CN109453655A - Boiler smoke low-temp desulfurization method of denitration - Google Patents
Boiler smoke low-temp desulfurization method of denitration Download PDFInfo
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- CN109453655A CN109453655A CN201811490471.XA CN201811490471A CN109453655A CN 109453655 A CN109453655 A CN 109453655A CN 201811490471 A CN201811490471 A CN 201811490471A CN 109453655 A CN109453655 A CN 109453655A
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- 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
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- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
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- 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
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Abstract
The present invention relates to a kind of boiler smoke low-temp desulfurization method of denitration, mainly solves the problem of that existing boiler flue gas desulfurization denitration operating cost is high and generate secondary pollution.The boiler smoke of sulfur compound and nitrogen oxides that the present invention is drawn by using boiler flue, into the denitrating tower comprising denitrating catalyst, after catalysis reduction, into heat exchanger, by with remove the flue gas heat exchange of chimney after, into the adsorption tower comprising crystallite adsorbent, after adsorbing sulfide and nitrogen oxides, into smoke stack emission；Nitrogen oxides in effluent and sulfide after regeneration carry out the technical solution of salt manufacturing processing, preferably solve the above problem, this method can be used in the industrial production of boiler flue gas desulfurization denitration.
Description
Technical field
The invention belongs to desulphurization denitration technical fields, and in particular to a kind of boiler smoke low-temp desulfurization method of denitration.
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, pot
Kiln gas is the important pollution sources of atmosphere.
Current boiler flue gas desulfurization 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 denitration of boiler smoke 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 boiler 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, deposits 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 boiler smoke2And NOX, and be worth with certain recycling.
Summary of the invention
The technical problem to be solved by the present invention is in existing coke-oven plant's boiler smoke governance process, operating cost height is produced
The technical issues of raw secondary pollution, provides a kind of boiler smoke low-temp desulfurization method of denitration, which has process short,
Low equipment investment, regeneration is simple, and low energy consumption, advantage without secondary pollution.
In order to solve the above technical problems, the present invention uses a kind of boiler smoke low-temp desulfurization method of denitration, including following step
It is rapid:
A) boiler smoke of boiler flue is drawn sulfur compound and nitrogen oxides, is denoted as material flow A, the temperature of the material flow A
It is 120 ~ 320 DEG C；
B) material flow A enters the denitrating tower comprising denitrating catalyst, after catalysis reduction, forms flow B；
C) stream B enters heat exchanger, by with remove the flue gas heat exchange of chimney after, form flow C, the temperature of the flow C is 80 ~
160℃；
D) flow C enters the adsorption tower comprising crystallite adsorbent, after adsorbing sulfide and nitrogen oxides, forms logistics D；
E) logistics D enters smoke stack emission；
F) adsorption tower after adsorbing sulfide and nitrogen oxides saturation in step d), with 100 ~ 10000 m3The logistics or heat of/h
Air regenesis, regenerated flue gas form logistics D, wherein the temperature of the logistics F is 120 ~ 350 DEG C；
G) logistics F enters the oxidizing tower comprising oxidation catalyst, after catalysis oxidation, forms logistics G；
H) logistics G enters regeneration tail gas desulfurizing tower, after water or lye spray, forms logistics H, spray liquid enters wastewater treatment
System or salt extraction system；
I) logistics H enters step the cooling tower in c).
In the above-mentioned technical solutions, preferred technical solution is that the temperature of the material flow A is 140 ~ 280 DEG C；Nitrogen oxidation
Object content is 100 ~ 1000mg/m3, sulfide content is 30 ~ 3000 mg/m3。
In the above-mentioned technical solutions, preferred technical solution is that the denitrating catalyst includes being selected from SSZ-13 molecule
Sieve, TS-1, Ti-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 zeolite/modenite, ZSM-5/ β zeolite/at least one of Y zeolite or ZSM-5/Y zeolite/modenite.
