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Quantitative analysis of trace levels of β-ionone in water by liquid-liquidphase extraction-gas chromatography-mass spectrometry(LLE-GC-MS) 被引量:1

Quantitative analysis of trace levels of β-ionone in water by liquid-liquidphase extraction-gas chromatography-mass spectrometry(LLE-GC-MS)
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摘要 A simple and rapid technique based on liquid-liquid extraction coupled to gas chromatography-mass spectrometric detection(LLE-GC-MS) was developed for analysis of taste and odour compound β-ionone in water. Instrument parameters including programmed oven temperature, injection temperature and ion source temperature were evaluated and optimized. Effects of extraction time, ionic strength and p H on the detection efficiency were investigated and optimum conditions were 8 min of extraction time, without Na Cl addition at p H=9. Good linearity(R2=0.9997) was obtained when the linear range was 10-500 μg/L. The recoveries of β-ionone in ultrapure water and tap water samples were 88%-95% and 110%-114%, respectively. The relative standard deviations(RSD) were less than 10%. The method detection limit(MDL) and rejection quality level(RQL) were achieved at1.98 μg/L and 6.53 μg/L, respectively. LLE-GC-MS was demonstrated to be a rapid and convenient method for the determination ofβ-ionone in water samples. A simple and rapid technique based on liquid-liquid extraction coupled to gas chromatography-mass spectrometric detection(LLE-GC-MS) was developed for analysis of taste and odour compound β-ionone in water. Instrument parameters including programmed oven temperature, injection temperature and ion source temperature were evaluated and optimized. Effects of extraction time, ionic strength and p H on the detection efficiency were investigated and optimum conditions were 8 min of extraction time, without Na Cl addition at p H=9. Good linearity(R^2=0.9997) was obtained when the linear range was 10-500 μg/L. The recoveries of β-ionone in ultrapure water and tap water samples were 88%-95% and 110%-114%, respectively. The relative standard deviations(RSD) were less than 10%. The method detection limit(MDL) and rejection quality level(RQL) were achieved at1.98 μg/L and 6.53 μg/L, respectively. LLE-GC-MS was demonstrated to be a rapid and convenient method for the determination ofβ-ionone in water samples.
出处 《Journal of Central South University》 SCIE EI CAS CSCD 2015年第2期472-477,共6页 中南大学学报(英文版)
基金 Project(51178321)supported by the National Natural Science Foundation of China Project(2012ZX07403-001)supported by the National Science and Technology Major Project,China Project(20120072110050)supported by the Research Fund for the Doctoral Program of Higher Education of China
关键词 紫罗兰酮 气相色谱 痕量水 质谱法 液萃取 定量分析 注射温度 最佳工艺条件 liquid-liquid extraction gas chromatography-mass spectrometry β-ionone water
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  • 1PETER A, VON GUN TEN U. Oxidation kinetics of selected taste and odor compounds during ozonation of drinking water[J]. Environmental Science & Technology, 2007, 41(2): 626-631.
  • 2KRISTIN K, HILMAR B, ECKHARD W. Photoinitiated oxidation of geosmin and 2-methylisobomeol by irradiation with 254 nm and 185 nm UV light[J]. Water Research, 2009, 43(8): 2224-2232.
  • 3HO L, NEWCOMBE G. Effect of NOM, turbidity and floc size on the PAC adsorption of MIB during alum coagulation[J]. Water Research, 2005, 39(15): 3668-3674.
  • 4lKAWA M, SASNER J J. HANEY J F. Activity of cyanobacterial and algal odor compounds found in lake waters on green alga Chiarella pyrenoidosa growth[J]. Hydrobiologia, 2001, 443(112/3): 19-22.
  • 5DAVIES J M, ROXBOROUGH M, MAZUMDER A. Origins and implications of drinking water odours in lakes and reservoirs of British Columbia, Canada[J]. Water Research, 2004, 38(7): 1900-1910.
  • 6COTSARIS E, BRUCHET A, MALLEVIALLE J, BURSILL DB. The identification of odorous metabolites produced from algal monocultures[J]. Water Science Technology, 1995,31(11): 251-258.
  • 7JIN Xing. Research on typical odorous compounds from algae metabolites and the variation rule[DJ. Nanjing: Department of Environmental Science of Nanjing University of Science & Technology, 2009. (in Chinese).
  • 8ZHANG Li-feng, HU Rui-kang, YANG Zhao-guang. Routine analysis of off-flavor compounds in water at sub-part-per-trillion level by large-volume injection GC/MS with programmable temperature vaporizing inlet[J]. Water Research, 2006, 40(4): 699-709.
  • 9MCGUIRE M J, KRASNER S W, HWANG C J, IZAGUIRRE G. Closed-loop stripping analysis as a tool for solving taste and odor problems[J]. American Water Works Association, 1981, 73(10): 530-537.
  • 10US Environmental Protection Agency Method 600/4-88/039. Methods for the determination of organic compounds in drinking water[S].

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