EP0502945A1 - Verfahren und vorrichtung zur abgasreinigung - Google Patents

Verfahren und vorrichtung zur abgasreinigung

Info

Publication number
EP0502945A1
EP0502945A1 EP91900391A EP91900391A EP0502945A1 EP 0502945 A1 EP0502945 A1 EP 0502945A1 EP 91900391 A EP91900391 A EP 91900391A EP 91900391 A EP91900391 A EP 91900391A EP 0502945 A1 EP0502945 A1 EP 0502945A1
Authority
EP
European Patent Office
Prior art keywords
particles
absorbent
gas
venturi device
carrier gas
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.)
Ceased
Application number
EP91900391A
Other languages
English (en)
French (fr)
Inventor
Nils Bringfors
Lars-Erik Johansson
Stefan Ahman
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.)
UK Secretary of State for Defence
ABB Technology FLB AB
Original Assignee
UK Secretary of State for Defence
ABB Flaekt AB
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 UK Secretary of State for Defence, ABB Flaekt AB filed Critical UK Secretary of State for Defence
Publication of EP0502945A1 publication Critical patent/EP0502945A1/de
Ceased legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/50Sulfur oxides
    • B01D53/508Sulfur oxides by treating the gases with solids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23JREMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES 
    • F23J15/00Arrangements of devices for treating smoke or fumes
    • F23J15/003Arrangements of devices for treating smoke or fumes for supplying chemicals to fumes, e.g. using injection devices

