Big Chemical Encyclopedia

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

Articles Figures Tables About

Stable front

Which portion of the breakthrough wave has the potential for formation of a thermally stable front ... [Pg.85]

The column is equilibrated with the carrier mobile phase (I), and the injection of a sample (F) of a binary mixture (components A and A2) is performed diu-ing a finite period of time (tq — utj,J L), after which the displacer (P3) stream is pumped into the column. There are two concentration shocks one at the origin (0, 0), the stable front shock of the first component, the other at the end of the injection (0, To), the front shock of the displacer. Thus, two wave solutions appear in the x, t) plane. According to Eq. 9.25, for an initially empty bed, the characteristic parameters are I ai,a2, cif). State F represents the injection of A and A2 into the column according to Eq. 9.26, the characteristic parameters are F(co, ui2,as), where... [Pg.455]

What about ascending fronts If a front were to propagate upward, then the hot polymer-monomer solution in the reaction zone could rise because of buoyancy, removing enough heat at the polymer-monomer interface to quench the front. With a front that produces a solid product, the onset of convection is more complicated than the cases that we considered in Chapter 9, because the critical Rayleigh number is a function of the velocity (Volpert et al., 1996). Bowden et al. (1997) studied ascending fronts of acrylamide polymerization in dimethyl sulfoxide. As in the iodate-arsenous acid fronts, the first unstable mode is an antisymmetric one followed by an axisymmetric one. Unlike that system, in the polymerization front the stability of the front depends on both the solution viscosity and the front velocity. The faster the front, the lower the viscosity necessary to sustain a stable front. [Pg.242]

Below we discuss a particular case of coexisting stable front waves and calculate two-parameter bifurcation diagrams determining wave velocity vs. physical parameter relations. These results are then related to spatiotemporal patterns obtained by directly solving the partial differential equations which describe a bounded system. This system gives rise to an alternating pattern of fronts moving back and forth in the reactor. At the boundaries one type of front is transformed into the other one and is reflected back to the reactor. Such a pattern exists for the reaction-diffusion system (with Neumann boundary conditions) as well as for the reaction-diffusion-convection system (with Danckwerts boundary conditions). Observed zig-zag dynamics is both of theoretical and practical interest for operation of chemical reactors. [Pg.726]

The change in the excess work for establishing the stable front (SF) from SSI equals at equistability the change in excess work of establishing the stable front from SS3... [Pg.64]

These predictions are in good agreements with the recent experiments of Quinard al (1983). Furthermore the induced velocity field has been recently recorded in the unburnt mixture by Searby al (1983) in the case of stable fronts stabilized in weakly turbulent flows. As predicted by the theory for planar stable flames, the induced velocity field is found to be out of phase with the front corrugations leading to a blocking of the... [Pg.112]

If the mobility ratio is greater than 1.0, then there will be a tendency for the water to move preferentially through the reservoir, and give rise to an unfavourable displacement front which is described as viscous fingering. If the mobility ratio is less than unity, then one would expect stable displacement, as shown in Figure 8.16. The mobility ratio may be influenced by altering the fluid viscosities, and this is further discussed in Section 8.8, when enhanced oil recovery is introduced. [Pg.203]

Antimony Trioxide. Antimony(III) oxide (antimony sesquioxide) [1309-64-4] Sb203, is dimorphic, existing in an orthorhombic modification valentinite [1317-98-2] is colorless (sp gr 5.67) and exists in a cubic form and senarmontite [12412-52-17, Sb O, is also colorless (sp gr 5.2). The cubic modification is stable at temperatures below 570°C and consists of discrete Sb O molecules. The molecule is similar to that of P40 and As O and consists of a bowed tetrahedron having antimony atoms at each corner united by oxygen atoms lying in front of the edges. This solid crystallizes in a diamond lattice with an Sb O molecule at each carbon position. [Pg.202]

Overdriven detonation is the condition that exists during a DDT before a state of stable detonation is reached. Transition occurs over the length of a few pipe diameters and propagation velocities np to 2000 m/s have been measnred for hydrocarbons in air. This is greater than the speed of sonnd as measnred at the flame front. Overdriven detonations are typically accompanied by side-on pressnre ratios (at the pipe wall) in the range of 50-100. A severe test for detonation flame arresters is to adjust the mn-np distance so that DDT occurs at the arrester, subjecting it to the overdriven detonation impulse. [Pg.66]

