KR101567746B1 - Apparatus for treating exhaust gas - Google Patents
Apparatus for treating exhaust gas Download PDFInfo
- Publication number
- KR101567746B1 KR101567746B1 KR1020150084945A KR20150084945A KR101567746B1 KR 101567746 B1 KR101567746 B1 KR 101567746B1 KR 1020150084945 A KR1020150084945 A KR 1020150084945A KR 20150084945 A KR20150084945 A KR 20150084945A KR 101567746 B1 KR101567746 B1 KR 101567746B1
- Authority
- KR
- South Korea
- Prior art keywords
- plasma reactor
- exhaust gas
- microwave
- microwave plasma
- reducing agent
- Prior art date
Links
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D47/00—Separating dispersed particles from gases, air or vapours by liquid as separating agent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D50/00—Combinations of methods or devices for separating particles from gases or vapours
-
- 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
- B01D53/32—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 electrical effects other than those provided for in group B01D61/00
-
- 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
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/50—Sulfur oxides
-
- 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
- B01D53/46—Removing components of defined structure
- B01D53/54—Nitrogen compounds
- B01D53/56—Nitrogen oxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION 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
- B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03C3/00—Separating dispersed particles from gases or vapour, e.g. air, by electrostatic effect
Abstract
Description
The present invention relates to an exhaust gas treating apparatus.
Generally, it is necessary to maintain the atmospheric environment in a clean state by reducing various kinds of particulate matter, sulfur oxides, and nitrogen oxides, which are harmful exhaust products, from products produced by fossil fuel combustion in a factory or a combustion apparatus to a maximum extent It is a reality that is emerging.
In particular, currently known methods of reducing nitrogen oxides include selective catalytic reduction and selective non-catalytic reduction. Such selective catalytic reduction and selective non-catalytic reduction are well known and avoid detailed description.
Basically, selective catalytic reduction (SCR) is performed by supplying ammonia, which is a reducing agent, through the ammonia injection unit (AIG) to the downstream of the combustion apparatus to cause a reduction reaction in the catalytic reaction tower to reduce nitrogen oxides. Such a selective catalytic reduction process typically causes a phenomenon in which the combustion apparatus is in a low load state or the temperature of the exhaust gas to be introduced into the catalytic reaction tower is low, the reaction of nitrogen oxides is significantly lowered, There is a problem that a bad effect may be caused in the rear end facility.
In addition, the selective non-catalytic reduction (SNCR) method can directly reduce ammonia water or urea water into the combustion apparatus and react with nitrogen oxides generated through combustion of fossil fuel in the combustion apparatus . This selective non-catalytic reduction method is to supply ammonia or urea water of liquid phase into the combustion apparatus as described above. Therefore, when the reducing agent is sprayed into the combustion apparatus and water droplets come into contact with the boiler tube, There are always risks involved, and in fact some companies have suffered large losses.
In addition, the denitrification system using the selective non-catalytic reduction method has a limitation in that the denitrification rate is lowered while the combustion apparatus can achieve high efficiency when the combustion apparatus is at a low load.
An object of the present invention is to remove harmful pollutants contained in exhaust gas by using a combined process of a desulfurization facility and a denitration facility.
The present invention relates to a treatment apparatus capable of reducing various harmful emissions contained in exhaust gas discharged from an exhaust gas generating source.
In order to attain the above object, an exhaust gas treating apparatus according to a first embodiment of the present invention includes: an exhaust gas generating source for exhausting exhaust gas; A dust collecting facility disposed downstream of the exhaust gas generating source; A low temperature plasma reactor disposed downstream of the dust collecting facility for oxidizing the nitrogen monoxide discharged from the exhaust gas generating source into nitrogen dioxide; A desulfurization facility disposed downstream of the low temperature plasma reactor; A reservoir for storing the reducing agent; A microwave plasma reactor for supplying exhaust gas containing nitrogen oxide discharged from a desulfurization facility to a transfer pipe and converting a reducing agent supplied to a supply pipe of the storage tank into a hot gas phase to help dissociate nitrogen oxides; A microwave generator for generating a microwave according to application of power; And a plasma generator disposed between the microwave generator and the microwave plasma reactor, for generating a flame by guiding the microwave into the microwave plasma reactor through the induction tube. The exhaust gas discharged from the exhaust gas generator is collected by a dust collecting apparatus And is designed to be able to remove contaminants contained in the exhaust gas by sequentially passing through a low temperature plasma reactor, a desulfurization facility, and a high-temperature microwave plasma reactor.
