SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Yu Guan,Guolang Zhou,Lin Li,Yexin Jiang,Jingzhou Yin,Cheng Liu,Lili Zhang,Qiaofeng Han,Edison Huixiang Ang
This research focused on creating oxygen vacancy-enriched copper-doped LaFeO 3 perovskite using a Prussian blue MOF template. This new material, LFO-Cu, showed outstanding Bisphenol A (BPA) degradation with 98 % efficiency in just 30 min, ten times faster than pure LaFeO 3 (LFO). Moreover, the LFO-Cu/peroxymonosulfate (PMS) system worked effectively at pH levels from 4 to 10, breaking down various pollutants (TC, PhOH, MV, MB), and removing 85 % TOC in BPA and 50 % in TC. Density Functional Theory (DFT) calculations revealed that copper strengthened the catalyst-PMS interaction, leading to the generation of highly reactive oxygen species (ROS), primarily singlet oxygen ( 1 O 2 ) and superoxide radicals (O 2 – ·). A degradation pathway was proposed, showing less toxic intermediates than BPA. In summary, copper-doped oxygen-rich vacancy MOFs-derived perovskite has significant potential for improving refractory organic mineralization.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
ANALYTICA CHIMICA ACTA
·
2025
·
IF 6
Feng Zhang,Sen Zhang,Xing Liu,Wei Gao,Jun Luo,Yi-fan Pan,Wei-Juan Zheng,Xin Hu,Hong-zhen Lian
Background Glycoproteins are critical in various biological processes and attract lots of attention of researchers. It still remains a challenge to detect glycopeptides by mass spectrometry because of their low abundance with heterogeneity and lability, as well as signal suppression by non-glycopeptides. The boronate affinity-based enrichment is an effective solution for detecting cis -diols-containing compounds including glycopeptides in complex matrices. However, there has not been any report about absolute quantitation of boron in the absorbent materials for glycopeptides, which obstructed the tailored design of boronate affinity materials and deeper understanding of interaction mechanisms. Results This work presents the development of a boronic acid-functionalized magnetic zirconium metal-organic framework (mMOF–AAPBA) with actual boron content for specific capture of glycopeptides. The synthesized nanocomposite could enrich glycopeptides by magnetic solid-phase extraction (MSPE) via the synergistic effect of hydrophilic interaction and boronate affinity. After full characterization including quantitative analysis of boron by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), mMOF–AAPBA was applied as MSPE absorbent to capture glycopeptides. Under the optimized conditions, it could enrich 28 glycopeptides both from horseradish peroxidase and immunoglobulin digests, with a limit of detection of 1 fmol μL −1 coupled with matrix-assisted laser desorption/ionization time of flight mass spectrometry. The boronate affinity absorbent also possessed great ability of anti-interference and good reusability. Furthermore, it possessed high performance in enriching glycopeptides in real samples including human saliva and traditional Chinese medicine injections. Significance In the preparation of the boron-containing nanocomposites, there is a special interest that an accurate protocol was established to assay boron based on LA-ICP-MS assisted by home-made matrix reference substances for the first time. These findings highlight the quantitative boron-containing mMOF–AAPBA as a robust affinity material for glycopeptide enrichment in real biological samples, offering potential applications in glycoproteomics and other cis -diols compound related researches.
研究领域:
分析化学
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生物化学
·
纳米技术
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质谱学
·
糖蛋白质组学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Xuebi Du,Shichao Feng,Jianquan Luo,Yongbing Zhuang,Weijie Song,Xuewei Li,Yinhua Wan
Amine-functionalized and metal doped metal–organic frameworks (MOFs) will enable further enhancement of CO 2 adsorption, which holds great promise in mixed matrix membranes (MMMs) for CO 2 /N 2 separation. Four kinds of UiO66 with different sizes have been successfully fabricated by introduction of Ce and/or amino groups in UiO66. The influence of Ce doping on the UiO66 is greatly related to the ligand. Compared with ZrUiO66, the CeZrUiO66 has bigger particle size, lower BET specific surface area and pore volume and a worse CO 2 adsorption capacity. Interestingly, the tendency of Ce-doped ZrUiO66-NH 2 is contrary to the aforementioned. In particular, bimetallic CeZrUiO66-NH 2 has an ultramicroporous structure, small particle size, rich crystal defect, superb CO 2 capture capacity and high CO 2 /N 2 adsorption selectivity, suggesting that the simultaneous introduction of Ce and amino groups is conducive to the enhancement of CO 2 separation. The intrinsic ultramicroporous structure of CeZrUiO66-NH 2 not only offers fast and low resistance transport channels for CO 2 , but also supplies more sites for CO 2 adsorption owning to the doping of Ce and the amino groups. As a result, Pebax/CeZrUiO66-NH 2 (3 wt%) MMMs show the CO 2 permeability of 100.7 Barrer and the CO 2 /N 2 ideal selectivity of 76.4, which is close to Robeson upper bound from 2008. Meanwhile, the Pebax/CeZrUiO66-NH 2 (3 wt%) MMMs present relatively good pressure resistance, which would be advantageous in terms of industrial application.
