![]() Method of producing aluminium oxide
专利摘要:
公开号:SU1232143A3 申请号:SU792730952 申请日:1979-02-12 公开日:1986-05-15 发明作者:Ре Лотар;Пласс Лудольф;Маршессо Филипп;Суд Раман 申请人:Металлгезельшафт Аг (Фирма); IPC主号:
专利说明:
The invention relates to metallurgy, in particular to methods for producing alumina (alumina). The purpose of the removal is to simplify the utilization of gases from the heat treatment of aluminum hydrochloride by separately removing the gaseous decomposition products of hydrochloride from the first stage of heat treatment and using it as a heat transfer fluid fed to the fluidized bed in the first stage calcined alumina from the second stage. The drawing shows a schematic diagram of the method. The original aluminum hydrochloride through the supply section 1 is sent to the fluidized bed reactor 2 (first heat treatment stage), equipped with a separator 3 and a return pipe 4. The gas product withdrawn from the first heat treatment stage 2 is sent to the separator 3, electric filter 5 and yes to the installation of the absorption of chlorine hydrogen (not shown). The drink separated in the separator 3 and the electric sill 5 is returned via pipelines 4 and 6 to reactor 2. Heat is supplied to reactor 2 by returning hot calcined product, alumina, through pipeline 7. Partially decomposed aluminum hydrochloride from reactor 2 through line 8 and through separators 9 and 10 through line 11 by pneumatic transport enters the second heat treatment stage: into decomposition reactor 12 with vortex fluidized bed (fluidized bed), then into low-boiling reactor 13 (extract) through pipeline 14. A controlled return to the reactor 13 of the vortex layer is carried out via a circulation pipeline 15. The selection of the finished production alumina is carried out from the reactor 13 via line 16 to a fluidized bed cooler t7. The cooled alumina is discharged from refrigerator 17 through line 18. From the reactor 12, the hot calcined alumina is partially directed to the first heat treatment stage to the reactor 2 via line 7. The gases from the second stage of decomposition from the reactor 13 are directed through the pipeline 19 through the separator 10 and the electrostatic precipitator 20 to the consumer. The solid phase, separated in the electrostatic precipitator 20, is returned to pfeaK-torus 13 via conduit 21. Example. Through section 1 of the feed to the reactor 2 serves every hour 54 t AfCfj-eHjO with a surface moisture of about 15% and an average grain diameter of about 150 p m. The reactor 2 is supplied with 300Q nm / h of steam with a temperature of 180 ° C via the steam line 22. The heating of the fluidized bed reactor 2 is carried out by supplying 180 t / h of calcinate with a temperature of 950 ° C via line 7. The temperature in the reactor 2 is set at 400 ° C. The gas flow rate supporting the fluid bed is 4.6 m / s. Due to the high velocity of the gas flow to the upper part of the reactor 2 together with the gas a significant amount of solids is carried out. After separation in the separator 3, the solid is returned to the reactor 2. The average suspension density is set at about 100 kg / m and a pressure drop of 1800 mm aq. The average residence time is about 0.5 h. Based on the above conditions, the degree of decomposition of aluminum chloride is about 98%. The exhaust gas in the amount of 38400 nm / h is directed to the 5 dp electrodustry of dedusting. The concentration of exhaust chloride hydrogen is 37% and the gas temperature is 250 C. From the reactor 2, 194 t / h of solid matter are taken and transported using pneumatic conveying through the separators 9 and 10 to the second heat treatment stage (into the reactor 12 of the vortex fluidized bed). In the vortex fluidized bed reactor 12 and in the weak boiling reactor 13 (latching), the final decomposition of aluminum chloride to alumina occurs. Dp of supporting the fluidized bed in the reactor 12 is the air supplied in the amount of 5000 nm / h through the pipeline 23 through the gas distribution device. The supply air is heated to 550 s by 31 heat transfer in the fluidized bed refrigerator 17. The reactor 12 is supplied through the pipeline 24 at a height of 4.0 m above the gas distribution device secondary air in the amount of 36230 .. Of this amount, 9700 air with temperature enters the pipeline 25 from the air separator 9, 5600 nm / h at 600 ° C - from the refrigerator 17 through line 26 and 20930 with — through line 27 from heat exchanger 28. With this, the ratio between the gas to support the fluidized bed and the secondary gas is 1: 7.2. 