CN110180602A - Low-temperature denitration catalyst and preparation method thereof - Google Patents

Low-temperature denitration catalyst and preparation method thereof Download PDF

Info

Publication number
CN110180602A
CN110180602A CN201910567194.6A CN201910567194A CN110180602A CN 110180602 A CN110180602 A CN 110180602A CN 201910567194 A CN201910567194 A CN 201910567194A CN 110180602 A CN110180602 A CN 110180602A
Authority
CN
China
Prior art keywords
low
catalyst
temperature denitration
added
molybdenum
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
CN201910567194.6A
Other languages
Chinese (zh)
Inventor
杨银春
郝新宇
曹成松
陈广忠
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.)
High Chemical (jiangsu) Chemical New Material Co Ltd
Original Assignee
High Chemical (jiangsu) Chemical New Material 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 High Chemical (jiangsu) Chemical New Material Co Ltd filed Critical High Chemical (jiangsu) Chemical New Material Co Ltd
Priority to CN201910567194.6A priority Critical patent/CN110180602A/en
Publication of CN110180602A publication Critical patent/CN110180602A/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
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/002Mixed oxides other than spinels, e.g. perovskite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/24Chromium, molybdenum or tungsten
    • B01J23/28Molybdenum
    • 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
    • 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
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2523/00Constitutive chemical elements of heterogeneous catalysts

Landscapes

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

Abstract

The invention discloses a kind of low-temperature denitration catalyst, including carrier and active material, for the carrier by mangaic acid praseodymium and titanium dioxide, active material is neodymia, molybdenum oxide and yttrium oxide.Low-temperature denitration catalyst of the invention has good NOxConversion temperature, to NOxThere are lower initiation temperature and catalytic performance, also there is excellent water resistant heat aging performance;Mangaic acid praseodymium and titanium dioxide collaboration of the present invention is used as catalyst carrier, greatly improves the specific surface area and Kong Rong of carrier, makes it have more active adsorption sites, is conducive to the desulphurization denitration performance for improving catalyst;Neodymia, molybdenum oxide and yttrium oxide collaboration are used as active material, improve to NH3Chemical adsorption capacity extend the service life of low-temperature denitration catalyst to improve catalyst activity.

