FOOD CHEMISTRY
·
2025
·
IF 9.8
An-qi Tang,Xuechao Xu,Cao-wei Chen,Mengyuan Tan,Lu Gao,Zhen-quan Yang
Enterobacter hormaechei , A zoonotic pathogen with escalating prevalence in global food sources, severely jeopardizes food safety, necessitating the development of high-performance detection methods. Herein, a novel colorimetric detection strategy integrating phages and nanozymes was proposed for foodborne E. hormaechei . Initially, four homologous phages (EhpYZU05, EhpYZU08, EhpYZU9–1 and EhpYZU10), which were isolated using E. hormaechei YZU05 as the host bacterium, were modified on the surface of NH 2 -MIL-88B(Fe) to fabricate four phage@NH 2 -MIL-88B(Fe) nanozymes. These nanozymes exhibit peroxidase-like activity, catalyzing 3,3′,5,5′-tetramethylbenzidine (TMB) chromogenic reaction in presence of H 2 O 2 . With introduction of multiple host or non-host E. hormaechei strains, TMB chromogenic reaction catalyzed by phage@NH 2 -MIL-88B(Fe) nanozymes can be specifically inhibited. This inhibition occurs due to the specific phage adsorption of phage@NH 2 -MIL-88B(Fe) nanozymes towards these host or non-host E. hormaechei strains, indirectly blocking their catalytic sites. Leveraging this principle, colorimetric broad-spectrum detection of E. hormaechei was achieved. Additionally, this method demonstrated reliable recoveries (96.7 % ~ 103.3 %) when applied to detect real food matrices, highlighting its high reliability in practical scenarios. This approach not only clarifies the intrinsic mechanism of phage-modified nanozymes for target bacteria detection but also provides a robust and reliable method for early pathogen detection, thereby significantly contributing to food safety enhancement
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高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2021
·
IF 8.742
Yixuan Gao,Siming Yan,Yi He,Yi Fan,Liyun Zhang,Jing Ma,Ruitong Hou,Li Chen,Jingyu Chen
Herein, a novel membrane with polyacrylic acid (PAA), NH 2 -MIL-88B(Fe) (NM88B), and graphene oxide (GO) was fabricated via a simple vacuum filter method equipped with the nylon membrane substrate. The composite membrane (PAA@NM88B/GO membrane) retained the laminated structure of GO, and PAA@NM88B was used as the photo-Fenton catalytic nano-filler to intercalate GO. Through a series of material characterization and membrane separation performance tests, the results showed that by introducing porous NM88B and PAA cross-linking modification, PAA@NM88B/GO membrane had excellent hydrophilicity, water flux and dye rejection performance. The flux of the PAA@NM88B/GO membrane was 68.21 L m −2 h −1 bar −1 , which is about 15 times higher than that of GO membrane. In addition, the composite membrane had a high rejection (over 97%) for methylene blue (MB), crystal violet (CV) and Congo red (CR). More importantly, PAA@NM88B/GO membrane can also be used to degrade textile wastewater in real life. The membrane can be used as a catalyst to degrade contaminants, and had a high removal of MB in 40 min (98.79%) under the synergistic effect of membrane adsorption and photocatalysis . Therefore, the results indicated that this new type of PAA@NM88B/GO membrane had potential applications in water purification and actual textile wastewater treatment .
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JOURNAL OF MATERIALS SCIENCE
·
2020
·Vol. 55
·期 26
·12041-12052
·
IF 3.553
Yi Xuerui,He Xiaobo,Yin Fengxiang,Yang Tong,Chen Biaohua,Li Guoru
The global NH 3 production is dominated by Haber–Bosch process, requiring high temperature and pressure. Electrochemical N 2 reduction reaction (NRR) under ambient conditions is a greener path for artificial N 2 fixation to NH 3 but calling for efficient catalyst to increase activity and selectivity. Herein, we report the iron-based metal–organic frameworks (MOFs), i.e., MIL-88B–Fe and amine-functionalized MIL-88B–Fe (NH 2 –MIL-88B–Fe) as efficient catalysts for electrochemical NRR under ambient temperature and pressure in neutral electrolyte. NH 2 –MIL-88B–Fe shows higher NH 3 yield rate of 1.205 × 10 –10 mol s −1 cm −2 than MIL-88B–Fe (3.575 × 10 –11 mol s −1 cm −2 ). Furthermore, NH 2 –MIL-88B–Fe exhibits the highest Faradaic efficiency of 12.45% at 0.05 V versus RHE. The control experiments prove that NH 3 is produced through electrocatalytic NRR. This work may trigger the interest of using MOFs as highly efficient catalysts for electrochemical NH 3 production.
