Journal of Materials Chemistry A
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2024
·Vol. 12
·期 46
·32030-32044
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IF 10.7
Xue Bi,Kunpeng Song,Qianlong Li,Tao Lin,Ye-Tang Pan,Wei Wang,Jiyu He,Rongjie Yang
In recent years, there have been few reports on the application of zeolites in the field of flame retardants, although their excellent thermal stability indicates great potential as flame retardants. However, a key challenge that needs to be solved urgently is the compatibility between molecular sieves as inorganic fillers and polymer matrices, which directly affects their performance and stability in practical applications. In this work, ZSM-5 zeolite was used as the carrier, Ce ions were introduced through ion exchange, and the growth of Ce-MOF was restricted on its surface, and a Ce-MOF@ZSM-5 hybrid material was designed to improve the flame retardant and ultraviolet resistance properties of thermoplastic polyurethane elastomer (TPU). The absorbance value of TPU composites in the whole region is significantly higher than that of pure TPU, and its absorbance reaches 1.33. Compared with pure TPU, the peak heat release rate and peak smoke production rate of TPU/Ce-MOF@ZSM-5 composites were reduced by 26.0% and 34.8%, respectively. In addition, the chemical resistance of TPU composites has been significantly improved. This work provides the possibility of preparing three-proofing TPU materials with UV resistance, chemical resistance and fire resistance, and is expected to expand the application of TPU materials in other fields.
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2024
·
IF 4.1
Liping Deng,Liangmei Rao,Xinyu Lu,Yutang Wang,Weiming Zhang,Xuemin Duan,Yangping Wen,Zhuohua Kong,Jingkun Xu
The accumulation of heavy metal cadmium (Cd) in the food chain poses a serious threat to human health, necessitating the development of rapid, on-site, and portable detection methods for Cd (II). Herein, we developed a smartphone-based electrochemical sensor for portable determination of Cd (II) in vegetables using a bismuth metal–organic framework (Bi-MOF) nanocomposite. Prismatic rod-like Bi-MOF was hydrothermally synthesized using trimesic acid as organic ligands, and subsequently, carboxyl-functionalized multi-walled carbon nanotubes (COOH-MWCNTs) were incorporated to form Bi-MOF nanocomposite network. The smartphone-based electrochemical sensor enables rapid, sensitive, and portable detection of Cd (II) in vegetable samples using Bi-MOF/COOH-MWCNTs-modified screen-printed carbon electrodes (SPCE). A comparative analysis of traditional electrochemical sensors coupled with desktop computer for linear voltametric responses for Cd (II) in the range of 0.2–500 ng/mL with a limit of detection (LOD) of 0.07 ng/mL using Bi-MOF/COOH-MWCNTs-modified glassy carbon electrodes (GCE), the portable sensor demonstrated good linear range in 0.7–350 ng/mL with a LOD of 0.22 ng/mL. This work introduces a novel approach for on-site and portable detection of Cd (II) in agricultural products.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Lei Zhu,Hongye Lu,Tianci Huo,Dongxiao Liu,Zechen Yan,Jianqiang Zhang
The frequent oil leakage accidents cause huge loss of natural resources and serious damage to the ecosystem. Although all kinds of modified sponges have been invented to deal with the offshore oil spills, it is difficult to separate high viscosity crude oil and water-in-oil emulsions. To address these challenges, a modified polyurethane (PU) sponge (PDMS/MOF-74@PU) coated by polydimethylsiloxane (PDMS) with ultra-low surface energy after growing spindle-shaped metal–organic framework structure (MOF-74) on the PU sponge surface was prepared. With the advantages of super-hydrophobic and high porosity, the prepared sponge can selectively and effectively absorb various oils from oil/water mixtures and it has good oil adsorption capacity (18–55 g/g). Meanwhile, the black MOF-74 endows the PDMS/MOF-74@PU photothermal properties for the separation of high viscosity crude oil under the light conditions. As well as, the prepared sponge shows excellent separation performance for the water-in-oil emulsions, the amount of water in the oil could reduce to less than 20 ppm and the separation efficiency could reach as high as 99.9 % after separation. In addition, we used molecular dynamics to verify the mechanism by which PDMS coatings change the surface wettability of materials. With the excellent mechanical property, chemical stability, and thermal stability in various harsh environments, the PDMS/MOF-74@PU have a broad application prospect in the treatment of offshore oil spills.
