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MIL-101(Fe)
MATERIALS CHEMISTRY AND PHYSICS · 2020 · IF 3.408

Influence of microwave-assisted synthesis on the structural and textural properties of mesoporous MIL-101(Fe) and NH2-MIL-101(Fe) for enhanced tetracycline adsorption

Yanan Dong,Tianding Hu,Manoj Pudukudy,Hongying Su,Lihong Jiang,Shaoyun Shan,Qingming Jia

In this paper, the effect of conventional solvothermal and a microwave-assisted method for the synthesis of MIL-101(Fe) and NH 2 -MIL-101(Fe) as adsorbents for the removal of tetracycline in wastewater is reported for the first time. The results had shown that the microwave treatment led to a significant reduction in the material synthesis time, which greatly saved the energy. It was also found that the microwave-assisted synthesized material exhibited small particle size, high specific surface area and better adsorption capacity. The introduction of amino group further enhanced the adsorption capacity of MIL-101(Fe). The adsorption capacity of MIL-101(Fe) and NH 2 -MIL-101(Fe) samples for tetracycline adsorption by microwave assisted synthesis method reached up to 332 mg/g and 378 mg/g, respectively. Moreover, the adsorption isotherm was well-fit with Freundlich model, indicating a multilayer adsorption . The kinetic studies indicated that the reaction followed pseudo second-order reaction kinetics with a best fit to the theoretical value. Due to the higher adsorption efficiency and lower energy consumption of the synthesis, the as-prepared microwave assisted materials could be used as potential adsorbents for different pollutants in wastewater.

研究领域: 环境科学 · 材料科学
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MOLECULES · 2022 ·Vol. 27 ·期 7 ·2288 · IF 4.927

Anti-Influenza Virus Study of Composite Material with MIL-101(Fe)-Adsorbed Favipiravir

Mengyuan Xu,Xi Li,Huiying Zheng,Jiehan Chen,Xiaohua Ye,Tiantian Liu

Nanomaterial technology has attracted much attention because of its antibacterial and drug delivery properties, among other applications. Metal-organic frameworks (MOFs) have advantages, such as their pore structure, large specific surface area, open metal sites, and chemical stability, over other nanomaterials, enabling better drug encapsulation and adsorption. In two examples, we used the common pathogenic bacteriumStaphylococcus aureusand highly infectious influenza A virus. A novel complex MIL-101(Fe)-T705 was formed by synthesizing MOF material MIL-101(Fe) with the drug favipiravir (T-705), and a hot solvent synthesis method was applied to investigate the in vitro antibacterial and antiviral activities. The results showed that MIL-101(Fe)-T705 combined the advantages of nanomaterials and drugs and could inhibit the growth ofStaphylococcus aureusat a concentration of 0.0032 g/mL. Regarding the inhibition of influenza A virus, MIL-101(Fe)-T705 showed good biosafety at 12, 24, 48, and 72 h in addition to a good antiviral effect at concentrations of 0.1, 0.2, 0.4, 0.8, 1.6, and 3 μg/mL, which were higher than MIL-101(Fe) and T-705.Keywords:MIL-101(Fe);favipiravir;antibacteria;antiviral

CAS / MDL: 56-81-5 25618-55-7
研究领域: 纳米技术 · 药学 · 病毒学
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JOURNAL OF SOLID STATE CHEMISTRY · 2022 · IF 3.656

Cu-doped MIL-101(Fe) with enhanced photocatalytic nitrogen fixation performance

Zhipeng Zhang,Feifei Li,Guoqiang Li,Rui Li,Yunfang Wang,Yawen Wang,Xiaochao Zhang,Lulu Zhang,Fangfang Li,Jianxin Liu,Caimei Fan

The bottlenecks of photocatalytic nitrogen fixation are adsorption and activation of nitrogen, because N–N bond in dinitrogen is one of the strongest bonds in chemistry . Herein, for the first time, Cu-doped MIL-101(Fe) was applications in photocatalytic nitrogen fixation. The photocatalytic nitrogen fixation activity of Cu-MIL-101(Fe) is three times that of MIL-101(Fe). Characteristic of MIL-101(Fe) and Cu-MIL-101(Fe) are systematically compared by XRD , SEM, TEM, BET, PL and energy band structure . These results indicated that the Cu doping not only enlarge the specific surface area from 1413 ​m 2 /g to 2097 ​m 2 /g, but also increase the photoreduction capability from −0.13 ​V to −0.7 ​V. These results indicated that nitrogen adsorption and activation capacity can be improved by Cu doping. By combining metal ions doping and components regulation of MOFs , this work provides many future opportunities for enhance photocatalytic nitrogen fixation activity.

