Mambo Moyo

Recent Advances in Polymeric Materials Used as Electron Mediators and Immobilizing Matrices in Developing Enzyme Electrodes

Different classes of polymeric materials such as nanomaterials, sol-gel materials, conducting polymers, functional polymers and biomaterials have been used in the design of sensors and biosensors. Various methods have been used, for example from direct adsorption, covalent bonding, crossing-linking with glutaraldehyde on composites to mixing the enzymes or use of functionalized beads for the design of sensors and biosensors using these polymeric materials in recent years. It is widely acknowledged that analytical sensing at electrodes modified with polymeric materials results in low detection limits, high sensitivities, lower applied potential, good stability, efficient electron transfer and easier immobilization of enzymes on electrodes such that sensing and biosensing of environmental pollutants is made easier. However, there are a number of challenges to be addressed in order to fulfill the applications of polymeric based polymers such as cost and shortening the long laboratory synthetic pathways involved in sensor preparation. Furthermore, the toxicological effects on flora and fauna of some of these polymeric materials have not been well studied. Given these disadvantages, efforts are now geared towards introducing low cost biomaterials that can serve as alternatives for the development of novel electrochemical sensors and biosensors. This review highlights recent contributions in the development of the electrochemical sensors and biosensors based on different polymeric material. The synergistic action of some of these polymeric materials and nanocomposites imposed when combined on electrode during sensing is discussed.

An amperometric biosensor based on horseradish peroxidase immobilized onto maize tassel-multi-walled carbon nanotubes modified glassy carbon electrode for determination of heavy metal ions in aqueous solution.

A biosensor for trace metal ions based on horseradish peroxidase (HRP) immobilized on maize tassel-multiwalled carbon nanotube (MT-MWCNT) through electrostatic interactions is described herein. The biosensor was characterized using Fourier transform infrared (FTIR), UV-vis spectrometry, voltammetric and amperometric methods. The FTIR and UV-vis results inferred that HRP was not denatured during its immobilization on MT-MWCNT composite. The biosensing principle was based on the determination of the cathodic responses of the immobilized HRP to H₂O₂, before and after incubation in trace metal standard solutions. Under optimum conditions, the inhibition rates of trace metals were proportional to their concentrations in the range of 0.092-0.55 mg L⁻¹, 0.068-2 mg L⁻¹ for Pb²⁺ and Cu²⁺ respectively. The limits of detection were 2.5 μg L⁻¹ for Pb²⁺ and 4.2 μg L⁻¹ for Cu²⁺. Representative Dixon and Cornish-Bowden plots were used to deduce the mode of inhibition induced by the trace metal ions. The inhibition was reversible and mixed for both metal ions. Furthermore, the biosensor showed good stability, selectivity, repeatability and reproducibility.

Kinetic and equilibrium modelling of lead sorption from aqueous solution by activated carbon from goat dung

The potential of goat dung-derived activated carbon as an adsorbent for the removal of lead from aqueous solution in a batch system was studied. Physicochemical properties of the biosorbent were characterized by means of X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. Batch adsorption experiments were carried out as a function of pH, contact time, adsorbent dosage, initial concentration and temperature. The adsorption showed a pH dependent profile and an optimum value at pH 4.5. The adsorption isotherm modelling showed that the equilibrium data fitted better to the Freundlich than the Langmuir model. Kinetic data were properly fitted with the pseudosecond-order kinetic model. Furthermore, the thermodynamic parameters indicated that the adsorption reaction was endothermic and a spontaneous process.

Adsorption of cadmium from aqueous solution using Rooibos shoots as adsorbent

The use of Rooibos shoots, a natural adsorbent, for cadmium removal from wastewater is proposed. The effects of initial pH, adsorbent dosage, contact time, and initial concentration were investigated in the batch adsorption mode. The optimum pH was found to be 5.5. Isotherm and kinetic data were modeled; the data fitted best to the Freundlich model, and, kinetically, the adsorption was of pseudo-second order as shown by the high R2 value of 0.9928 along with close agreement between the experimental qe (13.9 mg g−1) and calculated qe (14.24 mg g−1) values. The studied biomass material was found to be effectively used for removal of cadmium from contaminated mine wastewater.

