CN1207329A - Preparation and use method of catalyst for synthesis of 2,6-dimethylaniline - Google Patents

Preparation and use method of catalyst for synthesis of 2,6-dimethylaniline Download PDF

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Publication number
CN1207329A
CN1207329A CN 97108179 CN97108179A CN1207329A CN 1207329 A CN1207329 A CN 1207329A CN 97108179 CN97108179 CN 97108179 CN 97108179 A CN97108179 A CN 97108179A CN 1207329 A CN1207329 A CN 1207329A
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dimethylaniline
catalyst
weighing
carrier
preparation
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CN 97108179
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CN1087970C (en
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刘智凌
廖文文
王宇
谭卫宁
陈平
邹德元
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Hunan Research Institute of Chemical Industry
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Hunan Research Institute of Chemical Industry
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Abstract

A process for preparing the catalyst used to synthesize 2,6-dimethylaniline includes immersing gamma-A2O3 as carrier skeleton in Mg(NO3)2.6H2O and Al(NO3)3 solution to obtain spinel-type carrier (Al2O3-MgO), and impregnating in the solution of PdCl2 and hydrochloric acid to obtain said catalyst Pb/Al2O3-MgO/Al2O3. Its application process includes loading the catalyst in stainless steel tube, filling ceramic rings to both ends of the stainless steel tube, heating it by resistance wire, and introducing 2,6-dimethylphenol, hydrogen and ammonia. Its advantages are simple process, easy operation, high activity, strength, selectivity and product yield and long service life.