In an embodiment of the present invention, the dust collection facility may comprise an electrostatic precipitator. The electrostatic precipitator can be expected to have an effect of partially modifying the nitrogen monoxide contained in the exhaust gas with nitrogen dioxide.
The desulfurization facility may be a wet desulfurization system.
The feed pipe of the reservoir further comprises an improved feed module, which can supply the reducing agent stored in the reservoir according to the amount of nitrogen oxide to be fed into the microwave plasma reactor. This can optimize the amount of reducing agent used.
Specifically, the microwave plasma reactor is arranged such that the tube end of the transfer tube is disposed toward the upper part of the microwave plasma reactor to cause the exhaust gas to flow upward, while the end of the induction tube penetrates from the upper part to the lower part of the microwave plasma reactor, The direction can be made to be downward. The pipe end portion of the transfer pipe and the pipe end portion of the induction pipe may be arranged on the same axis line to improve the contact between the down stream reducing agent and the flame and the upward flow exhaust gas. In order to be selectable, the supply pipe may be penetrated downward from the upper part of the microwave plasma reactor to supply the reducing agent downward, or may be joined to the induction pipe and guided into the microwave plasma reactor through the induction pipe.
An exhaust gas treating apparatus according to a second embodiment of the present invention includes an exhaust gas generating source for exhausting exhaust gas; A desulfurization facility disposed downstream of the exhaust gas generating source; A dust collection facility disposed downstream of the desulfurization facility; A low temperature plasma reactor disposed downstream of the dust collecting facility for oxidizing the nitrogen monoxide discharged from the exhaust gas generating source into nitrogen dioxide; A reservoir for storing the reducing agent; A microwave plasma reactor supplied with the exhaust gas containing the nitrogen oxide discharged from the low temperature plasma reactor to the transfer tube and converting the reducing agent supplied to the supply pipe of the storage tank into the high temperature gas phase to help dissociate the nitrogen oxide; A microwave generator for generating a microwave according to application of power; And a plasma generator disposed between the microwave generator and the microwave plasma reactor, for generating a flame by guiding the microwave into the microwave plasma reactor through the induction tube. The exhaust gas discharged from the exhaust gas generator is supplied to the desulfurization equipment And a high-temperature microwave plasma reactor in order to remove contaminants contained in the exhaust gas.
In an embodiment of the present invention, the dust collection facility may comprise an electrostatic precipitator. The electrostatic precipitator can be expected to have an effect of partially modifying the nitrogen monoxide contained in the exhaust gas with nitrogen dioxide.
The desulfurization facility may be a dry desulfurization system.
The feed pipe of the reservoir further comprises an improved feed module, which can supply the reducing agent stored in the reservoir according to the amount of nitrogen oxide to be fed into the microwave plasma reactor. This can optimize the amount of reducing agent used.
Specifically, the microwave plasma reactor is arranged such that the tube end of the transfer tube is disposed toward the upper part of the microwave plasma reactor to cause the exhaust gas to flow upward, while the end of the induction tube penetrates from the upper part to the lower part of the microwave plasma reactor, The direction can be made to be downward. The pipe end portion of the transfer pipe and the pipe end portion of the induction pipe may be arranged on the same axis line to improve the contact between the down stream reducing agent and the flame and the upward flow exhaust gas. In order to be selectable, the supply pipe may be penetrated downward from the upper part of the microwave plasma reactor to supply the reducing agent downward, or may be joined to the induction pipe and guided into the microwave plasma reactor through the induction pipe.
The features and advantages of the present invention will become more apparent from the following detailed description based on the accompanying drawings.
Prior to that, terms and words used in the present specification and claims should not be construed in a conventional and dictionary sense, and the inventor may properly define the concept of the term in order to best explain its invention It should be construed as meaning and concept consistent with the technical idea of the present invention.
As described above, according to the present invention, abatement facilities for treating harmful exhaust substances such as organic substances or particulate matter, sulfur oxides, and nitrogen oxides contained in exhaust gas are arranged in line in an in-line form And to reduce it collectively.
The present invention can remarkably reduce the amount of the reducing agent used and improve the denitration rate through the low temperature plasma reactor and the high temperature microwave plasma reactor.
In particular, the present invention uses a high-temperature plasma flame as a heat source for a microwave plasma reactor, so that the denitration process can be continuously performed without stopping the operation of the denitration system according to the replacement of the igniter or the like required for flame generation in the prior art.
