Photoresponsive superabsorber particles containing a crosslinked hydrophilic core and a hydrophobic azobenzene‐containing shell were used to prepare photoresponsive polymeric nanomats, thus combining photoresponsivity with high porosity, toughness, and hydrophilicity. The properties of the nanomat composites were highly dependent upon the amount of the superabsorber photochromic particles added. Stable, highly elastic composite nanomats with very high loading (up to ≈50 wt.‐%), good water absorption capacity (4 000%) and relatively good tensile strength (3 MPa) were obtained. The photoresponsive behavior of the composites is demonstrated, which leads to relatively fast water desorption.
Copolymers of 3,4‐ethylenedioxythiophene and 3‐methylthiophene have been prepared by recurrent potential pulses using monomer mixtures with various concentration ratios, their properties being compared with those of the corresponding homopolymers. In addition, different technological applications have been tested for the generated copolymers. Results indicate that the properties of the copolymers are closer to those of poly(3,4‐ethylenedioxythiophene) than to those poly(3‐methylthiophene). Furthermore, the ability of the copolymers to store charge and to interact with plasmid DNA suggest that they are very promising materials.
In this comparative study, the charge storage performance of commercial high‐temperature polymer films was evaluated and correlated with their chemical structure. Isothermal surface potential decay measurements after annealing periods at 90 °C revealed that amorphous polyetherimide (PEI) films showed the best charge storage behavior. Polyimide films showed reduced charge storage performance, whereas sulfur‐containing polymer films are not suitable as electrets due to their fast charge decay. Additionally, the effect of water content in PEI films in the range of 0.02–0.79 wt.‐% was studied. Increasing amounts of water decreased the charge storage properties proportionally, but only by a relatively smaller amount: the highest investigated water content of 0.79 wt.‐% reduced the charge by only 30%.
A method that combines UV irradiation and pausing was developed to manipulate the regularity and the length scales of the morphology generated by phase separation in full‐interpenetrating polymer networks of polystyrene and poly(methyl methacrylate). Upon increasing the pause time of photopolymerization and photo‐crosslink processes, the morphology gradually changes from hexagonal‐like packing to random structures. The width of the loss tan δ obtained for these phase‐separated materials changes with the morphological regularity, suggesting a potential technique for fabrication of mechanical bandgap materials.
The morphology of molded parts is the result of a competition between deformation rate, crystallization kinetics, relaxation times, and cooling. In this work, samples are solidified isothermally, so that the differences in morphology can be ascribed only to flow, and after a step shear, so that the effect of crystallinity on flow can be neglected. The resulting morphology is characterized, so that the data can be adopted for any further analysis. A comparison is conducted among the resulting structures and an attempt is made to identify a key parameter able to justify the differences. It is found that the main morphological features can be correlated to a single rheological parameter: the maximum attained value of molecular strain during the pulse of flow.
CNF‐reinforced PP nanocomposites were fabricated from CNFs dispersed in a boiling PP/xylene solution. Their thermal properties were characterized by TGA and DSC and shown to exhibit improved thermal stability and higher crystallinity. They were further processed into thin films by compression molding. The electrical conductivity and dielectric property of the PP/CNF nanocomposite thin films were studied. Both electric conductivity and real permittivity increased with increasing fiber loading. Electrical conductivity percolation is observed between 3.0 and 5.0 wt.‐% fiber loading. The rheological behavior of the nanocomposite melts were also investigated. It was found that a small fiber concentration affects the modulus and viscosity of PP melt significantly.
Nature offers interesting examples of structures with a gradually changing composition that provides unique mechanical properties. Today, the transfer of biological principles to technical applications is gaining increasing attention. One prominent example of the transfer of biomimetic principles to materials science is the mussel byssus. Byssus threads possess gradually changing mechanical properties from soft to stiff in order to efficiently attach the mussel to the rock. This design is the basis for polymer gradient materials. Herein, we give a comprehensive overview of the most recent developments in the field of PGMs. In addition to basic terminology and definitions, selected highlights of PGMs are presented, followed by experimental techniques and characterization methods.
