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Water decomposition potential

Arsine is highly volatile and there is little risk of direct residual contamination. However, potential persistent decomposition products include arsenic and arsenic oxides. Wash the remains with soap and water. Pay particular attention to areas where agent may get trapped, such as hair, scalp, pubic areas, fingernails, folds of skin, and wounds. If remains are heavily contaminated with residue, then wash and rinse waste should be contained for proper disposal. Once the remains have been thoroughly decontaminated, no further protective action is necessary. Body fluids removed during the embalming process do not pose any additional risks and should be contained and handled according to established procedures. Use standard burial procedures. [Pg.252]

A thermal stability study was first carried out to determine the following information (1) the solidification temperature as a function of the concentration of the sulfonate (2) the enthalpy of decomposition by DTA (3) the autocatalytic nature of the decomposition by Dewar flask (4) kinetic data for decomposition by Dewar flask (5) the time to maximum rate by ARC, and (6) the heat generation as a function of temperature, also by ARC. In addition, the enthalpy of dilution was determined for various potential water leak rates. These data were useful in defining emergency response times. [Pg.170]

The potential required to split water into and O, i.e., (E - E is equal to 1.229 V. Though the theoretical potential is 1.23 V for water electrolysis, in practice the actual water decomposition will occur only above 1.7 V. The extra potential, which is essential for the water decomposition, is called overpotential. Overvoltages are composed of activation or charge transfer overvoltage, concentration or diffusion or mass transfer overvoltage and resistance overvoltage. Overvoltage is evaluated mainly as a function of current and temperature (Viswanathan, 2006). [Pg.116]

One other important criterion for successful water cleavage that must be considered is the solution pH. Although the potential difference between the two half reactions for water decomposition is fixed at 1.23 V and is independent of pH, the half-cell reactions are dependent upon pH (Figure 4). Thus, by altering the pH of a solution it is sometimes possible to alter the half-cell potentials to be compatible with the redox properties of a photosensitizing catalyst. The oxidant must have a redox potential above the oxygen line, whilst the reductant must have a redox potential below the hydrogen line. The effect of pH is illustrated in subsequent sections of this chapter. [Pg.491]

Tris(2,2 -bipyridyl)ruthenium(II) dication ([Ru(bipy)3]2+) is one of the most extensively studied coordination compounds in chemistry due to its potential for use in cyclic photochemical water decomposition. An extensive review of the complex appears elsewhere.116... [Pg.499]

Temperatures up to 1500 °C reduce the reversible thermodynamic potential for water decomposition from a room temperature value of 1.23 V to 0.7 V (43%). The cost of electrolytic hydrogen varies linearly with the potential of the cell at the current density being used, since cost of the electricity is the dominating item in the cost of electrolytic hydrogen, high-temperature steam electrolysis would greatly improve the economics. Heat is needed to maintain the temperature of the system, but heat costs only a third of the cost of electricity. So far, very high temperature cells are research items, but 1000 °C cells have been developed in Europe under the nickname Hot Elly. ... [Pg.487]

The reversible potential ofBr2 + 2e —> 2 Br is 1.08 V atm. The pH of sea water is near 7 and 25 °C hence the reversible potential of 2H+ + 2e —> Hj is about -0.42 V. The reversible cell potential would be then about 1.5 V. The idea here is to reduce the potential below the thermodynamically reversible value by photoillumination ofthe anode (photoassisted water decomposition Szklarczyk, 1983). [Pg.491]

The decrease of the decomposition voltage is at first sight difficult to comprehend and it cannot be explained by Nemst s equation, according to which the equilibrium deposition potentials of hydrogen and oxygen increase with increased pressure. The equation (X—8) expresses the relation between the reversible water decomposition potential and the gas pressure at 25 °C ... [Pg.228]

This equation shows that, theoretically the water decomposition potential will rise by 0.0435 V at a pressure increase from 1 to 10 atm., or from 10 to 100 atm. [Pg.229]

Peroxidases Used as an enzymatic rinse process after reactive dyeing, oxidative splitting of hydrolysed reactive dyes on the fibre and in the liquor, providing better wet fastness, decolourised waste water and potentially toxic decomposition compounds (aromatic nitro-compounds)... [Pg.182]

One of the more recent technologies in pollution treatment and remediation is based on the electrokinetic decontamination of soils [126-128], in which a dc potential (a few volts per centimeter) is applied across two inert electrodes embedded in a soil mass. This applied potential causes decomposition of the soil water to occur at the two electrodes. The migration of contaminants in the electric field, water transport, and reactions at the electrodes, as well as reactions caused by the induced pH gradient, can effectively clean soils. Acar et al. [127] reviewed electrokinetic remediation for the removal of metals and other inorganic contaminants from soil as well as its use in the extraction of organics from contaminated soils. [Pg.407]

Saracco and Specchia [84] noted that inorganic membranes have great potential in gas separation, catalytic reactors, gasification of coal, water decomposition, and solid electrolyte fuel cells [81-89]. Inorganic membranes are usually made from alumina, sUica, carbon, and zeolites [85]. We will only assess porous membranes since fouling is virtually absent in dense membranes [81]. [Pg.338]

The reversible potential of the water decomposition reaction is 1.23 V at 25° C. The overpotential for OERR in aqueous alkaline solutions... [Pg.495]

Figure 7.8. Stability field diagram for soluble and solid forms of Mn under a range of redox potential and pH conditions, assuming a dissolved CO concentration of 10 M. Shaded areas delineate conditions that are unattainable because of water decomposition. (Adapted from W. Stumm and J. J. Morgan. 1981. Aquat/c Chemistry. 2nd ed. New York Wiley.)... Figure 7.8. Stability field diagram for soluble and solid forms of Mn under a range of redox potential and pH conditions, assuming a dissolved CO concentration of 10 M. Shaded areas delineate conditions that are unattainable because of water decomposition. (Adapted from W. Stumm and J. J. Morgan. 1981. Aquat/c Chemistry. 2nd ed. New York Wiley.)...
Thermodynamic and over potential region For a terminal voltage smaller than the water decomposition potential Ud (Ud 2 V), no significant electrolysis happens and no current flows between the electrodes. [Pg.62]

If the terminal voltage U is higher than the water decomposition potential Ud, electrolysis takes place and the current is related to U according to (3.40) and (3.22) by ... [Pg.64]

The bifunctional mechanism proposes that a foreign metal, M, promotes water decomposition at lower potentials than that of platinum, by the following reactions ... [Pg.257]


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