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Determination of dissolved manganese(II) in coastal and estuarine waters by differential pulse cathodic stripping voltammetry

机译:差分脉冲阴极溶出伏安法测定沿海和河口水中的溶解态锰

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摘要

A method for the determination of dissolved manganese(II) in seawater utilizing cathodic stripping voltammetry on a rotating glassy carbon disk electrode is presented which is suitable for coastal and estuarine waters. The technique was accurate to within 2% in measuring manganese concentrations in CASS-3 Nearshore Seawater Reference Material, and manganese values determined on Narragansett Bay samples by this technique and by graphite furnace atomic absorption spectroscopy were in close agreement. Analytical conditions involve an oxidative deposition at a potential of +0.75 V and a pH of 8.5, followed by cathodic stripping in the differential pulse mode with a pulse modulation amplitude of 100 mV and a scan rate of 20 mV s(-1). The sensitivity is 11 nA nM(-1) min(-1), and the detection limit 6 nM. This technique can be used to examine organic complexation of manganese, as it measures kinetically labile inorganic species, while Mn-organic chelates such as MnEDTA(2-) are inert. A preliminary examination of South San Francisco Bay water, however, found no evidence of organic complexation of manganese.
机译:提出了一种在旋转玻璃碳盘电极上利用阴极溶出伏安法测定海水中锰的方法,该方法适用于沿海和河口水域。该技术在测量CASS-3近岸海水参考材料中的锰浓度时精确到2%以内,并且通过该技术和石墨炉原子吸收光谱法在Narragansett湾样品上测定的锰值非常一致。分析条件包括在+0.75 V的电势和pH值为8.5的氧化沉积,然后在差分脉冲模式下以100 mV的脉冲调制幅度和20 mV s(-1)的扫描速率进行阴极剥离。灵敏度为11 nA nM(-1)min(-1),检测极限为6 nM。该技术可用于检测锰的有机络合物,因为它可测量动力学不稳定的无机物,而Mn-有机螯合物(如MnEDTA(2-))是惰性的。然而,对南旧金山湾水的初步检查没有发现锰有机络合的证据。

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