CN109078488A - A kind of method of catalytic denitration - Google Patents

A kind of method of catalytic denitration Download PDF

Info

Publication number
CN109078488A
CN109078488A CN201810991373.8A CN201810991373A CN109078488A CN 109078488 A CN109078488 A CN 109078488A CN 201810991373 A CN201810991373 A CN 201810991373A CN 109078488 A CN109078488 A CN 109078488A
Authority
CN
China
Prior art keywords
reaction
catalytic denitration
gas
ammonia
catalyst
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
CN201810991373.8A
Other languages
Chinese (zh)
Inventor
张福顺
陈江涛
李奎中
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.)
Zhengzhou Kangningte Environmental Engineering Technology Co Ltd
Original Assignee
Zhengzhou Kangningte Environmental Engineering Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhengzhou Kangningte Environmental Engineering Technology Co Ltd filed Critical Zhengzhou Kangningte Environmental Engineering Technology Co Ltd
Priority to CN201810991373.8A priority Critical patent/CN109078488A/en
Publication of CN109078488A publication Critical patent/CN109078488A/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
    • B01D53/8628Processes characterised by a specific catalyst
    • 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
    • B01D53/14Separation 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 absorption
    • 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
    • B01D53/14Separation 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 absorption
    • B01D53/18Absorbing units; Liquid distributors therefor
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/38Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of titanium, zirconium or hafnium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03CMAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C3/00Separating dispersed particles from gases or vapour, e.g. air, by electrostatic effect
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/10Oxidants
    • B01D2251/104Ozone
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/20Reductants
    • B01D2251/206Ammonium compounds
    • B01D2251/2062Ammonia
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/40Nitrogen compounds
    • B01D2257/406Ammonia
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2258/00Sources of waste gases
    • B01D2258/02Other waste gases
    • B01D2258/0233Other waste gases from cement factories

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Environmental & Geological Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Exhaust Gas Treatment By Means Of Catalyst (AREA)

Abstract

The present invention provides a kind of methods of catalytic denitration, belong to environmentally friendly science and technology and environmental technology field.The method of catalytic denitration provided by the invention, nitrogenous exhaust gas is first passed through into dust removal process, the particle being avoided that in exhaust gas makes catalyst poisoning and blocking catalyst hole, then it by exhaust gas figure reaction kettle, is reacted with ammonia and ozone by catalyst, realizes the conversion of nitrogenous gas, then the ammonia of escape is absorbed by tail gas pond, reach discharge standard to be discharged, treatment effect is good, actual use value with higher.

