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Capsaicinoids (CPCs) is a special ingredient with pungent smell in condiments, which can also be used as an exogenetic marker for kitchen waste oil. Development of immunoassay for CPCs remains a challenging due to relatively difficult preparation of the broad-spectrum antibody (Ab). In this work, a broad-spectrum polyclonal antibody (pAb) which can simultaneously recognize capsaicin (CPC), dihydrocapsaicin (DCPC), nordihydrocapsaicin (NDCPC), and N-vanillylnonanamide (N-V) is produced, and a non-enzyme immunoassay (NISA) based on this Ab, dendritic mesoporous silica nanomaterials (DMSNs), polydopamine (PDA), and high catalytic efficiency of Pt nanoparticles to prepare signal probe (DMSNs@PDA@Pt) is established. Here, the limit of detection (LOD) of NISA for CPC is as low as 0.04 μg L -1 . It is worth mentioning that the LOD of the proposed NISA is at least 23 times lower than that of traditional enzyme-linked immunosorbent assay (ELISA) based on horseradish peroxidase (HRP). Moreover, the proposed NISA is applied to detect CPCs in edible oil samples, the result has good consistency with that of ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). The proposed NISA based on DMSN@PDA@Pt and broad-spectrum Ab is an ideal tool for highly effective screening CPCs for kitchen waste oil abuse surveillance., 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.)

A new ferrofluid extractant (Fe 3 O 4 @SiO 2 -WDES) was ingeniously prepared by coating magnetic Fe 3 O 4 @SiO 2 microspheres with water-based deep eutectic solvent (WDES) and used for dispersive liquid-liquid microextraction (DLLME) and HPLC determination of naphthalene-derived plant growth regulators (PGRs, i.e., 1-naphthylacetic acid, 2-naphthylacetic acid, 1-naphthoxy acetic acid, 2-naphthyloxyacetic acid and 1-naphthylacetamide) in edible oil. Herein, mass transfer of the analytes in DLLME was significantly enhanced via increasing the contact surface by employing the microspheres as the supporter and dispersant of WDES, and phase separation can be efficiently achieved using an external magnet rather than centrifugation in traditional DLLME. Response surface methodology (RSM) based on Box-Behnken design (BBD) was employed for the optimization of core experimental conditions, and Analytical Eco-Scale and Analytical GREEnness Metric Approaches were adopted to evaluate the degree of greenness of the procedure. Under the optimal conditions, satisfactory performances of linearity ranged from 5 to 100 μg/L (R 2 ≥ 0.9982), limit of detection (0.58-0.91 μg/L), limit of quantitation (1.9-3.0 μg/L), precision (RSDs ≤ 5.5%), recovery (81.3%-108.1%) and negligible matrix effect were achieved, which introduced a promising alternative route for the determination of naphthalene-derived plant growth regulators in edible oil., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Long term exposure to silica particles leads to various diseases, among which silicosis is of great concern. Silicosis is an interstitial lung disease caused by inhalation of silica particles in production environments. However, the mechanisms underlying silicosis remains unclear. Our previous studies revealed that progranulin (Pgrn) promoted the expression of pro-inflammatory factors in alveolar macrophages treated with silica particles and the secretion of extracellular matrix of pulmonary fibroblasts. Nevertheless, the role of Pgrn in silica particles-induced silicosis in vivo was unknown. This study found that silica particles increased Pgrn expression in silicosis patients. Pgrn deficiency reduced lung inflammation and fibrosis in silica particles-induced silicosis mouse models. Subsequently, based on transcriptional sequencing and interleukin (Il) -6 knockout mouse models, results demonstrated that Pgrn deficiency might decrease silicosis inflammation by reducing the production of Il-6, thereby modulating pulmonary fibrosis in the early stage of silicosis mouse models. Furthermore, another mechanism through which Pgrn deficiency reduced fibrosis in silicosis mouse models was the regulation of the transforming growth factor (Tgf) -β1/Smad signaling pathway. Conclusively, Pgrn contributed to silicosis inflammation and fibrosis induced by silica particles, indicating that Pgrn could be a promising therapeutic target., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

