CN109464908A - Coke oven flue gas low-temp desulfurization method of denitration - Google Patents
Coke oven flue gas low-temp desulfurization method of denitration Download PDFInfo
- Publication number
- CN109464908A CN109464908A CN201811490461.6A CN201811490461A CN109464908A CN 109464908 A CN109464908 A CN 109464908A CN 201811490461 A CN201811490461 A CN 201811490461A CN 109464908 A CN109464908 A CN 109464908A
- Authority
- CN
- China
- Prior art keywords
- flue gas
- coke oven
- logistics
- nitrogen oxides
- temperature
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D49/00—Separating dispersed particles from gases, air or vapours by other methods
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation 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
- B01D53/02—Separation 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 by adsorption, e.g. preparative gas chromatography
- B01D53/04—Separation 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 by adsorption, e.g. preparative gas chromatography with stationary adsorbents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/77—Liquid phase processes
- B01D53/78—Liquid phase processes with gas-liquid contact
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation 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
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
- B01D53/8621—Removing nitrogen compounds
- B01D53/8625—Nitrogen oxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/30—Sulfur compounds
- B01D2257/302—Sulfur oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Environmental & Geological Engineering (AREA)
- Analytical Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Treating Waste Gases (AREA)
Abstract
The present invention relates to a kind of method of coke oven flue gas desulphurization denitration, mainly solves the problem of that existing coke oven flue gas desulphurization denitration operating cost is high and generate secondary pollution.The present invention removes nitrogen oxides and sulfide in coke oven flue gas by using the method that micro crystal material adsorbs, into the coke-stove gas or blast furnace gas of coke oven combustion, before entering coke oven, first remove sulfide, it burns again, again with the nitrogen oxides and sulfide in the method removing coke oven flue gas of absorption, nitrogen oxides in effluent and sulfide after regeneration is through peroxidating, carry out the technical solution of resource utilization, preferably solves above-mentioned technical problem, this method can be used in the industrial production of coking flue gas desulfurization and denitrification.
Description
Technical field
The invention belongs to desulphurization denitration technical fields, and in particular to a kind of desulfurization denitration method of coke oven flue gas.
Background technique
SO2And NOXIt is the important atmosphere pollution in China, excessive discharge will cause haze, acid rain and photochemical fog
Deng serious harm ecological environment and human health.The burning of fossil fuel is SO2And NOXMain source.Coal be China most
Important natural energy source, as the second largest coal field in China, carbonization of coal is one of industrial coal field primary pollution source, burnt
Kiln gas is the important pollution sources of atmosphere.
Current coke oven flue gas desulfuration field is using more for ammonia process, lime/lime stone method, Dual alkali, magnesium oxide method etc.
For the Wet Flue Gas Desulfurization Technique and semi-dry desulphurization technology of representative.Wet desulphurization absorption rate is high, but such as lime/lime
Stone-gypsum, Dual alkali contain small hydrophilic ionic in magnesium oxide method slurries, are taken out of by flue gas, and are emitted into big
In gas, while these particle surfaces are easily absorbing sulfur dioxide, sulfur trioxide, hydrogen chloride, hydrogen fluoride, nitrogen oxides, nocuousness
Organic matter and bacterium etc. cause atmosphere suspended particles (usually said PM100, PM10, PM2.5 etc.) content to dramatically increase,
And cause haze and atmospheric photochemical reaction phenomenon, cause serious environmental pollution.Sodium sulfite (potassium) method sulfur removal technology, Wei Er
Man-Luo Defa Desulfovibrio technique, organic acid-acylate buffer-solution method sulfur removal technology, regeneration steam energy consumption is big and regenerates
Rate is low, therefore it is big to industrialize difficulty.Ammonia corrosion is big in the ammonia process of desulfurization, the production process of equipment burn into and ammonia is caused to be high energy
Consumption, high pollution process.Semi-dry desulphurization equipment corrosion compared with wet desulphurization is small, spreads without obvious temperature drop, conducive to chimney exhaust,
But desulfuration efficiency is relatively low, reaction speed is slow.
The mainstream technology in coke oven flue gas denitration field is NH3SCR denitration, SCR technology use catalyst, and catalytic action makes
Reaction activity reduces.In coke-oven plant, since flue gas self-temperature is very low (200 DEG C ~ 300 DEG C), it need to be urged using low-temperature denitration
Agent carries out denitration reaction during this temperature, and need to spray into ammonia into flue gas and make reducing agent.
Individual desulphurization and denitration technique not only takes up a large area, but also invests, operating cost height.Simultaneous SO_2 and NO removal skill
Art, which has, reduces device configuration, saves space, material source is wide, and price is low, renewable the advantages that recycling.Wherein, with work
Property charcoal (coke) technology be representative dry desulfurization denitrification integral technology be the technology most to the heat energy utilization in flue gas.
