CN1363550A - Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor - Google Patents

Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor Download PDF

Info

Publication number
CN1363550A
CN1363550A CN 02112535 CN02112535A CN1363550A CN 1363550 A CN1363550 A CN 1363550A CN 02112535 CN02112535 CN 02112535 CN 02112535 A CN02112535 A CN 02112535A CN 1363550 A CN1363550 A CN 1363550A
Authority
CN
China
Prior art keywords
aniline
reactor
liquid
gas
heating
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 02112535
Other languages
Chinese (zh)
Other versions
CN1169779C (en
Inventor
张金泉
曹宏生
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CNB02112535XA priority Critical patent/CN1169779C/en
Publication of CN1363550A publication Critical patent/CN1363550A/en
Application granted granted Critical
Publication of CN1169779C publication Critical patent/CN1169779C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A process for synthesizing biphenylamine from phenylamine includes such steps as metering phenylamine, heating it so 330-370 deg.C, reacting with catalyst and nitrogen gas at 320-360 deg.C, 1.6-2.5 MPa and 0.15-0.2 /h of space speed, cooling by heat exchange with raw material, gas-liquid separation to obtain intermediate liquid, heating, feeding in phenylamine rectifying tower, and purifying in biphenylamine rectifying tower. Its advantages include simple equipment, low cost, and high safety.

Description

The aniline syntehsizing diphenylamine method that adds nitrogen in the reactor
Technical field:
The present invention relates to be a kind of with aniline as raw material synthetic pentanoic method, prepared product is used for synthetic rubber anti-aging agent, dyestuff intermediate and important stablizer etc.Belong to the fine chemical technology field.
Background technology:
Prior art such as CN1186802A, denomination of invention is a continous diphenylemine synthesizing industrial system by using phenylamine as material.Its structure includes reactor and outlet is connected in series gas-liquid separator successively, the absorption device, inhale the nitrogen device, air water separator, dry cleaner was set before reactor, this dry cleaner inlet connects from syngas for synthetic ammonia (being refinery gas), the clean gas outlet of clean cleaner is connected to reactor, the gas phase import, the 1 grade of import that is connected to synthetic ammonia installation high-pressure unit operation is returned in the stripping gas outlet, Detoxicating device is set after air water separator, this Detoxicating device inlet connects from air water separator works off one's feeling vent one's spleen, V level (or the IV level) import that is connected to synthetic ammonia installation high-pressure unit operation is returned in the Detoxicating device air outlet, it designs by synthetic ammonia installation, that is to say, it is the hydrogen consumption that utilizes in the technical process of synthetic ammonia installation minimizing syntehsizing diphenylamine, reaches the purpose that reduces cost.Yet because it needs synthetic ammonia installation, and not thorough to reducing hydrogen consumption yet, so its cost is still very high.
Summary of the invention:
The object of the invention is the defective at above-mentioned existence, proposes a kind of cancellation synthetic ammonia installation, fundamentally reaches the aniline syntehsizing diphenylamine method that adds nitrogen in reactor that reduces cost, the preparation pentanoic.Technical solution of the present invention: its processing step is followed successively by: the metering of (1) aniline, the aniline raw material is measured and sends into the aniline well heater by aniline scale tank, volume pump; (2) aniline heating, the aniline raw material after the metering is heated to 330-370 ℃; (3) reaction, the raw material aniline after heating is located in the reactor that catalyzer is housed, and carries out chemical reaction, lowers the temperature by the raw produce interchanger then, makes temperature below 150 ℃; (4) gas-liquid separation, decompression afterreaction intermediate liquid carries out gas-liquid separation in gas-liquid separator; (5) intermediate liquid heating through the liquid phase behind the gas-liquid separator, is carried out heat temperature raising by medial launder, fresh feed pump, well heater; (6) separation and purification, enter aniline distillation tower to the intermediate liquid behind the heat temperature raising, liquid phase wherein enters the pentanoic rectifying tower and is purified to the pentanoic finished product, it is characterized in that processing step (3) reaction, in reactor, add nitrogen, pressure in the reactor is 1.6-2.5MPa, and aniline is 0.15-0.2/h with the air speed ratio of catalyzer, and temperature is 320-360 ℃.Advantage of the present invention: compared with prior art, owing to cancelled synthetic ammonia installation, number of devices is reduced, greatly reduce production cost, the condition operation at no hydrogen has reduced anti-hazard classification, has improved safety performance.
Accompanying drawing is a process flow sheet of the present invention.
Among the figure 1 is aniline metering, the 2nd, aniline heating, the 3rd, reaction, the 4th, gas-liquid separation, the 5th, intermediate liquid heating, the 6th, separation and purification, the 7th, finished product packing.
Embodiment
Aniline is by aniline scale tank volume (v=6m 3), volume pump (ram pump), the metering back is with the 2t/h flow, through nitrogen buffering gas bag (P=2.0MPa, V=0.3m 3) after enter raw produce interchanger preheating in the aniline heating 2, be heated to 340 ℃ through electric heater again and enter in the reactor, add nitrogen in the reactor, the pressure in the reactor is 2MPa, adds catalyzer 10m in the reactor 3Be 0.2/h with the air speed ratio of aniline, temperature is 340 ℃.The model of catalyzer is selected FD-20, it is to be produced by Fushun petrochemical industry research institute, reactor outlet material is reduced to below 150 ℃ through the raw produce interchanger, after be decompressed to below the 0.1MPa, enter the high-temperature separator in the gas-liquid separator 4, gas phase in the high-temperature separator is cooled to below 40 ℃ through condenser and enters low-temperature separator, the liquid phase of high-temperature separator and low-temperature separator enters the middle liquid bath of reaction in the intermediate liquid heating 5, through fresh feed pump (process pump), heat exchanger, well heater (heat interchanging area S=30m 2) be heated to 184 ℃, enter aniline distillation tower and separate, cat head aniline is cooled to below 100 ℃ through heat exchanger, condenser, partial reflux, the aniline scale tank that part is returned in the aniline metering 1 is recycled.The material that the tower still is 300 ℃ is purified for a collection of pentanoic rectifying tower that enters for per 5 tons, earlier light component is boiled off, and can steam finished product pentanoic, finished product packing then.