Polymer/clay composite hydrogels were prepared based on PVA hydrogels containing 3–10 wt.‐% MOM. Their microstructure and morphology were studied by FT‐IR, WAXS and SEM, whereas the interactions between MOM and PVA were evaluated by thermal analyses. The swelling ratios for the PVA/MOM hydrogels decrease with increasing MOM content. WAXS results indicate that MOM was intercalates, and DSC results show a strong interaction between PVA and MOM. This interaction results in a stable network, which is confirmed by the elastic modulus and the thermal decomposition behavior of the hydrogels. Therefore, MOM acts as a co‐crosslinker, improving the stability of the network.
Summary: One of the important applications of PUEs is as damping materials such as the spring aids used in cars, which need to have excellent cyclic fatigue durability. Our results show that the fatigue durability of PUE can be significantly improved by incorporating organoclay. The best result was obtained for 3 wt.‐% organoclay, and the fatigue durability of the PUE‐organoclay nanocomposites was increased on an average to about ten times that of pure PUE. The addition of organoclay resulted in a reduction in the size of hard‐segment domains. The organoclay nanoplatelets show reversible deformation behaviour during a fatigue test confirmed by WAXD and computer simulation. These could benefit in stopping crack propagation, releasing concentrated stress and giving rise to fatigue resistance.
Schematic diagram of d‐spacing on nanoscale change during stretching. 相似文献
Summary: Biomimetic scaffolds are appealing products for the repair of bone defects using tissue engineering strategies. The present study prepared novel biomimetic composite scaffolds with similar composite to natural bone using bioactive glass, collagen, hyaluronic acid, and phosphatidylserine. The microstructure, swelling ratio, biodegradability, and biomineralization characteristic of the composite scaffolds with and without hyaluronic acid and phosphatidylserine were compared and analyzed by SEM/EDAX, XRD, and FTIR techniques and in vitro test, and the properties can be influenced by 1‐ethyl‐3‐(3‐dimethylaminopropyl) carbodiimide (EDC)/N‐hydroxysuccinimide (NHS) crosslinking. The optimized properties of the crosslinked composite scaffolds observed in this study show the possibility of their use of bioactive and bioresorbable scaffolds in bone tissue engineering.
SEM micrographs of BG‐COL‐HYA‐PS composite scaffolds after immersion in SBF for 1 d. 相似文献
p‐tert‐Butylcalix[6]arene was acylated with different carboxylic acid anhydrides to improve their solubility in dimethacrylate cross‐linkers. An esterification of p‐tert‐butylcalix[6]arene 1 with octanoic anhydride followed by methacrylation of the residual hydroxy groups with methacrylic anhydride resulted mainly in the formation of a pentaoctanoatemonomethacrylate 2a . In the radical polymerization of methyl methacrylate the inhibition effect of residual hydroxy groups in 2a was evaluated. Dimethacrylate containing composites based on a monomer matrix of cross‐linking dimethacrylates and 0–30 wt.% of 2a were prepared. The addition of 2a resulted in a significant decrease of the polymerization shrinkage, whereas the modulus of elasticity of the visible light cured composites was not affected.
A bilayer‐structured PEI/CNF composite fabricated by a facile solution casting method is described, showing dramatically improved static dissipation properties at a rather low loading level. Compared to the conventional monolayer nanocomposite with high static dissipation rate, the bilayer‐structured composite exhibited a 91.4 wt.‐% reduction in CNF loading, while it is volumetric and surface static dissipation rates were ca. 1 000 and 20 times higher, respectively. The interface region in the bilayer structure accounts for such a remarkable improvement. It is believed that this design could significantly benefit the applications requiring high antistatic capability of polymeric materials.
The preparation of nanofibrillar composite (NFC) materials using single‐polymer nanofibrils as starting materials is described. Such a possibility is offered by (i) the concept of polymer/polymer NFCs, which have recently been manufactured and represent a further development in the field of microfibril‐reinforced composites, and (ii) the opportunity to isolate neat nanofibrils through selective dissolving of the second blend component. The resulting nanofibrillar single‐polymer composites are characterized by superior mechanical properties (the tensile modulus and strength are improved up to 350%), competing with glass‐fiber‐reinforced PET.
