LANGMUIR
·
2022
·
IF 4.331
Zhiliang Jin,Xiaohong Li,Teng Li,Youji Li
Graphdiyne (g-CnH2n–2) is a new carbon material composed of sp and sp2 hybrid carbon atoms. Since the synthesis by Li’s team, graphdiyne has been widely studied in other fields because of its excellent properties. In this paper, graphdiyne was synthesized from copper-containing materials and the composite GDY/CuI/MIL-53(Al) S-scheme heterojunction is prepared for photocatalytic cracking of water to produce hydrogen. First, GDY/CuI was prepared by organic synthesis, and then GDY/CuI was anchored on the surface of MIL-53(Al) by in situ ultrasonic stirring. After the continuous optimization of experimental conditions, the final hydrogen evolution rate is much higher than that of MIL-53(Al). This efficient photocatalytic performance can be attributed to the S-scheme heterojunction formed by the unique energy band arrangement. At the same time, the mechanism of charge transfer was demonstrated by in situ irradiation X-ray photoelectron spectroscopy. The strong interaction among the three strongly promotes the separation and transfer of photogenerated electron–hole pairs.
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高影响因子
Journal of Environmental Chemical Engineering
·
2023
·
IF 7.7
Shuya Liu,Xinjie Ma,Yuxin Liu,Weiwei Chen,Yuejie Ai,Kexin Li,Xiushen Ye,Ming Fang,Xiaoli Tan
To fully utilize the customizable characteristics of metal-organic framework (MOF) materials in environmental applications, it is important to precisely modulate the branching groups of MOFs for improved performance. In this work, MIL-53(Al) was modulated by different numbers of nitrogen atoms and carboxyl groups/phosphite groups (MOF-N 2 -(COOH) 3 , MOF-N 3 -(COOH) 4 , and MOF-N 2 -(PO(OH) 2 ) 3 ) via a post-synthesis modification method, and the influence of functional groups and chain length on adsorption and the mechanism of modified groups on the adsorption of uranium (U) are demonstrated. Batch experiments suggest the removal of U(VI) reaches 37%, 27%, and 90% for MOF-N 2 -(COOH) 3 , MOF-N 3 -(COOH) 4 and MOF-N 2 -(PO(OH) 2 ) 3 , respectively (pH = 4.0, T = 25 ℃, I = 0.01 M NaNO 3 ). The surface complexation between UO 2 2+ and the surface of functional groups on the modulated MOF dominates the adsorption. Nevertheless, the steric hindrance in MOF porous structure can explain the inferiority of U(VI) adsorption on MOF-N 3 -(COOH) 4 (27%) to MOF-N 2 -(COOH) 3 (37%). MOF-N 2 -(PO(OH) 2 ) 3 is more conducive to uranyl adsorption than MOF-N 2 -(COOH) 3 or MOF-N 3 -(COOH) 4 , which is due to better affinity of U(VI) to phosphate group than the carboxyl group by density functional theory (DFT) calculation. Moreover, the excellent regeneration performance and U(VI) adsorption of MOF-N 2 -(PO(OH) 2 ) 3 in natural water or wastewater further confirmed the practical application of modulated MOFs in practical application.
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2022
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IF 6.76
Liwei Sun,Meilin Yin,Zhen Li,Shaokun Tang
To alleviate environment issues derived from CO 2 emission, developing effective and economical methods for CO 2 capture has attracted much attention for decades. Metal-organic frameworks possess high porosity and stability, which is favorable to the adsorption of small molecules. Herein, an aluminum-based MOF, aluminum terephthalate [MIL-53(Al)], was synthesized with H 2 O and N , N′ -dimethylformamide as co-solvent via microwave-assisted method for CO 2 adsorption. The parameters including pre-mixing mode, microwave temperature, microwave power and reaction time were varied to study their influences on crystal structure, morphology and CO 2 adsorption capacity of MW-MIL-53(Al). Wherein, MW-MIL-53(Al) prepared with pre-mixing mode of stirring at 130 °C, 200 W and 3 h presents high crystallinity and rod-like morphology. The synthesized MW-MIL-53(Al) possesses relatively high BET surface area (961 m 2 /g), pore volume (0.46 cm 3 /g) and thermal stability (up to 480 °C), and its CO 2 adsorption capacity is 2.16 mmol CO 2 /g adsorbent under 25 °C and 0.1 MPa, which is higher than CS-MIL-53(Al) synthesized via conventional solvothermal method at 130 °C for 48 h.
