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NH 2 -functionalized metal-organic frameworks (NH 2 -functionalized MOFs) can abate organic pollutants, predominantly favored by their chemical, mechanical, and thermal stabilities. The present review stated the chemistry of identifying NH 2 -functionalization and its role in enhancing the properties of bare MOFs. The integration of the amine group bestows several advantages: 1.) enabling band structure modification, 2.) establishing strong metal-NH 2 bonds, 3.) preserving MOF structures from reactive oxygen species, and 4.) shielding MOF structures against pH alterations. Consequently, the NH 2 -functionalized MOFs are promising materials for the photodegradation of organic contaminants. The following section illustrates the two approaches (pre-synthetic and post-synthetic) for NH 2 -functionalized MOFs. Nevertheless, specific intrinsic limitations, entailing a high recombination rate of charge carriers and inadequate optical adsorption, restrain the applicability of NH 2 -functionalized MOFs. Accordingly, the succeeding segment presents strategies to elevate the photocatalytic activities of NH 2 -functionalized MOFs via heterojunction fabrication. The importance of the NH 2 -functionalized MOFs-based heterojunction has been evaluated in terms of the effect on the enhancement of charge separation, optical adsorption, and redox ability of charge carriers. Subsequently, the potential application for organic pollutant degradation via NH 2 -functionalized MOFs-based heterojunctions has been scrutinized, wherein the organic pollutants. Eventually, the review concluded with challenges and potential opportunities in engaging and burgeoning domains of the NH 2 -functionalized MOFs-based heterojunctions., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

The present study explores visible light-assisted photodegradation of ciprofloxacin hydrochloride (CIP) antibiotic as a promising solution to water pollution. The focus is on transforming the optical and electronic properties of BiOCl through the generation of oxygen vacancies (OVs) and the exposure of (110) facets, forming a robust S-scheme heterojunction with WS 2 . The resultant OVs mediated composite with an optimal ratio of WS 2 and BiOCl-OV (4-WS 2 /BiOCl-OV) demonstrated remarkable efficiency (94.3%) in the visible light-assisted photodegradation of CIP antibiotic within 1.5 h. The CIP degradation using 4-WS 2 /BiOCl-OV followed pseudo-first-order kinetics with the rate constant of 0.023 min -1 , outperforming bare WS 2 , BiOCl, and BiOCl-OV by 8, 6, and 4 times, respectively. Density functional theory (DFT) analysis aligned well with experimental results, providing insights into the structural arrangement and bandgap analysis of the photocatalysts. Liquid chromatography-mass spectrometry (LC-MS) analysis utilized for identifying potentially degraded products while scavenging experiments and electron paramagnetic resonance (EPR) spin trapping analysis elucidated the S-scheme charge transfer mechanism. This research contributes to advancing the design of oxygen vacancy-mediated S-scheme systems in the realm of photocatalysis, with potential implications for addressing water pollution concerns., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Inc. All rights reserved.)

Arsenic (As) contaminated water, especially groundwater reservoirs, is a major issue worldwide owing to its hazardous consequences on human health and the global environment issues. Also, irrigating agricultural fields with As-contaminated water not only produces an accumulation of As in the soil but also compromises food safety due to As entering into agricultural products. Hence, there is an urgent need to develop an efficient method for As removal in water. Fe-based MOFs have attained special attention due to their low toxicity, high water stability, better physical and chemical properties, and high abundance of iron. The arsenic species removal by Fe-MOF follows the adsorption and oxidation mechanism where As (III) converts into As (V). Moreover, the adsorption mechanism is facilitated by electrostatic interactions, H-bonding, acid-base interaction, hydrophobic interactions, van der Waals forces, π-π stacking interactions, and coordinative bindings responsible for Fe-O-As bond generation. This review thoroughly recapitulates and analyses recent advancements in the facile synthesis and potential application of Fe-based MOF adsorbents for the elimination of As ions. The most commonly employed hydro/solvothermal, ultrasonic, microwave-assisted, mechanochemical, and electrochemical synthesis for Fe-MOF has been discussed along with their adsorptive and oxidative mechanisms involved in arsenic removal. The effects of factors like pH and coexisting ions have also been discussed. Lastly, the article also proposed the prospects for developing the application of Fe-based MOF in treating As-contaminated water., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Nanostructured materials are fascinating since they are promising for intensely enhancing materials' performance, and they can offer multifunctional features. Creating such high-performance nanocomposites via effective and mild approaches is an inevitable requirement for sustainable materials engineering. Nanocomposites, which combine two-star nanomaterials, namely, cellulose nanofibrils (CNFs) and graphene derivatives (GNMs), have recently revealed interesting physicochemical properties and excellent performance. Despite numerous studies on the production and application of such systems, there is still a lack of concise information on their practical uses. In this review, recent progress in the production, modification, properties, and emerging uses of CNFs/GNMs hybrid-based nanocomposites in various fields such as flexible energy harvesting and storage, sensors, adsorbents, packaging, and thermal management, among others, are comprehensively examined and described based on recent investigations. Nevertheless, numerous challenges and gaps need to be addressed to successfully introduce such nanomaterials in large-scale industrial applications. This review will certainly help readers understand the design approaches and potential applications of CNFs/GNMs hybrid-based nanocomposites for which new research directions in this emerging topic are discussed., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier B.V. All rights reserved.)

The sustainable utilization of resources motivate us to create eco-friendly processes for synthesizing novel carbon nanomaterials from waste biomass by minimizing chemical usage and reducing energy demands. By keeping sustainability as a prime focus in the present work, we have made the effective management of Parthenium weeds by converting them into carbon-based nanomaterial through hydrothermal treatment followed by heating in a tube furnace under the nitrogen atmosphere. The XPS studies confirm the natural presence of nitrogen and oxygen-containing functional groups in the biomass-derived carbon. The nanostructure has adopted a layered two-dimensional structure, clearly indicated through HRTEM images. Further, the nanomaterials are analyzed for their ability towards the electrochemical detection of mercury, with a detection limit of 6.17 μM, while the limit of quantification and sensitivity was found to be 18.7 μM and 0.4723 μM μA -1 cm -2 , respectively. The obtained two-dimensional architecture has increased the surface area, while the nitrogen and oxygen functional groups act as an active site for sensing the mercury ions. This study will open a new door for developing metal-free catalysts through a green and sustainable approach by recycling and utilization of waste biomass., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The COVID-19 pandemic has caused unprecedented global health and economic crises. The emergence of long COVID-19 has raised concerns about the interplay between SARS-CoV-2 infections, climate change, and the environment. In this context, a concise analysis of the potential long-term effects of the COVID-19 epidemic along with the awareness aboutenvironmental issues are realized. While COVID-19 effects in the short-term have reduced environmental air pollutants and pressures, CO 2 emissions are projected to increase as the economy recovers and growth rates return to pre-COVID-19 levels. This review discusses the systematic effects of both the short-term and long-term effects of the pandemic on the clean energy revolution and environmental issues. This article also discusses opportunities to achieve long-term environmental benefits and emphasizes the importance of future policies in promoting global environmental sustainability. Future directions for growth and recovery are presented to cope with long COVID-19 epidemic along with the critical findings focussing on various aspects: waste management, air quality improvement., (© 2023. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)

