Abstract
Eight
granular
activated
carbons
(GAC),
four
anion
exchange
(IX)
resins,
and
two
alternative
adsorbents
(AAs)
were
tested
for
the
removal
of
per‐
polyfluoroalkyl
substances
(PFAS)
from
a
groundwater
source
used
drinking
water.
The
study
was
conducted
using
pilot(meter)‐scale
columns
operated
in
continuous‐flow
mode
16–26
months.
Comparison
between
GAC
showed
that
bituminous
GACs
exhibited
higher
adsorption
than
non‐/sub‐bituminous
GACs.
Testing
reactivated
new
no
significant
differences
with
respect
to
PFAS
adsorption.
Of
IX
resins
tested,
one
resin
superior
when
compared
all
three
resins.
A
surface‐modified
bentonite
adsorbent
efficiencies
over
types
here.
These
results
provide
benchmark
performance
capacities
at
pilot‐scale
various
highlight
promise
AAs
remove
water
sources
low
(ng/L)
concentrations.
Environmental Science & Technology,
Год журнала:
2021,
Номер
55(22), С. 15162 - 15171
Опубликована: Окт. 29, 2021
Harmful
per-
and
polyfluoroalkyl
substances
(PFAS)
are
ubiquitously
detected
in
aquatic
environments,
but
their
remediation
remains
challenging.
Metal–organic
frameworks
(MOFs)
have
been
recently
identified
as
an
advanced
material
class
for
the
efficient
removal
of
PFAS,
little
is
known
about
fundamentals
PFAS@MOF
adsorption
process.
To
address
this
knowledge
gap,
we
evaluated
performance
3
different
MOFs
8
PFAS
classes
from
aqueous
film-forming
foam-impacted
groundwater
samples
obtained
11
U.S.
Air
Force
installations.
Due
to
pore
sizes/shapes
identity
metal
node,
NU-1000,
UiO-66,
ZIF-8
were
selected
investigate
role
MOF
structures,
properties,
water
matrix
on
We
observed
that
(i)
dominated
by
electrostatic
acid–base
interactions
anionic
non-ionic
respectively,
(ii)
preferred
long-
over
short-chain
(iii)
strongly
dependent
nature
head
group
functionality,
(iv)
compromised
presence
ionic
neutral
co-contaminants
competing
ion-exchange
sites
binding.
With
study,
elucidate
mechanism
complex
sources
guide
design
more
treatment
PFAS-contaminated
bodies.
Environmental Science & Technology,
Год журнала:
2022,
Номер
56(10), С. 6699 - 6709
Опубликована: Апрель 27, 2022
The
water
shortage
crisis,
characterized
by
organic
micropollutants
(OMPs),
urgently
requires
new
materials
and
methods
to
deal
with
it.
Although
heteroatom
doping
has
been
developed
into
an
effective
method
modify
carbon
nanomaterials
for
various
heterogeneous
adsorption
catalytic
oxidation
systems,
the
active
source
regulated
intrinsic
electron
spin
structures
is
still
obscure.
Here,
a
series
of
nonmetallic
element-doped
(such
as
P,
S,
Se)
covalent
triazine
frameworks
(CTFs)
were
constructed
applied
remove
pollutants
using
adsorption-photocatalysis
process.
external
mass
transfer
model
(EMTM)
homogeneous
surface
diffusion
(HSDM)
employed
describe
It
was
found
that
sulfur-doped
CTF
(S-CTF-1)
showed
25.6-fold
increase
in
saturated
capacity
(554.7
μmol/g)
169.0-fold
surge
photocatalytic
kinetics
(5.07
h-1),
respectively,
compared
pristine
CTF-1.
A
positive
correlation
between
accumulation
at
site
(N1
atom)
energy
further
demonstrated
experimental
results
theoretical
calculations.
Meanwhile,
degradation
rates
greatly
enhanced
forming
built-in
electric
field
driven
polarization.
In
addition,
S-CTF-1
maintained
98.3%
removal
2,2',4,4'-tetrahydroxybenzophenone
(BP-2)
97.6%
regeneration
after
six-cycle
sequencing
batch
treatment
real
matrices.
This
work
established
relation
photocatalysis,
paving
way
design
modified
control
OMPs.
Microbial Biotechnology,
Год журнала:
2021,
Номер
15(3), С. 773 - 792
Опубликована: Сен. 27, 2021
Poly-
and
perfluorinated
chemicals,
including
alkyl
substances
(PFAS),
are
pervasive
in
today's
society,
with
a
negative
impact
on
human
ecosystem
health
continually
emerging.
These
chemicals
now
subject
to
strict
government
regulations,
leading
costly
environmental
remediation
efforts.
Commercial
polyfluorinated
compounds
have
been
called
'forever
chemicals'
due
their
strong
resistance
biological
chemical
degradation.
Environmental
cleanup
by
bioremediation
is
not
considered
practical
currently.
Implementation
of
will
require
uncovering
understanding
the
rare
microbial
successes
degrading
these
compounds.
This
review
discusses
underlying
reasons
why
degradation
heavily
fluorinated
rare.
Fluorinated
chlorinated
very
different
respect
chemistry
physiology.
Moreover,
end
product
biodegradation,
fluoride,
much
more
toxic
than
chloride.
