GB2121700A - Decontamination of combustion gases in fluidized bed - Google Patents

Decontamination of combustion gases in fluidized bed Download PDF

Info

Publication number
GB2121700A
GB2121700A GB08216492A GB8216492A GB2121700A GB 2121700 A GB2121700 A GB 2121700A GB 08216492 A GB08216492 A GB 08216492A GB 8216492 A GB8216492 A GB 8216492A GB 2121700 A GB2121700 A GB 2121700A
Authority
GB
United Kingdom
Prior art keywords
sorbent
sulfur
fluidized bed
contact zone
pollutants
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.)
Withdrawn
Application number
GB08216492A
Inventor
Albert M Leon
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.)
Dorr Oliver Inc
Original Assignee
Dorr Oliver Inc
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 Dorr Oliver Inc filed Critical Dorr Oliver Inc
Priority to GB08216492A priority Critical patent/GB2121700A/en
Publication of GB2121700A publication Critical patent/GB2121700A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01FCOMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
    • C01F11/00Compounds of calcium, strontium, or barium
    • C01F11/46Sulfates
    • C01F11/464Sulfates of Ca from gases containing sulfur oxides
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Analytical Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Treating Waste Gases (AREA)
  • Fluidized-Bed Combustion And Resonant Combustion (AREA)

Abstract

Atmospheric pollutants such as sulphur and sulphur dioxide are removed from an exhaust gas stream (14) (such as that produced in a fluidized bed combustion system (10)) by providing a fluidized bed (30) of particulate sorbent material, e.g. limestone and/or dolomite, wherein countercurrent contacting between upwardly directed combustion gases and descending sorbent particulate material creates a concentration gradient across the vertical extent of the bed giving a progressively decreasing concentration of pollutants such as sulphur and sulphur dioxide upwards and a decreasing concentration of sorbent, e.g. calcium oxide, downwards. <IMAGE>