研究领域:
材料科学
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化学工程
·
环境科学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2022
·
IF 7.968
Qinglian Sun,Sheng Huang,Zaoyuan Li,Donghua Su,Jinfei Sun
Metal-organic frameworks (MOFs) effectively remove hazardous contaminants and are widely used for wastewater treatment . In this work, Co-doped bimetallic MIL-88B(Fe/Co) was synthesized via the hydrothermal method to activate potassium persulfate (KPS) for methylene blue (MB) degradation. XRD , IR, XPS, and SEM were conducted to investigate the crystalline structure, chemical valence state, and morphology of MIL-88B(Fe/Co). The synthesis time and Fe 3 + /Co 2 + molar ratio were optimized. Results showed that 10% Co-doped MIL-88B(Fe/Co) could efficiently activate KPS to achieve 100% MB removal in 15 min, thereby indicating that Co 2 + could accelerate metal-to-metal charge transfer during activation. A quadratic model was established by fitting the experimental data to optimize the degradation parameters. The reaction system with a temperature of 70 °C, KPS concentration of 30 mM, MOFs concentration of 0.8 g/L, and initial pH of 10 could effectively remove 99.85% MB in 5 min. Quenching experiments and EPR analysis revealed that·OH, 1 O 2 , and·O 2 − were the dominant reactive oxygen species (ROS) during MB degradation. The active sites (N15, N7, S10, and N18) most vulnerable to ROS attack in MB were identified by DFT calculation. MB degradation intermediates were identified through MALDI.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2023
·
IF 15.1
Zhiyuan Liu,Linmeng Wang,Changan Wang,Rushuo Li,Peiyun Zhou,Hongyi Gao,Ge Wang
Strong metal-support interaction (SMSI) plays an important role in heterogeneous catalysis, but the influence of the chemical microenvironment of metal on it is often neglected. In this study, a mesoporous Ce-MOFs with pyridine N sites and open metal sites (OMS) were constructed, and highly dispersed Pt nanoclusters (NCs) and Pt-N x interface were subsequently introduced and constructed via SMSI effect for hydrogenation of dicyclopentadiene (DCPD). The spectroscopic results and density functional theory (DFT) computations demonstrate that pyridine N and OMS can regulate the SMSI effect between Ce-PyDC and Pt through Pt-N x interface and electronic interaction between Pt and OMS, which increase electron cloud density of Pt nanoclusters, promote DCPD adsorption, H 2 activation. The optimal Pt NCs@Ce-PyDC-3 can efficiently convert DCPD to tetrahydrodicyclopentadiene (THDCPD) at 50 °C, giving a 100 % DCPD conversion and 99 % THDCPD selectivity. This work provides an in-depth understanding of the correlation between the metal nanoparticle microenvironment and SISM effect.
研究领域:
催化化学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2022
·
IF 16.744
Zimo Wang,Yaohan Chen,Li Wang,Jifu Zheng,Yong Fan,Suobo Zhang
The development of new adsorbent materials to improve adsorption capacity and selectivity constitutes a significant research direction for removing toxic ions from water. In this study, a series of Zr-based metal–organic framework hierarchical porous nanofibre membranes (MOFs@PIM-W) was designed and successfully synthesised, and their adsorption properties and mechanism for fluoride ions in water were investigated. The formation of Zr–F bonds in Zr-based MOFs is a primary reason for the rapid, effective, and stable removal of fluoride ions from water. Moreover, in contrast to common powder adsorbents and the conventional static adsorption process, the obtained hierarchical porous nanofibre membranes improve the removal rate of fluoride ions, which may be attributed to the formation of hierarchical porous structures. Specifically, by modifying the types of MOFs, the obtained nanofibre membranes can effectively remove Hg(II) ions from water under a wide range of pH environments (pH = 2–10) with a removal rate of up to 99 %. This indicates that the hierarchical porous design of nanofibre membranes incorporated with their specific adsorption provides a viable option for rapidly and efficiently removing toxic ions from water.
