Мобильная версия

Доступно журналов:

3 288

Доступно статей:

3 891 637

 

Скрыть метаданые

Автор T F Young
Автор J Kieffer
Автор G Borchardt
Дата выпуска 1994-11-14
dc.description In this work we have improved the kinetic model of Kieffer and Borchardt for diffusion in silicate melts, which takes into account both the diffusion of individual polyanions and the reaction of different polyanions through condensation and splitting events. Making assumptions for the individual condensation reactions, similar to those by Masson, the equilibrium polyanion distributions in silicate melts were calculated by solving a system of coupled first-order differential equations, describing the reactions between polyanions of various sizes. The concentration dependence of the SiO<sub>4</sub><sup>4-</sup> monomers, determined by our approach, is identical to that resulting from the thermodynamic treatment by Masson. Furthermore, by allowing for local changes in the isotope distributions of the elements, and by assuming that migration of all species present in the system occurs due to random motion, the self-diffusion of silicon and oxygen in CoO-SiO<sub>2</sub> melts has been simulated. The parameters for the model have been estimated by fitting me simulation results to our experimental data of Si and O tracer diffusion. While the simulated concentration profiles were in good agreement with our experimental tracer diffusion measurements in the CoO-SiO<sub>2</sub> system, their shape could not be described by the standard solution of Fick's law. Conversely, for the CaO-SiO<sub>2</sub> and PbO-SiO<sub>2</sub> systems, the simulated profiles were in much better agreement with the standard solution. This difference in diffusional transport properties can be qualitatively interpreted as due to the structural differences of CoO-SiO<sub>2</sub> as compared to the two other systems.
Формат application.pdf
Издатель Institute of Physics Publishing
Название Application of a kinetic model to tracer diffusion of silicon and oxygen in silicate melts
Тип paper
DOI 10.1088/0953-8984/6/46/004
Electronic ISSN 1361-648X
Print ISSN 0953-8984
Журнал Journal of Physics: Condensed Matter
Том 6
Первая страница 9835
Последняя страница 9852
Аффилиация T F Young; Inst. fur Allgemeine Metall., Tech. Univ. Clausthal, Germany
Аффилиация J Kieffer; Inst. fur Allgemeine Metall., Tech. Univ. Clausthal, Germany
Аффилиация G Borchardt; Inst. fur Allgemeine Metall., Tech. Univ. Clausthal, Germany
Выпуск 46

Скрыть метаданые