CN106582268A - Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat - Google Patents

Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat Download PDF

Info

Publication number
CN106582268A
CN106582268A CN201611030182.2A CN201611030182A CN106582268A CN 106582268 A CN106582268 A CN 106582268A CN 201611030182 A CN201611030182 A CN 201611030182A CN 106582268 A CN106582268 A CN 106582268A
Authority
CN
China
Prior art keywords
flue gas
heat
room
heat exchange
slag
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
CN201611030182.2A
Other languages
Chinese (zh)
Inventor
唐晓龙
高凤雨
易红宏
王建根
赵顺征
孟小谜
宋爽
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.)
University of Science and Technology Beijing USTB
Original Assignee
University of Science and Technology Beijing USTB
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 University of Science and Technology Beijing USTB filed Critical University of Science and Technology Beijing USTB
Priority to CN201611030182.2A priority Critical patent/CN106582268A/en
Publication of CN106582268A publication Critical patent/CN106582268A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/86Catalytic processes
    • B01D53/8621Removing nitrogen compounds
    • B01D53/8625Nitrogen oxides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/50Sulfur oxides
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F27FURNACES; KILNS; OVENS; RETORTS
    • F27DDETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
    • F27D17/00Arrangements for using waste heat; Arrangements for using, or disposing of, waste gases
    • F27D17/008Arrangements for using waste heat; Arrangements for using, or disposing of, waste gases cleaning gases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2258/00Sources of waste gases
    • B01D2258/02Other waste gases
    • B01D2258/025Other waste gases from metallurgy plants
    • 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
    • Y02P10/00Technologies related to metal processing
    • Y02P10/25Process efficiency

Abstract

This invention provides a flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat, and belongs to the steel industry surplus heat utilization and the pollution control fields. The flue gas multi-pollutant collaborative purification process using the blast furnace slag sensible heat relates to a first induced draft fan, a secondary induced draft fan, a molten slag lead-in groove, a quantitative flow diverter, a molten slag granulating device, a solid slag conveying device, a first heat exchange chamber, a secondary heat exchange chamber, a dust collector, a SCR denitration device, a heat exchange boiler, a desulfurization device and a chimney, part of flue gas is sent by the first induced draft fan into the first heat exchange chamber, blast furnace molten slag introduced in by the molten slag lead-in groove is sent by the quantitative flow diverter to the molten slag granulating device for crushing into liquid droplets; then, the blast furnace slag is sent by the solid slag conveying device to the secondary heat exchange chamber, the flue gas out of the first heat exchange chamber and the secondary heat exchange chamber enters the SCR denitration device via the dust collector, then passes through the heat exchange boiler, then sent by the secondary induced draft fan to the desulfurization device and then discharged by the chimney. The flue gas multi-pollutant collaborative purification process can be used for full use of steel industry blast furnace slag sensible heat surplus energy and collaborative removal of typical multi-pollutants.