Description

Low-temperature denitration catalyst and preparation method thereof
Technical field
The present invention relates to a kind of catalyst technical fields, more particularly to a kind of low-temperature denitration catalyst and its preparation side Method.
Background technique
Nitrogen oxides (NOX) it is one of main atmosphere pollution, including NO, NO2Etc. a variety of nitrogen oxides, to human body Health and animals and plants existence can all cause certain injury, such as form acid rain, photochemical fog, but also can generate a variety of two Secondary pollution.Nitrogen oxides be generate ozone one of important as precursors object and forming region fine particles pollution and haze it is important Reason, so that the developed areas such as China's Delta of the Pearl River atmospheric visibility be made to decline increasingly, haze number of days is continuously increased.? Environmental consciousness and require more more and more intense today, how to remove the discharge of nitrogen oxides, becomes more and more urgent problem.
Be directed to exhaust gas from diesel vehicle denitration technology maturation the most at present is SCR denitration technology.Traditional SCR technology is will to contain Ammonia additive (such as ammonia, urea) sprays into about 300~420 DEG C of temperature of flue gas, under the effect of the catalyst, adds containing ammonia Add agent to react with NOx, generates N2And H2O.Traditional SCR method is a kind of higher method of conversion rate of NOx, up to 60%- 90%.But the problem of traditional SCR technology, essentially consists in: (1) additive containing ammonia under the high temperature conditions with O2It burns, or with Sulfur oxide reaction generates more particulate matters, if host uses high sulphur content diesel oil, SCR has to be generated during catalyst reduction Ammonium sulfate blocking danger.(2) SCR denitration used at present is mainly with vanadium titanium-based (V2O5/TiO2) based on, it is living Property group is divided into vanadic anhydride, and carrier is titanium dioxide.Although the denitration activity of catalytic component based on vanadium and resisting sulfur dioxide Ability is very high, but it must be just active under very high temperature (300-400 DEG C), and belonging to additionally, due to vanadic anhydride has Noxious material is highly soluble in water, in this way polluted underground water and soil etc. in order to prevent, discarded catalyst cannot at will fill or Air storage.(3) unobvious for the denitration effect of low temperature diesel oil.
Summary of the invention
In view of the above shortcomings, it is an object of the invention to develop a low-temperature denitration catalyst, there is high activity, low The advantages that poison, good hydrothermal stability, and the NOx removal activity with higher in low temperature environment.
Technical solution of the present invention is summarized as follows:
A kind of low-temperature denitration catalyst, wherein including carrier and active material, the carrier is by mangaic acid praseodymium and titanium dioxide Titanium, the active material are neodymia, molybdenum oxide and yttrium oxide.
Preferably, the low-temperature denitration catalyst, wherein the catalyst further includes lubricant, binder, plasticizing Agent, anti-wear agent and surfactant.
Preferably, the low-temperature denitration catalyst, wherein by weight, the catalyst includes following weight The material of part:
Preferably, the low-temperature denitration catalyst, wherein the lubricant includes the molybdenum disulfide of 55~60wt% With the cobalt dioxide of 40~45wt%.
Preferably, the low-temperature denitration catalyst, wherein the binder includes the manganese dioxide of 76~80wt% With the bentonite of 20~24wt%.
Preferably, the low-temperature denitration catalyst, wherein the plasticiser includes the epoxidation four of 60~65wt% The decanedioic acid two (two-ethylhexyls) of hydrogen diisooctyl phthalate and 35~40wt%.
Preferably, the low-temperature denitration catalyst, wherein the anti-wear agent includes 40~50wt% titanium carbide and 50 ~60wt% tetrapropanate fluorine rubber powder.
Preferably, the low-temperature denitration catalyst, wherein the surfactant includes 40~50wt% octadecane Base sodium sulphate and 50~60wt% monostearate sorb are smooth.
Preferably, the low-temperature denitration catalyst, wherein further include 12~16 parts of stannous chloride.
A kind of preparation method of low-temperature denitration catalyst, wherein the following steps are included:
1) mangaic acid praseodymium and titanium dioxide are taken, in 70~75 DEG C of 6~8h of vacuum oven, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in, continues 2~3h of stirring;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500~550 DEG C, is obtained in corresponding oxide active The heart: neodymia, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 18~20h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
The beneficial effects of the present invention are:
(1) low-temperature denitration catalyst of the invention has good NOxConversion temperature, to NOxThere is lower initiation temperature And catalytic performance, also there is excellent water resistant heat aging performance.
(2) mangaic acid praseodymium and titanium dioxide collaboration of the present invention is used as catalyst carrier, greatly improves the specific surface of carrier Long-pending and Kong Rong, makes it have more active adsorption sites, is conducive to the desulphurization denitration performance for improving catalyst;Neodymia, oxygen Change molybdenum and yttrium oxide collaboration is used as active material, improves to NH3Chemical adsorption capacity extend to improve catalyst activity The service life of low-temperature denitration catalyst.
Specific embodiment
The present invention will be further described in detail below with reference to the embodiments, to enable those skilled in the art referring to specification Text can be implemented accordingly.
This case proposes a kind of low-temperature denitration catalyst, wherein including carrier and active material, carrier is by mangaic acid praseodymium and dioxy Change titanium, active material is neodymia, molybdenum oxide and yttrium oxide.
Titanium dioxide is carrier, specific surface area, suitable pore structure and water absorption rate with higher, is had stronger mechanical strong Degree and stability, heat resistance, acid resistance are good, and mangaic acid praseodymium and titanium dioxide synergistic effect greatly improve the ratio table of carrier Area and Kong Rong make it have more active adsorption sites, are conducive to the desulphurization denitration performance for improving catalyst.Neodymia, Molybdenum oxide and yttrium oxide collaboration are used as active material, and the effect of neodymia is under the action of reducing agent NH3, by NO and NO2Also It originally is N2, wherein molybdenum oxide helps to improve the fast reaction step of neodymia, and improves the selectivity of neodymia, and yttrium oxide has Help improve to NH for (150 DEG C~280 DEG C) at low temperature3Chemical adsorption capacity, to improve catalyst activity, and can reduce SO2/SO3Conversion ratio, extend the service life of low-temperature denitration catalyst.
