Light-absorbing components
of atmospheric organic aerosols, which
are collectively termed “brown carbon” (BrC), are ubiquitous
in the atmosphere. They affect absorption of solar radiation by aerosols
in the atmosphere and human health as some of them have been identified
as potential toxins. Understanding the sources, formation, atmospheric
evolution, and environmental effects of BrC requires molecular identification
and characterization of light-absorption properties of BrC chromophores.
Identification of BrC components is challenging due to the complexity
of atmospheric aerosols. In this study, we employ two complementary
ionization techniques, atmospheric pressure photo ionization (APPI)
and electrospray ionization (ESI), to obtain broad coverage of both
polar and nonpolar BrC components using high-resolution mass spectrometry
(HRMS). These techniques are combined with chromatographic separation
of BrC compounds with high performance liquid chromatography (HPLC),
characterization of their light absorption with a photodiode array
(PDA) detector, and chemical composition with HRMS. We demonstrate
that this approach enables more comprehensive characterization of
BrC in biomass burning organic aerosols (BBOAs) emitted from test
burns of sage brush biofuel. In particular, we found that nonpolar
BrC chromophores such as PAHs are only detected using positive mode
APPI. Meanwhile, negative mode ESI results in detection of polar compounds
such as nitroaromatics, aromatic acids, and phenols. For the BrC material
examined in this study, over 40% of the solvent-extractable BrC light
absorption is attributed to water insoluble, nonpolar to semipolar
compounds such as PAHs and their derivatives, which require APPI for
their identification. In contrast, the polar, water-soluble BrC compounds,
which are detected in ESI, account for less than 30% of light absorption
by BrC.