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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Headspace single-drop microextraction and cuvetteless microspectrophotometry for the selective determination of free and total cyanide involving reaction with ninhydrin
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Headspace single-drop microextraction and cuvetteless microspectrophotometry for the selective determination of free and total cyanide involving reaction with ninhydrin

机译:顶空单滴微萃取和无比色皿分光光度法选择性测定涉及茚三酮反应的游离氰和总氰

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摘要

Headspace single-drop microextraction has been used for the determination of cyanide with ninhydrin in combination with fibre-optic-based cuvetteless microspectrophotometry which accommodates sample volume of 1 μL placed between the two ends of optical fibres, and has been found to avoid salient drawbacks of batch methods. This method involved hydrocyanic acid formation in a closed vial, and simultaneous extraction and reaction with 2 μL drop of ninhydrin in carbonate medium suspended at the tip of a microsyringe needle held in the headspace of the acidified sample solution. The method was linear in range 0.025-0.5 mg L~(-1) of cyanide. The headspace reaction was free from the interference of substances, e.g., thiocyanate, hydrazine sulphate, hydroxylammonium chloride and ascorbic acid. Sulphide was masked by cadmium sulphate, nitrite by sulphamic acid, sulphite by N-ethylmaleimide, and halogens by ascorbic acid. The limit of detection was found to be 4.3 μg L ~(-1) of cyanide which was comparable to existing most sensitive methods for cyanide. However, the present method is far more simple. The method was applied to acid-labile and metal cyanides complexes by treatment with sulphide when metal sulphides were precipitated setting cyanide ion free, and to iron(II) and (III) cyanide complexes by their decomposition with mercury(II), the mercury(II) cyanide formed was then determined. These pre-treatment methods avoided cumbersome pre-separation of cyanide by methods such as distillation or gas diffusion. The overall recovery of cyanide in diverse samples was 97% with RSD of 3.9%.
机译:顶空单滴微萃取已与茚三酮结合使用,基于光纤的无比色管微分光光度法用于测定氰化物,该分光光度法可容纳位于光纤两端之间的1μL样品量,并发现避免了显着的缺点批处理方法。该方法包括在一个封闭的小瓶中形成氢氰酸,并同时萃取并与2μL茚三酮在悬浮在酸化样品溶液顶部空间中的微型注射器针尖上悬浮的碳酸盐培养基中反应。该方法在0.025-0.5 mg L〜(-1)氰化物范围内是线性的。顶空反应不受物质的干扰,例如硫氰酸盐,硫酸肼,氯化羟铵和抗坏血酸。硫化物被硫酸镉掩盖,亚硝酸被氨基磺酸掩盖,亚硫酸盐被N-乙基马来酰亚胺掩盖,卤素被抗坏血酸掩盖。发现检出限为4.3μgL〜(-1)的氰化物,与现有的最敏感的氰化物方法相当。但是,本方法要简单得多。该方法适用于酸不稳定的金属氰化物配合物,当金属硫化物沉淀而无氰化物离子沉淀时,通过硫化物处理,并通过与汞(II),汞(分解)的分解作用应用于铁(II)和(III)氰化物配合物。 II)然后确定形成的氰化物。这些预处理方法避免了通过蒸馏或气体扩散等方法进行的氰化物繁琐的预分离。各种样品中氰化物的总回收率为97%,RSD为3.9%。

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