As the another embodiment of this case, wherein catalyst further includes lubricant, binder, plasticiser, anti-wear agent and surface Activating agent.
As the another embodiment of this case, wherein by weight, catalyst includes the material of following parts by weight:
As the another embodiment of this case, wherein lubricant includes the molybdenum disulfide and 40~45wt% of 55~60wt% Cobalt dioxide.Lubricant and polymer have good compatibility, its cohesion between polymeric inner plays and reduces polymer molecule The effect of power, so as to improve the internal frictional heat generation of melt and the mobility of melt.The preferred lubricant of this case be molybdenum disulfide and Cobalt dioxide.
As the another embodiment of this case, wherein binder includes the manganese dioxide and 20~24wt% of 76~80wt% Bentonite.Binder improves the adhesion strength of polymer and catalyst, improves burst temperature when its drying, and resistance to compression can be improved Intensity, the preferred binder of this case are that manganese dioxide and bentonite act synergistically.
As the another embodiment of this case, wherein plasticiser includes the epoxidation tetrahydrophthalic acid two of 60~65wt% The decanedioic acid two (two-ethylhexyls) of isodecyl ester and 35~40wt%.Epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems two Sour two (two-ethylhexyls) synergistic effect, improves the flexility for being kneaded product, reduces hardness.
As the another embodiment of this case, wherein anti-wear agent includes 4 third fluorine of 40~50wt% titanium carbide and 50~60wt% Rubber powder.Anti-wear agent improves the hydrothermal stability and wear-resisting property of catalyst, to improve its service life, this case is preferably resistance to Grinding agent is titanium carbide and tetrapropanate fluorine rubber powder.
As the another embodiment of this case, wherein surfactant include 40~50wt% sodium stearyl sulfate and 50~ 60wt% monostearate sorb is smooth.Due to having wetting, emulsification, this case is mentioned surfactant by the way that surfactant is added The compatibility performance of high polymer and solid.
As the another embodiment of this case, wherein further include 12~16 parts of stannous chloride.By the way that stannous chloride is added, keep away Exempt from the situation that the ammonium sulfate that additive containing ammonia generates in reduction process is easy blocking pipeline, so that denitrification rate is higher, pipeline More easy cleaning.
A kind of preparation method of low-temperature denitration catalyst, wherein the following steps are included:
1) mangaic acid praseodymium and titanium dioxide are taken, in 70~75 DEG C of 6~8h of vacuum oven, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in, continues 2~3h of stirring;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500~550 DEG C, is obtained in corresponding oxide active The heart: neodymia, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 18~20h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Specific embodiment and comparative example is listed below:
Embodiment 1:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide, further includes lubricant, binder, plasticiser, anti-wear agent and surfactant.
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 55wt% and the cobalt dioxide of 45wt%;Binder includes the titanium dioxide of 76wt% The bentonite of manganese and 24wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 40wt% of 60wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 40wt% titanium carbide and 60wt% tetrapropanate fluorine rubber powder;Surfactant includes 40~50wt% sodium stearyl sulfate and 50~60wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 70 DEG C of vacuum oven 6h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in continues to stir 2h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 18h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Embodiment 2:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide, further includes lubricant, binder, plasticiser, anti-wear agent and surfactant;
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 58wt% and the cobalt dioxide of 42wt%;Binder includes the titanium dioxide of 78wt% The bentonite of manganese and 22wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 37wt% of 63wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 45wt% titanium carbide and 55wt% tetrapropanate fluorine rubber powder;Surfactant includes 46wt% sodium stearyl sulfate and 54wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 72 DEG C of vacuum oven 7h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in continues to stir 2.5h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 19h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Embodiment 3:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide;It further include lubricant, binder, plasticiser, anti-wear agent and surfactant;
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 60wt% and the cobalt dioxide of 40wt%;Binder includes the titanium dioxide of 80wt% The bentonite of manganese and 20wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 35wt% of 65wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 50wt% titanium carbide and 50 tetrapropanate fluorine rubber powder;Surfactant includes 50wt% sodium stearyl sulfate and 50wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 75 DEG C of vacuum oven 8h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in continues to stir 3h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 550 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 20h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Comparative example 1:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier are titanium dioxide, and the active material is oxygen Change neodymium, molybdenum oxide and yttrium oxide, further includes lubricant, binder, plasticiser, anti-wear agent and surfactant.
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 55wt% and the cobalt dioxide of 45wt%;Binder includes the titanium dioxide of 76wt% The bentonite of manganese and 24wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 40wt% of 60wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 40wt% titanium carbide and 60wt% tetrapropanate fluorine rubber powder;Surfactant includes 40~50wt% sodium stearyl sulfate and 50~60wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) titanium dioxide is taken, in 70 DEG C of vacuum oven 6h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) titanium dioxide pre-processed in continues to stir 2h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 18h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Comparative example 2:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia and yttrium oxide, further includes lubricant, binder, plasticiser, anti-wear agent and surfactant.
