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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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2024
·Vol. 171
·期 4
·047503
·
IF 3.1
Zhengjie Zhang,Yiheng Zhang,Yangchun Li,Yurong Wang
An electrochemical sensor for the simultaneous detection of magnolol (MAG) and honokiol (HON) was constructed based on the metal-organic framework, UIO-66-NH2, and electroreduced carboxylated graphene oxide (ErGO-GOOH). The UIO-66-NH2@ErGO-COOH coating was characterized by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and electrochemical impedance spectroscopy. Cyclic voltammetry was applied to investigate the electrochemical behavior of MAG and HON on UIO-66-NH2@ErGO-COOH/GCE. The electroanalytical method for the simultaneous determination of MAG and HON was established using linear sweep voltammetry. Under optimal experimental conditions, a linear range of 0.05 ∼ 8 μM and limits of detection of 16 and 7.0 nm for MAG and HON, respectively, were obtained. The sensor exhibited good repeatability, reproducibility, stability and anti-interference ability. The sensor was successfully applied to the simultaneous detection of MAG and HON in urine and serum samples with good recovery.
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RENEWABLE ENERGY
·
2024
·
IF 9
Wenli Zhang,Jifei Liu,Hongwei Gu,Cheng Pan,Yifei Long,Qunpeng Cheng,Guozhi Fan
The metal-organic framework materials ZIF-8 and UiO-66-NH 2 , synthesized by hydrothermal methods, were characterized in detail and combined to catalyze the transfer hydrogenation of 5-hydroxymethylfurfural (5-HMF) to 2,5-di(hydroxymethyl)furan (2,5-DHMF) using isopropanol as the hydrogen source. The ZIF-8/UiO-66-NH 2 catalyst mixture exhibited abundant Lewis acid-base sites and a hierarchical multiporous structure with a large specific surface area (564.0 m 2 /g). The conversion of 5-HMF reached 98.2 %, and the selectivity and yield of 2,5-DHMF were 96.2 % and 94.5 %, respectively. The recycling performance of ZIF-8/UiO-66-NH 2 was also investigated, and the conversion of 5-HMF and selectivity of 2,5-DHMF significantly decreased to 78.4 % and 79.1 % in the second run, respectively. The loss of −NH 2 groups was found to be the main reason for the decrease in activity. However, the catalytic activity of the recovered catalyst can be almost completely restored by the addition of a small amount of fresh UiO-66-NH 2 and ZIF-8, and the conversion of 5-HMF and selectivity of 2,5-DHMF were increased to 89.4 % and 95.5 %, respectively. In the proposed reaction mechanism, Lewis acid-base sites play important roles and exhibit a synergistic catalytic effect in the selective conversion of 5-HMF to 2,5-DHMF.
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ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Ying Gao,Qinqin Chen,Xinhao Shen,Shuang Yao,Zhiwen Jiang,Sanjian Ma,Hailiang Yang,Juanhong Li,Zixia Lin,Xin Liu
Both the sluggish kinetics of Fe(II) regeneration and usage restriction of H2O2 have severely hindered the scientific progress of the Fenton reaction toward practical applications. Herein, a reduction strategy of activated hydrogen, which was used to simultaneously generate H2O2 and accelerate the regeneration of ferrous in a Fenton-like reaction based on the reduction of activated hydrogen derived from H2, was proposed. Two types of composite catalysts, namely, Pd/UiO-66(Zr)-2OH and Pd@UiO-66(Zr)-2OH, were successfully prepared by loading nano-Pd particles onto the outer and inner pores of UiO-66(Zr)-2OH in different loading modes, respectively. They were used to enhance the reduction of activated hydrogen. The characterization results based on the analysis of scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy revealed that the materials were successfully prepared. By using a trace amount of ferrous iron and without adding H2O2, trimethoprim (C0 = 20 mg·L–1), as a target pollutant, could be nearly 100% degraded within 180 min in the reaction system composed of these two materials. The cycle of iron and the self-generation of H2O2 were verified by the detection of ferrous H2O2 in the system. Density functional theory calculation results further confirmed that the pore-filled Pd0 NPs, as the main catalytic site for Pd@UiO-66(Zr)-2OH, could produce H2O2 under the combined action of hydrogen and oxygen. The Pd@UiO-66(Zr)-2OH system had excellent stability after multiple applications (at least 6 cycles), all of which resulted in 100% removal of trimethoprim. The degradation efficiency of the Pd/UiO-66(Zr)-2OH system for TMP gradually decreased from 97 to 80% after six cycles. The results of electron paramagnetic resonance combined with classical radical burst experiments revealed the degradation pathways in the reaction system with hydroxyl radicals and singlet oxygen as the main reactive oxygen particles.
