Surfaces and Interfaces
·
2026
·
IF 6
Wuxiu Ding,Duo Sun,Lan Zhang,Hongyi Wang,Yang Zhao,Weiguo He,Zhigang Du,Yongyan Yan
Applying protective coatings to the surface of stone heritage is one of the most common methods for its preservation. To enhance the weathering resistance of the limestone heritages, MIL-53@FS, a hydrophobic metal-organic framework (MOF) composite, was prepared through fluorosilane modification of MIL-53-OH synthesized via a solvothermal method. Characterization analyses were conducted using SEM, XRD, TGA, and FTIR techniques. The results indicated that MIL-53@FS maintained its well-ordered framework structure and certain porosity, while forming a continuous and uniform hydrophobic coating, leading to a significant increase of water contact angle to 127.14° and enhanced thermal stability. It exhibited excellent corrosion resistance, anti-icing performance, and color compatibility in the application tests, holding a promising outlook for protecting limestone-based heritages.
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RSC Advances
·
2021
·Vol. 11
·期 4
·2397-2404
·
IF 3.361
Jing Chen,Yali Xu,Shuying Li,Fanghong Xu,Qian Zhang
Tetracycline detection has been a great concern because of its overuse and difficulty in degrading. Here, a detection method with ratio fluorescence was developed by synthesizing Eu3+ doped nanocomposites with NH2-MIL-53(Al) nanosheets. After adding tetracycline, the fluorescence intensity at 616 nm characteristic emission peak of Eu3+ was sensitized by the antenna effect generated from coordinating Eu3+ with tetracycline, but the fluorescence of NH2-MIL-53(Al) at 433 nm was quenched by the fluorescence resonance energy transfer between the Eu3+-tetracycline composition and NH2-MIL-53(Al). Therefore, the efficient detection of tetracycline was achieved based on this change of ratio fluorescence signal. The experimental results show that Eu3+/NH2-MIL-53(Al) has excellent selectivity, a wider linear range and a lower detection limit for detecting tetracycline. This method can afford favorable ideas for developing advanced chemical and biological sensors.
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ANALYTICAL LETTERS
·
2020
·
IF 1.467
Meijuan Ren,Huan Wang,Yuanyuan Liu,Qin Ma,Wenjing Jia,Mingzhu Liu,Huiju Wang,Yongchang Lu
Amino-MIL-53(Al) nanosheets were synthesized by a hydrothermal reaction and were employed as a fluorescent probe because of their high quantum yield and excellent stability. The amino-MIL-53(Al) nanosheets have a maximum fluorescence emission peak at 435 nm using an excitation wavelength of 335 nm. The fluorescent intensity of luminophor at 435 nm was linearly quenched when mercury (II) (Hg2+) was added, which occurred due to the adsorption of Hg2+ onto the luminophor surface. Under these conditions, the fluorescent signal of the system is in the “turn-off” state. Following the addition of glutathione (GSH) into the system, the quenched fluorescence intensity may be partially restored based on the reaction between glutathione and Hg2+. In this condition, the fluorescent signal of the amino-MIL-53(Al)-Hg2+ system is in the “turn-on” state. Therefore, the amino-MIL-53(Al) nanosheets were successfully used as a “turn-off-on” fluorescent sensing system to determine the concentrations of Hg2+ in Tibetan medicine and glutathione in rabbit serum. A good correlation coefficient was obtained between the quenching of the fluorescence intensity of luminophor and the concentration of Hg2+ using the optimized conditions. A linear range was acquired from 1.96 nM to 38.27 μM with a detection limit of 0.23 nM of Hg2+ based upon a signal-to-noise ratio of three. For glutathione, the linear dynamic range was from 210 nM to 15.25 μM with a detection limit equal to 8.11 nM based upon a signal-to-noise ratio of three. This developed sensor system has the advantages of high selectivity, favorable sensitivity and simple operation for the determination of Hg2+ and glutathione in real samples.
