Facile Pretreatment of Three-Dimensional Graphene through Electrochemical Polarization for Improved Electrocatalytic Performance and Simultaneous Electrochemical Detection of Catechol and Hydroquinone

Three-dimensional graphene (3DG) with macroporous structure has great potential in the field of electroanalysis owing to a large active area, excellent electron mobility and good mass transfer. However, simple and low-cost preparation of 3DG electrodes with high electrocatalytic ability is still a challenge. Here, a fast and convenient electrochemical polarization method is established to pretreat free-standing 3DG (p-3DG) to offer high electrocatalytic ability. 3DG with monolithic and macroporous structure prepared by chemical vapor deposition (CVD) is applied as the starting electrode. Electrochemical polarization is performed using electrochemical oxidation (anodization) at high potential (+6 V) followed with electrochemical reduction (cathodization) at low potential (−1 V), leading to exposure of edge of graphene and introduction of oxygen-containing groups. The as-prepared p-3DG displays increased hydrophilicity and improved electrocatalytic ability. As a proof of concept, p-3DG was used to selective electrochemical detection of two isomers of benzenediol, hydroquinone (p-BD) and catechol (o-BD). In comparison with initial 3DG, p-3DG exhibits increased reversibility of redox reaction, improved peak current and good potential resolution with high potential separation between p-BD and o-BD. Individual or selective determination of p-BD or o-BD in single substance solution or binary mixed solution is realized. Real analysis of pond water is also achieved.

STUDY OF ELECTRODEPOSITION OF NICKEL FROM ALKALINE GLYCINE ELECTROLYTES

The essay is about studies of the electrochemical reduction of nickel ions from a glycine electrolyte by the method of recording cyclic and linear potentiodynamic polarization curves. The effect of the concentration of the main components, potential sweep and temperature on the electrodeposition process of nickel has been studied. It has been found that at the beginning of the process the electrodeposition of the nickel ions from glycine electrolyte is controlled by electrochemical polarization, which turns into concentration polarization

Corrosion Behavior of Zn, Fe and Fe-Zn Powder Materials Prepared via Uniaxial Compression

Powder metallurgy is one of the most prevalent ways for metallic degradable materials preparation. Knowledge of the properties of initial powders used during this procedure is therefore of great importance. Two different metals, iron and zinc, were selected and studied in this paper due to their promising properties in the field of biodegradable implants. Raw powders were studied using scanning electron microscopy (SEM) coupled with energy dispersive spectrometry (EDX). Powders (Fe, Zn and Fe-Zn in a weight ratio of 1:1) were then compressed at the pressure of 545 MPa to the form of pellets with a diameter of 1.7 cm. Surface morphology and degradation behavior in the Hanks´ solution were studied and evaluated. Electrochemical polarization tests along with the static immersion tests carried out for 21 days were employed for corrosion behavior characterization. The highest corrosion rate was observed for pure Zn powder followed by the Fe-Zn and Fe, respectively. A mixed Fe-Zn sample showed similar properties as pure zinc with no signs of iron degradation after 21 days due to the effect of galvanic protection secured by the zinc acting as a sacrificial anode.

Nano-TiO2 Coating Layers with Improved Anticorrosive Properties by Aerosol Flame Synthesis and Thermophoretic Deposition on Aluminium Surfaces

TiO2 in the form of nanoparticles is characterized by high photocatalytic activity and high resistance to oxidation, making it an excellent candidate to realize coatings for improving the corrosion resistance of aluminium surfaces. Different coating technologies have been proposed over the years, which often involve the use of toxic compounds and very high temperatures. In this work, an alternative and novel one-step method for the coating of aluminium alloy surfaces with titania nanoparticles is presented. The method is based on the combination of aerosol flame synthesis and direct thermophoretic deposition and allows to produce nanostructured thin coating layers of titania with different features. Specifically, 3.5 nm anatase nanoparticles were synthesized and deposited onto aluminium alloy AA2024 samples. The thickness of the coating was changed by modifying the total deposition time. A thermal annealing treatment was developed to improve the adhesion of nano-titania on the substrates, and the morphology and structures of the coatings were characterized using (ultra violet) UV-vis absorption, scanning electron microscopy, transmission electron microscopy and Raman spectroscopy. The corrosion resistance behavior of the coatings was evaluated by means of electrochemical polarization measurements, coupled with a numerical analysis using COMSOL software. Both the experimental and numerical electrochemical polarization curves showed a significant increase in the corrosion potential of coated substrates with respect to the bare aluminium and a decrease in the current density. The coatings obtained with higher deposition time and greater thickness showed the best performances in terms of the resistance of the aluminium surfaces to corrosion.

Corrosion Behavior of Cold-Formed AA5754 Alloy Sheets

In this work, the influence of bending an AA5457 alloy sheet and the resulting microstructural changes on its corrosion behavior was investigated. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to perform detailed microstructural analyses of the alloy in its original form and after bending. After immersion in naturally-aged NaCl under open-circuit conditions (0.5 M, adjusted to 3 by HCl), post-corrosion observations were made, and electrochemical polarization measurements were performed to investigate the corrosion mechanisms occurring on both surfaces. The results showed that the corrosion of AA5457 is a complex process that mainly involves trenching around coarse Si-rich particles, crystallographically-grown large pits, and the formation of multiple tiny pits around Si-rich nanoparticles. The experimental data showed that bending AA5457 changed the shape and distribution of Si-rich coarse particles, cumulated a higher dislocation density in the material, especially around Si-rich nanoparticles, and all of these factors caused that corrosion behavior of the AA5754 in the bending area was lowered.