The survival of humanity is severely threatened by the massive accumulation of waste in the ecosystem. One plausible solution for the management and upcycling of waste is conversing waste at the molecular level and deriving carbon-based nanomaterial. The field of carbon nanomaterials with distinctive properties, such as exceptionally large surface areas, good thermal and chemical stability, and improved propagation of charge carriers, remains a significant area of research. The study demonstrates recent developments in high-value carbon-based photocatalysts synthesis from various waste precursors, including zoonotic, phytogenic, polyolefinic, electronic, and biomedical, highlighting the progression as photocatalysts and adsorbents for wastewater treatment and water splitting applications. This review highpoints the benefits of using waste as a precursor to support sustainability and circular economy and the risks associated with their use. Finally, we support that a sustainable society will eventually be realized by exploring present obstacles and potential steps for creating superior carbon-based nanomaterials in the future., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Background: Azole and sulfonamide molecular frameworks are endowed with potent antimicrobial activity. Materials & methods: A series of azole-sulfonamide conjugates were synthesized using click reaction of N-propargylated imidazole with azide of sulfonamide and its antimicrobial efficacy was evaluated. Results: The compounds 7c , 7i and 7r displayed promising antibacterial activities, better than the standards sulfonamide and norfloxacin. All molecules exhibited promising antifungal activity, more potent than fluconazole. Docking studies of the active conjugates signified the importance of hydrophobic interactions in hosting the molecules in the active site of dihydrofolate reductase. Conclusion: Azole-sulfonamide conjugates are more active than single sulfonamide moieties and 7c , 7i and 7r may prove valuable leads for further optimization as novel antimicrobial agents.

Constructing an effective multi-heterojunction photocatalyst with maximum charge carrier separation remains challenging. Herein, a high-efficient Co 3 O 4 /MIL-88A/Mn-SrTiO 3 (Co 3 O 4 /MIL/Mn-STO) n-p-n heterojunction photocatalyst was successfully prepared by a simple hydrothermal method for the photodegradation of sulfamethoxazole (SMX). The combination of MIL and Co 3 O 4 /Mn-STO established an internal electric field and heterojunction, accelerating the separation of carriers, and thus improved photocatalytic performance. In the Co 3 O 4 /MIL/Mn-STO photocatalytic system, 95.5 % of SMX was degraded in 90 min. The photocatalytic kinetic removal rate of Co 3 O 4 /MIL/Mn-STO reached 0.0337 min -1 , 8 times of Co 3 O 4 (0.0041 min -1 ), 5.2 times of Mn-STO (0.0062 min -1 ), 4.6 times of MIL (0.0078 min -1 ), and 3.6 times of MIL/Mn-STO (0.0095 min -1 ). Remarkably, superoxide radicals ( • O 2 - ) and holes (h + ) have been recognized as the main active species in the degradation process through reactive species elimination experiments and electron spin resonance (ESR) tests. The experimental and theoretical proved the in-built interfacial contact and synergistic effect between the photocatalyst accomplished with low bandgaps, high specific surface area, more reaction sites, high electron-hole pair separation, and maximum solar-light utilization. The molecular structure and possible degradation routes with intermediate products in the photocatalytic system were investigated using a liquid chromatography-mass spectrometer (LC-MS) and DFT calculations. This work provided new insight into the guidelines of rational design/growth of new multicomponent photocatalysts to remove antibiotics and other emerging contaminants in wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Herein, we have reported a photocatalytic Bi 5 O 7 I, protonated g-C 3 N 4 heterojunction with directional charge transfer channels provided by tea waste biochar to achieve effective e - /h + pair isolation for the improved degradation of Methylene blue (MB) and Doxycycline hydrochloride (DCHCl). An S-scheme heterojunction was fabricated via the novel method that combined hydrothermal and ultrasonic dispersion, followed by an electrostatic self-assembly route. The as-fabricated Bi 5 O 7 I/protonated g-C 3 N 4 /Tea waste biochar heterojunction formed a strong contact at the interface, as supported by the electron microscopic results. As per the adsorption and photocatalytic degradation kinetics study, Bi 5 O 7 I/Tea waste biochar/protonated g-C 3 N 4 (40 wt%) heterojunction showed a higher adsorption rate of 41.56% and 32% for MB and DCHCl within 30 min in the dark. Also, 92.02% MB and 90.21% DCHCl degradation rates in 60 and 90 min, respectively, are approximately 43 and 32 times higher than bare Bi 5 O 7 I and protonated g-C 3 N 4 photocatalysts. The highest adsorption and degradation rate was achieved owing to the addition of Tea waste biochar and protonated g-C 3 N 4 in a controlled ratio, and the sufficient interfacial contact between Bi 5 O 7 I and protonated g-C 3 N 4 is for the improved isolation rate of e - /h + pairs as evidenced by zeta potential values photoluminescence spectra as well as from scanning and transmission electron microscopy. Moreover, Bi 5 O 7 I/Tea waste biochar/protonated g-C 3 N 4 (40 wt%) possessed high stability and recyclability after four consecutive cycles without much altering the degradation ability. Therefore, we believe that the as-fabricated Bi 5 O 7 I/Tea waste biochar/protonated g-C 3 N 4 (40 wt%) provides new insight into the highly efficient S-scheme mechanisms significant for accelerating multicomponent photocatalytic redox reactions; while forming an effective visible light responsive candidate for treating wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

