CHEMICAL ENGINEERING JOURNAL
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2023
·
IF 15.1
Huilin Li,Jingying Yang,Xiaochun Hu,Ran Han,Shuo Wang,Mingfei Pan
Amantadine (AMD) is an antiviral drug used to treat animal-based infectious diseases such as avian influenza. However, its illegal use in animal-derived food industries endangers human health. Therefore, an efficient, portable, and visual sensor to detect AMD in food is crucial for ensuring food safety. A multifunctional nanocomposite NH 2 -UiO-66@PtNPs was exploited to design a smartphone-assisted fluorescence-colorimetric immunosensing microarray for multidimensional detection of AMD in animal-derived foods. Platinum nanoparticles (NPs) were immobilized on a Zr-based metal–organic framework (NH 2 -UiO-66). Pt NPs exhibited peroxidase-like activity, whereas NH 2 -UiO-66 stabilized Pt NPs and improved the colorimetric signal of the sensor. Moreover, the fluorescence ligand NH 2 -BDC in NH 2 -UiO-66 was released via alkaline hydrolysis, amplifying the fluorescence signal and improving detection sensitivity. The smartphone-assisted color recognition system accurately identified the color changes of the microarray. The immunocompetitive reaction of AMD and the antibody (Ab) in the microarray NH 2 -UiO-66@PtNPs@Ab 2 allowed the quantitative and visual detection of AMD in a wide concentration range (0.1–1000 ng/mL) with high sensitivity [limit of detection = 0.0022 ng/mL (fluorescence), 0.069 ng/mL (colorimetric), and 0.68 ng/mL (smartphone)]. This detection strategy was verified in AMD-spiked food samples with satisfactory recoveries (82.0–103.0%) and stability (RSD: ≤7.1%, n = 3), showing its great potential for visual screening and portable detection of other food contaminants.
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CHINESE JOURNAL OF CHEMICAL ENGINEERING
·
2023
·
IF 3.8
Xiaoxia Ye,Rixin Huang,Zhihong Zheng,Juan Liu,Jie Chen,Yuancai Lv
Membrane separation strategies offer promising platform for the emulsion separation. However, the low mechanical strength of membrane separation layers and the trade-off between separation flux and efficiency present significant challenges. In this study, we report a CFM@UiO-66-NH 2 membrane with high separation flux, efficiency and stability, through utilizing a robust anti-abrasion collagen fiber membrane (CFM) as the multifunctional support and UiO-66-NH 2 by an in-situ growth as the separation layer. The high mechanical strength of the CFM compensated for the weakness of the separation layer, while the charge-breaking effect of UiO-66-NH 2 , along with the size sieving of its constituent separating layers and the capillary effect of the collagen fibers, contributed to the potential for efficient separation. Additionally, the CFM@UiO-66-NH 2 membrane exhibited superhydrophilic properties, making it suitable for separating oil-in-water microemulsions and nanoemulsions stabilized by anionic surfactants. The membrane demonstrated remarkable separation efficiencies of up to 99.960% and a separation flux of 370.05 L m –2 h –1 . Moreover, it exhibits stability, durability, and abrasion resistance, maintaining excellent separation performance even when exposed to strong acids and alkalis without any damage to its structure and performance. After six cycles of reuse, it achieved a separation flux of 417.97 L m –2 h –1 and a separation efficiency of 99.747%. Furthermore, after undergoing 500 cycles of strong abrasion, the separation flux remained at 124.39 L m –2 h –1 , with a separation efficiency of 99.992%. These properties make it suitable for the long-term use in harsh operating environments. We attribute these properties to the electrostatic effect resulting from the amino group on UiO-66-NH 2 and its in-situ growth on the CFM, which forms a size-screening separation layer. Our work highlights the potential of the CFM@UiO-66-NH 2 membrane as an environmentally friendly size-screening material for the efficient emulsion wastewater separation.
