11 research outputs found
Facile Preparation of Nickel Phosphide (Ni<sub>12</sub>P<sub>5</sub>) and Synergistic Effect with Intumescent Flame Retardants in Ethylene–Vinyl Acetate Copolymer
In
this paper, nanoporous nickel phosphide (Ni<sub>12</sub>P<sub>5</sub>) was synthesized by using a novel hydrothermal method, and
its structure was characterized by X-ray diffraction (XRD) and transmission
electron microscopy (TEM). Then it was used as a synergistic agent
with intumescent flame retardant (IFR) in the ethylene–vinyl
acetate (EVA) copolymer. With the addition of 2 wt % Ni<sub>12</sub>P<sub>5</sub> and 28 wt % IFR, the LOI value increased from 30.5
to 34.5. The UL-94 test showed that EVA with 25 wt % IFR burned and
had no rating, but with the addition of 2 wt % Ni<sub>12</sub>P<sub>5</sub> and 23 wt % IFR, it could reach V-0 rating. The CCT results
revealed that the Ni<sub>12</sub>P<sub>5</sub> and IFR system could
result in excellent flame retardance. The TGA data indicate that Ni<sub>12</sub>P<sub>5</sub> can increase the thermal degradation temperature
and the charred residues after burning. Moreover, the mechanical and
electrical properties of EVA composites are also investigated
Highly Effective P–P Synergy of a Novel DOPO-Based Flame Retardant for Epoxy Resin
A novel
flame retardant (FR) DOPO-PEPA, which was synthesized via
Atherton–Todd reaction between 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide
(DOPO) and 1-oxo-4-hydroxymethyl-2,6,7-trioxa-l-phosphabicyclo[2.2.2]Âoctane
(PEPA), was used as an additive-type FR in epoxy resin (EP). The results
of the limiting oxygen index (LOI), vertical burning test, and cone
calorimeter test indicated that the flame retardance of FR-EP composites
is dependent on the chemical structure of phosphorus-based FRs. EP/DOPO-PEPA
shows pretty good mechanical properties and a relatively high degree
of cross-linking. Furthermore, the synergy as DOPO-PEPA was more efficient
than that of DOPO or PEPA alone to flame retardant EP. When the FR
additives were 9.1%, the EP/DOPO-PEPA acquired a LOI value of 35%,
UL94 V-0 rating, and the lowest peak of heat release rate (PHRR) of
595 kW/m<sup>2</sup>. Furthermore, its continuous and firm char residue
layer also reinforced this kind of action
Nacre-Inspired Tunable Electromagnetic Interference Shielding Sandwich Films with Superior Mechanical and Fire-Resistant Protective Performance
With
the rapidly increasing development of portable device hardware
and flexible electronics, ultrathin electromagnetic interference (EMI)
shielding films with a combination of high flexibility and excellent
mechanical properties are noticeably required. In addition to minimizing
the electromagnetic wave pollution problem, the fire hazards caused
by accidental electrical leakage or aging are also a cause of extensive
concern. Inspired by nacre and sandwich structure, herein, we fabricated
for the first time an electrical insulating sandwich-structured film
based on Ca ion cross-linked sodium alginate (SA)–montmorillonite
(MMT) and Ti3C2Tx MXene through a step-by-step vacuum-assisted filtration process.
This novel design strategy not only maintains the inner EMI shielding
network but also can act as an excellent fire-resistant barrier to
protect the electronic device in case of accidental fire. Compared
with the pure Ti3C2Tx layer, such kind of sandwich film can effectively maintain the EMI
shielding performance (50.01 dB), dramatically enhance the mechanical
properties (84.4 MPa), and exhibit excellent fire-resistant performance.
Especially, compared with the film composed of mixture, the EMI shielding
effectiveness value is only 55% that of sandwich films. Besides, it
functions well under long-term heat aging test at 80 °C. Therefore,
this unique design provides a novel EMI material strategy to facilitate
its future applications in flexible electronics
Nacre-Inspired Tunable Electromagnetic Interference Shielding Sandwich Films with Superior Mechanical and Fire-Resistant Protective Performance
With
the rapidly increasing development of portable device hardware
and flexible electronics, ultrathin electromagnetic interference (EMI)
shielding films with a combination of high flexibility and excellent
mechanical properties are noticeably required. In addition to minimizing
the electromagnetic wave pollution problem, the fire hazards caused
by accidental electrical leakage or aging are also a cause of extensive
concern. Inspired by nacre and sandwich structure, herein, we fabricated
for the first time an electrical insulating sandwich-structured film
based on Ca ion cross-linked sodium alginate (SA)–montmorillonite
(MMT) and Ti3C2Tx MXene through a step-by-step vacuum-assisted filtration process.
