![]() Method for cleaning exhaust and industrial gases
专利摘要:
In this specification there is described a process for the purification of gases containing noxious constituents and especially the catalytic purification of gases containing noxious oxides of nitrogen. A gas containing the noxious oxides and including oxygen and a gaseous reducing fuel, is passed at a temperature above the ignition temperature of the gas and the fuel through a catalyst comprising an inert material impregnated or coated with a mixture or alloy of platinum and rhodium metals and rhodium is present in an amount of between 20 and 50 weight percent of the total metal content of the catalyst. The invention also includes catalysts for carrying out the above process. 公开号:SU1069606A3 申请号:SU1619887 申请日:1971-02-10 公开日:1984-01-23 发明作者:Джеймз Кейт Экрис Гари;Митчел Хатчингз Роберт 申请人:Джонсон,Мэтти Энд Ко.,Лимитед (Фирма); IPC主号:
专利说明:
e ABOUT) with The invention relates to methods for purifying waste industrial gases and exhaust gases of internal combustion engines from impurities of carbon monoxide and organic compounds and may find application in industries associated with wire enameling, with painting and drying of machine parts, in printing and other industries using organic solvents, as well as in the chemical industry in the vapor-phase oxidation of organic compounds, in the production of ethylene and ethylene oxide, in the operation of washed furnaces and engines combustion it. A known method of purification of gases from organic substances by burning 1. However, this method is not always justified due to the need to simultaneously burn the fuel 1. The closest in technical essence and the achieved result to the proposed method is the purification of industrial waste gases and exhaust gases of internal combustion engines, including passing them through a catalyst containing platinum or palladium or rhodium or ruthenium and a refractory catalytically active metal oxide (I - IX groups of the periodic system of elements on an inert carrier 2. It is known that, for example, platinum catalysts are stable close to temperatures of at least 750 ° C and are resistant to poisoning in most catalysts, excluding lead and phosphorus. The initial temperature of the gas stream supplied to the catalytic purification, i.e. ignition temperature, is 230-480s by a known method, i.e. quite high. The aim of the invention is to reduce the ignition temperatures of impurities during the cleaning process. The goal is achieved by the method of purification of exhaust and industrial gases from carbon monoxide and organic compounds by passing them through a catalyst containing platinum and a refractory catalytically active metal oxide II - IX groups of the periodic system of elements on an inert carrier, and using a catalyst containing platinum mixed with rhodium or in the form of their alloy at a concentration of rhodium 20-50 May. of their total content, and as an inert carrier, a ceramic material selected from the group including zirconmullite, mullite, i-alumina, silimanite, magnesium silicates, zircon, petalite, spodumene, cordierite, and aluminosilicates. The catalyst on the carrier, used according to the proposed method of gas cleaning, consists of a refractory oxide deposited on an inert ceramic material and catalytically active metals of platinum and rhodium. The inert carrier of the cat aggler used is a rigid, porous, cellular refractory ceramic material, such as, for example, ziru equulite, mullite, alpha-alumina, silimanite, magnesium silicates, zircon, petalite, spodumene, cordierite, and silicates. A suitable proprietary product is Torvex, sold by DuPont, and is a refractory honeycomb structure made from llit ceramics. The refractory catalytically active oxides are 1-50%, preferably 5-30% relative to the total weight of the supported catalyst. These oxides are one or more of the metal oxides H, P and fX of periods of the periodic system of elements that have atomic numbers not exceeding 40. Platinum and rhodium make up 0.0510% by reference to the total weight of the supported catalyst, preferably 0.5-2.0%. Externally, the catalyst is a rigid honeycomb structure or blocks with multiple openings or channels. Honeycombs usually occupy almost the entire cross section of a catalytic reactor with a seal between them and the walls to prevent bypassing part of the gas flow. It is convenient to use regularly spaced systems of tightly adjoining units or sequentially spaced separate units for reactors with a large cross-sectional area. The catalyst units are placed in the reactor so that the overall direction of the cellular channels coincides with the direction of the gas flow through the reactor. Blocks can be / positioned so that the flow of gas through the reactor is radial or transverse with respect to the total flow of gas. Lreemer 1. To determine ignition temperatures, i.e. inlet temperatures at which the oxidation reactions of impurities "become self-sustaining, as well as for determining the inlet temperatures 5 required for 90% oxidation impurities, use catgie-eator, states of platinum alloy and rhodium with the content of the latter 35 wt.