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This research proposes a simple and novel strategy for the green detection of antibiotics along with the reduction of microplastic and humic acid (HA) hazards. The entire process is based on a single-step solvent-sieving method to separate HA into insoluble (IHA) and soluble (SHA) components, subsequently recombining and designing the application according to the original characteristics of selected fractions in accordance with the zero-waste principle. IHA was applied as a dispersive solid phase extraction (DSPE) sorbent without chemical modification for the enrichment of trace MACs in complex biological matrices. The recovery of MACs was 74.06-100.84 % in the range of 2.5-1000 μg∙kg -1 . Furthermore, SHA could be combined with biodegradable polyvinyl alcohol (PVA) to prepare multifunctional composite films. SHA endows the PVA film with favorable mechanical properties, excellent UV shielding as well as oxidation resistance performance. Compared with pure PVA, the tensile strength, toughness, antioxidant and UV-protection properties were increased to 157.3 Mpa, 258.6 MJ·m -3 , 78.6 % and 60 % respectively. This study achieved a green and economically valuable utilization of all components of waste HA, introduced a novel approach for monitoring and controlling harmful substances and reducing white pollution. This has significant implications for promoting sustainable development and recovering valuable resources., 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.)

Green synthesis of silver (Ag) and gold (Au) nanoparticles (NPs) has acquired huge popularity owing to their potential applications in various fields. A large number of research articles exist in the literature describing the green synthesis of Ag and Au NPs for biomedical applications. However, these findings are scattered, making it time-consuming for researchers to locate promising advancements in Ag and Au NPs synthesis and their unexplored biomedical applications. Unlike other review articles, this systematic study not only highlights recent advancements in the green synthesis of Ag and Au NPs but also explores their potential unexplored biomedical applications. The article discusses the various synthesis approaches for the green synthesis of Ag and Au NPs highlighting the emerging developments and novel strategies. Then, the article reviews the important biomedical applications of green synthesized Ag and Au NPs by critically evaluating the expected advantages. To expose future research direction in the field, the article describes the unexplored biomedical applications of the NPs. Finally, the articles discuss the challenges and limitations in the green synthesis of Ag and Au NPs and their biomedical applications. This article will serve as a valuable reference for researchers, working on green synthesis of Ag and Au NPs for biomedical applications., Competing Interests: The authors declare no conflicts of interest in this work., (© 2024 Ahmad et al.)

Preparation of nano-rod aluminosilicate Mazzit (MAZ) zeolite under low-cost and environmental-friendly route is attractive, but still challenging. Herein, we report a green route for synthesizing nano-rod MAZ zeolite (MAZ-N) using low-cost and environmental-friendly choline chloride as template. Various characterizations including powder X-ray diffraction (XRD), scanning electron microscope (SEM), N 2 sorption, and thermogravimetry-differential thermal analysis (TG-DTA) show that MAZ-N samples have good crystallinity and uniform porous structures. Furthermore, the crystallization process and impact of synthesis conditions of MAZ-N samples have been investigated in detail. These results suggest the potential applications of MAZ-N zeolites as supporting catalyst compounds in industrial processes.

Wearable sensors for sweat biomarkers can provide facile analyte capability and monitoring for several diseases. In this work, a green wearable sensor for sweat absorption and chloride sensing is presented. In order to produce a sustainable device, polylactic acid (PLA) was used for both the substrate and the sweat absorption pad fabrication. The sensor material for chloride detection consisted of silver-based reference, working, and counter electrodes obtained from upcycled compact discs. The PLA substrates were prepared by thermal bonding of PLA sheets obtained via a flat die extruder, prototyped in single functional layers via CO 2 laser cutting, and bonded via hot-press. The effect of cold plasma treatment on the transparency and bonding strength of PLA sheets was investigated. The PLA membrane, to act as a sweat absorption pad, was directly deposited onto the membrane holder layer by means of an electrolyte-assisted electrospinning technique. The membrane adhesion capacity was investigated by indentation tests in both dry and wet modes. The integrated device made of PLA and silver-based electrodes was used to quantify chloride ions. The calibration tests revealed that the proposed sensor platform could quantify chloride ions in a sensitive and reproducible way. The chloride ions were also quantified in a real sweat sample collected from a healthy volunteer. Therefore, we demonstrated the feasibility of a green and integrated sweat sensor that can be applied directly on human skin to quantify chloride ions.

