Method of preparing aluminium chloride
专利摘要:
An improved method is disclosed for producing aluminum chloride by contacting chlorine with aluminum oxide and a reducing agent, each of which is present in an amount in excess of the stoichiometric amount of the chlorine in a molten bath of aluminum chloride and metal halide to form aluminum chloride which is recovered from the bath by sublimation. The improvement comprises increasing the rate of formation of aluminum chloride by adding a source of metal selected from the group consisting of iron, chromium, copper, europium and cerium to the molten bath. 公开号:SU738506A3 申请号:SU762430108 申请日:1976-12-16 公开日:1980-05-30 发明作者:Алан Волебер Дэвид;Норман Кочран Чарльз 申请人:Алюминум Компани Оф Америка (Фирма); IPC主号:
专利说明:
The invention relates to methods for producing aluminum chloride, which can be used as a catalyst in the cracking of petroleum products, as well as a number of organic syntheses. A known method of producing aluminum chloride by chlorination in a fluidized bed of aluminum-containing raw materials in the presence of a gaseous booster and melted particles of sodium aluminum chloride [1]. There is also a method of producing aluminum chloride by chlorination of aluminum-containing raw materials in the presence of a reducing agent in a melt of aluminum and sodium chlorides [2]. The disadvantage of this method is not sufficiently high speed Xia chloride (rirovaniya (at a flow rate 'chlorine Umino 300 cm) completeness of its conversion is 41-52%. The purpose of this invention is to increase the rate of chlorination. . The goal is achieved by the described method for producing aluminum chloride by chlorinating an aluminum-containing raw material in the presence of a reducing agent in a melt of aluminum and sodium chlorides or iron chloride, or monovalent copper chloride, or divalent copper chloride, or chromium chloride, which take, respectively, the weight. %: 0.05-10; 0.05—5; 0.07 7-1. A significant difference of the invention is that the process is conducted in the presence of either iron chloride, or monovalent copper chloride, or divalent copper chloride, or chromium chloride. It is preferable to take them in an amount, respectively, wt.%: 0.05-10; 0.05-5; 0.077-1. These differences can significantly increase the rate of chlorination (at a rate of transmission of chlorine of 300 cm e / min> the completeness of its conversion is 84%. Example 1. In a salt melt containing 390 g of NaCC, 920 g of AECE ^, at a temperature of 788 ^ 0, 325 g of coke, crushed to 100 mesh, and 50 g of A6 2 Oj, also crushed to 100 mesh, are introduced. Chlorine gas is passed through the melt, which enters the lower part of the melt bath at a speed of 300 cm ^ / min. The completeness of the conversion of chlorine to aluminum chloride · ν 4 1%. In the next experiment, the melt is introduced Ciss 2, in an amount of 1.0 g per 100 g NaCE-Al'CC ,. while the completeness of the conversion of chlorine to A8. SC for the same time as in the first case, increased to 84%. Example 2. The process is carried out in the same way as in example 1, but subsequently CuBR is introduced into the melt in the amount of 0.077 g per 100 g of NaCe-Atce 3 , while the completeness of chlorine conversion in the forest, at the same time, increased to 73%. Example 3. The process is carried out as in example 1, but subsequently 1.0 g of FeCC ^ per 100 g of NaCe-A £ Ce d is introduced into the melt. The completeness of the conversion of chlorine 69%. Example 4. The process is carried out as in example 1, but 1.0 g of chromium chloride is introduced into the melt. The completeness of the conversion of chlorine is 53%.
