SE534269C2 - Method of heating a blast furnace heater for use with a blast furnace - Google Patents
Method of heating a blast furnace heater for use with a blast furnace Download PDFInfo
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- SE534269C2 SE534269C2 SE0950901A SE0950901A SE534269C2 SE 534269 C2 SE534269 C2 SE 534269C2 SE 0950901 A SE0950901 A SE 0950901A SE 0950901 A SE0950901 A SE 0950901A SE 534269 C2 SE534269 C2 SE 534269C2
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- combustion
- oxidant
- fuel
- combustion gases
- stove
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- 238000000034 method Methods 0.000 title claims abstract description 26
- 238000010438 heat treatment Methods 0.000 title claims abstract description 17
- 238000002485 combustion reaction Methods 0.000 claims abstract description 109
- 239000007800 oxidant agent Substances 0.000 claims abstract description 64
- 230000001590 oxidative effect Effects 0.000 claims abstract description 64
- 239000000567 combustion gas Substances 0.000 claims abstract description 59
- 239000000446 fuel Substances 0.000 claims abstract description 56
- 239000001301 oxygen Substances 0.000 claims abstract description 34
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 34
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000011819 refractory material Substances 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 238000007865 diluting Methods 0.000 claims abstract description 4
- 239000007789 gas Substances 0.000 claims description 52
- 238000004064 recycling Methods 0.000 claims description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 14
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 13
- 239000001569 carbon dioxide Substances 0.000 claims description 6
- 239000012298 atmosphere Substances 0.000 claims description 3
- 238000012546 transfer Methods 0.000 claims description 3
- 238000010790 dilution Methods 0.000 claims description 2
- 239000012895 dilution Substances 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 239000000306 component Substances 0.000 claims 2
- 239000000463 material Substances 0.000 abstract description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 10
- 239000003546 flue gas Substances 0.000 description 10
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 5
- 229960004424 carbon dioxide Drugs 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000009471 action Effects 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000002737 fuel gas Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- RVCKCEDKBVEEHL-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzyl alcohol Chemical compound OCC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl RVCKCEDKBVEEHL-UHFFFAOYSA-N 0.000 description 1
- 101100161752 Mus musculus Acot11 gene Proteins 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- OYIKARCXOQLFHF-UHFFFAOYSA-N isoxaflutole Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C1=C(C2CC2)ON=C1 OYIKARCXOQLFHF-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229960003903 oxygen Drugs 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000009628 steelmaking Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B9/00—Stoves for heating the blast in blast furnaces
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
Abstract
23 Abstract Method for heating a blast furnace stove (300,400,500,600) by combusting a fuel with a lower heating value (LHV) of 7,5 MJ/Nm? or less in a combustion zone, arranged in a combustion chamber (30l,40l,50l,60l), in the stove, and causing the combustion gases to flow through and thereby heat refractory(302,402,502,602) material in the stove. The invention is characterized in that the fuel is combusted with an oxidant comprising at least 85% oxygen, and in that combustion gases that have (302,402,502,602) flowed through the refractory material are caused. to be recycled. backinto the combustion zone and thereby diluting the mixture offuel and oxidant therein sufficiently for the combustion to be flameless. H:\DOCWORK\Ansökningstext.doc, 2009-11-26
Description
The present invention relates to a method for heating a blast furnace stove for use with a blast furnace.
The combustion air supplied to a blast furnace is typically preheated using a stove, comprising refractory material which is heated using a burner. When the material is hot enough, combustion air is passed through the stoves to pre-heat it before injection into the blast furnace. Usually, several stoves are operated in parallel and cyclically so that atleast one stove is operated for heating combustion air while the refractory material of at least one stove is heated.
Conventionally, the top gas leaving the blast furnace has atemperature of around llO-l20°C and contains about 20-25% each of CO and CO2. Typically, 3-5% H2 and some H20 will also be present, but the other major constituent of the top gas isN2 (typically 45-57%). The gas constitutes a low grade fuel,having a relatively low heating value, and is commonly used to fuel the stoves.
The top gas is normally combusted using air-fuel burners inthe stoves. In order to ensure the necessary high air blast temperatures needed. by the blast furnace, it is known to enrich the top gas with a high calorific value gas, such ascoke oven gas or natural gas. The combustion of such addi-tional fuel leads to larger overall emissions of carbon dio-xide from the plant, and is therefore not desirable.It is also known to oxygen enrich the combustion air used in stack burners. Usually, the enrichment levels needed to re- duce or eliminate the need for additional, high-calorificfuels are such as to result in a final oxidant oxygen content in the combustion air of around 28-30%.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 Such methods may in some cases render peak flame temperatureshigh enough to damage the refractory material of the stove,and it may be necessary for example to supply an excess airrate to suppress the flame temperature.