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CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Yuexin Wang,Zhen Zhong,Yaseen Muhammad,Hui He,Zhongxing Zhao,Shuangxi Nie,Zhenxia Zhao
Engineering of monodentate ligands induced defects was proposed to modify NH 2 -MIL-88B(Fe) in order to promote its synergetic photo-Fenton catalytic degradation performance for acetamiprid (ACTM) as model neonicotinoid insecticides. Three monodentate ligands with different coordination groups (benzoic acid, pyrrole and pyrrole-2-carboxylic acid) were applied to in-situ induce ligand vacancies on NH 2 -MIL-88B(Fe). Effect of defect coordination mode on its photo-Fenton catalytic performance was investigated through the ACTM degradation reaction. Ligand defects on NH 2 -MIL-88B(Fe) would generate three merits: (1) it can modulate surface properties to enhance adsorption affinity towards ACTM; (2) it can introduce large amount of monodentate ligands and ligand vacancies in MOFs to promote light absorption and electron-hole separation capacity for photo-catalysis; (3) it can increase the amount of Fe Lewis acid sites to improve redox capacity of Fe 2+ /Fe 3+ for Fenton-catalysis. In this work, Pyrrole-2-carboxylic acid (Pac) was proved to introduce more monodentate ligands in MOFs and generate more ligand vacancies as well. As a result, ACTM can be easily captured by defective NH 2 -MIL-88B(Fe) and degraded by in-situ triggered oxidative reaction through the synergistic “photo-Fenton catalysis”. Performance measurements showed that Pac-MIL88(Fe) achieved 7.3 times higher adsorption rate and 5.5 times higher catalytic rate for ACTM than that of pristine MIL88(Fe). Moreover, total organic carbon (TOC) conversion reached 97.0% within only 90 min using Pac-MIL88(Fe) as photo-Fenton catalyst, showing 1.7 times higher than pristine MIL88(Fe). Thus, the in-situ fabrication of ligand defect-containing MIL88(Fe) can be foreseen of potential for designing new MOFs for wider practical applications.
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INORGANIC CHEMISTRY
·
2021
·
IF 5.165
Dianfa Zhao,Jie Liu,Lijuan Zhang,Yunshan Zhou,Yuxu Zhong,Yang Yang,Chengcheng Huang,Yong’an Wang
Maintaining a long-term continuous and stable reactivator blood concentration to treat organophosphorus nerve agent poisoning using acetylcholinesterase (AChE) reactivator pralidoxime chloride (2-PAM) is very important yet difficult. Because the flexible framework of MIL-88B(Fe) nanoparticles (NPs) can swell in polar solvents, pralidoxime chloride (2-PAM) was loaded in MIL-88B(Fe) NPs (size: ca. 500 nm) by stirring and incubation in deionized water to obtain 2-PAM@MIL-88B(Fe), which had a maximum drug loading capacity of 12.6 wt %. The as-prepared composite was characterized by IR, powder X-ray diffraction (P-XRD), scanning electron microscopy (SEM), ζ-potential, Brunauer–Emmett–Teller (BET), and thermogravimetry/differential thermal analysis (TG/DTA). The results showed that under constant conditions, the maximum drug release rates of 2-PAM@MIL-88B(Fe) in absolute ethanol, phosphate-buffered saline (PBS) solution (pH = 7.4), and PBS solution (pH = 4) at 150 h were 51.7, 80.6, and 67.1%, respectively. This was because the composite showed different swelling behaviors in different solvents. In PBS solution with pH = 2, the 2-PAM@MIL-88B(Fe) framework collapsed after 53 h and released 100% of 2-PAM. For mice after intragastric poisoning with sarin (a neurotoxic agent), an atropine-assisted 2-PAM@MIL-88B(Fe) treatment experiment revealed that 2-PAM@MIL-88B(Fe) continuously released 2-PAM for more than 72 h so that poisoned AChE was continuously and steadily reactivated. The reactivation rate of AChE was 56.7% after 72 h. This composite is expected to provide a prolonged, stable therapeutic drug for the mid- and late-stage treatment of neurotoxic agent poisoning.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Hui He,Yuexin Wang,Juan Li,Shanliang Jiang,Subhan Sidra,Wenxue Gong,Ying Tang,Yang Hu,Rule Wei,Dongxiao Yang,Xuesheng Li,Zhongxing Zhao