This study investigates the extent and spatial distribution of Potentially Toxic Elements (PTEs) in the Djebel Onk phosphate mine area in south-eastern Algeria, as well as the associated risks to human health. Various scales are considered and sampled, including tailing waste (n = 8), surrounding farmland soil (n = 21), and sediments (n = 5). The samples were mineralogically and chemically analyzed using XRD, FTIR, XRF, and ICP-MS techniques. Principal Component Analysis (PCA) was applied after transforming the raw data into centered-log ratios (clr) to identify the dominant factors controlling the distribution of PTEs. Furthermore, pollution assessment was conducted using several indices, including geo-accumulation, pollution load, contamination security indices, and enrichment and contamination factors. The results reveal that the analyzed samples are mostly P-enriched in the mine tailings, farmland soil, and sediments, with P 2 O 5 concentrations ranging from 13.37 wt% to 26.17 wt%, 0.91-21.70 wt%, and 17.04-29.41 wt%, respectively. The spatial distribution of PTEs exhibits clearly a decrease in the contents of CaO, P 2 O 5 , Cr, Sr, Cd, and U with increasing distance from the mine discharge site, while other oxides, such as MgO, Al 2 O 3 , SiO 2 , K 2 O, and Fe 2 O 3 , and associated elements (Cu, Co, Pb, and Zn), show an increase. PCA confirms the influence of minerals such as, apatite, dolomite, and silicates on the distribution PTEs. It denoted that the highest contamination level of all PTEs in soils and sediments was observed in the southern part of the plant and mine tailings compared to the northern part. In terms of human health risks, the assessment reveals that the hazard index (HI) values for both non-carcinogenic and carcinogenic risks associated with PTEs in the study area are below 1, suggesting no significant risk. However, regardless of the sample type, the lifetime cancer risk (LCR) values vary from 1.69E-05-2.11E-03 and from 1.03E-04-2.27E-04 for Cr, Ni, As (children) and Cd (adults), respectively, exceeding the safe levels recommended by the United States Environmental Protection Agency. The study highlights that oral ingestion poses the greatest risk, followed by dermal contact and particle inhalation. Importantly, all these indices decrease with increasing distance from the sampling site to the waste discharge point and the factory, which indicates that the phosphate mining activity had caused some extent risks. These findings provide valuable insights for mitigating the adverse health impacts and guiding environmental management efforts., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

The potential use of engineered dietary nanoparticles (EDNs) in diet has been increasing and poses a risk of exposure. The effect of EDNs on gut bacterial metabolism remains largely unknown. In this study, liquid chromatography-mass spectrometry (LC-MS) based metabolomics was used to reveal significantly altered metabolites and metabolic pathways in the secretome of simulated gut microbiome exposed to six different types of EDNs (Chitosan, cellulose nanocrystals (CNC), cellulose nanofibrils (CNF) and polylactic-co-glycolic acid (PLGA); two inorganic EDNs including TiO 2 and SiO 2 ) at two dietary doses. We demonstrated that all six EDNs can alter the composition in the secretome with distinct patterns. Chitosan, followed by PLGA and SiO 2 , has shown the highest potency in inducing the secretome change with major pathways in tryptophan and indole metabolism, bile acid metabolism, tyrosine and phenol metabolism. Metabolomic alterations with clear dose response were observed in most EDNs. Overall, phenylalanine has been shown as the most sensitive metabolites, followed by bile acids such as chenodeoxycholic acid and cholic acid. Those metabolites might be served as the representative metabolites for the EDNs-gut bacteria interaction. Collectively, our studies have demonstrated the sensitivity and feasibility of using metabolomic signatures to understand and predict EDNs-gut microbiome interaction., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

Environmental pollution caused by tetracycline antibiotics (TCs) is a major concern for public health worldwide. Trace detection and reliable discrimination of tetracycline and its analogs are consequently essential to determine the distribution characteristics of various tetracycline family members. Here, a dual-response sensor was constructed by integrating the fluorescence emission of fluorescein isothiocyanate (FITC) doped SiO 2 and Eu 3+ . A portable Lab-on-Paper device is further fabricated through probe immobilization, which allows convenient visual detection of tetracycline using a smartphone. In addition, for the coexistence of multiple tetracycline analogs, dimensionality reduction via principal component analysis is applied to the spectra, realizing accurate differentiation of the four most widely used tetracycline analogs (tetracycline (TC), chlortetracycline (CTC), oxytetracycline (OTC), and doxycycline (DOX)). The dual-response nanoplatform enabled a wide-gamut color variation crossing from green to red, with limit of detection (LOD) of 2.9 nM and 89.8 nM for spectrometer- and paper-based sensors, respectively. Analytical performance was examined in multiple real samples, including food, environmental, and biological settings, confirming robust environmental adaptability and resistance. Compared to previous TC sensors, this method has several notable improvements, including improved ecological safety, accessibility, reproducibility, practicality, and anti-cross-interference capacity. These results highlight the potential of the proposed "two birds with one stone" strategy, providing an integrated methodology for synchronous quantitative detection and derivative identification toward environmental contaminants., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