It is further known to pre-heat, using heat recovery units, the fuel and air fed to the stove burners.
All the above-described methods add complexity to the process and require costly equipment.
The blast furnace itself is a highly efficient counter-current reactor that has evolved over many years. It is ap-proaching the limits of thermodynamic efficiency, why it is difficult to reduce energy' consumption. relative to current best operating practices. Moreover, the blast furnace and its ancillary equipment, such as stoves, are the largest energy consumers in an integrated iron and steel works. Furthermore, the energy' consumed. in iron making' is the dominant factor determining' the carbon. consumption. of the integrated. steel making process, and therefore the emissions of carbon dio- xide. Therefore, it would be desirable to increase thermal efficiency of blast furnace stoves.Using so-called “carbon capture” techniques, it is possible to separate carbon dioxide from the stove flue gas, in order to lessen emissions. However, such separation is relatively expensive. Therefore, it would be desirable to design a blast furnace stove allowing cheaper carbon capture.
In addition. to the problen1 of high. peak temperatures men-tioned above, too low flame temperatures or heat input rateswill lead to long heating cycles, which is undesirable. In other words, the flame temperature needs to be moderated.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 The present invention solves the above described problems.Thus, the present invention relates to a method for heating ablast furnace stove by combusting a fuel with a lower heating(LHV) of 9 MJ/Nm3 or less i11 a combustion value zone, ar- ranged in a combustion chamber in the stove, and causing thecombustion gases to flow through and thereby heat refractorymaterial in the stove, and is characterized in that the fuelis combusted with an oxidant comprising at least 85% oxygen,and in that combustion gases are caused to be recirculatedinto the combustion zone and thereby diluting the mixture offuel and oxidant therein sufficiently for the combustion tobe flameless.
In the following, the invention will be described in detail,with reference to exemplifying embodiments of the inventionand to the appended drawings, in which:Figure l is a simplified illustration of a blast furnace andthree stoves in a conventional iron works; Figure 2 is a section view illustrating a conventional stoveof a modern type with external combustion chamber; Figure 3 is a section view of a stove with additional lancesaccording to the present invention; Figure 4 is a detail section view of a stove with. an oxyfuelburner according to the present invention; Figure 5 is a section view of a stove with combustion gasrecycling according to the present invention; andFigure 6 is a detail section view of a stove with an ejectorlance according to the present invention. illustrates Figure l the principal arrangement of a blast furnace 120 and three stoves 100 in an iron works. The opera- H:\DOCWORK\Ansökningstext.doc, 2009-11-26 tion of the blast furnace 120 produces blast furnace top gas, which is fed, using a fuel supply control device 110, to eachstove 100 to be used as fuel to heat the stove 100 in ques-tion. The top gas is combusted with an oxidant in the form ofair, which is supplied by an air supply control device 130.
Each stove 100 comprises refractory material in the form ofceramic bricks or the like, which is first heated and thenused to heat blast air which is fed into the blast furnace.When operated in refractory material heating mode (“on gas” mode), the top gas is combusted in the stove 100 with the oxidant, and the combustion gases are fed to a flue gas treatment device 150, possibly including a conventional car-bon capture step.
When operated in blast air heating mode (“on blast” mode),air is led through the refractory material in the oppositedirection, and then on to the blast furnace 120.The stoves 100 are operated cyclically, so that at any pointin time at least one stove is operated on blast and the rest of the stoves are operated on gas.
Figure 2 is a section view through a conventional stove 100of a modern type. The stove 100 comprises an external combus-tion chamber 101, refractory næterial 102 and aa dome 103.When operated on gas, it is critical that the temperature inthe dome 103 does not become too high, since there is then arisk of damage to the stove 100. It is to be understood thatthere are also stoves with internal combustion chambers, andthat the present invention is equally applicable to the oper- ation of such stoves.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 When operated on gas, top gas and air is fed into a combus- tion zone of the combustion chamber 101, in which combustion takes place, via an air burner 108. The burner 108 comprises a fuel inlet 105 and an air inlet 104. The hot combustion gases then stream up through the chamber 101, past the dome103 and. down through. the refractory' material 102, therebyheating the latter. When exiting through the port 106, thetemperature of the combustion gases is conventionally about 200-350°C.
When the refractory material has reached a predetermined temperature, the operation is switched to on blast operation.