1 is a schematic process diagram of an exhaust gas treating apparatus according to a first embodiment of the present invention.
2 is a schematic process diagram of an exhaust gas treating apparatus according to a second embodiment of the present invention.
3 is a longitudinal sectional view schematically showing the interior of a microwave plasma reactor to be employed in the exhaust gas treating apparatus of the present invention.
4 is a cross-sectional view of a microwave plasma reactor taken along the line AA in Fig.
BRIEF DESCRIPTION OF THE DRAWINGS The advantages, features, and ways of accomplishing the same will become apparent from the following description of embodiments taken in conjunction with the accompanying drawings. In the specification, the same reference numerals denote the same or similar components throughout the specification. In the following description, well-known functions or constructions are not described in detail since they would obscure the invention in unnecessary detail.
Now, an exhaust gas treating apparatus according to the present invention will be described in detail with reference to the accompanying drawings.
Figure 1 is the (
The exhaust
Here, the exhaust gas generating
The exhaust gas generated through the combustion of the exhaust gas generating
In the first embodiment of the present invention, the low temperature plasma reactor (200) is disposed at the rear end of the dust collecting apparatus (100). The low-
In addition, the exhaust gas that has escaped through the
The exhaust gas treatment apparatus according to the first embodiment of the present invention includes a
In particular, the exhaust gas treating apparatus according to the first embodiment of the present invention decomposes nitrogen oxides contained in the exhaust gas discharged from the exhaust
The
The
The present invention can force various reducing agents, such as ammonia or urea, into the
The
After the reaction as in formula (2), ammonia and cyanuric acid are produced. In order to realize such a thermal decomposition reaction, the
In other words, the
The products, ammonia and cyanuric acid, react with nitrogen oxides in denitrification equipment such as microwave plasma reactors. Is converted to a gaseous ammonia reducing agent through various reaction mechanisms so that the denitrification reaction of the nitrogen oxides takes place in the
As shown in Formula 3, ammonia is hydrolyzed in the
A cyano supplied from
Alternatively, the reducing agent contained in the reservoir (600) is preferably composed of a water-soluble (water-soluble) reducing agent. The water-soluble reducing agent has a hydroxyl group (OH < - & gt ; ) generated in a humidity as shown in Chemical Formula 4, so chemical bonding with other reactors can be easily performed. Specifically, the hydroxyl group, which is an anion, is rapidly combined with hydrogen (H + ) to be converted into water, and the contact reaction efficiency of the nitrogen oxide can be improved to reduce the residence time of the nitrogen oxide in the
The present invention is a reduction zone capable of simultaneously converting various kinds of reducing agents into gaseous and ammonia in a high temperature
It is noted that the
The
The
As is widely known, the plasma generating gas can be air, nitrogen, or combustion gas, but the present invention aims at reducing nitrogen oxides in a microwave plasma reactor. That is, in order to prevent nitrogen (N 2 ) from being converted into nitrogen monoxide in the air in the reactor, it is preferable to use steam, micro-injection water or an inert gas as the plasma generating gas.
As described above, since the
As described above, the exhaust gas and the gaseous reducing agent cause a denitration reaction through the chemical formula and the like already described in the microwave plasma reactor (400). After the nitrogen oxides are removed, the hot exhaust gas is vented to the
FIG. 2 is a schematic view showing a process flow of an exhaust gas treating apparatus according to a second embodiment of the present invention. The exhaust gas treating apparatus 1 'according to the second embodiment of the present invention includes: As another modification of the
The exhaust gas processing apparatus 1 'according to the second embodiment of the present invention is configured to exhaust the exhaust gas discharged from the exhaust
The exhaust gas generated through the combustion of the exhaust
The desulfurized exhaust gas is guided to a
In the second embodiment of the present invention, the low-temperature plasma reactor (200) is disposed at the rear end of the dust collecting apparatus (100). The low-
In addition, the exhaust gas that has escaped through the
The exhaust gas treatment apparatus according to the second embodiment of the present invention can reduce the nitrogen oxide contained in the exhaust gas discharged from the exhaust
The
The
The present invention can force various reducing agents, such as ammonia or urea, into the
The
After the reaction as in formula (2), ammonia and cyanuric acid are produced. In order to realize such a thermal decomposition reaction, the
In other words, the
The products, ammonia and cyanuric acid, react with nitrogen oxides in denitrification equipment such as microwave plasma reactors. Is converted to a gaseous ammonia reducing agent through various reaction mechanisms so that the denitrification reaction of the nitrogen oxides takes place in the
Ammonia is hydrolyzed in the
A cyano supplied from
Alternatively, the reducing agent contained in the reservoir (600) is preferably composed of a water-soluble (water-soluble) reducing agent. The water-soluble reducing agent has a hydroxyl group (OH < - & gt ; ) generated in a humidity as shown in Chemical Formula 4, so chemical bonding with other reactors can be easily performed. Specifically, the hydroxyl group, which is an anion, is rapidly combined with hydrogen (H + ) to be converted into water, and the contact reaction efficiency of the nitrogen oxide can be improved to reduce the residence time of the nitrogen oxide in the
The present invention is a reduction zone capable of simultaneously converting various kinds of reducing agents into gaseous and ammonia in a high temperature
It is noted that the
The
The
As is widely known, the plasma generating gas can be air, nitrogen, or combustion gas, but the present invention aims at reducing nitrogen oxides in a microwave plasma reactor. That is, in order to prevent nitrogen (N 2 ) from being converted into nitrogen monoxide in the air in the reactor, it is preferable to use steam, micro-injection water or an inert gas as the plasma generating gas.
