专利摘要:
This invention relates to methods for producing high-purity magnesium oxide from magnesite ore containing impurities of calcium compounds. The goal is to reduce energy costs. The ore is calcined and the resulting magnesium oxide in the leaching stage is converted into magnesium chloride and magnesium carbonate trihydrate is precipitated from the magnesium chloride solution by treatment with ammonium carbonate to form ammonium chloride, and ammonium is precipitated from ammonium chloride during regeneration and the precipitated magnesium carbonate trihydrate is precipitated. filtered, washed, dried and calcined to magnesium oxide. 1 il.
公开号:SU1519528A3
申请号:SU853979507
申请日:1985-11-26
公开日:1989-10-30
发明作者:Стюарт Энскау Вильям;Баскар Гадгил Балкришна
申请人:Гебрюдер Зульцер Аг (Фирма);
IPC主号:
专利说明:

This invention relates to a process for the production of high purity magnesium oxide from magnesite ore containing calcium compounds.
The aim of the invention is to reduce energy costs.
The drawing shows the scheme of the proposed method.
The method is carried out as follows.
The crushed magnesite ore, containing CaCO ,, FeO ,, ,, SiO, is fed through conduit 1 to furnace 2 and is burned to produce magnesium oxide. The latter is divided into two streams, one of which, in the amount of 7 kg (4.1 kg of MgO, 0.2 kg of CaO, 2.7 kg, ,, SiO,), via conduit 3, directs reactor 4, where it is treated 15 % solution of ammonium chloride coming PA this stage through the pipeline 5 from the apparatus 6. In the reactor 4 oxides
magnesium and calcium interact with by reaction
IlgO + 2 NH4.C1 - MgCl + MN3 + CaO + 2 NH4C1 - CaClj + NH,
A 15% solution of 5gCl2 containing 0.6% CaClj and ammonia is obtained, which is distilled off from the reaction medium with steam supplied through line 7.
In order to remove the CaClj impurity from the MgCl solution, the solution through pipeline 8 is sent to tank 9, where it is mixed with a second stream of magnesium oxide and carbon dioxide is supplied to this stage, resulting in the interaction of magnesium oxide with calcium chloride and SSG. CaCO3 by reaction.
 + CaCl2 + CO2 - MgClj; CaCO R. Due to the fact that the concentration of CaCli in the solution of MgClj is very

CM
For example, for a fiaCr precipitated / 1Pi, the requirement — ioct, would be prolonged, one time (the expense of the introduction of an additional amount of CaCl to 1% gtg to the pipeline 10 to 10%)
/ Carbon dioxide at this stage is fed to adjust the pH of the medium, which should not be lower than 5.5. The resulting suspension, containing less than 0.1% CaCl1, is fed through line 11 to filter 12, which separates the precipitate CaC j from chloride solution magni. 65 kg of a solution containing 16Z MgCl1 and less than 0.1% SLS, via line 13, are sent to reactor 14, where, when reacting with ammonium carbonate, the reaction
MpClj + CNH) CO, + 3HjO- -bMgCOj ЗН ,, 0
magnesium carbonate trihydrate is formed.
Ammonium carbonate is prepared in the absorber 15 from ammonia coming from reactor A and CO. In the reactor 14, it is supported by a temperature in the range of 25-5 ° C and a pH of 7.5-8.5. The suspension obtained in it in an amount of 81 kg, containing 16% MSCO, and 15%, is fed through conduit 16 to a bilter 6. The filtrate is sent to reactor 4, and the sediment is washed with water supplied through conduit 17, and then through conduit 18 to roasting in kiln 19 to obtain .gO. During roasting, CO is extracted, which is fed through conduit 20 to tank 9.
The result for the I method is compared with the g, prototype, which reduces the energy consumption of the process by 20% due to the elimination of the CaCO burning stage.
权利要求:
Claims (2)
[1]
1. A method of producing magnesite magnesium oxide containing calcium compounds, including calcining magnesite, treating the calcine product with a chloride solution, precipitating calcium carbonate from the resulting carbon dioxide solution, separating the precipitate from the mother liquor, treating the latter with ammonium carbonate to obtain a precipitate of magnesium carbonate trihydrate and solution ammonium chloride, washing the precipitate, its thermal decomposition to magnesium oxide and carbon dioxide, characterized in that, in order to reduce energy consumption, the calcined product is divided into two streams, one of which is sent for treatment with ammonium chloride solution from the stage of precipitation of magnesium carbonate trihydrate while simultaneously stripping ammonia with water vapor, and the second stream is fed to the stage of precipitation of calcium carbonate with additional introduction of calcium chloride to this stage.
[2]
2. The method according to claim 1, wherein the precipitation of magnesium carbonate trihydrate is carried out with ammonium carbonate obtained by reacting carbon dioxide from the stage of thermal decomposition of magnesium carbonate trihydrate with ammonia from the stage of processing the product about
gigum ammonium chloride.
类似技术:
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SU1519528A3|1989-10-30|Method of producing magnesium oxide from magnesite
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同族专利:
公开号 | 公开日
BR8505919A|1986-08-19|
PT81551A|1985-12-01|
ZA858855B|1986-08-27|
AT50548T|1990-03-15|
EP0182931A1|1986-06-04|
EP0182931B1|1990-02-28|
ES549121A0|1987-10-01|
AU578504B2|1988-10-27|
IN164603B|1989-04-22|
US4720375A|1988-01-19|
PT81551B|1987-11-11|
DE3481413D1|1990-04-05|
YU43951B|1989-12-31|
NO854725L|1986-05-28|
AU5043985A|1986-06-05|
ES8708200A1|1987-10-01|
YU183085A|1988-04-30|
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法律状态:
优先权:
申请号 | 申请日 | 专利标题
EP84114353A|EP0182931B1|1984-11-27|1984-11-27|Process for the preparation of very pure magnesium oxide|
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