Drill core materials from contrasting lithologies (sandstone, coarse granite, peridotite and siliceous breccia), were analysed to benchmark analytical conditions for XRF, XRD, hyperspectral and Raman spectrometers for on-linereal-time-on-mine analyses in the frame of the SOLSA project (http://www.solsa-mining.eu) sponsored by the EU-H2020 Raw Material program. We tested: (1) a multi-technique approach on sample surfaces (20 x 20 mm2 ); (2) surface roughness effects on the different analyses. Five surface states were selected: (1) sonic and diamond drilled, (2) diamond-saw cut, (3) 6 mm polished, (4) 0.25 mm polished (5) powdered (< 80 mm). The following techniques were used: (1) portable X-ray fluorescence spectroscopy (pXRF), (2) portable infra-red spectroscopy (pIR), (3) Raman spectroscopy (4) laboratory XRD. The results obtained on the selected lithologies can be summarised as follows: Peridotite hosts 57 wt.% serpentine, 29 wt.% forsterite, 11 wt.% enstatite, 3 wt.% talc and traces of amphibole (XRD), while pIR only indicate serpentine. Raman spectroscopy clearly detects the ubiquitous presence of lizardite and forsterite. Grains of enstatite, quartz, anatase, rutile, pyrite, magnetite, maghemite and goethite were detected in selected regions. pXRF analyses on powders indicate 22 wt.% Si, 21 wt.% Mg, 6 wt.% Fe, 90 ppm V, 40 ppm Ti, 2200 ppm Ni, 1400 ppm Cr, 40 ppm Zn and 900 ppm Mn. Analyses on the drilled, cut and polished surfaces show higher values for Si, Mg and Ti, similar contents of Fe, Ni, Zn, Mn, and variable contents of V and Cr compared to those on the powder sample. Granite (XRD) is composed of 27 wt.% quartz, 20 wt.% microcline, 28 wt.% albite, 24 wt.% mica and/or illite and 1 wt.% chlorite. pIR shows the presence of bound water and illite, in agreement with XRD analyses. Raman spectroscopy confirms the presence of quartz, albite, precises muscovite as mica, and detects gypsum, magnesium sulphate, rutile, anatase, calcite and hematite. pXRF on powder surface indicate 39 wt.% Si, 9.2 wt.% Al, 0.55 wt.% Ca, 4.2 wt.% K, 95 ppm Zr, 60 ppm Sr, 300 ppm Ba, 43 ppm Zn, 38 ppm Pb, 0.9 wt.% Fe, 136 ppm V, 960 ppm Ti. Analyses on drilled, cut and polished surfaces show higher Si contents (42-46 wt.%), and variable contents of the other elements. Cr was detected during polished surface analyses (235–324 ppm). These heterogeneous results are due to the coarse grain size. Sandstone is composed of 100 wt.% quartz (XRD). pIR indicates the presence of bound water, illite or montmorillonite. Raman spectroscopy, besides quartz, detects anatase, pyrite, maghemite, goethite and zircon. pXRF on powder shows 55 wt.% Si, 132 ppm Zr, 0.02 wt.% Fe, 55 ppm V, 358 ppm Ti and traces of Ca and K. Analyses on the drilled, cut and polished surfaces give lower concentrations, in particular for Zr (50-100 ppm), Ti (99-256 ppm). Fe, heterogeneously distributed (260-600 ppm), is related to iron oxihydroxides. Breccia contains 100 vol.% of quartz with traces of hematite and goethite (XRD). pIR shows water molecules and goethite. Raman spectroscopy confirms quartz, and hematite and goethite, and adds hedenbergite, forsterite, calcite, magnetite and maghemite. pXRF on powder indicate 53 wt.% Si, 1.7 wt.% Fe, 3700 ppm Ni and 780 ppm Cr. Sawn surfaces give lowest trace element values. As for sandstone, analyses on the drilled, cut and polished surfaces give generally lower concentration and highly variable (241-1520 ppm Ni; 12 ppm–1.2 wt.% Fe, 86-480 ppm Cr). The major challenges of combined on-line sensor are the different sizes probed by techniques (from cm (IR) to mm (pXRF) down to micron (Raman spectroscopy)). Heterogeneous and coarse grained materials need a high number of analyses to give reliable results (time consuming). Methods, such as IR and XRF, need a surface proximity. in order to have maximum signal output. Major technological developments are needed for optimizing the on-line setup. Finally, it is recommended to build-up an adequate Raman database.

