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Biodegradation is recognized as the main route for the decomposition of phthalic acid esters (PAEs) in nature, but the fate of PAEs in marine ecosystems is not well understood. Herein, a novel marine bacterium, Gordonia sihwaniensis RL-BY03, was identified and analyzed for its ability to degrade PAEs. Furthermore, the metabolic mechanism of di-(2-ethylhexyl) phthalate (DEHP) was examined through UPLC-MS/MS and genomic analysis. RL-BY03 could rely solely on several types of PAEs as its sole carbon source. Initial pH and temperature for DEHP degradation were optimized as 8.0 and 30 °C, respectively. Surprisingly, RL-BY03 could simultaneously degrade ethyl acetate and DEHP and they could increase the cell surface hydrophobicity. DEHP degradation kinetics fitted well with the first-order decay model. The metabolic pathway of DEHP was deduced following the detection of five metabolic intermediates. Further, genes that are related to DEHP degradation were identified through genomic analysis and their expression levels were validated through RT-qPCR. A co-related metabolic pathway at biochemical and molecular level indicated that DEHP was turned into DBP and DEP by β-oxidation, which was further hydrolyzed into phthalic acid. Phthalic acid was utilized through catechol branch of β-ketoadipate pathway. Additionally, RL-BY03 exhibited excellent bioremediation potential for DEHP-contaminated marine samples. In general, these findings have the potential to enhance our understanding of the fate of PAEs in marine ecosystems., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Utilizing metal luminescence enhancement to design fluorescent probes is a very sensible strategy. Herein, a fluorescent probe based on europium (III)-functionalized silver nanoparticles-conjugated homocysteine (AgNPs-Hcy-Eu 3+ ) was proposed for the selective and sensitive detection of tetracycline (TC). In this probe, Eu(III) was employed as the detection signal unit for TC, while AgNPs-Hcy was used as the ligand of fluorescence enhancement. When TC exists, it can bind to Eu 3+ immobilized in AgNPs-Hcy, leading to an enhanced fluorescence signal from Eu 3+ through energy transfer. Under optimal conditions, the fluorescence intensity of AgNPs-Hcy-Eu 3+ increased linearly with increasing TC concentration in the range of 0.1-30 μM (R 2  = 0.9964). The fluorescent probe own fluorescence enhancement, paving the way for sensitive detection with a low detection limit of 0.083 μM. It also has good selectivity for common antibiotics and anions. This work can be applied to the determination of TC in tap water and milk with recoveries of 94-98.5%. We expect AgNPs-Hcy-Eu 3+ to have potential applications in environmental testing and food safety., 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. Published by Elsevier Ltd.)

Fe 3 O 4 has the advantages of unique magnetic stability and low biological toxicity, which can improve pollutants separation efficiency. MXenes are two-dimensional materials and easy surface functionalization that can provide suitable carriers for Fe 3 O 4 . In this work, we synthesized magnetic MXene composites by a one-pot method that relies on doping Fe 3 O 4 particles onto Ti 3 C 2 MXene nanosheets by heat treatment. The Fe 3 O 4 /Ti 3 C 2 MXene was analyzed by SEM, XRD, FTIR and XPS techniques, which showed that the material has good tetracycline (TC) removal properties and magnetic separation ability. The results showed that the adsorption capacity of it was 46.42 mg g -1 , and the removal efficiency of 0.06 g adsorbent for 50 mL of 30 mg L -1 TC could reach 92.1% in a wide pH range of 4-10, when the adsorption temperature was 25 °C, and the adsorption time was 3 h. The adsorption data were consistent with Langmuir and the proposed second-order kinetic model, and the thermodynamic experiments confirmed that the adsorption of TC was a monolayer physicochemical adsorption coexisting heat-trapping process (ΔH = 15.72 kJ mol -1 ). In addition, the adsorption of TC by Fe 3 O 4 /Ti 3 C 2 MXene was attributed to the synergistic effect of electrostatic attraction, hydrogen bonding and π-π packing. In conclusion, the saturation magnetization of Fe 3 O 4 /Ti 3 C 2 MXene is 27.3 emu/g and it can not only be separated from water using its strong magnetic properties to avoid secondary contamination, but also can be used as a promising material to effectively remove antibiotics from aqueous media., 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. Published by Elsevier Ltd.)

In recent years, microplastics (MPs) have been widely found in the environment and pose potential risks to ecosystems, which attracted people's attention. Using bioindicators has been a great approach to understanding the pollution levels, bioavailability, and ecological risks of pollutants. However, only few studies have investigated MPs in mangrove ecosystems, with few bioindicators of MPs. Herein, the distribution of MPs in mangrove sediments and fiddler crabs (Tubuca arcuata) in mangroves was investigated. Results showed that the abundance values of MPs are 1160‒12,120 items/kg and 11-100 items/ind. in mangrove sediments and fiddler crabs, respectively. The dominant shape of MPs detected in mangrove sediments and fiddler crabs was fragments with sizes of 20‒1000 μm, larger MPs of 50-1000 μm were found in abundance. Polypropylene (PP), which is one of the most commonly used plastic materials, was the main polymer type. The distribution of MPs in fiddler crabs closely resembled that in surface mangrove sediments with a strong linear correlation (R 2  > 0.8 and p < 0.05) between their abundance. Therefore, the MP contamination level in mangrove sediments can be determined by studying MP pollution in fiddler crabs. Moreover, the results of the target group index (TGI) indicated that fiddler crabs prefer feeding specific MPs in mangrove sediments. Our findings demonstrate the suitability of fiddler crabs as bioindicators for assessing MP pollution in mangrove sediments., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

