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End use of hydrogen

The risk to the public during consumer end use of hydrogen derives from the possibility of accidental fire and explosion, a direct consequence of the physical and chemical properties of hydrogen. These properties help to define the kinds of safety issues that must be addressed, the fundamental design goals for hydrogen systems, and the operational limitations of these systems. Table 9-1 summarizes the properties of hydrogen in contrast with those of other commonly used fuels. [Pg.125]

Given the huge costs involved in building and operating the hydrogen production and distribution infrastructure, a major question is what end use of hydrogen could justify the cost that would be incurred in its massive production and distribution ... [Pg.194]

Synthesis gas generally refers to a mixture of carbon monoxide and hydrogen. The ratio of hydrogen to carbon monoxide varies according to the type of feed, the method of production, and the end use of the gas. [Pg.121]

Polyalphaolefin Hydraulic Fluids. Polyalphaolefms are made by oligomerizing alphaolefins such as 1-decene in the presence of a catalyst (Newton 1989 Shubkin 1993 Wills 1980). The crude reaction mixture is quenched with water, hydrogenated, and distilled. The number of monomer units present in the product polyalphaolefin oil depends on a number of reaction parameters including the type of catalyst, reaction temperature, reaction time, and pressure (Shubkin 1993). The exact combination of reaction parameters used by a manufacturer is tailored to fit the end-use of the resulting polyalphaolefin oil. A typical polyalphaolefin oil prepared from 1-decene and BF3- -C4H9OH catalyst at 30 °C contains predominantly trimer (C30 hydrocarbons) with much smaller amounts of dimer, tetramer, pentamer, and hexamer. While 1-decene is the most common starting material, other alphaolefins can be used, depending on the needs of the product oil. [Pg.286]

Hydrocarbon sulfonates, 23 531 Hydrocarbon surfactants, 24 133 Hydrocarbon waxes, 26 220 Hydrocarbyl complexes of thorium, 24 773 of uranium, 25 441-442 Hydrochloric acid, 13 808-809, 821-822. See also Hydrogen chloride in ascorbic acid manufacture, 25 757 chlorine from, 6 172-175 constant boiling, 13 814t density and concentration of, 13 808t end use of chlorine, 6 135t for fermentation, 11 38... [Pg.448]

Phosphorus pentachloride, 79 40, 42-44 end use of chlorine, 6 135t sodium reactions with, 22 766 Phosphorus pentafluoride, 79 33 Phosphorus pentahalides, 79 31-33 Phosphorus pentoxide, 79 49, 69. See also Phosphorus(V) oxides as cellulose solvent, 77 272 in hydrogen fluoride manufacture, 74 11 vapor of, 79 49... [Pg.699]

It follows that biomass will play a role complementary to other resources such as electricity from nuclear and hydraulic sources, as well as relatively inexhaustible supplies of natural gas, non-conventional oil and oil sands. The end use of these forms will be dictated by a combination of historic development and technological inertia such that substitution products electricity, methanol, hydrogen, or tonnage chemicals like ammonia, will provide the major outlets for biomass carbon... [Pg.179]

The kinetics of radiation-induced polymerization of bulk nitroethylene was also studied at 10° C by the use of hydrogen bromide as an anion scavenger (27). The value of Gt (yield of the initiation by 100 eV energy absorbed) was found to be about 3, which was much larger than the value obtained for many radiation-induced cationic polymerizations. The propagation rate constant, kp, was estimated to be 4 x 107 M-1 sec-1. The large kp value was attributed to the concept that the propagating chain ends were free ions in contrast to the existence of counter ions in catalytic polymerization. [Pg.409]

The front end section of hydrogen, methanol, and ammonia plants is shown in Figure 4.4. The secondary reformer is used only in an ammonia plant. The feed gas is desulfurized in carbon steel equipment. When the metai temperature exceeds 800 to 850° F (425 to 455°C), lCr-V Mo(2) or IViCr-VfeMo are used to avoid long-term deterioration of the mechanical properties by graphitization. Preheat coils in the top of the reformer furnace are usually 21/4Cr-1Mo up to 1,200°F (650° C) metal Temperature and type 304H... [Pg.77]

Rejtrmces. Blicke and Burckhalter, J. Am. Chem. Sec., 44, 478 (1942). The method has been checked in the Socony-Vacuum Laboratories. In cases where di-(2-thienyl)methane can be conveniently separated irom the end-products, the crude reaction mixture can be conveniently utilized without resorting to distillation of the 2-thenyl chloride. Over-all yields normally are improved in this manner. The author has found that it is convenient to prepare this compound using equimolar quantities of hydrochloric acid, thiophene, and formaldehyde, omitting the use of hydrogen chloride. The yields tire comparable when the above proced ire is employed. [Pg.5]


See other pages where End use of hydrogen is mentioned: [Pg.248]    [Pg.198]    [Pg.24]    [Pg.24]    [Pg.130]    [Pg.149]    [Pg.198]    [Pg.282]    [Pg.282]    [Pg.1128]    [Pg.248]    [Pg.198]    [Pg.24]    [Pg.24]    [Pg.130]    [Pg.149]    [Pg.198]    [Pg.282]    [Pg.282]    [Pg.1128]    [Pg.380]    [Pg.246]    [Pg.437]    [Pg.5]    [Pg.29]    [Pg.144]    [Pg.258]    [Pg.68]    [Pg.27]    [Pg.406]    [Pg.89]    [Pg.108]    [Pg.425]    [Pg.508]    [Pg.800]    [Pg.801]    [Pg.154]    [Pg.437]    [Pg.7]    [Pg.33]    [Pg.1515]    [Pg.50]    [Pg.128]    [Pg.42]    [Pg.5963]    [Pg.508]    [Pg.4]    [Pg.396]    [Pg.5]    [Pg.103]   
See also in sourсe #XX -- [ Pg.282 ]




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