科研之友
微信
新浪微博
Facebook
分享链接
摘要
High accuracy procedures for the determination of arsenic are needed for assigning reference values to certified reference materials (CRMs). There are a number of problems associated with the determination of total arsenic by inductively coupled plasma-mass spectrometry. Arsenobetaine (AsB) (the major species in fish) gives an enhanced response (9%) when compared to inorganic arsenic(V) and is very difficult to decompose. Chloride causes interference at m/z 75 by the formation of ArCl+ and chloride levels can be significant in marine fish. Also residual carbon in digests can lead to enhancement of arsenic signals by charge transfer effects. This can easily lead to erroneous quantification when compared to standards that do not contain carbon. This newly developed procedure overcomes these issues by complete mineralisation of the matrix leaving insignificant amounts of residual carbon and by removal of chlorine by evaporation. A detection limit of 30ng/g was achieved. Recoveries for the following CRMs: DORM 2 100.1 +/- 4.3%, SRM1548 96.1 +/- 4.6%, BCR 422 103.6 +/- 6.2% and SRM2976 105.9 +/- 6.2% were obtained. The digestion procedure uses open vessel wet digestion with a mixture of sulfuric and nitric acid held at 300 degrees C. The decomposition of AsB was confirmed by speciation analysis of the digest. Carbon (m/z 13) was monitored to demonstrate the efficiency of the digestion. Instrumentation for the reduction of ArCl+ interference was not required and this view is supported by the recovery data. Measurements were performed by external calibration using tellurium as an internal standard.
- 出版日期2006-4
