Photocatalytic degradation technology has received much attention from researchers in the last few decades, due to its easy and cost-effective nature. A lot of review articles have been published on dyes via photocatalytic degradation, but most of the review articles lack a detailed and in-depth photocatalytic degradation mechanism of dyes. Numerous review articles are available on photocatalysis. Here, in this review article, we are mainly focused on the complete and in-depth photocatalytic degradation mechanism of four commonly used dyes such as Malachite Green, Methylene Blue, Congo Red and Rhodamine B, which will be highly useful for the new researchers that work on dyes’ photocatalytic degradation. Initially, various aspects of dyes have been included in this review article, comprehensively. The main focus was on the covalent organic framework-based photocatalysts for dyes’ photocatalytic degradation, due to their porous nature and various unique properties. Various synthesis routes and the photocatalytic performance of covalent organic frameworks and composite of covalent organic frameworks have been highlighted in this review article. In the last section of this review article, the main stimulus was the four mentioned dyes’ properties, uses, and toxicity, and the photocatalytic degradation mechanism through various paths into environmentally friendly and less-harmful compounds in the presence of photocatalysts. Factors effecting the photocatalytic degradation, economic cost, challenges and future aspects of photocatalytic technology were also included in this review article. This review article will be highly useful for those researchers that work on the photocatalytic degradation of various dyes and search for the complete degradation of complex dye molecules.

Eriochrome Black T (EBT) is mutagenic and carcinogenic, and thus its presence in water may result in severe illnesses. This study was aimed at adsorbing EBT from simulated water samples by using a batch adsorption process, onto native (GP) and washed garlic peel (WGP). Surface and structural characterization of native and washed GP was performed using FTIR, SEM, BET, and BJH analysis. The effects of several parameters, affecting the process of adsorption, like pH, temperature, contact time, adsorbent dose, and initial dye concentration, were also examined. Freundlich and Langmuir isotherms were applied to the equilibrium data. Pseudo-first and pseudo-second order models were used to study the adsorption kinetics. The Langmuir isotherm and pseudo-second order model perfectly explained the equilibrium data. ΔG°, ΔH°, ΔS° studies indicated that adsorption of EBT onto GP and WGP was a favorable, spontaneous, and physical process. Maximum dye removal by GP (96%) and WGP (82%) was observed at pH 2. Similarly Maximum adsorption capacities were found to be 99.5 mg/g and 89.4 mg/g for GP and WGP, respectively. It is concluded from these results that garlic peel can be used as a cheaper and more efficient material for the adsorptive removal of EBT from contaminated water samples.

The outbreak of SARS-CoV-2, also known as the COVID-19 pandemic, is still a critical risk factor for both human life and the global economy. Although, several promising therapies have been introduced in the literature to inhibit SARS-CoV-2, most of them are synthetic drugs that may have some adverse effects on the human body. Therefore, the main objective of this study was to carry out an in-silico investigation into the medicinal properties of Petiveria alliacea L. (P. alliacea L.)-mediated phytocompounds for the treatment of SARS-CoV-2 infections since phytochemicals have fewer adverse effects compared to synthetic drugs. To explore potential phytocompounds from P. alliacea L. as candidate drug molecules, we selected the infection-causing main protease (Mpro) of SARS-CoV-2 as the receptor protein. The molecular docking analysis of these receptor proteins with the different phytocompounds of P. alliacea L. was performed using AutoDock Vina. Then, we selected the three top-ranked phytocompounds (myricitrin, engeletin, and astilbin) as the candidate drug molecules based on their highest binding affinity scores of −8.9, −8.7 and −8.3 (Kcal/mol), respectively. Then, a 100 ns molecular dynamics (MD) simulation study was performed for their complexes with Mpro using YASARA software, computed RMSD, RMSF, PCA, DCCM, MM/PBSA, and free energy landscape (FEL), and found their almost stable binding performance. In addition, biological activity, ADME/T, DFT, and drug-likeness analyses exhibited the suitable pharmacokinetics properties of the selected phytocompounds. Therefore, the results of this study might be a useful resource for formulating a safe treatment plan for SARS-CoV-2 infections after experimental validation in wet-lab and clinical trials.

This comprehensive review extensively explores the potential applications of MXenes as versatile materials in the realm of photocatalysis, with a specific focus on their efficacy in mitigating hazardous dyes and CO₂ to less harmful and friendly by-products. The review systematically investigates the unique properties that render MXenes well-suited for photocatalytic purposes and provides a thorough examination of their current state of research. It meticulously summarizes the successes and breakthroughs achieved thus far, offering insights into the advancements that have propelled these materials into the spotlight of photocatalytic research. In addition to highlighting achievements, the review critically addresses the challenges and hurdles that impede the full realization of the potential inherent in MXenes. Here, we have also highlighted the stability problem of MXenes and how to overcome this problem for efficient photocatalysis. The mechanism of photocatalysis was also the main theme of this review article and how to overcome the recombination of photogenerated charges. By identifying these challenges, the review serves as a valuable resource for researchers, providing a roadmap for future endeavours to unlock the untapped capabilities of these materials. It serves as a beacon for environmental researchers, offering valuable insights into the pivotal role these materials can play in creating a more environmentally friendly and safe world. Ultimately, this review contributes significantly to the collective knowledge base and will prove instrumental for researchers and professionals dedicated to environmental protection and sustainable living. Graphical Abstract

Fluorinated heterocycles have attracted extensive attention not only in organic synthesis but also in pharmaceutical and medicinal sciences due to their enhanced biological activities than their non-fluorinated counterparts. Triazole is a simple five-membered heterocycle with three nitrogen atoms found in both natural and synthetic molecules that impart a broad spectrum of biological properties including but not limited to anticancer, antiproliferative, inhibitory, antiviral, antibacterial, antifungal, antiallergic, and antioxidant properties. In addition, incorporation of fluorine into triazole and its derivatives has been reported to enhance their pharmacological activity, making them promising drug candidates. This mini-review explores the current developments of backbone-fluorinated triazoles and functionalized fluorinated triazoles with established biological activities and pharmacological properties.