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Dimensions, direct determination

Direct determination of the rate of the C- or Y-Dye formation reaction in the individual microdroplets has been made possible by potential application of the laser trapping-spectroscopy-electrochemistry technique. Furthermore, the dye formation reaction efficiency in each droplet could be controlled arbitrarily by the distance between the droplet and the electrode. Under the present experimental conditions (i.e., pH 10 and [SO] ] =20mM), the diffusion length of QDI within its lifetime is only several micrometers, so the distance dependence of the reaction is unique in the micrometer dimension. The present approach will therefore lead to a new methodology to control chemical reaction in micrometer-size volumes. [Pg.218]

Some other unceitainties associated with packed-bed catalytic membrane reactors arc the following. The reaction rate in the membrane layer is not easy to assess and it is likely to be different from that in the catalyst bed. The extremely small thickness of the membrane layer compared to the dimensions in the tubular and the annular regions makes the direct determination of the membrane-related parameters difficult, if not impossible in some cases. Furthermore, obtaining accurate data of the effective diffusivity for the membrane, particularly in the presence of a support layer, is not straightforward and often involves a high degree of uncertainty. [Pg.427]

ESD induced by electrons extracted at the tip of a scanning tunnelling microscope (STM) has recently applied to the study of the H-Si and Cl-GaAs(l 10) systems by Shen and Avouris [98]. A feature of the STM is the capability to provide an intense electron density (lO A/cm ) of atomic dimensions directly at the surface atoms. Under these conditions, desorption can also proceed with multiple-vibrational excitation. A combination of ESD and STM holds promise as a tool for atomistic DIET, also as a means to asses the influence of electron irradiation at surfaces [99]. In ESDIAD an interesting aspect is the determination of the trajectory of the ion on leaving the surface, which will be discussed later in relation to the TiOa surface. [Pg.616]

The advance of synthetic techniques in the last decade made possible the synthesis of model branched polymers of known and controlled structure and, equally important, relatively homogeneous in molecular weight and structure (204, 221, 228). Investigations (101, 136, 141, 196) (Fig. 9) of a variety of branched polymers of different branched chain configurations but of the same chemical stmctiure and total molecular weight permits direct determination of the effect of coil dimensions and configurations on rj. [Pg.284]

Direct Determination of Unperturbed Polyelectrolyte Coil Dimensions... [Pg.358]

Direct Determination of Unperturbed Polyel ti Iyte Coil Dimensions (under 0 Conditions)... [Pg.374]

The third form (Fig. 7) differs only in detail from the second it was preferred for the experiments with liquid hydrogen, because it could be made of much smaller dimensions. The platinum wire was wound on the outside of the cylindrical silver vessel and covered, to avoid thermal losses, with silver foil which was soldered at the edges to give a better thermal contact this form has the advantage that the platinum wire docs not have to be introduced vacuum-tight into the inside of the silver vessel. In a small size and at low temperatures this form of calorimeter proved to be excellent. The heat capacity of the silver vessel could be calculated with good accuracy, but it was also directly determined by a series of... [Pg.31]

There are two basic ways in which measurements of the unperturbed dimensions are obtained (1) determination of unperturbed dimensions directly, by measurements in theta solvents and (2) determination of the perturbed dimensions in a good solvent and extrapolation of the values to the unperturbed state using one of the existing theories. Both methods have been widely used as will be shown. [Pg.4]

Eq. 5.16 represents the model of steady-state operation of CPBR. It allows the determination of the steady-state X for any given combination of M at/F. This equation reduces in one the number of degrees of freedom of the system but there are still two degrees of freedom that allows flexibility of operation, since from the three operational variables Meat, F and Si, two can be established separately. A common situation is the use of Eq. 5.16 to determine the enzyme load required (Meat of the biocatalyst) to obtain the desired substrate conversion (X) for a certain mass flow of substrate (F Si). This equation can also be used for reactor design, since its dimensions are determined by the biocatalyst bed volume, which directly depends on biocatalyst mass, according to ... [Pg.216]

VII. Enthalpic and Entropic Contributions to Rubber Elasticity Force-Temperature Relations Vtn. Direct Determination of Molecular Dimensions IX. Single-Molecule Elasticity References... [Pg.157]

If the charges are isotropically deformable the proportionality factor a is a characteristic material constant independent of direction it is termed the polarizability of the substance and has volume dimensions. To determine polarizability experimentally, we start with the dielectric constant of the substance to be investigated a is related under certain generally valid suppositions to e by the Clausius-Mosotti equation... [Pg.24]

Every product failure demands individual treatment, which usually starts with simple visual examination, careful measurement of its dimensions and determination of its condition compared with an equivalent intact component. Comparison is a simple way of checking if the parts really are identical and, if not, the reason for divergence. Many products are now identifiable from logos, date stamps and manufacturing codes either printed or embossed on the product outer surface. If the material is unknown, or degradation is suspected, it must be analyzed for the constituent parts the matrix polymer, filler and any minor additives (such as UV absorbent). The analysis shonld aim to be non-destructive, but, if necessary, sampling needs to be away from critical features such as fracture surfaces. Although direct comparison with... [Pg.185]


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Dimensions, direct determination molecular

Direct Determination of Molecular Dimensions

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