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Hydrogen water system

The upper limit of efficiency of the biophotolysis of water has been projected to be 3% for weU-controUed systems. This limits the capital cost of useful systems to low cost materials and designs. But the concept of water biophotolysis to afford a continuous, renewable source of hydrogen is quite attractive and may one day lead to practical hydrogen-generating systems. [Pg.19]

Ammonia—water systems operate under moderate pressures and care must be taken to avoid leaks of the irritating and toxic ammonia (qv). Sometimes a third material with a widely different density, eg, hydrogen, is added to the cycle in order to eliminate the need for mechanical pumping. [Pg.508]

Hydrogen Chloride—Water System. Hydrogen chloride is highly soluble in water and this aqueous solution does not obey Henry s law at ah concentrations. Solubhity data are summarized in Table 5. The relationship between the pressure and vapor composition of unsaturated aqueous hydrochloric acid solutions is given in Reference 12. The vapor—Hquid equiHbria for the water—hydrogen chloride system at pressures up to 1632 kPa and at temperatures ranging from —10 to +70° C are documented in Reference 13. [Pg.439]

The thermodynamic data pertinent to the corrosion of metals in aqueous media have been systematically assembled in a form that has become known as Pourbaix diagrams (11). The data include the potential and pH dependence of metal, metal oxide, and metal hydroxide reactions and, in some cases, complex ions. The potential and pH dependence of the hydrogen and oxygen reactions are also suppHed because these are the common corrosion cathodic reactions. The Pourbaix diagram for the iron—water system is given as Figure 1. [Pg.275]

In work with the hydrogen chloride-air-water system, Dobratz, Moore, Barnard, and Mever [Chem. Eng. Prog., 49, 611 (1953)] using a cociirrent-flowsystem found that /cg (Eig. 14-77) instead of the 0.8 power as indicated by the Gilliland equation. Heat-transfer coefficients were also determined in this study. The radical increase in heat-transfer rate in the range of G = 30 kg/(s m ) [20,000 lb/(h fH)] was similar to that obsei ved by Tepe and Mueller [Chem. Eng. Prog., 43, 267 (1947)] in condensation inside tubes. [Pg.1402]

Certain anaerobic bacteria capable of producing hydrogen may, under special circumstances, contribute to hydrogen embrittlement of some alloys. Once again, if such mechanisms operate, they have very limited applicability in most cooling water systems. [Pg.125]

Glaze, W. H., Kang, J. W., and Aieta, M. "Ozone-Hydrogen Peroxide Systems for Control of Organies in Munieipal Water Supplies Proceedings of the Second International Conference in the Role of Ozone on Water and Wastewater Treatment, TekTran International Ltd., Kitchener, Ontario, Canada, pp. 233-244, 1987. [Pg.59]

Finally, a special example of transition metal-catalyzed hydrogenation in which the ionic liquid used does not provide a permanent biphasic reaction system should be mentioned. The hydrogenation of 2-butyne-l,4-diol, reported by Dyson et al., made use of an ionic liquid/water system that underwent a reversible two-... [Pg.231]

Figure 4-469 shows the effect on corrosion rates of 1020 steel in different water systems with dissolved hydrogen sulfide. The difference in corrosion rates is due to different corrosion products formed in different solutions. In solution I, kansite forms. Kansite is widely protective as the pyrrhotite coats the surface giving slightly more protection until a very protective pyrite scale is formed. In solution II, only kansite scale forms, resulting in continued increase in the corrosion rate. Finally, in solution 111, pyrite scale is formed as in solution I however, continued corrosion may be due to the presence of carbon dioxide. [Pg.1308]

Figure 4-469. Corrosion rates in hydrogen sulfide-water systems. (From Ref. [197].)... Figure 4-469. Corrosion rates in hydrogen sulfide-water systems. (From Ref. [197].)...
In sea-water systems such attack may occur under dead barnacles or shellfish, the decomposing organic matter assisting corrosion. Pitting is most likely to occur in polluted in-shore waters, particularly when hydrogen sulphide is present. In such contaminated waters non-protective sulphide scales are formed and these tend to stimulate attack. [Pg.697]

Excess Volume Comparison Figure 7.5 compares V for the three systems for which we have compared H, G, and 5, plus the (cyclohexane + decane) system.5 The comparatively large negative for the (ethanol + water) system curve (4) can be attributed to the decrease in volume resulting from the formation of hydrogen-bonded complexes in those mixtures. The negative for the (hexane + decane) system curve (3) reflects an increased packing... [Pg.332]

Bottinga, Y. 1969 Calculated fractionation factors for carbon and hydrogen isotope exchange in the system calcite-carbon dioxide-graphite-methane-hydrogen-water vapour. Geochimica et CosmochimicaActa 33 49-64. [Pg.137]

Table 14.6 Parameter Estimates for the Hydrogen Sulfide-Water System... Table 14.6 Parameter Estimates for the Hydrogen Sulfide-Water System...
VLE data and calculated phase diagram for the hydrogen sulfide-water system [reprinted from Industrial Engineering Chemistiy Research with permission from the American Chemical SocietyJ. [Pg.260]

The water dimer is probably the most intensively studied intermolecular hydrogen bonded system of all. Hence, ample theoretical and experimental data is available for this system,... [Pg.235]

Lundell, J., Latajka, Z., 1997, Density Functional Study of Hydrogen-Bonded Systems The Water-Carbon Monoxide Complex , J. Phys. Chem. A, 101, 5004. [Pg.294]


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See also in sourсe #XX -- [ Pg.395 ]




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Hydrogen + water

Hydrogen chloride-water system

Hydrogen systems

Hydrogen-methane-water system

Hydrogenous systems

Production of Hydrogen using a Coupled Water Electrolyzer-Solar Photovoltaic System

Ternary System Water - Hydrogen Peroxide-Jet Propulsion Fuel

The Hydrogen Sulfide-Water System

Water hydrogenation

Water-hydrogen sulfide system, liquid-vapor

Water-hydrogen sulfide system, liquid-vapor equilibria

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