On-line coupling of fizzy extraction with gas chromatography

被引:13
作者
Yang, Hao-Chun [1 ,2 ]
Urban, Pawel L. [1 ,3 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem, 101 Sect 2,Kuang Fu Rd, Hsinchu 30013, Taiwan
[2] Natl Chiao Tung Univ, Dept Appl Chem, 1001 Univ Rd, Hsinchu 300, Taiwan
[3] Natl Tsing Hua Univ, Frontier Res Ctr Fundamental & Appl Sci Matters, 101 Sect 2,Kuang Fu Rd, Hsinchu 30013, Taiwan
关键词
Extraction; Gas chromatography; Sample preparation; Volatile organic compounds; VOLATILE COMPOUNDS; TRAP EXTRACTION; BUBBLE; PLANTS; FRUIT;
D O I
10.1007/s00216-019-01755-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fizzy extraction (FE) is carried out by first dissolving a carrier gas (typically, carbon dioxide) in a liquid sample at a moderate pressure (typically, 150kPa) and then rapidly depressurizing the sample. The depressurization leads to instant release of numerous microbubbles in the liquid matrix. The abruptly released gas extracts the volatile solutes and elutes them toward a detector in a short period of time. Here, we describe on-line coupling of FE with gas chromatography (GC). The two platforms are highly compatible and could be combined following several modifications of the interface and adjustments of the extraction sequence. The analytes are released within a short period of time (1.5s). Thus, the chromatographic peaks are satisfactorily narrow. There is no need to trap the extracted analytes in a loop or on a sorbent, as it is done in standard headspace and microextraction methods. The approach requires only minor sample pretreatment. The main parameters of the FE-GC-mass spectrometry (MS) method were optimized. The results of FE were compared with those of headspace flushing (scavenging headspace vapors), and the enhancement factors were in the order of 2 to 13 (for various analytes). The limits of detection for some of the tested analytes were lower in the proposed FE-GC-MS method than in FE combined with atmospheric pressure chemical ionization MS. The method was further tested in analyses of selected real samples (apple flavor milk, mixed fruit and vegetable juice drink, mango flavored drink, pineapple green tea, toothpaste, and yogurt).
引用
收藏
页码:2511 / 2520
页数:10
相关论文
共 32 条
[1]   Studies of edible Amazonian plants part 4 -: Chemical characterization of the fruit of Annona squamosa L. occurring in the amazon [J].
Andrade, EHA ;
Zoghbi, MDB ;
Maia, JGS ;
Fabricius, H ;
Marx, F .
JOURNAL OF FOOD COMPOSITION AND ANALYSIS, 2001, 14 (02) :227-232
[2]  
[Anonymous], 2003, SEP SCI TECHNOL
[3]   Supercritical CO2 technology applied to the production of flavor ester compounds through lipase-catalyzed reaction: A review [J].
Baiao Dias, Arthur Luiz ;
dos Santos, Philipe ;
Martinez, Julian .
JOURNAL OF CO2 UTILIZATION, 2018, 23 :159-178
[4]  
Baranowska I, 2016, HDB TRACE ANAL
[5]   Development and validation of automatic HS-SPME with a gas chromatography-ion trap/mass spectrometry method for analysis of volatiles in wines [J].
Barros, Elisabete Paula ;
Moreira, Nathalie ;
Pereira, Giuliano Elias ;
Ferreira Leite, Selma Gomes ;
Rezende, Claudia Moraes ;
de Pinho, Paula Guedes .
TALANTA, 2012, 101 :177-186
[6]   Fizzy Extraction of Volatile and Semivolatile Compounds into the Gas Phase [J].
Chang, Cheng-Hao ;
Urban, Pawel L. .
ANALYTICAL CHEMISTRY, 2016, 88 (17) :8735-8740
[7]   Simultaneous Preconcentration and Desalting of Organic Solutes in Aqueous Solutions by Bubble Bursting [J].
Chingin, Konstantin ;
Cai, Yunfeng ;
Liang, Juchao ;
Chen, Huanwen .
ANALYTICAL CHEMISTRY, 2016, 88 (10) :5033-5036
[8]   Mass spectrometry-based metabolomics [J].
Dettmer, Katja ;
Aronov, Pavel A. ;
Hammock, Bruce D. .
MASS SPECTROMETRY REVIEWS, 2007, 26 (01) :51-78
[9]   High yield of ethyl valerate from the esterification of renewable valeric acid catalyzed by amino acid ionic liquids [J].
Dong, Lin-Lin ;
He, Ling ;
Tao, Guo-Hong ;
Hu, Changwei .
RSC ADVANCES, 2013, 3 (14) :4806-4813
[10]   STATISTICAL APPROACH TO CHROMATOGRAPHIC THEORY [J].
FRITZ, JS ;
SCOTT, DM .
JOURNAL OF CHROMATOGRAPHY, 1983, 271 (02) :193-212