CN104150508B - A kind of method that ammonia synthesis catalyst low pressure heats up - Google Patents

A kind of method that ammonia synthesis catalyst low pressure heats up Download PDF

Info

Publication number
CN104150508B
CN104150508B CN201410388751.5A CN201410388751A CN104150508B CN 104150508 B CN104150508 B CN 104150508B CN 201410388751 A CN201410388751 A CN 201410388751A CN 104150508 B CN104150508 B CN 104150508B
Authority
CN
China
Prior art keywords
ammonia
synthesis catalyst
ammonia synthesis
gas
low pressure
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.)
Expired - Fee Related
Application number
CN201410388751.5A
Other languages
Chinese (zh)
Other versions
CN104150508A (en
Inventor
冯尚武
杨少忠
刘青宝
杜以凤
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.)
SHANDONG SHUNTIAN CHEMICAL GROUP CO Ltd
Original Assignee
SHANDONG SHUNTIAN CHEMICAL GROUP CO Ltd
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 SHANDONG SHUNTIAN CHEMICAL GROUP CO Ltd filed Critical SHANDONG SHUNTIAN CHEMICAL GROUP CO Ltd
Priority to CN201410388751.5A priority Critical patent/CN104150508B/en
Publication of CN104150508A publication Critical patent/CN104150508A/en
Application granted granted Critical
Publication of CN104150508B publication Critical patent/CN104150508B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • Y02P20/129Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines

Landscapes

  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Catalysts (AREA)

Abstract

The invention discloses a kind of method that ammonia synthesis catalyst low pressure heats up, namely system pressure is supplemented to and is greater than 0.5MPa by synthesis system after being communicated with liquid ammonia storage tank, then gas is delivered to oil separator by open cycle compressor, deliver to synthetic tower after separating greasy dirt to heat up for ammonia synthesis catalyst, then through waste heat recoverer, heat exchanger, water cooler is sent to cool after water heater recovery waste heat, by Optimization Technology method, ammonia synthesis catalyst is heated up, do not need gas making, desulfurization, conversion, decarburization (or carbonization), compression, alcohol alkanisation system cloud gray model, liquid ammonia storage tank overbottom pressure is directly utilized to enter synthesis system, eliminate the process that above system repeats to drive, corresponding power consumption and coal consumption of having saved the compression of this system gas.