In recent years, there has been much interest in developing advanced and innovative approaches for sensing applications in various fields, including agriculture and environmental remediation. The development of novel sensors for detecting heavy metals using nanomaterials has emerged as a rapidly developing research area due to its high availability and sustainability. This review emphasized the naturally derived and engineered nanomaterials that have the potential to be applied as sensing reagents to interact with metal ions or as reducing and stabilizing agents to synthesize metallic nanoparticles for the detection of heavy metal ions. This review also focused on the recent advancement of nanotechnology-based detection methods using naturally derived and engineered materials, with a summary of their sensitivity and selectivity towards heavy metals. This review paper covers the pros and cons of sensing applications with recent research published from 2015 to 2022.

In this experimental study on self-compacting concrete (SCC), the Manufactured sand (M-sand) and Fly ash (FA) were utilised for partial replacement of Natural sand (N-sand) and Ordinary Portland Cement (OPC), respectively. N-sand was partially replaced by M-sand at various percentage levels, after the dose of FA in the mix was optimised. In terms of compressive strength, the optimum replacement level of OPC by FA was 20%, whilst for replacement of N-sand by M-sand it was 50%. Two types of mixes were prepared to compare the macro and micro level properties of SCC, i.e., SCC-I (100%OPC + 100%N-sand) and SCC-II (80%OPC + 20%FA + 50%N-sand + 50%M-sand). The characteristics of fresh concrete mixes were determined using Slump flow, T 50 time, V-funnel, L-box, U-box, and J-ring tests. After 28 days of curing in tap water, both types of specimens were exposed to a solution of ammonium sulphate [(NH 4 ) 2 SO 4 ] containing sulphate salt concentration of 2.0 g/l for 360 days to test their durability. Loss in compressive strength, weight change, sorptivity, and micro-structural changes (XRD, SEM, and EDS) all were evaluated for up to 360 days. It was found that the use of FA and M-sand in concrete makes it more environmental-friendly and durable, as well as have better performance in a sulphate environment., (© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

The pandemic of the novel coronavirus disease 2019 (COVID-19) is continuously causing hazards for the world. Effective detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can relieve the impact, but various toxic chemicals are also released into the environment. Fluorescence sensors offer a facile analytical strategy. During fluorescence sensing, biological samples such as tissues and body fluids have autofluorescence, giving false-positive/negative results because of the interferences. Fluorescence near-infrared (NIR) nanosensors can be designed from low-toxic materials with insignificant background signals. Although this research is still in its infancy, further developments in this field have the potential for sustainable detection of SARS-CoV-2. Herein, we summarize the reported NIR fluorescent nanosensors with the potential to detect SARS-CoV-2. The green synthesis of NIR fluorescent nanomaterials, environmentally compatible sensing strategies, and possible methods to reduce the testing frequencies are discussed. Further optimization strategies for developing NIR fluorescent nanosensors to facilitate greener diagnostics of SARS-CoV-2 for pandemic control are proposed., 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 B.V. All rights reserved.)

Oil leakage is a global environmental issue and happens frequently, resulting in a waste of oil resources and even threatening the safety of marine creatures and humans. Because of unidirectional oil transportation performance, "oil-diode" Janus membranes have attracted lots of attention for oil/water separation. However, the hydrophobic side of traditional "oil-diode" Janus membrane is completely hydrophobic, resulting in an easy permeation of oil, which hampers light oil recycling. Herein, we provide a facile approach to develop "oil-diode" Janus membranes with the special wettable structure for fast oil refining. The material characteristics and surface wettability of the membranes that generate superimposed efforts are vital to fabricate "oil-diode" Janus membranes. Interestingly, the manufactured membranes exhibit extra-high oil intrusion pressure up to 12 kPa and present high permeance of about 2993 L m -2 h -1 bar -1 in separating stable water-in-oil emulsion containing surfactant and separation efficiency up to 99.6%, thereby showing promising potential in oil recovery and refining.

