Adding
burning-rate
catalysts
(BRCs)
is
highly
effective
for
enhancing
ammonium
perchlorate
(AP)
thermal
decomposition.
To
mitigate
BRCs’
agglomeration
and
enhance
their
catalytic
activity
AP
pyrolysis,
five
metal
carbonyl
compounds
(Mo(CO)6,
Cr(CO)6,
W(CO)6,
Fe2(CO)9,
Mn2(CO)10)
were
refined
into
oxidized
carbon
nanotube
(CNTs)
cavities,
respectively,
by
ultrasonication.
The
structures
of
the
as-prepared
nanocomposites
examined
with
TEM,
SEM,
XPS,
Raman,
etc.,
confirming
successful
filling
compounds.
Electrochemical
studies
revealed
that
Mo(CO)6@CNTs(N1)
exhibited
an
enhanced
electron
transfer
rate
superior
electrocatalytic
performance
compared
to
CNTs(N1).
Their
evaluated
DSC
showed
5
wt.%
exhibits
best
effect,
increasing
heat
release
1850.62
J·g-1,
advancing
its
peak
temperature
80.6
oC,
decreasing
activation
energy
100.45
KJ·mol-1.
degradation
mechanism
catalyzed
was
probed
through
TG-FTIR-MS,
in-situ
solid
FTIR,
theoretical
calculations.
investigations
suggested
promoter
in
generates
nanotubes-confined
MoO3
nanoparticles
featuring
numerous
Lewis
Brønsted
acidic
sites,
which
not
only
improves
NH3
adsorption
but
also
enhances
accelerates
O2
conversion
O2-,
thereby
facilitating
pyrolysis.
Finally,
a
plausible
decomposition
postulated.
Adding
burning-rate
catalysts
(BRCs)
is
highly
effective
for
enhancing
ammonium
perchlorate
(AP)
thermal
decomposition.
To
mitigate
BRCs’
agglomeration
and
enhance
their
catalytic
activity
AP
pyrolysis,
five
metal
carbonyl
compounds
(Mo(CO)6,
Cr(CO)6,
W(CO)6,
Fe2(CO)9,
Mn2(CO)10)
were
refined
into
oxidized
carbon
nanotube
(CNTs)
cavities,
respectively,
by
ultrasonication.
The
structures
of
the
as-prepared
nanocomposites
examined
with
TEM,
SEM,
XPS,
Raman,
etc.,
confirming
successful
filling
compounds.
Electrochemical
studies
revealed
that
Mo(CO)6@CNTs(N1)
exhibited
an
enhanced
electron
transfer
rate
superior
electrocatalytic
performance
compared
to
CNTs(N1).
Their
evaluated
DSC
showed
5
wt.%
exhibits
best
effect,
increasing
heat
release
2904.63
J·g-1,
advancing
its
peak
temperature
80.6
oC,
decreasing
activation
energy
100.45
KJ·mol-1.
degradation
mechanism
catalyzed
was
probed
through
TG-FTIR-MS,
in-situ
solid
FTIR,
theoretical
calculations.
investigations
suggested
promoter
in
generates
nanotubes-confined
MoO3
nanoparticles
featuring
numerous
Lewis
Brønsted
acidic
sites,
which
not
only
improves
NH3
adsorption
but
also
enhances
accelerates
O2
conversion
O2-,
thereby
facilitating
pyrolysis.
Finally,
a
plausible
decomposition
postulated.
The
carrier
can
widely
affect
or
even
dominate
the
catalytic
activity
and
selectivity
of
nanoparticles
for
ammonium
perchlorate.
In
this
work,
a
novel
catalyst
was
fabricated
using
two-dimensional
MXene
as
through
simple
hydrothermal
method
NiO@TiO2/MXene
(TN)
nanocomposite.
System
characterization
indicates
that
supports
promote
good
dispersion
NiO
nanoparticles.
TiO2/MXene
itself
has
large
specific
surface
area,
thus
it
regulate
NiO.
