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Front kinetics

Interesting is the Multidimensional Reactive Flow model developed by Tarver et al. [5,103,104) it is based on the Non-Equilibrium Zeldovich-von Neuman-Dhring theory. This model starts from the primary chemical changes occurring in the adiabaticaUy compressed thin layer of molecules of the given EM and multiphonon up-pumping due to shock, but in the mathematical description it works with experimental data of thermal explosion of EM [5,103,104) it considers the induction period of initiation of detonation. However, the induction period of the EM decomposition in front of the detonation wave makes the front kinetically unstable and pulsating [101 ]. [Pg.262]

Sorbed pesticides are not available for transport, but if water having lower pesticide concentration moves through the soil layer, pesticide is desorbed from the soil surface until a new equiUbrium is reached. Thus, the kinetics of sorption and desorption relative to the water conductivity rates determine the actual rate of pesticide transport. At high rates of water flow, chances are greater that sorption and desorption reactions may not reach equihbrium (64). NonequiUbrium models may describe sorption and desorption better under these circumstances. The prediction of herbicide concentration in the soil solution is further compHcated by hysteresis in the sorption—desorption isotherms. Both sorption and dispersion contribute to the substantial retention of herbicide found behind the initial front in typical breakthrough curves and to the depth distribution of residues. [Pg.223]

The strong shock regime is the classic archetype and is characterized by a single narrow shock front that carries the material from its initial condition into a new high pressure, elevated temperature, high kinetic energy state. Following a quiescent period at peak pressure, whose duration depends upon... [Pg.16]

In this section we discuss the basic mechanisms of pattern formation in growth processes under the influence of a diffusion field. For simphcity we consider the sohdification of a pure material from the undercooled melt, where the latent heat L is emitted from the solidification front. Since heat diffusion is a slow and rate-limiting process, we may assume that the interface kinetics is fast enough to achieve local equihbrium at the phase boundary. Strictly speaking, we assume an infinitely fast kinetic coefficient. [Pg.888]

Column efficiency (number of theoretical plates) As in batch chromatography, one needs to determine the efficiency of the column in order to evaluate the dispersion of the fronts due to hydrodynamics dispersion or kinetics limitations. The relationship of N proportional to L can be expressed in terms of the equation for height equivalent to a theoretical plate (HETP) as ... [Pg.263]

Until the early 1970s, the absence of suitable techniques for probing the detailed microstructure of polymers or for examining the selectivity and rates of radical reactions prevented the traditional view front being seriously questioned. In more recent times, it has been established that radical reactions, more often than not, are under kinetic rather than thermodynamic control and the preponderance of... [Pg.4]

Fluid flow and reaction engineering problems represent a rich spectrum of examples of multiple and disparate scales. In chemical kinetics such problems involve high values of Thiele modulus (diffusion-reaction problems), Damkohler and Peclet numbers (diffusion-convection-reaction problems). For fluid flow problems a large value of the Mach number, which represents the ratio of flow velocity to the speed of sound, indicates the possibility of shock waves a large value of the Reynolds number causes boundary layers to be formed near solid walls and a large value of the Prandtl number gives rise to thermal boundary layers. Evidently, the inherently disparate scales for fluid flow, heat transfer and chemical reaction are responsible for the presence of thin regions or "fronts in the solution. [Pg.376]

OS 63] [R 27] [R 18] [P 46] Using a slit-type interdigital micro mixer prior to a liquid/liquid reaction system improves the conversion to 80%, hence close to the kinetic limits [117]. This is an improvement over using a microgrid in front of the reactor (see the Section Conversion/selectivity/yield - benchmarking to batch processing/kinetics, above). [Pg.510]


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See also in sourсe #XX -- [ Pg.244 , Pg.249 ]




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