This study uses waste coconut husk to synthesize carbon quantum dots decorated graphene-like structure for sustainable detection and removal of ofloxacin. The XRD spectrum shows the carbon nanomaterial's layered structure with turbostratic carbon stacking on its surface. The FESEM and HRTEM studies claim the successful development of quantum dots decorated 2D layered structure of carbon nanomaterial. The functionalization of sulfur and nitrogen is well observed and studied through XPS, while Raman spectra have provided insight into the surface topology of the as-synthesized nanostructure. The BET surface area was found to be 1437.12 m 2 /g with a microporous structure (pore width 2.0 nm) which interestingly outcompete many reported carbon-based nanomaterials such as graphene oxide, reduced graphene oxide and quantum dots. The detection and removal processes are monitored through UV-visible spectroscopy and the obtained detection limit and adsorption capacity were 2.7 nM and 393.94 mg/L respectively. Additionally, 1 mg carbon nanomaterial has removed 49 % ofloxacin from water in just 1 h. In this way, this study has successfully managed the coconut husk waste after its utilization for environmental remediation purposes., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Photocatalytic hybrid carbon nanotubes (CNTs)-mediated Ag-CuBi 2 O 4 /Bi 2 WO 6 photocatalyst was fabricated using a hydrothermal technique to effectively eliminate organic pollutants from wastewater. The as-prepared samples were characterized via Fourier transform infrared spectroscopy (FTIR), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction patterns (XRD), high-resolution transmission electron microscope (HR-TEM), UV-vis Diffuse Reflectance spectrum (UV-Vis DRS), and photoluminescence (PL) studies. The photocatalytic performance of fabricated pristine and hybrid composites was examined by photo-degradation of toxic dye viz. Rhodamine B (RhB) under visible light. Photo-degradation results revealed that the fabricated Ag-CuBi 2 O 4 /CNTs/Bi 2 WO 6 semiconductor photocatalyst followed pseudo-first-order kinetics and displayed a higher photocatalytic rate, which was found to be approximately 3.33 and 2.35 times higher than the pristine CuBi 2 O 4 and Bi 2 WO 6 semiconductor photocatalyst, respectively. Re-cyclic results demonstrated that the formed composite owns excellent stability, even after five consecutive cycles. As per the matched Fermi level of CNTs in between Ag-CuBi 2 O 4 and Bi 2 WO 6 , carbon nanotubes severed as electron transfer-bridge, Ag doping on CuBi 2 O 4 surface successfully increased photon absorption all across CuBi 2 O 4 surface. Also, it hindered the assimilation of photoinduced electron-hole pairs. The increased photocatalytic efficiency is contributed to the uniform dispersion of photo-generated electron-hole pairs via the construction of an S-scheme system. ROS trapping and ESR experiments suggested that (∙OH) and (O 2 - ∙) were the main radical species for enhanced photo-degradation of RhB dye. The current investigation, from our perspective, highlights the new insights for the fabrication of practical CNTs-mediated S-scheme-based semiconductor photocatalyst for the resolution of environmental issues based on practical considerations., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

This work successfully fabricated graphitic carbon nitride and magnetically recoverable α-Fe 2 O 3 /g-C 3 N 4 /SiO 2 photo-Fenton catalysts using thermal polycondensation and in situ-simple precursor drying-calcination process, respectively, was examined for model synthetic rhodamine B (RhB) dye in the presence of H 2 O 2 and acidic pH under simulated visible light irradiation. An aqueous suspension of the reaction mixture of dye-containing wastewater was fully degraded and reached 97% of photo-Fenton degradation efficiency within 120 min followed by the production of hydroxyl radical ( • OH). The dominant hydroxyl radical position generated surface charge, electrostatic potential distribution, and average local ionization potential, which contributed to the complete mineralization of RhB dye, according to the density functional theory (DFT) calculations. HPLC and GCMS experiments were performed to examine the degradation fragments of RhB and draw a plausible mechanistic pathway which showed that RhB degradation generated a series of N-deethylated products, followed by a one-time ring-opening, which indicated that photosensitization induced a photocatalysis reaction mechanism., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

Recently, there has been a significant increase in the interest of using photocatalysis for environmental clean-up applications. In this research, potassium, and phosphorus co-doped graphitic carbon nitride (KPCN) photocatalyst modified with graphene oxide (GO) and heterostructured with ZnFe 2 O 4 was synthesized via the hydrothermal method (KPCN/GO/ZnFe 2 O 4 ). The photoactivity of KPCN/GO/ZnFe 2 O 4 photocatalyst was examined for the photocatalytic degradation of target pollutants such as methylene blue (MB) dye, rhodamine B (RhB) dye, and tetracycline (TC) antibiotic. Furthermore, the chemical oxygen demand (COD) removal efficiency for real wastewater was determined to explore the practical application of KPCN/GO/ZnFe 2 O 4 photocatalyst. The degradation efficiencies of bare graphitic carbon nitride, KPCN, KPCN/GO, and KPCN/GO/ZnFe 2 O 4 photocatalysts for tetracycline antibiotics were 30%, 42%, 57%, and 87% within 60 min, respectively. Moreover, KPCN/GO/ZnFe 2 O 4 photocatalyst showed 71% COD removal efficiency within 240 min. The • OH and • O 2 - were the major reactive species in the photocatalytic process. Results showed that the degradation efficiencies of graphitic carbon nitride were greatly enhanced upon doping and further improved with the addition of GO and ZnFe 2 O 4 . Doping improved light harvesting, GO enhanced the adsorption ability and heterojunction with ZnFe 2 O 4 enhanced the charge separation as well as the reusability of synthesized KPCN/GO/ZnFe 2 O 4 photocatalyst., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Nature-derived or biologically encouraged hydrogels have attracted considerable interest in numerous biomedical applications owing to their multidimensional utility and effectiveness. The internal architecture of a hydrogel network, the chemistry of the raw materials involved, interaction across the interface of counter ions, and the ability to mimic the extracellular matrix (ECM) govern the clinical efficacy of the designed hydrogels. This review focuses on the mechanistic viewpoint of different biologically driven/inspired biomacromolecules that encourages the architectural development of hydrogel networks. In addition, the advantage of hydrogels by mimicking the ECM and the significance of the raw material selection as an indicator of bioinertness is deeply elaborated in the review. Furthermore, the article reviews and describes the application of polysaccharides, proteins, and synthetic polymer-based multimodal hydrogels inspired by or derived from nature in different biomedical areas. The review discusses the challenges and opportunities in biomaterials along with future prospects in terms of their applications in biodevices or functional components for human health issues. This review provides information on the strategy and inspiration from nature that can be used to develop a link between multimodal hydrogels as the main frame and its utility in biomedical applications as the primary target., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Parthenium hysterophorus, one of the seven most hazardous weeds is widely known for its allergic, respiratory and skin-related disorders. It is also known to affect biodiversity and ecology. For eradication of the weed, its effective utilization for the successful synthesis of carbon-based nanomaterial is a potent management strategy. In this study, reduced graphene oxide (rGO) was synthesized from weed leaf extract through a hydrothermal-assisted carbonization method. The crystallinity and geometry of the as-synthesized nanostructure are confirmed from the X-ray diffraction study, while the chemical architecture of the nanomaterial is ascertained through X-ray photoelectron spectroscopy. The stacking of flat graphene-like layers with a size range of ∼200-300 nm is visualized through high-resolution transmission electron microscopy images. Further, the as-synthesized carbon nanomaterial is advanced as an effective and highly sensitive electrochemical biosensor for dopamine, a vital neurotransmitter of the human brain. Nanomaterial oxidizes dopamine at a much lower potential (0.13 V) than other metal-based nanocomposites. Moreover, the obtained sensitivity (13.75 and 3.31 μA μM -1  cm -2 ), detection limit (0.6 and 0.8 μM), the limit of quantification (2.2 and 2.7 μM) and reproducibility calculated through cyclic voltammetry/differential pulse voltammetry respectively outcompete many metal-based nanocomposites that were previously used for the sensing of dopamine. This study boosts the research on the metal-free carbon-based nanomaterial derived from waste plant biomass., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Inc. All rights reserved.)

