BIOMEDICAL CHROMATOGRAPHY
·
2022
·Vol. 36
·期 11
·e5454
·
IF 1.911
Yong Zhang,Kaifang Wei,Litao Wang,Guihua Gao
In this work, MIL-53(Al), as an inorganic “filler” component, was embedded in polyvinylidene difluoride (PVDF) and polystyrene-block-polybutadiene (SBS) matrices to prepare two mixed-matrix membranes (MMMs), using a simpler method than that previously reported. The PVDF and SBS membranes retained much of the properties of PVDF, SBS, and native MIL-53(Al). The prepared MMMs were then placed in a vortex-stirred sample solution to develop a membrane solid-phase extraction method to extract estrogens and parabens, which were determined by high-performance liquid chromatography with fluorescence detection. The extraction efficiencies of the two membranes were compared, with the PVDF membrane exhibiting superior performance. In addition, the PVDF membrane was more freestanding and flexible, and its preparation method was also more facile and simple. The extraction conditions were optimized, and the analytical method showed low limits of detection (0.005–0.18 ng/mL), good linearity, and high accuracy, with recoveries ranging from 90.7% to 102.5%. As a result, this membrane solid-phase extraction method indicated its potential for application in aqueous sample pretreatment. For metal–organic framework–based MMM used in this method, in addition to being durable, freestanding, mechanically stable, and possessing a large area, it should also exhibit high metal–organic framework incorporation, good flexibility, and appropriate thickness and weight.
研究领域:
分析化学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Catalysis Science & Technology
·
2017
·Vol. 7
·期 5
·1129-1140
·
IF 5.773
Mengjie Pu,Yongwen Ma,Jinquan Wan,Yan Wang,Jiumei Wang,Mark L. Brusseau
In this work, a novel and effective heterogeneous catalyst, the metal–organic framework MIL-53(Fe), has been synthesized for the purpose of activating persulfate (PS). The catalytic performance of MIL-53(Fe) activated under different vacuum conditions was investigated; the stability and reusability of the catalyst were evaluated, and the activation mechanism was also investigated. The results indicated that vacuum activation could cause variation of the FeII/FeIII relative amount ratio of the catalyst, and thus would change the catalytic activity of MIL-53(Fe), because FeII and FeIII CUS (coordinatively unsaturated metal sites) are alternative active sites. It was found that MIL-53(Fe)-2 exhibits good performance in PS activation and could be used for multiple cycles; an OG removal rate of 98% was obtained within 120 min (95.7% mineralization efficiency) and 94.3% was achieved in the fifth cycle. The mechanism of activation of PS by MIL-53(Fe) was also suggested, which involved a predominant heterogeneous reaction and an auxiliary homogeneous reaction. The findings of this study provide a new insight into the application of reactive metal–organic frameworks in activating persulfate for the degradation of environmental contaminants.
研究领域:
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
DALTON TRANSACTIONS
·
2023
·Vol. 52
·期 31
·10662-10671
·
IF 4
Dan Wen,Yan Ma,Guomei Mu,Qiuping Huang,Xuefeng Luo,Dunmin Lin,Chenggang Xu,Fengyu Xie,Guangzhao Wang,Wenhan Guo
Improving the efficiency of the anodic oxygen evolution reaction (OER) is important to solve the global energy crisis and greenhouse gas emission problems. In this paper, a preparation method for a MIL-53(Fe)@ZIF-67(Co) composite electrode is proposed. The hierarchical structure formed by the combination of MIL-53(Fe) and ZIF-67(Co) provides a rich channel for the transport of electrons and mass in the OER process. XPS analysis and DFT calculations revealed that Fe electrons in MIL-53(Fe) were transferred to Co in ZIF-67(Co) through O, which confirmed the rapid charge transfer effect of this transport channel. The MIL-53(Fe)@ZIF-67(Co) electrode has significant OER performance. When the current density reaches 10 mA cm−2, the overpotential is only 193 mV. This study inaugurates a new way for the rational design of a multiphase interface and the construction of new MOF channel structures.
