SK915086A3 - Removal method of harmful substances from waste gases - Google Patents
Removal method of harmful substances from waste gases Download PDFInfo
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- SK915086A3 SK915086A3 SK9150-86A SK915086A SK915086A3 SK 915086 A3 SK915086 A3 SK 915086A3 SK 915086 A SK915086 A SK 915086A SK 915086 A3 SK915086 A3 SK 915086A3
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- fluidized bed
- solids
- sorbent
- waste gases
- waste gas
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- 238000000034 method Methods 0.000 title claims abstract description 19
- 239000002912 waste gas Substances 0.000 title claims description 29
- 239000000126 substance Substances 0.000 title description 4
- 239000007787 solid Substances 0.000 claims abstract description 26
- 239000004568 cement Substances 0.000 claims abstract description 18
- 239000002594 sorbent Substances 0.000 claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 claims abstract description 13
- 239000007789 gas Substances 0.000 claims abstract description 8
- 238000002485 combustion reaction Methods 0.000 claims abstract description 7
- 238000012545 processing Methods 0.000 claims abstract description 5
- 239000004575 stone Substances 0.000 claims abstract description 5
- 239000003344 environmental pollutant Substances 0.000 claims description 14
- 231100000719 pollutant Toxicity 0.000 claims description 14
- 239000000843 powder Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- 239000002689 soil Substances 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 3
- 235000019738 Limestone Nutrition 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 239000006028 limestone Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims 1
- 235000011941 Tilia x europaea Nutrition 0.000 claims 1
- 235000010216 calcium carbonate Nutrition 0.000 claims 1
- ZQNPDAVSHFGLIQ-UHFFFAOYSA-N calcium;hydrate Chemical compound O.[Ca] ZQNPDAVSHFGLIQ-UHFFFAOYSA-N 0.000 claims 1
- 239000002737 fuel gas Substances 0.000 claims 1
- 239000004571 lime Substances 0.000 claims 1
- 238000011144 upstream manufacturing Methods 0.000 claims 1
- 239000002245 particle Substances 0.000 abstract description 6
- 238000004064 recycling Methods 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 14
- 239000000428 dust Substances 0.000 description 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 229910001385 heavy metal Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 235000011116 calcium hydroxide Nutrition 0.000 description 2
- 238000006477 desulfuration reaction Methods 0.000 description 2
- 230000023556 desulfurization Effects 0.000 description 2
- 238000005108 dry cleaning Methods 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 230000005405 multipole Effects 0.000 description 2
- 238000005200 wet scrubbing Methods 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 238000012994 industrial processing Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/50—Sulfur oxides
- B01D53/508—Sulfur oxides by treating the gases with solids
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Biomedical Technology (AREA)
- Analytical Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treating Waste Gases (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Processing Of Solid Wastes (AREA)
- Gas Separation By Absorption (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
Abstract
Description
Spôsob odstraňovania škodlivín z odpadných plynovMethod of removing pollutants from waste gases
Oblasť technikyTechnical field
Vynález sa týka spôsobu suchého odstraňovania škodlivín, ako oxidu siričitého, kyseliny chlorovodíkovej, chlóru, fluorovodíka a ťažkých kovov, z odpadných plynov priemyslu spracovávajúceho kameň a zeminu.The invention relates to a method for dry removal of pollutants such as sulfur dioxide, hydrochloric acid, chlorine, hydrogen fluoride and heavy metals from the waste gases of the stone and soil processing industry.
Doterajší stav technikyBACKGROUND OF THE INVENTION
Pri použití známych spôsobov čistenia za mokra sa odpadne plyny, obvykle po odstránení prachu, spracovávajú kvapalinou vedenou v okruhu a pri tom sa ochladia do tej miery, že je nevyhnutné ich opäť na teplotu prevyšujúcu asi o 20 °C teplotu tavenia, aby sa zabránilo poškodeniu v dôsledku korózie. Odpadajúce množstvo reakčných produktov je spravidla rovnako príliš velké, než ako by bolo možné celé toto množstvo vracať späť do výrobného procesu. Spôsoby čistenia za mokra sú preto najčastejšie spojené s vysokými nákladmi na zariadenie a prevádzku, ktoré často bránia plynulej reakcii čistenia odpadných plynov.Using known wet scrubbing processes, the gases, usually after dust removal, are treated with the liquid circulating in the circuit and cooled to the extent that they are again necessary to a temperature in excess of about 20 ° C to prevent damage due to corrosion. The dropping amount of reaction products is generally as much too large as it would be possible to return the entire amount to the production process. Therefore, wet scrubbing processes are most often associated with high equipment and operating costs, which often hinder a continuous waste gas treatment reaction.
