RESUMO
Understanding graphene oxide's stability (or lack thereof) in liquid solvents is critical for fine-tuning the material's characteristics and its potential involvement in future applications. In this work, through the use of structural and surface investigations, the alteration of the structural and edge-surface properties of 2D graphene oxide nanosheets was monitored over a period of eight weeks by involving DLS, zeta potential, XRD, XPS, Raman and FT-IR spectroscopy techniques. The samples were synthesized as an aqueous suspension by an original modified Marcano-Tour method centred on the sono-chemical exfoliation of graphite. Based on the acquired experimental results and the available literature, a phenomenological explanation of the two underlying mechanisms responsible for the meta-stability of graphene oxide aqueous dispersions is proposed. It is based on the cleavage of the carbon bonds in the first 3-4 weeks, while the bonding of oxygen functional groups on the carbon lattice occurs, and the transformation of epoxide and hydroxyl groups into adsorbed water molecules in a process driven by the availability of hydrogen in graphene oxide nanosheets.
RESUMO
New very stable composites prepared by deposition of resorcinol-formaldehyde polymer (RF-) or carbon (C-) xerogels into walls of commercial porous tubular ceramics (TiO2-ZrO2 and alphaAl2O3-gammaAl203) were obtained by a sol-gel process followed by a drying and a pyrolytic (only for C-xerogel/ceramic composites) step. They were characterized by nitrogen adsorption-desorption, SEM and XRD, and tested for gas (H2, CH4, CO2 and CO) separation applications. Additional morpho-structural information about the open-interconnected ultramicropore structure of composites was found by gas permeation investigation. Interesting results for H2 permeance was obtained especially for RF-polymer/ceramic composites respecting Knudsen diffusion mechanism of gas permeance: H2 > CH4 > CO > CO2. The coexistence of Knudsen and surface diffusion mechanisms were confirmed.
