Cooling polar

All these features were observed experimentally for solutions of 3-amino-/V-methylphthalimide, 4-amino-/V-methylphthalimide, and for nonsubstituted rhoda-mine. The results were observed for cooled, polar solutions of phthalimides, in which the orientational relaxation is delayed. Exactly the same spectral behavior was observed [50] by picosecond spectroscopy for low viscosity liquid solutions at room temperature, in which the orientational relaxation rate is much higher. All experimental data indicate that correlation functions of spectral shifts Av-l(t), which are used frequently for describing the Time Dependent Stokes Shift, are essentially the functions of excitation frequency. 

Friedrich, B. and Herschbach, D.R. (1991). On the possibility of orienting rotationally cooled polar molecules in an electric field, Z. Phys. D—Atoms, Molecules and Clusters, 18, 153-161. 

Because of the rotation of the Earth and because of the warm equatorial and cool polar regions, the atmosphere divides itself into six regions (roughly corresponding to the climatic zones). These atmospheric regions are called the northern and southern Polar, Ferrel, and Hadley cells (so called because they are roll cells ) see Figure 3.2. This division of the atmosphere tends to slow the mixing... 

Friedrich, B., Herschbach, D.R., On the possibbity of orienting rotationally cooled polar... 

Since the 1971 balloon flights the major advance in the direct measurement of the background spectrum has been made by Woody, Mather, Nishioka, and Richards of Berkeley [10]. They flew a liquid helium-cooled polarizing Fourier transform... 

Dalibard J and Cohen-Tannoudji C 1989 Laser cooling belowthe Doppler limit by polarization gradients simple theoretical models J.Opt.Soc.Am. B 6 2023-45... 

Above the solution treatment temperature (ca 1250°C), the alloy is single phase with a bcc crystal stmcture. During cooling to ca 750—850°C, the sohd solution decomposes spinodally into two other bcc phases a and lattice parameter composition. The matrix a-phase is rich in Ni and Al and weakly magnetic as compared with which is rich in Fe and Co. The a -phase tends to be rod-like in the (100) dkection and ca 10 nm in diameter and ca 100 nm long. As the temperature is decreased, segregation of the elements becomes mote pronounced and the difference between the saturation polarizations of the two phases increases. 

Internal surfactant antistats ate physically mixed with the plastic resin prior to processing. When the resin is melted, the antistat distributes evenly in the polymer matrix. The antistat usually has some degree of solubiUty in the molten polymer. However, when the polymer is processed (extmded, molded, etc) into its final form and allowed to cool, the antistat migrates to the surface of the finished article due to its limited solubiUty in the solidified resin. The molecule of a surface-active agent is composed of a polar hydrophilic portion and a nonpolar hydrophobic portion. The hydrophilic portion of the surfactant at the surface attracts moisture from the atmosphere it is the moisture that has the static dissipative effect. 

Alumina is the most frequently employed adsorbant. Its activity (i.e., the extent to which it adsorbs polar compounds) is largely a function of the amount of water present. Alumina of Activity I is prepared by heating the material in an oven to 200-230° and allowing it to cool in a desiccator. Addition of water to the extent of 3%, 6%, 10%, or 15% to the dry material gives alumina of Activity II, III, IV, and V, respectively. 

The performance of soluble oils is made possible not only by their high specific heat and thermal conductivity but by their low viscosity, which permits good penetration into the very fine clearances around the cutting zone. Consequently, these fluids are used mainly where cooling is the primary requirement. Lubricating properties can be improved by polar additives, which are agents that enhance the oiliness or anti-friction characteristics. Further improvements can be effected by EP (extreme-pressure) additives, which are usually compounds of sulfur or chlorine. 

Crystalline non-polar polymers and amorphous solvents Most polymers of regular structure will crystallise if cooled below a certain temperature, i.e. the melting point T. This is in accordance with the thermodynamic law that a process will only occur if there is a decrease in Gibbs free energy (-AF) in going from one state to another. Such a decrease occurs on crystallisation as the molecules pack regularly. 

Amorphous non-polar polymers and crystalline solvents This situation is identical to the previous one and occurs, for example, when paraffin wax is mbced into rubber above its melting point. On cooling the paraffin wax tends to crystallise, some of it on the surface of the rubber. Such a bloom is one way of protecting a diene rubber from ozone attack. 

The Electrical A nalogue of Magnetic Cooling. Three Processes bg Which Ions Are Introduced into Solution.. 1 Polar Dielectric in an Electrostatic Field. The Concepts of Faraday and Maxwell. The Electrostatic Energy in the Fields of Ions. The. Charging of a Condenser. The Amount of Free Energy Lost, by a Dielectric. The Behavior of Solvents in an Electrostatic Field. A Dielectric in the Field of a Charged Sphere. Two Types of Process Contrasted. 

The behavior of a polar dielectric in an electric field is of the same kind. If the dielectric, is exposed to an external electric field of intensity X, and this field is reduced in intensify by an amount SX, the temperature of the dielectric will not remain constant, unless a certain amount of heat enters the substance from outside, to compensate for the cooling which would otherwise occur. Alternatively, when the field is increased in intensity by an amount SX, we have the converse effect. In ionic solutions these effects are vciy important in any process which involves a change in the intensity of the ionic fields to which the solvent is exposed—that is to say, in almost all ionic processes. When, for example, ions are removed from a dilute solution, the portion of the solvent which was adjacent to each ion becomes free and no longer subject to the intense electric field of the ion. In the solution there is, therefore, for each ion removed, a cooling effect of the kind mentioned above. If the tempera-... 

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