SENSORS AND ACTUATORS B-CHEMICAL
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2021
·
IF 7.46
Lei Guo,Zhaode Mu,Bin Yan,Jie Wang,Jing Zhou,Lijuan Bai
Non-small cell lung cancer (NSCLC) is the most common type of lung cancer with poor survival, in part because that half of the cases are already in advanced stage when they are diagnosed. In response to this issue, the present work constructed a novel electrochemical biosensor for sensitive detection of circulating tumor DNA (ctDNA) related to NSCLC. Specifically, polyethyleneimine (PEI) and covalent organic framework (COF TAPB-TFPB ) functionalized nitrogen-doped graphene (NG) nanocomposite (NG-PEI-COF TAPB-TFPB ) was designed and employed as sensing platform for the first time. NG-PEI-COF TAPB-TFPB with porous structure and good conductivity showed a synergistic effect on promoting electron transfer, which could provide large specific surface area and active sites to increase the immobilization of capture probe (CP). In addition, gold nanoparticles (AuNPs) decorated Fe-based metal-organic framework (Fe-MOF) were labeled with signal probe (SP) to form tracer label, which would attach to the electrode surface by sandwich hybridization of target probe (TP) with CP and SP. Consequently, Fe III from Fe-MOF could react with K 4 [Fe(CN) 6 ] to form electroactive prussian blue, generating a significantly amplified electrochemical detection signal. Under optimum conditions, the proposed DNA biosensor displayed a broad linear range for ctDNA determination from 100 fM to 100 nM with a detection limit of 7.65 fM. Moreover, the biosensor was successfully fabricated to assay ctDNA in human serum, indicating the potential for cancer diagnosis. More importantly, the high sensitivity and satisfactory stability of this biosensor make it a promising method to detect other biomolecules by changing the corresponding sequences of CP and SP.
研究领域:
生物医学工程
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癌症生物学
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分析化学
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纳米技术
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产品关联
DOI
高影响因子
MICROPOROUS AND MESOPOROUS MATERIALS
·
2024
·
IF 4.8
Mengkun Luan,Xiangjie Lei,Yu Fan
To increase the yield of light olefins during the catalytic pyrolysis of alkanes, a novel hierarchical Fe-incorporated ZSM-5 molecular sieve (FeM-Z5) was synthesized using an Fe-based metal-organic framework (Fe-MOF) as a mesoporogen and iron source through the dry gel conversion (DGC) method. In contrast to the conventional method of incorporating Fe species into ZSM-5 via impregnation, the DGC method incorporates Fe species into the framework of ZSM-5, decreasing the amount of Brønsted (B) acid sites and thereby inhibiting the side reactions of hydrogen transfer during the catalytic pyrolysis of alkanes. Compared with the FeN-Z5 catalyst prepared by the DGC method with Fe(NO 3 ) 3 as an iron source, FeM-Z5 had a larger amount of strong B acid sites and more mesopores with a size range of 10–40 nm originating from the decomposition of Fe-MOF; these aspects improved n-pentane pyrolysis and ethylene and propylene diffusion. As a result, the optimal FeM-Z5 catalyst exhibited the highest yield of ethylene and propylene (33.4 wt%) and the lowest deactivation rate (0.07 %/h) among the prepared catalysts during the catalytic pyrolysis of n-pentane.