In the above-mentioned technical solutions, preferred technical solution is that also containing in the denitrating catalyst 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 above-mentioned technical proposal, preferred technical solution is, before the step c), flue gas carries out UTILIZATION OF VESIDUAL HEAT IN, adopts
With steam boiler, the vapor (steam) temperature of production is 140 ~ 180 DEG C；The flue gas that waste heat boiler comes out enters back into heat exchanger, and described changes
Hot device is shell and tube or finned heat exchanger；Cooling tower in the step d) is spray column or heat exchanger types；Object
The temperature for flowing D is 30 ~ 100 DEG C.
In above-mentioned technical proposal, preferred technical solution is that the temperature of the logistics E is 30 ~ 100 DEG C；Nitrogen oxides
Content is 1 ~ 200mg/m3, sulfide content is 0.1 ~ 100 mg/m3。
In above-mentioned technical proposal, preferred technical solution is that the logistics E and material flow A exchange heat after heating up, temperature 80
~200℃。
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 the step C) in UTILIZATION OF VESIDUAL HEAT IN use steam boiler, it is raw
The vapor (steam) temperature of production is 150 ~ 170 DEG C；The step C) in cooling tower be spray column or heat exchanger types；Flow C
Temperature is 40 ~ 60 DEG C.In above-mentioned technical proposal, preferred technical solution is, in step d), the quantity of adsorption tower is at least more than two
A, adsorbent 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 ~ 3000 mg/m3。
In the above-mentioned technical solutions, preferred technical solution is, in step c), the quantity of adsorption tower at least more than two,
Adsorbent bed operation temperature is 30 ~ 80 DEG C, and operating pressure gauge pressure is 0.5 ~ 5Kpa.
In the above-mentioned technical solutions, preferred technical solution is that it includes X-type molecular sieve, Y that the crystallite adsorbent, which is selected from,
Type molecular sieve, A type molecular sieve, SSZ-13 molecular sieve, TS-1, Ti-MWW, Ti-MOR, ZSM type molecular sieve, modenite, β type point
Sub- 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 zeolite/Y zeolite or ZSM-
At least one of 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, 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 be 30 ~ 50 DEG C, operating pressure be 1 ~
3Kpa, 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, after the adsorbent of molecular sieve adsorption saturation, heat first
Water rinses, then with 100-300 DEG C of nitrogen regeneration.
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 boiler smoke low-temp desulfurization method of denitration of the invention.
1 is boiler smoke in Fig. 1, and 2 be denitrating tower, and 3 be waste heat steam boiler, and 4 be cooling tower, and 5 be adsorption tower, and 6 be wind
Machine, 7 be oxidizing tower, and 8 be spray column, and 9 be sedimentation basin, and 10 be wastewater biochemical pond, and 11 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 flue gas of 16 240 DEG C of ten thousand steres, amount of nitrogen oxides 500mg/m3, sulfide content is 200 mg/m3, flue gas into
Enter denitrating tower, at 240 DEG C, under ZSM-5 molecular sieve catalyst action, nitrogen oxides is reduced into nitrogen, the flue gas after reaction into
Enter waste heat boiler, generate steam, flue-gas temperature is reduced to 180 DEG C or so；Then flue gas enters from heat exchanger, and enters chimney
Cold flue gas heat exchange, temperature are reduced to 110 DEG C or so；By spraying cooling to 50 DEG C, shower water is made 110 DEG C of flue gas by circulation
After being neutralized with, effluent part, biochemical system is removed；After flue gas after cooling passes through defogging equipment, into adsorption tower；Using 3
200m3Adsorption tower, two open one standby, and 120m is loaded in each adsorption tower3Micro crystal material amounts to 360 m3The boiling of micro crystal material mercerising
Stone；Adsorption tower specification is 4.8 meters of diameter, 12.0 meters high；After flue gas removes sulfide and nitrogen oxides, into from heat exchanger, and
After hot fume heat exchange, reach 100 DEG C or more, into smoke stack emission, nitrogen oxides in effluent content is 50mg/m3, sulfide content
For 20 mg/m3.Desulphurization and denitration, dedusting crystallite adsorbent are loaded in adsorption tower, automatically switch circular regeneration after adsorption saturation；Often
Automatically switch within 7 days a tower regeneration, the adsorption tower 3000m of saturation3The hot fume of/h is regenerated, the nitrogen oxides of desorption and
Sulfide enters oxidizing tower, is oxidized to sulfur trioxide and nitrogen dioxide；It after mixed gas cooling, is absorbed with water spray, part is useless
After water neutralizes, it is discharged into biochemical system or going produces salt extraction workshop, tail gas enters flue gas spray column.
