Journal of Environmental Chemical Engineering
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2025
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IF 7.2
Yisha Zheng,Shuoling Lei,Wenjie Guo,Wenlong Xiang,Yanmei Chen,Yanhui Zhang
The high toxicity and persistence of nitroaromatic pollutants pose a serious threat to aquatic ecosystems. In this study, inert SiO 2 was employed as an "inactive enhancer" to construct core-shell MIL-125-NH 2 @ZIF-67/SiO 2 (M@Z/SiO 2 ) heterogeneous MOF catalysts via an epitaxial-wet impregnation method, enabling the efficient reduction of p -nitrophenol ( p -NP) under ambient temperature and pressure. Although SiO 2 itself lacks catalytic activity, the micro-mesoporous network it forms effectively disperses Co active sites and prevents their aggregation. The conversion rate of p -NP increased from 92.5% to 98.4% within 6 min and retained 98% activity after three consecutive cycles. Moreover, the catalyst exhibited excellent stability across a wide pH range (3-11) and in various anionic environments. Mechanistic studies revealed that the interfacial electron transfer between ZIF-67 and MIL-125-NH 2 significantly reduces the activation energy barrier of NaBH 4 . Additionally, the incorporation of SiO 2 not only enhances the mechanical stability of the composite but also optimizes pore structure and substrate mass transfer by modulating surface hydrophilicity. This work provides valuable insights for the precise design of MOF-on-MOF heterostructures and the synergistic engineering of interfacial and surface properties in environmental catalytic materials.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
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2025
·
IF 8.5
Sina Seifi,Azadeh Ghaee
In this study, a novel nanocomposite scaffold comprising pectin, gelatin, and amoxicillin trihydrate-loaded UiO-66-NH 2 metal-organic frameworks (UiO-66-NH 2 @AMX) was fabricated for skin tissue engineering applications. UiO-66-NH 2 nanoparticles were synthesized hydrothermally and subsequently loaded with amoxicillin trihydrate. Finally, UiO-66-NH 2 @AMX nanoparticles were incorporated into pectin-gelatin scaffolds using the freeze-drying method. FE-SEM imaging confirmed the octahedral morphology of the nanoparticles before and after drug loading. FTIR analysis demonstrated successful drug incorporation via non-covalent interactions. DLS and zeta potential measurements showed that UiO-66-NH 2 nanoparticles had a mean size of 218.5 ± 14 nm and a surface charge of +44.1 ± 2.7 mV. After drug loading, the size slightly increased to 248.8 ± 19 nm, and the surface charge decreased to +32.6 ± 2.5 mV, while maintaining colloidal stability. All of the scaffolds showed porous structures with interconnected pores in SEM imaging. The incorporation of UiO-66-NH 2 @AMX nanoparticles into the pectin-gelatin scaffolds up to 3 % (w/w) increased the tensile strength and Young's modulus of the scaffolds 37.6 % and 56.7 %, respectively. Antibacterial activity was evaluated by CFU assay, where UiO-66-NH 2 @AMX containing scaffolds revealed significant bacterial reduction against E. coli and S. aureus colonies. MTT, cell adhesion, and cell scratch assays conducted on L929 fibroblasts. All of the scaffolds demonstrated >85 % cell viability after 3 days of culture. Furthermore, scaffolds with 3 % (w/w) UiO-66-NH 2 @AMX enhanced cell adhesion and increased migration rate in scratch closure assay. Overall, the results indicate that the novel nanocomposite scaffolds are promising candidates for skin tissue engineering and wound healing applications.
