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.
Environmental Science & Technology,
Год журнала:
2024,
Номер
58(17), С. 7493 - 7504
Опубликована: Апрель 18, 2024
Samples
of
brown
carbon
(BrC)
material
were
collected
from
smoke
emissions
originating
wood
pyrolysis
experiments,
serving
as
a
proxy
for
BrC
representative
biomass
burning
emissions.
The
acquired
samples,
referred
to
"pyrolysis
oil
(PO
ACS ES&T Air,
Год журнала:
2024,
Номер
1(5), С. 426 - 437
Опубликована: Апрель 9, 2024
Light-absorbing
secondary
organic
aerosols
(SOAs),
also
known
as
brown
carbon
(BrC),
are
major
components
of
wildfire
smoke
that
can
have
a
significant
impact
on
the
climate
system;
however,
how
environmental
factors
such
relative
humidity
(RH)
influence
their
formation
is
not
fully
understood,
especially
for
heterocyclic
precursors.
We
conducted
chamber
experiments
to
investigate
BrC
from
nighttime
oxidation
furan
and
pyrrole,
two
primary
precursors
in
wildfires,
presence
pre-existing
particles
at
RH
<
20%
∼
50%.
Our
findings
revealed
increasing
significantly
affected
size
distribution
dynamics
both
SOAs,
with
pyrrole
SOA
showing
stronger
potential
generate
ultrafine
via
intensive
nucleation
processes.
Higher
led
increased
mass
fractions
oxygenated
compounds
suggesting
enhanced
gas-phase
and/or
multiphase
under
humid
conditions.
Moreover,
higher
reduced
absorption
coefficients
BrC,
contrasting
those
homocyclic
precursors,
due
non-absorbing
high-molecular-weight
decreasing
molecular
chromophores.
Overall,
our
demonstrate
unique
dependence
which
may
critically
modulate
radiative
effects
change.
Environmental Science & Technology,
Год журнала:
2024,
Номер
58(46), С. 20588 - 20597
Опубликована: Ноя. 7, 2024
The
linkages
between
BrC
optical
properties
and
chemical
composition
remain
inadequately
understood,
with
quantified
chromophores
explaining
less
than
25%
of
ambient
aerosol
light
absorption.
This
study
characterized
38
typical
in
aerosols
collected
Xi'an,
absorption
contributions
to
ranging
from
1.6
±
0.3
5.8
2.6%
at
365
nm.
Based
on
these
chromophores,
an
interpretable
machine
learning
model
the
Shapley
Additive
Explanation
(SHAP)
method
were
employed
explore
relationships
composition.
attained
high
accuracy
Pearson
correlation
coefficients
(
Atmospheric chemistry and physics,
Год журнала:
2025,
Номер
25(2), С. 1401 - 1432
Опубликована: Янв. 31, 2025
Abstract.
This
study
investigated
the
effect
of
relative
humidity
(RH)
on
chemical
composition
gas
and
particle
phases
formed
from
photooxidation
1,3-butadiene
(13BD)
in
presence
NOx
under
acidified
non-acidified
seed
aerosol.
The
experiments
were
conducted
a
14.5
m3
smog
chamber
operated
steady-state
mode.
Products
identified
by
high-performance
liquid
chromatography,
chromatography–mass
spectrometry,
ultrahigh-performance
chromatography
coupled
with
high-resolution
mass
spectrometry.
More
than
50
oxygenated
products
identified,
including
33
organics,
10
organosulfates
(OSs),
PAN,
APAN,
glyoxal,
formaldehyde,
acrolein.
Secondary
organic
aerosol
(SOA)
reaction
depended
RH
acidity
Based
Extended
Aerosol
Inorganics
Model
(E-AIM),
originated
solutions
was
found
to
exist
aqueous
solid
phases,
respectively.
Although
terms
“acidified”
“non-acidified”
are
true
for
which
seeds
atomized,
there
far
more
fundamental
differences
between
phase
states
species
partition
or
(aqueous/solid),
considerably
affects
their
partitioning
formation
mechanisms.
SOA
most
(i)
higher
conditions,
where
particles
deliquescent,
did
not
contain
any
phase;
(ii)
increased
conditions;
(iii)
decreased
increasing
RH.
