JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 15
·D882
·
IF 3.12
Da-Wei Yang,Ke-Ke Chang,Xiao-Fei Hu,Ya-Lan Liu,Tai-Qi Yin,Shi-Lin Jiang,Mei Li,Wei Han,Zhi-Fang Chai,Wei-Qun Shi
The objective of this work is to explore the electrochemical and electrodeposition behaviors of Eu (III) cation at the liquid binary Al-Ga alloy cathode. In addition, the co-reduction behaviors of Eu (III), Al (III) and Ga (III) were also systematically studied on a W electrode. The results indicated that Eu (III) can be reduced on the binary Al-Ga alloy cathode, and Eu (III), Al (III) and Ga (III) also can be co-reduced on the W electrode to form Al-Eu/Ga-Eu intermetallic compounds. At the same time, the isothermal section phase diagram of the Al-Ga-Eu ternary system at 773 K was also calculated. In addition, Al-Eu and Ga-Eu alloys were prepared by potentiostatic and galvanostatic electrolyses in the LiCl-KCl-EuCl3 melt. Finally, the electrodeposition products were characterized by X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) coupled with Energy Dispersive Spectroscopy (EDS).
研究领域:
材料科学
·
电化学
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DOI
高影响因子
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
·
2024
·
IF 1.5
Wang Xuebin,Mao Guoshu,Yu Shengjie,Fu Zhihai,Yue Yuanzhen,Zhang Shengdong,Ding Youqian,Huang Kun,Zhang Xian,Sun Xiaoyi
Responding to the need for radioactive waste disposal, the static and dynamic adsorption of Eu 3+ on TODGA-C resin in HNO 3 was investigated. The findings indicated that the adsorption of Eu 3+ on TODGA-C adheres to the quasi-second-order kinetic model. Additionally, the distribution coefficient for Eu 3+ adsorption on TODGA-C reaches 10 5 mL/g in 4 mol/L HNO 3 . Under the conditions of 3.5 mol/L HNO 3 , a flow rate of 3.6 mL/min, and an initial Eu 3+ concentration of 10 mg/L, the Thomas rate constant was found to be 1.2 mL/(mg·min), with a dynamic saturation capacity of 15 mg/mL.
研究领域:
放射性废物处理
·
化学工程
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高影响因子
ANALYTICA CHIMICA ACTA
·
2025
·
IF 6
Jingyi Xiao,Yi Ren,Menglong Liu,Yiyao Liu,Litao Chen,Jiayan Gao,Jinyang Li,Xue Gao
This study intends to create a ratiometric fluorescence probe utilizing aptamers for the detection of Vibrio parahaemolyticus ( V. parahaemolyticus ) in aquatic products. In this design, aptamer-functionalized magnetic nanoparticles specifically capture V. parahaemolyticus , while boric acid on Eu (III)-Based Metal-Organic Framework (Eu-MOF) interacts with glycolipids present on bacterial cells, thereby achieving dual recognition of V. parahaemolyticus . This fluorescent probe quantitatively detects V. parahaemolyticus by measuring the intensity of ratio fluorescence. The sensor demonstrates a detection range from 77 to 7.7×10 7 CFU/mL, possessing a detection threshold down to 1 CFU/mL. Moreover, the developed method based on Eu-MOF had been successfully applied to real samples. To achieve rapid on-site detection of V. parahaemolyticus , the study designed a portable smartphone sensor that confirms its capability for rapidly detecting pathogens and contributes significantly to establishing a system for regulating safety in detecting food and environment.
研究领域:
生物传感
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食品安全检测
·
微生物学
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DOI
PubMed
高影响因子
JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY
·
2024
·Vol. 333
·期 4
·2195-2206
·
IF 1.5
Li Junze,Zhao Chuang,Guo Wenbin,Gao Yang,Liu Tingting,Zhou Yu,Hou Hongguo,Jiao Caishan,Zhang Meng
Using DMDODGA as the carrier, the transportation and separation behavior of Eu(III) and La(III) were studied using a plate-type supported liquid membrane. La(III) and Eu(III) reach their maximum transport rates at feed phase nitric acid concentrations of 2 and 4 mol/L, which are 72.41 (± 2.12)% and 77.80 (± 2.45)%; Increasing the concentration of NO 3 − in feed phase will promote the transport of both ions. The change of HNO 3 concentration in feed phase had major effect on the separation of Eu(III)/La(III), and the co-transport of Eu(III)/La(III) was observed when the concentration of NO 3 − was 3 mol/L.
