ELECTROCHEMISTRY COMMUNICATIONS
·
2025
·
IF 4.2
Jie Zhang,Yuanying Shi,Liming Liu,Bin Qiu,Yue Tian,Guodong Guo
In this work, a novel homogeneous electrochemical (HEC) sensing strategy was developed for carcinoembryonic antigen (CEA) detection, addressing limitations of traditional electrochemical platforms that necessitate complex electrode modifications and receptor immobilization protocols. This approach integrates platinum nanoparticle-loaded UiO-66 metal-organic frameworks (Pt/UiO) as an oxidase-like nanozyme with CEA-specific aptamer (Apt) as recognition element, establishing a target-responsive catalytic mechanism. In solution-phase operation, the Pt/UiO nanozyme facilitates the oxidation of 1,2-diaminobenzene into electroactive diaminophenazine (DAP), generating measurable reduction current at unmodified electrode. Apt adsorption onto Pt/UiO surfaces effectively inhibits this enzymatic activity through steric hindrance, resulting in current suppression proportional to Apt coverage. The presence of CEA induces specific Apt-CEA binding, resulting Apt away from the nanozyme surface and restoring catalytic activity in a concentration-dependent manner. Optimization of experimental parameters (e.g., nanozyme concentration, incubation time) enabled the sensor to achieve a detection limit of 3 pg mL −1 with a linear range spanning 0.01–11 ng mL −1 , demonstrating potential for point-of-care applications in tumor biomarker analysis.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Jinlong Li,Zihuan Zhao,Qihang Wei,Hongman Hou,Gongliang Zhang,Jingran Bi
This study integrates UiO-66-COOH metal–organic frameworks (MOFs) with pectin (Pec) to precisely release potassium cinnamate (PC) to develop a pectinase-responsive active fruit-preservation system (UiO-66-COOH@PC/Pec). Carboxylated UiO-66 with nanoporosity was fabricated to achieve a high loading amount of PC (235 mg·g −1 ) via the synergistic effects of hydrogen bonding, as shown by the loading kinetics and reduced density gradient analyses. A gatekeeper was established by grafting Pec onto the surface of the MOF (UiO-66-COOH@PC/Pec), thereby “locking” PC to prevent leakage. Moreover, an enzyme-responsive controlled-release behavior was developed under pectinase stimulation, achieving up to 95 % PC release within 9 h through Fickian diffusion and only 25.3 % in enzyme-free conditions by non-Fickian diffusion and matrix erosion. With significant long-term inhibiting activity against both bacteria and fungi, UiO-66-COOH@PC/Pec successfully extended the shelf life of strawberries from 2 to 5 days at 25 °C. Moreover, UiO-66-COOH@PC/Pec exhibited good water solubility and negligible toxicity, indicating that it can be easily removed from fruit surfaces and offers high consumer acceptance. These results provide a novel MOF-based controlled-release strategy for smart food-packaging applications.
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JOURNAL OF MEMBRANE SCIENCE
·
2025
·
IF 9
Ziheng Li,Fengting Yao,Yan Dai,Xuehua Ruan,Xiaobin Jiang,Xuemei Wu,Wenji Zheng,Gaohong He
Metal-organic frameworks (MOFs) offer exceptional pore tunability for targeted separations. Moving beyond conventional defect engineering which often sacrifices selectivity for permeability, we propose to construct functionalized defects that synergistically integrate hierarchical low-resistance gas transfer pathways with tailored ultra-CO 2 -philic molecular domains. This strategy is achieved by in-situ embedding β-cyclodextrin (β-CD) as a multifunctional modulator during the crystallization of NH 2 -UiO-66 (NUiO). The macrocyclic cavities of β-CD induced structural defects cooperatively optimize the pore architecture of NH 2 -UiO-66, significantly enhancing gas permeability. Concurrently, exposed Zr 6 clusters and hydroxyl groups from β-CD enhance CO 2 adsorption capacity. Furthermore, defect-induced incomplete coordination promotes hydrogen bonding between the β-CD@NUiO and Pebax, improving interfacial compatibility for MMMs. The prepared β-CD 20 @NUiO MMM at 5 wt.% filler loading exhibits a CO 2 permeability of 125.5 Barrer and a CO 2 /N 2 selectivity of 112.4, exceeding the 2019 McKeown upper bound. The in-situ construction of defects via functional molecules transcends the limitations of single-parameter optimization for mass transfer pathways and active sites in porous materials, establishing a universal design principle for multifunctional coupled separation materials.
