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Liquid immersion development

The sample chamber of a DAC is filled with a medium that is able to transfer to the sample a homogeneous pressure, and is transparent in the spectral region of interest. At low temperatures, He, Ne and Xe and also homonu-clear molecules (H2, D2, N2 or O2) have been used as pressure-transmitting media. The hydrostatic behaviour of He and H2 allows experiments at low temperature up to 60 GPa (The kbar unit, traditionally used in many experiments with DACs, is close to 0.1 GPa) and N2 can be used up to 13 GPa. Loading the sample chamber with the sample and the pressure transmitting medium is usually performed by the liquid-immersion technique [40]. Hydrostatic pressure measurements in absorption experiments can be obtained from a calibration of the DAC using the pressure-induced shift of Ri and R2 fluorescence lines of Cr3+of a ruby chip near 694 nm, developed by [8]. However, this calibration is performed at RT and it must be extrapolated at low temperatures. It has been shown by Hsu [16] that the shift of the vibrational lines of the CO2 impurities contained in N2 used for pressure transmission could be used to measure pressure at low temperature. [Pg.118]

When a rotating rod is immersed in a molten polymer or a fairly concentrated polymer solution, the liquid will actually climb up the rod. This phenomenon, the Weissenberg effect, is contrary to what is observed in nonpolymer liquids, which develop a curved surface profile with a lowest point at the rod, as the material is flung outward by centrifugal force. [Pg.3]

Note If the chromatogram developed by method B was exposed to ammonia vapors for 10 min before being immersed in liquid paraffin— -hexane (1 -I- 2) the fluorescence of the chromatogram zones became deep red. Glucose and fructose also appeared red. [Pg.183]

The statics and dynamics of microstructures are governed by the forces that create or maintain them. Rarely can the forces be measured directly. But forces between special surfaces immersed in fluid can now be accurately gauged at separations down to 0.1 nm with the direct force measurement apparatus, an ingenious combination of a differential spring, a piezoelectric crystal, an interferometer, and crossed cyhndrical surfaces covered by atomically smooth layers of cleaved mica (Figure 9.4). This recent development is finding more and more applications in research on liquid and semiliquid microstructures, thin films, and adsorbed layers. [Pg.185]

Impregnation prior to the chromatographic development by immersing the PLC plate in a solution of the liquid stationary phase in a suitable solvent, with subsequent evaporation of the solvent. This method results in a homogeneous distribution of the liquid stationary phase all over the PLC layer. [Pg.54]

Thiolex A process for removing hydrogen sulfide from a light hydrocarbon liquid by extraction with aqueous sodium hydroxide passed through a bundle of hollow fibers immersed in it. Developed by the Merichem Company, Houston, TX. In 1991, 52 units were operating. Variations are known as Thiolex/Regen and Thiolex/Regen/Mericat. See also Mericat. [Pg.269]

The concept of the pH electrode has been extended to include other ions as well. Considerable research has gone into the development of these ion-selective electrodes over the years, especially in studying the composition of the membrane that separates the internal solution from the analyte solution. The internal solution must contain a constant concentration of the analyte ion, as with the pH electrode. Today we utilize electrodes with 1) glass membranes of varying compositions, 2) crystalline membranes, 3) liquid membranes, and 4) gas-permeable membranes. In each case, the interior of the electrode has a silver-silver chloride wire immersed in a solution of the analyte ion. [Pg.403]

To model this, Duncan-Hewitt and Thompson [50] developed a four-layer model for a transverse-shear mode acoustic wave sensor with one face immersed in a liquid, comprised of a solid substrate (quartz/electrode) layer, an ordered surface-adjacent layer, a thin transition layer, and the bulk liquid layer. The ordered surface-adjacent layer was assumed to be more structured than the bulk, with a greater density and viscosity. For the transition layer, based on an expansion of the analysis of Tolstoi [3] and then Blake [12], the authors developed a model based on the nucleation of vacancies in the layer caused by shear stress in the liquid. The aim of this work was to explore the concept of graded surface and liquid properties, as well as their effect on observable boundary conditions. They calculated the hrst-order rate of deformation, as the product of the rate constant of densities and the concentration of vacancies in the liquid. [Pg.76]


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See also in sourсe #XX -- [ Pg.165 ]




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