研究领域:
材料科学
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催化化学
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产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Liyun Zhang,Yi He,Pingya Luo,Lan Ma,Shuangshuang Li,Yiling Nie,Fei Zhong,Yuqi Wang,Li Chen
Developing the high-efficient and robust antifouling membranes for oily emulsions to achieve the purpose of prolonging the service life of the membrane shows great demand because of the restriction of hydration anti-fouling mechanism strategy to against pollution. Herein, a hydrophilic photo-Fenton-like catalyst – GO/Fe-MOF assembled stabilized polyacrylonitrile (SPAN) nanofibrous membrane with underwater superoleophobicity, robust mechanical strength and photo-Fenton self-cleaning performance was firstly designed and fabricated via ultrasonic assistance, mussel-inspired fixation and low temperature hydrothermal synthesis methods. In this work, benefiting by the regulable amounts of GO nanosheets on the SPAN@GO/M88A membrane surface, the obtained membrane possessed sub-micrometer skin layer, which guarantees the balance of fast permeation flux (920–7083 ± 47 L m −2 h −1 ) and separation efficiency (>99.2%) for diesel/water emulsion with small emulsified oils. Moreover, introduced hydrophilic Metal-organic frame nanoparticles (MIL-88A (Fe)) into modified membrane endowed underwater anti-oil-fouling and photo-Fenton catalytic degradation performance for organic contaminants. Meanwhile, the charged GO/M88A heterostructure can assist to achieve demulsification for separation of surfactant-stabilized emulsions by strong electrostatic force. More importantly, attached and irremovable contaminants on the membrane can be quickly removed by photo-Fenton self-cleaning method, and achieved over 96% of recovery flux recovery ratio, which effectively prolonged the service life of the membrane. We believe the newly designed SPAN@GO/M88A membrane with hydration antifouling and photo-Fenton self-cleaning properties can stimulate more studies on revivable separation membranes for multifunctional applications.
研究领域:
材料科学
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环境工程
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化学工程
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DOI
高影响因子
Food Chemistry-X
·
2024
·
IF 6.5
Yi Xia,Juan He,Long Tang,Miao Hu,Jie Zhou,Yao-Yu Xiao,Zhi-Chao Jiang,Xue Jiang
The assessment of total antioxidant capacity (TAC) is crucial for evaluating overall antioxidant potential, predicting the risk of chronic diseases, guiding dietary and nutritional interventions, and studying the effectiveness of antioxidants. However, achieving rapid TAC assessment with high sensitivity and stability remains a challenge. In this study, Ce/Fe-MOF with abundant oxygen vacancies was synthesized using microplasma for TAC determination. The microplasma synthesis method was rapid (30 min) and cost-effective. The presence of oxygen vacancies and the collaboration between iron and cerium in Ce/Fe-MOF not only enhanced the catalyst's efficiency but also conferred multiple enzyme-like properties: peroxidase-like, oxidase-like, and superoxide dismutase mimetic activities. Consequently, a simple colorimetric assay was established for TAC determination in vegetables and fruits, featuring a short analysis time of 15 min, a good linear range of 5–60 μM, a low detection limit of 1.3 μM and a good recovery of 91 %-107 %. This method holds promise for rapid TAC assessment in agricultural products.
研究领域:
食品科学
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生物化学
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材料科学
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产品关联
DOI
PubMed
高影响因子
COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING
·
2022
·
IF 9.463
Huidong Zhao,Bihe Yuan,Yuanyuan Zhan,Fangzhou Yang,Juanjuan Zhou,Congrui Qi,Chunying Lei,Yaoqiang Li
The combustion of polystyrene (PS) releases enormous amounts of toxic fumes and heat, which seriously affects human health and property safety. This research firstly proposes an efficiently feasible surgery to prepare a porous metal–organic framework (P-Fe-MOF) with macroporous based on the microporous MIL-53 and then uses its excellent porous structure to adsorb triethyl phosphate (TEP) as a flame retardant for PS to reduce its fire hazard. Scanning electron microscope images reveal that P-Fe-MOF has a distinct macroporous structure compared with original metal–organic framework (MOF). X-ray photoelectron spectra indicate that TEP has been successfully adsorbed into P-Fe-MOF. The combustion performance of PS composites is analyzed and the results suggest that the prepared PS composite has better flame-retardant performance than pure PS. This research presents a convenient method to fabricating a novel macroporous MOF , which provides a valuable enlightenment for broadening the application field of MOF and improving the comprehensive properties of polymers.