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
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2023
·
IF 6.1
Jiayi Chen,Zehao Yang,Jianpeng Zhang,Xing Shen,Zhenlin Xu,Xiangmei Li,Hongtao Lei
Herein, the UiO-66-NH2@quantum dot (NU66@QD) was synthesized with excellent fluorescence intensity and biocompatibility, which was used to develop a multiple immunochromatographic assay (ICA) for the detection of aflatoxin B1 (AFB1), fumonisin B1 (FB1), deoxynivalenol (DON), T-2 toxins (T-2), and zearalenone (ZEN) in cereals and feed. Five monoclonal antibodies and NU66@QD were efficiently labeled by a one-step mixed method to form a multiple detection probe. The limits of detection of the proposed NU66@QD-ICA for AFB1/FB1/DON/T-2/ZEN were 0.04/0.28/0.25/0.09/0.08 μg/kg. The recoveries ranged from 82.83–117.44%, with the coefficient of variation from 2.88–11.80%. A parallel analysis in 35 naturally contaminated cereal and feed samples was confirmed by LC-MS/MS, and the results showed a good correlation (R2 > 0.9), indicating the practical reliability of the multiple NU66@QD-ICA. Overall, the introduction of the novel nanomaterial NU66@QD provides a highly sensitive and efficient multiplex detection strategy for the development of ICA.
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PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2021
·Vol. 45
·期 20
·9264-9273
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IF 3.591
Chaowei Wang,Zhe Liu,Guangfa Hu,Ruimin Gao,Jianshe Zhao
In this study, the novel magnetic core–shell composites Fe3O4@UiO-66-HPA, consisting of magnetic Fe3O4@UiO-66 and vanadium-substituted Keggin-type heteropolyacid active species supported by Zr-MOF, were successfully prepared via a one-pot method and fully investigated using FT-IR, XRD, SEM, TEM, TEM-EDX, ICP, VSM and N2 adsorption–desorption isotherms. The synthetic composites were employed as catalysts in an ODS system of simulated fuel under oxygen. The catalyst Fe3O4@UiO-66-PW9V3 exhibits the supreme catalytic performance in this work, with sulfur removal of 99.85% and a TOF value of 31.16 h−1 under optimal reaction conditions (0.2 g catalyst mass, 60 °C reaction temperature, 500 rpm stirring speed, 1 L min−1 oxidant quantity and 180 min reaction time), and can also be recycled ten times without apparent loss of catalytic performance. Furthermore, the kinetic study shows that the ODS process accords with the pseudo-first-order model.
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CHEMICAL ENGINEERING JOURNAL
·
2020
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IF 10.652
Dechao Wang,Yangyang Xin,Xiaoqian Li,Feng Wang,Yudeng Wang,Weirui Zhang,Yaping Zheng,Dongdong Yao,Zhiyuan Yang,Xingfeng Lei
Porous liquids (PLs), an emerging class of liquid materials with permanent porosity and good fluidity, have shown great potential in gas capture and separation. However, directly turning metal–organic frameworks (MOFs) into type 1 PLs via post-synthetic modification (PSM) strategy with corona-canopy species has not been reported till now. Moreover, challenges including reducing the cost and simplifying the synthesis process are daunting. In present study, we propose a universal approach to turn UiO-66 into PLs via post-synthetic modification strategy with core-corona-canopy structure using organosilane (OS) corona and oligomer canopy species. The ionically-tethered canopy species endow UiO-66 with good liquid-like behaviors at room temperature. CO 2 and N 2 adsorption–desorption behaviors revealed that PLs possessed great potential in CO 2 selective adsorption separation. Meanwhile, the enhanced CO 2 selective capture sites were determined. As a proof-of-concept, the as-prepared UiO-66-liquid-M2070 PL was incorporated into Pebax-1657 polymer matrix to prepare mixed matrix membranes (MMMs). The excellent dispersion ability, porous structures, and corona-canopy species contributed to the enhanced CO 2 selective permeation. Therefore, the CO 2 permeability and CO 2 /N 2 selectivity of MMM P-UiO-66-liquid-50 increased by 396.5% and 81.3%, respectively, compared with that of pure Pebax membrane, showing attracting prospect in membrane separation. Moreover, the generality of this PSM strategy was confirmed using other different types of canopy species. Remarkably, this PSM strategy could be applied to synthesize other types of advanced porous materials (APMs)-based (e.g., covalent organic frameworks (COFs)) PLs by utilizing the rich library of oligomer species, thus undoubtedly advancing the applications of porous liquids in gas storage and separation.