Definitions

  • the present invention relates to a method and an apparatus for cleaning a process gas, such as flue gas, of gaseous pollutants, such as sulphur dioxide, sulphur trioxide, hydrogen chloride and hydrogen fluoride, by contacting the gas with an absorbent, such as lime, which is reactive with the gaseous pollutants, for conversion of these pollutants into separable, particulate pollutants.
  • a process gas such as flue gas
  • gaseous pollutants such as sulphur dioxide, sulphur trioxide, hydrogen chloride and hydrogen fluoride
  • Limestone or dolomite in the form of a finely milled or slightly coarser powder is generally added in the com ⁇ bustion chamber.
  • finely milled limestone or slaked lime in water suspension is most often added.
  • the reactivity of most absorbents that are available at reasonable costs is low at low temperatures and low relative humidity, which makes these techniques using a dry absorbent insuf ⁇ ficiently effective.
  • wet-dry flue gas cleaning involves lower investment costs but necessitates a more refined and thus more expen ⁇ sive absorbent as compared with the wet flue gas scrub ⁇ bers.
  • the absorbent is supplied, in the wet-dry methods, loosely or suspended in an amount of water which is smaller than the amount which is necessary to cool the flue gas to a temperature below the saturation tempera ⁇ ture. Since the suspended absorbent must be supplied to the flue gas in the form of fine water droplets so that the formed surface of evaporation will be large enough to ensure complete evaporation of the supplied amount of water, the suspension cannot be made thicker than as to allow fine division.
  • SE-7908674-0 suggests separate moisten ⁇ ing of the flue gases before being introduced in a bag filter whose bags have been coated with a dust cake of calcium hydroxide.
  • SE-8504675-3 suggests instead that the absorbent be moistened with water, before being supplied to the flue gas. The amount of water must then not be greater than as to allow maintaining the powder form of the absorbent. Otherwise the absorbent cannot be dis ⁇ charged to the flue gas by means of the feed screw shown in the drawing.
  • None of these techniques makes the flue gas cleaning sufficiently effective according to current environmental standards. Summary of the Invention Technical Problem It thus constitutes a problem to provide satisfactory separation of the gaseous pollutants, such as sulphur dioxide, of the flue gas, without using an absorbent sus ⁇ pended in water.
  • One object of the present invention therefore is to provide a simple method for effective separation of gaseous pollutants from e.g. flue gas, without supplying an absorbent suspended in water to the polluted gas.
  • a further object of the present invention is to pro ⁇ vide a simple apparatus for carrying out this method.
  • the above-men ⁇ tioned problem of providing satisfactory separation o f gaseous pollutants, such as sulphur dioxide, from a pro ⁇ cess gas, such as flue gas is solved in that a particu- late absorbent, such as lime, which is reactive with the gaseous pollutants, is dispersed in a carrier gas, such as air, and that said carrier gas and the absorbent particles dispersed therein are accelerated and subsequently are at high velocity contacted with a pressurised flow of liquid, such as water, which is finely divided on the surface of said particles, before the particles are contacted with the process gas for conversion of the pollutants thereof into separable, particulate pollutants.
  • a particu- late absorbent such as lime, which is reactive with the gaseous pollutants
  • a carrier gas such as air
  • a pressurised flow of liquid such as water
  • the absorbent which is contacted with the flue gases thus consists of fine, moistened high reactivity particles which quickly react with the gaseous pollutants of the gas and, by an absorption process, convert these into separable particulate pollutants.
  • the carrier gas and the moistened particles dispersed therein are preferably retarded, before being supplied to the process gas.
  • the flow of liquid is preferably supplied in such an amount to the carrier gas that the mass ratio of the sup ⁇ plied liquid to the absorbent particles dispersed in the carrier gas is in the range of 0.1-10, especially about 0.5.
  • a means for dis ⁇ persing the particles of the absorbent in a carrier gas is arranged in connection with a space for contacting a process gas, such as flue gas, containing gaseous pollutants with a particulate absorbent, such as lime, which is reactive with the gaseous pollutants.
  • This means communicates with at least one Venturi device posi ⁇ tioned in said space and having a convergent inlet portion for accelerating the carrier gas and the particles dis ⁇ persed therein, at least one intake opening arranged down- stream of the inlet portion and adapted to supply a pres ⁇ surised flow of liquid, such as water, to the carrier gas and the accelerated particles dispersed therein, and an outlet portion for supplying the carrier gas and the mois ⁇ tened particles dispersed therein to said space.
  • a pres ⁇ surised flow of liquid such as water
  • the Venturi device is preferably formed with a throat having a constant cross-sectional area, i.e. a constant hydraulic inner diameter.