A fluorescent-colorimetric dual-signal platform, N, S co-doped carbon dots functionalized silver nanoparticles (NS-CDs-AgNPs), was designed in situ by reducing AgNO 3 in the presence of N, S co-doped carbon dots (NS-CDs) under the assistance of microwave irradiation for glucose determination. With the formation of silver nanoparticles (AgNPs), the intrinsic fluorescence of NS-CDs was quenched, showing the fluorescence state was off. Whereas the fluorescence of NS-CDs can be switched on when a trace amount of H 2 O 2 was added. Based on this novel phenomenon, the peroxidase-like activity of NS-CDs-AgNPs by using 3,3',5,5'-tetramethylbenzidine (TMB) chromogen and H 2 O 2 as substrates was evaluated. The K m values of the prepared probe for H 2 O 2 and TMB were 0.84 mM and 0.01 mM with the V m of 6.65 × 10 -8  M S -1 and 3.01 × 10 -8  M S -1 , respectively. The results showed that NS-CDs-AgNPs had good peroxidase-like activity and strong affinity to TMB and H 2 O 2 . It confirmed that there is a redox interaction between AgNPs and H 2 O 2 , and H 2 O 2 can oxidize Ag to produce Ag + , which is the main reason that the fluorescence of NS-CDs-AgNPs can be activated by H 2 O 2 . The hydroxyl radical (·OH) was formed in the process of reaction, which can further oxidize TMB for color reaction. Meanwhile, glucose can be oxidized to produce H 2 O 2 in the presence of glucose oxidase (GOx). Based on the phenomenon, a fluorimetric and colorimetric dual-mode sensor for glucose detection was established. Satisfactory results were obtained with the linear range of 0.1-80 μM for fluorimetric mode and 0.5-5 μM for colorimetric mode, respectively. Additionally, the LOD was below 0.32 μM and 0.21 μM, respectively. The method was successfully applied to determine the glucose in human serum with satisfactory recovery and RSD., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Industrial wastewater containing heavy metal Cr(VI) seriously affects the health of organisms and may even lead to cancer. Developing efficient adsorbents that can quickly separate heavy metals is crucial for treating wastewater. In this study, magnetic multiwalled carbon nanotubes (MMWCNTs) with moderate particle size and abundant surface active sites were prepared by coating multiwalled carbon nanotubes with magnetic nanoparticles. The results of FTIR, XRD, TG, VSM, BET, and EDS showed MWCNTs completely encapsulated on the surface of the magnetic nanoparticles, with a particle size of approximately 30 nm. Oxygenated groups provided abundant surface active sites and formed numerous mesopores. The response surface methodology was used to optimize the adsorbent dose, adsorption contact time and adsorption temperature, and the removal rate of Cr(VI) was more than 95%. The quasi-second order kinetics and Freundlich adsorption isotherm model explained the adsorption process to Cr(VI). MMWCNTs interacted with Cr(VI) through electrostatic attraction, reduction reactions, complexation, and other means. The extensive hydrogen bonding of the green solvent deep eutectic solvent (DES) was employed to desorb the MMWCNTs and desorption rate exceed 90%. Even after five adsorption-regeneration cycles, the adsorbent maintained a high capacity. In conclusion, these novel MMWCNTs, as efficient adsorbents paired with DES desorption, hold broad potential for application in the treatment of Cr(VI)-contaminated wastewater., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The combination of fluorescent probe and colorimetric technique has become one of the most powerful analytical methods due to the advantages of visualization, minimal measurement errors and high sensitivity. Hence, a novel dual-modality sensing probe with both colorimetric and fluorescent capabilities was developed for detecting cobalt ions (Co 2+ ) based on homocysteine mediated silver nanoparticles and rhodamine 6G derivatives probe (AgNPs-Hcy-Rh6G2). The fluorescence of the AgNPs-Hcy-Rh6G2 probe turned on due to the opening of the Rh6G2 spirolactam ring in the presence of Co 2+ by a catalytic hydrolysis. The fluorescent intensity of probe is proportional to Co 2+ concentration in the range of 0.10-50 μM with a detection limit of 0.05 μM (S/N = 3). More fascinatingly, the color of AgNPs-Hcy-Rh6G2 probe changed from colorless to pink with increasing Co 2+ concentration, which allowing colorimetric determination of Co 2+ . The absorbance of AgNPs-Hcy-Rh6G2 probe is proportional to Co 2+ concentration in the range from 0.10 to 25 μM with a detection limit of 0.04 μM (S/N = 3). This colorimetric and fluorescent dual-modal method exhibited good selectivity, and reproducibility and stability, holding great potential for real samples analysis in environmental and drug field., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)

Tetracycline (TC) is extensively utilized in livestock breeding, aquaculture, and medical industry. TC residues seriously harm food security, the environment, and human health. There is an urgent need to exploit a highly efficient and sensitive testing method to monitor TC residue levels in aquatic environments. In this study, graphitic carbon nitride quantum dots (g-CNQDs) were successfully synthesized by a one-step microwave-assisted method using citric acid and urea as precursors. The as-prepared g-CNQDs with size of 1.25-3.75 nm exhibited bright yellow fluorescence at 523 nm when excited at 397 nm. Interestingly, this characteristic fluorescence emission of g-CNQDs could be selectively and efficiently quenched by TC. Based on this phenomenon, for TC detection was successfully explored and applied in real water samples. Wide linear scope of 7-100 μM, low detection limit (LOD) of 0.48 μM, satisfactory recovery of 97.77%-103.4%, and good relative standard deviation (RSD) of 1.05-5.87% were obtained. Mechanism investigations revealed that the static quenching and the inner filter effect (IFE) were responsible for this fluorescence quenching between g-CNQDs and TC. This work not only provided a facile approach for g-CNQDs synthesis but also constructed a g-CNQDs-based fluorescent sensor platform for the highly sensitive and selective detection of TC in aquatic environments., 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. Published by Elsevier Ltd.)

The magnetic Fe 3 O 4 /bamboo-based activated carbon/Zr-based metal-organic frameworks composite (Fe 3 O 4 /BAC/UiO-66) was prepared by hydrothermal method. The as-prepared material was analyzed via TEM, XRD, FT-IR, BET-BJH, VSM and XPS techniques, the results showed that it had good dispersion and magnetic separation capacity (Ms = 44.06 emu∙g -1 ). Then, the adsorption properties of materials for bisphenol A (BPA) were studied. The results revealed that the removal efficiency of 50 mg·L -1 BPA by 0.1 g of adsorbent can reach 87.18-95% in a wide pH range. Langmuir isotherm model and pseudo-second-order kinetic well fitted the adsorption data. The thermodynamic data indicated that the adsorption process was spontaneous and endothermic. Moreover, BAC as a supporter and UiO-66 as the functional part in the ternary composite may have a synergistic effect, which was beneficial for the removal of contaminants. The Fe 3 O 4 /BAC/UiO-66 can be simply separated from the water using its strong magnetism after finish adsorption process, which effectively avoids secondary contamination., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

The CuO/reduced graphene oxide foam (CuO/RGF) with excellent recyclability was prepared via hydrothermal method followed by freeze drying treatment for bisphenol A (BPA) removal via activating peroxydisulfate (PDS). SEM, XRD, XPS, FT-IR, BET, and TG techniques were used to investigate the structure and property of CuO/RGF. The effect of degradation conditions (pH, PDS amount, Cl - , HCO 3 , HA and FA) on BPA removal by CuO/RGF were investigated. The result presented that CuO nanosheet was inserted into the RGF carrier with three-dimensional structure. The degradation rate constant of BPA over CuO/RGF (0.00917 min - ) was 1.24 and 6.46 times higher than those of BPA over CuO (0.00714 min -1 ) and RGF (0.00142 min -1 ). More importantly, the pore structure of RGF can successfully limit the release of Cu (II) compared to pure CuO. According to quenching test as well as electron spin resonance (EPR) spectra, BPA degradation was triggered by -1 ). More importantly, the pore structure of RGF can successfully limit the release of Cu (II) compared to pure CuO. According to quenching test as well as electron spin resonance (EPR) spectra, BPA degradation was triggered by 1 O 2 OH and SO • , which was the combination of nonradical ( 4 •- ) and radical activation of PDS ( 1 OH and SO 2 ). The possible degradation route of BPA was proposed based on intermediates obtained by combining solid phase extraction pretreatment technique with high performance liquid-mass spectrometry. After assessing the viability of MCF-7 cells, we can see that the estrogenic activities of treated solution reduced without producing stronger endocrine disruptors.• OH and SO 4 •- ). The possible degradation route of BPA was proposed based on intermediates obtained by combining solid phase extraction pretreatment technique with high performance liquid-mass spectrometry. After assessing the viability of MCF-7 cells, we can see that the estrogenic activities of treated solution reduced without producing stronger endocrine disruptors., Competing Interests: Declaration of competing interest The authors declare that they have no competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier Ltd.)

