Microwave-Assisted Synthesis of Porous Aggregates of CuS Nanoparticles for Sunlight Photocatalysis.

Solvated two-dimensional nanosheets of copper hydroxy dodecylsulfate in 1-butanol react with thiourea under microwave irradiation to yield surfactant-free porous aggregates of CuS nanoparticles. These aggregates exhibit excellent photocatalytic activity toward degradation of methylene blue, methyl orange, and 4-chlorophenol in natural sunlight. While the high surface area (14.74 m2 g-1) and porosity increase the active reaction centers for adsorption and degradation of organic molecules, quantum confinement results in a low recombination of photogenerated electrons and holes. Chemical and photogenerated hydroxyl radicals cause the oxidation of the dyes and 4-chlorophenol.

Synthesis and anion-exchange reactions of a new anionic clay, α-magnesium hydroxide.

A new anionic clay, α-magnesium hydroxide, was synthesized by hydrolysis of magnesium acetate in propylene glycol. The structure of this α-hydroxide is similar to that of hydrotalcites. It consists of positively charged magnesium hydroxide layers arising out of partial protonation of the hydroxyl groups of the [Mg(OH)(2)] layers and loosely held anions in the interlayer region. As expected it ages readily in water to give ß-magnesium hydroxide, brucite. While anion-exchange reactions of α-magnesium hydroxide could not be carried out in aqueous medium a number of anion-exchange reactions could be carried out successfully in ethanol medium.

Delamination of surfactant-intercalated brucite-like hydroxy salts of cobalt and copper and solvothermal decomposition of the resultant colloidal dispersions.

Surfactant anion intercalated hydroxy salts of copper and cobalt of the formula M(OH)2- x (surf)x.mH2O [M = Cu, Co; surf = dodecyl sulfate, dodecyl benzene sulfonate, and x = 0.5 for Cu and 0.67 for Co] delaminate readily in 1-butanol to give translucent colloidal dispersions that are stable for months. The extent of delamination and the colloidal dispersion observed in these solids is higher than what had been observed for layered double hydroxides. The dispersions yield the corresponding nanoparticulate oxides on solvothermal decomposition. While the copper hydroxy salt forms approximately 300 nm dendrimer-like CuO nanostructures comprising nanorods of approximately 10 nm diameter, the cobalt analogue forms approximately 20 nm superparamagnetic particles of Co3O4.

Graphite oxide-intercalated anionic clay and its decomposition to graphene-inorganic material nanocomposites.

A graphite oxide-intercalated anionic clay (nickel zinc hydroxysalt) has been prepared using the aqueous colloidal dispersions of negatively charged graphite oxide sheets and aminobenzoate-intercalated anionic clay layers as precursors. When the two colloidal dispersions are reacted, the interlayer aminobenzoate ions are displaced from the anionic clay and the negatively charged graphite oxide sheets are intercalated between the positively charged layers of the anionic clay. The thermal decomposition of the intercalated solid at different temperatures yields graphene-metal oxide/metal nanocomposites. Electron microscopic analysis of the composites indicates that the nanoparticles are intercalated between the layers of graphite in many regions of these solids although the graphite layers are largely exfoliated and not stacked well together.