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Hydro-dynamic

Next we consider the situation of a coil which is unperturbed in the hydro-dynamic sense of being effectively nondraining, yet having dimensions which are perturbed away from those under 0 conditions. As far as the hydrodynamics are concerned, a polymer coil can be expanded above its random flight dimensions and still be nondraining. In this case, what is needed is to correct the coil dimension parameters by multiplying with the coil expansion factor a, defined by Eq. (1.63). Under non-0 conditions (no subscript), = a(rg)Q therefore under these conditions we write... [Pg.616]

The phase-field model and generalizations are now widely used for simulations of dendritic growth and solidification [71-76] and even hydro-dynamic flow with moving interfaces [78,79]. One can even use the phase-field model to treat the growth of faceting crystals [77]. More details will be given later. [Pg.879]

As known, SEC separates molecules and particles according to their hydro-dynamic volume in solution. In an ideal case, the SEC separation is based solely on entropy changes and is not accompanied with any enthalpic processes. In real systems, however, enthalpic interactions among components of the chromatographic system often play a nonnegligible role and affect the corresponding retention volumes (Vr) of samples. This is clearly evident from the elution behavior of small molecules, which depends rather strongly on their chemical nature and on the properties of eluent used. This is the case even for... [Pg.445]

In SEC, universal calibration is often utilized to characterize a molecular weight distribution. For a universal calibration curve, one must determine the product of log(intrinsic viscosity molecular weight), or log([7j] M). The universal calibration method originally described by Benoit et al. (9) employs the hydro-dynamic radius or volume, the product of [tj] M as the separation parameter. The calibration curves for a variety of polymers will converge toward a single curve when plotted as log([7j] M) versus elution volume (VJ, rather than plotted the conventional way as log(M) versus V, (5). Universal calibration behavior is highly dependent on the absence of any secondary separation effects. Most failures of universal calibration are normally due to the absence of a pure size exclusion mechanism. [Pg.565]

The fact that a flowing catalyst-vapor mixture acted just as a traditional liquid was a crucial point. It meant that the cracking plant was in essence a hydro-dynamic system readily controlled over a range of... [Pg.993]

Figure 52.1 Journal positions during start-up while a hydro-dynamic oil wedge is being established... Figure 52.1 Journal positions during start-up while a hydro-dynamic oil wedge is being established...
As regards general principles, the main effects are manifested in the region of comparatively high degrees of filling, it does not matter if the case at hand is a hydro-dynamic interaction of the flows around them or a direct intermolecular interaction of the filler s particles. Here we should bear in mind the following decisive principles. [Pg.85]

Hydrodynamic Equations.—Before deriving the hydro-dynamic equations, some integral theorems that are useful in the solution of the Boltzmann equation will be proved. Consider a function of velocity, G(Vx), which may also be a function of position and time let... [Pg.20]

B14. Becker, K. M., Jahnberg, S., Haga, I., Hansson, P. T. and Mathisen, R. P., Hydro-dynamic instability and dynamic burn-out in natural circulation two-phase flow. An experimental and theoretical study, Nukleonik 6, 224 (1964). [Pg.288]

In 1999, Luo and Domfeld [110] proposed that there are two typical contact modes in the CMP process, i.e., the hydro-dynamical contact mode and the solid-solid contact mode [110]. When the down pressure applied on the wafer surface is small and the relative velocity of the wafer is large, a thin fluid film with micro-scale thickness will be formed between the wafer and pad surface. The size of the abrasive particles is much smaller than the thickness of the slurry film, and therefore a lot of abrasive particles are inactive. Almost all material removals are due to three-body abrasion. When the down pressure applied on the wafer surface is large and the relative velocity of the wafer is small, the wafer and pad asperity contact each other and both two-body and three-body abrasion occurs, as is described as solid-solid contact mode in Fig. 44 [110]. In the two-body abrasion, the abrasive particles embedded in the pad asperities move to remove materials. Almost all effective material removals happen due to these abrasions. However, the abrasives not embedded in the pad are either inactive or act in three-body abrasion. Compared with the two-body abrasion happening in the wafer-pad contact area, the material removed by three-body abrasion is negligible. [Pg.259]

Sivashinsky, G.I., On a distorted flame front as a hydro-dynamic discontinuity, Acta Astronaut., 3, 889, 1976. [Pg.127]

Starting with the causes of particle stress, the following report discussed the hydro-dynamic principles of the most frequently used model reactors and bioreactors, which are required for an approximate calculation of stress. [Pg.35]

