SK278406B6 - Removing method of harmful substances from waste gases - Google Patents
Removing method of harmful substances from waste gases Download PDFInfo
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- SK278406B6 SK278406B6 SK9150-86A SK915086A SK278406B6 SK 278406 B6 SK278406 B6 SK 278406B6 SK 915086 A SK915086 A SK 915086A SK 278406 B6 SK278406 B6 SK 278406B6
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- fluidized bed
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- 239000002912 waste gas Substances 0.000 title claims abstract description 32
- 238000000034 method Methods 0.000 title claims abstract description 18
- 239000000126 substance Substances 0.000 title abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 28
- 239000002594 sorbent Substances 0.000 claims abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims abstract description 4
- 238000002347 injection Methods 0.000 claims abstract description 3
- 239000007924 injection Substances 0.000 claims abstract description 3
- 239000004568 cement Substances 0.000 claims description 18
- 239000003344 environmental pollutant Substances 0.000 claims description 14
- 231100000719 pollutant Toxicity 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 239000000843 powder Substances 0.000 claims description 7
- 238000002485 combustion reaction Methods 0.000 claims description 6
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 4
- 239000002689 soil Substances 0.000 claims description 4
- 239000004575 stone Substances 0.000 claims description 4
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 3
- 239000000920 calcium hydroxide Substances 0.000 claims description 3
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 3
- 235000019738 Limestone Nutrition 0.000 claims description 2
- 239000000292 calcium oxide Substances 0.000 claims description 2
- 235000012255 calcium oxide Nutrition 0.000 claims description 2
- 238000012994 industrial processing Methods 0.000 claims description 2
- 239000006028 limestone Substances 0.000 claims description 2
- 239000012530 fluid Substances 0.000 abstract 4
- 238000010992 reflux Methods 0.000 abstract 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 12
- 239000000428 dust Substances 0.000 description 10
- 239000007789 gas Substances 0.000 description 7
- 239000002245 particle Substances 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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-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
- 238000006477 desulfuration reaction Methods 0.000 description 3
- 230000023556 desulfurization Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 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
- 238000004140 cleaning Methods 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
- 239000002994 raw material Substances 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
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 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
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010419 fine particle Substances 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
- 239000007788 liquid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 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
- 230000001105 regulatory effect Effects 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
- 150000003463 sulfur Chemical class 0.000 description 1
- -1 sulphide 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
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- 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
Oblasť technikyTechnical field
Vynález sa týka spôsobu suchého odstraňovania škodlivín, ako oxidu siričitého, kyseliny chlorovodíkovej, chlóru, fluorovodíka a ťažkých kovov, z odpadových plynov priemyslu spracúvajúceho 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 odpadové plyny, obvykle po odstránení prachu, spracovávajú kvapalinou vedenou v okruhu a pri tom sa ochladia do tej miery, že je nevyhnutné ich opäť zohriať na teplotu prevyšujúcu asi o 20°C teplotu tavenia, aby sa zabránilo poškodeniu v dôsledku korózie. Odpadajúce množstvo reakčných produktov je spravidla rovnako príliš veľké na to, aby 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 odpadových plynov.Using known wet scrubbing processes, the waste gases, usually after dust removal, are treated with the liquid circulating in the circuit and cooled to the extent that they need to be reheated to a temperature above about 20 ° C to prevent melting. corrosion damage. The dropping amount of reaction products is generally also too large to be returned to the production process. Wet scrubbing processes are therefore most often associated with high equipment and operating costs, which often hinder a continuous waste gas cleaning reaction.
Pri výrobe cementu sa už tiež robili pokusy čistiť odpadové plyny pri teplote 300 až 850°C za sucha. Pri tom vyšlo ale najavo, že odpadové 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 aje 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 dry. However, it became apparent that, at temperatures above 500 ° C, the waste gases often contained 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 fuel is absorbed by the crude cement powder and bound in clinker.
Takéto priaznivé pomery sa ale pri iných spaľovacích 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 odpadových plynov, pričom vlastný produkt tu nevykazuje žiadnu schopnosť absorbovať škodliviny, ktorá by stála za zmienku.However, such favorable proportions do not occur in other combustion processes in the industrial processing of stone and soil. There, the 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 has no worth mentioning ability to absorb the pollutants.