Over the past several decades, the increase in industrialization provoked the discharge of harmful pollutants into the environment, affecting human beings and ecosystems. ZnO-based photocatalysts seem to be the most promising photocatalysts for treating harmful pollutants. However, fast charge carrier recombination, photo corrosion, and long reaction time are the significant factors that reduce the photoactivity of ZnO-based photocatalysts. In order to enhance the photoactivity of such photocatalysts, a combined process i.e., sonocatalysis + photocatalysis = sonophotocatalysis was used. Sonophotocatalysis is one of several different AOP methods that have recently drawn considerable interest, as it produces high reactive oxygen species (ROS) which helps in the oxidation of pollutants by acoustic cavitation. This combined technique enhanced the overall efficiency of the individual method by overcoming its limiting factors. The current review aims to present the theoretical and fundamental aspects of sonocatalysis and photocatalysis along with a detailed discussion on the benefits that can be obtained by the combined process i.e., US + UV (sonophotocatalysis). Also, we have provided a comparison of the excellent performance of ZnO to that of the other metal oxides. The purpose of this study is to discuss the literature concerning the potential applications of ZnO-based sonophotocatalysts for the degradation of pollutants i.e., dyes, antibiotics, pesticides, phenols, etc. That are carried out for future developments. The role of the produced ROS under light and ultrasound stimulation and the degradation mechanisms that are based on published literature are also discussed. In the end, future perspectives are suggested, that are helpful in the development of the sonophotocatalysis process for the remediation of wastewater containing various pollutants., Competing Interests: Declaration of competing interest The authors declare that they have no known competing for financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Doping-induced vacancy engineering of graphitic carbon nitride (GCN) is beneficial for bandgap modulation, efficient electronic excitation, and facilitated charge carrier migration. In this study, synthesis of oxygen and sulphur co-doped induced N vacancies (OSGCN) by the hydrothermal method was performed to activate peroxymonosulfate (PMS) for sulfamethoxazole (SMX) antibiotic degradation and H 2 production. The results from experimental and DFT simulation studies validate the synergistic effects of co-dopants and N-vacancies, i.e., bandgap lowering, electron-hole pairs separation, and high solar energy utilization. The substitution of sp 2 N atom by O and S co-dopants causes strong delocalization of HOMO-LUMO distribution, enhancing carrier mobility, increasing reactive sites, and facilitating charge-carrier separation. Remarkably, OSGCN/PMS photocatalytic system achieved 99.4% SMX degradation efficiency and a high H 2 generation rate of 548.23 μ mol g -1 h -1 within 60 min and 36 h, respectively under visible light irradiations. The SMX degradation kinetics was pseudo-first-order with retained recycling efficiency up to 4 catalytic cycles. The results of EPR and chemical scavenging experiments revealed the redox action of reactive oxidative species, wherein 1 O 2 was the dominant reactive species in SMX degradation. The identification of formed intermediates and the SMX stepwise degradation pathway was investigated via LC-MS analysis and DFT studies, respectively. The results from this work anticipated deepening the understanding of PMS activation by substitutional co-doping favoring N-vacancy formation in GCN lattice for improved photocatalytic activity., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The current research includes the synthesis, improvement of NaCMC-cl-DMAA/AAc hydrogel and in-situ controlled release of gentamicin within various pH environments. The prepared hydrogel was then modified using boron nitride nanosheets aiming to enhancement in the adsorption rate. The prepared hydrogels were investigated by FTIR, XRD, FESEM, TGA/DSC, swelling and cell viability analysis. Cytotoxicity study indicated that prepared sample has a cytocompatibility nature towards healthy normal human cell line (FR2 cells). By changing the pH environment, the drug release properties of the hydrogels can be controlled. The cumulative rate of release for NaCMC-cl-DMAA/AAc hydrogel was 76.5 % at pH = 2.2 and 87.5 % at pH = 7.4. Whereas drug release rate for NaCMC-cl-DMAA/AAc-BNNSs hydrogel composite was 78.6 % at pH = 2.2 and 97.3 % at pH = 7.4 within 4320 min. Gentamicin release kinetics have been determined using the Korsemeyar-Peppas model, which confirms the drug release mechanism., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier B.V.)

Dual-pore covalent organic frameworks (COFs) offer a molecular scaffold for introducing building blocks into periodically organized polygonal skeletons to produce fascinating structural features. The rapid development of this material has attracted intensive interest from researchers with diverse expertise. This review selects the leading scientific findings about dual-pore COFs and highlights their functions and perspectives on design, structure properties, and synthesis strategies. Dual-pore COFs, as newly hetero-pore COFs by integrating particular pores into one polygonal skeleton, have been compared to conventional COFs. Dual-pore COFs display hierarchical/heterogeneous porosities and homogeneous porosity, which endow them with exceptional features involving mass diffusion, charge transfer, and large surface area with abundant active sites. Additionally, the strategic dual-pore design by opting for different approaches, such as integration of [D 2h  + C 2 ] symmetries, kagome-type lattices, and other symmetric arrangements of monomers, are inclusively discussed. Identification and construction of dual-pores in COFs via optimal synthetic methods, such as desymmetrization, multiple linking sites, and orthogonal reactions, are highlighted as the primary pore engineering routes to simultaneously regulate the growth and alter the characteristics of COFs for promising applications. Lastly, a focused discussion on various challenges and critical fundamentals of dual-pore engineering is successfully outlined, with potential prospects of introducing dual-pore in COFs., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

