Covalent grafting of chitosan onto stainless steel through aryldiazonium self-adhesive layers.

Although the conventional methods for strong attachment of chitosan onto stainless steel require many steps in different solvents, it has been demonstrated in this work that covalent grafting of chitosan on a steel surface can be easily achieved through the formation of a self-adhesive surface based on aryldiazonium seed layers. Initially, a polyaminophenyl layer is grafted on a stainless steel surface by means of the one-step GraftFast(TM) process (diazonium induced anchoring process). The grafted aminophenyl groups are then converted to an aryldiazonium seed layer by simply dipping the substrate in a sodium nitrite acidic solution. That diazonium-rich grafted layer can be used as a self-adhesive surface for subsequent spontaneous coating of chitosan onto the steel surface. X-ray photoelectron and impedance electrochemical spectroscopies were used to characterize the pristine and modified steel samples. As evidenced from impedance and linear polarization results, the primary polyaminophenyl layer characterized by a high charge transfer resistance contributed to better protection against corrosion of the resulting chitosan-coated steel in sulfuric acid medium.

Decoration of graphitic surfaces with Sn nanoparticles through surface functionalization using diazonium chemistry.

Composites of tin nanoparticles (Sn NP) and graphene are candidate materials for high capacity and mechanically stable negative electrodes in rechargeable Li ion batteries. A uniform dispersion of Sn NP with controlled size is necessary to obtain high electrochemical performance. We show that the nucleation of Sn particles on highly ordered pyrolitic graphite (HOPG) from solution can be controlled by functionalizing the HOPG surface by aryl groups prior to Sn deposition. On the contrary, we observe heterogeneous deposition of micrometer sized Sn islands on HOPG subjected to oxidation prior to deposition in the same conditions. We demonstrate that functional groups act as nucleation sites for Sn NP nucleation, and that homogeneous nucleation of small particles can be achieved by combining surface functionalization with diazonium chemistry and appropriate stabilizers in solution.

Surface homogeneity of anion exchange membranes: a chronopotentiometric study in the overlimiting current range.

Electrotransport of sodium chloride near and through the ASV anion exchange membrane was first investigated. Chronopotentiometric and current-voltage characteristics results have shown that the ASV membrane acts as a totally conducting plane with respect to the transport of NaCl electrolyte. SEM and AFM images contributed to confirm the overall homogeneous surface of the membrane. Further chronopotentiometric studies of the membrane were evaluated in the presence of different alkaline chloride solutions in order to explore the influence of alkali co-ions on the transport phenomena. Membrane characterization led to determine the transport number of chloride counterion in the membrane. It is reported in this work that chronopotentiometry using the Sand equation toward the homogeneous ion exchange membrane is a simple and efficient method for determination of the diffusion coefficient of the electrolytes in the bulk solution. Discussions on the transport properties of the electrolyte solutions in relation with the hydrated ion sizes allowed us to verify the diffusion coefficient of the electrolytes determined by means of chronopotentiometric method.

Permselectivity and microstructure of anion exchange membranes.

The water content, the ion exchange capacity, the transport number of counter-ion of the AMV and AMX anion exchange membranes were determined. The two-phase model (gel phase and interstitial phase) of structure microheterogeneity was validated by means of conductivity measurements. The chronopotentiometric results allowed us to affirm the overall surface homogeneity of the membranes. According to the two-phase model, the influence of the gel phase and the interstitial phase on the membrane permselectivity was discussed in detail. Majorities of co-ions exist in the interstitial phase, thus they have no influence on the transport of counter-ions in the gel phase. The determination of the KCl amount sorbed in the interstitial phase confirmed the existence of partition equilibrium between the interstitial phase and the external solution. Such partition equilibrium can be considered within the microheterogeneous model in order to represent the internal structure of the electromembranes.