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On the kinetic of crystallization of zinc oxalate (II). Determination of the specific surface energy at the crystal solution interface by kinetic studies
Author(s) -
Kirkova E.,
Djarova M.
Publication year - 1977
Publication title -
kristall und technik
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.377
H-Index - 64
eISSN - 1521-4079
pISSN - 0023-4753
DOI - 10.1002/crat.19770120802
Subject(s) - supersaturation , nucleation , crystallization , chemistry , kinetic energy , thermodynamics , surface energy , crystal growth , oxalate , crystal (programming language) , kinetics , zinc , crystallography , inorganic chemistry , organic chemistry , physics , quantum mechanics , computer science , programming language
An apparatus based on turbidimetry was constructed for studying the kinetics of crystallization of sparingly soluble salts. The kinetics of crystallization of zinc oxalate was investigated at various supersaturations and p Hs of the medium. The specific surface energy at the crystal‐solution interface was determined from the induction periods of the S‐shaped curves by means of the classical theory of nucleation. The calculations were made using the slope of the logarithmic dependence of I or τ, respectively, on supersaturation (equations 1 and 2) and the critical supersaturation which was also determined on the basis of kinetic data. Various values of σ were found for the different supersaturations. Different values for this quantity were also obtained when supersaturation was presented by the concentration ratio ( S = C / C 0 ) or by the ratio of the product of the two ions concentrations in the supersaturated solution to that in the saturated one ( S = ab /L p ). These σ values were lower than those obtained using the critical supersaturations at the two different solution p Hs. For the present it is impossible to give a definite explanation of the results obtained. The experiments for determining the specific surface energy at the crystal‐solution interface will be continued.