  • the outlet portion of the Venturi device can be divergent in order to retard the carrier gas and the moistened particles dispersed therein before they are supplied to the process gas, and its intake opening can be positioned in the outlet portion, preferably immediately downstream of the throat.
  • the outlet portion of the Venturi device can have a constant cross-sectional area and its intake opening can be formed in the throat, preferably immediately upstream of its outlet portion.
  • the Venturi device preferably is of circular cross- section and is formed with intake openings which can be symmetrically arranged in the inner surface of the diver ⁇ gent outlet portion or in the throat inner surface in a plane perpendicular to the symmetry axis of the Venturi device.
  • Each intake opening preferable forms a mouth of an intake duct whose centre line makes an angle in the range of 10°-80°, especially 45°, with the symmetry axis of the Venturi device.
  • Fig. 1 is a schematic view of a plant for cleaning flue gases from a coal-fired central boiler plant, said flue gas cleaning plant comprising an apparatus according to the present invention.
  • Fig. 2 is a detailed view of a portion of the appa ⁇ ratus in Fig. 1.
  • Fig. 3 is a detailed view of a different embodiment of the portion in Fig. 2.
  • the flue gas formed during the combustion of coal in the central boiler plant 1 shown in Fig. 1 is conducted to an air preheater 2 adapted to transfer heat from the hot flue gas to combustion air which through a duct 2a is sup- plied to the' central boiler plant by means of a fan 3.
  • the flue gas is then, without preceding separation of its fly ash, led through a duct 4 to an elongate tubular reactor 5 in which the flue gas is mixed with an absorbent which is reactive with the gaseous pollutants of the flue gas.
  • the absorbent is supplied to the reactor via a Ven ⁇ turi device 6 positioned in the lower part of the reactor, see Fig. 2 or 3, in the form of fine, moistened particles. The production of these particles will be described fur ⁇ ther down in the specification.
  • the absorbent particles are effectively mixed with the flue gas, the amount of mois ⁇ ture supplied with the particles being evaporated during its contact with the flue gas, at the same time as the gaseous pollutants, such as a sulphur dioxide, of the flue gas react with the particles and are converted into parti ⁇ culate pollutants.
  • the amount of moisture supplied is selected relative to the temperature of the flue gas so that the flue gas is not cooled to a temperature below the saturation temperature, thereby avoiding precipitation of moisture.
  • the velocity of the flue gas does not significantly decrease when conducted into the tubular reactor.
  • the flue gas thus maintains a sufficiently high velocity to entrain also the heavier particles of the particulate pollutants formed during the reaction, the unreacted absorbent particles and the fly ash of the flue gas to an electrostatic precipitator 7 positioned downstream of the tubular reactor.
  • the particles of the flue gas are separated, whereupon the flue gas cleaned of particulate and gaseous pollutants is passed through a duct 8 to a flue gas fan 9.
  • the fan 9 discharges via a duct 10 the cleaned flue gas to a chimney 11 for emission into the atmosphere.
  • the particles which are separated in the precipitator 7 are collected in three dust hoppers 12, 13 and 14 formed in the bottom of the precipitator.
  • the particles collected in the first dust hopper 12, about 90% of the total amount of dust, are supplied via a conduit 15 to a recycling silo 16.
  • the particles collected in the hoppers 13 and 14 are instead conducted via a conduit 17 to a storage silo (not shown).
  • the separated particles which are stored in the recycling silo 16 are, in a conduit 19, mixed with fresh, dry absorbent particles, preferably calcium hydroxide, which are stored in a silo 18.
  • the amount of fresh absor- bent supplied from the silo 18 to the conduit 19 is deter ⁇ mined in conventional manner by the residual emission which is measured in the duct 8 after the precipitator.
  • the amount of recycled absorption material supplied to the conduit 19 is determined according to the amount of fresh absorption material supplied, so that, at a certain load, a constant amount of absorption material is supplied to the tubular reactor 5.
  • a fan or compressor 20 supplies fresh air to the con ⁇ duit 19 at such a pressure, about 0.5 bar, that the air can mix the fresh absorbent particles with the recycled particles and supply these in dispersed form to the Ven ⁇ turi device 6 which is mounted in the upper end of the conduit 19.
  • the Venturi device 6 consists of two circular parts 21 and 22 which are interconnected by means of a nut 23.
  • the first part 21 which is fixedly mounted in the upper end of the conduit 19, comprises a convergent inlet portion 21a having a length which is between 40 and 90 mm, usually about 60 mm, and an inner diameter which is between 40 and 120 mm,, usually about 80 mm, at its upstream end, and a throat portion 21b having a constant inner diameter which is between 20 and 60 mm, usually about 40 mm.
  • the part 22 also comprises a throat portion 22a having the same inner diameter as the throat portion 21b and forming, together with the throat portion 21b, a throat having a length which is between 20 and 40 mm, usually about 30 mm, and a divergent outlet portion 22b having a length which is between 20 and 80 mm, usually about 30 mm, and an inner diameter which is between 30 and 80 mm, usually about 5.0 mm, at its downstream end.
