Cutting-edge developments in MXene-derived functional hybrid nanostructures: A promising frontier for next-generation water purification membranes.

A novel family of multifunctional nanomaterials called MXenes is quickly evolving, and it has potential applications that are comparable to those of graphene. This article provides a current explanation of the design and performance assessment of MXene-based membranes. The production of MXenes nanosheets are first described, with an emphasis on exfoliation, dispersion stability, and processability, which are essential elements for membrane construction. Further, critical discussion is also given to MXenes potential applications in Vacuum assisted filtration, casting method, Hot press method, electrospinning and electrochemical deposition and layer-by-layer assembly for the creation of MXene and MXene derived nanocomposite membranes. Additionally, the discussion is carried forward to give an insight to the modification methods for the construction of MXene-based membrane are described in the literature, including pure or intercalated nanomaterials, surface modifiers and miscellaneous two-dimensional nanomaterials. Furthermore, the review article highlights the potential utilization of MXene and MXene based membranes in separation and purification processes including removal of small organic molecules, heavy metals, oil-water separation and desalination. Finally, the perspective use of MXenes strong catalytic activity and electrical conductivity for specialized applications that are difficult for other nanomaterials to accomplish are discussed in conclusion and future prospectus section of the manuscript. Overall, important information is given to help the communities of materials science and membranes to better understand the potential of MXenes for creating cutting-edge separation and purification membranes.

Electrochemical nitrate reduction over bimetallic Pd-Sn nanocatalysts with tunable selectivity toward benign nitrogen.

Nitrate is recognized as a highly impactful water contaminant among various pollutants in water. To address the ever-growing demand for water purification, this work investigates the bimetallic palladium (Pd) and tin (Sn) catalysts, which are electrochemically deposited on stainless steel mesh support (Pd-Sn/SS) for the selective conversion of harmful nitrate (NO3-) into benign nitrogen (N2) gas. Results indicate that the bimetallic composition in Pd-Sn/SS electrodes substantially influenced the reaction route for nitrate reduction as well as the performance of nitrate transformation and nitrogen selectivity. It is found that the electrode prepared from Pd:Sn = 1:1 (mole ratio) demonstrates an outstanding nitrate conversion of 95%, nitrogen selectivity of 88%, and nitrogen yield of 82%, which outperform many reported values in the literature. The electrochemically synthesized bimetallic electrode proposed herein enables a new insight for promoting the reactivity and selectivity of nitrate reduction in water.

Graphitic carbon nitride derived probes for the recognition of heavy metal pollutants of environmental concern in water bodies.

Graphitic carbon nitride (g-CN) has a number of valuable features that have been recognized during the studies related to its photocatalytic activity enhancement derived by visible light. Because of these characteristics, g-CN can be used as a detecting signal transducer with different transmission modalities. The latest up-to-date detection capabilities of modified g-CN nanoarchitectures are covered in this study. The structural features and synthetic methodologies have been discussed in a number of reports. Herein, employment of the g-CN as a promising probing modality for the recognition of different toxic heavy metals is the promising feature of the present study.

Guar gum-based stimuli responsive hydrogels for sustained release of diclofenac sodium.

In the current study, hydrogels for the controlled release of diclofenac sodium were synthesized from graphene oxide-reinforced guar gum and poly (N-vinyl-2-pyrrolidone) using the Solution Casting Technique. Varying concentrations of 3-Glycidyloxypropyl trimethoxysilane (GLYMO) were employed for the crosslinking of hydrogels. Further, the characterization of hydrogels was carried out using different techniques such as Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction, thermal analysis and scanning electron microscope. The FTIR investigations reveals particular functionalities and development of hydrogel interfaces. While thermal analysis prophesied that, improvement in forces among hydrogel components is directly proportional to the GLYMO concentration. In-vitro biodegradation test and cell viability assay against HEK-293 cell lines confirmed their biodegradable and biocompatible nature. GPG-32 demonstrated maximum antibacterial activity against P.aeruginosa and E.coli strains. The maximum swelling 2001 % and 1814 % in distilled water were recorded for GPG (control) and GPG-8 respectively that obeyed Fick's law. Hydrogels displayed high swelling responses at pH 6 in buffer and non-buffer solutions. In 2.5 h, 88.7 % diclofenac sodium was released which was determined by UV visible spectrophotometer. In conclusion, guar gum-based non-toxic, biocompatible and biodegradable hydrogels would be a model platform for targeting inflammation and pains. Furthermore, improved mechanical and viscoelastic behavior of hydrogels could also be explored for making drug loaded dressings for wound healing applications.

