In this work, the removal of Methyl Orange (MO) from aqueous solution was studied using a new nonconventional
and eco-friendly adsorbent, spent tea leaves (STL). Untreated and acid treated STL were
used as bio-adsorbent for removal of MO using batch method. Effects of different STL dosages (1 – 4
g), pH solutions (2–11) and initial dye concentrations (10 – 60 mg/L) were investigated. Adsorption
experiments conducted using acid treated STL resulted in higher MO removal efficiency ranging from
79 to 92% for 1-4 g of adsorbent dosage compared to the untreated ones which resulted in only 18 to
56% of removal for the similar amount of dosage. In addition, acidic condition favours the MO removal
as compared to alkaline medium. Experimental data were analysed using the Langmuir and Freundlich
models of adsorption and it was found that adsorption isotherm was best described by Freundlich model
and pseudo-first order equation with high correlation coefficient. Results revealed that acid treated STL,
being a waste, has the greater potential to be used as adsorbent for MO removal from aqueous solution.
The use of nanosized titanium dioxide (TiO2) and zinc oxide (ZnO) in the suspension form during treatment makes the recovering and recycling of photocatalysts difficult. Hence, supported photocatalysts are preferred for practical water treatment applications. This study was conducted to investigate the efficiency of calcium alginate (CaAlg) beads that were immobilized with hybrid photocatalysts, TiO2/ZnO to form TiO2/ZnO-CaAlg. These immobilized beads, with three different mass ratios of TiO2:ZnO (1:1, 1:2, and 2:1) were used to remove Cu(II) in aqueous solutions in the presence of ultraviolet light. These beads were subjected to three cycles of photocatalytic treatment with different initial Cu(II) concentrations (10-80ppm). EDX spectra have confirmed the inclusion of Ti and Zn on the surface of the CaAlg beads. Meanwhile, the surface morphology of the beads as determined using SEM, has indicated differences of before and after the photocatalytic treatment of Cu(II). Among all three, the equivalent mass ratio TiO2/ZnO-CaAlg beads have shown the best performance in removing Cu(II) during all three recycling experiments. Those TiO2/ZnO-CaAlg beads have also shown consistent removal of Cu, ranging from 7.14-62.0ppm (first cycle) for initial concentrations of 10-80ppm. In comparison, bare CaAlg was only able to remove 6.9-48ppm of similar initial Cu concentrations. Thus, the potential use of TiO2/ZnO-CaAlg beads as environmentally friendly composite material can be further extended for heavy metal removal from contaminated water.
This paper presents a scalable method of developing ultrasensitive electrochemical biosensors. This is achieved by maximizing sensor conductivity through graphene wrapping of carbonized electrospun nanofibers. The effectiveness of the graphene wrap was determined visually by scanning electron microscopy and chemically by Fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray diffraction. The sensing performance of different electrode samples was electrochemically characterized using cyclic voltammetry and electrochemical impedance spectroscopy, with the graphene-wrapped carbonized nanofiber electrode showing significantly improved performance. The graphene-wrapped carbonized nanofibers exhibited a relative conductivity of ∼14 times and an electroactive surface area of ∼2 times greater compared to the bare screen-printed carbon electrode despite experiencing inhibitive effects from the carbon glue used to bind the samples to the electrode. The results indicate potential for a highly conductive, inert sensing platform.
In this study, a composite material, manganese oxide/reduced titania nanotubes (Mn2O3/R-TNTs), was synthesized through incorporation of Mn2O3 onto R-TNTs via the reverse pulse electrodeposition technique. The influence of pulse reverse duty cycles on the morphological, structural and electrochemical performance of the surface was studied by varying the applied duty cycle from 10% to 90% for 5 min total on-time at an alternate potential of -0.90 V (E on) and 0.00 V (E off). FESEM analysis revealed the uniform deposition of Mn2O3 on the circumference of the nanotubes. The amount of Mn2O3 loaded onto the R-TNTs increased as a higher duty cycle was applied. Cyclic voltammetry and galvanostatic charge-discharge tests were employed to elucidate the electrochemical properties of all the synthesized samples in 1 M KCl. The specific capacitance per unit area was greatly enhanced upon the incorporation of Mn2O3 onto R-TNTs, but showed a decrease as a high duty cycle was applied. This proved that low amounts of Mn2O3 loading enhanced the facilitation of the active ions for charge storage purposes. The optimized sample, Mn2O3/R-TNTs synthesized at 10% duty cycle, exhibited high specific capacitance of 18.32 mF cm-2 at a current density of 0.1 mA cm-2 obtained from constant current charge-discharge measurements. This revealed that the specific capacitance possessed by Mn2O3/R-TNTs synthesized at 10% duty cycle was 6 times higher than bare R-TNTs.