CHINESE JOURNAL OF CHEMICAL ENGINEERING
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2024
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IF 3.7
Sijia Wang,Ye Liu,Liang He,Yu Sun,Qing Huang,Shoudong Xu,Xiangyun Qiu,Tao Wei
Solid polymer composite electrolytes possess the benefits of superior compatibility with electrodes and good thermal characteristics for more secure energy storage equipment. Herein, a new gel polymer electrolyte (GPE) containing NH 2 -MIL-53(Al), [PP 13 ][TFSI], LiTFSI, and PVDF-HFP was prepared using a simple method of solution casting. The effects of encapsulating different ratios of ionic liquid ([PP 13 ][TFSI]) into the micropores of functionalized metal-organic frameworks (NH 2 -MIL-53(Al)) on the electrochemical properties were compared. XRD, SEM, Nitrogen adsorption-desorption isotherms and electrochemical measurements were conducted. This GPE demonstrates a superior ionic conductivity of 8.08×10 –4 S cm –1 at 60 °C and can sustain a discharge specific capacity of 156.6 mAh g –1 at 0.2 C for over 100 cycles. This work might offer a potential approach to alleviate the solid-solid contact with the solid-state electrolyte and electrodes, and broadens up new window for the creation of all-solid-state batteries.
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ANALYTICA CHIMICA ACTA
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2024
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IF 5.7
Huanhuan Zhu,Shuo Chen,Xiaoying Huang,Xi Chen,Zhengjun Gong
Background Organophosphate flame retardants (OPFRs) are notorious emerging contaminants threatening the environment and human health. Triphenyl phosphate (TPHP), which has an extremely serious biotoxicity, is a typical harmful OPFR. Due to its wide use, TPHP has been discovered in various environmental mediums. Moreover, it is pretty recalcitrant to the removal process, resulting in the need for a technique to understand it better. Hence, accurate and quick discrimination of TPHP in the environment is critical to further evaluate its potential effect on ecosystems and human health. Results An ingenious oxidant-free chemiluminescence (CL) sensor based on the oxidant-free UV/MIL-100(Fe) gel system was established for TPHP detection. The oxidation of luminol in the UV-activated MIL-100(Fe) gel has resulted in remarkable CL emission, which is contributed by reactive oxygen species (ROS) generated by it. Notably, the CL intensity was inhibited significantly after introducing TPHP. An investigation into the mechanism underlying the effect of CL suppression demonstrated that TPHP competed with luminol to consume ROS from UV-activated MIL-100(Fe) gel, contributing to CL inhibition. The subsequent sensing performance experiments demonstrated the advantages of environmentally friendly, economic efficiency, user-friendly operation, rapid determination, potential for compact size, high selectivity, and sensitivity. Additionally, these investigations confirmed the low limit of detection (210 ng L −1 ) and wide linear range (10–1000 μg L −1 ). Significance In this paper, a green, economical, and oxidant-free CL sensing strategy for TPHP has been established. It has the advantage of being rapid, having the potential for compact size, high selectivity, and sensitivity. This ingenious method has promising applications in real-time and online environmental monitoring, and it paves the way for the rapid and environmentally friendly identification of emerging contaminants that are structurally stable and recalcitrant to remove.
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JOURNAL OF SOLID STATE CHEMISTRY
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2024
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IF 3.2
Xiaolan Guo,Xiaoman Li,Yuxin Huang,Yongjun Peng,Tongke Hu,Yazhen Chen,Jianhua Cheng
In this study, we synthesized a convenient and efficient composite photocatalyst, In 2 O 3 /Co 3 O 4 from the pyrolysis of Co-doped MIL-68(In). Structural characterization indicates that the composite material exhibited a rod-like hollow structure, thus increasing the specific surface area. Meanwhile, In 2 O 3 /Co 3 O 4 forms a PN heterojunction, which reduces the recombination rate of photogenerated hole-electron pairs. Moreover, the visible light absorption ability of this material is enhanced and it has good catalytic properties. Under visible light, the removal rate of tetracycline (TC) reaches 94% by the In 2 O 3 /Co 3 O 4 in 90 min, and the reaction constant is 0.02393 min −1 , which is 6.86 and 5.56 times of the single component In 2 O 3 and Co 3 O 4 , respectively. As shown by free radical quenching experiments and electron paramagnetic resonance (EPR) test, h + and •O 2 − play an important role in degrading TC into small molecule intermediates in the catalytic process.
