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Crystallizers drive system

Floudas et al. [135] also studied the isothermal crystallization of PEO and PCL blocks within PS-b-PEO-h-PCL star triblock copolymers. In these systems the crystallization occurs from a homogeneous melt Avrami indexes higher than 1 are always observed since the crystallization drives structure formation and does not occur under confined conditions. A reduction in the equilibrium melting temperature in the star block copolymers was also observed. [Pg.70]

Figure 6. Schematic of driving forces for flows in Czochralski crystal growth system, which shows the regions where the driving forces will produce the strongest motions. The shape functions describing the unknown interface shapes are listed also. Figure 6. Schematic of driving forces for flows in Czochralski crystal growth system, which shows the regions where the driving forces will produce the strongest motions. The shape functions describing the unknown interface shapes are listed also.
Convection in the crystal growth systems discussed earlier cannot be characterized by analysis with either perfectly aligned vertical temperature gradients or slender cavities, because these systems have spatially varying temperature fields and nearly unit aspect ratios. Even when only one driving force is present, such as buoyancy-driven convection, the flow structure can be quite complex, and little insight into the nonlinear structure of the flow has been gained by asymptotic analysis. [Pg.65]

The surprising result is that our liquid crystal model system with just these three broken symmetries of life knows time, another feature of living systems. It does not learn about time after it has been pushed far from equilibrium and is close to turbulence. It knows time as soon as the nonequilibrium driving force is strong enough to enforce a pattern. Even its first pattern is characterized by a frequency, co. When i 0, the interface reverts back to its featureless dead state = 0 and co = 0. [Pg.486]

SAXS spectra and the intensity of the most intense WAXD reflection (110) increase simultaneously, indicating that the PCL crystallization drives the microphase separation in this system ns well. [Pg.452]

The drive system on a scraped surface continuous crystallizer must allow free turning of the driven shaft. The shaft must also be sealed against leakage of the process fluids. The drive system used is illustrated in Fig. 054. [Pg.207]

The primary driving forces behind investigation of new solvents include environmental concerns and the abiUty to form Hquid crystals in the new solvent systems. By analogy with Kevlar, a synthetic aromatic polyamide fiber, spinning from a Hquid crystalline solution should yield cellulose fibers with improved strength, as has been demonstrated in laboratory experiments. [Pg.243]

Evaporative crystalli rs generate supersaturation by removing solvent, thereby increasing solute concentration. These crystallizers may be operated under vacuum, and, ia such circumstances, it is necessary to have a vacuum pump or ejector as a part of the unit. If the boiling poiat elevation of the system is low (that is, the difference between the boiling poiat of a solution ia the crystallizer and the condensation temperature of pure solvent at the system pressure), mechanical recompression of the vapor obtained from solvent evaporation can be used to produce a heat source to drive the operation. [Pg.356]

Another velocity finally appears in a system where a liquid is in contact with an interface. The interface energy 7 then works as a static driving force. This can trigger a current which is damped by a dynamic force, the viscous friction, in the case of density difference between crystal and liquid. Taking the ratio... [Pg.903]

Secondly, I wish to counteract anticipated despondency which some of the complexities on the present theoretical scene may perhaps provoke. For this purpose, I wish to invoke the decisive simplicity and definiteness of some of the experimental effects observed within the confines of the above, near ideal systems. This, as I often pointed out elsewhere, is unmatched in the field of crystal growth of simple substances. Complicated as polymers may seem, and subtle as some of the currently relevant theoretical issues, this should not obscure the essential simplicity and reproducibility of the core material. To be specific, the appropriate chains seem to want to fold and know when and how, and it is hardly possible to deflect them from it. Clearly, such purposeful drive towards a predetermined end state should continue to give encouragement to theorists for finding out why Those who are resolved to persevere or those who are newly setting out should find the present review a most welcome source and companion. [Pg.220]


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See also in sourсe #XX -- [ Pg.77 ]




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