CHARACTERIZATION OF OVERLAPPED CHROMATOGRAPHIC PEAKS BY THEIR 2ND DERIVATIVE - THE LIMIT OF THE METHOD

被引:27
作者
GRUSHKA, E
ISRAELI, D
机构
[1] Department of Inorganic and Analytical Chemistry, Hebrew University, Jerusalem
关键词
D O I
10.1021/ac00206a014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The second derivative of a chromatographic signal can aid In the recognition of composite peaks. In the case of a two-component composite, the second derivative has three maxima and two minima. The time position of the second of the three maxima is indicative of the point where the peak envelope of each component cross each other. This second maximum can be used to trigger the end of integration of the first component and the beginning of the integration of the second component. In theory, the second derivative approach works well. The present paper Investigates the limits of the method. It was found that, depending on the separation between the two components in the composite, there is a peak height ratio below which the method falls to recognize the existence of a composite system. The greater the separation, the smaller the height ratio. At 4σ separation, the minimum height ratio that the method can still recognize as a composite Is around 10−5. However, the useful range of the approach may extend to a lower range of height ratios due to the small changes in the area with relatively large changes In the peak height ratio. Noise also affects the useful range of the method. In general, as the noise increases, the method fails at higher peak height ratios. A surface describing the useful range of the method is given as a function of the signal-to-noise ratio, the separation, and the height ratio. © 1990, American Chemical Society. All rights reserved.
引用
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页码:717 / 721
页数:5
相关论文
共 16 条
[1]  
ASHLEY JW, 1965, ANAL CHEM, V35, P626
[2]  
ASHLEY JW, 1965, ANAL CHEM, V35, P627
[4]   RAPID-SCANNING, MULTI-CHANNEL HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC DETECTION OF ZIMELDINE AND METABOLITES WITH 3-DIMENSIONAL GRAPHICS AND CONTOUR PLOTTING [J].
CLARK, BJ ;
FELL, AF ;
SCOTT, HP ;
WESTERLUND, D .
JOURNAL OF CHROMATOGRAPHY, 1984, 286 (MAR) :261-273
[5]   VALIDATION AND CALIBRATION IN HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY (HPLC) [J].
EBEL, S .
CHROMATOGRAPHIA, 1986, 22 (7-12) :373-378
[6]   COMPUTER-AIDED MULTICHANNEL DETECTION IN HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
FELL, AF ;
SCOTT, HP ;
GILL, R ;
MOFFAT, AC .
CHROMATOGRAPHIA, 1982, 16 :69-78
[7]   NOVEL TECHNIQUES FOR PEAK RECOGNITION AND DECONVOLUTION BY COMPUTER-AIDED PHOTODIODE ARRAY DETECTION IN HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
FELL, AF ;
SCOTT, HP ;
GILL, R ;
MOFFAT, AC .
JOURNAL OF CHROMATOGRAPHY, 1983, 282 (DEC) :123-140
[8]   APPLICATIONS OF RAPID-SCANNING MULTICHANNEL DETECTORS IN CHROMATOGRAPHY - PLENARY LECTURE [J].
FELL, AF ;
SCOTT, HP ;
GILL, R ;
MOFFAT, AC .
JOURNAL OF CHROMATOGRAPHY, 1983, 273 (01) :3-17
[9]   BACKGROUND SUBTRACTION FOR FLUORESCENCE DETECTION IN THIN-LAYER CHROMATOGRAPHY WITH DERIVATIVE SPECTROMETRY AND THE ADAPTIVE KALMAN FILTER [J].
GEROW, DD ;
RUTAN, SC .
ANALYTICA CHIMICA ACTA, 1986, 184 :53-64
[10]   APPLICATION OF DERIVATIVE SPECTROSCOPY TO THE DETERMINATION OF CHROMATOGRAPHIC PEAK PURITY [J].
GRANT, A ;
BHATTACHARYYA, PK .
JOURNAL OF CHROMATOGRAPHY, 1985, 347 (02) :219-235