Multiwalled carbon nanotubes (MWNTs) have been introduced into blends of polycarbonate (PC) and poly(styrene‐acrylonitrile) (SAN) by melt mixing in a microcompounder. Co‐continuous blends are prepared by either pre‐compounding low amounts of nanotubes into PC or SAN or by mixing all three components together. Interestingly, in all blends, regardless of the way of introducing the nanotubes, the MWNTs were exclusively located within the PC phase, which resulted in much lower electrical resistivities as compared to PC or SAN composites with the same MWNT content. The migration of MWNTs from the SAN phase into the PC phase during common mixing is explained by interfacial effects.
Poly(propylene) (PP) nanocomposites filled with shorter‐ and longer‐aspect‐ratio multiwalled carbon nanotubes (MWNTs) were compounded using a twin‐screw extruder and an injection moulding machine. It is shown that with only 1 vol.‐% of MWNTs, creep resistance of PP can be significantly improved with reduced creep deformation and creep rate at a long‐term loading period. Additionally, the creep lifetime of the nanocomposites has been considerably extended by 1 000% compared to that of a neat PP. Three possible mechanisms of load transfer were considered that could contribute to the observed enhancement of creep resistance, which are: (1) fairly good interfacial strength between MWNTs and polymer matrix, (2) increasing immobility of amorphous regions due to nanotubes acting as restriction sites, and (3) high aspect ratio of MWNTs. DSC results showing crystallinity changes in the specimens before and after creep deformation present evidence to confirm these mechanisms. Our results should lead to improved grades of creep resistant polymer nanocomposites for engineering applications.
The copolymerization system of oxetane and tetrahydropyran is reinterpreted with the aid of computer simulations. The original claim that this system is a “living” and/or controlled pseudoperiodic copolymerization 1 is not confirmed by the simulation results. It is suggested that the formation of branched oxonium cations and the statistical nature of THP incorporation are the reasons for the observed discrepancies between the simulation results and experimental data.
Nanocomposites based on an ethylene–vinyl acetate copolymer (27 wt.‐% vinyl acetate) and multiwall carbon nanotubes (MWNTs) have been prepared by melt blending and their thermal degradation and flame retardant properties have been evaluated. Special attention has been paid to the influence of the nanotube nature on the flammability properties and more particularly on the time to ignition (TTI) as measured by cone calorimetry. It has been shown that there is a strong influence of the nature of carbon nanotubes on the fire behaviour of the composites, especially previous MWNTs crushing proved to substantially delay the TTI while maintaining much reduced heat release rate (HRR). Such a remarkable behaviour might be explained by the chemical reactivity of radical species present at the surface/extremities of crushed MWNTs during the combustion process.
We report a facile method to accomplish the crosslinking reaction of PVA with SWNTs, MWNTs, and C‐60 using MW irradiation. Nanocomposites of PVA crosslinked with SWNT, MWNT and C‐60 were prepared expeditiously by reacting the respective carbon nanotubes with 3 wt.‐% PVA under MW irradiation, maintaining a temperature of 100 °C, representing a radical improvement over literature methods to prepare such crosslinked PVA composites. This general preparative procedure is versatile and provides a simple route to manufacture useful SWNT, MWNT and C‐60 nanocomposites.
Water‐soluble single‐ and multi‐walled carbon nanotubes (CNTs) were prepared by grafting polyacrylamide chains from the graphitic surface via ceric ion‐induced redox radical polymerization. The reducing functionalities were covalently attached to the tubes by peroxide‐assisted radical reaction. The results showed that polymer chains were grafted onto CNTs by the redox process. The redox radical polymerization initiated by carbon nanotube‐bearing functionalities not only provides a powerful strategy for modifying the carbon nanostructures but also gives us the knowledge of their sidewall chemistry.
A simple method to fabricate polymer nanocomposites with single‐walled carbon nanotubes is reported, in which the nanotubes were reacted with poly(L ‐lysine) by using high‐speed vibration milling. The nanocomposites obtained were characterized by Fourier transform infrared (FT‐IR), UV–Vis spectroscopy, and thermogravimetric methods. The morphology as well as the dispersion of the carbon nanotubes were determined by scanning and transmission electron microscopy.
Camphor sulfonic acid (CSA) doped polyaniline (PANI) nanotubes (175 nm in outer diameter and 120 nm in inner diameter) were synthesized successfully by a self‐assembly method. It is found that the room‐temperature conductivity of an individual PANI nanotube is 30.5 S · cm−1; in particular, the intrinsic resistance of an individual nanotube (30 kΩ) is much smaller than the contact resistance of crossed nanotubes (500 kΩ).