As described above, since the
As described above, the exhaust gas and the gaseous reducing agent cause a denitration reaction through the chemical formula and the like already described in the microwave plasma reactor (400). After the nitrogen oxides are removed, the hot exhaust gas is vented to the
FIG. 3 is a longitudinal sectional view schematically showing the inside of the microwave plasma reactor shown in FIG. 1 or FIG. 2, and FIG. 4 is a cross-sectional view of the microwave plasma reactor shown in FIG.
As shown, the
The reducing agent supply pipe T2 extending in the
In addition, the
In the present invention, the
In the present invention, a tube end portion of an exhaust gas transfer tube (T1) opened upward and a tube end portion of an induction tube (T3) injectable downwardly are arranged in the same direction along the longitudinal direction of the reactor so as to double the direct contact between the reducing agent and the exhaust gas So as to be disposed on the axis line.
Optionally, the
In the exhaust gas treating apparatus according to the present invention, nitrogen oxide can be reduced to a low level of nitrogen monoxide and nitrogen dioxide while continuously passing through the oxidizing region of the low
In addition, the exhaust gas treatment apparatus according to the present invention can reduce the amount of sulfur oxides discharged by means of the
While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. It will be apparent to those skilled in the art that various modifications and variations can be made in the present invention. It is evident that the person skilled in the art can change or improve it.
It will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention as defined by the appended claims.
100 ----- Dust collection facility,
200 ----- low temperature plasma reactor,
300 ----- Desulfurization equipment,
400 ----- Microwave Plasma Reactor
500 ----- Chimney,
600 ----- Storage tank,
700 ----- Improved supply module,
800 ---- Microwave generator,
900 ----- Plasma generator,
1000 ----- Source of exhaust gas.
Claims (10)
A dust collecting apparatus 100 disposed downstream of the exhaust gas generating source 1000;
A low temperature plasma reactor (200) disposed downstream of the dust collecting apparatus (100) for oxidizing nitrogen monoxide (NO) emitted from the exhaust gas generating source (1000) to nitrogen dioxide (NO 2 );
A desulfurization facility 300 disposed downstream of the low temperature plasma reactor 200;
A storage tank 600 for storing the reducing agent;
The exhaust gas containing nitrogen oxide discharged from the desulfurization facility 300 is supplied to the transfer pipe T 1 and the reducing agent supplied to the supply pipe T 2 of the storage tank 600 is converted into a high temperature gas phase, A microwave plasma reactor (400) for assisting dissociation of the substrate;
A microwave generator 800 generating a microwave according to application of a power source; And
A microwave plasma generator 400 disposed between the microwave generator 800 and the microwave plasma reactor 400 for generating a flame by guiding the microwave into the microwave plasma reactor 400 through an induction tube T3, (900). ≪ / RTI >
The dust collecting apparatus (100) comprises an electrostatic precipitator.
Wherein the desulfurization facility (300) comprises a wet desulfurization system.
Wherein the supply pipe (T2) of the storage tank (600) further comprises an improved supply module (700).
The end of the transfer tube T 1 is installed upward in the microwave plasma reactor 400,
The induction tube T3 is penetrated downward from the upper part of the microwave plasma reactor 400,
And the supply pipe (T2) joins the induction pipe (T3) to guide the reducing agent to the microwave plasma reactor (400) downward.