研究领域:
环境科学
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材料科学
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水处理
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纳米技术
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
·
2022
·
IF 4.598
Qi Zhang,Tao Wei,Jiahao Lu,Cheng Sun,Yanyan Zhou,Mengting Wang,Ye Liu,Beibei Xiao,Xiangyun Qiu,Shoudong Xu
All solid-state lithium-ion batteries (ASSLBs) are thought to benefit from using solid composite electrolytes (SCEs) to increase their energy density and safety. In this study, we firstly introduce the PVB additives to SCEs and prepared a SCE composed of a mixture of nanostructured MOFs (UiO-67), PVDF-HFP, PVB, and LiTFSI. Electrochemical characterizations of the SCEs (EIS, LSV, CV and battery test) were also conducted. The SCE UBP-2 (PVB:PVDF-HFP = 1:10) shows a high lithium-ion transference number (t Li + =0.72) and good ionic conductivity (3.27×10 −4 S cm −1 at 60 °C). A symmetric Li cell with SCE UBP-2 can be continuously cycled at 0.1 mA cm −2 for more than 2500 h without experiencing a short circuit. The full cell (LiFePO 4 /UBP-2/Li) also maintained a high reversible discharge capacity of 154.9 mAh g −1 at 0.1C after 200 cycles at 60 °C. At 3C, a capacity of around 100 mAh g −1 was also achieved. This work might help to enhance the development of the forthcoming all solid-state batteries.
研究领域:
材料科学
·
能源存储
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF FOOD COMPOSITION AND ANALYSIS
·
2023
·
IF 4.3
Yuanqian Xiong,Dong Zhang,Cuizhu Ye,Yu Wang,Xiangrui Deng,Danwen Deng,Chunhong Xiong,Jinsheng Zhang,Qianhui Gu,Ganhui Huang
Ciprofloxacin hydrochloride is widely used to treat animal diseases. However, its chronic abuse has caused severe accumulation in animal-derived foods , which has seriously damaged human health. Thus, in this study, a novel molecularly imprinted electrochemical sensor (MIES) was designed for selective and ultra-sensitive detection of ciprofloxacin hydrochloride (CPFX) in milk. The sensor was based on the molecularly imprinted polymers (MIPs) synthesized with poly-pyrrole (PPy) as the functional monomer , AuNPs and S-CoFe-MOFs (CoFe-Metal organic frameworks coated with chitosan) as the Supporting materials , and CPFX as the template molecule. The electrochemical behavior of MIPs/S-CoFe-MOFs/AuNPs/GCE was studied by several electrochemical methods, which showed a wider detection linear range (0.05 ∼ 500 ng·mL -1 ) and lower detection limit (0.0033 ng·mL -1 ) than those in previous reports. The optimization of experiments confirmed the good selectivity and stability of the sensors----- with the milk sample recovery of 89.04∼110.26%, and the relative standard deviations (RSD) of less than 5.5%, which was close to HPLC. In conclusion, the sensor we constructed has a high selectivity and stability potential in detecting CPFX in milk.
研究领域:
食品科学
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分析化学
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生物医学
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2021
·Vol. 11
·期 6
·3371-3379
·
IF 3.361
Zesheng Chen,Kun-huan He,Runzhi Wei,Yiju Lv,Zheng Liu,Guo-Cheng Han
A new metal–organic framework (MOF) compound [Mn2(2,2′-bca)2(H2O)2]n (Mn-MOFs) was successfully synthesized by solvothermal method, and Mn-MOFs@Zn material was prepared by loading zinc phosphate onto Mn-MOFs by ball milling, then Mn-MOFs@Zn was added to the water-based acrylic paint to prepare Mn-MOFs@Zn@acrylic coating. The AC impedance test results showed Mn-MOFs@Zn@acrylic coating has higher corrosion inhibition performance and stability to mild steel when compared with blank coating. The impedance modulus of the blank coating in the low frequency region decreased by 90%, and the Rct showed a trend of first increasing and then decreasing over time, the maximum Rct was only 303.8 Ω, which was only Mn-MOFs@Zn@acrylic coating one-seventh of the Rct value. The artificial scratch experiment showed that the Mn-MOFs@Zn@acrylic coating only slightly corrodes at the scratches, because Mn-MOFs@Zn material made the coating a self-repairing function and improved the durable anticorrosion performance of the acrylic coating.
