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Due to the extremely low concentration, complex composition and easy to be converted into each other in water and air of water-soluble volatile organic compounds (VOCs), it is a great challenge to the traditional detection technology, pollution control and traceability, etc. Therefore, developing a convenient, swift and on-site detection method for simultaneous quantification of multiple VOCs is highly anticipated. In this paper, a multifunctional sensor array with adsorption and sensing of VOCs has been constructed by four fluorescence channels of small-sized Eu@Uio-66 and Tb@Uio-66. Due to the obvious cross-reactive characteristics between 4 fluorescence channels and VOCs, the sensor array could detect 8 VOCs simultaneously with all detection limits as low as ppb level. In addition, the detection results of sensor array for actual water samples coexisting with multiple VOCs confirmed that it has strong anti-interference performance and could be used for simultaneous detection of multiple VOCs in real water. The construction of sensor array with VOC adsorption function not only helps to reduce the detection limit of VOCs benefiting from the pre-concentration of materials, but also has significant value to reduce the harmfulness of pollutants. Predictably, this work is of great significance for VOC traceability, analysis of ecotoxicological effects and monitoring of pollution distribution characteristics., 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 threat of tetracycline antibiotics to the environment and human health is attracting widespread attention. The development of morphological analysis and quantitative techniques of multiple tetracyclines is of great significance for the evaluation of biochemical toxicity, wide-spectrum antibacterial property and degradation cycle between different tetracyclines. In this study, the white fluorescent Eu/Tb@CDs was synthesized and applied successfully to the identification and detection of the most widely used tetracycline antibiotics (tetracycline (TC), oxytetracycline (OC), chlortetracycline (CC) and doxycycline (DC)) with detection limits all below 1 nM. For the actual water samples with coexistence of the above 4 tetracyclines, their simultaneous morphology identification and accurate quantitative detection can also be realized through simple spectrometric measurement. In addition, the selective and competitive experiments have been carried out on the pollutants widely present in water, and the results have also confirmed that other pollutants could not interfere with the detection of the above 4 tetracyclines. It is undeniable that this work will conveniently and visually reveal the existence information and geographical distribution characteristics of different tetracycline antibiotics in the environment and their action mechanism on organisms., 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.)

Aniline has attracted much concern for its long degradation half-life and huge toxicity to the environment and human beings. Therefore, the development of a multi-functional device for visual detection and efficient removal of aniline was highly anticipated. In our work, the small-size Eu@UiO-66(COOH) was obtained by post-synthesis modification (PSM), and then the film-based fluorescent sensor was prepared by crosslinking reaction. The films not only showed incredible mechanical stability and potential for large-scale preparation, but also have excellent fluorescence response to aniline in solutions and gas phase. As the concentration of aniline increased, the fluorescence of films gradually increased at 350 nm, while the fluorescence gradually quenching at 620 nm, and the detection limits (LOD) of aniline in water and air were 0.27 ppb and 0.086 ppb, respectively. In addition, the adsorption performance of the film for aniline has also been confirmed and the maximum adsorption capacity was 32.6 mg/g, which is a strong guarantee for the realization of ultra-trace detection and toxicity reduction of aniline. In summary, the multi-functional film sensor has been designed for ultra-trace detection and efficient removal of aniline in solutions and gas phase, and have significant value for pollutant treatment, ecological restoration and early prevention., (Copyright © 2022 Elsevier B.V. All rights reserved.)

In Fenton or Fenton-like processes, the key step is to catalyze H 2 O 2 and produce highly reactive OH radicals. More efforts are then focus on designing efficient heterogeneous Fenton catalysts by activating H 2 O 2 to generate OH at the highest possible steady state concentration. In this study, using the antibiotic ofloxacin as target organic pollutant, we firstly demonstrate a point of view for improving OH utilization efficiency by regulating surface chemical reactions to minimizing its migration distance to the target pollutant. C doped g-C 3 N 4 incorporated CuFeO 2 (CCN/CuFeO 2 ) exhibited almost ten times higher ofloxacin degradation rate constant than our previously reported CuFeO 2 {012} catalyst (0.1634 vs 0.0179 min -1 ). Since similar amount of OH was generated, the different inhibition effect of tert-butyl alcohol and nitrobenzene on the ofloxacin degradation confirmed that the much-enhanced ofloxacin degradation was attributed to the surface Fenton reaction process. According to XPS and EXAFS characterization, the C-O-Cu bond between g-C 3 N 4 and CuFeO 2 established a closed-circuit surface Fenton reaction mechanism. H 2 O 2 was adsorbed and decomposed into OH/O 2 - over ≡Cu  +  site in CuFeO 2 . The successful construction of CCN/CuFeO 2 creates a negative surface potential and benefits the enrichment of target antibiotics from water, which greatly reduces the migration distance of OH/O 2 •- to adjacent pollutant and then increases the OH/O 2 - utilization efficiency by avoiding the unwanted quenching. Hence, CCN/CuFeO 2 possesses superior Fenton catalytic activity and long-term stability., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

