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Order activities

B = Basic salt M = melting. Results expressed as (order) activation energy/kJ mole-1 (temperature range/K)... [Pg.228]

Based on the experimental data kinetic parameters (reaction orders, activation energies, and preexponential factors) as well as heats of reaction can be estimated. As the kinetic models might not be strictly related to the true reaction mechanism, an optimum found will probably not be the same as the real optimum. Therefore, an iterative procedure, i.e. optimization-model updating-optimization, is used, which lets us approach the real process optimum reasonably well. To provide the initial set of data, two-level factorial design can be used. [Pg.323]

It can be expected that, if a highly dispersed, poorly ordered active catalyst has been prepared, and if the reaction conditions (T, pc0) refer to low-equilibrium segregation, a deactivation will also proceed initially through reverse segregation. [Pg.172]

Both 1st- and 2nd-order rate expressions gave statistically good fits for the control samples, while the treated samples were statistically best analyzed by 2nd-order kinetics. The rate constants, lst-order activation parameters, and char/residue yields for the untreated samples were related to cellulose crystallinity. In addition, AS+ values for the control samples suggested that the pyrolytic reaction proceeds through an ordered transition state. The mass loss rates and activation parameters for the phosphoric acid-treated samples implied that the mass loss mechanism was different from that for the control untreated samples. The higher rates of mass loss and... [Pg.335]

In this review, we compare the transition state which does not involve HFTP-participation [TS(e,0)] with single-HFIP involvement [TS(e,l) and TS(e,l) ] (Fig. 14). Particular emphasis is then put on the twofold HFlP-activated complex (Fig. 15) for a detailed inspection of the hydrogen bond assisted epoxidation. All relevant characteristics of higher order activation (as shown, e.g., in Fig. 16) are already present in the transition states TS(e,2) and TS(e,2) (Fig. 15). [Pg.20]

Figure 7. Comparison between H-Beta zeolites (open circles and dashed lines) and HY zeolites (continuous lines) for gas-oil cracking (a) First-order activity constant by specific surface area vs, Si/Al ratio (b) and (c) Average total conversion vs. gas-oil ratio for a H-Beta with Si/Al=27 and a HY Si/Al=35, and for a H-Beta with Si/Al=10 and a Hy with Si/Al=7.7 respectively. Solid circles correspond to the H-Beta steamed at 750 C and 1 atmosphere of water pressure. Figure 7. Comparison between H-Beta zeolites (open circles and dashed lines) and HY zeolites (continuous lines) for gas-oil cracking (a) First-order activity constant by specific surface area vs, Si/Al ratio (b) and (c) Average total conversion vs. gas-oil ratio for a H-Beta with Si/Al=27 and a HY Si/Al=35, and for a H-Beta with Si/Al=10 and a Hy with Si/Al=7.7 respectively. Solid circles correspond to the H-Beta steamed at 750 C and 1 atmosphere of water pressure.
Rate determining step Order Activation energy Surface area Pore volume... [Pg.124]

Transfer RNAs Order Activated Amino Acids on the mRNA Template... [Pg.730]

Besides the elimination of the sample-and-hold, oversampling converters also reduce the complexity of the anti-aliasing filter. Previous anti-aliasing filters required the use of high order active filters (11th order elliptic for example) that resulted in phase... [Pg.116]

Apoptosis Apoptosis is an ordered, active process that brings about the death of a cell as an important part of the maintenance of organismal homeostasis. Apoptosis can be assayed, in flow cytometry, by, for example, looking at the expression of phosphatidylserine on the cell surface, by looking for nuclei with less-than-normal (sub-GO/Gl) amounts of DNA, and by looking for an increase in DNA fragment termini. [Pg.237]