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CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
·
2022
·
IF 1.193
Linli HOU,Li WANG,Yonghai SONG,Limin LIU
A luminescent hydroxyl-functionalized MIL-53(Al) (OH-MIL-53(Al)) was prepared by one-step solvent thermal method for multiresponsive fluorescence sensor. The OH-MIL-53(Al) exhibited uniform nanospheres with average diameter of 150±20 nm, flexible three-dimensional frameworks, and good dispersion in water. The OH-MIL-53(Al) emitted green fluorescence with a maximum wavelength of 515 nm which showed good fluorescence quenching response for sensing F − and fluorescence enhancement response for water, with good day-to-day stability. The mechanism was based on protonation/deprotonation of hydroxyl group located on OH-MIL-53(Al). Good linear relationship could be found between the luminescence intensity of 515 nm and F − concentrations in the range of 0–60 µM with a determination limit of 70 nM. At the concentrations from 0% to 100%, the fitting curve for water content was in good agreement with the linear equation, and the detection limit was 0.10%. OH-MIL-53(Al) demonstrated excellent fluorescence sensing performance, indicating that it could be used as a multiresponsive sensor to practical application.
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DALTON TRANSACTIONS
·
2021
·Vol. 50
·期 24
·8540-8548
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IF 4.39
Zixuan Li,Deyi Zhan,Abdul Saeed,Nanjing Zhao,Junfeng Wang,Weihong Xu,Jinhuai Liu
Due to their ultra-thin morphology, larger specific surface area and more exposed active sites, two-dimensional (2D) metal–organic framework (MOF) nanosheets can break the limitations of three-dimensional (3D) MOFs in sensitivity, response speed and the limit of detection for sensing applications. In this work, fluorescent NH2-MIL-53(Al) nanosheets were developed as a fluoride detection sensor compared with the 3D bulk counterpart. The morphological and structural characteristics of the obtained products were systematically characterized, and the favourable chemical and fluorescence stability of the NH2-MIL-53(Al) nanosheets were explored. The fluorescent NH2-MIL-53(Al) nanosheets showed high sensitivity, fast response speed (as short as 10 seconds), low limit of detection (15.2 ppb), and wide linear detection range (5–250 μM), and all performances were better than those of their bulk counterpart. In addition, the sensing mechanism was investigated to be based on the transformation of the NH2-MIL-53(Al) framework that induced the release of fluorescent ligands, resulting in an exceptionally enhanced fluorescence. This work highlights the advantages of 2D MOF nanosheets in fluorescence sensing applications.
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CHEMOSPHERE
·
2023
·
IF 8.8
Hao Li,Canyuan Lin,Ruhui Ma,Yuancai Chen
In this study, the selective adsorption of aromatic compounds on mesoporous MIL-53(Al) was investigated, and followed the order: Biphenyl (Biph) > Triclosan (TCS) > Bisphenol A (BPA) > Pyrogallol (Pyro) > Catechol (Cate) > Phenol (Phen), and exhibited high selectivity toward TCS in binary compounds. In addition to hydrophobicity and hydrogen bonding, π–π interaction/stacking predominated, and more evidently with double benzene rings. TCS-containing halogens could increase π interaction on the benzene rings via forming Cl–π stacking with MIL-53(Al). Moreover, site energy distribution confirmed that complementary adsorption mainly occurred in the Phen/TCS system, as evidenced by Δ Q pri (the decreased solid-phase TCS concentration of the primary adsorbate) < Q sec (the solid-phase concentrations of the competitor (Phen)) . In contrast , competitive sorption occurred in the BPA/TCS and Biph/TCS systems within 30 min due to Δ Q pri = Q sec , followed by substitution adsorption in the BPA/TCS system, but not for the Biph/TCS system, likely attributed to the magnitude of energy gaps (E g ) and bond energy of TCS (1.80 eV, 362 kJ/mol) fallen between BPA (1.74 eV, 332 kJ/mol) and Biph (1.99 eV, 518 kJ/mol) according to the density-functional theory of Gaussian models. Biph with a more stable electronic homeostasis than TCS lead to the occurrence of substitution adsorption in the TCS/BPA system, but not in the TCS/Biph system. This study provides insight into the mechanisms of different aromatic compounds on MIL-53(Al).
