Determination of silicon and aluminum in silicon carbide nanocrystals by high-resolution continuum source graphite furnace atomic absorption spectrometry

被引:23
作者
Dravecz, Gabriella [1 ]
Bencs, Laszlo [1 ]
Beke, David [1 ,2 ]
Gali, Adam [1 ,3 ]
机构
[1] Hungarian Acad Sci, Wigner Res Ctr Phys, Inst Solid State Phys & Opt, H-1525 Budapest, Hungary
[2] Budapest Univ Technol & Econ, Fac Chem Technol & Biotechnol, H-1111 Budapest, Hungary
[3] Budapest Univ Technol & Econ, Dept Atom Phys, H-1111 Budapest, Hungary
基金
匈牙利科学研究基金会;
关键词
Electrothermal atomic absorption spectrometry; Nanomaterials; Refractory elements; Chemical modification; Atomization mechanism; PLASMA-MASS SPECTROMETRY; EMISSION-SPECTROMETRY; DRINKING-WATER; TRACE-ELEMENTS; SAMPLES; URINE; AAS; PALLADIUM; CHROMIUM; NICKEL;
D O I
10.1016/j.talanta.2015.09.067
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The determination of Al contaminant and the main component Si in silicon carbide (SiC) nanocrystals with the size-distribution of 1-8 nm dispersed in an aqueous solution was developed using high-resolution continuum source graphite furnace atomic absorption spectrometry (HR-CS-GFAAS). The vaporization/atomization processes were investigated in a transversally heated graphite atomizer by evaporating solution samples of Al and Si preserved in various media (HCl, HNO3). For Si, the best results were obtained by applying a mixture of 5 mu g Pd plus 5 mu g Mg, whereas for Al, 10 mu g Mg (each as nitrate solution) was dispensed with the samples, but the results obtained without modifier were found to be better. This way a maximum pyrolysis temperature of 1200 degrees C for Si and 1300 degrees C for Al could be used, and the optimum (compromise) atomization temperature was 2400 degrees C for both analytes. The Si and Al contents of different sized SiC nanocrystals, dispersed in aqueous solutions, were determined against aqueous (external) calibration standards. The correlation coefficients (R values) of the calibrations were found to be 0.9963 for Si and 0.9991 for Al. The upper limit of the linear calibration range was 2 mg/l Si and 0.25 mg/l Al. The limit of detection was 3 mu g/l for Si and 0.5 mu g/l for Al. The characteristic mass (m(0)) was calculated to be 389 pg Si and 6.4 pg Al. The Si and Al content in the solution samples were found to be in the range of 1.0-1.7 mg/l and 0.1-0.25 mg/l, respectively. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:271 / 275
页数:5
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