Transmission Electron Microscopy (TEM) Through Focused ION Beam (FIB) from Vitrified Chromium Wastes

This study shows how the Focused Ion Beam (FIB) has been applied to vitrified materials obtained from chromium wastes. Due to the issues arising during conventional Ar+ ion milling, it was necessary to thin these samples using FIB. Difficulties came from the heterogeneous size between chromium spine...

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Detalles Bibliográficos
Autores: S. Ballesteros-Elizondo, J. R. Parga-Torres, J. Ma. Rincón-López, E. Palacios-González
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:México
Institución:Instituto Mexicano del Petróleo
Repositorio:Redalyc-IMP
OAI Identifier:oai:redalyc.org:47419293009
Acceso en línea:https://www.redalyc.org/articulo.oa?id=47419293009
Access Level:acceso abierto
Palabra clave:Ingeniería
Focused Ion beam (FIB)
Transmission Electron Microscopy (TEM)
Selected Area Diffraction Patterns(SADP)
Descripción
Sumario:This study shows how the Focused Ion Beam (FIB) has been applied to vitrified materials obtained from chromium wastes. Due to the issues arising during conventional Ar+ ion milling, it was necessary to thin these samples using FIB. Difficulties came from the heterogeneous size between chromium spinels and the residual glass phase. The FIB was applied to obtain thin foils from vitrified materials. These brittle and heterogeneous samples result in specimens with many perforations and chipping when using conventional thinning below 100 nanometers. Alternatively, FIB allowed thinning in the range of 60 - 80 nanometers from specifically selected areas such as the areas containing spinel crystals Mg(Al,Cr)2O4 in order to facilitate the final Transmission Electron Microscopy (TEM) observations. In this paper, FIB is shown to be a very powerful microtool as a brittle samples preparation method as well as providing an alternative way for performing conventional ceramography and Ar+ ion milling. FIB is a much less destructive method with greater observed capacity in the quantity and analysis of microcrystalline phases.