DD250059A5 - PROCESS FOR CLEANING GAS MIXTURES - Google Patents
PROCESS FOR CLEANING GAS MIXTURES Download PDFInfo
- Publication number
- DD250059A5 DD250059A5 DD86295071A DD29507186A DD250059A5 DD 250059 A5 DD250059 A5 DD 250059A5 DD 86295071 A DD86295071 A DD 86295071A DD 29507186 A DD29507186 A DD 29507186A DD 250059 A5 DD250059 A5 DD 250059A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- gases
- phase
- contact
- catalysts
- foam
- Prior art date
Links
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
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
-
- 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
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
- B01D53/8603—Removing sulfur compounds
- B01D53/8609—Sulfur oxides
-
- 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
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/86—Catalytic processes
- B01D53/8643—Removing mixtures of carbon monoxide or hydrocarbons and nitrogen oxides
- B01D53/8646—Simultaneous elimination of the components
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Analytical Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Catalysts (AREA)
- Treating Waste Gases (AREA)
- Separation Of Gases By Adsorption (AREA)
- Silicon Compounds (AREA)
Abstract
Description
gelassen, ein Teilstrom abgezweigt und nach allfälligem Durchleiten durch einen Wärmetauscher auf Katalysatordichte geprüft und erforderlichenfalls der Katalysator ergänzt. Bei Entfernung von Stickoxiden kann dem Gas ein mit diesen reagierenden Substrat, vorzugsweise Ammoniak, in stöchiometrischem Verhältnis beigemengt werden. Als derartige Reaktionssubtrate eignen sich außer Ammoniak auch z.B. Kohlenmonoxid und Kohlenwasserstoffe.left, diverted a partial flow and tested for any passage through a heat exchanger on the catalyst density and, if necessary, the catalyst complements. When nitrogen oxides are removed, the gas may be admixed with a substrate which reacts with these, preferably ammonia, in a stoichiometric ratio. As such reaction substrates, besides ammonia, e.g. Carbon monoxide and hydrocarbons.
Die Einhaltung eines intensiven Gas-Flüssigkeits-Phasenkontaktes bei möglichst geringem Druckverlust ermöglicht die Ausführung des erfindungsgemäßen Verfahrens im industriellen Ausmaß. Zur Erzielung dieses Effektes eignen sich insbesondere Vorrichtungen mit Phasenkontaktböden, welche mithelfen, einen hydrostatischen Druck der über dieser lastenden Flüssigkeitssäule zu überwinden und zu regulieren. Eine solche Vorrichtung ist z.B. in der veröffentlichten PCT-Anmeldung WO 82/03184 (veröffentlicht als EP Nr. 73801,16.3.1983) beschrieben.The maintenance of an intensive gas-liquid phase contact with the lowest possible pressure loss allows the execution of the inventive method on an industrial scale. To achieve this effect, in particular devices with phase contact bottoms, which help to overcome and regulate a hydrostatic pressure of the liquid column overlying this liquid are suitable. Such a device is e.g. in published PCT application WO 82/03184 (published as EP No. 73801, 16.3.1983).
Es ist bekannt, daß Metallphthalocynine als Katalysatoren zur Hydrierung von Kohlenmonoxid zu C1-Cg Kohlenwasserstoffen eingesetzt werden können, und daß Kobalt oder Eisenphthalocyanine, auf Kohle aufgebrcht, zur Entfernung von Stickoxiden aus Zigarettenrauch dienen können. Bei dem bisherigen Stand der Technik war jedoch die große Wirksamkeit von in Flüssigkeiten suspendierten oder gelösten Metallphthalocyaninen und anderen Katalysatoren in intensivem Phasenkontakt mit zu reinigenden Gasgemischen überraschend.It is known that metal phthalocynines can be used as catalysts for the hydrogenation of carbon monoxide to C 1 -Cg hydrocarbons, and that cobalt or iron phthalocyanines, based on charcoal, can serve to remove nitrogen oxides from cigarette smoke. In the prior art, however, the great effectiveness of suspended in liquids or dissolved metal phthalocyanines and other catalysts in intensive phase contact with gas mixtures to be cleaned was surprising.
Die erfindungsgemäß erzielte erhöhte Aktivierung von Katalysatoren ist von großer technischer Bedeutung. So ist bei etwa 1 000 ppm Stickoxide enthaltenden Abgasen von Kraftwerken bei erfindungsgemäßem Einsatz von Eisenphthalocynanin bei 1500C unter Verwendung von etwa 10 Phasenkontaktböden ein Wirkungsgrad von 90% erreichbar, wobei dieser Wirkungsgrad bei Verwendung einer größeren Anzahl von Kontaktböden noch erhöht und bis auf 99% gebracht werden kann. Bei einer Umlaufmenge von 2001 Trägerflüssigkeit werden 10kg Katalysator benötigt.·The inventively achieved increased activation of catalysts is of great industrial importance. Thus, with about 1,000 ppm nitrogen oxides-containing exhaust gases from power plants according to the invention using Eisenphthalocynanin at 150 0 C using about 10 phase contact surfaces, an efficiency of 90% achievable, this efficiency when using a larger number of contact plates still increased and up to 99 % can be brought. For a circulation volume of 2001 carrier liquid 10kg of catalyst are required.