TN
is
superior
to
in
promoting
high
temperature
decomposition
AP.
By
increasing
concentration
Ni2+
precursor,
load
on
increased,
ability
AP
improved.
With
increase
load,
decreased
from
437.3°C
313.3°C,
Ea
216.1kJ/mol
114.6kJ/mol,
heat
release
increased
by
118%.
NH3-TPD
O2-TPD
have
shown
stronger
adsorption
capacity
catalysts
NH3
O2
surface,
better
their
performance,
indicating
differences
performance.
TG/FT-IR
further
nanocomposites
accelerate
conversion
N2O
NO,
which
beneficial
rapid
The
practical
utility
of
bismuth
and
tin
compounds,
as
promising
green
combustion
catalysts,
is
constrained
by
their
substantial
particle
agglomeration.
Herein,
we
reported
a
straightforward
ultrasonication-assisted
method
to
incorporate
compounds
into
the
inner
spaces
carbon
nanotubes
(CNTs),
giving
CNTs-confined
(tin)
compounds.
as-prepared
nanocomposites
were
structurally
completely
characterized.
electrochemical
property
investigations
showed
that
introduction
increases
catalytic
active
sites
inhibits
nanoparticle
agglomeration
effectively.
theoretical
calculations
revealed
synergistic
effects
between
Bi2O3
can
improve
efficiency
electron
transfer
in
Bi(NO3)3@A-CNTs(M1)
composite.
evaluation
results
performance
on
ammonium
perchlorate
(AP)
pyrolysis
suggested
adding
5
wt.
%
DBT@A-CNTs(M1)
(DBT
=
Dibutyltin
dichloride)
AP
brought
about
more
concentrated
thermal
decomposition
process,
advancing
peak
high-temperature
stage
from
420.4
°C
328.9
325.9
°C,
respectively,
boosting
its
heat
release
976.42
J·g-1
2251.2
2452.03
J·g-1,
respectively.
studies
degradation
mechanism
AP,
probed
kinetics,
in-situ
solid
FTIR
TG-FTIR-MS,
concluded
critical
steps
ClO4-
NH4+
O2
O2-
accelerated
interaction
formed
nanoparticles
nanotubes,
relative
contents
stable
gases,
ultimately
promoting
pyrolysis.
A
tentative
finally
proposed.
Adding
burning-rate
catalysts
(BRCs)
is
highly
effective
for
enhancing
ammonium
perchlorate
(AP)
thermal
decomposition.
To
mitigate
BRCs’
agglomeration
and
enhance
their
catalytic
activity
AP
pyrolysis,
five
metal
carbonyl
compounds
(Mo(CO)6,
Cr(CO)6,
W(CO)6,
Fe2(CO)9,
Mn2(CO)10)
were
refined
into
oxidized
carbon
nanotube
(CNTs)
cavities,
respectively,
by
ultrasonication.
The
structures
of
the
as-prepared
nanocomposites
examined
with
TEM,
SEM,
XPS,
Raman,
etc.,
confirming
successful
filling
compounds.
Electrochemical
studies
revealed
that
Mo(CO)6@CNTs(N1)
exhibited
an
enhanced
electron
transfer
rate
superior
electrocatalytic
performance
compared
to
CNTs(N1).
Their
evaluated
DSC
showed
5
wt.%
exhibits
best
effect,
increasing
heat
release
1850.62
J·g-1,
advancing
its
peak
temperature
80.6
oC,
decreasing
activation
energy
100.45
KJ·mol-1.
degradation
mechanism
catalyzed
was
probed
through
TG-FTIR-MS,
in-situ
solid
FTIR,
theoretical
calculations.
investigations
suggested
promoter
in
generates
nanotubes-confined
MoO3
nanoparticles
featuring
numerous
Lewis
Brønsted
acidic
sites,
which
not
only
improves
NH3
adsorption
but
also
enhances
accelerates
O2
conversion
O2-,
thereby
facilitating
pyrolysis.
Finally,
a
plausible
decomposition
postulated.