Description

The flue gas multiple pollutant synergistic purification technique that blast-furnace cement sensible heat is utilized
Technical field
The present invention relates to steel industry UTILIZATION OF VESIDUAL HEAT IN and pollution control field, particularly relate to what a kind of blast-furnace cement sensible heat was utilized Flue gas multiple pollutant synergistic purification technique, it is adaptable to plan to build steel mill or exemplary process flue gas (sintering/pelletizing/coking etc.) and blast furnace The existing iron and steel enterprise for adjoining.
Background technology
Count according to Chinese Ministry of Environmental Protection, the SO of steel industry in 20142、NOx180.7 ten thousand tons are respectively with smoke-dust discharge capacity, 56.6 Ten thousand tons and 101.5 ten thousand tons, 10.4%, 4% and the 7% of industrial source total release is accounted for respectively.In steel and iron industry production process The typical flue gas such as sintering, pelletizing and coking is the main source of iron and steel enterprise's Air Pollutant Emission.Except above-mentioned pollution beyond the region of objective existence, allusion quotation Type flue gas also endangers gas containing a large amount of bioxin and 1~3vol.% carbon monoxides (CO) etc..
Using the more ripe dedusting of Thermal Power Generation Industry, desulfurization technology, through appropriate improvement, steel industry is widely used in Flue gas desulfurization and dedusting engineering.In recent years, it is that leading iron and steel typical case flue gas ash removal is increasingly turned to electricity and changes bag or pocket type with electric precipitation Dedusting.Through dry method/semidry methods such as exploration for many years and long-term engineering practice, recirculating fluidized bed, rotating spraying, dense-phase towers Sulfur removal technology reaches its maturity, and has some superiority in terms of operation stability and economic serviceability.Chinese patent (CN202398282U, CN102210973A) is disclosed for semi-dry desulphurization dust removal integrated plant, is widely used to head Steel, Baosteel, elder brother's steel and climb steel etc. sinter flue gas dust-removal and desulfurizing engineering.
However, for steel industry denitrating flue gas work, comprehensively into technical scheme demonstration stage, engineer applied compared with For limited.During steel industry is typical low-temperature flue gas (100~180 DEG C of agglomerates of sintered pellets, 210~250 DEG C of coking) because its undulatory property, Should not directly using (the vanadium titanium system catalysis of the ripe SCR technology of thermal power plant without the drawback such as suitable thermal source or heating operating cost height Agent, temperature window is at 300~400 DEG C).Therefore, developing low-temperature SCR catalyst, or find suitable thermal source heating low-temperature flue gas is The Important Action of steel industry denitrating flue gas is solved at present.Additionally, substantial amounts of CO gases are He the harm gas such as bioxin in flue gas Reduction of discharging will also become the emphasis of Environmental capacity.
Related data shows that (fume afterheat, product sensible heat, slag show the residual heat resources in China's steel and iron industry production process Heat) recycling inefficiency.Wherein, blast-furnace slag is a large side-product-silicic acid in blast furnace ironmaking production process Salt, is characterized in molten state, and temperature is at 1450~1600 DEG C.The cooling treatment of molten blast furnace slag adopts water quenching mostly at present, Its shortcoming has:A large amount of sensible heats of blast furnace slag cannot be recycled;The waste and pollution of flushing cinder water resource;Sulfur-bearing, volatile gas Deng a large amount of precipitations and directly discharge of pollutant, surrounding enviroment are caused to pollute.Water quenching technology carries out chilling and is cooled to solid slag Process is related to the recycling of blast furnace slag and sensible heat heat recovery.Chinese patent (CN101418950A, CN102787186A, CN103820588A, CN103060496A, CN104745751A) disclose blast-furnace cement sensible heat or washing slag water The exhaust heat recovering method and device of steam.Blast furnace slag is except making the cement compared with high added value somehow succedaneum, China is specially Sharp (CN103922787A, CN104556097A, CN102698737A, CN101797467A, CN101745309) is individually disclosed Titanium-containing blast furnace slag prepares porous material, houghite and zeolite, SCR denitration and its raw material titanium tungsten powder, flue gas desulfurization and inhales The method for receiving agent.
Chinese patent CN102228774A invents a kind of blast-furnace cement sensible heat and reclaims the method for being sintered flue gas desulfurization simultaneously And device.Specifically, liquid slag carries out first desulphurization reaction and first time heat after being granulated reactor and be broken with sintering flue gas Amount is exchanged, and then Jing vibrations bed carries out secondary desulfuration reaction and second heat recovery of heat again, finally in the cooling bay sending out The form of electricity carries out the third time of heat and recycles.Patent CN103787277A discloses one kind and carries out first using blast-furnace cement sensible heat The method and device of alkane preparing synthetic gas by reforming.The side heated by above-mentioned utilization blast-furnace cement sensible heat directly contact object gas Method, is not directed to tap cinder amount, speed of slagging tap and target gas flow and the problems such as matching of flow velocity, is also not directed to many pollutions Collaboration administer.