Organothiophosphate pesticides (OPPs) are the most common water contaminants, significantly endangering human health and bringing serious public safety issues. Thus, developing effective technologies for the removal or trace detection of OPPs from water is urgent. Herein, a novel graphene-based silica-coated core-shell tubular magnetic nanocomposite (Ni@SiO 2 -G) was fabricated for the first time and used for the efficient magnetic solid-phase extraction (MSPE) of the OPPs chlorpyrifos, diazinon, and fenitrothion from environmental water. The experimental factors affecting extraction efficiency such as adsorbent dosage, extraction time, desorption solvent, desorption mode, desorption time, and adsorbent type were evaluated. The synthesized Ni@SiO 2 -G nanocomposites showed a higher preconcentration capacity than the Ni nanotubes, Ni@SiO 2 nanotubes, and graphene. Under the optimized conditions, 5 mg of tubular nano-adsorbent displayed good linearity within the range of 0.1-1 μg·mL -1 , low limits of detection (0.04-0.25 pg·mL -1 ), low limits of quantification (0.132-0.834 pg·mL -1 ), good reusability (n = 5; relative standard deviations between 1.46% and 9.65%), low dosage (5 mg), and low real detection concentration (< 3.0 ng·mL -1 ). Moreover, the possible interaction mechanism was investigated by density functional theory calculation. Results showed that Ni@SiO 2 -G was a potential magnetic material for the preconcentration and extraction of formed OPPs at ultra-trace levels from environmental water., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

The increasing amount of europium in aqueous environment from rare earth industry has become a serious environmental challenge. Significant efforts have been focused on ion-imprinting membranes (IIMs) for selective separation of ions from analogues. Based on ion-imprinting technique, we have developed Eu 3+ -imprinted nanocomposite membranes (Eu-IIMs) for selectively separating Eu 3+ from La 3+ , Gd 3+ and Sm 3+ . Polydopamine (pDA) was previously synthesized on basal membranes to augment the interfacial adhesion. Grapheme oxide (GO) and modified silicon dioxide (kSiO 2 ) were synergistically stacked on pDA-modified substrates to form hydrophilic nanocomposite membranes. Ag nanoparticles were modified on the surface to enhance anti-fouling performance. The temperature-controlled selective recognition sites were formed using N-isopropylacrylamide (NIPAm) and acrylamide (Am) as functional monomers as well as europium ions as templates by RAFT (reversible addition-fragmentation chain transfer) method. Large enhanced Eu 3+ -rebinding capacity (101.14 mg g −1 ), adsorptive selectivity (1.82, 1.57, 1.45 for Eu 3+ /La 3+ , Eu 3+ /Gd 3+ , Eu 3+ /Sm 3+ ) and permselectivity (3.82, 3.47, 3.34 for La 3+ /Eu 3+ , Gd 3+ /Eu 3+ , Sm 3+ /Eu 3+ ) were achieved on Eu-IIMs with superior regeneration performance. Additionally, the negligible damage of the membranes after buried for 20 d indicated the superior anti-fouling property of the Eu-IIMs. The ion-imprinted nanocomposite membranes synthesized in this work have shown great potentials for selective separation of rare earth ions. [ABSTRACT FROM AUTHOR]

A new type of dry powders with capsular structure was fabricated for fire suppression, in which the content of water approached 60%. The capsules with the size of 3–5 μm consisted of liquid core and solid shell, where the core was water droplet and the shell was assembled silicon dioxide particles with surface hydrophobic modification. The shell of close-packed silica particles surrounding each water droplet provided the structural rigidity of the capsules and enabled their application as powder fire suppressants. Two different scaled real fire tests showed that thus-prepared solid powders could extinguish 0.21 MW gasoline pool fire in 2.0 s with agent mass of 0.055 kg, and 1.0 MW gasoline pool fire in 5.0 s with agent mass of 0.49 kg. Such fire extinguishing performance greatly outperformed the conventional monoammonium phosphate (ABC) powders, neat silica powders and water mist, with significantly reduced fire extinguishing time and mass of agent consumed. Mechanism of the core-shell particles in fire suppression was discussed based on established theories and experimental results. [ABSTRACT FROM AUTHOR]

