ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(26), P. 33451 - 33460
Published: June 20, 2024
Pillar-layered
metal-organic
frameworks
(PLMOFs)
are
promising
gas
adsorbents
due
to
their
high
designability.
In
this
work,
CO2
storage
capacity
as
well
controllable
C2H2/CO2
separation
ability
acquired
by
rationally
manipulating
the
interlayer
stacking
in
pillar-layered
MOF
materials.
The
rational
construction
of
MOFs
started
from
2D
Ni-BTC-pyridine
layer,
an
isomorphic
structure
pioneering
MOF-1
reported
1995.
replacement
terminal
pyridine
groups
bridging
pyrazine
linkers
under
optimized
solvothermal
conditions
led
three
3D
PLMOFs
with
different
types
between
adjacent
Ni-BTC
layers,
named
PLMOF
1
(ABAB
stacking),
2
(AABB
and
3
(AAAA
stacking).
Regulated
layer
arrangements,
C2H2
adsorption
capacities
(273
K
bar)
1-3
vary
173.0/153.3,
185.0/162.4,
203.5/159.5
cm3
g-1,
respectively,
which
surpass
values
most
adsorbents.
Dynamic
breakthrough
experiments
further
indicate
that
have
performance,
can
successfully
overcome
challenge.
Specially,
remove
trace
(3%)
mixture
produce
high-purity
ethylene
(99.9%)
one
step
productivities
1.68,
2.45,
3.30
mmol
respectively.
GCMC
simulations
superior
unique
performance
mainly
ascribed
degrees
agglomeration
ultramicropores
these
PLMOFs.
This
study
reports
on
the
rational
design
of
hydroxyl-functionalized
covalent
organic
framework
nanofibers
(HO-COFs:
PyTA-2,3-NA(OH)2
and
PyTA-2,6-NA(OH)2)
by
a
scalable
solvothermal
method.
The
resulting
HO-COF
is
more
hydrophilic
than
PyTA-2,6-NA(OH)2
HO-COF,
which
can
effectively
enhance
sensitivity
sensor
toward
basic
ethylenediamine
(EDA).
fabricated
nanofiber-based
quartz
crystal
microbalance
exhibits
rapid
sensing
response
distinguished
selectivity
EDA
vapor,
arising
from
strong
hydrogen
bonding
interactions
with
NH2
groups
EDA,
as
investigated
wide
variety
chemical
analysis
techniques
density
functional
theory
calculations.
presence
exposed
neighboring
hydroxyl
that
face
same
direction
in
present
exhibited
efficient
interactions.
nanofiber
1.6
times
higher
to
100
ppm
(ppm)
opposite
directions,
low
limit
detection
2.9
ppm.
structure
has
abundant
active
facing
direction,
making
them
favorable
sites
for
binding
molecules
through
bond
color
changed
after
exposure
colorimetric
assessment
naked-eye
detection.
These
exhibit
remarkable
other
interfering
vapors
show
high
stability
only
6.4%
drop
6
months.
adsorption
follows
pseudo-first-order
kinetic
model,
an
rate
about
8.0
faster
nanofibers.
findings
this
highlight
potential
use
COFs,
particularly
those
close
groups,
effective
materials
selective
harmful
EDA.
ACS Applied Materials & Interfaces,
Journal Year:
2024,
Volume and Issue:
16(26), P. 33451 - 33460
Published: June 20, 2024
Pillar-layered
metal-organic
frameworks
(PLMOFs)
are
promising
gas
adsorbents
due
to
their
high
designability.
In
this
work,
CO2
storage
capacity
as
well
controllable
C2H2/CO2
separation
ability
acquired
by
rationally
manipulating
the
interlayer
stacking
in
pillar-layered
MOF
materials.
The
rational
construction
of
MOFs
started
from
2D
Ni-BTC-pyridine
layer,
an
isomorphic
structure
pioneering
MOF-1
reported
1995.
replacement
terminal
pyridine
groups
bridging
pyrazine
linkers
under
optimized
solvothermal
conditions
led
three
3D
PLMOFs
with
different
types
between
adjacent
Ni-BTC
layers,
named
PLMOF
1
(ABAB
stacking),
2
(AABB
and
3
(AAAA
stacking).
Regulated
layer
arrangements,
C2H2
adsorption
capacities
(273
K
bar)
1-3
vary
173.0/153.3,
185.0/162.4,
203.5/159.5
cm3
g-1,
respectively,
which
surpass
values
most
adsorbents.
Dynamic
breakthrough
experiments
further
indicate
that
have
performance,
can
successfully
overcome
challenge.
Specially,
remove
trace
(3%)
mixture
produce
high-purity
ethylene
(99.9%)
one
step
productivities
1.68,
2.45,
3.30
mmol
respectively.
GCMC
simulations
superior
unique
performance
mainly
ascribed
degrees
agglomeration
ultramicropores
these
PLMOFs.