Surfaces and Interfaces
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2022
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IF 6.137
Chong Wang,Wendong Xing,Yilin Wu,Yunhui Li,Yongsheng Yan,Jianwei Zhu
Sulfamethoxazole (SMX) is a widespread organic contaminant that threatens the ecological environment and human health. Therefore, it is of great significance to develop an effective method for selective separation of SMX from the aquatic environments. Herein, a novel in-situ synthesis of CNT/UiO-66-NH 2 based molecularly imprinted nanocomposite membranes (CUMIMs) is designed for selective removal of SMX. The CNT/UiO-66-NH 2 nanocomposite is prepared through in-situ growth of MOFs in the presence of CNT . The CNT around the MOFs can effectively avoid the aggregation of CNT/UiO-66-NH 2 nanocomposite and introduce unique properties into the PVDF/PVA membrane, which simultaneously benefit in both hydrophilicity and water flux. More importantly, the well dispersed CNT/UiO-66-NH 2 nanocomposite with huge specific in the membrane can facilitate the selectivity toward SMX. The selective separation performance of CUMIMs is evaluated by static adsorption and permeselectivity experiments. The results showed that the synthesized CUMIMs afford an ideal rebinding selectivity (α SMX/SMM = 2.01, α SMX/TC = 4.34, and α SMX/CIP = 4.65) and permselectivity factor (β = 2.15) toward SMX. The presented strategy on CUMIMs fabrication would potentially enrich the application of CNT/MOFs-based molecularly imprinted nanocomposite membrane in the field of contaminant separation.
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高影响因子
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2023
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IF 6.1
Xiaobo Zhang,Zhiru Li,Lili Yang,Bing Hu,Qiuyue Zheng,Jiang Man,Jijuan Cao
The sensitive and accurate detection of ochratoxin A (OTA) is crucial for public health due to its high toxicity. Herein, using Au nanoparticle (NP)-attached CdS/UiO-66-NH2 heterostructures as photoactive materials, a photoelectrochemical (PEC) aptasensor was presented for the ultrasensitive assay of OTA based on a competitive displacement reaction triggering the trans-cleavage ability of CRISPR/Cas12a. In this sensing strategy, methylene blue-labeled single-stranded DNA (MB-ssDNA) was immobilized on the Au NPs/CdS/UiO-66-NH2 electrode to accelerate the separation of the photogenerated carrier, thus producing a significantly increased PEC response. In the presence of OTA, it specifically bound with the aptamer (Apt) and resulted in the release of the activation chain, triggering the trans-cleavage characteristics of CRISPR/Cas12a. MB-ssDNA was cut randomly on the electrode surface to convert the PEC signal from the “on” to the “off” state, thereby achieving a quantitative and accurate detection of OTA. The CRISPR/Cas12a-derived PEC aptasensor exhibited excellent sensitivity and specificity, with a linear range from 100 to 50 ng/mL and a detection limit of 38 fg/mL. Overall, the proposed aptasensor could provide a rapid, accurate, and sensitive method for the determination of OTA in actual samples.
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高影响因子
RSC Advances
·
2020
·Vol. 11
·期 1
·48-56
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IF 3.119
Yingjie Hu,Yuxin Mei,Baining Lin,Xuhong Du,Fan Xu,Huasheng Xie,Kang Wang,Yonghua Zhou
The one-pot synthesis of methyl isobutyl ketone (MIBK) and methyl isobutyl methanol (MIBC) from acetone and hydrogen is a typical cascade reaction comprised of aldol condensation-dehydration-hydrogenation. Pd loss and aggregation during long term operation are typical problems in industrial application. In this paper, an active and stable catalyst was achieved with defective UiO-66 as a support for Pd, which was synthesized with the ratio 15 : 1 of ZrOCl2·8H2O to ZrCl4 as Zr-precursors. The resultant Pd catalyst remained active for at least 1000 h with a MIBK + MIBC selectivity of 84.87–93.09% and acetone conversion of 45.26–53.22% in a continuous trickle-bed reactor. Besides the increased Brønsted acid amount generated by the defect sites was favorable for the activity, the cavity confinement in the UiO-66 (R = 15 : 1) structure also efficiently prevented Pd loss and aggregation during the long term run. The contrast of the characterization of the fresh and used Pd/UiO-66 (R = 15 : 1) indicated that the deactivation of the catalyst was attributed to carbonaceous accumulation on the catalyst surface, which could be easily regenerated by calcination. This work supplied a new alternative for the design and utilization of industrial catalysts for MIBK and MIBC synthesis.