Pri výrobe cementu sa už tiež robili pokusy čistiť odpadné plyny pri teplote 300 až 850 °C za sucha. Pri tom vyšlo ale na javo, že odpadné plyny obsahujú pri teplotách nad 500 °C často menej ako 100 mg/Nm3 oxidu siričitého SO2, ktorý tu stojí v popredí škodlivín, lebo najväčšia časť síry zavedenej do výrobného procesu spolu s palivom sa absorbuje surovým cementovým práškom a je viazaná v slinku.In the manufacture of cement, attempts have already been made to purify the waste gases at a temperature of 300 to 850 ° C in the dry state. However, it has become clear that, at temperatures above 500 ° C, the waste gases often contain less than 100 mg / Nm 3 of SO 2 , which is at the forefront of the pollutants, since most of the sulfur introduced into the production process together with the fuel is absorbed. raw cement powder and bound in clinker.
Takéto priaznivé pomery sa ale pri iných spalovacích procesoch pri priemyselnom spracovaní kameňa a zemín nevyskytujú. Tam sa musia, skôr ako síra obsiahnutá v palive, odstraňovať iné škodliviny, ako chloridy a fluoridy, z odpadných plynov, pričom vlastný produkt tu nevykazuje žiadnu schopnosť absorbovať škodliviny, ktorá by stála za zmienku.However, such favorable ratios do not occur in other combustion processes in the industrial processing of stone and soil. There, pollutants other than chlorides and fluorides must be removed from the waste gases, rather than the sulfur contained in the fuel, and the product itself does not have any worth mentioning ability to absorb.
Pri procese výroby cementu sa síra ale tiež znáša do spalovacieho procesu surovinovým práškom. Táto síra pochádza zčasti z organických prípadne sulfidických zlúčenín síry, ktoré sa už pri nízkych teplotách rozpadajú a vedú behom predohrievania k uvolňovaniu oxidu siričitého S02 , pričom obsahy oxidu siričitého môžu dosiahnuť až 6000 mg/Nm3. V dôsledku toho, že pri procese výroby cementu, pri obvyklých teplotách odpadných plynov nedochádza prakticky k žiadnej sorpcii oxidu siričitého SO2 surovým materiálom, musia sa aj cementárne vybaviť zariadaním na odsírenie odpadných plynov, aj keď je síra zanesená spolu s palivom, v závislosti na postupe je v odpadných plynoch obsiahnutá len v minimálnom množstve.In the cement production process, however, sulfur is also carried into the combustion process by the raw powder. The sulfur is derived in part from organic sulphide or sulfur compounds to be at low temperatures disintegrate during the preheating and result in the release of sulfur dioxide S0 2, wherein the content of sulfur dioxide may be up to 6000 mg / Nm3. As a result, the the process of the cement, the usual temperatures of the waste gases there virtually no uptake of sulfur dioxide SO2 raw material, it must be the cement plant provided with zariadaním desulfurization waste gases, while the sulfur is clogged with the fuel, depending on the The process is only contained in the waste gases in a minimal amount.
Čistenie za sucha pri teplotách 200 až 400 °C je nezávislé na použitom sorbentu a nezávislé na pomere sorbentu k množstvu škodliviny,ale nie je tiež príliš účinné. Obyčajne je možné odstrániť len menej ako 60 % škodlivín z odpadného plynu, pokiaí sa ale nechce prejsť k drahým a s ohladom na najčastejšie sa vyskytujúcu vysokú prašnosť, len za určitých podmienok prevádzkovo bezpečným spôsobom čistenia pomocouDry cleaning at 200 to 400 ° C is independent of the sorbent used and independent of the sorbent to pollutant ratio, but is also not very effective. Usually, only less than 60% of the pollutants can be removed from the waste gas, but unless they want to switch to expensive and high dust levels, the only way to do this is to use an operationally safe method of cleaning under certain conditions.