UV-H 2 O 2 is the most widely used oxidizing system with established effectiveness and a high level of technical development for practical application. However, little attention was paid on the effect of suspended particles in natural water on organic contaminants removal via UV-H 2 O 2 technique. In this study, this effect of suspended particles to enhance the contaminant degradation was explored using silica/alumina-based oxides (MCM-41 and Al@MCM-41) as the representative. The results showed that MCM-41 had no effect on OFX degradation compared with UV-H 2 O 2 . While the degradation efficiency and reaction rate were greatly enhanced at a pH range of 3.0-9.0 especially at acidic pH values (3.0-5.0) in the presence of Al@MCM-41. The probe experiments proved that OFX adsorption followed by surface reaction process played an important role to enhance the performance of UV-H 2 O 2 . Based on the characterization results, the positive effect of suspended particles was not related to their surface area and pore size distribution, but dependent on the chemical composition and surface acid-base property. The suspended particles can provide an active surface composed of acid and base sites. The base site can create a local basic micro-environment by producing more • OH et al. While the dissociated acid sites in Al@MCM-41 with a negative charged surface favor OFX adsorption and then reaction with produced ROS. Our findings suggest that the enhanced performance of UVA-H 2 O 2 induced by suspended particles should be concerned., (Copyright © 2021. Published by Elsevier B.V.)

An analytical challenge that arises in environmental and food analysis is to quantify heterogeneous nanoparticles especially in polydisperse and complex samples. The method stated herein based on the reinjection asymmetrical flow field-flow fractionation (AF4 × AF4) coupled with inductively coupled plasma-mass spectrometer (ICP-MS) and statistical deconvolution allowed for identifying the molecular weight (Mw) and selenium abundance of the low Mw protein fractions (ca. < 132 kDa) in an unknown and complex sample (e.g., selenium-rich soybean protein isolates (Se-SPI)). A non-linear decay crossflow program was also developed to get better resolution and shorter elution time for both low and high Mw components. The concept of the reinjection method was based on the excellent ability for reducing sample complexity regarding the size fractionation, and peak reproducibility under the identical conditions of AF4 system. The standard protein mixture was used as a proof-of-principle sample. The results showed the underlying peaks predicted by the reinjection method were agreed with the separation result using the standard mixture (the relative standard deviation of peak locations < 1%), which indicated the reinjection method could provide an accurate assessment of the underlying peak number and location, and was promising to minimize the overfitting problem for statistic deconvolution. Interestingly, significant differences of Se abundance in protein fractions were observed in the low Mw range for Se-SPI, ranging from 0.28 to 1.66 cps/V with the Mw ranging from 13.75 kDa to 104.17 kDa, which indicated significant differences in the ability of binding Se for these selenium-rich proteins in Se-SPI., 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. Published by Elsevier B.V.)

As(iii) pollution has caused increasing concern due to its significant impact in environmental safety and human health. Carbon dots (CDs)-MnO2 nanocomposites were prepared and characterized for As(iii) detection. The intense blue fluorescence of CDs can be greatly quenched by functionalization with MnO2 nanosheets due to the existence of the fluorescence resonance energy transfer (FRET) effect. CDs-MnO2 nanocomposites were then used as a fluorescence sensor for As(iii) detection with high detection sensitivity and selectivity. The redox reaction between As(iii) and MnO2 nanosheets can induce the decomposition of MnO2 and termination of the FRET process. Then the blue fluorescence originating from CDs can be recovered. The detection limit of CDs-MnO2 nanocomposites toward As(iii) was calculated to be 16.8 nM (1.40 ppb) in a linear concentration range of 0-200 nM. CDs-MnO2 nanocomposites were also found to possess highly selective ability toward As(iii) detection. In addition, the spiked and recovery test also confirmed the practicality and reliability of CDs-MnO2 nanocomposites toward As(iii) detection in real water samples, such as groundwater etc. Our research has provided a reliable tool and strategy for visual detection of As(iii) with outstanding sensing ability.