研究领域:
材料科学
·
电化学
·
能源材料
·
催化
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2015
·
IF 4.529
Ruowen Liang,Fenfen Jing,Lijuan Shen,Na Qin,Ling Wu
A bifunctional photocatalyst-Fe-benzenedicarboxylate (MIL-53(Fe)) has been synthesized successfully via a facile solvothermal method. The resulting MIL-53(Fe) photocatalyst exhibited an excellent visible light ( λ ≥ 420 nm) photocatalytic activity for the reduction of Cr(VI), the reduction rate have reached about 100% after 40 min of visible light irradiation, which has been more efficient than that of N-doped TiO 2 (85%) under identical experimental conditions. Further experimental results have revealed that the photocatalytic activity of MIL-53(Fe) for the reduction of Cr(VI) can be drastically affected by the pH value of the reaction solution, the hole scavenger and atmosphere. Moreover, MIL-53(Fe) has exhibited considerable photocatalytic activity in the mixed systems (Cr(VI)/dyes). After 6 h of visible light illumination, the reduction ratio of Cr(VI) and the degradation ratio of dyes have been exceed 60% and 80%, respectively. More significantly, the synergistic effect can also be found during the process of photocatalytic treatment of Cr(VI) contained wastewater under the same photocatalytic reaction conditions, which makes it a potential candidate for environmental restoration. Finally, a possible reaction mechanism has also been investigated in detail.
研究领域:
环境科学
·
材料科学
·
化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
FOOD CHEMISTRY
·
2023
·
IF 8.8
Huilin Li,Jingying Yang,Ran Han,Yueyao Wang,Xintong Han,Shuo Wang,Mingfei Pan
Rapid, sensitive, specific and stable detection of mycotoxin in food remains an extremely crucial issue. Herein, a magnetic-fluorescent immunosensing platform for the detection of zearalenone (ZEN) was proposed. The platform utilized Au nanoparticles (AuNPs) heterogeneous fluorescent metal–organic framework (MIL-53(Al)@AuNPs) labeled with ZEN-bovine serum albumin (ZEN-BSA) as signal probe and ZEN mono-antibodies coupled with magnetic NPs (MNPs-mAbs) as capture probe. Specifically, the heterogenization of AuNPs on the MIL-53(Al) surface improved its biocompatibility, and facilitated the loading of ZEN-BSA conjugates. The MNPs-mAbs could rapidly capture the target ZEN, simplify the immunoassay process and further improve the detection efficiency. The established competitive magnetic-fluorescent immunosensing platform had a wider linear response to ZEN in the range of 0.001–100 ng/mL with a lower limit of detection (LOD) at 0.0035 ng/mL, and could finish the whole detection process within 20 min, showing great potential for rapid and sensitive detection of food contaminants.
研究领域:
分析化学
·
食品科学
·
纳米技术
·
毒理学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
OPTICAL MATERIALS
·
2023
·
IF 3.9
Zhuofan Han,Dengjie Zhong,Yunlan Xu,Haixing Chang,Yi Liu,Lin Dong,Nianbing Zhong
In this research, MIL-53(Fe)@BiOBr/TCN/Ti photoanode was created using the secondary silica sol drop coating method, and assembled with Cu cathode to form photocatalytic fuel cell (PFC) to degrade rhodamine B and generate electricity. The resulting PFC has high visible light response and photocatalytic activity . It has a rhodamine B degradation efficiency of 92.19%, a maximum power density of 6.2 μW cm −2 , and a maximum photocurrent density of 0.11 mA cm −2 . Its strong photocatalysis capabilities benefits from the wider light absorption range and lower charge carrier recombination rate of the photoanode. The double Z-scheme heterojunction formed among BiOBr, MIL-53(Fe) and TCN in the composite catalyst of the photoanode provide more transfer channels for photogenerated e − and encourage the separation of e − -h + pairs. ∙OH and ∙O - 2 are the main active substances for rhodamine B degradation. This study offers a novel approach to the development of high-efficiency photoanodes for PFC.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Qiong Wu,Yining Liu,Haochuan Jing,Hongbin Yu,Ying Lu,Mingxin Huo,Hongliang Huo
Special enhanced synergistic effect of ultra-small γ-Fe 2 O 3 and graphene oxide (GO) on MIL-53 (Fe) was achieved for boosting photocatalysis. Compared to traditional methods of surface coverage, the incorporation of γ-Fe 2 O 3 (average size 2–3 nm) inside MOFs particles not only increased the light absorption of catalyst, but also formed numerous micro-heterojunctions with MOFs units and thus effectively facilitated the separation of photogenerated carriers. By supplying attachment sites for MOFs crystal, the functionalized GO reduced the size of MOFs particles to 100–200 nm, meanwhile improved their dispersibility. The active sites and quantum yield of photocatalytic reaction were also intensified benefiting from the large surface area and high electronic conductivity of GO. Therefore, the novel γ-Fe 2 O 3 -MIL-53(Fe)-GO composite exhibited the highest photocatalytic activity towards norfloxacin, with a removal rate of 92.8% in 90 min. The kinetic constant was 4.49-fold higher than that using pure MIL-53 (Fe), and 1.43-time greater than that in the system of MIL-53 (Fe) and hydrogen peroxide, which usually acted as efficient electron acceptors to increase the quantum yield and final photocatalytic performance of MOFs. Based on the identified intermediates, three NOR degradation pathways including the cleavage of piperazine ring, defluorination and decarboxylation, as well as the conversion of quinolones group were proposed. Photocatalytic mechanism investigation revealed the holes and hydroxyl radicals came from the reaction of electrons with oxygen played the important role in γ-Fe 2 O 3 -MIL-53(Fe)-GO photocatalysis. Moreover, the utilization of magnetic nanoparticles improved the recovery and recyclability of ternary catalyst.