研究领域: 材料科学 · 化学工程
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Journal of Chemistry · 2020 · IF 1.79

Hydrothermal Catalytic Conversion of Glucose into Lactic Acid with Acidic MIL-101(Fe)

Xiaofang Liu,Zhigang Liu,Qiuyun Zhang,Hongguo Wu,Rui Wang

MIL-101(Fe) was explored for the first time for the catalytic conversion of glucose into lactic acid (LA). The as-synthesized MIL-101(Fe) was successfully characterized, and its higher specific surface area, porosity, and feasible acid properties were confirmed to determine the remarkable catalytic activity in glucose-to-LA conversion (up to 25.4% yield) compared with other catalysts like MIL-101(Cr, Al) and UiO-66(Zr). The reaction parameters including temperature, reaction time, and substrate species as well as catalyst reusability were discussed.

研究领域: 化学工程 · 材料科学 · 生物化学
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JOURNAL OF SOLID STATE CHEMISTRY · 2022 · IF 3.656

Cracked spindle morphology of MIL-101(Fe) for improved photocatalytic nitrogen reduction

Lijun Guo,Feifei Li,Jianxin Liu,Rui Li,Zhuobin Yu,Qing Xi,Lulu Zhang,Yaru Li,Caimei Fan

Morphology regulation is a simple way to improve photocatalytic activity. In this work, a MIL-101(Fe) photocatalyst with cracked spindle morphology has been successfully prepared by EG pre-coordination solvothermal method . The cracking degree of MIL-101(Fe) can be regulated by adjusting pre-coordination time. The MIL-101(Fe) with the optimal uniform crack displays a best NH 3 evolution rate of 592 ​μmol ​h −1  ​g −1 under the visible light irradiation . Cracked MIL-101(Fe) is similar to a semi-exposed model, which can increase the number of reactive sites, improve refraction and reflection of light, and ultimately enhance the photocatalytic nitrogen fixation activity. This work developed a convenient strategy to improve the photocatalytic activity of nitrogen reduction by controlling morphology.

研究领域: 材料科学 · 环境科学 · 化学工程
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CANADIAN JOURNAL OF CHEMICAL ENGINEERING · 2022 ·Vol. 101 ·期 6 ·3262-3272 · IF 2.5

Removal of glyphosate from aqueous solution by CuO coated MIL-101(Fe)

Dongmei Jia,Jia Guo,Jing Li,Yongzheng Duan

The composite of CuO coated MIL-101(Fe) (CuO@MIL-101(Fe)) was successfully prepared using a one-pot hydrothermal technology. X-ray diffraction (XRD), Fourier transform infrared spectrum (FTIR), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), Brunauer–Emmett–Teller (BET), and TG technologies were used to characterize its structural, morphological, and physicochemical properties. CuO@MIL-101(Fe) exhibited a better pH adaptivity, a faster removal ratio of 95.8% for glyphosate within 10 min at pH 7, and a higher selectivity of adsorption capacity, even reaching 231.6 and 233.5 mg g −1 with coexisting Cl − (10 mmol L −1 ) and SO 4 2− (10 mmol L −1 ). The enhanced adsorption performances of CuO@MIL-101(Fe) may be caused by Cu forming a coordination interaction with glyphosate. A possible mechanism of glyphosate removal was discussed on the basis of the FTIR and X-ray photoelectron spectroscopy (XPS) analysis. CuO@MIL-101(Fe) composite would be more favourable to capture glyphosate from wastewater.