A desulfurization facility 300 disposed downstream of the exhaust gas generating source 1000;
A dust collection facility 100 disposed downstream of the desulfurization facility 300;
A low temperature plasma reactor (200) disposed downstream of the dust collecting apparatus (100) for oxidizing nitrogen monoxide (NO) emitted from the exhaust gas generating source (1000) to nitrogen dioxide (NO 2 );
A storage tank 600 for storing the reducing agent;
The exhaust gas containing nitrogen oxide discharged from the low temperature plasma reactor 200 is supplied to the transfer tube T 1 and the reducing agent supplied to the supply tube T 2 of the storage tank 600 is converted into a high temperature gas phase, A microwave plasma reactor (400) for assisting dissociation of the oxide;
A microwave generator 800 generating a microwave according to application of a power source; And
A microwave plasma generator 400 disposed between the microwave generator 800 and the microwave plasma reactor 400 for generating a flame by guiding the microwave into the microwave plasma reactor 400 through an induction tube T3, (900). ≪ / RTI >
The dust collecting apparatus (100) comprises an electrostatic precipitator.
The desulfurization facility (300) comprises a dry desulfurization system.
Wherein the supply pipe (T2) of the storage tank (600) further comprises an improved supply module (700).
The end of the transfer tube T 1 is installed upward in the microwave plasma reactor 400,
The induction tube T3 is penetrated downward from the upper part of the microwave plasma reactor 400,
And the supply pipe (T2) joins the induction pipe (T3) to guide the reducing agent to the microwave plasma reactor (400) downward.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020150084945A KR101567746B1 (en) | 2015-06-16 | 2015-06-16 | Apparatus for treating exhaust gas |
CN201680035416.4A CN108064187A (en) | 2015-06-16 | 2016-06-15 | Emission-control equipment |
PCT/KR2016/006368 WO2016204516A1 (en) | 2015-06-16 | 2016-06-15 | Exhaust gas processing device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020150084945A KR101567746B1 (en) | 2015-06-16 | 2015-06-16 | Apparatus for treating exhaust gas |
Publications (1)
Publication Number | Publication Date |
---|---|
KR101567746B1 true KR101567746B1 (en) | 2015-11-09 |
Family
ID=54605194
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020150084945A KR101567746B1 (en) | 2015-06-16 | 2015-06-16 | Apparatus for treating exhaust gas |
Country Status (3)
Country | Link |
---|---|
KR (1) | KR101567746B1 (en) |
CN (1) | CN108064187A (en) |
WO (1) | WO2016204516A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109499286A (en) * | 2018-12-28 | 2019-03-22 | 中科新天地(合肥)环保科技有限公司 | One kind administering vulcanization exhaust gas technique and device based on lower temperature plasma technology |
KR102237217B1 (en) * | 2020-12-01 | 2021-04-07 | 한국에너지기술연구원 | Decomposition accelerator composition for exhaust gas decomposition and exhaust gas treatment method using the same |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107583422A (en) * | 2017-10-23 | 2018-01-16 | 安徽金森源环保工程有限公司 | A kind of low-temperature plasma desulfuring and denitrifying apparatus and desulfurization denitration method |
CN111389190B (en) * | 2020-04-17 | 2024-02-09 | 大唐环境产业集团股份有限公司 | Plasma-based ship tail gas desulfurization and denitrification system and method |
CN114471066A (en) * | 2020-10-23 | 2022-05-13 | 陕西青朗万城环保科技有限公司 | Microwave denitration method and control system thereof |
GB2600691A (en) * | 2020-11-02 | 2022-05-11 | Edwards Ltd | Plasma abatement |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001070749A (en) | 1999-09-09 | 2001-03-21 | Babcock Hitachi Kk | Waste gas treatment system |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100213812B1 (en) * | 1997-03-08 | 1999-08-02 | 박운서 | Removal method of sulfur and nitrogen with low temperature plasma reactor |
KR200207679Y1 (en) * | 2000-08-08 | 2000-12-15 | 한국중공업주식회사 | Combined Equipment with Plasma Reactor for Treatment of Hazardous Gas and Electrostatic Precipitator for Collection of Fly-ash and Byproducts |
KR100473335B1 (en) * | 2001-10-17 | 2005-03-07 | 한국전력공사 | The Selective Removal of Elemental Hg from Gas Mixture by Plasma |
