Song Xinjian, Wang Bing, Huang Yina, Li Liqing, Li Ting, Li Chunya, Zhang Shenghui
Key Laboratory of Biologic Resources Protection and Utilization of Hubei Province, Hubei University for Nationalities, Enshi 445000, China.
Key Laboratory of Analytical Chemistry of the State Ethnic Affairs Commission, College of Chemistry and Materials Science, South-Central University for Nationalities, Wuhan 430074, China.
Talanta. 2014 Feb;119:606-12. doi: 10.1016/j.talanta.2013.11.055. Epub 2013 Nov 27.
A polymeric film modified glassy carbon electrode was electrochemically fabricated with potential step technique using 1-butyl-3-[3-(N-pyrrole)propyl] imidazolium tetrafluoroborate ionic liquid as a monomer. Followed by being treated with sodium dodecyl sulfonate solution, a hydrophobic film bearing poly{1-butyl-3-[3-(N-pyrrolyl)propyl]imidazolium dodecyl sulfonate} moiety was modified onto electrode surface. The substitution was confirmed by X-ray photoelectron spectroscopy. The morphology of the polymeric film electrode surface was characterized with scanning electron microscopy. Electrochemical behaviors of magnolol at the hydrophobic polymeric film electrode were systematically investigated with voltammetry. Compared with the unmodified glassy carbon electrode, the oxidation peak shift slightly towards positive potential and the oxidation peak current significantly increased. Under optimal conditions, the oxidation peak current was linearly related to the magnolol concentration in the range of 1.0 × 10(-8) to 1.0 × 10(-6) mol L(-1) and 1.0 × 10(-6) to 5.0 × 10(-5) mol L(-1). The detection limit was estimated to be 4.55 × 10(-9) mol L(-1) (S/N=3). The polymerized ionic liquid film electrode was successfully used to analysis magnolol in M. officinalis. The result was consistent with that obtained by high performance liquid chromatography.
采用电位阶跃技术,以1-丁基-3-[3-(N-吡咯基)丙基]咪唑四氟硼酸盐离子液体为单体,电化学制备了聚合物膜修饰玻碳电极。随后用十二烷基磺酸钠溶液处理,在电极表面修饰了带有聚{1-丁基-3-[3-(N-吡咯基)丙基]咪唑十二烷基磺酸盐}部分的疏水膜。通过X射线光电子能谱证实了取代反应。用扫描电子显微镜对聚合物膜电极表面的形貌进行了表征。用伏安法系统研究了厚朴酚在疏水聚合物膜电极上的电化学行为。与未修饰的玻碳电极相比,氧化峰向正电位略有偏移,氧化峰电流显著增加。在最佳条件下,氧化峰电流在1.0×10(-8)至1.0×10(-6)mol L(-1)和1.0×10(-6)至5.0×10(-5)mol L(-1)范围内与厚朴酚浓度呈线性关系。检测限估计为4.55×10(-9)mol L(-1)(S/N=3)。该聚合离子液体膜电极成功用于厚朴中厚朴酚的分析。结果与高效液相色谱法一致。