RSC Advances,
Journal Year:
2025,
Volume and Issue:
15(11), P. 8287 - 8292
Published: Jan. 1, 2025
We
demonstrate
complete
photo-assisted
electrocatalytic
defluorination
of
PFAS
in
AFFF
using
nonprecious
materials.
High-salt
LiOH
electrolyte
prevents
foaming,
and
pulsed
electrolysis
with
tailored
potential
modulation
optimizes
defluorination.
Ecotoxicology and Environmental Safety,
Journal Year:
2023,
Volume and Issue:
267, P. 115663 - 115663
Published: Nov. 1, 2023
Per-
and
polyfluoroalkyl
substances
(PFAS)
are
synthetic
chemicals
that
have
been
widely
utilized
in
various
industries
since
the
1940s,
now
emerged
as
environmental
contaminants.
In
recent
years,
perfluorooctanoic
acid
(PFOA)
perfluorooctane
sulfonate
(PFOS)
restricted
replaced
with
several
alternatives.
The
high
persistence,
bioaccumulation,
toxicity
of
these
contributed
to
their
emergence
contaminants,
aspects
behavior
remain
largely
unknown
require
further
investigation.
trace
level
PFAS
makes
development
a
monitoring
database
challenging.
Additionally,
potential
health
issues
associated
not
yet
fully
understood
due
ongoing
research
inadequate
evidence
(experimental
epidemiological
studies),
especially
regard
combined
effects
exposure
mixtures
human
risks
from
drinking
water
consumption.
This
in-depth
review
offers
unprecedented
insights
into
pathways
toxicological
impacts
PFAS,
addressing
critical
knowledge
gaps
behaviors
implications.
It
presents
comprehensive
NABC—Needs,
Approach,
Benefits,
Challenges—analysis
guide
future
strategies
for
sustainable
management
pervasive
ACS ES&T Water,
Journal Year:
2023,
Volume and Issue:
3(4), P. 1201 - 1211
Published: March 15, 2023
Per-
and
polyfluoroalkyl
substances
(PFAS)
are
persistent
synthetic
contaminants
that
present
globally
in
water
exceptionally
difficult
to
remove
during
conventional
treatment
processes.
Here,
we
demonstrate
a
practical
train
combines
foam
fractionation
concentrate
PFAS
from
groundwater
landfill
leachate,
followed
by
an
electrochemical
oxidation
(EO)
step
degrade
the
PFAS.
The
study
combined
up-scaled
experimental
approach
with
thorough
characterization
strategies,
including
target
analysis,
sum
parameters,
toxicity
testing.
Additionally,
EO
kinetics
were
successfully
reproduced
newly
developed
coupled
numerical
model.
mean
total
degradation
over
designed
reached
50%,
long-
short-chain
degrading
up
86
31%,
respectively.
resulted
decrease
toxic
potency
of
water,
as
assessed
transthyretin
binding
bacterial
bioluminescence
bioassays.
Moreover,
extractable
organofluorine
concentration
decreased
44%.
Together,
these
findings
provide
improved
understanding
promising
for
on-site
remediation
PFAS-contaminated
water.
Chinese Journal of Chemistry,
Journal Year:
2024,
Volume and Issue:
42(16), P. 1913 - 1928
Published: April 24, 2024
Comprehensive
Summary
Organic
fluorine
compounds
are
ubiquitous
and
pivotally
important
organic
molecules,
yet
their
activation
transformation
have
long
been
a
formidable
challenge
due
to
the
high
energy
low
reactivity
of
C—F
bonds.
electrosynthesis,
an
environmentally
benign
synthetic
method
in
chemistry,
enables
myriad
chemical
transformations
without
need
for
external
redox
reagents.
In
recent
years,
electrochemistry
has
emerged
as
powerful
tool
achieving
bonds
fluorine‐containing
compounds.
This
review
aims
succinctly
recapitulate
latest
advancements
electrochemical
defluorinative
delve
into
reaction
design,
mechanistic
insights,
developmental
prospects
these
methods.
Key
Scientists
1959,
Lund
was
first
pioneer
electroreduction
CF
3
CH
group.
Electrochemistry
lately
provided
new
opportunities
efficient
conversion
fluorides.
