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Selection catalytic

Hydrogenation. Acetylene can be hydrogenated to ethylene and ethane. The reduction of acetylene occurs in an ammoniacal solution of chromous chloride (20) or in a solution of chromous salts in H2SO4 (20). The selective catalytic hydrogenation of acetylene to ethylene, which proceeds... [Pg.374]

Process Licensors. Some of the well-known nitric acid technology licensors are fisted in Table 3. Espindesa, Grande Paroisse, Humphreys and Glasgow, Rhfyne Poulenc, Uhde, and Weatherly are all reported to be licensors of weak acid technology. Most weak acid plant licensors offer extended absorption for NO abatement. Espindesa, Rhfyne Poulenc, Weatherly, and Uhde are also reported (53,57) to offer selective catalytic reduction (SCR) technology. [Pg.45]

Fig. 7. NO reduction using selective catalytic recovery (SCR) (a) basic principles of the SCR process where represent gas particles and (b) effect of... Fig. 7. NO reduction using selective catalytic recovery (SCR) (a) basic principles of the SCR process where represent gas particles and (b) effect of...
R. L. Stevens, J. L. Goff, and A. H. Thomas, "Santa Maria Cogeneration Project Selective Catalytic Reduction for NO Control," presented at the... [Pg.205]

When NO destmction efficiencies approaching 90% are required, some form of post-combustion technology appHed downstream of the combustion 2one is needed to reduce the NO formed during the combustion process. Three post-combustion NO control technologies are utilized selective catalytic reduction (SCR) nonselective catalytic reduction (NSCR) and selective noncatalytic reduction (SNCR). [Pg.510]

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 H2O using ammonia as the reducing agent in the presence of a catalyst. [Pg.510]

G. S. Shareef, D. K. Stone, K. R. Perry, K. L. Johnson, and K. S. Locke "Selective Catalytic Reduction NO Control for Small Natural Gas-Pired Prime Movers," paper 92-136.06, in Ref. 16. [Pg.516]

C VRT Center for Waste Reduction Technologies SCR Selective catalytic reduction... [Pg.2153]

TABLE 25-25 Advantages and Disadvantages of Selective Catalytic Reduction of Nitrogen Oxides... [Pg.2181]

Selective Catalytic Reduction of Nitrogen Oxides The traditional approach to reducing ambient ozone concentrations has been to reduce VOC emissions, an ozone precurssor. In many areas, it has now been recognized that ehmination of persistent exceedances of the National Ambient Air Qnality Standard for ozone may reqnire more attention to reductions in the other ingredients in ozone formation, nitrogen oxides (NOJ. In such areas, ozone concentrations are controlled by NO rather than VOC emissions. [Pg.2195]

NO Emission Control It is preferable to minimize NO formation through control of the mixing, combustion, and heat-transfer processes rather than through postcombustion techniques such as selective catalytic reduction. Four techniques for doing so, illustrated in Fig. 27-15, are air staging, fuel staging, flue-gas recirculation, and lean premixing. [Pg.2381]

In a recent paper Pijpers et al. [2.42] have reviewed the application of XPS in the field of catalysis and polymers. Other recent applications of XPS to catalytic problems deal with the selective catalytic reduction of using Pt- and Co-loaded zeolites. Although the Al 2p line (Al from zeolite) and Pt 4/ line interfere strongly, the two oxidation states Pt and Pt " can be distinguished after careful curve-fitting [2.43]. [Pg.23]

Flue gas treatment (FGT) is more effective in reducing NO, emissions than are combustion controls, although at higher cost. FGT is also useful where combustion controls are not applicable. Pollution prevention measures, such as using a high-pressure process in nitric acid plants, is more cost-effective in controlling NO, emissions. FGT technologies have been primarily developed and are most widely used in Japan. The techniques can be classified as selective catalytic reduction, selective noncatalytic reduction, and adsorption. [Pg.28]

Selective catalytic reduction (SCR) is cmrently the most developed and widely applied FGT technology. In the SCR process, ammonia is used as a reducing agent to convert NO, to nitrogen in the presence of a catalyst in a converter upstream of the air heater. The catalyst is usually a mixture of titanium dioxide, vanadium pentoxide, and hmgsten trioxide. SCR can remove 60-90% of NO, from flue gases. Unfortunately, the process is very expensive (US 40- 80/kilowatt), and the associated ammonia injection results in an ammonia slip stream in the exhaust. In addition, there are safety and environmental concerns associated with anhydrous ammonia storage. [Pg.28]

Nitric Acid Plant - Nitrogen oxide levels should be controlled to a maximum of 1.6 kg/t of 100% nitric acid. Extended absorption and technologies such as nonselective catalytic reduction (NSCR) and selective catalytic reduction (SCR) are used to eontrol nitrogen oxides in tail gases. [Pg.66]

