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机构地区:[1]北京师范大学化学系
出 处:《分析科学学报》1995年第4期24-27,共4页Journal of Analytical Science
基 金:国家自然科学基金
摘 要:在HAC-NaAC底液中,卡可西灵在汞电极上有两个还原峰,第一峰峰电位Epct=0.04V(vs.Ag/AgCl),为2电子转移的可逆过程;第二峰峰电位Epc2=0.39v,为4电子转移的不可逆过程。第二峰具有明显的吸附性。本文探讨了该峰的吸附特性,认为吸附型体为中性分子,属于不可逆吸附体系。测得其电极反应动力学参数αnα和卡可西灵在汞电极上的饱和吸附量,估计了每个卡可西灵分子所占的面积。建立了测定卡可西灵的吸附伏安法。in a supporting electrolyte of HAc-NaAc, cyclic voltammetry of cacotheline showed two cathodic pobs at Hg electrode. The peak potentials of them were 0. 04V and-0. 39V(vs.AS/AgCl),respectively.The first Peak .represents a reversible process involving 2 electrons,while,the second is an irreversible process inchuding 4 elections. The second peak showed obvious adsorptive properties, which was discussed in detail in this paper. The adsorbed species was bly neutral cacotheline molecule. Under the conditions Of longer preconcentration time, smaller cacotheline concentration and faster scan rate, the reduedon of cacotheline We. almost toeflly controlled by adsotption. It this easel it belongs to the irrevendble adsorptive stystem. to value of an. and the saturated amount of cacotheline adsorbed on Hg surface were determined. The area occupied by each cacotheline molecule adsorbed was estimated. The method of determination of cacotheline by adsotptive stripping voltummetry was established.
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