In this study, we report on an easy-to-assemble amperometric electrochemical biosensor incorporating thylakoid membranes for the detection of photosynthetic herbicides. These molecules interfere with the light-induced photosynthetic electron transport occurring at the level of the photosystems within the thylakoid membranes, thus reducing the current of the associated bioelectrode. Thylakoid membranes isolated from pea plants were adsorbed directly on a bare carbon paper working electrode and placed in the measurement cell in the absence of any electrochemical mediator, obtaining a fully environmental-friendly biodevice capable of photocurrent densities up to 14 μA/cm 2 . Three photosynthetic herbicides inhibiting Photosystem II and belonging to different chemical classes, namely diuron, terbuthylazine and metribuzin, were detected by measuring the electrode photocurrent, which decreased reproducibly in a concentration-dependent manner in a range between 10 -7 - 5 × 10 -5  M of each herbicide. The limit of detection for the three herbicides was between 4-6 × 10 -7  M. Storage stability tests revealed for the biosensor a half-life longer than 15 days at 4 °C and full stability up to 4 months at -80 °C. This study provides a simple, environmental-friendly and cost-effective procedure for the fabrication of a mediatorless carbon paper-based electrochemical biosensor characterized by high photocurrents, long storage stability, reproducible detections and good sensitivity., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Stimulus-responsive pesticide or fertilizer systems have been emerged to improve the use efficiency of agrochemicals, reduce over-application and ensuing environmental problems. However, environmental-friendly synthesis of these systems still remain challenging. In this work, an environmental-friendly synthesis strategy has been developed to form a pesticide and fertilizer combination to achieve the integration of plant protection and nutrient supply. This pesticide-fertilizer combination system was fabricated using ammonium zinc phosphate (ZNP) and in-situ synthesized zeolitic imidazolate framework-8 (ZIF-8) as nutrients resources, and dinotefuran (DNF) as a pesticide. DNF was encapsulated in-situ (loading capacity of 12.32 ± 0.46%) during the ZIF-8 crystal synthesis process, rather than loaded by further adsorption, which improved its stability and prevented premature or rapid release. The hydrophobic ZIF-8 provided a pH-responsive slow-release behavior. The cumulative released DNF within seven days at pH 4.0, 7.0 and 10.0 was 66.30%, 40.41%, and 37.44%, respectively. The pesticide-fertilizer combination system showed significant effects on corn seed pre-cultivation, soil cultivation and pest control. This work provides a strategy for the integration of pesticide and fertilizer, which will reduce negative environmental effects caused by their over-applications and have great potential in modern sustainable agriculture., 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 © 2021 Elsevier B.V. All rights reserved.)

It is of great importance to safely dispose nuclear wastes with the development of nuclear industries. Past approaches to this problem have included immobilizing radioactive cesium in Portland cement-based matrices; however, the leaching rates of cesium are relatively high, especially as the leaching temperature increases. This paper explores a high-efficiency and cost-effective approach for encapsulating cesium using a sulfoaluminate cement (SAC) matrix, which was prepared via synergetic use of industrial solid wastes. Leaching results showed that, the apparent diffusion coefficient values of cesium were only ~1.4 × 10 -15 cm 2 /s and ~5 × 10 -18 cm 2 /s at 25 ℃ and 90 ℃ leaching conditions, respectively. These values were several orders of magnitude lower when compared with previously reported values, indicating the excellent encapsulation performance of the solid-waste-based SAC for cesium. Moreover, the heavy metals contained in the industrial solid waste were also effectively immobilized. A mechanistic analysis revealed that cesium was encapsulated in the SAC matrices stably by a physical effect. Finally, a life cycle assessment and economic analysis indicated that this approach was environmental-friendly, cost-effective, and energy-saving. This work provides a promising strategy for effective encapsulation of cesium and synergetic treatment of industrial solid wastes., (Copyright © 2021 Elsevier B.V. All rights reserved.)

