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Temperature termination

These MTD (or LMTD) correction factors are read from the appropriate chart, which descrihes the exchanger mechanical and temperature terminal operational conditions. The P and R ratios must he calculated as represented in the diagrams otherwise the factor read will have no meaning. A true counterflow or parallel flow exchanger does not require any correction to the LMTD. [Pg.72]

Check the condenser temperature terminal difference (CTTD) and compare with design specifications. This is the difference between the LP exhaust steam temperature and the CW outlet temperature. Changes here will reflect one or more of the problems dis-... [Pg.118]

Generally similar but NiMH transitions are more subtle. Backup temperature termination recommended Similar, but with NiMH, cold temperature charge limit is 15°C NiMH slightly higher than NiCd... [Pg.1319]

In contrast to the kinetic approach, deviations from the terminal model have also been treated from a thermodynamic viewpoint [Kruger et al., 1987 Lowry, 1960 Palmer et al., 2000, 2001]. Altered copolymer compositions in certain copolymerizations are accounted for in this treatment in terms of the tendency of one of the monomers (M2) to depropagate. An essential difference between the kinetic and thermodynamic treatments is that the latter implies that the copolymer composition can vary with the concentrations of the monomers. If the concentration of monomer M2 falls below its equilibrium value [M]c at the particular reaction temperature, terminal M2 units will be prone to depropagate. The result would be a... [Pg.515]

Several chemical transformations of this acyl complex were carried out in order to prove its structure. The reaction of carbon monoxide with the complex gave acyl halide and chlorocarbonylbis (triphenylphosphine)-rhodium (XII). The thermal decomposition of the acyl complex gave rise to a mixture of isomeric olefins. The formation of olefin from the complex can be carried out more smoothly by adding iodine. When iodine was added to the solution of the acyl complex at room temperature, terminal olefin was obtained in high yield. These reactions are summarized below... [Pg.162]

Since the Sastry density is an absolute (thermodynamic) limit to vitrification as T 0, it follows that the point (f>.. P = 0) is the low-temperature termination of the Kauzmann curve. Since materials are vitrified by cooling and/or compression, the Kauzmann curve is expected to have a positive slope... [Pg.72]

Of course, the approximations made by the spin wave theory are reasonable at very low temperatures only, and thus it is plausible that this line of critical temperatures terminates at a transition point 7 Kt, the Kosterlitz-Thouless (1973) transition, while for T > 7kt one has a correlation function that decays exponentially at large distances. This behavior is recognized when singular spin configurations called vortices (fig. 33 Kawabata and Binder, 1977) are included in the treatment (Berezinskii, 1971, 1972). Because 0(x) is a multivalued function it is possible that a line integral such... [Pg.202]

In Fig. 10.3-2 we have plotted, for various fixed compositions, the bubble and dew point pressures of this mixture as a function of temperature. The leftmost curve in this figure is the vapor pressure of pure ethane as a function of temperature, terminating in the critical point of ethane (for a pure component, the coexisting vapor and liquid are necessarily of the same composition, so the bubble and dew pressures are identical and equal to the vapor pressure). Similarly, the rightmost curve is the vapor pressure of pure propylene, terminating at the propylene critical point. The intermediate curves (loops) are the bubble and dew point curves relating temperature and pressure for various fixed compositions. Finally, there is aline in Fig. 10.3-2 connecting the critical points of the mixtures of various compositions this line is the critical locus of ethane-propylene mixtures. [Pg.558]

The alkoxides hydrolyze vigorously in water. The fe/7-butoxide is a cyclic dimer (9-V) in solvents, whereas the isopropoxide is tetrameric (9-VI) at ordinary temperatures but trimeric at elevated temperatures. Terminal and bridging alkoxyl groups can be distinguished by nmr spectra. Other alkoxides can exist also as dimers and trimers. [Pg.272]

Tip 16 Polymerization of methyl methacrylate, styrene, and vinyl acetate. MMA, when polymerized, exhibits termination by both combination and disproportionation (in fact, disproportionation is promoted at higher temperatures). Termination by disproportionation leads to the formation of radicals and, eventually, polymer molecules with a TDB. We also know that TDBs will become competitive with the monomer vinyl bonds for radicals as conversion increases. TDB polymerization (characterized by rate constants close (in value) to propagation rate constants) leads to trifunctional LCB. Yet, upon analysis, poly(MMA) chains are linear. How come What is the explanation/reasoning for this observation We also know that styrene terminates predominantly via combination. Styrene also exhibits transfer to monomer, which is enhanced at higher temperature levels. Transfer to monomer generates chains with TDBs. Yet, polystyrene is linear. What is the explanation ... [Pg.262]

Figure 3.6 The MetAP2-PROTAC-l complex is degraded in Xenopus extracts. The MetAP2-PROTAC-l mixture or MetAP2 alone was added to Xenopus egg extract. Reactions were incubated for the indicated times at room temperature, terminated by adding SDS-PAGE loading buffer, and evaluated by SDS-PAGE followed by western blotting with an anti-MetAP2 antibody. Where indicated, reactions were further supplemented with 50 pM LLnL or 10 pM epoxomicin (Epox.). Reprinted, with permission, from Sakamoto et al 2001 National Academy of Sciences, U.S.A. Figure 3.6 The MetAP2-PROTAC-l complex is degraded in Xenopus extracts. The MetAP2-PROTAC-l mixture or MetAP2 alone was added to Xenopus egg extract. Reactions were incubated for the indicated times at room temperature, terminated by adding SDS-PAGE loading buffer, and evaluated by SDS-PAGE followed by western blotting with an anti-MetAP2 antibody. Where indicated, reactions were further supplemented with 50 pM LLnL or 10 pM epoxomicin (Epox.). Reprinted, with permission, from Sakamoto et al 2001 National Academy of Sciences, U.S.A.
Isomers of linear internal olefins give practically the same product distribution at higher temperatures. However, at lower temperatures terminal olefins give a higher proportion of linear aldehydes than internal olefins (see fig. 9, p. 49). [Pg.38]

Keywords Terminal alkynes, potassium iodide, copper(I) iodide, triethyi amine (Et3N), (diace toxyiodo)benzene, acetonitrile, room temperature, terminal iodination, 1-iodoalkenes... [Pg.307]

Qz) lies between 830 C and 840 C at 500 bars. Its high temperature termination is the invariant point phlogopite-sanidine-enstatite-forsterite-liquid-gas, as described by Luth (1967). Schairer (1954) indicated that the solubility of MgO in KAlSi303-Si02 melts was very small. Curves (Ph) and (En) are assumed to be identical to the curve sanidine-quartz-liquid-gas described by Shaw (1963). The data in Table 3 indicate that this is the case for (En) within the uncertainties of this body of data. [Pg.234]


See other pages where Temperature termination is mentioned: [Pg.982]    [Pg.567]    [Pg.127]    [Pg.51]    [Pg.34]    [Pg.89]    [Pg.151]    [Pg.591]    [Pg.424]    [Pg.269]    [Pg.73]    [Pg.567]    [Pg.45]    [Pg.25]    [Pg.194]    [Pg.1469]    [Pg.136]   
See also in sourсe #XX -- [ Pg.262 ]




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