Glyceric
acid,
threitols,
threonic
acids,
four
dimers,
three
unknowns,
among
main
measured
either
conditions
across
all
levels.
Total
secondary
carbon
yield
both
conditions.
photochemical
reactivity
13BD
our
systems
faster
To
determine
contribution
ambient
aerosol,
we
analyzed
PM2.5
samples
collected
at
European
monitoring
stations
located
Poland.
occurrence
several
(e.g.,
glyceric
tartronic
tartaric
OSs)
field
suggests
that
could
contribute
formation.
Atmospheric chemistry and physics,
Год журнала:
2023,
Номер
23(23), С. 15077 - 15096
Опубликована: Дек. 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.
Atmosphere,
Год журнала:
2024,
Номер
15(11), С. 1294 - 1294
Опубликована: Окт. 28, 2024
Brown
carbon
aerosols
(BrC),
a
subfraction
of
organic
aerosols,
significantly
influence
the
atmospheric
environment,
climate
and
human
health.
The
North
China
Plain
(NCP)
is
hotspot
for
BrC
research
in
China,
yet
our
understanding
optical
properties
rural
regions
still
very
limited.
In
this
study,
we
characterize
chemical
components
light
absorption
at
site
during
winter
NCP.
average
mass
concentration
PM1
135.1
±
82.3
μg/m3;
organics
nitrate
are
main
PM1.
coefficient
(babs,BrC)
53.6
45.7
Mm−1,
accounting
39.5
10.2%
total
370
nm.
Diurnal
variations
reveal
that
babs,BrC
lower
afternoon,
attributed
to
evolution
planetary
boundary
layers.
mainly
emitted
locally,
both
aqueous
phase
photooxidation
reactions
can
increase
babs,BrC.
Notably,
reduced
when
RH
>
65%.
During
foggy
conditions,
facilitate
formation
secondary
contribute
bleaching
BrC.
This
process
ultimately
causes
decrease
Ångström
exponent
(AAE)
efficiency
(MAE).
contrast,
babs,BrC,
along
with
AAE
MAE,
rise
due
substantial
primary
emissions.
study
enhances
polluted
ACS Earth and Space Chemistry,
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 16, 2024
The
atmospheric
oxidation
of
naphthalene,
found
in
automobile
exhaust
and
biomass
burning
smoke,
forms
a
secondary
organic
aerosol
(SOA)
with
high
yield.
In
this
study,
near-explicit
gas
mechanism
for
the
photooxidation
naphthalene
presence
NOx
was
derived
using
box
model
platform.
initiated
by
an
OH
radical
produces
various
products,
including
naphthols,
nitronaphthols,
naphthoquinones,
ring-opening
organonitrates.
resulting
applied
to
UNIfied
Partitioning
Aerosol-phase
Reaction
(UNIPAR)
predict
SOA
formation
via
multiphase
reactions
naphthalene.
Semiexplicitly
predicted
products
were
sorted
construct
volatility-reactivity-based
two-dimensional
(2D)
lumping
species,
which
used
process
partitioning
organics
their
heterogeneous
chemistry
form
SOA.
performance
demonstrated
data
obtained
from
under
varying
conditions
(NOx
levels,
humidity,
temperature,
seed
types)
large
outdoor
photochemical
smog
chamber.
Major
mechanisms
compared
tentatively
identified
proton
transfer
reaction-mass
spectrometry.
simulated
organic-to-carbon
ratio
(0.72)
functional
groups
(0.70
±
0.7)
constructed
analysis
chamber-generated
Fourier
transform
infrared
Among
environmental
variables,
temperature
are
influential
formation.
A
strong
negative
relationship
appeared
between
levels
hydrocarbon
(HC)-limited
regions
(HC
ppbC/NOx
ppb
<5)
but
weakly
positive
at
NOx-limited
regions.
impact
aqueous
on
growth
insignificant
regardless
inorganic
types
(inorganic
liquid
water
content
acidity)
due
poor
solubility
phase.
Under
is
dominated
organic-phase
reactive,
low-volatile
multifunctional
aldehydes.
Both
are,
however,
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.