Coupled Mineralogy and Chemistry on drill core samples: benchmarking on-line-real-time analyses / Orberger, Beate; Duée, Cedric; Maubec, Nicoalas; Laperche, Valérie; Capar, Laure; Bouruignon, Anne; Bourrat, Xavier; El Mendili, Yassine; Gascoin, Stephanie; Chateigner, Daniel; Rodriguez, Celine; Salaün, Anne; Le Guen, Monique; Mariotto, Gino; Giarola, Marco; Kumar, Arun; Daldasso, Nicola; Zanatta, Marco; Lutterotti, Luca; Borovin, Evgeny; Bortolotti, Mauro; Secchi, Maria; Montagna, Maurizio; Pillière, Henry; Lefevre, Thomas; Eijkelkamp, Fons; Nolte, Harm; Koert, Peter; Grazulis, Saulius; Trotet, Fabien; Kadar, Mohammed; Devaux, Karen. - ELETTRONICO. - 6:(2017), p. 70. (Intervento presentato al convegno AMAM-ICAM tenutosi a Castellaneta Marina, Taranto, Italy nel 5-9 June 2017).

Coupled Mineralogy and Chemistry on drill core samples: benchmarking on-line-real-time analyses

Luca Lutterotti;Evgeny Borovin;Mauro Bortolotti;Maria Secchi;Maurizio Montagna;
2017-01-01