Cyanobacteria blooms are crucial environmental issues by threatening both aquatic ecosystem and human health. A biomass by-product with antimicrobial activity, pyroligneous acid (PA) was tested for its suitability for removal of the cyanobacteria Microcystis aeruginosa (M. aeruginosa) in this work. Results show that the removal efficiency could reach up to 90% in the presence of 0.45% of PA and the inhibition to M. aeruginosa growth could extend to at least 40 days. The removal mechanism was studied. Both organic acids and phenols are functional content in M. aeruginosa removal and acetic acid is the most important one. Zeta potential analysis and morphology study show that the damage of cells dominates the flocculation and sedimentation of M. aeruginosa under low PA concentration (<0.7%), and increasing PA (≥0.7%) resulted in a trend of zeta potential to zero, thus removing any "shield" and triggering flocculation. Finally, study on the phenols residual after M. aeruginosa treatment shows that it could be close to 0 in 70 h. Therefore, this work proposes a possible method for world-wide treatment of cyanobacteria bloom and a new way for further utilization of PA., (Copyright © 2020 Elsevier Inc. All rights reserved.)

In this work, the poly(vinylidene fluoride) (PVDF) hollow fiber membranes with switchable pore size were fabricated by melt-spinning and stretching (MS-S) process based on a completely green and sustainable route. The membrane preparation process and pore formation mechanism were discussed and investigated in detail. Meanwhile, the effect of stretching ratio on the membrane structure and property was studied based on scanning electron microscopy (SEM), pore size distribution, N 2 flux, pure water flux, mechanical property and so on. The prepared membranes with different stretching ratios exhibited excellent tensile strength in the range from 23.0 to 62.6 MPa. The mean pore size of the prepared membranes with stretching 100 % (M-100) was about 0.317 μm, which showed a high dye rejection (<93.9 %) for Direct Black 19. Specifically, there were not any organic solvent and low-molecular-weight diluent used during the preparation process. The recycled PEO and water were obtained after treating the wastewater by membrane filtration. In addition, the recycled PEO could be reused as pore forming agent, which could achieve completely green and sustainable membrane preparation process., 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 © 2020 Elsevier B.V. All rights reserved.)

The development of highly efficient and green catalytic oxidation process based on peroxymonosulfate (PMS) activation has been identified to be a significant yet challenging objective in the environmental catalysis field. A simple, environmentally benign and highly effective catalytic oxidation system was innovatively constructed by coupling NaBO 2 and PMS for the removal of Acid Red 1. The catalytic mechanism in the NaBO 2 /PMS system was elucidated by electron paramagnetic resonance (EPR) combined with several radical capture reagents (ascorbic acid, methanol, tert-butyl alcohol, ethanol and l -histidine). The experimental results indicated that singlet oxygen ( 1 O 2 ) severed as the predominant reactive oxygen species (ROS) rather than the HO or during the catalytic oxidation process, at variance with the reported radical pathway in the Co 2+ /PMS system. Inspiringly, p-benzoquinone (p-BQ) as a trapping agent in most advanced oxidation process could be turned into the positive one in the NaBO 2 /PMS system, achieving a nearly 3-times enhancement in terms of the rate constant for AR1 removal. More interestingly, sodium chloride (NaCl) presented the same enhancement effect as p-benzoquinone due to generation of hypochlorous acid (HOCl) and more 1 O 2 , which was completely different from the reported. This study develops a highly efficient green oxidation process and opens up a new insight in the remediation of contaminated water., (Copyright © 2019. Published by Elsevier Ltd.)

A novel environmental-friendly unpacking powder for fireworks which has no sulfur, no magnesium, no aluminum or their alloys has been prepared in this study: potassium perchlorate (75%), potassium hydrogen terephthalate (13%), micronano porous silicon (9%), carbon (2%), ferrocene (1%). The PM2.5 and PM10 were collected by the ambient air particulate sampler, and the gas product was tested with a smoke analyzer and gas chromatograph to investigate its environmental-friendly performance. The detonation radius was measured by similar triangulation method, and p-t curves were measured in a closed bomb to investigate its practicality. The heat of combustion, sensitivity and hygroscopicity of the formula were measured according to China fireworks industry standard to verify the safety of the novel unpacking powder. The test results suggest that new unpacking powder using micronano porous silicon can effectively reduce the PM content and the product does not contain SO 2 , so it can be applied to export., (Copyright © 2019 Elsevier B.V. All rights reserved.)