研究领域:
材料科学
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化学工程
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产品关联
DOI
高影响因子
Separations
·
2024
·Vol. 11
·期 12
·356
·
IF 2.5
Zhaowei Wu,Meiyi Hu,Pengfan Zhuo,Jie Wang,Shaoping Tong
A composite Fe-MOF-C/N was prepared with Fe-MOF and g-C3N4precursors, and its activation property of peroxymonosulfate (PMS) in the degradation of Sulfamethoxazole (SMX) was studied. XRD, SEM, and TEM analyses showed that Fe-MOF-C/N was porous and mainly composed of phases of Fe3N, C0.08Fe1.92, and graphite. XPS indicated that Fe-MOF-C/N mainly had Fe, C, N, and O elements, among which Fe existed in the form of Fe2+and Fe3+. Fe-MOF-C/N was used to activate PMS to degrade SMX, and the result showed that Fe-MOF-C/N had excellent catalytic performance and 84.17% of SMX could be removed in 8 min. Free radical quenching experiments showed that1O2was the main active species in Fe-MOF-C/N/PMS. The stability experiment showed that Fe-MOF-C/N had good stability, and the degradation rate of SMX only decreased by 5.8% after five times of use.
研究领域:
环境科学
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催化材料
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产品关联
DOI
高影响因子
Toxics
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2024
·Vol. 12
·期 7
·524
·
IF 3.9
Yuanzhen Li,Yinming Fan,Yanhong Wang,Yinian Zhu,Zongqiang Zhu,Shengpeng Mo,Xiaobin Zhou,Yanping Zhang
VOCs can be used instead of ammonia as a reducing agent to remove NO, achieving the effect of removing VOCs and NO simultaneously. Due to the high energy consumption and low photocatalytic efficiency required for conventional thermocatalytic purification, photothermal coupled catalytic purification can integrate the advantages of photocatalysis and thermocatalysis in order to achieve the effect of pollutants being treated efficiently with a low energy consumption. In this study, samples loaded with Co and Mn catalysts were prepared using the hydrothermal method on Fe-MOF with various morphologies. The catalytic performance of each catalyst was analyzed by studying the effects of their physicochemical properties through various characterizations, including XRD, SEM, BET, XPS, H2-TPR, TEM and O2-TPD. The characterization results demonstrated that the specific surface area, pore volume, high valence Co and Mn atoms, surface adsorbed oxygen and the abundance of oxygen lattice defects in the catalysts were the most critical factors affecting the performance of the catalysts. Based on the results of the performance tests, the catalysts prepared with an octahedral-shaped Fe-MOF loaded with Co and Mn showed a better performance than those loaded with Co and Mn on a rod-shaped Fe-MOF. The conversions of acetone and NO reached 50% and 64%, respectively, at 240 °C. The results showed that the catalysts were capable of removing acetone and NO at the same time. Compared with the pure Fe-MOF without Co and Mn, the loaded catalysts showed a significantly higher ability to remove acetone and NO simultaneously under the combination of various factors. The key reaction steps for the catalytic conversion of acetone and NO on the catalyst surface were investigated according to the Mars–van Krevelen (MvK) mechanism, and a possible mechanism was proposed. This study presents a new idea for the simultaneous removal of acetone and NOxby photothermal coupling.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2024
·
IF 4.9
Changchang Li,Yue Zhi,Minnan Zhu,Chengyu Yang,Yayang Tian,Tao Chen,Yuan Zhao,Jie Gao,Linfeng Chen
The development of simple, efficient and low-cost methods for rapid on-site monitoring have always been a challenging topic in the field of analysis. Here, we successfully constructed a selective, sensitive and rapid colorimetric sensor for the sensing of diethylstilbestrol (DES) by using molecular imprinting technology to construct specific recognition sites on the surface of Fe-based metal organic frameworks (Fe-MOF) peroxidase-like nanozyme. The surface of obtained sensor (Fe-MOF@MIP) had abundant channels and imprinted cavities that allowed the substrate to enter and responded with Fe-MOF core to drive the chromogenic reaction of 3,3′,5,5′-tetramethylbenzidine (TMB). When DES was present, it could specifically enter the cavities and obstruct the channels of substrate into the Fe-MOF core, thereby inhibiting the chromogenic reaction. The experimental results demonstrate that the sensor had excellent selectivity, anti-interference and catalytic stability. In the linear range of 0 – 1.67 μ M, the detection limit is as low as 8.43 nM, which is superior to peer sensors. To better adapt to in-situ analysis, we have further developed a rapid analysis method based on photo colorimetry, which performed well in real sample analysis and recovery test with the results consistent with the gas chromatograph-mass spectrometer (GC–MS), demonstrating its great potential for rapid on-site monitoring.
