Adsorption of congo red from aqueous solution using various TiO2 nanoparticles

In this work, TiO2 nanopowder (TIP600) was prepared by a sol-gel method and titanium isopropoxide, glacial acetic acid, and deionized water were used as the starting materials. Adsorption of congo red (CR) on Degussa-P25 (P25), commercial TiO2 (C-TiO2), and TIP600 was investigated. But, photochemical and photocatalytic event were not used for this adsorption process. Adsorption of CR onto the adsorbents was studied at different temperatures (25.0, 40.0, and 50.0 degrees C) and various adsorbent doses (0.1, 0.05, and 0.025g). The kinetics of dye adsorption has been investigated in terms of pseudo-first order, pseudo-second order, and intra-particle diffusion rate. The results indicate that pseudo-second order plays a significant role in the adsorption mechanism. The adsorptive capacity of TIP600 is much higher than that of other adsorbents. The value of H-# was obtained as positive, therefore the nature of adsorption was found endothermic. Equilibrium isotherm of CR was fitted to the Freundlich and Langmuir models. The equilibrium data of adsorbate were found to best fit the Langmuir model. For CR, TIP-600 was demonstrated as the best adsorption capacity (q(max) 112mgg(-1))

Catalytic dehydrogenation of tetradecanol over copper/barium oxide catalysts

The liquid phase dehydrogenation of tetradecanol to tetradecanal has been studied over a series of CuO/BaO catalysts. Catalytic activity and selectivity to tetradecanal was found to depend on the ratio of easily reducible copper sites to less easily reducible copper sites. The catalysts have been characterized by X-ray diffraction, temperature programmed reduction, and thermo-gravimetric analysis. TPR results have shown that there were at least two types of copper oxides with varying reducibility. The relationship between the activity and area ratio of various copper oxide sites and a scheme for the conversion of tetradecanol were discussed

Dioxomolybdenum(VI) Complexes of 2-hydroxybenzaldehyde 4-phenyl-S-methylthiosemicarbazone(1)

Mixed ligand complexes of dioxomolybdenum(VI) with 2-hydroxybenzaldehyde 4-phenyl-S-methylthiosemicarbazone (H2L) were prepared with the formula [MoO2(L)D] (D = H,O, methyl, n-butyl, and n-undecyl alcohol, DMF, DMSO, pyridine, 4-picoline, and 3,5-lutidine). The compounds were characterized by elemental analysis, IR and H-1 NMR spectroscopy. The thermal decomposition of the compounds were investigated by using TGA, DTG, and DTA methods in air, and the thermal behavior depending on the second ligand molecule was discussed. A single crystal of the DMF coordinated complex was studied by X-ray diffractometry