Organic Covalent Interaction-based Frameworks as Emerging Catalysts for Environment and Energy Applications: Current Scenario and Opportunities.

The term "covalent organic framework" (COF) refers to a class of porous organic polymeric materials made from organic building blocks that have been covalently bonded. The preplanned and predetermined bonding of the monomer linkers allow them to demonstrate directional flexibility in two- or three-dimensional spaces. COFs are modern materials, and the discovery of new synthesis and linking techniques has made it possible to prepare them with a variety of favorable features and use them in a range of applications. Additionally, they can be post-synthetically altered or transformed into other materials of particular interest to produce compounds with enhanced chemical and physical properties. Because of its tunability in different chemical and physical states, post-synthetic modifications, high stability, functionality, high porosity and ordered geometry, COFs are regarded as one of the most promising materials for catalysis and environmental applications. This study highlights the basic advancements in establishing the stable COFs structures and various post-synthetic modification approaches. Further, the photocatalytic applications, such as organic transformations, degradation of emerging pollutants and removal of heavy metals, production of hydrogen and Conversion of carbon dioxide (CO2 ) to useful products have also been presented. Finally, the future research directions and probable outcomes have also been summarized, by focusing their promises for specialists in a variety of research fields.

Metal organic frameworks as promising sensing tools for electrochemical detection of persistent heavy metal ions from water matrices: A concise review.

Water bodies are being polluted rapidly by disposal of toxic chemicals with their huge entrance into drinking water supply chain. Among these pollutants, heavy metal ions (HMIs) are the most challenging one due to their non-biodegradability, toxicity, and ability to biologically hoard in ecological systems, thus posing a foremost danger to human health. This can be addressed by robust, sensitive, selective, and reliable sensing of metal ions which can be achieved by Metal organic frameworks (MOF) based electrochemical sensors. In the present era, MOFs have caught greater interest in a variety of applications including sensing of hazardous pollutants such as heavy metal ions. So, in this review article, types, synthesis and working mechanism of MOF based sensors is explained to give general overview with updated literature. First time, detailed study is done for sensing of metal ions such as chromium, mercury, zinc, copper, manganese, palladium, lead, iron, cadmium and lanthanide by MOFs based electrochemical sensors. The use of MOFs as electrochemical sensors has attractive success story along with some challenges of the area. Considering these challenges, we attempted to highlight the milestone achieved and shortcomings along with future prospective of the MOFs for employing it in electrochemical sensing devices for HMIs. Finally, challenges and future prospects have been discussed to promote the development of MOFs-based sensors in future.

Parametric optimization and structural feature analysis of humic acid extraction from lignite.