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高影响因子
JOURNAL OF CHROMATOGRAPHY A
·
2020
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IF 4.049
Jiayang Zhang,Birong Zhang,Xueping Dang,Zhiyong Song,Yuling Hu,Huaixia Chen
A Poly (3,4-ethylenedioxothiophene) (PEDOT)/UiO-66 composite was electrodeposited on an etched stainless-steel wire as head-space solid-phase microextraction (HS-SPME) coating. A robust, well controlled thickness, and uniform coating of metal organic framework composites can be realized by the electrodeposited strategy. The incorporated UiO-66 not only enhanced the uniformity and stability of the composite coating, but also effectively decreased the stacking phenomenon of PEDOT and improved its extraction efficiency, which was over 100 times higher than that of the PEDOT coating without UiO-66. The composite coating was used to enrich seven types of volatile organic compounds (VOCs) in ion-exchange resins, including methyl cyclohexane, benzene, toluene, ortho-xylene, styrene, para-xylene and divinyl-benzene. The results of adsorption isotherm analysis showed that π stacking effect played dominant role between the composite coating and VOCs in the extraction process. The composite coating was characterized by scanning electron microscopy, X-ray diffraction, Fourier transform infrared and thermogravimetric analysis, respectively. A determination method for seven kinds of VOCs was established by HS-SPME coupled with gas chromatography-flame ionization detection (GC-FID). Under the optimal experimental conditions, the detection linear range (LRs) was 0.09-100 ng mL −1 , and the detection limit (LODs) was 0.03-0.06 ng mL −1 (S/N = 3). The method was applied for the migration detection of VOCs in four types of ion-exchange resin, which showed satisfactory recovery (84.5-117.2%).
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高影响因子
CHROMATOGRAPHIA
·
2020
·Vol. 83
·期 9
·1121-1131
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IF 1.596
Pang Xiaoya,Liu Haiyan,Yu Huan,Zhang Miaomiao,Bai Ligai,Yan Hongyuan
A method for preparing a metal–organic framework (MOF)–polymeric monolith was established by in situ radical polymerization with derivatized UiO-66-2COOH and N- isopropylacrylamide (NIPAAm) as co-monomers. It was worth noting that the obtained monolith possessed characteristics of relatively uniform porous structure and a high surface area (84.16 m 2 g −1 ). The adsorption capacity of the monolith increased from 22.87 to 44.92 mg −1 due to the addition of MOF. The monolith was used as adsorbent and coupled with HPLC for the online purification and extraction of ursolic acid (UA) in medicinal plant. The limit of detection (LOD, S / N = 3) and the limit of quantification (LOQ, S / N = 10) were 0.17 μg mL −1 and 0.57 μg mL −1 , respectively; the relative standard deviation (RSD) of intra-day and inter-day assays for five plant samples were 1.00–3.67% and 2.43–5.76%, respectively; a good accuracy was demonstrated by the recovery of 92.2–103.28%. The results indicated that the MOF–polymer monolith was feasible for the online enrichment and purification of UA in plant.
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高影响因子
JOURNAL OF SEPARATION SCIENCE
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2019
·Vol. 42
·期 16
·2679-2686
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IF 2.516
Weixuan Yao,Zhefeng Fan,Suling Zhang
A zirconium terephthalate metal-organic framework-incorporated poly( N -vinylcarbazole- co -divinylbenzene) monolith was fabricated in a capillary by a thermal polymerization method. The optimized monolith had a homogeneous structure, good permeability, and stability. The monolith could be used for the effective enrichment of fungicides through π-π interactions, electrostatic forces, and hydrogen bonds. The potential factors that affect the extraction efficiency, including ionic strength, solution pH, sample volume, and eluent volume, were investigated in detail. The monolith-based in-tube solid-phase microextraction coupled with ultra-high-performance liquid chromatography and high-resolution Orbitrap mass spectrometry was performed for the analysis of five fungicides (pyrimethanil, tebuconazole, hexaconazole, diniconazole, and flutriafol) in environmental samples. Under the optimized conditions, the linear ranges were 0.005–5 ng/mL for pyrimethanil, 0.01–5 ng/mL for flutriafol, and 0.05–5 ng/mL for other fungicides, respectively, with coefficients of determination ≥0.9911. The limits of detection were 1.34–14.8 ng/L. The columns showed good repeatability (relative standard deviations ≤9.3%, n = 5) and desirable column-to-column reproducibility (relative standard deviations 5.3–9.4%, n = 5). The proposed method was successfully applied for the simultaneous detection of five fungicides in water and soil samples, with recoveries of 90.4–97.5 and 84.0–95.3%, respectively.