Then, air is introduced through the port 106, streams through the hot refractory material 102, via the dome 103 and thecombustion chamber 101, and out through an outlet port 107.At this point, 1100-l200°C. the blast air has a typical temperature of It is preferred, in the context of the present invention, to heat the stove with blast furnace top gas, as described above. It is furthermore preferred. to use top gas from. a blast furnace to which blast air is provided from the stove.This allows for the arrangement of the stove near the blastfurnace, is energy efficient and leads to low total emissionsfrom the plant.
However, it is to be understood that the present inventioncan be equally advantageously applied to stoves heated withother low-grade fuels.
By way of example, typical chemical compositions (percentage values) and lower heating values (LHV) are provided. in Tables I and II, respectively, for blast furnace top gas and converter off-gas.
Table 1 H:\DOCWORK\Ansökningstext.doc, 2009-11-26 N2 02 H2 co c02 cH4 cmHn H20Top gas 52.5 0.55 2.3 23.5 20 - - 1.15Off-gas 17.2 0.1 2.5 64.5 15.6 - - 0.1Table 2LHV (MJ/NHP) LHV (MJ/kg)Top gas 3.2 2.4Off-gas 6.3 8.4 According to the present invention, the stove is heated with a gaseous fuel the LHV value of which is not higher than 9 MJ/Nmê. Use of such low-grade fuel will draw maximum benefit from the possible cost benefits of the present invention. The fuel may comprise a certain addition of another, more high- grade fuel, as long as the LHV value of the mixture is equal to or less than 9 MJ/Nm3. In order to minimize cost and emis- sions, it is however preferred not to add high grade fuels prior to combustion.According to the present invention, such a low-grade fuel isused for heating the stove by combusting it, not with air or slightly oxygen-enriched air, but with an oxidant comprising at least 85% by weight, preferably at least 95% by weight,oxygen, where the oxidant most preferably' is industrially pure oxygen having an oxygen content of essentially 100%.This will increase fuel efficiency, since the nitrogen bal-last present in air does not need to be heated. Moreover, Byreducing the nitrogen ballast in the combustion products, thenecessary flame temperatures can be attained without the needto supplement the low-grade fuel gas with high calorific fuels. The reduced energy demand will facilitate increased H:\DOCWORK\Ansökningstext.doc, 2009-11-26 power* generation. and/or lead. to a reduced. need. for import gas, thus improving fuel management.
Normally, using an oxidant with such large oxygen contents would. lead. to peak temperatures high. enough. to damage the dome and refractory material of the stove.
However, the present inventors have discovered. that it is possible to use this type of oxidant under condition that thestove combustion gases are recirculated into the combustion zone to such. extent that the mixture of fuel and. oxidant therein. is diluted. sufficiently' for the combustion. in the combustion zone to be of the type normally referred to as “flameless”. Herein, a “flameless” combustion denotes a flameless oxidation mode, achieved by the oxidant and fuelgas being' heavily' diluted. with recirculated. exhaust fumesbefore the main part of the combustion process takes place inthe combustion a combustion is achieved zone. In this way, with no visible flame, in other words a flame which is not oralmost not visible to the human eye. Another way to express this is that the combustion reactants are so diluted that the combustion is a “volume type” combustion, without a stableflame.That “combustion gases are recirculated into the combustion zone” herein refers to that combustion gases located outsideof the combustion zone are recirculated back into the combus-tion zone. Such combustion gases may originally be locatedinside the combustion chamber itself, but outside of the partof the combustion chamber occupied by the zone in which com-(the Thus, in bustion mainly takes place “combustion zone”). this case combustion gases are in fact recirculated within the combustion chamber. Alternatively, such combustion gases H:\DOCWORK\Ansökningstext.doc, 2009-11-26 may be recirculated from outside of the combustion chamber back to the combustion zone.
As will be described in further detail in the following, the dilution of the reactants may be achieved either by creating heavy turbulence inside the combustion chamber using high- velocity lancing of oxidant, possibly using a staged combus- tion scheme, and/or the recycling' of flue gases from. the stove back into the combustion zone.
It has been found that, using such flameless combustion with an oxidant with very large oxygen contents, it is possible to achieve sufficiently low peak flame temperatures so as not to damage the stove. Also, sufficiently high flame temperatures are achievable.
Additionally, when a high-oxygen oxidant is used to combust low-grade fuels such as blast furnace top gas, the C02 con- tents of the combustion gases become considerably higher ascompared to when using air or slightly oxygen-enriched air as the oxidant. Since conventional carbon capture techniques tend to be considerably cheaper per unit captured C02 when the treated gas contains a larger share of carbon dioxide, this leads to considerable cost savings when using such a carbon capture step to treat the stove combustion gases.