JP2004330001A (en) * | 2003-04-30 | 2004-11-25 | Nittetsu Mining Co Ltd | Method and apparatus for treating nitrogen oxide-containing gas |
US7368094B2 (en) * | 2004-09-23 | 2008-05-06 | General Motors Corporation | Plasma-assisted NOx reduction |
JP3937356B1 (en) * | 2006-03-29 | 2007-06-27 | 株式会社日立プラントテクノロジー | Exhaust gas treatment method and equipment |
CN103961987B (en) * | 2014-05-16 | 2015-12-09 | 电子科技大学 | A kind of oxynitrides based on microwave plasma removes device |
CN104437040B (en) * | 2014-12-16 | 2017-01-04 | 江苏国苏检测有限公司 | Removal of nitrogen oxide device based on dielectric barrier discharge reactor and removal methods thereof |
-
2015
- 2015-06-16 KR KR1020150084945A patent/KR101567746B1/en active IP Right Grant
-
2016
- 2016-06-15 WO PCT/KR2016/006368 patent/WO2016204516A1/en active Application Filing
- 2016-06-15 CN CN201680035416.4A patent/CN108064187A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001070749A (en) | 1999-09-09 | 2001-03-21 | Babcock Hitachi Kk | Waste gas treatment system |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109499286A (en) * | 2018-12-28 | 2019-03-22 | 中科新天地(合肥)环保科技有限公司 | One kind administering vulcanization exhaust gas technique and device based on lower temperature plasma technology |
KR102237217B1 (en) * | 2020-12-01 | 2021-04-07 | 한국에너지기술연구원 | Decomposition accelerator composition for exhaust gas decomposition and exhaust gas treatment method using the same |
Also Published As
Publication number | Publication date |
---|---|
WO2016204516A1 (en) | 2016-12-22 |
CN108064187A (en) | 2018-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR101567746B1 (en) | Apparatus for treating exhaust gas | |
KR101902331B1 (en) | NOx reduction system using microwave plasma based on Selective Non-Catalytic Reduction | |
US9114357B2 (en) | Treatment of nitrogen oxides in flue gas streams | |
US20140165888A1 (en) | SIMULTANEOUS TREATMENT OF FLUE GAS WITH SOx ABSORBENT REAGENT AND NOx REDUCING AGENT | |
CN102500206A (en) | System and method for desulfurizing and denitrating smoke based on action of hydrogen peroxide | |
CN102459833A (en) | Combustion flue gas nox treatment | |
CN103463978A (en) | Device and method for smoke simultaneous desulfurization and denitrification based on hydrogen peroxide catalytic oxidation | |
GB2446045A (en) | Reducing NOx emissions in industrial combustion systems | |
CN102355934A (en) | Combined waste gas treatment of waste gas streams containing ammonia and nitrogen oxides in industrial plants | |
CN110711470A (en) | Desulfurization and denitrification purification process for incineration flue gas of biomass boiler | |
CN102371113A (en) | Flue gas purifying treatment method and system | |
KR20170075514A (en) | System for denitrification using plasma and method for denitrification u sing plasma | |
KR101591229B1 (en) | NOx reduction system using microwave plasma based on selective catalytic reduction | |
CN112955243A (en) | Integrated waste gas treatment device using metal filter | |
KR101311834B1 (en) | The disposal system of perfluorinated compounds | |
CN211302635U (en) | Biomass boiler burns flue gas desulfurization denitration clean system | |
CN109260919A (en) | The integration desulfurization denitration device and its desulfurization denitration method of ozone combination urea | |
KR101567745B1 (en) | NOx reduction system using microwave plasma | |
KR101606257B1 (en) | Apparatus and Method for Denitrifying and Desulfurizing Exhaust Gas using Fluidized Bed | |
JP5640120B1 (en) | Simultaneous reduction method of nitrogen oxide and nitrous oxide by multistage reaction in fluidized bed combustion furnace | |
KR102474846B1 (en) | Sncr-based plasma nitrogen oxide reduction device for ships | |
KR100437875B1 (en) | NOx reduction system by selective catalytic reduction available for urea as reducing agent | |
KR100681161B1 (en) | Apparatus for removing nitrogen oxides using peroxy radical and method thereof | |
CN100434142C (en) | Process for realizing medium temperature dry-method direct denitration of flue gas by using ethanol | |
KR102122253B1 (en) | Apparatus for treating exhaust gas |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20191105 Year of fee payment: 5 |