[embodiment 2]
Specific embodiment device process as shown in Fig. 1, the flue gas of 15 260 DEG C of ten thousand steres, amount of nitrogen oxides are
400mg/m3, sulfide content is 100 mg/m3, flue gas enters denitrating tower, at 240 DEG C, in ZSM-5 molecular sieve catalyst action
Under, nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat boiler, generates 150 DEG C of steam, and flue-gas temperature is reduced to
140 DEG C or so；Then flue gas enters spraying cooling to 40 DEG C, and shower water after effluent part neutralizes, removes biochemistry by being recycled
System；After flue gas after cooling passes through defogging equipment, into adsorption tower；Using 3 200m3Adsorption tower, two open it is one standby, each
120m is loaded in adsorption tower3Micro crystal material amounts to 360 m3Micro crystal material ZSM-5 molecular sieve；Adsorption tower specification is 4.8 meters of diameter,
It is 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 with
On, into smoke stack emission, nitrogen oxides in effluent content is 50mg/m3, sulfide content is 20 mg/m3.Filling is de- in adsorption tower
Sulphur, denitration, dedusting crystallite adsorbent, automatically switch circular regeneration after adsorption saturation；Automatically switch within every 7 days a tower regeneration, satisfies
The adsorption tower 3000m of sum3The 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
Person goes to salt extraction workshop, and tail gas enters flue gas spray column.
[embodiment 3]
Specific embodiment device process as shown in Fig. 1, the flue gas of 14 300 DEG C of ten thousand steres, amount of nitrogen oxides are
450mg/m3, sulfide content is 200 mg/m3, flue gas enters denitrating tower, at 300 DEG C, urges in the ZSM-5 molecular sieve of copper load
Under agent effect, nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat boiler, generates 160 DEG C of steam, flue gas again into
Enter from heat exchanger, and enter the cold flue gas heat exchange of chimney, temperature is reduced to 110 DEG C or so；110 DEG C of flue gas passes through flue-gas temperature
It is reduced to 110 DEG C or so；110 DEG C of flue gas is by spraying cooling to 50 DEG C, and by being recycled, effluent part neutralizes shower water
Afterwards, biochemical system is removed；After flue gas after cooling passes through defogging equipment, into adsorption tower；Using 3 200m3Adsorption tower, two open
One is standby, and 120m is loaded in each adsorption tower3Micro crystal material amounts to 360 m3Micro crystal material ZSM-5 molecular sieve；Adsorption tower specification is
It is 4.8 meters of diameter, 12.0 meters high；After flue gas removes sulfide and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reach
To 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
Interior filling desulphurization and denitration, dedusting crystallite adsorbent after adsorption saturation, automatically switch circular regeneration with high-temperature flue gas；Every 7 days certainly
One tower regeneration of dynamic switching, the adsorption tower 3000m of saturation3240 DEG C of flue gases of/h are regenerated, the nitrogen oxides and sulphur of desorption
Compound enters the oxidizing tower containing vanadium series catalyst, is oxidized to sulfur trioxide and nitrogen dioxide；After mixed gas cooling, sprayed with water
Leaching absorbs, and 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, flue gas enters denitrating tower, at 180 DEG C, under mordenite catalyst effect,
Nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat boiler, generates 10 tons of 165 DEG C of steam, flue-gas temperature 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
1000 mg/m3, sulfide content is 500 mg/m3, flue gas enters denitrating tower, at 180 DEG C, in the ZSM-5 molecule of copper zinc load
Under sieve catalyst effect, nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat boiler, generates 150 DEG C of steam, flue gas
170 DEG C are cooled to, then flue gas enters from heat exchanger, and enters the cold flue gas heat exchange of chimney, and temperature is reduced to 130 DEG C or so；
Flue gas enters spray column, and by spraying cooling to 40 DEG C, shower water is by being recycled, after effluent part neutralizes, what going produced
Salt extraction system；After flue gas after cooling passes through defogging equipment, into adsorption tower；Using 4 200m3Adsorption tower, three open it is one standby,
120m is loaded in each adsorption tower3Micro crystal material, amount to 480 m3Micro crystal material copper ZSM-5 molecular sieve；Adsorption tower specification is straight
It is 4.8 meters of diameter, 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.In adsorption tower
Desulphurization and denitration, dedusting crystallite adsorbent are loaded, 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 260 DEG C of 200,000 sides rice, amount of nitrogen oxides are