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NEW JOURNAL OF CHEMISTRY
·
2025
·Vol. 49
·期 7
·2889-2897
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IF 2.5
Yanan Zhu,Yongchang Yang,Shiqiang Li,Chang Zhu,Zegang Qiu,Qianqian Zhu
The development of efficient materials for adsorption desulfurization has attracted much attention for the safety of humans and the ecosystem. Metal–organic frameworks have shown promise in removing organic sulfur compounds in liquid fuels, while another star material – MXene has rarely been applied in this field. In this study, Ti3C2Tx MXene/Cu-MOF composites with different MXene contents (3.3%, 6.7%, and 13.3%) were synthesized via an in situ precipitation method. Characterization showed that the Cu-MOF was successfully coated on the surface of Ti3C2Tx MXene and partially embedded between the MXene nanosheets, restraining the agglomeration of both MXene and the Cu-MOF. The optimal composite-3.3%MXene/Cu-MOF presented the largest surface area of 166.6 m2 g−1. Compared to MXene and Cu-MOF, 3.3%MXene/Cu-MOF exhibited an enhanced adsorption performance for methyl phenyl sulfide in the model fuel with an equilibrium adsorption capacity of 87.4 mg g−1. Furthermore, the effects of adsorption parameters, adsorption kinetics, adsorption isotherms, and the adsorption mechanism, and regenerative performance of 3.3%MXene/Cu-MOF were comprehensively discussed. A pseudo-second order kinetic model and the Langmuir adsorption isotherm were found to better explicate the adsorption behavior on 3.3%MXene/Cu-MOF, which exhibited a theoretical maximum adsorption capacity of 183.9 mg g−1. This work hopes to shed light on the material design for adsorption desulfurization.
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JOURNAL OF MEMBRANE SCIENCE
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2025
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IF 9
Weihao Liu,Xu Jiang,Yan Yang,Lei Guo,Haoyang Wang,Lu Shao
Constructing high-performance mixed matrix membranes (MMMs) with highly permeable polymers of intrinsic microporosity (PIMs) and metal-organic frameworks (MOFs) faces critical challenge of poor interfacial compatibility between MOF fillers and the polymer matrix and difficulty in maintaining a defect-free interface at high filler loading (over 30 %). In this study, a Bi-HHTP loading as high as 50 wt% and uniform dispersion with excellent interfacial integrity is achieved in our high-performance MMMs through the elaborate design of multiple synergistic interfacial interactions, including hydrogen bonding between the phenolic hydroxyl groups of the 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP) ligand in the Bi-HHTP filler and the cyano groups in the PIM-1 matrix and π-π stacking between their benzene ring structures. The optimized MMM exhibits a remarkable CO 2 permeability up to 4021 Barrer with an ideal CO 2 /N 2 selectivity of 42.1 which substantially outperforms the neat PIM-1 membrane and exceeds the 2019 upper bound. The enhanced separation performance of the MMMs stems mainly from the significant increase in CO 2 solubility selectivity with Bi-HHTP loading, which benefits from the inherent CO 2 affinity of Bi-HHTP and the effective suppression of N 2 dissolution by the rigidification of PIM-1 chain segments induced by strong interfacial interactions. Most importantly, the resulted high-loading MMMs exhibited remarkable structural stability, showing strong resistance to both physical aging and CO 2 -induced plasticization. This strategy overcomes the loading bottlenecks of state-of-the-art MMMs and contributes advanced membrane materials for efficient CO 2 capture.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2025
·
IF 9
Huanhuan Dong,Xiaoyu Ji,Zhao Li,Junxiang Guo,Shan Peng
Viscous oil spills (e.g., petroleum and diesel) in marine environments and domestic oily wastewater pose seriously ecological and public health risks owing to their high viscosity and poor fluidity, making the remediation a very urgent challenge. To address these issues, we designed an inherently hydrophobic MXene/hollow CuCo-MOF (H-CuCo-MOF)@PDMS sponge featuring an instantly photothermal response and a multiscale wrinkled structure. The confined effects of H-CuCo-MOF and MXene synergistically generate an efficient electron transport network, where interfacial charge transfer enhances carrier lifetime, thereby prolonging photothermal conversion efficiency. In Addition, the high specific surface area of H-CuCo-MOF and the layered structure of MXene increase confined adsorption sites while preventing MOF aggregation. Stress mismatch between flexible PDMS and rigid MXene form a highly wrinkled architecture, effectively mitigating MXene stacking. Under 1-sun irradiation, the sponge’s surface temperature quickly reaches ∼80 °C within 20 s, altering surface tension and inducing the Marangoni effect to accelerate oil absorption. Moreover, taking advantages of high match between the coated sponge and the viscous oil, the separation efficiencies are exceeding 95 % for diesel oil and rapeseed oil, and 82.7 % for crude oil. The material also proves superior durability, maintaining stable hydrophobicity after 150 friction cycles, exceptional mechanical recovery (99.2 % after 10 compressions), and notable salt resistance and antibacterial properties.
