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Hydrogenation components, typical

The gaseous component typically contains hydrocarbons, hydrogen sulfide, ammonia, mercaptans, solvents, and other constituents, and is either discharged directly to the atmosphere or is combusted in a flare. The major air emissions from blowdown systems are hydrocarbons in the case of direct discharge to the atmosphere and sulfur oxides when flared. [Pg.100]

Figure 12.12. Coaxial nanosecond flashlamp components. Typical conditions for red and near-IR operation are high voltage (V= 5 kV), gas pressure P = 0.8 B of equal volumes of argon and hydrogen, repetition rate R = 40 kHz, and electrode separation... Figure 12.12. Coaxial nanosecond flashlamp components. Typical conditions for red and near-IR operation are high voltage (V= 5 kV), gas pressure P = 0.8 B of equal volumes of argon and hydrogen, repetition rate R = 40 kHz, and electrode separation...
The component typically analyzed in plants is cellulose, which is the major structural carbohydrate in plants (Epstein et al. 1976, 1977). Cellulose contains 70% carbon-bound hydrogen, which is isotopically non-exchangeable and 30% of exchangeable hydrogen in the form of hydroxyl groups (Epstein et al. 1976 Yapp and Epstein 1982). The hydroxyl-hydrogen readily exchanges with the enviromnen-tal water and its D/H ratio is not a useful indicator of the D/H ratio of the water used by the plants. [Pg.180]

The oxidative dimerization has recently attracted attention, both from a fundamental viewpoint and as a means for synthesizing aromatics from lower olefins. The reaction is essentially a combination of allyl radicals, by which the oxidation is limited to the abstraction of one hydrogen atom. Typically, the catalysts applied here do not contain Mo03 or a similar component that promotes the selective incorporation of oxygen. [Pg.136]

Isosbestic points are commonly met when electronic spectra are taken (a) on a solution in which a chemical reaction is in progress (in which case the two absorbing components concerned are a reactant and a product, A + B) or (b) on a solution in which the two absorbing components are in equilibrium and their relative proportions are controlled by the concentration of some other component, typically the concentration of hydrogen ions, e.g., an acid-base indicator equilibrium. [Pg.147]

Typical levels are 25-50%, the weight of zeolite in the catalysts, with the remainder being the hydrogenation component and a silica (Si02) or alumina (AI2O3) binder. Exact recipes are guarded as trade secrets. [Pg.1287]

Typical catalysts of this type contain 60-80% of silica alumina, with the remainder being the hydrogenation component. The compositions of these catalysts are closely held secrets. Over the years, broad ranges of silica/alumina molar ratios have been used in various cracking applications, but silica is almost always in excess for high acidity and stability. A typical level might be 25% alumina (AI2O3). [Pg.1287]

Chain Extenders and Cross-linkers. In addition to the two principal components of most urethane coatings, isocyanate and polyol components, a number of di- or polyfunctional, active hydrogen components may be used as chain extenders or cross-linkers. The most important classes of compounds for this use are diols or polyols (monomers or oligomers), diamines, and alkanolamines. Typical examples of diols are ethylene, dlethylene, dlpropylene glycol, 1,4-butanedio1, 1,5-hexanediol, neopentyl glycol,... [Pg.1004]

The catalysts for these demanding ketone syntheses must possess at least mild basicity/acidity and a selective hydrogenation component(s). The presence of Lewis acid sites, which act as acceptors for the enolate intermediates that are formed at the basic sites, is beneficial when basic sites predominate. However, the majority of the selective catalysts appear to be mostly acidic in nature catalysts with strongly basic sites are typically non-selective to ketones,except at low ( 310-330 K) temperatures concomitant with low reaction rates and the inability to dehydrate the ketoalcohol (e.g, diamino-functionalized MCM-41, or quaternary ammonium ion exchange polymer). ... [Pg.312]

Most modern hydrocracking processes are catalytic, and the catalyst employed is usually dual functional with both a hydrogenation component and an acidic component. Typical acidic components include amorphous silica-alumina, alumina, and a large family of zeolites. Typical hydrogenation components are noble metals such as palladium and platinum and nonnoble metals such as nickel, cobalt, tungsten, and molybdenum. The latter metals are usually in sulfided form. [Pg.294]

Typically, approximately 70% of the heating value of the feedstock fuel is associated with the carbon monoxide and hydrogen components of the gas, but can be higher depending upon the gasifier type. Hydrogen must be separated from the gas product stream (which also contains carbon dioxide and carbon monoxide as well as other trace contaminants) and polished to remove remaining sulfur, carbon monoxide, and other contaminants to meet the requirements for various end uses. [Pg.773]


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See also in sourсe #XX -- [ Pg.294 ]




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Hydrogen Components

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