High light adsorption and fast charge separation are crucial for photo-Fenton catalytic activity of MOFs. Herein, bottom-up design was proposed to fabricate polypyrrole (PPy C ) nanowires in MIL-88B(Fe) cages as photo-Fenton catalyst for Sulfamethoxazole (SMX) efficient degradation. Pyrrole was prior anchored into MIL-88B(Fe) cluster via Fe-N coordination, and then the additional monomer pyrrole was further triggered bottom-up polymerization in confined cages of MIL-88B(Fe) and formed PPy C @Py-MIL(Fe) composite. These PPy C nanowires were dispersed in Py-MIL(Fe) cages and tightly connected with MOFs clusters via Fe-N bonding. Characterization proved that: (1) Interfacial Fe-N can significantly promote the efficient electron transport from PPy C nanowires to Py-MIL(Fe), enhance optical absorption property, and construct strong Lewis acidic sites and ligand vacancies in PPy C @Py-MIL(Fe). (2) The confined PPy C nanowire via Fe-N connection remarkably promote photo-generated electron-hole separation, Fe 2+ |Fe 3+ redox ability of MOF, and improved photo-electric corrosion ability. As a result, it significantly enhanced the photo-Fenton catalytic performance for SMX degradation. Catalytic oxidation was attributed to the generation of ‧OH species that oxidized 93% SMX in 60 min, showing ultra-rapid degradation and TOC removal rates of 33.7 min −1 ·mg·g −1 and 8.68 min −1 ·mg·g −1 respectively, which was about 4–220 times higher than those reported state-of-the-art catalysts. Additionally, the PPy C @Py-MIL(Fe) catalyst showed minimal loss in catalytic activity even after recycling for 10 times, exhibiting good recycling stability compared to many MOFs. Systematic analysis shown that in-situ anchored growth of polypyrrole in confined porous cages of MOF can effectively enhance the catalytic activity and stability of MIL-88B(Fe), and has great development potential applications for photo-Fenton catalytic degradation of organic pollutants.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2022
·Vol. 33
·期 17
·14228-14239
·
IF 2.779
Liu Jieling,Yang Jiaji,An Shuyue,Wen Meiqi,Wang Xian,Gong Rongzhou,Nie Yan
Metal-organic framework (MOF) crystals have promising applications in a number of different fields, but the growth of MOF crystals with controllable morphology and high uniformity remains a major challenge. By taking the advantage of the synergistic effects of water molecules in the mixed solvent and polyvinylpyrrolidone (PVP) surfactants, this work demonstrates an approach for the preparation of NH 2 -MIL-88B(Fe) MOF crystals with both highly customizable size and aspect ratios and high uniformity. The effects of the concentration of water in the mixed solvent and the amount of PVP surfactants on the morphology and size of the MOF crystals were investigated. The morphology and crystalline properties were characterized by scanning electron microscopy and X-ray diffraction techniques. The data showed that through controlling the concentration of water in the solvent and the amount of the PVP surfactant, the size of the MOF crystals can be tuned rather widely, over 344–5.14 μm, while the aspect ratio of the crystals can be varied widely over 1.0–7.1. Possible mechanisms for such high tunability were discussed. As an example of potential applications, the complex permeability and permittivity of MOF-derived composites (25 wt%) were measured over a wide frequency range of 2–18 GHz. The parameters were then used to evaluate the potential for electromagnetic wave absorption. The results indicate that the composite with a thickness of only 1.2 mm exhibits a “− 10 dB” absorption bandwidth of 4.1 GHz and a minimum reflection of − 20 dB. Such bandwidth and reflection properties provide inspiration for future design of lightweight, broadband electromagnetic wave absorbers from the perspective of fine morphology control.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 36
·17438-17455
·
IF 3.925
Qingcan Xiang,Zongxue Yu,Xuyang Li,Pingquan Wang,Niandan He,Yao Pang,Qiuxiang Wang,Yucheng Liu