研究领域:
化学工程
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分离科学
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DOI
高影响因子
TALANTA
·
2025
·
IF 6.1
Shuyun Zhu,Kunming Sun,Shuyi Liu,Qian Wang,Jiatong Fan,Xian-En Zhao,Guobao Xu
Flavonoid glycosides are formed by dehydration condensation of aglycones and sugar molecules. Therefore, discrimination of flavonoid glycosides from their corresponding aglycones is a challenging task because they contain the same aglycone part in their molecular structures. Herein, boric acid-functional Eu(III)-organic framework (BA-Eu-MOF) was applied to discriminate flavonoid glycosides including baicalin (Bai), wogonoside (Wog), rutin (Rut), puerarin (Pue), quercitrin (Que) and astragalin (Ast) from their corresponding aglycones for the first time. Besides as organic ligand to sensitize the luminescence of Eu 3+ through “antenna” effect, 5-boronobenzene-1,3 dicarboxylic acid provided recognition site for flavonoid glycosides. Infrared, fluorescence, UV–vis, and mass spectra were used to investigate the recognition reaction between BA-Eu-MOF and flavonoid glycosides. The data indicated that the cis -diols of flavonoid glycosides from sugars covalently bonded to boric acid group to form cyclic boronic esters, which quenched the fluorescence of BA-Eu-MOF at 620 nm through decreasing the intersystem efficiency, inner filter effect and photoelectron transfer. In contrast, aglycones could not alter the fluorescence of BA-Eu-MOF because of no covalent bond between them. This probe exhibited high sensitivity towards flavonoid glycosides with the low detection limits of 3.3 nM, 3.5 nM, 33 nM, 56 nM, 5.1 nM and 5.5 nM for Bai, Que, Wog, Ast, Pue and Rut, respectively. The unique recognition ability of boric acid group enables selective and sensitive detection of flavonoid glycosides without the interference of their corresponding aglycones.
研究领域:
化学
·
药理学
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DOI
PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2024
·
IF 4.3
Xuequan Jing,Meina Guo,Jiarong Li,Wei Xu,Haonan Qin,Weidong Xiao,Yinhua Wan,Jieliang Chen,Zhangwei Yao,Weijie Song,Hongdong Yu,Kang Hu,Tinggang Li
The overuse of quinolone antibiotics has led to a series of health and environmental issues. Herein, we combine the distinct luminescence properties of Eu 3+ with the unique structure of covalent organic frameworks (COFs) to develop a precise and sensitive fluorescent probe for detecting Flumequine (Flu) in water. Eu 3+ is thoroughly anchored into the channels of COFs as recognition sites, while the synthesized probe material still maintains its intact framework structure. The unique structure of COFs provides excellent support and protection for Eu 3+ . Therefore, COF-Eu can rapidly bind with Flu which can transfer the absorbed energy to Eu 3+ through an “antenna effect”, resulting in red fluorescence. Moreover, there is a good linear relationship between Flu concentration in the range of 0–30 µM, with a detection limit of 41 nM. Simultaneously, the material maintains remarkable reproducibility, with its performance remaining almost unchanged after five cycles of use. Remarkably, the probe demonstrates excellent Flu recovery rates in real samples. This study provides a viable approach for the recognition of flumequine in the environment through a customized fluorescence detection method.