Table XXIII shows that increasing octane numbers were obtained in the following order activated carbon, alumina and synthetic aluminum silicate, fuller s earth. Branching of paraffin hydrocarbons will be parallel to changes in octane number. It should be remarked that these experiments were made in 1941 and that newer aluminum silicates might produce more branched paraffin hydrocarbons. Table XXIII shows that increasing octane numbers were obtained in the following order activated carbon, alumina and synthetic aluminum silicate, fuller s earth. Branching of paraffin hydrocarbons will be parallel to changes in octane number. It should be remarked that these experiments were made in 1941 and that newer aluminum silicates might produce more branched paraffin hydrocarbons.
Mushiake, H., Saito, N., Furusawa, Y., Izumiyama, M., Sakamoto, K., Shamoto, H., Shimizu, H., and Yoshimoto, T. (2002). Orderly activations of human cortical areas during path-planning task. [Pg.15]

Examples of studies on multiphoton absorption processes and nonlinear second-and third-harmonic generation processes will be discussed along with some possible radiative and nonradiative processes. The selection rules for multiphoton absorption will be mentioned in Section 7.3, and molecular examples will be shown along with their correlating photophysical properties in Section 7.4. The effect of some parameters relating to second-order activity along the lanthanide... [Pg.161]

Very similar, though rather less extensive, studies have been made of decomposition reactions of MnRe(C0)jg (15), Tc2(C0)iq (17), and Re2(C0)jg (13). All the kinetics are consistent with the rather stringent predictions of rate eq 9 for the homolytic fission mechanism and are totally inconsistent with a simple C0-dissociative mechanism. Other workers have studied substitution reactions of Mn2(CO)10 (18) and MnRe(CO)10 (19) and have commented, correctly, that their kinetic results are consistent with the dissociative reaction. This seems to have led to some doubts about the correctness of our conclusion that the reactions of all the decacarbonyls proceed mainly or totally via homolytic fission. These doubts do not arise from the kinetics because the kinetics observed by these workers (18, 19) are equally consistent with the homolytic fission mechanism or, indeed, virtually any first-order activation of the complexes. The conditions under which the reactions were followed were simply not those capable of leading to a kinetic distinction between the various mechanisms proposed. The absence of any homonuclear products of the reactions of MnRe(C0)jg was offered (19) as evidence against the homolytic fission mechanism. This point had been raised before (15, 17) when it was countered by emphasizing the absence of sufficient data on... [Pg.139]

Reaction Order Activation Energy (kcal/mole) Frequency-Factor (min ) ... [Pg.238]

For nth-order activity decay and m order in a gas-phase concentration of species i,... [Pg.667]

Much better stability was reported for AsFg-doped polyacetylene coated with poly(p-xylylene) (26), which is an excellent barrier toward oxygen and water. Samples having conductivities of 260 S/cm were coated by vacuum deposition thus, the initial concentration of oxygen in the sample was low. After 24 h in air, a conductivity loss of 10% was observed for treated films, whereas the conductivity of uncoated control samples decreased by a factor of 3. After 1 month, the coated samples had a conductivity of 150 S/cm, whereas that of the control was only 11 S/cm. From isothermal aging studies, the poly(p-xylylene) coating was found to increase the first-order activation energy for conductivity loss by 2.4 Kcal/mol, from 17.2 to 14.8. These data... [Pg.278]

Figure 1. Schematic view of the wave propagation in a second-order active crystal... Figure 1. Schematic view of the wave propagation in a second-order active crystal...
In this chapter we report on some novel strategies that have been pursued to obtain efficient second-order nonlinear molecules starting from the well-known phthalocyanines. In principle, these planar centrosymmetric molecules do not present second-order activity and have been extensively studied for third-order applications. In order to induce asymmetry, two main approaches have been followed a) peripheral substitution of the macrocycle with donor and acceptor groups and b) structural modifications of the Pc core to reduce the symmetry, the resulting-noncentrosymmetric compounds (i.e. subphthalocyanines) presenting variable degrees of dipolarity/octupolarity in the nonlinear response. [Pg.511]


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See also in sourсe #XX -- [ Pg.108 ]




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