A g-C3N4/NH2-MIL-88B(Fe)/CD@GO membrane (M2) was prepared by a simple vacuum filtration method. By embedding a Z-scheme heterojunction composite photocatalyst into graphene oxide (GO) nanosheets, not only can the water molecule transport channel be regulated, but the membrane can also be endowed with photocatalytic activity and membrane fouling is effectively alleviated. The pure water permeation flux of M2 (253.26 L m−2 h−1 bar−1) was 13 times that of the original GO membrane (18.83 L m−2 h−1 bar−1). What's more, even after 10 cycles, M2 still maintains excellent separation efficiency and flux. After six cycles, the rejection of Congo Red (CR), Malachite Green (MG) and Rhodamine B (RhB) by M2 was over 95%. At the same time, under the conditions of an extreme pH value and high salt concentration, the rejection of dye remained at the original level after six cycles. Therefore, the novel photocatalytic membrane has excellent separation performance, stability and photocatalytic activity, and can be used as a potential membrane for wastewater purification and environmental protection.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2019
·
IF 14.229
Munir Ahmad,Xie Quan,Shuo Chen,Hongtao Yu
Iron containing MOFs have been currently estimated as greater candidates for heterogeneous Fenton catalysts due to their open pores and well dispersed metallic components. However, metals in majority of MOFs are bounded by organic linkers, which reduces Lewis acid sites and make them not available for H 2 O 2 activation. Creating coordinatively unsaturated metal centers (CUCs), acting as Lewis acid sites, is a feasible approach for efficient photo-Fenton activity. Here, we successfully synthesized a photo-Fenton CUCs-MIL-88B-Fe catalyst with mixed-valence (Fe II /Fe III ) on ultrathin Ti 3 C 2 nanosheets. The Lewis acidity was probed by TPD-NH 3 and IR-pyridine analysis and tested for pollutants degradation. The results showed that CUCs-MIL-88B-Fe/Ti 3 C 2 displayed highest photo-Fenton activity under visible light irradiation at pH 3.0 and 10 mM H 2 O 2 . This could be attributed with the CUCs, fast H 2 O 2 activation, high Lewis acidity and carrier separation with Ti 3 C 2 nanosheets due to its high charge mobility. Furthermore, CUCs-MIL-88B-Fe/Ti 3 C 2 exhibited a good stability and reusability.
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高影响因子
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING
·
2021
·Vol. 127
·期 12
·1-11
·
IF 2.584
Fu Manjun,Chai Bo,Yan Juntao,Wang Chunlei,Fan Guozhi,Song Guangsen,Xu Fang
Hydrogen peroxide (H 2 O 2 ) was widely applied as the bactericide and bleach agent in food industry due to its strong oxidation, whose residue had also posed a hazard to public health at the same time. Therefore, it was indispensable to establish a simple, highly effective and accurate method for the detection of H 2 O 2 in foods. Herein, the MIL-88B-Fe metal–organic framework (MOF) was prepared by a facile solvothermal process and utilized as the peroxidase mimic for H 2 O 2 detection. The resultant MIL-88B-Fe MOF exhibited an excellent peroxidase mimetic activity to effectively catalyse the oxidation of 3,3’,5,5’-tetramethylbenzidine (TMB) in the presence of H 2 O 2 , generating a blue coloured product. Under the optimal testing conditions, the linear absorbance response is well correlated with the H 2 O 2 concentration ranging from 10 to 100 μM with a detection limit of 0.60 μM. The catalytic kinetic assay suggested that the MIL-88B-Fe MOF possessed the higher affinity towards both the substrate TMB and H 2 O 2 than horseradish peroxidase. Moreover, the MIL-88B-Fe MOF also displayed a high selectivity and anti-interference performance towards H 2 O 2 detection. In addition, the peroxidase mimetic catalytic oxidation TMB mechanism over the MIL-88B-Fe MOF was clarified by the photoluminescence test. Benefitting from the sensitive response and good anti-interference capacity, this method was applied in real milk and beer samples for H 2 O 2 detection and showed a favourable reproducibility and feasibility. These results indicated that the proposed method based on MIL-88B-Fe as peroxidase mimic might be a promising candidate for H 2 O 2 detection in food field.