Tým je teda daná úloha navrhnúť spôsob odstraňovania škodlivín z odpadných plynov spalovacích procesov priemyselného spracovania kameňa a zemín, ktorý by bol všeobecne použitelný a ekonomickejší ako doteraz známe spôsoby.Thus, it is an object of the present invention to provide a process for the removal of pollutants from the waste gases of the combustion processes of industrial stone and soil processing, which is generally applicable and more economical than the known methods.
katalyzátorov.catalysts.
Podstata vynálezuSUMMARY OF THE INVENTION
S prekvapením sa zistilo, že je možné tento ciel dosiahnúť, ak sa odpadné plyny privedú pri 50 až 100 °C vo fluidnom reaktore do styku so sorbentom pozostávajúcim z delia z prúdu pevných čiastíc, pevné častice sa odplynu a vrátia sa späť do fluidného reaktora, ako sorbent sa použije surový cementový prášok, vápenec s obsahom viac ako 90 % uhličitanu vápenatého CaCO^, pálené vápno, hydratované vápno alebo čiastočne kalcinovaný surovinový prášok a do okruhu sa kontinuálne pridáva nový sorpčný prostriedok a z okruhu sa vynáša vyčerpaný sorpčný prostriedok.Surprisingly, it has been found that this objective can be achieved if the waste gases are brought into contact with a sorbent consisting of a stream of solid particles at 50 to 100 ° C in a fluidized bed reactor, the solid particles are degassed and returned to the fluidized bed reactor, As a sorbent, a raw cement powder, limestone containing more than 90% calcium carbonate CaCO 2, quicklime, hydrated lime or partially calcined raw powder is used and a new sorbent is continuously added to the circuit and the spent sorbent is discharged from the circuit.
S výhodou sa odpadné plyny pred vstupom do fluidného reaktora ochladzujú na 50 až 100 °C. Alternatívne sa môžu odpadné plyny ochladzovať aj vo fluidnom reaktore na 50 až 100 °C vstrekovaním vody. Okrem toho sa pamätá na to, aby sa teplota vo fluidnom reaktore a prídavok sorpčného prostriedku regulovali v závislosti na obsahu škodlivín v čistom plyne. Ďalšou výhodou spôsobu je, že sa sorpčné prostriedky vynášané z okruhu môžu bez ďalšieho vracať do proce3 su výroby cementu. S výhodou sa častice pevných látok oddelujú v klasicky pracujúcom odlučovači pevných látok, najmä viacpólovom elektrofiltri, z prúdu plynu, pričom sa jemne zrnitý podiel pevných látok, obohatený ťažkými kovmi, vynáša a používa sa ako prísada hotového cementového slinku.Preferably, the waste gases are cooled to 50-100 ° C prior to entering the fluidized bed reactor. Alternatively, the waste gases may also be cooled to 50-100 ° C in a fluidized bed reactor by water injection. In addition, it is remembered that the temperature in the fluidized bed reactor and the addition of sorbent are controlled depending on the pollutant content of the pure gas. A further advantage of the process is that the sorbents discharged from the circuit can be recycled to the cement production process without further delay. Preferably, the solid particles are separated from the gas stream in a conventionally operating solids separator, in particular a multipole electrofilter, whereby the finely divided solids enriched with heavy metals are discharged and used as an additive of ready-made cement clinker.
Pomocou spôsobu podlá vynálezu sa môžu nielen lubovolne predĺžiť doby styku, ktoré sú často pri iných spôsoboch čistenia za sucha pri dolnom rozsahu teplôt príliš krátke, ale získa sa aj produkt, ktorý nevyžaduje žiadne zvláštne cťalšie spracovanie alebo deponovanie, čím je často zaťažená ekonomičnosť doterajších spôsobov.With the method according to the invention, not only can the contact times, which are often too short for other dry cleaning processes at the lower temperature range, be prolonged arbitrarily, but also a product that does not require any particular further processing or depositing is obtained. .