Description

A kind of method of catalytic denitration
Technical field
The present invention relates to environmentally friendly science and technology and environmental technology fields, in particular to a kind of method of catalytic denitration.
Background technique
With the continuous improvement of national atmosphere pollutants emission standards, the cognition of haze harmfulness is deepened, NOx is as mist The predecessor of haze, acid rain, discharge standard are possible to more stringent.The denitration technology that cement industry generallys use at present is low nitrogen Burning, SNCR, and in order to cope with tighter discharge standard, it is necessary to increase SCR denitration on the basis of this denitration, realizes SNCR- SCR combined denitration.Domestic cement industry is seldom to the research of SCR denitration technology, but SCR technology is widely used in Thermal Power Generation Industry. Although the smoke transportation of the two has the dustiness of larger difference, especially cement industry to be much higher than Thermal Power Generation Industry, it is easy to make It is blocked at catalyst dust stratification.
The denitration technology technique of cement industry is also immature at present, is badly in need of developing effective catalytic denitration technology.
Summary of the invention
The purpose of the present invention is to provide a kind of method of catalytic denitration, the efficient photocatalytic cements kiln exhaust gas of this method energy Nitrogenous exhaust gas conversion, reaches discharge standard.
In order to realize above-mentioned purpose of the invention, using following technical scheme:
A kind of method of catalytic denitration, the method for catalytic denitration the following steps are included:
Nitrogenous exhaust gas is passed through into electrostatic precipitation processes, dust-removing waste gas is obtained, dust-removing waste gas is passed through in the reaction kettle of preheating;
It is passed through ammonia and ozone in a kettle and heats reaction, obtains reaction gas, reaction gas is passed through tail gas pond Reaction.
Compared with prior art, the beneficial effect comprise that the method for catalytic denitration provided by the invention, will first contain Nitrogen exhaust gas passes through dust removal process, and the particle being avoided that in exhaust gas makes catalyst poisoning and blocking catalyst hole, then will give up It in gas figure reaction kettle, is reacted with ammonia and ozone by catalyst, realizes the conversion of nitrogenous gas, then pass through tail gas pond The ammonia for absorbing escape, reaches discharge standard and is discharged, and treatment effect is good, actual use value with higher.
Specific embodiment
Embodiment of the present invention is described in detail below in conjunction with embodiment, but those skilled in the art will Understand, the following example is merely to illustrate the present invention, and is not construed as limiting the scope of the invention.It is not specified in embodiment specific Condition person carries out according to conventional conditions or manufacturer's recommended conditions.Reagents or instruments used without specified manufacturer is The conventional products that can be obtained by commercially available purchase.
A kind of method of catalytic denitration of the embodiment of the present invention is specifically described below.
A kind of method of catalytic denitration, the method for catalytic denitration the following steps are included:
Nitrogenous exhaust gas is passed through into electrostatic precipitation processes, dust-removing waste gas is obtained, dust-removing waste gas is passed through in the reaction kettle of preheating;
It is passed through ammonia and ozone in a kettle and heats reaction, obtains reaction gas, reaction gas is passed through tail gas pond Reaction.
The reaction principle of denitration catalyst is as follows:
4NO+4NH3+O2=4N2+6H2O;
2NO2+4NH3+O2=3N2+6H2O;
By the catalytic action of catalyst, so that the temperature of reaction reduces, nitric oxide or nitrogen dioxide and ammonia and prolong Phase reaction generates harmless nitrogen and water, reaches the standard of processing exhaust gas.
Further, in preferred embodiments of the present invention, the operating voltage of electrostatic precipitation is 50-65kv.
Electrostatic precipitation is one kind of dedusting method.Dusty gas by being electrically isolated when high-voltage electrostatic field, grit with In anion junction belt after negative electricity, tends to anode surface electric discharge and deposit.In the industry such as metallurgy, chemistry to purification gas or Recycle useful grit.Make gas ionization using electrostatic field to make dust particles be adsorbed onto the collecting method on electrode.In forceful electric power Air molecule is ionized as cation and electronics in, and electronics, which marches on towards, encounters grit in anode process, make the negatively charged absorption of grit It is collected to anode.
Using higher voltage, play the effect of ionized air, the negative ions of air ionization and input it is to be processed Charged particle in nitrogenous gas combines, and gradually reunites, achievees the purpose that dedusting.
Further, in preferred embodiments of the present invention, the concentration of solid particles of dust-removing waste gas is less than 20g/Nm3
The concentration of solid particle in gas after controlling dedusting, avoids excessive concentration from influencing the use of catalyst.Due to urging Agent has more hole, and solid particle is more, the hole of interests blocking catalyst, and the catalytic efficiency of catalyst is caused to drop It is low;In addition, solid particle contains more poisonous and harmful substance, interests lead to catalyst poisoning, also will affect urging for catalyst Change efficiency and plays the role of guard catalyst so needing to control the solid particle in gas.
