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Abstract Despite the widespread use of titanium dioxide (TiO2) in photocatalytic applications, its inherent limitations, such as low efficiency under visible light and rapid recombination of electron-hole pairs, hinder its effectiveness in environmental remediation. This study presents a comparative investigation of TiO2-based composites, including TiO2/ZrO2, ZnO, Ta2O3, SnO, Fe2O3, and CuO, aiming to assess their potential for enhancing photocatalytic applications. Photocatalysis holds promise in environmental remediation, water purification, and energy conversion, with TiO2 being a prominent photocatalyst. To improve efficiency and broaden applicability, various metal oxide composites have been explored. Composites were synthesized and characterized using techniques such as XRD, SEM, TEM, and zeta potential analysis to evaluate their structural and morphological properties. Photocatalytic performance was assessed by degrading herbicide Imazapyr under UV illumination. Results revealed that, the photo-activity of all prepared composites were more effective than the photo-activity of commercial hombikat UV-100. The photonic-efficiency is arranged according to the order TiO2/CuO > TiO2/SnO > TiO2/ZnO > TiO2/Ta2O3 > TiO2/ZrO2 > TiO2/Fe2O3 > Hombikat TiO2-UV100. All composites exhibited superior performance, attributed to enhanced light absorption and charge separation. The study underscores the potential of these composites for environmental remediation and energy conservation, offering valuable insights for the development of advanced photocatalysts.

Abstract Green nanotechnology offers several possibilities to bridge the nano and sustainability domains and help us achieve the Sustainable Development Goals (SDGs) and address major global concerns. In this review, we detail the fundamentals and applications of GNT toward SDGs goals. This includes energy production, pollution abatement, water treatment, and eco-friendly agricultural practices. The discussion includes challenges related to legal, ethical and safety aspects as well as limits of the technology. Prospects call for collaborative efforts across various disciplines and policy guidelines in bridging eco-friendly nanotechnology with UN SDGs. We hope that the insights provided in this review can help guide future research and policies toward more environmentally responsible practices, improving global environmental stewardship with a special emphasis on nanotechnology. Graphical Abstract

Abstract The development of photocatalysts must be meticulous, especially when they are designed to degrade hazardous dyes that cause mutagenesis and carcinogenesis. In this meticulous approach, Ni-based metal–organic frameworks with different ligands, including terephthalic acid (NTP), 2-aminoterephthalic acid (NATP), and their composite with g-C3N4 (NTP/GCN, and NATP/GCN) have been synthesized using hydrothermal method. Structural analysis by XRD and ATR-IR revealed synergistic properties due to robust chemical interactions between the NATP-MOFs and GCN systems. A flower-like morphology was observed for both NTP and NATP, while their composites showed mixed-particulate structures mimicking the morphology of GCN. Optical analyses indicated visible-light driven properties with modulated recombination resistance in the system. Among the synthesized bare and composite systems, NATP/GCN exhibited the highest photocatalytic degradation efficiency for the cationic rhodamine B dye (~ 93% in 120 min), while it was relatively less efficient for the anionic Congo red dye, (~ 64% in 120 min). The insights gained from the fundamental characterizations including Mott–Schottky, scavenger, and electrochemical impedance analysis revealed that the amino-groups in NATP/GCN composite offered the band edge potentials suitable for the effective generation of energetic radical species with the improved carrier delocalization, recombination resistance, and charge transfer properties in the composite system through Z-scheme formation. Parametric investigations by varying the concentration of catalyst, dye, and pH along with recycle studies, demonstrated the excellent stability of the developed composites for sustainable photocatalytic applications.

Gold nanoclusters (AuNCs), with sizes below 2 nm, have emerged as remarkable nanomaterials exhibiting unique optical, electronic, and chemical properties. Their ultra-small size imparts advantageous characteristics, including high surface area, tunable fluorescence, and excellent biocompatibility, making AuNCs highly promising for diverse applications. This article explores recent advancements in leveraging AuNCs to address critical challenges in clean energy storage and environmental remediation. For energy storage, AuNCs boost the performance of Li-based batteries by facilitating rapid electron transfer kinetics and limiting polysulfide shuttling. The review delves into mechanistic insights governing AuNC–hydrogen interactions, various synthetic approaches for tailoring AuNCs, and their emerging applications as advanced electrodes, efficient catalysts, and conductive additives enabling improved charge storage capabilities. Additionally, using plasmonic effects and hot carrier generation induced by AuNCs shows tremendous potential in photocatalytic water splitting for clean hydrogen fuel production. For environmental applications, AuNCs enable the degradation of persistent organic pollutants, heavy metal ion detection at part-per-trillion levels, and solar-driven water purification, relying on plasmon-enhanced hot carrier processes. However, the long-term ecological impacts of AuNCs remain unclear. This study thus underscores the need for further toxicological assessments and life cycle analyses to promote sustainable AuNC-based technologies through responsible research and innovation. Overall, it highlights the versatile applicability of AuNCs in addressing critical energy and environmental challenges.

• A dual atomic Mn and S co-doping C 3 N 4 was synthesized by thermal polymerization. • Mn and S doping adjusts the band structure improving the separation of photo-generated electrons and holes. • Mn and S doping promotes O 2 adsorption and electron transfer to generate active species. • Mn/S-C 3 N 4 shown excellent degradation efficiency for various organic pollutants. Oxygen activation leading to the generation of reactive oxygen species (ROS) is essential for photocatalytic environmental remediation. The limited efficiency of O 2 adsorption and reductive activation significantly limits the production of ROS when employing C 3 N 4 for the degradation of emerging pollutants. Doping with metal single atoms may lead to unsatisfactory efficiency, due to the recombination of photogenerated electron-hole pairs. Here, Mn and S single atoms were introduced into C 3 N 4 , resulting in the excellent photocatalytic performances. Mn/S-C 3 N 4 achieved 100% removal of bisphenol A, with a rate constant 11 times that of pristine C 3 N 4. According to the experimental results and theoretical simulations, S-atoms restrict holes, facilitating the photo-generated carriers' separation. Single-atom Mn acts as the O 2 adsorption site, enhancing the adsorption and activation of O 2 , resulting the generation of ROS. This study presents a novel approach for developing highly effective photocatalysts that follows a new mechanism to eliminate organic pollutants from water. [Display omitted] [ABSTRACT FROM AUTHOR]

The extensive use of synthetic dyes in the textile industry has resulted in severe water contamination, with methylene blue (MB) being a prevalent pollutant. This study presents the development of an eco-friendly nanocomposite, Activated Carbon Thin Film-Zeolitic Imidazolate Framework-8 (ACTF@ZIF-8), synthesized through an in-situ growth method for efficient MB removal from aqueous solutions. The composite's structural and physicochemical properties were thoroughly characterized using Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TGA), X-ray Diffraction (XRD), High-Resolution Transmission Electron Microscopy (HR-TEM), and Brunauer-Emmett-Teller (BET) surface area analysis. The nanocomposite exhibited a high specific surface area of 384.4 m2/g and an adsorption capacity of 156.83 mg/g, achieving a removal efficiency of 98.8%. Kinetic studies indicated that MB adsorption followed a pseudo-second-order model (R2 = 0.9994), suggesting chemisorption as the primary mechanism. The adsorption isotherms conformed to the Freundlich model (R2 = 0.999), indicating multilayer adsorption on a heterogeneous surface. Thermodynamic analysis indicated an endothermic process, characterized by a positive enthalpy change and an increase in entropy. The process was confirmed to be spontaneous, as demonstrated by negative Gibbs free energy values. The composite also demonstrated high reusability, maintaining efficiency across multiple cycles. These findings position ACTF@ZIF-8 as a promising material for sustainable wastewater treatment, aligning with advancements in nanomaterial-based environmental remediation. [ABSTRACT FROM AUTHOR]