Humic acid (HA) is a complex organic compound made up of small molecules. A variety of raw materials are used to manufacture HA, due to which the structure and composition of HA vary widely. In this study, nitric acid oxidation of two coal samples from Lakhra (Pakistan) was followed by HA extraction using 2.5, 3.0 and 3.5% KOH solutions. The impact of different operating parameters such as; the effect of KOH concentrations, KOH-coal proportion, extraction time and pH range influencing the HA extraction efficiency was optimally investigated. Commercial HA applications possess numerous challenges, including valuable applications and sub-optimal extraction techniques. A significant limitation of conventional experimental methods is that they can only investigate one component at a time. It is necessary to improve the current processing conditions, this can only be achieved by modelling and optimization of the process conditions to meet market demands. A comprehensive evaluation and prediction of HA extraction using Response Surface Methodology (RSM) are also being reported for the first time in this study. The maximum HA extraction efficiency of 89.32% and 87.04% for coal samples 1 and 2 respectively was achieved with the lowest possible pH of 1.09 (coal sample 1) and 1(coal sample 2), which is remarkably lower as compared to those reported in the literature for conventional alkaline extraction process. The model was evaluated for two coal samples through the coefficient of determination (R2), Root Means Square Error (RMSE), and Mean Average Error (MEE). The results of RSM for coal sample 1 (R2 = 0.9795, RMSE = 4.784) and coal sample 2 (R2 = 0.9758, RMSE = 4.907) showed that the model is well suited for HA extraction efficiency predictions. The derived humic acid from lignite coal was analyzed using elemental analysis, UV-Visible spectrophotometry and Fourier-transformed infrared (FTIR) spectroscopy techniques. Scanning Electron Microscopy (SEM) was applied to analyze the morphological modifications of the extracted HA after treatment with 3.5% KOH solution. For agricultural objectives, such as soil enrichment, enhancing plant growth conditions, and creating green energy solutions, this acquired HA can be made bioactive. This study not only establishes a basis for research into the optimized extraction of HA from lignite coal, but it also creates a new avenue for the efficient and clean use of lignite.

Water stable MOFs as emerging class of porous materials for potential environmental applications.

Metal-organic frameworks (MOFs) are extensively recognized for their wide applications in a variety of fields such as water purification, adsorption, sensing, catalysis and drug delivery. The fundamental characteristics of the majority of MOFs, such as their structure and shape, are known to be sensitively impacted by water or moisture. As a result, a thorough evaluation of the stability of MOFs in respect to factors linked to these property changes is required. It is quite rare for MOFs in their early stages to have strong water-stability, which is necessary for the commercialization and development of wider applications of this interesting material. Also, numerous applications in presence of water have progressed considerably as a "proof of concept" stage in the past and a growing number of water-stable MOFs (WSMOFs) have been discovered in recent years. This review discusses the variables and processes that affect the aqueous stability of several MOFs, including imidazolate and carboxylate frameworks. Accordingly, this article will assist researchers in accurately evaluating how water affects the stability of MOFs so that effective techniques can be identified for the advancement of water-stable metal-organic frameworks (WSMOFs) and for their effective applications toward a variety of fields.

Metal-Organic Framework-Based Composites for the Detection and Monitoring of Pharmaceutical Compounds in Biological and Environmental Matrices.

The production of synthetic drugs is considered a huge milestone in the healthcare sector, transforming the overall health, aging, and lifestyle of the general population. Due to the surge in production and consumption, pharmaceutical drugs have emerged as potential environmental pollutants that are toxic with low biodegradability. Traditional chromatographic techniques in practice are time-consuming and expensive, despite good precision. Alternatively, electroanalytical techniques are recently identified to be selective, rapid, sensitive, and easier for drug detection. Metal-organic frameworks (MOFs) are known for their intrinsic porous nature, high surface area, and diversity in structural design that provides credible drug-sensing capacities. Long-term reusability and maintaining chemo-structural integrity are major challenges that are countered by ligand-metal combinations, optimization of synthetic conditions, functionalization, and direct MOFs growth over the electrode surface. Moreover, chemical instability and lower conductivities limited the mass commercialization of MOF-based materials in the fields of biosensing, imaging, drug release, therapeutics, and clinical diagnostics. This review is dedicated to analyzing the various combinations of MOFs used for electrochemical detection of pharmaceutical drugs, comprising antibiotics, analgesics, anticancer, antituberculosis, and veterinary drugs. Furthermore, the relationship between the composition, morphology and structural properties of MOFs with their detection capabilities for each drug species is elucidated.

Graphitic carbon nitride nanosheets as promising candidates for the detection of hazardous contaminants of environmental and biological concern in aqueous matrices.

