【摘要】 采用浸涂流延法制得ＰＶＣ膜修饰碳微电极，用 Ｋ３ Ｆｅ（ＣＮ）６的循环伏安图考察了电 极的电化学性能，并用此电极建立了环境水样中痕量汞的阳极溶出伏安法测定。在０．０６ ｍｏｌ／Ｌ ＫＳＣＮ＋ ０．０１ ｍｏｌ／Ｌ ＫＣＩ介质中，富集电位－０．８０Ｖ，搅拌富集时间 ３００ｓ，扫描电压范围 －０．２０～０．４０Ｖ，扫描速率３１４ ｍＶ／ｓ，溶出峰电流与 Ｈｇ２＋浓度在 ０．０１～ ２．０ ｍｇ／Ｌ的范围内有 良好的线性关系，本电极成本低廉、制做简单、使用方便、性能稳定，工作电位范围宽、无汞污 染，是一种可用于阳级溶出伏安法的新型电极。更多还原

【Abstract】 By the flow-spreading over the carbon powder microelectrode with the tetrahydrofuran solution of 1.5% polyvinyl chloride (PVC) and 1% dioctylphthalate, a polyvinyl chloride film modified carbon microelectrode (PCFMCE) has been prepared. The cyclic voltammetry of PCFMCE in 10 mmol/L K3Fe(CN)6+1 mol/L KCI solution showed that the electrode process was semi-reversible, and the main process was diffusion controlled. An anodic stripping volammetry (ASV) technique by using PCFMCE for the determination of trace amounts of Hg2+ in water samples has been established. In a supporting electrolyte of 0.06 mol/L KSCN and 0.01 mol/L KCI, a sensitive oxidation wave of mercury was found by ASV. The peak potential was at + 0. 12(vs. SCE). Under the conditions of enriching potential - 0. 8 V, strirring time 300 s, scaning potential range - 0.20 - 0. 40 V and scan rate 314 mV/s, the linear relationship between the anodic stripping current and concentration for mercury existed over the range of 0.01 - 2.0 mg/L. The detection limit was 0.01 mg/L. This method has ho successfully applied to the direct determination of trace amounts of mercury in environmental waters. The novel microelectrode shows high stability and selectivity. The electrode is easy to make, and inexpensive.更多还原