研究领域:
材料科学
·
环境科学
·
纳米技术
·
催化
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2020
·
IF 9.038
Shi-Wen Lv,Jing-Min Liu,Ning Zhao,Chun-Yang Li,Zhi-Hao Wang,Shuo Wang
Nowadays, designing highly active photocatalysts for pollutant degradation under visible light still remains a challenging problem. Herein, a novel benzothiadiazole functionalized Co-doped MOF-based photocatalyst with electron deficient unit was first synthesized via a feasible step-by-step assembly strategy. Benzothiadiazole, as typical electron deficient group, could effectively promote the separation and transfer of photoinduced charge carriers. The implantation of Co ion could be served as an effective mediator to further facilitate the charge transfer through a Co 3+ /Co 2+ redox pathway. Interestingly, the as-synthesized Co-MIL-53-NH-BT exhibited significantly enhanced photocatalytic degradation capacity for BPA and OFX under visible light irradiation, with removal efficiency as high as 99.9 % and 99.8 % within 120 min. TOC analysis suggested that majority of contaminants had been degraded into CO 2 and H 2 O. The important parameters influencing the photocatalytic activity were investigated, and the kinetics study was also conducted. The possible degradation pathways and the possible photocatalytic mechanism were proposed. More importantly, the as-synthesized Co-MIL-53-NH-BT showed good reusability, stability as well as universal applicability. To sum up, current work not only developed an efficient and visible-light active photocatalyst for treating organic-contaminated wastewater, but also afforded some novel insight into the utilization of benzothiadiazole in MOF-based photocatalyst towards improving photocatalytic activity.
研究领域:
环境科学
·
材料科学
·
化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF MOLECULAR STRUCTURE
·
2025
·
IF 4.7
Ying Wang,Tengfei He,Jingguo Cao,Ke Li,Chengqian Wang,Qun Liu,Yu Zhang
This study demonstrates a sustainable strategy for synthesizing MIL-53(Al) and ZSM-5 zeolite through dual-waste synergy using coal fly ash (CFA) and waste polyethylene terephthalate (PET). A sequential alkaline fusion-acid leaching protocol selectively fractionated CFA into aluminum-rich solutions and silica residues, while alkaline hydrolysis of PET liberated terephthalic acid (PTA) as organic ligands. The Al 3+ -PTA coordination under solvothermal conditions produced MIL-53(Al)(CFA-PET) exhibiting well-defined 1D rhombic channels with a high BET surface area (1303 m 2 ·g −1 ), whereas hydrothermal crystallization of silica residues yielded ZSM-5(CFA), which formed spherical aggregates composed of 100 nm nanosheets with 89.9 % yield and a surface area of 311 m 2 ·g −1 . Structural advantages were evidenced by exceptional adsorption performance: MIL-53(Al)(CFA-PET) achieved 96.24 % methylene blue removal at pH 7 (250 mg·L −1 ), outperforming rhodamine B (30.8 %) and methyl orange (66.4 %), as well as reagent-synthesized MIL-53(Al) Che (91.99 %). Both materials demonstrated exceptional CO 2 capture capacities (4.23 mmol·g −1 for MIL-53(Al)(CFA-PET) vs. 2.37 mmol·g −1 for ZSM-5(CFA) at 273 K/1 bar), attributable to MIL-53′s flexible framework enabling dynamic pore adjustment and ZSM-5′s rigid microporous channels favoring molecular sieving. This work establishes a closed-loop strategy for converting industrial and plastic wastes into functionally differentiated porous materials through element-targeted process design.