Monitoring of pollutant and toxic substances is essential for cleaner environment and healthy life. Sensing of various environmental contaminants and biomolecules such as heavy metals, pharmaceutics, toxic gases, volatile organic compounds, food toxins, and pathogens is of high importance to guaranty the good health and sustainable environment to community. In recent years, graphitic carbon nitride (g-CN) has drawn a significant amount of interest as a sensor due to its large surface area and unique electrochemical properties, low bandgap energy, high thermal and chemical stability, facile synthesis, nontoxicity, and electron rich property. Furthermore, the binary and ternary nanocomposites of graphitic carbon nitride further enhance their performance as a sensor making it a cost effective, fast, and reliable gadget for the purpose, and opens a wide area of research. Numerous reviews addressing a variety of applications including photocatalytic energy conversion, photoelectrochemical detection, and hydrogen evolution of graphitic carbon nitride have been documented to date. But a lesser attention has been devoted to the mechanistic approaches towards sensing of variety of pollutants concerned with environmental and biological aspects. Herein, we present the sensing features of graphitic carbon nitride towards the detection of various analytes including toxic heavy metals, pharmaceuticals, phenolic compounds, nitroaromatic compounds, volatile organic molecules, toxic gases, and foodborne pathogens. This review will undoubtedly provide future insights for researchers working in the field of sensors, allowing them to investigate the intriguing graphitic carbon nitride material as a sensing platform that is comparable to several other nanomaterials documented in the literature. Therefore, we hope that this study could reveal some intriguing sensing properties of graphitic carbon nitride, which may help researchers better understand how it interacts with contaminants of environmental and biological concern. Graphitic carbon nitride Nanosheets as Promising Analytical Tool for Environmental and Biological Monitoring of Hazardous Substances.

In-house fabrication of macro-porous biopolymeric hydrogel and its deployment for adsorptive remediation of lead and cadmium from water matrices.

A novel adsorbent was prepared by blending chitosan (CS) and acrylic acid (AA) while using formaldehyde as a cross linker in the form of hydrogel beads. The adsorption properties of these hydrogel beads for the removal of toxic metal ions (Pb2+ and Cd2+) from aqueous solutions were evaluated. The hydrogel beads have a 3D macro-porous structure whose -NH2 groups were considered to be the dominant binding specie for Cd and Pb ions. The equilibrium adsorption capacity (qe) of beads was significantly affected by the mass ratio of sorbent and sorbate. The percentage removal of Cd and Pb ions was observed to be enhanced with the increase in sorbate concentration. The hydrogel beads maintained good adsorption properties at adsorption-desorption equilibrium. The Langmuir and Freundlich models were used to elaborate the isotherms as well as isotherm constants. Adsorption isothermal data is well explained by the Freundlich model. The data of experimental kinetics is interrelated with the second-order kinetic model, which showed that the chemical sorption phenomenon is the rate limiting step. The results of intraparticle diffusion model described the adsorption process occurred on a porous substance that proved chitosan/Formaldehyde beads to be the favorable adsorbent.

Polymerization kinetics of bicyclic olefins and mechanism with symmetrical ansa-metallocene catalysts associated with active center count: relationship between their activities and structure and activation path.

