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Restricted paths identity

In the second method, i.e., th particle method 546H5471 a spray is discretized into computational particles that follow droplet characteristic paths. Each particle represents a number of droplets of identical size, velocity, and temperature. Trajectories of individual droplets are calculated assuming that the droplets have no influence on surrounding gas. A later method, 5481 that is restricted to steady-state sprays, includes complete coupling between droplets and gas. This method also discretizes the assumed droplet probability distribution function at the upstream boundary, which is determined by the atomization process, by subdividing the domain of coordinates into computational cells. Then, one parcel is injected for each cell. [Pg.326]

Depending on the identity of the peroxyl radicals involved, reactions (47)-(50) may occur in differing proportions. In particular, the product-forming self reaction of tertiary peroxyl radicals is restricted to path (49) and (50), since path (47) and (48) require the existence of C-H a to the peroxyl function. The exact mechanism of these reactions is still controversial, that is, whether the productforming processes are sequential or concerted. Reaction (47) has been described by Russell (1957) as a concerted process, and this process bears his name. It is formulated as having a six-membered transition state. [Pg.174]

S.3. Diaphragm Resistance. The calculation of the resistance across a separator, such as an asbestos or a polymeric diaphragm, is identical to the method employed to determine the resistance of an electrolyte between two parallel plates. However, the distance between the two faces of a separator is not equal to its thickness, as the liquid path in the separator is tortuous and the area is restricted by the finite porosity. Therefore, the 1/A term in the parallel plate configuration should be modified to read as [tortuosity x length]/[porosity x area] or as the ratio of tortuosity to porosity, which is called the MacMullin number. The MacMullin number, characterizing a... [Pg.156]

However, it could be argued that, despite the discovery of the new transient, the net chemical products are identical with those in (24). Possible reactions of the long lived radical complex are poorly characterized but they will most likely influence the quantum yield and product formation depending on the reaction conditions and available reaction partners. In laboratory systems such reactions could involve dissolved O2, other Fe(III) species, or back-electron transfer reaction paths in the atmospheric aqueous phase would be less restricted. [Pg.24]

Due to collisions of the emitted photoelectrons with atoms in the solid, only electrons from the near-surface region can leave the sample, i.e. the mean free path of the electrons is restricted to a few numbers of atomic layers, which is the reason that this technique is surface sensitive. After leaving the sample, collisions of the electrons and the gas environment must be avoided. Therefore, XPS is routinely used in ultra-high vacuum at a pressure below 10 mbar. Yet, catalytic reactions proceed at ambient or even higher pressure. This pressure gap implies that the surface features analysed by conventional XPS are not necessarily identical with those prevailing under catalytic reaction conditions. [Pg.523]

Since each photon behaves by definition like every other photon in the field, certain criteria must be met. Each photon must be identical with every other photon of this class, and the system of particles with which this class of photons interacts must be composed of exactly the same kind of individual particles (in terms of dimensions, refractive index, etc.) in order that the separate interactions be identical. If more than one interaction per photon takes place, the order, number, and character of these interactions must be the same for each photon. In order to circumvent the inordinate complexity imposed by the last requirement, the volume element, dE, must be restricted to dimensions considerably smaller than the mean free path of an individual photon, so that only single interactions are possible in dV. [Pg.30]


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