ANALYTICA CHIMICA ACTA
·
2014
·
IF 4.517
Xia Hao,Jing Lei Lei,Nian Bing Li,Hong Qun Luo
A simple and effective method for the detection of electrochemically inactive sodium dodecyl sulfate (SDS) has been designed, based on different binding affinity of polyethyleneimine (PEI) toward electrochemically active eosin Y and electrochemically inactive SDS. The stronger binding affinity of the PEI toward SDS than eosin Y results in the decrease of the redox peak current of surface confined eosin Y and provides a quantitative readout for the SDS. The difference in value of the cathodic peak current showed a linear relationship with SDS concentration in a concentration range from 1 to 40 μg mL −1 , and a detection limit of 0.9 μg mL −1 for SDS was obtained. Furthermore, the method has been successfully applied to the detection of SDS in real samples. The developed approach provided a simple and reliable detection for SDS and might have potential applications in electrochemical methods for inactive molecules.
研究领域:
分析化学
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电化学
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DOI
PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2025
·
IF 2.5
Xiaoxia Liu,Sa Yang,Yanli Cheng,Donglei Wei,Hou Chen,Liangjiu Bai,Wenxiang Wang,Huawei Yang,Lixia Yang,Kun Yin
A hydrogel-based photocatalyst is synthesized by the construction of a hydrogel skeleton using common monomers and subsequent in situ generation of Zn–Cu–S photocatalyst particles. The photocatalytic degradation performance of the hydrogel-based photocatalyst is systematically studied, and the photocatalyst exhibits good removal ability for eosin Y. The composite photocatalyst shows high efficiency at low loading, with a removal rate of up to >98% in 3 hours under sunlight irradiation, without the need for a preliminary dark adsorption process. High removal efficiency was observed, remaining above 95% even after 10 recycling runs, demonstrating the excellent stability of the composite photocatalyst. We thus provide a facile method to construct hydrogel-based photocatalysts that show high application potential in the photocatalytic removal of eosin Y.
研究领域:
环境科学
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材料科学
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化学工程
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光催化
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DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·
IF 1.5
Shengbiao Zheng,Yu Liu,Jing Liu,Jing Tang
The electrodeposition of eosin Y (EY) on graphene oxide (GO) modified glassy carbon electrode (GCE) was performed and the modified platform applied for the simultaneous determination of dopamine (DA) and epinephrine (EP). The EY/GO modified GCE was characterized using electrochemical impedance spectra. The modified electrode exhibited excellent electroanalytical performance for DA and EP by cyclic voltammetry due to the synergistic effect of the good electrical conductivity of GO and electrochemical activity of EY. The linear responses were found by differential pulse voltammetry (DPV) between 0.2 and 100 μM concentration range for DA and EP, with detection limits of 50 nM for DA and 30 nM for EP (S/N = 3), respectively. Further experiments were investigated for electrode selectivity, stability and reproducibility. In addition, in order to evaluate electrochemical activities for this proposed electrode, the simultaneous determination of DA and EP at EY/GO/GCE was explored in diluted human urine samples.
研究领域:
分析化学
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生物医学工程
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DOI
高影响因子
ANALYTICAL CHEMISTRY
·
2013
·
IF 5.695
Ting Wen,Nian Bing Li,Hong Qun Luo
A novel sensing system has been designed for the detection of sodium dodecyl sulfate (SDS) based on the recovered fluorescence signal of eosin Y and polyethyleneimine (PEI) complex. The eosin Y reacted with PEI to form a complex by virtue of hydrophobic interaction as well as the electrostatic interaction, which resulted in a strong fluorescence quenching of the eosin Y. Subsequently, with the addition of SDS to the eosin Y/PEI system, a strong surface interaction and electrostatic interactions between PEI and SDS resulted in the formation of the PEI/SDS complex and the dissociation of the eosin Y/PEI complex, which led to the significant fluorescence recovery. Herein, we have demonstrated that this facile methodology can offer a rapid, reliable, and selective detection of SDS with a detection limit as low as 0.02 μg mL–1 and a linear range from 0.4 to 6 μg mL–1. Furthermore, the method has been successfully applied to the detection of SDS in real samples with satisfied recovery and accuracy. Overall, these results demonstrate that this method has great promise for environmental applications.
研究领域:
分析化学
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环境科学
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DOI
PubMed
高影响因子
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
·
2016
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IF 2.653
Huan Wu,Yanmei Zhao,Xuanping Tan,Xiaoqing Zeng,Yuan Guo,Jidong Yang
A convenient fluorescence quenching method for determination of Quizalofop-p-ethyl(Qpe) was proposed in this paper. Eosin Y(EY) is a red dye with strong green fluorescence (λex/λem = 519/540 nm). The interaction between EY, Pd(II) and Qpe was investigated by fluorescence spectroscopy, resonance Rayleigh scattering(RRS) and UV–Vis absorption. Based on changes in spectrum, Pd(II) associated with Qpe giving a positively charged chelate firstly, then reacted with EY through electrostatic and hydrophobic interaction formed ternary chelate could be demonstrated. Under optimum conditions, the fluorescence intensity of EY could be quenched by Qpe in the presence of Pd(II) and the RRS intensity had a remarkable enhancement, which was directly proportional to the Qpe concentration within a certain concentration range, respectively. Based on the fluorescence quenching of EY-Pd(II) system by Qpe, a novel, convenient and specific method for Qpe determination was developed. To our knowledge, this is the first fluorescence method for determination of Qpe was reported. The detection limit for Qpe was 20.3 ng/mL and the quantitative determination range was 0.04–1.0 μg/mL. The method was highly sensitive and had larger detection range compared to other methods. The influence of coexisting substances was investigated with good anti -interference ability. The new analytical method has been applied to determine of Qpe in real samples with satisfactory results.
研究领域:
分析化学
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环境科学
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DOI
高影响因子
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2016
·Vol. 408
·期 19
·5247-5259
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IF 3.125
Pan Ziyu,Peng Jingdong,Zang Xu,Lei Gang,He Yan,Liu Di
A novel, highly selective, and sensitive resonance light scattering (RLS) detection approach coupled with high performance liquid chromatography (HPLC) was researched and developed for the synchronous analysis of three kinds of benzimidazole anthelmintics, including mebendazole (MBZ), albendazole (ABZ), and fenbendazole (FBZ) for the first time. In the pH range of 3.5–3.7 Britton-Robinson buffer medium, three kinds of anthelmintics, which were separated by HPLC, reacted with eosin Y (EY) to form 1:1 ion-association complexes, resulting in significantly enhanced RLS signals and the maximum peak located at 335 nm. The enhanced RLS intensity was in proportion to the MBZ, ABZ, and FBZ concentration in the range 0.2–25, 0.2–23, and 0.15–20 μg/mL, respectively. The limit of detection was in the range of 0.064–0.16 μg/mL. In addition, human urine was determined to validate the proposed method by spiked samples and real urine samples. Satisfactory results were obtained by HPLC-RLS method.
The diagram mechanism of generating resonance between emitted light and scattered light
研究领域:
分析化学
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药物分析
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生物医学工程
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产品关联
DOI
PubMed
高影响因子