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A novel bifunctional Ti–Fe kaolinite composite with excellent adsorption and photocatalytic properties was synthesized by a simple precipitation method. X-ray diffraction analysis and high-resolution transmission electron microscope analysis confirmed the existence of rutile phase TiO 2 and amorphous iron in the composite. The specific surface area of the Ti–Fe kaolinite composite is 5.5 times higher than that of the original kaolinite. The composite was used as an adsorbent as well as photocatalyst for Cr(VI) removal. The results indicate that the low pH is favorable to the Cr(VI) removal by the composite and the removal rate of Cr(VI) reached 87% at pH 3.0. Visible light irradiation obviously increased the removal of Cr(VI) by the composite and greatly shortened reaction equilibrium time, which may be attributed to the photocatalytic reduction of Cr(VI) to Cr(III) by TiO 2 associated with simultaneous redox cycle of Fe(III)/Fe(II). Various common co-existing ions did not show obvious effects on the removal of Cr(VI) by the composite. The composite exhibited very high stability for the Cr(VI) removal. The adsorption models and thermodynamics of Cr(VI) onto the composite were studied. [ABSTRACT FROM AUTHOR]

Two new three-dimensional 12-connected metal–organic coordination polymers, [Zn2(bptc)(H2O)]·C2H5OH·H2O (1) and [Cd4(bptc)2(bbi)(H2O)]·H2O (2) (H4bptc=biphenyl-2,5,2′,5′-tetracarboxylic acid, bbi=1,1′-(1,4-butanediyl)bis(imidazole)), have been solvothermally synthesized and structurally characterized by single crystal X-ray diffraction analyses. All compounds are also characterized by elemental analyses, IR spectra, thermogravimetric (TG) analyses and X-ray powder diffraction (XRD). Topological analysis indicates that both 1 and 2 are 12-connected frameworks with fcu topology, which are based on cuboid cage and rob-like {Cd3} subunit as 12-connected nodes, respectively. Furthermore, the luminescence properties of the two compounds were discussed in detail. [ABSTRACT FROM AUTHOR]

Abstract: A large new family of rare-earth metal–cadmium–germanides RE2CdGe2 (RE=Y, Pr, Nd, Sm, Gd–Yb) has been synthesized and structurally characterized. All eleven structures have been established from single-crystal X-ray diffraction data and have been found to belong to the tetragonal Mo2FeB2 structure type (ordered ternary variant of the U3Si2 structure type—space group P4/mbm (No. 127), Z=2; Pearson symbol tP10). The structural variations among the three series of isostructural RE2MgGe2, RE2InGe2, and RE2CdGe2 compounds are discussed, as well as the crystal chemistry changes as a function of the decreasing size of the rare-earth metals (lattice constants a=7.176(2)–7.4589(12)Å and c=4.1273(14)–4.4356(13)Å). The experimental results have been complemented by tight-binding linear muffin-tin orbital (TB–LMTO) electronic structure calculations. [Copyright &y& Elsevier]