Journal of Environmental Sciences
·
2021
·
IF 5.565
Jiaqi Shi,Rui Han,Shuangchun Lu,Qingling Liu
A series of highly-hydrophobic MIL-53-Al (MIL = Materials of Institut Lavoisier) frameworks synthesized via decoration of the Al-OH groups by alkyl phosphonic acid were developed as adsorbents for removing acetone from humid gas streams. The newly prepared materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscope (SEM), N 2 adsorption-desorption and thermogravimetric analysis (TGA). Their adsorption behaviors toward acetone vapor under dry and wet conditions were studied subsequently. Results showed that alkyl phosphonic acid was successfully grafted into MIL-53-Al skeleton through coordinating interaction with Al 3+ generating MIL-53-Al@C x ( x = 12, 14, 18). The MIL-53-Al@C x exhibited similar crystal structure and thermal stability to parent MIL-53-Al. Furthermore, the modified materials showed significantly enhanced hydrophobicity . The water vapor uptake of MIL-53-Al@C 14 decreased by 72.55% at 75% relative humidity (RH). Dynamic adsorption experiments demonstrated that water vapor had almost no effect on the acetone adsorption performance of MIL-53-Al@C 14 . Under the condition of 90% RH, the acetone adsorption capacity of MIL-53-Al@C 14 was 102.98% higher than that of MIL-53-Al. Notably, MIL-53-Al@C 14 presented excellent adsorption reversibility and regeneration performance in 10 adsorption-desorption cycles. Taken together, the strategy of metal-OH group modification is an attractive way to improve the acetone adsorption performance over metal-organic frameworks (MOFs) under humid conditions. Besides, MIL-53-Al@C 14 would be deemed as a promising candidate for capturing acetone in high moisture environment.
研究领域:
材料化学
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环境科学
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吸附分离
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多孔材料
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配位化学
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2023
·Vol. 47
·期 17
·8334-8346
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IF 3.3
Peifu Sun,Xiao Zhang,Zhiren Guo,Xinyue Liu,Yuanming Lan,Dongxiang Zhang,Hansheng Li,Jinying Li,Helei Liu,Xiyan Xu
The excessive discharge of isothiazolinone bacteriostatic agent-containing wastewater has posed serious threats to human health and environmental safety. As 1,2-benzisothiazolin-3-one (BIT) is one of the most commonly used isothiazolinones, its effective degradation is necessary and urgent. In the current study, a NH2-MIL-53(Fe)-based adsorptive photo-Fenton-like system was constructed for efficiently adsorbing and photodegrading BIT under solar light. The equilibrium BIT adsorption capacity Qe of NH2-MIL-53(Fe) reached 1140.89 mg g−1. The adsorptive photo-Fenton-like system has achieved more than 90% removal of BIT using NH2-MIL-53(Fe) in the presence of H2O2 under solar light irradiation, and the band gap of NH2-MIL-53(Fe) was calculated by UV-Vis analysis to be 2.10 eV. The influences of pH, dosage of photocatalysts and H2O2 were also assessed. It was found that H2O2 reduced the recombination of electron–hole pairs, and the radical quenching experiments and EPR testing result confirmed that h+, ˙OH and O2˙− played a crucial role in the photocatalytic process. This study supports the application of Fe-based MOF materials for simultaneous adsorption and the solar light photocatalytic degradation of BIT.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2022
·
IF 9.136
Zihan Kang,Mengshi Chen,Enzhu Lin,Jiang Wu,Kanghui Ke,Ni Qin,Dinghua Bao
Carbon-based composites with high activity and selectivity have broad prospects in the field of synthesis and catalysis. This work describes the controllable encapsulation of Bi 2 WO 6 (BWO) piezocatalysts with the mixture of derivatives and frameworks obtained by calcining MIL-53 metal–organic frameworks (MOFs). The mesoporous carbon and multi-functional groups of C/Fe 3 O 4 derived from the pyrolysis of MIL-53(Fe) can mediate the magnetic recyclability of catalysts and act as electron transfer units. Due to the high thermal stability, MIL-53(Al) mixed together still retains the frameworks and shows ameliorated hydrophobicity induced by porous carbon , which ensures the continuous generation of active radicals. The MOFs-assembled BWO nanoflowers possess the characteristics of complete adsorption-release and piezocatalytic degradation of organic pollutants, and the piezocatalytic degradation efficiency reaches 3.7 times higher than that of pure BWO nanoflowers. We also proposed a magnetic modulation method to obtain efficient macroporous MOFs/BWO-PVDF membranes. The magnetic composite powders can be highly exposed to the membrane surface to form more active sites for piezocatalytic reaction, which can overcome the problem of catalysts embedding in the membrane. This work not only proposes a novel way of synthesizing carbon composite piezocatalysts, but also provides the possibility to obtain more convenient, recyclable and high-performance piezocatalytic membrane, which is of great significance to explore the extensive application of piezocatalyst in sewage treatment.
