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Physico-chemical basis

In physico-chemical terms, metals in these different forms are held by chemical bonds of different strengths. According to the strength of the chemical bonds, the forms of metals may be divided into four groups  [Pg.18]

The capacity of metals to disperse in space is clearly related to this classification weakly-confined metals are able to disperse for greater distances than strongly-confined metals, and so on. In particular, mobile forms are able to migrate far from their sourcesprovided that some natural or artificial physical field is exerted to effect migration. However, all forms are in a state of dynamic equilibrium and can transform into other forms. One consequence is that, with increasing concentration of metals in the more mobile forms, there is a simultaneous increase in concentration of metals in the forms with stronger chemical bonds. For example, dissolved Pb, Mo and Cu will interact with oxides and hydroxides of Fe and Mn under certain physico-chemical conditions of pH and Eh. First, due to adsorption of these metals from solution, the metals are [Pg.18]

Mobile and weakly-confined forms of metals make up only a minor part, less than 2%, of the total content of heavy metals in rocks and their weathering products. However, it is these mobile forms of metals that can migrate for significant distances from sources, and thereby convey information about deep ore bodies and oil and gas reservoirs. Weakly-confined forms have direct and steady equilibrium with mobile forms, and thus to a certain degree acquire the same property. Moderately-confined forms also share this property, but only to a small extent. [Pg.19]

These features of the jet halo enhance the prospecting depth of the geoelectrochemical methods. A number of field experiments have verified that the prospecting depth for an ore body attains some hundred metres and for oil and gas reservoirs several kilometres. Similar results have been obtained with data for relatively-confined forms of metals, although the widths of halos are greater than those for mobile and weakly-confined forms of metals. [Pg.20]

Detailed studies of the distributions of concentrations of metals in jet halos reveal apparent non-uniformity of anomaly structure (Fig. 2-2). Maximum concentrations of anomalies on the diurnal surface correspond to the zones of enhanced concentrations of mobile forms of metals at depth, which extend almost vertically and have a complicated [Pg.20]


As part of the studies undertaken in our laboratory it was necessary to be able to determine quantitatively the surfactant present in large numbers of samples (> 100 per week) arising, for example, from core flooding experiments. The chosen method needed to be rapid to reduce analysis time, and to require little manipulation of the sample to reduce errors. In this paper we report the development of a method for the determination of anionic surfactants based upon autotitration and comment on the physico-chemical basis of the technique. [Pg.260]

V.B. Fenelonov, Physico-Chemical Basis, Doctoral dissertation, Institut Kataliza, Novosibirsk, 1987 (in Russian). [Pg.329]

Albert, A. (1985) Selective Toxicity The Physico-Chemical Basis of Therapy, 7th edn, Chapman and Hall, London. [Pg.187]

Wilson, N.S., Dolan, J.W, Snyder, L.R., Carr, P.W., and Sander, L.C., Colnmn selectivity in reversed-phase liqnid chromatography iii. The physico-chemical basis of selectivity, J. Chromatogr. A, 961, 217, 2002. [Pg.292]

What is the physico-chemical basis for the point of inflection being taken as the equivalence point ... [Pg.99]

Clearly, between these two extremes, the conditions are such that [Cl ] = [Ag" "]. The shapes of the emf-V curve on either side of the point of inflection are the same - a mirror image in fact - implying that the two regimes, above and below N inflection represent deviations from a common position. The only situation existing between the two extremes that could have any physico-chemical basis is that where [C/ ] = [Ag ]. [Pg.99]

Farr, S.J., The physico-chemical basis of radiolabelling metered dose inhalers with Tc, J. Aerosol Med., 9(Suppl. 1) S27-S36 (1996). [Pg.267]

Albert, A. 1973. Structure-activity relations. In Selective Toxicity the Physico-Chemical Basis of Therapy. London Chapman and HaU chapter 7. [Pg.305]

Mac Kenzie, A. P The physico-chemical basis for the freeze-drying process. Developments in Biological Standardization Vol. 74, p. 51-67. Acting Editors Joan C. May, F. Brown S. Karger AG, CH 4009-Basel (Switzerland) 1992... [Pg.120]

MacKenzie APThe physico-chemical basis for the freeze drying process. Dev Biol Std 1977 36 51-67. [Pg.289]

