JP3999995B2 - Dry smoke purification system - Google Patents
Dry smoke purification system Download PDFInfo
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- JP3999995B2 JP3999995B2 JP2002103109A JP2002103109A JP3999995B2 JP 3999995 B2 JP3999995 B2 JP 3999995B2 JP 2002103109 A JP2002103109 A JP 2002103109A JP 2002103109 A JP2002103109 A JP 2002103109A JP 3999995 B2 JP3999995 B2 JP 3999995B2
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- JP
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- Prior art keywords
- desulfurization
- flue gas
- reactor
- denitration
- moving bed
- 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.)
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- 238000000746 purification Methods 0.000 title claims description 10
- 239000000779 smoke Substances 0.000 title claims description 3
- 239000003546 flue gas Substances 0.000 claims description 43
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 41
- 238000006477 desulfuration reaction Methods 0.000 claims description 34
- 230000023556 desulfurization Effects 0.000 claims description 34
- 239000000843 powder Substances 0.000 claims description 34
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 33
- 239000002250 absorbent Substances 0.000 claims description 31
- 230000002745 absorbent Effects 0.000 claims description 31
- 239000002245 particle Substances 0.000 claims description 24
- 239000007789 gas Substances 0.000 claims description 16
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 claims description 14
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 claims description 14
- 239000000428 dust Substances 0.000 claims description 8
- 238000011144 upstream manufacturing Methods 0.000 claims description 6
- 230000003009 desulfurizing effect Effects 0.000 claims description 4
- 239000006096 absorbing agent Substances 0.000 claims description 3
- 239000004071 soot Substances 0.000 claims description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical group [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 19
- 239000000292 calcium oxide Substances 0.000 description 11
- 235000012255 calcium oxide Nutrition 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000000034 method Methods 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000011575 calcium Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000010883 coal ash Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
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- Devices And Processes Conducted In The Presence Of Fluids And Solid Particles (AREA)
Description
【0001】
【産業上の利用分野】
本発明は、排煙ガス中の硫黄酸化物(SOx)、窒素酸化物(NOx)、及びばい塵を除去するための、乾式排煙浄化システムであり、従来から用いられている湿式排煙脱硫装置と集塵装置の組合せに比較してローコストなものである。
【0002】
【従来の技術】
従来、排煙脱硫においては、大容量の排煙脱硫装置は、石灰石膏法が広く普及し、また中小容量の排煙脱硫装置は水酸化マグネシウム法(水マグ法)が採用されている。
以上の2方式は、何れも湿式法であり、用水を多量に使用し、また、排煙温度も再加熱はしているが、100℃〜90℃であり、通常ボイラーの排出温度140℃〜130℃より低下するため、排煙ガスの有効上昇高さが低くなる欠点を有している。
