JPH10509914A - Method for separating gaseous pollutants from heat treatment gas - Google Patents
Method for separating gaseous pollutants from heat treatment gasInfo
- Publication number
- JPH10509914A JPH10509914A JP8517170A JP51717096A JPH10509914A JP H10509914 A JPH10509914 A JP H10509914A JP 8517170 A JP8517170 A JP 8517170A JP 51717096 A JP51717096 A JP 51717096A JP H10509914 A JPH10509914 A JP H10509914A
- Authority
- JP
- Japan
- Prior art keywords
- dust
- mixer
- quicklime
- heat treatment
- supplied
- 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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Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/50—Sulfur oxides
- B01D53/508—Sulfur oxides by treating the gases with solids
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/81—Solid phase processes
Abstract
(57)【要約】 熱処理ガスは、ガス状の汚染物質を分離可能な塵に変えるため、ガス内のガス状の汚染物質との間で反応性を有する粒状の吸収材が熱処理ガスに導入される接触反応器(10)に通される。熱処理ガスはそれから、塵分離器(5)に通される。塵分離器(5)内にて分離された塵の大半は、その内部で混合および湿潤化がなされるミキサー(11)に通され、さらにこの塵の一部は、新たな吸収材とともに熱処理ガスに導入されることにより吸収材として再循環する。新たな吸収材としては生石灰が追加される。塵は、ミキサー内における湿った状態での生石灰の総滞留時間が、生石灰とミキサーに供給される水とが略完全に反応し、かつ生石灰から消石灰が形成されるのに十分な時間となるよう、ミキサー内で長時間にわたって留まり、かつ多数回にわたって再循環する。 (57) [Summary] In order to convert gaseous pollutants into separable dust, a particulate absorber that is reactive with gaseous pollutants in the gas is introduced into the heat treatment gas. Through a contact reactor (10). The heat treatment gas is then passed to a dust separator (5). Most of the dust separated in the dust separator (5) is passed through a mixer (11) in which mixing and wetting is performed. Recirculates as an absorbent by being introduced into Quicklime is added as a new absorbent. The dust is such that the total residence time of the quicklime in the wet state in the mixer is sufficient for the quicklime and the water supplied to the mixer to react almost completely and for slaked lime to be formed from the quicklime. , Stay in the mixer for a long time and recycle many times.
Description
【発明の詳細な説明】 熱処理ガスからガス状の汚染物質を分離する方法 本発明は、煙道ガスのような熱処理ガスから二酸化硫黄のようなガス状の汚染 物質を分離する方法であって、熱処理ガスは、ガス状の汚染物質を分離可能な塵 に変えるため、ガス状の汚染物質との間で反応性を有する粒状の吸収材が湿った 状態で熱処理ガスに導入される接触反応器に通され、さらに熱処理ガスは、その 内部で熱処理ガスから塵が分離されるとともに浄化処理済みガスが排出される塵 分離器に通され、この塵分離器内にて分離された塵の一部は、その内部で混合が なされるとともに湿潤化のために水が供給されるミキサーに通され、さらにこの 塵の一部は、新たな吸収材の追加分とともに熱処理ガスに導入されることにより 吸収材として再循環する方法に関する。 熱処理ガスからガス状の汚染物質を分離する上述した方法は例えば、SE−8 504675−3およびSE−8904106−5において知られている。これ ら2つの文献によれば、新たな吸収材としては好ましくは粒状の消石灰(水酸化 カルシウム)が用いられる。この吸収材は塵分離器内にて熱処理ガスから分離さ れた塵と混合され、さらにこの混合物には接触反応器内の煙道ガスに湿った状態 で導入されるよう水が供給される。消石灰は比較的高価であり、このような消石 灰の代わりに比較的安価な生石灰(酸化カルシウム)を用いるための各種の試み がなされている。これらの試みにおいては、生石灰が浄化工程に導入される前に 、生石灰を消化するプラント、すなわち酸化カルシウムと水とを反応させて水酸 化カルシウムを形成させるプラントを用いなければならない。このような石灰消 化プラントは高価であり、このことは消石灰から生石灰に代替した際に予想され る利益が出ないということを意味している。 本発明の目的は、生石灰を消化するための高価でかつ別個のプラントを必要と することなく消石灰を生石灰に代替することができる、熱処理ガスからガス状の 汚染物質を分離する方法を提供することを目的とする。 本発明によれば、このような目的は導入部に述べた種類の方法であって、生石 灰が新たな吸収材として追加され、かつ塵分離器内にて分離された塵の大半はミ キサーに対して略連続的な流れとして供給および排出され、この塵は、ミキサー 内における湿った状態での生石灰の総滞留時間が、生石灰とミキサーに供給され る水とが略完全に反応し、かつ生石灰から消石灰が形成されるのに十分な時間と なるよう、ミキサー内で長時間にわたって留まり、かつ多数回にわたって再循環 することを特徴とする方法により達成される。 