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 55wt% and the cobalt dioxide of 45wt%;Binder includes the titanium dioxide of 76wt% The bentonite of manganese and 24wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 40wt% of 60wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 40wt% titanium carbide and 60wt% tetrapropanate fluorine rubber powder;Surfactant includes 40~50wt% sodium stearyl sulfate and 50~60wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 70 DEG C of vacuum oven 6h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the yttrium oxide ingredient in catalyst is provided by yttrium nitrate; The aequum for calculating various raw materials, weighs raw material according to quantity, and neodymium nitrate is added in deionized water, is stirred evenly, and nitric acid is added Yttrium continues to stir evenly, and the mangaic acid praseodymium and titanium dioxide pre-processed in 1) is added, and continues to stir 2h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500 DEG C, obtains corresponding oxide active center: oxidation Neodymium and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 18h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Comparative example 3:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide, further includes lubricant, binder, plasticiser, anti-wear agent and surfactant;
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 58wt% and the cobalt dioxide of 42wt%;Binder includes the titanium dioxide of 78wt% The bentonite of manganese and 22wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 37wt% of 63wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 45wt% titanium carbide and 55wt% tetrapropanate fluorine rubber powder;Surfactant includes 46wt% sodium stearyl sulfate and 54wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 72 DEG C of vacuum oven 7h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum; The aequum for calculating various raw materials, weighs raw material according to quantity, and neodymium nitrate is added in deionized water, stirs evenly, is then added Nitric acid molybdenum, stirs evenly, and the mangaic acid praseodymium and titanium dioxide pre-processed in 1) is added, and continues to stir 2.5h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 19h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Comparative example 4:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide, further includes lubricant, binder, plasticiser, anti-wear agent and surfactant;
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 58wt% and the cobalt dioxide of 42wt%;Binder is bentonite;Plasticiser packet Include the epoxidation diisodecyl tetrahydrophthalate of 63wt% and the decanedioic acid two (two-ethylhexyls) of 37wt%;Anti-wear agent Including 45wt% titanium carbide and 55wt% tetrapropanate fluorine rubber powder;Surfactant include 46wt% sodium stearyl sulfate and 54wt% monostearate sorb is smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 72 DEG C of vacuum oven 7h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in continues to stir 2.5h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, molybdenum disulfide, cobalt dioxide, bentonite, epoxidation tetrahydrophthalic acid are successively added Diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, monostearate mountain Pears are smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 19h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Comparative example 5:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide;It further include lubricant, binder, plasticiser, anti-wear agent and surfactant;
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 60wt% and the cobalt dioxide of 40wt%;Binder includes the titanium dioxide of 80wt% The bentonite of manganese and 20wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 35wt% of 65wt% Diacid two (two-ethylhexyls);Anti-wear agent is tetrapropanate fluorine rubber powder;Surfactant include 50wt% sodium stearyl sulfate and 50wt% monostearate sorb is smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 75 DEG C of vacuum oven 8h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in continues to stir 3h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 550 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), tetrapropanate fluorine rubber powder, sodium stearyl sulfate, monostearate mountain Pears are smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 20h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Comparative example 6:
A kind of low-temperature denitration catalyst, including carrier and active material, carrier is by mangaic acid praseodymium and titanium dioxide, the activity Substance is neodymia, molybdenum oxide and yttrium oxide;It further include lubricant, binder, plasticiser, anti-wear agent and surfactant;
Catalyst includes the material of following parts by weight:
Lubricant includes the molybdenum disulfide of 60wt% and the cobalt dioxide of 40wt%;Binder includes the titanium dioxide of 80wt% The bentonite of manganese and 20wt%;Plasticiser includes epoxidation diisodecyl tetrahydrophthalate and the last of the ten Heavenly stems of 35wt% of 65wt% Diacid two (two-ethylhexyls);Anti-wear agent includes 50wt% titanium carbide and 50 tetrapropanate fluorine rubber powder;Surfactant includes 50wt% sodium stearyl sulfate and 50wt% monostearate sorb are smooth.
A kind of preparation method of low-temperature denitration catalyst, comprising the following steps:
1) mangaic acid praseodymium and titanium dioxide are taken, in 75 DEG C of vacuum oven 8h, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, Yttrium oxide ingredient in catalyst is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, by neodymium nitrate It is added in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added 1) the mangaic acid praseodymium and titanium dioxide pre-processed in continues to stir 3h;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 550 DEG C, obtains corresponding oxide active center: oxidation Neodymium, molybdenum oxide and yttrium oxide;
4) into said components, it is adjacent that molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro are successively added Phthalic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, list Stearic acid sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 20h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
Above embodiments 1-3 and traditional SCR catalyst comparative example are subjected to active evaluation test.Experimental condition is as follows:
Gas volume composition: nitric oxide: 500ppm, ammonia: 500ppm, carbon dioxide: 5%, vapor: 4.5%, oxygen Gas: 14%, nitrogen: Balance Air;Air speed: 40000h-1
Activity evaluation such as table 1:
Table 1:
Denitrating catalyst of the invention has good NOxConversion temperature, Examples 1 to 3 are real compared with comparative example 1~6 Catalyst in example 1~3 is applied to all have to NOxLower initiation temperature and catalytic performance.And low temperature diesel oil denitration of the invention After weathering, performance decline is not obvious catalyst, therefore catalyst of the present invention has good water resistant heat aging performance.
Although the embodiments of the present invention have been disclosed as above, but its is not only in the description and the implementation listed With it can be fully applied to various fields suitable for the present invention, for those skilled in the art, can be easily Realize other modification, therefore without departing from the general concept defined in the claims and the equivalent scope, the present invention is simultaneously unlimited In specific details.

