treated withsulphuric acid or also bisulphate, whereby one equivalent of alkali is taken from the neutral chromate and separated in the form of valkali sulphate. When sodium dichromate is manu-' factured in this manner this causes a quite considerable loss of alkali since sodium sulphate can no longer be passed back into the process. As it also always contains small quantitiesoi chromate which render it discoloured the sulphate is mostly a troublesome valueless secondary product and is consigned as waste. m
The method also proposed hitherto of effecting the conversion of the neutral chromate into dichromate with the aid of carbon dioxide forthe purpose of separating half of the alkali in the form of sodium bicarbonate has hitherto failed on account of the difficulties of effecting this conversion in anything like a satisfactoryyield. It needs very high carbon dioxide pressure in order to displace the equilibrium in the favor-of bicarbonate formation and by this means the econ- I omy of this process is reduced considerably. 1
Another method is that through calcium chromate which is obtained by the oxidizing opening up of chrome ore with lime at very high temperature. In this case the excess of lime must be neutralized and the calcium chromate treated with sodium bisulphate. Accordingly very large quantities of bisulphate are necessary. Now however since the manufacture of nitric acid from ammonia the bisulphate is obtained less and less as a waste product so that the calcium chromate process is greatly endangered.
If for lack of bisulphate sulphuric acid were to be employed, then on account of the high acid costs the process would no longer be economic. V
In accordance with the present invention these a difiiculties can be avoided. According to the process of the invention alkali chromate obtained in the known manner is treatedin the aqueous phase together with an equivalent quantity of chromium hydroxide, hydrated chromiumi oxide, chromium oxide or also metallic chromium or alloys or mixtures containing chromium at temperatures above 100 C. under pressure with oxygen or gases containing oxygen.
It is however not atall necessary that the chromate should be present in the pure state but,
and herein lies the great advantage of the invention, it suffices to employ a chrome ore irit obtained in the known manner whereby the cost of extraction can be saved.
Prior to the further working up of the chromat'e frit to dichromate the content of chromate and if desired also the content offree alkali maybe determined and the addition. of trivalent chromi'um containing oxygen correspondingly ascertained. Instead of trivalent chromium oxygen compounds also chromium metal or its alloys such as ferrochrome can be added. 7
The mixture is nowheated in the aqueous phase with gases containing oxygen underpressure to a temperature above 100 C. suitably to 250300 C; whereby the whole of the chromium added is converted into dichromate. The alkali infree' state or combined under the form of monochromate is thereby entirely utilized and the cost of sulphuric acid or bi'sulphate'is saved.
' The trivalent chromium oxygen compound, in theform of chromium hydroxide, hydrated chromium oxide or chromium oxide can be produced by known processes and it is also in this case quite unnecessary that it should be isolated in the purecondition prior'to the further'working up. If it-is obtained for example by reduction of a chromate frit then after reduction the mass is extracted with water'in' order to removethe alkali'content and the residue is conveyed to the oxidation process. Even if it is possible directly to convert a reduced fritin the presence of an equivalent quantity of. alkali by pressure oxidation into dichromate, yet it is much more economic to effect the oxidationin the presence of chrornate or chromatic frit since thereby the cost of reduction is saved. 1 As already mentioned instead of trivalent chromium oxygen compounds, chromium metal, alloys, or mixtures, thus for eX- ample ferrochrome can be subjected to the pressure oxidation in the aqueous phase in the presence of chromate or a chromate frit.
This process is rendered very simple and economic on account of the fact that the opening-up of the chromium ore canalso be effected without disadvantage withconsiderable alkali excess since the latter is again combined by the ierro chrome in the pressure oxidation.
It may further be remarked that the execution of the process is in no way dependent upon the absence. of lime. It istherefore quite possible to employthe roasted product obtained according to the lime-soda process. Also in the reductionand the subsequent application of the reduction product a content of lime is not detrimental.
stage, extracting the chromate from the roast by leaching and subjecting the residu e to a further exhaustive oxidation. The roast finally obtained is reduced in the known manner, freed from alkali and together with the extracted chromate of the first operation subjected to the pressure oxidation. In this manner it is also possible to effect the exhaustive oxidation without loss of alkali by means of an excess of alkali which is recovered.
From the above description it is seen that there is concerned in the case of the present invention a method of manufacture of unexpected elasticity, since it is possible, according to the conditions, to proceed by the most advantageous method.