研究领域:
分析化学
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环境科学
·
材料科学
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DOI
PubMed
高影响因子
APPLIED CLAY SCIENCE
·
2021
·
IF 5.467
Junming Zhou,Hongmei Liu,Dong Liu,Peng Yuan,Hongling Bu,Peixin Du,Wenxiao Fan,Mengyuan Li
Weathered crust elution-deposited rare earth (WED-RE) ores are important rare earth element (REE) resources around the world. In these ores, the REE are believed to mainly exist as exchangeable REE(III) ions on the surfaces of clay minerals, such as tubular halloysite and platy kaolinite . However, the mechanisms underlying the sorption and desorption of REE(III) ions on clay minerals in the environment of weathered crusts remain ambiguous. In this study, the sorption/desorption characteristics of Eu(III) ions onto halloysite and kaolinite were investigated. The results revealed that Eu(III) was adsorbed onto both clay minerals through inner-sphere complexation and outer-sphere complexation, where the former was the primary sorption mechanism. Halloysite displayed a higher sorption capacity for Eu(III) than kaolinite in a weakly acidic environment (pH 4–6). The desorption efficiency increased with the increasing concentration of NH 4 + ions. When the NH 4 + concentration was 0.002 mol/L, which is similar to the typical cation concentration of groundwater/rainwater, the amount and rate of Eu(III) desorption from halloysite were lower than those from kaolinite. The desorption of Eu(III) ions from the two clay minerals is proposed to be governed by the attraction between the outer-sphere complexes and clay minerals when the NH 4 + concentration is 0.002 mol/L. Therefore, halloysite has a higher sorption capacity and stronger retention capacity for Eu(III) than kaolinite, which suggests that halloysite may play a greater role in REE(III) enrichment in WED-RE ores than kaolinite owing to the similar chemical properties of REE(III) ions. The fundamental results obtained in this study afford new insights into the migration of REE and the role of clay minerals in REE enrichment during ore formation.
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INORGANIC CHEMISTRY
·
2015
·
IF 4.762
Jingyan Sun,Bo Song,Zhiqiang Ye,Jingli Yuan
Singlet oxygen (1O2) plays a key role in the photodynamic therapy (PDT) technique of neoplastic diseases. In this work, by using a 9,10-dimethyl-2-anthryl-containing β-diketone, 1,1,1,2,2-pentafluoro-5-(9′,10′-dimethyl-2′-anthryl)-3,5-pentanedione (Hpfdap), as a 1O2-recognition ligand, a novel β-diketonate–europium(III) complex that can act as a luminescence probe for 1O2, [Eu(pfdap)3(tpy)] (tpy = 2,2′,2″-terpyridine), has been designed and synthesized for the time-gated luminescence detection of 1O2 in living cells. The complex is weakly luminescent due to the quenching effect of 9,10-dimethyl-2-anthryl groups. After reaction with 1O2, accompanied by the formation of endoperoxides of 9,10-dimethyl-2-anthryl groups, the luminescence quenching disappears, so that the long-lived luminescence of the europium(III) complex is switched on. The complex showed highly selective luminescence response to 1O2 with a remarkable luminescence enhancement. Combined with the time-gated luminescence imaging technique, the complex was successfully used as a luminescent probe for the monitoring of the time-dependent generation of 1O2 in 5-aminolevulinic acid (a PDT drug) loaded HepG2 cells during the photodynamic process. In addition, by coloading the complex and a mitochondrial indicator, Mito-Tracker Green, into HepG2 cells, the specific localization of [Eu(pfdap)3(tpy)] molecules in mitochondria of HepG2 cells was demonstrated by confocal fluorescence imaging measurements.
研究领域:
生物化学
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医学影像
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药物化学
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DOI
PubMed
高影响因子
SENSORS AND ACTUATORS B-CHEMICAL
·
2024
·
IF 8
Yu Kang,Ludi Wang,Yaoyang Liu,Runquan Shi,Xiaoyan Tang,Li Wang
Efficient and selective sensing of lanthanides are crucial for identifying valuable lanthanide streams and designing effective extraction/masking agents for mining and nuclear waste management. Luminescence-based sensing often struggles with interference from water molecules. Common approaches to improve emissive lanthanide complexes in water involve increasing ligand lipophilicity and enclosing the emitting metal center. Herein, we have demonstrated that lipophilic ligands do not always lead to higher emissions. When strong coordinating groups are involved in the ligand, the complex may adapt special architecture to compensate the hydrophilic nature of the ligand by creating lipophilic microenvironment and lead to higher emissions. Our findings highlight the importance of the overall lipophilicity of both the ligand and the final complex, which could serve as important reference for future design of efficient lanthanide sensing and emissive complexes.
研究领域:
化学
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材料科学
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环境科学
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DOI
高影响因子
POLYMER INTERNATIONAL
·
2024
·
IF 2.9
Fang Wu,Xinfei Zhang,Qi Wang,Dayang Yu,Pan Zheng,Rongli Zhu,Xu Wang,Zejun Pu,Jiachun Zhong
In order to expand the application of biobased polycarbonate in optical components, a series of isosorbide polycarbonate (PICC)/rare earth ion complex fluorescent composites were prepared by using PICC as a macromolecular ligand and Eu 3+ and Tb 3+ as rare earth luminescence centers. The coordination system between rare earth ions and PICC was investigated by Fourier transform infrared spectroscopy, DSC and TGA. On adjusting the ratio of Eu 3+ and Tb 3+ , a PICC/rare earth ion composite with adjustable fluorescence color was obtained. Also, the thermal, mechanical and optical properties of a series of PICC/rare earth ion fluorescent films with different ratios were tested. A transparent fluorescent composite material with excellent mechanical properties and tunable fluorescent colors has been prepared. © 2024 Society of Industrial Chemistry.
