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首页> 外文期刊>Journal of AOAC International >Simultaneous determination of nickel and copper by H-point standard addition method-first-order derivative spectrophotometry in plant samples after separation and preconcentration on modified natural clinoptilolite as a new sorbent
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Simultaneous determination of nickel and copper by H-point standard addition method-first-order derivative spectrophotometry in plant samples after separation and preconcentration on modified natural clinoptilolite as a new sorbent

机译:改进的天然斜发沸石作为新吸附剂分离和预富集后,通过H点标准添加方法-一阶导数分光光度法同时测定植物样品中的镍和铜

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摘要

For the simultaneous determination of nickel(II) and copper(II) in plant samples, a rapid and accurate method was developed. In this method, solid-phase extraction (SPE) and first-order derivative spectrophotometry (FDS) are combined, and the result is coupled with the H-point standard addition method (HPSAM). Compared with normal spectrophotometry, derivative spectrophotometry offers the advantages of increased selectivity and sensitivity. As there is no need for carrying out any pretreatment of the sample, the spectrophotometry method is easy, but because of a high detection limit, it is not so practical. In order to decrease the detection limit, it is suggested to combine spectrophotometry with a preconcentration method such as SPE. In the present work, after separation and preconcentration of Ni(II) and Cu(II) on modified clinoptilolite zeolite that is loaded with 2-[1-(2-hydroxy-5-sulforphenyl)-3-phenyl-5-formaza-no]-benzoic acid monosodium salt (zincon) as a selective chromogenic reagent, FDS-HPSAM, which is a simple and selective spectrophotometric method, has been applied for simultaneous determination of these ions. With optimum conditions, the detection limit in original solutions is 0.7 and 0.5 ng/mL, respectively, for nickel and copper. The linear concentration ranges in the proposed method for nickel and copper ions in original solutions are 1.1 to 3.0 x 10(3) and 0.9 to 2.0 X 10(3) ng/mL, respectively. The recommended procedure is applied to successful determination of Cu(II) and Ni(II) in standard and real samples.
机译:为了同时测定植物样品中的镍(II)和铜(II),开发了一种快速而准确的方法。该方法将固相萃取(SPE)和一阶导数分光光度法(FDS)相结合,并将结果与​​H点标准添加法(HPSAM)耦合。与常规分光光度法相比,导数分光光度法具有提高选择性和灵敏度的优势。由于不需要对样品进行任何预处理,因此分光光度法很容易,但是由于检测限高,因此不太实用。为了降低检测限,建议将分光光度法与预浓缩方法(例如SPE)结合使用。在目前的工作中,在负载有2- [1-(2-羟基-5-磺基苯基)-3-苯基-5-甲酰胺-的改性斜发沸石上分离和预富集Ni(II)和Cu(II)。作为选择性显色试剂的No]-苯甲酸单钠盐(zincon),FDS-HPSAM是一种简单且选择性的分光光度法,已用于同时测定这些离子。在最佳条件下,原始溶液中镍和铜的检出限分别为0.7和0.5 ng / mL。对于原溶液中的镍和铜离子,建议的方法中的线性浓度范围分别为1.1至3.0 x 10(3)ng和0.9至2.0 X 10(3)ng / mL。推荐的方法适用于成功测定标准样品和实际样品中的Cu(II)和Ni(II)。

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