中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
DETERMINATION OF GEOSMIN AND 2-METHYLISOBORNEOL IN WATER BY HEADSPACE LIQUID-PHASE MICROEXTRACTION COUPLED WITH GAS CHROMATOGRAPHY-MASS SPECTROMETRY

文献类型:期刊论文

作者Ma, Jiping2; Lu, Wenhui1,2; Li, Jinhua1; Song, Zhiwen2; Liu, Dongyan1; Chen, Lingxin1
刊名ANALYTICAL LETTERS
出版日期2011
卷号44期号:8页码:1544-1557
关键词Gas Chromatography-mass Spectrometry Geosmin Headspace Liquid-phase Microextraction 2-methylisoborneol Single-drop Microextraction Water Samples
ISSN号0003-2719
产权排序[Lu, Wenhui; Li, Jinhua; Liu, Dongyan; Chen, Lingxin] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Environm Proc, Yantai 264003, Peoples R China; [Ma, Jiping; Lu, Wenhui; Song, Zhiwen] Qingdao Technol Univ, Inst Environm & Municipal Engn, Key Lab Environm Engn Shandong Prov, Qingdao, Peoples R China
通讯作者Chen, LX, Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Environm Proc, Yantai 264003, Peoples R China.lxchen@yic.ac.cn
文献子类Article
英文摘要Geosmin (GSM) and 2-methylisoborneol (MIB) were extracted from water samples, adsorbed in organic solvent microdrop by headspace liquid-phase microextraction (HS-LPME), and were analyzed by gas chromatography-mass spectrometry (GC-MS). Influence factors such as the extraction solvent types, headspace and microdrop volumes, stirring rate, equilibrium and extraction time, and ionic strength for HS-LPME efficiency were thoroughly evaluated. Under optimized extraction and detection conditions, the calibration curves of GSM and MIB were linear in the range of 5-1000 ng/L. The detection limits of GSM and MIB were 1.1 and 1.0 ng/L, respectively. Average recoveries of 95.45-113.7% (n=5) were obtained and method precisions were also satisfactory. Trace levels of the off-flavor compounds at ng/L in tap water and raw water were successfully quantified.; Geosmin (GSM) and 2-methylisoborneol (MIB) were extracted from water samples, adsorbed in organic solvent microdrop by headspace liquid-phase microextraction (HS-LPME), and were analyzed by gas chromatography-mass spectrometry (GC-MS). Influence factors such as the extraction solvent types, headspace and microdrop volumes, stirring rate, equilibrium and extraction time, and ionic strength for HS-LPME efficiency were thoroughly evaluated. Under optimized extraction and detection conditions, the calibration curves of GSM and MIB were linear in the range of 5-1000 ng/L. The detection limits of GSM and MIB were 1.1 and 1.0 ng/L, respectively. Average recoveries of 95.45-113.7% (n=5) were obtained and method precisions were also satisfactory. Trace levels of the off-flavor compounds at ng/L in tap water and raw water were successfully quantified.
学科主题Chemistry ; Analytical
WOS关键词MUSTY ODOROUS COMPOUNDS ; SINGLE-DROP ; EXTRACTION ; SAMPLES ; EARTHY ; CYANOBACTERIA ; INLET ; PONDS ; MIB
WOS研究方向Chemistry
语种英语
WOS记录号WOS:000291644300015
资助机构National Natural Science Foundation of China [40906045]; Yantai Science and Technology Plan Program, Yantai, China [2008155]
公开日期2011-07-22
源URL[http://ir.yic.ac.cn/handle/133337/4842]  
专题烟台海岸带研究所_山东省海岸带环境工程技术研究中心
烟台海岸带研究所_中科院海岸带环境过程与生态修复重点实验室
作者单位1.Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Environm Proc, Yantai 264003, Peoples R China
2.Qingdao Technol Univ, Inst Environm & Municipal Engn, Key Lab Environm Engn Shandong Prov, Qingdao, Peoples R China
推荐引用方式
GB/T 7714
Ma, Jiping,Lu, Wenhui,Li, Jinhua,et al. DETERMINATION OF GEOSMIN AND 2-METHYLISOBORNEOL IN WATER BY HEADSPACE LIQUID-PHASE MICROEXTRACTION COUPLED WITH GAS CHROMATOGRAPHY-MASS SPECTROMETRY[J]. ANALYTICAL LETTERS,2011,44(8):1544-1557.
APA Ma, Jiping,Lu, Wenhui,Li, Jinhua,Song, Zhiwen,Liu, Dongyan,&Chen, Lingxin.(2011).DETERMINATION OF GEOSMIN AND 2-METHYLISOBORNEOL IN WATER BY HEADSPACE LIQUID-PHASE MICROEXTRACTION COUPLED WITH GAS CHROMATOGRAPHY-MASS SPECTROMETRY.ANALYTICAL LETTERS,44(8),1544-1557.
MLA Ma, Jiping,et al."DETERMINATION OF GEOSMIN AND 2-METHYLISOBORNEOL IN WATER BY HEADSPACE LIQUID-PHASE MICROEXTRACTION COUPLED WITH GAS CHROMATOGRAPHY-MASS SPECTROMETRY".ANALYTICAL LETTERS 44.8(2011):1544-1557.

入库方式: OAI收割

来源:烟台海岸带研究所

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