乾式排煙脱硫は、装置外への排水は全く無く、また排煙ガス温度の低下を生じないなどの長所を有するが、装置価格が湿式法に比較してコスト高であるため、日本では現在(2002年)、その実用機としては火力発電所において、石炭灰・石灰脱硫法で一例、活性炭法で一例の2例あるのみである。
【0003】
【発明が解決しようとする課題】
本発明の乾式排煙浄化システムは、従来の技術における湿式脱硫装置と集塵装置の組合せに対して、コスト的に十分対抗し得る乾式排煙浄化システムを提供するものである。従来からの乾式排煙浄化装置は、その吸収剤と排煙ガスとの固気反応において、吸収剤は粒状化して直交流移動層として固気接触するものとしている。排煙ガスの移動層を通過するときの圧力損失の上昇を抑制するため吸収剤の粒径分布は粒径5〜9mm程度として粉体の混在をさけるものとし、またガス流速も0.4〜0.6m/秒の低速度としているため、固気反応装置の移動層が大型化する。そのため、吸収剤の製造コスト、及び固気反応装置(SOx・NOx吸収塔)コストが上昇要因となっていた。
【0004】
【課題を解決するための手段】
上記の課題を解決すべく、本発明は以下の構成を提供する。請求項1に係る発明は、脱硫・脱硝用粉体吸収剤により、排煙ガス中の硫黄酸化物(SOx)、及び、窒素酸化物(NOx)を除去するための乾式排煙浄化システムであって、
上流側に設置される噴流層反応器と、下流側に設置される移動層反応器とを具備し、
前記噴流層反応器は、反応器本体にガス流入部を備え、前記ガス流入部から前記反応器本体内に、排煙ガスと共に脱硫・脱硝用粉体吸収剤を流入させ、前記反応器本体内で前記排煙ガスの脱硫・脱硝を行なわせるように構成されると共に、前記反応器本体は多段に構成され、各段に前記脱硫・脱硝用粉体吸収剤を捕集するサイクロンを備え、前記サイクロンによって捕集した脱硫・脱硝用粉体吸収剤を前記反応器本体の上流側の前段に搬送して再利用するように構成され、
前記移動層反応器は、反応器本体内に粒子を充填した移動層を備え、前記噴流層反応器から前記排煙ガスと共に流出した前記脱硫・脱硝用粉体吸収剤を前記移動層の前記粒子間に貫入させて捕集させ、前記脱硫・脱硝用粉体吸収剤を捕集させた前記移動層によって、前記排煙ガスの脱硫・脱硝を行なわせると共に、前記排煙ガス中のばい塵を捕集させるように構成されていることを特徴とする乾式排煙浄化システムを提供するものである。
更に、本発明の構成について説明する。
(1)吸収剤は、粒体を製造するための歩留まり低下に全く関係することのない粉体とした。
(2)粉体とすることにより、噴流層の適用を容易にし、排煙ガスの流速は4m/sec以上にすることができる。
(3)粉体吸収剤の集塵捕集を考慮し、粒体移動層によるものとし、その移動層は2重円環構造であり、また、排ガスの流入速度0.8m/sec以上とすることにより、直交流移動層の小型化をはかることが可能となった。2重円環構造の直交流移動層は、「移動層粒状集塵装置、特許第3028466号・平成12年2月4日」を援用する。
(4)従来、粉体吸収剤により、バグフィルターを用いてバグフィルター表面に粉体層を形成して、SOx吸収部を形成する方法もあるが、バグフィルターを用いるとき、バグフィルターへの流入速度は通常1.6〜2cm/秒であるため、粉体のバグフィルターへの付着の確実性が得られないため、脱硫剤の利用率が低下する。
(5)粉体吸収剤は脱硫用としてCa利用率(Ca/S)を70〜60%以下とするとき脱硫効率は90%以上、脱硝効率は60%以上を有する。(図1参照)
(6)本発明においては、粒体移動層を適用していることより、排煙ガスの流入速度は80cm/秒以上にすることにより、粉体吸収剤は、確実に移動層粒子間に貫入し、脱硫・脱硝反応に寄与し得る。
【0006】
【実施例】
本発明の乾式排煙浄化システムを、図−2により説明する。
図2、図3、図4の1〜8Aの各部分は、粉体吸収剤製造装置であり、9〜18の各部分は排煙ガス処理装置である。
粉体吸収剤製造の原料は、生石灰(CaO)サイロ1、石炭灰サイロ2より、生石灰計量機1A、石炭灰計量機2Aにて粉体計量し、粉体混合機4を経て、混練機5に供給され、また混練水は給水タンク3より給水計量機3Aより供給された水により混練される。このときの給水量は生石灰(CaO)に水を加えて水酸化カルシウム(Ca(OH)2)にするときの理論水量(CaO+H2O→Ca(OH)2においてCaO,1.0に対してH2O,0.32)の1.5倍以上とする。
【0007】
混練物は水和養生装置6において、湿度100%、温度80〜98℃で水和養生により硬化する。その水和硬化物を粉砕乾燥機7により粉体状の吸収剤を製造し、吸収剤サイロ8に貯溜する。粉体吸収剤は、排煙ガス中の硫黄酸化物(SOx)濃度に応じ吸収剤供給機8Aより供給され、排煙ガスと共にガス流入部9より噴流層反応器10内に流入し、排煙ガスと脱硫・脱硝反応をする。噴流層反応器10を排出した排煙ガスは2重円環状の移動層反応器11に供給される。移動層反応器11に充填している移動層粒子11Cは粒子供給部11Dより供給され、移動層反応器11の下部にある粒子排出部11Eより排出されるため、移動層粒子は上部より下部へ移動層を形成する。
【0008】
一方排煙ガスは、移動層反応器11の内筒部11Aより外筒部11Bへ移動層内を直交流する。排煙ガスに随伴している粉体吸収剤は、移動層粒子間に貫入し、移動層内で捕集され、移動層内で排煙ガス中のSOx・NOxを吸収する。
SOx・NOxを吸収した、使用済粉体吸収剤は、粒子排出部11Eより移動層粒子11Cとともに排出し、分級機12により使用済粉体吸収剤と移動層粒子11Cは分離され、移動層粒子11Cは、粒子搬送部14,及び粒子搬送用送風機14Aにより粒体移動層11の上部にある粒子供給部11Dに空気搬送され、循環使用される。
移動層反応器11で浄化されて流出した排煙ガスは、誘引通風機15を経て煙突16より大気放出される。
【0009】
噴流層反応器10を、図5に示す多段構成として、第1段噴流層反応器10A,第2段噴流層反応器10B,第3段噴流層反応器10Cとするとき、各段毎のサイクロン10Dにより粉体脱硫剤を捕集し、その粉体脱硫剤を上流側の前段に搬送して、脱硫剤の利用率向上をはかるものである。即ち、排煙ガスは、10A→10B→10Cの各噴流層反応器を流れ、粉体脱硫剤は10C→10B→10Aの各段の噴流層反応器を搬送され、固気反応は全体として対向流反応となる。石炭灰、及びカルシウムを原料とした吸収剤は、図1に示すように脱硫におけるCa利用率(Ca/S)60〜70%以下において、SOx・NOxの同時吸収性能を有することより、脱硫・脱硝剤として適用し得る。図1においては、固気反応が20時間以上になると脱硝性が低下し、脱硫性能のみの特性となる。
