[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN1923338A - Fume desulfurizing process with enhancement limestone method - Google Patents

Fume desulfurizing process with enhancement limestone method Download PDF

Info

Publication number
CN1923338A
CN1923338A CN 200610053076 CN200610053076A CN1923338A CN 1923338 A CN1923338 A CN 1923338A CN 200610053076 CN200610053076 CN 200610053076 CN 200610053076 A CN200610053076 A CN 200610053076A CN 1923338 A CN1923338 A CN 1923338A
Authority
CN
China
Prior art keywords
flue gas
absorption
slurry
limestone
concentration
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
CN 200610053076
Other languages
Chinese (zh)
Other versions
CN100469418C (en
Inventor
吴忠标
莫建松
程常杰
李福才
王凯南
程斌
徐卫平
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.)
Zhejiang Tianlan Environmental Protection Technology Co Ltd
Original Assignee
Zhejiang Tianlan Desulfurization And Dust-Removal 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 Zhejiang Tianlan Desulfurization And Dust-Removal Co Ltd filed Critical Zhejiang Tianlan Desulfurization And Dust-Removal Co Ltd
Priority to CNB2006100530766A priority Critical patent/CN100469418C/en
Publication of CN1923338A publication Critical patent/CN1923338A/en
Application granted granted Critical
Publication of CN100469418C publication Critical patent/CN100469418C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Treating Waste Gases (AREA)

Abstract

The invention relates to a method for desulfurising smoke, especially a strengthen limestone smoke desulfurising method. Wherein, it comprises adding limestone and additive into reactor, to be mixed and reacted with water to generate adsorption slurry; inputting slurry into adsorption tower; the sulfur smoke enters into tower to react with slurry; the purified smoke is discharge outside the tower; the slurry with sulfur dioxide will be discharged at the bottom of tower to be recycled. The invention can improve desulfurising efficiency at 5-10% and improve the absorber utilization at 1-10%.