研究领域:
分析化学
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生物医学工程
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环境科学
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产品关联
DOI
高影响因子
DESALINATION
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2024
·
IF 8.3
You Zhou,Lei Xu,Sheng-Jie Han,Cai-Hua Liu,Yi-Bin Li,Ming-Lai Fu,Baoling Yuan
Solar-driven interfacial photothermal evaporation (SIPE) has been considered as a green and sustainable technology for obtaining fresh water, and the exploring efficient photothermal materials is crucial. Nanocomposite derived from metal-organic framework exhibits high light absorption properties and excellent chemical stability, making it an ideal candidate in the SIPE. Herein, Fe 3 O 4 /C nanocomposite was obtained using MIL-101 (Fe) as a precursor, and Fe 3 O 4 /C-based porous hydrogel (Fe 3 O 4 /C-PH) was subsequently prepared through chemical crosslinking foaming polymerization. The obtained Fe 3 O 4 /C-PH exhibited an evaporation rate of 3.33 kg m −2 h −1 under one sun intensity. Fe 3 O 4 /C-PH demonstrated outstanding desalination and salting out resistance when treating real seawater. Moreover, it could remove over 99 % of dyes from wastewater. The photothermal mechanisms are molecular thermal vibration of C component and semiconductor relaxation of Fe 3 O 4 . Meanwhile, the hydrophilic and porous skeleton structure of the hydrogel ensure Fe 3 O 4 /C-PH to transport water rapidly and exhibit good light absorption properties. This research broadens the candidate of photothermal materials for applications in SIPE, and also provides new avenues for desalination and wastewater purification.
研究领域:
材料科学
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环境科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
International Journal of Applied Ceramic Technology
·
2026
·Vol. 23
·期 3
·e70206
·
IF 2.6
Weiwei Pei,Hongli Liu,Guanqi Xu,Junjie Zhang,Boshi Gao,Wenshuo Cao,Mingwei Li,Xianlin Xiao,Mingda Liu,Yuhao Liu,Xiaoxiao Huang
Driven by the rapid development of microelectronics and aerospace engineering, lightweight, ultrathin, broadband microwave absorption (MA) materials are urgently required for advanced electromagnetic protection and stealth technologies. Conventional ceramic-derived MA absorbers face inherent bottlenecks of incompatible impedance matching and insufficient attenuation efficiency, severely restricting their application in miniaturized aerospace and electronic systems. A novel bubble coral-like Fe-MOF modified carbonaceous nanofiber composite (BF@CNFs) is fabricated via electrospinning, thermal curing, and high-temperature carbonization, with its microstructure precisely tailored by optimizing polyacrylonitrile/phenolic resin ratio and carbonization heating rate. The optimized BF@CNF-2 delivers a minimum reflection loss of −36.2 dB at 1.3 mm thickness, with an effective absorption bandwidth nearly covering the entire Ku-band (12.0–18.0 GHz). This outstanding performance stems from the synergistic effect of conductive carbon nanofiber scaffolds and Fe-MOF-derived magnetic phases. The work provides a scalable, ceramic-compatible strategy for high-performance MA materials, addressing long-standing technical challenges, with promising prospects in aerospace stealth and electromagnetic shielding.