[Display omitted] • Dual-functional paper-based materials are fabricated through a surface engineering strategy. • Rapid and sensitivity detection towards Cr 2 O 7 2− is achieved through multiple detection methods. • N and B co-doped MXene quantum dots possess longer maximum emission wavelengths and strong oxidation stability. • Outstanding enrichment capacity towards Cr 2 O 7 2− (162.4 mg g−1) is exhibited. Dichromate ion (Cr 2 O 7 2−) is a highly toxic chromium-containing compound that poses significant hazards to the digestive, respiratory systems, skin, and mucous membranes. Currently, the detection and adsorption of Cr 2 O 7 2− face significant challenges, including the time-consuming and low sensitivity nature of traditional analytical methods. The limited efficiency and capacity of existing adsorbents hinder their practical application in real-time water quality monitoring and environmental remediation. Herein, using polyethyleneimine-functionalized (PEI) pulp fiber paper as the substrate, we developed smart paper-based materials (designated as NB-MQDs@PP) incorporated with nitrogen and boron co-doped MXene quantum dots (NB-MQDs) for rapid adsorption and sensitive detection of Cr 2 O 7 2−. Compared to undoped MQDs, NB-MQDs exhibited longer excitation wavelength and enhanced oxidation stability. As anticipated, NB-MQDs achieved rapid (response time of 10 s) and sensitive (detection limit of 1.2 μM) recognition of Cr 2 O 7 2− within a wide pH range with a quenching efficiency of 99.9%. Simultaneously, two on-site detection methods, immersion and cyclic filtration, were constructed based on NB-MQDs@PP. The detection limit of the immersion method was 17.0 nM, while the cyclic filtration method had a detection limit as low as 3.8 nM, surpassing the majority of those reported literatures. Remarkably, NB-MQDs@PP exhibited outstanding enrichment capacity towards Cr 2 O 7 2−, with an adsorption capacity of up to 162.4 mg/g. This work provides a novel strategy for creating unique paper-based materials with excellent capture and monitoring dual-function, which can be customized according to the requirements of various application scenarios. [ABSTRACT FROM AUTHOR]

The treatment of dye-contaminated wastewater is essential for mitigating environmental and health risks. In this study, we developed a novel nanocomposite, TiO₂-incorporated graphene oxide (TiO₂@GOn), aimed at enhancing the photocatalytic degradation of neutral red dye, which served as the target analyte. The photocatalysis technique was employed, leveraging the excitation of TiO₂ under UV light to generate reactive oxygen species for efficient dye degradation. TiO₂ nanorods were combined with graphene oxide to form the TiO₂@GOn nanocomposite, designed to improve charge separation and enhance catalytic activity. Nanocomposite characterization was carried out using X-ray diffraction (XRD) to determine crystallographic structure, scanning electron microscopy (SEM) to visualize surface morphology, and UV–Vis spectroscopy to evaluate the optical properties and photocatalytic behavior. The TiO₂@GOn nanocomposite demonstrated a synergistic catalytic effect, outperforming pristine TiO₂ and graphene oxide individually in dye degradation. This study introduces a highly efficient nanomaterial for environmental applications, offering a sustainable approach to the treatment of dye pollutants in wastewater.Highlights: Development of TiO2-incorporated graphene oxide nanocomposite (TiO2@GOn). Catalytic degradation ability towards neutral red dye has been explored. Highly exposed surface area for the photocatalytic degradation process. Highly effective in the photocatalytic degradation of neutral red dye. Explored the possibility of employing TiO2@GOn in dye degradation applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • Fe 3 O 4 @P-C 3 N 4 can activate the PMS-assisted photocatalysis (PAP) system. • P doping and tubular morphology enhance the light response and carrier separation. • Heterogeneous electron acceptors promote the formation of reactive species. • The Fe 3 O 4 @P-C 3 N 4 /PAP system exhibits low toxicity and stability for TC removal. • This system has strong adaptability to actual water environments. Photocatalytic wastewater purification is essential for environmental remediation, but rapid carrier recombination and limited oxidative capacity hinder progress. This study proposes an innovative strategy by integrating homogeneous and heterogeneous electron acceptors into a g-C 3 N 4 −based photocatalytic system, significantly enhancing the multipath utilization of photogenerated electrons. A novel Fe 3 O 4 @P-C 3 N 4 was developed to activate an advanced peroxymonosulfate−assisted photocatalysis (PAP) system, achieving complete degradation and significant mineralization of tetracycline (TC) in real water environments, outperforming others reported in the last five years. Phytic acid, as a key precursor, modifies the hollow tubular morphology and introduces phosphorus (P) heteroatoms as electronic trapping centers, enhancing the visible light response and carrier separation, thereby promoting the Fe2+/Fe3+ cycle and the formation of reactive species. Density functional theory (DFT) calculations pinpointed TC's vulnerable sites and synergically identified reactive species, revealing almost non-toxic degradation processes. Moreover, the recyclable magnetic Fe 3 O 4 @P-C 3 N 4 /PAP system demonstrates practical application potential and leaching stability in cyclic and continuous testing. This study offers unique insights into the strategic design of photocatalysts and catalytic environments, potentially advancing practical wastewater remediation. [ABSTRACT FROM AUTHOR]

Schematic presentation of synthesis of Cu- BDC MOF nanosheets and rGO/ Cu- BDC MOF nanosheets. [Display omitted] • Two-dimensional rGO/Cu-BDC MOF nanocomposites were successfully synthesized. • An efficient catalytic reduction of 4-NP to 4-AP is accomplished using rGO/Cu-BDC MOF. • The synergy between Cu-BDC MOF and rGO enhances both the 4-nitrophenol reduction and electrochemical properties. Two-dimensional nanosheets, with their distinct characteristics, are widely used in various applications such as water splitting, supercapacitors, catalysis etc. In this research, we produced Cu-BDC MOF nanosheets by using Cu 2 O nanotubes for metal ions and H 2 BDC as the organic linker. We combined these Cu-BDC MOF nanosheets with reduced graphene oxide (rGO) to form a nanocomposite. The collaboration between Cu-BDC MOF and rGO boosts both the catalytic reduction of 4-nitrophenol and the electrochemical capabilities. The conversion of 4-nitrophenol to 4-aminophenol is achieved using sodium borohydride as both a reducing agent and a catalyst. The study explores the impact of different concentrations of 4-nitrophenol and sodium borohydride on catalytic efficiency. The increase in sodium borohydride concentration enhances catalytic efficiency by providing more BH 4 − ions and electrons for the reduction process. The catalytic reduction process adheres to the Langmuir–Hinshelwood mechanism with apparent pseudo-first-order kinetics. Specifically, Cu-BDC MOF and rGO/Cu-BDC MOF exhibit specific capacities of 468.4 mA h/g and 656.4 mA h/g at a current density of 2 A/g, respectively, while also enhancing the operating voltage window. Therefore, electrodes based on rGO/Cu-BDC MOF nanosheets present a novel approach for environmental remediation and energy storage applications across various fields. [ABSTRACT FROM AUTHOR]