Description

Enhanced limestone method flue gas desulfurization process
Technical Field
The invention relates to a flue gas desulfurization process, in particular to an enhanced limestone flue gas desulfurization process which is mainly applied to the technical field of atmospheric pollution treatment and prevention.
Background
The history of flue gas desulfurization has been long and studies have been made by people as early as over a hundred years ago. Currently, desulfurization techniques can be classified into three major categories: (1) desulfurization before combustion, such as coal washing and microbial desulfurization; (2) desulfurizing during combustion, such as industrial briquette sulfur fixation and in-furnace calcium injection; (3) post-combustion desulfurization, i.e., Flue Gas Desulfurization (FGD). The FGD process is the only large-scale commercial desulfurization technology in the world. FGD technology, mainly uses absorbent or adsorbent to remove SO in flue gas2And converting it to a more stable sulfur compound. FGD technology is widely varied, but the wet limestone/lime process is dominant in today's technology.
The wet limestone/lime fume desulfurizing technology is to utilize low cost lime and limestone as absorbent to absorb SO in fume2To produce calcium sulfite hemihydrate or gypsum. The technology influences the application of the technology in thermal power plants in the 70 s due to the problems of large investment, high operating cost, corrosion, scaling, blockage and the like. After years of practice and improvement, the working performance and reliability are greatly improved, the investment and operating cost are obviously reduced, and the method is a main method for flue gas desulfurization in devices introduced in China at present. The method has the main advantages that: a. the desulfurization efficiency is high (when the Ca/S of some devices is 1, the desulfurization efficiency is more than 95%); b. the utilization rate of the absorbent is high and can be more than 95 percent; c. the equipment running rate is high (can reach more than 95 percent). 2 sets of wet limestone/gypsum method flue gas desulfurization technology and method introduced into Nissan Mitsubishi heavy industry and matched with 2X 360MW unit in Chongqing Lopa Huang power plant during 'seventy five' periodThe equipment is firstly built into the flue gas desulfurization demonstration project of a large-scale power plant boiler and is put into commercial operation in 1992 and 1993, the desulfurization rate of the system reaches more than 95 percent, and the purity of the byproduct gypsum is higher than 90 percent.
However, the existing wet limestone/lime flue gas desulfurization technology has the main disadvantages of high investment, and the need of carrying out oxidation control (forced oxidation or inhibition oxidation) on sulfite generated in the desulfurization process to ensure the reliable operation of the system, which results in higher operation cost.
Disclosure of Invention
The invention provides an enhanced limestone flue gas desulfurization process which can improve the utilization rate of a desulfurizer, reduce the desulfurization cost and avoid system scaling without oxidation control.
A enhanced limestone method flue gas desulfurization process comprises respectively inputting limestone and additive into a digestion reactor, mixing the limestone and additive in the digestion reactor, and reacting with water to generate absorption slurry; inputting the absorption slurry into an absorption tower, and discharging purified flue gas out of the absorption tower after the sulfur-containing flue gas enters the absorption tower and reacts with the absorption slurry; the absorption slurry absorbing the sulfur dioxide is discharged from the bottom of the absorption tower and recycled or subjected to post-treatment.
The post-treatment process comprises the following steps: discharging the absorption slurry absorbing sulfur dioxide from the bottom of the absorption tower, then feeding the absorption slurry into a hydrocyclone for solid-liquid separation, returning the top flow of the hydrocyclone into the absorption tower or mechanically applying the top flow to a digestion reactor, feeding the bottom flow of the hydrocyclone into a vacuum belt filter for further dehydration to prepare low-moisture-content desulfurized slag, discharging the desulfurized slag, and discharging the filtrate or mechanically applying the desulfurized slag to the digestion reactor.
The additive is organic acid and/or inorganic additive, and the organic acid is: at least one of adipic acid, citric acid, humic acid, benzoic acid, and acetic acid; the inorganic additive is: at least one of magnesium oxide, sodium sulfate and sodium nitrate.
Theabsorption tower is a packed tower, a sieve plate tower, a rotational flow plate tower or a Venturi. The bottom of the absorption tower is provided with a lateral stirring device to prevent the absorption slurry from precipitating.
The desulfurization process conditions are as follows: the pH value of absorption slurry entering the tower is 5.0-9.0, and the liquid-gas ratio is 2.0-20.0L/m3The concentration of the inorganic additive is 0-100000mg/L, the concentration of the organic acid is 0-3000mg/L, and the concentrations of the inorganic additive and the organic acid are not 0mg/L at the same time. The calcium ion concentration is 600-2000mg/L, the absorption slurry mass percentage concentration is 1-35%, and the desulfurization efficiency can be more than 95%.
