Abstract.
Secondary
organic
aerosols
(SOA)
formed
by
oxidation
of
typical
precursors
largely
emitted
biomass
burning,
such
as
PAHs
and
furans,
are
still
poorly
characterized
in
terms
formation
yields,
physical
light
absorption
properties,
particularly
those
generated
at
night
following
reaction
with
nitrate
radicals
(NO3).
In
the
present
study,
we
evaluated
compared
effective
density
(ρeff),
Ångström
exponent
(α),
mass
coefficient
(MAC)
laboratory-generated
SOA
from
three
furan
compounds
(furan,
2-methylfuran,
2,5-dimethylfuran)
four
(naphthalene,
acenaphthylene,
fluorene,
phenanthrene).
were
an
flow
reactor
between
hydroxyl
(OH;
0.1–20
equivalent
aging
days)
or
NO3
(0.05–6
nights
14
h)
single
PAH.
The
ρeff,
α,
MAC
varied
depending
on
precursor
oxidant
considered.
ρeff
OH
tended
to
increase
particle
size
before
reaching
a
“plateau”.
This
was
evident
for
nighttime
chemistry
experiments
(1.2
1.6
average
particles
>
100
nm).
Such
results
highlighted
potential
differences
chemical
composition
SOA,
well
probably
their
morphology,
according
size.
Three
times
lower
yields
obtained
OH.
PAH
(18
76
%)
5
6
higher
than
furans
(3–12
%).
While
showed
low
negligible
found
have
significant
impact
UV-Visible
region,
implying
contribution
atmospheric
brown
carbon
(BrC).
No
values
observed
processes,
due
nitrogen-containing
chromophores
through
homogeneous
gas
phase
processes
only
(without
NOx).
Overall,
this
work
demonstrated
that
both,
day-
substantial
aerosol
properties
so
climate.
ACS ES&T Air,
Journal Year:
2024,
Volume and Issue:
1(7), P. 690 - 703
Published: May 3, 2024
Although
atmospheric
organic
pollutants
have
been
extensively
studied
to
elucidate
summertime
urban
photochemical
air
pollution,
uncertainties
remain
concerning
the
quality
of
wintertime
in
large
northern
North
American
cities.
Here,
we
used
online
mass
spectrometric
measurements
volatile
compounds
(VOCs)
and
aerosol
(OA),
combined
with
positive
matrix
factorization
(PMF),
identify
sources
downtown
Toronto,
Canada
during
February–March
2023.
In
some
cases,
comparable
PMF
factors
were
identified
for
both
VOCs
OA,
such
as
from
traffic,
cooking,
background
oxygenated
sources.
However,
VOC
yielded
additional
information,
a
factor
associated
human-related
emissions
VOCs.
Additionally,
yields
two
traffic
factors:
one
likely
related
gasoline
diesel
use.
Despite
cold
relatively
dark
conditions,
OA
grow
intensity
daytime,
indicative
activity,
whereas
cooking
enhanced
morning
late
evening
due
timing
vehicle
use,
boundary
layer
effects.
This
study
illustrates
benefits
that
arise
parallel
source–receptor
analyses
gases
particles.
Atmospheric chemistry and physics,
Journal Year:
2025,
Volume and Issue:
25(6), P. 3737 - 3752
Published: March 28, 2025
Abstract.
Biomass
burning
is
a
major
global
source
of
both
primary
brown
carbon
(BrC)
and
reactive
trace
gases
in
the
atmosphere
thus
has
significant
impact
on
climate
regional
atmospheric
chemistry.
However,
substantial
gap
remains
our
understanding
nighttime
evolution
biomass
emissions.
Here
we
present
prominent
formation
secondary
organic
aerosol
(Night-OA)
with
strong
absorptivity
but
markedly
different
spectral
dependence
from
that
aerosols,
which
was
observed
during
autumn
Pearl
River
Delta
region
China
when
plumes
prevailed.
Our
results
demonstrate
Night-OA
appeared
to
have
high
magnitudes
emissions
at
nightfall
available
oxidants
NO2
O3.