The efficient elimination of synthetic dyes from industrial wastewaters continues to be a significant environmental issue. This paper describes one-pot synthesis of zinc titanate nanocomposites exhibiting dual adsorption and photocatalytic properties, achieved using precipitation/calcination and solvothermal techniques from a common precursor solution. Methylene blue (MB), a frequently utilized cationic dye, was chosen as the model contaminant. The zinc titanate composites exhibited significant adsorption capabilities; consistently attaining > 4 mg of MB adsorbed per gram of material for all Zn/Ti ratios within the initial 30 min in the absence of UV light exposure. Composites having a Zn/Ti ratio of 0.5 exhibited superior performance, with Z-0.5c attaining the maximum photocatalytic degradation under UV illumination. Phase analysis indicated that calcination resulted in increased crystallinity, which was associated with improved photocatalytic activity, while solvothermally generated samples preserved nanoscale morphologies that facilitated adsorption. The results underscore the efficacy ofzinc titanate nanocomposites as dual-function materials for wastewater treatment, facilitating fast adsorption and prolonged photocatalytic degradation to enhance dye elimination. This study offers significant insights into the optimization of Zn/Ti ratios and synthesis techniques for improved environmental applications. [ABSTRACT FROM AUTHOR]

The application of semiconductor photocatalysis powered by renewable energy sources for environmental remediation of emerging contaminants has gained significant research interest in recent years. Lanthanum-substituted bismuth vanadate (La-BiVO4)/graphitic carbon nitride (g-C3N4) heterojunctions were synthesized for the photocatalytic degradation of emerging water contaminants. Significantly, La³+ substitution serves as a model system for exploring the broader concept of cationic substitutions on BiVO4. By strategically replacing a portion of Bi(III) with various cations, we can potentially tailor the electronic structure of BiVO4 for enhanced photocatalytic performance. Photoelectrochemical analysis confirmed rapid charge separation and reduced resistance, leading to effective contaminant degradation. The La-BiVO4/g-C3N4 nanocomposite exhibited exceptional photocatalytic performance under simulated solar light irradiation (Xe-350W, AM 1.5 G), achieving 87.66% photooxidation of roxarsone within 150 min, surpassing g-C3N4, BiVO4, LaVO4, La-BiVO4, BiVO4/g-C3N4, and LaVO4/g-C3N4 by factors of 1.94, 1.26, 2.25, 1.39, 1.13, and 2.51, respectively. Moreover, it demonstrated 99.61% degradation of Cr(VI) after 60 min, outperforming g-C3N4, BiVO4, LaVO4, La-BiVO4, BiVO4/g-C3N4, and LaVO4/g-C3N4 by factors of 1.11, 1.81, 1.62, 1.67, 1.20, and 1.13, respectively. These findings underscore the superior photocatalytic efficacy of the La-BiVO4/g-C3N4 nanocomposite. The efficient photocatalytic activity of La-BiVO4/g-C3N4 type-II heterojunctions demonstrates its potential for real-world environmental remediation. This material offers a promising strategy for removing harmful water contaminants, thereby mitigating risks associated with water consumption. [ABSTRACT FROM AUTHOR]

[Display omitted] In the last decades, 4-nitrophenol is regarded as one of highly toxic organic pollutants in industrial wastewater, which attracts great concern to earth sustainability. Herein, atomically dispersed ternary FeCoNb active sites were incorporated into nitrogen-doped honeycomb-like mesoporous carbon (termed FeCoNb/NHC) by a two-step pyrolysis strategy, whose morphology, structure and size were characterized by a set of techniques. Further, the catalytic activity and reusability of the as-prepared FeCoNb/NHC were rigorously examined by using 4-NP catalytic hydrogenation as a proof-of-concept model. The influence of the secondary pyrolysis temperature on the catalytic performance was investigated, combined by illuminating the catalytic mechanism. The resultant catalyst exhibited significantly enhanced catalytic features with a normalized rate constant (k app) of 1.2 × 104 min-1g−1 and superior stability, surpassing the home-made catalysts in the control groups and earlier research. This study provides some constructive insights for preparation of high-efficiency and cost-effectiveness single-atom nanocatalysts in organic pollutants environmental remediation. [ABSTRACT FROM AUTHOR]

[Display omitted] • The Al 6 Si 2 O 13 /WO 2.72 nanocomposites exhibits excellent photocatalytic activity and stability in degrading triazophos pesticides, reducing the rate from 100.0% to 13.7% in 140.0 min. • The S-scheme heterojunction significantly enhances photocatalytic performance by improving charge separation and minimizing recombination. • Abundant oxygen vacancies combined with the S-scheme heterojunction accelerate charge separation, further enhancing photocatalytic degradation activity. The environmental contamination caused by organophosphorus pesticides (for example, triazophos) is an escalating concern. To mitigate this issue, this study introduces a novel Al 6 Si 2 O 13 /WO 2.72 (ASO/WO) nanocomposite photocatalyst, which markedly enhances the photocatalytic degradation of triazophos. The optimized nanocomposite material with a 60.0 % ASO loading (60-ASO/WO) achieves a degradation rate of 86.3 % for triazophos within 140.0 min, marginally exceeding 60-ASO/WO 3 (72.6 %) and significantly outperforming individual ASO (65.0 %), WO (59.5 %), and WO 3 (56.2 %). This catalyst retains 88.9 % of its activity after five cycles, showcasing exceptional efficiency and stability. Additionally, its electrochemical surface area (ECSA, 310.0 cm2), total organic carbon (TOC, removal rate of 73.7 %), photocurrent, and electrochemical impedance are all optimal. X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), and theoretical calculations elucidate the critical role of oxygen vacancies and the S-scheme heterojunction in augmenting charge separation and photocatalytic performance, corroborating the synergistic effect of oxygen defects and the S-scheme. While individual factors can enhance photocatalytic activity, their combination results in a more pronounced effect. Liquid chromatography-mass spectrometry (LCMS) identifies the principal degradation intermediates, including 1-phenyl-3-hydroxy-1, 2, 4-triazole, diethyl thiophosphate, and 3, 5, 6-trichloro-2-pyridinol, underscoring the material's potential in environmental remediation. [ABSTRACT FROM AUTHOR]

Dibromoethane is a widespread, persistent organic pollutant. Biochars are known mediators of reductive dehalogenation by layered FeII-FeIII hydroxides (green rust), which can reduce 1,2-dibromoethane to innocuous bromide and ethylene. However, the critical characteristics that determine mediator functionality are lesser known. Fifteen biochar substrates were pyrolyzed at 600 °C and 800 °C, characterized by elemental analysis, X-ray photo spectrometry C and N surface speciation, X-ray powder diffraction, specific surface area analysis, and tested for mediation of reductive debromination of 1,2-dibromoethane by a green rust reductant under anoxic conditions. A statistical analysis was performed to determine the biochar properties, critical for debromination kinetics and total debromination extent. It was shown that selected plant based biochars can mediate debromination of 1,2-dibromoethane, that the highest first order rate constant was 0.082/hr, and the highest debromination extent was 27% in reactivity experiments with 0.1 µmol (20 µmol/L) 1,2-dibromoethane, ≈ 22 mmol/L FeII GR , and 0.12 g/L soybean meal biochar (7 days). Contents of Ni, Zn, N, and P, and the relative contribution of quinone surface functional groups were significantly (p < 0.05) positively correlated with 1,2-dibromoethane debromination, while adsorption, specific surface area, and the relative contribution of pyridinic N oxide surface groups were significantly negatively correlated with debromination. [ABSTRACT FROM AUTHOR]