Description

SPECIFICATION Decontamination of combustion gases in fluidized bed incinerators The invention relates to the in-situ treatment of noxious, gaseous, combustion products produced within a fluidized bed combustion system to effectively remove sulfur-containing atmospheric pollutants (i.e. sulfur dioxide) therefrom.
Fluidized bed combustion systems are recognized as providing highly effective means for generating heat. As such, they are industrially applied to a variety of unit operations ranging from the generation of hot gases for the extraction of sensible heat therefrom to the incineration of combustible sewage sludge and oil refinery wastes. In the operation of such incineration systems, air is passed through a gas distribution or constriction plate to fluidize inert bed particles supported by such plate. After raising the bed temperature to a predetermined level, fuel is injected into the bed and ignited to raise the temperature to the operating range. Thereupon, the sewage, oil refinery waste stream or the like is introduced to the bed and undergoes combustion with the evolution of substantial quantities of heat.Heat generation may be sufficient to eliminate any further necessity for auxiliary fuel.
So called "clean" fuels as typified by natural gas and No. 2 fuel oil, are becoming increasingly more costly to the extent of becoming economically prohibitive. Cheaper fuel, as typified by high sulfur coal, high sulfur residual oil (Bunker C, No. 6, for example) containing generally about 1/2% by weight or more of sulfur, are proposed alternatives. However, though feasible from both operational and economic standpoints, their use entails the possible risk of environmental pollution since SO, and similarly noxious sulfur containing materials resulting from the combustion of fuel or waste material would be emitted with the incinerator stack gases. Emission of such pollutants may, in fact, violate governmental regulations thereby invoking possible civil and/or criminal sanctions.
Generally, the removal of sulfur pollutants produced as described is attempted by the use of sorbents such as calcium carbonate (limestone), calacium oxide (lime), and dolomite either as the bed material as described in U.S. Patent No. 3,982,901 or as a pre-added material introduced at some stage prior to incineration. In either case the sulfur material reacts with the sorbent material, for example limestone to form the salt, CaSO4, and is removed as such from the incineration unit. In accordance with current technology, as exemplified by the foregoing patents, essentially homogeneous bed systems are achieved. Due to significant back mixing, the distribution of the limestone, lime and/or dolomite sorbent, as well as pollutant gases, is relatively uniform throughout the contact zone defined by the fluidized bed.In such systems, even though employing a countercurrent mode of contacting bed material and pollutant gases, discriminatory contacting between bed particles and pollutants can neither be predetermined nor controlled. Thus, substantially spent and thus ineffective limestone may contact a sulfur atmosphere at or near the freeboard side of the contact zone thereby resulting in the discharge of sulfur pollutant to the atmosphere through the incinerator stack. In addition, any possible in-situ calcination of limestone to CaO, the latter being generally recognized to be the more effective sulfur sorbent, most probably occurs undesirably in an 502 rich atmosphere. A separate precalcination unit is required unless the more expensive CaO is used in the first instance as the bed material.
In any event, processing of the aforedescribed type, to be effective, requires the use of relatively large amounts of sorbent.
According to the present invention there is provided a process for removing sulfur, sulfur dioxide and like atmospheric pollutants from a gaseous stream produced by the incineration of one or more combustible feed materials containing molecular and/or combined sulfur comprising, passing said stream upwardly through a high temperature contact zone defined by a fluidized bed of countercurrent, descending sorbent particulate material capable of combining at the high temperature with said pollutants to provide a solid adduct, the opposed points of entry of said sorbent particulate and combustible feed materials respectively being such that said sorbent and combustion products of said combustible feed materials traverse at least about 90% of the vertical extent of said contact zone and wherein concentration gradients are maintained vertically.
Back-mixing is minimized by maintaining a sufficiently large height-diameter ratio of said contact zone, i.e. greater than about 5:1.
An embodiment of the invention will now be described, by way of an example, with reference to the accompanying drawings, in which Figure 1 is a schematic illustration of an embodiment of the invention, and Figure 2 is a schematic illustration indicating generally a concentration gradient obtained in accordance with an embodiment of the invention.
In the accompanying drawings, like reference numerals designate similar parts in each of the figures. Reference numeral 10 generally designates a fluidized bed combustion unit in which the process of the invention can be carried out. In general, the combustion unit 10 comprises an outer shell 12 having an exhaust gas outlet 14 provided in a roof portion 16, which outlet 14 communicates with a reactive chamber 18 of the combustion unit 10. In general, the outer shell 12 is of steel construction and is provided, internally, with a refractory lining (not shown). A conical wall 20 forms the bottom of the combustion unit 10 and is provided with a clean out port 22. An air inlet 24, such as a blower unit, supplies fluidizing gas to a windbox 26 preferably through headers (not shown).A horizontat constriction or perforate plate 28, which may be provided with tuyeres (not shown) as is known in the art, horizontally divides the combustion unit 10 into the reaction chamber portion 18 and the windbox portion 26. Constriction plate 28 is capable of supporting a fluidized bed 30, the latter defining a sorbent gas contact zone. As illustrated, reaction chamber 18 comprises the fluidized bed contact zone 30 and a freeboard zone 32. One or a plurality of fuel feeds 34 and sorbent feeds 36 are disposed about the periphery of the combustion unit 10 (usually of generally cylindrical shape) and communicate directly with the reaction chamber 18. Fuel feed(s) 34 may be such as to deliver solid, liquid and/or gas material as well as any additional air which may be necessary to support combustion. An underflow 38 enables withdrawal of solid materials from the reaction chamber 18.Apparatus useful herein of the type described is well known in the art and in this regard reference is made to the fluidized bed incinerator described in, for example, U.S. Patent No.
4,1 68,670, the relevant portions of which are incorporated herein by reference. As will be made clear hereinafter, the described apparatus may be further modified in accordance with prior art reachings to enhance particular aspects and obtain specific advantages.
It is essential that the fluidized bed 30 not be fully back-mixed by maintaining a height diameter ratio in excess of about 5:1. These parameters, height and diameter, are indicated by designations H s D, respectively in Fig. 1. The utilization of diameter is appropriate since the combustion unit 10 will generally be approximately cylindrical in shape. In accordance with the invention, it is found that vertical back mixing of the upwardly-flowing pollutant gases and descending sorbent particles is minimized when maintaining a fluidized bed within the stated height-dimater ratio. "Back-mixing" as used herein refers essentially to the tendency of the sorbent particles to undergo haphazard flow.The consequent "teetering" effect results in a random, relatively disoriented, distribution of the particles throughout the contact zone 30 with the establishment of secondary flowpaths often directly opposed to the primary flow direction. In effect then, many of the particles "back-up". This phenomenon is undersired since there is no assurance that sulfur-poor atmospheres in the proximity of a freeboard boundary 44 of fluidized bed 30 will necessarily contact fresh sorbent material, the latter being the ideal situation.
