EP0421979A1 - Procédé pour diminuer l'émission du soufre dans des procédés de frittage - Google Patents
Procédé pour diminuer l'émission du soufre dans des procédés de frittage Download PDFInfo
- Publication number
- EP0421979A1 EP0421979A1 EP90890268A EP90890268A EP0421979A1 EP 0421979 A1 EP0421979 A1 EP 0421979A1 EP 90890268 A EP90890268 A EP 90890268A EP 90890268 A EP90890268 A EP 90890268A EP 0421979 A1 EP0421979 A1 EP 0421979A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- coke
- sulfur
- slurry
- lime
- sintered
- 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.)
- Granted
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/16—Sintering; Agglomerating
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
- C10L9/00—Treating solid fuels to improve their combustion
- C10L9/10—Treating solid fuels to improve their combustion by using additives
Definitions
- the invention relates to a method for reducing pollutant emissions in thermal processes, such as in particular sintering processes, in which a fuel-containing mixture, in particular a coke bed, is ignited.
- EP-A1 39 305 has already disclosed a method for reducing pollutant emissions during sintering, in which an extraneous rust coating is applied as an intermediate layer between the raw sintered layer and the sintered grate.
- the proposed intermediate layer consists of granular material which should be able to remove pollutants. This granular sorbent material is moistened for significant pollutant emissions, with particularly large effects being achieved with basic slurries or liquids. Lime milk was preferably given as the basic slurry, a correspondingly larger volume of sulfur-containing waste products being formed in addition to the coke ash.
- the invention now aims to provide a method of the type mentioned, in which, without increasing the amount of materials to be handled, enriched with pollutants, a reduction in pollutant emissions, in particular an almost complete desulphurization of the exhaust gases can be achieved without expensive flue gas desulfurization.
- the invention consists in essential in that the pore-rich fuel fraction, especially the coke, of the mixture is rolled with Ca (OH) 2 or soaked with a slurry of hydrated lime before the fuel-containing mixture is given up.
- the process according to the invention is preferably carried out in such a way that, based on the amount of coke, 5-30% by weight Ca (OH) 2, preferably 10-25% by weight, are used in dry form and the coke is rolled together with the hydrated lime .
- Ca (OH) 2 preferably 10-25% by weight
- an almost unchanged ignition temperature of the coke could be maintained in the case of rolling coke with dry lime hydrate, with the treatment of dried coke with a lime hydrate slurry in the stated proportions by weight lowering the ignition temperature by 40-45 ° C was observed.
- Such a lower ignition temperature had a higher reak activity and led to particularly good sulfur incorporation in the ashes.
- a slurry of Ca (OH) 2 is preferably used in 1 to 3 parts by weight of water per part by weight of Ca (OH) 2.
- slurries with one part by weight of Ca (OH) 2 and one part by weight of H2O as well as slurries with one part by weight of Ca (OH) 2 and three parts by weight of H2O resulted in a particularly strong reduction in the ignition temperature, whereas a treatment of coke with a slurry from one part by weight of Ca (OH) 2 to two parts by weight of H2O still resulted in a lowering of the ignition temperature by about 35 ° C.
- Sinter coke is primarily used for such sintering purposes, as mentioned above, and in the process according to the invention it is preferred to use sinter coke in a grain size of 0.5-5 mm, preferably 1 to 3 mm.
- the sintered coke to be used is dried before rolling or before treatment with the hydrated lime slurry, temperatures around 100 ° C. appearing particularly suitable as drying temperatures.
- a high level of sulfur incorporation can be achieved with the least use of foreign material in that the hydrated lime slurry in an amount of 20-50, preferably 25 to 50 wt .-%, based on coke, is used.
- the sulfur incorporation could be further optimized by controlling the process temperatures and, according to a preferred procedure, the sintering temperatures are kept low.
- a sample of the coke mixed with lime sludge or hydrated lime was placed in a retort and heated in a tube furnace with air supply at a heating rate of approx. 5 ° C./min.
- the exhaust gas composition was continuously measured during the heating phase.
- the ignition point of the sample mixtures was characterized by a significantly faster rise in the sample temperature and the beginning of CO2 development.
- the ignition temperatures of the individual samples were 450 ° C. in the case of example 1, 455 ° C. in the case of example 2 and 450 ° C. in the case of example 3.
- the ignition temperature of the sample of Example 4 was not determined and that of Example 5 was 495 ° C.
- the ignition temperature of the untreated coke with a grain size of 1 to 3 mm is 490 ° C.
