Effects of Hairy Nanoparticles on Polymer Crystallization Kinetics
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Crystallization kinetics of molten binary and ternary oxide systems
Samples of Pd(40)Ni(40)P(20) glass, produced by cooling the melt at 1 or 800 K/s, are heated in a differential scanning calorimeter to determine the crystallization kinetics. Optical microscopy shows that eutectic crystallization proceeds both by growth from the surface of the samples and by the growth of spherical regions around preexisting nuclei in the interior. A modified Kissinger (1957) analysis is used to obtain the activation energy for crystal growth (3.49 eV). The steady state homogeneous nucleation frequency at 590 K is about 10 million/cu m per sec. This is estimated to be the maximum nucleation frequency: it is too low to account for the observed population of quenched-in nuclei, which are therefore presumed to be heterogeneous. The major practical obstacle to glass formation in this system is heterogeneous nucleation.
Viscosity, electric resistivity, and Youngs modulus measurements of glass compositions for crystallization kinetics of oxide systems
Crystallization kinetics of molten binary and ternary oxide systems
Glass formation studied from crystallization kinetics of molten binary and ternary oxide system
Investigation of glass formation by studies of molten binary and ternary oxide systems crystallization kinetics
Glass composition preparation and research on crystallization kinetics of molten binary and ternary oxide systems of glass
Crystallization kinetics and impact tests of glass fiber-epoxy composites
The crystal growth rates of NH4H2PO4, KH2PO4, (NH4)2SO4, KAl(SO4)2 central dot 12H2O, NaCl, and glycine and the nucleation rates of KBr, KCl, NaBr central dot 2H2O, (NH4)2Cl, and (NH4)2SO4 were expressed in terms of the fundamental driving force of crystallization calculated from the activity of supersaturated solutions. The kinetic parameters were compared with those from the commonly used kinetic expression based on the concentration difference. From the viewpoint of thermodynamics, rate expressions based on the chemical potential difference provide accurate kinetic representation over a broad range of supersaturation. The rates estimated using the expression based on the concentration difference coincide with the true rates of crystallization only in the concentration range of low supersaturation and deviate from the true kinetics as the supersaturation increases.
Crystal growth kinetics of molten oxides containing yttria or lanthana
Kinetics of crystallization of molten binary and ternary oxide systems
Dynamic crystallization and kinetic melting tests have been conducted for a lunar soil that resembles the bulk composition of the matrices of melt-rock breccias. The melting tests indicate that plagioclase and olivine can exist for finite times above their equilibrium liquidus temperatures; within 20-30 C below its liquidus temperature the sample is choked with crystals. A range of textures from radiate to porphyritic pyroxene-plagioclase granophyric to subophitic to intergranular to intersertal to very fine-grained poikilitic is found in the dynamic crystallization experiments. The number of nuclei, as deduced from the textures, increases as the melting temperature deceases from above the liquidus to below.
Kinetics of crystallization of high temperature glass systems