Claims (10)

1. a kind of low-temperature denitration catalyst, which is characterized in that including carrier and active material, the carrier is by mangaic acid praseodymium and dioxy Change titanium, the active material is neodymia, molybdenum oxide and yttrium oxide.
2. low-temperature denitration catalyst according to claim 1, which is characterized in that the catalyst further includes lubricant, glues Tie agent, plasticiser, anti-wear agent and surfactant.
3. according to claim 1 or 2 described in any item low-temperature denitration catalysts, which is characterized in that by weight, described to urge Agent includes the material of following parts by weight:
4. low-temperature denitration catalyst according to claim 3, which is characterized in that the lubricant includes 55~60wt%'s The cobalt dioxide of molybdenum disulfide and 40~45wt%.
5. low-temperature denitration catalyst according to claim 3, which is characterized in that the binder includes 76~80wt%'s The bentonite of manganese dioxide and 20~24wt%.
6. low-temperature denitration catalyst according to claim 3, which is characterized in that the plasticiser includes 60~65wt%'s The decanedioic acid two (two-ethylhexyls) of epoxidation diisodecyl tetrahydrophthalate and 35~40wt%.
7. low-temperature denitration catalyst according to claim 3, which is characterized in that the anti-wear agent includes 40~50wt% carbon Change titanium and 50~60wt% tetrapropanate fluorine rubber powder.
8. low-temperature denitration catalyst according to claim 3, which is characterized in that the surfactant include 40~ 50wt% sodium stearyl sulfate and 50~60wt% monostearate sorb are smooth.
9. low-temperature denitration catalyst according to claim 3, which is characterized in that further include 12~16 parts of stannous chloride.
10. the preparation method of described in any item low-temperature denitration catalysts according to claim 1~3, which is characterized in that including with Lower step:
1) mangaic acid praseodymium and titanium dioxide are taken, in 70~75 DEG C of 6~8h of vacuum oven, is cooled to room temperature;
2) the neodymia ingredient in catalyst is provided by neodymium nitrate, and the molybdenum oxide ingredient in catalyst is provided by nitric acid molybdenum, catalysis Yttrium oxide ingredient in agent is provided by yttrium nitrate;The aequum for calculating various raw materials, weighs raw material according to quantity, and neodymium nitrate is added It in deionized water, stirs evenly, nitric acid molybdenum is then added, stirs evenly, yttrium nitrate is added, continues to stir evenly, be added in 1) The mangaic acid praseodymium and titanium dioxide pre-processed, continues 2~3h of stirring;
3) by the said goods, it is put into Muffle furnace, calcines 5h at 500~550 DEG C, obtains corresponding oxide active center: oxygen Change neodymium, molybdenum oxide and yttrium oxide;
4) into said components, molybdenum disulfide, cobalt dioxide, manganese dioxide, bentonite, epoxidation tetrahydro neighbour benzene two are successively added Formic acid diisodecyl ester, decanedioic acid two (two-ethylhexyls), titanium carbide, tetrapropanate fluorine rubber powder, sodium stearyl sulfate, single tristearin Sour sorb is smooth to be kneaded, and material is kneaded uniform;
5) it will be kneaded the material come out, after curing 18~20h, is added in filtering pre-extruded and squeezes out, be filtered to remove material
6) it by the material after filtering pre-extruded, is formed by mold integral extrusion, and be dried;
7) the said goods are immersed in stannous chloride aqueous solution, after impregnating 8h under room temperature, is dried;
8) according to the length of regulation, above-mentioned finished product is cut, and carries out front end hardened artiwear processing;
9) product is packed.
CN201910567194.6A 2019-06-27 2019-06-27 Low-temperature denitration catalyst and preparation method thereof Pending CN110180602A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910567194.6A CN110180602A (en) 2019-06-27 2019-06-27 Low-temperature denitration catalyst and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910567194.6A CN110180602A (en) 2019-06-27 2019-06-27 Low-temperature denitration catalyst and preparation method thereof

