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Due to the dearth of extremely capable, sensitive, and stable catalysts, the efficient detection and catalytic removal of 4-nitrophenol (4-NP) in industrial wastewater remains a serious challenge. The detection and determination of 4-nitrophenol (4-NP) presence in the environment is a matter of paramount importance because it is a high-priority hazardous pollutant that can affect people, animals, and plants. Here, we present a promising and economically viable green synthetic route for fabricating CuFe2O4 and CuFe2O4@Ag hybrid nanocomposites from the leaf extract of Senna didymobotrya. The UV–Vis, FTIR, XRD, FE-SEM, EDXA, BET and VSM analysis were performed to characterize the synthesis of CuFe2O4@Ag nanocomposite. To evaluate the electrocatalytic capacity of CuFe2O4@Ag, electrochemical sensing stratergy was performed with cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The modified CuFe2O4@Ag glassy carbon electrode (GCE) (CuFe2O4@Ag/GCE) demonstrated a linear response in the range of 0.01-15 μg/ml (71 nm-107 μM) and the ability to detect 4-NP at low concentration (0.006 μg/ml (43 nM)). Due to the increased surface area of CuFe2O4@Ag/GCE by ̴ 1.5-fold, a greater cathodic current response (-16 μA/cm2) at a low potential of -0.81 V was observed compared to CuFe2O4/GCE alone for the detection of 4-NP. Additonally, CuFe2O4@Ag showed excellent reduction ability towards 4-NP using NaBH4 with an efficiency of 96.4 % which was higher than the CuFe2O4 (only 87.3 %) in 12 min due to the synergistic relationship among Ag NPs and CuFe2O4 nanostructures. The outcomes from this study shows that the bi-functional electrocatalyst holds vast potential for environmental remediation.

This work demonstrates recent advancements in the phytosynthetic and environmentally friendly method of preparing ZnFe2O4 and ZnFe2O4@Ag hybrid nanocomposites using Pedalium murex L leaf extract as a stabilizing and reducing agent. The synthesized nanocomposite was characterized with UV–vis, FTIR, TGA/DSC, XRD, FE-SEM, and EDX to investigate the electronic as well as morphological properties. Moreover, the photocatalytic behaviour of ZnFe2O4 and ZnFe2O4@Ag hybrid nanocomposites was evaluated with a breakdown of 2,4-dichlorophenoxyacetic acid (2,4-DPA) by exposing to UV–Vis light. The results obtained suggest that ZnFe2O4@Ag hybrid nanocomposite exhibited photocatalytic activity for the degradation of 2,4-DPA by approximately 94% in 60 min compared to ZnFe2O4. The hybrid nanostructure of ZnFe2O4@Ag significantly promoted charge transfer and prevented electron and hole recombination resulting in the enhancement of photocatalytic activity. Furthermore, ZnFe2O4@Ag nanocomposite showed the fair recyclable capacity for up to five catalytic cycles with an acceptable degradation percentage of 2,4-DPA. The findings of this study identify efficient charge transfer factor as a major contributor to the catalytic activity, with promising possibilities for the design of environmental remediation nanocomposite for harmful contaminants.