In the present invention, back-mixing is minimized since the countercurrent streams undergo essentially laminar flow. In this manner and as illustrated in Fig. 2, relatively uniform concentration gradients are established across the fluidized bed 30 having a direction coincident with the vertical axis of combustion unit 10. As indicated by a directional arrow 42, SO2 concentration decreases while CO2 concentration increases as the pollutant gas stream proceeds upwardly through the fluidized bed 30. On the other hand, the CaO concentration decreases while CaSO4 concentration increases in the downward direction through the fluidized bed 30 as indicated by a directional arrow 40.Accordingly, progressively decreasing sulfur atmospheres encounter progressively increasing CaO concentration regions assuring contact between sorbent bed particles having maximum sorbency and gaseous atmospheres having reduced sulfur concentrations at or near the freeboard boundary 44 of fluidized bed 30.
The temperature maintained across fluidized bed 30 may vary within ranges customarily used in such incineration processes as is well known. The temperature selected should enable substantial calcination of limestone occurring under the conditions described. As is evident from Fig. 2, in-situ calcination of limestone is desirably achieved in the relatively sulfur-poor atmosphere extant in the region of freeboard boundary 44. This is highly conducive to rapid and efficient calcination. In effect, the calcination conditions are in all essential aspects similar to those which would prevail, were a separate calcination unit used. The present invention thus obviates any necessity for a separate pre-calcination unit.
This is an important advantage over prior art techniques wherein it is often necessary to use calcined limestone as the feed material to the combustion unit. Moreover, relatively less particulate sobent material is needed herein since, as previously described, the "freshest" sorbent is available where the sulfur, sulfur dioxide, etc. concentration levels are at their lowest within fluidized bed 30.
The fule and sorbent materials are fed to the combustion unit 10 at or near the respective lower and upper boundaries of fluidized bed 30. The points of entry are selected to insure that the sorbent feed material and consequent combustion bases traverse at least about 90% of the height H of fluidized bed 30 to insure effective resuls. Reduction of the H:D ratio below the minimum value stated materially increases the likelihood of backmixing and disruption of the aforementioned concentration gradients. Compliance with the hereinbefore stated parameters is thus esential in order to maximize operational efficacy.
The sorbent bed materials suitable for use herein are refractory particulate substances, well known in the art and include e.g. limestone and/or dolomite. The particle size and bulk density of these materials as commercially supplied are standard in the art for fluidized bed use. Generally, the particle size of the sorbent material is such that preferred particles have a diameter of less than about 1/8 inch.
In accordance with the instant process, air is admitted at inlet 24 to windbox 26 at a temperature of generally up to 650 F at a velocity sufficient to fluidize the sorbent particles. The fluidized bed 30 is preferably composed of limestone or dolomoite as described.
Crushed coal containing sulfur is injected into fluidized bed 30 through fuel feeds 34. The coal is ignited in the fluidized bed 30 which reaches a controlled temperature of about 1600 F generating a stream of gaseous sulfur oxidation products such as SO2. These products proceed upwardly as indicated by directional arrow 42 in Fig. 2. Particulate sorbent is fed, preferably continuously, through sorbent feeds 36 to replenish that withdrawn from the underflow 38 primarily as CaSO4.
Formation of the latter occurs as follows. At the high bed temperature the limestone, or more accurately, CaO, having a high surface area due to its relatively fine state of subdivision and pore structure, readily reacts with the sulfur pollutants to form CaSO4 according to the following equation: CaO + SO2 + 0.502#CaSO4 It is generally advisable to provide an excess of CaO over the theroretical CaO requirement for neutralization of the sulfur-containing pollutants. The product calcium sulfate after removal from combustion unit 10 may be reheated by suitable means (not shown) to drive off SO, as the initial step in the production of sulfuric acid and the resultant CaO reclaimed for recycle to fluidized bed 30.The combustion gases from which the sulfur containing pollutants have been substantially, that is effectively removed, are discharged to the atmosphere through exhaust gas outlet 14 in essentially non-polluting form. Generally, the sulfur content of gases discharged to the atmosphere is substantially less, in terms of volume per cubic foot of discharged gas, than the minimum limits imposed by environmental regulations.
In operation, it is observed that a substantial portion of the feed limestone is effectively calcined during the initial phase of its descent through the contact zone 30, that is after tranversing but a relatively minor portion of its vertical path. This occurs inherently under the operating conditions prescribed herein.
The aforedescribed embodiment can be used to burn high sulfur coal as a fuel to generate hot gases capable, for example, of driving a gas turbine which, in turn, drives a generator which produces electric power. Effective reduction of sulfur gases is important here also since such gases are highly corrosive to turbine blades.
In yet another application of the invention, combustible sludge and oil refinery wastes can be effectively incinerated. These can be added to combustion unit 10 along with the fuel feed or separately introduced as desired.
In many instances, refuse to be incinerated likewise contains appreciable quantities of sulfur. The instant process is particularly effective with respect thereto.
Thus, the present invention enables the feasible use of high sulfur fuels in a wide variety of operations capable of implementation utilizing a fluidized bed combustion unit.
By virtue of the instant process, savings are attributable not only to the use of less costly fuel but additionally to such other aspects as enhanced efficiency of sorbent use and inherent calcination as discussed.
The process can be effectively carried out with apparatus incorporating, for example, the heat exchange means described in U.S. Patent No. 3,982,901. Generally, a given apparatus is suitable provided it be equipped as generaly described herein. The particular type of means used for delivering fuel, be it liquid or solid, particulate sorbent, refuse and the like, to the combustion unit as well as for withdrawing gaseous and solid combustion and other products, are largely optional and in any event are described in detail in the relevant prior art.
Furthemore, although the present invention has been described with particular reference to preferred embodiments, it will be apparent to those skilled in the art that variations and modification may occur to one skilled in the art without departing from the scope of the invention as defined in the appended claims.