Figure 3 shows a jpreferred. embodiment of the invention. A stove 300, which is similar to the conventional one 200 shownin figure 2, comprises a combustion chamber 301, a dome 303, refractorymaterial 302, an inlet 304 used for combustionair when the stove is operated in a conventional manner withair combustion, another inlet 305 used. for low-grade fuelsuch as top gas, 207. and ports 306, 307 similar to ports 206, Instead of combusting the low-grade fuel with air, one H:\DOCWORK\Ansökningstext.doc, 2009-11-26 or several lances 310, 311, 312 are inserted into the combus- tion chamber, and are used to supply the above defined high- oxygen oxidant into the combustion zone. The oxidant may be provided by local oxygen production or using an externally provided oxidant.
In all embodiments described. herein, the total amount of oxidant per time unit is balanced against the amount of sup- plied low-grade fuel, so as to create the desired combustion conditions in terms of stoichiometry.
It is preferred that each lance 310, 311, 312 supplies oxi- dant to the combustion zone at high velocity, preferably at least 200 m/s, more preferably at least sonic velocity. Such high-velocity lancing leads to heavy turbulence in the com- bustion chamber, in turn entraining combustion gases into the combustion zone and thereby diluting the flame so as to achieve flameless combustion.
According' to one preferred. embodiment, a lance 310 is ar- ranged with its orifice in close proximity to the orifice of the fuel inlet 305. According to another preferred embodi- ment, a lance 311 is arranged at a position at a distance fron1 the orifice of the fuel inlet 305. Depending' on the geometry of the combustion chamber 301, one of these arrange- ments, or a combination of both, may provide the best recir- culation of combustion gases into the combustion zone. A arranged further downstream in rela- 311, supplementary lance 312,tion to the other lance or lance 310, can be used toprovide a staged combustion process, whereby the total flamemore than one 311, 312 may be volume can be made even larger. Naturally,lance of each of the described types 310,arranged. to complement each. other. In case the oxidant is lanced in close proximity to the fuel inlet 305, it is pre- H:\DOCWORK\Ansökningstext.doc, 2009-11-26 ferred. to also lance oxidant further downstrean1 so as tocreate a staged combustion process.an overview Figure 4 is illustration. of another* preferred embodiment, in which a blast furnace stove 400 comprises acombustion chamber 401, 406. refractory material 402 and a port Low grade fuel is supplied via a supply conduit 411, a supply device 412 and an inlet 413. Oxidant is supplied via a supply conduit 414, a supply device 415 and a lance comprising an orifice 416. The lance is arranged so that its orifice 416 is arranged adjacent to the fuel inlet 413. Preferably, the lance runs coaxially to the fuel inlet 413, as depicted in figure 6. By such an adjacent arrangement, especially when coaxial, and. when the oxidant is lanced. at the above de- scribed. high. velocities, the fuel is efficiently' entrained into the combustion zone by ejector action on the part of theAs a result, high velocity oxidant. heavy recirculation of combustion. products is achieved. in the combustion chamber 401, in particular recirculating combustion gases into the combustion zone expanding the flame front. When such a high-velocity lance is arranged adjacent to the fuel inlet 413, itis preferred to simultaneously use a secondary oxidant lance312, providing part of the totally supplied oxygen at anotherlocation in the combustion chamber 401 downstream of the fuelinlet 413, creating a staged combustion of the low-grade fueland thereby facilitating the achievement of a flameless com-bustion.
According to a very preferred embodiment, an existing, con- ventional, air burner, which was used to heat the existing stove 400 previously, is in an initial step replaced by an oxyfuel burner 410 comprising the above described fuel inlet H:\DOCWORK\Ansökningstext.doc, 2009-11-26 11413 and oxidant lance. An “oxyfuel” burner herein refers to a burner driven with a fuel and an oxidant, wherein the oxidant comprises a large part oxygen, preferably at least 85% oxy-gen, more preferably at least 95% oxygen.According to an alternative, very preferred embodiment, the existing air burner described above is, in an initial step,supplemented with one or several high-velocity oxidant lances as described above, and the air supply is terminated.
As described above, such high velocity lancing yields heavy turbulence inside the combustion chamber 301, 401, leading toa flameless combustion and hence sufficiently low peak flame temperatures.
However, the mass flow rate of the combustion gases will belower when using a high-oxygen oxidant as compared to whenusing air as the oxidant. This will lead to smaller convec-tive heat transfer to the refractory material and hence long-Therefore, er heating cycle times. when converting an exist- ing stove for high-oxygen oxidant operation, it is preferredto recycle flue gases from the stove back into the combustion zone as described below in connection to figures 5 and 6.