Description

A kind of method that ammonia synthesis catalyst low pressure heats up
Technical field
The invention belongs to chemical production technical field, particularly relate to a kind of method that ammonia synthesis catalyst low pressure heats up.
Background technology
The ammonia synthesis catalyst intensification technology that current industry generally adopts is after the whole production system of synthetic ammonia has been overhauled, gasification system first Gas-making Furnace temperature raising gas, after semi-water gas composition is qualified, open desulphurization system, compression system heats up for transformation system, transformation system heats up and terminates, pressure swing adsorption decarbonization (or carbonization) system is opened after conversion gas composition is qualified, alcohol alkanisation system is opened after unstripped gas composition is qualified, after alkane gas trace qualified after import synthesis system, synthesis system pressure is risen to 5.0MPa, then ammonia synthesis catalyst starts to heat up, ammonia synthesis catalyst temperature rise rate is generally 60 DEG C/h, maintenance terminates rear synthetic catalyst temperature and is generally 40 DEG C, 460 DEG C of ability need be warming up to normally produce, period approximately needs 7-8 hour, gas after alkane again could be supplemented Deng the qualified rear synthesis system of synthetic catalyst temperature index, gas making during this period, desulfurization, conversion, decarburization (or carbonization), compression, alcohol alkanisation system cloud gray model is a kind of waste, restarting after out of service is also a kind of waste.
The synthesis system of our company's prior art is through gas making, desulfurization, conversion, decarburization (or carbonization), compression, after alcohol alkanisation system cloud gray model, system pressure is supplemented to 5.0MPa, then gas is delivered to oil separator by open cycle compressor, deliver to synthetic tower after separating greasy dirt to heat up for ammonia synthesis catalyst, then through waste heat recoverer, heat is handed over, water cooler is sent to cool after water heater recovery waste heat, ammonia condenser is sent to lower the temperature further again after sending ammonia separator to separate part liquefied ammonia after cooling, then send cool exchanger to be separated liquefied ammonia and after reclaiming cold, return recycle compressor and carry out next one circulation, gas circulation is normally opened electric furnace afterwards and is suitably adjusted the electric current of electric furnace and voltage according to furnace temperature rising situation and reach the object that ammonia synthesis catalyst heats up, the liquefied ammonia separated send liquid ammonia storage tank.Ammonia synthesis catalyst heats up and carries out under gas making, desulfurization, conversion, decarburization (or carbonization), compression, alcohol alkanisation system operation too, causes the significant wastage of the energy.
Summary of the invention
The object of the invention is by optimized process flow, provide a kind of ammonia synthesis catalyst to heat up, do not need the method that the ammonia synthesis catalyst low pressure of carrying out under gas making, desulfurization, conversion, decarburization (or carbonization), compression, alcohol alkanisation system operation conditions heats up.
The object of the invention is to be achieved through the following technical solutions,
System pressure is supplemented to and is greater than 0.5MPa by synthesis system after being communicated with liquid ammonia storage tank, then gas is delivered to oil separator by open cycle compressor, deliver to synthetic tower after separating greasy dirt to heat up for ammonia synthesis catalyst, then through waste heat recoverer, heat is handed over, water cooler is sent to cool after water heater recovery waste heat, now suitably should control water cooler cooling temperature below 55 DEG C, ammonia condenser is sent to lower the temperature further again after sending ammonia separator to separate part liquefied ammonia after cooling, now suitably should control ammonia condenser cooling temperature below 55 DEG C, then send cool exchanger to be separated liquefied ammonia and after reclaiming cold, return recycle compressor and carry out next one circulation, gas circulation is normally opened electric furnace afterwards and is suitably adjusted the electric current of electric furnace and voltage according to furnace temperature rising situation and reach the object that ammonia synthesis catalyst heats up, the liquefied ammonia separated send liquid ammonia storage tank.
Preferably, system pressure is supplemented to 1.0-1.5MPa by synthesis system after being communicated with liquid ammonia storage tank.
Preferably, control water cooler cooling temperature 40-50 DEG C to be advisable.
Preferably, control ammonia condenser cooling temperature 40-50 DEG C to be advisable.
Beneficial effect of the present invention: by Optimization Technology method, ammonia synthesis catalyst is heated up, do not need gas making, desulfurization, conversion, decarburization (or carbonization), compression, alcohol alkanisation system cloud gray model, liquid ammonia storage tank overbottom pressure is directly utilized to enter synthesis system, eliminate the process that above system repeats to drive, save power consumption and the coal consumption of the compression of this system gas accordingly.
Accompanying drawing explanation
Fig. 1 is process flow sheet of the present invention
Fig. 2 is the process flow sheet of prior art.
Embodiment
As shown in Figure 1, after whole synthesis ammonia system has overhauled, according to gas making, desulfurization, conversion, decarburization (or carbonization), compression, the time of alcohol alkanisation system cloud gray model, synthesis system be communicated with liquid ammonia storage tank in advance, synthesis system pressure is supplemented to 1.0-1.5MPa, then gas is delivered to oil separator by open cycle compressor, deliver to synthetic tower after separating greasy dirt to heat up, then through waste heat recoverer for ammonia synthesis catalyst, heat is handed over, water cooler is sent to cool after water heater recovery waste heat, now suitably should control water cooler cooling temperature 40-50 DEG C, ammonia condenser is sent to lower the temperature further again after sending ammonia separator to separate part liquefied ammonia after cooling, now should suitably control ammonia condenser temperature 40-50 DEG C, then send cool exchanger to be separated liquefied ammonia and after reclaiming cold, return recycle compressor and carry out next one circulation, gas circulation is normally opened electric furnace afterwards and is suitably adjusted the electric current of electric furnace and voltage according to furnace temperature rising situation and reach the object that ammonia synthesis catalyst heats up, and makes the basic and gas making of ammonia synthesis catalyst heating-up time, desulfurization, conversion, decarburization (or carbonization), compression, the time of alcohol alkanisation system cloud gray model matches, and reaches whole synthesis ammonia system and once drives normally to run, energy-saving and cost-reducing object.

Claims (3)

1. the method for an ammonia synthesis catalyst low pressure intensification, it is characterized in that system pressure is supplemented to 1.0-1.5MPa by synthesis system after being communicated with liquid ammonia storage tank, then gas is delivered to oil separator by open cycle compressor, deliver to synthetic tower after separating greasy dirt to heat up for ammonia synthesis catalyst, then through waste heat recoverer, heat is handed over, water cooler is sent to cool after water heater recovery waste heat, now suitably should control water cooler cooling temperature below 55 DEG C, ammonia condenser is sent to lower the temperature further again after sending ammonia separator to separate part liquefied ammonia after cooling, now suitably should control ammonia condenser cooling temperature below 55 DEG C, then send cool exchanger to be separated liquefied ammonia and after reclaiming cold, return recycle compressor and carry out next one circulation, gas circulation is normally opened electric furnace afterwards and is suitably adjusted the electric current of electric furnace and voltage according to furnace temperature rising situation and reach the object that ammonia synthesis catalyst heats up, the liquefied ammonia separated send liquid ammonia storage tank.
2. the method for a kind of ammonia synthesis catalyst low pressure intensification according to claim 1, is characterized in that controlling water cooler cooling temperature 40-50 DEG C is advisable.
3. the method for a kind of ammonia synthesis catalyst low pressure intensification according to claim 1, is characterized in that controlling ammonia condenser cooling temperature 40-50 DEG C is advisable.
CN201410388751.5A 2014-08-10 2014-08-10 A kind of method that ammonia synthesis catalyst low pressure heats up Expired - Fee Related CN104150508B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410388751.5A CN104150508B (en) 2014-08-10 2014-08-10 A kind of method that ammonia synthesis catalyst low pressure heats up