Prehlad obrázkov na výkresochOverview of the drawings
Ďalšie podrobnosti sú vysvetlené pomocou prí kladu odsírenia odpadných plynov cementu a pomocou schématu spôsobu dnodušene na obr. 1.Further details are explained by way of an example of the desulfurization of cement waste gases and by way of a method diagram in FIG. First
z procesu výroby znázorneného zjePríklady prevedenia vynálezuThe manufacturing process illustrated in the Examples
Cirkulačný systém pre pevnú látku, pozostávajúci z fluidného reaktora 1, odlučovača 2 pevných látok a zo spätného vedenia 3 sa zásobuje cez vedenie 4 vodou na rozprašovanie, cez vedenie 5 sorpčnými prostriedkami a cez vedenie 7 odpadným plynom, ktorý sa má odsíriť. Maximálne odsírený odpadný plyn opúšťa hore fluidný reaktor 1, zbaví sa v odlučovači 2 na pevné látky prachu a dostáva sa cez dúchacie zariadenie 8 a vedenie 9 do komína. Pod odlučovačom 2 pevných látok je usporiadané dopravné zariadenie, pomocou ktorého sa oddelený prach dopravuje ku spätnému vedeniu 3 a konečne sa opäť privádza do fliudného reaktora 1. Časť množstva cirkulujúcich pevných častíc sa cez vedenie 7 vynáša z cirkulačného systému na pevné látky a na vhodnom mieste sa privádza do výroby cementu.The solids circulating system, consisting of the fluidized bed reactor 1, the solids separator 2 and the return line 3, is supplied with water for atomisation, through the line 5 with sorption means and through the line 7 with the waste gas to be desulfurized. The maximum desulphurized waste gas exits the fluidized bed reactor 1, is freed from dust in the solids separator 2 and enters the stack through the blower device 8 and the line 9. A conveyor device is arranged below the solids separator 2, by means of which the separated dust is conveyed to the return line 3 and finally fed back to the fluidized bed reactor 1. Part of the quantity of circulating solids is discharged through the line 7 to the solids at a suitable location. is fed to cement production.
Jednotlivé zložky obsiahnuté v zostatkovej látke, napríklad ťažké kovy, sa môžu po selektívnom odlúčení od ostatných látok vyniesť cez vedenie 10. Odpadné plyny odchádzajú s teplotou 100 až 450 °C, vždy podlá toho či a ktoré zariadenia na spätné získanie tepla sú usporiadané (kotol na odpadné teplo, príprava teplej vody, mlyn). V prípade, že plyny nie sú vedené cez mlyn, je ich obsah prachu 100 g/Nm3.The components contained in the residual substance, for example heavy metals, can be discharged via line 10 after selective separation from the other substances. The waste gases leave at a temperature of 100 to 450 ° C, depending on whether and which heat recovery equipment is arranged (boiler). for waste heat, hot water preparation, mill). If the gases are not passed through the mill, their dust content is 100 g / Nm 3 .
V posledne uvedenom byť až 1000 g/Nm3 a bežne prach pomocou prípade môže zaťaženie prachom môže mať zmysel odstrániť pred elektrofiltra alebo mechanického odlučovača, aby bolo možné obmedziť cirkuláciu pev ných látok v cirkulačnom systéme na pevné látky na také množstvo, ktoré je optimálne na odsírenie.In the latter, up to 1000 g / Nm 3, and normally dust by case, the dust load may make sense to remove the electrofilter or mechanical separator in order to limit the circulation of solids in the circulation system to solids to an amount that is optimal for desulphurisation.
Prípadne je tiež možné v takýchto prípadoch celkom alebo zčasti upustiť od zvláštneho prídavku sorbčných prostriedkov. Obsah prachu v odpadných plynoch sa redukuje v odlučovači 2 pevných látok na množstvo nižšie ako 50 mg/Nm3.It is also possible, in such cases, to dispense wholly or in part with the special addition of sorbents. The dust content of the waste gases is reduced in the solids separator 2 to an amount of less than 50 mg / Nm 3 .
Obsah oxidu siričitého S02 v odpadnom plyne je v závislosti na zložení surového materiálu až 6000 mg/Nm3. Tento sa môže v čistom plyne znížiť spôsobom podía vynálezu až na hodnotu nižšiu ako 50 mg/Nm3. Prípustné množstvá oxidu siricitého sa podía zákonných predpisov pohybujú v Nemecku okolo 400 mg/Nm3, vo Švajčiarsku okolo 500 mg/Nm3.The sulfur dioxide content of the SO 2 in the waste gas is up to 6000 mg / Nm 3 , depending on the composition of the raw material. This can be reduced in the pure gas by the process according to the invention up to a value of less than 50 mg / Nm 3 . The permissible amount of sulfur dioxide according to the statutory regulations in Germany range of about 400 mg / Nm 3, Switzerland about 500 mg / Nm3.
