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ANALYTICAL SCIENCES · 2024 ·Vol. 40 ·期 6 ·1081-1087 · IF 1.8

Sandwich-type electrochemical immunosensing of CA125 by using nanoribbon-like Ti3C2Tx MXenes and toluidine blue/UIO-66-NH2

Mei Xuqiao,Zeng Zhenhua,Xu Wenxin,Yang Huicong,Zheng Yuanhai,Gao Haimin,Wu Chuncai,Zheng Yanping,Xu Qiaoli,Wang Guowei,Xu Yuhuang,Wu Ayang

CA125 (carbohydrate antigen 125) is an important biomarker of ovarian cancer, so developing effective method for its detection is of great significance. In the present work, a novel sandwich-like electrochemical immunosensor (STEM) of CA125 was constructed by preparing nanoribbon-like Ti 3 C 2 T x MXenes (Ti 3 C 2 T x NR) to immobilize primary antibody (PAb) of CA125 and UIO-66-NH 2 MOFs structure to immobilize second antibody (SAb) and electroactive toluidine blue (Tb) probe. In this designed STEM assay, the as-prepared Ti 3 C 2 T x NR nanohybrid offers the advantages in large surface area and conductivity as carrier, and UIO-66-NH 2 provided an ideal platform to accommodate SAb and a large number of Tb molecules as signal amplifier. In the presence of CA125, the peak currents of Tb from the formed STEM structure increase with the increase of CA125 level. After optimizing the related control conditions, a wide linear range (0.2–150.0 U mL −1 ) and a very low detection limit (0.05 U mL −1 ) of CA125 were achieved. It’s thus expected the developed STEM strategy has important applications for the detection of CA125. Graphical abstract

研究领域: 生物医学工程 · 分析化学 · 肿瘤学
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ACS Applied Materials & Interfaces · 2021 · IF 9.229

NH2-UiO-66 Coated with Two-Dimensional Covalent Organic Frameworks: High Stability and Photocatalytic Activity

Yongchao Wang,Qing Yang,Fangli Yi,Ruowei Lu,Yanxia Chen,Cheng Liu,Xinyu Li,Cuijuan Wang,Hongjian Yan

The poor stability and low catalytic activity of NH2-UiO-66 in basic solutions require the reactions to be conducted in acidic solutions, which seriously hinders its potential photocatalytic application. Herein, we report that NH2-UiO-66 coated with two-dimensional covalent organic frameworks (COFs) via imine bond connection presents not only high photocatalytic activity but also high stability and adaptability to the solution environment. The NH2-UiO-66/COF hybrid material was fabricated through the Schiff base reaction of NH2-UiO-66 with 4,4′,4″-(1,3,5-triazine-2,4,6-triyl)trianiline (TAPT) and 2,4,6-triformylphloroglucinol (TP). The hybrid material showed high stability in an alkaline environment, with only 4.7% of NH2-UiO-66 decomposed after the photocatalytic reaction. The optimum photocatalytic H2 evolution rate was 8.44 mmol·h–1·g–1 when triethanolamine was used as an electron-donating agent. The results presented here illustrate the possibility for effectively improving both the photocatalytic performance and stability of NH2-UiO-66 by coupling with COFs.

研究领域: 材料科学 · 光催化领域
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Immobilization of Nickel- and Cobalt-Based Complexes in NH2-UiO-66 for Efficient CO2 Photoreduction

Yu Jiang,Si-Chao Liu,Li-Ping Zhang,Guo-Wei Guan,Yi-Tao Li,Shuang Ni,Run-Yuan Jiang,Su-Tao Zheng,Hao-Ran Liu,Hao-Ling Lan,Qing-Yuan Yang