Thus, figure 5 ii; an overview illustration of za stove 500 according to another preferred embodiment, comprising a com- bustion chamber 501, refractory material 502 and a dome 503.
During on gas operation, the combustion gases leave the stove 500 through a port 506. However, part of the combustion gases are recycled back to the combustion zone in the combustionchamber 501 via a recycling device 511. The feedback device 511 may include a propelling device, such as a fan, to feed the recycled combustion gas to the combustion chamber 501.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 12 The recycling device 511 is also arranged to mix the recycledcombustion gas with a high-oxygen oxidant of a composition asThe mix- described above, provided via a supply conduit 512. ing may take place using conventional diffusers. The mixtureof recycled combustion gas and oxidant is then supplied tothe combustion chamber 501 via an inlet 513. fuel, A. low-grade such as top gas, is provided, via a supply conduit 514, a supply device 515 and an inlet 516. In the combustion zone,the fuel is hence combusted with the oxidant in the presenceof the combustion gases that have been recycled. into thecombustion zone after they have already past the stove 500.This way, the flame in the combustion chamber 501 is diluted.Using such flue gas recycling, it has been found that it ispossible to reach convective heat transfer rates high enoughso as to be able to nmintain the heating cycle time of anexisting stove in which a næthod according to the presentinvention is applied. This is achieved by recycling a suffi-cient amount of combustion gases to maintain the gas mass orthermal energy flow per time unit through the stove 500, at alevel which is at least the same as the gas mass or thermalenergy flow per time unit which was used when the existingstove was operated, prior to conversion to operation accord-ing to the present invention, using a low-oxygen oxidant withno recycling.This involves balancing' the amount of recycled. combustiongases to the provided amount of low-grade fuel and oxidantper time unit. Table 3 illustrates an example of such a bal- ance, in which a first mode of operation, in which coke oven gas enriched. blast furnace top gas is combusted. with. air, without recycling, is described and compared to a correspond- ing second mode of operation, in which industrially' pure H:\DOCWORK\Ansökningstext.doc, 2009-11-26 13 oxygen is used as the oxidant and a certain amount of recy-cling is introduced in accordance to the present invention.As can be seen from Table 3, the flame temperature and gasmass flow through the refractory material 502 of the stove500 are maintained at essentially the same level when apply-ing the inventive method, at the same time as the combustion heat is reduced.
Table 3 a s M % ß'^ \ 0 bi -lJ Gå w V n E 3m Ü O G) GE V w H > O^ z H Q w Ug V H n H H wG) \ E (U -IJ A U EU M \ m w m s E > n ~O E m IU .Cl H O -v-l O v-lE ë å °" q 8 G 5 33 8 8E V n ^ o E mo 3 w g -H w m x m ^ m m'I'| O (Û > \ -U -U (D V (U 'G (U A (UH H m o M m m m \ m g mm m m E n w E w M \H w å E > w E w M ww H m x m m o n z n E n AQ-a -v-l O O N O v-l IU -lJ v-l V v-l Z v-l dPo 4 H 0 o o E o m E. V E ~V m ~VConventional 48502 40408 4045 0 208 1448 1988 O 86567 23J. reC C eW th l 0 60222 0 8538 194 1372 1939 21345 60991 43In the “conventional” operation mode of Table 3, four stoves are operated in order to deliver 195000 Nm?/h of blast air at a. temperature of 1125°C. To heat this volume of air from ambient temperature requires 308 GJ of energy per hour, pro- vided by having two stoves *on blast'. Hence, the overall (energy in blast air)/(heat ofis 308/(2°208) stove efficiency, defined as combustion supplied to stoves), or about 74%.
Some of this inefficiency' is associated. with. the flue gas sensible heat.
The recycle device 511 is arranged to recycle enough combus-tion gases so as to render the combustion in the combustionzone flameless by lowering the oxygen concentration in the combustion chamber 501.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 14 In order to render the combustion. in the combustion zone flameless, it has been found that a total oxygen percentageby volume of not more than about 12%, preferably not morethan 10%, of the inert part of the atmosphere in the combus-tion chamber 501, not counting the fuel components combustion gases, will effectively yield a flameless combustion. There- fore, it is preferred. that a sufficiently' large amount ofcombustion gases is recycled to yield a continuous concentra-tion of oxygen in the combustion chamber 501 which is equal to or lower than this percentage.