To reveal the fate of anthracene (ANT) in soil, the photodegradation behavior of ANT was systematically studied using SiO 2 to simulate a soil environment. Under xenon lamp irradiation, more than 90% of ANT loaded on SiO 2 could be removed after 240 min. Moreover, the effects of water content, chloride ions (Cl-) and humic acid (HA) were examined. It was found that the presence of water and HA can significantly inhibit the photolysis of ANT on SiO 2 , while the addition of chloride alone has no obvious effect. However, when water is present, the inhibition effect of chloride became more obvious. According to radical quenching experiments and electron paramagnetic resonance (EPR) spectra, hydroxyl radicals (•OH) and chlorine radicals (Cl•) were formed in the system. Possible reaction pathways were speculated based on products identified by mass spectrometry. ANT was attacked by •OH to form hydroxylated products, which can be further hydroxylated and oxidized with the final formation of ring-opening products. ANT directly excited by light may also react with Cl• to produce chlorinated polycyclic aromatic hydrocarbons (Cl-PAHs). Finally, the experimental results were verified on real soil. This study provides important information for understanding the photochemical transformation mechanism of ANT at the soil/air interface. [Display omitted] • Co-existing chloride inhibited the photolysis of ANT on moist silicon dioxide. • ANT was attacked by •OH to form hydroxylated products. • In presence of Cl-, excited ANT may react with Cl• to produce Cl-PAHs. • The formation of •Cl was attributed to the reaction of •OH with Cl-. • DFT calculation provided evidence for ANT excitation and the radical reaction site. [ABSTRACT FROM AUTHOR]

The interest in removing contagious viruses from indoor air using ventilation and filtration systems is increasing rapidly because people spend most of the day indoors. The development of an effective platform to regenerate the antiviral function of air filters during use and safe abrogation of used filters containing infectious viruses is a challenging task, because an on-demand safe-by-design manufacture system is essential for in-place antiviral coatings, but it has been rarely investigated. With these considerations, an electrically operable dispenser was prepared for decorating continuous ultrafine Fe-Zn, Fe-Ag, or Fe-Cu particles (<5 nm) onto SiO 2 nanobeads (ca. 130 nm) to form nanobulges (i.e., nanoroughness for engaging coronavirus spikes) in the aerosol state for 3 min direct deposition on the air filter surfaces. The resulting nanobulges were exposed to human coronaviruses (HCoV; surrogates of SARS-CoV-2) to assess antiviral function. The results were compared with similar-sized individual Zn, Ag, and Cu particles. The nanobulges exhibited comparable antiviral activity to Zn, Ag, and Cu particles while retaining biosafety in both in vitro and in vivo models because of the significantly smaller metallic fractions. This suggests that the bimetallic bulge structures generate reactive oxygen species and Fenton-mediated hydroxyl radicals for inactivating HCoV., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

The presence of organic contaminants (OCs) in aquatic systems is a threat to ecological and human health. Adsorption by graphene-based adsorbent is a promising technique for OC removal and we previously fabricated crumpled graphene balls (CGBs), via a novel nano-spray drying technique, which show robust adsorptive performance. Yet, since CGBs contain non-accessible surface area due to 2D graphene stacking, the goal of this research was to investigate the efficacy of maximizing the accessible CGB surface by synthesizing a nanocomposite composed of metal oxide nanoparticles encapsulated by crumpled graphene oxide (MGC). The metal oxides reduce graphene oxide stacking, expand the internal adsorptive surface area, and boost the adsorptive capacity of the MGC. MGC (fumed SiO 2 or SiO 2 ) exhibit an enhanced Langmuir adsorption capacity (q m , normalized by the % carbon) for an OC model, methylene blue (MB), achieving improvements of 60-86% compared to CGB, 3-4 fold compared to powder activated carbon (PAC) and 6-7 fold compared to granular activated carbon (GAC). MGCs display rapid adsorption reaching equilibrium after 9-12 min of contact and remaining stable in wastewater effluent /surface water. A cost-efficiency comparison reveals MGCs achieve one ton of MB removal at similar or lower material costs than that of PAC/GAC., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Surfactant foam (SF) can be used to remediate petroleum-contaminated soil because of its easy transfer to inhomogeneous and low-permeability formations. Nanoparticles (NPs) not only stabilize SF under extreme conditions but also impart various functions, aiding the removal of petroleum contaminants. This review discusses the stabilization mechanisms of nanoparticle-stabilized SF (NP-SF) as well as the effects of NP size, chargeability, wettability, and NP-to-surfactant ratio on foam stability. SF stabilized by inert SiO 2 NPs is most commonly used to remediate soil contaminated with crude oil and diesel. Low dose of SF stabilized by nano zero-valent iron is cost-effective for treating soil contaminated with chlorinated organics and heavy metal ions. The efficiency and recyclability of Al 2 O 3 /Fe 3 O 4 NPs in the remediation of diesel and crude oil contamination could be enhanced by applying a magnetic field. This review provides a theoretical basis and practical guidelines for developing functional NP-SF to improve the remediation of petroleum-contaminated soils. Future research should focus on the structural design of photocatalytic NPs and the application of catalytic NP-SF in soil remediation., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier B.V.)

