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电活化玻碳电极差分脉冲伏安法测定水杨酸的研究 被引量:3

Determination of Salicylic Acid by Differential Pulse Voltammetry with an Electro-activated Glassy Carbon Electrode
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摘要 采用循环伏安法和差分脉冲伏安法对水杨酸在电活化玻碳电极上的电化学行为进行研究。在pH 7.0的PBS溶液中,将玻碳电极用恒电位法在+1.7 V电位阳极氧化400 s。在0.2 mol.L-1NaOH溶液中,水杨酸在0.602 V处有一良好的氧化峰,其氧化峰电流与扫描速率在0.02~0.2 V.s-1范围内呈良好线性关系,表明电极过程为受吸附控制的不可逆过程。差分脉冲伏安法的氧化峰电流(Ipa)与水杨酸的浓度在5.0×10-6~2.0×10-3 mol.L-1范围内呈良好的线性关系,相关系数为0.986 3,检出限为1.2×10-7 mol.L-1。该方法操作简便,重复性较好,将其用于阿司匹林片剂中水杨酸含量的检测,结果满意。 The electrochemical behavior of salicylic acid (SA) on an electro-activated glassy carbon electrode (EGCE) was studied by cyclic voltammetry(CV) and differential pulse vohammetry (DPV). The glassy carbon electrode ( GCE ) was activated in pH 7.0 PBS buffer for 400 s by poteutiostatic method at + 1.7 V. In 0.2 mol · L^-1 NaOH solution, a well-defined oxidative peak of SA was observed at 0. 602 V (vs. Ag/AgCl) on the activated electrode. The anodic peak current increased linearly with scan rate from 0. 02 V · s^- 1 to 0.2 V · s^- 1, revealing that the reaction was a absorptioncontrolled process. The experimental parameters were optimized and the correlation between peak current (Ipa) and concentration was studied by differential pulse vohammetry. Under the optimal conditions, the linear range for SA was in the range of 5.0 × 10^-6 - 2.0 × 10^ -3 mol · L^-1 with a correlation coefficient of 0. 986 3, and the detection limit(S/N =3) was 1.2 × 10^-7 mol · L^-1 The activated glassy carbon electrode showed the advantages of simple preparation procedure and good reproducibility, and was applied in the determination of salicylic acid in pharmaceutical drugs with satisfactmy results.
出处 《分析测试学报》 CAS CSCD 北大核心 2011年第11期1306-1310,共5页 Journal of Instrumental Analysis
基金 贵州省科学技术基金资助项目(黔科合J字[2009]2023号) 贵州省教育厅自然科学研究基金资助项目(黔教科2010025) 贵州民族学院应用化学创新团队资助项目(2011)
关键词 水杨酸 电活化玻碳电极 差分脉冲伏安法 salicylic acid electro-activated glassy carbon electrode differential pulse vohammetry
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