Conversion of chromium(III) propionate to chromium(VI) by the Advanced Oxidation Process Pretreatment of a biomimetic complex for metal analysis.

The use of H(2)O(2) and UV irradiation to remove organic ligands in a chromium(III) complex for the subsequent chromium analysis is reported. The Advanced Oxidation Process (AOP) using a 5.5-W UV lamp, H(2)O(2) and Fe(2+)/Fe(3+) as catalyst (photo Fenton process) was found to give complete and quantitative Cr(III)-->Cr(VI) conversion and removal of ligands in chromium(III) propionate [Cr(3)O(O(2)CCH(2)CH(3))(6)(H(2)O)(3)]NO(3), a biomimetic chromium species, as subsequent chromium analyses by the 1,5-diphenylcarbazide method and atomic absorption revealed.

Studies of the oxidation of palladium complexes by the advanced oxidation process Pretreatment of model catalysts for precious metal analysis.

The advanced oxidation process (AOP) for the pretreatment of model palladium catalysts has been studied. Most standard metal analysis techniques are for metal ions free of organic ligands. Spent palladium catalysts contain organic ligands that need to be removed prior to analysis.

Conversion of Chromium(III) Propionate to Chromate/dichromate(VI) by the Advanced Oxidation Process. Pretreatment of a Biomimetic Complex for Metal Analysis.

The use of H(2)O(2) and UV irradiation to remove organic ligands in a chromium(III) complex for the subsequent chromium analysis is reported. The Advanced Oxidation Process (AOP) using a 5.5-W UV lamp, H(2)O(2) and Fe(2+)/Fe(3+) as catalyst (photo Fenton process) was found to give complete and quantitative Cr(III) → Cr(VI) conversion and removal of ligands in chromium(III) propionate [Cr(3)O(O(2)CCH(2)CH(3))(6)(H(2)O)(3)]NO(3), a biomimetic chromium species, as subsequent chromium analyses by the 1,5-diphenylcarbazide method and atomic absorption revealed.

Palladium and the electrochemical quartz crystal microbalance: a new method for the in situ analysis of the precious metal in aqueous solutions.

A new method for the quantitative determination of palladium(II) by the electrochemical quartz crystal microbalance (EQCM) technique has been developed. Using a bare carbon-coated quartz crystal, Pd(II) ions are directly deposited from aqueous solution as palladium metal onto the crystal surface, and the Pd(II) concentration is determined with a detection limit of 0.0156 mM, or 1.

Electrochemical deposition of sol-gel films for enhanced chromium(VI) determination in aqueous solutions.

A pyridine-functionalized sol-gel film has been formed by electrodeposition at a glassy carbon electrode surface. When this protonated film is exposed to a Cr(VI) solution, the Cr(VI) anions are preconcentrated at the electrode surface. Using square wave voltammetry, the Cr(VI) species are reduced to Cr(III), and a peak current corresponding to this reduction is generated at 0.

Inorganic sensing using organofunctional sol-gel materials.

This Account describes recent work in the development and applications of sol-gel sensors for concentrated strong acids and bases and metal ions. The use of sol-gel films doped with organic indicators for the optical sensing of concentrated strong acids (HCl, 1-10 M) and bases (NaOH, 1-10 M) has been explored, and the development of dual optical sensor approaches for ternary systems (HCl-salt-H 2O and NaOH-alcohol-H 2O) to give acid and salt, as well as base and alcohol, concentrations is discussed. The preparation of transparent, ligand-grafted sol-gel monoliths is also described, and their use in the analysis of both metal cations (Cu (2+)) and metal anions [Cr(VI)] is presented.

Optical determination of Cr(VI) using regenerable, functionalized sol-gel monoliths.

Transparent, pyridine-functionalized sol-gel monoliths have been formed and their use in Cr(VI) sensing applications is demonstrated. The monoliths were immersed in acidic Cr(VI)-containing solutions, and the Cr(VI) uptake was monitored using UV-vis and atomic absorption spectroscopies. At concentrations at the ppm level, the monoliths exhibit a yellow color change characteristic of Cr(VI) uptake, and this can be measured by monitoring the absorption change at about 350 nm using UV-vis spectroscopy.

Quantitative analysis of trace chromium in blood samples. Combination of the advanced oxidation process with catalytic adsorptive stripping voltammetry.

A new method for pretreating blood samples for trace Cr analysis is described. The advanced oxidation process (AOP with H2O2 and 5.5-W UV irradiation for 60 min) is used to remove biological/organic species for subsequent analysis.

Predicting second gas-solid virial coefficients using calculated molecular properties on various carbon surfaces.

Gas-solid chromatography was used to obtain values of the second gas-solid virial coefficient, B2s, in the temperature range from 343 to 493 K for seven adsorbate gases: methane, ethane, propane, chloromethane, chlorodifluoromethane, dimethyl ether, and sulfur hexafluoride. Carboxen-1000, a 1200 m2/g carbon molecular sieve (Supelco Inc.), was used as the adsorbent.