Pri procese výroby cementu sa síra ale tiež znáša do spaľovacieho procesu surovinovým práškom. Táto síra pochádza sčasti z organických, prípadne sulfidických zlúčenín síry, ktoré sa už pri nízkych teplotách rozpadajú a vedú behom predhrievania k uvoľňovaniu oxidu siričitého SO2 , pričom obsahy oxidu siričitého môžu dosiahnuť až 6000 mg/Nm3. V dôsledku toho, že pri procese výroby cementu, pri obvyklých teplotách odpadových plynov nedochádza prakticky k žiadnej sorpcii oxidu siričitého SO2 surovým materiálom, musia sa aj cementárne vybaviť zariadením na odsírenie odpadových plynov, aj keď je síra zanesená spolu s palivom, v závislosti od postupu je v odpadových plynoch obsiahnutá len v minimálnom množstve.In the cement production process, however, sulfur is also carried into the combustion process by the raw powder. This sulfur originates in part from organic or sulphide sulfur compounds which decompose already at low temperatures and lead to SO 2 evolution during preheating, with sulfur dioxide contents of up to 6000 mg / Nm 3 . As a result, the the process of the cement, the conventional exhaust gas temperature there virtually no uptake of sulfur dioxide SO2 raw material, must be the cement plant provided with a device for desulfurization of waste gases, while the sulfur is clogged with the fuel, according to the of the process is contained in the waste gases only in a minimal amount.
Čistenie za sucha pri teplotách 200 až 400°C je nezávislé od použitého sorbentu a nezávislé od pomeru sorbentu k množstvu škodliviny, ale nie je tiež príliš účinné. Obyčajne je možné odstrániť len menej ako 60 % škodlivín z odpadového plynu, pokiaľ sa ale nechce prejsť k drahým a s ohľadom na najčastejšie sa vyskytujúcu vysokú prašnosť, len za určitých podmienok prevádzkovo bezpečným spôsobom čistenia pomocou katalyzátorov.Dry 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 off-gas, unless, however, to switch to expensive and, in view of the most commonly occurring, high dust levels, only under certain conditions an operationally safe catalyst cleaning process.
Tým jc teda daná úloha navrhnúť spôsob odstraňovania škodlivín z odpadových plynov spaľovacích procesov priemyselného spracovania kameňa a zemín, ktorý by bol všeobecne použiteľný a ekonomickejší ako doteraz známe spôsoby.Thus, the task is to propose a method for removing pollutants from the waste gases of the combustion processes of industrial stone and soil processing, which would be generally applicable and more economical than the known methods.
Podstata vynálezuSUMMARY OF THE INVENTION
S prekvapením sa zistilo, že je možné tento cieľ dosiahnuť, ak sa odpadové plyny privedú pri 50 až 5 100°C vo fluidnom reaktore do styku so sorbentom pozostávajúcim z pevných častíc, pevné častice sa oddelia z prúdu plynu a vrátia sa späť do fluidného reaktora, ako sorbent sa použije surový cementový prášok, vápenec s obsahom viac ako 90 % uhličitanu vápenatelo ho CaCO3, 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 solid particles at 50-500 ° C in a fluidized bed reactor, the solid particles are separated from the gas stream and returned to the fluidized bed reactor. For example, raw cement powder, limestone containing more than 90% calcium carbonate CaCO 3 , quicklime, hydrated lime or partially calcined feedstock powder are used as sorbent and a new sorbent is continuously added to the circuit and the spent sorbent is discharged from the circuit.
Výhodne sa odpadové plyny pred vstupom do flu15 idného reaktora ochladzujú na 50 až 100°C. Alternatívne sa môžu odpadové 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 20 závislosti od obsahu škodlivín v čistom plyne. Ďalšou výhodou spôsobu je, že sa sorpčné prostriedky vynášané z okruhu môžu bez ďalšieho vracať do procesu výroby cementu. Výhodne sa častice pevných látok oddeľujú v klasicky pracujúcom odlučovači pevných látok, 25 najmä viacpólovom elektrofiltri, z prúdu plynu, pričom sa jemne zrnitý podiel pevných látok, obohatený ťažkými kovmi, vynáša a používa 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 the sorbent are regulated in dependence on the pollutant content of the pure gas. A further advantage of the process is that the sorbents removed from the circuit can be recycled to the cement production process without further action. Preferably, the solids particles are separated from the gas stream in a conventionally operating solids separator, in particular a multi-pole electrostatic filter, from which the fine-grained solids enriched in heavy metals are discharged and used as an additive to the finished cement clinker.