The process of the invention comprises the following steps:
the absorbent limestone and the additive enter the digestion reactor through respective feeding and metering devices. Limestone and additives react with water in the digestion reactor to form an absorbent slurry (the additives being magnesium oxide for example).
The absorption slurry after the digestion reaction enters an absorption tower through an absorption slurry conveying pump, the sulfur-containing flue gas enters the absorption tower, and the sulfur-containing flue gas and the absorption slurry are subjected to desulfurization reaction inside the absorption tower:
if the additive is an organic acid, the reaction is as follows:
in the desulfurization tower, the organic acid reacts with limestone to obtain regeneration:
the purified flue gas is discharged from the upper part of the absorption tower, and the absorption slurry absorbing the sulfur dioxide is recycled through a main circulating pump or subjected to aftertreatment after reaching the bottom of the absorption tower.
After-treatment is required when the absorption slurry reaches a certain concentration and cannot be recycled.
And (3) discharging a part of slurry from the bottom of the absorption tower, passing the part of slurry through a desulfurization residue delivery pump, entering a hydrocyclone, separating in the hydrocyclone, returning the top flow of the hydrocyclone to the absorption tower, or mechanically using a digestion reactor as make-up water, and further removing water from the bottom flow by a vacuum belt filter to obtain desulfurization residues.
The enhanced limestone method flue gas desulfurization process adopts limestone and a certain proportion of additives to carry out desulfurization together, improves the pH buffer capacity of desulfurization absorption slurry and the concentration of sulfite ions in the desulfurization absorption slurry, effectively reduces the concentration of calcium ions, avoids thescaling of calcium sulfite and calcium sulfate, improves the utilization rate of the limestone and reduces the desulfurization cost. Compared with the traditional limestone method, the desulfurization efficiency can be improved by about 5-10% under the same liquid-gas ratio condition, and the utilization rate of the absorbent is improved by 1-10%.
Drawings
FIG. 1 is a flow diagram of an enhanced limestone process wherein:
1. absorption tower 2, sulfur-containing flue gas 3 and process flushing water
4. Purified flue gas 5, limestone bin 6 and additive bin
7. Screw conveyer 8, digestion reactor 9, absorption slurry delivery pump
10. Cyclone 11, vacuum belt filter 12, filtrate pump
13. Filtrate tank 14, desulfurized slag delivery pump 15 and main circulating pump
16. Process make-up water 17, discharged part filtrate 18 and limestone grinder
Detailed Description
Example 1
Referring to fig. 1, the absorbent limestone powder and the additive are stored in a limestone bin 5 and an additive bin 6, respectively, and enter a digestion reactor 8 through respective screw conveyors 7 and metering devices. If the limestone blocks are pulverized by a limestone grinder 18 and then enter the limestone silo 5. If a liquid additive, the additive may be delivered directly to the digestion reactor 8 via a liquid delivery line.
Limestone and additives are reacted with water (which may be process make-up water 16 or filtrate from filtrate tank 13 or the overhead stream of cyclone 10) in digestion reactor 8 to produce an absorption slurry.
The absorption slurry after the digestion reaction is conveyed to an output pipeline of a main circulating pump 15 through an absorption slurry conveying pump 9 or directly enters the absorption tower 1.
The sulfur-containing flue gas 2 enters the absorption tower 1 and reacts with the absorption slurry in the absorption tower 1, the purified flue gas 4 is discharged from the upper part of the absorption tower 1, and the absorption slurry which absorbs sulfur dioxide enters the main circulating pump 15 through an output pipeline for recycling or post-treatment after reaching the bottom of the absorption tower 1. The bottom of the absorption tower is provided with a lateral stirring device to prevent the absorption slurry from precipitating.
When the absorbed slurry needs post-treatment after reaching a certain concentration, the slurry enters a hydrocyclone 10 through a desulphurization residue delivery pump 14 for solid-liquid separation, the bottom flow of the hydrocyclone 10 enters a vacuum belt filter 11 for further dehydration, and the desulphurization residue with low water content is prepared and discharged. The top of the cyclone 10 flows back into the absorption tower 1 and can also be used as make-up water for the digestion reactor 8. The filtrate of the vacuum belt filter 11 is conveyed to the digestion reactor 8 for reuse through a filtrate pump 12, and the filtrate 17 is discharged out of the digestion reactor 12 after the ion concentration in the absorbed slurry is accumulated to a certain degree.
The process rinse water 3 can clean the equipment when needed.