Electrodeposition of zinc oxide nanoparticles on multiwalled carbon nanotube-modified electrode for determination of caffeine in wastewater effluent

ABSTRACT We report on the development of an electrochemical sensor based on electrodepositing zinc oxide on multiwalled carbon nanotube-modified glassy carbon electrode for the detection of caffeine in pharmaceutical wastewater effluents. The measurements were carried out using cyclic voltammetry, electrochemical impedance spectroscopy, chronoamperometry and differential pulse voltammetry (DPV). DPV measurements showed a linear relationship between oxidation peak current and concentration of caffeine in 0.1 M HClO4 (pH 1.0) over the concentration range 0.00388–4.85 mg/L and a detection limit of 0.00194 mg/L. The diffusion coefficient and Langmuir adsorption constant for caffeine were calculated to be 3.25 × 10−6 cm2 s−1 and 1.10 × 103 M−1, respectively. The sensor showed satisfactory results when applied to the detection of caffeine in wastewater effluents.

Removal of nickel(II) from aqueous solution by Vigna unguiculata (Cowpea) pods biomass

The potential to remove nickel(II) ions from aqueous solution using a biosorbent prepared from Vigna unguiculata pods (VUPs) was investigated in batch experiments. The batch mode experiments were conducted utilising the independent variables of pH (2 to 8), contact time (5 to 120 min), dosage concentration (0.2 to 1.6 g), nickel(II) concentrations (10 to 80 mg L(-1)) and temperature (20 to 50°C). The biosorption data fitted best to the Freundlich biosorption model with a correlation coefficient (R(2)) of 0.993 and lowest chi-squared value of 31.89. The maximum sorption capacity of the VUP for nickel(II) was 27.70 mg g(-1). Kinetics studies revealed that the biosorption process followed the pseudo-second-order model as it had the lowest sum of square error value (0.808) and correlation coefficient close to unity (R(2) = 0.998). The calculated thermodynamic parameters showed that the biosorption process was feasible, spontaneous and endothermic. Consequently, the study demonstrated that VUP biomass could be used as a biosorbent for the removal of nickel(II) from aqueous solution.

Simultaneous oxidative determination of antibacterial drugs in aqueous solutions using an electrode modified with MWCNTs decorated with Fe3O4 nanoparticles

The present study describes a simple sensor developed from Fe3O4 and MWCNT nanoparticles for the simultaneous detection of sulfamethoxazole (SMX) and trimethoprim (TMP). Determination was carried out using cyclic voltammetry, electrochemical impedance spectroscopy, chronoamperometry and differential pulse voltammetry. Oxidation peaks were obtained at 910 mV (SMX) and 1120 mV (TMP) in Britton–Robinson buffer (pH 6.0). LODs of 1.10 × 10−8 M (SMX; 2.79 μg L−1) and 2.10 × 10−8 M (TMP; 6.10 μg L−1) were obtained. The Fe3O4/MWCNT/GCE showed good stability and selectivity. Furthermore, the simultaneous detection of SMX and TMP in tablets, urine and water was possible using the standard addition method.

Preparation of poly(methyl methacrylate)–grafted Hyparrhenia hirta for methyl red removal from colored solutions

ABSTRACT Poly(methyl methacrylate)–grafted Hyparrhenia hirta (PMMA-g-Hh) biopolymer was prepared through radical polymerization using potassium persulfate (KPS) and applied in adsorption of methyl red from colored solutions. Solvent amount, initiator concentration, monomer concentration, temperature, and reaction time were the reaction parameters investigated for grafting. The biopolymer was characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and x-ray diffraction spectroscopy (XRD). The adsorption process was investigated with respect to pH, contact time, initial concentration, adsorbent dosage, and temperature. The optimum adsorption parameters were pH 6, contact time 90 min, adsorbent dosage 0.6 g, and initial concentration 50 mg/L. The Langmuir adsorption model best fitted the adsorption process, with maximum adsorption capacities of 19.95, 6.89, and 4.02 mg/g at adsorbent dosages of 0.2, 0.6, and 1.0 g, respectively. The pseudo-second-order model described the kinetics data better. The adsorption process was physical, spontaneous, and endothermic. The adsorbent was still active after 10 adsorption-desorption cycles, showing its suitability for use in colored solutions treatment.