Summary: Polyaniline nanobelts have been synthesized by a self‐assembly process using the chemical oxidative polymerization of aniline in a surfactant gel. The morphologies of polyaniline nanostructures were characterized by field‐emission scanning electron microscopy and transmission electron microscopy. The effects of the concentrations of cetyltrimethylammonium bromide on the morphologies of polyaniline nanostructures have also been investigated.
A scanning electron microscopy image of polyaniline nanobelts synthesized with 0.12 M cetyltrimethylammonium bromide at −7 °C. 相似文献
Macroporous temperature‐sensitive poly(N‐isopropylacrylamide) (PNIPA) hydrogels were prepared by a novel phase‐separation technique to improve the response properties. In comparison with a conventional PNIPA hydrogel prepared in water, these macroporous hydrogels, prepared by polymerization in aqueous sucrose solutions, have higher swelling ratios at temperatures below the lower critical solution temperature and exhibit much faster response rates to temperature changes.
Scanning electron microscopy image of the surface of a PNIPA hydrogel, prepared in 1.50 M aqueous sucrose solution. 相似文献
New aromatic compounds with a pyridazine core have been synthesized. Four electron‐withdrawing monomers have been easily prepared from simple condensation reactions and ring closure procedures. Optimized HOMO, LUMO, and bandgap energy levels have been obtained. The resulting conjugated polymers have been tested in organic solar cells. First studies have revealed power conversion efficiencies up to 0.5% for an active area of 1.0 cm2.
Antiseptics based on phenol and phenolic derivatives were chemically incorporated into polyanhydrides as pendant groups via ester linkages. Polyanhydrides with antiseptic loadings of 46–58 wt.‐% were obtained with molecular weights ranging from 9 400–23 000. In general, polymers with the bulkier antiseptics were more difficult to polymerize and yielded lower molecular weights. All polyanhydrides were amorphous with glass transition temperatures ranging from 27–58 °C. Polymers were deemed noncytotoxic after culturing L929 mouse fibroblast cells in media containing the polymers at two concentrations (0.10 and 0.01 mg · mL−1) over three days. In summary, mono‐functional bioactives can be chemically incorporated into noncytotoxic polyanhydrides.
We describe an enzyme‐responsive polymeric vehicle, which is of great interest in controlled drug delivery, biosensing, and other related areas. The polymer synthesized using lipase as catalyst in DMSO has a favorable molecular structure that is quickly hydrolyzed by lipase in aqueous phase, and allows a fast release of encapsulated molecules.
Highly efficient and well‐controlled ambient temperature reversible addition–fragmentation chain transfer (RAFT) polymerization is readily carried out under environmentally friendly mild solar radiation. This discovery has significantly extended studies from man‐made separated‐spectroscopic‐emission UV‐vis radiation (Macromolecules 2006 , 39, 3770) to natural continuous‐spectroscopic‐emission solar radiation for ambient temperature RAFT polymerization.
Poly(methyl methacrylate) nanosize particles were synthesized by a differential microemulsion polymerization process. Sodium dodecylsulfate and ammonium persulfate were used as the surfactant and initiator, respectively. The effects of reaction conditions on the particle size have been investigated. A particle size of less than 20 nm in diameter has been achieved with surfactant/monomer and surfactant/water weight ratios of 1:18 and 1:120, i.e. much milder conditions than those previously reported in the literature.
TEM image of nanoparticles prepared via differential microemulsion polymerization. 相似文献
Green nanocomposite coatings based on renewable plant oils have been developed. An acid‐catalyzed curing of epoxidized plant oils with 3‐glycidoxypropyltrimethoxysilane produced transparent nanocomposites. The hardness and mechanical strength improved by incorporating the silica network into the organic polymer matrix, and good flexibility was observed in the nanocomposite. The nanocomposites showed high biodegradability.
With the development of nanotechnology, there is a growing demand for advanced electronics based on functional nanomaterials. In this respect, owing to their unique properties, conducting polymers (CP) synthesized in the form of one‐dimensional (1D) nanostructures are of particular interest. In this feature paper, we first report one of the most powerful techniques, the hard templating synthesis, for elaborating a large number of uniform 1D CP nanotubes or nanowires with precise control over lengths and diameters. Then, recent advances in the preparation, through electrochemical template synthesis, of various multi‐segmented nanowires containing a combination of metallic and polymeric components are discussed. Hybrid metal‐CP nanowires are promising high tech materials as they exhibit enhanced performances compared to their bulk counterparts and are of direct interest for developing novel multifunctional systems for a wide range of applications. Finally, some future directions for research in the area of multi‐segmented nanowires are proposed.