This novel design strategy not only maintains the inner EMI shielding
network but also can act as an excellent fire-resistant barrier to
protect the electronic device in case of accidental fire. Compared
with the pure Ti3C2Tx layer, such kind of sandwich film can effectively maintain the EMI
shielding performance (50.01 dB), dramatically enhance the mechanical
properties (84.4 MPa), and exhibit excellent fire-resistant performance.
Especially, compared with the film composed of mixture, the EMI shielding
effectiveness value is only 55% that of sandwich films. Besides, it
functions well under long-term heat aging test at 80 °C. Therefore,
this unique design provides a novel EMI material strategy to facilitate
its future applications in flexible electronics
Effect of Rare Earth Hypophosphite Salts on the Fire Performance of Biobased Polylactide Composites
In this work, two kinds of rare earth
hypophosphites (REHP), lanthanum hypophosphite (LaHP) and cerium hypophosphite
(CeHP), were synthesized and characterized. Subsequently, LaHP and
CeHP were added into polylactide to improve its flame retardant properties.
Thermal gravimetric analysis was employed to investigate the thermal
decomposition behavior of REHP and flame retardant polylactide composites
(FR-PLA). The fire performance evaluated by microscale combustion
calorimetry and cone calorimeter clearly demonstrated that the addition
of LaHP and CeHP resulted in significant reduction of the heat release
rate, low total heat release, and compact intumescent char layer.
Thermogravimetric analysis–infrared spectrometry testing indicated
that the addition of REHP significantly decreased the yields of pyrolysis
products. Furthermore, the crystallization behaviors of FR-PLA composites
were investigated by differential scanning calorimetry. The char residue
of FR-PLA composites after cone calorimeter testing were also be investigated
by scanning electron microscope, Fourier transform infrared spectroscopy,
and X-ray photoelectron spectroscopy
Graphite-like Carbon Nitride/Polyphosphoramide Nanohybrids for Enhancement on Thermal Stability and Flame Retardancy of Thermoplastic Polyurethane Elastomers
Many
efforts have been made to enhance the fire safety of thermoplastic
polyurethane elastomers (TPUs) by reducing the heat release rate and
smoke emission. Suppressing the emission of smoke and reducing toxic
gases generated in the case of TPU burning play a key role to enable
TPU meet the eco-friendly and safety requirements. In this work, poly
diaminodiphenyl phosphonic methane (PDMPD) with higher thermal stability
and catalytic char formation capacity was synthesized; graphitic carbon
nitride/PDMPD (CPDMPD) hybrids were fabricated, and their effect on
the thermal behavior and flame retardancy of TPU composites was studied.
The peak heat release rate (PHRR), the total heat release, the CO
yield, and the smoke release of TPU show an obvious reduction on account
of addition of CPDMPD hybrids according to the cone tests. TPU/CPDMPD4
is endowed with a reduction of 49.0% of the PHRR. In this work, molecular
designing and physical function are integrated to prepare versatile
additives of polymers with optimized thermal stability and flame retardancy
Processable Dispersions of Graphitic Carbon Nitride Based Nanohybrids and Application in Polymer Nanocomposites
Graphitic
carbon nitride (g-C<sub>3</sub>N<sub>4</sub>) nanosheets
are endowed with extraordinary chemical and thermal stability and
good optical and photoelectrochemical properties and are expected
to be used in a wide range of fields. The direct dispersion of hydrophobic
g-C<sub>3</sub>N<sub>4</sub> nanosheets in water or organic solvents
without the assistance of dispersing agents is considered to be a
great challenge. Here we report novel g-C<sub>3</sub>N<sub>4</sub>/organic-modified montmorillonite (OMMT) nanohybrids, which were
synthesized through electrostatic interaction and then introduced
into polystyrene (PS) matrix to fabricate nanocomposites by a simple
solvent blending–precipitation method. Hybridizing g-C<sub>3</sub>N<sub>4</sub> with OMMT could easily form stable aqueous colloids
through electrostatic stabilization. These nanohybrids were evenly
dispersed in PS and showed strong interfacial interactions with the
polymer matrix. It is noted that the generation of total gaseous products