The content of the invention
The technical problem to be solved in the present invention is to provide the flue gas multiple pollutant synergistic purification that a kind of blast-furnace cement sensible heat is utilized Technique, realizes flue gas multiple pollutant while reducing discharging and blast furnace slag waste heat efficient utilization, it is adaptable to plan to build steel mill or exemplary process cigarette The existing iron and steel enterprise that gas (sintering/pelletizing/coking etc.) is adjoined with blast furnace.
The technique equipment therefor includes air-introduced machine, secondary air-introduced machine, slag lead-in groove, quantitative diverter, a liquid slag Pelletizer, solid slag conveyer device, first Heat Room, secondary heat exchange room, cleaner unit, SCR denitration device, heat exchange boiler, desulfurization Device and chimney, before No. one time air-introduced machine is arranged on first Heat Room, slag is imported quantitative diverter by slag lead-in groove, quantitatively Diverter is followed by liquid slag pelletizer, and liquid slag pelletizer is located at first Heat Room top, and first Heat Room bottom arranges solid-state Slag conveyer device, the solid slag conveyer device other end access secondary heat exchange room, first Heat Room and secondary heat exchange room cigarette out Gas enters cleaner unit, and cleaner unit is followed by SCR denitration device, and SCR denitration device is followed by heat exchange boiler, and heat exchange boiler is drawn by secondary Blower fan is connected with desulfurizer, and desulfurizer is followed by chimney.
Wherein, secondary heat exchange room could be arranged to multi-stage heat exchanger room.
SCR denitration device is controlled at 250~450 DEG C using wide temperate zone SCR technology, the operating temperature of catalyst.
In the case where the process flue gas before first heat exchange completes desulfurization, desulfurizer can be saved.
No. one time air-introduced machine is used for control into the heat exchange exhaust gas volumn of first Heat Room.
The quantitative diverter of molten blast furnace slag is to carry out accurately determining according to the process exhaust gas volumn and heat-exchange temperature of first Heat Room The granulation amount of amount control blast furnace slag.
High-temperature molten slag is broken into drop by liquid slag pelletizer, increases the directly contact area with flue gas, improves heat exchange Efficiency.
The flue gas of first Heat Room and the heating of secondary heat exchange room is realized converging by secondary air-introduced machine;Secondary air-introduced machine is prevented Process slag inlet and the slag notch blowby of the first Heat Rooms of flue gas Jing and secondary heat exchange room.
The specific embodiment of the technique is as follows:
Partial fume is delivered to first Heat Room through an air-introduced machine by pending flue gas, the height imported by slag lead-in groove Stove liquid slag is delivered to liquid slag pelletizer through quantitative diverter and is broken into drop;Into first Heat Room pending flue gas with Blast furnace drop slag directly contact after granulation, realizes the intensification of flue gas;Convey through solid slag through the blast furnace slag of first cooling Device enters secondary heat exchange room, for the remaining flue gas Direct Contact Heating for being introduced into first Heat Room;In first Heat Room Under the directly contact of the high temperature thermal-state blast furnace slag of secondary heat exchange room, CO in flue gas is He the gaseous contaminant direct oxidation such as bioxin For CO2, oxidation, purification is realized, and the heat of combustion process release further lifts flue-gas temperature;First Heat Room and secondary change Hot cell heating flue gas out carries out dedusting by cleaner unit, into SCR denitration device, realizes NO in flue gasxRemoving;Denitration Flue gas afterwards realizes the recycling of fume afterheat by heat exchange boiler, and then flue gas is delivered to desulfurization dress by secondary air-introduced machine Put, further realize SO in flue gas2Removing, subsequent flue gas Jing smoke stack emissions are to atmospheric environment.
The technique makes full use of what slag high-temperature residual heat and CO oxidizing fires discharged by flue gas and blast furnace slag directly contact Heat realizes the lifting of cigarette temperature, provides preference temperature for follow-up denitrating flue gas.The technique be provided simultaneously with flue gas in CO He bioxin Deng the removal effect of pollutant.Specifically, flue gas is processed by straight with blast furnace slag in first Heat Room and secondary heat exchange room Contact, CO is He the pollutant such as bioxin are direct oxidation into CO under the hot environment that blast furnace slag is provided2, CO is realized He bioxin Deng multi-pollutant oxidation, purification.
Heat in the heat transfer process of the technique is accounted by being carried out as follows:
Process exhaust gas volumn Q1(m3/ h), CO contents x% (volume fraction, combustion heat value q=283KJ/mol), average density is ρ1(kg/m3), mean temperature is T1(DEG C), mean specific heat are c1(KJ/kg/ DEG C), first Heat Room exhaust gas volumn Q1-1(m3/ h), Secondary heat exchange room exhaust gas volumn Q1-2=Q1–Q1-1(m3/h)。
Molten blast furnace slag particle amount m2(kg), mean temperature is T2(DEG C), mean specific heat are c2(KJ/kg/℃).Through Blast furnace slag temperature T after first Heat Room2-1(DEG C), it is c to spend for mean specific heat2-1(KJ/kg/℃).Behind secondary heat exchange room Blast furnace slag temperature T2-2(℃)。
Flue-gas temperature T after first Heat Room1-1(DEG C), flue-gas temperature T behind secondary heat exchange room1-2(℃)。 The directly contact sensible heat utilization efficiency of first Heat Room is η1(%), the oxidizing fire efficiency eta of CO3;Secondary heat exchange room directly connects Tactile sensible heat utilization efficiency is η1(%), the oxidizing fire efficiency eta of CO4
Computing formula is Q=c × m × △ T.
First Heat Room:
(Q1-1×t×ρ1)×c1×(T1-1–T1)=m2×c2×(T2–T2-1)×η1+Q1-1× x% × 103×t×q/ [22.4×(273+T1-1)/273]×η3
Secondary heat exchange room:
[(Q1–Q1-1)×t×ρ1]×c1×(T1-2–T1)=m2×c2-1×(T2-1–T2-2)×η2+(Q1–Q1-1) × x% × 103×t×q/[22.4×(273+T1-1)/273]×η4
Wherein t is the unit time (1h).
Preferably, by adjusting flue gas sendout, blast furnace slag granulation amount and enhanced heat exchange efficiency, optimization improves first heat exchange The heat-exchange temperature T of flue gas1-1With the heat-exchange temperature T of secondary heat exchange flue gas1-2, it is ensured that through first Heat Room and secondary heat exchange room Flue gas converge after cigarette temperature T1-3Meet 300~400 DEG C, SCR denitration device may be selected tradition vanadium Titanium series catalyst.
Alternatively, by adjusting flue gas sendout, blast furnace slag granulation amount and enhanced heat exchange efficiency, optimization improves first heat exchange The heat-exchange temperature T of flue gas1-1With the heat-exchange temperature T of secondary heat exchange flue gas1-2, it is ensured that through first Heat Room and secondary heat exchange room Flue gas converge after cigarette temperature T1-3Meet 250~350 DEG C, SCR denitration device may be selected middle low temperature catalyst.
The above-mentioned technical proposal of the present invention has the beneficial effect that:
In such scheme, steel industry typical case multi-pollutant (NOx, SO can be realized2, CO, bioxin, dirt etc.) collaboration Remove, flue gas is heated using blast-furnace cement sensible heat directly contact and the heat release of CO oxidizing fires, solve cigarette temperature low and cannot adopt The problem of SCR technique denitrations, while realizing CO He the direct oxidation of the pollutant such as bioxin purification, process avoids existing The utilization rate of waste heat of blast furnace water quenching cooling method is low, flushing cinder water resource waste and secondary pollution problem.
Description of the drawings
Fig. 1 is the flue gas multiple pollutant synergistic purification apparatus structure schematic diagram that the blast-furnace cement sensible heat of the present invention is utilized.
Wherein:1-1:Air-introduced machine;1-2:Secondary air-introduced machine;2-1:Slag lead-in groove;2-2:Quantitative diverter;2-3: Liquid slag pelletizer;2-4:Solid slag conveyer device;3-1:First Heat Room;3-2:Secondary heat exchange room;4:Cleaner unit;5:SCR Denitrification apparatus;6:Heat exchange boiler;7:Desulfurizer;8- chimneys.
Specific embodiment
To make the technical problem to be solved in the present invention, technical scheme and advantage clearer, below in conjunction with accompanying drawing and tool Body embodiment is described in detail.
The present invention provides the flue gas multiple pollutant synergistic purification technique that a kind of blast-furnace cement sensible heat is utilized.
As shown in figure 1, before in the technique equipment therefor, an air-introduced machine 1-1 is arranged on first Heat Room 3-1, slag is led Enter groove 2-1 and slag is imported into quantitative diverter 2-2, quantitative diverter 2-2 is followed by liquid slag pelletizer 2-3, liquid slag pelletizer 2-3 is located at first Heat Room 3-1 tops, and first Heat Room 3-1 bottoms arrange solid slag conveyer device 2-4, solid slag conveying dress Put the 2-4 other ends and access secondary heat exchange room 3-2, first Heat Room 3-1 and secondary heat exchange room 3-2 flue gas out enters cleaner unit 4, cleaner unit 4 is followed by SCR denitration device 5, and SCR denitration device 5 is followed by heat exchange boiler 6, and heat exchange boiler 6 passes through secondary air-introduced machine 1- 2 are connected with desulfurizer 7, and desulfurizer 7 is followed by chimney 8.
Wherein, secondary heat exchange room 3-2 could be arranged to multi-stage heat exchanger room.SCR denitration device 5 adopts wide temperate zone SCR technology, The operating temperature of catalyst is controlled at 250~450 DEG C.
Present invention process is specific as follows:
Process flue gas (Q1, m3/ h) through an air-introduced machine 1-1 by partial fume (Q1-1, m3/ h) deliver to first Heat Room 3- 1, the molten blast furnace slag imported by slag lead-in groove 2-1 is delivered to liquid slag pelletizer 2-3 through quantitative diverter 2-2 and is broken into liquid Drop;First Heat Room 3-1's processes flue gas by the directly contact with granulated blast-furnace drop slag, realizes the intensification of flue gas;Through The blast furnace slag Jing solid slag conveyer devices 2-4 of first cooling enters secondary heat exchange room 3-2, for being introduced into first Heat Room 3-1 Remaining flue gas (Q1-2, m3/ h) Direct Contact Heating;In the hot height of high temperature of first Heat Room 3-1 and secondary heat exchange room 3-2 Under the directly contact of slag, CO in flue gas is He the direct oxidation of the gaseous contaminant such as bioxin is CO2, realize oxidation, purification, and oxygen The heat for changing combustion process release further lifts flue-gas temperature;By first Heat Room 3-1 and secondary heat exchange room 3-2 out Heating flue gas realizes NO in flue gas by cleaner unit 4 into SCR denitration device 5xRemoving;Flue gas after denitration is by heat exchange Boiler 6 realizes the recycling of fume afterheat, and then flue gas is delivered to desulfurizer 7 by secondary air-introduced machine 1-2, further real SO in existing flue gas2Removing, with after, Jing chimneys 8 are emitted into atmospheric environment.
Embodiment 1
Existing Q1=100 ten thousand m3The sintering flue gas of/h, CO contents 1% (volume fraction) not yet carry out flue gas desulfurization, flue gas Mean temperature T1=150 DEG C, flue gas mean specific heat c1=1.077KJ/kg/ DEG C, flue gas average density ρ1=0.9kg/m3.Enter Enter exhaust gas volumn Q of first Heat Room1-1Ten thousand m of=X3/ h, remainder (100-X) ten thousand m3/ h flue gases enter secondary heat exchange room.
Molten blast furnace slag temperature T2=1500 DEG C, mean specific heat is c2=1.05KJ/kg/ DEG C, liquid slag granulation amount m2 (kg), mean temperature T after first heat exchange2-1=600 DEG C, the sensible heat utilization efficiency eta of first Heat Room1=80%, first Heat Room CO oxidizing fire efficiency etas3=90%, unit interval t are 1h.
First Heat Room:
(Q1-1×t×ρ1)×c1×(T1-1–T1)=m2×c2×(T2–T2-1)×η1+Q1-1× x% × 103×t×q/ [22.4×(273+T1-1)/273]×η3
That is,
Q1-1×0.9×1.077×(T1-1- 150)=m2× 1.05 × (1500-600) × 80%+Q1-1× 1% × 103× 283 × 90% × 273/ (273+T1-1)/22.4 (formula 1)
The mean specific heat c of 600 DEG C of blast furnace slag2-1=1.05KJ/kg/ DEG C, the slag temperature after secondary heat exchange T2-2=200 DEG C.Secondary heat exchange exhaust gas volumn Q1-2=100-Q1-1Ten thousand m of=(100-X)3/ h, cigarette temperature T after secondary heat exchange1-2℃。 The sensible heat utilization efficiency eta of secondary heat exchange room2=70%, secondary heat exchange room CO oxidizing fire efficiency etas4=80%, the unit interval, t was 1h。。
Secondary heat exchange room:
[(Q1–Q1-1)×t×ρ1]×c1×(T1-2–T1)=m2×c2-1×(T2-1–T2-2)×η2+(Q1–Q1-1) × x% × 103×t×q/[22.4×(273+T1-1)/273]×η4
That is,
(Q1–Q1-1)×0.9×1.077×(T1-2- 150)=m2× 1.05 × (600-200) × 70%+ (Q1–Q1-1)× 1% × 103× 283 × 80% × 273/ (273+T1-1)/22.4 (formula 2)
Preferably, T1-1=T1-2When=300 DEG C, calculated with formula (2) according to formula (1), exhaust gas volumn X=of first Heat Room 73.4 ten thousand m3/ h, into 26.6 ten thousand m of secondary heat exchange room exhaust gas volumn3/ h, theoretical required unit interval (1h) granulated bf slag quality m2 =79392kg ≈ 79.4t.
Embodiment 2
Existing Q1=100 ten thousand m3The sintering flue gas of/h, CO contents 1% (volume fraction) have completed flue gas desulfurization, and flue gas is put down Equal temperature T1=100 DEG C, flue gas mean specific heat c1=1.077KJ/kg/ DEG C, flue gas average density ρ1=0.9kg/m3.Into Exhaust gas volumn Q of first Heat Room1-1Ten thousand m of=X3/ h, remainder (100-X) ten thousand m3/ h flue gases enter secondary heat exchange room.
Molten blast furnace slag temperature T2=1500 DEG C, mean specific heat is c2=1.05KJ/kg/ DEG C, liquid slag granulation amount m2 (kg), mean temperature T after first heat exchange2-1=600 DEG C, the sensible heat utilization efficiency eta of first Heat Room1=80%, first Heat Room CO oxidizing fire efficiency etas3=90%, unit interval t are 1h.
First Heat Room:
(Q1-1×t×ρ1)×c1×(T1-1–T1)=m2×c2×(T2–T2-1)×η1+Q1-1× x% × 103×t×q/ [22.4×(273+T1-1)/273]×η3
That is,
Q1-1×0.9×1.077×(T1-1- 100)=m2× 1.05 × (1500-600) × 80%+Q1-1× 1% × 103× 283 × 90% × 273/ (273+T1-1)/22.4 (formula 1)
The mean specific heat c of 600 DEG C of blast furnace slag2-1=1.05KJ/kg/ DEG C, the slag temperature after secondary heat exchange T2-2=200 DEG C.Secondary heat exchange exhaust gas volumn Q1-2=100-Q1-1Ten thousand m of=(100-X)3/ h, cigarette temperature T after secondary heat exchange1-2℃。 The sensible heat utilization efficiency eta of secondary heat exchange room2=70%, secondary heat exchange room CO oxidizing fire efficiency etas4=80%, the unit interval, t was 1h。。
Secondary heat exchange room:
[(Q1–Q1-1)×t×ρ1]×c1×(T1-2–T1)=m2×c2-1×(T2-1–T2-2)×η2+(Q1–Q1-1) × x% × 103×t×q/[22.4×(273+T1-1)/273]×η4
That is,
(Q1–Q1-1)×0.9×1.077×(T1-2- 100)=m2× 1.05 × (600-200) × 70%+ (Q1–Q1-1)× 1% × 103× 283 × 80% × 273/ (273+T1-1)/22.4 (formula 2)
Preferably, T1-1=T1-2When=300 DEG C, calculated with formula (2) according to formula (1), exhaust gas volumn X=of first Heat Room 72.8 ten thousand m3/ h, into 27.2 ten thousand m of secondary heat exchange room exhaust gas volumn3/ h, theoretical required unit interval (1h) granulated bf slag quality m2 =134516kg ≈ 134.6t.
Embodiment 3
