Short temperature dependence

Sludge is destroyed by microorganisms and the kinetics of their life processes is temperature dependent. Short anaerobic digestion detention times are obtained at 35°C. Even shorter detention times are possible at 52—54°C, but detention in this range is costly. An increase in detention time occurs at 35—43°C and then a progressive decrease takes place until 52—54°C. This variation is caused by a change in character of the dominant process organisms. 

Recently, Dinwiddie et al. [14] reported the effects of short-time, high-temperatme exposures on the temperature dependence of the thermal conductivity of CBCF. Samples were exposed to temperatures ranging from 2673 to 3273 K, for periods of 10, 15, and 20 seconds, to examine the time dependent effects of graphitization on thermal conductivity measured over the temperature range from 673 to 2373 K. Typical experimental data are shown in Figs. 7 and 8 for exposure times of 10 and 20 seconds, respectively. The thermal conductivity was observed to increase with both heat treatment temperature and exposure time. 

The effects of temperature on the color development of the porous film in chlorobenzene were shown in Table 6 [23]. The coloration was reversible thermochromism. The refractive index of the materials generally decreases as the temperature increases, and the temperature dependence of the liquid is greater than that of the solid. For example, the temperature dependence (A/id/°C) of PVA and chlorobenzene was found to be 3.0 x 10 and 4.5 x 10" at 589.3 nm. Consequently, it is interpreted that the wavelength of the crosspoint between the dispersion curves of PVA and chlorobenzene shifts from the long side to the short side with increasing tem-... 

Do not infer from the above discussion that all the catalyst in a fixed bed ages at the same rate. This is not usually true. Instead, the time-dependent effectiveness factor will vary from point to point in the reactor. The deactivation rate constant kj) will be a function of temperature. It is usually fit to an Arrhenius temperature dependence. For chemical deactivation by chemisorption or coking, deactivation will normally be much higher at the inlet to the bed. In extreme cases, a sharp deactivation front will travel down the bed. Behind the front, the catalyst is deactivated so that there is little or no conversion. At the front, the conversion rises sharply and becomes nearly complete over a short distance. The catalyst ahead of the front does nothing, but remains active, until the front advances to it. When the front reaches the end of the bed, the entire catalyst charge is regenerated or replaced. 

Mass-spectrometric research on silane decomposition kinetics has been performed for flowing [298, 302-306] and static discharges [197, 307]. In a dc discharge of silane it is found that the reaction rate for the depletion of silane is a linear function of the dc current in the discharge, which allows one to determine a first-order reaction mechanism in electron density and temperature [302, 304]. For an RF discharge, similar results are found [303, 305]. Also, the depletion and production rates were found to be temperature-dependent [306]. Further, the depletion of silane and the production of disilane and trisilane are found to depend on the dwell time in the reactor [298]. The increase of di- and trisilane concentration at short dwell times (<0.5 s) corresponds to the decrease of silane concentration. At long dwell times, the decomposition of di- and trisilane produces... 

The activation energy for Region III was not estimated because this region is very short or disappears completely especially at higher temperatures though the temperature dependence of this range should be given by the coefficient R3 = R30(T)t1/2. 

For liquids, as the temperature increases, the degree of molecular motion increases, reducing the short-range attractive forces between molecules and lowering the viscosity. The viscosity of various liquids is shown as a function of temperature in Appendix A. For many liquids, this temperature dependence can be represented reasonably well by the Arrhenius equation ... 

Isotactic PHEMA was found to possess negative temperature dependence in water (Oh and Jhon, 1989). While atactic PHEMA is not expected to have a strong negative temperature dependence, the mechanisms of this behavior can still exist over short ranges and may effect the phase behavior. As such, increased temperatures may also function to control the pore morphology by allowing the polymer to phase separate early on in the reaction. 

Thermotropic cholesterics have several practical applications, some of which are very widespread. Most of the liquid crystal displays produced use either the twisted nematic (see Figure 7.3) or the supertwisted nematic electrooptical effects.6 The liquid crystal materials used in these cells contain a chiral component (effectively a cholesteric phase) which determines the twisting direction. Cholesteric LCs can also be used for storage displays utilizing the dynamic scattering mode.7 Short-pitch cholesterics with temperature-dependent selective reflection in the visible region show different colors at different temperatures and are used for popular digital thermometers.8... 

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