研究领域: 环境科学 · 材料科学
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 20 ·9185-9195 · IF 2.7

Construction of an MIL-101(Fe)/layered bimetallic oxide heterojunction for enhanced ciprofloxacin removal

Shikai Xue,Dongying Zhu,Qing Zuo,Shuangfeng Yang,Haiyan Wang,Qiujun Lu,Guoxing Yin,Guihua Ruan,Fuyou Du

A novel MIL-101(Fe)/ZnCrZr-LBMO heterojunction was successfully constructed and used for the removal of ciprofloxacin (CIP) in this work. The MIL-101(Fe)/ZnCrZr-LBMO composite exhibited significantly enhanced photocatalytic degradation activity, with reaction rates approximately 3.4 and 3.1 times faster than those observed with pristine MIL-101(Fe) and ZnCrZr-LBMO, respectively. The effect of different amounts of ZnCrZr-LBMO, sample pH, CIP concentration, inorganic cations, and anions on CIP removal was investigated, and the possible intermediates and degradation pathways of CIP were speculated. The·O2− radicals dominated CIP degradation, with minor contributions from 1O2, h+, and ·OH radicals. The composite exhibited high removal rates for CIP (94.7%), ofloxacin (86.8%), and tetracycline (96.3%), respectively, within 60 min of light irradiation, and excellent reusability, retaining over 85.1% CIP degradation rate after five cycles. Our work provides a new reference to construct highly efficient and easily recyclable MIL-101(Fe)/ZnCrZr-LBMO photocatalysts for the removal of antibiotic pollutants, promising advancements in real water treatment applications.

研究领域: 环境科学 · 材料科学
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LANGMUIR · 2024 · IF 3.7

Photocatalytic Selective Oxidation of Toluene over Chlorine-Coordinated MIL-101(Fe) under Ambient Conditions

Zeqi Wu,Feng Niu,Wenhao Yao,Siyuan Gao,Da Chen,Yuexiang Huang

The activation of an inert C(sp3)–H bond in selective oxidation of hydrocarbons under mild conditions is a critical and challenging process. Herein, we report a stable chlorine-coordinated metal–organic framework (MOF) photocatalyst, MIL-101(Fe), for efficient visible-light-driven photocatalytic selective oxidation of toluene to benzaldehyde in air under ambient conditions. Encouragingly, a benzaldehyde formation yield of 3.11 mmol·g–1·h–1 with a selectivity of 92.1% is achieved in 5 h, which is superior to most of the reported works. Based on the experimental results and characterizations, the high catalytic performance is mainly due to the promoted rate-limiting step of C(sp3)–H bond activation by a chlorine radical (Cl·) from the coordinated −Cl in the MIL-101(Fe) structure. In addition, the present photocatalyst possesses good substrate tolerance for photocatalytic selective oxidation of various toluene derivatives under optimized conditions.

研究领域: 化学 · 材料科学 · 环境科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2019 · IF 6.361

Adsorption behavior of arsenicals on MIL-101(Fe): The role of arsenic chemical structures

Zongchen Li,Xuemin Liu,Wei Jin,Qingsong Hu,Yaping Zhao

Arsenic species are regarded as typical water pollutants due to their toxicity. The chemical structures of arsenic species greatly influence their migration and transformation in the environment. Metal-organic frameworks (MOFs) are used as reliable adsorbents to control arsenic contamination, so it is urgently needed to study the effect of chemical structure of arsenic species during adsorption process. The adsorption behaviors of arsenate (As(V)) and its organic forms such as roxarsone (ROX), p-arsanilic acid (p-ASA) and dimethyl arsenate (DMA) by MIL-101(Fe), a type of highly porosity iron-based MOFs in aqueous environment were detailed investigated. The adsorption kinetics of those arsenic species on MIL-101(Fe) is rapid followed with pseudo-second-order kinetic model. MIL-101(Fe) exhibits excellent adsorption capacities for As(V), ROX, p-ASA and DMA with maximum adsorption capacities of 232.98, 507.97, 379.65 and 158.94 mg g −1 , respectively. The formed Fe O As inner-sphere coordination between arsenic species and the incomplete-coordinated cationic Fe in the MIL-101(Fe) cluster is the primary adsorption mechanism based on FTIR and XPS analysis. Substituent aromatic units in ROX and p-ASA strengthen the adsorption on MIL-101(Fe) through hydrogen bonds and π-π stacking interaction, resulting in higher adsorption capacities far beyond that of As(V) and DMA. The reusability of MIL-101(Fe) is limited by the strong Fe O As coordination. These results confirm MIL-101(Fe) a reliable adsorbent to control the aqueous arsenic species contamination and emphasize the significant role of the chemical structure of arsenic speciation on adsorption performances of MOFs.

