H
H.G. Miller
Researcher at University of Pretoria
Publications - 87
Citations - 807
H.G. Miller is an academic researcher from University of Pretoria. The author has contributed to research in topics: Phase transition & Canonical ensemble. The author has an hindex of 14, co-authored 87 publications receiving 754 citations. Previous affiliations of H.G. Miller include Council for Scientific and Industrial Research & National University of La Plata.
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A semi-empirical determination of the properties of nuclear matter
TL;DR: The temperature dependence of the coefficients in the semi-empirical mass formula has been determined from a least squares fit to the canonical ensemble average of the excitation energy for nuclei throughout the periodic table.
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On the cut-off prescriptions associated with power-law generalized thermostatistics
TL;DR: In this article, the authors revisited the cut-off prescriptions which are needed in order to specify completely the form of Tsallis' maximum entropy distributions and discussed some of its basic mathematical properties.
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Minimum kullback entropy approach to the fokker-planck equation
TL;DR: In this article, a minimum Kullback entropy approach was proposed to determine approximate, time-dependent solutions to the Fokker-Planck (FP) equation, and it was shown that the ensuing approximate solutions can be derived from a variational principle.
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Chemical equilibration in heavy-ion collisions
TL;DR: In this paper, the authors examined the question of chemical equilibration in heavy-ion collisions by comparing hadron production ratios from the NA35 and WA85 Collaborations with those calculated in an equilibrium thermodynamic model of hadron product.
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Kappa-deformed Statistics and the Formation of a Quark-Gluon Plasma
TL;DR: The effect of statistical mechanics on the formation of quark-gluon plasma (QGP) has been investigated in this article, where it was shown that for small deviations from Boltzmann-Gibbs (BG) statistics in the QGP phase, the critical temperature of a QGP does not change substantially for a large variation of the chemical potential.