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高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Jiaxin Yang,Deng Wang,Jihui Wang,Wenbin Hu
A novel self-healing composite coating was fabricated on magnesium alloy by using polycaprolactone (PCL) as resin matrix and iron-based metal-organic framework MIL-53 modified with tannic acid (TA) as function filler. The surface morphology, structure and wettability of composite coating were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FT-IR) and sessile water droplet static contact angle. The corrosion resistance and healing performance of PCL coatings was determined by electrochemical impedance spectroscopy (EIS) and photothermal tests. Results indicate that MIL-53@TA/PCL coating possesses a flatter surface, a higher corrosion resistance and better photothermal effect than that of blank PCL coating and MIL-53/PCL coating. Under the near-infrared (NIR) laser irradiation with the wave length of 808 nm, the scratched MIL-53@TA/PCL coating could be healed within 10 min because of the excellent photothermal conversion ability of MIL-53@TA component.
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高影响因子
RSC Advances
·
2021
·Vol. 11
·期 18
·10540-10547
·
IF 3.361
Anxia Li,Xiaoxin Yang,Juan Chen
Metal–organic frameworks (MOFs), such as MIL-53(Fe), have considerable potential as drug carriers in cancer treatment due to their notable characteristics, including controllable particle sizes, high catalytic activity, biocompatibility and large porosity, and are widely used in a broad range of drugs. In this study, a new approach for the synthesis of MIL-53(Fe) nanocrystals with controlled sizes has been developed using a non-ionic surfactant PVP as the conditioning and stabilizing agent, respectively. During the nucleation of MIL-53(Fe), the PVP droplet, as a nano-reactor, controlled the growth of the crystal nucleus. The size and aspect ratio (length/width) of nanocrystals increased with an increase in PVP in the synthetic mixture. The MIL-53(Fe) nanocrystals showed a homogeneous morphology, with approximately 190 nm in length and 100 nm in width. MIL-53(Fe) not only was used to load the anticancer drug doxorubicin (DOX) but also generated hydroxyl radicals (˙OH) via a Fenton-like reaction for ROS-mediated/chemo-therapy of cancer cells. The approach was expected to synthesize numerous types of nano-size iron(III)-based MOFs, such as MIL-53, 89, 88A, 88B and 101. The MIL-53(Fe) nanocrystals hold great promise as a candidate to improve the controlled release of drugs and treatment effect for cancer therapy.
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PubMed
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Yong Tang,Jianhao Qiu,Dingliang Dai,Guanglu Xia,Yixin Li,Biyao Fang,Jianfeng Yao
Sluggish charge transfer dynamics are still the key issue limiting the development of photocatalysis. In this study, CdS/ZnIn 2 S 4 /MIL-53-NH 2 ternary hierarchical heterostructures were constructed via a building block approach, where ZnIn 2 S 4 lamellae first grow on MIL-53-NH 2 followed by CdS nanoparticle deposition. The favorable interfacial compatibility and ternary heterostructures contribute to rapid and multistep spatial charge transfer, which suppresses charge recombination. Therefore, ultrahigh H 2 O 2 production of 1792 μmol·L −1 was obtained over CdS/Znln 2 S 4 /MIL-53-NH 2 composites with visible light, pure water and ambient air, which is not only higher than that of each monomer and binary heterostructure but also better than those of most reported references. Notably, the apparent quantum yield reached 4.5 % at 400 nm, and the solar-to-H 2 O 2 conversion efficiency was 0.081 % in pure water and ambient air. Additionally, H 2 O 2 generation over CdS/Znln 2 S 4 /MIL-53-NH 2 composites involves two-electron O 2 reduction with ·O 2 - as an intermediate. This work may encourage heterostructure design for efficient photocatalytic H 2 O 2 production.