% and active alumina on torvex. The results are shown in Table. one. As follows from the table. 1, the ignition temperature of impurities in the gas to be purified, with the exception of hydrogen, is 150-425 s, which is lower than the corresponding values of a known method (230-480 s). For the 90% oxidation of impurities most commonly encountered in practice, temperatures of 150-500 ° C are necessary. Note 2. A gas containing, in May.%: Methane 1.5, oxygen 3, the rest is nitrogen, with an insignificant amount of oxides of nitrogen and argon is fed to the purification. Use the catalyst, as in example 1, but with a different ratio of platinum and rhodi. Ignition temperatures are determined at a rhodium content of 0-100% of the total metal content. The results are shown in Table. 2 From tab. 2, it follows that the cattoi interval of low ignition temperatures corresponds to a rhodium content of 20–50 wt.% (Optimally 30–40;. Wt.%), An extremely low value is observed at 35 wt.%. Example 3. Catalyst efficiency was tested in the purification of exhaust gases from a laboratory single-cylinder diesel engine operating indoors. Engine performance is given in Table. 3 The tests are carried out in three operating modes - idle, medium and high loading. The characteristics of exhaust compositions in these modes (average for 10 tests) are given in Table 5. four When using the idle mode, the exhaust gas temperature of 950 ° C is too low for the catalytic reaction to take place. Tests show that the catalyst becomes spectacular at 170 ° C and its activity rapidly increases with increasing exhaust gas temperature. The catalyst is less efficient with respect to the purification of particles of a shaft, however, they are continuously removed from the catalyst during its operation due to catalytic oxidation, 0 therefore the catalyst does not lose its activity. Example 4. A loop gas of nitric acid production at a pressure of 5.3 kg / cm, containing 3% by volume of oxygen and 2000 hours per million of oxides of nitrogen, into which 1.78% by volume of methane or natural gas is introduced through the catalyst. . The catalyst contains 35% rhodium and 65% platinum 0 on mullite (Torvex). The ignition temperature is 25 ° C, the oxidation state of methane is 90%. As follows from the examples, the proposed method of gas cleaning ensures the reduction of the ignition temperature of impurities to 150-425 ° C against 230-480 ° C by a known method. Table 1 Hydrogen Carbon dioxide Benzene Toluene Xylene Alpha pinen Mesityl oxide Ethanol n-heptane Methylisobutyl ketone Methyl ethyl ketone 20 150-200 250-300 250-300 250-300 250-300 250-300 250-300 250-300 300-350 300-350 DO1 methylformamide Ethyl acetate Methane (air) Methane (3% Oj / N5} Thiophene Pyridine Chlorbutan Hydrogen sulphide Carbon disulfide Ratio Fh: Pt .. in “, 0: 100 5:95 20:80 35:65 50:50 100: 0 i J lIntensity of the T test of the brake, the efficiency of the run of the top Liv, kg / h 0.23 7.5 2.33 11.0 2.81 Continued table. one 350-400 400-450 400-450 400-450 400-450 400-450 450-500 400-425 375-400 33.9 600 96 54.0 1,190 487 52.6 1,170 597 Table The temperature of ignition, with m. "(. 425. 410 330 315 325 400 Table 3 Consumption 1 Air temperature, rev / min exhaust kg / C, C Note. Dma concentration is expressed in flue Cartridge units. Table 4
权利要求:
Claims (1) [1] (57) METHOD FOR CLEANING EXHAUST AND INDUSTRIAL GASES from impurities of carbon monoxide and organic compounds by passing them through a catalyst containing platinum and refractory catalytically active metal oxide of groups IX of the periodic system of elements on an inert carrier, characterized in that, in order to reduce the ignition temperature of impurities during the cleaning process, use a catalyst containing platinum mixed with rhodium or their alloy at a concentration of rhodium 20-50 wt.% of their total content, and as an inert carrier nomic material selected from. § a group including zirconmachllite, mullite, oC-alumina, silymanite, magnesium silicates, zircon, petalite, spodumene, cordierite and aluminosilicates.