Chinese patent 201410119747.9 recycles stack gases waste heat using stack gases waste-heat recovery device, reduces
The temperature of stack gases, the activated adoption ability having using coke and low-temperature denitration catalytic capability realize the de- of stack gases
Sulphur, denitration integration.The concrete operation step of the invention is that 1) stack gases first pass through waste gas residual heat recovery unit, and flue is useless
The waste heat of gas is recovered, and temperature is reduced to 100 DEG C ~ 150 DEG C, is subsequently entered in low-temperature SCR desulphurization denitration unit, in flue gas
SO2It by coke adsorbing and removing, is mixed by the flue gas of desulfurization with ammonia, take coke as the catalyst of SCR method, denitration reduction occurs
NO is completed in reactionXRemoving;2) coke in low-temperature SCR desulphurization denitration unit is supplied from by elevator and grader leveling blade
The coke feed unit of conveyer composition, the coke after denitration reduction reaction is expelled in coke main tank, periodically by outlet vehicle
It sends outside;3) flue gas of low-temperature SCR desulphurization denitration unit discharge is sent after gas cleaning unit dust separation to chimney, realizes flue
The qualified discharge of exhaust gas.The waste heat recycled in the waste gas residual heat recovery unit is sent in ammonia steaming device, is generated to coke-oven plant
Remained ammonia carries out ammonia still process processing, provides necessary ammonia for the denitration reduction reaction in low-temperature SCR desulphurization denitration unit.
Chinese patent 201810438291.0 discloses a kind of low-sulfur flue gas desulfurization and denitrification device.The device includes adsorption tower
And vibrating screen, adsorption tower are successively arranged the firstth area, the secondth area and third area along flue gas circulating direction, the firstth area is equipped with flue gas air inlet
Mouthful and positioned at smoke air inlet ammonia-spraying grid, third area is equipped with the gas outlet of flue gas, the active carbon flowed is equipped in the secondth area
Layer, active carbon layer are flowed into from the top entry of adsorption tower, outlet at bottom outflow;The connection of the outlet at bottom of vibrating screen and adsorption tower,
And it is connected by the top entry of conveying mechanism and adsorption tower.
Chinese patent CN201611269710.X discloses a kind of sintering flue gas ammonia charcoal combined desulfurization and denitration method, sintering
Flue gas is after the desulfurization of absorbing liquid containing ammonia again through activated carbon adsorption;Carbonaceous raw material, the gold that the active carbon is 2:1 ~ 5:1 by mass ratio
Belong to oxide source to roast to obtain in 850 ~ 1100 DEG C of countrysidies;The carbonaceous raw material is semicoke, or is the mixed of coal and biomass
Close material.In the present invention, the active carbon as made from by ammonia and the method for the invention is combined, can effective desulphurization denitration, also
Help reduce secondary pollution, reduction technique.
Document above is active carbon (coke) simultaneous SO_2 and NO removal, but can not all be detached from ammonia as this step of reducing agent denitration
Suddenly.Since coke oven flue flow field is uneven, temperature field is uneven, catalyst failure degree is uneven, the volume fraction of escape ammonia is difficult low
In design discipline.Escape ammonia is exceeded to will cause secondary pollution, and corrosion pipeline material, and there is danger in the use process of ammonia
Property, it is very important to the body harm of people.
In view of the above problems, not using ammonia, simultaneously the invention proposes the technology of molecular sieve adsorption simultaneous SO_2 and NO removal
Adsorb the SO in coke oven flue gas2And NOX, and be worth with certain recycling.
Summary of the invention
The technical problem to be solved by the present invention is to during existing coke-oven plant's Coke-oven flue gas governing, operating cost height is produced
The technical issues of raw secondary pollution, provides a kind of method of coke oven flue gas desulphurization denitration, which has process short, if
Standby with low investment, regeneration is simple, and low energy consumption, advantage without secondary pollution.
In order to solve the above technical problems, a kind of method that the present invention uses coke oven flue gas low-temp desulfurization denitration, including it is following
Step:
A) coke-stove gas or blast furnace gas for entering coke oven combustion first remove sulfide, then burn before entering coke oven;
B) coke oven flue gas of coke oven flue is drawn sulfur compound and nitrogen oxides, is denoted as material flow A, the temperature of the material flow A
It is 180 ~ 320 DEG C;
C) material flow A carries out UTILIZATION OF VESIDUAL HEAT IN, produces steam, and the flue gas after cooling forms flow B, and the temperature of the flow B is 120
~180℃;
D) flow B enters cooling tower, after supercooling, dedusting, forms flow C, the temperature of the flow C is 30 ~ 100 DEG C;
E) flow C enters the adsorption tower comprising crystallite adsorbent B, after adsorbing sulfide and nitrogen oxides, forms logistics D;
F) logistics D enters smoke stack emission after heating up;
G) adsorption tower after adsorbing sulfide and nitrogen oxides saturation in step e), with 500 ~ 5000m3The material flow A of/h regenerates, then
Raw flue gas forms logistics E, wherein the temperature of the logistics E is 120 ~ 350 DEG C;
H) logistics E enters the catalysis oxidizing tower comprising oxidation catalyst, after catalysis oxidation, forms logistics F;
I) after logistics F is sprayed with lye, logistics G is formed, spray liquid enters waste water treatment system;
J) logistics G enters step the cooling tower in d).
In the above-mentioned technical solutions, preferred technical solution is that UTILIZATION OF VESIDUAL HEAT IN uses steam boiler in the step c),
The vapor (steam) temperature of production is 140 ~ 180 DEG C;Cooling tower in the step d) is spray column or heat exchanger types;Flow C
Temperature be 30 ~ 100 DEG C.
