STUDIES ON THE APPLICATION OF PLATFORM ATOMIZATION TO FURNACE ATOMIC NONTHERMAL EXCITATION SPECTROMETRY FOR THE SIMULTANEOUS MULTIELEMENT ANALYSIS OF ENVIRONMENTAL MATERIALS

被引:8
作者
BAXTER, DC [1 ]
NICHOL, R [1 ]
LITTLEJOHN, D [1 ]
LUDKE, C [1 ]
SKOLE, J [1 ]
HOFFMANN, E [1 ]
机构
[1] INST SPEKTROCHEM & ANGEW SPEKTROSKOPIE,SPEKTROSKOP METHODEN UMWELTANALYT LAB,W-1199 BERLIN,GERMANY
关键词
FURNACE ATOMIC NONTHERMAL EXCITATION SPECTROMETRY; PLATFORM ATOMIZATION; MULTIELEMENT ANALYSIS; INTERFERENCE; ENVIRONMENTAL SAMPLE;
D O I
10.1039/ja9920700727
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Response surface methodology was used to optimize the discharge current and pressure with respect to detection limits for the simultaneous multi-element determination of Al, Cd, Cr, Cu, Fe, Ni and Pb by furnace atomic non-thermal excitation spectrometry (FANES). Comparison of wall and platform atomization showed improved detection limits for most elements with the latter. Despite the use of automatic background correction by wavelength modulation, residual background signals were observed at all lines, those on the Cd, Cu, Fe and Pb channels being rectified by including an 'autozero' procedure in the data processing software. For the remaining elements, spectral interferences disrupted the baseline during the atomization step, although blank subtraction provided satisfactory correction. Nevertheless, the presence of structured background emission poses a potentially serious source of error in FANES measurements. In the multi-element analysis of microwave-assisted digests of three environmental reference materials [National Institute of Standards and Technology (NIST) Standard Reference Material (SRM) 1572 Citrus Leaves, SRM 1575 Pine Needles and SRM 1645 River Sediment] by platform-equipped FANES, non-spectral interferences arose for all analytes except Cd and Pb. The use of the standard additions method was thus necessary for calibration purposes.
引用
收藏
页码:727 / 734
页数:8
相关论文
共 35 条
[21]   MICROWAVE DIGESTION TECHNIQUES IN THE SEQUENTIAL EXTRACTION OF CALCIUM, IRON, CHROMIUM, MANGANESE, LEAD, AND ZINC IN SEDIMENTS [J].
MAHAN, KI ;
FODERARO, TA ;
GARZA, TL ;
MARTINEZ, RM ;
MARONEY, GA ;
TRIVISONNO, MR ;
WILLGING, EM .
ANALYTICAL CHEMISTRY, 1987, 59 (07) :938-945
[22]  
MARSHALL J, 1983, ANALYST, V108, P178, DOI 10.1039/an9830800178
[24]   APPLICATIONS OF MICROWAVE-OVEN SAMPLE DISSOLUTION IN ANALYSIS [J].
NADKARNI, RA .
ANALYTICAL CHEMISTRY, 1984, 56 (12) :2233-2237
[25]   MULTIVARIATE OPTIMIZATION OF SIMULTANEOUS MULTI-ELEMENT ANALYSIS BY FURNACE ATOMIC NON-THERMAL EXCITATION SPECTROMETRY (FANES) [J].
NAUMANN, B ;
KNULL, B ;
KERSTAN, F ;
OPFERMANN, J .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1988, 3 (08) :1121-1126
[26]  
NICHOL R, 1990, 5TH BIENN NAT AT SPE
[28]   DATA-ANALYSIS OF HEAVY-METAL POLLUTION IN THE SEA BY USING PRINCIPAL COMPONENT ANALYSIS AND PARTIAL LEAST-SQUARES REGRESSION [J].
PIEPPONEN, S ;
LINDSTROM, R .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 1989, 7 (1-2) :163-170
[29]   EMISSION CHARACTERISTICS OF CHROMIUM IN HOLLOW ANODE-FURNACE ATOMIZATION NONTHERMAL EXCITATION SPECTROMETRY [J].
RIBY, PG ;
HARNLY, JM ;
STYRIS, DL ;
BALLOU, NE .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1991, 46 (02) :203-215
[30]   A COMBINATION OF A PULSED CONTINUUM LIGHT-SOURCE, A HIGH-RESOLUTION SPECTROMETER, AND A CHARGE COUPLED DEVICE DETECTOR FOR MULTIELEMENT ATOMIC-ABSORPTION SPECTROMETRY [J].
SCHMIDT, KP ;
BECKERROSS, H ;
FLOREK, S .
SPECTROCHIMICA ACTA PART B-ATOMIC SPECTROSCOPY, 1990, 45 (11) :1203-1210