The flue gas desulfurization process matched with the boiler at 410t/h is carried out according to the process, and the SO is arranged at the flue gas inlet of the boiler2The concentration is 2037mg/m3The flue gas temperature is 155 ℃, the pH value of the flue gas entering the tower is 7.0, and the liquid-gas ratio is 3.0L/m3The concentration of magnesium ions is 100000mg/L, the concentration of calcium ions is 668mg/L, the mass ratio of the concentration of absorption slurry is 18.0 percent, and the desulfurization efficiency reaches 95.0 percent.
Example 2
The 220t/h boiler matching flue gas desulfurization is carried out according to the technical process described in the embodiment 1. Boiler flue gas inlet SO2The concentration is 9690mg/m3The temperature is 160 ℃, the pH value of the mixture entering the tower is 5.0, and the liquid-gas ratio is 20.0L/m3The concentration of sodium sulfate ions is 2852mg/L, the concentration of calcium ions is 620mg/L, the mass ratio of the absorption slurry concentration is 11.7 percent, and the desulfurization efficiency reaches 97.0 percent.
Example 3
The 130t/h boiler matched flue gas desulfurization process is carried out according to the technical process described in the embodiment 1, and the SO is arranged at the flue gas inlet of the boiler2The concentration is 2050mg/m3The temperature is 155 ℃, the pH value of the mixture entering the tower is 6.5, and the liquid-gas ratio is 5.0L/m3The concentration of sodium nitrate is 5096mg/L, the concentration of calcium ions is 600mg/L, the mass ratio of the absorption slurry concentration is 13.0 percent, and the desulfurization efficiency is 96.1 percent.
Example 4
The process described in example 1 was followed for 170t/h boiler matched flue gas desulfurization. Boiler flue gas inlet SO2The concentration is 1800mg/m3The temperature is 152 ℃, the pH value of the mixture entering the tower is 6.0, and the liquid-gas ratio is 4.0L/m3The concentration of adipic acid is 3000mg/L, the concentration of calcium ions is 600mg/L, the mass ratio of the concentration of the absorption serosity is 11.0 percent, and the desulfurization efficiency is 95.8 percent.
Example 5
The 75t/h boiler matched flue gas desulfurization was carried out according to the process described in example 1. Boiler flue gas inlet SO2The concentration is 2060mg/m3The temperature is 155 ℃, the pH value of the mixture entering the tower is 6.0, and the liquid-gas ratio is 5.0L/m3The concentration of citric acid is 1960mg/L, the concentration of calcium ions is 940mg/L, the mass ratio of the concentration of the absorption serosity is 12.0 percent, and the desulfurization efficiency is 96.0 percent%。
Example 6
The process described in example 1 was followed for 170t/h boiler matched flue gas desulfurization. Boiler flue gas inlet SO2The concentration is 1050mg/m3The temperature is 160 ℃, the pH value of the mixture entering the tower is 6.5, and the liquid-gas ratio is 2.0L/m3The concentration of humic acid is 100mg/L, the concentration of calcium ions is 2000mg/L, the concentration-mass ratio of absorption serosity is 15.0 percent, and the desulfurization efficiency is 95.1 percent.
Example 7
The 220t/h boiler matching flue gas desulfurization is carried out according to the technical process described in the embodiment 1. Boiler flue gas inlet SO2The concentration is 2590mg/m3The temperature is 165 ℃, the pH value of the mixture entering the tower is 7.0, and the liquid-gas ratio is 5.0L/m3The concentration of magnesium ions is 4203mg/L, the concentration of adipic acid is 500mg/L, the concentration of calcium ions is 600mg/L, the concentration-mass ratio of absorption serosity is 13.0 percent, and the desulfurization efficiency is 97.0 percent.
Example 8
The process described in example 1 was followed for 170t/h boiler matched flue gas desulfurization. Boiler flue gas inlet SO2The concentration is 1700mg/m3The temperature is 165 ℃, the pH value of the mixture entering the tower is 5.8, and the liquid-gas ratio is 5.0L/m3The concentration of magnesium ions is 4416mg/L, the concentration of citric acid is 300mg/L, the concentration of calcium ions is 560mg/L, the concentration-mass ratio of absorption serosity is 12.6 percent, and the desulfurization efficiency is 98.4 percent.
Example 9
The 130t/h boiler complete flue gas desulfurization was carried out according to the process described in example 1. Boiler flue gas inlet SO2The concentration is 9900mg/m3The temperature is 168 ℃, the pH value of the mixture entering the tower is 9.0, and the liquid-gas ratio is 20.0L/m3The magnesium ion concentration is 7332mg/L, the humic acid concentration is 1000mg/L, and the calcium ion concentration is600mg/L, the mass ratio of the absorption slurry concentration is 17.0 percent, and the desulfurization efficiency is 98.8 percent.
Example 10
The 410t/h boiler matching flue gas desulfurization is carried out according to the technical process described in the example 1. Boiler flue gas inlet SO2The concentration is 1900mg/m3The temperature is 156 ℃, the pH value of the mixture entering the tower is 7.0, and the liquid-gas ratio is 4.0L/m3Sulfuric acid, sulfuric acidThe concentration of sodium is 2368mg/L, the concentration of adipic acid is 100mg/L, the concentration of calcium ions is 1120mg/L, the mass ratio of the absorption slurry concentration is 13.0%, and the desulfurization efficiency is 96.0%.