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Journal of Environmental Chemical Engineering
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2024
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IF 7.4
Hongbin He,Bolong Liang,Shumin Lin,Yan Chen,Xin Zhang,Shu-Xuan Liang
The residues of oxytetracycline hydrochloride (OTC) in water have potential adverse effects on human health and ecological environment. Photocatalytic degradation has been widely studied in the treatment of antibiotic pollution due to its environmentally friendly and efficient characteristics. However, the band gap of traditional photocatalysts is too wide, and the recombination of photogenerated electrons and holes is serious, which has negative effects on photocatalysis . Therefore, the Z-scheme heterojunction g-C 3 N 4 @MIL-101(Fe) composite photocatalyst was synthesized by high temperature calcination combined with solvothermal method. g-C 3 N 4 @MIL-101(Fe) was characterized by XRD, FTIR , SEM, TEM and other tests. All the results showed that the compound was successful A series of photoelectric tests showed that g-C 3 N 4 @MIL-101(Fe) has a narrower band gap, stronger light absorption ability, and improved the separation rate of photogenerated electrons and holes. Under visible light irradiation, g-C 3 N 4 @MIL-101(Fe) could remove 87.68% of OTC in 300 min. g-C 3 N 4 @MIL-101(Fe) showed good potential for practical application in five real water samples and stability after six cycles. Finally, superoxide radicals and hole radicals were identified as the main reactive species in the photodegradation process. The mechanism and pathway of the photocatalytic degradation of OTC by g-C 3 N 4 @MIL-101(Fe) are proposed. This work expands the construction and application of Fe-MOF based Z-scheme heterostructure and provides a new idea for water pollution remediation.
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Journal of Water Process Engineering
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2025
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IF 6.7
Jincheng Dai,Shuyue He,Xiyu Song,Chuliang Shen,Hongjuan Zhang,Ruyi Xie
The application of Fe-based metal-organic frameworks in photo-Fenton antibiotic degradation is limited by the low charge separation efficiency and slow Fe 3+ /Fe 2+ transition. In this study, a novel Z -scheme porous carbon nitride/mixed-valent MIL-53(Fe) (KCM-20) heterojunction photocatalyst was successfully constructed for degradation of high concentration tetracycline. On the one hand, the Z -scheme heterojunctions system is conducive to the rapid separation of photogenerated electron-hole pairs. On the other hand, the cyclic conversion of Fe 3+ /Fe 2+ in the MIL-53(Fe) photo-Fenton system can be accelerated. The KCM-20 showed the highest degradation efficiency for tetracycline. The KCM-20/light/H 2 O 2 system degraded more than 93 % of tetracycline (150 mg·L −1 ) within 75 min and exhibited the highest degradation kinetic constant, which is 8.0 and 2.4 times higher than those of carbon nitride and MIL-53(Fe), respectively. Its excellent catalytic performance can be attributed to the efficient synergy between photocatalytic reaction and Fenton reaction, producing more active species for tetracycline degradation. EPR and activity capture experiments indicate that ·O− 2, ·OH and h + are the main active species for tetracycline degradation. By analyzing the intermediate products, three degradation pathways for tetracycline were proposed. This work provides a new pathway for the preparation of efficient and cost-effective photocatalysts for the degradation of organic pollutants.
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MOLECULES
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2024
·Vol. 29
·期 14
·3417
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IF 4.2
Pengfei Zhu,Zhaoxia Hu,Shouwen Chen
The development of economical catalysts that exhibit both high activity and durability for chlorinated volatile organic compounds (CVOCs) elimination remains a challenge. The oxidizing and acidic sites play a crucial role in the oxidation process of CVOCs; herein, praseodymium (Pr) was introduced into CrOx catalysts via in situ pyrolysis of MIL-101(Cr). With the decomposition of the ligand, a mixed micro-mesoporous structure was formed within the M-Cr catalyst, thereby reducing the contact resistance between catalyst active sites and the 1,2-dichloroethane molecule. Moreover, the synergistic interaction between chromium and praseodymium facilitates Oβspecies and acidic sites, significantly enhancing the low-temperature catalytic performance and durability of the M-PrCr catalyst for 1,2-dichloroethane (1,2-DCE) oxidation. The M-30PrCr catalyst possess enhanced active oxygen sites and acid sites, thereby exhibiting the highest catalytic activity and stability. This study may provide a novel and promising strategy for practical applications in the elimination of 1,2-DCE.