Claims (1)

1, add the aniline syntehsizing diphenylamine method of nitrogen in the reactor, its processing step is followed successively by: the metering of (1) aniline, the aniline raw material is measured and sends into the aniline well heater by aniline scale tank, volume pump; (2) aniline heating, the aniline raw material after the metering is heated to 330-370 ℃; (3) reaction, the raw material aniline after heating is located in the reactor that catalyzer is housed, and carries out chemical reaction, lowers the temperature by the raw produce interchanger then, makes temperature below 150 ℃; (4) gas-liquid separation, decompression afterreaction intermediate liquid carries out gas-liquid separation in gas-liquid separator; (5) intermediate liquid heating through the liquid phase behind the gas-liquid separator, is carried out heat temperature raising by medial launder, fresh feed pump, well heater; (6) separation and purification, enter aniline distillation tower to the intermediate liquid behind the heat temperature raising, liquid phase wherein enters the pentanoic rectifying tower and is purified to the pentanoic finished product, it is characterized in that processing step (3) reaction, in reactor, add nitrogen, pressure in the reactor is 1.6-2.5MPa, and aniline is 0.15-0.2/h with the air speed ratio of catalyzer, and temperature is 320-360 ℃.
CNB02112535XA 2002-01-14 2002-01-14 Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor Expired - Lifetime CN1169779C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB02112535XA CN1169779C (en) 2002-01-14 2002-01-14 Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB02112535XA CN1169779C (en) 2002-01-14 2002-01-14 Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor

Publications (2)

Publication Number Publication Date
CN1363550A true CN1363550A (en) 2002-08-14
CN1169779C CN1169779C (en) 2004-10-06

Family

ID=4742084

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB02112535XA Expired - Lifetime CN1169779C (en) 2002-01-14 2002-01-14 Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor

Country Status (1)

Country Link
CN (1) CN1169779C (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102250651A (en) * 2011-06-17 2011-11-23 西安聚德新能源技术有限公司 Production process and device of large-proportion methanol gasoline for molecular sieve catalytic synthesis vehicle
CN105384683A (en) * 2015-12-17 2016-03-09 南通新邦化工科技有限公司 2-Methyl-pyridine and 4-methylpyridine production method
CN107935862A (en) * 2017-11-27 2018-04-20 南通新邦化工科技有限公司 A kind of method of aniline continuous synthesizing diphenylamine