研究领域: 环境科学 · 材料科学 · 化学
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JOURNAL OF POROUS MATERIALS · 2025 · IF 3.2

Degradation of tetracycline by MIL-101(Fe)/CoFe2O4 activated persulfate under visible light

Rui Guofen,Hu Zihao,Wu Huiqi,Ma Jianfeng

Composites of MIL-101(Fe)/CoFe 2 O 4 were prepared by a simple solvothermal approach and these composites were explored for tetracycline (TC) degradation by using light and persulfate (PS). MIL-101(Fe)/CoFe 2 O 4 catalyst showed superior catalytic performance when combined with photocatalysis and chemical catalysis. Experimental results suggest that the degradation efficiency reached 83% within 40 min. The TC adsorption ability of MIL-101(Fe)/CoFe 2 O 4 was tightly associated with pH, which can be interpreted through isoelectric point. Oxygen-active species, containing singlet oxygen ( 1 O 2 ) or superoxide radicals (O· 2‾), were also generated when there was dissolved oxygen, which could decompose the TC organic contaminant in solution. To be specific, MIL-101(Fe)/CoFe 2 O 4 /PS/Vis catalytic system was capable of eliminating TC through forming h + , 1 O 2 , O· 2‾, hydroxyl radicals (·OH) and sulfate radicals (·SO 4 ‾) species. Moreover, MIL-101(Fe)/CoFe 2 O 4 composite material showed outstanding stability.

研究领域: 环境科学 · 催化材料
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International Journal of Electrochemical Science · 2023 · IF 1.5

MIL-101 (Fe) modified carbon paste electrode for the efficient simultaneous detection of hydroquinone and catechol

Mengting Zhu,Ruli Xu,Xueyang Wang,Jie Liu Qianli Zhang,Jie Wei

Four Fe-based metal-organic frameworks (MIL-101(Fe), MIL-53(Fe), MIL-88(Fe), and MIL-100(Fe)) were synthesized using a solvothermal method, and further characterized by X-ray diffraction, Fourier transforms infrared spectroscopy, Scanning electron microscopy, and X-ray photoelectron spectroscopy. The synthesized Fe-MOFs were used to fabricate the modified carbon paste electrodes (CPE) for simultaneous detection of hydroquinone and catechol. Among the MILs (Fe) modified CPEs, MIL-101(Fe)/CPE exhibited extraordinary electrochemical sensitivity because of MIL-101 (Fe)’s excellent conductivity. The oxidation potential separation of hydroquinone and catechol achieved 190 mV. Compared with CPE, the oxidation currents of hydroquinone and catechol at MIL-101/CPE were 10-fold higher and the reduction currents were 5-fold higher. The linear range was 2 - 90 μM for hydroquinone and 2 - 100 μM for catechol, and the detection limit was 0.58 μM and 0.62 (S/N = 3) μM for hydroquinone and catechol. Furthermore, the application of MIL-101 (Fe)/CPE has been validated in an actual river water sample with the satisfied recoveries of 90.21 - 102.36% and 91.11 - 102.19% for hydroquinone and catechol, respectively.

研究领域: 分析化学 · 环境科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2022 · IF 5.518

Fabrication of Au nanostar/MIL-101(Fe) architecture for surface-enhanced Raman scattering detections

Tianze Cong,Hui Huang,Hao Zhang,Chengwei Li,Yongpeng Zhao,Zeng Fan,Lujun Pan

In the surface-enhanced Raman scattering (SERS) measurements, it is very important to fabricate “hot spots” and concentrate the analytes into these regions. In this work, a hybrid structure of Au nanostars (NSs) with high SERS sensitivity and metal-organic framework MIL-101(Fe) with high molecular adsorption capability was constructed as high performance SERS substrate. The MIL-101(Fe) shell between AuNSs is several nanometers, promoting the construct of “hot spots” and the aggregation of target molecules. The as-prepared AuNS/MIL-101(Fe) has achieved high SERS sensitivity, long-time stability, reproducibility, and capability of universal detections. The limit of detection for rhodamine 6 G is down to 0.29 nM. Meanwhile, the SERS activity of AuNS/MIL-101(Fe) is kept for at least 30 days. Furthermore, the relative standard deviations of signals on five substrates are all less than 10 %. The as-prepared AuNS/MIL-101(Fe) also exhibit the SERS activities for various molecules including dyes, organic contaminants, pesticides, and amino acids , indicating that the AuNS/MIL-101(Fe) substrates have wide applications in chemical analysis and environmental monitoring.

研究领域: 材料科学 · 分析化学 · 环境科学
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