Environmental inequalities are often large and consequential, exacerbating vertical inequalities of income and class and horizontal inequalities along lines of race and ethnicity. Climate policies can widen these inequalities as well as mitigate them, depending on their design. Decarbonization of the US electricity sector illustrates these possibilities. A strategy narrowly focused on carbon reduction alone is likely in some regions to increase disparities in exposure to localized co-pollutants emitted by fossil fuel combustion and, in some cases, to increase exposure in absolute terms. Strategies that in addition explicitly mandate improvements in air quality, both overall and specifically for frontline communities, can couple decarbonization with remediation of environmental inequalities and broad-based gains in public health. [ABSTRACT FROM AUTHOR]

Despite the long tradition of mining activities in Kosovo, there is still the a lack of policies for post-mining. Specifically, focusing on coal mining, this research analyzes the sustainable transition and post-mining management in the Ruhr Region, exploring the potential for knowledge transfer to enhance mining practices in Kosovo. The research aims to identify transferable strategies for sustainable mining transitions by examining environmental, social, and economic dimensions. Through comparative analysis, the study assesses the applicability of Ruhr’s experiences in fostering environmentally responsible mining practices in Kosovo and beyond. Similarities and possible challenges are discussed based on the environmental and socio-economic points of view. The findings contribute insights into effective post-mining strategies, facilitating knowledge transfer to regions undergoing similar transitions and thereby fostering sustainable mining practices globally.

Highlights Challenges and future directions for 3D-printed metal-organic frameworks (MOFs) monoliths in environmental applications are discussed. Various strategies for fabrication of 3D-printed MOF monoliths are summarized. Advancements in 3D printing enable customizable and high-performance MOF monoliths. 3D orienting of MOFs opens avenues for applications in water treatment and gas adsorption.

Multiphase microfluidic has emerged as a powerful platform to produce novel materials with tailor-designed functionalities, as microfluidic fabrication provides precise controls over the size, component, and structure of resultant materials. Recently, functional materials with well-defined micro-/nanostructures fabricated by microfluidics find important applications as environmental and energy materials. This review first illustrated in detail how different structures or shapes of droplet and jet templates are formed by typical configurations of microfluidic channel networks and multiphase flow systems. Subsequently, recent progresses on several representative energy and environmental applications, such as water purification, water collecting and energy storage, were overviewed. Finally, it is envisioned that integrating microfluidics and other novel materials will play increasing important role in contributing environmental remediation and energy storage in near future.

The application of soft materials, including gels, in different material and biological chemistry domains has gained momentum in the past few years. Environmental remediation, drug resistance, and delivery are significant concerns that are being investigated widely nowadays. In this work, we report the multifunctionality of a gelator molecule A2 (5,5′-((6-(phenylamino)-1,3,5-triazine-2,4-diyl)-bis-(azanediyl))-diisophthalic acid) in the gel state. The gelator molecule A2 was used to fabricate organogel and two metallogels using copper perchlorate and a Ru-based anticancer drug molecule, respectively. The organogel and Cu-metallogel show efficient adsorption capabilities of iodine in the vapor and solution phases. These iodine-loaded gel composites were utilized as efficient antibacterial agents against Escherichia coli and Helicobacter pylori (I10) bacterial strains. Additionally, owing to the pH-responsive nature of the gel material, the Ru-based anticancer drug-loaded metallogel, Ru-A2, was fabricated, and its activity in pH-responsive drug delivery to the cancerous cells was also investigated. [ABSTRACT FROM AUTHOR]

Autonomous micro/nanorobots capable of performing programmed missions are at the forefront of next-generation micromachinery. These small robotic systems are predominantly constructed using functional components sourced from micro- and nanoscale materials; therefore, combining them with various advanced materials represents a pivotal direction toward achieving a higher level of intelligence and multifunctionality. This review provides a comprehensive overview of advanced materials for innovative micro/nanorobotics, focusing on the five families of materials that have witnessed the most rapid advancements over the last decade: two-dimensional materials, metal–organic frameworks, semiconductors, polymers, and biological cells. Their unique physicochemical, mechanical, optical, and biological properties have been integrated into micro/nanorobots to achieve greater maneuverability, programmability, intelligence, and multifunctionality in collective behaviors. The design and fabrication methods for hybrid robotic systems are discussed based on the material categories. In addition, their promising potential for powering motion and/or (multi-)functionality is described and the fundamental principles underlying them are explained. Finally, their extensive use in a variety of applications, including environmental remediation, (bio)sensing, therapeutics, etc., and remaining challenges and perspectives for future research are discussed. [ABSTRACT FROM AUTHOR]

The rapid development of technology and industries has led to environmental pollution and caused serious harm to living beings. Photocatalysis has attracted widespread attention as an efficient way to increase the purity of air and water by controlling environmental pollution. Several materials such as metal oxides, chalcogenides, and semiconductors have emerged as outstanding photocatalysts because of their cleaner processes, low cost, chemical stability, high photo-catalytic ability, non-toxicity, and ability to absorb UV/visible radiations. In this review, photocatalytic activities of metal oxides and other materials are studied for environmental remediation and other applications. Some major materials used as photocatalysts include TiO2, ZnO, CuO, Fe2O3, ZnS, MOFs, COFs, graphene, g-C3N4, CNTs and bismuth oxides. The present article discusses the size, structure, surface area, morphology, and band gap of photocatalysts. These are the crucial factors for photocatalysis and influence photocatalytic kinetics. This review summarizes the use of various materials as photocatalysts in numerous applications such as the degradation of inorganic or organic pollutants, environmental remediation, air purification, CO2 photoreduction and water splitting for hydrogen production. Finally, a conclusion is drawn regarding future research plans to make photocatalyst materials more efficient and stable for environmental and industrial applications. [ABSTRACT FROM AUTHOR]