类似技术:
公开号 | 公开日 | 专利标题 SU1069606A3|1984-01-23|Method for cleaning exhaust and industrial gases US3951860A|1976-04-20|Catalyst JP2017127867A|2017-07-27|Catalyzed soot filter with layered design US4849399A|1989-07-18|Catalyst for the reduction of the ignition temperature of diesel soot US6613299B2|2003-09-02|Catalyzed diesel particulate matter exhaust filter US3963827A|1976-06-15|Catalysis JPH0611381B2|1994-02-16|Exhaust gas purification method KR20060093102A|2006-08-23|A catalyzed diesel particulate matter filter with improved thermal stability US3809743A|1974-05-07|Process for treating automotive exhaust US4077913A|1978-03-07|Catalyst JP2003521363A|2003-07-15|Catalyst and method for reducing exhaust emissions JP2773428B2|1998-07-09|Exhaust gas purification method EP0622107A2|1994-11-02|Exhaust gas purifying catalyst in diesel engines US4710487A|1987-12-01|Diesel exhaust gas catalyst EP0664149B1|1998-08-19|Method of purifying exhaust gas JP2000176249A|2000-06-27|Purifying device of exhaust gas from internal combustion engine, purifying method of exhaust gas, and purifying catalyst of exhaust gas US3072458A|1963-01-08|Method of catalytically purifying exhaust gases of internal combustion engines and cyclically regenerating the lead-contaminated catalyst KR940003609A|1994-03-12|Catalysts for treating exhaust gases from internal combustion and stationary supply lines JPH07829A|1995-01-06|Non-metal catalyst system for lean-burn engine JPH11107744A|1999-04-20|Exhaust emission control catalyst device WO2004103554A1|2004-12-02|Catalyst for oxidizing and removing methane in exhaust gas method for clarifying exhaust gas JP2000117058A|2000-04-25|Decreasing method of the discharge quantity of nitrogen oxides in stoichiometric excess medium by oxidizing agent JP2000042369A|2000-02-15|Purifying device for exhaust gas from internal combustion engine, purifying method of exhaust gas and purifying catalyst for exhaust gas JP4106762B2|2008-06-25|Exhaust gas purification catalyst device and purification method JP3395525B2|2003-04-14|Internal combustion engine exhaust gas purification catalyst and purification method
同族专利:
公开号 | 公开日 NL7013587A|1971-03-18| BE756151A|1971-02-15| JPS5621645A|1981-02-28| ES383629A1|1973-05-01| DE2045487A1|1971-03-25| CA960017A|1974-12-31| JPS5319554B1|1978-06-21| NL170375C|1982-11-01| CA984125A|1976-02-24| DE2045488A1|1971-04-08| GB1330841A|1973-09-19| SU375830A3|1973-03-23| ES383628A1|1973-05-01| US3806582A|1974-04-23| DE2045487C2|1985-05-23| NL170809C|1983-01-03| NL170809B|1982-08-02| FR2061385A5|1971-06-18| PL81040B1|1975-08-30| FR2061384A5|1971-06-18| PL76451B1|1975-02-28| NL7013586A|1971-03-18| US4289737A|1981-09-15| NL170375B|1982-06-01| BE756150A|1971-02-15| DE2045488C3|1978-10-05| DE2045488B2|1978-01-26| SU402198A3|1973-10-12|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 BE566487A| GB411655A|1933-03-28|1934-06-14|Richard Blum|Improvements in and relating to methods of and apparatus for purifying the exhaust gases of internal combustion engines| US3118727A|1956-10-12|1964-01-21|Engelhart Ind Inc|Method of removing nitrogen oxides from gases| GB883945A|1957-04-05|1961-12-06|Engelhard Ind Inc|A process for the removal of free oxygen and the catalytic reduction of oxides of nitrogen in waste gases| US3056646A|1959-07-14|1962-10-02|Engelhard Ind Inc|Method of effecting the catalytic contact of gases containing oxygen and methane| US3161605A|1961-03-31|1964-12-15|Du Pont|Preparation of supported catalysts| US3259453A|1962-07-19|1966-07-05|Du Pont|Method and apparatus