JOURNAL OF MATERIALS CHEMISTRY
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2012
·Vol. 22
·期 15
·7449-7455
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IF 5.968
Shu-Hui Huo,Xiu-Ping Yan
The adsorption of malachite green from aqueous solution on a highly porous metal–organic framework MIL-100(Fe) was studied in view of the adsorption isotherm, thermodynamics, kinetics, and regeneration of the sorbent. The adsorption isotherms of malachite green on MIL-100(Fe) followed the Freundlich model, and MIL-100(Fe) possessed heterogeneous surface caused by the presence of different functional groups on the surface. The adsorption of malachite green on MIL-100(Fe) is controlled by an entropy effect rather than an enthalpy change, and obeyed a pseudo-second-order kinetics. Analysis of the intraparticle diffusion plots revealed that more than one process affected the adsorption, and film (boundary layer) diffusion controlled the adsorption rate at the beginning. Evidence from zeta potential and X-ray photoelectron spectroscopic data showed that the adsorption of malachite green was also driven by electrostatic attraction and the interaction between the Lewis base –N(CH3)2 in malachite green and the water molecule coordinated metal sites of MIL-100(Fe). MIL-100(Fe) gave much higher adsorption capacity for malachite green than other conventional adsorbents such as activated carbon and natural zeolite. The high adsorption capacity, good solvent stability, and excellent reusability make MIL-100(Fe) attractive for the removal of MG from aqueous solution.
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BIOMACROMOLECULES
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2024
·
IF 5.5
Yidan Chen,Tiantian Feng,Xiaohong Zhu,Yuting Tang,Yao Xiao,Xiuhua Zhang,Sheng-Fu Wang,Dong Wang,Wei Wen,Jichao Liang,Huayu Xiong
Reactive oxygen species (ROS) have emerged as a promising treatment option for antibacterial and biofilm eradication. However, their therapeutic efficacy is significantly hampered by the unique microenvironments of diabetic wounds. In this study, we designed and synthesized porphyrin-based Fe covalent organic frameworks (Fe-COF) through a Schiff base condensation reaction. Subsequently, Fe-COF were encapsulated with hyaluronic acid (HA) through electrostatic adsorption, resulting in a novel formulation named HA-Fe-COF for diabetic wound healing. HA-Fe-COF were engineered to respond to hyaluronidase in the infected wound, leading to the controlled release of Fe-COF. Those released Fe-COF served a dual role as photosensitizers, generating singlet oxygen and localized heating when exposed to dual light sources. Additionally, they acted as peroxidase-like nanozymes, facilitating the production of ROS through enzymatic reactions. This innovative approach enabled a synergistic therapeutic effect combining photodynamic, photothermal, and chemodynamic modalities. Furthermore, the sustained release of HA from HA-Fe-COF promoted angiogenesis, collagen deposition, and re-epithelialization during the diabetic wound healing process. This “all-in-one” strategy offers a novel approach for the development of antimicrobial and biofilm eradication strategies that minimize damage to healthy tissues in vivo.
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Journal of the Taiwan Institute of Chemical Engineers
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2024
·
IF 5.5
Lowell Toku Kokuloku,Elvis Djam Miensah,Aotian Gu,Kaiwei Chen,Peng Wang,Chunhui Gong,Yan Jiao,Kai Chen,Yi Yang
Background Activated carbon (AC) is commonly used to remove many pollutants from water due to its appealing adsorption properties. However, the pristine surface properties of AC limit its ability to effectively remove 2,4,6-trinitrotoluene (TNT, a widely used explosive water contaminant). Modifying AC with Fe nanoparticles (NPs) can significantly improve the surface properties of the Fe/AC composite, thereby enhancing its adsorption capabilities. Method Commercial charcoal-based AC was modified with Fe NPs via wet impregnation followed by a one-step carbothermal synthesis (labeled Fe-AC-800). A detailed characterization of Fe-AC-800 and its counterparts, pristine AC and thermally modified AC (AC-800, without Fe NPs doping) was performed using XRD, Raman Spectroscopy, SEM, EDS, BET, XPS, and FTIR. Then, the adsorption characteristics and performances of Fe-AC-800 were analyzed to determine its effectiveness in removing TNT and compared to AC and AC-800, considering the impact of in-situ Fe-modification and carbothermal treatment. Significant findings Fe-AC-800 displayed a higher adsorption capacity for TNT (387.74 mg/g) than the pristine AC (265.52 mg/g) but only slightly higher than AC-800 (339.64 mg/g). This was ascribed to the combined effect of the carbothermal treatment and Fe NPs doping, which constructed a richer porous structure that improved the Fe-AC-800 surface features and favored TNT removal. The optimal adsorption capacity of Fe-AC-800 was 464.13 mg/g under ambient conditions. TNT adsorption onto Fe-AC-800 and AC-800 conformed to only the Langmuir isotherm model, indicating uniform monolayer adsorption, whereas on the pristine AC, it satisfied both Langmuir and Freundlich isotherm models, respectively. The primary mechanism of TNT adsorption onto Fe-AC-800 was physical adsorption through pore filling, hydrogen bonding, and π-π EDA interactions, respectively.