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高影响因子
Journal of Environmental Chemical Engineering
·
2016
·
IF 0
Fang Wang,Yong Tao Zhang,Yanli Xu,Xing Wang,Sunfeng Li,Hanbiao Yang,Xueting Liu,Fengyu Wei
N-K 2 Ti 4 O 9 /g-C 3 N 4 /UiO-66 ternary composites were successfully synthesized by a solvothermal method, and were characterized by powder X-ray diffraction, UV–vis diffuse reflectance spectroscopy, the valence band X-ray photoelectron spectroscopy, field emission transmission electron microscopy , photoluminescence emission spectra and N 2 adsorption-desorption. Photocatalytic activities of N-K 2 Ti 4 O 9 , g-C 3 N 4 , UiO-66, N-K 2 Ti 4 O 9 /g-C 3 N 4 binary composites and the ternary composites were investigated by the degradation of Rhodamine B (RhB) under visible light irradiation. The results show that the ternary composites exhibit higher photocatalytic activity as compared with the binary composites and the pure materials. The synergistically enhanced photocatalytic activity of the ternary composites is due to coupling direct solid-state Z-scheme N-K 2 Ti 4 O 9 /g-C 3 N 4 heterojunction with high adsorption capacity of UiO-66 for RhB.
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Journal of Materials Chemistry A
·
2025
·
IF 9.5
Fajie Hu,Danfeng Zhao,Rushuo Li,Yunqi Zhang,Tianyu Zhang,Xiubing Huang,Ge Wang
The hierarchical porous and chemical microenvironmental properties of Metal–Organic Frameworks (MOFs) have been emphasized in catalytic applications. In this work, after selectively removing ligands from frameworks of Ce-UiO-66 by monocarboxylic acid etching, they exhibit obvious mesoporous properties with essentially unchanged crystallinity. Distinguishing from other pore-making methods, the MOFs have abundant missing sites after etching, and Ni nanoparticles (NPs) can be efficiently anchored in the framework of defective Ce-UiO-66, resulting in the formation of Ce–O–Ni heterogeneous interfaces. The chemical environments of Ni NPs can be modulated through the Ce–O–Ni interfaces, and the metal–support interaction improves the charge densities between the active sites. The prepared catalysts showed high conversion and selectivity in the hydrogenation reaction of dicyclopentadiene, and also had good cycling performance. The present work provides new insights into the construction of hierarchical porous defective MOFs with abundant heterogeneous interfaces for hydrogenation reactions.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
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2025
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IF 13.2
Wenqi Zhao,Yue Qiao,Hang Jia,Yu Zhang,Enmao Zhang,Xigao Jian,Cheng Liu
The interfacial bonding between carbon fiber (CF) and the matrix in carbon fiber-reinforced high-performance thermoplastic (CFRHPTP) composites is weak, owing to the chemical inertness of the CF surface and nonreactivity of the thermoplastic resin. Hence, the applications of these composites are severely limited. In this study, a 2D GO/3D NH 2 -UiO-66 nanohybrid coating was hierarchically assembled via a two-step method. First, GO was assembled on CF (G-CF) via electrophoretic deposition to provide nucleation sites, and the NH 2 -UiO-66 was assembled in situ on the G-CF surface to obtain modified CF (G-N-CF) via electrochemical deposition. The chemical compositions, surface morphologies, and wettabilities of the CFs were systematically analyzed. Using poly(bisphthalazinone ether sulfone ketone) (PBPESK) as a matrix, a series of CF/PBPESK composites were prepared using G-N-CF, G-CF, and D-CF. The flexural strength and interlaminar shear strength of the G-N-CF-2/PBPESK composite increased by 28.5% and 48.3%, respectively, compared with those of the D-CF/PBPESK composite. The interfacial failure mechanism changed from adhesive failure to cohesive failure after treating CF with the 2D GO/3D NH 2 -UiO-66 nanohybrid coating. This study provides an effective strategy for the interphase design of CFRHPTP composites based on multiple physical and chemical interactions.
