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Low-temperature crystallization

Crystallization. Low temperature fractional crystallization was the first and for many years the only commercial technique for separating PX from mixed xylenes. As shown in Table 2, PX has a much higher freezing point than the other xylene isomers. Thus, upon cooling, a pure solid phase of PX crystallizes first. Eventually, upon further cooling, a temperature is reached where solid crystals of another isomer also form. This is called the eutectic point. PX crystals usually form at about —4° C and the PX-MX eutectic is reached at about —68° C. In commercial practice, PX crystallization is carried out at a temperature just above the eutectic point. At all temperatures above the eutectic point, PX is still soluble in the remaining Cg aromatics liquid solution,... [Pg.417]

Mechanical properties depend upon the chemical structure of both the hard- and soft-segment constituents. Properties such as melting point, modulus, solubility, and resistance to creep and set are influenced primarily by the nature of the hard segment, its concentration, and its state of crystallization. Low-temperature flexibility as well as tensile and tear strength also vary with hard-segment composition and concentration but, in addition, strongly depend on the composition of the amorphous phase. [Pg.62]

The structure was determined on a single crystal low-temperature modification... [Pg.235]

For jet fuels, the elimination of free water using filters and coalescers by purging during storage, and the limit of 5 ppm dissolved water are sufficient to avoid incidents potentially attributable to water contamination formation of micro-crystals of ice at low temperature, increased risk of corrosion, growth of micro-organisms. [Pg.250]

The pour point is the lowest temperature at which an oil can still pour while it is cooled, without agitation, under standardized conditions. The pour point of paraffinic bases is linked to the crystallization of n-paraffins. The pour point of naphthenic bases is related to a significant viscosity increase at low temperatures. This property can be improved by additives. [Pg.283]

C3.5.6.5 POLYATOMIC MOLECULES IN LOW-TEMPERATURE CRYSTALS—FREQUENCY DEPENDENCE... [Pg.3046]

Much of our knowledge of the frequency dependence of VER rates in polyatomic molecules stems from low-temperature studies of molecular crystals [2] such as pentacene (PTC 221 4) guest molecules in a crystalline naphthalene (N C,., H ) host. In naphthalene, the phonon cut-off frequency is -180 cm [97]. At low temperature,... [Pg.3046]

Hill J R, Chronister E L, Chang T-C, Kim H, Postlewaite J C and DIott D D 1988 Vibrational relaxation and vibrational cooling in low temperature molecular crystals J. Chem. Phys. 88 949-67... [Pg.3053]

By cooling the solution in a freezing mixture (ice and salt, ice and calcium chloride, or solid carbon dioxide and ether). It must be borne in mind that the rate of crystal formation is inversely proportional to the temperature cooling to very low temperatures may render the mass... [Pg.129]

High vacuum distillation gave a crystalline product, containing small amounts of impurities, inter alia some 2-butynoic acid. Crystallization from a 3 1 mixture of pentane and diethyl ether at low temperature gave the pure acid, m.p. 77°C, in 38-45 yields. [Pg.49]

This class of smart materials is the mechanical equivalent of electrostrictive and magnetostrictive materials. Elastorestrictive materials exhibit high hysteresis between strain and stress (14,15). This hysteresis can be caused by motion of ferroelastic domain walls. This behavior is more compHcated and complex near a martensitic phase transformation. At this transformation, both crystal stmctural changes iaduced by mechanical stress and by domain wall motion occur. Martensitic shape memory alloys have broad, diffuse phase transformations and coexisting high and low temperature phases. The domain wall movements disappear with fully transformation to the high temperature austentic (paraelastic) phase. [Pg.252]

The entropy value of gaseous HCl is a sum of contributions from the various transitions summarized in Table 4. Independent calculations based on the spectroscopic data of H Cl and H Cl separately, show the entropy of HCl at 298 K to be 186.686 and 187.372 J/(mol K) (44.619 and 44.783 cal/(mol K), respectively. The low temperature (rhombic) phase is ferroelectric (6). SoHd hydrogen chloride consists of hydrogen-bonded molecular crystals consisting of zigzag chains having an angle of 93.5° (6). Proton nmr studies at low temperatures have also shown the existence of a dimer (HC1)2 (7). [Pg.439]

Iron(III) fluoride ttihydrate [15469-38-2] FeF3-3H2 0, crystallizes from 40% HF solution ia two possible crystalline forms. At low temperature the a-form, which is isostmctural with a-AlF 3H2O, is favored. High temperatures favor P-FeF 3H2O, the stmcture of which consists of fluoride-bridged octahedra with one water of hydration per unit cell. [Pg.436]


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See also in sourсe #XX -- [ Pg.274 ]




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Crystal structures at low temperature

Crystallization at low-temperature

Crystallization temperature

Crystals, low-temperature

Single Crystal Diffraction Studies at Low Temperatures

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