A new melt‐processable PTFE material is presented and characterized that provides new and economical solutions in polymer technology while bridging the gap between perfluorinated PTFE and fluorothermoplastic materials such as perfluoroalkoxy resins. Thermal transitions, MW and MWD, and microstructures of the melt‐processable PTFE materials are investigated and compared to standard PTFE, modified PTFE, and PFA materials. The influence of the polymerization type used for the preparation of the melt‐processable PTFE (emulsion and suspension polymerization) on the MWD and the comonomer distribution are discussed.
Long‐aliphatic‐segment polyamides were prepared based on hexamethylenediamine and α,ω‐(CH2)x biosynthetic diacids (x = 10, 11, 12). The pertinent monomers (salts) were isolated as solids, thoroughly characterized for the first time, and then submitted to an anhydrous melt prepolymerization technique. The obtained prepolymers exhibited in the range of 5 100–11 800 g · mol?1, and the molecular weight was further increased by up to 55% through solid‐state finishing. The suggested overall polyamidation cycle was conducted at short melt‐reaction times, so as to avoid any thermal degradation, and was proved efficient, indicating similar reactants polymerizability independently of the methylene content.
Cyano‐OPV moieties were covalently incorporated into a PETG backbone to create ductile amorphous polymers which change their PL and absorption color as a function of deformation. The cyano‐OPV concentration was systematically varied, and the composition was related to the material's optical response. This approach afforded PETG/dye copolymers which upon annealing display characteristics of aggregated dye molecules. The materials exhibit a significant color change upon compression, consistent with disassembly of the dye aggregates. This mechanochromic response is irreversible and can be detected by the unassisted eye.
This is the first report on a thermoformable bionanocomposite based on a natural nanocrystal and formed by grafting long polymer chains onto the surface of microcrystalline cellulose. For the cellulose nanocrystal‐graft‐poly(ε‐caprolactone), the “graft from” strategy contributed to long and dense “plasticizing” PCL tails onto the CN surface as the key of thermoforming. The grafted PCL chains shielded the hydrophilic surface of CN and, hence, showed high water‐resistance. Moreover, a strategy for developing new bionanocomposite materials based on natural nanocrystals has been presented.
Summary: A method that takes into account the entire molecular weight distribution (MWD) for the prediction of polymer point properties and/or indexes is presented. The method is based on the convolution of the polymer mass molecular weight distribution and an empirical kernel function. Thus, the problem of relating the polymers properties to the MWD is reduced to the estimation of this empirical function. The proposed methodology is able to successfully predict melt indexes (MI) of a set of poly(propylene) samples.
Three series of composite films based on polyimide and MWNTs were prepared by conversion of pyromellitic dianhydride and 4,4′‐oxydianiline in the presence of the nanotubes, followed by thermal imidization. Carboxy‐ and amino‐functionalized as well as unmodified nanotubes were used. It was demonstrated that just 0.5 wt.‐% of nanotubes increased the tensile properties of the composite films distinctly. Surprisingly, a significant influence of the functional groups on the mechanical performance of the composite films could not be demonstrated. However, it was shown that functional groups may reduce the conductivity of the films. Furthermore, the influence of ultrasonication is discussed.
Summary: The swelling equilibrium of poly(acrylamide) [PAAm] and poly[acrylamide‐co‐(itaconic acid)] [P(AAm/IA)] hydrogels was studied as a function of temperature and IA content in aqueous solutions of surfactants: sodium dodecyl sulfate (SDS, anionic) and hexadecyltrimethylammonium bromide (HTAB, cationic). P(AAm/IA) hydrogels in water exhibited reentrant conformational transitions depending on temperature, whereas PAAm hydrogels were not affected with the change of temperature. The equilibrium‐volume‐swelling ratio of P(AAm/IA) hydrogels increased sharply in SDS solutions, with an increase of the mole percent of IA. However, in HTAB solution, the equilibrium‐volume‐swelling ratio of these hydrogels decreased with an increase of IA content.
The equilibrium volume‐swelling ratios of the hydrogels in water shown as a function of temperature. 相似文献