In above-mentioned technical proposal, preferred technical solution is that the temperature of the logistics D is 30 ~ 100 DEG C;Nitrogen oxides
Content is 1 ~ 200mg/m3, sulfide content is 0.1 ~ 100 mg/m3。
In the above-mentioned technical solutions, preferred technical solution is, into the coke-stove gas or blast furnace gas of coke oven combustion,
Hydrogen sulfide content is 0 ~ 20 mg/m3, 0 ~ 20 mg/m of organic sulfur content3。
In the above-mentioned technical solutions, preferred technical solution is, into the coke-stove gas or blast furnace gas of coke oven combustion,
Hydrogen sulfide content is 0 ~ 10 mg/m3, 0 ~ 10 mg/m of organic sulfur content3。
In the above-mentioned technical solutions, preferred technical solution is, into the coke-stove gas or blast furnace gas of coke oven combustion,
Hydrogen sulfide content is 0 ~ 5 mg/m3, 0 ~ 5mg/m of organic sulfur content3。
In above-mentioned technical proposal, preferred technical solution is that the heating mode of the logistics D is heated up using heated by gas
Mode or logistics D and material flow A heat exchange heating mode, for logistics D after heating up, temperature is 80 ~ 200 DEG C.
In above-mentioned technical proposal, preferred technical solution is, in step e), the quantity of adsorption tower is inhaled at least more than two
Attached bed operation temperature is 30 ~ 100 DEG C, and operating pressure is 0.1 ~ 20KPa.
In above-mentioned technical proposal, preferred technical solution is that the temperature of the material flow A is 200 ~ 300 DEG C;Nitrogen oxides
Content is 100 ~ 1000mg/m3, sulfide content is 40 ~ 3000mg/m3。
In the above-mentioned technical solutions, preferred technical solution is step ed) in, the quantity of adsorption tower at least more than two,
Adsorbent bed operation temperature is 30 ~ 100 DEG C, and operating pressure gauge pressure is 0.5 ~ 10Kpa.
In the above-mentioned technical solutions, preferred technical solution is the crystallite adsorbent A or the choosing of crystallite adsorbent B
From including X-type molecular sieve, Y type molecular sieve, A type molecular sieve, SSZ-13 molecular sieve, TS-1, Ti-MWW, Ti-MOR, ZSM type molecule
Sieve, modenite, beta molecular sieve, SAPO type molecular sieve, MCM-22, MCM-49, MCM-56, ZSM-5/ modenite, ZSM-5/
β zeolite, ZSM-5/Y, MCM-22/ modenite, ZSM-5/Magadiite, ZSM-5/ β zeolite/modenite, ZSM-5/ β boiling
At least one of stone/Y zeolite or ZSM-5/Y zeolite/modenite.
In the above-mentioned technical solutions, preferred technical solution is that also containing in the crystallite adsorbent includes element week
At least one of Ith A, II A, V A, I B, II B, III B, IV B, V B, VI B, VII B or the VIIIth race's element element in phase table.
In the above-mentioned technical solutions, preferred technical solution is that containing in the oxidation catalyst includes period of element
At least one of Ith A, II A, V A, I B, II B, III B, IV B, V B, VI B, VII B or the VIIIth race's element element in table.
In the above-mentioned technical solutions, preferred technical solution is that the lye is sodium hydroxide solution, ammonium hydroxide, residue
At least one of ammonium hydroxide, sodium carbonate liquor, calcium hydroxide solution.
In the above-mentioned technical solutions, preferred technical solution, it includes SSZ-13, TS- that the adsorbent of molecular sieve B, which is selected from,
1, Ti-MWW, Ti-MOR, ZSM type molecular sieve, modenite, beta molecular sieve, SAPO type molecular sieve, MCM-22, ZSM-5/ mercerising
Zeolite, ZSM-5/ β zeolite, ZSM-5/Y, MCM-22/ modenite, ZSM-5/ β zeolite/modenite, ZSM-5/ β zeolite/Y boiling
At least one of stone or ZSM-5/Y zeolite/modenite.
In the above-mentioned technical solutions, the silica alumina ratio of preferred technical solution, the molecular sieve is greater than 2.
In the above-mentioned technical solutions, preferred technical solution, the IIth element A is selected from magnesium and calcium in the periodic table of elements
At least one of;Ith B race element is selected from least one of copper, silver;IIIth B race element in lanthanum, cerium, yttrium at least
It is a kind of.
In the above-mentioned technical solutions, preferred technical solution, ZSM type molecular sieve is selected from packet in the adsorbent of molecular sieve
At least one of ZSM-5, ZSM-23, ZSM-11, ZSM-48 are included, wherein the silica alumina ratio of the molecular sieve is greater than 20.
In the above-mentioned technical solutions, preferred technical solution, adsorbent bed operation temperature are 0 ~ 100 DEG C, operating pressure 0.5
~ 10Kpa, gauge pressure.
In the above-mentioned technical solutions, preferred technical solution is passed through air, ozone, double water oxygen water in regeneration gas oxidizing tower
At least one of.
In the above-mentioned technical solutions, preferred technical solution first uses hot water after the adsorbent of molecular sieve adsorption saturation
It rinses, then with 100 ~ 300 DEG C of nitrogen regenerations.