Abundances of lUPAC (the International Union of Pure and Applied Chemistry). Their most recent recommendations are tabulated on the inside front fly sheet. From this it is clear that there is still a wide variation in the reliability of the data. The most accurately quoted value is that for fluorine which is known to better than I part in 38 million the least accurate is for boron (1 part in 1500, i.e. 7 parts in [O ). Apart from boron all values are reliable to better than 5 parts in [O and the majority arc reliable to better than I part in 10. For some elements (such as boron) the rather large uncertainty arises not because of experimental error, since the use of mass-spcctrometric measurements has yielded results of very high precision, but because the natural variation in the relative abundance of the 2 isotopes °B and "B results in a range of values of at least 0.003 about the quoted value of 10.811. By contrast, there is no known variation in isotopic abundances for elements such as selenium and osmium, but calibrated mass-spcctrometric data are not available, and the existence of 6 and 7 stable isotopes respectively for these elements makes high precision difficult to obtain they are thus prime candidates for improvement. [Pg.17]

When dezincification occurs in service the brass dissolves anodically and this reaction is electrochemically balanced by the reduction of dissolved oxygen present in the water at the surface of the brass. Both the copper and zinc constituents of the brass dissolve, but the copper is not stable in solution at the potential of dezincifying brass and is rapidly reduced back to metallic copper. Once the attack becomes established, therefore, two cathodic sites exist —the first at the surface of the metal, at which dissolved oxygen is reduced, and a second situated close to the advancing front of the anodic attack where the copper ions produced during the anodic reaction are reduced to form the porous mass of copper which is characteristic of dezincification. The second cathodic reaction can only be sufficient to balance electrochemically the anodic dissolution of the copper of the brass, and without the support of the reduction of oxygen on the outer face (which balances dissolution of the zinc) the attack cannot continue. [Pg.189]

English physicist and electrochemist Michael Faraday in 1823. You can make it by bubbling chlorine gas through calcium chloride solution at 0°C the hydrate comes down as feathery white crystals. In the winter of 1914, the Geiman army used chlorine in chemical warfare on the Russian front against the soldiers of the Tsar. They were puzzled by its ineffectiveness not until spring was deadly chlorine gas liberated from the hydrate, which is stable at cold temperatures. [Pg.66]

In spin trapping, radicals are trapped by reaction with a diamagnetic molecule to give a radical product.476 This feature (i.e. that the free spin is retained in the trapped product) distinguishes it from the other trapping methods. The technique involves EPR detection of the relatively stable radicals which result front the trapping of the more transient radicals. No product isolation or separation is required. The use of the technique in studies of polymerization is covered in reviews by Kamachi477 and Yamada ft a/.478... [Pg.134]


See other pages where Stable front is mentioned: [Pg.925]    [Pg.237]    [Pg.77]    [Pg.79]    [Pg.278]    [Pg.282]    [Pg.475]    [Pg.292]    [Pg.51]    [Pg.194]    [Pg.442]    [Pg.443]    [Pg.139]    [Pg.199]    [Pg.925]    [Pg.237]    [Pg.77]    [Pg.79]    [Pg.278]    [Pg.282]    [Pg.475]    [Pg.292]    [Pg.51]    [Pg.194]    [Pg.442]    [Pg.443]    [Pg.139]    [Pg.199]    [Pg.205]    [Pg.273]    [Pg.1106]    [Pg.377]    [Pg.262]    [Pg.5]    [Pg.427]    [Pg.197]    [Pg.323]    [Pg.516]    [Pg.521]    [Pg.526]    [Pg.2301]    [Pg.311]    [Pg.345]    [Pg.398]    [Pg.400]    [Pg.402]    [Pg.64]    [Pg.517]    [Pg.579]    [Pg.581]   
See also in sourсe #XX -- [ Pg.64 ]




SEARCH



© 2024 chempedia.info