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DESALINATION
·
2020
·
IF 7.098
Haojie Zeng,Zongxue Yu,Liangyan Shao,Xiuhui Li,Meng Zhu,Yuchuan Liu,Xiaofang Feng,Ximei Zhu
A novel photocatalytic membrane was prepared by using graphene oxide (GO), UiO-66-NH 2 and Ag 2 CO 3 as basic materials on the surface of PVDF membrane by vacuum filtration self-assembly. The prepared Ag 2 CO 3 @UiO-66-NH 2 /GO (AgCO@UiO/GO) membrane was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The AgCO@UiO/GO membrane possessed the photocatalytic effects, which significantly enhanced the separation effect of dyes and Cr(VI) wastewater. In particular, the AgCO@UiO/GO membrane can achieve complete removal of MB , RB ,MR and Cr(VI) under light conditions maintaining the fluxes during filtration process reach about 50 L · m −2 · h −1 . In addition, after long-time experiments, the AgCO@UiO/GO membrane retained a higher removal rate and maintained a high flux under light conditions than without light for all dyes and Cr(VI). The unique structure of AgCO@UiO/GO membrane with a large number of screening structures and photocatalytic activity resulting a better removal rate for pollutants and reducing membrane fouling . Furthermore, the AgCO@UiO/GO membrane shows a great potential in improving membrane removal performance and a solution to balance trade-off effect.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2019
·
IF 4.175
Ying Zhang,Jie Xiong,Chao Chen,Qizheng Li,Jingjing Liu,Zhicheng Zhang
The novel humidity sensor , fabricated from inorganic electrolyte doped porous metal-organic framework composite (denoted as LiCl@UiO-66-NH 2 ), is reported in the present work. The humidity sensing properties of LiCl@UiO-66-NH 2 composites have been investigated. The much higher comprehensive sensing properties of composites are obtained in LiCl@UiO-66-NH 2 with 12.5 wt% LiCl. It shows the excellent linearity (R 2 = 0.994) in a broad relative humidity (RH) range. The impedance modulus of LiCl@UiO-66-NH 2 (12.5 wt%) decreases nearly four orders of magnitude from 33% RH to 95% RH at 100 Hz. Besides, the LiCl@UiO-66-NH 2 (12.5 wt%) humidity sensor exhibits fast response (6s) and recovery (18s) speed and excellent long-term stability. The sensing mechanism was discussed through the investigation of complex impedance curves. These results suggest that LiCl@UiO-66-NH 2 have the potential application in humidity sensing. Our work offers a promising strategy for the fabrication of high performance humidity sensors.
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JOURNAL OF HAZARDOUS MATERIALS
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2019
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IF 7.65
Chun-Yang Li,Jing-Min Liu,Zhi-Hao Wang,Shi-Wen Lv,Ning Zhao,Shuo Wang
Aflatoxins have been a hot topic in the field related into public health and ecosystem protection, and great effort has been made in developing of adsorptive materials for effective probing the target aflatoxins. Conventional materials, like metal-organic frameworks (MOFs) showed promising application in separation science. However, the cumbersome separation process, competitive adsorption are also major challenges. Regarding this, a novel magnetic micro-composite denoted as Fe 3 O 4 @UiO-66-NH 2 @MON with core-shell structure was constructed. The core of Fe 3 O 4 microspheres was coated with MOFs crystals, and then microporous organic network (MON) was introduced onto the surface of Fe 3 O 4 @UiO-66-NH 2 through a sonogashira coupling reaction. It exhibited good magnetic separation ability, which effectively simplified the pre-treatment steps. The proposed method possessed excellent selectivity and sensitivity, with detection limits in the range of 0.15-0.87 μg L −1 combination with HPLC analysis. More importantly, the MON coating significantly improved the hydro-stability of whole adsorbents, thus enhancing the adsorption efficiency and favoring the practical application of the materials. The developed Fe 3 O 4 @UiO-66-NH 2 @MON-based solid extraction method has been well-applied for real sample analysis, with the recovery of 87.3%–101.8%. We believe the newly-constructed hybrid nano-adsorbents hold great potential in further application in various analytical methods for different target analytes.
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PubMed
高影响因子
FUEL
·
2019
·
IF 5.128
Lulu Yan,Tingting Duan,Tingting Huang,Bingbing Zhao,Yu Fan
This article proposes a novel strategy for producing highly dispersed H 3 PW 12 O 40 (HPW) on metal-organic frameworks (MOFs) via the anchoring action of amino groups originating from 2-amino terephthalic acid (APTA) in the MOF ligand. Under this method, amino groups are introduced into the linker of UiO-66 materials through a one-pot synthesis to disperse supported HPW, which has a negligible impact on the crystal structure of UiO-66. The acidic densities in the HPW/UiO-66 catalysts are effectively modified by adjusting the molar APTA/PTA (terephthalic acid) ratio in the mixed ligand and HPW loading. Consequently, the dispersion and stability of supported HPW are significantly enhanced, which make the as-prepared catalyst with 40 wt% of HPW present superior sec -butyl acetate (SBAC) yield (38.6 wt%) and selectivity (98 wt%) for the direct esterification of olefins. This strategy provides a new approach for preparing supported HPW with high dispersion and stability to be applied in olefin esterification.
