JOURNAL OF HAZARDOUS MATERIALS
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2017
·
IF 6.065
Songjian Zhao,Jian Mei,Haomiao Xu,Wei Liu,Zan Qu,Yong Cui,Naiqiang Yan
Metal-organic frameworks (MOFs) adsorbent Mil-101(Cr) was introduced for the removal of elemental mercury from sintering flue gas. Physical and chemical characterization of the adsorbents showed that MIL-101(Cr) had the largest BET surface area, high thermal stability and oxidation capacity. Hg 0 removal performance analysis indicated that the Hg 0 removal efficiency of MIL-101(Cr) increased with the increasing temperature and oxygen content. Besides, MIL-101(Cr) had the highest Hg 0 removal performance compared with Cu-BTC, UiO-66 and activated carbon, which can reach about 88% at 250 °C. The XPS and Hg-TPD methods were used to analyze the Hg 0 removal mechanism; the results show that Hg 0 was first adsorbed on the surface of Mil-101(Cr), and then oxidized by the open metal site Cr 3+ . The generated Hg 2+ was then combined surface adsorbed oxygen of adsorbent to form HgO, and the open metal site Cr 2+ was oxidized to Cr 3+ by surface active oxygen again. Furthermore, MIL-101(Cr) had good chemical and thermal stability.
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高影响因子
DALTON TRANSACTIONS
·
2018
·Vol. 47
·期 18
·6394-6403
·
IF 4.099
Yanqin Li,Qi Gao,Lijuan Zhang,Yunshan Zhou,Yuxu Zhong,Ying Ying,Mingcai Zhang,Chunqian Huang,Yong'an Wang
Currently extensive effort is compulsively expended to decontaminate efficiently banned chemical war agents. In this work, H5PV2Mo10O40 molecules have been encapsulated in mesoporous MIL-101(Cr), which features two types of mesoporous cages (internal diameters of 29 Å and 34 Å) and microporous windows (diameters of 12 Å and 16 Å), leading to the formation of a new composite H5PV2Mo10O40@MIL-101(Cr) through a simple impregnation method. The composite was characterized thoroughly by elemental analysis, FT-IR spectroscopy, powder X-ray diffraction, scanning electron microscopy, energy dispersive X-ray spectroscopy, TG/DTA, and textural analysis thereby confirming the encapsulation of the H5PV2Mo10O40 into MIL-101(Cr). The decontamination efficiency of sulfur mustard (4 μL HD in 40 μL of petroleum ether) by 20 mg of the composite is found to be 97.39% in 120 min under ambient conditions. GC-MS analysis on the decontaminated products using 2-chloroethyl ethyl sulfide (CEES), which has been widely used as a simulant of sulfur mustard, showed that MIL-101(Cr) just decontaminates CEES by adsorption, while CEES can be decontaminated under ambient conditions by a synergetic combination of adsorption of MIL-101(Cr) and subsequent chemical oxidation degradation to nontoxic 2-chloroethyl ethyl sulfoxide (CEESO) due to the presence of highly dispersed H5PV2Mo10O40 within the composites.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
·
IF 5.518
Chong Chen,Fengqing Wang,Qiuhao Li,Yunlong Wang,Jun Ma
A robust heterogeneous catalyst SIL-PW/MIL-101(Cr) for biodiesel production was fabricated via a bottom-up strategy using phosphotungstic acid (HPW) as a bridge to integrate SO 3 H-functionalized ionic liquid (SIL) with MIL-101(Cr). The characterization results indicated that HPW was well dispersed in the cavities of MIL-101(Cr). The subsequently introduced ionic liquid reacted with HPW to form heteropolyanion-based ionic liquid, which could be embedded in the mesoporous cages. These newly-developed SIL-PW/MIL-101(Cr) exhibited considerable catalytic activity, with 94.3 % conversion of oleic acid . The comparison experiments manifested the enhanced catalytic performance was attributed to the Brønsted acid sites originating from -SO 3 H groups together with the Lewis acid sites. Moreover, the mesoporous structure of MIL-101(Cr) remained intact during immobilization process, which was beneficial for diffusion of large-sized reactants. Due to the bridging function of HPW, no obvious leaching of active component during recycling was observed and the conversion maintained 91.8 % after reused for five times, displaying satisfactory reusability. This study could open new avenues for designing heterogeneous catalysts with multiple active sites through bridging strategy.