In the present study, Ni-UiO-66 was synthesized to improve the adsorption efficiency of tetracycline (TC) in wastewater treatment. To this end, nickel doping was performed in the preparation process of UiO-66. The synthesized Ni-UiO-66 was characterized by XRD, SEM and EDS, BET, FTIR, TGA, and XPS for obtaining the lattice structure, surface topography, specific surface area, surface functional groups, and thermostability. More specifically, Ni-UiO-66 has a removal efficiency and adsorption capacity of up to 90% and 120 mg g -1 , respectively, when used to treat TC. The presence of ions HCO 3 - , SO 4 and PO 2- , NO 3 humic acid reduces the removal efficiency from 80% to 60%. The performed analyses revealed that Ni-UiO-66 had similar adsorption capacity in wastewater with different ion strengths. The variation of adsorption capacity with the adsorption time was fitted using a pseudo-second-order kinetic equation. Meanwhile, it is found that the adsorption reaction occurs only on the monolayer of the UiO-66 surface so the adsorption process can be simulated using the Langmuir isotherm model. The thermodynamic analysis indicates that the adsorption of TC is an endothermic reaction. Electrostatic attraction, hydrogen-bond interaction, and π-π interaction might be the main reasons for the adsorption. The synthesized Ni-UiO-66 has well adsorption capacity and stable structure. Accordingly, it is expected to achieve a good prospect in industrial applications and wastewater treatment plants.- and PO 4 3- slightly affects the TC adsorption. A 20 mg L -1 humic acid reduces the removal efficiency from 80% to 60%. The performed analyses revealed that Ni-UiO-66 had similar adsorption capacity in wastewater with different ion strengths. The variation of adsorption capacity with the adsorption time was fitted using a pseudo-second-order kinetic equation. Meanwhile, it is found that the adsorption reaction occurs only on the monolayer of the UiO-66 surface so the adsorption process can be simulated using the Langmuir isotherm model. The thermodynamic analysis indicates that the adsorption of TC is an endothermic reaction. Electrostatic attraction, hydrogen-bond interaction, and π-π interaction might be the main reasons for the adsorption. The synthesized Ni-UiO-66 has well adsorption capacity and stable structure. Accordingly, it is expected to achieve a good prospect in industrial applications and wastewater treatment plants., 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 Ltd.)

An off-on fluorescent probe (NS-CDs-AgNPs) was synthesized based on a one-pot microwave process by utilizing N, S co-doping carbon dots (NS-CDs) and silver nitrate as precursors. The significant peak of NS-CDs-AgNPs at 393 nm in ultraviolet spectrum indicated silver nanoparticle (AgNPs) were successfully synthesized. A faint blue fluorescence emission (442 nm) was displayed when excited NS-CDs-AgNPs at 371 nm. A remarkable fluorescence recovery was observed upon adding of trance Hg 2+ , whereas the other heavy metal ions did not elicit this response. The reason for this phenomenon was revealed in this work that a spontaneous redox reaction occurred between NS-CDs-AgNPs and Hg 2+ , which leaded to the formation of NS-CDs-Ag n -2NPsHg complexes. On the basis of this mechanism, a new off-on fluorescent analytical method was constructed for Hg 2+ detection with linear range of 10-400 nM (R 2  = 0.9941), and the detection limit (LOD) of 5.16 nM. Additionally, satisfactory recovery (90.28%-106.13%) and the relative standard deviation (RSD) (RSD＜5.21%) were obtained in water sample detection. More importantly, the NS-CDs-AgNPs exhibited lower cytotoxicity and better biocompatibility, indicating a huge potential in cell imaging and clinical medicine., 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 Ltd.)

A combination of magnetic κ-carrageenan nanoparticles and deep eutectic supramolecular solvents used for extraction of catechol from water was evaluated by the magnetic dispersion solid phase extraction method. The magnetic κ-carrageenan nanoparticles (KC@Fe 3 O 4 MNPs) and the deep eutectic supramolecular solvent (DESP) were characterised by 1 H NMR, FT-IR, XRD, SEM, VSM, TG, and BET. The adsorption kinetics, adsorption isothermal model, adsorption thermodynamics and effects of pH and salt concentration were investigated. Additionally, the factors used in the desorption process, such as the type, dosage, concentration and time, were analysed. Under the optimised conditions, the analytes were linear over the range 5-5000 ng mL -1 , with a correlation coefficient greater than 0.999 and detection and quantitation limits of 1.6 and 4.7 ng mL -1 , respectively. The procedure was successfully applied to determinations of the analytes of interest in spiked water samples with relative average recoveries ranging from 94.3% to 101.5%. These results indicated that the combination of functionalized magnetic nanoparticles and DESP had high specificity and extraction efficiency for catechol and will be a feasible alternative to conventional analyses of organic phenolic pollutants in 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 Ltd. All rights reserved.)

Employing cheap Cu nanoclusters to design a novel fluorescent probe have promising opportunities in the field of optical sensors. Here, we fabricated a highly photoluminescent D -tryptophan ( D -Trp)-coated Cu nanoclusters (Trp-Cu NCs) by rapid microwave-assisted method to achieve precise quantification of tetracyclines (TC). Due to protecting groups of Trp, the synthesized Trp-Cu NCs have remarkable fluorescence stability with a quantum yield reached 12.5%. A distinct fluorescence quenching with the incremental addition of TC via the internal filtration effect (IFE). Based on turn-off fluorescence within 1 min, a detection method for detecting TC was constructed with a linear range of 0.3-120 μM and a limit of detection (LOD) of 0.12 μM. Besides, the proposed fluorescent probe has been employed for the determination of practical samples such as water samples, milk and honey, and exhibited satisfactory recoveries of 96.1%-108.2%, with relative standard deviations (RSD) lower than 5.0%. This is a sensitive, rapid and easily recognizable Trp-Cu NCs based sensing platform for the determination of TC, which could offer a powerful tool for ensuring food safety., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Excessive phosphorus (P) and ammonia nitrogen (NH 3 -N) in water bodies can lead to eutrophication of the aquatic environment. Therefore, it is important to develop a technology that can efficiently remove P and NH 3 -N from water. Here, the adsorption performance of cerium-loaded intercalated bentonite (Ce-bentonite) was optimized based on single-factor experiments using central composite design-response surface methodology (CCD-RSM) and genetic algorithm-back propagation neural network (GA-BPNN) models. Based on the determination coefficient (R 2 ), mean absolute error (MAE), mean square error (MSE), mean absolute percentage error (MAPE), and root mean square error (RMSE), the GA-BPNN model was found to be more accurate in predicting adsorption conditions than the CCD-RSM model. The validation results showed that the removal efficiency of P and NH 3 -N by Ce-bentonite under optimal adsorption conditions (adsorbent dosage = 1.0 g, adsorption time = 60 min, pH = 8, initial concentration = 30 mg/L) reached 95.70% and 65.93%. Furthermore, based on the application of these optimal conditions in simultaneous removal of P and NH 3 -N by Ce-bentonite, pseudo-second order and Freundlich models were able to better analyze adsorption kinetics and isotherms. It is concluded that the optimization of experimental conditions by GA-BPNN has some guidance and provides a new approach to explore adsorption performance after optimizing the conditions., 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 Ltd.)

