Electrochemical Properties of Phytosynthesized Gold Nanoparticles for Electrosensing

Gold nanoparticles are widely used in electrosensing. The current trend is to phytosynthesize gold nanoparticles (phyto-AuNPs) on the basis of the “green” chemistry approach. Phyto-AuNPs are biologically and catalytically active, stable and biocompatible, which opens up broad perspectives in a variety of applications, including tactile, wearable (bio)sensors. However, the electrochemistry of phytosynthesized nanoparticles is not sufficiently studied. This work offers a comprehensive study of the electrochemical activity of phyto-AuNPs depending on the synthesis conditions. It was found that with an increase in the aliquot of the plant extract, its antioxidant activity (AOA) and pH, the electrochemical activity of phyto-AuNPs grows, which is reflected in the peak potential decrease and an increase in the peak current of phyto-AuNPs electrooxidation. It has been shown that AOA is an important parameter for obtaining phyto-AuNPs with desired properties. Electrodes modified with phyto-AuNPs have demonstrated better analytical characteristics than electrodes with citrate AuNPs in detecting uric and ascorbic acids under model conditions. The data about the phyto-AuNPs’ electrochemistry may be useful for creating highly effective epidermal sensors with good biocompatibility.

Measuring Practical Reversibility of Surface-Bound DNA for Mechanistic Insight into Folding-Based Sensors

In this paper, we characterize the mass-transport-limited response of surface-tethered redox moieties via flexible DNA linkers using measured voltammetric peak current and peak potential splitting. We demonstrate that peak splitting can be used to differentiate between reversible, quasi-reversible, and irreversible electrochemical regimes of the tethered redox molecule. Interestingly, the transition from one regime to another is dependent on the length and structure of the DNA probe. For example, as the probe length increases the transition from reversible to quasi-reversible occurs at lower scan rates. Additionally, we directly compare the dependence of the peak splitting and peak current as a function of scan rate for ssDNA, dsDNA, and other structured nucleic acids such as stem-loop and pseudoknot probes. Lastly, we find that by interrogating our surfaces with cyclic voltammetry we can observe quantitative differences in the peak splitting once the aptamer is in a bound state and correlate this to the extent of conformational change the sequence undergoes. The observations reported herein are consistent with the postulation that signaling in this class of sensor architectures is dictated by changes in nucleic acid structure and flexibility, which controls the mass transfer rate of the redox probe to the surface of the electrode.

Electrochemical Frequency Modulation: New Approach and Revision of Previous Model

A careful evaluation of the earlier model (1-2) for electrochemical frequency modulation (EFM) involving two sinusoidal applied potentials for the determination of corrosion parameters shows an algebraic error. Although the missing term in the original derivation appears to be insignificant, it is found that errors involved in corrosion current determination, and especially in evaluation of the Tafel slopes can be very significant, which is of consequence because of the rising popularity of this technique. The magnitude of error is found to be a function of the inherent corrosion characteristics (anodic and cathodic Tafel slopes) of the corroding material as well as the applied peak potential of the modulation. A corrected model with detailed steps showing the appropriate math is presented. In addition, using the experimental data available in the literature, the errors involved in estimating the corrosion parameters by the earlier EFM model of Bosch et al (1-2) are evaluated. The corrected corrosion current and the Tafel slopes can be recovered from the incorrect model without the benefit of the harmonic currents, as shown in this paper.The analysis is also presented for the case of only one applied sinusoidal frequency modulation, which offers several advantages over the multiple frequency modulation.