【0010】
【発明の効果】
従来、乾式脱硫は用水使用量が少なく、排水を生じない。また、排煙温度を低下させない等の長所を有しながら、湿式脱硫に比して、コスト高のため普及しなかった。本発明による乾式排煙浄化システムは、脱硫・脱硝・集塵の複合機能を有し、経済性で十分湿式脱硫に対抗し得るものであり、地球環境保全に貢献し得るものである。
【図面の簡単な説明】
【図1】 固定層における吸収剤のSOx・NOx吸収特性
【図2】 乾式排煙浄化装置構成図
【図3】 移動層反応器 X1−X1’断面図
【図4】 移動層反応器 X2−X2’断面図
【図5】 多段型噴流層構成図
【符号の説明】
1 生石灰(CaO)サイロ
1A 生石灰計量機
2 石炭灰サイロ
2A 石炭灰計量機
3 給水タンク
3A 給水計量機
4 粉体混合機
5 混練機
6 水和養生装置
7 粉砕乾燥機
8 吸収剤サイロ
8A 吸収剤供給器
9 ガス流入部
10 噴流層反応器
10A 第1段噴流層反応器
10B 第2段噴流層反応器
10C 第3段噴流層反応器
10D サイクロン
11 移動層反応器
11A 移動層内筒部
11B 移動層外筒部
11C 移動層粒子
11D 移動層粒子供給部
11E 移動層粒子排出部
12 分級機
13 使用済脱硫剤サイロ
14 粒子搬送部
14A 粒子搬送用送風機
15 誘引通風機
16 煙突[0001]
[Industrial application fields]
The present invention is a dry flue gas purification system for removing sulfur oxide (SOx), nitrogen oxide (NOx), and soot and dust in flue gas, and has been used in the past. Compared to the combination of the device and the dust collector, it is low cost.
[0002]
[Prior art]
Conventionally, in flue gas desulfurization, the lime gypsum method has been widely used for large-capacity flue gas desulfurization devices, and the magnesium hydroxide method (water mug method) has been adopted for medium- and small-capacity flue gas desulfurization devices.
The above two methods are both wet methods, use a large amount of water and reheat the flue gas temperature, but it is 100 ° C to 90 ° C, and the normal boiler discharge temperature is 140 ° C to Since it falls from 130 degreeC, it has the fault that the effective raise height of flue gas becomes low.
Dry flue gas desulfurization has the advantages that there is no drainage to the outside of the device and the temperature of the flue gas does not decrease, but the cost of the device is higher than that of the wet method. (2002) As a practical machine, there are only two examples in a thermal power plant, one example using the coal ash / lime desulfurization method and one example using the activated carbon method.
[0003]
[Problems to be solved by the invention]
The dry type flue gas purification system of the present invention provides a dry type flue gas purification system that can sufficiently compete with the combination of the wet desulfurization device and the dust collector in the prior art. In the conventional dry-type flue gas purifying apparatus, in the solid-gas reaction between the absorbent and the flue gas, the absorbent is granulated and brought into solid-gas contact as a cross-flow moving layer. In order to suppress an increase in pressure loss when passing through the moving layer of the flue gas, the particle size distribution of the absorbent should be about 5 to 9 mm to avoid mixing of powders, and the gas flow rate should also be 0.4. Since the low speed is set to ˜0.6 m / sec, the moving bed of the solid-gas reactor becomes large. For this reason, the manufacturing cost of the absorbent and the solid-gas reactor (SOx / NOx absorption tower) cost have been increasing factors.
