In Situ Hydrothermal Growth of Metal−Organic Framework 199 Films on Stainless Steel Fibers for Solid-Phase Microextraction of Gaseous Benzene Homologues

• Published in: Analytical chemistry (Washington) 2009-12, Vol.81 (23), p.9771-9777
• Main Authors: Cui, Xiao-Yan, Gu, Zhi-Yuan, Jiang, Dong-Qing, Li, Yan, Wang, He-Fang, Yan, Xiu-Ping
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Chemistry; Chromatographic methods and physical methods associated with chromatography; Exact sciences and technology; Extraction processes; Gas chromatographic methods; Hydrocarbons; Metals; Stainless steel
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac901663x

Metal−organic frameworks (MOFs) have received great attention due to their fascinating structures and intriguing potential applications in various fields. Herein, we report the first example of the utilization of MOFs for solid-phase microextraction (SPME). MOF-199 with unique pores and open metal sites (Lewis acid sites) was employed as the coating for SPME fiber to extract volatile and harmful benzene homologues. The SPME fiber was fabricated by in situ hydrothermal growth of thin MOF-199 films on etched stainless steel wire. The MOF-199-coated fiber not only offered large enhancement factors from 19 613 (benzene) to 110 860 (p-xylene), but also exhibited wide linearity with 3 orders of magnitude for the tested benzene homologues. The limits of detection for the benzene homologues were 8.3−23.3 ng L−1. The relative standard deviation (RSD) for six replicate extractions using one SPME fiber ranged from 2.0% to 7.7%. The fiber-to-fiber reproducibility for three parallel prepared fibers was 3.5%−9.4% (RSD). Indoor air samples were analyzed for the benzene homologues using the SPME with the MOF-199-coated fiber in combination with gas chromatography−flame ionization detection. The recoveries for the spiked benzene homologues in the collected indoor air samples were in the range of 87%−106%. The high affinity of the MOF-199-coated fiber to benzene homologues resulted from the combined effects of the large surface area and the unique porous structure of the MOF-199, the π−π interactions of the aromatic rings of the analytes with the framework 1,3,5-benzenetricarboxylic acid molecules, and the π-complexation of the electron-rich analytes to the Lewis acid sites in the pores of MOF-199.