Zwei Ausführungsweisen des erfindungsgemäßen Verfahrens seien an Hand einer Zeichnung näher beschrieben. Die Darstellung I zeigt die Mitverwendung von Ammoniak als Reaktionssubstrat.Two embodiments of the method according to the invention will be described in more detail with reference to a drawing. The representation I shows the concomitant use of ammonia as a reaction substrate.
Vor Einleitung in den Misch raum M wird das Abgas mit ammoniakalischer Lösung entstaubt und entschwefelt. Im Mischraum M wird, durch eine Meßsonde gesteuert, Ammoniak stöchiometrisch zugemischt.Before being introduced into the mixing space M, the waste gas is dedusted with ammoniacal solution and desulphurized. In the mixing chamber M, controlled by a probe, ammonia stoichiometrically added.
Im Reaktionsraum R wird der Katalysator als Suspension oder in Lösung in einerTrägerflüssigKeit, z. B. Wasser, Paraffinölen oder Silikonölen, umgewälzt und im Gegenstrom zum Abgas mit Hilfe von Kontaktelementen in einen intensiven Phasenkontakt (Schaumphase) gebracht. Dabei reagieren die Stickoxide mit dem zugesetzten NH3ZU Stickstoff und Wasser.In the reaction space R, the catalyst is added as a suspension or in solution in a carrier liquid, e.g. As water, paraffin oils or silicone oils, circulated and brought in countercurrent to the exhaust gas by means of contact elements in an intensive phase contact (foam phase). The nitrogen oxides react with the added NH 3 to form nitrogen and water.
Im Gaswäscher W werden aus den gereinigten Abgasen die verbleibenden Katalysatorreste mit gereinigter Trägerflüssigkeit ausgewaschen und dann in den Reaktionsraum R rückgeführt.In the gas scrubber W, the remaining catalyst residues are washed out with purified carrier liquid from the cleaned exhaust gases and then recycled to the reaction space R.
Die Konzentration des Katalysators liegt bei 1 bis 30Gew.-% der eingesetzten Trägerflüssigkeit, vorzugsweise 5Gew.-%. Die Temperatur des Katalysators liegt, unabhängig vom Katalysator, in einem Bereich von 20 bis 5000C, vorzugsweise 20 bis 1500C.The concentration of the catalyst is 1 to 30% by weight of the carrier liquid used, preferably 5% by weight. The temperature of the catalyst is, regardless of the catalyst, in a range of 20 to 500 0 C, preferably 20 to 150 0 C.
In Darstellung Il wird gezeigt, wie unter Verwendung des erfindungsgemäßen Verfahrens aus den Stickoxiden Ammoniumnitrat gewonnen werden kann, wobei NH3 nicht in den Reaktionsraum R, sondern in den Gaswäscher eingeleitet wird.Representation II shows how ammonium nitrate can be obtained from the nitrogen oxides using the process according to the invention, NH 3 not being introduced into the reaction space R but into the gas scrubber.
Bei Reinigung von Abgasen, die von stationären Dieselmotoren stammen, ist ein Entstauben und Entschwefeln nicht erforderlich. DerEntstickungsgrad liegt bei erfindungsgemäßer Reinigung solcher bis zu 10000 ppm NOx enthaltender Abgase nach dem erfindungsgemäßen Verfahren bei über 90%. Bei Erhöhung des derzeitigen CO-Gehaltes von Dieselmotoren können auch die Abgase von Lastkraftwagen unter Verwendung von CO als Reaktionssubstrat erfindungsgemäß'entstickt, das CO zu CO2 und die Kohlenwasserstoffe zu CO2 und H2O umgesetzt werden.When cleaning exhaust gases from stationary diesel engines, dedusting and desulfurization is not required. The degree of de-icing in the inventive purification of such up to 10,000 ppm NO x- containing exhaust gases by the novel process is over 90%. When increasing the current CO content of diesel engines and the exhaust gases of trucks using CO as a reaction substrate according to the invention'entstickt the CO to CO 2 and the hydrocarbons to CO 2 and H 2 O are implemented.