Active
NO3
radical
chemistry
characterized
by
quick
O3
depletion
almost
zero
concentration
NO.
The
rapid
decrease
coincident
nitrate
suggests
consumption
supplied
N2O5
reaction
chains.
quickest
occurred
ceased
relative
humidity
reached
maximum,
it
mainly
added
mass
water-abundant
diameter
ranges.
This
co-variation
gas-phase
reactions
precursors,
along
aqueous-phase
involving
preexisting
hygroscopic
aerosols
diluted
plume,
likely
work
concert
promote
Night-OA.
Preexisting
background
are
generally
much
more
than
directly
emitted
burning.
Incorporating
important
role
aging
would
be
valuable
future
laboratory
model
simulation
studies.
proposed
mechanisms
for
BrC
broad
implications
air
quality
impacts
burning,
including
interaction
between
humid
regions,
as
well
pyroconvection
clouds.
Atmospheric chemistry and physics,
Journal Year:
2023,
Volume and Issue:
23(13), P. 7461 - 7477
Published: July 10, 2023
Abstract.
Primary
emissions
from
wood
and
pellet
stoves
were
aged
in
an
atmospheric
simulation
chamber
under
daytime
nighttime
conditions.
The
aerosol
was
analyzed
with
online
mass
spectrometry
offline
Fourier
transform
infrared
spectroscopy
(FTIR).
Measurements
using
the
two
techniques
agreed
reasonably
well
terms
of
organic
(OA)
concentration,
OA:OC
trends,
concentrations
biomass
burning
markers
–
lignin-like
compounds
anhydrosugars.
Based
on
spectrometry,
around
15
%
primary
(POA)
underwent
some
form
transformation
during
oxidation
conditions
after
6–10
h
exposure.
A
lesser
extent
observed
oxidation.
decay
certain
semi-volatile
(e.g.,
levoglucosan)
less
volatile
lignin-like)
POA
components
substantial
aging,
highlighting
role
heterogeneous
reactions
gas–particle
partitioning.
Lignin-like
to
degrade
both
conditions,
whereas
anhydrosugars
degraded
only
Among
marker
fragments
OA
(bbPOA),
heavy
ones
(higher
m/z)
relatively
more
stable
aging.
secondary
(bbSOA)
became
oxidized
continued
aging
resembled
that
aerosols.
bbSOA
formed
dominated
by
acids.
Organonitrates
important
product
humid
dry
Our
results
underline
importance
changes
aerosols
their
Heavier
seldom
used
chemistry
can
be
as
tracers
bbPOA
and,
combination
established
levoglucosan
marker,
provide
indication
Atmospheric chemistry and physics,
Journal Year:
2023,
Volume and Issue:
23(23), P. 15077 - 15096
Published: Dec. 7, 2023
Abstract.
Secondary
organic
aerosols
(SOAs)
formed
by
oxidation
of
typical
precursors
largely
emitted
biomass
burning,
such
as
polycyclic
aromatic
hydrocarbons
(PAHs)
and
furans,
are
still
poorly
characterized.
We
evaluated
compared
the
formation
yields,
effective
density
(ρeff),
absorption
Ångström
exponent
(α),
mass
coefficient
(MAC)
laboratory-generated
SOAs
from
three
furan
compounds
four
PAHs.
were
generated
in
an
flow
reactor
under
day-
(OH
radicals)
or
nighttime
(NO3
conditions.
The
ρeff,
α,
MAC
varied
depending
on
precursor
oxidant
considered.
ρeff
with
OH
NO3
tended
to
increase
particle
size
before
reaching
a
“plateau”,
highlighting
potential
differences
SOA
chemical
composition
and/or
morphology,
according
size.
Three
times
lower
yields
obtained
OH.
PAH
(18
%–76
%)
five
six
higher
than
those
for
furans
(3
%–12
%).
While
showed
low
negligible
light
properties,
had
significant
impact
UV–visible
region,
implying
contribution
atmospheric
brown
carbon.