400mg/m3, sulfide content is 100 mg/m3, flue gas enters denitrating tower, at 250 DEG C or so, in rare earth mordenite catalyst
Under effect, nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat boiler, generates 170 DEG C of steam, and flue gas cool-down arrives
175 DEG C, then flue gas enters from heat exchanger, and enters the cold flue gas heat exchange of chimney, and temperature is reduced to 130 DEG C or so；Into spray
Leaching cools to 50 DEG C, and shower water after effluent part neutralizes, removes biochemical system by being recycled；Flue gas after cooling is by removing
After mist equipment, into adsorption tower；Using 3 200m3Adsorption tower, two open one standby, and 120m is loaded in each adsorption tower3Crystallite material
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 4.8
Rice is 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, are automatically switched after adsorption saturation
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 is regenerated,
The nitrogen oxides and sulfide of desorption enter oxidizing tower, are oxidized to sulfur trioxide and nitrogen dioxide at 250 DEG C；Mixed gas cooling
Afterwards, it 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, flue gas enters denitrating tower, at 240 DEG C, in rare-earth Y molecular sieve catalyst action
Under, nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat steam boiler, generates 145 DEG C of steam, and flue gas cool-down arrives
160 DEG C, by spraying cooling to 40 DEG C, shower water after effluent part neutralizes, removes biochemical system by being recycled；After cooling
Flue gas by after defogging equipment, into adsorption tower；Using 3 200m3Adsorption tower, two open one standby, and each adsorption tower is built-in
Fill out 120m3Micro 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；
After flue gas removes sulfide and nitrogen oxides, into from after heat exchanger and hot fume heat exchange, reaches 100 DEG C or more, arranged into chimney
It puts, nitrogen oxides in effluent content is 50mg/m3, sulfide content is 20 mg/m3.Desulphurization and denitration, dedusting are loaded in adsorption tower
Crystallite adsorbent automatically switches circular regeneration after adsorption saturation；Automatically switch within every 7 days a tower regeneration, the adsorption tower of saturation is used
3000m3The hot fume of/h is regenerated, and the nitrogen oxides and sulfide of desorption enter oxidizing tower, is oxidized to sulfur trioxide and two
Nitrogen oxide；It after mixed gas 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 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, flue gas enters denitrating tower, at 210 DEG C, in the ZSM-5 molecule of copper and tungsten load
Under sieve catalyst effect, nitrogen oxides is reduced into nitrogen, and the flue gas after reaction enters waste heat boiler, generates 160 DEG C of steam, flue gas
185 DEG C are cooled to, then flue gas enters from heat exchanger, and enters the cold flue gas heat exchange of chimney, and temperature is reduced to 130 DEG C or so；
By spraying cooling to 50 DEG C, shower water after effluent part neutralizes, goes to the salt extraction workshop of coking by being recycled；After cooling
Flue gas by after defogging equipment, into adsorption tower；Using 4 200m3Adsorption tower, three open one standby, and each adsorption tower is built-in
Fill out 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 (10)
1. a kind of boiler smoke low-temp desulfurization method of denitration, comprising the following steps:
A) boiler smoke of boiler flue is drawn sulfur compound and nitrogen oxides, is denoted as material flow A, the temperature of the material flow A
It is 120 ~ 320 DEG C；
B) material flow A enters the denitrating tower comprising denitrating catalyst, after catalysis reduction, forms flow B；
C) stream B enters heat exchanger, by with remove the flue gas heat exchange of chimney after, form flow C, the temperature of the flow C is 80 ~
160℃；
D) flow C enters the adsorption tower comprising crystallite adsorbent, after adsorbing sulfide and nitrogen oxides, forms logistics D；
E) logistics D enters smoke stack emission；
F) adsorption tower after adsorbing sulfide and nitrogen oxides saturation in step d), with 100 ~ 10000m3The logistics or heat of/h is empty
Gas regeneration, regenerated flue gas form logistics D, wherein the temperature of the logistics F is 120 ~ 350 DEG C；
G) logistics F enters the oxidizing tower comprising oxidation catalyst, after catalysis oxidation, forms logistics G；
H) logistics G enters regeneration tail gas desulfurizing tower, after water or lye spray, forms logistics H, spray liquid enters wastewater treatment
System or salt extraction system；
I) logistics H enters step the cooling tower in c).