Further, in preferred embodiments of the present invention, the temperature of preheating is 100-150 DEG C.
Further, in preferred embodiments of the present invention, the flow of ammonia is 1-2.5L/min.
The input of suitable ammonia flow is conducive to the progress of reaction, reasonably matches so that nitrogenous gas is formed with ammonia Than;Not only it had been avoided that ammonia deficiency caused exhaust-gas treatment incomplete, but also has been avoided that the problem of peace input excessively leads to waste.
Further, in preferred embodiments of the present invention, the volume fraction of ozone is 5%-7%.
Further, in preferred embodiments of the present invention, heating reaction is that gradient-heated is reacted, gradient-heated reaction packet Include warming up period, plateau and reaction phase.
Further, in preferred embodiments of the present invention, warming up period is heated to 120-160 DEG C, heating time 15- 20min;The time of plateau is 10-13min;The reaction phase is heated to 220-280 DEG C, heating time 10-15min.
It further, further include denitrating catalyst, denitrating catalyst master in reaction kettle in preferred embodiments of the present invention Will by titanium dioxide, montmorillonite, ammonium paratungstate, vanadic anhydride, stearic acid, ammonium metavanadate, polyethylene glycol oxide, monoethanolamine, Carboxymethyl cellulose, lactic acid, wood pulp and glass fibre and deionized water are prepared.
Further, in preferred embodiments of the present invention, the escape amount of ammonia is 3-8ppm.
Feature and performance of the invention are described in further detail with reference to embodiments.
Embodiment 1
The present embodiment provides a kind of method of catalytic denitration, catalytic denitration, which passes through in ability reaction kettle, adds denitrating catalyst, It is reacted by denitrating catalyst and nitrogenous exhaust gas, generates the gas of environmental sound, reach discharge standard.
The reaction principle of denitration catalyst is as follows:
4NO+4NH3+O2=4N2+6H2O;
2NO2+4NH3+O2=3N2+6H2O;
By the catalytic action of catalyst, so that the temperature of reaction reduces, nitric oxide or nitrogen dioxide and ammonia and prolong Phase reaction generates harmless nitrogen and water, reaches the standard of processing exhaust gas.
Denitrating catalyst, mainly by titanium dioxide, montmorillonite, ammonium paratungstate, vanadic anhydride, stearic acid, ammonium metavanadate, Polyethylene glycol oxide, monoethanolamine, carboxymethyl cellulose, lactic acid, wood pulp and glass fibre and deionized water are prepared.
The method of denitration catalyst, comprising the following steps:
Nitrogenous exhaust gas is carried out electrostatic precipitation by 1.1 in electrostatic field, and the voltage of electrostatic field is 50kv;
1.2 obtain dust-removing waste gas, and the concentration of solid particles of dust-removing waste gas is less than 20g/Nm3
1.3 preheating reaction kettles are to 100 DEG C;
1.4 are passed through dust-removing waste gas in the reaction kettle having been warmed up, while being passed through ammonia and ozone, and the flow of ammonia is 1L/min, the volume parts of ozone are 7%, and the escape amount for controlling ammonia is 3ppm;
1.5 reaction kettles start gradient-heated reaction, and gradient-heated reaction includes warming up period, plateau and reaction phase, preheating Phase is heated to 120 DEG C, heating time 15min;The time of plateau is 10min;The reaction phase is heated to 220 DEG C, heating time For 10min;Start to be reacted after being heated to 220 DEG C;
Reaction gas is obtained after 1.6 reactions, reaction gas is passed through tail gas pond.
Embodiment 2
The present embodiment provides a kind of method of catalytic denitration, catalytic denitration, which passes through in ability reaction kettle, adds denitrating catalyst, It is reacted by denitrating catalyst and nitrogenous exhaust gas, generates the gas of environmental sound, reach discharge standard.
The reaction principle of denitration catalyst is as follows:
4NO+4NH3+O2=4N2+6H2O;
2NO2+4NH3+O2=3N2+6H2O;
By the catalytic action of catalyst, so that the temperature of reaction reduces, nitric oxide or nitrogen dioxide and ammonia and prolong Phase reaction generates harmless nitrogen and water, reaches the standard of processing exhaust gas.
Denitrating catalyst, mainly by titanium dioxide, montmorillonite, ammonium paratungstate, vanadic anhydride, stearic acid, ammonium metavanadate, Polyethylene glycol oxide, monoethanolamine, carboxymethyl cellulose, lactic acid, wood pulp and glass fibre and deionized water are prepared.
The method of denitration catalyst, comprising the following steps:
Nitrogenous exhaust gas is carried out electrostatic precipitation by 1.1 in electrostatic field, and the voltage of electrostatic field is 65kv;
1.2 obtain dust-removing waste gas, and the concentration of solid particles of dust-removing waste gas is less than 20g/Nm3
1.3 preheating reaction kettles are to 150 DEG C;
1.4 are passed through dust-removing waste gas in the reaction kettle having been warmed up, while being passed through ammonia and ozone, and the flow of ammonia is 2.5L/min, the volume parts of ozone are 7%, and the escape amount for controlling ammonia is 8ppm;
1.5 reaction kettles start gradient-heated reaction, and gradient-heated reaction includes warming up period, plateau and reaction phase, preheating Phase is heated to 160 DEG C, heating time 20min;The time of plateau is 13min;The reaction phase is heated to 280 DEG C, heating time For 15min;It is persistently reacted after being heated to 280 DEG C;
Reaction gas is obtained after 1.6 reactions, reaction gas is passed through tail gas pond.