  • the throat portion 22a is formed with a circumferential cavity 24 into which a water conduit 25 opens.
  • the cavity 24 communicates with the interior of the Venturi device by means of four intake ducts 26 whose intake openings 27 are symmetrically arranged in the inner surface of the divergent outlet por- tion 22b immediately downstream of the throat portion 22a.
  • the air and the absorption particles dispersed therein flow into the convergent portion 21a of the Ven ⁇ turi device, the air and, thus, the particles are acce ⁇ lerated to a velocity which is in the range of 70-150 m/s, especially 100 m/s, before it flows into the throat 21b and 22a.
  • the air passes the intake openings 27, it is contacted with a flow of water which is, at a high pres ⁇ sure, about 15 bar, supplied to the interior of the Ven ⁇ turi device via the conduit 25, the cavity 24, the intake ducts 26 and the intake openings 27.
  • the powder form of the absorbent thus is maintained, although the absorbent now contains such an amount of moisture as to have high reactivity.
  • the moistened absorbent particles are then supplied via the divergent outlet portion 22b to the tubular reactor 5, see Fig. 1.
  • the intake ducts are formed in the divergent outlet portion in such manner that their centre lines make an angle of about 45° with the symmetry axis of the Ven ⁇ turi device, see Fig. 2, and since their intake openings are positioned immediately downstream of the throat por ⁇ tion 22a, water is prevented from being sprayed on the inside of the Venturi device and, consequently, no dust is built up thereon.
  • the building-up of dust is also counter- acted by the fly ash which is present in the recycled absorption material and contains aluminium and silicon dioxide which act as abrasives.
  • the Venturi device 6 consists of two circular parts 31 and 32.
  • the first part 31 which is fixedly mounted in the upper end of the con- duit 19 comprises a convergent inlet portion 31a having a length which is between 40 and 90 mm, usually about 60 mm, and an inner diameter which is between 40 and 120 mm, usually about 80 mm, at its upstream end, and a throat portion 31b having a constant inner diameter which is between 20 and 60 mm, usually about 40 mm.
  • the part 32 also comprises a throat portion 32a which has the same inner diameter as the throat portion 31b and forms, together with the throat portion 31b, a throat having a length which is.between 20 and 60 mm, usually about 40 mm, and an outlet portion 32b having a length which is between 1 and 5 mm, usually about 2 mm, and a constant inner dia ⁇ meter which is between 20 and 60 mm, usually about 40 mm.
  • the throat portion 32a is formed with a circumferential -cavity 34 into which a water conduit 35 opens.
  • the cavity 34 communicates with the interior of the Venturi device by means of four intake ducts 36 whose intake openings 37 are symmetrically arranged in the inner surface of the throat portion 32a immediately upstream of the outlet portion 32b. Further the intake ducts are formed in the throat portion 32a in such manner that their centre lines make an angle of about 45° with the symmetry axis of the Venturi device.
  • the parts 31 and 32 are interconnected by means of the left end portion 33 of the part 32, said end portion being formed as an internally threaded sleeve which is fastened on threads made on the outer surfaces of the throat portion 31b and the conduit 19.
  • Venturi device 6 which is shown in Fig. 3 functions in essentially the same manner as the Venturi device in Fig. 2, except that the moistened absor ⁇ bent particles are not retarded in a divergent outlet por ⁇ tion, before being supplied to the tubular reactor 5.
  • the tubular reactor 5 can be provided with several, e.g. four, Venturi devices instead of a single Venturi device. However, they should be arranged on the same level in the reactor, thereby eliminating the risk that they spray dust on each other.
  • the Venturi device 6 can be of rectan- gular cross-section, instead of circular.
  • the reactor can be a large vessle having a ratio of the reactor height/length to the hydraulic dia ⁇ meter in the order of 2-5, instead of an elongate tube having a corresponding ratio in the order of 10-40.
  • the Venturi devices will in this variant be positioned in the upper part of the reactor, instead of in the lower part thereof.
  • the precipitator 7 can be a fabric fil ⁇ ter, such as a bag filter, instead of an electrostatic precipitator.
  • the fresh absorbent can be calcium oxide instead of calcium hydroxide.
  • the flue gas cleaning plant can also be provided with a precipitator positioned upstream of the tubular reactor.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Biomedical Technology (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Treating Waste Gases (AREA)
  • Gas Separation By Absorption (AREA)
EP91900391A 1989-12-05 1990-11-23 Verfahren und vorrichtung zur abgasreinigung Ceased EP0502945A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8904106 1989-12-05
SE8904106A SE466943B (sv) 1989-12-05 1989-12-05 Foerfarande och anordning foer rening av en processgas