Magnetic graphene hybrid has encouraging application in environmental remediation. Herein, adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -graphene oxide (Fe 3 O 4 -GO) surface was inspected via both theoretical and experimental methods. In the theoretical level, acidity impact on Cr (Ⅵ) species evolution and Cr (Ⅵ)→Cr (Ⅲ) reduction was investigated with the methodology of equilibrium thermodynamics. In the experimental level, adsorption fittings and spectroscopic tests (FTIR, UV–Vis, XPS) were performed to clarify the adsorbent-adsorbate interaction. Results indicate: (1) Under acidic condition, Cr (Ⅵ) is adsorbed by Fe 3 O 4 -GO in the form of H 2 CrO 4. Afterwards, over three-fifths of H 2 CrO 4 is reduced to Cr (Ⅲ), reaching adsorption percent and quantity 95.53 % and 382.10 mg g−1 in 10 min (2) Under basic condition, Cr (Ⅵ) is adsorbed in the form of CrO 4 2− without reduction. In the context of environmental remediation, two special implications are thereby procured. (1) Under acidic condition, Cr (Ⅵ) removal efficiency at the first cycle is maximized, while magnetic recovery is deteriorated, resulting in unsatisfactory cyclic performance. (2) Under basic condition, Cr (Ⅵ) removal efficiency is inferior to that under acidic condition, while magnetic recovery is guaranteed, leading to satisfactory cyclic performance. Exploration of this work provides reference especially for developing Fe 3 O 4 -GO architecture towards efficient sequestering of hexavalent chromium. Adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -GO surface(a) Illumination of redox reaction between Cr (Ⅵ) and Fe 3 O 4 given by thermodynamic calculation. Under acidic condition: spontaneous reaction H2CrO4+3Fe 2+ +6H + ⇌Cr 3+ +3Fe 3+ +4H2O owing to highly negative standard molar Gibbs free energy change. Under basic condition, non spontaneous reaction CrO4 2− +3Fe 2+ +4H2O⇌Cr(OH)4 - +3Fe 3+ +4OH − owing to highly positive standard molar Gibbs free energy change. (b) Adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -GO surface deciphered by Cr (Ⅵ) species distribution and XPS test. Under acidic condition: five small orange balls symbolizing H 2 CrO 4 adsorbed onto the surface of the big green ball representing Fe 3 O 4 -GO. Subsequently, three out of five small orange balls were transformed into small violet balls representing Cr3+, approaching the molar ratio Cr (Ⅲ)/Cr (Ⅵ) = 1.52 of the sample Fe 3 O 4 -GO-Cr as determined by XPS test (Fig. 8). The big blue ball represents Fe 3 O 4 -GO oxidized by H 2 CrO 4. Under basic condition: five small pink balls symbolizing CrO 4 2− adsorbed onto the surface of the big green ball representing Fe 3 O 4 -GO ensued by no reduction, as confirmed by thermodynamic analysis. [Display omitted] • Adsorption-reduction behavior of Cr (Ⅵ) on Fe 3 O 4 -graphene oxide surface is inspected. • In acidic media, H 2 CrO 4 is adsorbed, three-fifths of which is reduced to Cr (Ⅲ). • In basic media, CrO 4 2− is adsorbed without reduction. • Superior Cr (Ⅵ) removal efficiency but unsatisfactory cyclic performance in acidic media. [ABSTRACT FROM AUTHOR]

The impact of surface area, pore volume, and heteroatom type on the performance of porous organic polymers (POPs) in various applications remains unclear. To investigate this, three isoreticular POPs were employed having one common building block, resulting in varying surface areas, pore volumes, and heteroatom compositions. This study aimed to establish a correlation between the structural features of POPs (surface area, pore volume, and heteroatom type) with their adsorption capacity, and catalytic efficiency. To explore this relationship, the Knoevenagel condensation reaction was used as a model system, testing various substituted aldehydes to further validate our findings. Additionally, the capture of radioactive iodine vapor at 75 °C was simulated to examine the correlation with adsorption capacity, comparing the gravimetric iodine uptake capacity of each POP to gain insights into this relationship. [ABSTRACT FROM AUTHOR]

Singlet oxygen (1O2) is important in the environmental remediation field, however, its efficient production has been severely hindered by the ultrafast self-quenching of the as-generated radical precursors in the Fenton-like reactions. Herein, we elaborately designed lamellar anthraquinone-based covalent organic frameworks (DAQ-COF) with sequential localization of the active sites (C-O) at molecular levels for visible-light-assisted peroxymonosulfate (PMS) activation. Theoretical and experimental results revealed that the radical precursors (SO5 ·-) were formed in the nearby layers with the migration distance less than 0.34 nm, via PMS donating electrons to the photogenerated holes. This interlayer synergistic effect eventually led to ultraefficient 1O2 production (14.8 µM s-1), which is 12 times that of the highest reported catalyst. As an outcome, DAQ-COF enabled the complete degradation of bisphenol A in 5 min with PMS under natural sunlight irradiation. This interlayer synergistic concept represents an innovative and effective strategy to increase the utilization efficiency of ultrashort-lived radical precursors, providing inspirations for subtle structural construction of Fenton-like catalysts. [ABSTRACT FROM AUTHOR]

The unsatisfied visible light harvesting, slow charge separation, and limited practical surface area of carbon nitride (CN) constrain its performance in photocatalytic water splitting and environmental remediation. Herein, the thermal vapor‐assisted π‐conjugation modification of CN by grafting with p‐aminophenoxy groups was developed to tune the photophysical properties of CN to enhance its photocatalytic activity. Besides extending the light absorption, the surface modification constructed a nanojunction across the depth direction, which leads to facilitated charge separation and transfer. In addition, the thermal vapor modification process thermally etches and trims the pristine CN to be a highly holey structure, resulting to >10 times increase in specific surface area. Photocatalysis results showed that the obtained modified CN yielded hydrogen from photocatalytic water splitting at a rate of 7.82 mmol/g/h, over 7‐folds as that of pristine CN, with a quantum yield of 3.28% at 400 nm. The π‐conjugation modified CN also demonstrated enhanced photocatalytic environmental remediation application, exemplified by much faster photodegradation of tetracycline hydrochloride. This work provides the thermal vapor surface chemical modification of CN as a promising integrated pathway of multiple favorable photophysical properties toward efficient photocatalysis application. [ABSTRACT FROM AUTHOR]

AbstractOur research described in this report introduces a multifunctional composite resin, TiO2/SiO2@poly(hexadecyl methacrylate-co-butyl methacrylate-co-methyl acrylate), synthesized to enhance oil absorption and demulsification for oily wastewater treatment. By incorporating hydrophobically modified nano-titanium dioxide (nano-TiO2) and nano-silicon dioxide (nano-SiO2) into a polyacrylate resin through suspension polymerization, we aimed to overcome the limitations of traditional oil absorbent resins. The resin’s formulation included hexadecyl methacrylate, butyl methacrylate, and methyl acrylate. Characterization was conducted through measurements of contact angle, Fourier-transform infrared spectroscopy, scanning electron microscopy, and Brunauer–Emmett–Teller surface area analyses. The study meticulously optimized the chemical synthesis conditions, focusing on the amount of monomer, initiator and crosslinker, which are crucial for the polymerization reaction. Additionally, the physical parameters, such as the particle size and quantity of the nano-materials, were carefully controlled to achieve the desired material properties. The inclusion of nano-TiO2 and nano-SiO2 significantly enriched the resin’s porous structure, boosting its oil absorption ratios for oil in various solvents, notably enhancing stability and recyclability. The resin exhibited superior oil absorption capacities (e.g. 54.7 g/g for trichloromethane) and improved emulsion separation efficiency (e.g. 98.10% for trichloromethane emulsions), marking a substantial advancement in materials for environmental remediation applications. [ABSTRACT FROM AUTHOR]