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高影响因子
FOOD CHEMISTRY
·
2023
·
IF 8.8
Huilin Li,Jingying Yang,Ran Han,Yueyao Wang,Xintong Han,Shuo Wang,Mingfei Pan
Rapid, sensitive, specific and stable detection of mycotoxin in food remains an extremely crucial issue. Herein, a magnetic-fluorescent immunosensing platform for the detection of zearalenone (ZEN) was proposed. The platform utilized Au nanoparticles (AuNPs) heterogeneous fluorescent metal–organic framework (MIL-53(Al)@AuNPs) labeled with ZEN-bovine serum albumin (ZEN-BSA) as signal probe and ZEN mono-antibodies coupled with magnetic NPs (MNPs-mAbs) as capture probe. Specifically, the heterogenization of AuNPs on the MIL-53(Al) surface improved its biocompatibility, and facilitated the loading of ZEN-BSA conjugates. The MNPs-mAbs could rapidly capture the target ZEN, simplify the immunoassay process and further improve the detection efficiency. The established competitive magnetic-fluorescent immunosensing platform had a wider linear response to ZEN in the range of 0.001–100 ng/mL with a lower limit of detection (LOD) at 0.0035 ng/mL, and could finish the whole detection process within 20 min, showing great potential for rapid and sensitive detection of food contaminants.
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高影响因子
POLYHEDRON
·
2019
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IF 2.284
Ning Tian,Yifang Dai,Qing Liu,Wei Dai
A general synthetic strategy for HS-Fe 3 O 4 @MIL-53(Al) adsorbent has been developed in this work. The composite material exhibits an efficient capture performance for rubidium ion due to sulfhydryl group and magnetic Fe 3 O 4 doped in its porous cavity. The results of X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and N 2 adsorption–desorption proved that the HS-Fe 3 O 4 was immobilized in the composite material. High Rb + uptake capacity over the HS-Fe 3 O 4 @MIL-53(Al) is attributed to the exchange of acidic protons between the sulfhydryl group and the Rb + . The pseudo-second-order and Freundlich model could make a good description of the adsorption process. The Rb + sorption selectivity was moderately influenced by any co-ions effect (K + , Na + and Cs + ) due to HS-Fe 3 O 4 doped. These results reveal that our novel composite material might be a promising industrial adsorbent for Rb + capture.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2016
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IF 2.567
Huimin Ruan,Changmeng Guo,Hongwei Yu,Jiangnan Shen,Congjie Gao,Arcadio Sotto,Bart Van der Bruggen
This study reports the fabrication of mixed matrix membranes (MMMs) using immersion precipitation phase inversion for promising application in desalination of dye solutions. Aromatic poly(m-phenylene isophthalamide) is used as the polymer material, and the metal–organic framework MIL-53(Al) is added to develop integrally skinned asymmetric membranes. Successful dispersion of MIL-53(Al) particles into the membrane-separating layer is confirmed by scanning electron microscopy. The optimum performance of the membranes is obtained at 0.5 wt % MIL-53(Al) concentration. In particular, the M-0.5 membrane is planned for use in separating dye/salt aqueous mixtures. It is observed that the M-0.5 membrane has a rejection for NaCl and Na2SO4 below 11% and 37%, respectively, in mixed salt/dye solutions. Additionally, the M-0.5 membrane is found to have a rejection rate of 83.9%, 98.3%, and 99.8% for nitroso-R salt, xylenol orange, and ponceau S, respectively, in mixed Na2SO4/dye solutions. The rejection rate for Na2SO4 is lower than that of some commercial nanofiltration membranes (NF90, NF270, and DK). The membrane is promising for dye desalination in industrial-scale applications.