The photocatalytic reduction of carbon dioxide (CO 2 ) to carbon-based materials is challenging because of its intricate nature and the generation of multiple byproducts. Hence, developing photocatalysts with a high CO 2 -reduction yield and selectivity is critical. In this study, new photocatalysts (U-B-M, M = Co, Ni) were synthesized by incorporating 1,2-benzisothiazolin-3-one (BIT) into NH 2 -UiO-66, to create N, N’-chelating sites via an amine–aldehyde condensation reaction, followed by metal-ion chelation. The introduction of BIT decreased the resistance of the catalyst and enhanced the separation of photogenerated carriers. The catalytic performance of U-B-Ni (rate: 3.10 mmol·g −1 ·h −1 ; selectivity: 97 %) surpasses those most of all previously reported MOF-based photocatalysts. Moreover, U-B-Ni shows high stability and negligible deactivation on catalytic cycling for over 16 h. This study expands the utility of metal–organic frameworks (MOF) in photocatalysis and highlights the importance of amine–aldehyde condensation in MOF modification.

研究领域: 材料科学 · 环境科学 · 化学工程
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TALANTA · 2025 · IF 6.1

Enhanced quenching efficiency of UiO-66-NH2 over UiO-66 to engineer high-performance fluorescence aptasensor for oxytetracycline monitoring

Mengting Liu,Zuncai Gu,Lu Qian,Kawtar Ettayri,Tao Deng,Chenhao Zhang,Jing Qian,Xingyi Huang,Chengquan Wang

Oxytetracycline (OTC), a broad class of antibacterial medication, has been widely utilized in poultry husbandry and fish farming. However, the presence of OTC residues in the food has become a matter of great concern. These residues have the potential to induce the emergence and spread of bacterial resistance, which can have far-reaching consequences for public health. In this work, we focused on the comparison of the quenching efficiency of UiO-66 and its amino group-modified counterpart UiO-66-NH 2 , towards the fluorescence of nitrogen-doped graphene quantum dots (NGQDs) labeled aptamer (NGQDs-apt). It was found that UiO-66-NH 2 demonstrated a more potent fluorescence quenching ability towards NGQDs-apt, as high as 98.8 %, compared to 69.7 % for UiO-66 without amino functionalization. This enhanced performance is attributed to the improved interaction between the amino groups on UiO-66-NH 2 and the NGQDs-apt, facilitating more effective electron transfer. Consequently, UiO-66-NH 2 was selected as the optimal quencher for the development of a highly sensitive aptasensor. This aptasensor demonstrates a quantitative detection range for OTC spanning from 0.001 to 200 μM with an exceptionally low detection limit of 0.25 nM, showing simplicity, accuracy, stability and great potential for antibiotic residue detection in food samples. This work addresses the urgent need to develop reliable methods for detecting OTC residues in food due to the potential of OTC to trigger bacterial resistance, which is crucial for food safety and public health.

研究领域: 生物传感 · 食品安全 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Constructing NH2-MIL-125(Ti) derived evaporator for simultaneous photocatalytic decontamination and water evaporation

Yong Li,Xinyue Yang,Mengyao Wang,Deyun Yue,Jun Wu,Haojie Song

The pollutants present in wastewater can cause structural damage to evaporators, thereby reducing their evaporation efficiency and hindering the application of solar-driven water evaporation technologies. Here, the TiO 2 -based evaporator (CPM-Air) with highly efficient photodegradation and solar-powered water evaporation performance for simultaneous freshwater production and decontamination was prepared by pyrolysis NH 2 -MIL-125(Ti) grown on the surface of Carbon Felt (CF). The evaporation rate of CPM-Air evaporator reached 2.21 kg m -2 h −1 under 1.0 kW/m 2 , and high solar-vapor conversion efficiency of 102.20 %. Meanwhile, the Anatase TiO 2 obtained by carbonized NH 2 -MIL-125 (Ti) has more active sites for removal pollutants. CF as the catalytic promoter to accelerate electron transport, and improve the photogenerated electron-hole separation efficiency. The photothermal-photocatalytic synergy removal efficiency of high concentration (50 mg/L) CIP was 2 times higher than photocatalytic only. In addition, the CPM-Air evaporator has high water evaporation rate in different harsh environments, the 99.9 % of metal ions removal and excellent salt resistance. More importantly, the growth experiments on soybean indicated that the products of photothermal-photocatalytic synergy degradation CIP of CPM-Air evaporator was non-biotoxic. This study provides valuable insights into the potential of photothermal-photocatalytic synergy for sustainable water production.

