Highly efficient formation of poly(propylene carbonate) can be achieved in the coupling of CO2 and propylene oxide assisted by 4‐(N,N‐dimethylamino)pyridine (DMAP) and catalyzed with salen chromium(III) chloride by using DMAP/Cr ratios of less than 2. Under these conditions a possible backbiting mechanism is suppressed, leading to only minor amounts of cyclic carbonate as a side product.
A continuum model is developed to investigate the microstructure‐dependent AC properties of MWCNT/polymer nanocomposites. The AC conductivity of the composite is increased by a higher curl ratio of MWCNTs. At a critical frequency ω0, the AC conductivity switches to a frequency‐dependent region. For high MWCNT content, the curl curliness of MWCNTs has only a weak influence on the AC conductivity. For medium MWCNT content, the AC conductivity became frequency‐dependent for low frequencies with decreasing curl ratio of MWCNTs, which cannot be explained by correlation length theory. An interpretation based on the linear circuit theory is given. With increasing size of MWCNT clusters, the critical frequency ω0 increases. It is also affected significantly by the crystallinity the polymer.
The present article reports on a strategy for the functionalization of multi‐walled carbon nanotubes (MWCNTs) by grafting with various polymer chains. Copolymers consisting of α‐methylstyrene (AMS) and a second monomer, that is glycidyl methacrylate (GMA) or styrene (St), were synthesized in advance. The copolymers were heated in the presence of MWCNTs in solution, decomposition of the AMS sequences occurred, providing macroradicals, which further attacked the double bonds on the MWCNT surfaces. Grafting of the copolymer chains onto the surface of the MWCNTs was thus achieved, as demonstrated by FT‐IR, XPS and Raman technologies. The resulting poly(AMS‐co‐GMA)‐g‐MWCNTs could be uniformly dispersed in N,N‐dimethylformamide (DMF) and acetone, and the poly(AMS‐co‐St)‐g‐MWCNTs also could be uniformly dispersed in DMF.
Summary: Nanofibrous membranes that possess reactive groups are fabricated by the electrospinning process from PANCAA solutions that contain MWCNTs. Field emission scanning electron microscopy is used to evaluate the morphology and diameter of the nanofibers. Potentials for applying these nanofibrous membranes to immobilize redox enzymes by covalent bonding are explored. It is envisaged that the electrospun nanofibrous membranes could provide a large specific area and the MWCNTs could donate/accept electrons for the immobilized redox enzymes. Results indicate that, after blending with MWCNTs, the diameter of the PANCAA nanofiber increases slightly. The PANCAA/MWCNT nanofibrous membranes immobilize more enzymes than that without MWCNTs. Moreover, as the concentration of the MWCNTs increases, the activity of the immobilized catalase is enhanced by about 42%, which is mainly attributed to the promoted electron transfer through charge‐transfer complexes and the π system of MWCNTs.
The covalent immobilization of redox enzymes, such as catalase, on a PANCAA/MWCNTs nanofiber. 相似文献
The preparation of associative networks containing multi‐walled carbon nanotubes (MWCNTs) with covalently attached cyclodextrin (CD) rings and poly[(isobutylene)‐co‐(maleic anhydride)‐co‐(maleic acid‐(4‐tert‐butylphenyl)amide)] in water is described in this study. The synthesis of CD containing MWCNTs is realized by an amidation reaction of oxidized MWCNTs with propargylamine followed by a 1,3‐dipolar cycloaddition with CD‐azide. Dispersion behavior indicated the high stability of these networks. An increase in viscosity compared to a solution of pure polymer as a cause of network formation is observed. The addition of a CD‐decomposing enzyme (taka‐diastase from Aspergillus oryzae) let the network collapse and results in sedimentation of the modified MWCNTs.
Summary: A rapid and eco‐friendly synthesis of poly(butylene succinate) (PBS) using microwaves was developed in the presence of 1,3‐dichloro‐1,1,3,3‐tetrabutyldistannoxane as catalyst. To determine the optimum conditions, the effect of catalyst concentration, bulk vs. solution polymerization, reaction time, temperature, and stoichiometry of the monomers were studied. Based on the optimum conditions, PBS with a weight‐average molecular weight of 2.35 × 104 was obtained in a short time of 20 min.
Synthesis of poly(butylene succinate) under microwave irradiation. 相似文献
A facile approach to polymer nanocomposites with single‐wall carbon nanotubes and cationic polymers is reported. The composite material was synthesized by producing carboxylic acid groups at the nanotube termini followed by a reaction with poly(allylamine) in water. Fourier transform infrared spectral and thermogravimetric analyses corroborate that the poly(allylamine) chains were wrapped on the surface of the carbon nanotubes. The scanning electron microscopic (SEM) image shows that the nanotubes were dispersed with little aggregation, thus, strongly suggesting that the poly(allylamine) chains have covered the single‐wall carbon nanotubes, which was further evidenced by transmission electron microscopy. The composites are soluble in water, and this solubilization process opens up new opportunities in the solution chemistry on pristine nanotubes.