生石灰の形態をなす新たな吸収材は、好ましくはミキサーに供給されるが、塵 分離器内にて分離されミキサーに供給される塵の一部に追加されるようにしても よい。また生石灰は、接触反応器内の煙道ガス内に直接導入されるようにしても よい。 混合された塵を流体化させ、これにより混合を促進させるために、好ましくは ミキサーに空気流が供給される。 以下、本発明について添付図面を参照してより詳細に説明する。ここで図面は 、石炭燃焼主要加熱プラントからの煙道ガスを浄化するためのプラントであって 、本発明による方法を実施するための設備が設けられた浄化プラントを摸式的に 示したものである。 図面は、石炭燃焼主要加熱プラント1からの煙道ガスを浄化するためのプラン トを示し、前記煙道ガスはフライアッシュのような塵と、二酸化硫黄のようなガ ス状の汚染物質とを含んでいる。予熱装置2は、熱い煙道ガスから、ダクト2a を介してファン3により主要加熱プラント1に供給される燃焼空気へ熱を移動さ せるために配置されている。 熱い煙道ガスはダクト4を通って塵分離器5に搬送される。図示された実施例 において塵分離器5は、煙道ガスを通すことにより浄化を行う3つの連続した集 塵器ユニットを有する静電集塵器である。このようにして浄化された煙道ガスは ダクト6を介して煙道ガスファン7に通され、この煙道ガスファン7はダクト8 を介して煙道ガスが大気に放出されるよう煙突9に煙道ガスを供給する。塵分離 器はまた、バッグフィルタであってもよい。 ダクト4は接触反応器10を形成する垂直部分を備えている。ミキサー11は 接触反応器10の下方部分と連通している。ミキサー11は煙道ガス内のガス状 の汚染物質との間で反応性を有する粒状の吸収材を湿った状態で接触反応器10 の下方部分に導入する。この吸収材はガス状の汚染物質を集塵器5内にて分離さ れる塵に変える。集塵器5内にて分離された塵粒子は集塵器ユニットのホッパ1 2内で集められる。集められた塵粒子の大半は、以下に詳細に説明する方法によ りシステム内で再循環する。集められた塵粒子の残りは、詳細には説明しないが 、例えばウォームコンベヤにより外部に搬送される。 ミキサー11はSE−9404104−3に記載された種類のものである。従 って、ミキサー11は本質的に二重底の箱形状を有している。これら2つの底の うち上部のものは張力がかけられたポリエステルの流体化布(fluidising cloth) からなる2つの底の間には、空気供給管15を通ってミキサー11内の粒状の吸 収材を流体化させるための空気が導かれるチャンバ14が設けられている。ミキ サー11には、ミキサーの上方部分に配置された水供給管16およびノズル17 を通って水が供給される。混合される粒状の材料はミキサーの入口側端部にある 2つの材料インレット18および19を通ってミキサー11に供給される。ミキ サー11はさらに、協働して用いられる2つの平行なアジテータ(このうち1つ のみが図面に示されている)であって各々が水平シャフトとこれに取り付けられ た複数の傾いた楕円板とを有するアジテータからなる機械的な混合機構20を備 えている。ミキサー11の出口側端部は、よく混合されかつ湿った吸収材を流し 口21から接触反応器10に連続的に供給するため、接触反応器10まで延びて いる。 システム内で再循環する、集塵器ユニットのホッパ12内で集められた塵粒子 の一部分は、インレット19を通ってミキサー11に供給される。粒状の生石灰 (酸化カルシウム)は、インレット19を通って供給される塵粒子に混合させる ため、インレット18を通ってミキサー11に供給される。混合物はノズル17 から供給される水により湿潤化される。ノズル17から供給される水はまた、ミ キサー11に供給される生石灰を消化するためのものでもある。機械的な混合機 構20の構造、およびミキサー11に供給される材料粒子の流体化により、ミキ サー11は、ミキサー11の流し口21を通って吸収材として連続的に接触反応 器10に供給される、均一に湿らされた均一な混合物を生成する。ミキサー11 内での材料粒子の滞留時間は約5乃至60秒、とりわけ10乃至20秒である。 ミキサー11内での材料粒子の上述したような滞留時間(10乃至20秒)、 すなわち石灰粒子が湿った状態にある時間は、生石灰と消化のために追加される 水とが完全に反応し、かつ生石灰から消石灰が形成されるのに十分な時間とはな っていない。このような反応は比較的遅く、数分を要する。 ここで、以下に示す理論上の実例により、本発明についてより詳細に説明する 。この実例では、図面の点A、BおよびC、すなわちそれぞれがミキサー11の 前方にあるダクト4内、ミキサー11の後方にある反応器10のうち集塵器5の 入口側、および集塵器5の出口側に該当する位置を支配する条件が示されている 。 点Aでの塵はほとんどフライアッシュであり、これに対し点Bでの塵はフライ アッシュおよび吸収材である。 点Dでは、単位時間あたり2930kgの塵が排出され、このうち2,000 kgはフライアッシュである。 この実例では従って、消化される生石灰を含む粒状の吸収材は、点Dで排出さ れる前にシステム内で平均して約35 って、生石灰を消化するのに十分な、ミキサー11内での吸収材の総滞留時間は 350乃至700秒、すなわち約6乃至12分である。 上述した実例における水の総消費量は3,366(l/h)であり、このうち 152(l/h)が石灰の消化に必要とされる。このような量の水が消費された ときには、ミキサー11から排出される吸収材の水分含有量は約6%である。し かしながら水分含有量は、混合物の組成に応じて好ましくは2乃至15%の範囲 で変化する。 上述した実例において、点Aでの煙道ガスのフライアッシュ含有量が0、すな わち点Dでの排出量が930(kg/h)である場合には、上述した場合からの 類推により、その循環数は、約110 間は1,100乃至2,200秒、すなわち約18乃至37分となる。