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DOI
高影响因子
Journal of Physical Chemistry C
·
2021
·
IF 4.126
Yao Li,Le Xin Song,Wei Ping Wang,Yue Teng,Juan Xia,Nan Ning Liu
In this work, we prepared a series of Fe-MOF polyhedra [metal organic framework (MOF)-1 ∼ −13] by introducing β-cyclodextrin (CD) as a morphology modifier using an interaction between ferric chloride and terephthalic acid in dimethylformamide. A novel structural evolution from a hexagonal bipyramid to a bipyramidal hexagonal prism was clearly observed. This evolution was gradual and could be well reflected by the height ratio of the prism and pyramid in these polyhedral structures. It is the relative concentration of β-CD that drives this structural evolution. Although the reaction temperature and time can also affect the height ratio to some extent, their influence can only be realized in the presence of β-CD. In the absence of β-CD, only hexagonal bipyramid structures were obtained. It is worth noting that Fe-MOF-1 with a bipyramidal hexagonal prism structure (prism height, ∼130 nm) showed typical paramagnetic characteristics, and its saturation magnetization was determined to be 23.1 emu·g–1. Furthermore, we found that Fe-MOF-1 exhibited good photocatalytic performance for different types of dyes (crystal violet with positives and methyl orange with negative charges). At the same time, a possible photocatalytic mechanism was proposed to explain the difference of degradation efficiency between the two dyes. Also, we use the combination of specific surface area and zeta potential to explain the differences in the catalytic properties of a series of Fe-MOF materials. In addition, MOF-1 shows the same electrocatalytic oxygen evolution reaction performance as some bimetallic MOFs such as Fe-Co-MOF. For example, the overpotential of MOF-1 is 398 mV at 10 mA·cm–2 current density, while that of Fe-Co-MOF is 410 mV. We believe that the current work can contribute to the adjustment, modification, and application of MOF nanostructures.
研究领域:
材料科学
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化学工程
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS A-GENERAL
·
2024
·
IF 4.7
Yuqi Li,Yue Zhang,Zhiyuan Wang,Chengxu Zhang,Fanming Meng,Jianqiang Zhao,Xinpei Li,Jue Hu
Metal-Organic Frameworks (MOFs) materials with unique properties have attracted much attention in various fields. However, the limited number of active sites and the time-consuming synthesis process hinder their widespread application. Herein, this work demonstrates the first preparation of highly efficient and stable MOF (Fe-MOF-U) catalysts with enhanced specific surface area , morphology and active sites, through ultrasonic-assisted solvothermal method for oxygen evolution reaction (OER) electrocatalysis . The results show that the crystal size of Fe-MOF-U decreases significantly, and the specific surface area and pore size increase. In addition, many oxygen vacancies are produced in the crystal, making the reaction intermediates easier to form and thus improving the catalyst's oxygen evolution performance. The overpotential of Fe-MOF-U catalyst at 10 mA cm −2 is 221 mV, which is lower than that of the conventional solvothermal synthesized Fe-MOF-S (237 mV). Furthermore, the turnover frequency of the Fe-MOF-U catalyst is 3.32 s −1 at the overpotential of 300 mV, which is 5 times higher than that of Fe-MOF-S (0.70 s −1 ). In situ Raman and methanol molecular probe tests indicate a weakened adsorption of *OH on the Fe-MOF-U surface. DFT calculations are consistent with the characterization results, both proving that the ultrasonic-assisted solvothermal method can generate specific oxygen vacancy (μ 3 -O defect) in Fe-MOF-U which improved OER performance. This study provides a new idea for the morphology controlling and defect introduction of MOF and a new approach for its application.
研究领域:
材料科学
·
电化学
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DOI
高影响因子