' The present process is distinguished economically by the fact that losses of alkaliand high costs for acid are avoided, whereby naturally a considerable reduction of the manufacturing costs is efiected. I
It is immaterial to the execution of the process in what manner the chromate is manufactured, and whether excess of caustic alkali, alkali carbonate or alkali carbonate in the presence 'of alkaline earths is employed.
It is likewise'immaterial in what manner and with what agent the reduction of the other part of the chromate is eiiected. It is essential that the ratio: trivalent chromium or metallic chromium alkali in free state or under form of alkali monochromate, is correctly adjusted, it being also optional to employ instead of the trivalent chromium metallic chromium or its alloys or mixtures.
According to the present invention it is therefore possible to solve the problem of the conversion of neutral chromate into acid chromate, so that one equivalent of alkali instead of being separated in a costly process as a valueless prodnot, is combined with a furtherequivalent of chromium in a useful manner. 7
The following examples illustrate the invention, the parts being by weight-'- Escample 1 (a) 300 parts of chrome ore 50 percent CrzOs content, 320 parts of fused caustic soda, and 100- 200 parts of iron oxide or roast residue are intimately mixed and subjected to an oxidizing roasting for about 68 hours at 450-500" C. A-95 percent opening up is effected.
(b) 3 parts or the roast material obtained are heated in an autoclave with about 8-10 parts of water for about 12 hours to 300 C.and the pressure maintained bythe supply of hydrogen at about kg. a
When the reduction is complete, the material containing chromium oxide hydrate is separated by filtration and washing from the caustic lye which, after suitable concentration, is again brought back into the process.
(0) The reduction product is now heated with one part of the chromate frit obtained according to"(a) with about 15 parts of water in an autoclave for 4.-3 hours to 280300 C. and the pressure adjusted by forcing in oxygen or air to about 100 kg; When the oxidation is complete, the sodium dichromate is separated from the residue by filtration and Worked up in the known manner. The dichromate obtained is pure and free from alumina.
Example 2 300 parts of chrome ore 50 percent CrzOs content, 220 parts of sodium carbonate, parts of 'C. and the pressure adjusted with oxygen to about '100 kg.
When the oxidation is complete, the dichromate solution is separated from the residue, by filtration and worked up in the known manner.
In the present case the carbon dioxide ob tained by oxidation of the carbon content is bound by the lime present.
The pressure oxidation can also take place with equal success by forcing in air. In this case the carbon dioxide is continuously removed with theair rich in nitrogen which is drawn off, and it is to be recommended at the end of the operation to convert the lime into carbonate by forcing in carbon dioxide and to decompose calcium chromate formed.
Example 3 300 parts of chrome ore 50 percent ClzOs, 220
parts of sodium carbonate, and 250-300 parts of slaked lime are subjected to an oxidizing opening up operation at 930-950 C. One half of the roast material is exhaustively extracted with water and the chromate lye adjusted to about 10-15 percent Cr content.
The other half is treated at d00-600 C. in the furnace a reducing atmosphere; thereby the alkali chroma-ta is reduced to chromite. If there is in the reducing gases at the same time sufiicient carbon dioxide, then all the alkali and also the lime are converted into carbonate. The reduced material, after cooling, is extracted with water, filtered, and in the presence of the chromate lye obtained above, heated in an autoclave for 6-8 hours to 280-300" C. and the pressure adjusted with oxygen or to about 100 kgs.
When the oxidation is complete, the sodium dichromate is separated by filtration fromthe residue and worked up in the known manner. The alkali obtained in leaching the reduced material passes back into the opening up operation. If the reduction is eirected exclusively with hydrogen, then free caustic soda is obtained.
In this case it is to be recommended to treat the material before or after oxidation, with carbon dioxide-for the purpose of converting the caustic lime into carbonate. I
NVhat I claim is: Q
1. Process for the manufacture of dichro'mates by treating an alkali metal chromatein the aqueous solution together with. an equivalent quantity of substances selected from the group consisting of hydrated chromium oxide, chromium oxide, metallic chromium, chromium alloys, and mixtures containing chromium, at temperature abovelO0' C. under pressure, with gases containing oxygen. 7
2. Process for the manufacture of dichromates which consists of treating aqueous extract of a frit obtained by an alkaline oxidizing operation of a material containing chromium, together with an equivalent quantity of a substance containing a trivalent chromium oxygen compound in the aqueous solution, at a temperature above 100 C. under pressure, with a gas containing oxygen.
