JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2016
·
IF 2.822
Fang Long,Jing Wang,Zhaohui Zhang,Liang Yan
A novel magnetic molecularly imprinted electrochemical sensor (MMIP-sensor) combined with magnetic molecularly imprinted solid-phase extraction (MMISPE) was constructed for rapid and sensitive detection of tetrabromobisphenol S (TBBPS) in water samples. The magnetic molecularly imprinted polymer based on magnetic graphene/multi-walled carbon nanotubes hybrid composite (MMIP/Gr-MWCNTs) was prepared as MMISPE sorbet to separate and enrich TBBPS from complex system. Adsorption results showed that the MMIP/Gr-MWCNTs possessed excellent selective adsorption toward TBBPS with a maximum adsorption capacity of 17.83 mg g − 1 . The magnetic imprinted sensor based on the magnetic Gr-MWCNTs composite modified electrode was prepared by electropolymerization of dopamine monomer . The high sensitivity of the MMIP-sensor was attributed to the large specific surface area and excellent electrical conductivity of the magnetic Gr-MWCNTs composites. The detection limit of the MIP-sensor toward TBBPS was calculated as 2.1 × 10 − 11 mol L − 1 (S/N = 3). Under the optimum conditions, the MISPE-MMIP-sensor combination system provided 10–12 fold preconcentration than that of MMIP-sensor alone determination. The MISPE-MMIP-sensor was successfully used for detection of TBBPS in drinking water , rain water , lake water and tap water with recoveries of 88.4–98.8%.
研究领域:
分析化学
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环境监测
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电化学传感
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分子印迹技术
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水处理
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污染物检测
✓ 已验证
DOI
高影响因子
ANALYTICA CHIMICA ACTA
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2014
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IF 4.517
Shan Liu,Maochao Wei,Xiangli Zheng,Shuai Xu,Changli Zhou
We are just beginning to exploit the fascinating potential of thionine , called electrochemical probe that can selectively recognize specific polycyclic aromatic hydrocarbons (PAHs), as tools for the detection of tricyclic aromatic hydrocarbons phenanthrene (PHE) and anthracene (ANT). A novel electrochemical sensing platform by modification of electroactive thionine functionalized graphene onto glass carbon electrode (Th/GRs/GCE) surface was constructed. The immobilized thionine showed a remarkable stability, which may benefit from the π–π stacking force with graphene. Under optimum conditions, the proposed electrochemical sensor exhibited high sensitivity and low detection limit for detecting PHE and ANT. The total amount of PHE and ANT could be quantified in a wide range of 10 pM–0.1 μM with a good linearity ( R 2 = 0.9979) and a low detection limit of 0.1 pM ( S / N = 3). Compounds which possess one or two benzene rings or PAHs with more than three rings, such as benzene, naphthalene (NAP), benzo[a]pyrene (BaP) and pyrene (PYR) show little interference on the detection. Consequently, a simple and sensitive electrochemical method was proposed for the determination of PHE and ANT, which was used to determine PHE and ANT in waste water samples. The electrochemical method provides a general tool that complements the commonly used spectroscopic methods and immune method for the detection of PAHs.
研究领域:
分析化学
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环境监测
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电化学传感器
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分子识别
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污染物检测
✓ 已验证
DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·Vol. 11
·期 12
·9868-9880
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IF 1.5
Hongying Li,Xueliang Wang,Tao Wang,Zhaoxia Wang,Wei Zhao
A modified electrode was fabricated by casting graphene oxide (GO) suspension onto the surface of active glassy carbon electrode (GCE), and it can significantly enhanced the oxidation peak currents of m-trihydroxybenzene (m-THB) and p-nitrophenol (p-NP). Based on this, a sensitive analytical method towards their simultaneous determination was established. Many influencing factors such as the type of electrolyte, acidity, scan rates and concentrations were explored. Under the optimal experimental conditions, the oxidation peak currents of m-THB and p-NP were linearly increased with their concentrations ranging from 9 to 100 μM, with the detection limits both of 1 μM. Comparing with other reported methods, this sensor showed wider linear range and lower detection limit. In addition, the proposed method was successfully used to analysis of real environmental water samples with satisfactory recoveries, which verified the practicability of the sensor.
