The perovskite structure is shown to be the single most versatile ceramic host. Inorganic perovskite type oxides are attractive compounds for varied applications due to its large number of compounds, they exhibit both physical and biochemical characteristics and their Nano-formulation have been utilized as catalysts in many reaction due to their sensitivity, unique long-term stability and anti-interference ability. Some perovskites materials are very hopeful applicants for the improvement of effective anodic catalysts performance. Depending Perovskite-phase metal oxides distinct variety of properties they became useful for various applications they are newly used in electrochemical sensing of alcohols, glucose, hydrogen peroxide, gases, and neurotransmitters. Perovskite organometallic halide showed efficient essential properties for photovoltaic solar cells. This review presents a full coverage of the structure, progress of perovskites and their related applications. Stress is focused particularly to different methods of perovskites properties and there related application.

A facile bottom-up “green” synthetic route of gold nanoparticles (Au NPs) is described, using a leaf extract of the Malvaceae plant Corchorus olitorius as a reducing and stabilizing agent. The size and shape of the obtained nanoparticles were modulated by varying the amounts of the metal salt and the broth extract in the reaction medium. Only one hour was required for the complete conversion to Au NPs, suggesting that the reaction rate was higher or comparable to those of nanoparticles synthesized by chemical methods. The obtained nanoparticles were characterized by UV–visible spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, and thermal gravimetric analysis (TGA). While infrared spectroscopy was employed to characterize the various functional groups in the organic layer that stabilized the particles, TEM images were used to optimize the conditions for NPs growth. A low concentration of the C. olitorius extract yielded mixed triangular and hexagonal shapes; in contrast, quasi-spherical shapes of Au NPs with an average size of 37–50 nm were obtained at a higher extract broth concentration. The Au NPs displayed Surface Plasmon Resonance (SPR) bands at 535 nm. An in vitro cytotoxic assay of the biocompatible Au NPs revealed a strong cytotoxic activity in three human cancer cell lines, namely, colon carcinoma HCT-116, hepatocellular carcinoma HepG-2, and breast adenocarcinoma MCF-7. In-silico bioactivity, drug-likeness, and ADMET (Absorption, Distribution, Metabolism, Excretion, and Toxicity) predictions were conducted in order to examine the pharmacokinetic behavior of the compounds present in the C. olitorius extract.

A series of novel pyridine and fused pyridine derivatives have been prepared starting from 6-(3,4-dimethylphenyl)-2-hydrazinyl-4-(thiophen-2-yl)-pyridine-3-carbonitrile 1 which on treatment with appropriate formic acid, acetic acid/acetic anhydride, benzoyl chloride and/or carbon disulfide afforded the corresponding triazolopyridine derivatives 2–5. Also, treatment of hydrazide 1 with diethyloxalate, chloroacetyl chloride, chloroacetic acid and/or 1,2-dichloroethane yielded the corresponding pyridotriazine derivatives 7–10. Further transformation of compound 1 with a different active methylene group, namely acetyl acetone, diethylmalonate, ethyl cyanoacetate, ethyl benzoylacetate and/or ethyl acetoacetate, produced the pyridine–pyrazole hybrid derivatives 11–15. These newly synthesized compounds (1–15) were subjected to in silico molecular docking screenings towards GlcN-6-P synthase as the target protein. The results revealed moderate to good binding energies of the ligands on the target protein. All the newly prepared products exhibited antimicrobial and antioxidant activity.

This review provides a critical and technically grounded assessment of continuous electrocoagulation processes (CEPs) for the treatment of industrial inorganic pollutants, emphasizing recent innovations, methodological developments, and practical outcomes. A comprehensive literature survey indicates that 53 studies published over the past 25 years have investigated CEPs for inorganic contaminant removal, with 36 focusing on standalone electrocoagulation systems and 17 exploring integrated CEPs approaches. Recent advancements in reactor design, such as enhanced internal mixing, optimized electrode geometry, and modular configurations, have significantly improved treatment efficiency, scalability, and operational stability. Evidence indicates that CEPs can achieve high removal efficiencies for a wide range of inorganic contaminants, including fluoride, arsenic, heavy metals (e.g., chromium, lead, nickel, iron), nitrates, and phosphates, particularly under optimized operating conditions. Compared to conventional treatment methods, CEPs offer several advantages, such as simplified operation, reduced chemical consumption, lower sludge generation, and compatibility with renewable energy sources and complementary processes like membrane filtration, flotation, and advanced oxidation. Despite these promising outcomes, industrial-scale implementation remains constrained by non-standardized reactor designs, variable operational parameters, electrode passivation, high energy requirements, and limited long-term field data. Furthermore, few studies have addressed the modeling and optimization of integrated CEPs systems, highlighting critical research gaps for process enhancement and reliable scale-up. In conclusion, CEPs emerge as a novel, adaptable, and potentially sustainable approach to industrial inorganic wastewater treatment. Its future deployment will rely on continued technological refinement, standardization, validation under real-world conditions, and alignment with regulatory and economic frameworks.

Production of biochar is accomplished by pyrolysis of corncobs at 350 °C (BC-350) and 450 °C (BC-450) under oxygen-limited conditions. The chemical and physical properties were investigated via XRD, FTIR, BET, SEM and EDX analysis. Batch experiments were conducted for the adsorption of Pb²⁺ ions from aqueous solution onto biochar with regards to pH, contact time, biochar dose and initial Pb²⁺ concentration. The adsorption efficiency of Pb²⁺ was increased as increasing pH and biochar dose up to 1.5 g/L. Kinetic and isothermal studies demonstrated that the experimental data were fitted with the pseudo-second-order model, Langmuir and Freundlich isotherms. The study emphasized the preferable pyrolysis temperature which is 450 °C. According to the Dubinin-Kaganer-Radushkevich (DKR) model, the adsorption process of Pb²⁺ was a chemical and endothermic reaction. Results showed the applicability of corncob based biochar to be used as an efficient and low cost adsorbent for Pb²⁺ ions removal.