In recent times, green chemistry or "green world" is a new and effective approach for sustainable environmental remediation. Among all biomaterials, cellulose is a vital material in research and green chemistry. Cellulose is the most commonly used natural biopolymer because of its distinctive and exceptional properties such as reproducibility, cost-effectiveness, biocompatibility, biodegradability, and universality. Generally, coupling cellulose with other nanocomposite materials enhances the properties like porosity and specific surface area. The polymer is environment-friendly, bioresorbable, and sustainable which not only justifies the requirements of a good photocatalyst but boosts the adsorption ability and degradation efficiency of the nanocomposite. Hence, knowing the role of cellulose to enhance photocatalytic activity, the present review is focused on the properties of cellulose and its application in antibiotics, textile dyes, phenol and Cr(VI) reduction, and degradation. The work also highlighted the degradation mechanism of cellulose-based photocatalysts, confirming cellulose's role as a support material to act as a sink and electron mediator, suppressing the charge carrier's recombination rate and enhancing the charge migration ability. The review also covers the latest progressions, leanings, and challenges of cellulose biomaterials-based nanocomposites in the photocatalysis field., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Air pollution is becoming a distinctly growing concern and the most pressing universal problem as a result of increased energy consumption, with the multiplication of the human population and industrial enterprises, resulting in the generation of hazardous pollutants. Among these, carbon monoxide, nitrogen oxides, Volatile organic compounds, Semi volatile organic compounds, and other inorganic gases not only have an adverse impact on human health both outdoors and indoors, but have also substantially altered the global climate, resulting in several calamities around the world. Thus, the purification of air is a crucial matter to deal with. Photocatalytic oxidation is one of the most recent and promising technologies, and it has been the subject of numerous studies over the past two decades. Hence, the photocatalyst is the most reassuring aspirant due to its adequate bandgap and exquisite stability. The process of photocatalysis has provided many benefits to the atmosphere by removing pollutants. In this review, our work focuses on four main themes. Firstly, we briefly elaborated on the general mechanism of air pollutant degradation, followed by an overview of the typical TiO 2 photocatalyst, which is the most researched photocatalyst for photocatalytic destruction of gaseous VOCs. The influence of operating parameters influencing the process of photocatalytic oxidation (such as mass transfer, light source and intensity, pollutant concentration, and relative humidity) was then summarized. Afterwards, the progress and drawbacks of some typical photoreactors (including monolithic reactors, microreactors, optical fiber reactors, and packed bed reactors) were described and differentiated. Lastly, the most noteworthy coverage is dedicated to different types of modification strategies aimed at ameliorating the performance of photocatalysts for degradation of air pollutants, which were proposed and addressed. In addition, the review winds up with a brief deliberation for more exploration into air purification photocatalysis., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Inc. All rights reserved.)

WBE has been a monitoring system that can give purposeful and inclusive real-time assessments of civic society as well as environmental health. This concept review introduces WBE as a surveillance scheme and initial warning outbreaks of contagious diseases caused by harmful SARS-CoV-2 with pandemic potential. Examining biomarkers of contagious diseases as evidence in polluted water taken from wastewater treatment plants suggests that these systems can be examined to get epidemiological data for checking the transmission of infectious B.1.1.529 to different areas. Thereafter, various benefits of surveillance are provided to analyse health information and pinpoint different problems that may be occurring in the workstation. Surveillance is followed by intervention steps that improved the work environment and prevent further progression of the disease. This information will help to improve early detection strategies, designing a prevention strategy to reduce their spread, infection control and therapies, thus, strengthening our global preparedness to fight future epidemics. In the end, a comprehensive discussion on the remaining challenges and opportunities for epidemiology has been given for future research perspectives., Competing Interests: Declaration of competing interest All authors declare no conflict interest., (Copyright © 2022 Elsevier B.V. All rights reserved.)

The present study used a free radical co-polymerization approach to synthesize a smart hydrogel of itaconic acid grafted poly(acrylic acid-co-aniline) (ItA-g-poly(AA-co-ANi)). ItA-g-poly(AA-co-ANi) hydrogel was characterized by Fourier transform infrared spectroscopy (FT-IR), Raman, X-ray diffraction (XRD), thermogravimetric analysis (TGA), field emission scanning electron microscope (FE-SEM), and X-ray photoelectron spectroscopy (XPS) analysis. Rhodamine B (RhB) dye was removed from an aqueous medium using ItA-g-poly(AA-co-ANi) hydrogel. To determine the maximum adsorption, the effect of parameters such as initial dye concentration, contact time, pH, and adsorbent dose were examined. The ItA-g-poly(AA-co-ANi) hydrogel had a high swelling percentage of 1755.3%. The high water penetration of ItA-g-poly(AA-co-ANi) hydrogel with a high swelling rate exposed the internal adsorption sites for RhB dye adsorption. The adsorption performance of ItA-g-poly(AA-co-ANi) hydrogel was explained by the pseudo-first-order and Freundlich adsorption isotherm models. Moreover, after four adsorption-desorption cycles, the ItA-g-poly(AA-co-ANi) hydrogel maintained an adsorption efficiency of 85.2%. The high water retention ability of ItA-g-poly(AA-co-ANi) hydrogel improved the moisture maintenance limit of soil for irrigation up to 23 days. As a result, ItA-g-poly(AA-co-ANi) hydrogel can be used in the elimination of toxic dyes as well as in irrigation systems., (Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Aqueous contaminants such as pharmaceuticals, dyes, personal care products, etc., are the common water contaminants that show adverse health effects. Photocatalysis is one of the well-known techniques to treat these water contaminants. Currently, most inorganic photocatalysts show a poor balance between adsorption and photocatalytic activity. In addition, heavy metal pollution and low biosafety are significant concerns in photocatalysis. Thus, environmentally friendly photocatalysts are required to avoid the secondary pollution caused by some inorganic semiconductor-photocatalysts. Organic polymer-based photocatalysts are low-cost, stable, non-toxic, and can utilize visible and NIR light for photocatalysis. In this review, we have discussed polypyrrole as a photocatalyst. Polypyrrole is a conducting organic polymer photocatalyst that is highly stable with high charge mobility and strong binding sites for photocatalytic reactions. Besides these advantages, polypyrrole has limitations, such as high charge recombination due to a small bandgap and poor dispersity. So we have explored the modifications to polypyrrole photocatalysts, such as doping and heterojunctions. Further, we have explained the applications of polypyrrole in photocatalysis as an adsorbent, sensitizer, degradation of pollutants, and energy production. Finally, the future aspects of polypyrrole photocatalysis are also explored to improve the path of future research., (Copyright © 2022. Published by Elsevier Ltd.)

In this study, using a new polymer combination of Chitosan(CH)/Xanthan Gum(XG) has been exhibited for wound dressing implementation by the 3D-Printing method, which was fabricated due to its biocompatible, biodegradable, improved mechanical strength, low degradation rate, and hydrophilic nature to develop cell-mimicking, cell adhesion, proliferation, and differentiation. Different concentrations of XG were added to the CH solution as 0.25, 0.50, 0.75, 1, and 2 wt% respectively in the formic acid/distilled water (1.5:8.5) solution and rheologically characterized to evaluate their printability. The results demonstrated that high mechanical strength, hydrophilic properties, and slow degradation rate were observed with the presence and increment of XG concentration within the 3D-Printed patches. Moreover, in vitro cell culture research was conducted by seeding NIH 3T3 fibroblast cells on the patches, proving the cell proliferation rate, viability, and adhesion. Finally, 1% XG and 4% CH containing 3D-Printed patches were great potential for wound dressing applications., (Copyright © 2022. Published by Elsevier B.V.)

