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1.
Diffuse reflectance spectroscopy in the UV, visible, and near-IR regions is found to allow the detection and identification of lanthanide oxides, fluorides, sulfides, and sulfofluorides without decomposing and dissolving samples. A nondestructive method for the detection and quantitative determination of more than 1 wt % of Eu(II) in the corresponding fluorides is proposed.  相似文献   
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The conditions of sensitization of the luminescence of Eu(III) by Tb(III) ions in complexes with inorganic (Na2WO4) and organic (nalidixic acid) ligands in sorbates on solid matrices (zeolite CaX and crystalline zirconium phosphate (ZrP)) and in coprecipitation with CaWO4 have been investigated. It has been established that the maximum sensitization of the europium luminescence is attained in the case where Eu and Tb are present in a 1:0.5 ratio. In this case, the integral intensity of luminescence of Eu(III) (the band with max = 612 nm) in the sorbate of its complex with nalidixic acid on ZrP accounts for more than 60% of the luminescence intensity of the industrial photoluminophor Y2O3:Eu (FL-612) possessing red luminescence, and the intensity of Tb(III) luminescence (the band with max = 545 nm) accounts for about 40% of the luminescence intensity of the photoluminophor Gd2O2S:Tb possessing green luminescence.  相似文献   
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Russian Physics Journal - The physical concept and the model of the construction of the plasma source of charged particles in crossed E × H fields are presented in which, due to the special...  相似文献   
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Polycrystalline hydroxyapatites Ca(10-x)REE(x)(PO(4))(6)(OH)(2-x)O(x) were synthesized and studied by X-ray powder diffraction, infrared absorption, diffuse-reflectance spectroscopy, and thermogravimetry. The solubility limits x(max) of rare earth elements (REE) in Ca hydroxyapatites decreases with an increasing REE atomic number from x(max) = 2.00 for La, Pr, and Nd to x(max) = 0.20 for Yb at 1100 °C. Refinements of X-ray diffraction patterns by the Rietveld method show that REE atoms substitute for Ca preferentially at the Ca(2) sites of the apatite structure. The substitution decreases the Ca(2)-O(4) atomic distances in the calcium coordination polyhedra and increases the Ca(2)-O(1,2,3) distances. This observation shows that interatomic distances depend not only on radii of the ions involved in the substitution but also on their charges.  相似文献   
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Conclusions The barriers of rotation around the C-N bond in the amides C5H5CoB9H9C2HCON(CH3)2, 1-(CH3)2NCO-1, 2-B10C2H11 and 1-(CH3)2NCO-1,7-B10C2H11 are substantially lower than in ordinary amides.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2119–2120, September, 1977.  相似文献   
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