Since all oxidant is supplied to the combustion chamber 501and. possibly' through. one or 312, via the recycling' device 511 several oxidant lances 310, 311, the amount of oxygen supplied per time unit is known. Hence, one may calculate theamount of combustion gases to recycle per time unit in orderto reach the above described, sufficiently low, oxygen con- centrations. concentration of 11% is 1/0.11 - 1 2 In the example of Table 3, an 02 desired, why for each unit volume O2, 8.1 units of inert gas is needed. For each volume unit top gas sup- plied, about 0.14 volume units of Og, in the form of an oxi- dant comprised of industrially pure oxygen, is supplied inorder to achieve the desired. Lambda of about 1.125. Thismeans that about 1/0.14 2 7.1 units of fuel is supplied foreach unit of oxygen. Since about 75% by volume of top gas isconstituted of inert gases, and keeping the decimal precision from previous calculation steps, each volume unit O2 in thecombustion chamber 501 is already diluted with about 7.1*0.75ß 5.4 units of inert gas only by providing the top gas fuel.In other words, an extra 8.1-5.4 = 2.7 units of inert gas in the form of combustion gas recycling will be needed per unit H:\DOCWORK\Ansökningstext.doc, 2009-11-26 lanced 02 into the combustion chamber 501. This means that atleast about 38% of the combustion gases should be recircu- lated in order to reach a maximum 02 concentration of 11%. concentration in which The corresponding' example reaching ll% (Lthe combustion chamber using converter off-gas as fuel,off-gas requires 0.33 volume units of 02 per volume unit off-gas and contains 1/3 per volume only about inert gases, yields a required. admixture of at least 7.1 volume unitscombustion gases per unit volume lanced 02, or a flue gasrecirculation of at least about 234%.
According to one preferred embodiment, all of the oxidant ispremixed with the recycled combustion gases before enteringthe combustion zone. However, additional oxidant may also besupplied through one or more lances in the combustion chamber501. In this case, it is the total amount of supplied oxygenper time unit which must be used as the basis for calculationof the amount of recycled combustion gases.
Moreover, as can be deduced from the figures given in Table3, the heat supplied by combustion can be reduced by some 7%,flow rate and while essentially' maintaining the gas mass flame temperature. It has been found that by operating the stoves in an integrated. iron and. steel works according' to this example, with flameless oxyfuel and capturing of the C02from the flue gas, it is possible to reduce the emissionsfrom the plant by around 20%.
According to a preferred embodiment, enough combustion gasesare recycled to essentially maintain or increase the gas mass flow per time unit through the refractory material.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 16 According to an alternative preferred embodiment, enough combustion gases are recycled to essentially maintain or increase the thermal energy throughput through the refractory material. This takes into consideration. the different heat capacities for various inert components in the combustion gases. In this case, it is also preferred that enough combus- tion gases are recycled. so that the flame temperature is essentially maintained or decreased.
As is also shown in Table 3, the C02 contents of the fluegases vented. fronl the stove 500 are much. higher* - 43% as compared to 23% in the conventional operation mode. The costs per unit weight captured C02 for conventional carbon capture techniques is significantly decreased as the C02 concentra- tion increases from low levels up to a level of roughly 50-60%. Concentrations increased beyond this limit will provide smaller gains. As a result, the costs for a carbon capturestep for treating the stove flue gases may be reduced signif-icantly per unit weight captured C02 when a high-oxygen oxi- dant is used in accordance with the present invention.
According to a very preferred embodiment, an existing, con- ventional, air burner, which was used to heat the existing stove 500 previously, is in an initialfuel 513, step replaced by ainlet 516 and. an inlet for recycled. combustion. gasesand the fuel is then combusted with the above describedhigh oxygen oxidant. To this end, it is preferred that theoxidant is submitted by premixing with the recycled combus-tion gases. It is alternatively preferred that such premixingis combined with one or several lances as described above. an overview Figure 6 is illustration. of another* preferred embodiment of the present invention, showing a blast furnace stove 600 with a combustion chamber 601, refractory material H:\DOCWORK\Ansökningstext.doc, 2009-11-26 17 602, a port 606, a conduit for recycled combustion gases 610, a recycle device 611, a fuel supply' conduit 616, a fuel supply device 617 and a fuel inlet 618.