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高影响因子
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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FOOD CHEMISTRY
·
2025
·
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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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 SOLID STATE CHEMISTRY
·
2021
·
IF 3.498
Meimei Zhou,Wei Zou,Xuemei Zhu,Huachen Ma,Pengbo Wang,Jiaxin Shang,Pingping Luo
UIO-66-NH 2 was successfully deposited on electrospun polyacrylonitrile (PAN) nanofibers treated by thermal oxidative stabilization (TOS) via a simple and effective in situ growth method. Owing to the formation of acridone rings, naphthyridinering rings and hydronaphthyridine rings during the TOS process, the thermally stabilized electrospun PAN (TSPAN) nanofibers were greatly improved in stability and heat resistance and could provide adequate nucleation points for MOFs growth, indicating an ideal MOFs deposition support without additional surface modifications. The results demonstrated that UIO-66-NH 2 crystals distributed relatively uniform and dense on the TSPAN nanofibers with mass loading up to 28.1 wt%. Compared with powdered UIO-66-NH 2 , the formed UIO-66-NH 2 @TSPAN nanofibers showed enhanced visible light driven photocatalytic activity towards reduction of Cr(VI) due to the improvement of visible light response, more excellent photothermal conversion ability and the increase of exposed active sites. The photocatalytic reduction rate of Cr(VI) over UIO-66-NH 2 @TSPAN was up to 93% within 180 min and the rate constant (k = 0.1362) was 2.3 times that of powdered UIO-66-NH 2 (k = 0.00576). Significantly, the mechanical flexibility and structural stability endowed the nanofibrous photocatalyst easy operation and outstanding reusable capability. The photocatalytic activity for Cr(VI) reduction still preserved 90% after five cycles. This work proposes a facile strategy for preparation of free-standing MOFs nanofibers and provides MOFs-based photocatalysts a new opportunitie for broad applications in water treatment.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2026
·
IF 9.1
Wei-Guang Yang,Xin-He Feng,Xuwen Wu,Zhong-Zhen Yu,Dongzhi Yang
Two typical chemical warfare agents—nerve agents and blister agents—pose a serious threat to human life. Under atmospheric conditions devoid of free water, however, the rapid degradation and complete elimination of these agents using anhydrous catalysts remain significant challenges. To overcome this limitation, a LiCl+AC-MOF composite catalyst with moisture-induced wetting surface is prepared by in-situ growing UiO-66-NH 2 on the activated carbon particles, and then confining LiCl crystallization in the nanocavities of UiO-66-NH 2 . In humid atmosphere (RH = 90%), the confined LiCl undergoes deliquescence within the UiO-66-NH 2 nanocavities, thereby generating a continuous wetting surface. This mechanism yields an impressive water uptake of 1.61 g g −1 , which significantly enhances the equilibrium water content at the gas-solid boundary of the composite catalyst. Leveraging the abundance of free water to the Zr sites, the composite catalyst facilitates the rapid hydrolytic degradation of the nerve agent simulant dimethyl 4-nitrophenyl phosphate with a half-life of 1.9 h at RH = 90%. For the blister agent simulant 2-chloroethyl ethyl sulfide, the catalyst not only cleaves the C S and C Cl bonds but also utilizes its wetting surface to accelerate the recombination of intermediate into final products (half-life = 0.4 min at RH = 70%). In summary, the highly efficient catalyst designed in this work spontaneously harvests atmospheric moisture to create a self-wetting surface. This distinctive surface chemistry enhances both the mass transfer of chemical warfare agent simulants and their subsequent active degradation at Zr sites, thereby substantially broadening the design scope for advanced chemical protective materials applicable to next-generation respirators and gas masks.