Claims (9)

1. An enhanced limestone flue gas desulfurization process, which comprises the following steps: respectively inputting limestone and an additive into a digestion reactor, mixing the limestone and the additive in the digestion reactor, and reacting with water to generate absorption slurry; inputting the absorption slurry into an absorption tower, and discharging purified flue gas out of the absorption tower after the sulfur-containing flue gas enters the absorption tower and reacts with the absorption slurry; the absorption slurry absorbing the sulfur dioxide is discharged from the bottom of the absorption tower and recycled or subjected to post-treatment.
2. The enhanced limestone method flue gas desulfurization process according to claim 1, characterized in that: the post-treatment comprises the following steps: discharging the absorption slurry absorbing sulfur dioxide from the bottom of the absorption tower, then feeding the absorption slurry into a hydrocyclone for solid-liquid separation, returning the top flow of the hydrocyclone into the absorption tower or mechanically applying the top flow to a digestion reactor, feeding the bottom flow of the hydrocyclone into a vacuum belt filter for further dehydration to prepare low-moisture-content desulfurized slag, discharging the desulfurized slag, and discharging the filtrate or mechanically applying the desulfurized slag to the digestion reactor.
3. The enhanced limestone method flue gas desulfurization process according to claim 1, characterized in that: the additive is organic acid and/or inorganic additive.
4. The enhanced limestone method flue gas desulfurization process of claim 3, characterized in that: the organic acid is at least one of adipic acid, citric acid, humic acid, benzoic acid and acetic acid.
5. The enhanced limestone method flue gas desulfurization process of claim 3, characterized in that: the inorganic additive is at least one of magnesium oxide, sodium sulfate and sodium nitrate.
6. The enhanced limestone method flue gas desulfurization process according to claim 1, characterized in that: the pH value of the absorption slurry entering the absorption tower is 5.0-9.0.
7. The enhanced limestone method flue gas desulfurization process according to claim 1, characterized in that: the liquid-gas ratio is 2.0-20.0L/m during the absorption reaction in the absorption tower3
8. The enhanced limestone method flue gas desulfurization process according to claim 1, characterized in that: the concentration of the inorganic additive is 0-100000mg/L and the concentration of the organic acid is 0-3000mg/L when the absorption reaction is carried out in the absorption tower, and the concentrations of the inorganic additive and the organic acid are not 0mg/L at the same time.
9. The enhanced limestone method flue gas desulfurization process according to claim 1, characterized in that: the concentration of calcium ions is 600-2000mg/L when the absorption reaction is carried out in the absorption tower.
CNB2006100530766A 2006-08-18 2006-08-18 Fume desulfurizing process with enhancement limestone method Active CN100469418C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2006100530766A CN100469418C (en) 2006-08-18 2006-08-18 Fume desulfurizing process with enhancement limestone method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2006100530766A CN100469418C (en) 2006-08-18 2006-08-18 Fume desulfurizing process with enhancement limestone method

Publications (2)

Publication Number Publication Date
CN1923338A true CN1923338A (en) 2007-03-07
CN100469418C CN100469418C (en) 2009-03-18

Family

ID=37816271

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2006100530766A Active CN100469418C (en) 2006-08-18 2006-08-18 Fume desulfurizing process with enhancement limestone method

Country Status (1)