Embodiment 3
The present embodiment provides a kind of method of catalytic denitration, catalytic denitration, which passes through in ability reaction kettle, adds denitrating catalyst, It is reacted by denitrating catalyst and nitrogenous exhaust gas, generates the gas of environmental sound, reach discharge standard.
The reaction principle of denitration catalyst is as follows:
4NO+4NH3+O2=4N2+6H2O;
2NO2+4NH3+O2=3N2+6H2O;
By the catalytic action of catalyst, so that the temperature of reaction reduces, nitric oxide or nitrogen dioxide and ammonia and prolong Phase reaction generates harmless nitrogen and water, reaches the standard of processing exhaust gas.
Denitrating catalyst, mainly by titanium dioxide, montmorillonite, ammonium paratungstate, vanadic anhydride, stearic acid, ammonium metavanadate, Polyethylene glycol oxide, monoethanolamine, carboxymethyl cellulose, lactic acid, wood pulp and glass fibre and deionized water are prepared.
The method of denitration catalyst, comprising the following steps:
Nitrogenous exhaust gas is carried out electrostatic precipitation by 1.1 in electrostatic field, and the voltage of electrostatic field is 55kv;
1.2 obtain dust-removing waste gas, and the concentration of solid particles of dust-removing waste gas is less than 20g/Nm3
1.3 preheating reaction kettles are to 130 DEG C;
1.4 are passed through dust-removing waste gas in the reaction kettle having been warmed up, while being passed through ammonia and ozone, and the flow of ammonia is 2L/min, the volume parts of ozone are 6%, and the escape amount for controlling ammonia is 5ppm;
1.5 reaction kettles start gradient-heated reaction, and gradient-heated reaction includes warming up period, plateau and reaction phase, preheating Phase is heated to 140 DEG C, heating time 17min;The time of plateau is 12min;The reaction phase is heated to 260 DEG C, heating time For 13min;It is persistently reacted after being heated to 260 DEG C;
Reaction gas is obtained after 1.6 reactions, reaction gas is passed through tail gas pond.
Embodiment 4
The present embodiment provides a kind of method of catalytic denitration, catalytic denitration, which passes through in ability reaction kettle, adds denitrating catalyst, It is reacted by denitrating catalyst and nitrogenous exhaust gas, generates the gas of environmental sound, reach discharge standard.
The reaction principle of denitration catalyst is as follows:
4NO+4NH3+O2=4N2+6H2O;
2NO2+4NH3+O2=3N2+6H2O;
By the catalytic action of catalyst, so that the temperature of reaction reduces, nitric oxide or nitrogen dioxide and ammonia and prolong Phase reaction generates harmless nitrogen and water, reaches the standard of processing exhaust gas.
Denitrating catalyst, mainly by titanium dioxide, montmorillonite, ammonium paratungstate, vanadic anhydride, stearic acid, ammonium metavanadate, Polyethylene glycol oxide, monoethanolamine, carboxymethyl cellulose, lactic acid, wood pulp and glass fibre and deionized water are prepared.
The method of denitration catalyst, comprising the following steps:
Nitrogenous exhaust gas is carried out electrostatic precipitation by 1.1 in electrostatic field, and the voltage of electrostatic field is 60kv;
1.2 obtain dust-removing waste gas, and the concentration of solid particles of dust-removing waste gas is less than 20g/Nm3
1.3 preheating reaction kettles are to 150 DEG C;
1.4 are passed through dust-removing waste gas in the reaction kettle having been warmed up, while being passed through ammonia and ozone, and the flow of ammonia is 1.5L/min, the volume parts of ozone are 6%, and the escape amount for controlling ammonia is 7ppm;
1.5 reaction kettles start gradient-heated reaction, and gradient-heated reaction includes warming up period, plateau and reaction phase, preheating Phase is heated to 150 DEG C, heating time 18min;The time of plateau is 11min;The reaction phase is heated to 270 DEG C, heating time For 14min;It is persistently reacted after being heated to 270 DEG C;
Reaction gas is obtained after 1.6 reactions, reaction gas is passed through tail gas pond.
Experimental example 1
This experimental example carries out denitration catalyst processing in the method for the embodiment 1-4 catalytic denitration provided, and comparative example 1 is not to remove The exhaust gas of dirt carries out denitration process (remaining is same as Example 1), and comparative example 2 is handled (its with 0.5L/min ammonia flow It is remaining same as Example 1), comparative example 3 is reacted (remaining is same as Example 1) with the ammonia flow of 5L/min, is counted respectively Calculate the service life and denitration efficiency of catalyst.Experimental result is shown in Table 1.
1 denitration experimental result of table
From table 1 can, the exhaust gas of non-dedusting significantly affects the service life and denitration efficiency of catalyst, and ammonia flow The too small or excessive service life and denitration efficiency that also can all influence catalyst.
In conclusion the method for catalytic denitration provided in an embodiment of the present invention, when the use of extension catalyst that can be opposite Between, opposite saving use cost simultaneously improves denitration efficiency, has higher practical application value and preferable promotion price Value.
Embodiments described above is a part of the embodiment of the present invention, instead of all the embodiments.Reality of the invention The detailed description for applying example is not intended to limit the range of claimed invention, but is merely representative of selected implementation of the invention Example.Based on the embodiments of the present invention, obtained by those of ordinary skill in the art without making creative efforts Every other embodiment, shall fall within the protection scope of the present invention.