Claims (7)

1. A process for removing sulfur, sulfur dioxide and like atmospheric pollutants from a gaseous stream produced by the incineration of one or more combustible feed materials containing molecular and/or combined sulfur comprising, passing said stream upwardly through a high temperature contact zone defined by a fluidized bed of countercurrent, descending sorbent particulate material capable of combining at the high temperature with said pollutants to provide a solid adduct, the opposed points of entry of said sorbent particulate and combustible feed materials respectively being such that said sorbent and combustion products of said combustible feed materials traverse at least about 90% of the vertical extent of said contact zone and wherein concentration gradients are maintained vertically.
2. A process as claimed in claim 1, in which the temperature of said contact zone during incineration is about 1600 F.
3. A process as claimed in claim 1 or claim 2, in which the bulk density of said sorbent particular material has a diameter of less than about 1/8 inch.
4. A process as claimed in any preceding claim, in which said sorbent particulate material is limestone and/or dolomite.
5. A process as claimed in any preceding claim, in which said combustible feed material is bituminous coal.
6. A process as claimed in claim 4, in which substantial calcination of said limestone occurs in the upper portion of said contact zone in an atmosphere having a low concentration of contaminant sulfur material.
7. A process for effectively removing sulfur, sulfur dioxide and like atmospheric pollutants from a gaseous stream, substantially as hereinbefore described with reference to the accompanying drawings.
GB08216492A 1982-06-07 1982-06-07 Decontamination of combustion gases in fluidized bed Withdrawn GB2121700A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB08216492A GB2121700A (en) 1982-06-07 1982-06-07 Decontamination of combustion gases in fluidized bed