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高影响因子
FOOD CHEMISTRY
·
2025
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IF 9.8
Yehong Han,Ruiyang Ma,Juntao Wang,Hongyuan Yan,Yufei Shan,Zihan Liu,Zhi Wang
In this study, for the effective determination of fipronil and ethiprole residues in milk, a new analytical approach, which was based on a tip solid-phase extraction (TSPE) by using a newly prepared ternary deep eutectic solvent-functionalized UiO-66 (TDES@UiO-66) as the adsorbent and HPLC-UV detection, was developed. The method integrated the advantages of both the high adsorption capability of the TDES@UiO-66 and the high efficiency of the TSPE, and enabled a rapid extraction of fipronil and ethiprole from milk samples within 8 min by utilizing only 3.0 mg of TDES@UiO-66 adsorbent. The developed method demonstrated an excellent analytical performance, including good linearity (linear rang: 0.02–10 μg/mL; r : 0.9990–0.9997), high precision (relative standard deviations: ≤ 9.9 %), good accuracy (recoveries: 91.1 %–109.8 %), and good sensitivity (limits of quantification: 0.011–0.018 μg/mL). This study provides a rapid and practical approach for the detection of fipronil and ethiprole in different milk samples.
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PubMed
高影响因子
Molecular Catalysis
·
2024
·
IF 3.9
Basiru O. Yusuf,Sulayman A. Oladepo,Saheed A. Ganiyu,Abdul Malik P. Peedikakkal
Metal-organic frameworks (MOFs) are excellent for immobilizing guest active species due to their high surface area and porosity. In this study, CuO/UiO-66 catalysts with varying amounts of CuO were successfully synthesized and used for converting waste cooking oil (WCO) to biodiesel. The catalysts were characterized using N 2 adsorption-desorption, XRD, NH 3 -TPD, SEM, TEM, TGA and FTIR. The biodiesel was characterized using NMR and GC–MS. The results showed that CuO/UiO-66 displayed high catalytic activity due to the synergistic effect between UiO-66 and copper oxide in the composite. Under optimum reaction conditions, we achieved a 90.1 % conversion with the 7 %CuO/UiO-66 catalyst. This catalyst also displayed good stability and reusability with a conversion of 81.06 % after three cycles. Our kinetic studies revealed a pseudo-first-order kinetics, with 32.26 kJ/mol in activation energy, consistent with a chemically controlled reaction.
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高影响因子
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2024
·Vol. 171
·期 3
·037526
·
IF 3.1
Deyong Kang,Shanbao Ma,Qiaoling Zheng
Squamous cell carcinoma antigen (SCCA) is an important biomarker in the diagnose of cancer, so developing effective methods for its detection is of great significance. In the present work, a novel sandwich-like electrochemical immunosensing assay (STEM) of SCCA was constructed by preparing gold nanoparticle/reduced graphene-oxide (Au NPs/rGO) to immobilize primary antibody (PAb) of SCCA and UIO-66-NH2 MOFs structure to immobilize second antibody (SAb) and electroactive toluidine blue (Tb) probe. In this designed STEM assay, the prepared Au NPs/rGO nanohybrid offers the advantages in large surface area and conductivity as carrier, and UIO-66-NH2 provided an ideal platform to accommodate SAb and a large number of Tb molecules as signal amplifier. In the existence of SCCA, the current peaks of Tb from the formed STEM structure increase with the increase of SCCA level. After optimizing the related control factors, a wide linear range (0.01 pg ml−1 and 15.0 ng ml−1) and very low detection limit (0.003 pg ml−1) of SCCA was achieved, it's thus expected the designed STEM strategy has important applications for the detection of SCCA.