Claims (10)

1. a kind of method of catalytic denitration, which is characterized in that the method for the catalytic denitration the following steps are included:
Nitrogenous exhaust gas is passed through into electrostatic precipitation processes, dust-removing waste gas is obtained, the dust-removing waste gas is passed through in the reaction kettle of preheating;
It is passed through ammonia and ozone in a kettle and heats reaction, obtains reaction gas, reaction gas is passed through the reaction of tail gas pond.
2. the method for catalytic denitration according to claim 1, which is characterized in that the operating voltage of the electrostatic precipitation is 50-65kv。
3. the method for catalytic denitration according to claim 2, which is characterized in that the concentration of solid particles of the dust-removing waste gas Less than 20g/Nm3
4. the method for catalytic denitration according to claim 2, which is characterized in that the temperature of the preheating is 100-150 DEG C.
5. the method for catalytic denitration according to claim 1, which is characterized in that the flow of the ammonia is 1-2.5L/ min。
6. the method for catalytic denitration according to claim 5, which is characterized in that the volume fraction of the ozone is 5%- 7%.
7. the method for catalytic denitration according to claim 1, which is characterized in that the heating reaction is that gradient-heated is anti- It answers, the gradient-heated reaction includes warming up period, plateau and reaction phase.
8. the method for catalytic denitration according to claim 7, which is characterized in that the warming up period is heated to 120-160 DEG C, Heating time is 15-20min;The time of the plateau is 10-13min;The reaction phase is heated to 220-280 DEG C, heating Time is 10-15min.
9. the method for catalytic denitration according to claim 1, which is characterized in that further include denitration catalyst in the reaction kettle Agent, the denitrating catalyst is mainly by titanium dioxide, montmorillonite, ammonium paratungstate, vanadic anhydride, stearic acid, ammonium metavanadate, poly- Ethylene oxide, monoethanolamine, carboxymethyl cellulose, lactic acid, wood pulp and glass fibre and deionized water are prepared.
10. the method for catalytic denitration as described in claim 1, which is characterized in that the escape amount of the ammonia is 3-8ppm.
CN201810991373.8A 2018-08-28 2018-08-28 A kind of method of catalytic denitration Pending CN109078488A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810991373.8A CN109078488A (en) 2018-08-28 2018-08-28 A kind of method of catalytic denitration

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810991373.8A CN109078488A (en) 2018-08-28 2018-08-28 A kind of method of catalytic denitration

Publications (1)

Publication Number Publication Date
CN109078488A true CN109078488A (en) 2018-12-25

Family

ID=64794989

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810991373.8A Pending CN109078488A (en) 2018-08-28 2018-08-28 A kind of method of catalytic denitration

Country Status (1)