Pomocou spôsobu podľa vynálezu sa môže nielen 30 ľubovoľne predĺžiť čas styku, ktorý· je často pri iných spôsoboch čistenia za sucha pri dolnom rozsahu teplôt príliš krátky, ale získa sa aj produkt, ktorý nevyžaduje žiadne zvláštne ďalšie spracovanie alebo deponovanie, čím je často zaťažená ekonomickosť doterajších spôso35 bov.With the method according to the invention, not only can the contact time, which is often too short for other dry cleaning processes at the lower temperature range, be arbitrarily prolonged, but also a product which does not require any particular further processing or depositing is obtained. the prior art35 bov.
Prehľad obrázkov na výkresochBRIEF DESCRIPTION OF THE DRAWINGS
Ďalšie podrobnosti sú vysvetlené pomocou príkladu odsírenia odpadových plynov z procesu výroby cementu a pomocou schémy spôsobu znázorneného zjednodušene na obr. 1.Further details are explained by way of an example of the desulfurization of the waste gases from the cement production process and by means of the process diagram shown in simplified form in FIG. First
Príklady uskutočnenia vynálezuDETAILED DESCRIPTION OF THE INVENTION
Cirkulačný systém pre pevnú látku, pozostávajúci z fluidného reaktora 1, odlučovača 2 pevných látok a zo 50 spätného vedenia 3 sa zásobuje cez vedenie 4 vodou na rozprašovanie, cez vedenie 5 sorpčnými prostriedkami a cez vedenie 7 odpadovým plynom, ktorý sa má odsíriť. Maximálne odsírený odpadový plyn opúšťa hore fluidný reaktor 1, zbaví sa v odlučovači 2 na pevné lát55 ky 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 fluidného reaktora 1. Časť 60 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 circulation system, consisting of a fluidized bed reactor 1, a solids separator 2 and a 50 return line 3, is supplied with water for atomization, via a line 5 with sorption means and via a line 7 with 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 conveying 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 60 of the amount of circulating solids is discharged via line 7 from the solids circulation system and a suitable it is brought to the cement production site.
Jednotlivé zložky obsiahnuté v zostatkovej látke, napríklad ťažké kovy, sa môžu po selektívnom odlúčení 65 od ostatných látok vyniesť cez vedenie 10. Odpadové plyny odchádzajú s teplotou 100 až 450°C, vždy podľa toho či a ktoré zariadenia na spätné získanie tepla sú usporiadané (kotol na odpadové teplo, príprava teplej vody, mlyn). V prípade, že plyny nie sú vedené cez mlyn, je ich obsah prachu 100 g/Nm3. V posledne uvedenom prípade môže zaťaženie prachom byť až 1000 g/Nm3 a môže mať zmysel odstrániť predbežne prach pomocou elektrofiltra alebo mechanického odlučovača, aby bolo možné obmedziť cirkuláciu pevných látok v cirkulačnom systéme na pevné látky na také množstvo, ktoré je optimálne na odsírenie. Prípadne je tiež možné v takýchto prípadoch celkom alebo sčasti upustiť od zvláštneho prídavku sorpčných prostriedkov. Obsah prachu v odpadových plynoch sa redukuje v odlučovači 2 pevných látok na množstvo nižšie ako 50 mg/Nm3.The individual components contained in the residual substance, for example heavy metals, can be discharged through line 10 after selective separation 65 from the other substances. The waste gases leave at a temperature of 100 to 450 ° C, depending on whether and which heat recovery devices are arranged ( waste heat boiler, hot water preparation, mill). If the gases are not passed through the mill, their dust content is 100 g / Nm 3 . In the latter case, the dust load can be up to 1000 g / Nm 3 and it may make sense to remove the preliminary dust by means of an electrofilter or mechanical separator in order to limit the solids circulation in the circulation system to solids to an amount optimal for desulfurization. Optionally, 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 less than 50 mg / Nm 3 .