[0004]
[Means for Solving the Problems]
In order to solve the above problems, the present invention provides the following configurations. The invention according to claim 1 is a dry type flue gas purification system for removing sulfur oxide (SOx) and nitrogen oxide (NOx) in flue gas with a powder absorbent for desulfurization / denitration. And
A spouted bed reactor installed on the upstream side and a moving bed reactor installed on the downstream side,
The spouted bed reactor has a gas inlet to the reactor body, the reactor body from the gas inlet, allowed to flow into a desulfurization and denitration powder absorber with flue gas, wherein the reactor body in the while being configured so as to perform the desulfurization and denitration of flue gases, the reactor body is configured in multiple stages, comprises a cyclone for collecting the desulfurizing DeNOx powder absorbent to each stage, the the powder absorbent for desulfurization and denitration were collected by the cyclone is conveyed in front of the upstream side of the reactor main body is configured to reuse,
The moving bed reactor includes a moving bed filled with particles in the reactor main body , and the desulfurization / denitration powder absorbent flowing out together with the flue gas from the spouted bed reactor is transferred to the particles of the moving bed . is penetrated by collecting in between, by the mobile phase was collected powder absorbent for the desulfurization and denitrification, causes rope rows desulfurization and denitrification of the flue gas, Soot dust the flue gas it is intended to provide a dry flue gas purification system, characterized in that is configured to make collect.
Further, the configuration of the present invention will be described.
(1) The absorbent was a powder that had nothing to do with yield reduction for producing granules.
(2) By using powder, application of the spouted bed can be facilitated, and the flow rate of the flue gas can be 4 m / sec or more.
(3) In consideration of dust collection of the powder absorbent, it shall be based on a granular moving layer, the moving layer has a double ring structure, and the exhaust gas inflow rate is 0.8 m / sec or more. This makes it possible to reduce the size of the cross-flow moving bed. For the cross-flow moving bed having a double annular structure, “moving bed granular dust collector, Japanese Patent No. 3028466 / February 4, 2000” is incorporated.
(4) Conventionally, there is a method of forming a SOx absorption part by forming a powder layer on the surface of the bag filter using a powder filter with a powder absorbent, but when using the bag filter, it flows into the bag filter. Since the speed is usually 1.6 to 2 cm / second, the certainty of adhesion of the powder to the bag filter cannot be obtained, so that the utilization rate of the desulfurizing agent is lowered.
(5) The powder absorbent has a desulfurization efficiency of 90% or more and a denitration efficiency of 60% or more when the Ca utilization rate (Ca / S) is 70 to 60% or less for desulfurization. (See Figure 1)
(6) In the present invention, since the particle moving layer is applied, the inflow rate of the flue gas is set to 80 cm / second or more, so that the powder absorbent can surely penetrate between the moving layer particles. And can contribute to desulfurization and denitration reactions.
[0006]
【Example】
A dry smoke purification system of the present invention will be described with reference to FIG.
2, 3, and 4, each part of 1 to 8 </ b> A is a powder absorbent manufacturing apparatus, and each part of 9 to 18 is a flue gas treatment apparatus.
The raw material for the production of the powder absorbent is a quick lime (CaO) silo 1 and a coal ash silo 2, powder is measured with a quick lime meter 1 A and a
[0007]
The kneaded product is cured by hydration curing in the hydration curing apparatus 6 at a humidity of 100% and a temperature of 80 to 98 ° C. A powdery absorbent is produced from the hydrated cured product by the crushing and drying
[0008]
On the other hand, the flue gas cross-flows in the moving bed from the
The used powder absorbent that has absorbed SOx / NOx is discharged together with the moving
The exhaust gas exhausted after being purified by the moving bed reactor 11 is discharged to the atmosphere from the chimney 16 through the
[0009]
When the spouted
[0010]
【The invention's effect】
Conventionally, dry desulfurization uses less water and does not produce drainage. In addition, while having the advantage of not lowering the flue gas temperature, it was not popular due to its high cost compared to wet desulfurization. The dry type flue gas purification system according to the present invention has a combined function of desulfurization, denitration, and dust collection, is economical and can sufficiently resist wet desulfurization, and can contribute to global environmental conservation.
