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1.
We present a review of our recent measurements of total cross sections (Q
T's) for the scattering of positrons by Na, K, and Rb, and positronium-formation cross sections (Q
Ps's) for Na and K. For our total cross section measurements, a beam transmission technique has been used. For ourQ
Ps measurements, our approach involves setting upper and lower limits onQ
Ps using a combination of (1) measuring the transmission of the positron beam with the angular discrimination of the apparatus made as poor as possible, and (2) measuring the 511 keV annihilation gamma rays in coincidence produced by the decay of para-Ps formed in the scattering cell. Comparison with theoretical calculations shows that our measuredQ
T's andQ
Ps's for Na and K agree reasonably well with a close coupling approximation (CCA) calculation which takes into account the formation of Ps in then=1 andn=2 states. In the 3–10 eV energy range, this calculation predicts a peak in theQ
T's andQ
Ps's for K which also appears in our measurements. The absence of such a peak in our measuredQ
T's andQ
Ps's (preliminary) for Na in this energy range is also consistent with the same theory. Comparisons with five-state CCA calculations ofQ
T which do not take Ps-formation into account also show good agreement with our positron-Na, K, and RbQ
T measurements for energies above 20 eV, but show dramatic departures from our measurements below 10 eV for K and Rb. 相似文献
2.
The role of filamentation instability of quark-gluon plasma, in explaining collective phenomena in relativistic heavy-ion
collisions, has been analyzed. Using equations of SU(2) two fluid color hydrodynamics it is shown that this instability can
significantly enhance nuclear stopping and might contribute to collective sideward flows. 相似文献
3.
4.
The aminolysis of a novel activated ester resin was utilized for kinetic study via continuous in situ fluorescence measurements. A variety of resin compositions (polystyrene, JandaJel, ArgoPore, TentaGel, NovaGel, and PEGA) and solvents (dimethylformamide, acetonitrile, tetrahydrofuran, 1,2-dichlorethane, and toluene) were tested to compare their effects on the reaction rate. A linear relationship between the reaction rate and (solvent polarity x swelling of resin) was elucidated for the aminolysis reaction. 相似文献
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7.
Brozell AM Muha MA Parikh AN 《Langmuir : the ACS journal of surfaces and colloids》2005,21(25):11588-11591
We report the formation of microscopic patterns of substrate-supported, 3D planar colloidal crystals using physical confinement in conjunction with surfaces displaying predetermined binary patterns of hydropholicity. The formation process involves a primary self-assembly wherein nano- and microscale colloids order into a photonic fcc lattice via capillary interactions followed by a secondary template-induced crystal cleavage step. Following this method, arbitrary arrays of pattern elements, which preserve structural and orientational properties of the parent crystal, can be easily obtained. 相似文献
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9.
Using petroleum ether as a precipitant and chloroform–acetone mixture as solvent, six fractions of cellulose triacetate were obtained by fractional precipitation. The molecular weight of each fraction was obtained from osmotic pressure measurements carried out on chloroform solutions. It was shown that virtual nonfractionability of cellulose triacetate with regard to molecular weight occurred in this system. This behavior was also observed in attempts to fractionate it from tetrachloroethane or acetic acid solutions. These results are explained by the hypothesis that specific polymer–solvent interaction takes place due to hydrogen bonding. 相似文献
10.
The solubility of cellulose triacetate in a range of solvents was measured, and the results for tetrachloroethane, chloroform, and acetic acid were compared with those from initial phase separation in solvent–nonsolvent mixtures and viscosity–concentration studies. The correlation found between solubilities, precipitation values, and values of the Huggins viscosity constant is discussed with reference to the type of polymer–solvent interaction proposed previously to explain fractionation behavior. A qualitative comparison of solubility–swelling behaviour was also made for a very low molecular weight cellulose triacetate sample in a wide range of solvents. Results are compared with those for higher molecular weight samples and discussed with regard to the cohesiveenergy densities of solvent and polymer. Some attempt has been made to predict suitable solvents for cellulose triacetate, based on consideration of their molecular structures. 相似文献