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Hydrogen production process control

Fernandez, J.R., Abanades, J.C., Murillo, R. and Grasa, G. (2012) Conceptual design of a hydrogen production process from natural gas with CO2 capture using a Ca-Cu chemical loop. International Journal of Greenhouse Gas Control, 6,126-141. [Pg.172]

Organization and Overview. The book is divided into two volumes. The first contains 14 chapters, which cover the origin and characterization of petroleum, major processes for fuel-production, and environmental pollution control. The second volume contains 13 chapters, which focus on lubricants, hydrogen production, process modeling, automation, and refining management. [Pg.466]

Miscellaneous. Hydrochloric acid is used for the recovery of semiprecious metals from used catalysts, as a catalyst in synthesis, for catalyst regeneration (see Catalysts, regeneration), and for pH control (see Hydrogen-ION activity), regeneration of ion-exchange (qv) resins used in wastewater treatment, electric utiUties, and for neutralization of alkaline products or waste materials. In addition, hydrochloric acid is also utilized in many production processes for organic and inorganic chemicals. [Pg.451]

Trichlorosilane. The primary production process for trichlorosilane is the direct reaction of hydrogen chloride gas and sihcon metal in a fluid-bed reactor. Although this process produces both trichlorosilane and sihcon tetrachloride, production of the latter can be minimi2ed by proper control of the reaction temperature (22). A significant amount of trichlorosilane is also produced by thermal rearrangement of sihcon tetrachloride in the presence of hydrogen gas and sihcon. [Pg.19]

Cobalt(II) complexes of three water-soluble porphyrins are catalysts for the controlled potential electrolytic reduction of H O to Hi in aqueous acid solution. The porphyrin complexes were either directly adsorbed on glassy carbon, or were deposited as films using a variety of methods. Reduction to [Co(Por) was followed by a nucleophilic reaction with water to give the hydride intermediate. Hydrogen production then occurs either by attack of H on Co(Por)H, or by a disproportionation reaction requiring two Co(Por)H units. Although the overall I easibility of this process was demonstrated, practical problems including the rate of electron transfer still need to be overcome. " " ... [Pg.287]

An understanding of the kinetics and catalytic mechanism of polymer hydrogenation is essential in order to optimize the reaction conditions, to control the reaction systems, and to design commercial production processes. Catalytic kinetic mechanisms for Rh-, Os- and Ru-complex polymer hydrogenation systems have been extensively investigated, and are summarized in the following sections. [Pg.565]

In any case, covering may be impracticable for other reasons. Many processes as they are currently designed depend upon at least visual access by operators for process control, and in other instances the production of odorous chemicals such as hydrogen sulphide can be accompanied by the formation of methane, giving a potential fire or explosion hazard. [Pg.145]

As an example, the propagation steps for the reductive alkylation of alkenes are shown in Scheme 7.1. For an efficient chain process, it is important (i) that the RjSi radical reacts faster with RZ (the precursor of radical R ) than with the alkene, and (ii) that the alkyl radical reacts faster with the alkene (to form the adduct radical) than with the silicon hydride. In other words, the intermediates must be disciplined, a term introduced by D. H. R. Barton to indicate the control of radical reactivity [5]. Therefore, a synthetic plan must include the task of considering kinetic data or substituent influence on the selectivity of radicals. The reader should note that the hydrogen donation step controls the radical sequence and that the concentration of silicon hydride often serves as the variable by which the product distribution can be influenced. [Pg.144]

On the other hand, the term carbon black is used for a group of well-defined, industrially manufactured products. They are produced under carefully controlled conditions. The physical and chemical properties of each type of carbon black are kept within narrow specifications. Carbon black is one form of highly dispersed elemental carbon with extremely small particles. Depending on the production process and the raw materials, carbon black also contains chemically bound hydrogen, oxygen, nitrogen, and sulfur. [Pg.143]

Because of problems encountered in blending whey products containing residual M. miehei rennet with materials containing casein, this rennet preparation has been modified to decrease its heat stability (Branner-Jorgensen et al 1980 Cornelius 1982). This process involves treatment of the rennet with hydrogen peroxide under controlled conditions. Some enzymic activity is lost but the modified enzyme has about the same stability as calf rennet. Nearly all M. miehei rennet used by the cheese industry is now modified (Ramet and Weber 1981). [Pg.617]

A mixture of palladium chloride and triphenylphosphine effectively catalyzes carboxylation of linoleic and linolenic acids and their methyl esters with water at 110°-140°C and carbon monoxide at 4000 psig. The main products are 1,3-and 1,4-dicarboxy acids from dienes and tricarboxy acids from trienes. Other products include unsaturated monocar-boxy and dicarboxy acids, carbomethoxy esters, and substituted a,J3-unsaturated cyclic ketones. The mechanism postulated for dicarboxylation involves cyclic unsaturated acylr-PdCl-PhsP complexes. These intermediates control double bond isomerization and the position of the second carboxyl group. This mechanism is consistent with our finding of double bond isomerization in polyenes and not in monoenes. A 1,3-hydrogen shift process for double bond isomerization in polyenes is also consistent with the data. [Pg.154]

Table II, the second example, shows the benefits of metals passivation at a FCCU in a refinery operating to maximize throughput. The FCC catalyst contained 490 ppm nickel and 1200 ppm vanadium, and the unit was operating against both its air blower and gas compressor limits. Hydrogen production was 92 SCF per barrel of FCCU feed with this amount of hydrogen in the gas to the compressor, it was difficult to maintain the compressor governor on control. The high concentration of hydrogen in the fuel gas also affected the steady state operation of the heat control of other processing units. Table II, the second example, shows the benefits of metals passivation at a FCCU in a refinery operating to maximize throughput. The FCC catalyst contained 490 ppm nickel and 1200 ppm vanadium, and the unit was operating against both its air blower and gas compressor limits. Hydrogen production was 92 SCF per barrel of FCCU feed with this amount of hydrogen in the gas to the compressor, it was difficult to maintain the compressor governor on control. The high concentration of hydrogen in the fuel gas also affected the steady state operation of the heat control of other processing units.

See other pages where Hydrogen production process control is mentioned: [Pg.380]    [Pg.291]    [Pg.460]    [Pg.639]    [Pg.639]    [Pg.428]    [Pg.352]    [Pg.985]    [Pg.106]    [Pg.66]    [Pg.139]    [Pg.287]    [Pg.293]    [Pg.518]    [Pg.575]    [Pg.263]    [Pg.35]    [Pg.235]    [Pg.95]    [Pg.142]    [Pg.169]    [Pg.129]    [Pg.140]    [Pg.515]    [Pg.506]    [Pg.533]    [Pg.150]    [Pg.391]    [Pg.713]    [Pg.476]    [Pg.280]    [Pg.2359]    [Pg.421]    [Pg.36]    [Pg.242]    [Pg.41]    [Pg.51]   
See also in sourсe #XX -- [ Pg.638 , Pg.639 ]




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