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410388751.5A CN104150508B (en) 2014-08-10 2014-08-10 A kind of method that ammonia synthesis catalyst low pressure heats up

Publications (2)

Publication Number Publication Date
CN104150508A CN104150508A (en) 2014-11-19
CN104150508B true CN104150508B (en) 2016-02-24

Family

ID=51876179

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410388751.5A Expired - Fee Related CN104150508B (en) 2014-08-10 2014-08-10 A kind of method that ammonia synthesis catalyst low pressure heats up

Country Status (1)

Country Link
CN (1) CN104150508B (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991009811A1 (en) * 1990-01-04 1991-07-11 Schwarzenbek Eugene F Synthetic ammonia process
CN102557075A (en) * 2010-12-07 2012-07-11 北京利达丰华科技有限公司 Method for circularly utilizing cooling capacity and method for increasing yield of synthesis ammonia
CN203307064U (en) * 2013-06-08 2013-11-27 浠水县福瑞德化工有限责任公司 Ammonia synthesis system
CN103570039A (en) * 2013-11-08 2014-02-12 安徽金禾实业股份有限公司 Novel refrigeration method and novel refrigeration device in synthetic ammonia production process
CN203683104U (en) * 2014-02-17 2014-07-02 孙经东 Low-pressure heating device of synthetic tower of ammonia synthesizing device
CN203715291U (en) * 2014-03-03 2014-07-16 四川隆桥化工集团有限公司 Warming system with temperature regulating valve in synthetic ammonia reaction process

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1991009811A1 (en) * 1990-01-04 1991-07-11 Schwarzenbek Eugene F Synthetic ammonia process
CN102557075A (en) * 2010-12-07 2012-07-11 北京利达丰华科技有限公司 Method for circularly utilizing cooling capacity and method for increasing yield of synthesis ammonia
CN203307064U (en) * 2013-06-08 2013-11-27 浠水县福瑞德化工有限责任公司 Ammonia synthesis system
CN103570039A (en) * 2013-11-08 2014-02-12 安徽金禾实业股份有限公司 Novel refrigeration method and novel refrigeration device in synthetic ammonia production process
CN203683104U (en) * 2014-02-17 2014-07-02 孙经东 Low-pressure heating device of synthetic tower of ammonia synthesizing device
CN203715291U (en) * 2014-03-03 2014-07-16 四川隆桥化工集团有限公司 Warming system with temperature regulating valve in synthetic ammonia reaction process

Also Published As

Publication number Publication date
CN104150508A (en) 2014-11-19

Similar Documents

Publication Publication Date Title
CN101899562B (en) Waste heat utilization steel strip heat treatment system
CN203489712U (en) Novel generating equipment with integrated application of waste heat in sintering, steel making and steel rolling
CN205145175U (en) Continuous degassing unit of lactic fermentation
CN104150508B (en) A kind of method that ammonia synthesis catalyst low pressure heats up
CN201390755Y (en) Surplus heat recovery system of blast furnace slag washing water
CN201770747U (en) Residual-heat utilization steel-tape heat treatment system
CN209631819U (en) One kind producing hot-rolled process residual neat recovering system for steel
CN204263424U (en) Tyre vulcanization dynamical system
CN203687472U (en) Cooling device in ammonium nitrate production device
CN202280490U (en) Device for converting heat energy of remained hot water
CN104195035A (en) Novel comprehensive waste heat utilization system of biogas engineering
CN203980740U (en) The energy saving water supply device of technique cold water
CN203429098U (en) Alcohol recycling device in pectin production
CN202204132U (en) Device for heating water by recycling heat of polycrystalline silicon reduction furnace
CN202099387U (en) Regenerated acid storage mechanism for cold rolling line
CN204958811U (en) Living beings microwave schizolysis system
CN204352738U (en) From heating control system
CN104261428A (en) Synthesis ammonia production method for improving net value of ammonia
CN204254728U (en) Vertical shaft preventing freeze in winter heating system
CN203048597U (en) Heating, unfreezing and blowing-out system for nitrogen generating equipment
CN204725705U (en) A kind of energy-conservation mixing device
CN203559151U (en) Rapid cooling device of single crystal furnace
CN202725156U (en) Improved structure of staticizing reactor
CN202175553U (en) Recycling structure for exhausted gas of zinc oxide desulfurizing tank
CN202297532U (en) Steam-free heating recycle oil benzene braising device

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20160224

Termination date: 20160810

CF01 Termination of patent right due to non-payment of annual fee