- the sintered coke samples pretreated according to Examples 1 to 5 were subjected to ashing.
- the ashing was carried out at three different temperatures, namely 900 ° C, 1000 ° C and 1100 ° C.
- the incorporation of sulfur into the ashes was created here a sulfur analysis before and after ashing.
- the results of the sulfur incorporation in the ashes are shown in Figure 1, which is a block diagram of the sulfur incorporation in the ashes.
- the percent sulfur incorporation is shown on the ordinate and on the abscissa, arranged side by side, the results of the three ashing tests carried out in each case with untreated coke and with the sintered coke breeze treated with hydrated lime.
- a particularly high sulfur incorporation value in the ash namely 96.5%, was achieved by ashing the sintered coke pretreated according to Example 2 at 900 ° C.
- the values of the sulfur incorporation at the ashing temperatures 1000 and 1100 ° C. were approximately in the range obtained for the ashing of the mixtures according to Example 1 and Example 3.
- the largest percentage of sulfur incorporation is achieved at the lowest incineration temperature and the relatively lowest percentage of sulfur incorporation can be achieved at the highest incineration temperature.
- the percentages of sulfur incorporation in the sinter coke pretreated according to the invention are at least four times as high as those which could be achieved in the ashing of untreated coke.
- the sulfur emission via sintered exhaust gases depends on the sulfur content of the sintered coke. This sulfur burns primarily to SO2. A reduction in SO2 formation is theoretically possible through a sulfidic bond in the sinter itself.
- the temporary setting of the coke sulfur in the sinter reduces the SO2 emissions through the sintered exhaust gas and helps to comply with or fall below the prescribed emission values.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Geochemistry & Mineralogy (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Metallurgy (AREA)
- Geology (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Combustion & Propulsion (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Treatment Of Sludge (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT2315/89A AT393095B (de) | 1989-10-06 | 1989-10-06 | Verfahren zum verringern der schwefelemission bei sinterprozessen |
| AT2315/89 | 1989-10-06 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0421979A1 true EP0421979A1 (fr) | 1991-04-10 |
| EP0421979B1 EP0421979B1 (fr) | 1994-03-30 |
Family
ID=3532090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP90890268A Expired - Lifetime EP0421979B1 (fr) | 1989-10-06 | 1990-10-05 | Procédé pour diminuer l'émission du soufre dans des procédés de frittage |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5116588A (fr) |
| EP (1) | EP0421979B1 (fr) |
| JP (1) | JPH03192194A (fr) |
| KR (1) | KR910008151A (fr) |
| AT (1) | AT393095B (fr) |
| DE (1) | DE59005179D1 (fr) |
| ES (1) | ES2053170T3 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0526446A3 (en) * | 1991-06-28 | 1993-04-07 | Voest-Alpine Stahl Donawitz Gmbh | Process for reducing harmful emissions in sintering processes |
| EP0992594A1 (fr) * | 1998-10-08 | 2000-04-12 | Sidmar N.V. | Procédé de réduction des émissions de dioxines et de furanes par les installations d'agglomération de minerais de fer |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100321621B1 (ko) * | 1997-12-27 | 2002-05-13 | 이구택 | 질소산화물및황산화물을저감할수있는소결광제조방법 |
| US20060127599A1 (en) * | 2002-02-12 | 2006-06-15 | Wojak Gregory J | Process and apparatus for preparing a diamond substance |
| AU2005262871B2 (en) * | 2004-06-28 | 2011-06-09 | Douglas C. Comrie | Reducing sulfur gas emissions resulting from the burning of carbonaceous fuels |
| JP5617766B2 (ja) * | 2011-06-08 | 2014-11-05 | 新日鐵住金株式会社 | 炭材の改質処理設備 |
| JP5598439B2 (ja) * | 2011-07-20 | 2014-10-01 | 新日鐵住金株式会社 | 焼結鉱の製造方法 |