for treating exhaust gases of internal combustion engines| US3245920A|1962-08-17|1966-04-12|Engelhard Ind Inc|Catalyst composition consisting of a noble metal on alumina| US3255027A|1962-09-07|1966-06-07|Du Pont|Refractory product and process| US3565830A|1963-02-07|1971-02-23|Engelhard Min & Chem|Coated film of catalytically active oxide on a refractory support| US3467492A|1964-11-06|1969-09-16|Chemical Construction Corp|Elimination of nitrogen oxides from gas streams| FR1479602A|1965-04-22|1967-05-05|Schneider & Co|Catalyst support| US3454355A|1966-05-20|1969-07-08|Chevron Res|Method of removing sulfur dioxide and nitrogen oxides from gases| US3554929A|1967-06-08|1971-01-12|Du Pont|High surface area alumina coatings on catalyst supports| US3425803A|1967-09-01|1969-02-04|Engelhard Ind Inc|Nitric acid tail gas purification| BE756151A|1969-09-16|1971-02-15|Johnson Matthey & Cy Ltd|CATALYSIS IMPROVEMENTS|BE756151A|1969-09-16|1971-02-15|Johnson Matthey & Cy Ltd|CATALYSIS IMPROVEMENTS| US4053556A|1971-06-16|1977-10-11|Johnson, Matthey & Co., Limited|Catalysis| US4025606A|1971-06-25|1977-05-24|Johnson Matthey & Co., Limited|Catalysis| GB1417544A|1971-11-22|1975-12-10|Johnson Matthey Co Ltd|Catalysts containing platinum and rhodium| IT971446B|1971-12-16|1974-04-30|Corning Glass Works|MATERIAL FOR CLEANING OR CHECKING WASTE GAS EXHAUST GAS FROM INTERNAL COMBUSTION AND SIMILAR ENGINES| US4076792A|1972-04-12|1978-02-28|Corning Glass Works|Catalyst systems for the reduction of the oxides of nitrogen| JPS5338715B2|1972-04-15|1978-10-17| GB1383896A|1972-06-14|1974-02-12|Grace W R & Co|Process of removing noxious components from exhaust gases with the aid of a catalyst| CA1001147A|1972-11-30|1976-12-07|Takashi Ohara|Method for the production of exhaust and waste gases purifying catalysts| DE2304831C3|1973-02-01|1978-06-22|Kali-Chemie Ag, 3000 Hannover|Process for the catalytic removal of carbon monoxide, unburned hydrocarbons and nitrogen oxides from car exhaust gases| JPS5057946A|1973-07-17|1975-05-20| US4198379A|1974-01-11|1980-04-15|James G Russell|Nitrogen oxide pollution abatement using catalytic combustion| JPS51110491A|1975-03-26|1976-09-30|Ube Industries| nox kangenjokayoshokubai| JPS6038179B2|1977-08-26|1985-08-30|Matsushita Electric Ind Co Ltd| JPS5824174B2|1977-08-31|1983-05-19|Mitsubishi Heavy Ind Ltd| US4257223A|1978-05-08|1981-03-24|Johnson, Matthey & Co., Limited|Engines| GB2024646B|1978-07-10|1983-05-05|Johnson Matthey Co Ltd|Catalytic oxidation of smoke in exhaust gases| US4199435A|1978-12-04|1980-04-22|Chevron Research Company|NOx Control in cracking catalyst regeneration| US4290878A|1978-12-08|1981-09-22|Chevron Research Company|NOx control in platinum-promoted complete combustion cracking catalyst regeneration| DE3020630C2|1980-03-10|1987-07-16|Bridgestone Tire Co. Ltd., Tokio/Tokyo, Jp| DE3348099C2|1983-10-03|1994-10-20|Wahlco Power Products Inc|Device for preheating a stream of combustion air| DE3335917C3|1983-10-03|1997-03-13|Wahlco Power Products Inc|Device for regeneratively preheating a stream of combustion air with a hot NO¶x¶-containing flue gas stream and for reducing the NO¶x¶ contained in the flue gases| US4950476A|1986-11-06|1990-08-21|Ford Motor Company|Method of catalytically oxidizing alcohol vapor accompanied by varying amounts of excess oxygen| US5254797A|1989-06-07|1993-10-19|Ngk Insulators, Ltd.