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Journal of Water Process Engineering
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2025
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IF 6.7
Mei Dong,Qiguang Cao,Song Li,Kebin Li
Designing stable and efficient heterogeneous catalysts for peroxymonosulfate (PMS) activation remains a critical challenge in advanced oxidation processes. Herein, we prepared a polyvinylpyrrolidone (PVP)-modified MIL-101(Fe)@CoZn-ZIF (PVP-MCZ) core-shell nanocomposite that synergistically combined enhanced catalytic activity with exceptional stability. The PVP-MCZ catalyst achieved complete degradation of 4-nitrophenol (4-NP) (20 mg/L) within 15 min, while suppressing metal leaching (<0.5 mg/L). Comprehensive characterization (XPS, EPR) revealed a dual-pathway mechanism: (i) radical-dominated SO 4 − generation via Co 2+ /Co 3+ and Fe 2+ /Fe 3+ redox cycling, and (ii) non-radical 1 O 2 production from PMS self-decomposition. This work provides a scalable strategy to design MOF-based catalysts for sustainable water remediation.
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JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS
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2025
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IF 3.1
Erxu Wang,Huiran Zhang,Xiangchuan Li,Lili Geng,Zhen Wang,Airong Chu,Bin Lu,Li Duan
Alzheimer’s disease (AD) is a common neurodegenerative disease, and is characterized by impaired acetylcholine-mediated neurotransmission. Acetylcholinesterase (AChE) inhibition is a well-established therapeutic strategy for AD. Medicinal plants exhibit multi-target effects, low toxicity, and cost-effectiveness. Therefore, screening AChE inhibitors from botanical sources holds considerable pharmacological potential. In this study, a metal-organic framework was used as a novel support for immobilizing AChE, resulting in the creation of AChE@MIL-88B-NH 2 , which served as a tool for screening potential AChE inhibitors. The immobilized enzyme exhibited excellent reusability, stability against pH fluctuations and thermal stress, and resistance to organic solvents. The constructed AChE@MIL-88B-NH 2 -based ligand fishing strategy coupled with mass spectrometry was applied to screen for AChE inhibitors in Nelumbinis plumula extracts. Seven compounds were identified as potent AChE inhibitors. Enzyme kinetic assays revealed that these ligands exhibit a mixed inhibition mechanism against AChE. Molecular docking demonstrated that the seven compounds effectively bound to the AChE active site, with binding affinities ranging from -9.7 to -8.5 kcal/mol. The established AChE@MIL-88B-NH 2 -based ligand fishing strategy provides a simple and efficient approach for screening potential AChE inhibitors from complex botanical matrices, offering a promising avenue for discovering novel therapeutic agents for AD.
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JOURNAL OF MATERIALS RESEARCH
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2025
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IF 2.9
Yang Wen,Wang Yujia,Gao Na,Zhu Zhengfa,Chen Yuanyuan,Wang Hao,Tang Xiaoning
Designing efficient visible light-driven photocatalytic antimicrobial agents presents significant challenges. In this study, S-shaped core–shell NH 2 -MIL-125/TiO 2 (NT-x) heterojunctions were constructed by simple in situ solvothermal method, as photocatalytic antimicrobial agents for efficient bactericidal use under visible light. Notably, 99.99% inhibition was achieved for both Escherichia coli and Staphylococcus aureus at low concentrations (0.02 and 0.035 mg mL −1 , respectively) after exposure to simulated sunlight for 20 min. Reasonable energy band configuration and built-in electric field of this structure provided improved photogenerated carrier transfer paths as well as enhanced separation and transport efficiency. Moreover, the core–shell structure enhanced the interaction between NH 2 -MIL-125 and TiO 2 , increased the total number of reactive sites, and promoted the efficient generation of reactive oxygen species. Finally, possible mechanisms for the inactivation of bacteria were discussed. This research offers new perspectives for the advancement of advanced metal–organic framework-based photocatalysts with antibacterial activity under visible light. Graphical abstract
