ABSTRACT
A facile and green method for trapping the hydrophobic reduced graphene oxide between the hydrophilic Kunipia F layers in order to attain stable aqueous dispersions of reduced graphene oxide is described. Initially stable aqueous dispersions of hydrophilic clay intercalated with hydrophilic graphene oxide sheets were formed providing well-organized heterostructures, as it was revealed by scanning electron microscopy images. These structures were preserved in the product obtained after hydrothermal treatment where the hydrophilic graphene oxide was converted to hydrophobic reduced graphene oxide. Ultraviolet measurements revealed the aforementioned conversion which was accompanied by a characteristic change in color from yellow-brown to black in the corresponding aqueous dispersions of these hybrids before and after hydrothermal treatment. The stability of these homogeneous dispersions was confirmed by Zeta Potential measurements implying interactions both in cases of graphene oxide and reduced graphene oxide with clay sheets that made feasible the effective interstratification of graphene-clay layered materials. In these stable dispersions chemistry in aqueous environment could be fully utilized making possible their incorporation e.g., as fillers to hydrophilic polymeric matrices extending thus the limits of application.
ABSTRACT
Palladium is usually supported on porous materials in the form of nanoparticles. The hydrogen storage capacity of such a system is usually much higher than the separated capacity of the metal (approximately 0.7 H/Pd) and the support. Pd nanoparticles provide a source of hydrogen atoms by dissociation. The atomic hydrogen spills over from the Pd structure to the support via surface diffusion and this phenomenon is known as hydrogen spillover. In this study commercial SWNTs were dispersed in PEG 200 solution. Then the precursor PdCl2 in PEG 200 was added and the whole left to react under stirring with reflux at 200 degrees C for 1 h. Succeeding washings with ethanol and centrifugation followed for several times and finally the sample was dried at 60 degrees C. Through this procedure a 3 wt% Pd loading was achieved whereas the TEM derived nanoparticle size distribution indicated a 50% percentage of Pd nanoparticles with diameter less than 8 nm. Hydrogen isotherms up to 2 MPa were carried out with the gravimetric method. The defined storage capacity of 1.2 wt% at 0.2 MPa was quite satisfactory. However, a 0.2 wt% portion of this storage capacity was attributed to the formation of water molecules through reaction of H atoms with the dissociatively adsorbed oxygen atoms on the Pd nanoparticles. This conclusion was educed from a series of thermal desorption experiments following the H2 adsorption/desorption cycles and regeneration. Through this set of experiments several other important parameters were defined as the temperature for complete hydrogen desorption and the optimum conditions for PEG removal.