Joonmok Shim

Optimized coverage of gold nanoparticles at tyrosinase electrode for measurement of a pesticide in various water samples

Gold nanoparticles (AuNPs) were electrodeposited onto a glassy carbon (GC) electrode to increase the sensitivity of the tyrosinase (TYR) electrode. By controlling the applied potential and time, the coverage of AuNPs at the TYR electrode was optimized with respect to the current response. The voltammetric measurements revealed a sensitive enzymatic oxidation and electrochemical reduction of substrate (phenol and catechol). The quantitative relationships between the inhibition percentage and the pesticide concentration in various water samples were measured at the TYR-AuNP-GC electrode, showing an enhanced performance attributed by the use of AuNPs.

Improvement of an enzyme electrode by poly(vinyl alcohol) coating for amperometric measurement of phenol

A poly(vinyl alcohol) film cross-linked with glutaraldehyde (PVA-GA) was introduced to the surface of a tyrosinase-based carbon paste electrode. The coated PVA-GA film was beneficial in terms of increasing the stability and reproducibility of the enzyme electrode. The electrode showed a sensitive current response to the reduction of the o-quinone, which was the oxidation product of phenol, by the tyrosinase, in the presence of oxygen. The effects of the PVA and PVA-GA coating, the pH, and the GA:PVA ratio on the current response were investigated. The sensitivity of the PVA-GA-Tyr electrode was 130.56microA/mM (1.8microA/microM cm(2)) and the linear range of phenol was 0.5-100microM. At a higher concentration of phenol (>100microM), the current response showed the Michaelis-Menten behavior. Using the PVA-GA-Tyr electrode, a two-electrode system was tested as a prototype sensor for portable applications.

Detoxification of simulated textile wastewater using a membraneless electrochemical reactor with immobilized peroxidase.

Simulated textile wastewater was degraded using a membraneless electrochemical reactor with immobilized peroxidase on the porous Celite. The optimal current density was 10 A m(-2), at which the highest amount of hydrogen (H(2)O(2)) could be generated. The decolorization efficiencies of the simulated wastewater using the electrochemical and electroenzymatic methods were 35% and 92%, respectively. Biodegradability, the ratio of 5-day biochemical oxygen demand to chemical oxygen demand (BOD(5)/COD), was enhanced about 1.88 times when using the electroenzymatic treatment rather than raw wastewater, which could not be achieved by the electrochemical treatment. The toxic unit (TU), calculated using the lethal concentration (LC(50)) of Daphnia magna (D. Magna), of effluent treated by electroenzymatic method was below 1, whereas those of simulated textile wastewater and effluent treated by electrochemical method were 11.4 and 3.9, respectively.

Effects of Electrolyte Concentration on Growth of Dendritic Zinc in Aqueous Solutions

In order to understand the nature of dendritic zinc growth, electrochemical zinc redox reaction on nickel plate was investigated in aqueous solutions containing different concentrations, 0.2, 0.1 and 0.02 (M), of zinc sulfate () or zinc chloride (). Zinc ion was efficiently reduced and oxidized on nickel in the high-concentration (0.2 M) solution, whereas relatively poor efficiency was obtained from the other low-concentration solutions (0,1 and 0.02 M). Cyclic voltammetry (CV) analysis revealed that the 0.2 M electrolyte solution decomposes at more positive potentials than the 0.1 and the 0.02 M solutions. These results suggested that the concentration of electrolyte solution and anion would be an important factor that suppresses the reaction of the zinc dendrite formation. Scanning Electron Microscopy (SEM) data revealed that the shape of dendritic zinc and its growing behavior were also influenced by electrolyte concentration.