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JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Cong Xie,Xiao Zhang,Wenbin Shi,Ping Yang
The poor stability of perovskite nanomaterials exposed in high temperature, moisture, light radiation, and polar solvent conditions severely restrict their commercial application. To address this issue, the growth in situ of CsPbX 3 (X = Cl, Br, I) nanocrystals (NCs) is carried out by using the stable aluminum (Al)-based metal-organic frameworks to create CsPbX 3 @MIL-53(Al) composites. Compared with pristine CsPbX 3 NCs prepared using room temperature ligand assisted re-precipitation synthesis, the CsPbX 3 @MIL-53(Al) composites exhibit narrow photoluminescence (PL) spectra and greatly improved stability. The green emitting CsPbBr 3 @MIL-53(Al) composite exhibit narrowed PL spectrum (the full width at half-maximum of PL spectra: 20 nm for the composite and 28 nm for CsPbBr 3 NCs) and a blue-shifted PL peak wavelength (517.6 nm for the composite and 527.6 nm for the CsPbBr 3 NCs). The relationship of microstructure, components, PL, fluorescence lifetime, and stability are discussed systematically. Anomalous stability against heat-treatment, polar solvent and humidity conditions indicated the composites retained their initial PL intensity after storge more than 4 months in ambient conditions and heat-treated to 120ºC for 5 cycles. The emitting color of CsPbBr 3 @MIL-53(Al) composites are easily adjusted from blue, green to red by controlling the halide components of precursors. The composite was used to create emitting coating and highly bright flexible emitting films which also reveal high stability, suggesting that in situ encapsulation of CsPbX 3 NCs in MIL-53(Al) would supply a novel platform for various emitting devices.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2026
·
IF 4.8
Haozhe Yang,Mo Yang,Fangrong Hu,Mingzhu Jiang,Longhui Zhang,Shangjun Lin,Ziheng Zhi,Wanting Zhu,Chenxi Liu,Lei Li
A MIL-53(Al)-functionalized terahertz metasurface sensor was developed for the room-temperature detection of styrene, a potential volatile biomarker associated with lung cancer. The sensor combines the localized electromagnetic field enhancement of the terahertz metasurface with the adsorption enrichment capability of MIL-53(Al). Benefiting from the flexible one-dimensional channels, the size-compatible pore environment of MIL-53(Al), and the possible π–π and host–guest interactions between styrene molecules and the terephthalate linkers, the functionalized metasurface exhibits an enhanced sensing response toward styrene. APTES was introduced as an interfacial coupling layer to improve the immobilization and dispersion of MIL-53(Al) nanocrystallites on the metasurface. SEM and FTIR characterizations confirmed the formation of a nanocrystallite-stacked MIL-53(Al) coating and the successful introduction of both APTES and MIL-53(Al) onto the sensor surface. The optimized sensor achieved a sensitivity of 0.37 GHz/ppm and a limit of detection of 1 ppm within the concentration range of 1–100 ppm. In addition, the sensor showed good selectivity against several interfering VOCs, as well as acceptable repeatability and stability. This work provides a feasible strategy for integrating flexible MOF adsorbents with terahertz metasurfaces, offering a potential platform for rapid, label-free, and room-temperature detection of trace aromatic VOCs.
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INORGANICA CHIMICA ACTA
·
2018
·
IF 2.264
Yebin Guan,Ming Xia,Xiaohong Wang,Weicheng Cao,Alessandro Marchetti
Nano-sized NH 2 -MIL-53(Al) particles were conveniently synthesized in aqueous solution at ambient temperature with a widely applicable mixing method, and the morphology and character were examined with a series of techniques. XRD patterns and TEM images showed that the obtained NH 2 -MIL-53(Al) material possessed rod-like shape, which is different from those obtained from N, N-dimethyl formamide (DMF). This nano-sized NH 2 -MIL-53(Al) matrix displayed enhanced efficiency for adsorptive elimination of methyl blue molecules in aqueous solution.