The development of efficient heterogeneous Fenton catalysts is mainly by "trial-and-error" concept and the factor determining H 2 O 2 activation remains elusive. In this work, we demonstrate that suitable facet exposure to elongate O-O bond in H 2 O 2 is the key parameter determining the Fenton catalyst's activity. CuFeO 2 nanocubes and nanoplates with different surface facets of {110} and {012} are used to compare the effect of exposed facets on Fenton activity. The results indicate that ofloxacin (OFX) degradation rate by CuFeO 2 {012} is four times faster than that of CuFeO 2 {110} (0.0408 vs 0.0101 min -1 ). In CuFeO 2 {012}-H 2 O 2 system, OFX is completely removed at a pH range 3.2-10.1. The experimental results and theoretical simulations show that • OH is preferentially formed from the reduction of absorbed H 2 O 2 by electron from CuFeO 2 {012} due to suitable elongation of O-O (1.472 Å) bond length in H 2 O 2 . By contrast, the O-O bond length is elongated from 1.468 to 3.290 Å by CuFeO 2 {110} facet, H 2 O 2 tends to be dissociated into -OH group and passivates {110} facet. Besides, the new formed ≡Fe 2+ * on CuFeO 2 {012} facet can accelerate the redox cycle of Cu and Fe species, leading to excellent long-term stability of CuFeO 2 nanoplates.

To develop an ultraefficient and reusable heterogeneous Fenton-like catalyst at a wide working pH range is a great challenge for its application in practical water treatment. We report an oxygen vacancy promoted heterogeneous Fenton-like reaction mechanism and an unprecedented ofloxacin (OFX) degradation efficiency of Cu doped Fe 3 O 4 @FeOOH magnetic nanocomposite. Without the aid of external energy, OFX was always completely removed within 30 min at pH 3.2-9.0. Compared with Fe 3 O 4 @FeOOH, the pseudo-first-order reaction constant was enhanced by 10 times due to Cu substitution (9.04/h vs 0.94/h). Based on the X-ray photoelectron spectroscopy (XPS), Raman analysis, and the investigation of H 2 O 2 decomposition, • OH generation, pH effect on OFX removal and H 2 O 2 utilization efficiency, the new formed oxygen vacancy from in situ Fe substitution by Cu rather than promoted Fe 3+ /Fe 2+ cycle was responsible for the ultraefficiency of Cu doped Fe 3 O 4 @FeOOH at neutral and even alkaline pHs. Moreover, the catalyst had an excellent long-term stability and could be easily recovered by magnetic separation, which would not cause secondary pollution to treated water.

Fe2O3 and/or Al2O3 were supported on mesoporous SBA-15 by wet impregnation and calcinations with AlCl3 and FeCl3 as the metal precursor and were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectra (FTIR) of adsorbed pyridine. Fe2O3/Al2O3@SBA-15 was found to be highly effective for the mineralization of ibuprofen aqueous solution with ozone. The characterization studies showed that Al-O-Si was formed by the substitution of Al(3+) for the hydrogen of surface Si-OH groups, not only resulting in high dispersion of Al2O3 and Fe2O3 on SBA-15, but also inducing the greatest amount of surface Lewis acid sites. By studies of in situ attenuated total reflection FTIR (ATR-FTIR), in situ Raman, and electron spin resonance (ESR) spectra, the chemisorbed ozone was decomposed into surface atomic oxygen species at the Lewis acid sites of Al(3+) while it was converted into surface adsorbed (•)OHads and O2(•-) radicals at the Lewis acid sites of Fe(3+). The combination of both Lewis acid sites of iron and aluminum onto Fe2O3/Al2O3@SBA-15 enhanced the formation of (•)OHads and O2(•-) radicals, leading to highest reactivity. Mechanisms of catalytic ozonation were proposed for the tested catalysts on the basis of all the experimental information.

A plasmonic photocatalyst Ag-AgI supported on mesoporous alumina (Ag-AgI/Al(2)O(3)) was prepared by deposition-precipitation and photoreduction methods. The catalyst showed high and stable photocatalytic activity for the degradation and mineralization of toxic persistent organic pollutants, as demonstrated with 2-chlorophenol (2-CP), 2,4-dichlorophenol (2,4-DCP), and trichlorophenol (TCP) under visible light or simulated solar light irradiation. On the basis of electron spin resonance, cyclic voltammetry analyses under a variety of experimental conditions, two electron transfer processes were verified from the excited Ag NPs to AgI and from 2-CP to the Ag NPs, and the main active species of O(2)(*-) and excited h(+) on Ag NPs were involved in the photoreaction system of Ag-AgI/Al(2)O(3). A plasmon-induced photocatalytic mechanism was proposed. Accordingly, the plasmon-induced electron transfer processes elucidated the photostability of Ag-AgI/Al(2)O(3). This finding indicates that the high photosensitivity of noble metal NPs due to surface plasmon resonance could be applied toward the development of new plasmonic visible-light-sensitive photocatalysts and photovoltaic fuel cells.