Di Junwei, Zhang Feng
Department of Chemistry, Suzhou University, Suzhou 215006, PR China.
Talanta. 2003 May 28;60(1):31-6. doi: 10.1016/S0039-9140(03)00062-6.
This paper described the determination of trace manganese using linear sweep voltammetry at a pretreatment glassy carbon electrode. The glassy carbon electrode pretreated by electrochemical method in the 0.1 moll(-1) NaOH solution greatly improved the electrode responsibility in the determination of manganese(II). The barrier to the detection of low manganese concentration was overcome by means of autocatalytic effect of manganese oxide deposited on the electrode in advance. Under the optimum experiments condition (0.04 moll(-1) NH(3)-NH(4)Cl buffer solution, pH 9.0), the linear range was 4x10(-8) to 1xl0(-6) moll(-1) Mn(II) for linear sweep voltammetry and 1x10(-9) to 4x10(-8) moll(-1) Mn(II) for convolution voltammetry. The relative standard deviation for 2x10(-8) moll(-1) Mn(II) is 3.4%. The proposed method is simple, rapid, sensitive and selective. It had been applied to the determination of trace manganese in samples with satisfactory results.
本文描述了采用线性扫描伏安法在预处理玻碳电极上测定痕量锰的方法。在0.1 moll(-1) NaOH溶液中通过电化学方法预处理的玻碳电极极大地提高了电极在测定锰(II)时的响应性能。通过预先沉积在电极上的氧化锰的自催化作用,克服了低锰浓度检测的障碍。在最佳实验条件(0.04 moll(-1) NH(3)-NH(4)Cl缓冲溶液,pH 9.0)下,线性扫描伏安法测定锰(II)的线性范围为4x10(-8)至1xl0(-6) moll(-1),卷积伏安法测定锰(II)的线性范围为1x10(-9)至4x10(-8) moll(-1)。2x10(-8) moll(-1) Mn(II)的相对标准偏差为3.4%。该方法简便、快速、灵敏且具有选择性。已应用于样品中痕量锰的测定,结果令人满意。