To reduce or eliminate the inhibition effect of natural organic matters (NOMs) in water on TiO 2 photocatalysis for removal of emerging contaminants, four activated carbon/titanium dioxide (AC/TiO 2 ) composites with different pore structure were prepared by hydrothermal method. The results showed that anatase TiO 2 particles were uniformly distributed in the pores or onto the surface of activated carbons. The total removal rate of 6 mg L -1 17α-ethinylestradiol (EE2) on the four AC/TiO 2 composites reached above 90%, 30% higher than that of EE2 on TiO 2 . The degradation rate constants of EE2 on four kinds of AC/TiO 2 were much higher than that on TiO 2 . Further study indicated that the adsorption removal ratio of EE2 on the composites was slightly reduced mainly because competitive adsorption between hydrophilic NOMs (HA and FA) and EE2 molecules when HA and FA coexisted with EE2 in water. But importantly, the obvious inhibitory effect of FA for TiO 2 photocatalysis was eliminated on four composites because the introduction of AC with excellent adsorption capacity can preferentially transfer hydrophobic EE2 molecules onto adsorption sites of TiO 2 /AC composites., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier Ltd. All rights reserved.)

Hazardous solid waste blast furnace dust (BFD) is rich in valuable metal components such as iron (Fe), zinc (Zn), manganese (Mn), and its recycling or harmless treatment is a major challenge. This paper creatively proposes the strategy of "treating waste with waste" by using BFD for desulfurization. The experimental results show that BFD slurry can achieve high-efficiency desulfurization and recovery of Zn resources. The characterization results indicate that ZnO and Fe 2 O 3 in BFD slurry are the main active components of desulfurization, and the consumption of active components is the main reason for the decline of BFD slurry activity. Further semi-continuous experimental research shows that Zn, Fe, and Mn ions in BFD slurry play a crucial role in the catalytic oxidation of sulfur dioxide (SO 2 ). Additionally, the effects of reaction temperature, stirring speed, inlet SO 2 concentration, and inlet gas flow rate on the leaching rate of Zn and Fe were investigated. Under optimal conditions (SO 2 concentration = 3000 mg‧m -3 , reaction temperature = 40 °C, inlet gas flow rate = 300 mL‧min -1 , solid-liquid ratio = 0.5 g/300 mL, stirring speed = 600 rpm), the desulfurization rate reaches 100%, and the maximum leaching rate of Zn can reach 44.6%. Based on the experimental and characterization results, the possible mechanism of BFD slurry desulfurization was proposed. This study provides a reference for the application of BFD in the field of wet desulfurization., 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 Ltd. All rights reserved.)

The wide application of fungicides is becoming one of the main causes of water pollution. Activated carbon (AC) is a frequently-used adsorbent in water treatment. In this work, aiming to obtain a better understanding of fungicides on AC, carbendazim was selected as a model fungicide in water. The effects of AC dosage, adsorption temperature, adsorption time and pH value of solution on carbendazim adsorption by AC were investigated. When the initial concentration of carbendazim was 500 mg L -1 and the volume of wastewater was 25 mL, the optimum dosage of AC and reaction time was determined to be 0.3 g and 150 min, respectively. The pH ranging from 3.0 to 10.0 exhibited little effect on the adsorption capability of AC. The higher the adsorption temperature was, the better adsorption capacity was. Adsorption capacity could reach 32.31 mg g -1 under the optimal adsorption conditions. The kinetics study reveals that the adsorption of carbendazim occurred on the surface of adsorbent during initial stage. The adsorption data was well fitted by Langmuir adsorption isotherm, indicating that the adsorption process was monolayer adsorption. The thermodynamic experiments confirmed that the adsorption of carbendazim was an endothermic process with the coexistence of physical and chemical adsorption. Because the main components of AC used in this research work is amorphous carbon with low impurity and its surface has not been modified with additional functional groups, the conclusion of the study was easy to be replicated by repeated experiments. Therefore, the findings of this study could guide the adsorption of carbendazim onto the other kinds of AC with high specific surface area, and provide useful information for application of commercial AC in treatment of fungicides wastewater., (Copyright © 2022. Published by Elsevier Ltd.)

Mercury ion (Hg 2+ ) is a heavy metal pollutant that can affect the safety of water environment and endanger human health. A novel detection strategy (GNPs- L -Cys-Rh6G2) for Hg 2+ based on a fluorescence "OFF-ON" was proposed. Gold nanoparticles (GNPs) were assembled with l -cysteine ( L -Cys), which was used as a "bridge" to link with rhodamine 6G derivatives (Rh6G2). The fluorescence state transition of GNPs- L -Cys-Rh6G2 switching from "OFF"-"ON" was observed because Hg 2+ opened the spirolactam ring through a catalytic hydrolysis mechanism. The fluorescence signal of the GNPs- L -Cys-Rh6G2 system mixed with Hg 2+ in the concentration range of 10-100 μM was analyzed and determined with a limit of detection (LOD) of 2 μM (S/N = 3). Moreover, the spiked Hg 2+ concentration in real water samples were successfully quantified by GNPs- L -Cys-Rh6G2, which was in line with the ideal average recovery rate and relative standard deviation. The proposed strategy exhibited high specificity, sensitivity and stability, providing a novel sensing platform for heavy metal ions detection in water environment., (Copyright © 2022. Published by Elsevier Ltd.)

In this study, using a convenient one-pot microwave-assisted method, we rapidly fabricated a N, S-codoped fluorescent carbon dots (NSCDs) through using citric acid (CA) and d -penicillamine (DPA) for the detection of tetracyclines (TC). To rapidly and efficiently optimize the various synthesis parameters and significantly decrease the number of experimental runs, the effect of the synthesis factors on quantum yield (QY) by NSCDs was implemented through means of response surface methodology (RSM). The as-synthesized NSCDs presented superior photoluminescence stability with a strong quantum yield (QY) of 91.55% under optimal conditions, which was consistent with the predicted value using RSM. The fluorescence intensity of the NSCDs could be quenched effectively after adding TC by the inner filter effect (IEE) and photoinduced electron transfer (PET). Thus, the determination of TC by using NSCDs as a facile fluorescent probe was constructed in the range of 0.2-70 μM with a limit detection of 0.072 μM. Moreover, this detection approach has been utilized to detect TC in actual samples with satisfactory results., (Copyright © 2022. Published by Elsevier Ltd.)