The present invention relates to a method for separating gaseous pollutants , such as sulfur dioxide, from a heat-treating gas, such as a flue gas. The heat treatment gas is used to convert gaseous pollutants into separable dust, so that a particulate absorber that is reactive with gaseous pollutants is introduced into the heat treatment gas in a wet state. The heat treatment gas is further passed through a dust separator in which dust is separated from the heat treatment gas and the purified gas is discharged, and a part of the dust separated in the dust separator is The mixture is passed through a mixer in which water is supplied for wetting, and a part of the dust is introduced into the heat treatment gas together with an additional portion of the new absorbent, thereby absorbing the absorbent. As to how to recirculate To. The above-described methods for separating gaseous contaminants from heat treatment gases are known, for example, from SE-8504675-3 and SE-8904106-5. According to these two documents, granular slaked lime (calcium hydroxide) is preferably used as the new absorbent. The absorber is mixed with dust separated from the heat treatment gas in a dust separator, and the mixture is supplied with water so as to be introduced wet to the flue gas in the contact reactor. Slaked lime is relatively expensive, and various attempts have been made to use relatively inexpensive quick lime (calcium oxide) in place of such slaked lime. In these attempts, a plant must be used to digest quicklime, ie, a reaction between calcium oxide and water to form calcium hydroxide, before the quicklime is introduced into the purification process. Such lime digestion plants are expensive, which means that the replacement of slaked lime with quicklime does not have the expected benefits. It is an object of the present invention to provide a method for separating gaseous contaminants from a heat treatment gas, which can replace slaked lime with quick lime without the need for an expensive and separate plant for digesting quick lime. With the goal. According to the invention, such an object is a method of the kind mentioned in the introduction, in which quicklime is added as a new absorbent and most of the dust separated in the dust separator is fed to the mixer. Is supplied and discharged as a substantially continuous stream, and this dust is generated by the total residence time of the quicklime in the mixer in the wet state when the quicklime and the water supplied to the mixer almost completely react with each other, and from the quicklime. This is achieved by a process characterized by staying in the mixer for an extended period of time and recirculating it multiple times so that the slaked lime has a sufficient time to form. The new absorbent in the form of quicklime is preferably fed to the mixer, but may be added to a portion of the dust that is separated in the dust separator and fed to the mixer. Quick lime may also be introduced directly into the flue gas in the contact reactor. An air flow is preferably provided to the mixer to fluidize the mixed dust and thereby facilitate mixing. Hereinafter, the present invention will be described in more detail with reference to the accompanying drawings. Here, the drawing schematically shows a plant for purifying flue gas from a coal-fired main heating plant, provided with equipment for carrying out the method