It is known in the art, coal gas is purified using traditional handicraft, using desulfurizing tower again during gas purification process
It is middle to use iron oxide desulfurization;Naphthalene is taken off with active carbon using in de- naphthalene tower;Benzene is taken off with active carbon using debenzolizing tower again;3 are used altogether
Absorbing unit successively purifies coal gas.In device operation, device exit hydrogen sulfide, benzene and naphthalene are dense, influence production effect
Rate.Using method of the invention, have the advantages that (1), can be by benzene, naphthalene and hydrogen sulfide, organic sulfur using adsorbent of molecular sieve
It can thoroughly remove completely, solve the problems, such as line clogging.(2) adsorbent is subjected to multifunction, can desulfurization simultaneously, de- benzene,
De- naphthalene can carry out comprehensive purifying process simultaneously, reduce the quantity of adsorption tower in this way, reduce production in an adsorption tower
Cost.
Using technical solution of the present invention: the coke-stove gas that coke oven comes out enters slightly de- benzene unit, slightly enters after de- benzene
Comprehensive purifying tower, purifying column is interior to contain molecular sieve adsorbent, while removing the aromatic hydrocarbons and sulfide in coal gas, enters back into coke
Furnace burning.De- naphthalene tower exit hydrogen sulfide content is 0 mg/m3, naphthalene content is 0 mg/m3, tar content 0 carries in gas
Organic sulfur be also removed, sulfur dioxide in flue gas is emitted on 10m g/m3Hereinafter, device is stable.It is de- to reduce end desulfurization
The cost of nitre.
By adopting the above technical scheme, using crystallite adsorbent desulphurization denitration, crystallite adsorbent to gas cleaning handle just like
Lower advantage: the sulfur dioxide and nitrogen oxides in flue gas can be effectively adsorbed, discharge standard is made up to;High temperature resistant, structure are steady
It is fixed, iterative regenerable;It is high to adsorb precision, other than adsorb sulfur dioxide, can also dedusting simultaneously remove the harmful substances such as dioxin,
Make up to discharge standard;Crystallite adsorbent long service life, does not generate dangerous waste.By setting up adsorption tower in exhanst gas outlet, benefit
Sulfur dioxide, the nitrogen oxides in flue gas are adsorbed with System of Silica/Aluminum Microparticle hydrochlorate crystallite adsorbent, System of Silica/Aluminum Microparticle in adsorption tower
After hydrochlorate crystallite adsorbent adsorption saturation, crystallite adsorbent is regenerated by high-temperature flue gas, the nitrogen oxides and sulphur of desorption
Compound enters oxidizing tower, is oxidized to sulfur trioxide and nitrogen dioxide, and regenerated flue gas is absorbed with water spray, after effluent part neutralizes,
It is discharged into biochemical system or goes to salt extraction workshop, tail gas enters flue gas spray column circulation.Entire treatment process process is short, equipment investment
It saves, regenerative operation is simple and reliable, and low energy consumption, flue gas emission nitrogen oxides≤50mg/m3, sulfur dioxide≤30mg/m3, dust content
Less than 5 mg/m3, achieve preferable technical effect.
Detailed description of the invention
Fig. 1 is the flow diagram of coke oven flue gas desulfurization denitration method of the invention.
1 is coke oven flue gas in Fig. 1, and 2 is are spray column from heat exchanger 3, and 4 be heat exchanger, and 5 be electric fishing mist, and 6 be adsorption tower, 7
It is heater for blower, 8,9 be oxidizing tower, and 10 be spray column, and 11 be sedimentation basin, and 12 be cooling tower, and 13 be chimney.
The present invention will be further described below by way of examples, but is not limited only to the present embodiment.
Specific embodiment
[embodiment 1]
The coke-stove gas that coke oven comes out enters slightly de- benzene unit, slightly forms logistics I after de- benzene, wherein benzene concentration exists in logistics I
1000~4000mg/m3Between, naphthalene concentration is in 200~500mg/m3Between, concentration of hydrogen sulfide is in 100~500mg/m3Between;Object
Stream I enters comprehensive purifying tower, ZSM molecular sieve class adsorbent is contained in the comprehensive purifying tower, while removing in coal gas
Aromatic hydrocarbons and sulfide form logistics II, and benzene concentration is less than 1000mg/m in logistics II3, naphthalene concentration is less than 4 mg/m3, hydrogen sulfide is dense
Degree is less than 4mg/m3;Organic sulfur concentration is less than 4mg/m3;Logistics II enters coke oven combustion.