A SEM image of two crossed PANI‐CSA nanotubes and the attached Pt electrodes. 相似文献
Summary: Covalent surface functionalization of carbon nanotubes with polypeptides is promising for possible medical applications. This work presents a graft‐from approach to perform the polypeptide modification of multiwalled carbon nanotubes (MWNTs). The raw MWNTs are first amine‐functionalized. The amine‐functionalized MWNTs are then used as the initiator to initiate the ring‐opening polymerization of γ‐benzyl‐L ‐glutamate N‐carboxyanhydride (BLG‐NCA), to result in the polypeptide‐grafted MWNTs. FT‐IR, XPS, and TGA data demonstrate that the functionalization is successful. The TEM images of the products show that the thickness of the polypeptide shell of the PBLG‐MWNT is about 4.5–22 nm. Using the facile route developed here, carbon nanotubes functionalized with other types of polypeptides can be easily fabricated using the corresponding NCAs.
Strategy for the polypeptide modification of multiwalled carbon nanotubes by a graft‐from approach. 相似文献
Summary: An initiator for nitroxide mediated ‘living’ free radical polymerization was prepared with a fluorescent tag attached to the initiating alkyl radical terminus. This was used to synthesize amphiphilic poly(acrylic acid)‐block‐polystyrene diblock copolymers, which self assembled in a tetrahydrofuran/buffer solution to form structures that are visible by fluorescence.
Poly(ethylene glycol) (PEG)‐based films, nanotubes, and nanotube arrays were successfully made using layer‐by‐layer (LbL) assembly ion‐containing PEO derivatives on porous templates and planar substrates. PEG nanotubes are challenging to produce because PEG dissolves into solutions and solvents used during nanotube processing, but our techniques circumvent the issue. Nanotube dimensions were verified using microscopy and the average observed diameter was 155 nm. The PEG‐based structures showed remarkable stability in water, salt water, and sodium hydroxide solution.
A long alkylsilyl group was attached to a thiophene ring system to overcome the instability of 2,5‐bis(halomethyl)thiophene monomers, by imparting steric hindrance and electronic delocalization. The resulting stable monomer could be used directly to prepare low‐band‐gap poly(thienylenevinylene) (1.57 eV) through heteroaromatic dehydrohalogenation polymerization.
The preparation, characterization and properties of novel millable polyurethane/organoclay nanocomposites are reported. Clay treated with methyl tallow bis(2‐hydroxyethyl) quaternary ammonium chloride was used as an organoclay for nanocomposite preparation. X‐ray diffraction indicated the intercalation of polymer chains inside the interlayer spacings of the clay. Dynamic mechanical analysis showed a significant increase in storage modulus, and tensile strength increases with increased organoclay loading.
X‐ray diffraction patterns of millable polyurethane/organoclay nanocomposites. 相似文献
The storage moduli, shear moduli and surface morphologies of poly(vinyl alcohol) (PVA) and alumina hybrid hydrogels were investigated. The storage moduli of hybrid hydrogels with higher alumina contents were found to be 1.5 times higher than those of PVA gels. This increase in modulus might be attributed to the cohesion of alumina to the PVA network.
SEM photograph of Al7 PVA/alumina hybrid hydrogel. The photograph was taken with a magnification of × 220. 相似文献
New multifunctional copoly(2‐oxazoline) nanoparticles were prepared for cell studies. The polymer contains double‐bond side chains as potential reaction sites for “thio”‐click reactions as well as a fluorescein label covalently bound to the polymer backbone. Using the nanoprecipitation technique, spherical nanoparticles of 200–800 nm were obtained. Confocal laser scanning microscopy measurements revealed the cellular uptake of the nanoparticles.
Summary: Dissipative particle dynamics simulation was performed to study the formation of multicompartment micelles from ABC star triblock copolymers in water. The study revealed some new morphologies that had not been observed before and also provided a direct visualization of the evolution of wormlike multicompartment micelles that follows the fusion process. Thus, this work provides molecular understanding of multicompartment micelles which will be useful for the future rational synthesis of novel micelles.
Multicompartment micelles formed from ABC star triblock copolymers in water by DPD simulations. 相似文献
Summary: Polypyrrole nanotubes with high electric conductivity and azo function have been fabricated in high yield via an in‐situ polymerization. During the process fibrillar complex of FeCl3 and methyl orange (MO), acting as a reactive self‐degraded template, directed the growth of polypyrrole on its surface and promoted the assembly into hollow nanotubular structures.
TEM image of uncompleted PPy nanotubes synthesized in MO solutions after reaction for 40 min. 相似文献
The carbon nitride poly(triazine imide) with intercalated bromide ions is a layered, graphitic material of 2D covalently bonded molecular sheets with an exceptionally large gallery height of 3.52 Å due to the intercalated bromide anions. The material can be cleaved both mechanically and chemically into thin sheets and scrolls analogous to the carbon‐only systems graphite and graphene.
