3 research outputs found
Nitrogen-Enriched Carbon Nanofiber Aerogels Derived from Marine Chitin for Energy Storage and Environmental Remediation
Nitrogen-enriched
(N-enriched) carbon nanofiber aerogels (NCNAs)
with an ultrafine nanofiber network structure were designed and prepared
by using chitin nanofiber aerogels as the precursor. Because of the
uniform nanofibrous architecture and nitrogen-rich composition of
chitin nanofiber aerogels, the NCNAs exhibited large specific surface
area (490–1597 m<sup>2</sup> g<sup>–1</sup>) and a high
nitrogen content (2.07–7.65%). As a consequence, supercapacitor
electrodes prepared from NCNA-900 showed specific capacitances as
high as 221 F g<sup>–1</sup> at the current density of 1.0
A g<sup>–1</sup> and good capacitance retention of 92% over
8000 cycles in a 6.0 mol L<sup>–1</sup> KOH electrolyte without
further activation. Moreover, the NCNA-900 could also be applied as
an effective adsorbent for dye adsorption, such as Congo red (496
mg g<sup>–1</sup>) and Rhodanine B (489 mg g<sup>–1</sup>). In view of an excellent electrochemical performance and high adsorption
capacities for dyes as well as cost-effective and eco-friendly approaches,
NCNAs derived from marine chitin show great potential for application
in energy storage and environmental remediation
Three-Dimensional Nanoporous Cellulose Gels as a Flexible Reinforcement Matrix for Polymer Nanocomposites
With
the world’s focus on utilization of sustainable natural
resources, the conversion of wood and plant fibers into cellulose
nanowhiskers/nanofibers is essential for application of cellulose
in polymer nanocomposites. Here, we present a novel fabrication method
of polymer nanocomposites by in-situ polymerization of monomers in
three-dimensionally nanoporous cellulose gels (NCG) prepared from
aqueous alkali hydroxide/urea solution. The NCG have interconnected
nanofibrillar cellulose network structure, resulting in high mechanical
strength and size stability. Polymerization of the monomer gave PÂ(MMA/BMA)/NCG,
PÂ(MMA/BA)/NCG nanocomposites with a volume fraction of NCG ranging
from 15% to 78%. SEM, TEM, and XRD analyses show that the NCG are
finely distributed and preserved well in the nanocomposites after
polymerization. DMA analysis demonstrates a significant improvement
in tensile storage modulus <i>E</i>′ above the glass
transition temperature; for instance, at 95 °C, <i>E</i>′ is increased by over 4 orders of magnitude from 0.03 MPa
of the PÂ(MMA/BMA) up to 350 MPa of nanocomposites containing 15% v/v
NCG. This reinforcement effect can be explained by the percolation
model. The nanocomposites also show remarkable improvement in solvent
resistance (swelling ratio of 1.3–2.2 in chloroform, acetone,
and toluene), thermal stability (do not melt or decompose up to 300
°C), and low coefficients of thermal expansion (in-plane CTE
of 15 ppm·K<sup>–1</sup>). These nanocomposites will have
great promising applications in flexible display, packing, biomedical
implants, and many others
Tough and Cell-Compatible Chitosan Physical Hydrogels for Mouse Bone Mesenchymal Stem Cells in Vitro
Most
hydrogels involve synthetic polymers and organic cross-linkers
that cannot simultaneously fulfill the mechanical and cell-compatibility
requirements of biomedical applications. We prepared a new type of
chitosan physical hydrogel with various degrees of deacetylation (<i>DD</i>s) via the heterogeneous deacetylation of nanoporous chitin
hydrogels under mild conditions. The <i>DD</i> of the chitosan
physical hydrogels ranged from 56 to 99%, and the hydrogels were transparent
and mechanically strong because of the extra intra- and intermolecular
hydrogen bonding interactions between the amino and hydroxyl groups
on the nearby chitosan nanofibrils. The tensile strength and Young’s
modulus of the chitosan physical hydrogels were 3.6 and 7.9 MPa, respectively,
for a <i>DD</i> of 56% and increased to 12.1 and 92.0 MPa
for a <i>DD</i> of 99% in a swelling equilibrium state.
In vitro studies demonstrated that mouse bone mesenchymal stem cells
(mBMSCs) cultured on chitosan physical hydrogels had better adhesion
and proliferation than those cultured on chitin hydrogels. In particular,
the chitosan physical hydrogels promoted the differentiation of the
mBMSCs into epidermal cells in vitro. These materials are promising
candidates for applications such as stem cell research, cell therapy,
and tissue engineering