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB08216492A GB2121700A (en) 1982-06-07 1982-06-07 Decontamination of combustion gases in fluidized bed

Publications (1)

Publication Number Publication Date
GB2121700A true GB2121700A (en) 1984-01-04

Family

ID=10530870

Family Applications (1)

Application Number Title Priority Date Filing Date
GB08216492A Withdrawn GB2121700A (en) 1982-06-07 1982-06-07 Decontamination of combustion gases in fluidized bed

Country Status (1)

Country Link
GB (1) GB2121700A (en)

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB596258A (en) * 1945-07-25 1947-12-31 Michael Henry Miller Arnold Improvements in and relating to the maintenance of beds of particulate solids at predetermined levels
GB2034448A (en) * 1978-11-11 1980-06-04 Ishikawajima Harima Heavy Ind Fluidised bed combustion furnace or reactor
EP0027398A1 (en) * 1979-10-08 1981-04-22 Air Industrie Process and installation for the treatment of a gas by contacting a stream of this gas with particles of solid matter
GB1600258A (en) * 1977-01-03 1981-10-14 Wormser Eng Inc Burning and desulphurizing coal
GB2074890A (en) * 1979-04-20 1981-11-11 Wormser Eng Inc Fluidized Bed Combustors

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB596258A (en) * 1945-07-25 1947-12-31 Michael Henry Miller Arnold Improvements in and relating to the maintenance of beds of particulate solids at predetermined levels
GB1600258A (en) * 1977-01-03 1981-10-14 Wormser Eng Inc Burning and desulphurizing coal
GB2034448A (en) * 1978-11-11 1980-06-04 Ishikawajima Harima Heavy Ind Fluidised bed combustion furnace or reactor
GB2074890A (en) * 1979-04-20 1981-11-11 Wormser Eng Inc Fluidized Bed Combustors
EP0027398A1 (en) * 1979-10-08 1981-04-22 Air Industrie Process and installation for the treatment of a gas by contacting a stream of this gas with particles of solid matter

Similar Documents

Publication Publication Date Title
JP2657896B2 (en) Fluid bed reactor and combustion method
SU1258334A3 (en) Method of chemical treatment of fuel in pseudoliquefied layer
US4346064A (en) Decontamination of combustion gases in fluidized bed incinerators
CA1254367A (en) Process of removing pollutants from flue gas
US4670237A (en) Process of removing pollutants from exhaust gases
US3625164A (en) Combustion of high-sulfur coal in a fluidized bed reactor
JPH0318923B2 (en)
IE52546B1 (en) Process of simultaneously producing fuel gas and process heat from carbonaceous materials
US4359005A (en) Fluidized bed incineration of waste
RU2139473C1 (en) Method of treatment of solid residues after burning sulfur-containing fuel and device for realization of this method
CA1096708A (en) Char separator
EP0021558A1 (en) Method and apparatus for removing sulfur dioxide from gas
CA1065193A (en) Low pollution incineration of solid waste
US3745207A (en) Process for the recovery of waste pickle liquor
EP0294024B1 (en) Process for removing nitrous oxides from a gas
US3904549A (en) Fluidized bed regeneration of powdered activated carbon
US5625119A (en) Method for treating sludge and soil contaminated with hydrocarbons
US5092929A (en) Process of treating residues obtained by purification of exhaust gas
GB2121700A (en) Decontamination of combustion gases in fluidized bed
US5551357A (en) Method and system for recycling sorbent in a fluidized bed combustor
JPH10267221A (en) Desulfurization method of exhaust gas of fluidized bed furnace
US4741890A (en) Gas scrubbing method
US3864458A (en) Fluid bed incineration of chloride-containing waste streams
JPH10194800A (en) Reduction of nox in cement kiln exhaust gas
CN113332851A (en) Moving bed dry flue gas desulfurization method

Legal Events

Date Code Title Description
WAP Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1)