Sensitivity enhancement of inorganic arsenic analysis byin situmicroplasma preconcentration coupled with liquid chromatography atomic fluorescence spectrometry
文献类型: 外文期刊
作者: Yao, Zhenzhen 1 ; Liu, Meitong 1 ; Liu, Jixin 1 ; Mao, Xuefei 1 ; Na, Xing 4 ; Ma, Zhihong 2 ; Qian, Yongzhong 1 ;
作者机构: 1.Chinese Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Minist Agr & Rural Affairs, Key Lab Agrofood Safety & Qual, Beijing 100081, Peoples R China
2.Dept Agr, Beijing Res Ctr Agr Stand & Testing, Agr Prod Qual & Safety Risk Assessment Lab, Beijing 100097, Peoples R China
3.Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
4.Beijing Abil Technol Co Ltd, Beijing 100081, Peoples R China
期刊名称:JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY ( 影响因子:4.023; 五年影响因子:3.827 )
ISSN: 0267-9477
年卷期: 2020 年 35 卷 8 期
页码:
收录情况: SCI
摘要: In this work, anin situdielectric barrier discharge trap (DBDT) was first utilized to preconcentrate inorganic arsenic (iAs) species coupled with liquid chromatography hydride generation atomic fluorescence spectrometry (LC-HG-AFS), and a novel LC-HG-in situDBDT-AFS instrument was thereby fabricated. Considering the relatively deficient sensitivity of LC-HG-AFS and retention of As(v) in a strong anion exchange column, As(v) was chosen as a model species for iAs preconcentration. During the extraction of arsenic species in a rice sample using 1% (v/v) HNO(3)and 1% (v/v) H2O2, As(iii) was oxidized to As(v) being regarded as iAs. After LC separation, according to the retention time, only As(v) was trapped by 11 kV discharging under 110 mL min(-1)air mixed with Ar; following sweeping by Ar gas for 190 s, iAs was released with 13 kV at 180 mL min(-1)H(2)-rich Ar to the AFS for measurement.Viapreconcentration, the limit of detection (LOD) of iAs reached 0.05 mu g L(-1)with similar to 10 times enhancement in analytical sensitivity; the linearity (r) was > 0.997 ranging from 0.5 mu g L(-1)to 50 mu g L(-1)with 1.9% RSD (5 mu g L-1,n= 6). The measured iAs in certified reference materials (CRMs) were all within their certified values, and the spike recoveries were in the range of 93-102%. With sensitivity, robustness, low power, small size and easy operation, the combination of LC and DBDT fulfilled the analysis of trace iAs in rice samples. In fact, other arsenic species can also be preconcentrated and detected to enhance the sensitivity by this proposed LC-HG-in situDBDT techniqueviaprecisely synchronizing DBD trap and release with chromatographic retention. To focus on the food safety, iAs was chosen as a model arsenic species to verify the availability ofin situDBDT. Considering the versatility of DBD,in situDBDT demonstrates a promising application for elemental speciation analysis and LC atomic spectrometry.
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