Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Polarization temperature

The polarity of the C—-OH bond, i.e., the basicity of the carbinol-amine, depends on its structure, particularly on the stability of the ring system (degree of aromatic character), and the electron affinity of the substituents on nitrogen and carbon. Of course, external factors also play an important role in the equilibrium temperature, polarity of the solvent, and presence or absence of catalysts (the solvent can also act as a catalyst). [Pg.170]

Predictably, the association between the ion-pair and the substrate is influenced by the choice of the organic phase and by the reaction temperature. Polar solvents will not only affect the interaction between the catalysts and substrate, they will also reduce the association of the ion-pair with a resultant increase in free anion over which there is no stereochemical control (Table 12.4). [Pg.521]

At high temperatures, ferroelectric materials transform to the paraelectric state (where dipoles are randomly oriented), ferromagnetic materials to the paramagnetic state, and ferroelastic materials to the twin-free normal state. The transitions are characterized through order parameters (Rao Rao, 1978). These order parameters are characteristic properties parametrized in such a way that the resulting quantity is unity for the ferroic state at a temperature sufficiently below the transition temperature, and is zero in the nonferroic phase beyond the transition temperature. Polarization, magnetization and strain are the proper order parameters for the ferroelectric. [Pg.383]

By carefully controlling the temperature we were able to obtain fairly good matching of thermally- and photo-induced absorption bands. Thus, it seems probable that low temperatures, polar solvents and irradiation with ultraviolet light all lead to the same absorbing species. [Pg.296]

Further supporting evidence is adduced from the observation that the anils of 2 -methoxy- 1-naphthaldehyde and 2-hydroxy-3-naphth-aldehyde show no marked spectral sensitivity to temperature, polarity... [Pg.296]

These possibilities could be due to a parameter inherent in a given method. Among these three isolation methods, the differences in parameters include pH, temperature, polarity of extraction solvents, moisture, and particle size. Any single parameter or combination of parameters could be affecting the yield in mutagen levels recovered from the sludge samples. Therefore, a series of experiments was conducted to examine possible effects of these parameters. [Pg.664]

H. The effect of temperature, polarity of solvent, and ionic strength on pJf/s of groups in enzymes and in solution... [Pg.431]

Polyelectrolytes change their conformation with the degree of dissociation which is varied with pH, temperature, polarity of solvent and ionic strength. [Pg.243]

This was qualitatively shown in investigations of conformational behaviour and intramolecular mobility (IMM) of cholesterol-containing polymers in dilute solutions as of a function of solvent quality 134-136,185-l88) and temperature. Polarization luminescence provides one of the most fruitful methods for the evaluation of IMM l75,176). The method permits to get direct information about rotational mobility of the macromolecule as a whole, as well as about the mobility of the main chains and side branches. This is achieved via the attachment to macromolecules of so called luminescent markers (LM) — anthracylacyloxymethane groups in the case reported. Below are shown the chain fragments with LM which give information on the mobility of main chains (LM-1) and of side groups (LM-2) ... [Pg.241]

Capillary Applied voltage Temperature Polarity Detection... [Pg.174]

WMAP also found a TE (temperature-polarization) cross-correlation. At small angles the TE amplitude was perfectly consistent with the standard picture of the recombination era. But there was also a large angle TE signal that gave an estimate for the electron scattering optical depth since reionization r = 0.17 0.04. Based on this the epoch of reionization was 200 million years after the Big Bang. [Pg.170]

The polarity reversal is sensitive to temperature. Polarity reversal occurs faster at higher temperature. [Pg.545]

The sequence of tripod-shaped TPA(OH) complexes down each channel is also polar, and the concept of a polar template may be appropriate. Furthermore, the concept of polar diffusion should be explored at low temperature, polar molecules should adopt a specific orientation during diffusion down a polar channel. [Pg.117]

The considerable electrical anisotropy of this salt is made still more evident on the room-temperature polarized infrared reflection spectra [30] (see also Chapter 6 and Fig. 1 of this chapter). In addition, these reflection spectra give a remarkably clear information on the existence of strong coupling between the quasi-one-dimensional electronic system and the symmetric ag vibrational modes of the TCNQ molecules. More precisely, under the effect of this coupling, these particular modes, which are normally Raman active but infrared nonactive, acquire an anomalous intense infrared activity together with an anomalous polarization [20,30,31]. [Pg.323]

The room-temperature polarization-field hysteresis of the ceramics shows well-saturated loops. The values of remnant polarization, spontaneous polarization and coercive field determined are reported in Table 3. The data of single crystal previously reported are also list in Table 3. [Pg.88]

Permeate flux decreases with an increase in feed concentration. This phenomenon can be attributed to the reduction of the driving force due to decrease of the vapor pressure of the feed solution and exponential increase of viscosity of the feed with increasing concentration. The DCMD flux gradually increases with an increase in temperature difference between feed and cooling water. Lagana et al. [63] reported that the viscosity of apple juice at high concentration induces severe temperature polarization. It may be noted that temperamre polarization is more important than concentration polarization, which is located mainly on the feed side. [Pg.525]

Mengual et al. have observed an Arrhenius type of dependence of the permeate flux on the feed temperature. An increase in the feed circulation velocity increases the heat transfer coefficient in the liquid boundary layer, which in turn increases the VMD flux due to the reduction in the temperature polarization. Concentration factors increased with a decrease in feed temperature during VMD, and for a decrease of 30°C to 10°C, increase in concentration factors from 7-15.5 to 21-31 were obtained for a highly volatile black currant aroma ester [17]. [Pg.529]

Concentration and temperature polarization can be reduced by the presence of spacers that are mrbulence promoters, which enhance the mass flux by increasing the film heat transfer coefficient. Spacers also change the flow characteristics and promote regions of turbulence thus improving boundary layer transfer [106]. DCMD in spacer-filled channels have been shown to improve flux by 31% 1% than that without spacers. The temperamre polarization coefficients are substantially increased and approach unity when the spacers are used in the channels. [Pg.539]

Cath et al. [97] have demonstrated that, careful design of membrane module and configuration of MD processes could simultaneously reduce temperature polarization and permeability obstmctions in the DCMD of salt solutions. Results have shown that fluxes almost double those that are observed in the traditional mode of DCMD, can be achieved at relatively low temperatures. [Pg.539]

Temperature Polarization—The difference in temperature of the bulk liquid and the membrane surface is called... [Pg.545]

The performance of membrane operations is diminished by polarization phenomena (concentration and temperature polarization), although the extent to which these phenomena can occur differs considerably. [Pg.1105]


See other pages where Polarization temperature is mentioned: [Pg.262]    [Pg.480]    [Pg.96]    [Pg.277]    [Pg.191]    [Pg.3]    [Pg.226]    [Pg.324]    [Pg.255]    [Pg.331]    [Pg.262]    [Pg.20]    [Pg.127]    [Pg.127]    [Pg.36]    [Pg.156]    [Pg.177]    [Pg.224]    [Pg.58]    [Pg.850]    [Pg.390]    [Pg.115]    [Pg.157]    [Pg.526]    [Pg.530]    [Pg.531]    [Pg.539]    [Pg.542]    [Pg.545]   
See also in sourсe #XX -- [ Pg.115 ]




SEARCH



© 2024 chempedia.info