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Microheterogenization

J. F. Rusling, in Electrochemistry in Micelles, Microemulsions and Related Microheterogeneous Fluids, Electroanalytical Chemistry, A Series of Advances, Marcel Dekker, New York, 1994. [Pg.223]

C1.5.4.5 CONJUGATED POLYMERS, CHROMOPHORE AGGREGATES, AND MICROHETEROGENEOUS MATERIALS... [Pg.2500]

Wang H, Bardo A M, Collinson M M and Higgins D A 1998 Microheterogeneity in dye-doped silicate and polymer films J. Chem. Phys. B 102 7231-7... [Pg.2510]

Carreto M L, Rubio S and Perez-Bendito D 1996 Organic microheterogeneous systems in kinetic anaiysis—Seif-assembied systems Analyst 121 33R-44R... [Pg.2606]

M. Grat2el and K. Kalyanasundaram, eds.. Kinetics and Catalysis in Microheterogenous Systems, Marcel Dekker, New York, 1991. [Pg.155]

Kinetics and Catalysis in Microheterogeneous Systems, edited by M. Gratzel and K. Kalyanasundaram... [Pg.953]

Kalyanasundaram K (1987) Photochemistry in microheterogeneous systems. Academic, New York... [Pg.93]

Considering that microwaves couple mainly with polar and amphiphilic molecules, it has been suggested that microwave irradiation of these microheterogeneous systems. [Pg.478]

Microheterogeneity below specified level Polyacrylamide gel electrophoresis C- and N-terminal analysis. Amino acid composition... [Pg.465]

Latch DE, K McNeill (2006) Microheterogeneity of singlet oxygen distributions in irradiated humic acid solutions. Science 311 1743-1747. [Pg.44]

An attractive way to overcome this problem is to use microheterogeneous photocatalytic systems based on lipid vesicles, i.e. microscopic spherical particles formed by closed lipid or surfactant bilayer membranes (Fig. 1) across which it is possible to perform vectorial photocatalytic electron transfer (PET). This leads to generation of energy-rich one-electron reductant A" and oxidant D, separated by the membrane and, thus, unable to recombine. As a result of such PET reactions, the energy of photons is converted to the chemical energy of spatially separated one electron reductant tmd oxidant. [Pg.39]

It may be possible to achieve an adequate solution of these problems by developing catalysts with snrface properties that have been tailored deliberately so as to provide a favorable catalytic action on all intermediate steps that need it. Such catalysts should be polyfunctional and exhibit a certain degree of chemical and structural surface microheterogeneity. Electrochemical nanoelectrochemistry (see Chapter 36) may be a possible approach for synthesizing snch snrfaces. For a detailed investigation and control of these catalytic surfaces, the tools available among the experimental physical methods (see Chapter 27) will be nsefnl. [Pg.553]

Kalyansundaram, K., 1987, Photochemistry in Microheterogeneous Systems , Academic press Inc., London. [Pg.186]

A detailed treatment of the transport and kinetics at microheterogeneous electrodes was given by Albery and Bartlett The electron transfer of MV to Pt-particles can be described by a bimolecular rate constant kj ... [Pg.120]

Kiwi, J., Kalyanasundaram, K., Grdtzel, M. Visible Light Induced Qeavage of Water into Hydrogen and Oxygen in Colloidal and Microheterogeneous Systems. Vol. 49, pp. 37-125. [Pg.193]

The microheterogenous and nanoheterogenous (mesoscopic) liquid-liquid systems may be concisely called the small systems. They comprise the micro- and nanodomains, described in colloidal chemistry as a variety of structures, e.g., micelles, rods, disks, vesicles, microemulsions, monolayers, and Langmuir Blodgett layers [6,17 19,70]. [Pg.35]

K. Kalyanasundaram. Photochemistry of Microheterogeneous Systems, Academic Press, London, 1987. [Pg.237]

For the remainder of this chapter, we discuss results for various studies of interfacial solvation dynamics. We first discuss studies at liquid liquid interfaces at planar interfaces and in microheterogeneous media in Section II. In Section III, we discuss solvation dynamics at liquid solid interfaces. In Section IV, we review theoretical models and simulations of solvation dynamics at liquid interfaces. Finally, we conclude with a discussion of future studies. [Pg.406]

Dynamics of polar solvation have been studied at a range of differing liquid-liquid interfaces. These include planar liquid-liquid, and liquid-air interfaces as well as those found in microheterogeneous media. We discuss each case separately. [Pg.407]

Biphasic media are macroheterogenous, with a well-defined liquid-liquid interface [25,63] [Fig. 1(g), (h)], or microheterogeneous consisting of an emulsion with a very important interface area [37,38] [Fig. 1-f]. The first medium is used for kinetic studies... [Pg.557]

The microheterogeneity coefficient was introduced only for the description of the microstructure of binary copolymers with symmetric units. At increased number of unit types and/or when account is taken of structural isomerism, the role of Km will be performed by other parameters analogous to it. A general strategy for the choice of these latter has been elaborated in detail [12], while their values have been measured via NMR spectroscopic techniques for a variety of polycondensation polymers [13]. [Pg.167]

A biologically formed protein or polynucleotide, while exhibiting some limited heterogeneity in length or microheterogeneity in the main chain sequence or in pendant prosthetic groups, has an essentially unique sequence. Different forms of a protein or polynucleotide often can be... [Pg.320]


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See also in sourсe #XX -- [ Pg.62 ]




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