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Rapid Determination of Picomolar Titanium in Seawater with Catalytic Cathodic Stripping Voltammetry

机译:催化阴极溶出伏安法快速测定海水中的痕量钛

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Titanium (Ti) is present as a trace element in seawater at extremely low concentrations (5-350 pM, where 1 pM velence 10~(-12) mol L~(-1)) throughout the water column. Presently, little is known about the marine biogeochemistry of Ti and there is a distinct lack of oceanic measurements of Ti, because of the combined difficulties of trace-metal clean sampling for an element at such low levels and the lack of a suitable shipboard method of analysis. Here, a new cathodic stripping voltammetry procedure is presented for the rapid determination of Ti at pM concentrations in seawater that is capable of being used directly at sea. This method utilizes the catalytic enhancement of the reduction of the complex formed between Cupferron (N-nitrosophenylhydroxylamine) and Ti(IV). While Cupferron itself acts as both a complexing agent and an oxidizing agent, it was found that the optimal sensitivity was with bromate as an auxiliary oxidant. An advantage of this method is that it is useable over the pH range of 5.5-8. Under the conditions employed in this work, detection limits ranged from 5 pM to 12 pM. This new catalytic method is significantly more sensitive than existing methods and has been extensively tested at sea in the Atlantic and Southern Oceans.
机译:钛(Ti)在海水中以极低的浓度(5-350 pM,其中1 pM的10〜(-12)mol L〜(-1)浓度)作为海水中的微量元素存在。目前,关于钛的海洋生物地球化学知之甚少,而且由于缺乏如此低含量的元素进行痕量金属清洁取样的综合困难,以及缺乏合适的船载方法,钛的海洋测量数据明显缺乏。分析。在此,提出了一种新的阴极溶出伏安法,可快速测定海水中pM浓度的Ti,该钛能够直接在海上使用。该方法利用催化增强作用来还原铜铁(N-亚硝基苯基羟胺)与Ti(IV)之间形成的络合物。虽然Cupferron本身既充当络合剂又充当氧化剂,但发现最佳灵敏度是使用溴酸盐作为辅助氧化剂。该方法的优点是可在5.5-8的pH范围内使用。在这项工作中采用的条件下,检测限范围为5 pM至12 pM。这种新的催化方法比现有方法灵敏得多,并且已经在大西洋和南大洋的海上进行了广泛测试。

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