Electrochemical Deposition of Polypyrrole in the Presence of Silanes as Adhesion Promoters.

Polypyrrole adhesion to indium-tin oxide electrodes was improved by adding pre-hydrolyzed alkoxysilanes to the electrodeposition media. The pyrrole oxidation and film growth rates were studied by potentiostatic polymerization in acidic media. The morphology and thickness of the films were studied by contact profilometry and surface-scanning electron microscopy. The bulk and surface semiquantitative chemical composition was studied by Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy. Finally, the adhesion was studied by scotch-tape adhesion test, where both alkoxysilanes showed a significant improvement in adhesion. We proposed a hypothesis for the improvement in adhesion, that involves the formation of siloxane material as well as in situ surface modification of the transparent metal oxide electrode.

Removal of Cu(II) ions from aqueous streams using poly(acrylic acid-co-acrylamide) hydrogels.

The adsorption of Cu(II) ions from aqueous solutions onto poly(acrylic acid-co-acrylamide) hydrogels was investigated. The hydrogels were prepared via free-radical solution polymerization using Irgacure 754 as a photoinitiator and ethylene glycol dimethacrylate as a cross-linking agent. Loading of acrylamide/acrylic acid moieties on the surfaces of hydrogels and the amount of cross-linking agent were varied to determine the maximum metal uptake. Polymerization kinetics was investigated by (1)H NMR. The physicochemical properties of hydrogels were investigated by nitrogen sorption measurements, elemental analysis, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). The (1)H NMR results demonstrated that the polymerization reaction was carried out almost to completion and confirmed the absence of residual monomers. Swelling results indicated that, by appropriate selection of cross-linking agent amount and monomer ratio, hydrogels can be swollen up to 70,000%. Further characterization of the hydrogels showed rapid adsorption kinetics and equilibrium Cu(II) adsorption capacities of 121 mg g(-1). Cu(II) adsorption kinetic data followed pseudo-first-order kinetics. Adsorption equilibrium data were better fitted by a Langmuir isotherm. FTIR and XPS results indicated the presence of a tetradentate copper complex on the surfaces of hydrogels. The copper uptake achieved suggests the potential use of hydrogels to extract toxic metals from industrial aqueous streams.

Surface characterization of electrodeposited silver on activated carbon for bactericidal purposes.

The use of an electrochemical reactor operated under different flow conditions to deposit silver from aqueous AgNO(3) solutions and tartaric acid as an organic additive on a commercial activated carbon with ultimate bactericidal applications in water purification processes is presented. The characterization of carbon/silver samples was studied by BET, FTIR, X-ray diffraction, XPS, and SEM techniques. The bactericidal activity of the carbon/silver samples was tested on drinking water samples inoculated with E. coli. A reduction of carbon surface area was detected and was caused by increased amounts of silver deposited on carbon samples. Adherent silver deposits were obtained on the carbon/silver samples. X-ray diffraction studies of carbon with electrodeposited silver showed two different preferential deposition planes, [111] and [220]. The FTIR results confirm the presence of carboxyl, phenolic, quinone, and ether surface groups. The XPS results suggest the formation of Ag(2)O and AgO surface species and confirm the reduction of silver to the metallic form. Antimicrobial activity toward E. coli indicated reductions by up to 7 orders of magnitude in the log CFU/mL in just 10 min contact time and for silver contents of 2.47 wt%.