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作 者:肖健林[1] 刘建允[1] 张鑫[1] 廖金金[1]
机构地区:[1]东华大学环境科学与工程学院,上海201620
出 处:《分析科学学报》2014年第1期35-38,共4页Journal of Analytical Science
基 金:国家自然科学基金(No.21105009);电分析化学国家重点实验室开放课题(No.SKLEAC201205)
摘 要:采用3-巯丙基三甲氧基硅烷(MPTS)为单一硅源合成有机硅纳米材料,将其组装到金电极表面,制备MPTS薄膜修饰电极。采用原子力显微镜和透射电镜表征有机硅纳米,粒径为3.3~5.7nm;采用方波溶出伏安法测定该修饰电极对汞的响应信号。结果表明,该修饰电极对痕量汞有高灵敏响应。在0.1mol/LHCl中,于-0.4V电位下富集10min,溶出峰电流与其浓度在1.5×10-12~75.0×10-12mol/L范围内呈线性关系,相关系数为0.9980,检出限为5.0×10-13mol/L。该方法用于实际水样中汞的测定,与原子荧光光谱法进行比较,结果基本一致。The organosilica nanomaterial was synthesized using (3-mercaptopropyl)-trimethoxysilane (MPTS) as a single silica source and the MPTS modified Au electrode was obtained by self-assembling. The organosilica particle size was about 3.3-5. 7 nm as measured by transmission electron microscope (TEM) and atomic force microscope(AFM). Mercury( Ⅱ ) stripping peak signal was investigated by square wave stripping voltammetry (SWV). The results showed that the modified electrode had a sensitive response to trace mercury (Ⅱ). Under the optimal experimental conditions, the linear relationship between peak current and mercury( Ⅱ ) concentration was achieved in range of 1.5 ×10-12 - 75.0 × 10-12 mol/L with 10 min preconcentration at - 0. 4 V in the 0. 1 mol/L hydrochloric acid solution. The detection limit was 5.0 × 10-13 mol/L. The prepared sensor was successfully applied for the determination of mercury( Ⅱ) in tap water and lake water, and the results were consistent with those obtained by atomic fluorescence spectrometry(AFS).
关 键 词:3-巯丙基三甲氧基硅烷 方波溶出伏安法 汞
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