The Preparation of Au NPs/RGO-MoO 2 Composite Modified Electrode and Simultaneous Detection of Acetaminophen and Dopamine

Dopamine (DA) exists in human body fluids and is the most basic metabolite of the human body, and it is an important neurotransmitter in the central nervous system of animals. Acetaminophen (AMP) is commonly used as cold medicine to treat fever and relieve pain. The safe dosage is very important to human health. Therefore, it is very important to construct an accurate, efficient and fast detection method for detecting AMP and DA. In this paper, Au NPs/RGO-MoO 2 composite modified electrode was prepared for the detection of AMP and DA , We can see that the synergy between RGO-MoO 2 nanomaterials and Au NPs and can promote the electrochemical reaction of AMP and DA, and the oxidation peak potential difference is greater than 180 mV. The linear range of the sensor for detecting AMP is 0.05~320 μmol/L while the linear range of DA is 0.6~260 μmol/L, and the detection limits are 7.2 nmol/L and 13 nmol/L (S/N=3) respectively. The Au NPs/ RGO-MoO 2 /GCE sensor can be used for the detection of AMP and DA in actual samples because of its excellent characteristics such as wide linear range, lower detection limit, excellent reproducibility, stability, and high selectivity

Electro-oxidation of formoterol fumarate on the surface of novel poly(thiazole yellow-G) layered multi-walled carbon nanotube paste electrode

The current study explicates the electro-oxidation behavior of formoterol fumarate (FLFT) in the presence of uric acid (UA) on the surface of poly thiazole yellow-G (TY-G) layered multi-walled carbon nanotube paste electrode (MWCNTPE). The modified (Poly(TY-G)LMWCNTPE) and unmodified (MWCNTPE) electrode materials were characterized through electrochemical impedance spectroscopy (EIS), field emission scanning electron microscopy (FE-SEM), and cyclic voltammetry (CV) approaches. The characterization data confirms the good conducting and electrocatalytic nature with more electrochemical active sites on the Poly(TY-G)LMWCNTPE than MWCNTPE towards the FLFT analysis in the presence of UA. Poly(TY-G)LMWCNTPE easily separates the two drugs (FLFT and UA) even though they both have nearer oxidation peak potential. The electro-catalytic activity of the developed electrode is fast and clear for FLFT electro-oxidation in 0.2 M phosphate buffer (PB) of pH 6.5. The Poly(TY-G)LMWCNTPE offered a well-resolved peak with the highest electro-oxidation peak current at the peak potential of 0.538 V than MWCNTPE. The potential scan rate and oxidation peak growth time studies show the electrode reaction towards FLFT electro-oxidation is continued through a diffusion-controlled step. The variation of concentration of FLFT in the range from 0.2 to 1.5 µM (absence of UA) and 3.0 to 8.0 μM (presence of UA) provides a good linear relationship with increased peak current and a lower limit of detection (LOD) values of 0.0128 µM and 0.0129 µM, respectively. The prepared electrode gives a fine recovery for the detection of FLFT in the medicinal sample with acceptable repeatability, stability, and reproducibility.

Electrical Potentials of Protoscoleces of the Cestode Echinococcus granulosus from Bovine Origin

Larval stages of the tenia Echinococcus granulosus are the infective forms of cystic echinococcosis or hydatidosis, a worldwide zoonosis. The protoscolex that develops into the adult form in the definitive host is enveloped by a complex cellular syncytial tegument, where all metabolic interchange takes place. Little information is available as to the electrical activity of the parasite in this developmental stage. To gain insight into the electrical activity of the parasite at the larval stage, here we conducted microelectrode impalements of bovine lung protoscoleces (PSCs) of Echinococcus granulosus in normal saline solution. We observed two distinct intra-parasitic potentials, a transient peak potential and a stable second potential, most likely representing tegumental and intra-parasitic extracellular space electrical potential differences, respectively. These values changed upon the developmental status of the parasite, its anatomical regions, or time course after harvesting. Changes in electrical potential differences of the parasite provide an accessible and useful parameter for the study of transport mechanisms and potential targets for the development of novel antiparasitic therapeutics .

Performance Evaluation of Extended Aeration-Based Sewage Treatment Plants at NCT of Delhi, India

Due to urbanization and industrialization huge amount of wastewater is being generated, which is causing water pollution. Nowadays water pollution is a serious problem. The present study has been carried out to evaluate the efficiency of a waste water treatment plants with Extended Aeration Sludge Process (EASP). This has been done by examining the various physiochemical characteristics of wastewater (BOD, COD, TSS & PO4), including a comparison of these characteristics at inlet and outlets of wastewater treatment plants and their variance over time. The examination of the competency of a technology is necessary for further optimization of the treatment units whilst complying with the Central Pollution Control Board (CPCB) requirements. In New Delhi’s Extended Aeration Plants are not working to their peak potential, but have still been able to treat the significant wastewater effectively. The study implies that the effluent released into the Yamuna River would not contribute to the river’s level of pollution.

