Temperature condition

Such a method does not require high working temperatures, making it possible to avoid thermodesorption processes. It also enables us to conduct measurements over a wide range of temperatures. [Pg.179]

Some authors have chosen to work at very low temperatures, while others have used the Kelvin method at a temperature of a few hundred degrees in the framework of studies on catalysts. [Pg.179]

If the system is no longer isothermal, it is possible to demorrstrate that the experimentally measrtred potential difference is the contact potential difference added to the electromotive force of thermoelectric origin. [Pg.179]

Figine 6.35 gives a diagrammatic representation of the system when its components are not at the same temperature. [Pg.179]

If the thermal gradient at the electrodes is weak, which is usually the case, the terms a(T, -T2) and a (T3 -T4) ate neghgible. Moreover, since the conductor connecting the two sohds R and S is metalhc, its thermoelectric power a is weak and the term a (Tj — T3) is small. This electromotive force, for systems at a temperature lower than 360°C, was estimated at a few mV by J.P. Beaufils. [Pg.180]

Most molecular dynamics simulations, and particularly those for proteins, use constant temperature conditions. [Pg.78]

The viscosity average molecular weight is not an absolute value, but a relative molecular weight based on prior calibration with known molecular weights for the same polymer-solvent-temperature conditions. The parameter a depends on all three of these it is called the Mark-Houwink exponent, and tables of experimental values are available for different systems. [Pg.42]

In view of item (2), experimental (subscript ex) values of s° are reduced to standard (subscript s) temperature conditions by the expression... [Pg.638]

The choice of the solvent also has a profound influence on the observed sonochemistry. The effect of vapor pressure has already been mentioned. Other Hquid properties, such as surface tension and viscosity, wiU alter the threshold of cavitation, but this is generaUy a minor concern. The chemical reactivity of the solvent is often much more important. No solvent is inert under the high temperature conditions of cavitation (50). One may minimize this problem, however, by using robust solvents that have low vapor pressures so as to minimize their concentration in the vapor phase of the cavitation event. Alternatively, one may wish to take advantage of such secondary reactions, for example, by using halocarbons for sonochemical halogenations. With ultrasonic irradiations in water, the observed aqueous sonochemistry is dominated by secondary reactions of OH- and H- formed from the sonolysis of water vapor in the cavitation zone (51—53). [Pg.262]

Supercritical Fluid Extraction. Supercritical fluid (SCF) extraction is a process in which elevated pressure and temperature conditions are used to make a substance exceed a critical point. Once above this critical point, the gas (CO2 is commonly used) exhibits unique solvating properties. The advantages of SCF extraction in foods are that there is no solvent residue in the extracted products, the process can be performed at low temperature, oxygen is excluded, and there is minimal protein degradation (49). One area in which SCF extraction of Hpids from meats maybe appHed is in the production of low fat dried meat ingredients for further processed items. Its apphcation in fresh meat is less successful because the fresh meat contains relatively high levels of moisture (50). [Pg.34]

Effects of Rate Conditions. It is essential for commercial a-quartz crystals to have usable perfection growth at a high rate and at pressure and temperature conditions that allow economical equipment design. The dependence of rate on the process parameters has been studied (8,14) and may be summarized as follows. Growth rate depends on crystallographic direction the (0001) is one of the fastest directions. Because AS is approximately linear with AT, the growth rate is linear with AT. Growth rate has an Arrhenius equation dependence on the temperature in the crystallization zone ... [Pg.520]

It is an axiom of sterilization technology that appropriate conditions must be estabUshed throughout the material to be sterilized. The time-at-temperature conditions are critical when considering any sterilization method using heat. [Pg.407]

Superheated steam results when steam is heated to a temperature higher than that which would produce saturated steam. The equiUbrium between hquid and vapor is destroyed, and the steam behaves as a gas. It loses its abiUty to condense into moisture when in contact with the cooler surface of the article to be sterilized. This process resembles dry-heat sterilization more than steam sterilization and, under ordinary time—temperature conditions for steam sterilization, does not produce stetihty. [Pg.408]

A minimum volatihty is frequently specified to assure adequate vaporization under low temperature conditions. It can be defined either by a vapor pressure measurement or by initial distillation temperature limits. Vaporization promotes engine start-up. Fuel vapor pressure assumes an important role particularly at low temperature. For example, if fuel has cooled to —40°C, as at arctic bases, the amount of vapor produced is well below the lean flammabihty limit. In this case a spark igniter must vaporize enough fuel droplets to initiate combustion. Start-up under the extreme temperature conditions of the arctic is a major constraint in converting the Air Force from volatile JP-4 to kerosene-type JP-8, the military counterpart of commercial Jet Al. [Pg.415]

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