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
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2017
·
IF 2.843
Mengqian Yuan,Fan Tian,Guangfang Li,Huiping Zhao,Yunling Liu,Rong Chen
In this work, hierarchical nanostructures Fe(III)-modified BiOBr were successfully prepared via a facile one-step route at room temperature. Compared with pure BiOBr, Fe(III)-modified BiOBr samples possess enhanced photocatalytic abilities for benzyl alcohol oxidation and organic dye degradation in the presence of H2O2 upon light illumination. The improved photocatalytic oxidation and degradation ability of Fe(III)-modified BiOBr is ascribed to the enhanced photogenerated carriers separation efficiency and promoted production of ·OH due to the generation of Fe2+ ions via interfacial charge transfer from Fe3+ ions. This work provides a facial approach to improve photocatalytic efficiency for organic synthesis and environmental remediation.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2025
·Vol. 36
·期 5
·1-14
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IF 2.8
Junlong Wang,Yimin Dai,Ling Cai,Siwen Yang,Yusong Yang,Lihui Xie,Li Wan
The frequent leakage of crude oil and the illegal discharge of industrial organic pollutants have caused serious damage to the ecological environment and the loss of valuable resources. In this paper, we introduce a sponge with magnetic and photothermal properties. Polydopamine and ferric oxide (Fe 3 O 4 ) were grafted onto the sponge, self-assembled on the three-dimensional (3D) skeleton surface by Zif material, and grafted with cetyltrimethoxysilane to make the modified sponge highly hydrophobic (water contact angle = 155°). Moreover, due to the dual photothermal conversion properties of polydopamine and ferric oxide (Fe 3 O 4 ), the modified sponge can be quickly heated to 110 °C under light (1.25 kw/m 2 ). The modified sponge demonstrated excellent crude oil adsorption capacity (44 g/g) and recyclability. Due to its magnetic properties (saturated magnetization = 4.43 emu/g), derived from the incorporation of Fe₃O₄, the sponge could be remotely controlled for adsorption. Moreover, it demonstrated the ability to continuously adsorb and collect light oil from the water surface with the aid of a peristaltic pump. The sponge also functioned as an efficient filter for separating heavy oil underwater through liquid gravity, achieving a separation efficiency of 97.2%. Therefore, this composite sponge not only presents a promising solution for crude oil spill remediation but also holds significant potential for industrial wastewater treatment, making it highly relevant for practical environmental applications.
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JOURNAL OF HAZARDOUS MATERIALS
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2024
·
IF 12.2
Yongzhen Dong,Jiawei Liu,Liqin Kong,Dongyang Deng,Long Wu,Yiping Chen
This study presents the development of a magnetic relaxation switching (MRS) immunosensor for the sensitive detection of chlorpyrifos (CPF) with a signal amplification strategy using Pd/Cu-TCPP(Fe) hybrid nanosheets and polydopamine (PDA). Pd/Cu-TCPP(Fe) nanosheets, which exhibit high peroxidase-like activity and excellent storage stability, making them suitable replacements for natural enzymes in biosensors, are further functionalized with goat anti-mouse IgG (Ab 2 ) to construct an immunosensor. The mechanism relies on the competition between free CPF and the immobilized bovine serum albumin-CPF conjugates for antibody binding, which modulates the aggregation of magnetic nanoparticles (MNPs) that are related to the transverse relaxation time. The optimized immunosensor shows a linear detection range from 0.5 ng/mL to 100 ng/mL and a limit of detection (LOD) of 0.24 ng/mL, outperforming traditional enzyme-linked immunosorbent assay (ELISA) methods by achieving an LOD that is about 9 times lower. Real sample analysis demonstrates the applicability of the Pd/Cu-TCPP(Fe)-PDA-MRS immunosensor for detecting CPF residues in tomato and water samples, with results well consistent with those obtained using gas chromatography. This work highlights the potential of nanomaterials in enhancing the performance of MRS immunosensors for pesticide residue analysis in environmental and food safety monitoring.