according to the invention. is there. The drawing shows a plant for purifying flue gas from a coal-fired main heating plant 1, said flue gas comprising dust such as fly ash and gaseous pollutants such as sulfur dioxide. I have. The preheating device 2 is arranged to transfer heat from the hot flue gas to the combustion air supplied to the main heating plant 1 by the fan 3 via the duct 2a. The hot flue gas is conveyed through a duct 4 to a dust separator 5. In the embodiment shown, the dust separator 5 is an electrostatic precipitator having three consecutive precipitator units that purify by passing flue gas. The flue gas thus purified is passed through a duct 6 to a flue gas fan 7, which passes through a duct 8 to a chimney 9 so that the flue gas is released to the atmosphere. Supply flue gas. The dust separator may also be a bag filter. The duct 4 has a vertical section forming a contact reactor 10. The mixer 11 is in communication with the lower part of the contact reactor 10. The mixer 11 introduces the particulate absorbent, which is reactive with the gaseous pollutants in the flue gas, into the lower part of the contact reactor 10 in a moist state. This absorber converts gaseous pollutants into dust that is separated in the dust collector 5. The dust particles separated in the dust collector 5 are collected in the hopper 12 of the dust collector unit. Most of the collected dust particles are recirculated in the system in a manner described in detail below. The remainder of the collected dust particles is transported outside, for example, by a worm conveyor, which will not be described in detail. The mixer 11 is of the type described in SE-9404104-3. Accordingly, the mixer 11 has an essentially double-bottom box shape. The upper one of these two bottoms is made of a tensioned polyester fluidizing cloth. Between the two bottoms, the granular absorbent in the mixer 11 is passed through the air supply pipe 15. A chamber 14 into which air for fluidization is introduced is provided. The mixer 11 is supplied with water through a water supply pipe 16 and a nozzle 17 arranged in the upper part of the mixer. The granular material to be mixed is supplied to the mixer 11 through two material inlets 18 and 19 at the inlet end of the mixer. The mixer 11 further comprises two parallel agitators (only one of which is shown in the drawing) used in cooperation, each having a horizontal shaft and a plurality of inclined elliptical plates attached thereto. And a mechanical mixing mechanism 20 composed of an agitator having The outlet end of the mixer 11 extends to the contact reactor 10 in order to continuously supply the well-mixed and wet absorbent from the outlet 21 to the contact reactor 10. A portion of the dust particles collected in the hopper 12 of the dust collector unit, which is recirculated in the system, is fed to the mixer 11 through an inlet 19. Granular quicklime (calcium oxide) is supplied to the mixer 11 through the inlet 18 for mixing with the dust particles supplied through the inlet 