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instrumental techniques applied to mineralogy and geochemistry

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X-ray Absorption Spectroscopy in Mineralogy <strong>and</strong> in the Earth <strong>and</strong> Environmental Sciences 51<br />

two orders of magnitude. Consequently, S/N is enhanced <strong>and</strong> XANES spectra on even<br />

very diluted heavy a<strong>to</strong>ms can be measured proficiently.<br />

v) Finally, it should be noted that XAS experiments can be performed on a highly<br />

flexible sample environment. In this way, XAS experiments can be performed under<br />

extreme conditions of temperature, different gas atmospheres, <strong>and</strong> even under high<strong>applied</strong><br />

pressure on solid, liquid <strong>and</strong> gaseosous samples.<br />

These characteristics make XAS an incomparable <strong>to</strong>ol <strong>to</strong> face different problems in<br />

Mineralogy <strong>and</strong> in the Earth <strong>and</strong> Environmental Sciences. Indeed, the flexible sample<br />

environment allows approach the temperature <strong>and</strong> pressure conditions of the Earth’s<br />

interior where phase transitions in minerals under high pressure are known <strong>to</strong> govern<br />

some of the major geophysical properties. In a similar way, XAS provides an unique<br />

insight in<strong>to</strong> the accurate knowledge of trace-element behaviour in rock-forming <strong>and</strong><br />

accessory minerals that results fundamental <strong>to</strong> underst<strong>and</strong> <strong>and</strong> model petrologic <strong>and</strong><br />

geochemical processes. These rock-forming minerals are always complex solid solutions<br />

<strong>and</strong>, therefore, the only approach capable of characterising the local coordination of the<br />

individual substituents is the use of element-selective spectroscopic methods like XAS.<br />

This is for example the case of the characterization of trace Nd <strong>and</strong> Ce site<br />

preference <strong>and</strong> coordination in natural melanites. The identification of the crystalchemical<br />

parameters controlling trace-element partitioning between minerals <strong>and</strong> silicate<br />

melts is a <strong>to</strong>pic of considerable interest. Garnets represent an important group of rockforming<br />

minerals in this regard, since they are stable over a wide range of physicochemical<br />

conditions <strong>and</strong> are able <strong>to</strong> incorporate several trace elements commonly used in<br />

geochemical modeling. For these reasons, aluminosilicate garnets (X 3 Al 2 Si 3 O 12 , X =<br />

Fe 2+ , Mn 2 +, Mg, Ca) have received much attention, regarding their complex crystal<br />

chemistry, their thermodynamic properties or trace-element behaviour. Despite the<br />

importance of the geochemical behavior of REE in garnets, little work has been done <strong>to</strong><br />

decipher their site preference <strong>and</strong> local coordination in trace or minor amounts. Indeed,<br />

there are no examples in the literature of direct structural investigations on the site<br />

location <strong>and</strong> geometry of REE in natural garnets, possibly due <strong>to</strong> their low<br />

concentrations. A recent work by Quartieri et al. has reported the XAS study of the site<br />

location <strong>and</strong> geometry of trace amounts of neodymium (from 176 <strong>to</strong> 1074 ppm) <strong>and</strong>

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