研究领域:
材料科学
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光催化
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纳米技术
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化学工程
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环境科学
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DOI
高影响因子
Journal of Analytical Methods in Chemistry
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2023
·
IF 2.6
Xiuzhen Yang,Changye Wang,Bin Zhou,Shuangchan Cheng
Iron-based organic frame material MIL-53 (Fe) was synthesized by the hydrothermal method with Cu2+ incorporated to obtain bimetallic composite MIL-53 (Fe, Cu). The structure and morphology of the material were characterized by SEM, XRD, BET, FTIR, XPS, and zeta potential. The adsorption performance of MIL-53 (Fe, Cu) on methyl orange was tested under a variety of conditions, including the effects of pH and material dosage, by the static adsorption test. The results show that under the condition of pH = 7, a temperature of 30°C, and an adsorbent dosage of 20 mg, the removal rate of MIL-53 (Fe, Cu) for methyl orange can reach more than 96% within 4 h, and the maximum adsorption capacity after fitting by the thermodynamic model can reach 294.43 mg/g, showing the excellent adsorption performance of MIL-53 (Fe, Cu) on methyl orange. In addition, by exploring the adsorption mechanism of MIL-53 (Fe, Cu) on methyl orange, it is found that the adsorption of MIL-53 (Fe, Cu) on methyl orange depends on chemical adsorption, as evidenced by combining Fe3+ and Cu2+ in the material with methyl orange molecules to form complexes to achieve adsorption. While the specific surface area of the material had no obvious effect on adsorption, the effects of pH, temperature, and concentration were explored. At a pH of 6.5, greater adsorption occurred at higher temperatures, as determined by thermodynamic model fitting, as well as with higher initial methyl orange molecule concentration.
研究领域:
材料科学
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环境化学
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分析化学
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DOI
高影响因子
DALTON TRANSACTIONS
·
2016
·Vol. 45
·期 19
·7952-7959
·
IF 4.177
Qiao Sun,Min Liu,Keyan Li,Yitong Han,Yi Zuo,Junhu Wang,Chunshan Song,Guoliang Zhang,Xinwen Guo
A series of MIL-53(Fe)-type materials, Fe(BDC)(DMF,F), were prepared by using different ratios of n(FeCl3)/n(FeCl2), which have varied amounts of Fe2+ in their frameworks. From FeCl3 to FeCl2, the structures of the synthesized samples transform from MIL-53(Fe) to Fe(BDC)(DMF,F). Along with this structure transformation, the crystal morphology goes through a striking change from a small irregular shape to a big triangular prism. This phenomenon indicates that the addition of FeCl2 is beneficial for the formation of a Fe(BDC)(DMF,F) structure. The catalytic activity of these iron-containing MOFs was tested in phenol degradation with hydrogen peroxide as an oxidant at near neutral pH and 35 °C. The degradation efficiency of these samples increases gradually from MIL-53(Fe) to Fe(BDC)(DMF,F). 57Fe Mössbauer spectra reveal that Fe2+ and Fe3+ coexist in the Fe(BDC)(DMF,F) framework, and the highest amount of Fe2+ in the sample prepared with mixed FeCl3 and FeCl2 is 26.0%. The result illustrates that the amount of Fe2+ in the samples can be controlled using varied n(FeCl3)/n(FeCl2) in the feed. The diverse amount of Fe2+ in this series of FeMOF materials exactly explains the distinction of reaction efficiency. The iron leaching tests, structures of the fresh and used catalysts, and the data of the recycling runs show that the Fe-containing MOFs are stable in this liquid-phase reaction.
研究领域:
材料科学
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环境化学
·
催化
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DOI
PubMed
高影响因子
ACS Sustainable Chemistry & Engineering
·
2026
·
IF 7.6
Jiaxin Wang,Shenghua Liu,Xiaoqian Feng,Lijiao Chen,Huan Wang,Yonghua Zhao,Qijian Zhang,Haiyan Wang,Xinwen Guo
Dry reforming of methane (DRM) is a promising route for the simultaneous conversion of CO2 and CH4; despite the effectiveness of C–H bond activation ability of Ni-based catalysts, they face serious challenges due to coking. Herein, two metal–organic frameworks (MOFs), NH2-MIL-53 and MIL-53 were loaded with Ni via impregnation and calcined at different temperatures to prepare Ni/Al2O3 catalysts. The results reveal that the Ni-based catalyst derived from NH2-MIL-53 possesses a higher specific surface area (SSA) due to the presence of –NH2 groups, which remarkably improved the dispersion of Ni. Additionally, the calcination temperatures are found to play an important role. Low-temperature calcination leads to weaker metal–support interaction (MSI) while high-temperature calcination results in lower specific surface area (SSA) and agglomeration of the active component Ni. The Ni/Al2O3 catalyst calcined at 850 °C exhibits moderate MSI and high SSA, leading to excellent catalytic activity (CH4 conversion ∼68%, CO2 conversion ∼80%) and stability (>50 h with coking ≈0.022 mmol C·gcat–1·h–1) at 750 °C with a GHSV of 96,000 mL/(gcat·h). The derived porous alumina restricts Ni sintering. In situ DRIFT results show that such a catalyst benefits the formation of key intermediate b-HCOO* due to high Ni dispersion. This work provides new insights and directions for optimizing the performance of MOF-derived catalysts.