19. The mixture is wetted by the water supplied from the nozzle 17. The water supplied from the nozzle 17 is also for digesting quicklime supplied to the mixer 11. Due to the structure of the mechanical mixing mechanism 20 and the fluidization of the material particles supplied to the mixer 11, the mixer 11 is continuously supplied to the contact reactor 10 as an absorbent through the outlet 21 of the mixer 11. , Producing a uniformly moistened, homogeneous mixture. The residence time of the material particles in the mixer 11 is about 5 to 60 seconds, especially 10 to 20 seconds. The residence time of the material particles in the mixer 11 as described above (10 to 20 seconds), i.e. the time during which the lime particles are wet, allows the quicklime and the water added for digestion to react completely, And it is not enough time for slaked lime to be formed from quicklime. Such a reaction is relatively slow and takes several minutes. Now, the present invention will be described in more detail with reference to the following theoretical examples. In this example, points A, B and C in the drawing, namely in the duct 4 respectively in front of the mixer 11, in the reactor 10 behind the mixer 11 the inlet side of the dust collector 5, and in the dust collector 5 The conditions governing the position corresponding to the exit side of are shown. The dust at point A is mostly fly ash, whereas the dust at point B is fly ash and absorbent. At point D, 2930 kg of dust is discharged per unit time, of which 2,000 kg is fly ash. In this example, therefore, the particulate absorbent, including the quicklime to be digested, averages about 35% in the system before being discharged at point D. Thus, the total residence time of the absorbent in the mixer 11 sufficient to digest quicklime is 350 to 700 seconds, ie about 6 to 12 minutes. The total water consumption in the example described above is 3,366 (l / h), of which 152 (l / h) is required for lime digestion. When such an amount of water is consumed, the water content of the absorbent discharged from the mixer 11 is about 6%. However, the moisture content preferably varies between 2 and 15% depending on the composition of the mixture. In the above example, if the fly ash content of the flue gas at point A is 0, that is, the emission at point D is 930 (kg / h), by analogy with the above case, the circulation Number is about 110 The interval is between 1,100 and 2,200 seconds, or about 18-37 minutes.
───────────────────────────────────────────────────── フロントページの続き (81)指定国 EP(AT,BE,CH,DE, DK,ES,FR,GB,GR,IE,IT,LU,M C,NL,PT,SE),OA(BF,BJ,CF,CG ,CI,CM,GA,GN,ML,MR,NE,SN, TD,TG),AP(KE,LS,MW,SD,SZ,U G),AL,AM,AT,AU,BB,BG,BR,B Y,CA,CH,CN,CZ,DE,DK,EE,ES ,FI,GB,GE,HU,IS,JP,KE,KG, KP,KR,KZ,LK,LR,LT,LU,LV,M D,MG,MK,MN,MW,MX,NO,NZ,PL ,PT,RO,RU,SD,SE,SG,SI,SK, TJ,TM,TT,UA,US,UZ,VN────────────────────────────────────────────────── ─── Continuation of front page (81) Designated countries EP (AT, BE, CH, DE, DK, ES, FR, GB, GR, IE, IT, LU, M C, NL, PT, SE), OA (BF, BJ, CF, CG , CI, CM, GA, GN, ML, MR, NE, SN, TD, TG), AP (KE, LS, MW, SD, SZ, U G), AL, AM, AT, AU, BB, BG, BR, B Y, CA, CH, CN, CZ, DE, DK, EE, ES , FI, GB, GE, HU, IS, JP, KE, KG, KP, KR, KZ, LK, LR, LT, LU, LV, M D, MG, MK, MN, MW, MX, NO, NZ, PL , PT, RO, RU, SD, SE, SG, SI, SK, TJ, TM, TT, UA, US, UZ, VN
