Arsenic distribution in waters and its geochemical behavior in sediment of Mahanadi estuary in India.

Distribution of arsenic in the marine environment is associated with its biogeochemical behavior. Indeed, very few studies have been conducted along the seasonal cycle to show its non-conservative behavior in the tropical estuary. The Mahanadi River, one of the major tropical rivers in the peninsular India, drains densely populated and industrialized region of Paradeep port. Over this 1-year study, the variations of inorganic arsenic were examined along the salinity gradient of the Mahanadi estuary, with the aim to provide some insights into the mechanisms that control arsenic concentrations and behavior under estuarine mixing. Arsenic in the estuary was derived from both natural and anthropogenic sources, and it displayed partial removal from the water in the mixing zone. Results of geo-accumulation index indicated that sediments were uncontaminated and they acted as a sink for arsenic. The diffusive fluxes from water to sediment were estimated to be 9.05 µg m(-2) day(-1) at Chaumohona, 9.83 µg m(-2) day(-1) at Kaudia, and 11.85 µg m(-2) day(-1) at Neherubunglow. The findings of the study suggest that both the removal of arsenic by biogeochemical processes and its diffusive transport from water to sediment are of major importance for both the non-conservative behavior of arsenic in the estuary and its export to the coastal water.

Immobilization of palladium in mesoporous silica matrix: preparation, characterization, and its catalytic efficacy in carbon-carbon coupling reactions.

Palladium(0) has been immobilized into the silica-based mesoporous material to develop catalyst Pd(0)-MCM-41, which is found to be highly active in carbon-carbon coupling reactions. [Pd(NH3)4]2+ ions have been incorporated into the mesoporous material during synthesis of MCM-41 and subsequently upon treatments with hydrazine hydrate Pd2+ ions present in mesoporous silica matrix were reduced to Pd(0) almost instantaneously. The catalyst has been characterized by small-angle X-ray diffraction, N2 sorption, and transmission electron microscopy (TEM). TEM and surface area measurements clearly demonstrate that the immobilization of Pd(0) into the mesoporous silica has a significant effect on pore structure of the catalyst. Nevertheless, after immobilization of palladium the meso-porosity of the material is retained, as evidenced in the nitrogen sorption measurement. The TEM micrograph shows that both MCM-41 and Pd(0)-MCM-41 have similar types of external surface morphology; however, Pd(0)-MCM-41 was less ordered. Pd(0)-MCM-41 showed high catalytic activity toward carbon-carbon bond formation reactions like Heck and Sonogashira coupling, as evidenced in high turn-over numbers. In contrast to many other Pd-based catalysts reported so far, Pd(0)-MCM-41 acts as a truly heterogeneous catalyst in C-C coupling reactions. Notably, the new heterogeneous catalyst is found to be efficient in the activation of arylchloride to give impressive conversion in cross coupling (15-45% for Heck and 30% for Sonogashira) reactions under mild conditions.

Anchoring of copper complex in MCM-41 matrix: a highly efficient catalyst for epoxidation of olefins by tert-BuOOH.

A complex moiety containing copper (II) has been anchored covalently into the organic-modified Si-MCM-41 to prepare a new catalyst. The amine group containing organic moiety 3-aminopropyl-triethoxysilane has been first anchored on the surface of Si-MCM-41 via silicon alkoxide route. The amine group upon condensation with salicyldehyde affords a bidentate ligand in the mesoporous matrix for anchoring copper(II) ions. The prepared catalyst has been characterized by UV-vis, electron paramagnetic resonance (EPR), and infrared (IR) spectroscopic analysis, small-angle X-ray diffraction, and N2 sorption study. A remarkable difference in the pore structure has been observed after the immobilization of copper(II) complex in Si-MCM-41. The catalyst showed excellent catalytic efficiency in epoxidation reactions with various olefinic compounds including styrene and allyl alcohol, using tert-BuOOH as oxidant. Notably, styrene shows unprecedented high conversion (97%) as well as epoxide selectivity (89%) with tert-BuOOH over the Cu-MCM-41 catalyst.