No
values
was
observed
processes,
probably
due
nitrogen-containing
chromophores
only
(without
NOx).
results
demonstrated
that
PAHs
through
both,
have
substantial
aerosol
properties.
Environmental Science Atmospheres,
Journal Year:
2023,
Volume and Issue:
3(9), P. 1319 - 1334
Published: Jan. 1, 2023
Pellet
combustion
in
residential
heating
stoves
has
increased
globally
during
the
last
decade.
Despite
their
high
efficiency,
widespread
use
of
pellet
is
expected
to
adversely
impact
air
quality.
The
atmospheric
aging
emissions
received
even
less
attention,
focusing
mainly
on
daytime
conditions,
while
degree
which
undergo
night-time
as
well
role
relative
humidity
remain
poorly
understood.
In
this
study,
environmental
simulation
chamber
experiments
were
performed
characterize
fresh
and
aged
organic
aerosol
(OA)
emitted
by
a
stove.
stove
PM1
(particulate
matter
with
an
aerodynamic
diameter
than
1
μm)
consisted
OA
(93
±
4%,
mean
standard
deviation)
black
carbon
(5
3%).
primary
(POA)
oxygen-to-carbon
ratio
(O
:
C)
was
0.58
0.04,
higher
that
logwood
emissions.
at
concentration
70
μg
m-3
(after
dilution
equilibration
chamber)
semi-volatile
(68%),
low
extremely
volatility
(16%)
intermediate-volatility
compounds.
oxidation
under
dark
conditions
investigated
injecting
nitrogen
dioxide
(NO2)
ozone
(O3)
into
chamber,
different
(10-80%)
(RH)
levels.
all
secondary
(SOA)
formation
observed,
increasing
levels
after
few
hours
exposure
NO3
radicals.
change
composition
extent
depended
RH.
For
RH,
SOA
mass
formed
up
30%
initial
OA,
accompanied
moderate
both
O
C
(7-8%
increase)
spectrum.
Aging
RH
(60-80%)
led
more
oxygenated
(increase
11-18%),
but
only
minor
(1-10%)
increase
mass.
indicates
importance
heterogeneous
aqueous
reactions
system,
oxidize
original
relatively
small
net
These
results
show
can
chemically
evolve
photochemical
activity
(e.g.
wintertime
period)
important
enhancement
certain
conditions.
Aerosol Science and Technology,
Journal Year:
2024,
Volume and Issue:
unknown, P. 1 - 23
Published: Oct. 11, 2024
Biomass
burning
(BB)
is
a
major
source
of
atmospheric
fine
carbonaceous
aerosols,
which
play
significant,
yet
uncertain,
role
in
modulating
the
Earth's
radiation
balance.
However,
accurately
representing
their
optical
properties
climate
models
remains
challenging
due
to
factors
such
as
particle
size,
mixing
state,
combustion
type,
chemical
composition,
aging
processes,
and
relative
humidity
(RH).
In
our
study,
we
investigated
BB
organic-rich
aerosols
generated
from
smoldering
sub-Saharan
African
biomass
fuels.
Fuel
samples
were
collected
Africa
laboratory.
We
quantified
key
parameters,
including
mass
cross-sections
for
extinction
(2.04
±
0.32
−
15.5
2.48
m2/g),
absorption
(0.04
0.01–0.3
0.1
scattering
(1.9
0.68–15.3
5.5
m2/g).
Wavelength-dependent
used
determine
Ångström
exponents.
The
single
albedo
these
ranged
0.8
0.03
1.0
0.04
observed
wavelength-dependent
behavior.
Extinction
emission
determined
at
wavelength
550
nm,
with
values
ranging
42
5
293
32
m2/kg.
Notably,
exhibited
fuel-type
dependence,
differences
between
hardwood
other
fuels,
grass
animal
dung.
Aging
increased
while
had
opposite
effect
across
all
Nitrate
radical
oxidation,
both
photo
dark
conditions,
also
influenced
properties.
findings
are
expected
close
gap
understanding
aerosol
emissions
one
least
studied
regions
world
–
providing
information
air
quality
region.