Country Link
CN (1) CN100469418C (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101947410A (en) * 2010-09-28 2011-01-19 浙江天达环保股份有限公司 Active activator of limestone powder
CN102000489A (en) * 2010-11-24 2011-04-06 东北电力科学研究院有限公司 Wet desulfurizer for thermal power plant and desulfurization method thereof
CN102019138A (en) * 2010-11-18 2011-04-20 华北电力大学(保定) Multifunctional composite additive for wet-method flue gas desulfuration process and using method thereof
CN101342460B (en) * 2008-08-20 2011-08-17 浙江天蓝环保技术有限公司 Automatically controlled desulphurizing agent slurry formulating device
CN102183518A (en) * 2011-01-26 2011-09-14 中节能六合天融环保科技有限公司 Method for quickly measuring sulfate radical content in magnesium method desulfurization process
CN102485323A (en) * 2011-04-15 2012-06-06 安徽理工大学 Rapid calcium desulphurization method for flue gas
CN102000481B (en) * 2009-08-31 2012-10-10 宝山钢铁股份有限公司 Method for treating desulfurization ash
CN109126409A (en) * 2018-10-30 2019-01-04 中冶焦耐(大连)工程技术有限公司 It is a kind of that desulfurization and decarburization technique being carried out to biogas with causticization liquid
CN111013345A (en) * 2019-12-05 2020-04-17 盛尼克能源环保技术(重庆)有限公司 Wet flue gas desulfurization method by adding magnesium limestone
CN114682161A (en) * 2020-12-26 2022-07-01 黄华丽 Solid-liquid different-weight mixed slurry material storage tank and application thereof

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101342460B (en) * 2008-08-20 2011-08-17 浙江天蓝环保技术有限公司 Automatically controlled desulphurizing agent slurry formulating device
CN102000481B (en) * 2009-08-31 2012-10-10 宝山钢铁股份有限公司 Method for treating desulfurization ash
CN101947410A (en) * 2010-09-28 2011-01-19 浙江天达环保股份有限公司 Active activator of limestone powder
CN102019138A (en) * 2010-11-18 2011-04-20 华北电力大学(保定) Multifunctional composite additive for wet-method flue gas desulfuration process and using method thereof
CN102019138B (en) * 2010-11-18 2013-02-13 华北电力大学(保定) Multifunctional composite additive for wet-method flue gas desulfuration process and using method thereof
CN102000489A (en) * 2010-11-24 2011-04-06 东北电力科学研究院有限公司 Wet desulfurizer for thermal power plant and desulfurization method thereof
CN102183518A (en) * 2011-01-26 2011-09-14 中节能六合天融环保科技有限公司 Method for quickly measuring sulfate radical content in magnesium method desulfurization process
CN102485323A (en) * 2011-04-15 2012-06-06 安徽理工大学 Rapid calcium desulphurization method for flue gas
CN109126409A (en) * 2018-10-30 2019-01-04 中冶焦耐(大连)工程技术有限公司 It is a kind of that desulfurization and decarburization technique being carried out to biogas with causticization liquid
CN111013345A (en) * 2019-12-05 2020-04-17 盛尼克能源环保技术(重庆)有限公司 Wet flue gas desulfurization method by adding magnesium limestone
CN114682161A (en) * 2020-12-26 2022-07-01 黄华丽 Solid-liquid different-weight mixed slurry material storage tank and application thereof