It is questionable if these results obtained with endothelial cells can be transferred to other non-endothelial cells. Because of their origin endothelial cell are structured to withstand hydro dynamical stress. [Pg.133]

In both plant (e.g. [57]) and animal (e.g. [86]) cell systems, cellular respiration has been shown to be a more sensitive indicator of system response to hydro-dynamic stress than membrane integrity, suggesting that intracellular enzymes and/or organelles may be affected at stress levels lower than those required to cause membrane damage. [Pg.150]

If the contribution of a polymer molecule to the viscosity of the solution is in reality proportional to the cube of its linear dimension, the intrinsic viscosity in a -solvent should be proportional to the square root of the molecular weight. The influence of intramolecular interactions on the configuration having been neutralized by this choice of solvent medium, it becomes possible to examine separately the hydro-dynamic aspects of the problem. [Pg.612]

GP 1] [R 1] A kinetic model for the oxidation of ammonia was coupled to a hydro-dynamic description and analysis of heat evolution [98], Via regression analysis and adjustment to experimental data, reaction parameters were derived which allow a quantitative description of reaction rates and selectivity for all products trader equilibrium conditions. The predictions of the model fit experimentally derived data well. [Pg.298]

D microfabricated micro mixers (see Section 4.1.5) may be connected to tubes for reasons of residence time prolongation, similar to chip-tube micro reactors (see Section 4.1.4). The tube may also have the function of creating distinct hydro-dynamic features (see Section 4.1.4). [Pg.399]

The chip micro reactor ([R 6]) was only one part of a complex serial-screening apparatus [20]. This automated system consists of an autosampler (CTC-HTS Pal system) which introduces the reactant solutions in the chip via capillaries. A pumping system (p-HPLC-CEC System) serves for fluid motion by hydro dynamic-driven flow. A dilution system [Jasco PU-15(5)] is used for slug dilution on-chip. The detection system was a Jasco UV-1575 and analysis was carried out by LC/MS (Agilent 1100 series capLC-Waters Micromass ZQ). All components were on-line and self-configured. [Pg.525]

It is important to note that the dilfnsion-layer thickness depends not only on hydro-dynamic factors but also (through the diffusion coefficient) on the nature of the diffusing species. This dependence is minor, of course, since the values of Dj differ little among the various substances, and in addition are raised to the power one-third in Eq. (4.37). [Pg.65]

Many of the electrochemical techniques described in this book fulfill all of these criteria. By using an external potential to drive a charge transfer process (electron or ion transfer), mass transport (typically by diffusion) is well-defined and calculable, and the current provides a direct measurement of the interfacial reaction rate [8]. However, there is a whole class of spontaneous reactions, which do not involve net interfacial charge transfer, where these criteria are more difficult to implement. For this type of process, hydro-dynamic techniques become important, where mass transport is controlled by convection as well as diffusion. [Pg.333]

Figure 16. Radius of gyration versus time for MPC dynamics (solid line) that includes hydro-dynamic interactions and Boltzmann sampling of velocities (dashed line) without hydrodynamic interactions. System parameters Nb — 200 and T — 0.8. From Kikuchi, et al., 2002. Figure 16. Radius of gyration versus time for MPC dynamics (solid line) that includes hydro-dynamic interactions and Boltzmann sampling of velocities (dashed line) without hydrodynamic interactions. System parameters Nb — 200 and T — 0.8. From Kikuchi, et al., 2002.
In a typical research and development setting, in the event that a new drug candidate is recognized by the drug-discovery group, then the dissolution rate constant K for that compound under specified hydro-dynamic conditions can be determined from powder dissolution data and practical size analysis by microscopy. [Pg.183]


See other pages where Hydro-dynamic is mentioned: [Pg.523]    [Pg.274]    [Pg.944]    [Pg.1509]    [Pg.157]    [Pg.87]    [Pg.615]    [Pg.89]    [Pg.855]    [Pg.93]    [Pg.263]    [Pg.254]    [Pg.119]    [Pg.137]    [Pg.130]    [Pg.147]    [Pg.150]    [Pg.14]    [Pg.131]    [Pg.147]    [Pg.254]    [Pg.67]    [Pg.15]    [Pg.228]    [Pg.546]    [Pg.336]    [Pg.376]    [Pg.261]    [Pg.177]   
See also in sourсe #XX -- [ Pg.25 ]




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