Many mortal organisms on this planet have developed the potential to merge all internal as well as external environmental cues to regulate various processes running inside organisms and in turn make them adaptive to the environment through the circadian clock. This moving rotator controls processes like activation of hormonal, metabolic, or defense pathways, initiation of flowering at an accurate period, and developmental processes in plants to ensure their stability in the environment. All these processes that are under the control of this rotating wheel can be changed either by external environmental factors or by an unpredictable phenomenon called mutation that can be generated by either physical mutagens, chemical mutagens, or by internal genetic interruption during metabolic processes, which alters normal functionality of organisms like innate immune responses, entrainment of the clock, biomass reduction, chlorophyll formation, and hormonal signaling, despite its fewer positive roles in plants like changing plant type, loss of vernalization treatment to make them survivable in different latitudes, and defense responses during stress. In addition, with mutation, overexpression of gene components sometimes supresses mutation effect and promote normal circadian genes abundance in the cell, while sometimes it affects circadian functionality by generating arrhythmicity and shows that not only mutation but overexpression also effects normal functional activities of plant. Therefore, this review mainly summarizes the role of each circadian clock genes in regulating rhythmicity, and shows that how circadian outputs are controlled by mutations as well as overexpression phenomenon., (© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

In solar photocatalysis, light utilization and recycling of powder from reaction solution are the main obstructions that hinder the photocatalytic efficacy of any photocatalyst. In this respect, a floatable system is effective for efficient solar photocatalysis by light utilization. Due to the maximum solar light absorption property, floating nanocomposite photocatalyst is an appealing substitute for effective wastewater treatment. Floating photocatalysts are a non-oxygenated and non-stirred solution that is a good light harvester, stable, non-toxic, biodegradable, naturally abundant in nature. They also have low density, a simple preparation process, no need to stir, and high porosity. Due to these characteristics, floating photocatalysts are widely favored and ideal candidates for practical environmental remediation. Several researchers have come up with new and innovative ways for immobilizing capable photocatalyst on a floatable substrate to produce floating nanocomposite photocatalytic material. In recent decades, g-C 3 N 4 -based floating photocatalysts have gained a lot of attention as g-C 3 N 4 is a visible light active photocatalyst with unique and exceptional properties. It also has good photocatalytic activity in waste water treatment and environmental remediation. Many previous reports have studied the logical design and manufacturing method for heterojunction floating photocatalysts and immobilized floating photocatalysts. Based on those studies, we have focused on the g-C 3 N 4 based immobilized and non-immobilized floating photocatalysts for pollutant degradation. We have also categorized immobilized floating photocatalyst based on several lightweight substrates such as expanded perlite and glass microbead. In addition, future challenges have been discussed to maximize solar light absorption and to improve the efficiency of broadband response floating photocatalysts. Floating photocatalysis is an advanced technique in energy conversion and environmental remediation thus requires special consideration., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Coronavirus disease-2019 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has been one of the most challenging worldwide epidemics of recent times. Semiconducting materials (photocatalysts) could prove effectual solar-light-driven technology on account of variant reactive oxidative species (ROS), including superoxide ( • O 2 - ) and hydroxyl ( • OH) radicals either by degradation of proteins, DNA, RNA, or preventing cell development by terminating cellular membrane. Graphene-based materials have been exquisitely explored for antiviral applications due to their extraordinary physicochemical features including large specific surface area, robust mechanical strength, tunable structural features, and high electrical conductivity. Considering that, the present study highlights a perspective on the potentials of graphene based materials for photocatalytic antiviral activity. The interaction of virus with the surface of graphene based nanomaterials and the consequent physical, as well as ROS induced inactivation process, has been highlighted and discussed. It is highly anticipated that the present review article emphasizing mechanistic antiviral insights could accelerate further research in this field., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2022 Elsevier Ltd. All rights reserved.)

The prevalence of global health implications from the COVID-19 pandemic necessitates the innovation and large-scale application of disinfection technologies for contaminated surfaces, air, and wastewater as the significant transmission media of disease. To date, primarily recommended disinfection practices are energy exhausting, chemical driven, and cause severe impact on the environment. The research on advanced oxidation processes has been recognized as promising strategies for disinfection purposes. In particular, semiconductor-based photocatalysis is an effective renewable solar-driven technology that relies on the reactive oxidative species, mainly hydroxyl (•OH) and superoxide (•O 2 - ) radicals, for rupturing the capsid shell of the virus and loss of pathogenicity. However, the limited understanding of critical aspects such as viral photo-inactivation mechanism, rapid virus mutagenicity, and virus viability for a prolonged time restricts the large-scale application of photocatalytic disinfection technology. In this work, fundamentals of photocatalysis disinfection phenomena are addressed with a reviewed remark on the reported literature of semiconductor photocatalysts efficacies against SARS-CoV-2. Furthermore, to validate the photocatalysis process on an industrial scale, we provide updated data on available commercial modalities for an effective virus photo-inactivation process. An elaborative discussion on the long-term challenges and sustainable solutions is suggested to fill in the existing knowledge gaps. We anticipate this review will ignite interest among researchers to pave the way to the photocatalysis process for disinfecting virus-contaminated environments and surfaces for current and future pandemics., (Copyright © 2022 Elsevier Inc. All rights reserved.)

Nanotechnology holds huge potential for the prevention of various viral outbreaks that have increased at a disquieting rate over the past decades. Metal oxide nanomaterials with oxidative capability are the effective materials that provide platforms as well as tools for the well understanding of the mechanism, its detection, and treatment of various viral diseases like measles, influenza, herpes, ebola, current COVID-19 etc. In this inclusive review, we survey various previous research articles on different notable photoactive transition metal oxides that possess enough potential to act as antiviral agents for the deactivation of harmful viruses. We investigated and highlighted the plausible photocatalytic oxidative mechanism of photoactive transition metal oxides in degrading viral coatings, genomic RNA using suitable free radical generation. The key finding of the present review article including the discovery of a vision on the suitable photocatalytic transition metal oxides that have been proven to be excellent against harmful viruses and consequently combatting deadly CoV-2 in the environment. This review intends to provide conclusive remarks and a realistic outlook on other advanced photocatalytic metal oxides as a potential solution in battling other similar upcoming pandemics., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

MXenes family has aroused marvelous consideration as a frontier photoactive candidate for solar energy transformation and environmental remediation. 2D Ti 3 C 2 exhibit a unique layered microstructure, large surface functional groups (-F, -OH, -O), substantial sorption selectivity, superior reduction efficiency, and electrical conductivity. Electronically conductive Ti 3 C 2 T x with tunable energy band gap (0.92-1.75eV) makes it one of the most potential photoactive materials for photodegradation. The present review paper aims to design cost-effective heterojunctions and Schottky junctions of Ti 3 C 2 with transition metal oxides, sulfides, g-C 3 N 4 , and other organic frameworks. The discussion mainly involves different aspects related to its tunable electronic structure, stability problems, and surface morphology control. In addition, the advantages of Ti 3 C 2 in fabricating highly efficient Ti 3 C 2 based catalytic junctions exhibiting suppressed charge carrier recombination are discussed with particular emphasis on their adsorption and redox properties for the removal of toxic dyes, heavy metal ions, and various pharmaceuticals. Finally, current challenges and research directions are outlined and prospected for the future development of Ti 3 C 2 based photocatalytic systems., (Crown Copyright © 2022. Published by Elsevier Ltd. All rights reserved.)

