Determination of cadmium in coal using solid sampling graphite furnace high-resolution continuum source atomic absorption spectrometry

被引:45
作者
da Silva, AF
Borges, DLG
Lepri, FG
Welz, B [1 ]
Curtius, AJ
Heitmann, U
机构
[1] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil
[2] ISAS, Inst Analyt Sci, Dept Berlin, D-12489 Berlin, Germany
关键词
high-resolution continuum source atomic absorption spectrometry graphite furnace atomic absorption spectrometry; solid sampling; cadmium determination; coal analysis; iridium permanent modifier;
D O I
10.1007/s00216-005-3327-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This work describes the development of a method to determine cadmium in coal, in which iridium is used as a permanent chemical modifier and calibration is performed against aqueous standards by high-resolution continuum source atomic absorption spectrometry (HR-CS AAS). This new instrumental concept makes the whole spectral environment in the vicinity of the analytical line accessible, providing a lot more data than just the change in absorbance over time available from conventional instruments. The application of Ir (400 mu g) as a permanent chemical modifier, thermally deposited on the pyrolytic graphite platform surface, allowed pyrolysis temperatures of 700 degrees C to be used, which was sufficiently high to significantly reduce the continuous background that occurred before the analyte signal at pyrolysis temperatures < 700 degrees C. Structured background absorption also occurred after the analyte signal when atomization temperatures of > 1600 degrees C were used, which arose from the electron-excitation spectrum (with rotational fine structure) of a diatomic molecule. Under optimized conditions (pyrolysis at 700 degrees C and atomization at 1500 degrees C), interference-free determination of cadmium in seven certified coal reference materials and two real samples was achieved by direct solid sampling and calibrating against aqueous standards, resulting in good agreement with the certified values (where available) at the 95% confidence level. A characteristic mass of 0.4 pg and a detection limit of 2 ng g(-1), calculated for a sample mass of 1.0 ing coal, was obtained. A precision (expressed as the relative standard deviation, RSD) of < 10% was typically obtained when coal samples in the mass range 0.6-1.2 mg were analyzed.
引用
收藏
页码:1835 / 1841
页数:7
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