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Chemical Engineering Journal Advances
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2023
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IF 0
Mengsi Cheng,Ying Fang,Zhaoguang Yang,Xinghao Liu,Bo Qiu,Tong Zhang,Haipu Li,Wenbo Zhao
MIL-100(Fe) was modified by amino groups (MIL - 100(Fe) - NH 2 ) to enhance the removal of antimonate (Sb(V)) with low concentration (50−200 μg/L) from natural water through batch adsorption experiments. With the initial Sb(V) concentration up to 200 μg/L, the residual Sb(V) concentration after treated by MIL - 100(Fe) - NH 2 was only 3.52 ± 0.131 μg/L, lower than the drinking water standards (5 μg/L) in China, while that was much higher (94.2 ± 3.52 μg/L) after pristine MIL-100(Fe) treatment. Based on results of XPS analysis, and adsorption kinetics and isotherms, we concluded that Sb(V) substituted the terminal −OH groups of MIL-100(Fe) to form inner-sphere complexes by coordination reactions with Fe nodes and be adsorbed by hydrogen bonding as well. The grafted amino groups (−NH 2 ) adsorbed Sb(V) by hydrogen bonding and facilitated the coordination reactions between Sb(V) and Fe nodes. The higher K L value (0.0116 ± 0.00,118 L/μg) obtained by fitting with the Langmuir isotherm model, while that of unmodified MIL-100(Fe) was 4.74 × 10 −4 ± 5.85 × 10 −5 L/μg, also confirmed that the −NH 2 groups greatly enhanced the affinity between MIL-100(Fe) and Sb(V). Furthermore, MIL - 100(Fe) - NH 2 still worked nicely in a wide pH range (2 − 12), with varied ionic strength (0.05 µmol/ L −1.5 mol/L), coexisting ions (CO 3 2− , NO 3 − , SO 4 2− , Cl − , H 2 PO 4 − ), and even in the real water bodies. Additionally, MIL - 100(Fe) - NH 2 exhibited good reusability and low Fe leaching (99.92 μg/L). We hope MIL - 100(Fe) - NH 2 become a candidate for effective removal of Sb(V), even other heavy metals from natural waterbodies.
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Journal of Nanomaterials
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2015
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IF 1.644
Tong Liu,Qingtao Wang,Bingzheng Yan,Mei Zhao,Wenbo Li,Haiyan Bie
Highly dispersed crystalline Ru nanoparticles (NPs) were successfully immobilized inside the pores of MIL-101 by a double solvents method (DSM). HRTEM clearly demonstrated the uniform distribution of the ultrafine Ru NPs throughout the interior cavities of MIL-101. The synthesized Ru@MIL-101 catalyst was also characterized by X-ray diffraction (XRD), N2 adsorption desorption, and ICP-AES. The catalytic test indicated that the Ru NPs supported MIL-101 material exhibited exceedingly high activity and excellent durability for hydrogen generation from the catalytic hydrolysis of amine boranes.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2019
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IF 5.107
Yuqi Cui,Li-chao Nengzi,Jianfeng Gou,Yan Huang,Bo Li,Xiuwen Cheng
Z-scheme heterojunction photocatalyst can simultaneously reduce the recombination of photo-generated electron-hole pairs and preserve its outstanding redox ability during the process of photocatalytic reaction. In this study, Z-scheme MIL-53(Fe)/α-Bi 2 O 3 /g-C 3 N 4 photocatalyst was successfully fabricated via an accessible method and comprehensive characterized by XRD, FT-IR, SEM, TEM, XPS, N 2 adsorption-desorption isotherms, UV–vis diffuse reflection spectroscopy and photoelectrochemical analysis. The as-obtained MIL-53(Fe)/α-Bi 2 O 3 /g-C 3 N 4 composite exhibited superior photocatalytic activity for amino black 10B degradation than that of pure g-C 3 N 4 , α-Bi 2 O 3 , MIL-53(Fe) and α-Bi 2 O 3 /g-C 3 N 4 binary composite under visible light irradiation and the photodegradation rate would achieve the maximum when the mass fraction of MIL-53(Fe) was 32% in ternary composite. The enhanced photocatalytic performance of MIL-53(Fe)/α-Bi 2 O 3 /g-C 3 N 4 ternary composite could be mainly ascribed to improved visible light absorption range and the construction of an effective interfacial heterojunction driven by direct solid-state dual Z-scheme mechanism, which significantly facilitates the separation and transfer of photo-generated charge carriers. Eventually, the as-prepared ternary composite was confirmed to have prominent stability and reusability after consecutive 4 recycling run.
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