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Selective catalytic reduction component

For some models adsorption or storage is important. For example, oxygen storage is important in a 3-way catalysis, a catalyst may contain a hydrocarbon storage component for improved low-temperature performance, and ammonia storage is important for ammonia SCR (selective catalytic reduction). Clearly, this sort of behaviour needs to be included in the final model. The nature of the measurements depends on the exact system being studied and will be discussed in more detail later. Suffice to say, from measurements at steady state, the heats of adsorption and coefficients of... [Pg.61]

Selective Catalytic Reduction. Selective catalytic reduction (SCR) is widely used in Japan and Europe to control NO emissions (1). SCR converts the NO in an oxygen-containing exhaust stream to molecular N2 and H20 using ammonia as the reducing agent in the presence of a catalyst. NOx removals of 90% are achievable. The primary variable is temperature, which depends on catalyst type (38). The principal components of an SCR... [Pg.510]

While the development of flue gas clean-up processes has been progressing for many years, a satisfactory process is not yet available. Lime/limestone wet flue gas desulfurization (FGD) scrubber is the most widely used process in the utility industry at present, owing to the fact that it is the most technically developed and generally the most economically attractive. In spite of this, it is expensive and accounts for about 25-35% of the capital and operating costs of a power plant. Techniques for the post combustion control of nitrogen oxides emissions have not been developed as extensively as those for control of sulfur dioxide emissions. Several approaches have been proposed. Among these, ammonia-based selective catalytic reduction (SCR) has received the most attention. But, SCR may not be suitable for U.S. coal-fired power plants because of reliability concerns and other unresolved technical issues (1). These include uncertain catalyst life, water disposal requirements, and the effects of ammonia by-products on plant components downstream from the reactor. The sensitivity of SCR processes to the cost of NH3 is also the subject of some concern. [Pg.164]

When biomass is co-fired with coal (even in small percentages), the alkali metals in biomass ash can alter the properties of the resulting mixed ash. This could have a significant impact on the coal plant s operating and maintenance costs or even operability. The addition of biomass to a coal-fired power plant can also nullify ash sales contracts for coal flyash. Biomass ash components in feedstocks may also reduce the long-term efficiency and effectiveness of certain (selective catalytic reduction, SCR) systems for the selective catalytic reduction ofNOx. [Pg.1523]

Also for oxidation reactions, the choice of the alumina support mainly depends on two criteria the stability of the phase at the reaction temperature and the reactivity (or better the lack thereof) toward feed components and products. For example, ethylene oxychlorination to ethylenedichloride is performed at approximately 220-250° C and 5-6 atm in the presence of a y-Al203-supported catalyst, which has a surface area of from 100 to 200 m and contains 10wt% CUCI2 and 3 wt% KCl, (423,424). Another example is a process called ammonia selective oxidation (ASO, or also selective catalytic oxidation, SCO), which converts small amounts of NH3 from waste gases to N2 at reaction temperatures of 150—300 °C. The process is used to abate the ammonia sHp after a selective catalytic reduction process with ammonia or urea in diesel-engine-exhaust after-treatment (425). The patented catalyst consists of Y-AI2O3 (60—300 m g ) loaded with 0.5-4 wt% platinum and 0.5—4 wt% vanadia and is coated onto the surface of a ceramic or metallic monoftthic structure (426). [Pg.389]

In order to decrease the number of bricks in the posttreatment exhaust line, some combinations can be found such as integrating catalytic treatment and filtration step. The aim of this single brick is to reduce the overall size of the posttreatment system and to reduce the cost of the final engine. One approach to achieve this goal is to coat the soot filter with a catalyst composition effective for the conversion of NO in innocuous components. With this selective catalytic reduction filtration (SCRF) concept, the catalyzed soot filter assumes two functions removal of the particulate and conversion of the NO species to N2 of the exhaust stream (Scheme 35.6). [Pg.807]

The selective catalytic reduction (SCR) of NO by CO over supported noble metal (Pt, Pd, or Rh) catalysts is an active area of interest because of the high prices and scarcity of noble metals. Therefore, it is an important task to find alternative catalytic components to reduce even replace the noble metals. Recent research reveals that the transition-metal oxides have high catalytic activity for reduction of NO by CO [154-162]. Copper oxide has been demonstrated to be an active species among the various transition-metal oxides for this reaction [158,163-166],... [Pg.234]

The aim of the project is to evaluate the perspective of a modified selective catalytic reduction process to reduce NO emissions from flue gas. In a previous study the activity of the equimolar NO/NO2 reduction was found to be higher then the NO reduction. The modified process is based on the equimolar NO/NO2 reduction. NO being the predominant NO component in flue gas from stationary sources, must then be partly oxidized to NO2. A desk study is carried out to review the literature on methods for flue gas composition modification with respect to the NO/NO2 ratio. The evaluation of the modified SCR process also requires more knowledge about the increase in catalytic activity of the equimolar NO/NO2 reduction as compared to the NO reduction and about the effect of catalyst composition on the reaction rate. In order to investigate these aspects, an experimental programme is carried out, using four different catalyst materials two commercial preparations and two self-prepared vanadium-titaniumdioxide catalysts. The results of activity measurements for NO, NO2 and the equimolar NO/NO2 reduction are reported, under conditions relevant for large scale applications. From these results some prehminary conclusions can be drawn with respect to the perspective of the modified process. [Pg.3]

In addition to four component condensation, several other applications of chiral primary ferrocenylalkyl amines have been published. Thus, an asymmetric synthesis of alanine was developed (Fig. 4-3la), which forms an imine from 1-ferrocenylethyl amine and pyruvic acid, followed by catalytic reduction (Pd/C) to the amine. Cleavage of the auxiliary occurs readily by 2-mercaptoacetic acid, giving alanine in 61% ee and allowing for recycling of the chiral auxiliary from the sulfur derivative by the HgClj technique [165]. Enantioselective reduction of imines is not limited to pyruvic acid, but has recently also been applied to the imine with acetophenone, although the diastereoisomeric ferrocenylalkyl derivatives of phenylethylamine were obtained only in a ratio of about 2 1 (Fig. 4-31 b). The enantioselective addition of methyl lithium to the imine with benzaldehyde was of the same low selectivity [57]. Recycling of the chiral auxiliary was possible by treatment of the secondary amines with acetic acid/formaldehyde mixture that cleaved the phenylethylamine from the cation and substituted it for acetate. [Pg.210]

In the triene series for the synthesis of the stereoisomers of (15 3)-anacardic acid, namely the 8(Z),11(Z),14 8(E),11(E),14 8(Z),11(E),14 and 8(Z),11(E),14 compounds by the alkylation of the ArC., intermediate (ethyl 2-methoxy-6-methybenzoate) with a 0 4 component these boration methods have been of value as an addition to selective catalytic hydrogenation and the use of terminal trimethylsilylation (ref. 167). At this stage for synthetic purposes the selective reductive use of boration methods has been mainly exploited. The chief use of combined addition/alkylation procedures is for obtaining 8(E), and 11 (E) isomers. For this, the sequence of synthons, for the side chain has to follow the different series, Ar9->ArCi2->ArCi5. [Pg.516]


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See also in sourсe #XX -- [ Pg.433 ]




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