A clue to the physico-chemical basis of the correlation comes from the observation from the crystal structures of various dehydrogenase-NAD+ complexes that those enzymes which bind NADH in the syrt-conformation [45a] transfer the pro-5 hydrogen whereas those enzymes that bind NADH in the a // -conformation [46b] transfer the pro-/ hydrogen (see e.g. You, 1984). The observed stereospecificities thus correspond to transfer of hydride towards the viewer from both rotamers of [45]... [Pg.136]

From the conceptual point of view, there are two general approaches to the molecular structure problem the molecular orbital (MO) and the valence bond (VB) theories. Technical difficulties in the computational implementation of the VB approach have favoured the development and the popularization of MO theory in opposition to VB. In a recent review [3], some related issues are raised and clarified. However, there still persist some conceptual pitfalls and misinterpretations in specialized literature of MO and VB theories. In this paper, we attempt to contribute to a more profound understanding of the VB and MO methods and concepts. We briefly present the physico-chemical basis of MO and VB approaches and their intimate relationship. The VB concept of resonance is reformulated in a physically meaningful way and its point group symmetry foundations are laid. Finally it is shown that the Generalized Multistructural (GMS) wave function encompasses all variational wave functions, VB or MO based, in the same framework, providing an unified view for the theoretical quantum molecular structure problem. Throughout this paper, unless otherwise stated, we utilize the non-relativistic (spin independent) hamiltonian under the Bom-Oppenheimer adiabatic approximation. We will see that even when some of these restrictions are removed, the GMS wave function is still applicable. [Pg.118]

A physico-chemical basis for the critical size requirement has been described. There is evidence that chemical events rather than diffusion can govern subsequent linear growth of zeolite crystals. [Pg.11]

Physico-chemical basis of the retention behaviour of compounds. 26... [Pg.25]

An alternative procedure to gain deeper insight into the physico-chemical basis of solvation consists of the partitioning of AGsoi into its enthalpic, A//soi, and en-tropic, A.S(o, components. Taken together, these quantities represent a substantial reservoir of information about the interactions between solute and solvent molecules. Moreover, these quantities are state functions and can be rigorously derived by using standard thermodynamic relationships, as noted in Eqs. 4-2 and 4-3. Finally, the availability of experimentally measured data for the enthalpy and entropy of solvation makes it possible to calibrate the reliability of theoretical models to predict those thermodynamic quantities. [Pg.104]

Forss (1) reviewed the relationship between sensory analysis and flavor chemistry, and provided a discussion of sensory characterization of flavor. Williams et al. (2) also addressed the problem of relating the many known flavor compounds to what is actually perceived by the individual on a physico-chemical basis. This chapter will center more on reviewing advances in sensory methodology as they have been adapted by the flavor and food industry. [Pg.2]

Dzisko, Vera and Karnaukhov, Anatolii and Tarasova, Djemma. Physico-Chemical Basis of Synthesis of Oxide Catalysts. Novosibirsk Nauka, 1978. [Pg.38]

N. S. Wilson, J. W. Dolan, L. R. Snyder, P. W. Carr, L. C. Sander, Column selectivity in reversed-phase liquid chromatography III. The physico-chemical basis of selectivity, /. Chromatogr. A 961 (2002), 217-236. [Pg.132]

Having laid down the physico-chemical basis of interface and colloid science in Volume I, we can now make a start with the systematic treatment. Solid-gas and, in particular, solid-liquid interfaces are selected as the first topics. The argument for this choice is that such Interfaces do not change their area upon adsorption and/or charging, and are therefore the simplest group of model systems. In Volume III, dealing with fluid-fluid Interfaces, this restriction will be relaxed. [Pg.8]

MacKenzie, A.P. The physico-chemical basis of the freeze drying process. Dev. Biol. 1976, 36, 51-67. [Pg.1849]

PHYSICO-CHEMICAL BASIS OF THE MEMBRANO-TROPIC ACTION... [Pg.173]

Chirife, J. and Favetto, G.J. 1992. Some physico-chemical basis of food preservation by combined methods. Food Research International 25 389-396. [Pg.238]


See other pages where Physico-chemical basis is mentioned: [Pg.3]    [Pg.171]    [Pg.49]    [Pg.120]    [Pg.122]    [Pg.7]    [Pg.170]    [Pg.148]    [Pg.1]    [Pg.195]    [Pg.298]    [Pg.17]    [Pg.46]    [Pg.53]   


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