Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Path velocity

Figure 2.10. Flow profiles in tubes and packed columns. (A) Laminar flow. r = tube radius, Vx =stream path velocity at radial position r. V = maximum flow velocity at tube center. (B) Turbulent flow. Figure 2.10. Flow profiles in tubes and packed columns. (A) Laminar flow. r = tube radius, Vx =stream path velocity at radial position r. V = maximum flow velocity at tube center. (B) Turbulent flow.
For species of differing mass and size, the mean free paths, velocities, and collision frequencies will be different. The derivation of the binary diffusivity is more complicated but may be expressed as [28] [74] [5] (sect 17-3) ... [Pg.316]

According to Uhlmann and Ardelt [9,10], greater changes in performance can be achieved by varying the path type than by varying the grinding pressure or path velocity. [Pg.264]

FIGURE 2.22 Flow profiles in tubes and packed columns. Segment A, laminar flow r = tube radius, Fj = stream path velocity at radial position r, Fmax = maximum flow velocity at tube center. Most open tubular columns operate with this profile. Segment B, turbulent flow 1 = laminar sublayer, 2 = buffer layer. Segment C, plug flow. Segment D, flow in a packed column. Effect is more pronounced with smaller tube diameter -particle size ratios. [Pg.60]

The basics of the method are simple. Reflections occur at all layers in the subsurface where an appreciable change in acoustic impedance is seen by the propagating wave. This acoustic impedance is the product of the sonic velocity and density of the formation. There are actually different wave types that propagate in solid rock, but the first arrival (i.e. fastest ray path) is normally the compressional or P wave. The two attributes that are measured are... [Pg.18]

One of the most usefiil applications of the mean free path concept occurs in the theory of transport processes in systems where there exist gradients of average but local density, local temperature, and/or local velocity. The existence of such gradients causes a transfer of particles, energy or momentum, respectively, from one region of the system to another. [Pg.671]

Molecular beam sample introduction (described in section (Bl.7.2)). followed by the orthogonal extraction of ions, results in improved resolution in TOP instruments over eflfrisive sources. The particles in the molecular beam typically have translational temperatures orthogonal to the beam path of only a few Kelvin. Thus, there is less concern with both the initial velocity of the ions once they are generated and with where in the ion source they are fonned (since the particles are originally confined to the beam path). [Pg.1354]

The initial energy - E XoA t), VoA(t)) - is a function of the coordinates and the velocities. In principle, the use of momenta (instead of velocities) is more precise, however, we are using only Cartesian coordinates, making the two interchangeable. We need to sample many paths to compute ensemble averages. Perhaps the most direct observable that can be computed (and measured experimentally) is the state conditional probability - P A B,t) defined below ... [Pg.275]

One of the advantages of the Verlet integrator is that it is time reversible and symplectic[30, 31, 32]. Reversibility means that in the absence of numerical round off error, if the trajectory is run for many time steps, say nAt, and the velocities are then reversed, the trajectory will retrace its path and after nAt more time steps it will land back where it started. An integrator can be viewed as a mapping from one point in phase apace to another. If this mapping is applied to a measurable point set of states at on(> time, it will... [Pg.300]

Here f denotes the fraction of molecules diffusely scattered at the surface and I is the mean free path. If distance is measured on a scale whose unit is comparable with the dimensions of the flow channel and is some suitable characteristic fluid velocity, such as the center-line velocity, then dv/dx v and f <<1. Provided a significant proportion of incident molecules are scattered diffusely at the wall, so that f is not too small, it then follows from (4.8) that G l, and hence from (4.7) that V v° at the wall. Consequently a good approximation to the correct boundary condition is obtained by setting v = 0 at the wall. ... [Pg.27]

At Che opposite limit, where Che density Is high enough for mean free paths to be short con ared with pore diameters, the problem can be treated by continuum mechanics. In the simplest ease of a straight tube of circular cross-section, the fluid velocity field can easily be obtained by Integrating Che Nsvler-Stokes equations If an appropriate boundary condition at Che... [Pg.179]

In molecular distillation, the permanent gas pressure is so low (less than 0 001 mm. of mercury) that it has very little influence upon the speed of the distillation. The distillation velocity at such low pressures is determined by the speed at which the vapour from the liquid being distilled can flow through the enclosed space connecting the still and condenser under the driving force of its own saturation pressure. If the distance from the surface of the evaporating liquid to the condenser is less than (or of the order of) the mean free path of a molecule of distillate vapour in the residual gas at the same density and pressure, most of the molecules which leave the surface will not return. The mean free path of air at various pressures is as follows —... [Pg.120]

After the skimmer, the ions must be prepared for mass analysis, and electronic lenses in front of the analyzer are used to adjust ion velocities and flight paths. The skimmer can be considered to be the end of the interface region stretching from the end of the plasma flame. Some sort of light stop must be used to prevent emitted light from the plasma reaching the ion collector in the mass analyzer (Figure 14.2). [Pg.95]

In (a), a pulse of ions is formed but, for illustration purposes, all with the same m/z value. In (b), the ions have been accelerated but, because they were not all formed in the same space, they are separated in time and velocity, with some ions having more kinetic energy than others. In (c), the ions approach the ion mirror or reflectron, which they then penetrate to different depths, depending on their kinetic energies (d). The ones with greater kinetic energy penetrate furthest. In (e), the ions leave the reflectron and travel on to the detector (f), which they all reach at the same time. The path taken by the ions is indicated by the dotted line in (f). [Pg.193]

In a vacuum (a) and under the effect of a potential difference of V volts between two electrodes (A,B), an ion (mass m and charge ze) will travel in a straight line and reach a velocity v governed by the equation, mv = 2zeV. At atmospheric pressure (b), the motion of the ion is chaotic as it suffers many collisions. There is still a driving force of V volts, but the ions cannot attain the full velocity gained in a vacuum. Instead, the movement (drift) of the ion between the electrodes is described by a new term, the mobility. At low pressures, the ion has a long mean free path between collisions, and these may be sufficient to deflect the ion from its initial trajectory so that it does not reach the electrode B. [Pg.375]


See other pages where Path velocity is mentioned: [Pg.130]    [Pg.1411]    [Pg.413]    [Pg.645]    [Pg.130]    [Pg.1411]    [Pg.413]    [Pg.645]    [Pg.148]    [Pg.542]    [Pg.664]    [Pg.669]    [Pg.686]    [Pg.848]    [Pg.1309]    [Pg.1424]    [Pg.1428]    [Pg.2005]    [Pg.2062]    [Pg.2084]    [Pg.2315]    [Pg.2911]    [Pg.41]    [Pg.42]    [Pg.271]    [Pg.161]    [Pg.18]    [Pg.29]    [Pg.88]    [Pg.121]    [Pg.161]    [Pg.369]    [Pg.36]    [Pg.165]    [Pg.171]    [Pg.171]    [Pg.196]    [Pg.199]   
See also in sourсe #XX -- [ Pg.413 ]




SEARCH



Optical path difference velocity

© 2024 chempedia.info