posted on 2016-06-30, 00:00authored byRian You, James G. Radney, Michael R. Zachariah, Christopher D. Zangmeister
Optical
absorption spectra of laboratory generated aerosols consisting
of black carbon (BC) internally mixed with nonabsorbing materials
(ammonium sulfate, AS, and sodium chloride, NaCl) and BC with a weakly
absorbing brown carbon surrogate derived from humic acid (HA) were
measured across the visible to near-IR (550 to 840 nm). Spectra were
measured in situ using a photoacoustic spectrometer and step-scanning
a supercontinuum laser source with a tunable wavelength and bandwidth
filter. BC had a mass-specific absorption cross section (MAC) of 7.89 ±
0.25 m2 g–1 at λ = 550 nm and an
absorption Ångström exponent (AAE) of 1.03 ± 0.09
(2σ). For internally mixed BC, the ratio of BC mass to the total
mass of the mixture was chosen as 0.13 to mimic particles observed
in the terrestrial atmosphere. The manner in which BC mixed with each
material was determined from transmission electron microscopy (TEM).
AS/BC and HA/BC particles were fully internally mixed, and the BC
was both internally and externally mixed for NaCl/BC particles. The
AS/BC, NaCl/BC, and HA/BC particles had AAEs of 1.43 ± 0.05,
1.34 ± 0.06, and 1.91 ± 0.05, respectively. The observed
absorption enhancement of mixed BC relative to the pure BC was wavelength
dependent for AS/BC and decreased from 1.5 at λ = 550 nm with
increasing wavelength while the NaCl/BC enhancement was essentially
wavelength independent. For HA/BC, the enhancement ranged from 2 to
3 and was strongly wavelength dependent. Removal of the HA absorption
contribution to enhancement revealed that the enhancement was ≈1.5
and independent of wavelength.