2020,
Zhou
coworkers
discovered
carboxylation
α‐CF
alkenes.
Lambert
colleagues
reported
electrophotocatalytic
amination
aryl
Electrochemical
hydrodefluorination
trifluoromethylketones
developed
by
Lennox
2021.
same
year,
Wang
Guo
disclosed
radical
alkylation
alkenes
with
Katritzky
salts
alkyl
precursors.
Subsequently,
Wu
Liao
described
transition‐metal‐free,
site‐selective
arylation
polyfluoroarenes
(het)arenes
using
paired
electrophotocatalysis.
2023,
numerous
efforts
were
made
achieve
bond
activation.
Xia
organoboron‐controlled
chemoselective
sequential
(deutero)hydrodefluorination
trifluoroacetamides.
Chemosphere,
Journal Year:
2024,
Volume and Issue:
357, P. 142088 - 142088
Published: April 20, 2024
Per-
and
poly-fluoroalkyl
substances
(PFAS)
are
synthetic
chemicals
widely
used
in
everyday
products,
causing
elevated
concentrations
drinking
water
posing
a
global
challenge.
While
adsorption
methods
commonly
employed
for
PFAS
removal,
the
substantial
cost
environmental
footprint
of
commercial
adsorbents
highlight
need
more
cost-effective
alternatives.
Additionally,
existing
exhibit
limited
effectiveness,
particularly
against
diverse
types,
such
as
short-chain
PFAS,
necessitating
modifications
to
enhance
capacity.
Biochar
can
be
considered
eco-friendly
alternative
conventional
adsorbents.
With
abundant
feedstocks
favorable
physicochemical
properties,
biochar
shows
significant
potential
applied
an
adsorbent
removing
contaminants
from
water.
Despite
its
effectiveness
adsorbing
different
inorganic
organic
environments,
some
factors
restrict
effective
application
adsorption.
These
related
characteristics
well
chemistry.
Therefore,
have
been
introduced
overcome
these
limitations
improve
biochar's
This
review
explores
preparation
conditions,
including
pyrolysis
process,
activation,
modification
techniques
capacity
types
PFAS.
It
addresses
critical
questions
about
performance
composites,
mechanisms
governing
adsorption,
challenges,
future
perspectives
this
field.
The
surge
research
on
indicates
growing
interest,
making
timely
valuable
resource
in-depth
exploration
remediation.
Journal of the American Chemical Society,
Journal Year:
2024,
Volume and Issue:
146(15), P. 10687 - 10698
Published: April 5, 2024
Perfluorooctanoic
acid
(PFOA)
is
an
artificial
chemical
of
global
concern
due
to
its
high
environmental
persistence
and
potential
human
health
risk.
Electrochemical
methods
are
promising
technologies
for
water
treatment
because
they
efficient,
cheap,
scalable.
The
electrochemical
reduction
PFOA
one
the
current
methodologies.
This
process
leads
defluorination
carbon
chain
hydrogenated
products.
Here,
we
describe
a
mechanistic
study
in
gold
electrodes.
By
using
linear
sweep
voltammetry
(LSV),
E0′
−1.80
V
vs
Ag/AgCl
was
estimated.
Using
scan
rate
diagnosis,
determined
electron-transfer
coefficient
(αexp)
0.37,
corresponding
concerted
mechanism.
strong
adsorption
into
surface
confirmed
by
Langmuir-like
isotherm
absence
(KA
=
1.89
×
1012
cm3
mol–1)
presence
negative
3.94
107
mol–1,
at
−1.40
Ag/AgCl).
Based
on
Marcus–Hush's
theory,
calculations
show
solvent
reorganization
energy
(λ0)
0.9
eV,
suggesting
large
electrostatic
repulsion
between
perfluorinated
water.
estimated
free
transition
state
electron
transfer
(ΔG‡
2.42
eV)
suggests
that
it
thermodynamically
reaction-limiting
step.
19F
–
1H
NMR,
UV–vis,
mass
spectrometry
studies
confirm
displacement
fluorine
atoms
hydrogen.
Density
functional
theory
(DFT)
also
support
mechanism
reductive
PFOA,
agreement
with
experimental
values.