The neutralization treatment of acid mine drainage involves the oxidation of Fe(II), but little is known about the effects of co-existing minerals on the oxidation and hydrolysis of Fe(II) to iron oxides. Here we investigated the transformation of fresh and heated Fe(II) oxidation coprecipitates, which were synthesized in the presence and the absence of five co-existing minerals (montmorillonite, kaolin, quartz (SiO 2 ) , aluminium oxide (Al 2 O 3 ) and calcium carbonate (CaCO 3 )). In the FeSO 4 system with montmorillonite or kaolin, the formation of lepidocrocite was inhibited with the increase of clay mineral contents. In the same system, heated coprecipitates of montmorillonite were mainly comprised of amorphous ferrihydrite and its transformation was retarded by the excess montmorillonite. In the FeCl 2 system with SiO 2 , Al 2 O 3 or CaCO 3 , akaganeite formation was inhibited with the increase in the corresponding mineral contents. In the same system, goethite formation was blocked by either CaCO 3 or Al 2 O 3 and the growth of lepidocrocite was inhibited by CaCO 3 or SiO 2 . However, magnetite formation was enhanced by addition of CaCO 3 . These findings are important for predicting products of abiotic Fe(II) oxidation during the neutralization of acid mine drainage and for better understanding the transformation of amorphous iron oxides in the complicated environmental matrix., Competing Interests: Declaration of Competing Interest There are no conflicts of interest to declare. 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. Declarations of interest There are no conflicts of interest to declare., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Freeze-thaw (FT) cycles would alter physical and chemical properties of soil and thus influence the transport of plastic particles (one type of emerging contaminant with great concerns). This study was designed to investigate the effects of FT treatment on the mobility of plastic particles (nanoplastics as representative) in columns packed with natural soils (i.e. loamy sand and sandy soil, quartz sand employed as comparison). We found that FT treatment of different types of porous media would induce different transport behaviors of plastic particles. Specifically, FT treatment of quartz sand did not affect plastic particles mobility. While FT treatment of loamy sand and sandy soil increased plastic particles transport. The increased pore sizes and disintegration of small soil particles from soils (the detached soil would serve as mobile vehicle for the transport of plastic particle) led to the facilitated mobility of plastic particles in two types of soils after FT treatment. The presence of preferential flow paths induced by FT treatment also drove to the enhanced mobility of plastic particles in sandy soil with FT treatment. This study clearly showed that the mobility of model plastic particles in two types of natural soils was greatly enhanced by FT treatment., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Nanoplastics (NPs) have become an emerging global environmental problem, and the toxicity of polystyrene nanoplastics (PS-NPs) in rice plants has received widespread attention. However, few studies have focused on silicon (Si)-mediated interactions between PS-NPs and rice. Thus, two forms of Si (organosilicon/inorganic silica) treated rice cells were exposure of positively or negatively charged NPs, PS-NH 2 and PS-COOH, to evaluate the effects of Si for defense against PS-NPs toxicity in rice. The result showed PS-NH 2 nanoparticles were accumulated at relatively low levels in cells compared with that of PS-COOH, but induced a higher accumulation of hydrogen peroxide (H 2 O 2 ) and superoxide radicals (O 2 •- ). However, both organosilicon and inorganic silica can generate more negative potential on the surfaces of cell wall to absorb large numbers of positively charged PS-NH 2 . In addition, they can prevent the uptake of both PS-NH 2 and PS-COOH through reducing the porosity on the surface of the cell walls. These finally alleviated the toxicity of oxidative stress caused by PS-NPs and improved the viability of rice cells. Our findings demonstrated the significant contribution of Si in combating PS-NPs in rice., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)