Ďalšia prednosť spôsobu spočíva v tom, že sa na zlepšenie hospodárnosti môžu pri spalovacích procesoch používať aj také palivá, ktoré obsahujú ťažké kovy, vrátane škodlivín I. triedy, ako kadmium, tálium, ortuť alebo podobne. Tieto škodliviny sa vo fluidnom reaktore 1 viažu prevažne na zvlášť jemnozrnné častice a môžu sa v klasicky pracujúcom odlučovači 2 pevných látok, napríklad vo viacpólovom elektrofiltre, takmer dokonale oddeliť od ostatných zostatkových látok, a nezávisle na reakčných produktoch, privedených späť do výrobného procesu cementu vynášať.A further advantage of the method is that fuels which contain heavy metals, including class I pollutants such as cadmium, thallium, mercury or the like, can also be used in the combustion process to improve economy. In the fluidized bed reactor 1, these pollutants are predominantly bound to particularly fine-grained particles and can be almost completely separated from other residual substances in a classically operating solids separator 2, for example in a multipole electrofilter, and independently of the reaction products brought back into the cement production process. .
Častice pevných látok vynesené týmto spôsobom, vykazujú jednak vysokú koncentráciu škodlivín, ale na druhej strane len malé množstvo všetkých odpadajúcich reakčných produktov. Tieto sa môžu - pokial to nie je pre ten ktorý produkt spaíovacieho procesu škodlivé - na vhodnom mieste vracať späť do procesu výroby produktu, lebo tieto sú samé o sebe viazané stabilne a nie sú rozpustné vo vode. Pri výrobe cementu sa ponúka možnosť ich primiešavať pri mletí slinku alebo cementu. Podía okolností prichádza do úvahy aj úprava pre spätné získanie škodlivín v kovovej alebo inak upotrebiteínej forme. Spôsobom podía vynálezu je možné odlúčiť 90 % škodlivín z odpadných plynov a postarať sa, aby nezaťažovali životné prostredie.The solid particles carried in this way show, on the one hand, a high concentration of pollutants, but, on the other hand, only a small amount of all the reaction products falling off. These may - if not harmful to the particular product of the combustion process - be recycled at a suitable point in the product production process, since they are themselves bound stably and are not soluble in water. In the manufacture of cement, it is possible to mix them in grinding clinker or cement. Alternatively, the treatment for recovering the pollutants in metallic or otherwise useful form is also contemplated. With the method according to the invention it is possible to separate 90% of the pollutants from the waste gases and to ensure that they do not burden the environment.
Spôsob podlá vynálezu bol použitý pri zariadení na výrobu cementu s dvomi rotačnými pecami, ktoré sú navezené 800 prípadne 1500 t cementového slinku. Vcelku odpadlo pri tom za hodinu 100 000 až 260 000 Nm3 odpadného plynu s teplotou 85 až 160 °C a obsahom prachu 700 až 1000 mg/Nm3. Okrem toho obsahoval odpadný plyn na Nm3 2000 až 3600 mg oxidu siričitého S02, 200 až 250 mg chlorovodíka HCI a 80 až 100 mg fluorovodíka HF ako aj malé, kvantitatívne nestanoví telné množstvá ortuti a kadmia.The process according to the invention was used in a cement production plant with two rotary kilns which are loaded with 800 or 1500 tons of cement clinker. In total, 100,000 to 260,000 Nm 3 of waste gas having a temperature of 85 to 160 ° C and a dust content of 700 to 1000 mg / Nm 3 were dropped per hour. In addition, the waste gas per Nm 3 contained 2000 to 3600 mg of SO 2 , 200 to 250 mg of HCl and 80 to 100 mg of HF, as well as small quantitatively non-quantifiable amounts of mercury and cadmium.
Rozprašovaním vody bezprostredne nad oblasť vstupu, ktorá sa rozširuje na spôsob Venturiho trysky, fluidného reaktora boli odpadné plyny ochladzované na 60 až 70 °C. Približne na rovakom mieste oblasti vstupu bol do fluidného reaktoru pridávaný sorbent, pozostávajúci z častíc pevnej látky, a síce na sorbent odvádzaný späť bolo pridávané za hodinu 2000 až 2300 ta na čerstvý sorbent za hodinu asi 300 kg hydrátu vápenatého a asi 2000 kg cementového surovinového prášku.By spraying water immediately above the inlet region, which extends in the manner of a venturi nozzle, of the fluidized bed reactor, the waste gases were cooled to 60-70 ° C. At about the same point of the inlet region, a sorbent consisting of particulate solids was added to the fluidized bed reactor, while the sorbent was returned to the fresh sorbent per hour about 300 kg of calcium hydrate and about 2000 kg of cement raw powder per hour. .