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MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Jianmei Li,Qi Sun,Tuyatsetseg Jambal,Dulguun Dorjgotov,Na Su,Qiuju Wu,Jirimutu
To identify adulterated camel meat in emerging markets, there is an urgent need for sensitive, rapid, and convenient detection methods. In this study, a novel fluorescent sensing platform was developed to effectively identify pork components adulterated in camel meat by regulating the surface charge properties of MIL-101(Cr). Our data demonstrated that the modification of polyethylenimine (PEI) had minimal impact on the crystal structure of MIL-101(Cr). However, it significantly affected the adsorption behavior of MIL-101(Cr) towards 6-carboxyfluorescein (FAM) labelled DNA, thereby influencing the response of fluorescence quenching-recovery. Under optimal conditions, the proposed turn-on fluorescent biosensor, based on PEI-MIL-101(Cr) exhibited high sensitivity with a detection limit of 42 pM. It also demonstrated excellent selectivity for specific target DNA, successfully detecting a pork fraction of 0.45 % (w/w) in camel meat. This study was aimed to provide a fresh perspective on the potential application of functional materials derived from metal-organic frameworks in detecting food adulteration .
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MICROPOROUS AND MESOPOROUS MATERIALS
·
2019
·
IF 4.182
Weina Shi,Yanqing Zhu,Cong Shen,Jifu Shi,Gang Xu,Xiudi Xiao,Runqiang Cao
Thermochemical heat storage based on inorganic salt hydrates is a promising approach to relieve the heat energy supply and demand conflicts, but there exist lots of defects of pure salts when applied to the thermochemical. This paper attempted to use functionalized Metal-Organic Frameworks (MOFs) as the porous matrices to improve the heat storage performance of inorganic salt hydrates. A series of MOFs/CaCl 2 composites based on MIL-101(Cr)-X (X = -NH 2 , –SO 3 H, H, –CH 3 , –F) were successfully synthesized and fully characterized by combining multiple techniques (i.e. powder X-ray diffraction, scanning electron microscopy , energy-dispersive X-ray analysis, N 2 adsorption-desorption, Fourier transform infrared spectroscopy , thermogravimetric and differential scanning calorimetry). The water sorption properties of the series of MOFs/CaCl 2 composites were studied during the hydration process, and a continuous adsorption/desorption experiment was also performed to investigate the cycle stability of the MOFs/CaCl 2 composites. The results show that the hydrophilic MOFs based composites have higher water sorption capacity (0.6 g(H 2 O)/g(sample) for MIL-101(Cr)–SO 3 H/CaCl 2 ) accompanied with higher heat storage density (1274 J/g for MIL-101(Cr)–SO 3 H/CaCl 2 ). Moreover, the series of MOFs all presented excellent cycle performance with little loss after continuous 17 adsorption/desorption cycles.
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ChemSusChem
·
2026
·Vol. 19
·期 7
·e202502250
·
IF 5.9
Junjie Zhang,Jingai Shao,Liwen Fu,Zhong Lin,Xiong Zhang,Shihong Zhang,Haiping Yang,Hanping Chen
Developing biomass-based solid acid catalysts and converting biomass-derived molecules into high-value chemicals has a dual promoting effect on the high-value utilization of waste biomass. This study introduces a groundbreaking one-pot hydrothermal strategy integrating biomass with MIL-101(Cr) precursor to fabricate hierarchical carbon-based catalysts for the highly efficient and selective dehydration of xylose to furfural, achieving 67.2%–72.0% furfural yield (a 33% enhancement over conventional biomass-derived catalysts) under optimized conditions (180°C, 3 h) in a toluene/water biphasic system. The modified hydrochar exhibits an ultra-high surface area of 2119.3 m 2 /g, abundant dual Lewis/Brønsted acid sites, and dispersed Cr 3+ active centers, enabled by synergistic MOF-templated modification engineering and biomass hydrothermal carbonization. Moreover, the correlation between the physicochemical properties and catalytic performance of modified hydrochar was analyzed. Notably, biomass feedstocks with low ash content and high nitrogen content can yield modified hydrochar with more acidic active sites, which exhibits superior catalytic activity. This study provides new ideas for the high-value utilization of waste biomass.
