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The experimental setup for the collection of synchrotron X-ray powder diffraction data from samples with high absorption (μR > 10) is described. It consists of a combination of a vacuum chamber with an image-plate system. A numerical absorption correction for the applied geometry has been derived and the data were corrected accordingly. Values for f ′(Er) and f ′′(Er) were refined from eight measurements on Er5Re2O12 above and below the Er LIII absorption edge. Successful refinement of the crystallographic data has verified the high quality of the collected intensities.

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