Dehydration synthesis and crystal structure of terbium oxychloride, TbOCl.

Terbium oxychloride, TbOCl, was synthesized via the simple heat-treatment of TbCl3·6H2O and its structure was determined by refinement against X-ray powder diffraction data. TbOCl crystallizes with the matlockite (PbFCl) structure in the tetra-gonal space group P4/nmm and is composed of alternating (001) layers of (TbO) n and n Cl-. The unit-cell parameters, unit-cell volume, and density were compared to the literature data of other isostructural rare-earth oxychlorides in the same space group and showed good agreement when compared to the calculated trendlines.

Crystal structures and comparisons of potassium rare-earth molybdates KRE(MoO4)2 (RE = Tb, Dy, Ho, Er, Yb, and Lu).

Six potassium rare-earth molybdates KRE(MoO4)2 (RE = Tb, Dy, Ho, Er, Yb, and Lu) were synthesized by flux-assisted growth in K2Mo3O10. The crystal structures were determined using single-crystal X-ray diffraction data. The synthesized molybdates crystallize with the ortho-rhom-bic Pbcn space group (No. 60). Trendlines for unit-cell parameters were calculated using data from the current study. The unit-cell parameters a and c increase linearly whereas b decreases with larger RE cations, based on crystal radii. The unit-cell volumes increase linearly and the densities decrease linearly with larger RE cations. The average distances between the RE cations and the nearest O atoms increase with larger cations whereas the average distances of Mo-O and K-O do not show specific trends.

Gaseous Iodine Sorbents: A Comparison between Ag-Loaded Aerogel and Xerogel Scaffolds.

Silver-exchanged aluminosilicate aerogels and xerogels were investigated as gaseous iodine [I2(g)] sorbents. The structures, morphologies, compositions, and porosities of aerogels (as-made and heat-treated at 350 °C) and xerogels are compared by using powder X-ray diffraction (PXRD), scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and specific surface area (SSA) as well as pore size analyses. The as-made aerogels, xerogels, and heat-treated aerogels were ion exchanged with Ag in AgNO3 solutions of deionized water and methanol (5:1 by volume), and PXRD patterns showed the presence of nanocrystalline Ag0 after the Ag exchange. Gravimetric iodine loadings of Ag-aerogels and Ag-xerogels were 0.33-0.41 g g-1. The Ag-aerogels without heat treatment showed an ∼8 mass % higher iodine loading than Ag-impregnated xerogels and ∼3 mass % higher than heat-treated Ag-impregnated aerogels. All gels after iodine uptake showed the presence of AgI, indicating chemisorption of iodine to silver. The SSA values of the as-made gels were 420-600 m2 g-1 but decreased significantly to 34-120 m2 g-1 after Ag impregnation and iodine uptake. Overall, changes in physical and chemical properties of aerogels and xerogels after iodine uptake were similar and the differences in iodine loading capacities of the aerogels and xerogels were minimal, providing a driver for using xerogels due to their less complex synthesis process as compared to aerogels.

Crystal structures and comparisons of huntite aluminum borates REAl3(BO3)4 (RE = Tb, Dy and Ho).

Three huntite-type aluminoborates of stoichiometry REAl3(BO3)4 (RE = Tb, Dy and Ho), namely, terbium/dysprosium/holmium trialuminium tetrakis(borate), were synthesized by slow cooling within a K2Mo3O10 flux with spontaneous crystallization. The crystal structures were determined using single-crystal X-ray diffraction (SC-XRD) data. The synthesized borates are isostructural to the huntite [CaMg3(CO3)4] structure and crystallized within the trigonal R32 space group. The structural parameters were compared to literature data of other huntite REAl3(BO3)4 crystals within the R32 space group. All three borates fit well into the trends calculated from the literature data. The unit-cell parameters and volumes increase linearly with larger RE cations whereas the densities decrease. All of the crystals studied were refined as inversion twins.

Metal-Organic Framework-Polyacrylonitrile Composite Beads for Xenon Capture.

Mechanically robust forms of HKUST-1 metal-organic frameworks (MOFs) were fabricated by embedding the MOF crystals in a passive polyacrylonitrile (PAN) matrix at different MOF loadings of 10-90 mass %. PAN is highly porous and acts as a scaffold that holds the active MOF adsorbent in place. These MOF-PAN composites were then evaluated for capturing Xe. Data presented herein show that the PAN matrix does not notably interfere with the Xe capture process, where the Xe capacities scale somewhat linearly with the increase in MOF loadings within the composites. Also, γ radiation exposures to the composites revealed that they are highly tolerant to these types of radiation fields.