Second-order bilinear calibration for determining polycyclic aromatic compounds in marine sediments by solvent extraction and liquid chromatography with diode-array detection

被引:40
作者
Gimeno, RA [1 ]
Comas, E [1 ]
Marcé, RM [1 ]
Ferré, J [1 ]
Rius, FX [1 ]
Borrull, F [1 ]
机构
[1] Univ Rovira & Virgili, Dept Quim Analit & Quim Organ, Tarragona 43005, Spain
关键词
polycyclic aromatic hydrocarbons; polycyclic aromatic sulfur heterocycles; marine sediment; second-order calibration; GRAM; standard additions; HPLC-DAD;
D O I
10.1016/j.aca.2003.08.057
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method based on solvent extraction followed by chromatographic separation with diode-array detection has been applied to determine polycyclic aromatic hydrocarbons (PAHs) in marine sediment samples. Because interfering substances coeluted with the compounds studied, second-order calibration using the Generalized Rank Annihilation Method (GRAM) was used for quantification. For calibration, a spiked sample was used instead of a standard solution because the complexity of the samples made us suspect the presence of matrix effect. With this method, the compounds do not need to be completely separated from the interferences and quantification can be carried out with only one spiked sample for calibration. Hence, the quantification process is shorter than the one based on univariate calibration. The ability of the method to quantify the studied compounds was evaluated by comparing the results with those of a univariate standard addition calibration, which involved the previous isolation of the analytes. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 53
页数:7
相关论文
共 21 条
[1]   COMPARISON OF LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY INTERFACES FOR THE ANALYSIS OF POLYCYCLIC AROMATIC-COMPOUNDS [J].
ANACLETO, JF ;
RAMALEY, L ;
BENOIT, FM ;
BOYD, RK ;
QUILLIAM, MA .
ANALYTICAL CHEMISTRY, 1995, 67 (22) :4145-4154
[2]  
[Anonymous], 1987, BINDING CONSTANTS ME
[3]   Comparison of different drying, extraction and detection techniques for the determination of priority polycyclic aromatic hydrocarbons in background contaminated soil samples [J].
Berset, JD ;
Ejem, M ;
Holzer, R ;
Lischer, P .
ANALYTICA CHIMICA ACTA, 1999, 383 (03) :263-275
[4]   Using second-order calibration to identify and quantify aromatic sulfonates in water by high-performance liquid chromatography in the presence of coeluting interferences [J].
Comas, E ;
Gimeno, RA ;
Ferré, J ;
Marcé, RM ;
Borrull, F ;
Rius, FX .
JOURNAL OF CHROMATOGRAPHY A, 2003, 988 (02) :277-284
[5]   Time shift correction in second-order liquid chromatographic data with iterative target transformation factor analysis [J].
Comas, E ;
Gimeno, RA ;
Ferré, J ;
Marcé, RM ;
Borrull, F ;
Rius, FX .
ANALYTICA CHIMICA ACTA, 2002, 470 (02) :163-173
[6]   Evaluation of on-line methodology for microwave-assisted extraction of polycyclic aromatic hydrocarbons (PAHs) from sediment samples [J].
Cresswell, SL ;
Haswell, SJ .
ANALYST, 1999, 124 (09) :1361-1366
[7]   Comparison of three-way resolution methods for non-trilinear chemical data sets [J].
de Juan, A ;
Tauler, R .
JOURNAL OF CHEMOMETRICS, 2001, 15 (10) :749-772
[8]   Solid-phase microextraction for detemnining the distribution of sixteen US Environmental Protection Agency polycyclic aromatic hydrocarbons in water samples [J].
Doong, R ;
Chang, S ;
Sun, Y .
JOURNAL OF CHROMATOGRAPHY A, 2000, 879 (02) :177-188
[9]   Recent developments in CANDECOMP/PARAFAC algorithms: a critical review [J].
Faber, NM ;
Bro, R ;
Hopke, PK .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2003, 65 (01) :119-137
[10]   Towards a rehabilitation of the generalized rank annihilation method (GRAM) [J].
Faber, NM .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2002, 372 (5-6) :683-687