Country Link
CN (1) CN109078488A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1923337A (en) * 2006-08-23 2007-03-07 浙江大学 Boiler smoke gas multipollutant ozonization and simultaneous elimination device and method therefor
CN103298540A (en) * 2010-11-09 2013-09-11 Geesco有限公司 System using selective catalytic reduction for improving low-temperature de-nox efficiency and reducing yellow plume
CN106237851A (en) * 2016-08-23 2016-12-21 华电电力科学研究院 A kind of utilize ozone to carry out SCR denitration to carry the System and method for of effect
JP6051673B2 (en) * 2012-08-13 2016-12-27 いすゞ自動車株式会社 Exhaust gas aftertreatment device and internal combustion engine equipped with the exhaust gas aftertreatment device
CN107051203A (en) * 2017-06-21 2017-08-18 重庆大学 A kind of middle low temperature sulfur-containing smoke gas efficient denitrifying device and method based on Fast SCR reactions

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1923337A (en) * 2006-08-23 2007-03-07 浙江大学 Boiler smoke gas multipollutant ozonization and simultaneous elimination device and method therefor
CN103298540A (en) * 2010-11-09 2013-09-11 Geesco有限公司 System using selective catalytic reduction for improving low-temperature de-nox efficiency and reducing yellow plume
JP6051673B2 (en) * 2012-08-13 2016-12-27 いすゞ自動車株式会社 Exhaust gas aftertreatment device and internal combustion engine equipped with the exhaust gas aftertreatment device
CN106237851A (en) * 2016-08-23 2016-12-21 华电电力科学研究院 A kind of utilize ozone to carry out SCR denitration to carry the System and method for of effect
CN107051203A (en) * 2017-06-21 2017-08-18 重庆大学 A kind of middle low temperature sulfur-containing smoke gas efficient denitrifying device and method based on Fast SCR reactions

Similar Documents

Publication Publication Date Title
CN101422692B (en) Method and device for pulse corona plasma reaction and absorption catalysis desulfurization denitration
CN109569228A (en) The exhaust system and technique of flue gas of garbage furnace
CN1011858B (en) Process for treating waste gas
CN107398153A (en) A kind of flue gas desulfurization and denitrification processing system
CN104759192A (en) Low-cost coal-fired flue gas various pollutant ultralow emission system and low-cost coal-fired flue gas various pollutant ultralow emission method
CN104437059A (en) Flue gas absorbent of desulfurization and denitrification, and desulfurization and denitrification method thereof
WO2019062455A1 (en) Flue gas desulfurization and denitration agent, preparation method therefor and applications thereof
CN102274680A (en) Steamer discharge ammonia flue gas desulfurization, denitration and demisting integrated method
CN103463944A (en) Electrostatic cooperative pollutant removing method and device
CN102716654A (en) Method and device for flue gas denitration by spray absorption and electrochemical reduction
CN108722141A (en) A kind of dust removal integrated method of desulphurization denitration
WO2020098574A1 (en) Method and apparatus for purifying waste incineration flue gas
CN108079758A (en) The drying of glutamic acid-fermented waste liquid concentrate is granulated organic fertilizer smoke treating method
CN206897142U (en) A kind of integrative coordinated removing sulfur trioxide device suitable for sulphur coal
CN107999024A (en) A kind of preparation method and applications of the efficiently copper-based demercuration adsorbent of sulfur resistive
CN109078488A (en) A kind of method of catalytic denitration
WO2021134925A1 (en) Semi-dry flue gas desulfurization and denitrification method
CN104258699B (en) The method of plasma and gas-solid or Gas-Liquid Dispersion system synergistic purification pollutant
CN102806083A (en) Catalyst for removing nitrogen oxide in high-temperature flue gas containing sulfur oxide and preparation method
CN113117484A (en) Dry-method integrated flue gas desulfurization and denitrification process
CN202893192U (en) High-temperature dustproof SCR (Selective Catalytic Reduction) denitration device for cement kiln smoke
CN114849434A (en) Prilling tower system and tail gas treatment device
CN104014228A (en) Light energy catalysis and ultraviolet (UV) photolysis oxidation combined high-efficiency waste gas treatment device
CN210584379U (en) VOCs processing apparatus
CN110433621B (en) Method and device for reduction denitration of kiln flue gas carbon

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

Application publication date: 20181225

RJ01 Rejection of invention patent application after publication