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INORGANIC CHEMISTRY
·
2024
·
IF 4.3
Yuhao Che,Wenhui Li,Chunqi Wang,Xuemin Zhang,Zilei Guo,Aziz Bakhtiyarovich Ibragimov,Junkuo Gao
The development of materials with superior thermal insulation and flame retardancy is critical for industrial applications and daily life. Metal–organic framework (MOF)@poly(vinyl alcohol) (PVA) (MOF@PVA) aerogel composites have demonstrated remarkable thermal insulation and flame retardancy properties. In this work, MIL-53(Al) was directly mixed with PVA and formed by freeze-drying, and the influence of the pore structure on the thermal insulation and flame retardancy properties of the materials was investigated. The incorporated MIL-53(Al) nanoparticles introduced abundant micro- and mesopores, enhancing the complexity of the pore structure and improving the thermal insulation and flame retardancy properties of the aerogels. The directionally freeze-cast aerogel achieved a thermal conductivity of 0.040 W·mK–1, and maintained excellent thermal insulation ability even at 220 °C. Furthermore, the aerogel exhibited nonflammable and self-extinguishing characteristics. This environmentally friendly manufacturing method provides new ideas for the design of MOF-based composites, thereby expanding their application areas.
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2025
·
IF 8.5
Le Zhong,Yuxiao Feng,Zichen Wang,Tian Tian,Yali Bi,Jiandong Cui
Enzymatic synthesis of flavor esters is crucial for applications in food, beverage, and cosmetics industries. However, the poor activity and stability of free lipase hinder these reaction. Inspired by the concept of lipase interface activation, MIL-53(Al)-NH 2 was modified with alkyl acid anhydrides of varying chain lengths to tailor its hydrophobicity, and Candida Rugosa lipase (CRL) was subsequently immobilized on this surface to achieve efficient interface activation. The resulting CRL@MIL-53(Al)-AM11 exhibited 3.5 times higher activity than the unmodified CRL@MIL-53(Al)-NH 2 . Moreover, CRL@MIL-53(Al)-AM11 enabled one-step purification of crude CRL via selective adsorption. It also showed enhanced storage and thermal stability as well as higher resistance to protease degradation and denaturants than free CRL. CRL@MIL-53(Al)-AM11 retained 75 % of its initial activity after 30 min treatment at 55 °C, whereas the free CRL retained only 41 %. After 11 days of storage, CRL@MIL-53(Al)-AM11 maintained 70 % of its initial activity, in contrast to 36 % for the free lipase. Notably, CRL@MIL-53(Al)-AM11 achieved a 97 % conversion rate in the esterification synthesis of the flavoring substance (butyl butyrate) within 24 h and retained over 40 % conversion after five consecutive cycles. Therefore, this strategy offers a feasible approach for constructing high-performance immobilized lipases for flavor ester synthesis.
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Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 2
·121220
·
IF 7.2
Mengjiao Yu,Xiong-Fei Zhang,Mengjie Li,Jianan Song,Jianfeng Yao
The valorization of cellulose into valuable platform chemicals necessitates efficient and sustainable catalytic systems, where the acid-base properties of catalysts are critical for directing reaction pathways. This work presents the one-pot synthesis of a series of aluminum-based metal-organic frameworks (MIL-53) with tunable acid-base functionalities, achieved by modulating organic linkers. The successful formation of cooperative acid-base sites was confirmed by comprehensive characterization, including X-ray diffraction, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy and pyridine adsorbed infrared spectra. Catalytic performance evaluations demonstrated that acid-base cooperative sites significantly enhance the oriented conversion of cellulose to 5-hydroxymethylfurfural (5-HMF). Under optimal conditions (190 °C, 8 h) in a tetrahydrofuran (THF)/NaCl-H 2 O biphasic system, MIL-53-NH 2 /SO 3 H yielded 63.8 % 5-HMF, 6.3 % levulinic acid (LA), and 23.9 % formic acid (FA). The catalytic transformation of cellulose is a cascade process encompassing hydrolysis of cellulose to glucose, isomerization of glucose to fructose, dehydration to 5-HMF, and rehydration of 5-HMF to LA and FA. These results provide a promising strategy for designing efficient acid-base bifunctional catalysts for biomass conversion.
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