Abstract

Drill core materials from contrasting lithologies (sandstone, coarse granite, peridotite and siliceous breccia), were analysed to benchmark analytical conditions for XRF, XRD, hyperspectral and Raman spectrometers for on-linereal-time-on-mine analyses in the frame of the SOLSA project (http://www.solsa-mining.eu) sponsored by the EU-H2020 Raw Material program. We tested: (1) a multi-technique approach on sample surfaces (20 x 20 mm2 ); (2) surface roughness effects on the different analyses. Five surface states were selected: (1) sonic and diamond drilled, (2) diamond-saw cut, (3) 6 mm polished, (4) 0.25 mm polished (5) powdered (< 80 mm). The following techniques were used: (1) portable X-ray fluorescence spectroscopy (pXRF), (2) portable infra-red spectroscopy (pIR), (3) Raman spectroscopy (4) laboratory XRD. The results obtained on the selected lithologies can be summarised as follows: Peridotite hosts 57 wt.% serpentine, 29 wt.% forsterite, 11 wt.% enstatite, 3 wt.% talc and traces of amphibole (XRD), while pIR only indicate serpentine. Raman spectroscopy clearly detects the ubiquitous presence of lizardite and forsterite. Grains of enstatite, quartz, anatase, rutile, pyrite, magnetite, maghemite and goethite were detected in selected regions. pXRF analyses on powders indicate 22 wt.% Si, 21 wt.% Mg, 6 wt.% Fe, 90 ppm V, 40 ppm Ti, 2200 ppm Ni, 1400 ppm Cr, 40 ppm Zn and 900 ppm Mn. Analyses on the drilled, cut and polished surfaces show higher values for Si, Mg and Ti, similar contents of Fe, Ni, Zn, Mn, and variable contents of V and Cr compared to those on the powder sample. Granite (XRD) is composed of 27 wt.% quartz, 20 wt.% microcline, 28 wt.% albite, 24 wt.% mica and/or illite and 1 wt.% chlorite. pIR shows the presence of bound water and illite, in agreement with XRD analyses. Raman spectroscopy confirms the presence of quartz, albite, precises muscovite as mica, and detects gypsum, magnesium sulphate, rutile, anatase, calcite and hematite. pXRF on powder surface indicate 39 wt.% Si, 9.2 wt.% Al, 0.55 wt.% Ca, 4.2 wt.% K, 95 ppm Zr, 60 ppm Sr, 300 ppm Ba, 43 ppm Zn, 38 ppm Pb, 0.9 wt.% Fe, 136 ppm V, 960 ppm Ti. Analyses on drilled, cut and polished surfaces show higher Si contents (42-46 wt.%), and variable contents of the other elements. Cr was detected during polished surface analyses (235–324 ppm). These heterogeneous results are due to the coarse grain size. Sandstone is composed of 100 wt.% quartz (XRD). pIR indicates the presence of bound water, illite or montmorillonite. Raman spectroscopy, besides quartz, detects anatase, pyrite, maghemite, goethite and zircon. pXRF on powder shows 55 wt.% Si, 132 ppm Zr, 0.02 wt.% Fe, 55 ppm V, 358 ppm Ti and traces of Ca and K. Analyses on the drilled, cut and polished surfaces give lower concentrations, in particular for Zr (50-100 ppm), Ti (99-256 ppm). Fe, heterogeneously distributed (260-600 ppm), is related to iron oxihydroxides. Breccia contains 100 vol.% of quartz with traces of hematite and goethite (XRD). pIR shows water molecules and goethite. Raman spectroscopy confirms quartz, and hematite and goethite, and adds hedenbergite, forsterite, calcite, magnetite and maghemite. pXRF on powder indicate 53 wt.% Si, 1.7 wt.% Fe, 3700 ppm Ni and 780 ppm Cr. Sawn surfaces give lowest trace element values. As for sandstone, analyses on the drilled, cut and polished surfaces give generally lower concentration and highly variable (241-1520 ppm Ni; 12 ppm–1.2 wt.% Fe, 86-480 ppm Cr). The major challenges of combined on-line sensor are the different sizes probed by techniques (from cm (IR) to mm (pXRF) down to micron (Raman spectroscopy)). Heterogeneous and coarse grained materials need a high number of analyses to give reliable results (time consuming). Methods, such as IR and XRF, need a surface proximity. in order to have maximum signal output. Major technological developments are needed for optimizing the on-line setup. Finally, it is recommended to build-up an adequate Raman database.
2017
Scientific Research abstracts
Bari, Italy
Digilabs
978-88-7522-090-7
Coupled Mineralogy and Chemistry on drill core samples: benchmarking on-line-real-time analyses / Orberger, Beate; Duée, Cedric; Maubec, Nicoalas; Laperche, Valérie; Capar, Laure; Bouruignon, Anne; Bourrat, Xavier; El Mendili, Yassine; Gascoin, Stephanie; Chateigner, Daniel; Rodriguez, Celine; Salaün, Anne; Le Guen, Monique; Mariotto, Gino; Giarola, Marco; Kumar, Arun; Daldasso, Nicola; Zanatta, Marco; Lutterotti, Luca; Borovin, Evgeny; Bortolotti, Mauro; Secchi, Maria; Montagna, Maurizio; Pillière, Henry; Lefevre, Thomas; Eijkelkamp, Fons; Nolte, Harm; Koert, Peter; Grazulis, Saulius; Trotet, Fabien; Kadar, Mohammed; Devaux, Karen. - ELETTRONICO. - 6:(2017), p. 70. (Intervento presentato al convegno AMAM-ICAM tenutosi a Castellaneta Marina, Taranto, Italy nel 5-9 June 2017).
Orberger, Beate; Duée, Cedric; Maubec, Nicoalas; Laperche, Valérie; Capar, Laure; Bouruignon, Anne; Bourrat, Xavier; El Mendili, Yassine; Gascoin, Stephanie; Chateigner, Daniel; Rodriguez, Celine; Salaün, Anne; Le Guen, Monique; Mariotto, Gino; Giarola, Marco; Kumar, Arun; Daldasso, Nicola; Zanatta, Marco; Lutterotti, Luca; Borovin, Evgeny; Bortolotti, Mauro; Secchi, Maria; Montagna, Maurizio; Pillière, Henry; Lefevre, Thomas; Eijkelkamp, Fons; Nolte, Harm; Koert, Peter; Grazulis, Saulius; Trotet, Fabien; Kadar, Mohammed; Devaux, Karen
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11572/203556
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