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Segregation function

Figure 7. Top, extension of Spencer and Leshaw s model to the case of a reactor having two inlets (unmixed feedstreams). In the general case, there are four environments (two entering, two leaving). Bottom, when the segregation function only depends on residence time, this representation is also valid (78). Three environment model with three parameters R s = exp(-R t ), ... Figure 7. Top, extension of Spencer and Leshaw s model to the case of a reactor having two inlets (unmixed feedstreams). In the general case, there are four environments (two entering, two leaving). Bottom, when the segregation function only depends on residence time, this representation is also valid (78). Three environment model with three parameters R s = exp(-R t ), ...
The complementary fraction in the L.E. is 1 - s. s(X,t ), which may also be written s(X,a), is known as the "segregation function". This term is somewhat confusing as the process above is concerned with segregation of ages (mixing earliness). However, s(X,a) also describes the decay of segregation in the physical sense under the additional (and often made) assumption that E.E. = macrofluid and L.E. = microfluid. In the particular tube considered above, the... [Pg.207]

Most models for "intermediate micromixing" can be compared by means of their "segregation" function s(A,a). Here are some examples taken from the literature ... [Pg.208]

As already mentioned above, the usual assumption is that the reactor comprises two Environments. The Entering (or Initial) Environment, which consist of a macrofluid, and the Leaving (or Final) Environment where the fluid behaves as a microfluid. The segregation function" presented above (Sec. 3-1) describes the transfer between these Environments. The first limiting case is that of Minimum Mixedness where the Entering Environment spreads out into the whole reactor. The tubes of the BPT-model remain insulated and (4-1) is still valid. The conversion for a single reaction is written... [Pg.217]

To evaluate the real behavior of fuels in relation to the segregation effect, the octane numbers of the fuel components can be determined as a function of their distillation intervals In this manner, new characteristics have been defined, the most well-known being the delta R 100 (A7 100) and the Distribution Octane Number (DON). Either term is sometimes called the Front-End Octane Number . [Pg.199]

In addition, many grades of paper and paperboard are used in direct or indirect contact with foods. Thus, many mills only use paper chemicals that have been cleared for use by the U.S. Pood and Dmg Administration (PDA) (3), so that it is not necessary to segregate machine broke (off-grade paper and edge clippings that are reclaimed for their fiber value) and white water. Most of the chemicals discussed in this article are approved by the PDA for use in paper and paperboard that are intended for appHcations in food processing and packaging. However, there are various restrictions on both the specific functional uses and amounts of paper chemical additives which can be used, so the PDA status should be confirmed by the suppHer before use. [Pg.15]

The lead-base babbitts ate based upon the lead—antimony—tin system, and, like the tin-base, have a stmcture of hard crystals ia a relatively soft matrix. The lead-base ahoys ate, however, mote prone to segregation, have a lower thermal conductivity than the tin-base babbitts, and ate employed genetahy as an iaexpensive substitute for the tin-base ahoys. Properly lined, however, they function satisfactorily as beatings under moderate conditions of load and speed. [Pg.62]

Crystallization is one of the oldest unit operations in the portfoho of industrial and/or laboratory separations. Almost all separation techniques involve formation of a second phase from a feed, and processing conditions must be selected that allow relatively easy segregation of the two or more resulting phases. This is a requirement for crystallization also, and there are a variety of other properties of the sohd product that must be considered in the design and operation of a crystallizer. Interactions among process, function, product, and phenomena important in crystallization ate iRustrated in Figure 1. [Pg.338]

The combination of reac tor elements is facihtated by the concept of transfer functions. By this means the Laplace transform can be found for the overall model, and the residence time distribution can be found after inversion. Finally, the chemical conversion in the model can be developed with the segregation and maximum mixed models. [Pg.2075]

FIG. 23 14 Comp arison of maximiim mixed, segregated, and ping flows, (a) Relative volumes as functions of variance or n, for several reaction orders, (h) Second-order reaction with n = 2 or 3. (c) Second-order, n = 2. (d) Second-order, n = 5. [Pg.2088]

The principal applications of REELS are thin-film growth studies and gas-surface reactions in the few-monolayer regime when chemical state information is required. In its high spatial resolution mode it has been used to detect submicron metal hydride phases and to characterize surface segregation and difRision as a function of grain boundary orientation. REELS is not nearly as commonly used as AES orXPS. [Pg.325]

Figure 2. Total energies of ordered (LIq structure, squares), random (circles) and segregated (triangles) fee RhsoPdso alloys as a function of the number of neighboring shells included in the local interaction zone. Values obtained by the LSGF-CPA method are shown by filled symbols and full lines. The energies obtained by the reference calculations are shown by a dashed line (LMTO, ordered sample), a dotted line (LMTO-CPA, random sample), and a dot-dashed line (interface Green s function technique, segregated sample). Figure 2. Total energies of ordered (LIq structure, squares), random (circles) and segregated (triangles) fee RhsoPdso alloys as a function of the number of neighboring shells included in the local interaction zone. Values obtained by the LSGF-CPA method are shown by filled symbols and full lines. The energies obtained by the reference calculations are shown by a dashed line (LMTO, ordered sample), a dotted line (LMTO-CPA, random sample), and a dot-dashed line (interface Green s function technique, segregated sample).
We will limit ourselves to the surface segregation energy of an impurity of atomic number Z + 1 in a BCC matrix of atomic number Z and study the variation of this energy as a function of the number Nj of d electrons per atom in the d band of e transition metal Z. [Pg.376]

Modification of the top electrode may also be achieved. This was done by adding a small amount of surfactant, such as an ether phosphate or an ether sulfate, to the spin-coal solution of the luminescent polymer [89[. The lipophobic ether chains segregate at the surface of the (predominantly) hydrocarbon polymer, becoming available for complexation with the aluminum cathode which is deposited on top. Thus, the dipole in the surfactant points away from the electrode and lowers its work function to improve the injection of electrons. [Pg.537]

In the final analysis, market price and sales volume are functions of the quality standards offered and the buyer s degree of confidence that the product will conform to the standards. Maintenance of buyer s confidence requires inspection to screen out all nonconforming products, or control over variability of quality during production and distribution to a degree where few, if any, products fail to meet the standards. Screening inspection of the finished product cannot improve quality it merely serves to segregate unacceptable from acceptable product, and results in loss of production capacity and costly waste and salvage. The second consideration provides the only sound basis for quality control in frozen food production and distribution. It operates on the old principle that an ounce of prevention is worth a pound of cure. ... [Pg.29]

While thin polymer films may be very smooth and homogeneous, the chain conformation may be largely distorted due to the influence of the interfaces. Since the size of the polymer molecules is comparable to the film thickness those effects may play a significant role with ultra-thin polymer films. Several recent theoretical treatments are available [136-144,127,128] based on Monte Carlo [137-141,127, 128], molecular dynamics [142], variable density [143], cooperative motion [144], and bond fluctuation [136] model calculations. The distortion of the chain conformation near the interface, the segment orientation distribution, end distribution etc. are calculated as a function of film thickness and distance from the surface. In the limit of two-dimensional systems chains segregate and specific power laws are predicted [136, 137]. In 2D-blends of polymers a particular microdomain morphology may be expected [139]. Experiments on polymers in this area are presently, however, not available on a molecular level. Indications of order on an... [Pg.385]


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