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四苯基硼酸铵-萘吸附剂用于合金和生物样品中铁的预富集及痕量测定,采用2-(5-溴-2-吡啶偶氮)-5-二乙氨基苯酚进行三阶导数分光光度法测定

Ammonium tetraphenylborate-naphthalene adsorbent for the preconcentration and trace determination of iron in alloys and biological samples using 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol by third derivative spectrophotometry.

作者信息

Ali Taher M, Krishan Puri B

出版信息

Talanta. 1996 Feb;43(2):247-53. doi: 10.1016/0039-9140(95)01759-3.

DOI:10.1016/0039-9140(95)01759-3
PMID:18966485
Abstract

A solid ion-pair material produced from ammonium tetraphenylborate on naphthalene (ATPB-naphthalene) provides a simple, rapid, economical and selective technique for preconcentrating iron from approximately 500 ml of aqueous solution of standard alloys and biological samples. Iron reacts with 2-(5-bromo-2-pryidlazo)-5-diethylaminophenol (5-Br-PADAP) to form a water-soluble cationic complex. When the aqueous solution of this cationic species in the pH range 3.2-8.5 is passed over the adsorbent ATPB-naphthalene at a flow rate of 1 ml min(-1), it is quantitatively retained on naphthalene as an uncharged ion-associated complex. The solid mass from the column was dissolved out with 5 ml of dimethylformamide (DMF) and iron is determined by third derivative spectrophotometry by measuring the signal d(3)A/ dlambda(3) between lambda(2)(773 nm) and lambda(3)(737 nm). The calibration curve is linear over the concentration range 0.10-25.0 mug of iron in 5 ml of DMF solution. Eight replicate determinations of 5 mug of iron gave a mean intensity (peak-to-peak signal between lambda(2) and lambda(3)) of 1.534 with a relative standard deviation of 0.90%. The sensitivity of the method is 0.307 (d(3)A/dnm(3) )/mug found from the slope of the calibration curve. The interference of a large number of anions and cations has been studied and the optimized conditions developed were utilized for the trace determination of iron in various standard alloys and biological samples.

摘要

由萘四苯基硼酸铵制备的固体离子对材料(ATPB-萘)为从约500毫升标准合金和生物样品的水溶液中预富集铁提供了一种简单、快速、经济且选择性高的技术。铁与2-(5-溴-2-吡啶偶氮)-5-二乙氨基苯酚(5-Br-PADAP)反应形成水溶性阳离子络合物。当该阳离子物种在pH值为3.2 - 8.5的水溶液以1毫升/分钟的流速通过吸附剂ATPB-萘时,它作为不带电荷的离子缔合络合物被定量保留在萘上。柱中的固体物质用5毫升二甲基甲酰胺(DMF)溶解,通过测量773纳米(λ₂)和737纳米(λ₃)之间的信号d³A/dλ³,用三阶导数分光光度法测定铁。校准曲线在5毫升DMF溶液中铁浓度为0.10 - 25.0微克的范围内呈线性。对5微克铁进行八次重复测定,得到的平均强度(λ₂和λ₃之间的峰-峰信号)为1.534,相对标准偏差为0.90%。该方法的灵敏度为0.307(d³A/dnm³)/微克,由校准曲线的斜率得出。研究了大量阴离子和阳离子的干扰情况,并将所建立的优化条件用于各种标准合金和生物样品中铁的痕量测定。

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