A new liquid chromatography–fluorescence method for determination of perfluorooctanesulphonyl fluoride upon derivatisation with 1-naphthol

International Journal of Environmental Analytical Chemistry

Volumn 94, Issue , 2014, Pages 1388-1393

  Meng, Xiangpeng ^a   Tang, Zhi ^a   Li, Qinghua ^a   Li, Charlie ^b   Cai, Zongwei ^a  

^a HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

^b CALIFORNIA DEPARTMENT OF PUBLIC HEALTH   (United States)

Author keywords

derivatisation; LC FLD; perfluorooctanesulphonyl fluoride; POPs

Indexed keywords

CHROMOPHORES; FLUORESCENCE; FLUORINE COMPOUNDS; MASS SPECTROMETRY; NAPHTHOL; NUCLEAR QUADRUPOLE RESONANCE; CHROMATOGRAPHY;

DERIVATISATION; INSTRUMENT DETECTION LIMITS; PERFLUOROOCTANESULPHONATE; PERFLUOROOCTANESULPHONYL FLUORIDE; POPS; PROTON NUCLEAR MAGNETIC RESONANCE; QUALITATIVE AND QUANTITATIVE ANALYSIS; TIME OF FLIGHT MASS SPECTROMETRY;

LIQUID CHROMATOGRAPHY;

EID: 84916896432     PISSN: 03067319     EISSN: 10290397     Source Type: Journal    
DOI: 10.1080/03067319.2014.954563     Document Type: Article

References (25)

1. Updated POPs list, (2014). .
2. POPRC (UNEP), Decision SC-4/10 to SC-4/18: The 9 New POPs Under the Stockholm Convention (UNEP, Geneva, 2009).
3. 3M, U.S. EPA Docket No. 2002-0043-0008. (1999).
4. R. Renner, Environ. Sci. Technol. 38, 264A–265A (2004). doi:10.1021/es040570p.
5. M.H. Russell, W.R. Berti, B. Szostek and R.C. Buck, Environ. Sci. Technol. 42, 800–807 (2008). doi:10.1021/es0710499.
6. C.P. Higgins, J.A. Field, C.S. Criddle and R.G. Luthy, Environ. Sci. Technol. 39, 3946–3956 (2005). doi:10.1021/es048245p.
7. C.A. Moody, W.C. Kwan, J.W. Martin, D.C.G. Muir and S.A. Mabury, Anal. Chem. 73, 2200–2206 (2001). doi:10.1021/ac0100648.
8. S.D. Richardson, Anal. Chem. 81, 4645–4677 (2009). doi:10.1021/ac9008012.
9. K. Wille, J.V. Bussche, H. Noppe, E. De Wulf, P. Van Caeter, C.R. Janssen, H.F. DeBrabander and L.J. Vanhaecke, J. Chromatogr. A. 1217, 6616–6622 (2010). doi:10.1016/j.chroma.2010.03.054.
10. M. Onghena, Y. Moliner-Martinez, Y. Picó, P. Campíns-Falcó and D. Barceló, J. Chromatogr. A. 1244, 88–97 (2012). doi:10.1016/j.chroma.2012.04.056.
11. S. Ullah, T. Alsberg and U. Berger, J. Chromatogr. A. 1218, 6388–6395 (2011). doi:10.1016/j.chroma.2011.07.005.
12. M. Shoeib, T. Harner, B.H. Wilford, K.C. Jones and J. Zhu, Environ. Sci. Technol. 39, 6599–6606 (2005). doi:10.1021/es048340y.
13. M. Loewen, F. Wania, F. Wang and G. Tomy, Environ. Sci. Technol. 42, 2374–2379 (2008). doi:10.1021/es702276c.
14. N.L. Stock, V.I. Furdui, D.C.G. Muir and S.A. Mabury, Environ. Sci. Technol. 41, 3529–3536 (2007). doi:10.1021/es062709x.
15. K. Kannan, S. Corsolini, J. Falandysz, G. Oehme, S. Focardi and J.P. Giesy, Environ. Sci. Technol. 36, 3210–3216 (2002). doi:10.1021/es020519q.
16. J.P. Giesy and K. Kannan, Environ. Sci. Technol. 35, 1339–1342 (2001). doi:10.1021/es001834k.
17. Y. Wang, S. Beesoon, J.P. Benskin, A.O. De Silva, S.J. Genuis and J.W. Martin, Environ. Sci. Technol. 45, 8907–8914 (2011). doi:10.1021/es2023434.
18. A.G. Paul, K.C. Jones and A. Sweetman, Environ. Sci. Technol. 43, 386–392 (2009). doi:10.1021/es802216n.
19. G.W. Olsen, J.M. Burris, J.H. Mandel and L.R. Zobel, J. Occup. Environ. Med. 41, 799–806 (1999). doi:10.1097/00043764-199909000-00012.
20. 3M. AR226-0681, 2000, 1063–1072.
21. J.W. Martin, D.C.G. Muir, C.A. Moody, D.A. Ellis, W.C. Kwan, K.R. Solomon and S.A. Mabury, Anal. Chem. 74, 584–590 (2002). doi:10.1021/ac015630d.
22. C. Sun, H. Sun, Y. Lai, J. Zhang and Z. Cai, Anal. Chem. 83, 5822–5826 (2011). doi:10.1021/ac201117k.
23. S. Shekhar, T.B. Dunn, B.J. Kotecki, D.K. Montavon and S.C. Cullen, J. Org. Chem. 76, 4552–4563 (2011). doi:10.1021/jo200443u.
24. G. Arsenault, B. Chittim, A. McAlees, R. McCrindle, N. Riddell and B. Yeo, Chemosphere 70, 616–625 (2008). doi:10.1016/j.chemosphere.2007.06.087.
25. S.M. Vyas, I. Kania-Korwel and H.J. Lehmler, J. Environ. Sci. Health Part A Toxic/Hazard. Subst. Environ. Eng. 42, 249 (2007).