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Physical phenomena contributing

Table 3.1 can be used to classify the solvents. These properties can lead to understanding of various physical phenomenon (Chiou and Kile, 1994). They can be used in selecting potential solvent alternatives. This is carried out, for example, through a group contribution molecular design of solvents (MOLDES) approach in molecular modeling (Pretel et al., 1994). [Pg.52]

These effects arise from the same physical phenomenon as those contributing to A S and consequently parallel them (Figure 7.12). [Pg.308]

The solvent polarization can be formally decomposed into different contributions each related to the various degrees of freedom of the solvent molecules. In common practice such contributions are grouped into two terms only [41,52] one term accounts for all the motions which are slower than those involved in the physical phenomenon under examination (the slow polarization), the other includes the faster contributions (the fast polarization). The next assumption usually exploited is that only the slow motions are instantaneously equilibrated to the momentary molecule charge distribution whereas the fast cannot readjust, giving rise to a nonequilibrium solvent-solute system. [Pg.173]

It was only the discovery of a new physical phenomenon known as radioactivity that presented scientists with a method which contributed to a considerable expansion of our knowledge of the properties and structure of matter and to a significant increase in the number of chemical elements in the periodic system. At the early stage of the studies of radioactivity three types of radiation were found alpha rays (fluxes of the nuclei of helium atoms with the positive charge of two), beta rays (fluxes of electrons with the negative charge of one), and gamma rays (these are in fact rays similar to X-rays). [Pg.174]

The same result can be obtained by nebuUzation of an analyte solution into small droplets that are then flash heated by exposure to hot gas, as in thermospray and APCI sources. Thus, it is conamon to find that a compound that will not 5deld a meaningful mass spectrum using conventional Cl (solid sample heated in an insertion probe) will do so when subjected to flash heating in APCI. Anotber physical phenomenon that contributes to this effect is the increase of vapor pressure of an analyte as the sample size becomes very small, as in a nebulized solution. This increase is described by the Kelvin equation (Thomson 1871, Moore 1972) ... [Pg.198]

One curious physical phenomenon associated with gases is the fact that when there is a mixture of gases in a given volume they behave independentiy so that their pressures are additive. In fact this raises the issue of what we mean by pressure. Common sense may lead us to expect that volumes are additive as indeed they are for macroscopic objects such as bricks. Thus, it is somewhat thought provoking that several gases can be easily confined in the same volume. This same sort of question also arises for mixtures of liquids to a much less extent as discussed later in Chapter 6. These considerations go to the very heart of the concept of the size of atoms and molecules and how much space is between them in a liquid or gas. As we will soon see, the space between gas molecules is about 100 times their size at 1 atm so there is plenty of space for other molecules. In addition, it will soon become evident that pressure is (force/area) caused by many collisions of gas molecules with the wall of the container. Cavendish in 1781 and Dalton in 1810 contributed to the concept now known as Dalton s law. ... [Pg.11]

Another phenomenon contributing to the great variability of organic compounds is isomerism. Isomers are compounds that have exactly the same molecular formula but differ in at least one of their chemical or physical properties. [Pg.13]

Mechanisms of Leukocyte Adsorption. The exact mechanism of leukocyte adhesion to filter media is not yet fuUy understood. Multiple mechanisms simultaneously contribute to the adhesion of cells to biomaterials, however, physical and biological mechanisms have been distinguished. Physical mechanisms include barrier phenomenon, surface tension, and electrostatic charge biological mechanisms include cell activation and cell to cell binding. [Pg.524]

In this chapter studies of physical effects within the elastic deformation range were extended into stress regions where there are substantial contributions to physical processes from both elastic and inelastic deformation. Those studies include the piezoelectric responses of the piezoelectric crystals, quartz and lithium niobate, similar work on the piezoelectric polymer PVDF, ferroelectric solids, and ferromagnetic alloys which exhibit second- and first-order phase transformations. The resistance of metals has been investigated along with the distinctive shock phenomenon, shock-induced polarization. [Pg.136]

Among the high-temperature superconductors one finds various cuprates (i.e., ternary oxides of copper and barium) having a layered structure of the perovskite type, as well as more complicated oxides on the basis of copper oxide which also include oxides of yttrium, calcium, strontium, bismuth, thallium, and/or other metals. Today, all these oxide systems are studied closely by a variety of specialists, including physicists, chemists, physical chemists, and theoreticians attempting to elucidate the essence of this phenomenon. Studies of electrochemical aspects contribute markedly to progress in HTSCs. [Pg.630]

In fact, the physical picture of the phenomenon is more subtle. The contribution of any trajectory with 0 is cancelled in the first order in B by the contribution of the time-reversed trajectory, since the values of SB — Sq are opposite for these paths [ Fig. 1(d), (e)]. The cancellation does not occur only at very small / . The integration in Eq. 3 over also give a quadratic in (3 contribution to the MR. This contribution is positive and comes from the second order term in the expansion of enSB —enS° in B. It follows from our results [Eqs. (1),(9)] that the contribution of small angles is dominant resulting in a negative parabolic MR [22], We find that the parabolic MR crosses over to linear at very small / ss 0.05/ o, which explains why the parabolic MR was not seen in numerical simulations [15] and experiment [16]. [Pg.70]


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