研究领域: 环境科学 · 材料科学 · 水资源管理
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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY · 2024 · IF 1.5

Highly efficient capture of thorium ion by graphene oxide modified UiO-66-NH2 from aqueous solution

Guo Dingge,Xiao Jing,Ning Yang,Yu Hongchao,Jin Tianxiang,Huang Bin,Qian Yong

The efficient removal of thorium from the environment is critical due to the risks it poses to organisms. Metal–organic frameworks are favored by scholars because of their potential to effectively adsorb a variety of heavy metal ions in wastewater treatment. In this work, the interaction of UiO-66-NH 2 surface with graphene, enhances adsorption capacity of MOFs. Optimal adsorption conditions have been identified, and a detailed adsorption mechanism has also been comprehensively discussed. The theoretical maximum adsorption capacity exhibited by UiO-66-GO is 119.57 mg g −1 . Moreover, it shows a fast adsorption rate and reached equilibrium within 20 min. The development of materials with good adsorption performance and fast adsorption for Th(IV) plays an important role in the development of Th(IV) adsorption in the future.

研究领域: 环境科学 · 材料科学
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Molecular Catalysis · 2024 · IF 3.9

Experimental and computational study on removal of nitric oxide using NH2-MIL-125: Revisiting removal mechanism

Jianfu Luan,Jiayou Liu,Xiaoxiang Huang,Zhongchao Tan,Hesheng Yu

The NH 2 -MIL-125 (NM-125) or modified NM-125 materials are used for photocatalytic removal of nitric oxide (NO). Most researchers attributed few NO 2 emission during NO photocatalysis to high selectivity towards the formation of nitrate ions due to the neglect of the principle of electroneutrality and pore structure of NM-125. This may cause misleading photocatalytic mechanism of NO removal. Herein, this work proposes a new mechanism behind NO removal using NM-125 based on experimental investigations and theoretical calculations. First, experimentally, the highest NO removal efficiency of 88.54 % with negligible NO 2 emission occurs at the anhydrous condition. In addition, in-situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) measurements verify the presence and accumulation of NO 2 as product during photocatalytic conversion of NO. Furthermore, density functional theory (DFT) calculations and grand canonical Monte Carlo (GCMC) computations demonstrate that there exist strong interactions between NO 2 and -NH 2 group within pores. Few NO 2 is detected during experiments is probably due to its subsequent adsorption in the pores of NM-125. The new NO removal mechanism including photocatalytic conversion NO into NO 2 and subsequent NO 2 adsorption in the pores of NM-125 is thus proposed. This work provides a deeper insight into photocatalytic NO removal over NM-125 and its variants.

CAS / MDL: 10312-55-7
研究领域: 环境科学 · 材料科学
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH · 2024 ·Vol. 31 ·期 6 ·9764-9783 · IF 0

Magnetically separable Co0.6Fe2.4O4/MIL-101-NH2 adsorbent for Congo red efficient removal