Existing Q1=100 ten thousand m3The sintering flue gas of/h, CO contents 1% (volume fraction) not yet carry out flue gas desulfurization, flue gas Mean temperature T1=150 DEG C, flue gas mean specific heat c1=1.077KJ/kg/ DEG C, flue gas average density ρ1=0.9kg/m3.Enter Enter exhaust gas volumn Q of first Heat Room1-1=100 ten thousand m3/ h, does not adopt secondary heat exchange room.
Molten blast furnace slag temperature T2=1500 DEG C, mean specific heat is c2=1.05KJ/kg/ DEG C, liquid slag granulation amount m2 (kg), mean temperature T after first heat exchange2-1=600 DEG C, the sensible heat utilization efficiency eta of first Heat Room1=80%, first Heat Room CO oxidizing fire efficiency etas3=90%, unit interval t are 1h.
First Heat Room:
(Q1-1×t×ρ1)×c1×(T1-1–T1)=m2×c2×(T2–T2-1)×η1+Q1-1× x% × 103×t×q/ [22.4×(273+T1-1)/273]×η3
That is,
Q1-1×0.9×1.077×(T1-1- 150)=m2× 1.05 × (1500-600) × 80%+Q1-1× 1% × 103× 283 × 90% × 273/ (273+T1-1)/22.4 (formula 1)
Preferably, T1-1When=300 DEG C, calculated according to formula (1), ten thousand m of exhaust gas volumn X=100 of first Heat Room3/ h, does not adopt Use secondary heat exchange room, theoretical required unit interval (1h) granulated bf slag quality m2=120668kg ≈ 120.7t.
Embodiment 4
Existing Q1=40 ten thousand m3The coking flue gas of/h, not yet carries out flue gas desulfurization, flue gas mean temperature T1=200 DEG C, flue gas Mean specific heat c1=1.22KJ/kg/ DEG C, flue gas average density ρ1=1.86kg/m3.Into exhaust gas volumn Q of first Heat Room1-1 Ten thousand m of=X3/h。
Molten blast furnace slag temperature T2=1500 DEG C, mean specific heat is c2=1.05KJ/kg/ DEG C, liquid slag granulation amount m2 (kg), mean temperature T after first heat exchange2-1=600 DEG C, the sensible heat utilization efficiency eta of first Heat Room1=80%, first Heat Room CO oxidizing fire efficiency etas3=90%, unit interval t are 1h.
First Heat Room:
(Q1-1×t×ρ1)×c1×(T1-1–T1)=m2×c2×(T2–T2-1)×η1+Q1-1× x% × 103×t×q/ [22.4×(273+T1-1)/273]×η3
That is,
Q1-1×1.86×1.22×(T1-1- 200)=m2× 1.05 × (1500-600) × 80%+Q1-1× 1% × 103× 283 × 90% × 273/ (273+T1-1)/22.4 (formula 1)
The mean specific heat c of 600 DEG C of blast furnace slag2-1=1.05KJ/kg/ DEG C, the slag temperature after secondary heat exchange T2-2=200 DEG C.Secondary heat exchange exhaust gas volumn Q1-2=100-Q1-1Ten thousand m of=(100-X)3/ h, cigarette temperature T after secondary heat exchange1-2℃。 The sensible heat utilization efficiency eta of secondary heat exchange room2=70%, secondary heat exchange room CO oxidizing fire efficiency etas4=80%, the unit interval, t was 1h。。
Secondary heat exchange room:
[(Q1–Q1-1)×t×ρ1]×c1×(T1-2–T1)=m2×c2-1×(T2-1–T2-2)×η2+(Q1–Q1-1) × x% × 103×t×q/[22.4×(273+T1-1)/273]×η4
That is,
(Q1–Q1-1)×1.86×1.22×(T1-2- 200)=m2× 1.05 × (600-200) × 70%+ (Q1–Q1-1)× 1% × 103× 283 × 80% × 273/ (273+T1-1)/22.4 (formula 2)
Preferably, T1-1=T1-2When=300 DEG C, calculated with formula (2) according to formula (1), exhaust gas volumn X=of first Heat Room 29.1 ten thousand m3/ h, into 10.9 ten thousand m of secondary heat exchange room exhaust gas volumn3/ h, theoretical required unit interval (1h) granulated bf slag quality m2 =66110kg ≈ 66.2t.
Embodiment 5
Existing Q1=20 ten thousand m3The coking flue gas of/h, not yet carries out flue gas desulfurization, flue gas mean temperature T1=200 DEG C, flue gas Mean specific heat c1=1.22KJ/kg/ DEG C, flue gas average density ρ1=1.86kg/m3.Into exhaust gas volumn Q of first Heat Room1-1 Ten thousand m of=X3/h。
Molten blast furnace slag temperature T2=1500 DEG C, mean specific heat is c2=1.05KJ/kg/ DEG C, liquid slag granulation amount m2 (kg), mean temperature T after first heat exchange2-1=600 DEG C, the sensible heat utilization efficiency eta of first Heat Room1=80%, first Heat Room CO oxidizing fire efficiency etas3=90%, unit interval t are 1h.
First Heat Room:
(Q1-1×t×ρ1)×c1×(T1-1–T1)=m2×c2×(T2–T2-1)×η1+Q1-1× x% × 103×t×q/ [22.4×(273+T1-1)/273]×η3
That is,
Q1-1×1.86×1.22×(T1-1- 200)=m2× 1.05 × (1500-600) × 80%+Q1-1× 1% × 103× 283 × 90% × 273/ (273+T1-1)/22.4 (formula 1)
The mean specific heat c of 600 DEG C of blast furnace slag2-1=1.05KJ/kg/ DEG C, the slag temperature after secondary heat exchange T2-2=200 DEG C.Secondary heat exchange exhaust gas volumn Q1-2=100-Q1-1Ten thousand m of=(100-X)3/ h, cigarette temperature T after secondary heat exchange1-2℃。 The sensible heat utilization efficiency eta of secondary heat exchange room2=70%, secondary heat exchange room CO oxidizing fire efficiency etas4=80%, the unit interval, t was 1h。。
Secondary heat exchange room:
[(Q1–Q1-1)×t×ρ1]×c1×(T1-2–T1)=m2×c2-1×(T2-1–T2-2)×η2+(Q1–Q1-1) × x% × 103×t×q/[22.4×(273+T1-1)/273]×η4
That is,
(Q1–Q1-1)×1.86×1.22×(T1-2- 200)=m2× 1.05 × (600-200) × 70%+ (Q1–Q1-1)× 1% × 103× 283 × 80% × 273/ (273+T1-1)/22.4 (formula 2)
Preferably, T1-1=T1-2When=350 DEG C, calculated with formula (2) according to formula (1), exhaust gas volumn X=of first Heat Room 14.5 ten thousand m3/ h, into 5.5 ten thousand m of secondary heat exchange room exhaust gas volumn3/ h, theoretical required unit interval (1h) granulated bf slag quality m2 =55635kg ≈ 55.7t.
The above is the preferred embodiment of the present invention, it is noted that for those skilled in the art For, on the premise of without departing from principle of the present invention, some improvements and modifications can also be made, these improvements and modifications Should be regarded as protection scope of the present invention.

