The effects of formation and functionalization of graphene-based membranes on their gas and water vapor permeation properties.

The gas and water vapor permeabilities of graphene-based membranes can be affected by the presence of different functional groups directly bound to the graphene network. In this work, one type of carboxylated graphene oxide (GO-COOH) and two types of graphene oxide synthesized i) under strong oxidative conditions directly from graphite (GO-1) and ii) under mild oxidative conditions from exfoliated graphene (GO-2) were used as precursors of self-standing membranes prepared with thicknesses in the range of 12-55 µm via slow-vacuum filtration preparation method. It was observed that the permeabilities for all tested gases decreased in order GO-2 > GO-1 > GO-COOH and depended on both the arrangement of graphene sheets and their functionalization. The GO-1 membrane with a high content of oxygen-containing groups showed the best performance for water vapor permeability. The GO-2 membrane with a thickness of 43 µm exhibited a disordered GO sheet morphology and, therefore, unique gas-separation performance towards H2/CO2 gas pair, showing high hydrogen permeability while keeping extremely high H2/CO2 ideal selectivity that exceeds the Robeson 2008 upper bound of polymer membranes.

Carbon and zeolite-based composites for radionuclide and heavy metal sorption.

Zeolites have been investigated as sorbents of heavy metals from water. Since graphene oxide was already reported as promising radionuclide sorbent, we developed composite materials containing both a synthetic zeolite (type A, P or Y) and graphene oxide to be multifunctional sorbents. The extension of multifunctionality of sorbents was done by presence of third component, exfoliated graphite, to have additional properties as conductivity. The changing sorption activities of a composite was studied depending on its composition and functional modification. The composites, characterized by X-ray powder diffraction, Raman, FTIR spectroscopy and scanning electron microscopy, were tested for sorption of selected radionuclides (134Cs+, 85Sr2+) and heavy metals (Pb2+, Cd2+). The dependency on composition was found in connection with a high sorption of Pb2+ and Cd2+. Finally, optimized multifunctional sorbents (Gr-GO-COOH-A in ratio 40:40:20 and Gr:GO:A in ratio 25:25:50) were found to keep interesting high sorption activities for heavy metals and radionuclides with good conductivity properties.

Influence of Inorganic Bases on the Structure of Titanium Dioxide-Based Microsheets.

Laboratory synthesis of microsheets of titanium dioxide from titanyl sulfate involves the use of ammonia solution, whereas another inorganic base is most likely to be employed at the industrial level, as ammonia is a toxic agent and therefore should be avoided according to European Union (EU) regulations. Selected nontoxic bases such as sodium, potassium, and lithium hydroxides have been tested as an alternative to ammonia solution to obtain amorphous and crystalline TiO2-based microsheets. The final products obtained at each step of the procedure (samples lyophilized and annealed at 230 and 800 °C) were analyzed with electron and atomic force microscopy, X-ray powder diffraction, thermal analysis, and Fourier transform infrared (FTIR) and Raman spectroscopies to determine their morphology and phase composition. The differences in the morphology of the obtained products were described in detail as well as phase and structural composition throughout the process. It was found that, in the last step of the synthesis, microsheets annealed at 800 °C were built of small rods and oval or platy crystalline particles depending on the base used. The temperature of formation of anatase, rutile, and alkali-metal titanates in correlation with the ionic radius of the alkali metal present in the sample was discussed.

New generation photocatalysts: how tungsten influences the nanostructure and photocatalytic activity of TiO2 in the UV and visible regions.

Tungsten-doped anatase was prepared by a thermal hydrolysis of aqueous solutions of peroxo complexes of titanium and tungsten. The synthesized samples included X-ray diffraction, high-resolution transmission electron microscopy, selected area electron diffraction, Raman spectroscopy, specific surface area, and porosity determination. W doping resulted in a decrease of the unit-cell volume of anatase at lower W contents and an increase at higher W contents. The position of the most intense Raman band of the E(g) mode (near 147 cm(-1)) also has a local minimum at medium-doped titania (1.1-3.6% W in titania). W doping increases the temperature of anatase-to-rutile transformation by about 100 °C compared with nondoped anatase. The photocatalytic activity of doped titania samples was determined by decomposition of Orange II dye during irradiation at 365 and 400 nm. Specimens with moderate W doping (1.0-3.3% W) perform best: they enhance the corresponding reaction rates 10 times at 365 nm and 5 times at 400 nm, respectively, compared with pure titania obtained under the same set of synthesis conditions.