The flue gas of 16 240 DEG C of ten thousand steres, amount of nitrogen oxides 500mg/m3, sulfide content is 200 mg/m3, into
Enter waste heat boiler, generate steam, flue-gas temperature is reduced to 180 DEG C or so;180 DEG C of flue gas, to 50 DEG C, is sprayed by spraying cooling
Water drenching after effluent part neutralizes, removes biochemical system by being recycled;After flue gas after cooling passes through defogging equipment, into suction
Attached tower;Using 3 200m3Adsorption tower, two open one standby, and 120m is loaded in each adsorption tower3Micro crystal material amounts to 360 m3It is micro-
Brilliant material modenite;Adsorption tower specification is 4.8 meters of diameter, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, enter
From after heat exchanger and hot fume heat exchange, reach 100 DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 50mg/m3,
Sulfide content is 20 mg/m3.Desulphurization and denitration, dedusting crystallite adsorbent are loaded in adsorption tower, are automatically switched after adsorption saturation
Circular regeneration;Automatically switch within every 7 days a tower regeneration, the adsorption tower 3000m of saturation3The hot fume of/h is regenerated, desorption
Nitrogen oxides and sulfide enter oxidizing tower, be oxidized to sulfur trioxide and nitrogen dioxide;After mixed gas cooling, water spray is used
It absorbs, after effluent part neutralizes, is discharged into biochemical system or going produces salt extraction workshop, tail gas enters flue gas spray column.
[embodiment 2]
The coke-stove gas that coke oven comes out enters slightly de- benzene unit, slightly forms logistics I after de- benzene, wherein benzene concentration exists in logistics I
1000~4000mg/m3Between, naphthalene concentration is in 200~500mg/m3Between, concentration of hydrogen sulfide is in 100~500mg/m3Between;Object
Stream I enters comprehensive purifying tower, ZSM molecular sieve class adsorbent is contained in the comprehensive purifying tower, while removing in coal gas
Aromatic hydrocarbons and sulfide form logistics II, and benzene concentration is less than 1000mg/m in logistics II3, naphthalene concentration is less than 4 mg/m3, hydrogen sulfide is dense
Degree is less than 4mg/m3;Organic sulfur concentration is less than 4mg/m3;Logistics II enters coke oven combustion.
Specific embodiment device process as shown in Fig. 1, the flue gas of 15 260 DEG C of ten thousand steres, nitrogen oxides contain
Amount is 400mg/m3, sulfide content is 100 mg/m3, into waste heat boiler, 150 DEG C of steam are generated, flue-gas temperature is reduced to
120 DEG C or so;By spraying cooling to 40 DEG C, shower water after effluent part neutralizes, is gone 120 DEG C of flue gas by being recycled
Biochemical system;After flue gas after cooling passes through defogging equipment, into adsorption tower;Using 3 200m3Adsorption tower, two open it is one standby,
120m is loaded in each adsorption tower3Micro crystal material amounts to 360 m3Micro crystal material ZSM-5 molecular sieve;Adsorption tower specification is diameter
It is 4.8 meters, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reach 100
DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 50mg/m3, sulfide content is 20 mg/m3.Adsorption tower is built-in
Desulphurization and denitration, dedusting crystallite adsorbent are filled out, automatically switches circular regeneration after adsorption saturation;One tower of automatic switchover in every 7 days is again
It is raw, the adsorption tower 3000m of saturation3The hot fume of/h is regenerated, and the nitrogen oxides and sulfide of desorption enter oxidizing tower, oxygen
It is melted into sulfur trioxide and nitrogen dioxide;It after mixed gas cooling, is absorbed with water spray, after effluent part neutralizes, is discharged into department of biochemistry
Salt extraction workshop is united or goes, tail gas enters flue gas spray column.
[embodiment 3]
The coke-stove gas that coke oven comes out enters slightly de- benzene unit, slightly forms logistics I after de- benzene, wherein benzene concentration exists in logistics I
1000~3500mg/m3Between, naphthalene concentration is in 200~500mg/m3Between, concentration of hydrogen sulfide is in 100~500mg/m3Between;Object
Stream I enters comprehensive purifying tower, and the ZSM-5 molecular sieve class adsorbent containing zinc modification in the comprehensive purifying tower removes simultaneously
Fall the aromatic hydrocarbons and sulfide in coal gas, forms logistics II, benzene concentration is less than 60mg/m in logistics II3, naphthalene concentration is less than 1 mg/m3,
Concentration of hydrogen sulfide is less than 1mg/m3;Toluene, dimethylbenzene, ethylbenzene, trimethylbenzene, naphthalene, anthracene, the concentration in Kun are less than 1 mg/m3;Vulcanization
Object is hydrogen sulfide, the concentration in sulfur dioxide, mercaptan, thioether, thiophene, methyl mercaptan, Dimethyl sulfide is less than 1 mg/m3, logistics
II, which enters coke oven, generates electricity.
Specific embodiment device process as shown in Fig. 1, the flue gas of 14 240 DEG C of ten thousand steres, nitrogen oxides contain
Amount is 450mg/m3, sulfide content is 200 mg/m3, into waste heat boiler, 160 DEG C of steam are generated, flue-gas temperature is reduced to
110 DEG C or so;By spraying cooling to 50 DEG C, shower water after effluent part neutralizes, is gone 110 DEG C of flue gas by being recycled
Biochemical system;After flue gas after cooling passes through defogging equipment, into adsorption tower;Using 3 200m3Adsorption tower, two open it is one standby,
120m is loaded in each adsorption tower3Micro crystal material amounts to 360 m3Micro crystal material ZSM-5 molecular sieve;Adsorption tower specification is diameter
It is 4.8 meters, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reach 110
DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 40mg/m3, sulfide content is 10 mg/m3.Adsorption tower is built-in
Desulphurization and denitration, dedusting crystallite adsorbent are filled out, after adsorption saturation, automatically switches circular regeneration with high-temperature flue gas;Automatically it cuts within every 7 days
Change a tower regeneration, the adsorption tower 3000m of saturation3240 DEG C of flue gases of/h are regenerated, the nitrogen oxides and sulfide of desorption
Into the oxidizing tower containing vanadium series catalyst, it is oxidized to sulfur trioxide and nitrogen dioxide;After mixed gas cooling, inhaled with water spray
It receives, after effluent part neutralizes, is discharged into biochemical system or goes to salt extraction workshop, tail gas enters flue gas spray column.