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Surfaces and Interfaces
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2024
·
IF 5.7
Zhihao Liu,Tingting Yang,Yuwen Yan,Yongtao Tang,Jianxin Meng,Fengyu Li
Colorimetry is to determine the component content usually comparing or measuring the “RGB” values, which has the advantages of quick response and visual comparison. However, the widely reported “RGB” models are limited by requiring professional operation such as accurate sampling, insufficient information, cumbersome calculation, etc., which has significantly restricted the promotional application. Inspired by the PAA-PVA gel with excellent absorbing-swelling ability and superior response ability, indefinite volume addition has a significant difference in the swelling phenomenon of PAA-PVA hydrogel, the extent of this enlargement is directly related to the amount of testing sample absorbed, which can be applied to reflect testing sample volume added. In addition, benefited from a comprehensive and precise parameter network, the deep learning (DL) algorithm solves the defects such as ambient light effect and manual extract RGB values of the colorimetric sensing analysis strategy. Considering Fe(II) is an essential element for life science and environmental monitoring, we have developed a self-calibrating colorimetric sensor assisted deep learning strategy for the Fe(II) detection with indefinite volume. It can directly complete the analysis of Fe(II) concentration via captured images, without going through a complicated process similar to the RGB model. Specifically, we integrated the advantages of colorimetric sensing strategy, absorbing-swelling hydrogel, and DL algorithm to develop a phenanthroline (PHEN) indicator doped PAA-PVA colorimetric sensor (PHEN-PAA-PVA). Then, 2,500 colorimetric response images were collected as the training dataset and assessed 2 DL algorithms and 7 machine learning (ML) algorithms. The convolutional neural network (CNN) model exhibited the most efficiency to quantify 1×10 −5 -9×10 −4 mol/L Fe(II), with a limit of detection (LOD) of 3.3×10 −6 mol/L. It provides a promising and blooming in-situ detection approach for Fe(II) analysis, contributes to health management and environment monitoring.
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CHEMICAL ENGINEERING JOURNAL
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2024
·
IF 13.3
Yingying Guo,Huiyong Wang,Qian Zhang,Shuaiqi Gao,Zhiyong Li,Yang Zhao,Zhimin Liu,Suojiang Zhang,Jianji Wang
Covalent organic frameworks (COFs) have great potential in solar hydrogen production to alleviate environmental pollution and global energy crisis. However, to achieve high H 2 yield is still a challenge. Herein, we designed and synthesized two Fe 3+ -coordinated imine type COFs (Fe-COFs) for photocatalytic H 2 production from water splitting. It was surprising to find that with the progress of H 2 evolution under visible light, the bulk powders of Fe-COFs (180–250 nm) were gradually stripped into covalent organic nanosheets (Fe-CONs, 0.3–1.9 nm), which in turn efficiently catalyzed H 2 production. As such, a self-driven mechanism was established in the catalytic system, and H 2 evolution rate increased with the increase of cyclic runs until the thickness of the nanosheet no longer changes in the regeneration and reuse process of the Fe-CON photocatalysts. The optimal Fe-CON catalyst exhibited a record high H 2 evolution rate of 67.94 mmol g −1 h −1 among the currently reported COFs loaded with other non-noble metals, due to the more exposed active sites, smaller charge-transfer resistance, and stronger separation ability of the photogenerated electrons and holes of Fe-CONs. This work provides the first example for the integration of self-driven photochemical exfoliation of 2D materials and their highly efficient photocatalytic hydrogen evolution.
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ENVIRONMENTAL RESEARCH
·
2025
·
IF 7.7
Li Zhao,Kangting Du,Mei Huang,Dong Tian,Jinsong He,Yongjia Lei,Yan Liu,Guochun Lv,Jianmei Zou,Fei Shen
Recycling paper packaging waste into Fe-biochar catalysts is a promising strategy for resource utilization. In this study, a dissolution-regeneration method using a DMAc/LiCl system was employed to synthesis Fe-biochar pellet catalyst (Fe-WPBC) with corrugated cardboard as a cheap carbon precursor. The Fe-WPBC possessed a spherical cage-like hollow structure with millimeter-size dimensions, making it suitable for practical application. An impressive rate constant of 0.2452 min -1 for tetracycline degradation via peroxymonosulfate activation was achieved, and Fe-WPBC showed high stability, maintaining close to 100% tetracycline removal efficiency even after five cycles. Mechanistic insights were obtained through radical quenching, electron paramagnetic resonance, and electrochemical analysis etc. Both electron transfer path and SO 4 · - and O 2 · - dominated radical path concurrently existed. Possible degradation pathways were further proposed in combination with LC-MS and DFT calculations. Besides, toxicity simulations using T.E.X.T and ECOSAR programs showed that the degradation intermediates were less toxic than tetracycline. Finally, the practical application potential of Fe-WPBC was evaluated through a continuous flow reactor, which achieved a 99% tetracycline degradation efficiency and maintained over 400 min. This study provides new insights into both the recycling of paper packaging waste and the development of pellet catalysts for pollution degradation.
