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Low cost adsorbents in ultrasound-assisted dispersive micro solid-phase extraction for simultaneous determination of indium and nickel by high-resolution continuum source graphite furnace atomic absorption spectrometry in soils and sediments

机译:超声辅助分散微相萃取中的低成本吸附剂,通过高分辨率连续源石墨炉原子吸收光谱法同时测定土壤和沉积物中的铟和镍

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摘要

As a sample preparation step, ultrasound-assisted dispersive micro solid-phase extraction (USA DMSPE) with low cost materials as an adsorbent is presented. The extraction capabilities of eight low cost materials were investigated. The best results were obtained for bentonite clay. The use of high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS GF AAS) for simultaneous determination of two elements after extraction was developed. The primary absorption line at 303.935 nm was used for the determination of indium, and an adjacent secondary line at 303.793 nm for nickel. Both absorption lines were within the wavelength interval covered by the linear chargecoupled device (CCD) array detector. Some essential parameters of the extraction technique such as the amount of adsorbent, pH of sample solution, ultrasonication and centrifugation time, and slurry solution preparation before injection to HR-CS GF AAS as well as main parameters of spectrometer were studied. Detection limits of 0.01 mg L-1 and 0.26 mg L-1 were found for In and Ni, respectively. The precision, expressed as the relative standard deviation during real sample analysis, ranged from 2 to 11%. To investigate the accuracy of the developed method, digested CRMs (soils and sediments) were evaluated with a recovery between 90% and 117% for both analytes. The values found for Ni and In (after spiking) were not significantly different from those of the certified or added ones. The presented method was applied to extraction and the simultaneous determination of trace amounts of In and Ni in soil and lake sediment samples.
机译:作为样品制备步骤,提出了作为吸附剂的低成本材料的超声辅助分散微相萃取(USA DMSPE)。研究了八种低成本材料的提取能力。为膨润土粘土获得了最佳结果。利用高分辨率连续源石墨炉原子吸收光谱法(HR-CS GF AAS)以在开发萃取后同时测定两种元素。 303.935nm的主要吸收线用于测定铟,镍铟,镍含量为303.793nm。两个吸收线在线性充电装置(CCD)阵列检测器覆盖的波长间隔内。研究了提取技术的一些基本参数,如吸附剂,样品溶液的pH值,超声波和离心时间,以及注射HR-CS GF AAS之前的浆料溶液制备以及光谱仪的主要参数。发现0.01mg L-1和0.26mg L-1的检测限为In和Ni。在真实样本分析期间表达为相对标准偏差的精度,范围为2〜11%。为了研究显影方法的准确性,评估消化的CRMS(土壤和沉积物),其分析物的回收率为90%至117%。为NI和(尖峰后)发现的值与认证或添加的值没有显着不同。呈现的方法应用于萃取和同时测定土壤和湖泊沉积物样品中的痕量和Ni。

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