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 21,279 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Quantitative in situ attenuated total internal reflection Fourier transform infrared (ATR FTIR) spectroscopy has been used to study the isotherm of poly(sodium 4-styrene sulfonate), PSS, adsorption to a TiO(2) surface in aqueous solution at a pH of 3.5. The effect of adding surfactant cetylpyridinium bromide monohydrate (CPBM) on the adsorption isotherm of PSS was investigated at CPBM concentrations of 3.60 x 10(-7), 1.02 x 10(-5), and 1.04 x 10(-4) M. The use of in situ ATR FTIR allowed for the calculation of the concentration of both PSS and CPBM at the TiO(2)/water interface over the entire course of all experiments. It was found that the addition of a small amount of CPBM, 3.60 x 10(-7) M, to PSS solutions resulted in 23 +/- 3% less PSS accumulating at the TiO(2)/water interface compared to isotherm studies with no CPBM present. The mole ratio of CPBM to PSS varies from 4 +/- 1 to 1 to 20 +/- 4 to 1 in a stepwise manner as the solution concentration of PSS is increased for solutions with a CPBM concentration of 3.60 x 10(-7). The addition of CPBM at concentrations of 1.02 x 10(-5) and 1.04 x 10(-4) M showed distinct differences in the behavior of the PSS isotherm, but at the highest solution PSS concentrations, the amount of PSS at the TiO(2)/water interface compared to that of PSS solutions with no CPBM added is indistinguishable within the experimental uncertainties. For these higher concentrations of CPBM, both PSS and CPBM appear to come to the TiO(2) surface as aggregates and the mole ratio of CPBM to PSS at the TiO(2)/water interface decreases as the concentration of PSS is increased. For a CPBM concentration of 1.02 x 10(-5) M, the mole ratio of CPBM to PSS changes from 139 +/- 29 to 1 to 33 +/- 7 to 1 as the solution PSS concentration is increased. For a CPBM concentration of 1.04 x 10(-4) M, the mole ratio of CPBM to PSS changes from 630 +/- 130 to 1 to 110 +/- 21 to 1 as the solution PSS concentration is increased. Despite the large differences in the CPBM to PSS mole ratios, the amount of PSS that adsorbs to the surface is statistically indistinguishable for CPBM concentrations of 0, 1.02 x 10(-5), and 1.04 x 10(-4) M, indicating that the structure of the PSS molecules in each of the systems does not significantly change in the presence of CPBM.
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PMID:Quantitative in situ attenuated total internal reflection Fourier transform infrared study of the isotherms of poly(sodium 4-styrene sulfonate) adsorption to a TiO2 surface over a range of cetylpyridinium bromide monohydrate concentration. 2006 83

The reactions of a zirconium salt with 1,2,4,5-benzenetetracarboxylate (btec), bathophenanthroline (Bphen) and thiocyanate ions were synthesized and studied by changing the mole ratio, the order of reactant and their pH. It is found that the coordination mode of btec acid depends on the control of reaction conditions. Monodentate, bidentate and bridging modes were investigated by FT-IR spectroscopy. The structures of Zr(btec) and Zr(btec)(Bphen) complexes were also characterized by UV-Vis, CHN, ICP-AES, (1)H NMR and cyclic voltammetry. The role of Bphen ligand in the photopysical properties of Zr(btec)(Bphen) complexes was investigated by DFT calculation. The photoluminescence (PL) emission of nine Zr(btec) complexes that have two peaks, a sharp and intense band for the first peak from 320 to 430 nm in comparison to the second peak with a less intensity and broadened in the regions of 650-780 nm. PL spectra of twelve Zr(btec)(Bphen) complexes also showed bands at 450, 550, 625 nm. LED devices with Zr complex as emitter layer and the structure ITO/PEDOT:PSS/PVK:PBD/zirconium complex/Al emitted a broad band centered at 550 and 650 originating from the Zr complexes. The EL spectra of Zr(btec) and Zr(btec)(Bphen) complexes indicated a long red shift rather than PVK:PBD blend. We believe that the electroplex occurring at PVK-Zr complexes interface is responsible for the green-red emission in the EL of the device. These observations suggest an important role for the Bphen ligand to improve EL performance.
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PMID:Enhancement of electroluminescence in zirconium poly carboxylic acid-based light emitting diodes by bathophenanthroline ligand. 2367 38

The present study investigates the possibility of inducing monovalent ion permselectivity on standard cation exchange membranes, by the layer-by-layer (LbL) assembly of poly(ethyleneimine) (PEI)/poly(styrenesulfonate) (PSS) polyelectrolyte multilayers. Coating of the (PEI/PSS)N LbL multilayers on the CMX membrane caused only moderate variation of the ohmic resistance of the membrane systems. Nonetheless, the polyelectrolyte multilayers had a substantial influence on the monovalent ion permselectivity of the membranes. Permselectivity comparable to that of a commercial monovalent-ion-permselective membrane was obtained with only six bilayers of polyelectrolytes, yet with significantly lower energy consumption per mole of Na(+) ions transported through the membranes. The monovalent ion permselectivity stems from an increased Donnan exclusion for divalent ions and hydrophobization of the surface of the membranes concomitant to their modification. Double-layer capacitance obtained from impedance measurements shows a qualitative indication of the divalent ion repulsion of the membranes. At overlimiting current densities, water dissociation occurred at membranes with PEI-terminated layers and increased with the number of layers, while it was nearly absent for the PSS-terminated layers. Hence, LbL layers allow switching on and turning off water splitting at the surface of ion exchange membranes.
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PMID:Layer-by-layer modification of cation exchange membranes controls ion selectivity and water splitting. 2440 Oct 42