2015
DOI: 10.1016/j.sab.2015.09.013
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Improving precision of X-ray fluorescence analysis of lanthanide mixtures using partial least squares regression

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Cited by 30 publications
(18 citation statements)
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“…More recently, the use of the lanthanides and other rare earths in electronics, optoelectronics, glasses, lighting, and permanent magnets has expanded greatly. Consequently, there is increased interest in analyzing lanthanide-bearing materials and ores by a variety of techniques including x-ray fluorescence analysis (XRF) [26][27][28][29]. Quantitative composition analysis by XRF requires knowledge of parameters such as line energies and shapes [30].…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…More recently, the use of the lanthanides and other rare earths in electronics, optoelectronics, glasses, lighting, and permanent magnets has expanded greatly. Consequently, there is increased interest in analyzing lanthanide-bearing materials and ores by a variety of techniques including x-ray fluorescence analysis (XRF) [26][27][28][29]. Quantitative composition analysis by XRF requires knowledge of parameters such as line energies and shapes [30].…”
Section: Introductionmentioning
confidence: 99%
“…Quantitative composition analysis by XRF requires knowledge of parameters such as line energies and shapes [30]. This knowledge is particularly critical when one uses common semiconductor detector systems whose spectral resolution is insufficient to fully separate relevant x-ray spectral features, for example x-ray lines from different lanthanides of interest and lines from the geologically more common 3d transition metals [29]. Uncertainty in line centers results in either systematic or statistical uncertainty when one fits overlapping spectra to extract peak areas, de-pending on whether the center energies are treated as fixed or free parameters, respectively [31].…”
Section: Introductionmentioning
confidence: 99%
“…For each data point, the microfluidic device was (i) fully flushed with twice its internal volume, in order to assure reaching a steady state; (ii) further flushed until 600 mL of each phase was retrieved in collecting output vials, for off-line XRF or ICP-OES analysis (see the ESI † for more details about the XRF analysis). 32,38,39 The necessary overall time required to obtain each sample varies according to the flow rate used (always equal, by construction, for both phases (Fig. 1)) which in our case varies from 34 mL min À1 to 0.57 mL min À1 (see Table S2 of the ESI †).…”
Section: Microfluidic Systemmentioning
confidence: 98%
“…Many works have tried to overcome this by applying multivariate statistical analyses as to separate the information given in the energy region of interest (ROI) in different parts, corresponding to the different spectral lines present. 5,6 Nevertheless, it would be useful to have a spectrometer capable of resolving the L emission lines successfully. Reviewing the emission lines of these elements, an energy resolution of around 10 eV is enough to allow for the desired discrimination.…”
Section: Articlementioning
confidence: 99%