Claims (4)

1. the flue gas multiple pollutant synergistic purification technique that a kind of blast-furnace cement sensible heat is utilized, it is characterised in that:The technique equipment therefor Including air-introduced machine (1-1), secondary air-introduced machine (1-2), slag lead-in groove (2-1), quantitative diverter (2-2), a melting slag particle Change device (2-3), solid slag conveyer device (2-4), first Heat Room (3-1), secondary heat exchange room (3-2), cleaner unit (4), SCR take off Nitre device (5), heat exchange boiler (6), desulfurizer (7) and chimney (8), pending flue gas is through an air-introduced machine (1-1) by portion Point flue gas delivers to first Heat Room (3-1), and the molten blast furnace slag imported by slag lead-in groove (2-1) is through quantitative diverter (2- 2) deliver to liquid slag pelletizer (2-3) and be broken into drop;Flue gas into first Heat Room (3-1) is directly connect with blast furnace drop slag Touch, realize the intensification of flue gas;Subsequently, the blast furnace slag lowered the temperature for the first time is through solid slag conveyer device (2-4) into secondary heat exchange room (3-2), for the remaining flue gas Direct Contact Heating for being introduced into first Heat Room (3-1);In first Heat Room (3-1) and two Under the directly contact of the high temperature thermal-state blast furnace slag of secondary Heat Room (3-2), CO in flue gas is He bioxin gaseous contaminant direct oxidation For CO2, oxidation, purification is realized, and the heat of combustion process release further lifts flue-gas temperature;First Heat Room (3-1) and two Secondary Heat Room (3-2) flue gas out carries out dedusting by cleaner unit (4);SCR denitration device (5) is entered back into, in realizing flue gas NOxRemoving;Flue gas after denitration realizes the recycling of fume afterheat by heat exchange boiler (6), and then passes through secondary air inducing Flue gas is delivered to desulfurizer (7) by machine (1-2), further realizes SO in flue gas2Removing, the discharge of subsequent flue gas Jing chimneys (8) To atmospheric environment.
2. the flue gas multiple pollutant synergistic purification technique that blast-furnace cement sensible heat according to claim 1 is utilized, it is characterised in that: The SCR denitration device (5) is controlled at 250~450 DEG C using wide temperate zone SCR technology, the operating temperature of catalyst.
3. the flue gas multiple pollutant synergistic purification technique that blast-furnace cement sensible heat according to claim 1 is utilized, it is characterised in that: The liquid slag pelletizer (2-3) is placed in first Heat Room (3-1) top, and secondary heat exchange room (3-2) is set to multi-stage heat exchanger room.
4. the flue gas multiple pollutant synergistic purification technique that blast-furnace cement sensible heat according to claim 1 is utilized, it is characterised in that: The flue gas that the first Heat Room (3-1) and secondary heat exchange room (3-2) are heated is realized converging by secondary air-introduced machine (1-2).
CN201611030182.2A 2016-11-15 2016-11-15 Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat Pending CN106582268A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611030182.2A CN106582268A (en) 2016-11-15 2016-11-15 Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611030182.2A CN106582268A (en) 2016-11-15 2016-11-15 Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat

Publications (1)

Publication Number Publication Date
CN106582268A true CN106582268A (en) 2017-04-26

Family

ID=58592571

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611030182.2A Pending CN106582268A (en) 2016-11-15 2016-11-15 Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat

Country Status (1)

Country Link
CN (1) CN106582268A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107281932A (en) * 2017-08-11 2017-10-24 钢研晟华科技股份有限公司 The process of denitrating flue gas is sintered using slag sensible heat and active ingredient
CN108607341A (en) * 2018-04-19 2018-10-02 杨清海 A kind of collaboration treatment process of sintering flue gas pollutant removing and Btu utilization
CN111603913A (en) * 2020-06-09 2020-09-01 周昊 System and method for treating liquid slag discharging boiler waste gas of ozone denitration coal-fired power plant
CN111603931A (en) * 2020-06-09 2020-09-01 周昊 SCR denitration coal-fired power plant liquid slag discharge boiler waste gas treatment system and method

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08245243A (en) * 1995-03-08 1996-09-24 Rasa Shoji Kk Treatment of harmful gas for water granulation system of blast furnace molten slag and treating equipment therefor
CN102228774A (en) * 2011-05-27 2011-11-02 中钢集团鞍山热能研究院有限公司 Method and device for sensible heat reclaiming of blast furnace slag and desulfurization of sintering flue gas
CN102997697B (en) * 2012-12-12 2014-08-27 武汉钢铁(集团)公司 Sinter waste-heat utilization process based on purification of sintering flue gas
CN105688667A (en) * 2016-01-22 2016-06-22 钢研晟华工程技术有限公司 Method for carrying out denitration on sintering flue gas by utilizing sensible heat of blast furnace slag

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08245243A (en) * 1995-03-08 1996-09-24 Rasa Shoji Kk Treatment of harmful gas for water granulation system of blast furnace molten slag and treating equipment therefor
CN102228774A (en) * 2011-05-27 2011-11-02 中钢集团鞍山热能研究院有限公司 Method and device for sensible heat reclaiming of blast furnace slag and desulfurization of sintering flue gas
CN102997697B (en) * 2012-12-12 2014-08-27 武汉钢铁(集团)公司 Sinter waste-heat utilization process based on purification of sintering flue gas
CN105688667A (en) * 2016-01-22 2016-06-22 钢研晟华工程技术有限公司 Method for carrying out denitration on sintering flue gas by utilizing sensible heat of blast furnace slag

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107281932A (en) * 2017-08-11 2017-10-24 钢研晟华科技股份有限公司 The process of denitrating flue gas is sintered using slag sensible heat and active ingredient
CN107281932B (en) * 2017-08-11 2019-10-25 钢研晟华科技股份有限公司 The process of denitrating flue gas is sintered using steel slag sensible heat and effective component
CN108607341A (en) * 2018-04-19 2018-10-02 杨清海 A kind of collaboration treatment process of sintering flue gas pollutant removing and Btu utilization
CN111603913A (en) * 2020-06-09 2020-09-01 周昊 System and method for treating liquid slag discharging boiler waste gas of ozone denitration coal-fired power plant
CN111603931A (en) * 2020-06-09 2020-09-01 周昊 SCR denitration coal-fired power plant liquid slag discharge boiler waste gas treatment system and method

Similar Documents

Publication Publication Date Title
CN104195326A (en) Sintering energy-saving technique and system capable of removing multiple pollutants
CN102997697B (en) Sinter waste-heat utilization process based on purification of sintering flue gas
CN106996702B (en) A kind of agglomeration for iron mine flue gas segmentation enrichment and UTILIZATION OF VESIDUAL HEAT IN emission reduction SOxAnd NOxMethod
CN106582268A (en) Flue gas multi-pollutant collaborative purification process using blast furnace slag sensible heat
CN103900391A (en) Selective sintering-machine flue-gas heat exchange and denitration system and method thereof
CN107131770B (en) A kind of agglomeration for iron mine waste heat recycling collaboration emission reduction SOxAnd NOxMethod
CN107115775B (en) Iron ore sintering flue gas sectional enrichment self-heat exchange emission reduction SOxAnd NOxMethod of producing a composite material
CN110813006A (en) Waste gas waste heat recovery and purification process of coke oven gas heating system
CN104229855A (en) Process for on-line heating and oxidation of desulfurized fly ash by virtue of flue gas from power generating boiler or sintering machine
CN112500003A (en) Novel method for reducing emission of nitrogen oxides through preheating and calcining
CN102537945B (en) Burning system and flue gas system for circulating fluidized bed boiler
CN102728332A (en) Regeneration method of desulphurization, denitration and demercuration combined activated coke and special-purpose device thereof
CN106839794B (en) Sintering flue gas desulfurization and denitrification and waste heat recovery integrated system and implementation method
CN111333290A (en) Cu-containing industrial sludge hazardous waste recycling treatment system and treatment method thereof
CN201589534U (en) Sintering machine head flue gas afterheat recycling device
CN110484283A (en) A kind of coking residual heat integrative recovery process and system
CN206583315U (en) A kind of sintering flue gas desulfurization denitration and residual neat recovering system
CN206139011U (en) System for desulfurization simultaneously of sintering flue gas is out of stock
CN102021316A (en) Two-stage roasting smelting process for arsenic-sulfur gold concentrates
CN103954140A (en) Flue gas low-temperature denitration system of sintering machine and method thereof
CN108870988A (en) A kind of sintering smoke purifying system and its purification method
CN210291885U (en) Melting pyrolysis system of industry and municipal solid waste
CN209541450U (en) A kind of comprehensive treatment of sintering flue gas and the system of utilizing
CN205156650U (en) Sintering plant flue gas integrated processing system
CN110205431A (en) Rotary kiln coal-based direct reduction oxygenation is molten to divide furnace short route molten iron making processes

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20170426