Melts mobility model

Melting point, 193, 203, 528 Meslin s theorem, 229 Metastable states, 181 Mixed liquids, 380 Mixture rule, 263 Mobile equilibrium, 304, 340 Model, thermodynamic, 240 Mol, 20, 135... 

Decreased mobility of adsorbed chains has been observed and proved in many cases both in the melt and in the solid state [52-54] and changes in composite properties are very often explained by it [52,54]. Overall properties of the interphase, however, are not completely clear. Based on model calculations the formation of a soft interphase is claimed [51], while in most cases the increased stiffness of the composite is explained by the presence of a rigid interphase [55,56]. The contradiction obviously stems from two opposing effects. Imperfection of the crystallites and decreased crystallinity of the interphase should lead to lower modulus and strength and larger deformability. Adhesion and hindered mobility of adsorbed polymer chains, on the other hand, decrease deformability and increase the strength of the interlayer. 

Fig. 11. Evidence that a membrane-associated immunochemical reaction (complement fixation) depends on the mobility of the target hapten (IX) in the plane of a model membrane. The extent of the immunochemical reaction, complement fixation, is measured by A Absorbance at 413 nm. Temperature is always 32°C, which is above the chainmelting temperature (23°C) of dimyristoylphosphatidylcholine used for the data given in A and below the chain-melting transition temperature (42°C) of dipalmitoylphosphatidyl-choline used for the data in B. Thus A refers to a fluid membrane and B refers to a solid membrane. The numbers by each curve are equal to c, the mole % of spin-label hapten IX in the plane of the lipid membrane. It will be seen that complement fixation, as measured by A Absorbance at 413 nm is far more effective in the fluid membrane than in the solid membrane at low hapten concentrations (i.e., c 0.3 mo e%). In C the lipid membrane host is a 50 50 mole ratio mixture of cholesterol and dipalmitoylphosphatidylcholine. The immunochemical data suggest that this membrane is in a state of intermediate fluidity. Specific affinity-purified IgG molecules were used in these experiments. (For further details, see Ref. 5.)... 

The order and mobility of a labeled flexible alkyl spacer in the linear thermotropic polymeric nematic liquid crystal poly(2,2 -dimethyl-4,4 -dioxyazoxybenzenedodecanedioyl-dj0) (poly[oxy(3-methyl-1,4-phenylene)azoxy 2-methyl-1,4-phenylene)oxy(1,12-dioxo-1,12-dodecanediyl-d2oll) is explored with deuterium NMR. The quadrupol splittings of the spacer methylene segments in the nematic melt of the polymer are reported as a function of the temperature and are contrasted with observations on model compounds solubilized in a nematic solvent. 

This applies, however, only within limits. Many solids are somewhat mobile and can flow very slowly. In that case methods and models of capillarity can be applied. One case where capillarity plays an important role is sintering. In sintering a powder is heated. At a temperature of roughly 2/3 of the melting point of the material the surface molecules become mobile and can diffuse laterally. Thereby the contact areas of neighbouring particles melt and menisci are formed. When cooling, the material solidifies in this new shape and forms a continuous solid. 

The microstructure and morphology of thick single-phase films have been extensively studied for a wide variety of metals, alloys, and refractory compounds. Structural models have been proposed (12,13). Three zones with different microstructure and surface morphology were described for thick (tens of micrometers) deposits of pure metal. At low temperature (< 0.3 Tm ), where Tm is the melting point (K) of the deposit metal, the surface mobility of the adatoms is reduced, and the deposit was reported to grow as tapered crystallites. The surface is not full density (Zone 1). At higher substrate temperature (0.3-0.45 Tm ), the surface mobility increases. The surface... 

Meyer (3) showed some time ago that the color of hot sulfur melts is caused mainly by the presence of S3 and S4. In this connection we should also mention recent sophisticated studies by Block and co-workers (10). Sulfur molecules S with 2-22 sulfur atoms have been desorbed from a condensed sulfur layer on a tungsten field emitter of a field ionization time-of-flight mass spectrometer. The condensed sulfur layer is in a highly mobile liquid-like steady state. The observation of these large sulfur molecules is important to the current models of liquid sulfur. 

The water molecules produced during mechanochemical dehydration of lepidocrocite facilitate the lithium mobility in a way similar to that found when LiOH melts and reacts with Fc20j. The structural transformation is explained within a model in which Li vacancies created during grinding promote the migration of Fe ions from octahedral to tetrahedral sites. 

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