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Water, absorptionally bound method

Functional property terminology is not well defined and is not universally agreed upon. Often, the same term is used to describe a variety of methods measuring different properties. For example, terms such as water hydration capacity, water absorption, water binding, and waterholding capacity are all used interchangeably to describe water bound or retained by a protein. It is therefore necessary to carefully define the terms under study and make sure the methods selected measure the desired parameters. [Pg.292]

It should be clear that the RM measured in this way, e. g. 0,1 %, must not be identical with residual moisture contents measured with other methods (see Section 1.3.1) because there will be always some water which cannot be desorbed at the end temperature of the drying. This content of bound water for one product and one temperature is a stable value which can be taken from the measurements of absorption isotherms. [Pg.81]

Earlier work (6) using this method yielded a second-order rate constant of 24.7 1.5 M""1 sec."1 for the reaction of dilute solutions of cesium with water in ethylenediamine. On the basis of optical absorption spectra (7) and other evidence (8, II), it was assumed that this reaction was that of the solvated electron as well as loosely bound electrostatic aggregates of electrons and cations with water. This permitted correlation with the results of aqueous radiation chemistry. [Pg.176]

Two methods of bonding a spiropyran to the surface of silica gel have already been mentioned the reaction of silica-bound salicylaldehyde with Fischer s base, and the reaction of 6-lithioBIPS with silica. Silica-bonded spiropyrans exhibited properties (reverse photochromism, visible light photobleaching, and color changes upon acid treatment due to salt formation) very similar to those of spiropyrans merely adsorbed onto silica. The differences in behavior were attributed to the different extent of absorption and desorption of atmospheric water caused by the difference in the number of free SiOH groups available in the two cases.86... [Pg.62]

EPA has used cancer risk data from human epidemiological studies to derive risk factors associated with oral exposure to benzene. Oral dose levels associated with specific carcinogenic risks have been extrapolated the risk value of 2.7x 10"2 for lifetime inhalation exposure to 1 ppm was converted to a slope factor of 2.9/10"2 for oral exposure of 1 mg/kg/day, assuming identical levels of absorption of benzene following both routes of exposure. Using the method described by EPA (IRIS 1996), the drinking water levels associated with individual upper-bound estimates of 10"4, 10"5, 10"6, and 10"7 have been calculated to be lxlO 1, lxlO"2, lxlO"3, and lxlO"4 mg/L, respectively, which are equivalent to dose levels of 3x 10"3,... [Pg.135]

Modem methods for study of metal-activated enzymes include NMR and ESR spectroscopy, water relaxation rates by pulsed NMR (PRR), atomic absorption, Mbssbauer, X-ray and neutron diffraction, high-resolution electron microscopy, UV/visible/IR spectroscopy, laser lanthanide pertubation methods, fluorescence, and equilibrium and kinetic binding techniques. Studies with Mg(II)-activated enzymes have been hampered by the lack of paramagnetic or optical properties that can be used to probe its environment, and the relative lack of sensitivity of other available methods initial velocity kinetics, changes in ORD/CD, fluorescence, or UV properties of the protein, atomic absorption assays for equilibrium binding, or competition with bound Mn(II) °. Recent developments in Mg and 0-NMR methodology have shown some promise to provide new insights . ... [Pg.672]

Metal-semiconductor phase transition (MSPT) in VO2 reflected in the interfacial behavior of bound water because of changes in the absorptivity of the materials with respect to water and efficiency of nuclear magnetic relaxation (Turov et al. 1995a). Therefore, the signal width and intensity of bound water strongly changed. However, these materials were not structurally characterized using adsorption or/and cryoporometry methods. [Pg.422]


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