Graphene oxide (GO) forms persistent dispersions in aqueous solutions up to concentrations of 0.2 mg mL(-1). Addition of methylene blue (MB) to these aqueous dispersion of GO gives rise to the observation in optical spectroscopy of new absorption bands that are indicative of the formation of MB/GO conjugates. Four new absorption maxima have been characterized, and their intensity varies depending on the relative concentration of MB with respect to GO. Two of these bands appearing at 677 and 757 nm correspond to individual MB molecules adsorbed on neutral or acid sites of GO, respectively. Two other bands at 615 and 580 nm are attributable to adsorbed MB molecules showing interaction with other neighbor dye molecules at incomplete (615 nm) or complete (580 nm) surface coverage. Complete coverage of GO surface by MB causes the formation of a precipitate and the separation of the MB/GO conjugate. EDS mapping of carbon and sulfur atoms of MB/GO conjugate indicates the homogeneous distribution of MB molecules coating GO sheets. A simple and reliable protocol for surface area measurement and determination of the level of aggregation for GO dispersions in water has been proposed by determining the amount of MB that leads to the maximum intensity of the 580 nm band and precipitation of the MB/GO conjugate. Specific surface area as high as 736.6 m(2) g(-1) in the range of the theoretical value for GO has been experimentally measured for diluted GO solutions, but aggregation levels of 15% were estimated for GO concentration of 50 μg mL(-1).
A coal-tar-derived mesophase was chemically activated to produce a high surface area (~3200 m(2)/g) carbon with a porosity made up of both micropores and mesopores. Its adsorption capacities were found to be among the highest ever reported in literature, reaching values of 860 mg/g and 1200 mg/g for the adsorption of benzene and toluene, respectively, and 1200 mg/g for the combined adsorption of benzene and toluene from an industrial wastewater. Such high values imply that the entire pore system, including the mesopore fraction, is involved in the adsorption process. The almost complete pore filling is thought to be due to the high relative concentrations of the tested solutions, resulting from the low saturation concentration values for benzene and toluene, which were obtained by fitting the adsorption data to the BET equation in liquid phase. The kinetics of adsorption in the batch experiments which were conducted in a syringe-like adsorption chamber was observed to proceed in accordance with the pseudo-second order kinetic model. The combined presence of micropores and mesopores in the material is thought to be the key to the high kinetic performance, which was outstanding in a comparison with other porous materials reported in the literature.
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