US2230592A - Process of preparing magnesia and sulphur dioxide - Google Patents

Process of preparing magnesia and sulphur dioxide Download PDF

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US2230592A
US2230592A US295052A US29505239A US2230592A US 2230592 A US2230592 A US 2230592A US 295052 A US295052 A US 295052A US 29505239 A US29505239 A US 29505239A US 2230592 A US2230592 A US 2230592A
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coal
zone
sulphur dioxide
gas
reducing
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Griessbach Robert
Bitterfeld Kreis
Sutterlin Walther
Zirngibl Hans
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WALTHER H DUISBERG
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WALTHER H DUISBERG
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F5/00Compounds of magnesium
    • C01F5/02Magnesia
    • C01F5/06Magnesia by thermal decomposition of magnesium compounds
    • C01F5/12Magnesia by thermal decomposition of magnesium compounds by thermal decomposition of magnesium sulfate, with or without reduction
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00Sulfur; Compounds thereof
    • C01B17/48Sulfur dioxide; Sulfurous acid
    • C01B17/50Preparation of sulfur dioxide
    • C01B17/501Preparation of sulfur dioxide by reduction of sulfur compounds

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  • PROCESS DF PREPARING MAGNSIA AND SULPHUR DIOXIDE l Filed sept. 15, 1939 THE: A-r oRNEYs Patented Feb. 4, 1941 UNITED STATES PATENT OFFICE PROCESS F PBEPARING MAGNESIA AND SULPHUB DIOmE Robert Griessbach, Wollen, Kreis Bitterfeld,
  • the present invention relates to a process of preparing magnesia and sulphur dioxide.
  • a revolvingfurnace with a Y gas-tight Aclosure at one side and an inlet for gas and air at different parts of the furnace.
  • an inlet for gas and air according to the conditions of the invention may likewise be mounted at other furnaces, for instance, a shaft kiln, a tunnel kiln or the-like.
  • heating and reducing gas there may be used a gas containing hydrogen, carbon monoxide or a gasied liquid reducing lagent.
  • the reducing coal should be poor in ash. ⁇
  • the upper end of a revolving furnace is charged with a mixture of 100 parts of kieserite and 8.5 parts of a granular coke from lignite.
  • the heating gas (generator gas) and the corresponding quantities of air are introduced through'burners one of which is mounted at .the 35 lowest end of the lower third of the furnace and is fed in a strongly reducing way (3 to 5 per cent.
  • magnesia thus obtained is to be furthe -treated so as to obtain sintered magnesite, its high temperature is with advantage directly utilized by heating the reaction product, which by the necessary flux of iron oxide (for instance, roasted pyrites) to the mixture of kieserite and coal has been given the usual composition, to about 1400 C. in a correspondingly lined prolonged part of the furnace in an oxidizing atmosphere.
  • iron oxide for instance, roasted pyrites
  • magnesia is obtained which is free from coal ash.
  • the material is heated, in the iirst oxidizing zone, to about 700 C., the temperature is then slowly raised to about 1000 C., 900 C. being not exceeded until the material contains about 50 to 70 per cent. of magnesia.
  • a process of preparing magnesia and sulphur dioxide by reduction of magnesium sulphate which comprises leading the material through an oxidizing preheating zone having a temperature of about 700 C. and reducing the material ina furnace heated in the interior at temperatures rising up to about 900 C.
  • a. reducing agent of the group consisting of coal and gas
  • said reducing agent being present in a quantity suilicient to effect full reduction of no more than about 50 to '70 per temperatures rising up to about 900 C.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)