3. Process for the manufacture of dichromates which consists of treating aqueous extract of a frit obtained by an alkaline oxidizing operation of a material containing chromium, together with an equivalent quantity of a substance containing metallic chromium in the aqueous solution, at a temperature above 100 C. under pressure, with a gas containing oxygen.
4. Process for the manufacture of dichromates which consists of treating a frit obtained by an alkaline oxidizing operation of a material containing chromium, together with an equivalent quantity of a trivalent chromium oxygen compound in the aqueous solution above 100 C. under pressure, with a gas containing oxygen.
5. Process for the manufacture of dichromates which consists of treating a irit obtained by an alkaline oxidizing operation of a material containing chromium, together with an equivalent quantity of a substance containing metallic chromium in the aqueous solution above 100 C. under pressure, with a gas containing oziygen.
6. Process for the manufacture of dichromates which consists of reducing a chromate frit obtained by an alkaline oxidizing operation of a material containing chromium, removing the basic compounds formed and oxidizing the product obtained, in the aqueous solution above 100 C. under pressure with a gas containing oxygen in the presence of an equivalent quantity of a basic compound.
7. Process for the ma ufacture of dichromates which consists of reducing a chromate irit obtained by an alkaline oxidizing operation of a material containing chromium, removing the basic compounds formed and oxidizing the product obtained, in the aqueous solution above 100 C. under pressure with a gas containing oxygen in the presence of an equivalent quantity of an alkali metal monochromate.
8. Process for the manufacture of dichromates which consists of reducing a chromate frit obtained by an alkaline oxidizing operation of a material containing chromium, removing the basic compounds formed and oxidizing the product obtained in the aqueous solution above 100 C. under pressure with a gas containing oxygen in the presence of an equivalent quantity of a chromate frit obtained by an alkaline oxidizing operation of a material containing chromium.
9. Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent, neutralizing said basic alkaline earth metal compound and then treating the said chromate frit together with an equivalent quantity of a trivalent chromium oxygen compound in the aqueous solution at a temperature above 100 C., under pressure, with a gas containing oxygen.
10. Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent,
treating the said chromate frit together with an equivalent quantity of a trivalent chromium oxygen compound in the aqueous solution at a temperature above 100 C., under pressure, with a gas containing oxygen and simultaneously neutralizing said basic alkaline earth metal compound.
11. Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent, neutralizing said basic alkaline earth metal compound and then treating the said chromate irit together with an equivalent quantity of a substance containing metallic chromium, in the aqueous solution at a temperature above 100 C., under pressure, with a gas containing oxygen.
12. Process for the manufacture of dichromates which consists of preparing a chromate frit by an alkaline oxidizing operation of a substance containing chromium in the presence of a basic alkaline earth metal compound used as a diluent, treating the said chromate frit together with an equivalent quantity of a substance containing metallic chromium, in the aqueous solution at a temperature above C., under pressure, with a gas containing oxygen and simultaneously neutralizing said basic alkaline earth metal compound.
13. Process for the manufacture of dichromates as claimed in claim 1 in which in place of an alkali metal chromate, an alkaline earth metal chromate is used.
14. Process for the manufacture of dichromates as claimed in claim 7 in which in place of an alkali metal chromate, an alkaline earth metal chromate is used.
JULES EMILE DEMANT.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1924710X | 1930-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1924710A true US1924710A (en) | 1933-08-29 |
Family
ID=9682285
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US512507A Expired - Lifetime US1924710A (en) | 1930-08-14 | 1931-01-30 | Process for the manufacture of dichromates |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1924710A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430261A (en) * | 1942-01-26 | 1947-11-04 | Marvin J Udy | Production of chromium compounds |
| US3715425A (en) * | 1970-10-19 | 1973-02-06 | Allied Chem | Process for the manufacture of chrome chemicals |
-
1931
- 1931-01-30 US US512507A patent/US1924710A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2430261A (en) * | 1942-01-26 | 1947-11-04 | Marvin J Udy | Production of chromium compounds |
| US3715425A (en) * | 1970-10-19 | 1973-02-06 | Allied Chem | Process for the manufacture of chrome chemicals |
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