scholarly journals Phase Change Enthalpies and Entropies of Liquid Crystals

2006 ◽  
Vol 35 (3) ◽  
pp. 1051-1330 ◽  
Author(s):  
William E. Acree ◽  
James S. Chickos
Keyword(s):  
1968 ◽  
Vol 20 (19) ◽  
pp. 1024-1025 ◽  
Author(s):  
J. J. Wysocki ◽  
J. Adams ◽  
W. Haas

Author(s):  
Rudolf Naef ◽  
William E. Acree Jr.

The calculation of the standard enthalpies of vaporization, sublimation and solvation of organic molecules is presented using a common computer algorithm on the basis of a group-additivity method. The same algorithm is also shown to enable the calculation of their entropy of fusion as well as the total phase-change entropy of liquid crystals. The present method is based on the complete break-down of the molecules into their constituting atoms and their immediate neighbourhood; the respective calculations of the contribution of the atomic groups by means of the Gauss-Seidel fitting method is based on experimental data collected from literature. The feasibility of the calculations for each of the mentioned descriptors was verified by means of a 10-fold cross-validation procedure proving the good to high quality of the predicted values for the three mentioned enthalpies and for the entropy of fusion, whereas the predictive quality for the total phase-change entropy of liquid crystals was poor. The goodness of fit (Q2) and the standard deviation (σ) of the cross-validation calculations for the five descriptors was as follows: 0.9641 and 4.56 kJ/mol (N=3386 test molecules) for the enthalpy of vaporization, 0.8657 and 11.39 kJ/mol (N=1791) for the enthalpy of sublimation, 0.9546 and 4.34 kJ/mol (N=373) for the enthalpy of solvation, 0.8727 and 17.93 J/mol/K (N=2637) for the entropy of fusion and 0.5804 and 32.79 J/mol/K (N=2643) for the total phase-change entropy of liquid crystals. The large discrepancy between the results of the two closely related entropies is discussed in detail. Molecules, for which both the standard enthalpies of vaporization and sublimation were calculable, enabled the estimation of their standard enthalpy of fusion by simple subtraction of the former from the latter enthalpy. For 990 of them the experimental enthalpy-of-fusion values are also known, allowing their comparison with predictions, yielding a correlation coefficient R2 of 0.6066.


1969 ◽  
Vol 8 (1) ◽  
pp. 471-487 ◽  
Author(s):  
J. Wysocki ◽  
J. Adams ◽  
W. Haas

2018 ◽  
Vol 2018 ◽  
pp. 1-8
Author(s):  
Eva Klemenčič ◽  
Mitja Slavinec

Thermal stabilization exploiting phase change materials (PCMs) is studied theoretically and numerically. Using the heat source approach in numerical simulations, we focus on phase change temperature as a key factor in improving thermal stabilization. Our focus is to analyze possible mechanisms to tune the phase change temperature. We use thermotropic liquid crystals (LCs) as PCMs in a demonstrative system. Using the Landau-de Gennes mesoscopic approach, we show that an external electric field or appropriate nanoparticles (NPs) dispersed in LCs can be exploited to manipulate the phase change temperature.


1969 ◽  
Vol 51 (3) ◽  
pp. 1258-1260 ◽  
Author(s):  
George H. Heilmeier ◽  
Joel E. Goldmacher

Author(s):  
M. Locke ◽  
J. T. McMahon

The fat body of insects has always been compared functionally to the liver of vertebrates. Both synthesize and store glycogen and lipid and are concerned with the formation of blood proteins. The comparison becomes even more apt with the discovery of microbodies and the localization of urate oxidase and catalase in insect fat body.The microbodies are oval to spherical bodies about 1μ across with a depression and dense core on one side. The core is made of coiled tubules together with dense material close to the depressed membrane. The tubules may appear loose or densely packed but always intertwined like liquid crystals, never straight as in solid crystals (Fig. 1). When fat body is reacted with diaminobenzidine free base and H2O2 at pH 9.0 to determine the distribution of catalase, electron microscopy shows the enzyme in the matrix of the microbodies (Fig. 2). The reaction is abolished by 3-amino-1, 2, 4-triazole, a competitive inhibitor of catalase. The fat body is the only tissue which consistantly reacts positively for urate oxidase. The reaction product is sharply localized in granules of about the same size and distribution as the microbodies. The reaction is inhibited by 2, 6, 8-trichloropurine, a competitive inhibitor of urate oxidase.


Author(s):  
Matthew R. Libera ◽  
Martin Chen

Phase-change erasable optical storage is based on the ability to switch a micron-sized region of a thin film between the crystalline and amorphous states using a diffraction-limited laser as a heat source. A bit of information can be represented as an amorphous spot on a crystalline background, and the two states can be optically identified by their different reflectivities. In a typical multilayer thin-film structure the active (storage) layer is sandwiched between one or more dielectric layers. The dielectric layers provide physical containment and act as a heat sink. A viable phase-change medium must be able to quench to the glassy phase after melting, and this requires proper tailoring of the thermal properties of the multilayer film. The present research studies one particular multilayer structure and shows the effect of an additional aluminum layer on the glass-forming ability.


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