JOURNAL OF SOLID STATE CHEMISTRY
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2022
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IF 3.656
Lichuan Tan,Peng Wang,Ruowei Lu,Siwen Feng,Guangsong Yuan,Cuijuan Wang
Hollow MOFs nanoreactors with controlled shape, size, pore volume , and shell thickness have been considered as emerging materials for a variety of applications. Selecting environmentally friendly and cheap colloidal carbon (CNs) as the template, bimetallic hollow Ce/Zr-UiO-66 nanoreactors were synthesized. The PXRD , TEM , EDS and other characterization analysis proved that hollow structure was formed, accompanied with incorporating of Ce(III) in UiO-66 and the crystal morphology was good. Furthermore, bimetallic hollow Ce/Zr-UiO-66 was studied as a catalyst to catalyze the conversion of furfural (FF) to furfuryl alcohol (FAL) without exogenous hydrogen. The results showed that the hollow structure and bimetallic UiO-66 was beneficial to the catalytic reaction by modulating the ratio of Ce(III) and Zr(IV). Among then, the 1:4 ratio of Ce(III) and Zr(IV) displayed good catalytic activity, the conversion rate of FF was 95% and selectivity of FAL was 94%. This study opens a new avenue for further rational design and construction of well-performing MOFs nanoreactors.
研究领域:
材料科学
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催化化学
✓ 已验证
DOI
高影响因子
DALTON TRANSACTIONS
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2024
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IF 3.5
Zhengyan Wang,Chenhao Yuan,Dong Yang,Mifen Cui,Jihai Tang,Zhuxiu Zhang,Xu Qiao
It is of great significance to develop catalysts for the degradation of hexachlorobenzene from the industrial thermal process. In this paper, formic acid was used as a modulator to generate defect sites in Ce/Zr-UiO-66 with intrinsic Brønsted acidity. The defective formate ligands were removed through methanol–water vapor treatment to expose additional open metal sites with Lewis acidity. The intrinsic Brønsted acid sites of the resulting Ce/Zr-UiO-66-FA-P achieved a hexachlorobenzene degradation efficiency of 99.5% at 250 °C. The generated Lewis acid sites facilitated the C–C cleavage of degradation intermediates. More than 95.0% of the final products were CO2/CO, coupled with chlorinated alkanes/alkenes, which outperformed other benchmark metal oxide catalysts. The Ce/Zr-UiO-66-FA-P catalyst maintained its catalytic activity in the model industrial flue gas and humid environment. The degradation pathway of hexachlorobenzene was tracked using in situ FT-IR spectra.
研究领域:
环境科学
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催化化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
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2021
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IF 13.273
Yun Fan,Haijun Zhang,Meihui Ren,Yichi Zhang,Yun Li,Longxing Wang,Jiping Chen
It is of great significance to develop the low-temperature catalysts for the reduction in emission of chlorinated aromatic hydrocarbons (CAHs) from the industrial thermal processes. In this work, the bimetallic Ce-Zr/UiO-66 catalysts were synthesized by a solvothermal method to degrade CAHs. Powder X-ray diffraction, Fourier transform infrared spectra and X-ray photoelectron spectroscopy analyses showed that cerium was successfully incorporated into the lattice of Zr/UiO-66 without destroying the structure of metal–organic frameworks. The activities of Ce-Zr/UiO-66 catalysts for CAHs degradation varied with the concentration of cerium. Ce 0.2 Zr 0.8 /UiO-66 with the highest surface area (1502 m 2 g −1 ) presented the highest efficiency (>85%) for hexachlorobenzene degradation at low heating temperature (100–150 °C) with less formation of polychlorinated dibenzo- p -dioxins and dibenzofurans. Appropriate amount of water (5 wt%) and nitrogen atmosphere were beneficial to improve degradation efficiency. The degradation products proved that hydrodechlorination and oxidation of CAHs both occurred on the catalysts.
研究领域:
环境化学
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催化
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材料科学
✓ 已验证
DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
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2023
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IF 5.2
Yunlong Li,Miao Liu,Yixian Liu,Lilong Zhou,Jilong Han,Zhengjie Li,Jimmy Yun,Runjing Liu
Two kinds of Ce-doped UiO-66 were synthesized by using CeCl 3 ·7H 2 O and (NH 4 ) 2 Ce(NO 3 ) 6 as cerium precursors, namely Ce(III)- and Ce(IV)-UiO-66. The effect of valence states of cerium precursors on adsorption performance towards Rhodamine B (RhB) was investigated for the first time. Ce atoms are in two valence states of +3 and + 4, where Ce 3+ ions turn their surfaces negatively charged. The higher cerium content (24.8%) and ratio of Ce 3+ /Ce 4+ ions (1.4:1) of Ce(IV)-UiO-66 made its surface more negatively charged, which is contributed to form stronger electrostatic interaction with cationic dyes. The adsorption amounts of RhB were 239.5 mg/g and 431.7 mg/g for Ce(III)- and Ce(IV)-UiO-66, which are 2.38 and 5.11 times higher than pristine UiO-66, respectively. The well-fit Langmuir model and pseudo-second-order model suggest a monolayer chemisorption process. The adsorption mechanism suggests that the electrostatic interaction and the complexation interaction between Ce 3+ and RhB are dominant factors affecting RhB adsorption. Since Ce 3+ severed as adsorption sites, the higher Ce content and stronger electrostatic interaction of Ce(IV)-UiO-66 together promoted its RhB adsorption than Ce(III)-UiO-66. The obtained results help to understand how the mixed-valences of incorporated metals affect the adsorption behaviors of bimetallic MOFs deeply.
研究领域:
材料科学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
FOOD CHEMISTRY
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2024
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IF 8.5
Yiming Dong,Yu Zhang,Puyue Liu,Shiyi Zhu,Xuewen Peng,Xiaobo Hu,Xiya Zhang,Yiping Chen
Ensuring the safety of animal-derived foods requires the reliable and swift identification of enrofloxacin residues to monitor the presence of antibiotics. In this regard, we synthesized, tuned, and investigated the optical properties of a bimetallic metal–organic framework (Ce/Zr-UiO 66). The investigation was facilitated by employing a polydopamine-coated pipette tip with high adsorption efficiency, serving as an immunoreactive carrier. Subsequently, an immunofunctionalized variant of Ce/Zr-UiO 66, referred to as Ce/Zr-UiO 66@ Bovine serum albumin-enrofloxacin, was developed as an optical probe for the rapid and sensitive identification of enrofloxacin across a variety of samples. The method can accurately detect enrofloxacin at concentrations as low as 0.12 ng/mL, with a determination time of under 15 min; furthermore, it demonstrates exceptional efficacy when applied to food, environmental, and clinical samples. The implementation of this methodology offers a valuable means for cost-effective, rapid, and on-site enrofloxacin determination.
研究领域:
分析化学
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食品安全
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材料科学
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生物化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子