Also Published As

Publication number Publication date
CN100469418C (en) 2009-03-18

Similar Documents

Publication Publication Date Title
CN1923339A (en) Fume desulfurizing process with enhancement lime method
CN1923338A (en) Fume desulfurizing process with enhancement limestone method
CN102019138B (en) Multifunctional composite additive for wet-method flue gas desulfuration process and using method thereof
CN103894047B (en) Flue gas pollutant controls integrated purifying recovery process
CN1807253A (en) Method for treating tail gas and waste water from rare earth finished ore acid method burning process
CN101073741A (en) Method and apparatus for combined removing sulfur-dioxide and nitrogenoxide by mixed solution
CN1883765A (en) Circulation desulfurization technology by ammonia-soda process
CN101053738A (en) Wet flue gas desulfurizing and hydrargyrum-removing technology based on two-stage oxidation reaction and system thereof
CN1830526A (en) Purification technology and equipment of waste gas containing high concentration nitrogen oxide
CN1939840A (en) Tail gas treatment and reutilization for calcium carbide stove
CN102225307A (en) Flue gas desulfurization process by using organic acid enhanced acetylene sludge
CN1887696A (en) Process and system of desulfurizing low concentration SO2 fume and producing sulfuric acid
CN1475298A (en) Concentrated alkali double alkali method stack gas desulfurizing technology
CN103861426B (en) A kind of flue gas desulfurization and dedusting also reclaims the method for sodium sulfite
CN107961658A (en) A kind of device and method for carrying out desulfurization and decarburization to flue gas using carbide slag
CN108261913B (en) Magnesium oxide semi-dry desulfurization process
CN1583230A (en) Flue desulfuriznig and dust collecting induction and crystallization process for reuse by concentrated slurry double alkali method
CN1248483A (en) Flue gas desulfurizing agent and method
CN1736556A (en) Method for desulfurizing waste gas and reutilizing sulfur source
CN1565709A (en) Technique for catalytic oxidating desulfurizing products of flue gas
CN1974430A (en) Method of recovering and regenerating waste gas desulfurizing and defluorinating absorbent liquid continuously
CN107970758A (en) A kind of device and method using carbide slag purifying smoke
CN1339332A (en) Sulphur dioxide removing electrolysis process
CN1102422C (en) Flue gas wet desulfuration and denitration purification process
CN1274390C (en) Low temperature plasma adsorption catalytic smoke desulfur device and its sulfur removal method

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
ASS Succession or assignment of patent right

Free format text: FORMER OWNER: WU ZHONGBIAO

C41 Transfer of patent application or patent right or utility model
C56 Change in the name or address of the patentee

Owner name: ZHEJIANG TIANLAN ENVIRONMENTAL PROTECTION TECHNOLO

Free format text: FORMER NAME: TIANLAN DESULFURIZATION DUSTPROOF CO., LTD., ZHEJIANG PROV.

COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 310012 ROOM 1019, WENSAN DIGITAL BUILDING, NO. 369, WENSAN ROAD, XIHU DISTRICT, HANGZHOU CITY, ZHEJIANG PROVINCE TO: 311202 XINGYI VILLAGE, BEIGAN SUBDISTRICT, XIAOSHAN DISTRICT, HANGZHOU CITY, ZHEJIANG PROVINCE

CP01 Change in the name or title of a patent holder

Address after: Hangzhou City, Zhejiang Province, Xihu District Wensanlu Road 310012 building room 1019, No. 369 digital

Co-patentee after: Wu Zhongbiao

Patentee after: ZHEJIANG TIANLAN ENVIRONMENTAL PROTECTION TECHNOLOGY Co.,Ltd.

Address before: Hangzhou City, Zhejiang Province, Xihu District Wensanlu Road 310012 building room 1019, No. 369 digital

Co-patentee before: Wu Zhongbiao

Patentee before: Zhejiang Tianlan Desulphurization & Dust-Removal Co.,Ltd.

TR01 Transfer of patent right

Effective date of registration: 20110222

Address after: Hangzhou City, Zhejiang province Xiaoshan District 311202 North Street Xingyi Village

Patentee after: ZHEJIANG TIANLAN ENVIRONMENTAL PROTECTION TECHNOLOGY Co.,Ltd.

Address before: Hangzhou City, Zhejiang Province, Xihu District Wensanlu Road 310012 building room 1019, No. 369 digital

Co-patentee before: Wu Zhongbiao

Patentee before: ZHEJIANG TIANLAN ENVIRONMENTAL PROTECTION TECHNOLOGY Co.,Ltd.

C56 Change in the name or address of the patentee
CP01 Change in the name or title of a patent holder

Address after: Hangzhou City, Zhejiang province Xiaoshan District 311202 North Street Xingyi Village

Patentee after: ZHEJIANG TIANLAN ENVIRONMENTAL PROTECTION TECHNOLOGY Co.,Ltd.

Address before: Hangzhou City, Zhejiang province Xiaoshan District 311202 North Street Xingyi Village

Patentee before: ZHEJIANG TIANLAN ENVIRONMENTAL PROTECTION TECHNOLOGY Co.,Ltd.