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高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Yuxin Li,Zhimin Wang,Yuanfeng Wei,Ting Wang,Maosong Zhao,Jie Luo,Jun Zhou,Zhaoshuang Li,Kai Yin,Chengbin Liu
Water decontamination from arsenic-contaminated groundwater is critical to the health of millions of households worldwide. However, efficiently removing the low-adsorbing As(III) remains challenging. Herein, a multifunctional biocomposite bead UiO-66-NH 2 -Cl@PCB integrating defects, oxidation and adsorption properties was prepared to effectively remove As(III). The N -chlorosulfonamide bound within the embedded UiO-66-NH 2 -Cl oxidizes the lower-adsorbing As(III) to As(V), which could be effectively adsorbed by the defect-rich MOF, while the porous chitosan bead (PCB) host ensures the utilisation of the reactive sites of UiO-66-NH 2 -Cl. Using 1 g/L of UiO-66-NH 2 -Cl@PCB, 1 mg/L of As(III) can be reduced to under 10 μg/L in 300 min. Furthermore, similar As(III) removal efficiencies were achieved across a wide pH spectrum (3–9) or in the presence of interfering substances (anions, cations, organic matter). High concentrations of phosphate will inhibit its performance. As(III) removal followed the Freundlich isotherm modal, and its maximum removal capacity reached 58.09 mg/g at pH 7. Furthermore, at equilibrium concentrations of 10 μg/L, its As(III) removal capacity exceeded 10 mg/g. UiO-66-NH 2 -Cl@PCB can purify the As(III)-spiked groundwater to meet the drinking standard level. Using NaOH solution for regeneration, the removal efficiency maintained above 70 % in the fifth cycle. Additional chlorination treatment can significantly improve reusability. 2.4 g of UiO-66-NH 2 -Cl@PCB packed fixed-bed column was capable of purifying 3820 BV of groundwater containing 100 μg/L of As(III). The proposed UiO-66-NH 2 -Cl@PCB has the potential to be an easy-to-use and reliable material for efficient As(III) removal.
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CRYSTENGCOMM
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2025
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IF 2.6
Huanxia Lin,Wensong Lin,Yeheng Zhang,Ran Gao,Yong He
BiOCl/UiO-66-NH2 photocatalysts were synthesized by a hydrothermal method. BUNH-8 (BiOCl/UiO-66-NH2 composite with 8% UiO-66-NH2) exhibits exceptional photocatalytic performance under visible-light illumination, degrading 92% of rhodamine B (RhB) within 60 minutes, which is 38.16% greater than that of pure BiOCl. The enhanced performance of the BiOCl/UiO-66-NH2 composite photocatalyst can be attributed to the distinct band structure difference between BiOCl and UiO-66-NH2, facilitating effective Z-scheme charge separation and transfer under light irradiation. Superoxide radicals were determined to be the crucial active species in the photocatalytic degradation process via electron paramagnetic resonance (EPR) analysis and a simulated photocatalytic degradation experiment of the dye RhB with scavengers added. Apart from its high efficiency, BUNH-8 demonstrates excellent stability as well. Even after being reused four times, it maintains its excellent photocatalytic performance, suggesting its high potential for application.
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CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Chaoting Shi,Ninghan Tang,Shan Pu,Hui Xin,Lan Wu,Xiandeng Hou
Metal-Organic Frameworks (MOFs) have been widely used for the antibiotic pollution control. However, it remains a challenge to simple design and synthesis of multifunctional MOFs for sensing and degradation antibiotics. Herein, a multifunctional UiO-66(Zr/Ce)-NH 2 ratiometric fluorescence sensing and photocatalytic degradation platform was rapidly and simply constructed at room temperature by a one-pot method using a dielectric barrier discharge device. The mixed-metal centers and mixed-ligands of this platform enabled effective ratiometric fluorescence sensing of tetracycline (TC), along with a visual fluorescence shift from blue to yellow-green color. The platform demonstrated a detection of TC ranged from 200 nM to 15 μM, with a detection limit of 43 nM. Moreover, the UiO-66(Zr/Ce)-NH 2 exhibited strong light absorption and efficient photogenerated carrier separation, thus offering excellent degradation performance of TC compared with that of MOFs with single metal center, mixed ligands or mixed metal centers. The mechanism of fluorescence detection and potential charge transfer pathways by the UiO-66(Zr/Ce)-NH 2 were analyzed. This work provided a new approach for the simple design and synthesis of multifunctional MOFs platforms.