Claims (5)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT0290685A AT383287B (en) | 1985-10-08 | 1985-10-08 | METHOD FOR PURIFYING GAS MIXTURES |
Publications (1)
Publication Number | Publication Date |
---|---|
DD250059A5 true DD250059A5 (en) | 1987-09-30 |
Family
ID=3542188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DD86295071A DD250059A5 (en) | 1985-10-08 | 1986-10-06 | PROCESS FOR CLEANING GAS MIXTURES |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0218574B1 (en) |
AT (2) | AT383287B (en) |
CA (1) | CA1295814C (en) |
CZ (1) | CZ726086A3 (en) |
DD (1) | DD250059A5 (en) |
DE (1) | DE3681110D1 (en) |
HU (1) | HUT43966A (en) |
PL (1) | PL261739A1 (en) |
ZA (1) | ZA867272B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3835161C2 (en) * | 1988-10-13 | 1996-08-14 | Werner Dipl Chem Fabian | Exhaust gas purification using catalytic oxidation with atmospheric oxygen |
US5288469A (en) * | 1992-03-16 | 1994-02-22 | Envirosurgical, Inc. | Surgery plume filter device |
AU4102493A (en) * | 1992-03-16 | 1994-11-08 | Envirosurgical, Inc. | Surgery plume filter device and method of filtering |
US5910291A (en) * | 1992-03-16 | 1999-06-08 | Envirosurgical, Inc. | Surgery plume filter device and method of filtering |
FR2701220B1 (en) * | 1993-02-08 | 1995-04-14 | Inst Francais Du Petrole | Process for catalytic deodorization and reduction of the nitrogen content of slurry tank effluents. |
CN116832873B (en) * | 2023-07-25 | 2024-02-27 | 西北大学 | Complex iron catalyst for removing hydrogen sulfide in industrial gas and preparation method thereof |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2385200A (en) * | 1942-06-25 | 1945-09-18 | Hooker Electrochemical Co | Methods and apparatus for reacting gases with liquids |
BE765087A (en) * | 1970-04-20 | 1971-08-16 | Becker Raymond O | METHOD AND APPARATUS AGAINST ATMOSPHERIC AIR POLLUTION |
CS160060B2 (en) * | 1971-07-21 | 1975-02-28 | ||
JPS5643771B2 (en) * | 1973-12-18 | 1981-10-15 | ||
FR2382923A1 (en) * | 1977-02-28 | 1978-10-06 | Percevaut Emile | Gas purifier, esp. for diesel engine exhaust gases - incorporates washer, decantation tank and wash-liquor treatment chamber, forming autonomous closed circuit unit |
CA1075879A (en) * | 1977-05-04 | 1980-04-22 | Gulf Canada Limited | Recovery of sulfur from gas streams containing sulfur and sulfur compounds in dilute concentration |
DE2736488C3 (en) * | 1977-08-12 | 1980-03-13 | Steag Ag, 4300 Essen | Process for removing sulfur oxides from flue gases |
US4238462A (en) * | 1978-01-31 | 1980-12-09 | Air Resources, Inc. | Autocirculation process and apparatus |
US4325923A (en) * | 1978-07-26 | 1982-04-20 | Rhone-Poulenc Industries | Contacting of plural phases |
US4374104A (en) * | 1980-09-30 | 1983-02-15 | Air Resources, Inc. | Composition and method for removing hydrogen sulfide from gas stream |
DE3108075A1 (en) * | 1981-03-04 | 1982-09-16 | Basf Ag, 6700 Ludwigshafen | METHOD FOR REMOVING DISTICKOXIDE OXIDE FROM SUCH CONTAINING EXHAUST GASES |
-
1985
- 1985-10-08 AT AT0290685A patent/AT383287B/en not_active IP Right Cessation
-
1986
- 1986-09-24 ZA ZA867272A patent/ZA867272B/en unknown
- 1986-10-06 DD DD86295071A patent/DD250059A5/en unknown
- 1986-10-06 PL PL1986261739A patent/PL261739A1/en unknown
- 1986-10-07 DE DE8686890275T patent/DE3681110D1/en not_active Expired - Fee Related
- 1986-10-07 HU HU864200A patent/HUT43966A/en unknown
- 1986-10-07 AT AT86890275T patent/ATE66632T1/en not_active IP Right Cessation
- 1986-10-07 CZ CS867260A patent/CZ726086A3/en unknown
- 1986-10-07 EP EP86890275A patent/EP0218574B1/en not_active Expired - Lifetime
- 1986-10-08 CA CA000520131A patent/CA1295814C/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
PL261739A1 (en) | 1988-05-26 |
CZ726086A3 (en) | 1995-06-14 |
CA1295814C (en) | 1992-02-18 |
DE3681110D1 (en) | 1991-10-02 |
AT383287B (en) | 1987-06-10 |
ATE66632T1 (en) | 1991-09-15 |
ZA867272B (en) | 1987-05-27 |
HUT43966A (en) | 1988-01-28 |
ATA290685A (en) | 1986-11-15 |
EP0218574A3 (en) | 1989-03-08 |
EP0218574A2 (en) | 1987-04-15 |
EP0218574B1 (en) | 1991-08-28 |
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