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高影响因子
Advanced Composites and Hybrid Materials
·
2022
·Vol. 5
·期 4
·2896-2905
·
IF 11.806
Xu Haitao,Zu Mei,Cheng Haifeng,Liu Dongqing,Xie Wei
The thermal management of electronic devices has attracted significant research attention in the recent year. However, the commonly used thermal management materials at this stage are mainly phase change materials (PCMs), which are limited by their relatively low enthalpy. In this study, the metal–organic framework MIL-101(Cr) was synthesised by an environmentally friendly and low-cost L-malic acid as the mineralising agent. The as-prepared MIL-101(Cr) composite coating was utilised as a sorbent for a passive thermal management strategy, through a vapour sorption–desorption process. By coating the as-prepared MIL-101(Cr) powder onto a metal substrate, a temperature drop for 25 min (maximum 8.6 °C) was achieved for 0.256 g of coating at a heating power of 2.5 W. The use of latent heat has emerged as an attractive method for intermittent heat dissipation. The equivalent enthalpy of the composite coating could reach as high as 1171.9 J/g coating , indicating a significant improvement in the thermal management performance compared with the conventional PCMs. Graphical abstract
Summary: A composite coating for thermal management was obtained by silicate solution and powder MIL-101(Cr).
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APPLIED CATALYSIS A-GENERAL
·
2013
·
IF 3.41
Zhiguo Sun,Gang Li,Hai-ou Liu,Liping Liu
A series of MOF-based catalysts, metal-salen complexes incorporated into amino-functionalized MIL-101 matrices by salicylaldehyde condensing to amino group and coordinating metal ion through one pot method, have been prepared and characterized. The successful preparation of catalysts demonstrates that postsynthetic modification (PSM) is a practical and powerful route to generate MOF-based catalyst with multiple active sites. The catalytic performances of prepared catalysts were investigated via selective oxidation of cyclohexane to cyclohexanone and cyclohexanol (KA-oil) by molecular oxygen in the absence of solvent. It was found that NH 2 -MIL-101(Cr)-Sal-Co, as a typical case, behaves as cooperative catalyst for cyclohexane selective oxidation. That is, salen-Co(II) attached to framework of MOF is able to assist in the generation of new radicals from peroxides via a Haber–Weiss catalytic cycle to promote conversion of cyclohexane while framework Cr ion is able to catalyze the dehydration of intermediate product cyclohexyl hydroperoxide (CHHP) to improve KA-oil selectivity. Furthermore, this catalyst exhibits good recyclability and behaves as truely heterogeneous catalyst.
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ACS Applied Nano Materials
·
2025
·
IF 5.5
Ai-Hui Cao,Xin-Tai Su,Min Zhang,Qi-Long Zhu
Photocatalytic water decomposition is a cost-effective way to convert sustainable solar energy into chemical energy. While semiconductor photocatalysis has generated considerable interest in photocatalytic hydrogen evolution, it is hampered by fast electron–hole complexation and suboptimal efficiency. Herein, an NH2-MIL-101(Cr)/doped-C3N4 heterojunction possessing a static internal electric field (IEF) is successfully prepared, characterized, and assessed for photocatalytic hydrogen production. The optimized photocatalytic H2 evolution rate of the resultant NH2-MIL-101(Cr)/O–C3N4 is 460 μmol g–1 h–1 under visible light, with an AQY of 2.5% at 450 nm. Spectral evidence indicates that the static IEF facilitates rapid electron transfer from NH2-MIL-101(Cr) to O–C3N4, achieving efficient photogenerated charge separation and a consequent significant enhancement in catalytic activity. This work not only presents a case of construction of an IEF through assembling NH2-MIL-101(Cr) with O–C3N4 but also deepens the insight of the rudimentary mechanisms of the static IEF in heterojunctions for photocatalytic hydrogen evolution.