The vaccine innovation is a ubiquitous preventive measure to the transmission of highly infectious SARS-COV-2. The ongoing mass coronavirus vaccination programmes have inadvertently become the bulk producers of biomedical and plastic waste triggering severe impact on the environment. The sustainable management of bio hazardous vaccine waste in particular; syringes, needles, used/un-used vials and single-use plastic equipment is of utmost importance. This perspective presents a critical point of view in terms of the generated vaccine waste and the subsequent knock-on effect on all aspects of ecosystem. The discussion includes dire consequences due to the release of huge amount of plastic-based personal protective equipment into marine environment. The pivotal crisis of CO 2 emission during the manufacture and storage of different vaccines has contributed to global warming. The unavoidable generation of microfibers upon incineration, autoclaving, pyrolysis and open dumping of vaccine waste has further jeopardized the environment. In this vein, exploration of biodegradable materials for vaccine inoculation and development of green technologies for sound waste management is suggested to mitigate the environment pollution., Competing Interests: Declaration of competing interest All Authors declare no conflict interest., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Removal of hazardous herbicides from the aqueous solution is critical for overcoming health-related issues across the wider population. In the current work, we have prepared sodium alginate (SAlg), dextrin, and acrylic acid (AA) based cross-linked hydrogels, composed of bentonite incorporated in the biocompatible hydrogel matrix. This hydrogel composite can remove highly toxic herbicide paraquat (PQ). As-synthesised hydrogel (SAlg/dextrin-cl-PAA) and hydrogel composite (SAlg/dextrin-cl-PAA/bentonite) were further analysed by infra-red spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and thermogravimetric analysis (TGA/DSC). For the first time, PQ adsorption onto sodium and dextrin-based hydrogel was also evaluated. The measured highest removal capacities were 76.923 and 90.909 mg g -1 for the SAlg/dextrin-cl-PAA and SAlg/dextrin-cl-PAA/bentonite, respectively. Pseudo-second-order (PSO) and Langmuir isotherm models have shown to be best suited for accurately describing the adsorption mechanism. A thermodynamics study verified that the adsorption of PQ on adsorbents is spontaneous, favourable and exothermic. Moreover, reusability analysis shows that the adsorbents possess good reproducibility even after six successive cycles. The adsorption results demonstrate that the synthesised adsorbents are very efficient for removing herbicides (PQ) from wastewater., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Industrial metal ion pollution has been considered the chief source of water contaminants all over the world. In the present research, we have prepared gum tragacanth cross-linked 2-hydroxyethyl methacrylate-co-acrylamide (GT-cl-(HEMA-co-AAm)) hydrogel and gum tragacanth cross-linked 2-hydroxyethyl methacrylate-co-acrylamide/zinc oxide (GT-cl-(HEMA-co-AAm)/ZnO) hydrogel composite with better Hg 2+ adsorption capability. GT-cl-(HEMA-co-AAm)/ZnO hydrogel composite (154.8 mg g -1 ) exhibited higher Hg 2+ adsorption than GT-cl-(HEMA-co-AAm) hydrogel. To address the performance of GT-cl-(HEMA-co-AAm) hydrogel and GT-cl-(HEMA-co-AAm)/ZnO hydrogel composite, batch adsorption experiments were successfully conducted under different optimised conditions. At last, in-vitro antibacterial activities of Hg 2+ loaded GT-cl-(HEMA-co-AAm) and GT-cl-(HEMA-co-AAm)/ZnO were performed in two different well Staphylococcus aureus (gram-positive) and Pseudomonas aeruginosa (gram-negative) bacteria. As a positive control, ampicillin was employed against both types of bacteria. This methodology for the reusability of material has a great ecofriendly impression for minimising secondary waste derived from adsorption and can help design upgraded antibacterial agents., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

As a result of environmental concerns and the depletion of biomass assets, eco-friendly, renewable biomass-based chemical extraction has recently received significant attention. Bio-based chemicals can be prepared using different renewable feedstockbio-resources through microbial fermentation. Chemicals produced from renewable feedstockscan reduce ecological consequences from improper disposal and repurpose them into valuable products. Biodegradability, biocompatibility and non-toxicity, particularly in biomedical applications, have inspired researchers towards developing novel technologies that have social benefit. Among semi-synthetic and synthetic polymeric materials, utilization of natural bio-based monomeric materials can provide opportunities for sustainable development of novel non-toxic, biodegradable and biocompatible products. The purpose of this work is to give a summary of research into the generation of natural bio-based succinic acid (SA) monomer, the development of poly(butylene succinate) (PBS) as biodegradable polymer, PBS-based nanocomposites and their innovative uses., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Reduced graphene oxide (RGO) was synthesized in this research via Tour's method for the use of filler in the hydrogel matrix. The copolymerization of N , N -dimethylacrylamide (DMA) onto the gum tragacanth (GT) was carried out to develop gum tragacanth-cl- N , N -dimethylacrylamide (GT-cl-poly(DMA)) hydrogel using N , N '-methylenebisacrylamide (NMBA) and potassium persulfate (KPS) as cross-linker and initiator correspondingly. The various GT-cl-poly(DMA) hydrogel synthesis parameters were optimized to achieve maximum swelling of GT-cl-poly(DMA) hydrogel. The optimized GT-cl-poly(DMA) hydrogel was then filled with RGO to form reduced graphene oxide incorporated gum tragacanth-cl- N , N -dimethylacrylamide (GT-cl-poly(DMA)/RGO) hydrogel composite. The synthesized samples were used for competent adsorption of Hg 2+ and Cr 6+ ions. Fourier transform infrared, X-ray powder diffraction, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy were used to characterize the gum tragacanth-cl- N , N -dimethylacrylamide hydrogel and reduced graphene oxide incorporated gum tragacanth-cl- N , N -dimethylacrylamide hydrogel composite. The experiments of adsorption-desorption cycles for Hg 2+ and Cr 6+ ions were carried out to perform the reusability of gum tragacanth-cl- N,N -dimethylacrylamide hydrogel and reduced graphene oxide incorporated gum tragacanth-cl- N,N -dimethylacrylamide hydrogel composite. From these two samples, reduced graphene oxide incorporated gum tragacanth-cl- N,N -dimethylacrylamide exhibited high adsorption ability. The Hg 2+ and Cr 6+ ions adsorption by gum tragacanth-cl- N,N -dimethylacrylamide and reduced graphene oxide incorporated gum tragacanth-cl- N,N -dimethylacrylamide were best suited for pseudo-second-order kinetics and Langmuir isotherm. The reported maximum Hg 2+ and Cr 6+ ions adsorption capacities were 666.6 mg g -1 and 473.9 mg g -1 respectively.