[Brief description of the drawings]
[Fig. 1] SOx / NOx absorption characteristics of absorbent in fixed bed [Fig. 2] Dry flue gas purifier configuration diagram [Fig. 3] Cross section of moving bed reactor X1-X1 '[Fig. 4] Moving bed reactor X2- X2 'cross section [Fig. 5] Multistage spouted bed configuration [Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Quick lime (CaO) silo 1A Quick lime meter 2
Claims (1)
上流側に設置される噴流層反応器と、下流側に設置される移動層反応器とを具備し、
前記噴流層反応器は、反応器本体にガス流入部を備え、前記ガス流入部から前記反応器本体内に、排煙ガスと共に脱硫・脱硝用粉体吸収剤を流入させ、前記反応器本体内で前記排煙ガスの脱硫・脱硝を行なわせるように構成されると共に、前記反応器本体は多段に構成され、各段に前記脱硫・脱硝用粉体吸収剤を捕集するサイクロンを備え、前記サイクロンによって捕集した脱硫・脱硝用粉体吸収剤を前記反応器本体の上流側の前段に搬送して再利用するように構成され、
前記移動層反応器は、反応器本体内に粒子を充填した移動層を備え、前記噴流層反応器から前記排煙ガスと共に流出した前記脱硫・脱硝用粉体吸収剤を前記移動層の前記粒子間に貫入させて捕集させ、前記脱硫・脱硝用粉体吸収剤を捕集させた前記移動層によって、前記排煙ガスの脱硫・脱硝を行なわせると共に、前記排煙ガス中のばい塵を捕集させるように構成されていることを特徴とする乾式排煙浄化システム。 A dry smoke purification system for removing sulfur oxide (SOx) and nitrogen oxide (NOx) in flue gas with a powder absorbent for desulfurization and denitration,
A spouted bed reactor installed on the upstream side and a moving bed reactor installed on the downstream side,
The spouted bed reactor has a gas inlet to the reactor body, the reactor body from the gas inlet, allowed to flow into a desulfurization and denitration powder absorber with flue gas, wherein the reactor body in the while being configured so as to perform the desulfurization and denitration of flue gases, the reactor body is configured in multiple stages, comprises a cyclone for collecting the desulfurizing DeNOx powder absorbent to each stage, the the powder absorbent for desulfurization and denitration were collected by the cyclone is conveyed in front of the upstream side of the reactor main body is configured to reuse,
The moving bed reactor includes a moving bed filled with particles in the reactor main body , and the desulfurization / denitration powder absorbent flowing out together with the flue gas from the spouted bed reactor is transferred to the particles of the moving bed . is penetrated by collecting in between, by the mobile phase was collected powder absorbent for the desulfurization and denitrification, causes rope rows desulfurization and denitrification of the flue gas, Soot dust the flue gas dry flue gas purification system, characterized by being configured to make collect.
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| JP2002103109A JP3999995B2 (en) | 2002-02-28 | 2002-02-28 | Dry smoke purification system |
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| JP2002103109A JP3999995B2 (en) | 2002-02-28 | 2002-02-28 | Dry smoke purification system |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103212281A (en) * | 2013-03-29 | 2013-07-24 | 江苏中显集团有限公司 | Smoke desulfurization and denitrification integration method and special device thereof |
| CN105617831A (en) * | 2015-12-31 | 2016-06-01 | 上海东化环境工程有限公司 | Flue gas low-temperature denitration and semi-dry desulfurization process |
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| WO2014110884A1 (en) * | 2013-01-18 | 2014-07-24 | 北京神雾环境能源科技集团股份有限公司 | Powdered solid fuel boiler and dry purification process system |
| WO2014110883A1 (en) * | 2013-01-18 | 2014-07-24 | 北京神雾环境能源科技集团股份有限公司 | Process system for performing dry desulfurization on fume of pellet fuel boiler |
| CN103537184B (en) * | 2013-10-30 | 2018-07-27 | 河北工业大学 | The method that compound scavenger carries out desulphurization denitration is prepared with pickling iron and steel waste residue |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103212281A (en) * | 2013-03-29 | 2013-07-24 | 江苏中显集团有限公司 | Smoke desulfurization and denitrification integration method and special device thereof |
| CN103212281B (en) * | 2013-03-29 | 2015-05-20 | 江苏中显集团有限公司 | Smoke desulfurization and denitrification integration method and special device thereof |
| CN105617831A (en) * | 2015-12-31 | 2016-06-01 | 上海东化环境工程有限公司 | Flue gas low-temperature denitration and semi-dry desulfurization process |
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