| JP5810836B2 (ja) * | 2011-10-28 | 2015-11-11 | 新日鐵住金株式会社 | 焼結鉱製造用の改質炭材の製造方法 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2154955A1 (de) * | 1971-11-05 | 1973-05-17 | Rheinische Braunkohlenw Ag | Verfahren und vorrichtung zur anwendung von feinkoernigen brennstoffen, insbesondere feinkoernigen braunkohlenkoksen, fuer die sinterung, insbesondere von eisenerzen |
| DE2501503A1 (de) * | 1975-01-16 | 1976-07-22 | Ruhrkohle Ag | Verfahren zur entschwefelung der abgase von wirbelbettfeuerungen |
| EP0039305A1 (fr) * | 1980-04-25 | 1981-11-04 | MANNESMANN Aktiengesellschaft | Procédé pour réduire l'émission de polluants pendant l'agglomération par frittage |
| DE3635206A1 (de) * | 1986-10-16 | 1988-04-21 | Westfaelische Berggewerkschaft | Verfahren zur verfeuerung fossiler festbrennstoffe unter entwicklung von rauchgasen mit herabgesetztem schwefelgehalt |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19591C (de) * | 1900-01-01 | Dr. TH. OPPLER in Doos bei Nürnberg | Verfahren zur Absorption von gas- und dampfförmigen Säuren durch Briquettes | |
| DE234059C (fr) * | ||||
| DE131959C (fr) * | ||||
| US4093451A (en) * | 1977-09-28 | 1978-06-06 | Cardd, Inc. | Coke agglomerate and method of utilizing same |
| DE3131959A1 (de) * | 1981-08-13 | 1983-02-24 | Johann Schaefer Kalkwerke, 6252 Diez | "verfahren zur herstellung einer homogenen mischung aus feinteiligem kalkhydrat und feuchter kohle" |
| JPS5876728A (ja) * | 1981-10-31 | 1983-05-09 | Tokyo Electric Co Ltd | ロ−ドセル式台秤 |
| DD234059A1 (de) * | 1985-01-18 | 1986-03-19 | Buna Chem Werke Veb | Verfahren zur entgiftung der rauchgase von feuerungsanlagen |
| SE457014B (sv) * | 1987-03-25 | 1988-11-21 | Abb Stal Ab | Saett att foerbaettra utnyttjningen av svavelabsorbent vid foerbraenning i en fluidiserad baedd och en kraftanlaeggning med foerbraenning i fluidiserad baedd |
-
1989
- 1989-10-06 AT AT2315/89A patent/AT393095B/de not_active IP Right Cessation
-
1990
- 1990-10-01 US US07/591,096 patent/US5116588A/en not_active Expired - Fee Related
- 1990-10-05 DE DE90890268T patent/DE59005179D1/de not_active Expired - Fee Related
- 1990-10-05 ES ES90890268T patent/ES2053170T3/es not_active Expired - Lifetime
- 1990-10-05 JP JP2268252A patent/JPH03192194A/ja active Pending
- 1990-10-05 EP EP90890268A patent/EP0421979B1/fr not_active Expired - Lifetime
- 1990-10-06 KR KR1019900015961A patent/KR910008151A/ko not_active Withdrawn
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2154955A1 (de) * | 1971-11-05 | 1973-05-17 | Rheinische Braunkohlenw Ag | Verfahren und vorrichtung zur anwendung von feinkoernigen brennstoffen, insbesondere feinkoernigen braunkohlenkoksen, fuer die sinterung, insbesondere von eisenerzen |
| DE2501503A1 (de) * | 1975-01-16 | 1976-07-22 | Ruhrkohle Ag | Verfahren zur entschwefelung der abgase von wirbelbettfeuerungen |
| EP0039305A1 (fr) * | 1980-04-25 | 1981-11-04 | MANNESMANN Aktiengesellschaft | Procédé pour réduire l'émission de polluants pendant l'agglomération par frittage |
| DE3635206A1 (de) * | 1986-10-16 | 1988-04-21 | Westfaelische Berggewerkschaft | Verfahren zur verfeuerung fossiler festbrennstoffe unter entwicklung von rauchgasen mit herabgesetztem schwefelgehalt |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0526446A3 (en) * | 1991-06-28 | 1993-04-07 | Voest-Alpine Stahl Donawitz Gmbh | Process for reducing harmful emissions in sintering processes |
| EP0992594A1 (fr) * | 1998-10-08 | 2000-04-12 | Sidmar N.V. | Procédé de réduction des émissions de dioxines et de furanes par les installations d'agglomération de minerais de fer |
Also Published As
| Publication number | Publication date |
|---|---|
| US5116588A (en) | 1992-05-26 |
| ES2053170T3 (es) | 1994-07-16 |
| JPH03192194A (ja) | 1991-08-22 |
| AT393095B (de) | 1991-08-12 |
| DE59005179D1 (de) | 1994-05-05 |
| KR910008151A (ko) | 1991-05-30 |
| EP0421979B1 (fr) | 1994-03-30 |
| ATA231589A (de) | 1991-01-15 |
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