Traditional batch configuration is not sustainable due to catalyst leaching and ineffective recovery. Herein, a novel membrane-based catalyst with oxygen vacancies is developed, which assembled metal-organic-framework cobalt ferrite nanocrystals (MOF-d Co x Fe 3-x O 4 ) on polyvinylidene fluoride membrane to activate peroxymonosulfate (PMS) for catalytic degradation of emerging pollutants. MOF-d Co x Fe 3-x O 4 are synthesized by one-step pyrolysis using Co/Fe bimetallic organic frameworks (Co x Fe 3-x bi-MOF) with tunable cobalt content as a template (x/3-x represented the molar ratio of Co and Fe in MOF). Intriguingly, MOF-d Co 1.75 Fe 1.25 O 4 membrane exhibits excellent PMS activation efficiency as indicated by 95.12% removal of the probe chemical (bisphenol A) at 0.5 mM PMS (∼100 L m -2  h -1  at the loading of 10 mg), which is significantly higher than the traditional Co 1.75 Fe 1.25 O 4 suspension system (34.16%). Experimental results show that the membrane has excellent anti-interference ability to anions and dissolved organic matter, and can effectively degrade a variety of emerging pollutants, and its performance is not inhibited by the change of solution pH (3-9) or the long-term (20 h) continuous flow operation. EPR and quenching experiments show that catalytic degradation is the result of the synergistic effect of radicals and non-radicals. The oxygen vacancy-mediated mechanism can explain the formation of active substances, and the formation of 1 O 2 plays an important role in the degradation of bisphenol A. This study provides a membrane-based strategy for effective and sustainable removal of emerging pollutants., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Graphene has found important applications in various areas and hundred tons of graphene materials are annually produced. It is crucial to investigate both the negative and positive environmental effects of graphene materials to ensure the safe applications and develop environmental applications. In this study, we reported the stimulating effects of reduced graphene oxide (RGO) to nitrogen-fixing bacterium Azotobacter chroococcum. RGO stimulated the cell growth of A. chroococcum at 0.010-0.500 mg/mL according to the growth curves and the colony-forming unit (CFU) increases. RGO wrapped over the A. chroococcum cells without inducing ultrastructural changes. RGO decreased the leakage of cell membrane, but slight oxidative stress was observed in A. chroococcum. RGO promoted the nitrogen fixation activity of A. chroococcum at 0.5 mg/mL according to both isotope dilution method and acetylene reduction activity measurements. Consequently, the increases of soil nitrogen contents were evidenced, in particular about 30% increase of organic nitrogen occurred at 0.5 mg/mL of RGO. In addition, RGO might possibly benefit the plant growth through enhancing the indoleacetic acid production of A. chroococcum. These results highlighted the positive environmental effects of graphene materials to nitrogen-fixing bacteria in nitrogen cycle., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The enrichment of various pollutants in mangrove has attracted widespread attention. Especially, microplastics accumulation in mangrove may provide a more challenging ecological colonization site by enriching pollutants, thus affecting the change of microplastics antibiotic resistance and increasing the risk of antibiotic failure. Herein, the antibiotic-resistant of microplastics and sediment from mangrove were investigated. The results show that isolates are mainly colonized by Vibrio parahemolyticus (V. parahemolyticus), Vibrio alginolyticus (V. alginolyticus), and Shewanella. 100% mangrove microplastics isolates are resistant to chloramphenicol, cefazolin, and tetracycline, especially amoxicillin clavulanate and ampicillin. Meanwhile, the multiple antibiotics resistance (MAR) indexes of V. parahaemolyticus, Shewanella, and V. alginolyticus in mangrove microplastics are 0.72, 0.77, and 0.77, respectively, which are far higher than the MAR index standard (0.2) and that of mangrove sediment isolates. Furthermore, compared with V. parahaemolyticus isolated from the same mangrove microplastics, Shewanella and V. alginolyticus show stronger drug resistance. It should be noted that there is a closely related relationship between the type of microplastics and the antibiotics resistance of isolated bacteria. For the antibiotics sensitivity test of norfloxacin, streptomycin, amoxicillin, and chloramphenicol, V. parahaemolyticus have the lower antibiotics resistance than that of V. alginolyticus isolated from the same mangrove microplastics. However, Vibrio isolated from PE has stronger antibiotics resistance. Results reveal that mangrove may be one of the potential risks for emergence and spread of bacterial antibiotics-resistant and multidrug-resistant, and microplastic biofilms may act as promoters of bacterial antibiotic resistance., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

Nutrients in centralized discharge area of treated sewage can cause high ecological risks to aquatic systems, thus a deep-level nutrient removal is necessary. Recently, periphyton has attracted increasing interests for its excellent performance in nutrient removal. In this study, the suitability and durability of basalt fiber (BF) as a new green carrier of periphyton was evaluated, and development process of basalt fiber-periphtyon (BFP) was tracked with bacterial community succession and physiological indicators. Then, well-developed BFP was applied to deeply purify water containing the same concentration of nutrient as the treated sewage. Results showed the periphyton could adapt to BF and formed in large quantities. In addition, the tensile strength of BF after being used as a carrier was still strong. Bacterial community and physiological indicators indicated that BFP was well developed in 40-50 days. LEfSE and random forest analysis revealed that Deinococcus-Deinococci, Spartobacteria and Chlamydiia at class-level, Rhizobiales and Rhodobacterales at order-level were the biomarkers for development of BFP. Moreover, application results showed BFP efficiently removed nitrogen and phosphorus from water and promoted the transformation of ammonia to nitrate. The concentration of ammonia and phosphorus severely decreased from 4.90 ± 0.11 mg/L to 0.51 ± 0.20 mg/L, from 0.66 ± 0.016 mg/L to 0.023 ± 0.013 mg/L, respectively. The efficient nutrient removal was attributed to accumulation of nitrogen and phosphorus metabolism related organisms in BFP as well as favorable water physic-chemical conditions created by BFP. These results suggest that BF is a suitable and durable green carrier of periphyton, and BFP could efficiently reduce ecological risk to aquatic systems receiving treated sewage., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Zr/CTAB/BAC was prepared by bamboo activated carbon (BAC) functionalised by zirconia chloride octahydrate (ZrOCl 2 ·8H 2 O) and Cetyltrimethylammonium bromide (CTAB). The effects of temperature, time, Zr dosage and CTAB concentration on removing phosphate and nitrate (H 2 PO 4 and NO - ) in wastewater were investigated. The structure of Zr/CTAB/BAC was characterized by SEM, BET, FTIR, XRD and TG, and the kinetics and thermodynamics of adsorption were discussed. The optimum preparation conditions were as follows: the modification temperature was 25 °C, the modification time was 4 h, the mass of the modifier Zr added was 0.40 g, and the concentration of the modifier CTAB was 0.6 mM. When the dosage of Zr/CTAB/BAC was in the range of 0.1 g-1.0 g, the removal efficiency of phosphate in simulated wastewater was between 59.32% and 99.42%, and the removal efficiency of nitrate was between 34.08% and 93.70%. Using NaOH as a regenerant, after four times adsorption and desorption experiments, the removal efficiency of phosphate and nitrate by Zr/CTAB/BAC can still reach more than 70%. The chemical adsorption was the primary cause of the adsorption, and the adsorption process was endothermic. Zr/CTAB/BAC had an obvious removal effect on phosphate and nitrate in water, which could be promoted to treat other anionic salts in sewage.3 - ) in wastewater were investigated. The structure of Zr/CTAB/BAC was characterized by SEM, BET, FTIR, XRD and TG, and the kinetics and thermodynamics of adsorption were discussed. The optimum preparation conditions were as follows: the modification temperature was 25 °C, the modification time was 4 h, the mass of the modifier Zr added was 0.40 g, and the concentration of the modifier CTAB was 0.6 mM. When the dosage of Zr/CTAB/BAC was in the range of 0.1 g-1.0 g, the removal efficiency of phosphate in simulated wastewater was between 59.32% and 99.42%, and the removal efficiency of nitrate was between 34.08% and 93.70%. Using NaOH as a regenerant, after four times adsorption and desorption experiments, the removal efficiency of phosphate and nitrate by Zr/CTAB/BAC can still reach more than 70%. The chemical adsorption was the primary cause of the adsorption, and the adsorption process was endothermic. Zr/CTAB/BAC had an obvious removal effect on phosphate and nitrate in water, which could be promoted to treat other anionic salts in sewage., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

