CN102898390A - Method for heating triamine reactor carrier gas with flue gas of molten salt furnace - Google Patents

Method for heating triamine reactor carrier gas with flue gas of molten salt furnace Download PDF

Info

Publication number
CN102898390A
CN102898390A CN2012104421439A CN201210442143A CN102898390A CN 102898390 A CN102898390 A CN 102898390A CN 2012104421439 A CN2012104421439 A CN 2012104421439A CN 201210442143 A CN201210442143 A CN 201210442143A CN 102898390 A CN102898390 A CN 102898390A
Authority
CN
China
Prior art keywords
molten salt
flue gas
salt furnace
carrier 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.)
Pending
Application number
CN2012104421439A
Other languages
Chinese (zh)
Inventor
马肃
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 CN2012104421439A priority Critical patent/CN102898390A/en
Publication of CN102898390A publication Critical patent/CN102898390A/en
Pending legal-status Critical Current

Links

Images

Abstract

The invention relates to the field of production of tripolycyanamide, in particular to a method for heating a reactor by using high-temperature flue gas generated by a molten salt furnace during production of tripolycyanamide. The method comprises the following steps of: arranging a shell and tube heat exchanger between the molten salt furnace and a dust remover; making normal-pressure flue gas discharged out of the molten salt furnace enter the shell side of the shell and tube heat exchanger; making ammonia gas of 0.1MP enter the shell side of the shell and tube heat exchanger at the normal temperature; heating to 320-350 DEG C by using high-temperature flue gas in the shell side; entering a carrier gas preheater; heating to 390-420 DEG C by using molten high-temperature molten salt; and entering the bottom of the reactor to obtain reaction carrier gas. Carrier gas is heated by using high-temperature flue gas generated by the molten salt furnace, so that waste of high-temperature flue gas is reduced, the using amount of molten salt is reduced simultaneously, coal consumption is lowered, the consumption of white coal is 3.9-4.0 tons needed for preparing every ton of tripolycyanamide in a refitted reaction system through practical production, and cost is saved greatly.

Description

Utilize the method for molten salt furnace flue gas heating triamine device carrier gas
Technical field
The present invention relates to the Melamine Production field, relate to specifically the method for the high-temperature flue gas reactor heating that utilizes the molten salt furnace generation in the Melamine Production.
Background technology
In the Melamine Production, the temperature of reaction of urea is about 390 ℃ in the reactor, in the general industrial production, directly utilize molten salt furnace heating fused salt, carrier gas in the high-temperature molten salt reactor heating that melts, the consumption of coal is high, and one ton of trimeric cyanamide of general every production on average needs to consume 4.2 tons anthracite.And the flue-gas temperature that molten salt furnace produces is up to more than 500 ℃, and in the existing production equipment, the molten salt furnace flue gas generally passes through preheated air behind the fly-ash separator, and high level heat has caused the waste of the energy as Lowlevel thermal energy usefulness.
Summary of the invention
The objective of the invention is to utilize the high-temperature flue gas of molten salt furnace generation, the reactor heating carrier gas improves temperature of reactor.
The present invention realizes by the following technical solutions:
Utilize the method for molten salt furnace flue gas heating triamine device carrier gas, technical process is:
Between molten salt furnace and fly-ash separator, increase a tube and shell heat exchanger, molten salt furnace normal pressure flue gas out enters the shell side of tube and shell heat exchanger, normal temperature, 0.1MP ammonia be introduced in the tube side of tube and shell heat exchanger, utilize the high-temperature flue gas in the shell side to be heated to 320-350 ℃, then enter carrier gas preheater, utilize the high-temperature molten salt that melts to be heated to 390-420 ℃, enter at last reactor bottom, as the reaction carrier gas.
The invention has the beneficial effects as follows: the high-temperature flue gas heating carrier gas that utilizes molten salt furnace to produce, reduced the waste of high-temperature flue gas, reduced simultaneously the consumption of fused salt, saved coal, through actual production, one ton of trimeric cyanamide of the every production of improved reactive system need to consume anthracite 3.9-4.0 ton, has greatly saved cost.
Description of drawings
Fig. 1 is original production technique;
Fig. 2 is improved production technique.
Embodiment
As shown in Figure 1, in original production technique, the high-temperature flue gas that molten salt furnace produces directly enters air preheater through fly-ash separator, high level heat has been wasted resource as Lowlevel thermal energy usefulness, and carrier gas utilizes the fused salt heating of thawing fully, the fused salt expense is large, and coal consumption is high.Technique after the improvement as shown in Figure 2, between molten salt furnace and fly-ash separator, increase a tube and shell heat exchanger, molten salt furnace normal pressure flue gas out enters the shell side of tube and shell heat exchanger, normal temperature, the ammonia of 0.1MP is introduced in the tube side of tube and shell heat exchanger, utilizes the high-temperature flue gas in the shell side to be heated to 320-350 ℃, then enter carrier gas preheater, utilize the high-temperature molten salt that melts to be heated to 390-420 ℃, enter at last reactor bottom, as the reaction carrier gas.