|Method of treating exhaust gas| US5010051A|1989-11-08|1991-04-23|Engelhard Corporation|Staged three-way conversion catalyst and method of using the same| DE69133164T2|1990-01-12|2003-04-10|Ngk Spark Plug Co|Poison-resistant catalytic composition| JP2897367B2|1990-01-12|1999-05-31|日本特殊陶業株式会社|Poisoning prevention body, catalyst with poisoning prevention layer, and exhaust gas purification device| US5212142A|1991-11-04|1993-05-18|Engelhard Corporation|High performance thermally stable catalyst| US6080377A|1995-04-27|2000-06-27|Engelhard Corporation|Method of abating NOx and a catalytic material therefor| US6471924B1|1995-07-12|2002-10-29|Engelhard Corporation|Method and apparatus for NOx abatement in lean gaseous streams| US5874057A|1995-07-12|1999-02-23|Engelhard Corporation|Lean NOx catalyst/trap method| US5743929A|1995-08-23|1998-04-28|The Boc Group, Inc.|Process for the production of high purity carbon dioxide| US5849256A|1996-04-26|1998-12-15|Engelhard Corporation|Method for oxidizing carbon monoxide in a gas stream containing oxidizable sulphur compounds| US5792436A|1996-05-13|1998-08-11|Engelhard Corporation|Method for using a regenerable catalyzed trap| US6037183A|1996-12-20|2000-03-14|Corning Incorporated|Automotive hydrocarbon sensor system| US6242263B1|1996-12-20|2001-06-05|Corning Incorporated|Automotive hydrocarbon sensor| JP3903598B2|1997-09-24|2007-04-11|トヨタ自動車株式会社|Exhaust gas purification catalyst and method for producing the same| US6344173B1|1998-12-07|2002-02-05|Corning Incorporated|Automotive hydrocarbon sensor| US6497848B1|1999-04-02|2002-12-24|Engelhard Corporation|Catalytic trap with potassium component and method of using the same| DE10006103A1|2000-02-11|2001-08-16|Krupp Uhde Gmbh|Catalyst for decomposing N¶2¶O, its use in nitric acid production and process for its production| JP4573320B2|2000-09-08|2010-11-04|昭和電工株式会社|Nitrous oxide decomposition catalyst, production method thereof, and decomposition method of nitrous oxide| US7856992B2|2005-02-09|2010-12-28|Headwaters Technology Innovation, Llc|Tobacco catalyst and methods for reducing the amount of undesirable small molecules in tobacco smoke| US7803201B2|2005-02-09|2010-09-28|Headwaters Technology Innovation, Llc|Organically complexed nanocatalysts for improving combustion properties of fuels and fuel compositions incorporating such catalysts| US7357903B2|2005-04-12|2008-04-15|Headwaters Heavy Oil, Llc|Method for reducing NOx during combustion of coal in a burner| US8115373B2|2005-07-06|2012-02-14|Rochester Institute Of Technology|Self-regenerating particulate trap systems for emissions and methods thereof| US20070078053A1|2005-09-30|2007-04-05|U.S.A. As Represented By The Administrator Of The National Aeronautics And Space Administration|Catalyst for decomposition of nitrogen oxides| US7758660B2|2006-02-09|2010-07-20|Headwaters Technology Innovation, Llc|Crystalline nanocatalysts for improving combustion properties of fuels and fuel compositions incorporating such catalysts| DE102009006404B3|2009-01-28|2010-08-26|Süd-Chemie AG|Diesel oxidation catalyst with good low temperature activity| GB201110850D0|2011-03-04|2011-08-10|Johnson Matthey Plc|Catalyst and mehtod of preparation| DE102015005238A1|2015-04-24|2016-10-27|Wolfgang Hölderich|Production of lactams by Beckmann rearrangement of oximes| CN105540661B|2015-12-31|2017-11-10|淄博广通化工有限责任公司|The recycle device of zircon sand fluidizing chlorination tail gas| CN105617809B|2015-12-31|2017-09-22|淄博广通化工有限责任公司|The tail gas recycle Application way of zircon sand fluidizing chlorination device discharge|
法律状态:
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 GB4554569|1969-09-16| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|