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FOOD CHEMISTRY
·
2024
·
IF 8.5
Rui Cheng,Yiqun Wan,Xuejin Mao,Hao Wan,Fan Liu,Lan Guo,Bingzhen Zhang
This work presents an efficient sorbent for plant growth regulators (PGRs) by regulating the defects of a metal–organic framework MIL-101(Cr). Using the regulated MIL-101(Cr), we developed a simple and effective method for the simultaneous determination of eleven PGRs in fresh fruit juice. The extraction conditions were optimized by an orthogonal array design. Under optimal conditions, the method showed a satisfactory limit of detection (0.1–1.2 ng/g), recovery rates (83.4–110.2 %), and precision (2.9–18.0 % for intra-day and 2.7–10.8 % for inter-day), as well as a greatly suppressed matrix effect. Notably, regulating the defects significantly enhanced the desorption of PGRs on MIL-101(Cr). The sorbent didn’t need to be destroyed to release the adsorbed PGRs and could be reused at least 6 times. Furthermore, the defects of MIL-101(Cr) and interactions between the sorbent and PGRs were studied by TGA, ATR-IR, XPS, NH 3 -TPD and UV–Vis DRS.
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高影响因子
JOURNAL OF SEPARATION SCIENCE
·
2025
·Vol. 48
·期 3
·e70118
·
IF 2.8
Yu Jiang,Hong Pan,Menghong Xie,Huifeng Deng,Guihua Ruan,Yipeng Huang
In this study, magnetic Fe 3 O 4 -coated metal-organic framework composites, CONH 2 -MIL-101(Cr)/Fe 3 O 4 , were synthesized by depositing Fe 3 O 4 particles on the surface of amidated MIL-101(Cr). The scanning electron microscope images show that the MIL-101(Cr) crystals were uniformly coated by Fe 3 O 4 particles. The magnetic hysteresis curve of CONH 2 -MIL-101(Cr)/Fe 3 O 4 reveals a saturated magnetization value of 23.47 emu/g. The water contact angle decreases from 61.00° to 12.88° after amidation and Fe 3 O 4 coating. The magnetic solid-phase extraction (MSPE) efficiency of CONH 2 -MIL-101(Cr)/Fe 3 O 4 for benzoic acid derivatives was studied. Under optimal conditions, the adsorption and desorption processes can be completed within 5 min, and the maximum adsorption capacity to protocatechuic acid (PCA) and vanillic acid (VA) is 10.31 and 17.30 mg/g. Coupling the MSPE with high-performance liquid chromatography-ultraviolet detection, the detection limit for PCA and VA was 0.29 and 0.58 ng/mL, respectively. The mean recoveries of PCA and VA in spiked samples ranged from 82.85%–91.27% with relative standard deviations lower than 0.33%–5.33%. This study provides inspiration for the fabrication of novel magnetic sorbents, and a reliable method for the adsorption and analysis of benzoic acid derivatives.
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FUEL
·
2024
·
IF 6.7
Xifeng Zhu,Longchun Zhong,Yi Xiao,Yuan Liu,Jiawei Wang,Tao Wang,Wei-Ping Pan
To enhance the elimination of trace elemental mercury (Hg 0 ) from coal-fired flue gas, silver nanoparticles (AgNPs) were directionally anchored into the pores of MIL-101(Cr) using the double-solvent method (DSM) to achieve a highly dispersed fixed-bed adsorbent Ag@MIL-101 at room temperature. Various experimental characterizations were conducted to verify the Physical and chemical properties of the adsorbent, and fixed bed adsorption experiments evaluated the Hg 0 removal efficiency. Within the temperature range of 30–70 °C, Ag@MIL-101(Cr) achieved nearly 100 % Hg 0 removal efficiency, maintaining stability even at high concentrations of SO 2 (1500 ppm) and H 2 O (9 %). Density functional theory (DFT) revealed that the introduction of AgNPs greatly enhanced the adsorption capacity of MIL-101(Cr) for Hg 0 , with an evident electron exchange between Ag and Hg, and the adsorption energy changed from −36.91 kJ/mol to −68.59 kJ/mol. The interaction between Ag and Hg was a relatively strong weak interaction, which allowed for easy desorption at moderate temperatures (∼200 °C), significantly saving energy. Tests conducted with flue gas from an actual coal-fired power plant demonstrated that 2Ag@MIL-101(Cr) exhibited superior Hg 0 removal efficiency compared to activated carbon at the WESP outlet under low-temperature (about 50 °C) and high-humidity conditions, providing an efficient and economical solution for flue gas purification.
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