Description

Feb- 4, 1941- R GRlEssBAcH Erm. 2,230,592
PROCESS DF PREPARING MAGNSIA AND SULPHUR DIOXIDE l Filed sept. 15, 1939 THE: A-r oRNEYs Patented Feb. 4, 1941 UNITED STATES PATENT OFFICE PROCESS F PBEPARING MAGNESIA AND SULPHUB DIOmE Robert Griessbach, Wollen, Kreis Bitterfeld,
Walther Siitterlln,
Bitterfeld, and Hans Application September 15, 1939, Serial No. 295,052 In Germany February 2, 1937 2 Claims.
The present invention relates to a process of preparing magnesia and sulphur dioxide.
The known processes of reducing magnesium sulphate by means of coal do not yet show an industrially useful way for obtaining magnesium oxide and onlyone uniform sulphur compound in a practically complete yield. The main difliculties reside in the fact that, on using a deficiency of coal, the reduction does not occur quantitatively; on usingan excess of coal, however,` S, HzS, COS .and CS2 are formed besides SO2. It has, therefore, been suggested to effect the re'- duction with an excess of coal, but to let follow as second operative step a chlorinating or oxidizing roasting. These processes, obviously, have the drawback that other sulphur compounds are formed besides sulphur dioxide, the working up of which compounds is very dicult.
Now we have found a process by which it is possible in one single operation to reduce magnesium sulphate practically completely so as to form magnesium oxide, a gas being simultaneously obtained which contains the sulphur only in the form of sulphur dioxide in such a concentration that sulphurtrioxide may be'prepared therefrom in a Contact apparatus attached 'to the reaction device.- This decomposition of the magnesium sulphate is attained by subdividing the reduction furnaceinto three zones. upper, feebly oxidizing zone the mixture of magnesium sulphate and coal introduced which contains a deficiency of coal is pre-heated. During its migration it passes the middle zone where the temperature rises from about 700 C. to 900 C. In this Zone the coal has a reducing action. The. gaseous phase is kept neutral in that zone of the furnace. When 'the contentof the fui'- nace reaches the lower zone the coal is already consumed. The unchanged magnesium sulphate still present is then completely reduced in a reducing gaseous medium. By the partial combustion of the gas introduced at the lower end of the furnace for the purpose of heating the interior of the furnace, carbon dioxide and/or steam are formed, the formation of magnesium sulphide being prevented thereby. The temperatures in this zone are at about 1000 C.
By this mode of working the above mentioned drawbacks of the known processes of decomposing magnesium sulphate are avoided. On the one hand the formation of sulphur and hydrogen sulphide is practically prevented by the use of a deficiency of coal in the middle zone and on the other hand the unchanged magnesium sulphate is likewise reduced so as to form magnesium In the oxide by the reducing action of the gases in the lower zone. Any reduced sulphur gases which may be formed in this zone are completely oxidized in the upper zone by the air blown in so as to form sulphur dioxide. 5
By the slowly rising temperatures in the middlezone it becomes also possible that in the range of higher temperatures a sufficient quantity of magnesium oxide is present to prevent the hitherto .technically inevitable agglutination of the charge of the furnace. Generally a content of 50 per cent. to 70 p er cent. of magnesium oxide is sufficient for the mixture when it enters the third zone of about 900 C. to 1000- C.
For carrying out the reduction there may, for instance, be used a revolvingfurnace with a Y gas-tight Aclosure at one side and an inlet for gas and air at different parts of the furnace.
Of course, an inlet for gas and air according to the conditions of the invention may likewise be mounted at other furnaces, for instance, a shaft kiln, a tunnel kiln or the-like. As heating and reducing gas there may be used a gas containing hydrogen, carbon monoxide or a gasied liquid reducing lagent. The reducing coal should be poor in ash.`
'll'lie following example serves to illustrate the invention, but it' is not intended to limit it thereto; the parts areby weight:
The upper end of a revolving furnace is charged with a mixture of 100 parts of kieserite and 8.5 parts of a granular coke from lignite. The heating gas (generator gas) and the corresponding quantities of air are introduced through'burners one of which is mounted at .the 35 lowest end of the lower third of the furnace and is fed in a strongly reducing way (3 to 5 per cent. of Hz--CO remain unburnt) in order to decompose the residues of MgSO4 Whereas the other burner is situated at the limit between the lower 40 third andthe middle zone, the'addition of air to the heatinggasbeing regulated there so that neither a reducing nor an oxidizing but solely a Y neutral burning atmosphere is formed by which the temperature is brought to about 900 C. At 45 the limit between the middle and the upper zone4 where the gases in the furnace have cooled to about 700 C. by the action of the material introduced a new oxidizing zone is created by the addition of air to such an extent that at the inlet end the waste gases are composed of about 1 per cent. of O2, 18 to 20 per cent. of CO2 and 8 to 10 per cent. of SO2. Under these working conditions the gases contain neither other sulv phur compounds nor elementary sulphur. The
product obtained is practically completelyl reduced and contains about 95 per cent. of MgO (residue: impurities from the kieserite and ash portions of Vthe coal.)
If the magnesia thus obtainedis to be furthe -treated so as to obtain sintered magnesite, its high temperature is with advantage directly utilized by heating the reaction product, which by the necessary flux of iron oxide (for instance, roasted pyrites) to the mixture of kieserite and coal has been given the usual composition, to about 1400 C. in a correspondingly lined prolonged part of the furnace in an oxidizing atmosphere. Y
It is also possible, instead of using coal and gas, to perform the reduction with the aid of gas `alone, whereby a magnesia is obtained which is free from coal ash. In this case the material is heated, in the iirst oxidizing zone, to about 700 C., the temperature is then slowly raised to about 1000 C., 900 C. being not exceeded until the material contains about 50 to 70 per cent. of magnesia.
The invention is of course not limited to the exact details described, for obvious modications may occur to a person skilled in the art.
What we claim is:
1. A process of preparing magnesia and sulphur dioxide by reduction of magnesium sulphate which comprises leading the material through an oxidizing preheating zone having a temperature of about 700 C. and reducing the material ina furnace heated in the interior at temperatures rising up to about 900 C. Without sintering inv the presence-of a. reducing agent of the group consisting of coal and gas, said reducing agent being present in a quantity suilicient to effect full reduction of no more than about 50 to '70 per temperatures rising up to about 900 C. Without sintering with coal in the presence ofv a neutral atmosphere, said coal being present in a quantity sumcient to effect full reduction of no more than about 50 to '70 per cent. of the magnesium sulphate to magnesi'aand completing the reduction at temperatures rising up to about 1000 C. while in contact with a gaseous reducing agent.
ROBERT GRIEssBAcH. WALTHER. s'I'rERLIN. HANS zIRNGIBL.
US295052A 1937-02-02 1939-09-15 Process of preparing magnesia and sulphur dioxide Expired - Lifetime US2230592A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2687947A (en) * 1950-04-04 1954-08-31 Ici Ltd Production of sulfur dioxide
US2776191A (en) * 1953-12-31 1957-01-01 Int Minerals & Chem Corp Process for the production of magnesium oxide from ores containing magnesium sulfate
US2951743A (en) * 1956-03-29 1960-09-06 Vaw Ver Aluminium Werke Ag Process of making alumina
US4990319A (en) * 1987-09-15 1991-02-05 Kuraray Co., Ltd. Process for producing ammonia and sulfur dioxide

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2687947A (en) * 1950-04-04 1954-08-31 Ici Ltd Production of sulfur dioxide
US2687946A (en) * 1950-04-04 1954-08-31 Ici Ltd Production of sulfur dioxide
US2776191A (en) * 1953-12-31 1957-01-01 Int Minerals & Chem Corp Process for the production of magnesium oxide from ores containing magnesium sulfate
US2951743A (en) * 1956-03-29 1960-09-06 Vaw Ver Aluminium Werke Ag Process of making alumina
US4990319A (en) * 1987-09-15 1991-02-05 Kuraray Co., Ltd. Process for producing ammonia and sulfur dioxide

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