Publications (1)

Publication Number Publication Date
CN110180602A true CN110180602A (en) 2019-08-30

Family

ID=67723725

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910567194.6A Pending CN110180602A (en) 2019-06-27 2019-06-27 Low-temperature denitration catalyst and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110180602A (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101560900A (en) * 2008-04-16 2009-10-21 北京有色金属研究总院 Vehicle exhaust catalytic cleaner and cold start pollution control application
CN101658793A (en) * 2009-09-29 2010-03-03 浙江三龙催化剂有限公司 Titania-based catalytic agent in coal steam-electric plant smoke SCR denitration and preparation method thereof
US20100222205A1 (en) * 2009-02-27 2010-09-02 Steven Bolaji Ogunwumi Method Of Manufacturing A Catalyst Body By Post-Impregation
CN103381362A (en) * 2013-07-22 2013-11-06 哈尔滨工业大学 Low-temperature manganese-based denitration catalyst and preparing method thereof
CN103433028A (en) * 2013-08-16 2013-12-11 南京工业大学 Three-way NOx, CO and HC removing catalyst used in marine engine, and preparation method thereof
CN104492422A (en) * 2014-12-25 2015-04-08 宜兴国电精辉环保设备有限公司 Denitration catalyst for high-temperature smoke and preparation method of denitration catalyst
CN104785102A (en) * 2015-03-26 2015-07-22 东华工程科技股份有限公司 Energy-saving and efficient N2O and NOx removing process
CN104971771A (en) * 2015-07-10 2015-10-14 山东海润环保科技有限公司 Low-temperature diesel oil SCR denitration catalyst and preparation method thereof
CN106423139A (en) * 2016-11-14 2017-02-22 包头稀土研究院 Rare-earth-based SCR denitration catalyst and preparation method thereof