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Molecular Catalysis
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2024
·
IF 3.9
Lina Sun,Ping Ning,Jie Yang,Xin Song,Kai Li
This study used metal oxide-modified metal-organic frameworks to examine H 2 S catalytic oxidation selectivity. The findings revealed that the oxidation mechanisms and products differed between Fe 2 O 3 /UiO-66 and Al 2 O 3 /UiO-66. The dithionates were intermediate products of H 2 S oxidation on Al 2 O 3 /UiO-66, whereas the bisulfates were intermediate products on Fe 2 O 3 /UiO-66. Fe 2 O 3 /UiO-66 showed stronger surface oxidation activity than Al 2 O 3 /UiO-66. The formation of sulfate/SO 2 was primarily attributable to surface oxygen, whereas elemental sulfur was primarily related to lattice oxygen. The product generation processes of H 2 S on Fe 2 O 3 /UiO-66 and Al 2 O 3 /UiO-66 surfaces were as follows: H 2 S → HSO 4 2− → SO 2 → S for Fe 2 O 3 /UiO-66, while H 2 S → S 2 O 4 2− → SO 2 for Al 2 O 3 /UiO-66. H 2 O and surface oxygen have the potential to alter H 2 S adsorption on the catalyst surface. For Fe 2 O 3 , the conversion of H 2 S to SO 2 involves both an oxidation process and a reduction process. For Al 2 O 3 , the conversion of H 2 S to SO 2 includes two oxidation processes. Due to the oxidation step of S 2 O 4 2− limiting the generation of SO 2 , the reduction process of SO 2 was also hindered, which in turn restricted the production of S over Al 2 O 3 . Fe 2 O 3 can achieve the oxidation and removal of H 2 S at lower reaction temperatures, while also creating elemental S.
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JOURNAL OF POWER SOURCES
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2025
·
IF 7.9
Wenwu Zhao,Xionghuan Yang,Ying Gu,Siqing Li,Yanqiang Hu,Yanfeng Tang,Minmin Wang
The development of highly efficient and stable electrocatalysts is crucial for the practical application of water splitting in renewable energy production. The Ni-Fe Phosphate electrocatalyst was synthesized through a simple and scalable electrodeposition method. This study presents a comprehensive investigation into the surface reconstruction engineering of an amorphous Ni-Fe phosphate electrocatalyst for enhancing its performance in alkaline water splitting. The reconstructed electrocatalyst exhibits significantly improved activity in alkaline water splitting. As expected, a low cell voltage of 1.86V was used to drive water splitting at 300 mA cm −2 , while the electrodes maintained high stability during 180 h continuous full water splitting at 70 mA cm −2 . This work provides insights into the mechanisms underlying the enhanced performance of the reconstructed Ni-Fe Phosphate based electrocatalyst and offers a promising approach for the design of advanced electrocatalysts for water splitting.
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Materials
·
2024
·Vol. 17
·期 11
·2488
·
IF 3.1
Dongmei Zhao,Xinyao Wang,Libin Wang,Jingzhen Wang,Xu Wang,Weipeng Cheng
Antibiotic residues have been found to have potentially harmful effects on ecological and human health. Carbon nitride-based photocatalysts have widely focused on antibiotic photocatalytic degradation. Herein, we prepared Fe-modified g-C3N4nanorod bunches (FCNBs) using chemical vapor co-deposition. Specifically, through the process of calcination, a blend of urea and chlorophyllin sodium iron salt underwent an intriguing transformation, resulting in the integration of Fe into the framework of the g-C3N4nanorod cluster. The resulting photocatalyst exhibited remarkable stability and superior dispersibility. The prepared FCNBs had a unique structure, which was beneficial for increasing light absorption. Furthermore, the Fe species formed a chemical coordination with the g-C3N4matrix, thereby altering the electronic structure of the matrix. This modification facilitated charge transfer, prolonged the carrier lifetime, and enhanced light absorption, all of which significantly increased the photocatalytic activity. The oxytetracycline degradation efficiency of FCNBs was 82.5%, and they demonstrated outstanding stability in cycle trials. This work introduces a promising photocatalyst for the degradation of antibiotics.
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