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作 者:王明艳[1] 许兴友[1] 马卫兴[1] 曹志凌[1,2] 许瑞波[1]
机构地区:[1]淮海工学院化学工程学院,连云港222005 [2]北京理工大学化学工程学院,北京100081
出 处:《理化检验(化学分册)》2010年第10期1125-1128,1131,共5页Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
基 金:江苏省海洋生物技术重点建设实验室(2007HS009);淮海工学院自然基金(Z2008021)
摘 要:利用分子自组装技术制备了4-(3-吡啶基)-2-巯基咪唑修饰金电极,用循环伏安法研究了抗坏血酸和槲皮素在该修饰电极上的电化学行为,发现该电极对两反应物均具有良好的催化作用。在抗坏血酸和槲皮素混合溶液中,采用一阶微分线性扫描伏安法进行检测,发现两物质氧化峰相差240 mV,建立抗坏血酸存在下槲皮素的直接测定方法。在抗坏血酸和槲皮素的共存溶液中,槲皮素峰电流的一阶微分与其浓度在2.0~200μmol.L-1范围内呈线性关系,方法的检出限(3S/N)为1.0μmol.L-1。方法的回收率在98.8%~102.0%之间。Pretreated gold electrode was modified by self-assembling in 4-(3-pyridyl)-2-mercapto-imidazole(abbreviated as PMIZ) alcoholic solution.Electrochemical behaviors of ascorbic acid and quercetin at this modified electrode(or designated as PMIZ/AuE) were studied by cyclic voltammetry.It was found that the PMIZ/AuE showed catalytic effect towards both the reactions of ascorbic acid and quercetin at the electrode,and that in a solution containing both ascorbic and quercetin,a potential difference of 240 mV was observed between the oxidation peak potentials of these 2 compounds,when measured by 1st derivative linear scanning voltammetry.Based on these facts,a direct method for determination of quercetin in the presence of ascorbic acid was proposed.Linear relationship between values of 1st derivative of peak current(ip) and concentration of quercetin was found in the range of 2.0 to 200 μmol·L-1,with its detection limit(3S/N) of 1.0 μmol·L-1.Values of recovery found were in the range of 98.8% to 102.0%.
关 键 词:线性扫描伏安法 修饰金电极 4-(3-吡啶基)-2-巯基咪唑 抗坏血酸 槲皮素
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