固相萃取掺氧空气-乙炔火焰原子吸收光谱法测定水和植物样品中的痕量镓  

Determination of Trace Ga in Water and Plant Samples by O2-doped Air-Acetylene FAAS with Solid Phase Extraction Preconcentration

作　　者：叶陆芳 宋小华 余代顺 杨小慢 谢文根 吴少尉 YE Lu-fang;SONG Xiao-hua;YU Dai-shun;YANG Xiao-man;XIE Wen-gen;WU Shao-wei(College of Chemistry and Environmental Engineering,Hubei University for Nationalities,Enshi 445000,China)

机构地区：[1]湖北民族大学化学与环境工程学院

出　　处：《岩矿测试》2020年第2期243-250,共8页Rock and Mineral Analysis

基　　金：国家自然科学基金项目(21565013);大学生创新创业训练项目

摘　　要：目前研究萃取分离富集镓大多偏向在强酸性体系中,一定程度上给操作带来安全风险,另需耐酸器皿设备,易污染,空白背景值高。本文开发了一种在弱酸性条件下萃取分离富集痕量镓的方法。以大孔吸附树脂为载体,十六烷基三甲基溴化铵调节其表面极性,热固化负载2-乙基己基磷酸(2-乙基己基)酯,制备了镓的萃取树脂。动态考察了固相萃取镓的吸附容量,优化选择固相萃取分离富集条件,实验表明萃取条件温和,分离富集痕量镓效果理想。当溶液酸度为pH 2.5时,Ga(Ⅲ)达到最大的回收率99%,并确定了掺氧空气乙炔火焰原子吸收光谱法(FAAS)测定镓的最佳参数,提升了常规空气乙炔FAAS测定镓的灵敏度。方法检出限(3σ)为2.6ng/mL,相对标准偏差(RSD,n=7)为2.87%,加标回收率在95.7%~102.0%之间,理论富集倍数为40。本方法已应用于自来水、中药材和水培蔬菜样品中痕量镓的测定,简便、快速、可靠。BACKGROUND:At present,research on the extraction separation and enrichment of gallium is mostly biased to the strong acidic system,which brings a safety risk to the operation and needs acid-proof apparatus.Furthermore,the procedure is easily contaminated,resulting in high background values.OBJECTIVES:To develop a method for extraction separation and preconcentration of trace Ga under weakly acidic condition.METHODS:Solid phase extraction medium for Ga was prepared by using modified large porous adsorption resin with cetyl-trimethyl-ammonium bromide and loading it with 2-ethylhexyl phosphonic acid-2-ethylhexyleste.The separation and enrichment conditions of solid phase extraction were studied in detail.RESULTS:Experiments showed that the separation and enrichment of trace gallium was ideal when the extraction conditions were mild.The maximum recovery(99%)of Ga was achieved in sample solution with pH of 2.5.The determination parameters of gallium were optimized for oxygen doped air-acetylene flame atomic absorption spectrometry(FAAS),and the sensitivity was improved on that of the current method.The detection limit of the overall method(3σ)was 2.6ng/mL by IUPAC definition and the relative standard deviation(RSD,n=7)was 2.87%.The recoveries for spiked solution ranged from 95.7%to 102.0%,and a theory enrichment factor of 40 was obtained.CONCLUSIONS:This method has been successfully applied to the determination of trace gallium in tap water,Chinese medicine and hydroponic vegetable samples.It is simple,quick and reliable.

关 键 词：水 植物 镓 固相萃取 掺氧空气乙炔火焰 原子吸收光谱法 

分 类 号：O657.31[理学—分析化学]