作者: Ching-Te Huang , Yang-Yao Su , You-Zung Hsieh
DOI: 10.1016/S0021-9673(02)01278-5
关键词: Calibration curve 、 Detection limit 、 Chemistry 、 Solid-phase microextraction 、 Gas chromatography 、 Chromatography 、 Flame ionization detector 、 Analytical chemistry 、 Sample preparation 、 Glycol ethers 、 Extraction (chemistry)
摘要: Abstract A headspace solid-phase microextraction (HS-SPME), in conjunction with gas chromatography–flame ionization detection for use the determination of six frequently used glycol ethers at μg/l level is described. 75 μm Carboxen–polydimethylsiloxane fiber was to extract analytes from an aqueous solution. Experimental HS-SPME parameters such as extraction temperature, time, salt concentration and sample volume, were investigated optimized by orthogonal array experimental designs. The relative standard deviations reproducibility method varied 1.48 7.59%. correlation coefficients calibration curves exceeded 0.998 range least two orders magnitude. limits deionized water 0.26 3.42 μg/l. also applied analysis urine blood samples ranged 1.74 23.2