was dramatically inhibited by combining g-C<sub>3</sub>N<sub>4</sub> with OMMT. Moreover, flame retardancy was improved upon incorporation
of the nanohybrids into PS host. These improvements were due to the
strong interactions at interface of ternary systems, synergism between
g-C<sub>3</sub>N<sub>4</sub> and OMMT, and physical barrier effect
of the two components. This work provides a new pathway to manufacture
well-dispersed polymeric materials with enhanced fire safety
Nacre-Inspired Tunable Electromagnetic Interference Shielding Sandwich Films with Superior Mechanical and Fire-Resistant Protective Performance
With
the rapidly increasing development of portable device hardware
and flexible electronics, ultrathin electromagnetic interference (EMI)
shielding films with a combination of high flexibility and excellent
mechanical properties are noticeably required. In addition to minimizing
the electromagnetic wave pollution problem, the fire hazards caused
by accidental electrical leakage or aging are also a cause of extensive
concern. Inspired by nacre and sandwich structure, herein, we fabricated
for the first time an electrical insulating sandwich-structured film
based on Ca ion cross-linked sodium alginate (SA)–montmorillonite
(MMT) and Ti3C2Tx MXene through a step-by-step vacuum-assisted filtration process.
This novel design strategy not only maintains the inner EMI shielding
network but also can act as an excellent fire-resistant barrier to
protect the electronic device in case of accidental fire. Compared
with the pure Ti3C2Tx layer, such kind of sandwich film can effectively maintain the EMI
shielding performance (50.01 dB), dramatically enhance the mechanical
properties (84.4 MPa), and exhibit excellent fire-resistant performance.
Especially, compared with the film composed of mixture, the EMI shielding
effectiveness value is only 55% that of sandwich films. Besides, it
functions well under long-term heat aging test at 80 °C. Therefore,
this unique design provides a novel EMI material strategy to facilitate
its future applications in flexible electronics
UV Grafting of a DOPO-Based Phosphoramidate Monomer onto Polyamide 66 Fabrics for Flame Retardant Treatment
A novel
DOPO-based phosphorus- and nitrogen-containing monomer
named DOPO-DAAM was synthesized and grafted onto the surface of polyamide
66 (PA 66) fabrics via UV grafting in order to improve the flame retardancy.
To facilitate the grafting efficiency, the PA66 fabric surface was
first modified through the HCl treatment. In the UL-94 vertical burning
test, the PA66 fabrics treated with DOPO-DAAM could stop the melt-dripping.
Cone calorimetry results showed that a 22% reduction in peak heat
release rate was achieved for PA66 fabrics grafted with 20 wt % DOPO-DAAM.
Thermogravimetric analysis indicated that the presence of grafted
monomer catalyzed the degradation pathway of virgin PA66 fabrics where
the initial decomposition temperature was reduced and the char yield
was enhanced for all treated fabric samples. Moreover, real time FTIR
analysis confirmed that the DOPO-DAAM decomposed ahead of virgin PA66
and catalyzed the formation of char residue
Effect of Functionalized Graphene Oxide with Organophosphorus Oligomer on the Thermal and Mechanical Properties and Fire Safety of Polystyrene
A novel
organophosphorus oligomer was synthesized to functionalize
graphene oxide. Subsequently, the functionalized graphene oxide (FGO)
was incorporated into polystyrene (PS) to enhance the integration
properties of the matrix. The effect of FGO on the thermal properties,
fire safety, and mechanical properties of PS nanocomposites was investigated.
The results showed that the introduction of FGO significantly increased
the maximum decomposition temperature (<i>T</i><sub>max</sub>) (25 °C increase), reduced the total heat release (20.8% reduction),
and peak heat release rate (38.2% reduction) of PS. In addition, the
thermogravimetric analysis/infrared spectrometry analysis results
indicated that the amount of organic volatiles and toxic carbon monoxide
of PS was remarkably reduced. The physical barrier effect of FGO and
the synergistic effects between the organophosphorus oligomer and
FGO were the main causations for these properties improvements. Homogeneous
dispersion of FGO into the polymer matrix improved the mechanical
properties of FGO/PS nanocomposites, as demonstrated by tensile tests
results