Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(8), P. 3776 - 3786
Published: Feb. 12, 2024
Phenols
emitted
from
biomass
burning
contribute
significantly
to
secondary
organic
aerosol
(SOA)
formation
through
the
partitioning
of
semivolatile
products
formed
gas-phase
chemistry
and
multiphase
in
liquid
water
clouds.
The
aqueous-phase
SOA
(aqSOA)
via
hydroxyl
radical
(•OH),
singlet
molecular
oxygen
(1O2*),
triplet
excited
states
compounds
(3C*),
which
oxidize
dissolved
phenols
aqueous
phase,
might
play
a
significant
role
evolution
(OA).
However,
quantitative
predictive
understanding
aqSOA
has
been
challenging.
Here,
we
develop
stand-alone
box
model
investigate
•OH
by
dissolution
followed
their
reactions
with
•OH,
1O2*,
3C*
cloud
droplets
water.
We
four
phenolic
compounds,
i.e.,
phenol,
guaiacol,
syringol,
guaiacyl
acetone
(GA),
represent
some
key
potential
sources
For
same
initial
precursor
gas
that
dissolves
aerosol/cloud
subsequently
reacts
phase
oxidants,
predict
(defined
as
per
unit
concentration)
these
is
higher
than
isoprene-epoxydiol
(IEPOX),
well-known
precursor.
Cloud
can
dissolve
broader
range
soluble
compared
aerosols,
since
contents
aerosols
are
orders
magnitude
smaller
droplets.
Our
simulations
suggest
highly
reactive
multifunctional
like
GA
would
predominantly
undergo
within
layers,
while
likely
be
more
important
for
less
phenols.
But
absence
clouds,
condensation
low-volatility
oxidation
reversible
dominates
formation,
increases
relative
humidity
(RH),
approaching
40%
sum
at
95%
RH
GA.
developments
biomass-burning
readily
implemented
regional
global
atmospheric
models
gases
atmosphere.
Environmental Science & Technology,
Journal Year:
2022,
Volume and Issue:
56(6), P. 3645 - 3657
Published: March 1, 2022
Wildfire-influenced
air
masses
under
regional
background
conditions
were
characterized
at
the
Mt.
Bachelor
Observatory
(∼2800
m
a.s.l.)
in
summer
2019
to
provide
a
better
understanding
of
aging
biomass
burning
organic
aerosols
(BBOAs)
and
their
impacts
on
remote
troposphere
western
United
States.
Submicron
aerosol
(PM1)
concentrations
low
(average
±
1σ
=
2.2
1.9
μg
sm–3),
but
oxidized
BBOAs
O/C
0.84)
constantly
detected
throughout
study.
The
BBOA
correlated
well
with
black
carbon,
furfural,
acetonitrile
comprised
above
50%
PM1
during
plume
events
when
peak
concentration
reached
18.0
sm–3.
Wildfire
plumes
estimated
transport
times
varying
from
∼10
h
>10
days
identified.
showed
ΔOA/ΔCO
values
ranging
0.038
0.122
ppb
ppb–1
significant
negative
relation
age,
indicating
loss
relative
CO
long-range
transport.
Additionally,
increases
average
sizes
seen
more
aged
plumes.
mass-based
size
mode
was
approximately
700
nm
(Dva)
most
that
likely
originated
Siberia,
suggesting
aqueous-phase
processing
This
work
highlights
widespread
wildfire
emissions
have
properties,
thus
climate,
Environmental Science & Technology,
Journal Year:
2022,
Volume and Issue:
56(14), P. 9959 - 9967
Published: July 1, 2022
Biomass
burning
(BB)
releases
large
quantities
of
phenols
(ArOH),
which
can
partition
into
cloud/fog
drops
and
aerosol
liquid
water
(ALW),
react,
form
aqueous
secondary
organic
(aqSOA).
While
simple
are
too
volatile
to
significantly
particle
water,
highly
substituted
ArOH
more
strongly
might
be
important
sources
aqSOA
in
ALW.
To
investigate
this,
we
measured
the
·OH
oxidation
kinetics
yields
for
six
from
BB.
Second-order
rate
constants
high,
range
(1.9-14)
×
109
M-1
s-1
at
pH
2
(14-25)
5
6.
Mass
also
with
an
average
(±1σ)
value
82
(±12)%.
ALW
solutes
have
a
impacts
on
phenol
by
·OH:
BB
sugar
some
inorganic
salts
suppress
oxidation,
while
nitrate
salt
transition
metals
enhance
oxidation.
Finally,
estimated
rates
aqueous-
gas-phase
formation
SOA
single
as
function
content
(LWC),
conditions
(0.1
g-H2O
m-3)
(10
μg-H2O
m-3).
Formation
is
significant
across
LWC
range,
although
becomes
dominant
under
conditions.
We
see
generally
discrepancy
between
modeled
concentrations
range.
Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(8), P. 3776 - 3786
Published: Feb. 12, 2024
Phenols
emitted
from
biomass
burning
contribute
significantly
to
secondary
organic
aerosol
(SOA)
formation
through
the
partitioning
of
semivolatile
products
formed
gas-phase
chemistry
and
multiphase
in
liquid
water
clouds.
The
aqueous-phase
SOA
(aqSOA)
via
hydroxyl
radical
(•OH),
singlet
molecular
oxygen
(1O2*),
triplet
excited
states
compounds
(3C*),
which
oxidize
dissolved
phenols
aqueous
phase,
might
play
a
significant
role
evolution
(OA).
However,
quantitative
predictive
understanding
aqSOA
has
been
challenging.
Here,
we
develop
stand-alone
box
model
investigate
•OH
by
dissolution
followed
their
reactions
with
•OH,
1O2*,
3C*
cloud
droplets
water.
We
four
phenolic
compounds,
i.e.,
phenol,
guaiacol,
syringol,
guaiacyl
acetone
(GA),
represent
some
key
potential
sources
For
same
initial
precursor
gas
that
dissolves
aerosol/cloud
subsequently
reacts
phase
oxidants,
predict
(defined
as
per
unit
concentration)
these
is
higher
than
isoprene-epoxydiol
(IEPOX),
well-known
precursor.
Cloud
can
dissolve
broader
range
soluble
compared
aerosols,
since
contents
aerosols
are
orders
magnitude
smaller
droplets.
Our
simulations
suggest
highly
reactive
multifunctional
like
GA
would
predominantly
undergo
within
layers,
while
likely
be
more
important
for
less
phenols.
But
absence
clouds,
condensation
low-volatility
oxidation
reversible
dominates
formation,
increases
relative
humidity
(RH),
approaching
40%
sum
at
95%
RH
GA.
developments
biomass-burning
readily
implemented
regional
global
atmospheric
models
gases
atmosphere.