Description

The Preparation of catalysts and the application process of Synthetic 2 .6-dimethylaniline
The present invention relates to a kind of Preparation of catalysts method that is used for Synthetic 2 .6-dimethylaniline and be used for Synthetic 2, the method for 6-dimethylaniline.
2.6-dimethylaniline is important meticulous organic chemical industry's intermediate, is mainly used in to produce agricultural chemicals, dyestuff and medicine, wherein commercial have bactericide, herbicide, an anesthetic etc.2.6-the early stage production method of dimethylaniline is a meta-xylene restore nitrification method, with the concentrated sulfuric acid, nitric acid nitrating and iron powder reducing, has a large amount of three wastes to produce; After be improved to hydrogenating reduction or electrochemical reduction, but principal product 2, the 4-dimethylaniline has restricted development (United States Patent (USP) U.S.P.3,965,182 of this process route; U.S.P.3,960,962; U.S.P.3,931298 etc.), adopt 2,6-xylenol liquid-phase catalysis amination Synthetic 2,6-dimethylaniline, and industrialization.European patent E.P.68 in 282 and Deutsche Bundespatent D.E.3,147,734, adopts Al 2O 3Be catalyst, 400 ℃ of 90 crust descends 2,6-xylenol gas phase catalysis amination preparation 2,6-dimethylaniline.Europe another piece patent E.P.53,817; E.P.53,819 adopt spinelle Al 2O 3-MgO is a carrier, and load 0.5% Metal Palladium is a catalyst, at 180 ℃-200 ℃, normal pressure, and by 2,6-xylenol gas phase catalysis preparation 2,6-dimethylaniline, product selectivity about 70%, but above all unexposed Preparation of catalysts method.
The purpose of this invention is to provide a kind of Synthetic 2 that is used for, gas phase Study on Catalytic Amination of Alcohols preparation 2 under the Preparation of catalysts method of 6-dimethylaniline and the normal pressure, the method for 6-dimethylaniline.
Task of the present invention is finished like this: take by weighing r-Al earlier 2O 3,,, take by weighing Mg (NO again as carrier framework 200 ℃ of dehydrations down 3) 26H 2O joins Al (NO 3) 3Dissolve in the solution, pour this solution into dress r-Al 2O 3In the burning of the carrier framework bosom, incipient impregnation, then 120 ℃ dry down, 800-1300 ℃ of roasting 6 hours obtains sharp crystal Al after the cooling 2O 3-MgO carrier; Take by weighing NaHCO again 3Wiring solution-forming, impregnated carrier again, 120 ℃ of following dried overnight; Take by weighing PdCl at last 2, to dissolve by 1+10 with watery hydrochloric acid, dissolving back and above-mentioned carrier incipient impregnation, the drying that makes obtain catalyst P d (0.5% weight)/Al 2O 3-MgO (4: 1 weight)/Al 2O 3With the catalyst that the makes internal diameter of packing into is in the stainless steel tube of φ 19mm, uses the resistance wire heating, and managing built-in external diameter is the thermocouple temperature measurement sleeve pipe of 6mm, catalyst loads the porcelain ring up and down, and normal pressure feeds 2 down, 6-xylenol, hydrogen, ammonia, catalyst loading is a 0.1-0.15 gram 2,6-xylenol/gram catalyst hour, reaction temperature 180-200 ℃, 2,6-xylenol conversion ratio reaches 97.9%, 2.6-dimethylaniline selectivity 74.3%, 2,6-dimethyl cyclohexyl amine selectivity is 2.52%.
Preparation technology of the present invention is simple, and raw material is easy to get, and is easy to operate, is being used for Synthetic 2, when the 6-dimethylaniline synthesizes, and the catalyst activity height, intensity is good, and the life-span is long, reaction condition gentleness, selectivity of product height.
The invention will be further described below in conjunction with embodiment: embodiment 1:
Take by weighing 25 gram φ 3mm * 5mmr-Al 2O 3, at 200 ℃ of following drying and dehydratings, be placed on as carrier framework and burn in the bosom standbyly, take by weighing 3.205 gram Mg (NO 3) 26H 2O joins 25.18 gram Al (NO 3) 3(contain Al in the solution 3+Be 4.1%) dissolving.Solution poured into r-Al is housed 2O 3Burning cherish medium volume dipping, 120 ℃ of following dried overnight reduce nitrate under 300 ℃, then 900 ℃ of following roastings 6 hours, after the cooling spinelle Al 2O 3-MgO carrier 27g takes by weighing 1.25 gram NaHCO then 3Be made into 10ml solution, dipping, 120 ℃ of following dried overnight.Take by weighing PdCl again 20.209 gram adds watery hydrochloric acid 10ml, dissolves, dissolving back and the 27 gram carrier impregnation that obtain earlier are washed with distilled water to no chlorion and sodium ion then, and be dry again, thereby make catalyst 20g, carries palladium amount 0.5% (weight), surfaces A l 2O 3: MgO=4: 1 (weight), surfaces A l 2O 3+ MgO pickup is 10%.
With the catalyst 20g that makes, in the internal diameter φ 19mm stainless steel tube of packing into, with the resistance wire heating, managing built-in external diameter is the thermocouple temperature measurement sleeve pipe of 6mm, and catalyst loads the porcelain ring up and down.Under the normal pressure, 2, the 6-xylenol carries out being 3.0g/hr, ammonia and hydrogen flow rate all are 80ml/min, 195 ℃ of reaction temperatures, 2,6-xylenol conversion ratio 97.9%, 2,6-dimethylaniline selectivity 74.3%, 2,6-dimethyl cyclohexyl amine selectivity is 25.2%.Embodiment 2
Catalyst preparation process is with embodiment 1, Al 2O 3The total pickup of+MgO is 8%, and 180 ℃ of reaction temperatures, in 2.0 gram/times of charging, other reaction condition is constant, 2, and 6-xylenol conversion ratio 96.39%, 2,6-dimethylaniline selectivity 24.91%, 2,6-dimethyl cyclohexyl amine selectivity 74.85%.Embodiment 3:
Catalyst is with embodiment 2,180 ℃ of reaction temperatures, charging 2.0 grams 2, the 6-xylenol/hour, hydrogen flowing quantity is 80 ml/min, ammonia flow is 40 ml/min, 2, and 6-xylenol conversion ratio 99.07%, 2,6-dimethylaniline selectivity 32.70%, 2,6-dimethyl cyclohexyl amine selectivity 66.20%.Embodiment 4:
Preparation of Catalyst is with embodiment 1, but 1050 ℃ of carrier sintering temperatures, loading catalyst 20 grams, 180 ℃ of reaction temperatures, 2,6-xylenol inlet amount 3.0 Grams Per Hours, ammonia and hydrogen flowing quantity are respectively 60 ml/min and 80 ml/min, 2,6-xylenol conversion ratio 96.72%, 2,6-dimethylaniline selectivity 40.20%, 2,6-dimethyl cyclohexyl amine selectivity 59.30%.Embodiment 5:
The same embodiment of Preparation of Catalyst, but 1300 ℃ of carrier sintering temperatures, the aminating reaction condition is with embodiment 4,2,6-xylenol conversion ratio 65.72%, 2,6-dimethylaniline selectivity 20.3%, 2,6-dimethyl cyclohexyl amine selectivity 78.50%.