An aptamer-based fluorometric assay is described for the determination of bisphenol A (BPA). The aptamer against BPA is first attached to the surface of the red AuNPs, and this prevents the AuNPs from salt-induced formation of a blue-colored aggregate. Hence, the blue fluorescence of added nitrogen-doped carbon dots (NCDots) is quenched via an inner filter effect (IFE) caused by the red AuNPs. After addition of BPA, the BPA/aptamer complex is formed, and the AuNPs are no longer stabilized agains aggregation. This weakens the IFE and results in the recovery of the fluorescence of the NCDots which is measured best at excitation/emission wavelengths of 300/420 nm. The recovered fluorescence increases linearly in the 10 to 250 nM and 250 to 900 nM BPA concentration ranges, and the detection limit is 3.3 nM. The method was successfully applied to the determination of BPA in spiked environmental tap water samples. Graphical abstract Schematic presentation of a fluorometric aptamer based assay for bisphenol A (BPA). It is based on the inner filter effect of gold nanoparticles (AuNPs) on the fluorescence of nitrogen-doped carbon dots (NCDots).

Aluminum-air batteries are a promising power supply for electronics due to their low cost and high energy density. However, portable coin-type Al-air batteries operating under ambient air condition for small electronic appliances have rarely been reported. Herein, coin cell-type Al-air batteries using cost-effective and eco-friendly chitosan hydrogel membranes modified by SiO 2 , SnO 2 , and ZnO have been prepared and assembled. The Al-air coin cell employing chitosan hydrogel membrane containing 10 wt % SiO 2 as a separator exhibits better discharge performance with a higher flat voltage plateau, longer discharge duration, and higher power density than the cells using a chitosan hydrogel membrane containing SnO 2 or ZnO. Moreover, we also demonstrate that the presented Al-air coin cell can be recycled by a series of eco-friendly procedures using food-grade ingredients, resulting in recycled products that are environmentally safe and ready for reuse. The Al-air coin cell adopting a recycled cathode from a fully discharged Al-air coin cell using the above-mentioned procedure has shown comparable performance to cells assembled with a new cathode. With these merits of enhanced electrochemical performance and recyclability, this new Al-air coin cell with modified chitosan hydrogel membrane can find wide applications for powering portable and small-size electronics.

A facile and environmental-friendly approach was developed to prepare magnetic nano-adsorbent for environmental pollutant removal. Based on the mussel-inspired polymerization, amino-coated Fe 3 O 4 nanoparticles were fabricated by simply immersing Fe 3 O 4 nanoparticles into an aqueous solution of catechol and hexanediamine with stirring at room temperature. The magnetic nano-adsorbent was characterized via Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), thermo gravimetric analysis (TGA), and Brunauer-Emmett-Teller's test (BET). The effects of initial mole ratio of catechol/hexanediamine and coating time on the adsorption capacity were investigated, using Congo red as a model organic dye. Under the optimal preparation condition, the absorption capacity of the amino-coated Fe 3 O 4 nanoparticles reached 97.3 mg/g for Congo red, and the adsorption reached about 80% of the equilibrium adsorption amount within 200 min. Adsorption kinetics and isotherm studies indicated that the absorption process fitted the pseudo-second-order kinetic and Langmuir isotherm models well. Besides, desired functional groups could be introduced onto the surface of Fe 3 O 4 nanoparticles, to tailor the adsorption capacity for Congo red, amaranths red, methylene blue and methylene violet. It is believed that the amino-coated magnetic nano-adsorbent prepared by the proposed method in this study has a good prospect for wastewater treatment., (Copyright © 2017 Elsevier Inc. All rights reserved.)

In the present work, cellulose acetoacetates (CAA) was used as a precursor for preparing diversely functionalized cellulose derivatives. Four amino-bearing compounds, namely hexylamine (HA), l-glutamic acid (Glu), cysteine (Cys), and tyramine (TA) were reacted with acetoacetyl groups providing alkyl-, carboxyl-, thiol-, or phenolic functionalized cellulose. The reaction was conducted under mild conditions without catalysts and UV light. The products were characterized with FT-IR, NMR and solubility measurement. 1 H NMR measurement demonstrated the conversion of acetoacetyl groups were ideal, and all the cellulose derivatives demonstrated good solubility in certain solvent. Besides, CAA held a good stability under room temperature. This approach offers broad possibilities for developing new cellulose based materials. Moreover, this protocol can also be applied to fabricate other polysaccharide derivatives., (Copyright © 2017 Elsevier Ltd. All rights reserved.)