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Determination of Selenium (IV) by Stripping Voltammetry at a Mercury-Film Electrode

机译:汞膜电极上溶出伏安法测定硒(IV)

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摘要

A procedure was proposed for the determination of selenium (IV) by stripping voltammetry on a mercury-film electrode at an electrolysis potential of + 0.4V versus the saturated silver-silver chloride reference electrode in a 1 M H_2SO_4 solution. The current of the cathodic peak is a linear function of the selenium (IV) concentration in the range from 5 * 10~(-3) to 3 * 10~(-1) mg/L (6.3 * 10~(-8) to 3.8 * 10~(-6)M) at a time of electrolysis of 30 s (tel). The detection limit for selenium is 1 * 10~(-4) mg/L (1.3 * 10~(-9)M) at tel = 300 s. It was shown that selenium (IV) can be determined in the presence of 10 mg/L Zn (II), 1 mg/L Cd (II), 0.5 mg/L Pb (II), and 0.2 mg/L Cu (II). A procedure for the determination of selenium in natural, mineral ,and potable water was proposed.
机译:提出了一种在1 M H_2SO_4溶液中,相对于饱和的银-氯化银参比电极,在+ 0.4V的电解电位下,通过汞膜电极上的溶出伏安法测定硒(IV)的方法。阴极峰电流是硒(IV)浓度在5 * 10〜(-3)至3 * 10〜(-1)mg / L(6.3 * 10〜(-8)电解30 s(tel)时达到3.8 * 10〜(-6)M)。在tel = 300 s时,硒的检出限为1 * 10〜(-4)mg / L(1.3 * 10〜(-9)M)。结果表明,在10 mg / L Zn(II),1 mg / L Cd(II),0.5 mg / L Pb(II)和0.2 mg / L Cu(II )。提出了一种测定天然,矿物质和饮用水中硒的方法。

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