It
imperative
understand
limitations,
elucidate
physiological
mechanisms
defluorination,
order
better
discover,
study,
engineer
bacteria
that
can
efficiently
degrade
Membranes,
Год журнала:
2022,
Номер
12(7), С. 662 - 662
Опубликована: Июнь 27, 2022
Per-
and
Polyfluoroalkyl
Substances
(PFAS)
are
anthropogenic
chemicals
consisting
of
thousands
individual
species.
PFAS
consists
a
fully
or
partly
fluorinated
carbon-fluorine
bond,
which
is
hard
to
break
requires
high
amount
energy
(536
kJ/mole).
Resulting
from
their
unique
hydrophobic/oleophobic
nature
chemical
mechanical
stability,
they
highly
resistant
thermal,
chemical,
biological
degradation.
have
been
used
extensively
worldwide
since
the
1940s
in
various
products
such
as
non-stick
household
items,
food-packaging,
cosmetics,
electronics,
firefighting
foams.
Exposure
may
lead
health
issues
hormonal
imbalances,
compromised
immune
system,
cancer,
fertility
disorders,
adverse
effects
on
fetal
growth
learning
ability
children.
To
date,
very
few
novel
membrane
approaches
reported
effective
removing
destroying
PFAS.
Therefore,
this
article
provides
critical
review
treatment
removal
by
separation
systems.
We
discuss
recently
techniques
for
include
detailed
discussion
parameters
affecting
destruction.
Moreover,
an
estimation
cost
analysis
also
included
each
technology.
Additionally,
technology
still
growing,
we
incorporated
several
future
directions
efficient
treatment.
ACS Central Science,
Год журнала:
2022,
Номер
8(5), С. 663 - 669
Опубликована: Май 16, 2022
Cross-linked
polymers
containing
β-cyclodextrin
(β-CD)
are
promising
adsorbents
with
demonstrated
removal
performances
for
per-
and
polyfluoroalkyl
substances
(PFASs)
from
contaminated
water
sources.
Despite
the
performance
of
some
β-CD-based
PFAS
removal,
many
these
materials
not
amenable
rational
improvement
or
addressing
fundamental
questions
about
adsorption
mechanisms.
These
ambiguities
arise
poorly
defined
structure
cross-linked
polymers,
especially
respect
to
random
substitution
patterns
cyclodextrins
as
well
side
reactions
that
modify
structures
cross-linkers.
Here,
we
report
a
new
β-CD
polymer
platform
in
which
styrene
groups
covalently
attached
form
discrete
monomer
is
radical
polymerization.
This
was
polymerized
methacrylate
comonomers
provide
three
high
specific
surface
areas
isolated
yields
(all
>93%).
A
copolymerized
bearing
cationic
functional
group
achieved
nearly
100%
eight
anionic
PFASs
(initial
concentration
1
μg/L
each
compound)
nanopure
at
an
exceedingly
low
adsorbent
loading
mg
L-1,
compared
previous
cyclodextrin
required
loadings
least
order
magnitude
higher
achieve
equivalent
degree
removal.
Furthermore,
when
were
studied
challenging
salt
matrix,
observed
long-chain
controlled
by
complementary
interplay
hydrophobic
electrostatic
interactions,
whereas
short-chain
primarily
relied
on
interactions.
approach
demonstrates
great
promise
anticipate
compositions
will
be
tailored
using
versatility
polymerization
simultaneously
target
other
classes
micropollutants
future.
ACS ES&T Water,
Год журнала:
2022,
Номер
2(12), С. 2258 - 2272
Опубликована: Ноя. 3, 2022
Per-
and
polyfluoroalkyl
substances
(PFAS)
are
a
group
of
manmade
chemicals,
which
persistent
in
the
environment,
bioaccumulative,
toxic
to
humans.
Various
treatment
technologies
have
been
used
remove
PFAS
from
water,
among
them
adsorption
membrane
filtration
shown
greater
effectiveness
removal.
Therefore,
main
objective
this
article
is
provide
review
on
current
literature
investigating
removal
by
technologies.
The
specific
focus
explore
separation
mechanisms
involved
existing
challenges
adsorbents/membranes.
This
highlights
research
needs
for
developing
more
efficient
ACS Materials Letters,
Год журнала:
2022,
Номер
4(5), С. 853 - 859
Опубликована: Апрель 4, 2022
Contamination
of
natural
water
resources
by
per-
and
polyfluorinated
alkyl
substances
(PFAS)
has
affected
millions
people
around
the
world
emphasized
need
for
development
novel
effective
adsorbent
materials.
We
demonstrate
how
atomistic
molecular
dynamics
(MD)
simulations
can
be
used
to
provide
scale
insight
into
role
electrostatic
hydrophobic
interactions
on
adsorption
perfluorooctanoate
(PFOA)
surfactant,
a
prominent
longer-chain
PFAS,
polymer-based
network
in
water.
Specifically,
ammonium
salt
been
investigated
β-cyclodextrin
(CD)
cross-linked
with
decafluorobiphenyl
linkers
as
an
example
absorbent
material
that
already
demonstrated
efficient
PFAS
adsorption.
Examination
pairwise
reveals
importance
dual
pronged
mechanism
involving
both
interactions.
The
counterions
CD
segments
facilitates
attraction
anionic
headgroup
PFOA
while
fluorinated
additional
tail
well
higher
affinity
toward
comparison
hydrocarbons.
These
competing
result
primarily
outside
cavity
mostly
interacting
linkers.
using
"what
if"
scenarios
are
powerful
approach
infer
different
PFAS.