3570 kg of heavy fuel oil are injected into the space between the gas distribution device and the secondary air supply line 24 (the lower heat of combustion is 39,800 kJ (kg) through the pipe 29. The solid that is removed from the reactor 12 of the vortex fluidized bed, is released from the gas in the upper part of the reactor 13, remains in the lower part of the reactor and forms a dense fluidized bed there. In the reactor 13, the state of the fluidized bed is provided by supplying 1100 nm / h of air preheated to AOO C in the fluidized bed cooler 17. Due to the circulation of solids in the reactor 12 of the vortex fluidized bed, as well as due to the return of solids from the reactor 13 through line 15 in the general circulation system, the same temperature is established. The distribution of the total residence time of alumina was made by the editor M. Petrov Compiled by T. Sokolova Tehred V. Kadar Proof-reader S. Cherni Order 2665/60 Circulation 450 Subscription VNIIPI USSR State Committee for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab., 4/5 Production and printing company, Uzhgorod, st. Project, 4 to fS 20 321434 About 2.26 hours for the reactor 12 of the vortex fluidized bed and the reactor 13, is determined by an approximate ratio of 1: 3.8 (38 minutes in the reactor 12 5 and 1.8 hours in the reactor 13). The pressure loss in reactor 12 is set at about 660 nm aq. The average density of the slurry in the zone between the gas distributor and the secondary air (gas) pipe 24 is 150 kg / m and the average slurry density in the zone above the secondary air (gas) pipe 24 is 5 kg / m. In the section of the reactor 13 with a high solids content, a suspension with a density of about 550 kg / m prevails. Aluminum oxide, whose production is at the level of 10 tons per hour, is transferred from the reactor 13 via pipeline 16 to the fluidized bed refrigerator 17. In this refrigerator, the state of the fluidized bed is maintained by supplying 5600 air, with 5000 or 1100 nm / h being sent to the cooling chambers, in addition, additional water cooling is used. As a result, when passing through the refrigerator 17, the alumina is cooled to a temperature. The exhaust gas from reactors 12 and 13 in the amount of 45,000 hours has a temperature of 950 ° C. Cooled by contact with the solid phase in the separator 10, the gas is sent to the heat exchanger 28 and then to the electrostatic precipitator 20. The 4500 exhaust gas at the OUTPUT of the electrostatic precipitator 20 has a temperature of 350 ° C and contains {~) cold {0.5) hydrogen of 0.5 vol. X. 25 thirty five 0
权利要求:
Claims (1) [1] METHOD FOR PRODUCING ALUMINUM OXIDE by two-stage thermal decomposition of aluminum hydrochloride with partial decomposition of the starting material in the first stage and obtaining a calcined product in the second stage, including processing in the vortex fluidized bed zone and in the low boiling zone (aging) with circulation of solid particles between the zones, cooling the calcine in fluidized bed, gas removal, separation of solid particles from the gas stream and return them to heat treatment, characterized in that, in order to simplify the disposal exhaust gases, separate the gaseous decomposition product obtained in the first stage, and the heat treatment in the first stage is carried out in a fluidized bed using calcined alumina 4 removed from the second heat treatment stage as a heat carrier supplied to the fluidized bed. SU „„ 1232143 AZ
类似技术:
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同族专利:
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引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 DE1667195C3|1968-01-31|1979-09-27|Metallgesellschaft Ag, 6000 Frankfurt|Process for the production of hydrohalic acids and metal oxides| DE1767628C3|1968-05-30|1985-03-14|Metallgesellschaft Ag, 6000 Frankfurt|Process for performing endothermic processes| AT315207B|1972-11-20|1974-05-10|Ruthner Ind Planungs Ag|Process for the production of hydrogen chloride| US4049788A|1972-12-14|1977-09-20|Metallgesellschaft Aktiengesellschaft|Thermal transformation of metal chlorides to oxides in a fluidized bed| DE2261083C3|1972-12-14|1979-05-31|Metallgesellschaft Ag, 6000 Frankfurt|Process for the thermal cracking of metal chlorides| DE2503142A1|1975-01-27|1976-07-29|Metallgesellschaft Ag|Metal oxides prodn from metal chlorides - by decomposition in fluidized bed with removal of liquid metal chloride impurities| DE2524541C2|1975-06-03|1986-08-21|Aluminium Pechiney, Lyon|Process for the thermal cracking of aluminum chloride hydrate| DE2524540C2|1975-06-03|1986-04-24|Metallgesellschaft Ag, 6000 Frankfurt|Process for performing endothermic processes| IL47643A|1975-07-04|1977-05-31|Yissum Res Dev Co|Oxidation of magnesium chloride| DE2636855C2|1976-08-16|1986-08-21|Aluminium Pechiney, Lyon|Process for the thermal cracking of aluminum chloride hydrate| DE2636854C2|1976-08-16|1986-08-21|Aluminium Pechiney, Lyon|Process for the thermal cracking of aluminum chloride hydrate|US4402932A|1982-05-07|1983-09-06|The United States Of America As Represented By The Secretary Of The Interior|Thermal decomposition of aluminum chloride hexahydrate| JPS601000U|1983-06-17|1985-01-07| DE10260739B3|2002-12-23|2004-09-16|Outokumpu Oy|Process and plant for producing metal oxide from metal compounds| DE10260741A1|2002-12-23|2004-07-08|Outokumpu Oyj|Process and plant for the heat treatment of fine-grained solids| DE10260733B4|2002-12-23|2010-08-12|Outokumpu Oyj|Process and plant for the heat treatment of iron oxide-containing solids| DE10260738A1|2002-12-23|2004-07-15|Outokumpu Oyj|Process and plant for conveying fine-grained solids| DE10260734B4|2002-12-23|2005-05-04|Outokumpu Oyj|Process and plant for the production of carbon coke| DE10260731B4|2002-12-23|2005-04-14|Outokumpu Oyj|Process and plant for the heat treatment of iron oxide-containing solids| DE10260737B4|2002-12-23|2005-06-30|Outokumpu Oyj|Process and plant for the heat treatment of titanium-containing solids| US7730633B2|2004-10-12|2010-06-08|Pesco Inc.|Agricultural-product production with heat and moisture recovery and control| DE102006062151A1|2006-12-22|2008-06-26|Outotec Oyj|Process and plant for the heat treatment of particulate solids, in particular for the production of metal oxide from metal hydroxide| BR112013028371A2|2011-05-04|2017-02-14|Orbite Aluminae Inc|process of recovering at least one rare earth element and / or at least one rare metal selected from in, zr, li and ga from at least one material| CN103534367A|2011-03-18|2014-01-22|奥贝特铝业有限公司|Processes for recovering rare earth elements from aluminum-bearing materials| CA2863755C|2011-06-03|2016-04-26|Orbite Aluminae Inc.|Methods for preparing hematite| JP2014526431A|2011-09-16|2014-10-06|オーバイトアルミナインコーポレイテッド|Preparation process for alumina and various other products| MY175471A|2012-07-12|2020-06-29|Orbite Tech Inc|Processes for preparing titanium oxide and various other products| RU2016104423A|2012-01-10|2018-11-22|Орбит Текнолоджис Инк.|METHODS FOR PROCESSING RED SLUR| US9181603B2|2012-03-29|2015-11-10|Orbite Technologies Inc.|Processes for treating fly ashes| US9353425B2|2012-09-26|2016-05-31|Orbite Technologies Inc.|Processes for preparing alumina and magnesium chloride by HCl leaching of various materials| EP2920114A4|2012-11-14|2016-03-02|Orbite Aluminae Inc|Methods for purifying aluminium ions| WO2019114922A1|2017-12-11|2019-06-20|OutotecOy|Process and plant for thermal decomposition of aluminium chloride hydrate into aluminium oxide| WO2020244782A1|2019-06-07|2020-12-10|OutotecOy|Process and plant for thermal decomposition of aluminium chloride hydrate into aluminium oxide|
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申请号 | 申请日 | 专利标题 DE2805906A|DE2805906C2|1978-02-13|1978-02-13|Process for the thermal cracking of aluminum chloride hydrate| 相关专利
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