Copolymerization of ethylene (E) with 5-vinyl-2-norbornene (VNB) catalyzed by ansa-metallocenes allows the precise control of essential polymeric properties such as comonomer incorporation, molecular weight (M w), and polydispersity (D). Significant efforts have been devoted to synthesizing and developing novel catalysts, cocatalysts, and activators, although the fundamental elements of catalytic processes remain unclear. For example, it is questionable how polymeric catalysts are divided across dormant and active sites and how this distribution affects the order of monomers for the propagation rate, which widely vary in the literature. Furthermore, although the empirical correlation between the monomers and average M w has been established in many systems, the fundamental processes of chain termination remain unknown. Furthermore, the involvement of ion-pairing in metallocene-catalyzed polymerization and the termination mechanisms are also contentious issues. In this study, we describe the use of a quenched-labeling technique based on acyl chloride to selectively quench the zirconium metal-polymeric bond, which can be used to study the kinetics, active site [Zr][C*] counting, copolymer microstructure, and molecular weight distribution (MWD) to determine the rate laws for chain initiation, chain propagation rate (R p), propagation rate constant (k p) and chain termination. In addition, we also predict previously unknown chemical characteristics of E/bicyclic copolymerization processes, where either a cis-endocyclic double bond with steric properties or a vinyl exocyclic double bond affects the activity, i.e., [Zr]/[*C], (R p) and (k p). All these properties require the implementation of a particular kinetic mechanism that assumes the low activity of the building copolymer chains incorporating a single ethylene/VNB unit, i.e., the Cp2Zr-C2H5 group, in the ethylene addition process in the Cp2Zr-C bond. Due to ß-agostic stabilization, the Cp2Zr-C2H5 group exhibits a distinct feature. These effects were confirmed experimentally, such as the E/VNB co-polymer activity and VNB mol%, propagation rate decrease in the polymerization time (t p) of 120 s to 1800 s, crystalline properties, and significant increase in molecular weight. The active center [Zr]/[*C] fraction considerably increased in the initial (t p) 840 s, and subsequently tended to the steady stage of 33%, which is lower than previously reported E homo- and E/P copolymerization. The lower [C*]/[Zr] in both the early and stable stages, decrease in VNB mol%, and R p with t p can be associated with the more significant fraction of Cp2Zr-CH2CH3-type dormant site by the ß-agostic hydrogen interaction with the Cp2Zr metal. The t p versus R pE, R pVNB, k pE, k pVNB, and [Zr]/[C*] count could be fitted to a model that invokes deactivation of the growing polymer chains. In the case of the thermal behavior of the copolymers (melting temperature (T m) and crystalline temperature (ΔH m)), T m varied from 101 °C to 121 °C, while ΔH m varied from 9 to 16 (J g-1).

Covalent Organic Frameworks-Based Membranes as Promising Modalities from Preparation to Separation Applications: An Overview.

Covalent organic frameworks (COFs) are a promising class of porous crystalline materials made up of covalently connected and periodically protracted network topologies through organic linkers. The tailorability of organic linker and intrinsic structures endow COFs with a tunable porosity and structure, low density, facilely-tailored functionality, and large surface area, attracting increasing amount of interests in variety of research areas of membrane separations. COF-based membranes have spawned a slew of new research projects, ranging from fabrication methodologies to separation applications. Herein, we tried to emphasis the major developments in the synthetic approaches of COFs based membranes for a variety of separation applications such as, separation of gaseous mixtures, water treatment as well as separation of isomeric and chiral organic compounds. The proposed methods for fabricating COF-based continuous membranes and columns for real world applications are also thoroughly explored. Finally, a viewpoint on the future directions and remaining challenges for COF research in the area of separation is provided.

Covalent organic frameworks as promising adsorbent paradigm for environmental pollutants from aqueous matrices: Perspective and challenges.

Covalent organic frameworks (COFs) are an emerging class of new porous crystalline polymers materials having robust framework, outstanding structural regularity, highly ordered aperture size, inherent porosity, and chemical stability with designer properties, making them an ideal material for adsorbing a variety of contaminants from water bodies. Presented study focusses on the current advances and progress of pristine COFs as well as COFs based composites as an emerging substitute for the adsorption and removal of a variety of pollutants including water desalination technique, heavy metals, pharmaceuticals, dyes and organic pollutants. The absorption capabilities of COFs-derived architecture are evaluated and equated with those of other commonly used adsorbents. The interaction between sorption ability and structural property as well as some regularly utilized ways to improve the adsorption performance of COFs-based materials are also reviewed. Finally, perspective and a summary about the challenges and opportunities of COFs and COFs-derived materials are discussed to deliver some exciting data for fabricating and designing of COFs and COFs-derived materials for remediation of environmental pollutants.

Electroactive polymeric nanocomposite BC-g-(Fe3O4/GO) materials for bone tissue engineering: in vitro evaluations.