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ACS Applied Nano Materials
·
2024
·
IF 5.3
Wenjing Li,Weichen Wang,Mingyue Zhu,Peiao Cong,Daowei Gao,Rongyao Wang,Guozhu Chen
Metal oxides@metal–organic framework (MOFs)-based core/shell nanostructures demonstrate promising potential in catalytic hydrogenations. However, the direct nucleation and growth of MOFs on the topologically diverse surfaces of metal oxides face significant challenges due to the high interfacial energy resulting from topological mismatches. Herein, we present a facile in situ growth strategy for directly assembling an MIL-53(Al) layer on the surface of CeO2 nanospheres at low temperatures by mixing and stirring CeO2 nanospheres and MIL-53(Al) precursors without requiring sacrificial templates or additional surface modifications. Moreover, key factors such as reaction time, temperature, and the types of aluminum salts and ligands are systematically explored to comprehensively understand the nucleation behavior of MOFs shells. Notably, when active Pt nanoparticles are sandwiched between the CeO2 core and the MIL-53(Al) shell, the MIL-53(Al) effectively stabilizes the Pt nanoparticles and enhances the selectivity of hydrocinnamaldehyde in cinnamaldehyde hydrogenation. CeO2/Pt@MIL-53(Al) achieved more than twice the selectivity for HCAL compared to CeO2/Pt and even outperformed Pt/MIL-53(Al). Undoubtedly, this study provides distinctive insights into the nucleation and growth mechanisms of MOFs on metal oxides, expands the strategies for fabricating metal oxides@MOFs core/shell nanostructure, and proposes innovative ideas and possibilities for broadening the application domains of MOFs-based materials.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
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IF 9
Xin-Ru Chen,Heng Mao,Qiu-Ying Zhang,Wei-Min Liu,Shen-Hui Li,Qian-Qian Li,Li-Hao Xu,Yan-Mei Zhang,Xin-Yue Zhang,Jun-Jie Liu,Ao Kou,Zhi-Ping Zhao
Interfacial engineering in mixed matrix membranes (MMMs) is essential to attain superior separation performance and ensure long-term operational stability. In this research, a range of novel MMMs were designed and fabricated for pervaporation (PV) separation of n-butanol/water solution by introducing the MIL-53(Al) particles and three variants (i.e., MIL-53(Al)–NH 2 , MIL-53(Al)–NO 2 , MIL-53(Al)–OH) into PEBA polymer matrix. These four MIL-53(Al) counterparts were synthesized via a microwave-assisted solvothermal method by selectively functionalizing the terephthalic acid linkers with different chemical groups. The functional MIL-53(Al) variants were employed to explore the relationship between membrane microstructures and PV performance by manipulating the interfacial interactions with PEBA matrix. The findings reveal that incorporating MIL-53(Al) variants not only displayed excellent interfacial compatibility and uniform dispersion within PEBA matrix, but also constructed the preferential transport pathways for n-butanol over water molecules. Impressively, in a 1 wt% n-butanol aqueous solution at 40 °C, the resultant membrane attained a permeation flux of 1483.3 g·m -2 ·h -1 and a separation factor of 18.1. Compared to the PEBA/PVDF membrane, the total flux was enhanced by 17.1 %, and the separation factor was improved by 46.4 %. Moreover, the embedding MIL-53(Al) variants boosted thermal and mechanical properties of the membrane, endowing it with considerable potential for practical applications.
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Journal of Environmental Chemical Engineering
·
2026
·Vol. 14
·期 5
·123915
·
IF 7.5
Jumeng Di,Xiaohua Li,Songyu Guan,Wenwen Ma,Wen Li,Jie Gao,Yuzhi Xu,Bing Yu,Hailin Cong
Nanoplastics (NPs) pose severe risks to aquatic environments, and adsorption technology provides a promising strategy for their removal. Metal-organic frameworks (MOFs) are promising adsorbents, but their practical application is limited by insufficient water stability and restricted pore accessibility. To bridge this gap, defect-engineered Al/Mn bimetallic MOFs were synthesized via mild post-synthetic ion exchange. n-Octanoic acid (OA) was employed to modulate the crystallization process of MIL-53(Al), inducing missing linker defects, suppressing excessive crystal growth, and generating mesoporous structure. Subsequently, the partial substitution of terephthalic acid linkers with manganese clusters could introduce additional active sites, alter the surface properties while maintain the overall crystallinity of MOFs. The optimized Mn-0.2-OA maintained high PS removal efficiency under acidic to neutral conditions, with removal efficiencies above 92% over pH 1–7. It also showed good tolerance to representative interference factors, retaining removal efficiencies above 97.5% in the presence of common cations and 89.37% at 40 mg/L humic acid. The adsorption of 500 nm polystyrene microspheres was mainly driven by the synergistic effects of electrostatic attraction, π-π interactions, enhanced hydrophobic affinity, and hierarchical pore structure. Meanwhile, Mn-0.2-OA achieved a Langmuir-fitted maximum adsorption capacity of 849.17 mg/g and exhibited rapid adsorption kinetics, removing 96.4% of PS within 10 min at an initial concentration of 25 mg/L. Regeneration tests further confirmed its acceptable reusability for repeated PS adsorption. This strategy provides a feasible approach for designing efficient and reusable adsorbents for nanoplastic removal from aquatic environments.
