[go: up one dir, main page]

CN102921403A - Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst - Google Patents

Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst Download PDF

Info

Publication number
CN102921403A
CN102921403A CN2012103319819A CN201210331981A CN102921403A CN 102921403 A CN102921403 A CN 102921403A CN 2012103319819 A CN2012103319819 A CN 2012103319819A CN 201210331981 A CN201210331981 A CN 201210331981A CN 102921403 A CN102921403 A CN 102921403A
Authority
CN
China
Prior art keywords
tio
preparation
filter cake
concentration
maceration extract
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.)
Granted
Application number
CN2012103319819A
Other languages
Chinese (zh)
Other versions
CN102921403B (en
Inventor
陈建立
豆君
孙亮
邱巧锐
赵海娟
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.)
Longbai Group Co.,Ltd.
Original Assignee
HENAN BAILILIAN CHEMICAL 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 HENAN BAILILIAN CHEMICAL CO Ltd filed Critical HENAN BAILILIAN CHEMICAL CO Ltd
Priority to CN201210331981.9A priority Critical patent/CN102921403B/en
Publication of CN102921403A publication Critical patent/CN102921403A/en
Application granted granted Critical
Publication of CN102921403B publication Critical patent/CN102921403B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Inorganic Compounds Of Heavy Metals (AREA)
  • Catalysts (AREA)

Abstract

The invention discloses a V2O5-WO3/TiO2powder for making a denitration catalyst, which comprises the following steps of: 1) making metatitanic acid into pulp at a concentration of 280 to 320g/L based on TiO2, heating the pulp to 60 DEG C, regulating the pH value to 5.0 with caustic soda, regulating the pH value to 5.5 to 5.7 with ammonia water, and filtering the pulp by pressure and washing the filter cake by water; 2) preparing an impregnation solution; 3) making the filter cake made by the step 1) into pulp at a concentration of 280 to 320g/L based on TiO2, heating to 60 DEG C, adding the pulp into the impregnation solution obtained by the step 2), stirring the mixture for 2 to 4 hours, and filtering the solution by pressure; 4) calcining the filter cake obtained by the step 3) at 400 to 550 DEG C for 2 to 5h; and 5) crushing the calcined material obtained by the step 4).