Downgrading in the yield of crop is due to the inadequate availability of water. The way out for this trouble is to construct synthetic resources dependent on natural polymers with great water absorption and preservation limits. The present study investigated the design of agar-agar (Agr) and gelatin (GE) copolymerized methyl acrylate (MA) and acrylic acid (AA) hydrogel (Agr/GE-co-MA/AA) as a soil conditioner for moisture maintenance in agriculture. Agr/GE-co-MA/AA hydrogel was prepared by utilizing microwave-assisted green synthesis following the most suitable reaction conditions to obtain a remarkable water swelling percentage. The fabricated Agr/GE-co-MA/AA hydrogel was investigated through field emission scanning electron microscopy (FESEM), fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The water holding capacity of the soil and sand was examined by mixing Agr/GE-co-MA/AA hydrogel with soil and sand. The result demonstrates that the water holding time extended from 10 to 30 days for soil and 6 to 10 days for sand by using Agr/GE-co-MA/AA hydrogel. This synthesized biodegradable, low-cost and non-toxic Agr/GE-co-MA/AA hydrogel shows novelty as soil water maintaining material for irrigation in agriculture.

Herein, porous sodium alginate/graphite based hybrid hydrogel was fabricated as an effective adsorbent for organic pollutant. Sodium alginate was modified through graft polymerization of acrylic acid and subsequently loaded with graphite powder to enhance its adsorption capability. The synthesized sodium alginate cross-linked acrylic acid/graphite (NaA-cl-AAc/GP) hydrogel composite was utilized in the removal of malachite green (MG) dye from aqueous solution using batch adsorption experiments. The NaA-cl-AAc/GP hydrogel composite was characterized by infrared spectroscopy, Raman spectroscopy, thermo-gravimetric analysis, scanning electron microscopy, x-ray photoelectron spectroscopy and x-ray diffraction. Under optimized experimental conditions, a maximum adsorption capacity of 628.93 mg g -1 was attained for malachite green dye. Moreover, the adsorption process could be well described by the Langmuir isotherm model and pseudo-second-order kinetic model. The hydrogel composite also showed 91% adsorption after three consecutive cycles of dye adsorption-desorption. Therefore, the NaA-cl-AAc/GP hydrogel composite is a potentially favourable material towards dye pollution remediation owing to its better swelling rate, environment friendliness, high adsorption potential and regeneration capability., (Copyright © 2020 Elsevier B.V. All rights reserved.)

The transformation of biomass using steam gasification is a chemical route to facilitate changes in organic or residue supported carbonaceous substances addicted to carbon mono-oxide, hydrogen including carbon-di-oxide, etc. However, to commercialize the method of steam gasification, the hurdles persist during the gasification as well as downstream processing. This article delivers a summary of the different approaches that are described in the previous studies to achieve H 2 refinement and adaptation within the gasifier system. These include advanced aspects in the research and development of biomass gasification (alike advancements under the gasification operation). The upshot of diverse operating conditions like steam flow rate, operating temperature, moisture content, gasifier agents, residence time, biomass to air, steam to biomass, equivalence ratio, etc. towards the execution of biomass gasifier. This review accomplishes that the interdependence of several issues must be considered in point to optimise the producer gas., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Pectin is one of the finest natural polymer which has drawn great attention because of its applications in different fields. Due to the quintessential structure of pectin, it can be transformed into variety of useful products. It can be utilized as a blend in many polymers to make a mixture or a composite material. Owing to considerable collection in chemical conformation and cross-linking mechanism, different pectin based hydrogels have been prepared for different characteristics in pharmaceutical and bio-medical sites. Inventive properties of hydrogels like volubility, swellability, solvability and hydrophilicity make them better alternative for wastewater treatment. Recently, pectin based hydrogels have demonstrated excellent performance to eliminate various metal ions and dyes from the polluted water. The adsorption characteristics of pectin based hydrogels can be upgraded by using nanoparticles, which prompts to the development of hydrogel nano-composites. In this review article, we have summarized a comprehensive assessment in the direction of using pectin based hydrogels to remove toxic pollutants from aqueous solution. Sodium acrylate-co-N-isopropylacrylamide based pectin hydrogel has demonstrated the maximum adsorption capacities of 265.49, 137.43, 54.86, 53.86, 51.72 and 50.01 mg g -1 for the adsorption of methyl violet, methylene blue, Pb(II), Cu(II), Co(II) and Zn(II) respectively. We have also discussed the pectin structure, properties and applications in this article., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

A sol-gel synthesis of nanocomposite adsorbent materials by dehydroxylation condensation of tetraethoxysilane (TEOS) in the presence of xanthan gum (XG) using base catalyst and ethanol as co-solvent is discussed. The synthesized nanocomposite material was evaluated for their ability to adsorb cationic dyes-methylene blue (MB) and bismarck brown Y (BB) from an aqueous solution. The XG/SiO 2 nanocomposite shows the ordered macro- and meso-porous structures and also exhibited large surface area, excellent chemical/mechanical stability and high binding capability for MB and BB dyes. Different parameters such as pH, adsorbent dose and initial concentration were studied. The adsorption behaviour of the nanocomposite was investigated by performing both kinetics and equilibrium studies under batch conditions. The maximum adsorption capacity (Q max ) of the nanocomposite for MB and BB was found to be significantly high (432.90mgg -1 and 448.43mgg -1 , respectively). The time taken for the removal of 99.4% of MB and 87.2% of BB from 100mgL -1 of dye solutions is only 35min. Thus, the proposed XG/SiO 2 nanocomposite is a very promising adsorbent for the fast and efficient removal of dye from aqueous solutions., (Copyright © 2017 Elsevier B.V. All rights reserved.)

Batch adsorption experiments were carried out for the removal of methylene blue (MB) cationic dye from aqueous solution using organic/inorganic hydrogel nanocomposite of titania incorporated sodium alginate crosslinked polyacrylic acid (SA-cl-poly(AA)-TiO2). The hydrogel was prepared by graft copolymerization of acrylic acid (AA) onto sodium alginate (SA) biopolymer in the presence of a crosslinking agent, a free radical initiator and TiO2 nanoparticles. The hydrogel exhibited a high swelling capacity of 412.98g/g. The factors influencing adsorption capacity of the absorbents such as pH of the dye solutions, initial concentration of the dye, amount of absorbents, and temperature were investigated and used to propose a possible mechanism of adsorption. The adsorption process concurs with a pseudo-second-order kinetics and with Langmuir isotherm equation. A very high adsorption capacity (Qmax=2257.36 (mg/g)) and a correlation coefficient of 0.998 calculated from isotherm equations show the high efficiency of the absorbent and thus expected to be a good candidate as an absorbent for water treatment., (Copyright © 2016 Elsevier Ltd. All rights reserved.)