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE9404105-0 | 1994-11-28 | ||
SE9404105A SE504440C2 (en) | 1994-11-28 | 1994-11-28 | Ways to separate gaseous pollutants from hot process gases |
PCT/SE1995/001403 WO1996016722A1 (en) | 1994-11-28 | 1995-11-24 | Method for separating gaseous pollutants from hot process gases |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10509914A true JPH10509914A (en) | 1998-09-29 |
JP3640674B2 JP3640674B2 (en) | 2005-04-20 |
Family
ID=20396125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP51717096A Expired - Lifetime JP3640674B2 (en) | 1994-11-28 | 1995-11-24 | Method for separating gaseous pollutants from heat treatment gas |
Country Status (20)
Country | Link |
---|---|
EP (1) | EP0804273A1 (en) |
JP (1) | JP3640674B2 (en) |
KR (1) | KR100384589B1 (en) |
CN (1) | CN1080137C (en) |
AU (1) | AU692014B2 (en) |
BR (1) | BR9509831A (en) |
CZ (1) | CZ157497A3 (en) |
EE (1) | EE04049B1 (en) |
FI (1) | FI972233A (en) |
HU (1) | HU220402B (en) |
MD (1) | MD1020C2 (en) |
PL (1) | PL320426A1 (en) |
RO (1) | RO115421B1 (en) |
RU (1) | RU2147919C1 (en) |
SE (1) | SE504440C2 (en) |
SI (1) | SI9520141A (en) |
SK (1) | SK66197A3 (en) |
UA (1) | UA52592C2 (en) |
WO (1) | WO1996016722A1 (en) |
ZA (1) | ZA959876B (en) |
Families Citing this family (20)
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AT404565B (en) * | 1997-06-05 | 1998-12-28 | Scheuch Alois Gmbh | METHOD FOR PURIFYING POLLUTANT-GASES |
SE514592C2 (en) * | 1998-05-18 | 2001-03-19 | Flaekt Ab | Method and apparatus for flue gas purification with extinguishing lime in immediate connection with flue gas purification |
SE512227C2 (en) * | 1998-06-24 | 2000-02-14 | Flaekt Ab | Ways to clean flue gases during the start-up of a boiler |
US6290921B1 (en) * | 1999-11-03 | 2001-09-18 | Foster Wheeler Enegeria Oy | Method and apparatus for binding pollutants in flue gas |
SE523667C2 (en) | 2002-09-20 | 2004-05-11 | Alstom Switzerland Ltd | Method and apparatus for separating gaseous pollutants from hot gases by particulate absorbent material and mixer for wetting the absorbent material |
ATE403487T1 (en) | 2006-02-06 | 2008-08-15 | Alstom Technology Ltd | METHOD AND DEVICE FOR CONTROLLING THE ABSORPTION OF GASEOUS IMPURITIES FROM HOT PROCESS GASES |
DE602006020030D1 (en) | 2006-07-04 | 2011-03-24 | Alstom Technology Ltd | Method and device for separating gaseous pollutants from hot exhaust gases |
AT504426B8 (en) * | 2006-10-24 | 2008-09-15 | Scheuch Gmbh | APPARATUS FOR MOISTURIZING A SORPTION AGENT |
US7766997B2 (en) | 2007-12-21 | 2010-08-03 | Alstom Technology Ltd | Method of reducing an amount of mercury in a flue gas |
US7850936B2 (en) | 2008-02-18 | 2010-12-14 | Alstom Technology Ltd | Dry sulfur dioxide (SO2) scrubbing |