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ChemistrySelect
·
2024
·Vol. 9
·期 13
·e202303633
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IF 1.9
Mingyan Chen,Wentao Wang,Xinkai Feng,Dehua Zhang,Yao Zhang,Yucheng Liu
Graphical This work describes the application of a highly efficient catalyst (NH 2 -UiO-66-Mo) to the catalytic oxidation desulfurization process. NH 2 -UiO-66-Mo can greatly improve the efficiency of oxidative desulfurization The optimum operating conditions of NH 2 -UiO-66-Mo are investigated through experiments, which prove the excellent performance of the catalyst, and the reaction mechanism is further studied through a series of characterizations. A highly efficient oxidative desulfurization composite catalyst NH 2 -Uio-66-Mo has been prepared and applied in the catalytic oxidative desulfurization. It was elucidated that Mo 6+ could increase the oxygen vacancies and active sites on the catalyst and increase the pore size of UiO-66. Meanwhile, the removal rate of dibenzothiophene (DBT) reached 99.2 % after 60 min under optimal conditions and remained above 90 % after 5 cycles, showing the composite catalyst's remarkable catalytic performance and satisfactory reusability NH 2 -UiO-66-Mo. In addition, kinetic studies revealed that the desulfurization process can present a pseudo-first-order kinetic process. The apparent activation energy was 10.6 kJ/mol. Finally, in combination with oxides, possible oxidation pathways were identified.
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ANALYTICAL SCIENCES
·
2024
·Vol. 40
·期 6
·1081-1087
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IF 1.8
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
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高影响因子
Heliyon
·
2022
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IF 3.776
Xuezhong Li,Yue Wang,Qi Guo
The porous iron-based metal organic frameworks (NH 2 -MIL-101(Fe)), which consists of 2-amino benzene dicarboxylic acid (H 2 BDC-NH 2 ) and ferrous ions were synthesized through one-step hydrothermal method. The surface area and pore volume of as-synthesized NH 2 -MIL-101(Fe) were 66.48 m 2 /g and 0.09 cm 3 /g, respectively. The excellent photocatalytic performance endows NH 2 -MIL-101(Fe) to generate hydroxyl radical ( OH), which then acting as efficiently active sites for azo dye degradation in wastewater. Meanwhile, the outstanding stability ability of NH 2 -MIL-101(Fe) indicates the potential candidate for wastewater treatment.
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高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
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2022
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IF 6.371
Danhua Guo,Huijun Li,Jiwei Wang,Zhouqing Xu
Leaching of fluoride in drinking water can lead to fluorosis. It is a good method to reduce the concentration of fluoride ion in drinking water by selecting the adsorption material with large adsorption capacity and good selectivity. Herein, the NH 2 -UiO-66 based loofah sponge modified porous composite was prepared. The composite material took loofah sponge (LS) as the carrier, and loaded NH 2 -UiO-66 on the surface of LS by in-situ growth method. The structure of the prepared NH 2 -UiO-66 @LS was investigated by PXRD , FTIR, SEM, and XPS. The influencing factors of different materials, contact time, adsorbent dosage, preliminary fluoride concentration, and co-existing anions were optimized. Compared with LS, the adsorption efficiency of NH 2 -UiO-66 @LS was greatly improved, and the adsorption capacity was 65.08 mg/g for fluoride ion. Moreover, the maximum removal efficiency of NH 2 -UiO-66 @LS was the initial fluoride concentration of 100 mg/L. Under the condition of the coexistence of other anions, the composite material has a specific adsorption performance for fluoride within 40 min. Furthermore, the data of fluoride adsorption was best fitted with pseudo-second-order kinetic model. The thermodynamic studies showed that the fluoride adsorption process on NH 2 -UiO-66 @LS was feasible, spontaneous and endothermic. In addition, synthesized NH 2 -UiO-66 @LS can be reused upto eight cycles. The plausible fluoride adsorption mechanism of NH 2 -UiO-66 @LS was majorly ruled by electrostatic attraction and complexation. Furthermore, the raw material is easy to obtain and the preparation process of NH 2 -UiO-66 @LS is simple. Hence, the large adsorption capacity of NH 2 -UiO-66 @LS compared with reported adsorbents for fluoride makes it have potential application prospect from wastewater on industrial scale.