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JOURNAL OF SOLID STATE CHEMISTRY
·
2022
·
IF 3.656
Chunfu Liu,Chenyu Zhu,Han Wang,Shenao Xie,Junyang Zhou,Hongjun Fang
Co-doped metal organic frameworks (MOFs) were fabricated by a facile route and applied to remove (tetracycline, congo red, methylene blue and rhodamine B) through integrated adsorption and photocatalysis . The assembled MOFs composite exhibited larger S BET (889 m 2 /g), broad light adsorption, and accelerated carrier kinetics, which helped to enhance adsorption and photocatalysis performance. Specifically, nearly 100% TC (40 mg/L) could be removed by the Co-MIL-10 within 12 min solar-light irradiation, significantly faster than that of solo MIL-53(Al) (82%) and CoAl-LDH (54%), separately. Furthermore the obtained rate constant (0.2064 min −1 ) was 4.8 times and 9.7 times greater than that of MIL-53(Al) and CoAl-LDH, respectively. The quenching/EPR characterization suggested that photo-generated h + / • O 2 − / • OH species were responsible for TC oxidation , of which h + showed the great impact. Cycling experiments verified the robust stability of the MOFs catalyst. As well, an underlying photocatalytic mechanism of the current system was investigated in detail.
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ENVIRONMENTAL RESEARCH
·
2022
·
IF 8.431
Luan Minh Nguyen,Ngoan Thi Thao Nguyen,Thuy Thi Thanh Nguyen,Dai Hai Nguyen,Duyen Thi Cam Nguyen,Thuan Van Tran
The global occurrence of textile dyes pollution has recently emerged, posing a serious threat to ecological systems. To abate dye contamination, we here developed a novel magnetic porous CoFe 2 O 4 @MIL–53(Al) nanocomposite by incorporating magnetic CoFe 2 O 4 nanoparticles with MIL–53(Al) metal–organic framework. This nanocomposite possessed a surface area of 197.144 m 2 g −1 and a pore volume of 0.413 cm 3 g −1 . The effect of contact time (5–120 min), concentration (5–50 mg L −1 ), dosage (0.1–1.0 g L −1 ), and pH (2–10) on Congo red adsorption was clarified. CoFe 2 O 4 @MIL–53(Al) could remove 95.85% of Cong red dye from water with an accelerated kinetic rate of 0.6544 min −1 within 10 min. The kinetic and isotherm models showed the predominance of Bangham and Temkin. According to Langmuir, the maximum uptake capacities of CoFe 2 O 4 @MIL–53(Al), CoFe 2 O 4 , and MIL–53(Al) adsorbents were 43.768, 17.982, and 15.295 mg g −1 , respectively. CoFe 2 O 4 @MIL–53(Al) was selected to optimize Cong red treatment using Box–Behnken experimental design. The outcomes showed that CoFe 2 O 4 @MIL–53(Al) achieved the highest experimental uptake capacity of 35.919 mg g −1 at concentration (29.966 mg L −1 ), time (14.926 min), and dosage (0.486 g L −1 ). CoFe 2 O 4 @MIL–53(Al) could treat dye mixture (methylene blue, methyl orange, Congo red, malachite green, and crystal violet) with an outstanding removal efficiency of 81.24% for 30 min, and could be reused up to five cycles. Therefore, novel recyclable and stable CoFe 2 O 4 @MIL–53(Al) is recommended to integrate well with real dye treatments systems.
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APPLIED CATALYSIS B-ENVIRONMENTAL
·
2021
·
IF 19.503
Huanan Zhao,Zipeng Xing,Siyi Su,Sijia Song,Zhenzi Li,Wei Zhou
NH 2 -MIL-53(Al)/CdS p-n heterojunctions are fabricated via facile two-step hydrothermal method. The formation of p-n heterojunctions could form built-in field, which favors spatial charge separation. The resultant NH 2 -MIL-53(Al)/CdS p-n heterojunctions with narrowed band gap extend the photoresponse, and have a high specific surface area of 417.7 m 2 g −1 , and a narrow pore size of 8.8 nm. Under visible light irradiation, the photocatalytic efficiency for reduction of Cr(VI) and removal of refractory pesticide trichlorophenol is up to 99.23 and 98.85 %, respectively. The photocatalytic oxygen evolution is also as high as 563.6 μmol g −1 h −1 . The excellent photocatalytic activity can be ascribed to the efficient p-n heterojunctions accelerating charge transfer and favoring spatial charge separation, and the special mesoporous structure supplying adequate surface-active sites and facilitating mass transfer. This facile strategy opens up new insights for fabricating other p-n heterojunctions photocatalysts with efficient solar energy conversion.
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