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高影响因子
Sustainable Materials and Technologies
·
2025
·
IF 9.2
Xianjin Qi,Guizhi Yan,Boyu Du,Mengmeng Wang,Yongkui Li
Arsenic (As) contamination is a global problem that requires innovative remediation, this study successfully synthesized a novel MnFe 2 O 4 -Zn/Co ZIFs@MIL-53(Fe) (MFZM) using a solvent method to remove As(V) from contaminated water. The MFZM exhibited a rhomboidal dodecahedron structure with a high specific surface area of 158.93 m 2 /g, which contributed to its exceptional adsorption performance under both acidic and neutral pH conditions. Notably, the adsorption capacity for As(V) reached approximately 599.90 mg/g at an equilibrium concentration of 500 mg/L, surpassing the performance of several previously reported adsorbents. The kinetic modelling results indicated that the adsorption process followed a pseudo-second-order mechanism, suggesting chemisorption as the dominant process. However, the isotherm studies demonstrate favorable single-layer adsorption, with the Langmuir model providing the best fit for the experimental data. The X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy with energy-dispersive spectroscopy (SEM-EDS) analysis revealed that the Fe/Mn/Co on the MFZM surface can hydrolyze and generate Fe/Mn/Co-OH groups under pH conditions ranging from 3 to 7, facilitating the formation of stable coordination complexes with As(V). Furthermore, the MFZM provided abundant positively charged adsorption sites that effectively attracted HAsO 4 2− via electrostatic interactions, leading to efficient As(V) removal. These findings underscore the potential of the MFZM as a promising adsorbent for the effective remediation of As-contaminated wastewater, supporting sustainable environmental management.
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高影响因子
MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Peixun Yang,Senwei Jiang,Zhen Wu,Daodong Pan,Hangzhen Lan
Metal-organic frameworks (MOFs) hold significant potential for sample preparation, but single-MOF materials often face limitations in selectivity and extraction efficiency. To overcome these, a mesoporous MIL-53(Al)–NH 2 @UiO-66 composites with a core–shell structure was synthesized using an epitaxial growth strategy. This composite leverages the complementary properties of both MOFs, offering enhanced active sites and interaction forces for analytes. The structure and integration of the composite were characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction, confirming their successful integration. To address the challenge of detecting alkylphenols (APs) in food matrices, known for their endocrine-disrupting properties and low concentrations, a new solid-phase microextraction (SPME) Arrow was fabricated using the MIL-53(Al)–NH 2 @UiO-66 composite combined with polyacrylonitrile as a binder. APs were detected using ultra-performance liquid chromatography and quadrupole time-of-flight tandem mass spectrometry (UPLC-ESI-Q-ToF/MS). The developed SPME Arrow-UPLC-ESI-Q-ToF/MS method exhibits good linearity (R 2 ≥ 0.9958), wide linear range (0.01–1000 μg L –1 ), and high sensitivity (limits of detection ranging from 0.005 to 0.01 μg L –1 ) for APs determination. This method was validated for determining nine APs in milk samples from various packing materials, with spiked recoveries ranging from 85.2 % to 115 % and relative standard deviations from 3.4 % to 13.6 %. This study demonstrates the potential of MOF-on-MOF composites in enhancing the performance of adsorbents for SPME pretreatment, offering a promising approach for improving analytical methodologies in food safety.
研究领域:
分析化学
·
食品安全
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高影响因子
International Journal of Environmental Research and Public Health
·
2022
·Vol. 20
·期 1
·715
·
IF 4.614
Gege Wu,Jiping Ma,Chenxi Wei,Shuang Li,Jinhua Li,Xiaoyan Wang,Lingxin Chen
Metal organic framework based mixed matrix membranes (MOF-MMMs) were synthesized and applied for dispersive membrane extraction (DME) of four neonicotinoid insecticides (nitenpyram, thiacloprid, imidacloprid, and acetamiprid) in environmental water, combined with high performance liquid chromatography (HPLC) for determination. Several experimental conditions were optimized in detail, involving dosage percentage of MOF, extraction time, sample pH, salinity, type and volume of eluent, and elution time. High sensitivity with limits of detection and quantification were achieved as 0.013–0.064 μg L−1and 0.038–0.190 μg L−1, respectively, and good precision with relative standard deviations were obtained as 3.07–12.78%. The proposed method has been successfully applied to determine four neonicotinoid insecticides in tap water, surface water, and seawater, satisfactory recoveries of spiked water samples were between 72.50 and 117.98%. Additionally, the MOF-MMMs showed good reusability with the extraction efficiencies almost remaining stable after 14 cycles. The MOF-MMMs based DME followed by the HPLC method can be a promising utility for the determination of neonicotinoid insecticides in environmental water samples, with high sensitivity and convenient operation.Keywords:metal-organic framework;neonicotinoid insecticides;dispersive membrane extraction;high performance liquid chromatography;environmental analysis
研究领域:
分析化学
·
环境科学
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DOI
PubMed
高影响因子
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