Hydrothermal carbonization (HTC) provides alternatives technique to produce a nanosize activated carbon from biomass with a high surface area. Herein, this study we prepared empty fruit bunch-based activated carbon (EFBHAC) using HTC technique. The activated carbon was then functionalized with K 2 CO 3 and Cu(NO 3 ) 2 to produce bifunctional nano-catalyst for simultaneous esterification-transesterification of waste cooking oil (WCO). The physicochemical properties were performed i.e. N 2 sorptions analysis, TPD-CO 2 /NH 3 , FESEM, EDX, FTIR and XRD analysis. The results revealed that produced EFBHAC possessed a BET surface area of 4056.17 m 2  g -1 , with pore volume of 0.827 cm 3  g -1 and 5.42 nm of pore diameter resulting from hydrolysis, dehydration decarboxylation, aromatization and re-condensation during HTC process. Impregnation of EFBHAC with K 2 CO 3 and Cu(NO 3 ) 2 granted a high amount of basicity and acidity of 9.21 mmol g -1 and 31.41 mmol g -1 , respectively, accountable to high biodiesel yield of 97.1%, produced at the optimum condition of 5 wt% of catalyst loading, 12:1 of methanol to oil molar ratio at 70 °C for 2 h. More than 80% of biodiesel was produced after the 5th cycle depicted the good reusability. The transformations from WCO to biodiesel was confirmed via 1 H NMR, FTIR and TGA analysis. Fuel properties revealed kinematic viscosity of 3.3 mm 2  s -1 , cetane number of 51, flash point of 160.5 °C, cloud and pour point of 11 °C and -3 °C, respectively. These results show the excellent potential of waste materials to prepare bifunctional nano-catalysts to produce higher biodiesel yield which has potential to be commercialized., (Copyright © 2021 Elsevier Ltd. All rights reserved.)

The contamination of groundwater by arsenic (As) in Bangladesh is the biggest impairing of a population, with a large number of peoples affected. Specifically, groundwater of Gangetic Delta is alarmingly contaminated with arsenic. Similar, perilous circumstances exist in many other countries and consequently, there is a dire need to develop cost-effective decentralized filtration unit utilizing low-cost adsorbents for eliminating arsenic from water. Morphological synthesis of carbon with unique spherical, nanorod, and massive nanostructures were achieved by solvothermal method. Owing to their intrinsic adsorption properties and different nanostructures, these nanostructures were employed as adsorption of arsenic in aqueous solution, with the purpose to better understanding the morphological effect in adsorption. It clearly demonstrated that carbon with nanorods morphology exhibited an excellent adsorption activity of arsenite (about 82%) at pH 3, remarkably superior to the two with solid sphere and massive microstructures, because of its larger specific surface area, enhanced acid strength and improved adsorption capacity. Furthermore, we discovered that iron hydroxide radicals and energy-induced contact point formation in nanorods are the responsible for the high adsorption of As in aqueous solution. Thus, our work provides insides into the microstructure-dependent capability of different carbon for As adsorption applications., 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 Ltd. All rights reserved.)

The adverse effects of glyphosate herbicide on plants are well recognised, however, potential hormetic effects have not been well studied. This study aimed to use tomato as a model organism to explore the potential hormetic effects of glyphosate in water (0-30 mg L -1 ) and in compost soil (0-30 mg kg -1 ). The growth-promoting effects of glyphosate at concentrations of 0.03-1 mg L -1 in water or 0.03-1 mg kg -1 in compost were demonstrated in tomato for the first time. These hormetic effects were manifest as increased hypocotyl and radicle growth of seedlings germinated on paper towel soaked in glyphosate solution and also in crops which had been sprayed with glyphosate. Increased rates of photosynthesis (up to 2-fold) were observed in 4-week old crops when seeds were sown in compost amended with glyphosate and also when leaves were sprayed with glyphosate. The examination of chloroplast morphology using transmission electron microscopy revealed that the hormetic effects were associated with elongation of chloroplasts, possibly due to lateral expansion of thylakoid grana., 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 Ltd. All rights reserved.)

In recent years, global climate change and pollution of the marine environment have caused large-scale coral deaths and severe damages to coral reef ecosystems. Numerous studies have shown that coral diseases are closely related to microorganisms. And microplastics (MPs) are a potential threat to corals. In marine ecosystems, MPs are an emerging contaminant. MPs have a strong adsorption effect on pollutants in the water environment, and they are very easily colonized by microorganisms to form biofilms. Biofilms may accumulate many pathogens, increasing the probability of coral disease. However, there is no report about the composition of biofilms on the surface of microplastics in coral growth areas. In this study, nine kinds of MPs were chosen in the experiments, which are commonly found in the ocean. Four stakeout points were selected in the coral area. Biofilms were cultivated in natural environment. The composition and distribution of biofilms on the surface of the MPs were analyzed by 16 S rRNA sequencing. The characteristics of biofilms were observed by scanning electron microscopy (SEM). The experimental results show that the species composition and abundance distribution of the biofilm on the MP surface are significantly different from the surrounding seawater. The type of MPs and the stake out point are important factors affecting the structure of the biofilm bacterial community. Compared to seawater samples, MPs are enriched with certain dominant bacteria such as Vibrionaceae, Rhodobacteraceae, Flavobacteraceae, Microtrichaceae and Sphingomonadaceae. Among them, Vibrionaceae, Rhodobacteraceae and Flavobacteraceae are closely related to the tissue damage of stony corals, and Vibrios are also the main pathogens of coral albinism. In addition, Pseudomonas and Bbellvibrio cholerae are also detected on the MPs biofilm. SEM graphs of the MPs after culture could clearly observe rod-shaped bacteria and Streptococci. This study can provide a new direction for the study of coral toxicology by MPs and provide basic data for the toxicology research of MPs., Competing Interests: Declaration of competing interest There are no conflicts of interest., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

A sulfur cycle-driven bioprocess was developed for co-treatment wet flue gas desulfurization wastes with municipal sewage, as a result of sludge minimization. In this process, organics removal (one of the main objectives in sewage treatment) is closely associated with biological sulfate/sulfite reduction (BSR). In the previous studies, both the pros and corns of sulfite (SO 3 ) in microbial activities were demonstrated. In this study, we are motivated to unveil the detailed role of SO 2- in organic compound removal in the sulfur conversion-associated process. In addition, the effect of internal recirculation (IR) of UASB reactor was also explored. The results demonstrated that sulfite does inhibit the organic removal rate via depressing the acetate oxidation to inorganic carbon. And the inhibition is reversible when influent sulfite concentration decreased from 400 to 132 mg S/L, corresponding to the relative sulfate/sulfite-reducing genera increased from 18.66 to 38.62%. And the fermenting-related bacteria significantly decreased when an internal recirculation was employed for the UASB reactor. The results of this study could shed light on the understanding of the roles of sulfite and IR in organic compound removal performance and microbial community structures in BSR, which could be in turn beneficial to optimize the organic removal capacity of the sulfur bionconversion-concerning sewage treatment technology.3 2- in organic compound removal in the sulfur conversion-associated process. In addition, the effect of internal recirculation (IR) of UASB reactor was also explored. The results demonstrated that sulfite does inhibit the organic removal rate via depressing the acetate oxidation to inorganic carbon. And the inhibition is reversible when influent sulfite concentration decreased from 400 to 132 mg S/L, corresponding to the relative sulfate/sulfite-reducing genera increased from 18.66 to 38.62%. And the fermenting-related bacteria significantly decreased when an internal recirculation was employed for the UASB reactor. The results of this study could shed light on the understanding of the roles of sulfite and IR in organic compound removal performance and microbial community structures in BSR, which could be in turn beneficial to optimize the organic removal capacity of the sulfur bionconversion-concerning sewage treatment technology., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