[embodiment 4]
Specific embodiment device process as shown in Fig. 1, the flue gas of 20 180 DEG C of ten thousand steres, amount of nitrogen oxides are
1000mg/m3, sulfide content is 500 mg/m3, into waste heat boiler, 10 tons of 165 DEG C of steam, flue-gas temperature are generated per hour
It is reduced to 120 DEG C or so;120 DEG C of flue gas is by spraying cooling to 40 DEG C, and by being recycled, effluent part neutralizes shower water
Afterwards, the salt extraction system that going produces;After flue gas after cooling passes through defogging equipment, into adsorption tower;Using 4 200m3Absorption
Tower, three open standby, a filling 120m in each adsorption tower3Micro crystal material amounts to 480 m3Micro crystal material SSZ-13 molecular sieve;Absorption
Tower specification is 4.8 meters of diameter, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, changed into from heat exchanger and hot fume
After heat, reach 100 DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 50mg/m3, sulfide content is 20 mg/
m3.Desulphurization and denitration, dedusting crystallite adsorbent are loaded in adsorption tower, automatically switch circular regeneration after adsorption saturation;Every 7 days automatic
Switch a tower regeneration, the adsorption tower 2000m of saturation3The hot fume of/h is regenerated, the nitrogen oxides and sulfide of desorption
Into the oxidizing tower containing Cu-series catalyst, it is oxidized to sulfur trioxide and nitrogen dioxide;After mixed gas cooling, inhaled with water spray
It receives, after effluent part neutralizes, being discharged into produces salt extraction workshop, and tail gas enters flue gas spray column.
[embodiment 5]
Specific embodiment device process as shown in Figure 1, the flue gas of 20 180 DEG C of ten thousand steres, amount of nitrogen oxides are
1000mg/m3, sulfide content is 500 mg/m3, into waste heat boiler, generate 150 DEG C of steam, flue gas cool-down is to 170 DEG C, cigarette
Gas enters spray column, and by spraying cooling to 40 DEG C, shower water is by being recycled, and after effluent part neutralizes, what going produced is mentioned
Salt system;After flue gas after cooling passes through defogging equipment, into adsorption tower;Using 4 200m3Adsorption tower, three open it is one standby, often
120m is loaded in a adsorption tower3Micro crystal material, amount to 480m3Micro crystal material copper ZSM-5 molecular sieve;Adsorption tower specification is diameter
It is 4.8 meters, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reach 100
DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 40mg/m3, sulfide content is 10 mg/m3.Adsorption tower is built-in
Desulphurization and denitration, dedusting crystallite adsorbent are filled out, automatically switches circular regeneration after adsorption saturation;One tower of automatic switchover in every 7 days is again
It is raw, the adsorption tower 3000m of saturation3180 DEG C of flue gases of/h are regenerated, and the nitrogen oxides and sulfide of desorption, which enter, contains copper
The oxidizing tower of series catalysts, is oxidized to sulfur trioxide and nitrogen dioxide;It after mixed gas cooling, is absorbed with water spray, part is useless
After water neutralizes, being discharged into produces salt extraction workshop, and tail gas enters flue gas spray column.
[embodiment 6]
Specific embodiment device process as shown in Figure 1, the flue gas of 180 DEG C of 200,000 sides rice, amount of nitrogen oxides are
400mg/m3, sulfide content is 100 mg/m3, into waste heat boiler, 170 DEG C of steam are generated, flue gas cool-down enters to 175 DEG C
For spraying cooling to 50 DEG C, shower water after effluent part neutralizes, removes biochemical system by being recycled;Flue gas after cooling passes through
After defogging equipment, into adsorption tower;Using 3 200m3Adsorption tower, two open one standby, and 120m is loaded in each adsorption tower3Crystallite
Material amounts to 360 m3Micro crystal material, micro crystal material include the ZSM-5 molecular sieve of lanthanum and zinc modification;Adsorption tower specification is diameter
It is 4.8 meters, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, into smoke stack emission, nitrogen oxides in effluent content is
30mg/m3, sulfide content 5mg/m3.Desulphurization and denitration, dedusting crystallite adsorbent are loaded in adsorption tower, it is automatic after adsorption saturation
Switch circular regeneration;Automatically switch within every 7 days a tower regeneration, the adsorption tower 4000m of saturation3180 DEG C of the flue gas of/h carries out
Regeneration, the nitrogen oxides and sulfide of desorption enter oxidizing tower, are oxidized to sulfur trioxide and nitrogen dioxide at 250 DEG C;Gaseous mixture
It after body cooling, is absorbed with water spray, after effluent part neutralizes, is discharged into biochemical system or goes to salt extraction workshop, tail gas enters flue gas
Spray column.