Zhang Zhenhong,Zhong Yuye,Sun Peng,Zhao Pingping,Li Houbin,Liu Xinghai

The development of effective and practical adsorbents for eliminating pollutants still remains a significant challenge. Herein, we synthesized a novel magnetically separable composite, Co 0.6 Fe 2.4 O 4 /MIL-101-NH 2 , through the in-situ growth of MIL-101-NH 2 on magnetic nanoparticles, designed specifically for the removal of Congo red (CR) from aqueous solutions. MIL-101-NH 2 possessed high BET surface area (240.485 m 2 •g −1 ) and facile magnetic separation function and can be swiftly separated (within 30 s) through an external magnetic field post-adsorption. The investigation systematically explored the influence of crucial parameters, including adsorbent dosage, pH, adsorption duration, temperature, and the presence of interfering ions, on CR adsorption performance. Findings indicate that CR adsorption adheres to the pseudo-second-order (PSO) kinetic model and the Langmuir isotherm model. Thermodynamic analysis reveals the spontaneity, endothermic nature, and orderly progression of the adsorption process. Remarkably, the adsorbent with 0.1 g•L −1 boasts an impressive maximum adsorption capacity of 1756.19 mg•g −1 for CR at 298.15 K, establishing its competitive advantage. The reuse of the adsorbent over 5 cycles remains 78% of the initial adsorption. The CR adsorption mechanisms were elucidated, emphasizing the roles of π-π interactions, electrostatic forces, hydrogen bonding, and metal coordination. Comparison with other dyes, such as methylene blue (MB) and methyl orange (MO), and exploration of adsorption performance in binary dye systems, demonstrates the superior capacity and selectivity of this adsorbent for CR. In conclusion, our magnetically separable metal–organic framework (MOF)based composite presents a versatile and effective solution for CR removal, with promising applications in water treatment and environmental remediation. Graphical

研究领域: 环境科学 · 材料科学 · 化学工程 · 纳米技术 · 物理化学
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES · 2024 ·Vol. 25 ·期 18 ·9855 · IF 4.9

Preparation of NH2-MIL-101(Fe) Metal Organic Framework and Its Performance in Adsorbing and Removing Tetracycline

Yiting Luo,Rongkui Su

Tetracycline’s accumulation in the environment poses threats to human health and the ecological balance, necessitating efficient and rapid removal methods. Novel porous metal–organic framework (MOF) materials have garnered significant attention in academia due to their distinctive characteristics. This paper focuses on studying the adsorption and removal performance of amino-modified MIL-101(Fe) materials towards tetracycline, along with their adsorption mechanisms. The main research objectives and conclusions are as follows: (1) NH2-MIL-101(Fe) MOF materials were successfully synthesized via the solvothermal method, confirmed through various characterization techniques including XRD, FT-IR, SEM, EDS, XPS, BET, and TGA. (2) NH2-MIL-101(Fe) exhibited a 40% enhancement in tetracycline adsorption performance compared to MIL-101(Fe), primarily through chemical adsorption following pseudo-second-order kinetics. The adsorption process conformed well to Freundlich isotherm models, indicating multilayer and heterogeneous adsorption characteristics. Thermodynamic analysis revealed the adsorption process as a spontaneous endothermic reaction. (3) An increased adsorbent dosage and temperature correspondingly improved NH2-MIL-101(Fe)’s adsorption efficiency, with optimal performance observed under neutral pH conditions. These findings provide new strategies for the effective removal of tetracycline from the environment, thus holding significant implications for environmental protection.

CAS / MDL: 64-75-5
研究领域: 环境科学 · 材料科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

UiO-66-NH2 decorated EVOH nanofiber substrate induces the formation of high-performance Janus PA nanofiltration membrane

Qin Cheng,Jinping Gan,Kai Cai,Ming Xia,Yi Wu,Shanshan He,Pan Cheng,Qihao Guo,Ke Liu,Dong Wang