CN101513589B (en) * | 2009-03-03 | 2011-07-20 | 桑德环境资源股份有限公司 | Method and device for purification of flue gases by semidry process |
US8192529B2 (en) * | 2009-03-10 | 2012-06-05 | Gatton Jr Lawrence H | Integrated dry scrubber system |
ES2593812T3 (en) | 2010-11-24 | 2016-12-13 | General Electric Technology Gmbh | Method of purifying a combustion gas rich in carbon dioxide and a boiler system |
US8728211B2 (en) | 2012-03-30 | 2014-05-20 | Alstom Technology Ltd | Nozzle for spraying liquid and a mixer comprising the nozzle |
US9457366B2 (en) * | 2012-07-13 | 2016-10-04 | General Electric Technology Gmbh | Spray lance arrangement |
US8663586B1 (en) | 2012-08-07 | 2014-03-04 | Alstom Technology Ltd | High performance mercury capture |
US9108152B2 (en) * | 2013-11-26 | 2015-08-18 | Alstom Technology Ltd | Dry scrubber system with low load distributor device |
US8906333B1 (en) * | 2013-11-27 | 2014-12-09 | Alstom Technology Ltd | Dry scrubber system with air preheater protection |
CN105617851B (en) * | 2016-03-16 | 2018-08-28 | 中国科学院城市环境研究所 | A kind of method and its device of efficient double tower semi-dry desulphurization |
JP7360378B2 (en) * | 2017-09-06 | 2023-10-12 | エス.ア.ロイスト ルシェルシュ エ デヴロップマン | Method of treating exhaust gas in CDS exhaust gas treatment |
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DE3308927A1 (en) | 1983-03-12 | 1984-09-13 | L. & C. Steinmüller GmbH, 5270 Gummersbach | Process for binding gaseous pollutants contained in flue gases |
SE453570B (en) * | 1985-10-09 | 1988-02-15 | Flaekt Ab | Plant for sepg. acid components from gas mixt. |
SE458095B (en) * | 1986-06-27 | 1989-02-27 | Flaekt Ab | Sepn. system for pollutants from gas-form medium |
FI76931B (en) * | 1986-12-12 | 1988-09-30 | Imatran Voima Oy | FOERFARANDE FOER RENING AV ROEKGASER. |
JP3035015B2 (en) * | 1991-08-13 | 2000-04-17 | 三菱重工業株式会社 | Desulfurization method |
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1994
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Also Published As
Publication number | Publication date |
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BR9509831A (en) | 1997-09-30 |
ZA959876B (en) | 1996-07-15 |
RU2147919C1 (en) | 2000-04-27 |
SI9520141A (en) | 1997-10-31 |
KR100384589B1 (en) | 2003-08-21 |
SE504440C2 (en) | 1997-02-10 |
WO1996016722A1 (en) | 1996-06-06 |
EE04049B1 (en) | 2003-06-16 |
SK66197A3 (en) | 1997-10-08 |
HUT77637A (en) | 1998-06-29 |
RO115421B1 (en) | 2000-02-28 |
CZ157497A3 (en) | 1997-11-12 |
CN1167450A (en) | 1997-12-10 |
SE9404105L (en) | 1996-05-29 |
UA52592C2 (en) | 2003-01-15 |
HU220402B (en) | 2002-01-28 |
PL320426A1 (en) | 1997-09-29 |
MD1020C2 (en) | 1999-07-31 |
FI972233A0 (en) | 1997-05-27 |
JP3640674B2 (en) | 2005-04-20 |
EP0804273A1 (en) | 1997-11-05 |
AU4126496A (en) | 1996-06-19 |
FI972233A (en) | 1997-05-27 |
AU692014B2 (en) | 1998-05-28 |
CN1080137C (en) | 2002-03-06 |
EE9700215A (en) | 1998-02-16 |
SE9404105D0 (en) | 1994-11-28 |
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