Metal organic frameworks (MOFs) have tunable chemical structures, orderly pore structures, and modifiable surface functional groups making them a promising material for environmental remediation. However, their rigid powder morphology poses significant challenges for customizing MOF structures with adjustable mechanical properties. Here, we synthesis the stretchable UV‐curable MOF hydrogels through high‐resolution digital light processing 3D printing, and evaluated its adsorption effect on seven common dyesand.The results showed that it had selective adsorption effect on methylene blue (MB), and the adsorption effect increased with the increase of the initial concentration of MB: its adsorption capacity on 6 mgL−1, 12 mgL−1 and 24 mgL−1 MB solution reached 13.55 mgg−1, 26.31 mgg−1 and 50.70 mgg−1 respectively. Compared to powdered MOFs, the 3D‐printed MOF (Cu‐BTC) exhibited superior adsorption for dye and radioactive pollution, with methylene blue adsorption increasing from 8.93 mgg−1 to 25.05 mgg−1 and I2 adsorption from 141.56 mgg−1 to 792.65 mgg−1. Furthermore, the 3D‐printed MOF structure proved easily cleanable with dilute HCl and reusable over five times without degradation. In addition, our study highlighted the suitability of the 3D‐printed MOF for CO2‐sensing devices, demonstrating its broad applicability in environmental remediation and sensing technology. [ABSTRACT FROM AUTHOR]

The high-throughput method based on the micron-level structure that 3D bioprinting technology offers for various environmental microbiological engineering applications is made possible by its several printing paths and precision programming control. This versatility makes it an on-demand manufacturing technology. A novel 3D manufacturing technique called 3D bioprinting may be used to precisely uptake and disperse bacteria to create microbial active substances with a variety of intricate functionalities for environmental applications. The technological challenges that the current 3D bioprinting technology must face include the mechanical properties of materials, the creation of specific bioinks to adapt to different strains, and the exploration of 4D bioprinting for intelligent applications. Therefore, this analysis delves deeply into the core technological ideas of 3D bioprinting, bioink materials, and their environmental applications. It also offers recommendations about the challenges and opportunities associated with 3D bioprinting. Combined with the present advancements in microbe enhancement technology, 3D bioprinting will provide an enabling platform for multifunctional microorganisms and facilitate the management of in situ directional responses in the environmental domain. This review highlights the applications of 3D bioprinting in the environmental monitoring and bioremediation. 3D printing in solid waste management is also discussed in detail. [ABSTRACT FROM AUTHOR]

Reconfigurability within hydrogels has emerged as an attractive functionality that can be used in information encryption, cargo/delivery, environmental remediation, soft robotics, and medicine. Here micro‐patterned polymer hydrogels capable of temperature‐dependent reconfigurability are fabricated. For this, the hydrogels are provided with micron‐sized Pickering emulsion droplets stabilized by magnetic particles, which are capable of harnessing energy from external force fields. The droplets can both migrate under magnetic field gradients and heat the environment when laser irradiated. These functions not only affect a single compartment but have higher‐order effects on the mesoscale, thanks to the temperature‐responsiveness of the polymeric network. This double responsiveness is exploited to control the spatial organization of hundreds of droplets within the hydrogel matrix and form predesigned and sophisticated patterns. Furthermore, pattern self‐reconfiguration driven by the droplets themselves upon laser irradiation is induced. Finally, we show that due to their internal liquid phase, the droplets can be used as reservoirs of hydrophobic nutrients for living cells (i.e., Yarrowia lipolytica yeast) in the solid‐like environment of the polymeric network, and demonstrate communication between the droplets and the cells to facilitate nutrient uptake. Altogether, the results provide opportunities for the development of stimuli‐sensitive polymer hydrogels with post‐synthesis reprogrammable response using micro‐compartments as building blocks. [ABSTRACT FROM AUTHOR]

In the face of escalating environmental challenges driven by human activities, the quest for innovative solutions to counter pollution, contamination, and ecological degradation has gained paramount importance. Traditional approaches to environmental remediation often fall short in addressing the complexity and scale of modern-day environmental problems. As industries transition towards sustainable paradigms, the exploration of novel materials and technologies becomes crucial. Lignin nanoparticles have emerged as a promising avenue of exploration in this context. Once considered a mere byproduct, lignin's unique properties and versatile functional groups have propelled it to the forefront of environmental remediation research. This review paper delves into the resurgence of lignin from an environmental perspective, examining its pivotal role in carbon cycling and its potential to address various environmental challenges. The paper extensively discusses the synthesis, properties, and applications of lignin nanoparticles in diverse fields such as water purification and soil remediation. Moreover, it highlights the challenges associated with nanoparticle deployment, ranging from Eco toxicological assessments to scalability issues. Multidisciplinary collaboration and integration of research findings with real-world applications are emphasized as critical factors for unlocking the transformative potential of lignin nanoparticles. Ultimately, this review underscores lignin nanoparticles as beacons of hope in the pursuit of cleaner, healthier, and more harmonious coexistence between humanity and nature through innovative environmental remediation strategies. [ABSTRACT FROM AUTHOR]

Over the past decade, remotely powered micro actuators have gained increased attention for biomedical and environmental remediation applications, owing to their ability to access confined regions and the nonintrusive nature of control. Recent studies focus on improving the functionality and versatility of micro actuators through the development of new fabrication and actuation techniques. However, there is a possibility that a limited understanding of the scaling impact of various physical principles governing design and control has affected the successful implementation of such devices in practical scenarios. Thus, the main focus of this review is to evaluate the most widely utilized manufacturing methods and remote actuation sources in light of various characteristics such as resolution, productivity, shape complexity, actuation speed, actuation mode, operating medium, and so on. State-of-the-art developments in each type of manufacturing and actuation are introduced and delineated. Finally, the limitations of current devices are reviewed, and the future direction to enable the full potential of this field is provided. [ABSTRACT FROM AUTHOR]

Previous research highlights the potential of polyaniline-based biocomposites as unique adsorbents for humidity sensors. This study examines several preparative routes for creating polyaniline (PANI) and chitosan (CHT) composites: Type 1—in situ polymerization of aniline with CHT; Type 2—molecular association in acidic aqueous media; and a control, Type 3—physical mixing of PANI and CHT powders (without solvent). The study aims to differentiate the bonding nature (covalent vs. noncovalent) within these composites, which posits that noncovalent composites should exhibit similar physicochemical properties regardless of the preparative route. The results indicate that Type 1 composites display features consistent with covalent and hydrogen bonding, which result in reduced water swelling versus Type 2 and 3 composites. These findings align with spectral and thermogravimetric data, suggesting more compact structure for Type 1 materials. Dye adsorption studies corroborate the unique properties for Type 1 composites, and 1H NMR results confirm the role of covalent bonding for the in situ polymerized samples. The structural stability adopts the following trend: Type 1 (covalent and noncovalent) > Type 2 (possible trace covalent and mainly noncovalent) > Type 3 (noncovalent). Types 2 and 3 are anticipated to differ based on solvent-driven complex formation. This study provides greater understanding of structure-function relationships in PANI-biopolymer composites and highlights the role of CHT as a template that involves variable (non)covalent contributions with PANI, according to the mode of preparation. The formation of composites with tailored bonding modalities will contribute to the design of improved adsorbent materials for environmental remediation to versatile humidity sensor systems. [ABSTRACT FROM AUTHOR]

