The
products
of
incomplete
destruction
(PIDs)
per-
and
polyfluoroalkyl
substances
(PFAS)
represent
a
substantial
ambiguity
when
employing
thermal
treatments
to
remediate
PFAS-contaminated
materials.
In
this
study,
we
present
new
information
on
PIDs
produced
in
both
inert
oxidative
environments
from
five
long-chain
PFAS,
including
three
now
regulated
under
the
U.S.
Safe
Drinking
Water
Act,
one
cationic
precursor
compound,
C10
PFAS.
data
did
not
support
generation
tetrafluoromethane
any
studied
carbonyl
fluoride
was
found
only
potassium
perfluorooctanesulfonate
(K-PFOS)
heated
air
narrow
temperature
range.
Oxidative
conditions
(air)
were
observed
facilitate
PFAS
degradation
accelerate
mineralization
K-PFOS.
Spectroscopic
suggest
that
is
initiated
by
cleavage
bonds
form
perfluoroalkyl
radicals,
leading
organofluorine
(e.g.,
perfluoroalkenes).
air,
radicals
react
with
oxygen
oxygen-containing
PIDs.
enhanced
adding
solid
additives,
which
categorized
as
highly
effective
granular
activated
carbon
(GAC)
certain
noble
metals),
moderately
effective,
noneffective.
Remarkably,
simply
GAC,
achieved
>90%
perfluorooctanoic
acid
at
300
°C
∼1.9
atm
within
just
60
min
without
using
water
or
solvents.
The
nonthermal
destruction
of
aqueous
film-forming
foam
(AFFF)
stockpiles,
one
the
major
culprits
responsible
for
water
and
soil
contamination
by
per-
polyfluoroalkyl
substances
(PFAS),
is
extremely
challenging
because
coexistence
mixed
recalcitrant
PFAS
complicated
organic
matrices
at
high
concentrations.
To
date,
complete
defluorination
undiluted
AFFF
ambient
conditions
has
not
been
demonstrated.
This
study
reports
a
novel
piezoelectric
ball
milling
approach
treating
with
total
fluorine
concentration
9080
mg/L
carbon
234
g/L.
Near-complete
(>95%
conversion
organofluorine
to
fluoride)
was
achieved
comilling
boron
nitride.
By
carefully
examining
experimental
data,
we
identified
liquid
film
thickness
(Z)
collision
interface
as
descriptor
treatment
performance.
We
further
validated
that
effective
proceeded
when
Z
less
than
criteria
value
2.3
μm.
In
light
this
new
understanding,
addition
SiO2
dispersant
pre-evaporation
solvents
reduce
have
strategies
promote
capacity.
ACS ES&T Water,
Journal Year:
2024,
Volume and Issue:
4(4), P. 1191 - 1205
Published: March 8, 2024
Recent
literature
has
seen
a
significant
surge
in
studies
focusing
on
new
adsorbent
materials
for
per-
and
polyfluoroalkyl
substances
(PFASg),
class
of
contaminants
found
natural
waters
worldwide
that
pose
considerable
threat
to
human
environmental
health.
Despite
growing
interest,
the
fundamental
mechanisms
PFAS
adsorption
these
are
not
fully
understood,
thus
hindering
progress
developing
effective
solutions
removal.
This
Review
aims
bridge
knowledge
gap
by
offering
critical
appraisal
recent
innovations
specifically
designed
treating
PFAS.
Strategies
aimed
at
enhancing
nanopore
capacity
or
introducing
anion-exchange
capabilities
have
shown
promise.
Innovative
such
as
carbon
nanotubes,
graphene,
graphene
oxide
evaluated.
Modified
clay-based
silica-based
adsorbents
demonstrated
efficacy
removing
PFAS,
driven
hydrophobic
effect,
Coulombic
interactions,
electrostatic
interactions.
Polymers,
ranging
from
types
synthetic
variants,
promise
removal
across
wide
pH
range.
We
discuss
including
F–F
ion-pair
adsorption,
ion
exchange
chemically
thermally
modified
provide
general
guideline
design
adsorbents.
offers
holistic
view
advances
related
materials.
Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(8), P. 3942 - 3952
Published: Feb. 13, 2024
Aqueous
film-forming
foams
(AFFFs)
are
used
in
firefighting
applications
and
often
contain
per-
polyfluoroalkyl
substances
(PFAS),
which
can
detrimentally
impact
environmental
biological
health.
Incineration
is
a
potential
disposal
method
for
AFFFs,
may
produce
secondary
PFAS
other
air
pollutants.
We
online
chemical
ionization
mass
spectrometry
(CIMS)
to
measure
volatile
emissions
from
incinerating
AFFF
concentrate
solutions.
quantified
perfluorinated
carboxylic
acids
(PFCAs)
during
the
incineration
of
legacy
contemporary
AFFFs.
These
included
trifluoroacetic
acid,
reached
mg
m–3
quantities
incinerator
exhaust.
PFCAs
likely
arose
as
products
incomplete
combustion
fluorosurfactants
with
lower
peak
furnace
temperatures
yielding
higher
PFCA
concentrations.
also
detected
short-chain
PFAS,
novel
emissions.