Description

A kind of denitrating catalyst V 2O 5-WO 3/ TiO 2The preparation method of powder
Technical field
The present invention relates to a kind of denitrating catalyst V 2O 5-WO 3/ TiO 2The preparation method of powder.
Background technology
The flue gas that coal combustion generates is the nitrogen oxide as leading take nitric oxide and nitrogen dioxide, and it is the major reason that forms photochemical fog and acid rain, also is a kind of important greenhouse gases simultaneously.So, in by the end of July, 2011 country put into effect " thermal power plant's air pollution emission standard ", the nitrogen oxide emission of all newly-built fired power generating unit must not surpass 100mg/m after this standard-required 2012 3, the nitrogen oxide emission of all fired power generating unit of key area must not surpass 100mg/m after 2014 3, non-key area must not surpass 200mg/m 3, therefore, it is the instant task of environmental protection that the denitration of flue gas is administered.The SCR(SCR) gas denitrifying technology is the effective technology of the solution Pollution Index in Air Nitric Oxides that generally adopts in the world at present.Under the effect of catalyst, by reducing agents such as ammonia, urea, nitrous oxides selectivity harmful in the flue gas is catalysed and reduced into clean harmless nitrogen G﹠W, its denitration efficiency can reach more than 90%.The key of this technology and core are exactly denitrating catalyst.
Denitrating catalyst is take nano titanium oxide as carrier, and active component vanadic anhydride and co-catalyst tungstic acid in the load have been reported many about WO at present 3-TiO 2The preparation of composite granule, but about V 2O 5-WO 3/ TiO 2Composite granule also rarely have report.This vanadium titanium tungsten composite powder is with active component V 2O 5With the even combination of carrier, avoided adding the inhomogeneous phenomenon of fashionable mixing at moulding process in advance, can bring into play better V 2O 5Catalytic activity.
Summary of the invention
The objective of the invention is to provide a kind of denitrating catalyst V 2O 5-WO 3/ TiO 2The preparation method of powder.
Technical scheme of the present invention is: a kind of denitrating catalyst V 2O 5-WO 3/ TiO 2The preparation method of powder, draw together following steps:
1) metatitanic acid is made slurries, concentration is with TiO 2Count 250-350g/L, be heated to 60 ℃, regulate its pH value to 4.0-5.0 with caustic soda, regulate the pH value to 5.0-6.0 with ammoniacal liquor again, then filter-press water-washing;
2) preparation maceration extract: oxalic acid is joined in 60 ℃ of water, stirring is dissolved oxalic acid fully, adds ammonium metatungstate again, stirs slowly to add ammonium metavanadate after ammonium metatungstate dissolves fully again, all add to leave standstill after the dissolving and be aged to color and no longer change ammonium metavanadate addition V 2O 5/ TiO 2=0.8-1.2: 88-94, ammonium metatungstate addition WO 3/ TiO 2=5-10: 88-94, the oxalic acid addition is 3 times of ammonium metavanadate quality;
3) the filter cake making beating that step 1) is obtained, concentration is with TiO 2Count 250-350g/L, be heated to 60 ℃, then add step 2) maceration extract that obtains, stir press filtration behind 2 ~ 4h;
4) filter cake that step 3) is obtained is at the lower calcining of 400-550 ℃ temperature 2-5h;
5) the calcining material that step 4) is obtained is pulverized.
Further, the metatitanic acid of step 1) is the intermediate product of Titanium White Production By Sulfuric Acid Process.
Further, the filtrate that obtains of step 3) is used for step 2) the preparation maceration extract.
The present invention uses NaOH to replace most of ammoniacal liquor, regulate metatitanic acid slip pH to 4.0-5.0 with NaOH first, be adjusted to 5.0-6.0 with a small amount of ammoniacal liquor again, and then washing is to remove sulfate radical and sodium ion free in the filter cake, the method can reduce the consumption of ammonia, reduce the ammonia-nitrogen content in the waste water, met the requirement of cleaner production.
Then adopt the method for dipping simultaneously the predecessor of vanadium tungsten to be combined with metatitanic acid, just be combined in equably titanium dioxide surface through vanadium tungsten component after the calcining, the powder of the method preparation has good denitration performance, under the condition of flue gas condition 100%, the denitration rate when temperature window is 320-400 ℃ can reach more than 95%.
And the press filtration dewatering process is easy and simple to handle compared to the evaporation drying mode after adopting dipping, is easy to large-scale production, has reduced energy consumption, and the vanadium tungsten component that contains in the filtrate simultaneously can recycle when the preparation maceration extract, has reduced the waste of raw material.
The specific embodiment
The present invention will be further described below in conjunction with embodiment.
Embodiment 1
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 250g/L, in the time of 60 ℃, regulate its pH value to 4.0 with caustic soda, regulate pH value to 5.0 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 10.5kg oxalic acid, join 23.5L, in 60 ℃ the water, the ammonium metatungstate that adds 14.6kg fully after the dissolving, the ammonium metavanadate that slowly adds again 3.49kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 250g/L adds the maceration extract that step 2 prepares in the time of 60 ℃, press filtration behind the stirring 2h;
4) filter cake that step 3) is obtained is at the lower calcining of 400 ℃ temperature 5h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 2
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 280g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.6 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 11.9kg oxalic acid, join 26.7L, in 60 ℃ the water, the ammonium metatungstate that adds 19.8kg fully after the dissolving, the ammonium metavanadate that slowly adds again 3.95kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 280g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 3h;
4) filter cake that step 3) is obtained is at the lower calcining of 500 ℃ temperature 3h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 3
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 280g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.7 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 12.0kg oxalic acid, join 26.9L, in 60 ℃ the water, the ammonium metatungstate that adds 23.4kg fully after the dissolving, the ammonium metavanadate that slowly adds again 4.00kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 280g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 4h;
4) filter cake that step 3) is obtained is at the lower calcining of 450 ℃ temperature 5h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 4
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 300g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.5 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 15.8kg oxalic acid, join 35.4L, in 60 ℃ the water, the ammonium metatungstate that adds 17.5kg fully after the dissolving, the ammonium metavanadate that slowly adds again 5.25kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 300g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 2h;
4) filter cake that step 3) is obtained is at the lower calcining of 550 ℃ temperature 2h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 5
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 300g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.6 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 15.9kg oxalic acid, join 35.8L, in 60 ℃ the water, the ammonium metatungstate that adds 21.2kg fully after the dissolving, the ammonium metavanadate that slowly adds again 5.31kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 300g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 3h;
4) filter cake that step 3) is obtained is at the lower calcining of 500 ℃ temperature 2h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 6
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 300g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.7 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 16.1kg oxalic acid, join 36.2L, in 60 ℃ the water, the ammonium metatungstate that adds 25.0kg fully after the dissolving, the ammonium metavanadate that slowly adds again 5.36kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 300g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 4h;
4) filter cake that step 3) is obtained is at the lower calcining of 450 ℃ temperature 4h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 7
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 320g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.5 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 20.2kg oxalic acid, join 45.4L, in 60 ℃ the water, the ammonium metatungstate that adds 18.6kg fully after the dissolving, the ammonium metavanadate that slowly adds again 6.73kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 320g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 2h;
4) filter cake that step 3) is obtained is at the lower calcining of 500 ℃ temperature 3h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 8
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 320g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 5.6 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 20.4kg oxalic acid, join 45.9L, in 60 ℃ the water, the ammonium metatungstate that adds 22.6kg fully after the dissolving, the ammonium metavanadate that slowly adds again 6.81kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 320g/L adds the maceration extract that step 2 prepares in the time of 60 ℃, press filtration behind the stirring 3h;
4) filter cake that step 3) is obtained is at the lower calcining of 450 ℃ temperature 5h;
5) the calcining material that step 4) is obtained is pulverized.
Embodiment 9
1) the intermediate product metatitanic acid of Titanium White Production By Sulfuric Acid Process is made slurries 500L, concentration is with TiO 2Count 350g/L, in the time of 60 ℃, regulate its pH value to 5.0 with caustic soda, regulate pH value to 6.0 with ammoniacal liquor again, filter-press water-washing after adjusting is finished.
2) preparation of maceration extract, take by weighing 23.3kg oxalic acid, join 52.5L, in 60 ℃ the water, the ammonium metatungstate that adds 42.9kg fully after the dissolving, the ammonium metavanadate that slowly adds again 7.78kg after the stirring and dissolving all leaves standstill after the dissolving and is aged to color and no longer changes and stablize, and this process can be produced a large amount of gases.
3) the filter cake making beating that the step 1) washing is obtained is that concentration is with TiO 2The slurries 500L of meter 350g/L adds step 2 in the time of 60 ℃) maceration extract for preparing, stir press filtration behind the 4h;
4) filter cake that step 3) is obtained is at the lower calcining of 550 ℃ temperature 2h;
5) the calcining material that step 4) is obtained is pulverized.
Above embodiment illustrates the technical scheme that the present invention puts down in writing, and is all in the situation that do not break away from the simple distortion that core of the present invention makes or revise and all fall into protection scope of the present invention.