研究领域:
材料科学
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腐蚀与防护
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表面工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2022
·
IF 9.965
Haiqing Gao,Qin Ji,Bin Chi,Caixue Lin,Gang Ding,Yingxi Wang,Xiaolan Yu,Zushun Xu,Run Zhang,Ling Li,Jing Wang
Targeting excess H 2 O 2 in the tumor microenvironment, nanotheranostic agents for catalytic therapy are designed based on Fenton reaction, catalyzing H 2 O 2 into oxygen and hydroxyl radical ( OH). But the catalytic efficiency in tumor microenvironment is not satisfactory. In order to solve the problem, a series of bimetallic-dual ligands metal-organic frameworks Fe/Tm-MOFs were designed, that Fe 3+ and Tm 3+ as metalions, 2-methylimidazole and trimesic acid as ligands. Due to the doped Tm 3+ in Fe/Tm-MOFs and the conjugated structures formed by two ligands, the rate of electron transfer was improved, thus promoting the generation of OH at some extent. In addition, the photothermal effect of Fe/Tm-MOFs further promotes the generation of OH, which was evidenced by the 3,3′,5,5′-tetramethylbenzidine(TMB). Combining the drug loading and release capabilities of Fe/Tm-MOFs, synergetic therapy of photothermal/chemo-/catalytic therapy can be achieved. In vitro results reveal that DOX release behaviors are both pH- and thermal-responsive. In vivo anti-cancer results show that the tumors of mice almost disappeared within 10 days, which were injected with Fe/Tm-MOFs/DOX and irradiated with 808 nm for 10 min. Thus, an excellent therapeutic performance has been achieved. Besides, Fe/Tm-MOFs can serve as a multimodality bioimaging contrast agent, covering fluorescence imaging, photothermal imaging and magnetic resonance imaging. Thus, an all-in-one nanotheranostic agent is constructed, improving the catalytic efficiency and providing a novel method to design an efficient nanotheranostic agent.
研究领域:
生物医学工程
·
纳米医学
·
肿瘤学
✓ 已验证
DOI
PubMed
高影响因子
LANGMUIR
·
2025
·
IF 3.9
Yuanbo Li,Taiming Zhang,Yanru Ding,Yuhao Chen,Yukui Rui
The iron-based metal–organic frameworks (Fe-MOFs) NH2-MIL-101(Fe) (MIL) has gained widespread attention as a drug carrier material in agriculture. In this study, a multifunctional nanocomposite, MIL@A@D@C, was successfully synthesized by loading the fungicide azoxystrobin (AZOX) and immunoinducer d-cellobiose (D) onto MIL, followed by surface modification with carboxymethyl cellulose (CMC). The loading capacity of MIL was optimized by varying solvent conditions and the mass ratio of MIL to AZOX, revealing that ethanol as the reaction solvent and a MIL: AZOX mass ratio of 1:4 resulted in the highest loading efficiency (6.73%). MIL@A@D@C exhibited pH- and cellulase-responsive controlled release behavior. In vitro antifungal assays demonstrated that MIL@A@D@C at a low concentration of 1 ppm effectively inhibited Colletotrichum graminicola (the causal agent of maize anthracnose). Foliar application experiments further confirmed that the composite formulation achieved significant inhibition at a low dosage of 10 ppm, outperforming commercial azoxystrobin products. Plant and animal safety assessments indicated that MIL@A@D@C possessed enhanced biosafety. These findings highlight the potential of MIL@A@D@C as an environmentally friendly and highly effective nanodelivery system for crop disease management.
研究领域:
农业纳米技术
·
植物病理学
·
药物递送系统
·
材料科学
·
环境科学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Haiyuan Chi,Chengjun Li,Mei Huang,Jinquan Wan,Xiaoxia Zhou,Bing Yan
Sulfate radicals-based advanced oxidation processes are regarded as effective methods for removing organic contaminants. However, current removal technologies are often unable to achieve satisfactory results due to the low concentrations and high stability that are frequently characteristics for many types of organic contaminants. To improve the efficacy of using sulfate radicals to remove organic contaminants, we designed metal–organic frameworks (Fe(II)-MOFs) modified with enrichment and specific recognition of molecular imprinting layer (Fe(II)-MOFs@MIP). Using dibutyl phthalate (DBP) as the model target contaminant, the selectivity coefficient towards DBP was 7.28 for adsorption and 4.46 for catalytic degradation of Fe(II)-MOFs@MIP, which is excellent for most of the imprinted material. Additionally, we achieved the accurate recognition (169.25 μg × g −1 ) and efficient degradation (0.071 min −1 ) of DBP reducing levels to 100 μg × L -1 . UV–vis analysis confirmed that specific recognition of DBP was mainly through hydrogen bonding and π-π interaction, while in-situ Raman and radical quenching experiments showed that the imprinting layer could accurately adsorb and produce the spatial confinement effects on target contaminants, thereby reducing the transfer distance of free radicals. As a result, we show that Fe(II)-MOFs@MIP can achieve efficient targeted degradation of DBP, opening up a new avenue for the removal of this and other highly stable organic contaminants present at low concentrations in environmental systems.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）