Cypermethrin (CP) is a kind of chiral pesticides that has been defined as endocrine disrupting chemical. The diversity in bioactivity, toxicity, metabolism, bioaccumulation, and degradation behaviors of CP enantiomers as well as the research deficiency had made the risk assessment of CP enantiomers very complicated. Herein, four CP enantiomers were separated as target chemicals to investigate their enantioselective endocrine disrupting effects. Firstly, dual-luciferase reporter gene assays were adopted to investigate their potential endocrine disrupting effects via various receptors. The expression levels of steroid hormones related genes and hormone secretion levels in H295R cell were measured to verify the results. Results from the reporter gene assay showed that 1R-cis-αS-CP (CP11) exhibited glucocorticoid receptor (GR), mineralocorticoid receptor (MR), and thyroid receptor (TR) antagonistic activity with the RIC 20 values of 9.22 × 10 -7 , 3.33 × 10 -7 , and 4.47 × 10 -7  M, respectively; 1R-trans-αS-CP (CP21) also showed androgen receptor (AR) agonist activity and estrogen receptor (ER) antagonistic activity with the REC 20 and RIC 20 values were 1.07 × 10 -4  M and 4.78 × 10 -6  M, respectively. Results of qRT-PCR and hormone measurement also showed that CP11 and CP21 could disturb the expression of steroid hormones related genes and hormone secretion accordingly. Results provided here can help to understand the enantioselective ecological and health risks of CP enantiomers comprehensively and provide constructive guidance for the safe use of chiral pesticides and the invention of green pesticides., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

In this study, the influences of feedstock and pyrolysis temperature on carbon fractions of biochar were investigated. Four types of organic wastes (rice straw (RS), pine wood (PW), pig manure (PM) and sewage sludge (SS)) were pyrolyzed at different temperatures (300 °C, 400 °C, 500 °C, 600 °C and 700 °C). Biochar produced at low temperature exhibited high yields, high dissolved organic carbon (DOC) content and unstable organic carbon content. In contrast, biochar formed at high temperature showed high C content and C stability with a low O/C and H/C ratios. In addition, the biochar pyrolyzed from PW contained the lowest DOC of the four biochar types. The properties of DOC fractions (F1, F2 and F3) released from biochar differed depending on feedstock, pyrolysis temperatures, and extraction procedures. The highest specific ultraviolet absorbance at 254 nm of the F1 and F2 fractions were observed for RS biochar, suggesting that more aromatic organic matter was present in sequentially extracted fractions of RS biochar than in extracts from the other biochars. In addition, the hot water extracts (F2) mostly showed higher aromaticity than cold water extracts (F1). The stability of biochars was greatly enhanced at pyrolysis temperatures >500 °C. If the biochars produced in this study were to be used for carbon sequestration in soil, the first priority should be PW, followed in order by RS and PM., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Herein, we utilized nanoscale zero-valent iron loaded on layered double hydroxide (NZVI/LDH) to immobilize Se(VI) and evaluated the enhancement role of LDH in the NZVI reaction system. The structural characterization indicated that LDH could stabilize and disperse NZVI as well as prevent NZVI from oxidation, thereby increasing iron reactivity. Batch experiments displayed that, compared with those by NZVI, both extent and rate of Se(VI) immobilized by NZVI/LDH significantly increased, owing to the prominent synergistic effect ascribing from adsorption and reduction. Kinetics studies under a series of conditions showed that Se(VI) reaction could be well described by pseudo first-order model. The performance of Se(VI) immobilization was inhibited to a considerable extent by most of co-existing ions, Nevertheless, the presence of Cu 2+ improved performance of NZVI/LDH due to its role as a catalyst or medium of charge transfer during reduction. XANES revealed that LDH acted as a promoter for complete reduction of Se(VI) into Se(0)/Se(-II) over a wide pH range, whereas EXAFS suggested that LDH acted as a scavenger for insoluble products, making more reactive sites exposure to Se(VI) for reduction. These results suggested that NZVI/LDH as a promising candidate exhibited potential application in remediation of wastewaters containing Se(VI)., (Copyright © 2017 Elsevier Ltd. All rights reserved.)

In vivo studies of the interactions of polybrominated diphenyl ethers (PBDEs) in plants have generally focused on uptake, translocation, metabolism and accumulation, but there were limited reports about the phytotoxicity and translocation of PBDEs in contaminated soil with the effects of nanoparticles. In this study, the effects of Ni/Fe bimetallic nanoparticles on translocation of polybrominated diphenyl ethers (PBDEs) in contaminated soil and its phytotoxicity to Chinese cabbage were investigated by soil culture experiments. The results showed that the plant biomass, germination rate, and shoot and root lengths of treated soil (S-5) increased by 0.0044 g, 15%, and 5 and 6 mm, respectively, compared with untreated soil (S-2B). The average Ni and Fe contents of the edible parts(stem and leaf) of the S-5 sample, which contained 0.03 g/g Ni/Fe and 10 mg/kg BDE209, were measured at 1.71 and 184 mg/kg, respectively. The superoxide dismutase, peroxidase and catalase activities in the S-5 sample decreased by 12%, 6.1% and 5.9%, respectively, while compared with the S-2B sample. In all treatments, the contents of BDE209 and the total PBDEs in sample S-5 were lowest, suggesting that the fresh Ni/Fe nanoparticles had higher toxicity than that of the aged nanoparticles. And the lower brominated PBDEs (tri-to nona-) were detected in samples, indicating uptake, debromination and/or metabolism of PBDEs existed in plants. The phytotoxicity and translocation of BDE209 in the contaminated soil decreased as a result of the effects of the Ni/Fe bimetallic nanoparticles., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

The decomposition efficiency of polychlorinated biphenyls (PCBs) was determined using elemental iron (Fe) and three iron (hydr)oxides, i.e., α-Fe2O3, Fe3O4, and α-FeOOH, as catalysts. The experiments were performed using four distinct PCB congeners (PCB-209, PCB-153, and the coplanar PCB-167 and PCB-77) at temperatures ranging from 180 °C to 380 °C and under an inert, oxidizing or reducing atmosphere composed of N2, N2+O2, or N2+H2. From these three options N2 showed to provide the best reaction atmosphere. Among the iron compounds tested, Fe3O4 showed the highest activity for decomposing PCBs. The decomposition efficiencies of PCB-209, PCB-167, PCB-153, and PCB-77 by Fe3O4 in an N2 atmosphere at 230 °C were 88.5%, 82.5%, 69.9%, and 66.4%, respectively. Other inorganic chlorine (Cl) products which were measured by the amount of inorganic Cl ions represented 82.5% and 76.1% of the reaction products, showing that ring cleavage of PCBs was the main elimination process. Moreover, the dechlorination did not require a particular hydrogen donor. We used X-ray photoelectron spectroscopy to analyze the elemental distribution at the catalyst's surface. The O/Fe ratio influenced upon the decomposition efficiency of PCBs: the lower this ratio, the higher the decomposition efficiency. X-ray absorption near edge structure spectra showed that α-Fe2O3 effectively worked as a catalyst, while Fe3O4 and α-FeOOH were consumed as reactants, as their final state is different from their initial state. Finally, a decomposition pathway was postulated in which the Cl atoms in ortho-positions were more difficult to eliminate than those in the para- or meta-positions., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

