A NiO-nanostructure-based electrochemical sensor functionalized with supramolecular structures for the ultra-sensitive detection of the endocrine disruptor bisphenol S in an aquatic environment.

Herein, NiO nanoparticles (NPs) functionalized with a para-hexanitrocalix[6]arene derivative (p-HNC6/NiO) were synthesized by using a facile method and applied as a selective electrochemical sensor for the determination of bisphenol S (BPS) in real samples. Moreover, the functional interactions, phase purities, surface morphologies and elemental compositions of the synthesized p-HNC6/NiO NPs were investigated via advanced analytical tools, such as Fourier-transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). Additionally, the synthesized p-HNC6/NiO NPs were cast on the surface of a bare glassy carbon electrode (GCE) via a drop casting method, which resulted in uniform deposition of p-HNC6/NiO/GCE over the surface of the GCE. Additionally, the developed p-HNC6/NiO/GCE sensor demonstrated an outstanding electrochemical response to BPS under optimized conditions, including a supporting electrolyte, a Briton-Robinson buffer electrolyte at pH 4, a scan rate of 110 mV s-1 and a potential window of between -0.2 and 1.0 V. The wide linear dynamic range was optimized to 0.8-70 µM to obtain a brilliant linear calibration curve for BPS. The limit of detection (LOD) and limit of quantification (LOQ) of the developed sensor were estimated to be 0.0059 and 0.019 µM, respectively, which are lower than those of reported sensors for BPS. The feasibility of the developed method was successfully assessed by analyzing the content of BPS in waste water samples, and good recoveries were achieved.

Fabrication of para-dimethylamine calix[4]arene functionalized self-assembled graphene oxide composite material for effective removal of 2, 4, 6-tri-Cholorphenol from aqueous environment.

Water pollution caused by the release of organic pollutants is a major environmental concern worldwide. These pollutants can have harmful effects on aquatic ecosystems and the organisms living within them, as well as on human health when contaminated water is consumed. It is essential to implement proper treatment and management strategies to prevent and mitigate water pollution. Moreover, the major untreated industrial effluents are synthetic organic compounds especially 2,4,6-trichlorophenol (TCP) which cause several environmental issues and heath related problems in humans. To cope with this problem, an excellent 2D porous material based on p-DMAC4/GO composite has been synthesized as adsorbent material for the effective removal of 2,4,6-trichlorophenol pollutant from wastewater. In this regard, the advanced analytical tools such as Fourier-Transform infrared (FT-IR), X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy-Dispersive X-ray spectroscopy (EDS) were used for its characterization. The results justified the chemical composition, excellent crystalline nature, surface morphology and elemental composition of the synthesized composite material. The synthesized adsorbent material showed 95% adsorption of TCP from wastewater system at optimal conditions i.e., pH (6), adsorbent dosage (30 mg) and shaking time (60 min). The mathematical models such as isotherms, thermodynamics and kinetics studies validate the nature of adsorption process of TCP pollutant. The adsorption data found to be best fitted with Langmuir isotherms (R2 = 0.99); whereas kinetic study suggested the pseudo-second-order nature of reaction with R2 = 0.99. The thermodynamics study confirmed the spontaneous and endothermic nature of the TCP pollutant onto the surface of p-DMAC4/GO material. Moreover, the results of current work were also compared with existing reported adsorbents and data suggested the higher efficiency, feasibility, and reusability of p-DMAC4/GO material to remove the TCP pollutant from the wastewater system.

Exploring the Mechanism of Anionic Chemosensing by Imidazoles: A Review.

Chemosensing of ions has gained considerable attention by chemists. Insight into the mechanism involved between sensors and ions always fascinates researchers to develop economical, sensitive, selective, and robust sensors. This review comprehensively explores the mechanism of interaction between Imidazole sensors and anions. With most of the research concentrating only on fluoride and cyanide, this review has highlighted a large gap in various anions detection including SCN-, Cr2O72-, CrO42-, H2PO4-, NO2-, and HSO4-.This study also includes a critical analysis of different mechanisms and their respective limits of detection, with a discussion of the reported results.

Sulfonamides as Optical Chemosensors.

Sulfonamides are auspicious chemosensors which are capable to bind with ionic species through various ways like complexation, charge transfer, proton transfer etc. and produce a detection signal in the form of an optical change either in visible or UV-light and for electronic as well as fluorimetric spectra. Sulfonamides have gained much attention of analytical chemists these days as these are inexpensive, robust, green in nature and some what sensitive and selective to many anionic and cationic species. Due to their promising versatility in sensing properties, these are under great consideration in forensic, environmental, analytical and biochemistry laboratories. This review narrates how sulfonamides are being used to optically sense ionic species.

