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ETAL-ORGANIC COMPOUNDS

The effect of the addition of various surface-active organic compounds (cyclohexanol, camphor) to an aqueous solution of Na2S04 in contact with Bi single-crystal faces has been studied by Raud etal 9 in using ellipsometry. SQ - was not specifically adsorbed, but at E> -0.5 V (SCE), slight oxidation of the Bi faces was possible. [Pg.119]

Nickel interacts with numerous inorganic and organic compounds (Schroeder etal. 1974 Nielsen 1980a USEPA 1980, 1985 USPHS 1993). Some of these interactions are additive or synergistic in producing adverse effects, and some are antagonistic. [Pg.448]

Wallace LC, Pellizzari D, Leaderer B, etal. 1987. Emissions of volatile organic compounds from building materials and consumer products. Atmosph Environ 21 385-393. [Pg.189]

Table 3.1. Major sources (in kg yr ) of prebiotic organic compounds in early Earth (from Ehrenfreund etal., 2002f... Table 3.1. Major sources (in kg yr ) of prebiotic organic compounds in early Earth (from Ehrenfreund etal., 2002f...
Figure 5.6 Illustration of the effect of a completely water-miscible solvent (CMOS, i.e., methanol) on the activity coefficient of organic compounds in water-organic solvent mixtures decadic logarithm of the activity coefficient as a function of the volume fraction of methanol. Note that the data for naphthalene (Dickhut et al., 1989 Fan and Jafvert, 1997) and for the two PCBs (Li and Andren, 1994) have been derived from solubility measurements whereas for the anilins (Jayasinghe etal., 1992), air-water partition constants determined under dilute conditions have been used to calculate y,f. Figure 5.6 Illustration of the effect of a completely water-miscible solvent (CMOS, i.e., methanol) on the activity coefficient of organic compounds in water-organic solvent mixtures decadic logarithm of the activity coefficient as a function of the volume fraction of methanol. Note that the data for naphthalene (Dickhut et al., 1989 Fan and Jafvert, 1997) and for the two PCBs (Li and Andren, 1994) have been derived from solubility measurements whereas for the anilins (Jayasinghe etal., 1992), air-water partition constants determined under dilute conditions have been used to calculate y,f.
The above mentioned sequence of mechanistic steps has been experimentally proven for nitration of a wide range of organic compounds (Ridd 1991 Ridd Sandall 1981 Clemens, Ridd, Sandall 1984,1985 Clemens, Helsby, Ridd, etal. 1985 Lehnig 1996,1997 Giffney Ridd 1979 Powell et al. 1990). Some examples deserve special consideration. [Pg.252]

Table 1. Degradability ofhalogenated organic compounds in the presence ofzerovalent iron (Adapted from Gavaskar etal., 1998 and EPA, 1998). Compounds indicated in bold face are among the 25 most frequently detected groundwater contaminants at hazardous waste sites (NRC, 1994). ... Table 1. Degradability ofhalogenated organic compounds in the presence ofzerovalent iron (Adapted from Gavaskar etal., 1998 and EPA, 1998). Compounds indicated in bold face are among the 25 most frequently detected groundwater contaminants at hazardous waste sites (NRC, 1994). ...
PALMER ETAL. Organic Sulfur Compounds in Coals and Macerals... [Pg.300]

Phosphorus in the form of phosphate is the principal source of P for plants. Phosphorus is commonly applied in fertilisers although its uptake by plants is much less than that of N and K and its availability is one of the most common nutritional limitations to crop yield (Bould etal., 1983). Some of the P in soils and soil solutions may be present in organic compounds. However, it is unlikely to be available to plants in its organic form and decomposition of organic matter releases P in its available... [Pg.40]

A reaction in which the oxidized or reduced form of a compound isomerizes via a first-order process on the voltammetric time-scale is common for a wide range of organometallic and organic compounds (for example Bard etal., 1973 Bond et al., 1986,1988,1992). An example from the field of organic chemistry involves the reduction of diethyl maleate to its radical anion which then isomerizes to the diethyl fumarate anion, again an overall EC mechanism (Bard et al., 1973). There is a wide range of examples of other EC mechanisms such as the reduction of the antibiotic chloramphenicol in which a nitro unit (-NO2) is reduced to a hydroxylamine (-NHOH) (E step) which rapidly converts into a nitroso (-NO) species (C step) (Kissinger and Heineman, 1983). [Pg.37]

Sun, R.G, Wang, Y.Z., Zheng, B.Q., etal. (2000) 1.54 mm infrared photoluminescence and electroluminescence from an erbium organic compound. Journal of Applied Physics, 87, 7589-7591. [Pg.471]

Photoreactions on titanium dioxide have been the focus of considerable interest for some time. Titania offers the opportunity to oxidize organic compounds in polluted environments, and has also been exploited to generate titania-supported nanoparticles of metals (e.g., silver) via photoreduction reactions [85]. While there is not enough room here to thoroughly treat photocatalytic processes, a brief introduction to the subject is presented below. Readers seeking detailed treatments of this subject are referred to a recent review by Yates etal. on titania-facilitated photocatalysis [86]. [Pg.437]


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