Supramolecular assemblies of carbon nanocoils and tetraphenylporphyrin derivatives for sensing of catechol and hydroquinone in aqueous solution

Non-enzymatic electrochemical detection of catechol (CC) and hydroquinone (HQ), the xenobiotic pollutants, was carried out at the surface of novel carbon nanocoils/zinc-tetraphenylporphyrin (CNCs/Zn-TPP) nanocomposite supported on glassy carbon electrode. The synergistic effect of chemoresponsive activity of Zn-TPP and a large surface area and electron transfer ability of CNCs lead to efficient detection of CC and HQ. The nanocomposite was characterized by using FT-IR, UV/vis. spectrophotometer, SEM and energy dispersive X-ray spectroscopy (EDS). Cyclic voltammetry, differential pulse voltammetry (DPV) and electrochemical impedance spectroscopy were used for the electrochemical studies. CNCs/Zn-TPP/GCE nanosensor displayed a limit of detection (LOD), limit of quantification (LOQ) and sensitivity for catechol as 0.9 µM, 3.1 µM and 0.48 µA µM−1 cm−2, respectively in a concentration range of 25–1500 µM. Similarly, a linear trend in the concentration of hydroquinone detection was observed between 25 and 1500 µM with an LOD, LOQ and sensitivity of 1.5 µM, 5.1 µM and 0.35 µA µM−1 cm−2, respectively. DPV of binary mixture pictured well resolved peaks with anodic peak potential difference, ∆Epa(CC-HQ), of 110 mV showing efficient sensing of CC and HQ. The developed nanosensor exhibits stability for up to 30 days, better selectivity and good repeatability for eight measurements (4.5% for CC and 5.4% for HQ).

Thiourea-Grafted Graphite Felts as Positive Electrode for Vanadium Redox Flow Battery

In this paper, thiourea was successfully grafted onto the surface of acid preprocessed graphite felts [sulfuric acid-treated graphite felt (SA-GFs)] by thiol-carboxylic acid esterification. The thiourea-grafted graphite felts (TG-GFs) were investigated as the positive electrode for vanadium redox flow battery (VRFB). X-ray photoelectron spectroscopy results suggested that thiourea was grafted into the surface of graphite felts. The cyclic voltammetry showed that the peak potential separation decreased by 0.2 V, and peak currents were greatly enhanced on TG-GF electrode compared with SA-GF electrode, implying improved electro-catalytic activity and reversibility of TG-GF electrode toward VO2+/VO2+ redox reaction. The initial capacity of TG-GF-based cell reached 55.6 mA h at 100 mA cm−2, 22.6 mA h larger than that of SA-GF-based cell. The voltage and energy efficiency for TG-GF-based cell increased by 4.9% and 4.4% compared with those of SA-GF-based cell at 100 mA cm−2, respectively.

Synthesis and characterization of terthiophene bearing stable radicals

The synthesis and characterization of a new terthiophene bearing stable radical II is described. Through a cross coupling reaction between 2-tributylstannylthiophene and 6-(2,5-dibromo-thiophene-3-yl)pyridine-2-carboxaldehyde (2), 6-[2,2′:5′,2″]terthiophen-3′-ylpyridine-2-carboxaldehyde (3) was prepared. The condensation of 3 with 2, 4-diisopropylcarbonohydrazide bis-hydrochloride affords the heterocyclic tetrazane (4), which was oxidized with 1,4-benzoquinone to form the stable radical II. II characterized by IR, ESR, and cyclic voltammetry. Oxidative electropolymerization of II and its precursor 4 at oxidation peak potential of the terthiophene using cyclic voltammetric scans produces radical functionalized polyterthiophene on a platinum electrode (poly(II)-Pt).