The effects of gas compositions on NOx reduction and NH3 slip by selective non-catalytic reduction (SNCR) with NH3 were investigated in a simulated cement precalciner atmosphere. The results show that the presence of H2O improves NOx reduction and widens the reduction temperature window significantly. O2 is indispensable for reducing NOx. The optimum reduction temperature decreases and the temperature window widens to a lower temperature with the increase of O2 content. In addition, the increase of O2 content also results in a decrease of the maximum NOx reduction efficiency. The effect of SO2 on NOx reduction is negligible in the simulated precalciner atmosphere. To increase CO concentration makes NO reduction take place at relatively low temperatures. However, NH3 will tend to be oxidized into NO instead of reducing NO after entering the stream containing O2 at high temperatures if it is initially blended with a high concentration of CO in an oxygen-free environment. The increase of H2O, O2, SO2 or CO concentration is helpful to reduce NH3 slip in the temperature region below 900°C. These effects are resulted from the fact that the generation and consumption of O and OH radicals which are crucial to NO reduction and formation can be influenced by the four gas compositions. In industrial operation of SNCR for cement precalciner, these effects should be taken into account to increase NOx reduction efficiency and avoid NH3 slip., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Our previous reports showed that nano zero-valent iron (nZVI), steel pickle liquor for the synthesis of nZVI (S-nZVI), nZVI immobilised in mesoporous silica microspheres (SiO2@FeOOH@Fe) and nano Ni/Fe bimetallic particles (Ni/Fe) have been proved to show good property for elimination of polybrominated diphenyl ethers (PBDEs). However, it is necessary to compare their reactivity, reusability and stability when applied to in situ remediation. In this study, the performances of different iron-based nanoparticles were compared through reusability, sedimentation and iron dissolution experiments. The SiO2@FeOOH@Fe and Ni/Fe nanoparticles were shown to have higher reusability and stability, as they could be reused more than seven times, and that the SiO2@FeOOH@Fe can effectively avoid leaching iron ions into the solution and causing secondary pollution in the reaction. This study may serve as a reference for PBDE remediation in the future., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

An activated carbon (AC) containing a high concentration (374mgg(-1)) of Fe was prepared by carbonization of an ion-exchange resin. To examine its chemical reactivity as a catalyst to decompose 2,2',4,4',5,5'-hexachlorobiphenyl (PCB-153), the decomposition parameters of temperature and time were varied under air or N(2). Decomposition at 350°C was achieved within 15min under air and 30min under N(2), and the efficiency of PCB-153 decomposition was 99.7% and 98.0%, respectively. An analysis of inorganic chloride ions revealed that PCB-153 was mineralized effectively during the decomposition. The Brunauer-Emmett-Teller (BET) surface area and pore volume of the AC were measured to assess the adsorption capacity before and after the decomposition. The differences between decomposition under air and N(2) reflected the differences in the BET surface and pore volume measurements. A decomposition pathway was postulated, and the reactive characteristics of chlorine atoms loaded on the benzene rings followed the order of para>meta>ortho, which agrees with the calculated results from a density functional theory study., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

A microorganism was isolated from oil field injection water and identified as Rhodobacter sphaeroides. It was used for the remediation of simulated cadmium-contaminated soil. The phytoavailability of Cd was investigated through wheat seedling method to determine the efficiency of remediation. It was found that after remediation, the accumulation of Cd in wheat roots and leaves decreased by 67% and 53%, respectively. The Cd speciation in soil was determined with Tessier extraction procedure. It was found that the total Cd content in soil did not change during the experiments, but the geo-speciation of Cd changed remarkably. Among the five fractions, the concentration of exchangeable phases decreased by 27-46% and that of the phases bound to Fe-Mn oxides increased by 22-44%. The decrease of Cd accumulation in wheat showed significant positive correlation with the decrease of exchangeable phases. It could be concluded that the remediation of R. sphaeroides was carried out through the conversion of Cd to more stable forms. The decrease of sulfate concentration in supernatant indicated that the R. sphaeroides consumed sulfate., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

A link tooth wheel-cylinder non-thermal plasma reactor was set up to investigate the degradation of phenol in the mists. In addition, the decomposition efficiency of phenol, TOC removal, and byproduct formation were investigated. The stable discharge was achieved in both air and the mist condition. The decomposition efficiency and TOC removal increased with increasing the input power. For the input power of 3.6 W, the phenol decomposition and TOC removal reached 90% and 47%, respectively. Phenol degradation byproducts were identified as small molecular organic acids, including formic acid, acetic acid, and oxalic acid. Their masses in the trapped solutions first increased and then decreased slightly with increasing the input power. Therefore, the biodegradation capacity of the phenol degradation byproducts can be improved., (Copyright © 2011 Elsevier Ltd. All rights reserved.)

Polysulfide was produced and tested for use as an inexpensive chemical agent for the solidification/stabilization of lead in fly ash, generating little hydrogen sulfide gas. According to the equations S(n)(2-)-->S+S(n-1)(2-) and S(n)(2-)+H(+)-->HS(-)+S(n-1), this agent was expected to achieve long-term stability of disposed Pb. The leachate concentration of Pb in fly ash after sulfide treatment showed a decrease-increase-decrease trend. We also compared Pb leaching behavior from an aging/weathering experiment to thermodynamic modeling using the database from the Geochemist's Workbench software. Thermodynamic modeling indicated the tendency that when the precipitate was formed in the order of PbO, PbCO(3).PbO, and PbCO(3), the total concentration of soluble Pb will be lowered. The leaching curve of Pb in fly ash without a lime slurry injection system was close to PbO, whose activity was initially near 1, but when leaching time increased, it shifted to that of PbCO(3).PbO, before finally ending at that of PbCO(3). However, Ca(OH)(2) sprayed on fly ash interfered with the carbonation process of Pb., (Copyright (c) 2010 Elsevier Ltd. All rights reserved.)

The behavior of non-thermal plasma (NTP) and combined plasma catalysis (CPC) was investigated for removal of low-concentration benzene, toluene and p-xylene (BTX mixture) in air using a link tooth wheel-cylinder plasma reactor. Combining NTP with MnO(x)/Al(2)O(3) catalyst after the discharge zone (CPC) significantly promoted BTX conversion and improved the energy efficiency. For a specific input energy (SIE) of 10 JL(-1), the conversion of benzene, toluene and p-xylene reached 94%, 97% and 95%, respectively. The introduction of MnO(x)/Al(2)O(3) catalyst also moved the BTX conversion towards total oxidation and reduced the emission of O(3) and NO(2) as compared to NTP alone. For an SIE of 10 JL(-1), the O(3) outlet concentration decreased from 46.7 for NTP alone to 1.9 ppm for CPC, while the NO(2) emission correspondingly decreased from 1380 to 40 ppb.