Tissue engineering is a cutting-edge approach for using advanced biomaterials to treat defective bone to get desired clinical results. In bone tissue engineering, the scaffolds must have the desired physicochemical and biomechanical natural properties in order to regenerate complicated defective bone. For the first time, polymeric nanocomposite material was developed using cellulose and co-dispersed nanosystem (Fe3O4/GO) by free radical polymerization to fabricate porous polymeric scaffolds via freeze drying. Various characterizations techniques, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM)/energy dispersive X-ray (EDX), and universal testing machine (UTM) were used to investigate structural, morphological, and mechanical properties. Swelling, biodegradation, and wetting analysis were also performed to evaluate their physicochemical behavior. Intercalation of Fe3O4 nanoparticles into GO-sheets promoted their dispersion into the polymeric matrix. All porous scaffolds possessed a well-interconnected porous structure, while the synergistic effect of Fe3O4/GO reinforces the mechanical strength of porous scaffolds. The compressive strength and Young's modulus were increased by increasing Fe3O4 amount, and maximum mechanical strength was found in HFG-4 and least in HFG-1. However, these porous scaffolds have different swelling and biodegradation behavior due to the variable Fe3O4 intercalations into GO-sheets. Antibacterial activities of porous scaffolds were studied against severe Gram-positive and Gram-negative pathogens and increased Fe3O4 amount in nanosystem increased the antibacterial activities. The cell viability and morphology of pre-osteoblast (MC3T3-E1) cell lines were studied against porous scaffolds and increased cell viability and proliferation were observed from HFG-1 to HFG-4. Hence, the electroactive material could be the potential material for bone tissue engineering.

Methods for Predicting Ethylene/Cyclic Olefin Copolymerization Rates Promoted by Single-Site Metallocene: Kinetics Is the Key.

In toluene at 50 °C, the vinyl addition polymerization of 4-vinyl-cyclohexene (VCH) comonomers with ethylene is investigated using symmetrical metallocene (rac-Et(Ind)2ZrCl2) combined with borate/TIBA. To demonstrate the polymerizations' living character, cyclic VCH with linear-exocyclicπ and endocyclicπ bonds produces monomodal polymers, but the dispersity (Ɖ) was broader. The copolymers obtained can be dissolved in conventional organic solvent and have excellent thermal stability and crystalline temperature (ΔHm), and their melting temperature (Tm) varies from 109 to 126 °C, and ΔHm ranges from 80 to 128 (J/g). Secondly, the distribution of polymeric catalysts engaged in polymer chain synthesis and the nature of the dormant state are two of the most essential yet fundamentally unknown aspects. Comprehensive and exhaustive kinetics of E/VCH have shown numerous different kinetic aspects that are interpreted as manifestations of polymeric catalysts or of the instability of several types of active center [Zr]/[C*] fluctuations and formation rates of chain propagation RpE, RpVCH, and propagation rate constants kpE and kpVCH, the quantitative relationship between RpE, RpVCH and kpE, kpVCH and catalyst structures, their constituent polymer Mw, and their reactivity response to the endocyclic and exocyclic bonds of VCH. The kinetic parameters RpE, RpVCH, kpE, and kpVCH, which are the apparent rates for the metallocene-catalyzed E/VCH, RpE, and kpE values, are much more significant than RpVCH and kpVCH at 120 s, RpE and RpVCH 39.63 and 0.78, and the kpE and kpVCH values are 6461 and 93 L/mol·s, respectively, and minor diffusion barriers are recommended in the early stages. Compared with previously reported PE, RpE and kpE values are 34.2 and 7080 L/mol·s. VCH increases the RpE in the initial stage, as we are expecting; this means that the exocyclic bond of VCH is more active at the initial level, and that the chain transfer reaction of cyclic internal π double is increased with the reaction time. The tp versus Rp, kp, and [Zr]/[C*] fraction count may be fitted to a model that invokes deactivation of growing polymer chains. At tp 120-360 s higher, the incorporation rate of VCH suppresses E insertion, resulting in reduced molecular weight.

Phytochemistry and Diverse Pharmacology of Genus Mimosa: A Review.