Composite track-etched membranes (CTeMs) emerged as a versatile and high-performance class of materials, combining the precise pore structures of traditional track-etched membranes (TeMs) with the enhanced functionalities of integrated nanomaterials. This review provides a comprehensive overview of the synthesis, functionalization, and applications of CTeMs. By incorporating functional phases such as metal nanoparticles and conductive nanostructures, CTeMs exhibit improved performance in various domains. In environmental remediation, CTeMs effectively capture and decompose pollutants, offering both separation and detoxification. In sensor technology, they have the potential to provide high sensitivity and selectivity, essential for accurate detection in medical and environmental applications. For energy storage, CTeMs may be promising in enhancing ion transport, flexibility, and mechanical stability, addressing key issues in battery and supercapacitor performance. Biomedical applications may benefit from the versality of CTeMs, potentially supporting advanced drug delivery systems and tissue engineering scaffolds. Despite their numerous advantages, challenges remain in the fabrication and scalability of CTeMs, requiring sophisticated techniques and meticulous optimization. Future research directions include the development of cost-effective production methods and the exploration of new materials to further enhance the capabilities of CTeMs. This review underscores the transformative potential of CTeMs across various applications and highlights the need for continued innovation to fully realize their benefits. [ABSTRACT FROM AUTHOR]

• A novel side-aerated reactor for in-situ H 2 O 2 electrosynthesis was designed. • Side-aerated reactor coupled with a composite cathode greatly improved H 2 O 2 production. • Different aeration system and cathodes were evaluated for comparison. • Key factors for in-situ H 2 O 2 electrosynthesis were determined. The active graphite felt (GF) catalytic layer was effectively synthesized through a wet ultrasonic impregnation-calcination method, modified with CB and PTFE, and implemented in a pioneering side-aeration electrochemical in-situ H 2 O 2 reactor. The optimal mass ratio (CB: PTFE 1:4) for the modified cathode catalytic layer was determined using a single-factor method. Operating under optimum conditions of initial pH 5, 0.5 L/min air flow, and a current density of 9 mA/cm2, the system achieved a remarkable maximum H 2 O 2 accumulation of 560 mg/L, with the H 2 O 2 production capacity consistently exceeding 95 % over 6 usage cycles. The refined mesoporous structure and improved three-phase interface notably amplified oxygen transfer, utilization, and H 2 O 2 yield. Side aeration led to an oxygen concentration near the cathode reaching 20 mg/L, representing a five-fold increase compared to the 3.95 mg/L achieved with conventional bottom aeration. In the final application, the reaction system exhibited efficacy in the degradation of landfill leachate concentrate. After a 60-minute reaction, complete removal of chroma was attained, and the TOC degradation rate surpassed 60 %, marking a sixfold improvement over the conventional system. These results underscore the substantial potential of the system in H 2 O 2 synthesis and environmental remediation. [ABSTRACT FROM AUTHOR]

Geopolymers derived from solid waste can effectively remediate heavy metal polluted sites, achieving the ideal fusion of solid waste utilization and environmental remediation. Red mud and blast furnace slag were used to develop a geopolymer for the remediation of composite heavy metal-contaminated soils, focusing on Cd(II)-, Pb(II)-, Cu(II)-, and Zn(II)-contaminated soils. Uniaxial compressive strength tests, toxicity characteristic leaching procedures, pH change characteristics, and pH gradient tests were performed on the solidified/stabilized soil. The results showed that increasing the red mud-blast furnace slag content and curing age significantly enhanced the unconfined compressive strength. Furthermore, it suppressed the leaching of heavy metals in the solidified/stabilized soil. Notably, the treatment effectiveness of Cu(II) and Zn(II) was superior to that of Cd(II) and Pb(II). The leaching concentrations of Cd(II), Pb(II), and Zn(II) decreased in acidic to weakly alkaline environments but increased in strongly alkaline environments. However, the impact of curing age and initial heavy metal content on the pH of the solidified/stabilized soil was the opposite. In conclusion, red mud and blast furnace slag exhibited superior solidification/stabilization effects compared to cement. As environmental protection awareness grows and technology continues to evolve, geopolymers derived from red mud and blast furnace slag will play a greater role in pollution control and remediation, showcasing broad application prospects. [ABSTRACT FROM AUTHOR]

Introduction: Overusing and misusing pesticides, including paraquat (PQ), have led to numerous environmental contamination complications. PQ is an emerging bio-accumulative contaminant that is present in environmental aqueous matrices. Adsorption techniques are part of a set of technologies applied in ecological remediation, known for their high effectiveness in removing aqueous PQ. A study of the PQ adsorption capacity of three cyclodextrin-silica nanocomposites (a-CDSi, p-CDSi, and y-CDSi) from contaminated waters is presented in this paper. Methods: The cyclodextrin-silica nanocomposites were synthesized via an esterification reaction between the inorganic matrix and cyclodextrins (CDs) (a, p, and Y) and were characterized physicochemically by spectroscopic, thermal, and surface methods. Their PQ removal performance from contaminated aqueous media was studied under different experimental conditions. Results and Discussion: The results showed a fast adsorptive response in removal treatment studies over time. Adsorption capacities of 87.22, 57.17, and 77.27 mg.g-1 were found for a-CDSi, p-CDSi, and Y-CDSi, respectively, at only 30 min of treatment. Thermodynamic studies indicated spontaneous and exothermic adsorption processes. The removal assays responded mainly to physisorption mechanisms with contributions from chemisorption mechanisms. Spectroscopic assays showed a strong interaction of PQ with the adsorbents used. Innovative CDSi nanocomposites have proven to be highly efficient in applying aqueous PQ remediation, thus proving to be sustainable adsorbents of contaminants of emerging importance worldwide. [ABSTRACT FROM AUTHOR]

Organophosphate pesticides (OPPs) are widely prevalent in the environment primarily due to their low cost and extensive use in agricultural lands. However, it is estimated that only about 5% of these applied pesticides reach their intended target organisms. The remaining 95% residue linger in the environment as contaminants, posing significant ecological and health risks. This underscores the need for materials capable of effectively removing, recovering, and recycling these contaminants through adsorption processes. In this research, adsorbent materials composed of electro-spun carbon nanofibers (ECNFs) derived from polyacrylonitrile was developed. The materials were characterized through several techniques, including scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Fourier Transform Infrared Spectroscopy (FTIR), Brunauer-Emmett-Teller (BET) analysis, and contact angle measurements. SEM analysis revealed details of the structural properties and inter-fiber spacing variations of the carbon nanofibers. The results revealed that ECNFs possess remarkable uniformity, active surface areas, and high efficiency for adsorption processes. The adsorption studies were conducted using batch experiments with ethion pesticide in aqueous solution. High-Performance Liquid Chromatography-Diode Array Detector (HPLC-DAD) was utilized to quantify the concentrations of the OPP. Various parameters, including adsorbent dosage, pH, contact time, and initial ethion concentration, were investigated to understand their impact on the adsorption process. The adsorption isotherm was best described by the Freundlich model, while the kinetics of adsorption followed a non-integer-order kinetics model. The adsorption capacity of the ECNFs for OPP removal highlights a significant advancement in materials designed for environmental remediation applications. This study demonstrates the potential of ECNFs to serve as effective adsorbents, contributing to the mitigation of pesticide contamination in agricultural environments. [ABSTRACT FROM AUTHOR]

