Voltammetric determination of hydrogen peroxide at decorated palladium nanoparticles/poly 1,5-diaminonaphthalene modified carbon-paste electrode.

In this work, palladium nanoparticles (PdNPs)/p1,5-DAN/ carbon paste electrode (CPE) and p1,5-DAN/CPE sensors have been developed for determination of hydrogen peroxide. Both sensors showed a highly sensitive and selective electrochemical behaviour, which were derived from a large specific area of poly 1,5 DAN and super excellent electroconductibility of PdNPs. PdNPs/p1,5-DAN/CPE exhibited excellent performance over p1,5-DAN/CPE. Thus, it was used for detecting hydrogen peroxide (H2O2) with linear ranges of 0.1 to 250 µM and 0.2 to 300 µM as well as detection limits (S/N = 3) of 1.0 and 5.0 nM for square wave voltammetry (SWV) and cyclic voltammetry (C.V) techniques, respectively. The modified CPE has good reproducibility, adequate catalytic activity, simple synthesis and stability of peak response during H2O2 oxidation on long run that exceeds many probes. Both reproducibility and stability for H2O2 detection are attributable to the PdNPs immobilized on the surface of p1,5-DAN/CPE. The modified CPE was used for determining H2O2 in real specimens with good stability, sensitivity, and reproducibility.

Modified electrode decorated with silver as a novel non-enzymatic sensor for the determination of ammonium in water.

Ammonium is an essential component of the nitrogen cycle, which is essential for nitrogen cycling in ecosystems. On the other hand, ammonium pollution in water poses a great threat to the ecosystem and human health. Accurate and timely determination of ammonium content is of great importance for environmental management and ensuring the safety of water supply. Here we report a highly sensitive electrochemical sensor for ammonium in water samples. The modified electrode is based on the incorporation of silver nitrate (AgNO3) into a carbon paste embedded with 1-aminoanthraquinone and supported by multi-walled carbon nanotubes, which are commercially available. A potential of 0.75 V is applied to the modified electrode, followed by activation in hydrochloric acid. The modified electrode was used for square wave voltammetry of ammonium in water in the potential range of - 0.4-0.2 V. The performance of ammonium analysis was determined in terms of square wave frequency, square wave amplitude and concentration of electrolyte solution (sodium sulphate). The calculation of the surface area according to the Randles-Sevcik equation resulted in the largest surface area for the Ag/pAAQ/MWCNTs/CPE. The modified electrode exhibited a linear range of 5-100 µM NH4+ in 0.1 M Na2SO4 with a detection limit of 0.03 µM NH4+ (3σ). In addition, the modified electrode showed high precision with an RSD value of 9.93% for 10 repeated measurements. No interfering effect was observed at twofold and tenfold additive concentrations of foreign ions. Good recoveries were obtained in the analysis of tap and mineral water after spiking with a concentration of ammonium ions.

Biosynthesized silver nanoparticles for electrochemical detection of bromocresol green in river water.

In this study, silver nanoparticles (AgNPs)-based electrochemical sensor has been reported for assessing bromocresol green (BG) in river water. Firstly, AgNPs were greenly produced using the aqueous extract of Ficus sycomorus leaves. Then, the AgNP-modified glassy carbon (GC) electrode was prepared using the sticking method. AgNPs were characterized using transmission electron microscope (TEM), X-ray diffraction (XRD), square wave voltammetry (SWV) and scanning electron microscope (SEM). TEM and SEM were used for determining the size of AgNPs before and after adsorption, respectively. The results show that there was an increase in AgNP size from 20 to 30 nm. Additionally, XRD was used for characterizing the crystal nature of AgNPs, while SWV exhibited a characteristic oxidation peak of AgNPs at 0.06 V. Moreover, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used for characterizing the catalytic effect of AgNPs. BG as a targeted pollutant was detected at AgNPs/GC based on its oxidation through proton and electron transfer. Two peaks corresponding to the monomer and polymer oxidation were detected. The monomer- and polymer-based sensors have revealed a linear range of 2.9 × 10-5 to 2.1 × 10-4 mole l-1 and low detection limits (LODs) of 1.5 × 10-5 and 1.3 × 10-5 mole l-1, respectively.