Publications (1)

Publication Number Publication Date
EP0502945A1 true EP0502945A1 (de) 1992-09-16

Family

ID=20377696

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91900391A Ceased EP0502945A1 (de) 1989-12-05 1990-11-23 Verfahren und vorrichtung zur abgasreinigung

Country Status (12)

Country Link
EP (1) EP0502945A1 (de)
JP (1) JPH05502617A (de)
KR (1) KR920703185A (de)
CN (1) CN1052261A (de)
AU (1) AU635597B2 (de)
CA (1) CA2070295A1 (de)
FI (1) FI922591A0 (de)
PL (1) PL288082A1 (de)
SE (1) SE466943B (de)
TR (1) TR25007A (de)
WO (1) WO1991008042A1 (de)
YU (1) YU230690A (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT404565B (de) * 1997-06-05 1998-12-28 Scheuch Alois Gmbh Verfahren zur reinigung von schadstoffbelasteten gasen
SE525344C2 (sv) * 2003-06-26 2005-02-08 Alstom Technology Ltd Sätt och anordning för avskiljning av svaveldioxid från en gas
CN100422643C (zh) * 2006-06-23 2008-10-01 杭州新世纪能源环保工程股份有限公司 生活垃圾焚烧炉的烟气净化装置
DE102006060156A1 (de) 2006-12-18 2008-06-19 Evonik Stockhausen Gmbh Wasserabsorbierende Polymergebilde, welche unter Einsatz von Polymerdispersionen hergestellt wurden

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4206186A (en) * 1975-02-06 1980-06-03 Holter Gesellschaft Fur Patentverwertungsverfahren Mbh Refuse pyrolysis
AT363918B (de) * 1975-05-06 1981-09-10 Hoelter Heinz Verfahren und vorrichtung zur gasreinigung
DE3136914A1 (de) * 1981-09-17 1983-03-31 Hölter, Heinz, Dipl.-Ing., 4390 Gladbeck "verfahren zur rauchgasreinigung hinter kraftwerken mit gleichzeitiger herstellung von gips im trockenprozess"
SE452413B (sv) * 1984-12-04 1987-11-30 Flaekt Ab Medieblandande dysa, avsedd att utnyttjas i en kontaktreaktor
FI78401B (fi) * 1985-04-24 1989-04-28 Tampella Oy Ab Foerfarande och anordning foer att bringa roekgasernas gasformiga svavelfoereningar saosom svaveldioxid att reagera till fasta foereningar som separeras fraon roekgaserna.
US4795619A (en) * 1987-03-20 1989-01-03 Lerner Bernard J Removal of acid gases in dry scrubbing of hot gases
DE3803652A1 (de) * 1987-10-01 1989-08-10 Hoelter Heinz Einsatz von alkalisch reagierenden poroesen traegermaterialien zur trockenen schadgasabscheidung unter erhoehung der feuchtigkeit

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9108042A1 *

Also Published As

Publication number Publication date
SE8904106L (sv) 1991-06-06
SE466943B (sv) 1992-05-04
FI922591A (fi) 1992-06-04
TR25007A (tr) 1992-09-01
SE8904106D0 (sv) 1989-12-05
CA2070295A1 (en) 1991-06-06
YU230690A (sh) 1994-05-10
CN1052261A (zh) 1991-06-19
AU635597B2 (en) 1993-03-25
WO1991008042A1 (en) 1991-06-13
JPH05502617A (ja) 1993-05-13
FI922591A0 (fi) 1992-06-04
KR920703185A (ko) 1992-12-17
AU6900591A (en) 1991-06-26
PL288082A1 (en) 1991-12-02

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