Sub‐nanoporous membranes with ion selective transport functions are important for energy utilization, environmental remediation, and fundamental bioinspired engineering. Although mono/multivalent ions can be separated by monovalent ion selective membranes (MISMs), the current theory fails to inspire rapid advances in MISMs. Here, we apply transition state theory (TST) by regulating the enthalpy barrier (ΔH) and entropy barrier (ΔS) for designing next‐generation monovalent cation exchange membranes (MCEMs) with great improvement in ion selective separation. Using a molecule‐absorbed porous material as an interlayer to construct a denser selective layer can achieve a greater absolute value of ΔS for Li+ and Mg2+ transport, greater ΔH for Mg2+ transport and lower ΔH for Li+ transport. This recorded performance with a Li+/Mg2+ perm‐selectivity of 25.50 and a Li+ flux of 1.86 mol ⋅ m−2 ⋅ h−1 surpasses the contemporary "upper bound" plot for Li+/Mg2+ separations. Most importantly, our synthesized MCEM also demonstrates excellent operational stability during the selective electrodialysis (S‐ED) processes for realizing scalability in practical applications. [ABSTRACT FROM AUTHOR]

Metal-organic frameworks (MOFs) are structures with high surface area that can be used to remove heavy metals (HMs) efficiently from the environment. The effect of MOFs on HMs removal from contaminated soils has not been already investigated. Monometallic MOFs are easier to synthesize with high efficiency, and it is also important to compare their structures. In the present study, Zn-BTC, Cu-BTC, and Fe-BTC as three metal-trimesic acid MOFs were synthesized from the combination of zinc (Zn), copper (Cu), and iron (Fe) nitrates with benzene-1,3,5-tricarboxylic acid (H3BTC) by solvothermal method. BET analysis showed that the specific surface areas of the Zn-BTC, Cu-BTC, and Fe-BTC were 502.63, 768.39 and 92.4 m2g-1, respectively. The synthesized MOFs were added at the rates of 0.5 and 1% by weight to the soils contaminated with 100 mgkg-1 of Zn, nickel (Ni), lead (Pb), and cadmium (Cd). Then quinoa seeds were sown in the treated soils. According to the results, the uptakes of all four HMs by quinoa were the lowest in the Cu-BTC 1% treated pots and the lowest uptakes were observed for Pb in shoot and root (4.87 and 0.39, μgpot-1, respectively). The lowest concentration of metal extracted with EDTA in the post-harvest soils was for Pb (11.86 mgkg-1) in the Cu-BTC 1% treatment. The lowest metal pollution indices were observed after the application of Cu-BTC 1%, which were 20.29 and 11.53 for shoot and root, respectively. With equal molar ratios, highly porous and honeycomb-shaped structure, the most crystallized and the smallest constituent particle size (34.64 nm) were obtained only from the combination of Cu ions with H3BTC. The lowest porosity, crystallinity, and a semi-gel like feature was found for the Fe-BTC. The synthesized Cu-BTC showed the highest capacity of stabilizing HMs, especially Pb in the soil compared to the Zn-BTC and the Fe-BTC. The highly porous characteristic of the Cu-BTC can make the application of this MOF as a suitable environmental solution for the remediation of high Pb-contaminated soils. [ABSTRACT FROM AUTHOR]

Microactuators, capable of executing tasks typically repetitive, hazardous, or impossible for humans, hold great promise across fields such as precision medicine, environmental remediation, and swarm intelligence. However, intricate motions of microactuators normally require high complexity in design, making it increasingly challenging to realize at small scales using existing fabrication techniques. Taking inspiration from the hierarchical-anisotropy principle found in nature, we program liquid crystalline elastomer (LCE) microactuators with multimodal actuation tailored to their molecular, shape, and architectural anisotropies at (sub)nanometer, micrometer, and (sub)millimeter scales, respectively. Our strategy enables diverse deformations with individual LCE microstructures, including expanding, contracting, twisting, bending, and unwinding, as well as re-programmable shape transformations of assembled LCE architectures with negative Poisson's ratios, locally adjustable actuation, and changing from two-dimensional (2D) to three-dimensional (3D) structures. Furthermore, we design tetrahedral microactuators with well-controlled mobility and precise manipulation of both solids and liquids in various environments. This study provides a paradigm shift in the development of microactuators, unlocking a vast array of complexities achievable through manipulation at each hierarchical level of anisotropy. [ABSTRACT FROM AUTHOR]

In this study, the pressing issue of persistent organic pollutants in wastewater was addressed by designing and fabricating a magnetically separable MnFe2O4/rGO heterostructure catalyst for efficient mineralization of bisphenol A (BPA) and dyes such as alizarin red S (anionic) and malachite green (cationic), which are known for their resistance to biodegradation and carcinogenic properties. Comprehensive structural and surface analyses using XRD, XPS, SEM, and TEM/HRTEM coupled with magnetic and optical property measurements revealed the formation of the MnFe2O4/rGO heterostructures. Among all, the MnFe2O4/rGO-10 catalyst with 10% wt% of rGO exhibited 100% efficiency in the mineralization of BPA and both dyes under visible light illumination within 60 min. The stability and recyclability of the catalyst, assessed through XRD and VSM studies, demonstrated its consistent performance over multiple uses. The cost-effectiveness and stability of this catalyst underscore its potential for practical application in wastewater treatment, offering a viable solution to the persistent challenge of removing stubborn organic contaminants. [ABSTRACT FROM AUTHOR]

A supramolecular low molecular weight organogelator (CNAZO) containing azobenzene and cholesterol units was synthesized, and its applications have been studied. The CNAZO gelator displays excellent gelation ability in six kinds of organic solvents with satisfactory transparency and lower critical gelation concentrations. Meanwhile, the chirality can be transferred from the cholesterol unit to the azobenzene group, which can be reversibly modulated through 365 nm UV light irradiation and heating‐cooling treatment. Compared with D‐limonene, CNAZO can form a stable organogel and exhibits obvious CD signals in the mixed solvent that containing L‐limonene, which can be used for chiral recognition of limonene. Owing to the phase‐selective ability and porous network structure, CNAZO can also be chosen for the separation and recovery of petrol from water and be utilized for rhodamine B (RhB) adsorption with removal efficiency (Re) of 99 %. These interesting insights indicated that the CNAZO gelator could be selected in the design of sensors and in environmental remediation fields. [ABSTRACT FROM AUTHOR]

MIL‐88 MOFs have gained considerable attention as photocatalysts in environmental remediation due to their advantages such as stability, reusability, efficient light absorption, and charge separation capabilities. This study explores the potential of MIL‐88A, MIL‐88B, and NH2‐MIL‐88B for degrading the reactive orange 16 (RO16). MIL‐88 s were synthesized via solvo(hydro)thermal method and characterized using FTIR, PXRD, SEM, zeta potential, and UV‐DRS techniques. Photocatalytic degradations were conducted under UVA radiation, revealed a remarkable 93 % degradation rate. MIL‐88 s demonstrated exceptional performance and reusability, maintaining high efficiency even at 300 mg/L catalyst concentration. The photodegradation efficiencies of MIL‐88 A, MIL‐88B and NH2‐MIL‐88B for RO16 reach nearly 85 % within 120 minutes, 92 % within 60 minutes, 90 % within 75 minutes respectively. Even at a high initial concentration of 15 mg/L, the results underscore the significance of evaluating both initial efficiency and stability over multiple cycles, with MIL‐88B initially exhibiting the highest efficiency declining to 77 % by the fifth cycle, while MIL‐88 A maintained 54 % efficiency and NH2‐MIL‐88B sustained 72 % efficiency over the same period. Mechanistic elucidation identified O2⋅− and ⋅OH as the primary reactive radicals. This study is unique in being the first to explore the photocatalytic removal of RO16 using MIL‐88 s, providing a pioneering approach to sustainable water treatment. [ABSTRACT FROM AUTHOR]