Claims (3)

1. denitrating catalyst V 2O 5-WO 3/ TiO 2The preparation method of powder is characterized in that, the method may further comprise the steps:
1) metatitanic acid is made slurries, concentration is with TiO 2Count 250-350g/L, be heated to 60 ℃, regulate its pH value to 4.0-5.0 with caustic soda, regulate the pH value to 5.0-6.0 with ammoniacal liquor again, then filter-press water-washing;
2) preparation maceration extract: oxalic acid is joined in 60 ℃ of water, stirring is dissolved oxalic acid fully, adds ammonium metatungstate again, stirs slowly to add ammonium metavanadate after ammonium metatungstate dissolves fully again, all add to leave standstill after the dissolving and be aged to color and no longer change ammonium metavanadate addition V 2O 5/ TiO 2=0.8-1.2: 88-94, ammonium metatungstate addition WO 3/ TiO 2=5-10: 88-94, the oxalic acid addition is 3 times of ammonium metavanadate quality;
3) the filter cake making beating that step 1) is obtained, concentration is with TiO 2Count 250-350g/L, be heated to 60 ℃, then add step 2) maceration extract that obtains, stir press filtration behind 2 ~ 4h;
4) filter cake that step 3) is obtained is at the lower calcining of 400-550 ℃ temperature 2-5h;
5) the calcining material that step 4) is obtained is pulverized.
2. a kind of denitrating catalyst V according to claim 1 2O 5-WO 3/ TiO 2The preparation method of powder is characterized in that, the metatitanic acid of step 1) is the intermediate product of Titanium White Production By Sulfuric Acid Process.
3. a kind of denitrating catalyst V according to claim 1 and 2 2O 5-WO 3/ TiO 2The preparation method of powder is characterized in that, the filtrate that step 3) obtains is used for step 2) the preparation maceration extract.
CN201210331981.9A 2012-09-11 2012-09-11 Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst Active CN102921403B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210331981.9A CN102921403B (en) 2012-09-11 2012-09-11 Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210331981.9A CN102921403B (en) 2012-09-11 2012-09-11 Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst

Publications (2)

Publication Number Publication Date
CN102921403A true CN102921403A (en) 2013-02-13
CN102921403B CN102921403B (en) 2014-06-25

Family

ID=47636412

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210331981.9A Active CN102921403B (en) 2012-09-11 2012-09-11 Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst

Country Status (1)

Country Link
CN (1) CN102921403B (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104415777A (en) * 2013-08-22 2015-03-18 上海郎特汽车净化器有限公司 Active powder preparation method
CN104415781A (en) * 2013-08-22 2015-03-18 上海郎特汽车净化器有限公司 Ship diesel engine gas exhaust denitration catalyst preparation method
CN105478133A (en) * 2015-12-11 2016-04-13 福建工程学院 Low-cost SCR denitration catalyst and preparation method thereof
CN107537545A (en) * 2017-09-27 2018-01-05 国电环境保护研究院 A kind of preparation method and application of high vanadium catalyst
CN108855044A (en) * 2018-04-18 2018-11-23 浙江工业大学 Preparation method of vanadium-tungsten catalyst
CN108906030A (en) * 2018-03-08 2018-11-30 湖南三丰钒业有限公司 A kind of recovery and treatment method of spent vanadium catalyst
CN109331802A (en) * 2018-11-16 2019-02-15 内蒙古工业大学 A kind of preparation method of vanadium-based denitration catalyst with nanoporous TiO2 prepared by polyether as carrier
CN109569093A (en) * 2018-12-12 2019-04-05 徐金宝 A kind of air purifier ceramic element and its production method
CN113457440A (en) * 2021-07-23 2021-10-01 凯盛晶华玻璃有限公司 Process and device for denitration of flue gas by catalyst filtering unit
CN114988467A (en) * 2022-07-01 2022-09-02 安徽迪诺环保新材料科技有限公司 Low-sulfur high-pH titanium dioxide and production method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1792650A1 (en) * 2005-11-28 2007-06-06 Haldor Topsoe A/S Process for the preparation of a paraffin isomerisation catalyst
CN101428215A (en) * 2008-12-18 2009-05-13 哈尔滨工业大学 Process for producing flue gas denitration catalyst and flue gas denitration catalyst produced with the process
CN102357535A (en) * 2011-08-31 2012-02-22 沈阳乾鼎机械制造有限公司 Adjustable speed transmission gearbox device

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1792650A1 (en) * 2005-11-28 2007-06-06 Haldor Topsoe A/S Process for the preparation of a paraffin isomerisation catalyst
CN101428215A (en) * 2008-12-18 2009-05-13 哈尔滨工业大学 Process for producing flue gas denitration catalyst and flue gas denitration catalyst produced with the process
CN102357535A (en) * 2011-08-31 2012-02-22 沈阳乾鼎机械制造有限公司 Adjustable speed transmission gearbox device

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104415777A (en) * 2013-08-22 2015-03-18 上海郎特汽车净化器有限公司 Active powder preparation method
CN104415781A (en) * 2013-08-22 2015-03-18 上海郎特汽车净化器有限公司 Ship diesel engine gas exhaust denitration catalyst preparation method
CN105478133A (en) * 2015-12-11 2016-04-13 福建工程学院 Low-cost SCR denitration catalyst and preparation method thereof
CN107537545A (en) * 2017-09-27 2018-01-05 国电环境保护研究院 A kind of preparation method and application of high vanadium catalyst
CN108906030A (en) * 2018-03-08 2018-11-30 湖南三丰钒业有限公司 A kind of recovery and treatment method of spent vanadium catalyst
CN108855044A (en) * 2018-04-18 2018-11-23 浙江工业大学 Preparation method of vanadium-tungsten catalyst
CN109331802A (en) * 2018-11-16 2019-02-15 内蒙古工业大学 A kind of preparation method of vanadium-based denitration catalyst with nanoporous TiO2 prepared by polyether as carrier
CN109331802B (en) * 2018-11-16 2021-04-02 内蒙古工业大学 Nano-porous TiO prepared from polyether2Preparation method of vanadium-based denitration catalyst as carrier
CN109569093A (en) * 2018-12-12 2019-04-05 徐金宝 A kind of air purifier ceramic element and its production method
CN113457440A (en) * 2021-07-23 2021-10-01 凯盛晶华玻璃有限公司 Process and device for denitration of flue gas by catalyst filtering unit
CN114988467A (en) * 2022-07-01 2022-09-02 安徽迪诺环保新材料科技有限公司 Low-sulfur high-pH titanium dioxide and production method thereof