High-quality polyamide (PA) nanofiltration (NF) membrane with excellent selectivity and permeability is of great research significant because of their high practical application value, especially for the precise separation of divalent and monovalent ions, such as Mg 2+ and Li + . Herein, UiO-66-NH 2 nanoparticles (NPs) decorated ethylene vinyl alcohol copolymer (EVOH) nanofiber substrate (M-NFM) was utilized to construct high-quality Janus NF membrane through interfacial polymerization (IP) reaction using polyethyleneimine (PEI) and piperazine (PIP) as aqueous phase monomers and trimesoyl chloride (TMC) as organic phase monomers. The incorporation of UiO-66-NH 2 NPs significantly influenced the hydrophilicity, surface morphology, and pore structure of the substrate, thereby enhancing the properties of the resulting NF. Optimally prepared membranes demonstrated improved separation performance, permeability, stability, and antifouling characteristics compared to the unmodified substrate. Notably, at a Mg 2+ /Li + ratio of 30, the resultant NF membrane achieved a separation factor (S Mg 2+ /Li + ) of 28.4 and a salt permeation flux of 156.8   L·m -2 ·h -1 ·MPa -1 . Additionally, the membrane exhibited over 98% rejection rates for FeCl 3 , CuSO 4 , CaCl 2 , MgSO 4 , MgCl 2 and Na 2 SO 4 with fluxes exceeding 150   L·m -2 ·h -1 ·MPa -1 , highlighting its effectiveness in rejecting multivalent ions. This research presents a simpler and more reliable approach to the fabrication of high-quality Janus PA NF membrane, offering promising potential for industrial-scale applications.

研究领域: 材料科学 · 环境工程 · 化学工程
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LANGMUIR · 2024 · IF 3.7

Layer-Point Structure of Si3N4–NH2@GO for Improving Corrosion and Wear Resistance of Waterborne Epoxy Coating

Jing Zhang,Changhua Li,Xiaofeng Zhang,Hao Chen,Rui Gou,Chao Zhang,Dan Sun,Yi He

The use of graphene-based materials as anticorrosion coatings to protect metals is always a topic of discussion. In this work, silicon nitride (Si3N4) was aminated to improve its water dispersibility. Then it is attached to the graphene oxide (GO) surface to improve compatibility with epoxy (EP) resin as well as conductivity. The results of Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and zeta potentials test analyses indicated that Si3N4–NH2@GO with a layer-point structure has been successfully prepared. The corrosion resistance of the composite coatings was characterized by electrochemical impedance spectroscopy (EIS) and polarization curve analysis, and the wear resistance of the composite coatings was tested by friction and wear tests. The results showed that 1.0% Si3N4–NH2@GO has excellent corrosion and wear resistance. The use of Si3N4–NH2@GO layer point structures in this study broadens the way for GO applications.

CAS / MDL: 12033-89-5 7647-01-0
研究领域: 材料科学 · 防腐蚀技术 · 表面工程
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Journal of Materials Chemistry B · 2015 ·Vol. 3 ·期 9 ·2006-2011 · IF 4.726

An ultrasensitive electrochemical immunosensor for CEA using MWCNT-NH2 supported PdPt nanocages as labels for signal amplification

Na Li,Yaoguang Wang,Wei Cao,Yunhui Zhang,Tao Yan,Bin Du,Qin Wei

The excellent catalytic activity of a novel nanomaterial was introduced to ultrasensitive sandwich-type electrochemical immunosensor applications for detection of carcinoembryonic antigen (CEA). Amino-functionalized multi-walled carbon nanotube (MWCNT-NH2) supported PdPt nanocages were used as catalytic labels of secondary anti-CEA. PdPt nanocages with hollow interiors and porous walls could efficiently enhance electrocatalysis for reduction of H2O2. Meanwhile, with good dispersion, large specific surface area and amino groups, MWCNT-NH2 can immobilize a large amount of PdPt nanocages to improve the sensitivity and amplify the signal of the immunosensor. For the immobilization of primary antibodies, 3-aminopropyltriethoxysilane functionalized graphene sheets were used as transducing materials to modify glassy carbon electrodes and to enhance the electron transfer efficiently. Under the optimal conditions, the electrochemical immunosensor exhibited a wide linear range of 0.001–20 ng mL−1 with a low detection limit of 0.2 pg mL−1 for CEA. The proposed sensing strategy enriches electrochemical immunoassays and may have a promising application in bioassay analysis.

研究领域: 生物医学工程 · 分析化学
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