Iron oxide-Copper oxide nanoparticles composite (Fe2O3CuO NPs) was synthesized through a green phytosynthetic approach using Ocimum sanctum Linn (commonly known as Tulsi) leaf extract. The evaluation of electrocatalytic properties were evaluated by carrying out electrochemical detection of amiprofos-methyl (APM), an organophosphorus herbicide. It is moderately toxic to mammals and aquatic biodiversity and is considered to be an acetylcholinesterase inhibitor. The presence of specific natural phytochemicals such as eugenol, naringenin, apigenin, quercetin, and high amount of ascorbic acid in the aqueous extract of Ocimum sanctum Linn plant parts, has been widely used for the synthesis of various metallic nanoparticles where these compounds serve as reducing, stabilizing, and capping agents. The synthesized Fe2O3CuO NPs were characterized using scanning electron microscope (SEM), energy dispersive X-ray analysis (EDX), X-ray diffraction analysis (XRD), UV–Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR) and thermogravimetric analysis (TGA). The modified electrode was electrochemically characterized by cyclic voltammetry and differential pulse voltammetry (DPV) techniques for the detection of APM. The electrochemical signals have increased by three folds in the detection of APM with Fe2O3CuO nanocomposite compared to the bare glassy carbon electrode. The electrochemical sensor showed a linear range of 0.05 to 30 µg/mL with a limit of detection of 0.0065 µg/mL. The developed electrochemical sensor was successfully applied for the detection of APM in different water and soil samples with recoveries ranging from 96.00−99.00%. The electrode showed good stability and reproducibility over a period of 10 days with a 95% of peak current than the former. The newly synthesized nanoparticles, thus, proved to be an interesting material for electrochemical and biological studies.

Butachlor is a herbicide that belongs to the acetanilide family. It is widely used as a granule-based post-emergence herbicide on rice in India. As a result of the ongoing usage of these synthetic substances, soil fertility and soil organisms are declining. Differential pulse voltammetry was used to determine butachlor herbicide in soil samples with a modified glassy carbon electrode voltammetric sensor with palladium-supported multiwalled carbon nanotubes (Pd@MWCNTs). Scanning electron microscopy, energy dispersive x-ray spectroscopy, and X-ray diffraction spectroscopy were used to investigate the morphology of Pd@MWCNTs, while cyclic and differential pulse techniques were used to investigate the voltammetric properties. The butachlor herbicide under voltammetric investigation involves irreversible, two-electron reduction based on the protonation of the carbonyl group (>C=O). The voltammetric method was developed for the determination of butachlor in phosphate buffer solution at pH 6.0 as a supporting electrolyte. A good linear response to butachlor in the concentration ranging from 0.10 μg⸳mL−1 to 32.0 μg⸳mL−1 was observed, and a limit of detection of 0.044 μg⸳mL−1 was obtained with the calculation based on signal/noise=3. The suggested method was efficaciously applied for the detection of butachlor in soil samples.

The goal of this research is to increase the performance of AA 7150 reinforced with TiO2 microparticles by optimizing the stir casting parameters. The response surface method's central composite design technique was used to optimize the three stir casting factors of stirring temperature (A), stirring speed (B), and stirring time (C). The ultimate tensile strength, hardness, impact strength, elastic modulus, and compressive strength were all tested. With the aid of analysis of variance, it was discovered that it had a substantial influence on the test samples' characteristics responses. 5 quadratic experiments were linked using factors' characteristics. At a level of 95% confidence, the models were found to be statistically important, and the variations were found to be less than 5%. The response surface was used to assess the parameter interaction profile. Each interaction's contour plots provided a range of stirring settings within which each property may be maximized. [ABSTRACT FROM AUTHOR]

Zinecard is used to prevent a toxic effect to heart caused by certain medicines that are used to treat cancer. Zinecard is also used to treat tissue damage caused by the leakage of certain medicines that are used to treat cancer. Differential pulse polarographic method developed for the quantitative determination of zinecard gives a peak at -0.32 V at DME. From the structural point of view zinecard contains a >C=O- moiety which can be electrochemically reduced at universal buffer (pH 4.0). Millicoulometric experiment is performed successfully in estimating the number of electrons and proton to understand reduction mechanism. The differential pulse polarographic peak was adequately well-resolved, reproducible and linear dependent with the zinecard concentration. For quantification the calibration plot for zinecard concentrations ranging between 1.0×10-5 mol dm-3 to 1.0×10-8 mol dm-3 at pH 4.0 was selected. The proposed differential pulse polarographic method was successfully applied to the determination of zinecard in pharmaceutical formulations and urine samples. [ABSTRACT FROM AUTHOR]