Obsah oxidu siričitého SO2 v odpadovom plyne je v závislosti od zloženia surového materiálu až 6000 mg/Nm3. Tento sa môže v čistom plyne znížiť spôsobom podľa vynálezu až na hodnotu nižšiu ako 50 mg/Nm3. Prípustné množstvá oxidu siričitého sa podľa zákonných predpisov pohybujú v Nemecku okolo 400 mg/Nm3, vo Švajčiarsku okolo 500 mg/Nm3.The SO 2 content of 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 in accordance with the 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 spaľovacích 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 jemnozmné častice a môžu sa v klasicky pracujúcom odlučovači 2 pevných látok, napríklad vo viacpólovom elektrofiltri, takmer dokonale oddeliť od ostatných zostatkových látok, a nezávisle od reakčných produktov, privedených späť do výrobného procesu cementu vynášať.A further advantage of the process 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 particles and can be almost completely separated from other residual substances in a conventional working solids separator 2, for example in a multi-pole electrofilter, and independently of the reaction products fed back to 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 - pokiaľ to nie je pre ten - ktorý produkt spaľovacieho procesu škodlivé na vhodnom mieste vracať späť do procesu výroby produktu, lebo tieto sú samé osebe viazané stabilne a nie sú rozpustné vo vode. Pri výrobe cementu sa ponúka možnosť primiešavať ich pri mletí slinku alebo cementu. Podľa okolností prichádza do úvahy aj úprava pre spätné získanie škodlivín v kovovej alebo inak upotrebiteľnej forme. Spôsobom podľa vynálezu je možné odlúčiť 90 % škodlivín z odpadových 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 - unless this is not detrimental to the product of the combustion process at the appropriate point - be returned to the production process of the product, since these are themselves bound stably and are not soluble in water. In cement production, it is possible to mix them in grinding clinker or cement. Depending on the circumstances, treatment for recovering the pollutants in metallic or otherwise usable 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 podľa vynálezu bol použitý pri zariadení na výrobu cementu s dvoma rotačnými pecami, ktoré sú navezené 800 prípadne 1500 t cementového slinku. Vcelku odpadlo pri tom za hodinu 100 000 až 260 000 Nm3 odpadového plynu s teplotou 85 až 160°C a obsahom prachu 700 až 1000 mg/Nm3. Okrem toho obsahoval odpadový plyn na Nm3 2000 až 3600 mg oxidu siričitého SO2, 200 až 250 mg chlorovodíka HCI a 80 až 100 mg fluorovodíka HF ako aj malé, kvantitatívne nestanoviteľné 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 tonnes 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 was 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, quantifiable amounts of mercury and cadmium.
Rozprašovaním vody bezprostredne nad oblasť vstupu, ktorá sa rozširuje na spôsob Venturiho dýzy, fluidného reaktora boli odpadové plyny ochladzované na 60 až 70 °C. Približne na rovnakom mieste oblasti vstupu bol do fluidného reaktora pridávaný sorbent, pozostávajúci z častíc pevnej látky, a to na sorbent odvádzaný späť bolo pridávané za hodinu 2000 až 2300 t a 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, a 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 solid particles was added to the fluidized bed reactor, and the sorbent removed back was added per hour 2000 to 2300 t and fresh sorbent per hour about 300 kg calcium hydrate and about 2000 kg cement raw powder .
Vyčistený odpadový plyn obsahoval na Nm3 menej ako 50 mg prachu, menej ako 400 mg oxidu siričitéhoThe purified waste gas contained less than 50 mg of dust per Nm 3 , less than 400 mg of sulfur dioxide
SO2, menej ako 5 mg chlorovodíka HCI a menej ako 1 mg fluorovodíka HF.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 true SK278406B6 (en) | 1997-04-09 |
| SK915086A3 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 |
| 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 |
| SK915086A3 (en) | 1997-04-09 |
| 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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