Oxidant is supplied via an oxidant supply conduit 613 and anoxidant supply device 614 to an oxidant lance arranged sothat the orifice 615 of the lance is arranged adjacent to anorifice 612 for supply of recycled combustion gases, supplied from the recycle device 611. Preferably, the oxidant lanceruns coaxially with the recycled combustion gas inlet 612. Ina way which is similar to the function of the coaxial lancesuch an effi- orifice 416 as described in connection to figure 4, adjacent arrangement, especially when coaxial, willciently entrain the recycled combustion gases into the com-bustion zone by ejector action on the part of the high veloc-recirculation in ity' oxidant, creating' more combustion. gas the combustion chamber 601. At the same time, there is noneed for a separate propelling device in the recycling device611, since the recycled combustion gases will be propelled by the ejector action at the orifice 615.
The embodiment shown in figure 6 is advantageously combinedwith an additional oxidant lance, providing additional oxi-dant at a location in the combustion zone located at a dis-tance from the orifice 615, thereby achieving a staged com-bustion in the combustion zone.
As indicated. above, it is furthermore preferred that the400, 500, 450, stove 300, 600 is connected to a respective carbon capture step 350, 550, 650, which may be conventional per se, separating the carbon dioxide contents of the combus-tion gases vented from the stove before the combustion gases are released into the environment.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26 l8 When the age of a blast furnace stove approaches its expecteduseful life, it is preferred to apply one of the herein de-scribed embodiments, or a combination of several of them, tothe stove. the useful life of the This way, stove may' be prolonged, operating it with lower flame temperatures, with maintainedproduction rates in terms of blast air, better fuel economyand lower emissions.
Thus, a method according to the present invention will allowa blast furnace stove to be operated only on a low grade fuelsuch as blast furnace top gas, with no need for higher calo- rific value fuel enrichment and no risk for temperature- induced. stove damage, while producing' flue gases that are better suited for carbon capture. In addition, it allows the useful life of a stove to be prolonged.
If sufficient recycling of combustion gases is used, it isalso possible to achieve the same amount and quality of blastin. an existing stove vflUxfl1 is converted, air according to what has been. described. above, for* operation. witri a high-oxygen oxidant, and which stove is provided with the combus- tion gas recycling arrangement described. in connection to figure 5 or 6.
Above, preferred embodiments have been described. However, itis apparent to the skilled person that many modifications maybe made to the described embodiments without departing fromthe idea of the present invention.
For example, any one of the methods for creating recircula-tion of combustion gases as described in connection to fig- ures 4-6 may advantageously be supplemented with one or sev- H:\DOCWORK\Ansökningstext.doc, 2009-11-26 l9 eral of the various oxidant lances as described in connectionto figure 3.
Moreover, the ejector-propelled recirculated combustion gasesmethod as described in connection to figure 6 may advanta-geously' be premixed. with a certain amount of high-oxygenoxidant in a way similar to the one described in connectionto figure 5.
Also, the ejector-propelling' of pre-mixed. or non-pre-mixedrecycled combustion gases as described in connection to fig-ure 6 may advantageously be combined with ejector-propellingof low-grade fuel as described in connection to figure 4. the Thus, invention. shall not be limited. to the described embodiments, but may be varied within the scope of the ap- pended claims.
H:\DOCWORK\Ansökningstext.doc, 2009-11-26
Claims (13)
1. l. Method(300,400,500,600) for heating a blast furnace stove by combusting a fuel with a lower heating value (LHV) of 9 MJ/Nm3 or less in a combustion zone, ar-ranged in a combustion chamber (30l,40l,50l,60l), in thestove, and causing the combustion gases to flow through andthereby heat refractory material (302,402,502,602) in thestove, c h a r a c t e r i z e d i n 'that the fuel is com-busted with an oxidant comprising at least 85% oxygen, and in that combustion gases that have flowed through the refractory material (302,402,502,602) are caused. to be recycled. back into the combustion zone and thereby diluting the mixture offuel and oxidant therein sufficiently for the combustion to be flameless.
2. Method according to claim l, c h a r a c t e r i z e d i n that the recycled. combustion gases are premixed. with said oxidant before entering the combustion zone.
3. Method according to claim 2, c h a r a c t e r i z e d i n that all of said oxidant is supplied via such premixing with the combustion gases.
4. Method according to claim 2, c h a r a c t e r i z e d i n that some oxidant is supplied. via such. premixing' via combustion gases, and that additional oxidant is also pro- vided at high velocity through a lance (3lO,3ll,3l2), thereby entraining combustion gases into the combustion zone to achieve additional dilution of the flame.
5. Method according to any one of the preceding claims, c h a r a c t e r i z e d i n that enough combustion gases are recycled for the total oxygen percentage by volume of the inert part of the atmosphere in the combustion chamber H:\DOCWORK\Ansökningstext.doc, 2009-11-26 21 (301,401,501,601), not counting the non-inert fuel compo- nents, is equal to or less than 12%.