Vyčistený odpadný plyn obsahoval na Nm3 menej ako 50 mg prachu, menej ako 400 mg oxidu siričitého S02, menej ako 5 mg chlorovodíka HCI a menej ako 1 mg fluorovodíka HF.The purified waste gas contained Nm 3 of less than 50 mg of dust, less than 400 mg of SO 2 , less than 5 mg of HCl and less than 1 mg of HF.
Claims (2)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19853544764 DE3544764A1 (en) | 1985-12-18 | 1985-12-18 | METHOD FOR REMOVING POLLUTANTS FROM EXHAUST GAS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK278406B6 SK278406B6 (en) | 1997-04-09 |
| SK915086A3 true SK915086A3 (en) | 1997-04-09 |
Family
ID=6288750
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK9150-86A SK915086A3 (en) | 1985-12-18 | 1986-12-10 | Removal method of harmful substances from waste gases |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0228111B2 (en) |
| JP (1) | JPH0753224B2 (en) |
| AT (1) | ATE46088T1 (en) |
| CA (1) | CA1284802C (en) |
| CZ (1) | CZ280413B6 (en) |
| DD (1) | DD252767A5 (en) |
| DE (2) | DE3544764A1 (en) |
| DK (1) | DK165736C (en) |
| ES (1) | ES2011251T5 (en) |
| HU (1) | HU200706B (en) |
| SK (1) | SK915086A3 (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2624399B1 (en) * | 1987-12-14 | 1992-01-24 | Champagnole Ciments | PROCESS FOR DECONTAMINATION OF HOT GASES OR FUMES EMITTED BY A FIREPLACE, INSTALLATION FOR ITS IMPLEMENTATION AND PRODUCT OBTAINED |
| DE3824880A1 (en) * | 1988-07-19 | 1990-01-25 | Noell Gmbh | METHOD AND DEVICE FOR TREATING GASES |
| AT394660B (en) * | 1989-07-28 | 1992-05-25 | Staudinger Gernot | METHOD FOR REMOVAL OR REDUCTION OF GASEOUS POLLUTANTS AND DEVICE FOR CARRYING OUT THIS PROCESS |
| DE3942092A1 (en) * | 1989-12-20 | 1991-06-27 | Metallgesellschaft Ag | METHOD FOR REDUCING NO (ARROW DOWN) X (ARROW DOWN) CONTENT IN EXHAUST GAS |
| DE4000795A1 (en) * | 1990-01-12 | 1991-07-18 | Krupp Polysius Ag | METHOD FOR PURIFYING THE EXHAUST GASES FROM PLANTS FOR PRODUCING CEMENT CLINKER |
| DE4018786A1 (en) * | 1990-06-12 | 1991-12-19 | Krupp Polysius Ag | METHOD FOR PURIFYING THE EXHAUST GASES FROM PLANTS FOR PRODUCING CEMENT CLINKER |
| DE4034498A1 (en) * | 1990-09-06 | 1992-03-12 | Metallgesellschaft Ag | METHOD FOR SEPARATING HEAVY METALS AND DIOXINES FROM COMBUSTION EXHAUST GASES |
| DE4206602C2 (en) * | 1992-03-03 | 1995-10-26 | Metallgesellschaft Ag | Process for removing pollutants from combustion exhaust gases and fluidized bed reactor therefor |
| DE4330593A1 (en) * | 1993-09-09 | 1995-03-16 | Krupp Polysius Ag | Process for cleaning flue gases |
| DE4401166A1 (en) * | 1994-01-17 | 1995-07-20 | Krupp Polysius Ag | Process for cleaning flue gases |
| DE19532862A1 (en) * | 1995-09-06 | 1997-03-13 | Graf Epe Gmbh | Plant cleaning waste gases by solids contacting in recirculated fluidised bed |
| PT1200176E (en) * | 1999-06-18 | 2003-08-29 | Smidth & Co As F L | METHOD AND DEVICE FOR DEFAULTS OF EXHAUSTIVE GASES |
| EP1546058A1 (en) * | 2002-10-02 | 2005-06-29 | F.L. Smidth A/S | Method and plant for manufacturing cement clinker |
