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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Simultaneous determination of zirconium and hafnium as ternary complexes with 5-Br-PADAP and fluoride using solid-phase extraction and reversed-phase liquid chromatography
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Simultaneous determination of zirconium and hafnium as ternary complexes with 5-Br-PADAP and fluoride using solid-phase extraction and reversed-phase liquid chromatography

机译:固相萃取-反相液相色谱法同时测定5-Br-PADAP和氟化物三元络合物中的锆和ha

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摘要

Solid-phase extraction (SPE) along with reversed-phase liquid chromatography (RP-LC) was used for the simultaneous determination of Zr(IV) and Hf(IV) by means of their ternary chelates with fluoride and 2-(4-bromo-2-pyridylazo)-5-diethylaminophenol (5-Br-PADAP). The conditions of SPE sorption were examined in detail: type of SPE column, volume of the sample, volume of the eluent, concentrations of metal ions, fluoride salt, chromogenic reagent, organic phase, and pH. It was established that the sorption of Zr(IV) and Hf(IV), as their ternary chelates, on SPE Zorbax SPE C18 (EC) cartridge was the most efficient, when the sample containing metal ion (Zr(IV), Hf(IV), both, up to 2 μg), 5-Br-PADAP 1.5 * 10~(-4), NaF 7.5 * 10~(-5) mol l~(-1), methanol 40%, pH 4.5 ± 1 was applied for the SPE sorption. The chelates were discarded from SPE cartridge using acetonitrile/water (99.75 + 0.25, v/v) eluent containing 3.8 * 10~(-4) mol l~(-1) sodium fluoride and subsequently separated by RP-LC method. The RP-LC separation of both chelates was optimized and Zorbax SB-C18 analytical LC column along with acetonitrile/water (65 + 35, v/v) eluent containing the 1.5 * 10~(-4) mol l~(-1) sodium fluoride was used. The established SPE/LC conditions allow Zr(IV) 0.08-2.0 μg and Hf(IV) 0.04-2.0 μg determination in a sample volume up to 150 ml. The detection limits, 0.03 μg Hf(IV) and 0.05 μg Zr(IV), were obtained. Recoveries, (94 ± 2)% for Hf(IV) chelate and (106 ± 2)% for Zr(IV) chelate were obtained, when 1 μg of Zr(IV) and Hf(IV) ions were determined by the present SPE/LC method from the sample volume of 100 ml. The established, pre-concentration SPE conditions, along with the LC separation and determination allow the assay of Zr(IV) and Hf(IV) in complicated matrix materials. The present SPE/LC method was applied to the determination of Zr(IV) and Hf(IV) in tap water and reference geological material (rock, NCS DC 73303; certified content: Zr, 27.7 * 10~(-3)% (w/w) and Hf, 6.5 * 10~(-4)% (w/w)).
机译:固相萃取(SPE)和反相液相色谱(RP-LC)用于同时测定Zr(IV)和Hf(IV)的方法是与氟和2-(4-溴)形成三元螯合物-2-吡啶基偶氮)-5-二乙基氨基苯酚(5-Br-PADAP)。详细检查了SPE的吸附条件:SPE柱的类型,样品的体积,洗脱液的体积,金属离子的浓度,氟化物盐,生色剂,有机相和pH。已确定,当样品中含有金属离子(Zr(IV),Hf(时)时,Zr(IV)和Hf(IV)作为三元螯合物在SPE Zorbax SPE C18(EC)柱上的吸附效率最高。 IV),最多2μg),5-Br-PADAP 1.5 * 10〜(-4),NaF 7.5 * 10〜(-5)mol l〜(-1),甲醇40%,pH 4.5±1将其用于SPE吸附。使用含有3.8 * 10〜(-4)mol l〜(-1)氟化钠的乙腈/水(99.75 + 0.25,v / v)洗脱液将螯合物从SPE柱中丢弃,然后通过RP-LC方法分离。优化了两种螯合物的RP-LC分离,并使用Zorbax SB-C18分析型LC色谱柱以及含1.5 * 10〜(-4)mol l〜(-1)的乙腈/水(65 + 35,v / v)洗脱液使用氟化钠。已建立的SPE / LC条件允许在最大150 ml的样品中测定Zr(IV)0.08-2.0μg和Hf(IV)0.04-2.0μg。检出限为0.03μgHf(IV)和0.05μgZr(IV)。当通过本SPE测定1μgZr(IV)和Hf(IV)离子时,回收率达到Hf(IV)螯合物的(94±2)%和Zr(IV)螯合物的(106±2)% / LC法从样品量为100毫升。既定的预浓缩SPE条件,以及LC分离和测定,可用于分析复杂基质材料中的Zr(IV)和Hf(IV)。本SPE / LC方法用于自来水和参考地质材料中的Zr(IV)和Hf(IV)的测定(岩石,NCS DC 73303;认证含量:Zr,27.7 * 10〜(-3)%( w / w)和Hf,6.5 * 10〜(-4)%(w / w))。

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