The potential of polymerization in a dispersed system as an attractive technique for polymer/graphene composite synthesis is discussed. This overview is focused on the preparation of graphene/polymer composite materials by two methods: (i) emulsion mixing or blending of polymer and graphene aqueous dispersions, and (ii) in situ polymerization in a dispersed system (emulsion, miniemulsion, microemulsion, and Pickering‐stabilized emulsion). Various methods for the stabilization of graphene nanoplatelets (GNPs) prior to composite preparation are presented, and the established specific interactions between the filler and the matrix are discussed. The determination of the electrical conductivity and the opportunity offered by polymerization in a dispersed system for the formation of a segregated network of graphene filler in the frame of a polymer matrix are presented. The mechanical and thermal properties of the composites are also discussed. A short summary of the open questions regarding the synthesis of water‐borne polymer/graphene composites is presented.
The last decade has seen a growing interest in hybrid electrically conducting nanocomposites. This article aims to provide a detailed overview of the present status of research in carbon nanotube–polyaniline (CNT/PANI) composites, from processing to structural and property evaluations. CNT/PANI are synthesized by electrochemical and chemical processing. When chemical methods are used, the main challenge is to obtain processable CNT/PANI in the emeraldine salt (ES) form composites. Stable dispersions of ES–CNT in organic media are prepared using the post doping method, inverse emulsion polymerization, or ex situ polymerizations. On the contrary, stable water dispersions of CNT/ES are prepared using hydrophilization of a preformed CNT/ES composite, direct synthesis of micelle–CNT hybrid templates, interfacial polymerization, covalent functionalization of CNT with a water soluble polymer, or using electrostatic interactions between two oppositely charged ES and CNT aqueous colloids. Moreover, the strategies for the synthesis of ternary CNT/PANI composites incorporating noble metal nanoparticles, metal oxide, or graphene sheets are also presented and analyzed in depth. Finally, we give a review of potential applications, including chemical sensors, capacitors, fuel cells and electronic devices. 相似文献
One of the most important applications of graphene-based materials is the formation of nanocomposite materials, where graphene in the bulk-polymer matrix transfers its properties onto the polymeric material. Control of the polymer/graphene interface by attached polymeric interlayers is essential to generate nanocomposites, thus avoiding the aggregation of graphene nanoparticles. Among all graphene materials graphene oxide (GO) and reduced graphene oxide (r-GO) can be prepared on large scales useful for mass production graphene/polymer composites. The direct use of graphene materials as both, the polymerization initiator or catalyst and additive not only diminishes the agglomeration of particles in composites but also reduces the process of composite production to one facile step, which in turn avoids further purification regarding to strong acid initiators and metal particles catalysts. Here, literature activities within the past ∼10 years using graphene-based materials either as initiator or catalyst in different polymerization reactions are reviewed. 相似文献
The morphology of composite materials made by polymerizing methyl methacrylate into chrome-tanned cattlehide was examined by both light and scanning electron microscopy. The composites were selected from a series previously prepared and characterized, and their kinetics were reported. Micrographs of the polymer phase of the composites, prepared by preferential removal of collageneous material with 6N hydrochloric acid, yielded negative replicas of the fiber conformations. These provided evidence in support of proposed mechanisms of polymer deposition for two different methods of composite preparation. One method involved emulsion polymerization of monomer into hydrated leather and the other, preferentially filling leather free space. Both light and scanning electron microscopy of all composites and replicas revealed poly(methyl methacrylate) deposited largely in coarse aggregates around individual fibers. In emulsion systems, fiber bundles expanded with continuous deposition. No difference was observed in the morphology of bound and deposited polymers. However, high magnification of bound-polymer replicas exposed polymer surrounding some fibril traces. Deposition of polymer in the fine structure of bulk or solution prepared composites was not found; instead, all free space was occupied. A theory specifying polymer location in previous publications of this series, and extended here to define replica parameters, was abundantly supported by measured physical properties. A dominant grafting mechanism was precluded because the large domains limited points of possible attachment. Water absorptivities of emulsion prepared composites and controls were identical when the data were corrected to neat leather, although the rates were slightly perturbed. In contrast, both rate and equilibrium absorption data of the bulk and solution composites were retarded by polymer presence. 相似文献
In the paper, poly(methyl methacrylate)(PMMA)/SBA-15 composite materials were prepared by four different methods, that is,
in-situ batch emulsion polymerization in the presence of mesoporous SBA-15, PMMA emulsion mixed with SBA-15 powder or dispersion
in water, PMMA powder mixed with SBA-15 powder, and the properties of the composite materials were determined and compared.
The composites were characterized by infrared spectroscopy (IR), X-ray diffraction (XRD), thermogravimetric analysis (TGA),
differential scanning calorimetry (DSC), dynamic mechanics analysis (DMA) and scanning electron microscope (SEM). The results
showed that the glass transition temperatures (Tg), the storage modulus and tensile strength of the PMMA/SBA-15 composites
were all improved obviously, while the thermal decomposition temperature did not influenced apparently. The composite made
by in-situ batch polymerization exhibited the most improvement in the mechanical properties and Tg while the composite prepared
by mixing PMMA emulsion and SBA-15 dispersion gave rise to the least improvement in the mechanical properties and Tg. These
results were contributed to introducing different amount of voids into polymer matrix which were demonstrated by dielectric
constant measurement and SEM morphology observation. 相似文献
Water-in-Oil (W/O) and Oil-in-Water (O/W) type water absorbent polymer emulsions were studied using two different polymerization methods. W/O type water absorbent polymer emulsions were prepared by the inverse emulsion polymerization of ammonium acrylate (AA), the quaternized salt of dimethyl-aminoethyl methacrylate (DMQ) and acrylamide (AM) with N,N-methylene-bisacrylamide (MBA) as a crosslinker. A pH sensitive water absorbent polymer emulsion was prepared by the conventional emulsion polymerization of diethyl-aminoethyl methacrylate (DEAEMA) with ethylene glycol dimethacrylate (EGDMA) as a crosslinker. It was confirmed that the water absorption capacity of crosslinked polymers in inverse emulsion was controlled by crosslink density and dissociative charge density, and the crosslinked polyDEAEMA particles had a phase transition property of swelling and shrinking with pH. The dispersions of these water swollen crosslinked polymer particles exhibited an increase in viscosity and thixotropic fluidity. 相似文献