| KR101015154B1 (en) * | 2010-10-05 | 2011-02-16 | 한국에너지기술연구원 | Internal and external circulating acid gas removal device for high temperature flue gas powder absorber containing sulfur oxide and boron compound and acid gas removal method using the same |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3038457C2 (en) * | 1980-10-11 | 1983-11-10 | L. & C. Steinmüller GmbH, 5270 Gummersbach | Use of a waste product from dry flue gas desulphurisation for the production of fly ash cement |
| DE3215793A1 (en) * | 1982-04-28 | 1983-11-03 | Klöckner-Humboldt-Deutz AG, 5000 Köln | METHOD AND DEVICE FOR REDUCING THE SULFURING CIRCUIT AND / OR THE SO (ARROW DOWN) 2 (ARROW DOWN) EMISSION IN A PLANT FOR BURNING FINE GRAIN GOODS |
| DE3235558A1 (en) * | 1982-09-25 | 1984-03-29 | Metallgesellschaft Ag, 6000 Frankfurt | METHOD FOR SEPARATING POLLUTANTS FROM EXHAUST GAS |
| DE3235559A1 (en) * | 1982-09-25 | 1984-05-24 | Metallgesellschaft Ag, 6000 Frankfurt | Process for the removal of sulphur oxides from flue gas |
| DE3322159A1 (en) * | 1983-06-21 | 1985-01-03 | Metallgesellschaft Ag, 6000 Frankfurt | METHOD FOR SEPARATING POLLUTANTS FROM EXHAUST GAS |
| DE3326935A1 (en) * | 1983-07-26 | 1985-02-07 | Krupp Polysius Ag, 4720 Beckum | Process for the elimination of pollutants from the exhaust gases of a rotary kiln |
| DK348583D0 (en) * | 1983-07-29 | 1983-07-29 | Smidth & Co As F L | METHOD AND APPARATUS FOR REMOVAL OF SULFUR OXIDES FROM HOT ROEGGAS BY THE TOUR METHOD |
| DE3415210C2 (en) * | 1984-01-07 | 1995-06-22 | Kloeckner Humboldt Deutz Ag | Process for the desulfurization of the flue gas from a furnace |
-
1985
- 1985-12-18 DE DE19853544764 patent/DE3544764A1/en not_active Withdrawn
-
1986
- 1986-11-27 AT AT86202110T patent/ATE46088T1/en active
- 1986-11-27 EP EP86202110A patent/EP0228111B2/en not_active Expired - Lifetime
- 1986-11-27 ES ES86202110T patent/ES2011251T5/en not_active Expired - Lifetime
- 1986-11-27 DE DE8686202110T patent/DE3665410D1/en not_active Expired
- 1986-12-10 CZ CS869150A patent/CZ280413B6/en unknown
- 1986-12-10 SK SK9150-86A patent/SK915086A3/en unknown
- 1986-12-11 JP JP61295702A patent/JPH0753224B2/en not_active Expired - Lifetime
- 1986-12-16 DD DD86297685A patent/DD252767A5/en not_active IP Right Cessation
- 1986-12-16 DK DK606386A patent/DK165736C/en not_active IP Right Cessation
- 1986-12-17 CA CA000525587A patent/CA1284802C/en not_active Expired - Lifetime
- 1986-12-17 HU HU865268A patent/HU200706B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0228111B1 (en) | 1989-09-06 |
| DK165736B (en) | 1993-01-11 |
| CZ915086A3 (en) | 1995-11-15 |
| CA1284802C (en) | 1991-06-11 |
| SK278406B6 (en) | 1997-04-09 |
| ES2011251T5 (en) | 1995-08-16 |
| HU200706B (en) | 1990-08-28 |
| DE3544764A1 (en) | 1987-06-19 |
| JPS62144736A (en) | 1987-06-27 |
| EP0228111A1 (en) | 1987-07-08 |
| DE3665410D1 (en) | 1989-10-12 |
| ATE46088T1 (en) | 1989-09-15 |
| DK606386D0 (en) | 1986-12-16 |
| CZ280413B6 (en) | 1996-01-17 |
| DD252767A5 (en) | 1987-12-30 |
| EP0228111B2 (en) | 1994-06-15 |
| DK165736C (en) | 1993-06-14 |
| DK606386A (en) | 1987-06-19 |
| ES2011251B3 (en) | 1990-01-01 |
| JPH0753224B2 (en) | 1995-06-07 |
| HUT49057A (en) | 1989-08-28 |
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