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Catalysts
·
2025
·Vol. 15
·期 9
·812
·
IF 4
Xinru Gao,Han Meng,Changan Wang,Jinzhang Tao,Hongyi Gao
The development of highly efficient catalysts for the hydrogenation of dicyclopentadiene (DCPD) remains a critical challenge. In this study, we designed a series of bimetallic Ce–Ni metal–organic framework (MOF)-derived nanocatalysts by precisely tuning the Ce/Ni ratio and calcination temperatures. The optimized catalyst, Ni–CeO2(7:3)@C–400 °C, featuring highly dispersed carbon-coated Ni nanoparticles, achieved complete hydrogenation of DCPD to tetrahydrodicyclopentadiene (THDCPD) with 100% conversion and nearly 100% selectivity within 2 h under 100 °C and 2 MPa. The porous carbon framework significantly facilitated the diffusion and accessibility of DCPD molecules, combined with Ce species reconstructing the electronic structure of Ni active centers through electronic interactions, synergistically enhancing the hydrogenation efficiency. Furthermore, the catalyst demonstrated good structural stability. This work not only provides a robust strategy for the rational design of bimetallic MOF-derived catalysts but also highlights their potential for practical applications in industrial hydrogenation processes.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2025
·
IF 3.9
Kangxin Bai,Yang Liu,Zhuangzhi Li,Jiajie Shi,Zhenggong Wang,Jian Jin
The separation of C2H4/C2H6 is crucial for the efficient production of C2H4. The energy-efficient membrane technology has great potential in this separation. However, the similar physical properties of the two molecules make them extremely difficult in membrane separation. Herein, a series of nanosized MOF-808 particles were incorporated into a polyimide matrix to fabricate mixed matrix membranes (MMMs) for C2H4/C2H6 separation. The well-defined pore architecture of MOF-808 enables effective C2H4 purification through molecular sieving, while the restricted diffusion of C2H6 molecules within the MOF-808 channels facilitates remarkable kinetic separation. Importantly, the nanosized MOF-808 can be dispersed more evenly in the polymer matrix, significantly improving the compatibility between the polymer matrix and filler, thereby maximizing the sieving effect of MOF-808. The resulting nanosized MOF-808-based MMM demonstrates a high C2H4 permeability of 1187 barrer and a C2H4/C2H6 selectivity of 2.8, which has exceeded most of the MMMs reported so far and surpassed the 2013 upper bound. Our MMMs also show excellent long-term stability and antiplasticization performance. Our work highlights the effectiveness of enhancing the separation performance of MMMs by using reducing nanosized MOF-808, providing valuable insights for the design of MMMs for C2H4/C2H6 separation.
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JOURNAL OF LUMINESCENCE
·
2025
·
IF 3.6
Bin Wu,Denggerile Ao,Jun Ai,Lu Ga
Herein, a simple wet-milling synthesis method is reported for the production of Eu/Tb-based bimetallic-organic frameworks (Eu/Tb-MOFs). The introduction of the ligand 2, 5-dibromoterephthalic acid significantly turned on the characteristic fluorescence of the Eu/Tb-MOF at 620 nm through the “antenna effect”. The material was used as a fluorescent probe to detect tetracycline. In the presence of tetracycline, the fluorescence emission of Eu/Tb-MOF was dramatically turned off, allowing ratiometric fluorescence quantification of tetracycline. In addition, the combination of Eu/Tb-MOF with hydrogel can observe the afterglow property, which lays the foundation for the application in the field of anti-counterfeiting. Finally, Eu/Tb-MOF as a multifunctional fluorescent probe can also be used for fingerprint identification.