2. boiler smoke low-temp desulfurization method of denitration according to claim 1, it is characterised in that the temperature of the material flow A
It is 140 ~ 280 DEG C；Amount of nitrogen oxides is 100 ~ 1000mg/m3, sulfide content is 30 ~ 3000 mg/m3。
3. boiler smoke low-temp desulfurization method of denitration according to claim 1, it is characterised in that the denitrating catalyst
Including being selected from SSZ-13 molecular sieve, TS-1, Ti-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, the boiling of ZSM-5/Y, MCM-22/ mercerising
Stone, ZSM-5/Magadiite, ZSM-5/ β zeolite/modenite, ZSM-5/ β zeolite/Y zeolite or ZSM-5/Y zeolite/mercerising boiling
At least one of stone.
4. the boiler smoke low-temp desulfurization method of denitration stated according to claim 3, it is characterised in that in the denitrating catalyst
Also containing including 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 in the periodic table of elements
At least one element.
5. boiler smoke low-temp desulfurization method of denitration according to claim 1, it is characterised in that the step C) in it is remaining
Heat utilization uses steam boiler, and the vapor (steam) temperature of production is 140 ~ 180 DEG C；Cooling tower in the step c) be spray column or
Person's heat exchanger types；The temperature of flow C is 30 ~ 100 DEG C；The temperature of the logistics D is 30 ~ 100 DEG C；Amount of nitrogen oxides is
1~200mg/m3, sulfide content is 0.1 ~ 100 mg/m3。
6. boiler smoke low-temp desulfurization method of denitration according to claim 1, it is characterised in that the heating of the logistics D
Mode is exchanged heat heating mode using heated by gas heating mode or logistics D and material flow A, logistics D after heating up, temperature is 80 ~
200℃；In step d), for the quantity of adsorption tower at least more than two, adsorbent bed operation temperature is 30 ~ 100 DEG C, and operating pressure is
0.1~20KPa。
7. boiler smoke low-temp desulfurization method of denitration according to claim 1, it is characterised in that micro- described in step e)
It includes X-type molecular sieve, Y type molecular sieve, A type molecular sieve, SSZ-13 molecular sieve, TS-1, Ti-MWW, Ti- that brilliant adsorbent, which is selected from,
MOR, ZSM type molecular sieve, modenite, beta molecular sieve, SAPO type molecular sieve, MCM-22, MCM-49, MCM-56, ZSM-5/
Geolyte, ZSM-5/ β zeolite, ZSM-5/Y, MCM-22/ modenite, ZSM-5/Magadiite, ZSM-5/ β zeolite/mercerising boiling
Stone, ZSM-5/ β zeolite/at least one of Y zeolite or ZSM-5/Y zeolite/modenite.
8. boiler smoke low-temp desulfurization method of denitration according to claim 7, it is characterised in that the crystallite adsorbent
In also containing including 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
At least one element.
9. boiler smoke low-temp desulfurization method of denitration according to claim 1, it is characterised in that the oxidation catalyst
In containing including 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
At least one element.
10. the boiler smoke low-temp desulfurization method of denitration stated according to claim 7, it is characterised in that lye described in step h)
For at least one of sodium hydroxide solution, ammonium hydroxide, remained ammonia, sodium carbonate liquor, calcium hydroxide solution.
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