权利要求:
Claims (2) [1] The invention relates to methods for producing aluminum chloride, which can be used as a catalyst in the cracking of petroleum products, as well as a number of organic syntheses. A method of producing aluminum chloride by chlorinating aluminum-containing gas in the fluidized bed in the presence of a gaseous reducing agent and molten sodium aluminum chloride particles 1 is known. A method of producing aluminum chloride by chlorinating aluminum-containing raw material in the presence of molten aluminum chloride in a molten aluminum chloride by means of chlorinating aluminum-containing raw materials in the presence of aluminium chloride 1 is also known. The chlorination rate is not high enough (at a chlorine transmission rate of 300 cm of umin), the completeness of its conversion is. The purpose of this invention is to increase the rate of chlorination. This goal is achieved by the described method of producing aluminum chloride by chlorinating aluminum containing raw materials in the presence of a reducing agent in a melt of aluminum and sodium chlorides or iron chloride. or monovalent copper chloride, or divalent copper chloride, or chromium chloride, which is taken in an amount of, respectively, wt.%: O., 05-10; 0.05-5; 0.077-1. The essential difference of the invention is that the process is carried out in the presence of either ferric chloride, or monovalent copper chloride, or divalent copper chloride, or chromium chloride. It is preferable to take them in quantity, respectively, wt.%: 0.05-10; 0.05-5; 0.077-1. These differences make it possible to significantly increase the rate of chlorination (at a rate of 300 cm / min. Chlorine, the conversion is 84% complete. Example 1. In a salt melt containing 390 g of NaC, 920 g AECE, 325 g coke crushed to 100 mesh, and 50 g ABjO.j, also crushed to 100 mesh. Chlorine gas is passed through the melt, which enters the bottom of the molten bath at a rate of 300. Conversion of chlorine to aluminum chloride 4 1%. following experiment, CuCCj i is introduced into the melt in the amount of 1, 0 g per 100 g of NaCE-AlCC ,, J ... 73 with This completes the conversion of chlorine to ASC for the same time as in the first case, increased to 84%. Example 2. The process is carried out as in Example 1, but later CWS is added to the melt in a quantity of 0.077 g per 100 g NaCe-Aece t in this case, the completeness of chlorine conversion in the forest increased to 73% over the same time. Example 3. The process is carried out as in Example 1, but 1.0 g of FeCg-j is introduced into the melt per 100 g of Nace-Aece,). Completeness of chlorine conversion 69%. Example 4. The process is carried out as in Example 1, but 1.0 g of chromium chloride is introduced into the melt. The chlorine conversion is 53%. Claim 1. Method for producing aluminin chloride by chlorinating an aluminum-containing raw material in the presence of a reducing agent in an aluminum and sodium chloride melt, characterized in that, in order to increase the rate of chlorination, the process is carried out in the presence of ferric chloride or monovalent copper chloride or divalent copper chloride, or chromium chloride. 2. The method according to p. 1, characterized in that the ferric chloride or cuprous chloride, or cupric chloride, or chloride of xp on take in the amount, respectively, wt.%: 0.05-10; 0.05-5 0.077-1. Sources of information taken into consideration 1 “1e in the examination 1.Angew. Chem 3nternat, Edit. t. 72, 1960, p. 73-79. [2] 2. US patent number 4039648, cl. 423-496, published, 02.08.77 (prototype).
类似技术:
公开号 | 公开日 | 专利标题 SU738506A3|1980-05-30|Method of preparing aluminium chloride Kinnear et al.1952|661. Formation of organo-phosphorus compounds by the reaction of alkyl chlorides with phosphorus trichloride in the presence of aluminium chloride Hoey et al.1991|A convenient synthesis of 1, 4-dihydro-2, 3-benzoxathiin 3-oxide, a useful precursor of o-quinodimethane SU786881A3|1980-12-07|Method of aluminium chloride production Spagnolo et al.1982|General route for the facile transformation of ortho-substituted lithiobithienyls into amino derivatives CS195659B2|1980-02-29|Process for preparing aluminium chloride from raw material containing aluminium,silicium and oxygen Ashcroft et al.1980|Homolytic displacement at carbon: V. Formation of cyclopropylcarbinylsulphones and trichloroethylcyclopropanes from but-3-enyl cobaloximes by a novel process involving homolytic attack at the δ-carbon of the butenyl ligand Uemura et al.1975|Selenocyanatodethallation in organothallium | compounds DE1668544A1|1971-02-11|Dimerization Catalyst and Process GB1374054A|1974-11-13|Process for the continuous production of sulphur tetrafluoride US2946828A|1960-07-26|Process for preparing aliphatic fluorine compounds US2469290A|1949-05-03|Process for making tetrachlorodifluoroethane GB1375329A|1974-11-27| Liu et al.1990|Direct Synthesis of Some Oiaryl Ditellurides from Aryl Halides US4434149A|1984-02-28|Acid melt treatment to activate carbon for use as reductant US4538011A|1985-08-27|Method for the preparation of halogen substituted methanes and ethanes US4150047A|1979-04-17|Process for preparing halogenated metal chelates SU363680A1|1972-12-25|METHOD OF OBTAINING CHLORINE ALLYL US3927125A|1975-12-16|Method of preparing 2,4,6-triiodoresorcinol SU548569A1|1977-02-28|The method of producing titanium dioxide SU423493A1|1974-04-15|CATALYST FOR L1ETHANE CHLORINATION |] qffn? -Cn; - r? 0, C and .. J and !! i. S; U w US2653965A|1953-09-29|Production of acrylonitrile US2440768A|1948-05-04|Production of tetrachloroethylene US2940832A|1960-06-14|Method for synthesizing chromium hexacarbonyl US3607934A|1971-09-21|Process for the manufacture of chlorophosphines
同族专利:
公开号 | 公开日 GB1570088A|1980-06-25| JPS5281096A|1977-07-07| FR2336349B1|1980-01-11| AU1957876A|1978-05-18| RO72143A|1982-02-26| FR2336349A1|1977-07-22| CA1077679A|1980-05-20| JPS5612252B2|1981-03-19| DE2657071A1|1977-07-07| DE2657071C2|1982-04-15| US4039647A|1977-08-02| IT1065562B|1985-02-25| AU498425B2|1979-03-15|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US1474479A|1921-06-10|1923-11-20|E C Klipstein & Sons Company|Manufacture of metal chlorides| US1541068A|1923-01-15|1925-06-09|Harry L Pelzer|Process for the manufacture of aluminum chloride| GB668620A|1949-10-24|1952-03-19|Basf Ag|Improvements in the production of aluminium chloride| DE1061757B|1958-02-12|1959-07-23|Basf Ag|Fluidized bed process for the production of anhydrous aluminum chloride| SU146301A1|1960-04-15|1961-11-30|Г.Л. Грошев|The method of obtaining anhydrous aluminum chloride| GB1270126A|1969-03-29|1972-04-12|British Titan Ltd Formerly Bri|Process for the purification of aluminium chloride| US3832452A|1973-04-10|1974-08-27|D Crouch|Purification of anhydrous aluminum chloride in situ in a salt melt| US3938969A|1973-12-07|1976-02-17|Toth Aluminum Corporation|Purification of aluminum chloride|US4179492A|1977-07-08|1979-12-18|Cato Research Corp.|Process for making rare earth metal chlorides| FR2496632B1|1980-12-24|1983-09-30|Pechiney Aluminium| GR75129B|1980-12-24|1984-07-13|Pechiney Aluminium| US4517037A|1981-11-02|1985-05-14|Aluminum Company Of America|Refractory composition comprising nitride filler and colloidal sol binder| US4460550A|1983-03-30|1984-07-17|Kerr-Mcgee Chemical Corporation|Process for production of titanium dioxide from titaniferrous ore| US4442075A|1983-03-30|1984-04-10|Kerr-Mcgee Chemical Corporation|Titanium ore chlorination process using a molten salt| US4493784A|1984-01-30|1985-01-15|Atlantic Richfield Company|Dehydration of aluminum chloride hexahydrate| US4541907A|1984-04-16|1985-09-17|Aluminum Company Of America|Process for decomposing chlorinated hydrocarbon compounds| DE19924495A1|1999-05-28|2000-11-30|Merck Patent Gmbh|Process and apparatus for the continuous production of NaDCI¶4¶| US6808695B1|2000-05-22|2004-10-26|Toth Aluminum Corporation|Process for continuously producing aluminum from clays| CN103936047B|2013-01-22|2017-07-25|贵阳铝镁设计研究院有限公司|A kind of preparation method of anhydrous Aluminum chloride|
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申请号 | 申请日 | 专利标题 US05/644,416|US4039647A|1975-12-24|1975-12-24|Production of aluminum chloride| 相关专利
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