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Analytical Methods
·
2025
·
IF 2.6
Jiaxi Deng,Yiyao Luo,Jia Zheng,Zirui Yuan,Yi Ma,Huibo Luo,Xiaogang Luo,Danqun Huo,Changjun Hou
Baijiu represents the pinnacle of traditional Chinese culinary culture. The influence of Baijiu is evident in various literary works, rituals and banquets, dishes and healthcare, and numerous other areas. The reduction of substances plays a pivotal role in the flavor, aroma, and quality control of Baijiu. Therefore, the present work focuses on Baijiu and the reducing substances in it. In this study, CDs@ZrFe-MOF and three distinct catalase nanase substrates (ABTS, OPD, and TMB) were employed to create fluorescence and colorimetric dual-mode sensor arrays. The oxidation of the enzyme substrate into the appropriate oxidation substrate is facilitated by CDs@MOF in the presence of H₂O₂. The reducing substance effectively inhibits the formation of the oxidation substrate, resulting in alterations in fluorescence and UV intensity. The dual-mode sensor array was found to be effective in detecting 15 different types of reducing chemicals. Furthermore, the colorimetric and fluorescence sensor array demonstrated exceptional detection capability in detecting 19 different types of Luzhou-flavor liquor samples, achieving a 100% accuracy rate. This study will provide an accurate and rapid method for differentiating Baijiu.
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PubMed
高影响因子
ENERGY & FUELS
·
2025
·
IF 5.3
Yun Zhang,Xuemei Wang,Shangqing Zhang,Bicheng Liang
Harvesting osmotic energy from seawater–river water interfaces remains challenging due to the intrinsic selectivity–permeability trade-off in conventional ion-exchange membranes. Here, we fabricate large-scale Universitetet i Oslo-66 (UiO-66)/aramid nanofiber (ANF) nanocomposite membranes via an in situ polymerization method as high-performance osmotic energy generators. The UiO-66 layer, with its negatively charged surfaces and subnanometer channels, achieves near-ideal cation selectivity (0.99 and 0.98 under 5-fold and 50-fold concentration gradients), while the ANF scaffold’s three-dimensional (3D) fibrous nanochannels enable ultrafast cation diffusion (ionic permeabilities: 3.40 × 104 and 1.97 × 105 S m–2). This synergy effect yields record power densities of 16.46 W m–2 (50-fold) and 100.12 W m–2 (500-fold), surpassing state-of-the-art metal–organic framework (MOF) membranes (Materials of Institute Lavoisiers (MIL), Zeolitic Imidazolate Frameworks (ZIF), etc.) through precise angstrom-scale charge screening. What’s more, the high mechanical properties (tensile strength: 314.26 MPa; Young’s modulus: 9.96 GPa) endow the composite membranes with the scalable possibility of large-scale salinity gradient power generation. Under an enlarged testing area of 7 mm2, the maximum power density achieved a breakthrough of 1.93 W m–2. Combined with pH-responsive adaptability (140.86 W m–2 at a pH of 11) and 94.6% 30 day stability in harsh salinity gradients (0.01/5 M sodium chloride (NaCl)), this work establishes a paradigm for designing mechanically durable, large-scale nanofluidic systems to harvest blue energy efficiently across estuarine and industrial brine environments.
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MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Ying-ying Hu,Caiyue Gao,Xiao-qin Wu
Environmental pollution is a hot topic of concern for countries around the world. Therefore, {[Ni(NDC)(phen)(H 2 O)]• n ( Ni-1 , NDC = 2,6-naphthalenedicarboxylic acid, phen = o-phenanthroline), a 1D Ni-MOF, was synthesized using the solvothermal method as an electrochemical-fluorescence dual sensor for detecting phenylenediamine isomers. By the difference in the position of the reduction peaks, it is possible to distinguish between isomers while detecting them. The electrochemical behavior of the Ni-1 /GCE sensing phenylenediamine isomers was analyzed by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The LODs of o-PDA, m-PDA and p-PDA were 2.567 μM, 1.984 μM and 0.4003 μM in the detection range of 5–50 μM, respectively. Ni-1 was highly stable in aqueous solution (H 2 O), so it was dissolved in H 2 O to fabricate the Ni-1 /H 2 O fluorescence sensor. Ni-1 /H 2 O exhibited Stern-Volmer quenching constants of 6.080 × 10 4 M −1 , 2.086 × 10 3 M −1 , and 6.417 × 10 3 M −1 for o-PDA, m-PDA, and p-PDA, respectively. In addition, this dual sensor still shown excellent immunity to interference under the organic interferents. This work provides an efficient, convenient, and sensitive dual sensing method for the detection and differentiation of phenylenediamine isomers, which is of great significance for the detection of aromatic amines in the fields of wastewater discharge, environmental protection, and food safety.
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