研究领域:
材料科学
·
环境科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
ANALYST
·
2020
·Vol. 146
·期 4
·1295-1302
·
IF 3.978
Defen Feng,Fucun Wei,Yeyu Wu,Xuecai Tan,Fang Li,Yongkuai Lu,Gaochao Fan,Heyou Han
An ultrasensitive electrochemiluminescence (ECL) biosensor was developed based on MIL-53(Al)@CdS QDs and SiO2@AuNPs for trichlorfon detection. Metal–organic frameworks (MOFs) were used as a loading platform that provided a large surface area to load targets and modified materials onto the electrode. At the same time, SiO2@AuNPs loaded plenty of AuNPs which effectively increased the ECL resonance energy transfer between the CdS QDs, so that the ECL signal was strongly quenched and resulted in an amplified response. In the range of 10−11–10−4 M, the ECL response showed a linear relationship with the concentration (logarithm) of trichlorfon, and the detection limit was 5.1 × 10−12 M (S/N = 3). When the biosensor was applied to detect trichlorfon in lettuce, broccoli, cucumber, and chives, the recoveries obtained from the spiked samples were 97%–105%, 102%–104%, 100%–104%, and 98%–104%, respectively. Thus, this novel ECL biosensor has potential applications for the analysis of trichlorfon in food samples.
研究领域:
分析化学
·
环境科学
·
材料科学
·
食品安全
✓ 已验证
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Ying Jiang,Hao Lu,Lingli Lei,Daniel Scherman,Yingshuai Liu
The design of nanomedicines targeting specific tumor microenvironment (TME) characteristics, such as low pH, hypoxia, and elevated glutathione (GSH) concentration, holds significant potential for selectively killing cancer cells. In this study, we have developed a TME-responsive nanoparticle, i.e. , MIL-53(Fe)@MnO 2 stabilized with polyethylene glycol (FMP), which is capable of depleting GSH and sustainably generating hydroxyl radical (•OH) for enhanced chemodynamic therapy of cancer. After endocytosis, the FMP nanoparticles undergo gradual decomposition, resulting in GSH depletion while releasing Fenton-active Fe 2+ and Mn 2+ ions. These ions then subsequently catalyze a Fenton-like reaction to generate highly toxic •OH, ultimately inducing oxidative cell death. As a synergistic effect, the depletion of GSH further enhances therapeutic efficacy by inhibiting intracellular •OH scavenging. In vivo experiments demonstrated that this synergistically chemotherapeutic approach efficiently suppressed tumor growth without inducing significant systemic toxicity. This work presents a promising nanotherapeutic strategy that simultaneously depletes intracellular GSH and sustains cytotoxic •OH generation for enhanced tumor treatment.
研究领域:
纳米医学
·
癌症治疗
·
生物无机化学
·
活性氧治疗
·
靶向药物递送
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ANALYTICAL CHEMISTRY
·
2020
·
IF 6.785
Lan Guo,Ya-Jie Zhang,Yong-Liang Yu,Jian-Hua Wang
Butyrylcholinesterase (BuChE), the primary source of serum cholinesterase activity, is an indispensable biochemical marker for clinical diagnosis of liver function and organophosphorus poisoning. The requirement for bulky and expensive instruments represents a huge hindrance for point-of-care testing (POCT) of BuChE, especially in resource-limited settings. Herein, an easy-operated, economic, and portable photothermal (PT) biosensing platform for high-throughput BuChE detection was rationally designed. BuChE could “light up” the PT signal through in situ generation of Prussian blue (PB) by MIL-53 (Fe), which allowed us to translate biological signals into temperature signals. Such temperature change signals could be monitored at high throughput (six samples for a single measurement) by a miniature self-made integrated PT device via combining separable 96-well plates, a three-dimensional (3D) printed sample bracket, 808 nm lasers, and thermometers, satisfying the requirement for rapid on-site detection in a large batch with low cost. In addition, the large specific surface area, 3D network structure, and high porosity of MIL-53 (Fe) offered a beneficial platform for its reaction with enzymatic hydrolysate, resulting in high sensing sensitivity and low detection limit (0.3 U L–1), which was at least 20 000 times lower than the normal human serum BuChE activity. This facile, affordable, and broad applicability PT sensing platform provides a beneficial reference for the rational design of other disease diagnostic approaches suitable for POCT.
研究领域:
生物化学
·
分析化学
·
医学诊断
·
材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）