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高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Yuxin Yuan,Quanlan Liao,Tianxiang Zhao
Metal-organic frameworks (MOFs) have been hybridized with other functional materials, such as ionic liquids, covalent organic frameworks (COFs), and metallic nanoclusters, to fabricate composite materials. These composites possess the structural characteristics of their individual components and exhibit synergistic properties. In this work, we demonstrate the synthesis of core-shell structure UiO-66-NH 2 @PILs-x composite materials by encapsulating MOFs within ionic polymers (PILs) with varying thicknesses of PILs shell. These hybrid materials serve as bifunctional catalysts for the conversion of CO 2 into cyclic carbonates under solvent- and additive-free conditions through a synergistic catalytic effect facilitating the conversion of CO 2 into cyclic carbonates under solvent- and additive-free conditions through synergistic catalytic effect, exhibiting superior catalytic performance and excellent recyclability. This MOFs-based composite material provides a competitive approach for CO 2 catalytic conversion.
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高影响因子
Journal of Environmental Chemical Engineering
·
2025
·
IF 7.2
Mengyao Hua,Siyi Wang,Meng Cheng,Guangming Liang,Yafen Zhou,Lei Xu,Guofang Zhang
Photocatalysts UiO-66-(OH) 2 /MnO 2 -TiO 2 with intimate contact interfaces were successfully synthesized by impregnation methods and all of the composites were characterized by a variety of analytical techniques. The results indicated that MnO 2 and TiO 2 form a heterojunction and tightly attached to the surface of UiO-66-(OH) 2 , the generation of MnO 2 -TiO 2 heterojunction improved the catalyst electron-hole separation efficiency, and there was a strong electronic interaction between MnO 2 -TiO 2 and UiO-66-(OH) 2 in the composite. The synergistic combination of high adsorption capacity of UiO-66-(OH) 2 , and efficient interfacial charge transfer between UiO-66-(OH) 2 and MnO 2 -TiO 2 have a significant impact on the enhanced photocatalytic performance for formaldehyde removal. Meanwhile, the hydroxyl radicals (·OH) and superoxide radicals (·O 2 - ) also play a major role in removal of formaldehyde. The formaldehyde removal rate of 70UO/MnO 2 -TiO 2 (1 g 0.15 m 3 ) in self-made closed system under high pressure mercury lamp irradiation is 88.19 % within 5.5 h, if the removal time is extended to 24 h, the formaldehyde removal rate can reach 95.19 %, and the continuous photocatalytic reaction showed that the composite is a highly stable catalyst.
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高影响因子
MATERIALS RESEARCH BULLETIN
·
2024
·
IF 5.3
Qingmei Qiao,Yunlan Xu,Dengjie Zhong,Xihong Ke,Yuqin Yang,Hanlu Zeng
In order to enhance the carrier separation efficiency and redox ability of photoanode, a dual Z-scheme heterojunction Ce-UiO-66/g-C 3 N 4 /Bi 2 WO 6 /Ti photoanode was prepared and assembled with Cu cathode to form PFC. The characterization results show that Ce-UiO-66/g-C 3 N 4 /Bi 2 WO 6 uniformly distributed on the Ti substrate, with average crystallite size of 9.04 nm and average particle size of 33.05 nm, which provides sufficient reactive active sites for RhB degradation. The RhB degradation rate, P max , J sc , V oc and FF of the PFC were 90.9 % (90 min), 7.53 µW cm -2 , 0.152 mA cm -2 , 0.37 V and 0.134, respectively. The turnover frequency (TOF) for RhB degradation by the PFC reached 0.98 h -1 . Fermi energy level analysis shows that a double-Z heterojunction is formed between Bi 2 WO 6 and g-C 3 N 4 , and between Bi 2 WO 6 and Ce-UiO-66, which not only effectively separates photogenerated e - - h + , but also retains the high redox ability of the composite. Moreover, with the introduction of Ce-UiO-66, the composite photoanode has larger specific surface area and wider visible light absorption range. In addition, because of the built-in electric field, the photogenerated electrons can migrate to the surface of composite particles more easily and react with dissolved oxygen to generate more •O 2 - to participate in the degradation of RhB. This work provides a valuable reference for developing PFC photoanode with high efficiency and visible light response.
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