The
headspace
above
solutions
contained
larger
(C
≥
8),
less
oxidized
by
CIMS.
identified
neutral
resembling
fluorotelomer
surfactants
(e.g.,
sulfonamide
alkylbetaines
thioether
amido
sulfonates)
alcohols
headspaces.
Directly
comparing
distinct
spaces
byproducts
measured
CIMS
provides
insight
toward
chemistry
thermal
treatment
Environmental Science & Technology,
Journal Year:
2024,
Volume and Issue:
58(25), P. 11162 - 11174
Published: June 10, 2024
Thermal
treatment
has
emerged
as
a
promising
approach
for
either
the
end-of-life
or
regeneration
of
granular
activated
carbon
(GAC)
contaminated
with
per-
and
polyfluoroalkyl
substances
(PFAS).
However,
its
effectiveness
been
limited
by
requirement
high
temperatures,
generation
products
incomplete
destruction,
necessity
to
scrub
HF
in
flue
gas.
This
study
investigates
use
common
alkali
alkaline-earth
metal
additives
enhance
mineralization
perfluorooctanesulfonate
(PFOS)
adsorbed
onto
GAC.
When
treated
at
800
°C
without
an
additive,
only
49%
PFOS
was
mineralized
HF.
All
tested
demonstrated
improved
mineralization,
Ca(OH)2
had
best
performance,
achieving
efficiency
98%
air
N2.
Its
ability
increase
reaction
rate
shift
byproduct
selectivity
suggests
that
role
may
be
catalytic.
Moreover,
reduced
gas
instead
reacting
additive
form
inorganic
fluorine
(e.g.,
CaF2)
starting
waste
material.
A
hypothesized
mechanism
is
proposed
involves
electron
transfer
from
O2–
defect
sites
CaO
intermediates
formed
during
thermal
decomposition
PFOS.
These
findings
advocate
GAC
disposal
reuse,
potential
reduce
operating
costs
mitigate
environmental
impact
associated
incinerating
PFAS-laden
wastes.
ACS ES&T Engineering,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 2, 2025
Recent
studies
of
thermal
PFAS
destruction
have
reported
seemingly
incoherent
temperatures
and
products,
often
because
decomposition
pathways
are
highly
dependent
on
the
respective
experimental
system.
Here,
we
applied
accurate
DLPNO–CCSD(T)
coupled
cluster
calculations
to
isolate
identify
major
processes
during
in
gas
phase,
with
relevance
incineration,
oxidation,
other
treatment
technologies
which
their
volatile
products
desorb
into
phase.
All
investigated
perfluoroalkyl
acids
decompose
via
unimolecular
headgroup
loss,
either
through
HF
elimination
or
homolytic
bond
cleavage
as
a
function
type.
In
contrast,
all
fluorotelomers
undergo
initial
hydrogen
abstraction
from
characteristic
C2H4
moiety
by
hydroxyl
radicals
under
representative
incineration
conditions,
followed
radical
decomposition.
Subsequent
formation
perfluoroalkanes,
including
CF4,
can
then
be
prevented
supplying
sufficient
donors
such
hydrocarbon
fuel
water
well
scavenging
released
fluorine.
This
leads
generation
stable
1H-perfluoroalkanes.
While
parent
proceeds
at
gas-phase
≤700
°C,
carbon–carbon
1H-perfluoroalkanes
requires
up
∼950
°C
2
s
residence
time,
making
this
step
kinetic
bottleneck
way
complete
mineralization.
Environmental Science & Technology Letters,
Journal Year:
2025,
Volume and Issue:
12(2), P. 104 - 112
Published: Jan. 23, 2025
Per-
and
polyfluoroalkyl
substances
(PFAS)
have
garnered
increasing
attention
in
recent
years,
non-targeted
analysis
(NTA)
has
become
essential
for
elucidating
novel
PFAS
structures.
NTA
research
been
dominated
by
liquid
chromatography–mass
spectrometry
(LC-MS)
with
gas
(GC-MS)
used
less
often
as
evidenced
bibliometrics.
However,
the
performance
of
GC-MS
studies
(GC-NTA)
rivals
that
LC-ESI-MS,
is
shown
to
cover
a
complementary
chemical
space.
An
LC-ESI-MS
amenability
model
applied
list
approximately
12,000
revealed
than
10%
known
chemistry
predicted
be
amenable
typical
LC-MS
analysis.
Therefore,
there
strong
potential
applying
methods
more
fully
assess
environmental
contamination
landscape,
uniquely
shedding
light
on
both
PFAS,
especially
within
space
realm
volatile
semivolatile
PFAS.
Waste
streams
from
fluorochemical
manufacturing
facilities
heavily
studied
using
targeted
GC-MS;
however,
GC-NTA
needed
discover
are
not
emitted
facilities.
Studies
incineration
PFAS-containing
materials,
such
aqueous
film
forming
foam,
focused
destruction
parent
compounds,
little
about
transformation
products
formed
during
processes.
holds
elucidate
when
incinerated.
Wastewater
treatment
plants
landfills
sources
environment,
yet
understand
air
emissions
these
sources.
Consumer
lead
indoor
exposures
via
dust,
but
this
area
either
or
GC-MS.
Despite
challenges
advancing
GC-NTA,
we
call
researchers,
grantors,
managers,
other
stakeholders
recognize
necessity
so
may
face
together.