HIGHLIGHTSOptical sensors are of great importance these days because of their optical detection properties rather using Hi-tech techniques.Optical sensors are economical, robust, selective, sensitive and green in nature.The color change, shifts in electronic spectra or alterations in fluorescence pattern may be attributed by interaction between species to be sensed and Sulfonamides by different mechanism i.e. electron transfer, fluorescence energy transfer, charge transfer, hydrogen bonding, etc.LOD data is a proof of their prodigious efficiency of Sulfonamides as optical sensors.

Carbon dots as naked eye sensors.

Optical sensors are always fascinating for chemists due to their selectivity, sensitivity, robustness and cost-effective nature. Moreover, these sensors provide the facility of onsite detection without employing any instrumental technique. A number of such visual sensors including carbon dots (CDs) have been reported for selective detection of many ionic and molecular species. This review elaborates the utilization of CDs as colorimetric sensors. Carbon dots (CDs) are being synthesized from a large number of natural and synthetic carbon source materials using a variety of methods. CDs can also be tuned chemically by doping, to impart the desired sensing properties. Therefore, the development of CDs with selective sensing properties enables extremely low detection limits and has thus gained substantial attention.

Phosphomolybdate-doped-poly(3,4-ethylenedioxythiophene) coated gold nanoparticles: synthesis, characterization and electrocatalytic reduction of bromate.

Phosphomolybdate, H3PMo12O40, (PMo12)-doped-poly(3,4-ethylenedioxythiophene) (PEDOT) coated gold nanoparticles have been synthesized in aqueous solution by reduction of AuCl4(-) using hydroxymethyl EDOT as a reducing agent in the presence of polystyrene sulfonate and PMo12. The resulting PMo12-doped-PEDOT stabilized Au nanoparticles are water soluble and have been characterized by UV-visible spectroscopy, scanning electron microscopy and electrochemistry. Glassy carbon electrodes modified with these Au nanoparticles show excellent stability and catalytic activity towards the reduction of bromate in an aqueous electrolyte solution containing 10mM H2SO4 and 0.1M Na2SO4.

Development and implication of a capillary electrophoresis methodology for ciprofloxacin, paracetamol and diclofenac sodium in pharmaceutical formulations and simultaneously in human urine samples.

This work studies the development of a simple and fairly rapid methodology for simultaneous determination/separation of three frequently co-administered drugs; ciprofloxacin (CIP), paracetamol (PCT) and diclofenac sodium (DIC) using capillary electrophoresis (CE) with UV detection at 260 nm. Separation was achieved in only 6.5 min with a simple buffer of sodium tetraborate (50 mM) at pH 9.0. The Parameters affecting the separation and detection were optimized. The calibration curves were linear in the range of 5-500 µg/mL for CIP, 5-250 µg/mL for PCT and 1-125 µg/mL for DIC sodium under the optimized conditions. The lower limit of detection (LOD) was found to be 1 µg/mL for CIP & PCT and 0.5 µg/mL for DIC. The method was successfully used for the analysis of drugs in commercial pharmaceutical formulations and simultaneously from patient's urine sample with RSD 0.5-2.4%. Results obtained with CE method are compared with standard HPLC procedure and were found in good agreement.

Ultra-fast catalytic reduction of dyes by ionic liquid recoverable and reusable mefenamic acid derived gold nanoparticles.

We synthesized mefenamic acid (MA) derived gold nanoparticles (MA-AuNps) in aqueous solution (MA-Au sol). Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) of the sol at 1, 5, 15 and 60 min showed changes in size and shape of formed AuNps. Fourier Transform Infrared (FTIR) Spectroscopy revealed the interaction between AuNps and MA. Each Au sol exhibited exceptional catalytic activity for the reduction of Methylene Blue (MB), Rose Bengal (RB) and Eosin B (EB) dye individually as well as collectively. However, complete reduction of dye(s) was accomplished by Au sol of 5 min in just 15s. The catalytic performance of Ma-Au sol was far superior to that adsorbed on glass. AuNps were recovered with the help of water insoluble room temperature ionic liquid and reused with enhanced catalytic potential. This finding is a novel, rapid and highly economical alternative for environmental safety against pollution by dyes and extendable for control of other reducible contaminants as well.