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APPLIED SURFACE SCIENCE
·
2025
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IF 6.9
Fajie Hu,Rushuo Li,Danfeng Zhao,Xiubing Huang,Ge Wang
The hydrogenation of dicyclopentadiene (DCPD) to synthesize tetrahydrodicyclopentadiene (THDCPD) is one of the key processes for the preparation of high-energy–density fuels, and the development of low-temperature and high-activity Ni catalysts is still challenging. In this work, hierarchical porous (HP) Ce-UiO-66 loaded Ni nanoparticles (NPs) catalysts were prepared based on the soft template method and liquid-phase in situ reduction method. The introduction of mesopores into Ce-UiO-66 can effectively enhance the transfer and adsorption of the substrate, and Ni NPs act as the main active centers. Furthermore, the modulation of the electronic structure of Ni NPs and the promotion of Ce-Ni interaction were effectively achieved by changing the in-situ deposition conditions. With a low loading of 3 wt% Ni NPs, the prepared 3Ni/HP-UiO-66 catalysts could achieve the observed complete DCPD conversion and 100 % selectivity of THDCPD within 1 h and retained good cycling stability. The results demonstrated preferential adsorption and hydrogenation of the norbornene ring, confirming the reaction pathway of the 3Ni/HP-UiO-66 catalyst for the hydrogenation of DCPD. The present work provides a guidance for exploring and designing non-noble metal catalysts for the hydrogenation of olefins and aromatics.
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JOURNAL OF CHROMATOGRAPHY A
·
2016
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IF 3.926
Saichai Lin,Ning Gan,Yuting Cao,Yinji Chen,Qianli Jiang
In this paper, a novel dispersive solid phase extraction (dSPE) adsorbent based on aptamer-functionalized magnetic metal-organic framework material was developed for selective enrichment of the trace polychlorinated biphenyls (PCBs) from soil sample. Firstly, we developed a simple, versatile synthetic strategy to prepare highly reproducible magnetic amino-functionalized UiO-66 (Fe 3 O 4 @PDA@UiO-66-NH 2 ) by using polydopamine (PDA) as covalent linker. Then amino-functionalized aptamers which can recognize 2,3′,5,5′-tetrachlorobiphenyl (PCB72), 2′,3′,4′,5,5′-pentachlorobiphenyl (PCB106) were covalent immobilized on UiO-66-NH 2 through coupling reagent of glutaraldehyde. Aptamer-functionalized adsorbent (Fe 3 O 4 @PDA@UiO-66-Apt) can specifically capture PCBs from complex matrix with high adsorption capacity based on the specific affinity of aptamer towards target. Moreover, the adsorbent can be easily isolated from the solution through magnetic separation after extraction. Afterwards, the detection was carried out with gas chromatography tandem mass spectrometry (GC–MS). The selective dSPE pretreatment coupled with GC–MS possessed high selectivity, good binding capacity, stability, repeatability and reproducibility for the extraction of PCBs. Furthermore, the adsorbent possessed good mechanical stability which can be applied in replicate at least for 60 extraction cycles with recovery over 80%. It provided a linear range of 0.02–400 ng mL −1 with a good correlation coefficient (R 2 = 0.9994–0.9996), and the limit of detection was found to be 0.010–0.015 ng mL −1 . The method was successfully utilized for the determination of PCBs in soil samples.
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高影响因子
CHEMOSPHERE
·
2022
·
IF 8.943
Yuhan Wang,Chang Liu,Chao Wang,Qing Hu,Longzhen Ding
Developing synergistic systems and taking environmental risks into account are two necessary aspects of being considered to remove persistent organic pollutants efficiently. Thus, a combined catalytic system uniting the Fenton-like process and simulated solar-light photocatalysis has been constructed. Moreover, a series of NiCo 2 O 4 /HP-UiO-66 catalysts (yNiCo-DUx) were also fabricated to improve tetracycline (TC) removal efficiency. The NiCo 2 O 4 nanoparticles (NPs) and hierarchically porous metal-organic frameworks (HP-MOFs) were synthesised using one-step calcination. The Z-scheme structure of the catalysts was confirmed by ESR, XPS, DRS, time-resolved PL (TR-PL) spectra and the quenching experiments. The NiCo 2 O 4 nanoparticles could be embedded and fixed into the defects of the MOF structure, and the leaching of toxic metals was also significantly suppressed. In the optimal reaction condition with 15NiCo-DU50, sunlight, and peroxymonosulfate (PMS), the total removal efficiency of TC could reach 98.5% within 8 min of irradiation, and the highest % RSE could reach 11.2%. Moreover, the corresponding reaction rate was 28.7, 3.6 and 1.3–10.2 times higher than photocatalysis, Fenton-like processes and other catalysts. Furthermore, the possible degradation mechanism, generation of reactive species and PMS excitation pathways were also investigated in depth. The present study sheds light on the fabrication of HP-MOFs based catalysts and the combination of various methods to eliminate organic pollutants.