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MICROPOROUS AND MESOPOROUS MATERIALS
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2020
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IF 4.551
Hao Guo,Jiaqin Liu,Yanhong Li,Jürgen Caro,Aisheng Huang
Due to their rationally controlled pore size and easy functionalization, metal-organic frameworks (MOFs) are a promising candidate for membrane separation . As one of the most stable MOFs, UiO-66 has attracted intense attention for the preparation of molecular sieving membranes. A new post-synthesis modification (PSM) strategy was developed to enhance the separation selectivity of supported UiO-66-NH 2 membranes on porous ceramic tubes called UiO-66-NH 2 @SA by using salicylaldehyde (SA) modification. The mixed gas separation factors of H 2 /CO 2 and H 2 /CH 4 can be improved due to constrictions of the pore size through reaction of –NH 2 with SA giving iminophenol moieties. Notably, SA-modified UiO-66-NH 2 membranes are rather stable, at a high operation temperature of 200 °C and 1 bar, mixture separation factors of 11.3 for H 2 /CO 2 and 22 for H 2 /CH 4 can be obtained. Further, no obvious performance degradation has been observed after 3 months storing in air. This high stability of UiO-66-NH 2 @SA membrane could provide possibility for the industrial applications of hydrogen separation and purification.
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MICROCHIMICA ACTA
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2025
·Vol. 192
·期 5
·1-9
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IF 5.3
Li Rui,Que Wenzhong,Han Haiyan,Shi Honghui,Wang Rongfeng,Qiu Bin
IL-17 (interleukin-17) is a common proinflammatory cytokine and can be adopted as an important biomarker for several diseases; it is thus very necessary to design an effective method for monitoring IL-17. Herein, by preparing silver nanoparticles/graphdiyne (Ag/GDY) with simple electroless deposition as the sensing platform and methylene blue/UiO-66-NH 2 MOFs (MB/MOFs) as the signaling-amplifier, a highly efficient sandwich-like electrochemical immunosensing (SLEI) platform was designed for IL-17 detection. The superior electrical property, easy preparation, large surface area, and high stability of Ag/GDY make it a desirable substrate to immobilize primary antibody of IL-17. Meanwhile, the unique structure of UiO-66-NH 2 is beneficial to immobilize MB probe and secondary antibody. By optimizing experimental conditions, the MB current obtained at the as-designed SLEI platform increases along with IL-17 increase, and the related linearity is 1.0 pg mL −1 –1.0 ng mL −1 coupled with a low detection limit of 0.3 pg mL −1 . It is expected that the SLEI platform based on Ag/GDY and MB/MOFs shows some potential application for IL-17 detection. Graphical abstract
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高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Jing Meng,Moustafa Zahran,Ahmed S. Abou-Elyazed,Xiaolin Li
Herein, we report a novel electrochemical sensor for determining glucose in sweat, employing a graphene/metal–organic framework (MOF) as a modifier for stainless steel (SS) electrode. The MOF structures, MIL-101(Cr), MIL-101(Cr)-NO 2 , and MIL-101(Cr)-NH 2 , were hydrothermally synthesized and then characterized using X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, N 2 adsorption/desorption isotherms, and scanning electron microscopy (SEM). XRD and SEM results proved the formation of the crystalline MIL-101(Cr) and MIL-101(Cr)-NO 2 , and the amorphous MIL-101(Cr)-NH 2 . Additionally, FT-IR and isotherms confirmed their composition and mesoporosity, respectively. The amorphous MIL-101(Cr)-NH 2 showed the best electrocatalytic activity towards glucose oxidation among the fabricated MOFs. The electrocatalytic activity was also boosted after incorporating conductive graphene. Under optimized conditions, graphene/MIL-101(Cr)-NH 2 /SS was used for glucose determination using square wave voltammetry and chronoamperometry with detection limits of 0.004 and 0.01 mM, respectively. Moreover, the modified electrode showed acceptable recovery values when it was applied to detect glucose in artificial sweat samples.
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