Determination of standard heats of polymorphic transformations and melting of some monovalent metal halides by the DTA technique

1976 ◽  
Vol 41 (11) ◽  
pp. 3350-3353 ◽  
Author(s):  
J. Rosický ◽  
S. Kmoníčková
1980 ◽  
Vol 11 (13) ◽  
Author(s):  
G. HENRION ◽  
D. MARQUARDT ◽  
B. STOECKER
Keyword(s):  

2011 ◽  
Vol 115 (34) ◽  
pp. 9620-9632 ◽  
Author(s):  
Satchin Soorkia ◽  
Niloufar Shafizadeh ◽  
Jacques Liévin ◽  
Marc-André Gaveau ◽  
Christophe Pothier ◽  
...  

2004 ◽  
pp. 537 ◽  
Author(s):  
Sarah H. Oakley ◽  
Delia B. Soria ◽  
Martyn P. Coles ◽  
Peter B. Hitchcock

1964 ◽  
Vol 42 (4) ◽  
pp. 770-780 ◽  
Author(s):  
Peter Grey ◽  
G. C. B. Cave

A new method is proposed for the determination of milligram amounts of each halide present in a mixture of alkali-metal halides. In some mixtures, thiocyanate also may be determined. A methanol solution of the sample is titrated in a closed-type cell, with a standard solution of silver nitrate in methanol. By using high-frequency titrimetry, and an appropriate concentration of the halide solution, sharp end points were obtained for each halide. Because of solid solutions, the accuracy of the determination of individual halides in mixtures depended on the mole ratios of the halides; the errors found in the titration of various binary, ternary, and quaternary mixtures are reported. For some binary mixtures, the total amount of halide titrated in 120 ml of methanol was varied from 0.5 to 500 micromoles. At the lower concentrations, addition of a small amount of sodium nitrate sharpened the end point. At all concentrations of halide, an excessive amount of indifferent electrolyte essentially eliminated the end points. The alkali-metal halides gave more satisfactory titration graphs than did some other metal halides. The effects of variation in temperature, and of solvent evaporation were noted.


Author(s):  
Yu. А. Taran ◽  
М. К. Zakharov ◽  
А. L. Тaran ◽  
R. N. Ivanov

The processes of granulation by crystallization of molten droplets in the flow of a cooling agent (prilling) and on the cooled surfaces of the granulators are widely used in the chemical and allied industries. The process of granulation (crystallization) of melts and qualitative indicators of granular products, their marketability is determined by the transfer phenomena in the phases and by the kinetics of crystallization and enantiotropic polymorphic transformations in the crystalline phase. Quantitatively the latter are given in the form of dependences of the rate of nucleation and growth of centers of transformation. The processes kinetics is usually less studied, but it determines the structure of the formed crystal phase and the maximum rate of the process. Therefore, most attention is focused on its study. The description of the scheme, of developed experimental laboratory facilities for the study of the rates of nucleation and growth of crystallization centers in the polycrystalline front of the growing group of crystals, as is the case when crystallization occurs in devices in real conditions (constrained growth of crystals) and single crystals in a thin layer (unrestricted growth of crystals) is given. The transfer of heat in the measuring cell and the sample and possible errors of experimental results were estimated using the natural scale method.


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