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102250651A (en) * 2011-06-17 2011-11-23 西安聚德新能源技术有限公司 Production process and device of large-proportion methanol gasoline for molecular sieve catalytic synthesis vehicle
CN102250651B (en) * 2011-06-17 2014-07-09 西安聚德新能源技术有限公司 Production process and device of large-proportion methanol gasoline for molecular sieve catalytic synthesis vehicle
CN105384683A (en) * 2015-12-17 2016-03-09 南通新邦化工科技有限公司 2-Methyl-pyridine and 4-methylpyridine production method
CN105384683B (en) * 2015-12-17 2018-04-10 南通新邦化工科技有限公司 A kind of 2 picoline, the production method of 4 picolines
CN107935862A (en) * 2017-11-27 2018-04-20 南通新邦化工科技有限公司 A kind of method of aniline continuous synthesizing diphenylamine

Also Published As

Publication number Publication date
CN1169779C (en) 2004-10-06

Similar Documents

Publication Publication Date Title
US10017438B2 (en) Method and device system for producing dimethyl oxalate through carbonylation of industrial synthesis gas and producing ethylene glycol through dimethyl oxalate hydrogenation
CN101569817B (en) Tail gas recycling method in trichlorosilane production
CN102923715A (en) Novel process for recycling tail gas generated in polycrystalline silicon production
CN111470941A (en) High-quality cyclohexanol production device and process
CN113045383A (en) System and process for preparing methanol by carbon dioxide hydrogenation
CN210356586U (en) Tail gas recovery equipment for process for preparing lithium hexafluorophosphate by anhydrous hydrogen fluoride solvent method
CN111330412A (en) System and process for absorbing and purifying byproduct hydrogen chloride gas in chlorination workshop section to form acid
CN1169779C (en) Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor
CN111013382B (en) Tail gas treatment device and method for adipic acid production device
CN212369872U (en) System for absorbing and purifying byproduct hydrogen chloride gas in chlorination workshop section to form acid
CN110183479B (en) System and process for hydrolyzing low-pressure dimethyldichlorosilane
CN1141290C (en) Process for preparing biphenylamine from phenylamine by vacuum rectification while heating
CN208932988U (en) A kind of purge drying system of food-grade carbon-dioxide
CN116143078A (en) System and method for recycling hydrogen chloride in polycrystalline silicon tail gas
CN215288580U (en) System for preparing methanol by carbon dioxide hydrogenation
CN212299665U (en) Device for recovering argon tail gas in monocrystalline silicon production
CN212609586U (en) Hydrocarbon removing purifier
CN212142124U (en) Adipic acid apparatus for producing tail gas processing apparatus
CN111732496B (en) System for producing 3, 5-trimethylcyclohexanol by hydrogenation of isophorone and application method thereof
CN207671691U (en) Prepare the device of carbon monoxide
CN220861410U (en) Methyl chloride synthesis system without byproduct hydrochloric acid
CN101481362B (en) Method for preparing hexamethylene imine
CN217504147U (en) Energy-conserving recovery system of polycrystalline silicon chlorosilane-containing tail gas
CN221130998U (en) Device for preparing high-purity silane gas by utilizing trichlorosilane
CN215138495U (en) Methyl nitrite recovery unit

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
C14 Grant of patent or utility model
GR01 Patent grant
EE01 Entry into force of recordation of patent licensing contract

Assignee: Jiangsu Feiya Chemical Industry Co., Ltd.

Assignor: Cao Hongsheng

Contract fulfillment period: 2009.2.8 to 2014.2.7

Contract record no.: 2009320000139

Denomination of invention: Process for synthesizing biphenylamine from phenylamine by adding nitrogen gas to reactor

Granted publication date: 20041006

License type: Exclusive license

Record date: 20090225

LIC Patent licence contract for exploitation submitted for record

Free format text: EXCLUSIVE LICENSE; TIME LIMIT OF IMPLEMENTING CONTACT: 2009.2.8 TO 2014.2.7; CHANGE OF CONTRACT

Name of requester: JIANGSU FEIYA CHEMISTRY INDUSTRY CO.,LTD.

Effective date: 20090225

CX01 Expiry of patent term
CX01 Expiry of patent term

Granted publication date: 20041006