The genus Mimosa belongs to the Fabaceae family and comprises almost 400 species of herbs, shrubs and ornamental trees. The genus Mimosa is found all over the tropics and subtropics of Asia, Africa, South America, North America and Australia. Traditionally, this genus has been popular for the treatment of jaundice, diarrhea, fever, toothache, wound healing, asthma, leprosy, vaginal and urinary complaints, skin diseases, piles, gastrointestinal disorders, small pox, hepatitis, tumor, HIV, ulcers and ringworm. The review covered literature available from 1959 to 2020 collected from books, scientific journals and electronic searches, such as Science Direct, Web of Science and Google scholar. Various keywords, such as Mimosa, secondary metabolites, medicines, phytochemicals and pharmacological values, were used for the data search. The Mimosa species are acknowledged to be an essential source of secondary metabolites with a wide-ranging biological functions, and up until now, 145 compounds have been isolated from this genus. Pharmacological studies showed that isolated compounds possess significant potential, such as antiprotozoal, antimicrobial, antiviral, antioxidant, and antiproliferative as well as cytotoxic activities. Alkaloids, chalcones, flavonoids, indoles, terpenes, terpenoids, saponins, steroids, amino acids, glycosides, flavanols, phenols, lignoids, polysaccharides, lignins, salts and fatty esters have been isolated from this genus. This review focused on the medicinal aspects of the Mimosa species and may provide a comprehensive understanding of the prospective of this genus as a foundation of medicine, supplement and nourishment. The plants of this genus could be a potential source of medicines in the near future.

Octylamine as environment friendlier colorimetric detection probe for hazardous 2,4,6-Trinitrophenol from wastewater samples.

The precise detection of hazardous 2,4,6-Trinitrophenol (TNP) is essential for the environment and human health. TNP is used as a precursor in whistling fireworks in ammunition, mining, agriculture and is a hazardous environmental pollutant generated from leather, chemical, and dye industries. Exploring rapid and low-cost approaches for the detection and quantification of TNP has attracted many scientists nowadays. The proposed chemosensor utilizes the concept of dispersive liquid-liquid micro-extraction coupled with a UV-visible spectrophotometer for its sensing at the ultra-trace level. Significant changes based on intramolecular interactions followed by a distinct color change to orange-red from yellow in the presence of TNP is an attractive feature for the present study. The successive addition of TNP shows ultra-trace sensitivity (3.9831 µA µM-1 cm-1) at detection limit (LOD) of 0.0015 ± 0.03 µM (S/N = 3), a linear range of 0 µM-70 µM, and a response time of <5 min. Different types of real samples such as creatinine testing kit reagent, fireflies crackers, serum, and water samples were used and recovery of TNP was calculated by spiking the known concentration of the standard analyte. The obtained recovery was 93.6-103.6% with RSD range of 1.6-4.53% (n = 3) in different samples. The analytical performance of the colorimetric Chemoprobe in terms of its recovery, linearity range, and limit of detection offers an excellent platform for monitoring hazardous TNP. The results show that the proposed colorimetric chemosensor is easy to use, low-cost, environmentally friendly and offers an easily observable visual color change. Based on these features, the chemosensor can be used for large-scale applications for the detection of TNP in water and other samples.

Covalent organic frameworks-based smart materials for mitigation of pharmaceutical pollutants from aqueous solution.

Covalent organic frameworks (COFs) are an emergent group of crystalline porous materials that have gained incredible interest in recent years. With foreseeable controllable functionalities and structural configurations, the constructions and catalytic properties of these organic polymeric materials can be controlled to fabricate targeted materials. The specified monomer linkers and pre-designed architecture of COFs facilitate the post-synthetic modifications for introducing novel functions and useful properties. By virtue of inherent porosity, robust framework, well-ordered geometry, functionality, higher stability, and amenability to functionalization, COFs and COFs-based composites are regarded as prospective nanomaterials for environmental clean-up and remediation. This report spotlights the state-of-the-art advances and progress in COFs-based materials to efficiently mitigate pharmaceutical-based environmental pollutants from aqueous solutions. Synthesis approaches, structure, functionalization, and sustainability aspects of COFs are discussed. Moreover, the adsorptive and photocatalytic potential of COFs and their derived nanocomposites for removal and degradation of pharmaceuticals are thoroughly vetted. In addition to deciphering adsorption mechanism/isotherms, the stability, regeneratability and reproducibility are also delineated. Lastly, the outcomes are summed up, and new directions are proposed to widen the promise of COF-based smart materials in diverse fields.