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ACS Applied Materials & Interfaces
·
2019
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IF 8.456
Wen Li,Kuncan Wang,Junjie Huang,Xiao Liu,Dun Fu,Jiale Huang,Qingbiao Li,Guowu Zhan
Metal–organic frameworks have been exploited as excellent solid precursors and templates for the preparation integrated nanocatalysts with multicomponent and hierarchical structures. Herein, a novel synthetic protocol has been developed to fabricate versatile Zr-based solid solutions (such as ZnO–ZrO2, Co3O4–ZrO2, and CuO–ZrO2) via pyrolysis of Schiff base-modified UiO-66 octahedrons (size <100 nm), which were then utilized as efficient catalysts for CO2 hydrogenation. The Schiff base serves as an effective bridge to dope secondary metal ions into UiO-66 frameworks with controlled amounts of 0.13–8.8 wt %, which are initially hard to achieve. Interestingly, by simply changing the loading metal ions, the selectivity of C1 hydrogenation products can be facilely tuned. For instance, the maximum CO2 conversion of ZnO–ZrO2, Co3O4–ZrO2, and CuO–ZrO2 solid solutions were 5.8, 11.4, and 22.5%, with the main product selectivity of 70% CH3OH, 92.5% CH4, and 86.7% CO, respectively. Moreover, in situ diffuse reflectance infrared Fourier transform spectra characterization reveals that the significant difference in C1 product selectivity is mainly determined by the balance of *HCOO, *CH3O, and *CO intermediate species over the Zr-based solid solutions.
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Journal of Materials Chemistry A
·
2018
·Vol. 6
·期 24
·11337-11345
·
IF 9.931
Wei-Ming Liao,Jian-Hua Zhang,Zheng Wang,Shao-Yun Yin,Mei Pan,Hai-Ping Wang,Cheng-Yong Su
Electron-deficient Ru/Rh half-sandwich units are optoelectronical, stereochemical, and redox and catalytically active in nature. Four different species of these units were designed and successfully incorporated into UiO-67 frameworks by post-synthetic exchange (PSE) method and employed for photocatalytic H2 evolution and CO2 reduction. Among them, the PSE-MOF catalysts containing [M–OH2] (M = Rh or Ru) groups show higher photocatalytic activity than those with [M–Cl], providing a new example of the exploitation of H2O molecules as small ancillary ligands for the construction of Ru/Rh half-sandwich units and subsequent incorporation into MOFs as photocatalytic centers. The application of TEOA (triethanolamine) and DMA (N,N-dimethylaniline) as sacrificial agents leads to different catalytic mechanisms and durations. A long-term hydrogen evolution lasting for 174 h without significant decrease in efficiency was achieved in the RhOH2@UiO-DMA system, showing the advantage of PSE-MOFs as highly stable photocatalytic platforms with superior self-protective properties.
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SENSORS AND ACTUATORS B-CHEMICAL
·
2019
·
IF 6.393
Xin Xiong,Yao Zhang,YinFang Wang,HaiFeng Sha,Nengqin Jia
By virtue of the metal organic framework UiO-66-NH 2, an ingenious electrochemiluminescence immunosensor was successfully constructed for subtle exploration of the breast cancer biomarker CA 15-3. In this protocol, Ru(bpy) 3 Cl 2 ·6H 2 O (Ru(bpy) 3 2+ ), as a conventional luminescent reagent, provides a stable and strong luminescent signal. The UiO-66-NH 2 serves as a carrier to provide a large specific surface area for enhancing the electrochemical luminescence signal response of Ru(bpy) 3 2+ . UiO-66-NH 2 , Ru(bpy) 3 2+ are fixed together with Nafion membrane, and CA 15-3 antibody is covalently conjugated onto the membrane through the amide reaction. Ru(bpy) 3 2+ @UiO-66-NH 2 is used as the detection system. The experimental results reveal that the ECL signal decreased obviously after the CA 15-3 antigen molecule is captured on the immunosensor, with the capture of manifesting the principle of electrochemical luminescence quenching detection. Under optimal conditions, the sensor is sensitive and selective for detecting CA 15-3 with the detection range from 5 × 10 −4 to 5 × 10 2 U mL -1 and the low LOD (1.7705 × 10 -5 U mL -1 ). Furthermore, multiple experiments elucidate that the as-prepared sensor could be used for susceptibly detect CA 15-3 in actual samples, which has underlying application prospects in biological analysis.
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