Claims (2)

1, a kind of Synthetic 2 that is used for, the Preparation of catalysts of 6-dimethylaniline and application process is characterized in that: take by weighing r-Al 2O 3At 200 ℃ of following drying and dehydratings,, take by weighing Mg (NO again as carrier framework 3) 26H 2O and Al (NO 3) 2Wiring solution-forming is with solution and r-Al 2O 3Incipient impregnation, then 120 ℃ down dry, 800 ℃ of-1300 ℃ of roastings 6 hours obtain spinelle Al after the cooling 2O 3-MgO carrier takes by weighing NaHCO again 3Wiring solution-forming, impregnated carrier again, 120 ℃ of following dried overnight take by weighing PdCl at last 2, to dissolve by 1+10 with watery hydrochloric acid, dissolving back and the above-mentioned carrier incipient impregnation that makes are washed with distilled water to no chlorion and sodium ion then, and be dry again, obtains catalyst P d (0.5% weight)/Al 2O 3-MgO (4: 1 weight)/Al 2O 3The catalyst that makes is packed in the stainless steel tube, use the resistance wire heating, pipe built-in thermoelectric idol temperature-measuring casing, catalyst loads the porcelain ring up and down, and normal pressure feeds 2 down, 6-xylenol, ammonia and hydrogen, thus make 2, the 6-dimethylaniline.
2, according to the described a kind of Synthetic 2 that is used for of claim 1, the Preparation of catalysts of 6-dimethylaniline and application process, it is characterized in that: the catalytic reaction Synthetic 2, during the 6-dimethylaniline, reaction temperature 180-200 ℃, hydrogen and ammonia flow velocity are 40ml/min-80ml/min, 2, and the inlet amount of 6-xylenol is 2-3g/hr.
CN97108179A 1997-08-06 1997-08-06 Preparation and use method of catalyst for synthesis of 2,6-dimethylaniline Expired - Lifetime CN1087970C (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7767855B2 (en) 2005-06-23 2010-08-03 Basf Se Method for the continuous production of an amine
CN101356150B (en) * 2006-01-05 2011-09-14 巴斯夫欧洲公司 Process for continuous preparation of a primary aromatic amine
CN107308955A (en) * 2017-07-10 2017-11-03 江苏宝灵化工股份有限公司 Synthesize catalyst of 2,6 diisopropyl anilines and its production and use
CN107335440A (en) * 2017-07-10 2017-11-10 江苏宝灵化工股份有限公司 Synthesize catalyst of 2,6 dimethylanilines and its production and use
CN109422655A (en) * 2017-08-24 2019-03-05 中国石油化工股份有限公司 A kind of method of the direct ammonification aniline of phenol

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2439189A1 (en) 2010-09-17 2012-04-11 Basf Se Method for manufacturing aromatic amines

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3045719A1 (en) * 1980-12-04 1982-07-08 Basf Ag, 6700 Ludwigshafen METHOD FOR PRODUCING CYCLOALIPHATIC AND / OR AROMATIC AMINES
JPS60130568A (en) * 1983-12-20 1985-07-12 Nippon Kayaku Co Ltd Production of 7-alkyl-8-hydroxyquinoline
DD297399A5 (en) * 1986-12-22 1992-01-09 Basf Schwarzheide Gmbh,De PROCESS FOR THE PREPARATION OF N, N-DIMETHYLCYCLOHEXYLAMINE IN THE LIQUID PHASE AND CATALYST FOR CARRYING OUT THE PROCESS
JPH01165556A (en) * 1987-12-22 1989-06-29 Mitsui Petrochem Ind Ltd Recovery of anilines
CN1022483C (en) * 1990-04-21 1993-10-20 浙江工学院 Process for preparing 2, 4-dimethylaniline and 2, 6-dimethylaniline
DE4428018A1 (en) * 1994-08-08 1996-02-15 Bayer Ag Process for the preparation of aromatic amines

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7767855B2 (en) 2005-06-23 2010-08-03 Basf Se Method for the continuous production of an amine
CN101356150B (en) * 2006-01-05 2011-09-14 巴斯夫欧洲公司 Process for continuous preparation of a primary aromatic amine
CN107308955A (en) * 2017-07-10 2017-11-03 江苏宝灵化工股份有限公司 Synthesize catalyst of 2,6 diisopropyl anilines and its production and use
CN107335440A (en) * 2017-07-10 2017-11-10 江苏宝灵化工股份有限公司 Synthesize catalyst of 2,6 dimethylanilines and its production and use
CN109422655A (en) * 2017-08-24 2019-03-05 中国石油化工股份有限公司 A kind of method of the direct ammonification aniline of phenol
CN109422655B (en) * 2017-08-24 2021-10-29 中国石油化工股份有限公司 Method for preparing aniline by directly ammoniating phenol

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