Analysis of co-eluted isomers of high-molecular weight polycyclic aromatic hydrocarbons in high performance liquid chromatography fractions via solid-phase nanoextraction and time-resolved Shpol'skii spectroscopy

Authors

    Authors

    W. B. Wilson;A. D. Campiglia

    Comments

    Authors: contact us about adding a copy of your work at [email protected]

    Abbreviated Journal Title

    J. Chromatogr. A

    Keywords

    High-molecular weight polycyclic aromatic hydrocarbons; Solid-phase; nanoextraction; Shpol'skii spectroscopy; Gold nanoparticles; Laser-excited time-resolved Shpol'skii spectroscopy; MULTIDIMENSIONAL FLUORESCENCE SPECTROSCOPY; IONIZATION; MASS-SPECTROMETRY; DRINKING-WATER SAMPLES; 15 PRIORITY POLLUTANTS; ENVIRONMENTAL-SAMPLES; DIBENZOPYRENE ISOMERS; NANO-EXTRACTION; HPLC; FRACTIONS; FACILE METHOD; CARBON-BLACK; Biochemical Research Methods; Chemistry, Analytical

    Abstract

    We present an accurate method for the determination of isomers of high-molecular weight polycyclic aromatic hydrocarbons co-eluted in HPLC fractions. The feasibility of this approach is demonstrated with two isomers of molecular weight 302 with identical mass fragmentation patterns, namely dibenzo[a,i]pyrene and naphtho[2,3-a]pyrene. Qualitative and quantitative analysis is carried out via laser-excited time-resolved Shpol'skii spectroscopy at liquid helium temperature. Unambiguous identification of co-eluted isomers is based on their characteristic 4.2 K line-narrowed spectra in n-octane as well as their fluorescence lifetimes. Pre-concentration of HPLC fractions prior to spectroscopic analysis is performed with the aid of gold nanoparticles via an environmentally friendly procedure. In addition to the two co-eluted isomers, the analytical figures of merit of the entire procedure were evaluated with dibenzo[a,l]pyrene, dibenzo[a,h]pyrene and dibenzo[a,e]pyrene. The analytical recoveries from drinking water samples varied between 98.2 +/- 5.5 (dibenzo[a,l]pyrene) and 102.7 +/- 3.2% (dibenzo[a,i]pyrene). The limits of detection ranged from 51.1 ng L(-1) (naphtho[2,3-a]pyrene) to 154 ng L(-1) (dibenzo[a,e]pyrene). The excellent analytical figures of merit associated to its HPLC compatibility makes this approach an attractive alternative for the analysis of co-eluted isomers with identical mass spectra. (C) 2011 Elsevier B.V. All rights reserved.

    Journal Title

    Journal of Chromatography A

    Volume

    1218

    Issue/Number

    39

    Publication Date

    1-1-2011

    Document Type

    Article

    Language

    English

    First Page

    6922

    Last Page

    6929

    WOS Identifier

    WOS:000295241500010

    ISSN

    0021-9673

    Share

    COinS
     

    Accessibility Statement

    This item was created or digitized prior to April 24, 2027, or is a reproduction of legacy media created before that date. It is preserved in its original, unmodified state specifically for research, reference, or historical recordkeeping. In accordance with the ADA Title II Final Rule, the University Libraries provides accessible versions of archival materials upon request. To request an accommodation for this item, please submit an accessibility request form.