Claims (1)

1. utilize the method for molten salt furnace flue gas heating triamine device carrier gas, it is characterized in that its technical process is:
Between molten salt furnace and fly-ash separator, increase a tube and shell heat exchanger, molten salt furnace normal pressure flue gas out enters the shell side of tube and shell heat exchanger, normal temperature, 0.1MP ammonia be introduced in the tube side of tube and shell heat exchanger, utilize the high-temperature flue gas in the shell side to be heated to 320-350 ℃, then enter carrier gas preheater, utilize the high-temperature molten salt that melts to be heated to 390-420 ℃, enter at last reactor bottom, as the reaction carrier gas.
CN2012104421439A 2012-11-07 2012-11-07 Method for heating triamine reactor carrier gas with flue gas of molten salt furnace Pending CN102898390A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012104421439A CN102898390A (en) 2012-11-07 2012-11-07 Method for heating triamine reactor carrier gas with flue gas of molten salt furnace

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012104421439A CN102898390A (en) 2012-11-07 2012-11-07 Method for heating triamine reactor carrier gas with flue gas of molten salt furnace

Publications (1)

Publication Number Publication Date
CN102898390A true CN102898390A (en) 2013-01-30

Family

ID=47570910

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012104421439A Pending CN102898390A (en) 2012-11-07 2012-11-07 Method for heating triamine reactor carrier gas with flue gas of molten salt furnace

Country Status (1)

Country Link
CN (1) CN102898390A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103570636A (en) * 2013-11-16 2014-02-12 安徽金禾实业股份有限公司 Method for heating melamine circulation carrying gas by flue gas produced by molten salt furnace
CN103601693A (en) * 2013-10-23 2014-02-26 李东田 One-step method used for production of melamine by circulating ammonia gas as carrying gas
CN104315871A (en) * 2014-10-30 2015-01-28 安徽金禾实业股份有限公司 Molten-salt-furnace outlet flue gas heat energy recovery method in melamine production

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1493565A (en) * 2003-09-17 2004-05-05 丁泽华 Trimeric cyanamide joint production method using one step method
CN202254890U (en) * 2011-09-25 2012-05-30 山东省舜天化工集团有限公司 Novel carrier gas preheater

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1493565A (en) * 2003-09-17 2004-05-05 丁泽华 Trimeric cyanamide joint production method using one step method
CN202254890U (en) * 2011-09-25 2012-05-30 山东省舜天化工集团有限公司 Novel carrier gas preheater

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103601693A (en) * 2013-10-23 2014-02-26 李东田 One-step method used for production of melamine by circulating ammonia gas as carrying gas
CN103570636A (en) * 2013-11-16 2014-02-12 安徽金禾实业股份有限公司 Method for heating melamine circulation carrying gas by flue gas produced by molten salt furnace
CN104315871A (en) * 2014-10-30 2015-01-28 安徽金禾实业股份有限公司 Molten-salt-furnace outlet flue gas heat energy recovery method in melamine production
CN104315871B (en) * 2014-10-30 2016-05-25 安徽金禾实业股份有限公司 Molten salt furnace outlet smoke heat energy recovery method in Melamine Production

Similar Documents

Publication Publication Date Title
US10422583B2 (en) Method for recycling residual heat and dust in flue gas during reclaimed copper refining
CN102898390A (en) Method for heating triamine reactor carrier gas with flue gas of molten salt furnace
CN203489712U (en) Novel generating equipment with integrated application of waste heat in sintering, steel making and steel rolling
CN102923649B (en) Reduction hydrogen production compound furnace and device and method for ammonium paratungstate tungsten production by using same
CN203411320U (en) Converter device
CN211233983U (en) Waste heat recycling system of tubular heating furnace
CN203922756U (en) A kind of reactive tank exhaust heat-energy recycling system
CN102966934B (en) Magnesium smelting reducing slag waste heat boiler
CN204509202U (en) Gas-conducting cells, gas operated device and pulverized coal pyrolysis device
CN201620039U (en) Heating system of production process of potassium manganate
CN202562306U (en) Tunnel kiln waste heat utilization device
CN104003426A (en) System for recycling heat energy of tail gas in reaction tank
CN104165349B (en) Device for utilizing waste of boiler
CN202057214U (en) Pipe heat exchanger by utilizing residual heat of thermal phosphoric acid device to produce inorganic salt
CN203392858U (en) Recovery system for sulfur dioxide conversion waste heat in acid production process through sulfuric acid
CN202791980U (en) Heat pipe type low pressure superheated steam mixed air device
CN101746831B (en) Heating system of potassium manganate production technology
CN203474458U (en) Roasting system capable of recovering waste heat
CN217560437U (en) Industrial waste heat recycling device
CN203513567U (en) High-temperature waste heat recycling device
CN202880859U (en) Reducing hydrogen production compound furnace and device for producing tungsten from ammonium paratungstate by using the same
CN202915343U (en) Heat pipe type low-pressure superheated steam mixing device
CN103673644A (en) Waste heat utilizing system of submerged-arc furnace
CN202709072U (en) Novel residual heat recycling system for methane chloride device
CN202947111U (en) Coking furnace heat pipe waste heat boiler

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130130