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Background, 77 interfaces

As has been noted, much of the interest in hlms of proteins, steroids, lipids, and so on, has a biological background. While studies at the air-water interface have been instructive, the natural systems approximate more closely to a water-oil interface. A fair amount of work has therefore been reported for such interfaces in spite of the greater experimental difhculties. [Pg.551]

For model A, the interfaces decouple from the bulk dynamics and their motion is driven entirely by the local curvature, and the surface tension plays only a background, but still an important, role. From this model A... [Pg.745]

High power pulsed lasers are used to produce plasmas and thus to sample and excite the surfaces of soHds. Improvements in minimum detectable limits and decreases in background radiation and in interelement interference effects result from the use of two lasers (99) (see Surface and interface analysis). [Pg.115]

ENHANCED SIGNAL-TO-BACKGROUND RATIO WITH A HIGHLY ORDERED PYROLYTIC CARBON FILM AS AN ELECTROCHEMICAL INTERFACE... [Pg.145]

The charging of the double layer is responsible for the background (residual) current known as the charging current, which limits die detectability of controlled-potential techniques. Such a charging process is nonfaradaic because electrons are not transferred across the electrode-solution interface. It occurs when a potential is applied across the double layer, or when die electrode area or capacitances are changing. Note that the current is the tune derivative of die charge. Hence, when such processes occur, a residual current flows based on die differential equation... [Pg.21]

The interface should give low chemical background, fhus minimizing possible interference wifh fhe analytes. [Pg.21]

An intense chemical background from the material from which the belt was made is often observed in the mass spectra generated by this type of interface unless adequate conditioning is carried out. [Pg.139]

In this chapter, we present a brief background account of recent progress in the application of ab initio methods to elucidating the fundamental physicochemical processes that take place at the electrified aqueous metal interface. Our focus is predominantly on model single-crystal surfaces at lower surface coverages. [Pg.96]

For adsorbates on a metal surface, an SFG spectmm is a combination of resonant molecular transitions plus a nonresonant background from the metal. (There may also be a contribution from the water-CaF2 interface that can be factored out by following electrode potential effects see below.) The SFG signal intensities are proportional to the square of the second-order nonlinear susceptibility [Shen, 1984] ... [Pg.381]

By using a multichamber system [129], exchange of residual gases between successive depositions will be strongly decreased, and very sharp interfaces can be made. Furthermore, the use of a load-lock system ensures high quality of the background vacuum, and thus low levels of contaminants in the bulk layers. Multichamber reactor systems have been used for the fabrication of solar cells, and considerable improvements in energy conversion efficiency have been achieved [130, 131]. [Pg.15]

In the past five years, it has been demonstrated that the QELS method is a versatile technique which can provide much information on interfacial molecular dynamics [3 9]. In this review, we intend to show interfacial behavior of molecules elucidated by the QELS method. In Section II, we present the principle and the experimental apparatus of the QELS along with the historical background. The dynamic collective behavior of molecules at liquid-liquid interfaces was first obtained by improving the time resolution of the QELS method. In Section III, we show the molecular collective behavior of surfactant molecules derived from the analysis of the time courses of capillary wave frequencies. Since the... [Pg.239]

Understanding the behavior of radionuclides in estuaries, as the dynamic interface between the continental hydrochemical systems and the ocean basins, requires consideration of broader chemical cycling in the hydrosphere. In this volume, the behavior of U- and Th-series isotopes in rivers is discussed by Chabaux et al. (2003), that in groundwaters by Porcelli and Swarzenski (2003), and that in oceans by Cochran and Masque (2003). General background information is provided by Bourdon et al. (2003). [Pg.578]


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