研究领域:
材料科学
·
光学工程
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DOI
高影响因子
MOLECULES
·
2024
·Vol. 29
·期 17
·4259
·
IF 4.2
Jing Li,Yu Liang,Chun Tian,Hongyan Zou,Lei Zhan,Lijuan Wang,Chengzhi Huang,Chunmei Li
Bacillus anthracisis a Gram-positive bacterium that can cause acute infection and anthracnose, which is a serious concern for human health. DeterminingBacillus anthracisthrough its spore biomarker dipicolinic acid (DPA) is crucial, and there is a strong need for a method that is rapid, sensitive, and selective. Here, we created Eu(III)-coordination polymers (Eu-CPs) with surfaces that have abundant carboxyl and hydroxyl groups. This was achieved by using citric acid and europium nitrate hexahydrate as precursors in a straightforward one-pot hydrothermal process. These Eu-CPs were then successfully utilized for highly sensitive DPA determination. The fluorescence (FL) emission of Eu-CPs, which is typically weak due to the coordination of Eu(III) with water molecules, was significantly enhanced in the presence of DPA. This enhancement is attributed to the competitive binding between DPA’s carboxyl or hydroxyl groups and water molecules. As a result, the absorbed energy of DPA, when excited by 280 nm ultraviolet light, is transferred to Eu-CPs through an antenna effect. This leads to the emission of the characteristic red fluorescence of Eu3+at 618 nm. A strong linear relationship was observed between the enhanced FL intensity and DPA concentration in the range of 0.5–80 μM. This relationship allowed for a limit of detection (LOD) of 15.23 nM. Furthermore, the Eu-CPs we constructed can effectively monitor the release of DPA from Bacillus subtilis spores, thereby further demonstrating the potential significance of this strategy in the monitoring and management of anthrax risk. This highlights the novelty of this approach in practical applications, provides a valuable determination technique for Bacillus anthracis, and offers insights into the development cycle of microorganisms.
研究领域:
微生物学
·
分析化学
·
生物医学
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DOI
PubMed
高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Zhen-Wen Zhang,Ao-Jun Qiu,Geng-Jin-Sheng Cheng,Yu Fan,Yu Xiao,Yan-Zhu Liu,Qian-Yong Cao
Tetracycline detection remains an important research topic in the bioenvironmental field today. This paper reports a novel amphiphilic Eu(III) complex DO 3 AC 12 -Eu for single signal and ratiometric fluorescence detection of tetracycline (TC) in aqueous solution. DO 3 AC 12 -Eu can self-assemble micelle-like nano-aggregation in aqueous solution with no fluorescence. After addition of TC, the Eu(III)-based emission was observed for the effective antenna effect from TC to Eu(III) center. In addition, DO 3 AC 12 -Eu can load 4-methylumbelliferone sodium (MU) as a fluorescence reference to form DO 3 AC 12 -Eu/MU co-assembly nano-aggregation with a blue emission at 450 nm. Based on the TC-induced antenna effect and inner filter effect mechanism between TC and MU, DO 3 AC 12 -Eu/MU exhibits a ratiometrically fluorescent response toward TC, with increasing Eu(III)-based emission at 615 nm, and decreasing MU-based emission at 450 nm. Importantly, DO 3 AC 12 -Eu/MU exhibits superior sensitivity and selectivity over DO 3 AC 12 -Eu . The detection limit of DO 3 AC 12 -Eu/MU toward TC is 0.82 nM, far lower than that of DO 3 AC 12 -Eu (9.5 nM). Furthermore, DO 3 AC 12 -Eu/MU assembly has been successfully used for on-site and real-time detection of TC in food samples by using the smartphone-based visualization method and test gel.
研究领域:
分析化学
·
环境监测
·
生物环境科学
·
荧光传感技术
·
纳米科技
·
配位化学
·
食品安全检测
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产品关联
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高影响因子