6. Method according to claim 5, c h a r a c t e r i z e d i n that enough combustion gases are recycled for the totaloxygen percentage by volume of the inert part of the atmos-phere in the combustion chamber (301,401,501,601), not count-ing the non-inert fuel components, 10%. is equal to or less than
7. Method according to any one of the preceding claims, c h a r a c t e r i z e d i n that the «oxidant. comprises at least 95% oxygen.
8. Method according to any one of the preceding claims, c h a r a c t e r i z e d i n that the fuel is blast furnace top gas.
9. Method according to claim 8, c h a r a c t e r i z e d i n that the blast furnace top gas is taken from a blast furnace which is with hot stove (300,400,500,600). supplied air by the
10. Method according to any of the preceding claims, c h a - r a c t e r i z e d i n in a (400) that an existing' air burnerstove(516)that the fuel is then combusted with said oxidant. in an initial step is replaced by a fuel inlet and an inlet for recycled combustion gases (513), and
11. Method according to claim. 10, c h a r a c t e r i z e di n that enough combustion gases are recycled to nwintainthe gas mass flow per time unit through the refractory ma-terial (302,402,502,602) at a level which. is at least thesame as the gas mass flow per time unit which was used when the existing air burner was operated without recycling. H:\DOCWORK\Ansökningstext.doc, 2009-11-26 22
12. Method according to claim. 10, c h a r a c t e r i z e d i n that enough combustion gases are recycled to nwintainthe flame temperature at a level which is the same or lower,the and. a thermal energy transfer to (302,402,502,602) refractory' materialat a level which is the same or higher, asthe flame temperature and the thermal energy throughput pertime unit, respectively, which was used when the existing air burner was operated without recycling.
13. Method according to any one of the preceding claims, c h a r a c t e r i z e d i n that the carbon dioxide contentstove is (350,450,550,650), of the combustion. gases fronl the separated. in a subsequent separation step which is con-ventional per se, before the combustion gases are released into the environment. H:\DOCWORK\Ansökningstext.doc, 2009-11-26
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0950901A SE534269C2 (en) | 2009-11-26 | 2009-11-26 | Method of heating a blast furnace heater for use with a blast furnace |
| PCT/SE2010/051301 WO2011065907A1 (en) | 2009-11-26 | 2010-11-25 | Method for heatng a blast furnace stove |
| EP10833669.4A EP2513345B1 (en) | 2009-11-26 | 2010-11-25 | Method for heatng a blast furnace stove |
| CN201710137440.5A CN107090530A (en) | 2009-11-26 | 2010-11-25 | The method of heating furnace hot-blast stove |
| ES10833669.4T ES2567784T3 (en) | 2009-11-26 | 2010-11-25 | Method for heating a blast furnace stove |
| AU2010325221A AU2010325221B2 (en) | 2009-11-26 | 2010-11-25 | Method for heating a blast furnace stove |
| BR112012012675-0A BR112012012675A2 (en) | 2009-11-26 | 2010-11-25 | method for heating a blast furnace air heater |
| JP2012541054A JP5717754B2 (en) | 2009-11-26 | 2010-11-25 | How to heat a blast furnace hot stove |
| US13/510,108 US9896735B2 (en) | 2009-11-26 | 2010-11-25 | Method for heating a blast furnace stove |
| RU2012126542/02A RU2548552C2 (en) | 2009-11-26 | 2010-11-25 | Method of heating of blast-furnace air heater |
| PL10833669T PL2513345T3 (en) | 2009-11-26 | 2010-11-25 | Method for heatng a blast furnace stove |
| KR1020127016527A KR101706053B1 (en) | 2009-11-26 | 2010-11-25 | Method for heating a blast furnace stove |
| CN2010800537613A CN102770564A (en) | 2009-11-26 | 2010-11-25 | Method for heating blast furnace hot blast stove |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0950901A SE534269C2 (en) | 2009-11-26 | 2009-11-26 | Method of heating a blast furnace heater for use with a blast furnace |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE0950901A1 SE0950901A1 (en) | 2011-05-27 |
| SE534269C2 true SE534269C2 (en) | 2011-06-21 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE0950901A SE534269C2 (en) | 2009-11-26 | 2009-11-26 | Method of heating a blast furnace heater for use with a blast furnace |
Country Status (1)
| Country | Link |
|---|---|
| SE (1) | SE534269C2 (en) |
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2009
- 2009-11-26 SE SE0950901A patent/SE534269C2/en unknown
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| Publication number | Publication date |
|---|---|
| SE0950901A1 (en) | 2011-05-27 |
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