研究领域:
分析化学
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环境科学
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电化学
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传感器技术
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污染物检测
✓ 已验证
DOI
高影响因子
International Journal of Electrochemical Science
·
2023
·Vol. 13
·期 2
·1556-1567
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IF 1.5
Zhihong Yan,Bo Fu,Jincheng Chen,Tailin Liu,Kang Li
Bisphenol A (BPA) was successfully electrodeposited on glassy carbon electrode modified with the chitosan-graphene (Chit-GR/GCE) by multiple sweep voltammetry under ultraviolet (UV) irradiation. The experimental conditions of the BPA deposits and the probable oxidation mechanism were investigated. Two oxidation peaks (peakII=0.12 V, peakIII=0.20 V) appeared in a suitable potential range of 0.0V and 0.2V at the Chit-GR/GC eletrode in the presence of UV light, and it could be seen that the oxidation peak current increased with the increase of UV irradiation time. The emerging peakIII was reported firstly in the work, which showed that the Chit-GR modified electrode had catalytic activity on the oxidation of BPA. Based on the oxidation peak (III) of BPA oxidative porducts on the Chit-GR/GC electrode under UV irradiation, the electrochemical sensor was fabiracated for determination of BPA. The calibration curve was obtained in the range of 5.0 to 200.0 μM with the limit of detection of 0.34 μM (S/N=3) and the response sensitivity of 0.33 μA μM -1 , which was higher than those of the method of determining BPA based on the direct oxidtation of BPA (0.98 μM (S/N=3), 0.12 μA μM -1 ). It was applied successfully for determination of BPA in lake, soil and plastic bottle samples. The new strategy, based on anodic electrodeposition and photocatalytic oxidation of BPA oxidation porducts, was provided for determination of BPA under UV irradiation. It was green, evironmental and effective.
研究领域:
分析化学
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环境监测
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电化学传感
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污染物检测
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材料科学
✓ 已验证
DOI
高影响因子
ENVIRONMENTAL SCIENCE & TECHNOLOGY
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2011
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IF 4.827
Dawei Li,Lulu Qu,Wenlei Zhai,Jinqun Xue,John S. Fossey,Yitao Long
A novel facile method for on-site detection of substituted aromatic pollutants in water using thin layer chromatography (TLC) combined with surface-enhanced Raman spectroscopy (SERS) was explored. Various substituted aromatics in polluted water were separated by a convenient TLC protocol and then detected using a portable Raman spectrometer with the prepared silver colloids serving as SERS-active substrates. The effects of operating conditions on detection efficacy were evaluated, and the application of TLC−SERS to on-site detection of artificial and real-life samples of aromatics/polluted water was systematically investigated. It was shown that commercially available Si 60-F254 TLC plates were suitable for separation and displayed low SERS background and good separation efficiency, 2 mM silver colloids, 20 mM NaCl (working as aggregating agent), 40 mW laser power, and 50 s intergration time were appropriate for the detection regime. Furthermore, qualitative and quantitative detection of most of substituted aromatic pollutants was found to be readily accomplished using the developed TLC−SERS technique, which compared well with GC−MS in terms of identification ability and detection accuracy, and a limit of detection (LOD) less than 0.2 ppm (even at ppb level for some analytes) could be achieved under optimal conditions. The results reveal that the presented convenient method could be used for the effective separation and detection of the substituted aromatic pollutants of water on site, thus reducing possible influences of sample transportation and contamination while shortening the overall analysis time for emergency and routine monitoring of the substituted aromatics/polluted water.
研究领域:
环境监测
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分析化学
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水质分析
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光谱学
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污染物检测
✓ 已验证
DOI
高影响因子
CHROMATOGRAPHIA
·
2018
·Vol. 82
·期 3
·683-693
·
IF 1.401
Shen Chen,Wu Tong,Zang Xiaohuan
In this work, a zeolitic imidazolate framework-based graphene oxide composite (ZIF-8@GO) was prepared and used as the adsorbent in hollow fiber stir bar sorptive extraction. The stir bar was constructed of a small section of hollow fiber filled with 5 mg ZIF-8@GO and a thin stainless wire of 1.5 cm long in its lumen, and used to extract the trace levels of phthalate esters from children’s food samples prior to gas chromatography–mass spectrometric detection. The ZIF-8@GO showed a high adsorption efficiency for the compounds containing aromatic rings. The main experimental parameters that can impact the extraction efficiency including extraction temperature, extraction time, stirring rate, sample salinity, and desorption conditions were investigated. Under the optimized conditions, the limits of detection (LODs) for the five phthalate esters (diethyl phthalate, dipropyl phthalate, diisobutyl phthalate, butylbenzyl phthalate, and di(2-ethylhexyl) phthalate) were 0.15–0.6 µg L −1 for CiCi beverage and pear juice samples, and 0.75–2.2 µg kg −1 for jam samples. The limits of quantitation (LOQs) were 0.5–2.0 µg L −1 for CiCi beverage and pear juice samples, and 2.5–7.5 µg kg −1 for jam samples. Wide linear ranges of 0.5–500.0 µg L −1 and 2.5–2000 µg kg −1 were obtained for CiCi beverage, pear juice samples and jam samples, respectively, with good repeatability (RSD < 11%) and high method recoveries (72%–100%). The lifetime test results showed that the ZIF-8@GO-based hollow fiber stir bar can be reused for 120 extraction cycles without a significant loss of extraction efficiency, indicating its high durability and stability. The established method was applied successfully for the determination of the phthalate esters (PAEs) in children’s food samples. Graphical abstract
研究领域:
分析化学
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食品安全
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环境毒理学
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暴露科学
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食品化学
·
污染物检测
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）