[embodiment 7]
Specific embodiment device process as shown in Fig. 1, the flue gas of 18 240 DEG C of ten thousand steres, amount of nitrogen oxides are
400mg/m3, sulfide content is 100 mg/m3, into waste heat steam boiler, generate 145 DEG C of steam, flue gas cool-down to 160 DEG C,
By spraying cooling to 40 DEG C, shower water after effluent part neutralizes, removes biochemical system by being recycled;Flue gas after cooling
After defogging equipment, into adsorption tower;Using 3 200m3Adsorption tower, two open one standby, and 120m is loaded in each adsorption tower3
Micro crystal material amounts to 360 m3Micro crystal material ZSM-5 molecular sieve;Adsorption tower specification is 4.8 meters of diameter, 12.0 meters high;Flue gas removes
After desulfuration compound and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reach 100 DEG C or more, into smoke stack emission, cigarette
Amount of nitrogen oxides is 50mg/m in gas3, sulfide content 20mg/m3.Filling desulphurization and denitration, dedusting crystallite are inhaled in adsorption tower
Attached dose, automatically switch circular regeneration after adsorption saturation;Automatically switch within every 7 days a tower regeneration, the adsorption tower 3000m of saturation3/
The hot fume of h is regenerated, and the nitrogen oxides and sulfide of desorption enter oxidizing tower, is oxidized to sulfur trioxide and nitrogen dioxide;
Mixed gas cooling after, absorbed with water spray, effluent part neutralize after, be discharged into biochemical system or go to salt extraction workshop, tail gas into
Enter flue gas spray column.
[embodiment 8]
Specific embodiment device process as shown in Fig. 1, the flue gas of 18 210 DEG C of ten thousand steres, amount of nitrogen oxides are
400mg/m3, sulfide content is 100 mg/m3, into waste heat boiler, 160 DEG C of steam are generated, flue gas cool-down passes through to 185 DEG C
For spraying cooling to 50 DEG C, shower water after effluent part neutralizes, goes to the salt extraction workshop of coking by being recycled;Cigarette after cooling
After gas passes through defogging equipment, into adsorption tower;Using 4 200m3Adsorption tower, three open one standby, filling in each adsorption tower
150m3Micro crystal material amounts to 600 m3Micro crystal material containing modenite and ZSM-5 molecular sieve;Adsorption tower specification is diameter
It is 4.8 meters, 12.0 meters high;After flue gas removes sulfide and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reach 100
DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 50mg/m3, sulfide content is 20 mg/m3.Adsorption tower is built-in
Desulphurization and denitration, dedusting crystallite adsorbent are filled out, automatically switches circular regeneration after adsorption saturation;One tower of automatic switchover in every 7 days is again
It is raw, the adsorption tower 4000m of saturation3240 DEG C of the flue gas of/h is regenerated, and the nitrogen oxides and sulfide of desorption enter oxidation
Tower is oxidized to sulfur trioxide and nitrogen dioxide;It after mixed gas cooling, is absorbed with water spray, after effluent part neutralizes, is discharged into life
Change system goes to salt extraction workshop, and tail gas enters flue gas spray column.
Claims (11)
1. a kind of method of coke oven flue gas low-temp desulfurization denitration, comprising the following steps:
A) coke-stove gas or blast furnace gas for entering coke oven combustion first remove sulphur with crystallite adsorbent A before entering coke oven
Compound enters back into coke oven combustion;
B) coke oven flue gas of coke oven flue is drawn sulfur compound and nitrogen oxides, is denoted as material flow A, the temperature of the material flow A
It is 140 ~ 320 DEG C;
C) material flow A carries out UTILIZATION OF VESIDUAL HEAT IN, produces steam, and the flue gas after cooling forms flow B, and the temperature of the flow B is
120~180℃;
D) flow B enters cooling tower, after supercooling, dedusting, forms flow C, the temperature of the flow C is 30 ~ 100 DEG C;
E) flow C enters the adsorption tower comprising crystallite adsorbent B, after adsorbing sulfide and nitrogen oxides, forms logistics D;
F) logistics D enters smoke stack emission after heating up;
G) adsorption tower after adsorbing sulfide and nitrogen oxides saturation in step e), with 500 ~ 5000m3The material flow A of/h regenerates, then
Raw flue gas forms logistics E, wherein the temperature of the logistics E is 120 ~ 350 DEG C;
H) logistics E enters the catalysis oxidizing tower comprising oxidation catalyst, after catalysis oxidation, forms logistics F;
I) logistics F enters spray column, after being sprayed with lye, forms logistics G, spray liquid enters waste water treatment system or salt extraction
System;
J) logistics G enters step the cooling tower in d).
2. the method for coke oven flue gas desulphurization denitration according to claim 1, it is characterised in that the temperature of the material flow A is
240~280℃;Amount of nitrogen oxides is 100 ~ 1000mg/m3, sulfide content is 30 ~ 3000 mg/m3。
3. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that into coke oven combustion
Coke-stove gas or blast furnace gas, hydrogen sulfide content are 0 ~ 20 mg/m3, 0 ~ 20 mg/m of organic sulfur content3。
4. UTILIZATION OF VESIDUAL HEAT IN uses waste heat steam boiler in step c) described in, and the vapor (steam) temperature of production is 140 ~ 180 DEG C;Described
Cooling tower in step d) is spray column or heat exchanger types;The temperature of flow C is 30 ~ 100 DEG C.
5. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that the temperature of the logistics D
Degree is 30 ~ 100 DEG C;Amount of nitrogen oxides is 1 ~ 200mg/m3, sulfide content is 0.1 ~ 100 mg/m3。
6. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that the liter of the logistics D
Warm mode is using heated by gas heating mode or logistics D and material flow A heat exchange heating mode, and after heating up, temperature is logistics D
80~200℃。
7. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that in step e), adsorption tower
Quantity at least more than two, adsorbent bed operation temperature be 30 ~ 100 DEG C, operating pressure be 0.1 ~ 20KPa.
8. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that the crystallite absorption
It includes X-type molecular sieve, Y type molecular sieve, A type molecular sieve, SSZ-13 molecular sieve, TS-1, Ti- that agent A or crystallite adsorbent B, which are selected from,
MWW, Ti-MOR, ZSM type molecular sieve, modenite, beta molecular sieve, SAPO type molecular sieve, MCM-22, MCM-49, MCM-56,
ZSM-5/ modenite, ZSM-5/ β zeolite, ZSM-5/Y, MCM-22/ modenite, ZSM-5/Magadiite, ZSM-5/ β boiling
Stone/modenite, ZSM-5/ β zeolite/at least one of Y zeolite or ZSM-5/Y zeolite/modenite.
9. the method for coke oven flue gas low-temp desulfurization denitration according to claim 7, it is characterised in that the crystallite absorption
Also containing including the Ith A, II A, V A, I B, II B, III B, IV B, V B, VI B, VII B or the VIIIth race's element in the periodic table of elements in agent
At least one of element.
10. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that in the oxidation catalyst
Containing include in the periodic table of elements in the Ith A, II A, V A, I B, II B, III B, IV B, V B, VI B, VII B or the VIIIth race's element extremely
A kind of few element.
11. the method for coke oven flue gas low-temp desulfurization denitration according to claim 1, it is characterised in that lye described in step i)
For at least one of sodium hydroxide solution, ammonium hydroxide, remained ammonia, sodium carbonate liquor, calcium hydroxide solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811490461.6A CN109464908A (en) | 2018-12-07 | 2018-12-07 | Coke oven flue gas low-temp desulfurization method of denitration |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811490461.6A CN109464908A (en) | 2018-12-07 | 2018-12-07 | Coke oven flue gas low-temp desulfurization method of denitration |
Publications (1)
Publication Number | Publication Date |
---|---|
CN109464908A true CN109464908A (en) | 2019-03-15 |
Family
ID=65675834
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201811490461.6A Pending CN109464908A (en) | 2018-12-07 | 2018-12-07 | Coke oven flue gas low-temp desulfurization method of denitration |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109464908A (en) |
-
2018
- 2018-12-07 CN CN201811490461.6A patent/CN109464908A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109806740A (en) | The method of coke oven flue gas desulphurization denitration | |
CN109806741A (en) | The low-temp desulfurization method of denitration of coke oven flue gas | |
CN109806742A (en) | The desulfurization denitration method of coke oven flue gas | |
CN109453652A (en) | The desulfurization denitration method of boiler smoke | |
CN109513346A (en) | Sintering flue gas low-temp desulfurization method of denitration | |
CN109453657A (en) | The desulfurization denitration method of boiler smoke | |
CN109464911A (en) | Coke oven flue gas low-temp desulfurization method of denitration | |
CN109550393A (en) | Sintering flue gas low-temp desulfurization method of denitration | |
CN109453650A (en) | Boiler smoke low-temp desulfurization method of denitration | |
CN109499310A (en) | The low temperature synthesis desulfurating method of denitration of boiler smoke | |
CN109464906A (en) | The desulfurization denitration method of coke oven flue gas | |
CN109499311A (en) | The low temperature of boiler smoke is without ammonia integration desulfurization denitration method | |
CN109453649A (en) | Boiler smoke low-temp desulfurization method of denitration | |
CN109499324A (en) | The low temperature desulfurization denitration method of boiler smoke | |
CN109464910A (en) | Coke oven flue gas low-temp desulfurization method of denitration | |
CN109499318A (en) | The low-temp desulfurization method of denitration of boiler smoke | |
CN109453659A (en) | The desulfurization denitration method of coke oven flue gas | |
CN109513347A (en) | Pelletizing flue gas low-temperature desulfurization denitration method | |
CN109464909A (en) | Coke oven flue gas low-temp desulfurization method of denitration | |
CN109513349A (en) | Sintering flue gas low-temp desulfurization method of denitration | |
CN109731463A (en) | Coke oven flue gas low-temp desulfurization method of denitration | |
CN109453655A (en) | Boiler smoke low-temp desulfurization method of denitration | |
CN109464908A (en) | Coke oven flue gas low-temp desulfurization method of denitration | |
CN109453647A (en) | Boiler smoke low-temp desulfurization method of denitration | |
CN109453651A (en) | Coke oven flue gas without ammonia by desulfurization and denitrification method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20190315 |