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A description of phase transitions as recorded by differential scanning calorimetry (DSC) is given. A new numberN is defined asN=h′/h, whereh is the height of a transition peak for a mass of samplem and a heating rate †p andh′ is the height of the same peak for a mass2m or a heating rate2† p.N is theoretically derived in the case of isothermal and nonisothermal first order phase transitions and of a second order phase transition. The equivalence of mass and heating rate is proved. An example of the possible use ofN is given.

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Simultaneous measurements of the rate of heat evolution and changes of the mechanical variable of a transformation such as volume or pressure, performed in a p-V-T controlled scanning calorimeter have been applied to investigations of phase transitions in liquid crystals. In the instrument, the phase transitions can be induced by a controlled change of pressure, volume or temperature under isothermal, isobaric or isochoric conditions respectively. The present investigations have ben performed on 4-n-penthyl-penthylthiol-4′-decycloxybenzoate which demonstrates in the liquid crystal state a nematic and three smectic phases

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Abstract  

The melting and crystallization behaviour of water restrained in polysulfone (PSF) hollow fibre has been investigated by DSC. The PSF hollow fibre was prepared by wet spinning. The morphology of the fibre was observed by scanning electron microscopy. The amount of water was varied by successive evaporation and it was observed that melting and crystallization shifted to temperatures lower than those observed for free water. DSC and NMR studies showed that water in hollow fibres is in a restricted state.

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Abstract  

The nature of the β to α phase transition in silver iodide was investigated by conventional and modulated temperature DSC and dielectric property measurements. On cooling, the high temperature phase remained stable 2.5C below its normal transition temperature even at a very slow cooling rate 0.2C h–1. Dielectric property measurements under conventional and microwave heating suggested an anomalous effect of the latter on the β to α phase transition in this material.

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Journal of Thermal Analysis and Calorimetry
Authors: K. Moriya, T. Yamada, K. Sakai, S. Yano, S. Baluja, T. Matsuo, I. Pritz, and Y. Vysochanskii
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Abstract  

A simple method of determination of kinetic parameters by analysis of DTA(t) function was developed for the case of systems undergoing transitions without mass change and when kinetic equation describing transition rate is known. The presented method also permits the determination of transition rate dα/dt (or α(t )) when the kinetic equation of transition is unknown. The developed method was tested using DTA data of crystallization of 2CaOAl2 O3 1.95SiO2 glass pure and doped with Cr3+ and Nd3+ .

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Abstract  

The aim of this work was to study the glass transition, the glass transition of the maximally freeze-concentrated fractions, the ice melting and the gelatinization phenomenon in dispersions of starch prepared using glycerol-water solutions. The starch concentration was maintained constant at 50 g cassava starch/100 g starch dispersions, but the concentration of the glycerol solutions was variable (C g= 20, 40, 60, 80 and 100 mass/mass%). The phase transitions of these dispersions were studied by calorimetric methods, using a conventional differential scanning calorimeter (DSC) and a more sensitive equipment (micro-DSC). Apparently, in the glycerol diluted solutions (20 and 40%), the glycerol molecules interacted strongly with the glucose molecules of starch. While in the more concentrated glycerol domains (C g>40%), the behaviour was controlled by migration of water molecules from the starch granules, due to a hypertonic character of glycerol, which affected all phase transitions.

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Abstract  

An adiabatic calorimetry was used for some investigations of equilibrium and non-equilibrium phase transitions. For one of the substances studied (4,4′-di-n-heptyloxyazoxybenzene) it was possible to determine temperature dependence of an order parameter and number of clusters of high temperature phase in a region of a phase transition. For another substance (liquid 3,4 dimethylpiridine) an anomaly on the specific heat curves was interpreted as being responsible for a decay of molecules’ clusters. Non-equilibrium phase transitions were investigated for some liquid crystal substances. The process of transformation between metastable and stable phases was described quantitatively. The conclusions obtained concern the stability of metastable phases.

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