Highly dispersed ZnO nanoparticles with variable particle sizes were successfully prepared within an amphiphilic hyperbranched polyetherpolyol matrix via decomposition of an organometallic precursor in the presence of air leading to stable nanocomposites. The high degree of stabilization during and after the synthesis by the polymer permits control over the nanoparticle size and therefore, due to the quantum‐size‐effect, the particle properties. Furthermore, these polymer‐inorganic nanocomposites can easily be dispersed in apolar solvents to yield highly transparent, stable solutions.
Hollow polyphosphazene microcapsules have been fabricated by the covalent layer‐by‐layer assembly of polydichlorophosphazene (PDCP) and hexamethylenediamine (HDA) on aminosilanized silica particles, followed by core removal in a HF/NH4F solution. The hollow and intact microcapsules in both wet and dry states have been characterized by transmission electron microscopy and confocal laser scanning microscopy. The chemical structure of the microcapsules has been verified by FT‐IR spectroscopy. The microcapsules could be hydrolytically degraded in a phosphate buffer at biological pH.
Summary: The end coupling of living PSLi chains in hydrocarbon media by the addition of monoalkylbromides has been examined. A very selective PS–PS coupling reaction was obtained with neo‐pentylbromide (94%) at a ratio of PSLi/alkylbromide equal to 1 while the secondary and tertiary bromine derivatives yield only very limited coupling. The coupling mechanism is likely to involve a lithium‐bromine interchange at the PS chain end, generating polystyryl‐bromide which then reacts selectively with the remaining polystyryllithium chains.
Enzymatic grafting of caprolactone was carried out from poly[styrene‐co‐(4‐vinylbenzyl alcohol)] containing 10% hydroxyl functional monomer and compared with the grafting of vinyl acetate. A molecular weight increase due to the grafting of polycaprolactone was observed by size exclusion chromatography. Closer investigation of the grafting density by 1H NMR revealed an upper limit to the amount of grafting of about 50–60% of the pendant hydroxyl groups leaving unreacted hydroxyl groups on the polymer backbone available for subsequent reactions. The higher grafting density (95%) obtained with vinyl acetate suggests that this is not due to limited accessibility of the backbone but sterical constrains. Moreover, the grafting action of polycaprolactone seems to be a combination of grafting from by monomer initiation and grafting onto by transesterification of polycaprolactone.
The preparation of nanosized, molecularly imprinted polymer particles by nonaqueous emulsion polymerization is presented. Monodisperse cross‐linked polymer nanospheres with a diameter of around 100 nm were synthesized using a standard monomer mixture of methacrylic acid and ethylene dimethacrylate, containing (±)‐propranolol as a template. The rebinding efficiency of the resulting particles was determined by batch rebinding tests and isothermal titration calorimetry (ITC). The results indicate that the proposed imprinting process under nonaqueous conditions lead to particles with an enhanced capacity of template rebinding compared to both nonimprinted ones and to particles obtained by more conventional emulsion polymerization in water.
Well‐defined poly(ethylene oxide)s (PEOs) bearing reactive sites regularly distributed along the chain have been synthesized by the polycondensation of PEO containing a central tertiary amino group with dichloromethane, followed by quaternization with suitable reagents to obtain polyzwitterionic or cationic PEOs with alkyl, allyl, or fluorocarbon pendant groups. The pendant allyl groups have been converted into primary amino groups by reaction with 2‐aminoethanethiol hydrochloride to obtain polyamino‐functionalized PEO.
Polyfunctional PEOs bearing different pendant groups. 相似文献
Atom transfer radical polymerization (ATRP) is a robust method for the preparation of well‐defined (co)polymers. This process has also enabled the preparation of a wide range of polymer brushes where (co)polymers are covalently attached to either curved or flat surfaces. In this review, the general methodology for the synthesis of polymer brushes from flat surfaces, polymers and colloids is summarized focusing on reports using ATRP. Additionally, the morphology of ultrathin films from polymer brushes is discussed using atomic force microscopy (AFM) and other techniques to confirm the formation of nanoscale structure and organization.
Summary: A composite film composed of porous polyurethane (PU) and polystyrene (PS) microspheres with both superhydrophobicity and superoleophilicity has been prepared. In this film, the dual‐scale structure enhances both the hydrophobicity and oleophilicity of the surface material. The composite film with such an ‘intelligent’ wettability property can be utilized to separate oil and water systems efficiently.
The composite film can be used to separate diesel oil and water. 相似文献
A PTFE film surface was modified using a combined plasma/ozone‐activated process. The modified PTFE film was further reacted with 2‐bromoisobutyryl bromide to incorporate ATRP initiators in the film surface. Surface‐initiated ATRP on PTFE films was performed using sodium styrene sulfate as a monomer. The poly(sodium styrene sulfate) chain length grafted onto PTFE film surfaces increased with increasing reaction time. Analysis using X‐ray photoelectron spectroscopy, scanning electron microscopy, atomic force microscopy and a contact angle analyzer gave evidence of the success of the PTFE surface modifications.