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高影响因子
APPLIED SURFACE SCIENCE
·
2019
·
IF 5.155
Liangyan Shao,Zongxue Yu,Xiuhui Li,Xuyang Li,Haojie Zeng,Xiaofang Feng
A one-pot strategy for the preparation of NH 2 -MIL-88B(Fe)/CDs composite was successfully developed via a simple solvothermal synthesis method. NH 2 -MIL-88B(Fe)/CDs composites were characterized by XRD, FT-IR, SEM, TEM, XPS, UV–vis DRS, PL, transient photocurrent response and Mott-Schottky plots. The synthesized NH 2 -MIL-88B(Fe)/CDs composites exhibit stronger photocatalytic activity than the original NH 2 -MIL-88B(Fe) in both photoreduction of Cr(VI) and photodegradation of MB. This is mainly because on the one hand, there is an interaction at the interface between CDs and NH 2 -MIL-88B(Fe), and on the other hand, CDs in the composite as local electron acceptors can effectively enhance charge transfer and inhibit electron-hole recombination. The experimental results show that the pH value greatly affects the reduction efficiency of Cr(VI) over photocatalyst, and the addition of hole trapping agent is beneficial to photocatalytic reduction. Moreover, we have proposed the possible photocatalytic mechanism on composites through trapping experiments of active species. Importantly, cycling experiments have also revealed that NH 2 -MIL-88B(Fe)/CDs photocatalysts have good chemical stability and reusability, and have broad industrial application prospects.
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Small
·
2024
·Vol. 20
·期 27
·2309541
·
IF 13
Tingting Liu,Kaiyue Hu,Yansheng Li,Yanhong Wang,Dongmei Han,Zhihua Wang,Fubo Gu
The Z-scheme MIL-88B/BiOBr (referred to as M x B y , whereas x and y are the mass of MIL-88B(Fe) and BiOBr) heterojunction photocatalysts are successfully prepared by a facile ball milling method. By adding low concentration H 2 O 2 under visible light irradiation, the Z-scheme heterojunction and photocatalytic-Fenton-like reaction synergistically enhance the degradation and mineralization of ciprofloxacin (CIP). Among them, M50B150 showed efficient photodegradation efficiency and excellent cycling stability, with 94.6% removal of CIP (10 mg L −1 ) by M50B150 (0.2 g L −1 ) under 90 min of visible light. In the M x B y heterojunctions, the rapid transfer of photo-generated electrons not only directly decomposed H 2 O 2 to generate · OH, but also improved the cycle of Fe 3+ /Fe 2+ pairs, which facilitated the reaction with H 2 O 2 to generate · OH and · O 2 − radicals. In addition, the effects of photocatalyst dosages, pH of CIP solution, and coexisting substances on CIP removal are systematically investigated. It is found that the photocatalytic- Fenton-like reaction can be carried out at a pH close to neutral conditions. Finally, the charge transfer mechanism of the Z-scheme is verified by electron spin resonance (ESR) signals. The ecotoxicity of CIP degradation products is estimated by the T.E.S.T tool, indicating that the constructed photocatalysis-Fenton-like system is a green wastewater treatment technology.
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