Also Published As

Publication number Publication date
CN102921403B (en) 2014-06-25

Similar Documents

Publication Publication Date Title
CN102921403B (en) Method for preparing V2O5-WO3/TiO2 powder for making denitration catalyst
CN103011272A (en) Method for concentrating and purifying titanium dioxide waste acid by using complex acid
CN102773090A (en) Integral honeycomb denitrification catalyst with novel WO3 addition process and preparation method thereof
CN102294273B (en) Preparation method for TiO2-WO3 composite powder used as catalyst carrier
CN102416333B (en) A special tungsten-added nano-titanium dioxide for flue gas denitrification catalyst and its manufacturing method
CN111468103B (en) A method for recycling waste SCR denitration catalyst to prepare new SCR denitration catalyst
CN106390990A (en) Method for modifying special exhaust gas denitrification catalyst
CN102327783B (en) Method for preparing denitration catalyst carrier TiO2-WO3 composite powder
CN102698737A (en) Method for preparing selective catalytic reduction SCR flue gas denitration catalyst and method for preparing raw material titanium-tungsten powder of SCR flue gas denitration catalyst
CN107537492A (en) A kind of method that iron system denitrating catalyst is directly prepared by the activation of red mud soda acid
CN102764642A (en) Preparation method of special titanium-tungsten-silicon composite powder for SCR (selective catalytic reduction) denitrification catalyst
CN107185554A (en) A kind of method that useless SCR denitration cleaning is recycled
CN102583522A (en) Preparation method for titanium dioxide serving as catalyst carrier
CN104741113B (en) A kind of inexpensive denitrating catalyst and preparation method thereof
KR20120041208A (en) Process for preparing ammonium metatungstate
CN110407249A (en) A kind of method that discarded honeycomb type denitrification catalyst prepares titanium dioxide
CN103736482A (en) Preparation method of continuous extrusion SCR (Selective Catalytic Reduction) denitration honeycomb catalyst
CN109399712A (en) A method of with hydrogen peroxide clean manufacturing high purity vanadic anhydride
CN102764662B (en) Preparation method of special titanium-tungsten powder for SCR (selective catalytic reduction) denitrification catalyst
CN104772137A (en) Ceramsite catalyst with high manganese dioxide content for ozone catalysis, and preparation method and application thereof
CN104275178A (en) Method for recycling waste SCR denitration catalyst and regenerated SCR catalyst carrier
CN108404900A (en) SCR denitration and preparation method thereof
CN102921472A (en) Preparation method for titanium-tungsten composite powder as denitrification catalyst carrier
CN104368361A (en) Low cost recovery and regeneration method of waste SCR catalyst, and regenerated SCR catalyst carrier
CN103071483A (en) Preparation method of titanium-tungsten-silicon composite powder for SCR (Selective Catalytic Reduction) denitration catalyst

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CP01 Change in the name or title of a patent holder
CP01 Change in the name or title of a patent holder

Address after: 454191 Henan Province, Jiaozuo City Station area three km west of Henan baililian chemical Limited by Share Ltd

Patentee after: Longmang group Limited by Share Ltd billions

Address before: 454191 Henan Province, Jiaozuo City Station area three km west of Henan baililian chemical Limited by Share Ltd

Patentee before: Henan Baililian Chemical Co., Ltd.

CP01 Change in the name or title of a patent holder
CP01 Change in the name or title of a patent holder

Address after: 454191 Henan baililian Chemical Co., Ltd

Patentee after: Longbai Group Co.,Ltd.

Address before: 454191 Henan baililian Chemical Co., Ltd

Patentee before: LOMON BILLIONS GROUP Co.,Ltd.

CP02 Change in the address of a patent holder
CP02 Change in the address of a patent holder

Address after: 454150 Fengfeng office, zhongzhan District, Jiaozuo City, Henan Province

Patentee after: Longbai Group Co.,Ltd.

Address before: 454191 Henan baililian Chemical Co., Ltd

Patentee before: Longbai Group Co.,Ltd.