One‐dimensional methyl orange fibrils can be easily prepared. They are stable in acidic aqueous solutions and soluble in neutral water. When used to synthesize conducting polymer microtubules, the fibrils act as “hard templates” formally but as “soft templates” effectively. Microtubular structures of polypyrrole, polyaniline, and poly(3,4‐ethylenedioxythiophene) have been achieved successfully via such water‐soluble versatile templates.
Reactions between the ethylene groups in the backbone of conjugated polymers under UV illumination and heat treatment result in the cross‐linking of the main polymer chains. The cross‐linking leads to two simultaneous results in the polymer: excellent solvent resistance and increased bandgap. Using this reaction, three‐color polymer light‐emitting diodes (PLEDs) with a multi‐layer structure can be easily realized by a dry photo‐pattern in an active‐gas‐free environment. Multi‐layer blue devices with dramatically enhanced efficiency can also be achieved conveniently.
In this communication, the synthesis, characterization, and properties of highly conductive core–shell nanocomposites of poly(N‐vinylcarbazole) (PNVC)–polypyrrole (PPY) copolymers with multi‐walled carbon nanotubes (MWCNTs) are described. A unique free‐radical coupling reaction between PNVC and PPY cation radicals in chloroform solvent, using feric chloride as an oxidant, in the presence of suspended MWCNTs in the reaction medium, was used for the synthesis of nanocomposite. Field‐emission scanning and transmission electron microscopy studies showed the formation of the core–shell nanocomposite. Raman spectrocopy results as well as thermogravimetric analysis supported the electron microscopic observations. The resulting PNVC–PPY copolymer‐coated MWCNTs showed an unprecedentedly increased value of direct electrical conductivity (bulk) compared to the conductivity of all samples even with pure MWCNTs.
Nanofiber scaffolds of collagen have been fabricated via electrospinning using benign solvent systems as a replacement for 1,1,1,3,3,3 hexafluoro‐2‐propanol. Simple binary mixtures of phosphate‐buffered saline and ethanol have been found to be highly effective for electrospinning. FTIR spectra suggest that the triple helical structure of collagen was conserved after dissolution and electrospinning. Crosslinking of the electrospun collagen scaffolds was achieved with standard methods.
The mixed Langmuir monolayers and Langmuir–Blodgett (LB) films of homo‐polystyrene (h‐PS) and the diblock copolymer polystyrene‐block‐poly(2‐vinylpyridine) (PS‐b‐P2VP) have been characterized by the Langmuir monolayer technique and tapping mode atomic force microscopy (AFM), respectively. When the content of h‐PS is below 80 wt.‐%, the mixed LB films of h‐PS/PS‐b‐P2VP mainly exhibit isolated circular nanoaggregates. With a further increase of the h‐PS content (80–95%), however, highly uniform and stable necklace‐network structures are observed in the mixed LB films.
A single stage electrospinning process can give rise to preferentially oriented induced dipoles in poly(vinylidene fluoride‐trifluoroethylene) [P(VDF‐TrFE)] nanofibers. The piezoelectricity of as‐electrospun P(VDF‐TrFE) nanofiber webs opens up new possibilities for their use as a flexible nanogenerators and nano‐pressure sensors. In this work, the origin of the piezoelectricity has been spotlighted by randomization of the induced dipoles at the Curie temperature and analyzed by polarized FT‐IR spectroscopic techniques as well as by detecting the piezoelectric signal from a nano‐pressure sensor.
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.
We report the formation of poly(propylene) spherical and ellipsoidal particles templated by carbon nanotubes via solution crystallization. With an increase in nanotube loading, the particle shape changes from sphere to ellipsoid. In the intermediate concentration range, both spherical and ellipsoidal shapes coexist. The particle size decreases with an increase in nanotube loading.
Summary: A feasible method for the preparation of antimicrobial ultrafine fibers with silver nanoparticles was developed by direct electrospinning of a cellulose acetate (CA) solution with small amounts of silver nitrate followed by photoreduction. Silver nanoparticles in ultrafine CA fibers were stabilized by interactions with carbonyl oxygen atoms in CA. Ultrafine CA fibers with silver nanoparticles showed very strong antimicrobial activity.
TEM image of an ultrafine CA fiber electrospun from 10 wt.‐% CA solution with 0.5 wt.‐% AgNO3. 相似文献
Transparent film materials with excellent mechanical and thermal properties were elaborated by drying a latex suspension of armored polymer/Laponite composite particles. Low‐temperature TEM observation of ultrathin cross‐sections of the films indicated a unique network morphology characterized by a “honeycomb” distribution of the Laponite platelets remindful of the original particles morphology.
Summary: We show in this communication that large‐scale necklace‐like single‐crystalline tetragonal perovskite PbTiO3 nanowires can be obtained via a simple electrospinning method. The morphology and the crystal structure are investigated by SEM, XRD, and HRTEM. The length of the necklace‐like PbTiO3 nanowires is from tens to several tens of micrometers, the wider the diameter of it is between 100 and 200 nm and the thinner the part is between 20 and 50 nm. The necklace‐like PbTiO3 nanowires exhibit high surface photovoltage under the action of external electric field, which is probably applicable in displaying photoelectric devices of heterojunction structure.
SEM image of the electrospinning necklace‐like PbTiO3 nanowires. 相似文献
