Combining SEM, EDS & EBSD: Challenges and considerations in the micro-analysis of rock thin sections

Author(s):  
Alexandra Stavropoulou ◽  
Matthew Hiscock ◽  
Balz Kamber ◽  
Juan-Diego Rodriguez-Blanco

<p>Quantitative modal analysis of rock thin sections or liberation analysis of minerals processing plant materials can be very complex as grain sizes can vary by more than 7 orders of magnitude: Thin sections of rocks may contain extremely coarse grains (mm-sized crystals) down to glassy material with no long-range order (ordered domains <1 nm).</p><p>Material characterisation and modal analysis have traditionally been carried out with a combination of solid-state, microscopic and spectroscopic techniques (e.g., optical / scanning electron microscopy, powder X-ray diffraction, X-ray fluorescence spectroscopy). These techniques require different sample preparation routines, data acquisition and evaluation - a time-consuming process that may be considered too complex to implement in mineral processing plants despite requiring the relevant sample preparation equipment. Scanning electron microscopy (SEM) coupled with energy dispersive spectroscopy (EDS provides an opportunity to carry out this characterisation in a more rigorous and, in certain cases, automated way. This process includes image thresholding (setting of grey levels of present phases by the analyst) and X-ray data collection with EDS. EDS is an ideal analytical technique for this work as it offers high acquisition speeds and the collection of the whole energy spectrum with a single detector, not requiring the selection of a fixed element list prior to data acquisition. Characterisation of coarse-grained rocks requires larger areas to be scanned in order to ensure representativity.</p><p>The analytical workflow can be further optimised by combining SEM-based analytical techniques for in situ, non-destructive, and potentially simultaneous bulk analysis. Electron backscatter diffraction (EBSD) is an SEM-based technique which can be used to determine the crystallographic properties and orientation of mineral grains, as well as to perform fabric analyses on polycrystalline materials. EBSD allows for crystallographic data to be collected simultaneously with chemical data and does not require powdered samples. As a result, the texture of the material can be fully preserved. The sample preparation requirements of the technique are similar to those for standard SEM-EDS, with an additional final polishing step, essential for the removal of surface imperfections, as the EBSD signal is generated on the sample surface. The coupling of EDS and EBSD datasets permits the enhanced interpretation of feature analysis data, allowing for a deeper understanding of the compositional, structural and textural properties of the sample. This, highly-efficient, in-situ, bulk material characterisation, is key for the mining industry, as it provides insights for optimising downstream procedures thereby saving time and resources and bolstering throughput and efficiency.</p>

2013 ◽  
Vol 457-458 ◽  
pp. 244-247
Author(s):  
Min Li ◽  
Li Guang Xiao ◽  
Hong Kai Zhao

Polyethylene/montmorillonite (PE/MMT) nanocomposites were prepared by in situ polymerization. The morphology of MMT/MgCl2/TiCl4 catalyst and PE/MMT nanocomposites was investigated by scanning electron microscopy (SEM). It can be seen that MMT/MgCl2/TiCl4 catalyst remained the original MMT sheet structures and many holes were found in MMT and the morphology of PE/MMT nanocomposites is part of the sheet in the form of existence, as most of the petal structure. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were carried out to characterize all the samples. XRD results reveal that the original basal reflection peak of PEI1 and PEI2 disappears completely and that of PEI3 become very weak. MMT/MgCl2/TiCl4 catalyst was finely dispersed in the PE matrix. Instead of being individually dispersed, most layers were found in thin stacks comprising several swollen layers.


2015 ◽  
Vol 1120-1121 ◽  
pp. 572-575
Author(s):  
Hong Wei Liu ◽  
Feng Wang ◽  
Qiang Zhang ◽  
Xi Wu Li ◽  
Zhi Hui Li ◽  
...  

An innovative spray deposition technique has been applied to produce in situ TiB2/Zn-30Al-1Cu composites. The microstructures of the spray-deposited composite were studied using optical microscopy, scanning electron microscopy, and X-ray diffraction. Both theoretical and experimental results have shown that the TiB2particulates are formed in the microstructure. It was found that the TiB2particles were distributed in Zn-30Al-1Cu matrix uniformly, and the TiB2particles are about 2 μm in size. Moreover, the presence of the TiB2particles was led to increasing of α’ phase with less 2 μm size in the composites which have a tendency to decompose to α+η structure.


2015 ◽  
Vol 817 ◽  
pp. 593-598
Author(s):  
Yan Feng Liang ◽  
Sheng Quan Dong ◽  
Gao Hong Li

In situ TiCp/Al-4.5wt.%Cu composites have been coated using an electro-less Ni-P plating technique. The morphology and composition of the plating coating have been examined by scanning electron microscopy, optical microscopy, and X-ray diffraction. The results indicated that the coating had a high-phosphorus amorphous microstructure. The coatings microstructures showed significantly changes when the citric acid concentration in the chemical bath was varied in the range 16-20g/L.


2011 ◽  
Vol 696 ◽  
pp. 290-295 ◽  
Author(s):  
Vladislav Kolarik ◽  
Maria del Mar Juez-Lorenzo ◽  
Harald Fietzek

Micro-sized spherical Al particles have recently attracted interest for the development of a new concept for coatings based on their capability to form hollow alumina spheres and aluminized diffusion zones in the substrate. For understanding better their oxidation behaviour, spherical µm-Al particles with different sizes were oxidized in air on heating up to 1300°C and under isothermal conditions at 800°C and 850°C. The oxide formation was studiedin situby high temperature X-ray diffraction and the oxidised particles were analysed by scanning electron microscopy. On heating the µm-Al particles begin to form a g-Al2O3scale before reaching the melting point and the molten Al is kept within the g-Al2O3shell. On further heating q-Al2O3is detected, which forms simultaneously with the g-Al2O3. The g-Al2O3/ q-Al2O3scale is stable and protective under isothermal conditions up to 800°C within the investigated times. On further heating the g-Al2O3and q-Al2O3transform simultaneously to a-Al2O3in a temperature range of 850°C to 1100°C. Under isothermal conditions the g à a-Al2O3transformation is observed after 160 min at 850°C. During the g à a-Al2O3transformation shrinkage occurs that leads to formation of pores. A model is proposed describing the mechanism that leads to the formation of the observed whiskers morphologies during the g à a-Al2O3transformation.


Sign in / Sign up

Export Citation Format

Share Document