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101560900A (en) * 2008-04-16 2009-10-21 北京有色金属研究总院 Vehicle exhaust catalytic cleaner and cold start pollution control application
US20100222205A1 (en) * 2009-02-27 2010-09-02 Steven Bolaji Ogunwumi Method Of Manufacturing A Catalyst Body By Post-Impregation
CN101658793A (en) * 2009-09-29 2010-03-03 浙江三龙催化剂有限公司 Titania-based catalytic agent in coal steam-electric plant smoke SCR denitration and preparation method thereof
CN103381362A (en) * 2013-07-22 2013-11-06 哈尔滨工业大学 Low-temperature manganese-based denitration catalyst and preparing method thereof
CN103433028A (en) * 2013-08-16 2013-12-11 南京工业大学 Three-way NOx, CO and HC removing catalyst used in marine engine, and preparation method thereof
CN104492422A (en) * 2014-12-25 2015-04-08 宜兴国电精辉环保设备有限公司 Denitration catalyst for high-temperature smoke and preparation method of denitration catalyst
CN104785102A (en) * 2015-03-26 2015-07-22 东华工程科技股份有限公司 Energy-saving and efficient N2O and NOx removing process
CN104971771A (en) * 2015-07-10 2015-10-14 山东海润环保科技有限公司 Low-temperature diesel oil SCR denitration catalyst and preparation method thereof
CN106423139A (en) * 2016-11-14 2017-02-22 包头稀土研究院 Rare-earth-based SCR denitration catalyst and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ZHANG, SHIBO ET AL.,: ""Synergistic Mercury Removal over the CeMnO3 Perovskite Structure Oxide as a Selective Catalytic Reduction Catalyst from Coal Combustion Flue Gas"", 《ENERGY & FUELS》 *

Similar Documents

Publication Publication Date Title
US9802180B2 (en) Catalyst for synergistic control of oxynitride and mercury and method for preparing the same
CN101979140A (en) Metal loaded catalyst used for selective catalytic oxidation of ammonia, preparation method and application thereof
CN105833901B (en) A kind of PrOx-MnOx/ SAPO-34 low-temperature SCR catalyst for denitrating flue gas and the preparation method and application thereof
CN103769083B (en) A kind of NO_x Reduction by Effective composite oxide catalysts and its preparation method and application
CN102631921A (en) Nitric acid exhaust gas denitration catalyst and preparation method thereof
CN110385023B (en) Low-temperature flue gas denitration agent and preparation method and application thereof
CN106582874A (en) High temperature resistant phosphotungstic acid adsorbed iron-based oxide catalyst and preparation method thereof
CN101972652A (en) Preparation method of compound SCR catalyst with zero-valent mercury conversion function
CN108722432A (en) Low-temperature SCR catalyst and preparation method thereof in a kind of high activity
CN101554589A (en) Copper and iron modified titanium dioxide pillared bentonite catalyst and preparation method thereof
CN107413350A (en) Mischmetal denitrating catalyst and preparation method thereof
CN108671931A (en) A kind of method of modifying of the denitrating catalyst with anti-toxicity energy
JPH0714484B2 (en) Nitrogen oxide reduction catalyst
CN111420702A (en) High-activity water-resistant sulfur-resistant low-temperature SCR denitration catalyst and preparation method thereof
CN108236943A (en) A kind of preparation method of vanadium oxide catalyst
CN112844467B (en) Denitration catalyst and preparation method and application thereof
CN114192158A (en) Preparation method of CO and NOx synergistic removal catalyst
CN112023908B (en) Nitrogen oxide removing catalyst and preparation method thereof
CN108579731A (en) A kind of preparation method of low-temperature denitration carbon-supported catalysts
CN110180602A (en) Low-temperature denitration catalyst and preparation method thereof
CN107537514A (en) Ferromanganese cobalt monoblock type SCR low temperature catalysts preparation method, product and its application
CN108236944A (en) A kind of vanadium oxide catalyst and its application
CN110152659A (en) Denitration takes off VOC catalyst, preparation method, regeneration method
CN114471532A (en) Preparation method and application of flower-like samarium-manganese composite oxide denitration catalyst
CN109821547A (en) A kind of samarium ferrotitanium composite oxides object denitrating catalyst and preparation method thereof

Legal Events

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

Application publication date: 20190830