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Food Frontiers
·
2026
·Vol. 7
·期 4
·e70334
·
IF 6.3
Zongda Li,Yukun Zhang,Youning Zhang,Yu Zhang,Jiangxia Xu,Fanxing Meng,Minwei Zhang
Combining high-electroactive nanomaterial with enzyme immobilization, the development of the electrochemical biosensor is a frontier approach to improve the sensitivity and selectivity for the detection of organophosphorus pesticides (OPs). In this study, a core–shell nanostructure (Ag-HMPB@UiO-66) was prepared with the Ag-HMPB as a core and a UiO-66 forming the shell as an advanced platform for acetylcholinesterase (AChE) immobilization. The innovation lies in the synergistic integration of the excellent electron transfer capability of Ag-HMPB with the good structural stability of UiO-66. Based on Lewis acid–base theory, the form of Zr─O─P coordination bond could improve the efficiency of aptamer (Apt) immobilization (131.65 nM mg −1 ) compared with physical adsorption. Electrochemical analysis revealed that the as-prepared biosensor exhibited exceptional substrate affinity, with a low K m of 0.234 mM. Under optimized conditions, the biosensor exhibited sensitive detection of trichlorfon over a wide range (1 × 10 −13 to 2.5 × 10 −9 g L −1 ), with a low LOD of 0.44 pg L −1 (3σ/slope). Additionally, the biosensor can also be applied to the cucumber with good recovery (97.34% to 103.35%), as well as good storage stability and reproducibility. This provides a reliable and powerful tool for the trace detection of OPs in complex agricultural products.
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TALANTA
·
2026
·
IF 6.7
Wanyi Zhang,Chenyu Zhou,Hanbo Wang,Yuhan Chen,Tingting Xia,Xingguang Su
Quercetin, a potent natural antioxidant, is gaining widespread attention for its remarkable health benefits, including the prevention of cardiovascular diseases, allergies, diabetes, and cancer. As a promising functional food ingredient, there is an urgent need for fast, sensitive, and portable methods to monitor quercetin levels in various products. In this study, we present a portable dual-mode nanozyme-driven sensor based on cerium dioxide nanoparticle-anchored metal-organic framework (CeO 2 @UiO-66-NH 2 ) nanocomposite. This nanocomposite exhibits impressive oxidase-like activity and intrinsic fluorescence properties, enabling it to catalyze the oxidation of colorless N, N-diethyl-p-phenylenediamine to a pink product, which in turn quenches the fluorescence of CeO 2 @UiO-66-NH 2 at 458 nm via an inner filter effect (IFE). The presence of quercetin inhibits reactive oxygen species generation, thus attenuating the oxidation and restoring fluorescence. A paper-based fluorescent-colorimetric dual-mode sensing platform was established for quercetin detection, enabling rapid and visual evaluation without complex instruments. The proposed method exhibited a broad linear response range of 1-60 μM. The limits of detection for the colorimetric/fluorescent and paper-based colorimetric/fluorescent were 0.35, 0.27, 0.37, and 0.29 μM, respectively. This dual-mode sensor demonstrates excellent analytical sensitivity and selectivity, with successful application in real vegetable and juice samples, offering a reliable, efficient tool for quercetin monitoring in food and functional food ingredients.
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Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 5
·124516
·
IF 7.5
Bingkun Liu,Juncheng Guo,Hongda Huang,Yuhan Yang,Jingtao Zhang,Junling Zhang,Yonghui Zhang
Constructing a robust interfacial electric field is crucial for efficient spatial separation and directional migration of photogenerated carriers, which further boosts the performance of photocatalytic systems. In this study, a novel CF-supported SnS 2 /UiO-66-NH 2 high-low junction with intimate interface was fabricated via an in-situ solvothermal process. The optimal CF@SnS 2 /UiO-66-NH 2 -2 catalyst shows the best photocatalytic efficiency of 99.5% Cr(VI) removal at pH of 2.0 and nearly complete E. coli inactivation within 150 min, revealing its good photocatalytic redox capability. Moreover, the as-prepared composite possesses remarkable stability and desirable recycling performance. Mechanism analysis reveals that the intense internal electric field (IEF) and energy band bending are pivotal for promoting the separation and migration of charge carriers in the CF@SnS 2 /UiO-66-NH 2 high-low junction. This work offers new insights into the preparation and application of high-low junction photocatalysts.
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