Selective Catalytic Reduction (SCR) SCE is a process to reduce NO, to nitrogen and water with ammonia in the presence of a catalyst between 540-840 F (282-449 C). Ammonia is usually injected at a 1 1 molar ratio with the NOx contaminants. Ammonia is used due to its tendency to react only with the contaminants and not with the oxygen in the gas stream. Ammonia is injected by means of compressed gas or steam carriers. Efficiencies near 90% have been reported with SCR. See Exxon Thermal DeNO. ... [Pg.546]

Another route to 5a compounds (57) proceeds from the dienol ether (58) by selective catalytic hydrogenation of the A -double bond with concomitant shift of the 3,4-double bond to the 2,3-position. If the hydrogenation is carried out in the presence of traces of base, double bond migration is suppressed and the difficultly accessible A -enol ethers of 5a-series (59) are thus obtained. [Pg.390]

Improvements in engine and turbine design, along with the use of auxiliary equipment such as catalytic converters, selective catalytic reduction (SCR) units and the use of steam and water injection into turbines, combine to reduce overall emission levels. [Pg.488]

Selective catalytic reduction is based on selective reactions of a continuous gaseous flow of ammonia or similar reducing agents with the exhaust stream in the presence of a catalyst. The reaction that occurs is as follows ... [Pg.490]

These optimization studies are an important step in the study of Simmons-Smith cyciopropanations since they allowed for the development of a selective, catalytic method for introduction of a simple methylene unit. However, they also provide insights into the basic mechanism of this process. Together with earlier studies regarding carbenoid structure, the true nature of the reactive carbenoid, lCH2Znl, was confirmed. On the basis of these results, a revised transition structure was proposed. Although there is no direct evidence for such a transition... [Pg.139]

Combustion modifications and postcombustion processes are the two major compliance options for NO., emissions available to utilities using coal-fircd boilers. Combustion modifications include low-NO burners (LNBs), overfire air (OFA), reburning, flue gas recirculation (FGR), and operational modifications. Postcombustion processes include selective catalytic reduction (SCR) and selective noncatalytic reduction (SNCR). The CCT program has demonstrated innovative technologies in both of these major categories. Combustion modifications offer a less-expensive appiroach. [Pg.447]

Postcombustion processes are designed to capture NO, after it has been produced. In a selective catalytic reduction (SCR) system, ammonia is mixed with flue gas in the presence of a catalyst to transform the NO, into molecular nitrogen and water. In a selective noncatalytic reduction (SNCR) system, a reducing agent, such as ammonia or urea, is injected into the furnace above the combustion zone where it reacts with the NO, to form nitrogen gas and water vapor. Existing postcombustion processes are costly and each has drawbacks. SCR relies on expensive catalysts and experiences problems with ammonia adsorption on the fly ash. SNCR systems have not been proven for boilers larger than 300 MW. [Pg.447]

Catalyst and products are quickly separated in the reactor. However, some thermal and non-selective catalytic reactions continue. A number... [Pg.8]

It is important to separate catalyst and vapors as soon as they enter the reactor. Otherwise, the extended contact time of the vapors with the catalyst in the reactor housing will allow for non-selective catalytic recracking of some of the desirable products. The extended residence time also promotes thermal cracking of the desirable products. [Pg.10]

Post-riser hydrocarbon residence time leads to thermal cracking and non-selective catalytic reactions. These reactions lead to degradation of valuable products, producing dry-gas and coke at the expense of... [Pg.282]

Selective catalytic reduction (SCR) and selective noncatalytic reduction processes (SNCR) are widely employed in large industrial and utility boiler plants, as well as in municipal waste incineration plants and other combustion processes. They are used to complement mechanical improvements (such as low NOx burners and furnace design modifications) as an aid to reducing the emission levels of NOx, S02, and other noxious gases into the atmosphere. [Pg.684]

Table 3.1 lists some of the anodic reactions which have been studied so far in small cogenerative solid oxide fuel cells. A more detailed recent review has been written by Stoukides46 One simple and interesting rule which has emerged from these studies is that the selection of the anodic electrocatalyst for a selective electrocatalytic oxidation can be based on the heterogeneous catalytic literature for the corresponding selective catalytic oxidation. Thus the selectivity of Pt and Pt-Rh alloy electrocatalysts for the anodic NH3 oxidation to NO turns out to be comparable (>95%) with the... [Pg.99]

T. Rebitzki, B. Delmon, and J.H. Block, Isothermal instability due to remote control A model for selective catalytic oxidation, AIChE Journal 41, 1543-1549 (1995). [Pg.109]


See other pages where Selection catalytic is mentioned: [Pg.876]    [Pg.9]    [Pg.391]    [Pg.429]    [Pg.43]    [Pg.43]    [Pg.353]    [Pg.9]    [Pg.91]    [Pg.122]    [Pg.530]    [Pg.2152]    [Pg.2185]    [Pg.26]    [Pg.101]    [Pg.490]    [Pg.491]    [Pg.1046]    [Pg.988]    [Pg.74]    [Pg.143]   


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