Mucilage-capped silver nanoparticles for glucose electrochemical sensing and fuel cell applications.

A simple, cost-effective and green mucilage-capped silver nanoparticles (Mucilage-AgNPs) modified glassy carbon electrode (GC) composite was constructed for efficient and facile electrochemical oxidation of glucose for the first time. Mucilage-AgNPs were synthesized through the direct chemical reduction of Ag+ by mucilage extracted from Opuntia ficus-indica. Mucilage-AgNPs were identified and characterized using ultraviolet-visible spectroscopy, transmission electron microscopy and square wave voltammetry. Modification of the GC with AgNPs was carried out via a transfer-sticking technique with an immobilization time of 1 h. The Mucilage-AgNPs/GC composite was studied as a possible anode for glucose oxidation in a biofuel cell. The composite resulted in glucose oxidation with a current density and power density of 85.7 µA cm-2 and 25.7 µW cm-2, respectively. Glucose sensing using the Mucilage-AgNPs/GC composite was achieved successfully via two pathways: glucose oxidation and AgNP inhibition. The glucose oxidation-based sensor showed a lower detection limit of 0.01 mM and a linear range of 0.01 to 2.2 mM. The AgNPs inhibition-based sensor provides an indirect determination pathway of glucose with a detection limit of 0.1 mM and a linear range of 0.1 to 1.9 mM. AgNP inhibition is a novel pathway that could be used for determining a large number of organic and inorganic molecules. Overall, the Mucilage-AgNPs/GC is considered a pioneering composite for glucose sensing and fuel cell applications.

Individual and Simultaneous Voltammetric Determination of Ultra-Trace Environmental Contaminant Dihydroxybenzene Isomers Based on a Composite Electrode Sandwich-like Structure.

An advanced electroanalytical technique for the simultaneous assessment of environmental contaminant dihydroxybenzene isomers, catechol (CC), hydroquinone (HQ), and resorcinol (RC), has been investigated using palladium nanoparticles (PdNPs) incorporated onto a poly(1,5-diaminonaphthalene) (DAN) matrix over a glassy carbon electrode (GCE). Concurrently, these types of phenols can be assessed by the PdDAN/GCE modified electrode employing square wave voltammetry and cyclic voltammetry (CV) techniques under optimal conditions. This modified electrode has demonstrated linear responses for CC, HQ, and RC from 50.0 to 1000.0 mM; concomitantly, low detection limits of 0.22, 0.22, and 0.47 nM and low quantification limits of 0.740, 0.758, and 1.590 nM, have been, respectively, shown. Successfully, the simultaneous assessment of the three isomers in river stream water, tap water, and underground water has been implemented via the modified electrode under investigation. In comparison to reported studies, the PdDAN catalytic electrode has shown an effective sensitivity, leverage reproducibility, long-term stability, and excellent anti-interference capability for the determination of dihydroxybenzene isomers.

Simultaneous and selective electrochemical determination of hydroquinone, catechol and resorcinol at poly(1,5-diaminonaphthalene)/glassy carbon-modified electrode in different media.

The electrochemical behavior of phenolic isomers hydroquinone (HQ), catechol (CC) and resorcinol (RC) was examined in poly(1,5-diaminonaphthalene)/glassy carbon-modified electrode (P1,5-DAN/GC M.E.) by cyclic voltammetry (CV), square wave voltammetry (SWV) and chronoamperometry (CA) techniques in perchloric acid (HClO4) and phosphate buffer solution (PBS, pH 7.0). P1,5-DAN/GC M.E. was investigated for simultaneous determination of HQ, CC and RC in single, binary and ternary systems. Oxidation peak potentials were negatively shifted with increasing oxidation peak current for HQ, CC and RC at P1,5-DAN/GC M.E. compared with bare GC electrode. The obtained results illustrate that the former electrode exhibits better performance towards the three isomers in PBS rather than in HClO4 solution. The catalytic currents for different concentrations of HQ, CC and RC showed good relationship in the range of 0.1-100 µM for all analytes and low detection limits (LOD) of 0.034, 0.059 and 0.14 µM for them, respectively, in a ternary system in PBS at pH 7.0. This method has been practically applied for the detection of these isomers in tap water with acceptable results.