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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:高分辨率连续流源石墨炉原子吸收光谱法在超声辅助分散微固相萃取中同时测定铟和镍中的低成本吸附剂

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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 charge-coupled 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,提出了以低成本材料为吸附剂的超声辅助分散微固相萃取(USA DMSPE)。研究了八种低成本材料的提取能力。膨润土获得了最佳结果。开发了高分辨率连续谱源石墨炉原子吸收光谱法(HR-CS GF AAS),用于同时测定萃取后的两种元素。 303.935 nm处的主要吸收线用于测定铟,镍303.793 nm处的相邻辅助线用于测定镍。两条吸收线都在线性电荷耦合器件(CCD)阵列检测器覆盖的波长范围内。研究了萃取技术的一些基本参数,例如吸附剂的量,样品溶液的pH值,超声和离心时间,注入HR-CS GF AAS之前的浆液制备以及光谱仪的主要参数。 In和Ni的检出限分别为0.01 mg L?1和0.26 mg L?1。精度表示为实际样品分析期间的相对标准偏差,范围为2%至11%。为了研究开发方法的准确性,评估了消化的CRM(土壤和沉积物)的回收率,两种分析物的回收率在90%至117%之间。 Ni和In(加标后)的值与认证或添加的值没有显着差异。该方法用于土壤和湖泊沉积物中样品中痕量In和Ni的提取和同时测定。

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