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高影响因子
NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 27
·13047-13053
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IF 3.925
Feng Xu,Chao Liu,Jia-Xin Li,Cai-Zhen Zhan,Qi-Ning Xun,Wen-Shen Zhang,Wen-Fang Xing,Gang-Gang Chang
γ-Valerolactone (GVL) is an important lignocellulosic platform molecule with huge potential for various industrial and chemical applications, which is usually produced using levulinic acid (LA) or its esters as raw materials. However, a two-step reaction process in which hydrogenation of the carbonyl groups on metal sites and subsequent lactonization catalyzed by acidic sites over multiple catalysts has generally been needed to realize this synthesis. In this work, a hierarchically multifunctional single catalyst of Ru/phosphotungstic acid/hierarchically porous UiO-66 (Ru/HPW/HP-UiO-66), simultaneously integrated with acidic and metal sites, has been fabricated via a simple strategy and successfully applied in the one-pot synthesis of GVL using methyl levulinate (ML) as the raw material. The hierarchically porous and nanosized (∼15 nm) HP-UiO-66 can not only provide sufficient space for the mass transfer of substrates but also favors the loading of bulk HPW molecules, which can effectively mediate the catalytic activities and stability of Ru NPs using the confined pore effect of UiO-66 and the strong interaction between HPW and Ru. When applied in the one-pot synthesis of GVL, the hierarchical Ru/HPW/HP-UiO-66 catalyst showed excellent catalytic activity (>97% yield) and stability (maintained after 7 successive cycles) for GVL. More importantly, the hierarchical catalyst also exhibited an extraordinary performance in the hydrogenation of different unsaturated hydrocarbons in aqueous solution. It is expected that our study offers a novel route to biomass upgrades involving metal/acid bifunctional synergistic catalysts.
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ENVIRONMENTAL RESEARCH
·
2025
·
IF 7.7
Yuxuan Zhao,Yueli Wen,Xiaonuo Xu,Maohong Fan,Shiyun Guo,Zhiju Chen,Xiaoxiao Zhao,Bin Wang,Wei Huang
The heavy metals discharged from electroplating wastewater, represented as copper and chromium ions, is harmful to aquatic lives and human beings, and will break the ecological balance. In this work, magnetic hybrid porous structure adsorbent of Fe 3 O 4 @SiO 2 -UiO-66-EDTA is prepared for recycling copper and chromium ions. The adsorbent exhibits a maximum adsorption capacity of 212.10 mg/g for Cu(II) and 118.10 mg/g for Cr(VI). Notably, it shows excellent regenerability of 87.12% after 5 cycles. The adsorption of Cu(II) and Cr(VI) on Fe 3 O 4 @SiO 2 -UiO-66-EDTA follows the pseudo-second-order model, where chemical adsorption is dominant and it occurs spontaneously and exothermally. Based on XRD, FTIR, XPS, and DFT calculations, the adsorption mechanisms are driven by electrostatic attraction, chelation, and redox reactions. This work provides a novel and promising strategy for designing highly efficient adsorbents, paving the way for more effective treatments of electroplating wastewater contaminated with Cu(II) and Cr(VI).
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Xiaoxia Liang,Jiakang Duan,Yu Tian,Yue Han,Zewan Qin,Huixia Zhu,Yating Lu,Dongyu Nie,Yingna Guo,Xia Yang
AgCl/Ag 0 shows great promise for the removal of environmental pollutants, while its photocatalytic performance is still a great challenge on account of the agglomeration. Herein, orientational deposited and octahedral AgCl/Ag 0 were obtained by etching the UiO-66-NH 2 template for the first time. The 0.35:1–AgCl/Ag 0 exhibited outstanding efficiency in the degradation of Diazinon (DZN), which was closely 300 times than that of UiO-66-NH 2 and 0.35:1–AgCl@Ag 0 prepared without a template. Its bigger surface area provided more active sites to promote mass transfer efficiency and large amounts of •OH and 1 O 2 were fabricated to offense specific positions of DZN determined through Fukui function. Meanwhile, a high removal rate of 91.0 % was obtained after 5 recycles. Finally, the results of HPLC-MS, T.E.S.T., TOC and IC indicated all intermediates had less toxicity than DZN and were rapidly mineralized. Our work developed a new strategy for designing superb performance AgCl/Ag 0 photocatalysts.
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