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Solid-phase spectrophotometric determination of trace copper after collection as its bathocuproinedisulfonate chelate anion on chitin

机译:甲壳素上的铜联双磺酸二磺酸根螯合阴离子固相分光光度法测定痕量铜

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A collection method for anionic species on protonated chitin has been applied to the solid-phase spectrophotometric determination of trace copper. Copper is easily collect ed as its colored bathocuproinedisulfonate chelate anion on 20 mg of chitin from 20 cm~3 of aqueous solution at pH 5.0. The reflection absorbance of the chitin phase at 484 nm was measured directly. The calibration curve was linear in the concentration up to l μg of copper on 20 mg of chitin. The relative standard deviation was 2.89 for 0.5 μg of copper with 9 measurements. The tolerance limit for VO_3~- is 200-times in the concen- tration that of copper, and for Fe~(3+) and Al~(3+) it is 500- and 1000-times in the concentra tion of copper, respectively, when 5 mg of F-- is added. Common metal ions, reducing agents and inorganic anions do not interfere in the concentration range of l000- to l0000- times that of copper. The present method can be applied to the determination of copper in biological standard samples.
机译:质子化几丁质上阴离子物种的收集方法已应用于固相分光光度法测定痕量铜。铜很容易从20 cm〜3的pH 5.0水溶液中以20 mg几丁质上的有色卤化铜二磺酸盐螯合阴离子的形式收集。直接测量几丁质相在484 nm处的反射吸光度。在20 mg几丁质中,最高浓度为1μg的铜,校准曲线是线性的。 0.5克铜的9次测量的相对标准偏差为2.89。 VO_3〜-的极限浓度是铜的200倍,而Fe〜(3+)和Al〜(3+)的极限浓度是铜的500倍和1000倍,当添加5 mg F--时。常见的金属离子,还原剂和无机阴离子在铜浓度的1000至10000倍范围内不会产生干扰。本方法可用于生物标准样品中铜的测定。

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