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This work focuses on flexible epoxy (EP) composites containing various amounts of neat and polydopamine (PDA)-coated paraffin microcapsules as a phase change material (PCM), which have potential applications as adhesives or flexible interfaces with thermal management capability for electronics or other high-value-added fields. After PDA modification, the surface of PDA-coated capsules (MC-PDA) becomes rough with a globular appearance, and the PDA layer enhances the adhesion with the surrounding epoxy matrix, as shown by scanning electron microscopy. PDA deposition parameters have been successfully tuned to obtain a PDA layer with a thickness of 53 ± 8 nm, and the total PDA mass in MC-PDA is only 2.2 wt %, considerably lower than previous results. This accounts for the fact that the phase change enthalpy of MC-PDA is only marginally lower than that of neat microcapsules (MC), being 221.1 J/g and 227.7 J/g, respectively. Differential scanning calorimetry shows that the phase change enthalpy of the prepared composites increases with the capsule content (up to 87.8 J/g) and that the enthalpy of the composites containing MC-PDA is comparable to that of the composites with MC. Dynamic mechanical analysis evidences a decreasing step in the storage modulus of all composites at the glass transition of the EP phase, but no additional signals are detected at the PCM melting. PCM addition positively contributes to the storage modulus both at room temperature and above Tg of the EP phase, and this effect is more evident for composites containing MC-PDA. As the capsule content increases, the mechanical properties of the host EP matrix also increase in terms of elastic modulus (up to +195%), tensile strength (up to +42%), Shore D hardness (up to +36%), and creep compliance (down to −54% at 60 min). These effects are more evident for composites containing MC-PDA due to the enhanced interfacial adhesion. [ABSTRACT FROM AUTHOR]

An investigation on the crystallization of composites based on poly(ethylene succinate) and unmodified single-walled carbon nanotube was made in this report. Both isothermal and non-isothermal modes were studied along with subsequent melting behavior using differential scanning calorimetry. Crystal morphology was then explored using X-ray scattering and infrared spectroscopy. It was observed during isothermal crystallization that carbon nanotube (CNT) could contribute to the crystallization rate through heterogeneous nucleation. Furthermore, nanotubes enhanced the crystallinity within low and high undercooling rather than medium undercooling. Similar findings were obtained in non-isothermal crystallization mode. At lower cooling rates, the crystallization rate was more strongly influenced by the nanotubes, while at higher cooling rates the crystallinity was affected to the greater extent. The onset of the cold crystallization of polymer remained unaffected in presence of the nanotube, while its extent was reduced. X-ray diffraction together with infrared spectroscopy found that the polymer crystalline morphology was of α type, and no transition from α to β occurred in presence of the CNT. [ABSTRACT FROM AUTHOR]

In this research, influence of incorporating LiClO4 salt on the crystallization, conformation, and ionic conductivity of poly(ethylene oxide) (PEO) in its miscible blend with poly(methyl methacrylate) (PMMA) is studied. Differential scanning calorimetry showed that the incorporation of salt ions into the blend suppresses the crystallinity of PEO. The X-ray diffraction revealed that the unit-cell parameters of the crystals are independent of the LiClO4 concentration despite of the existence of ionic interactions between PEO and Li cations. In addition, the complexation of the Li+ ions by oxygen atoms of PEO is investigated via Fourier transform infrared spectroscopy. The conformational changes of PEO segments in the presence of salt ions are studied via Raman spectroscopy. It is found that PEO chains in the blend possess a crown-ether like conformation because of their particular complexation with the Li+ ions. This coordination of PEO with lithium cations amorphize the PEO and is accounted for suppressed crystallinity of PEO in the presence of salt ions. Finally, electrochemical impedance spectroscopy is used to characterize the ionic conductivity of PEO in the PEO/PMMA/LiClO4 ternary mixture at various temperatures. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 [ABSTRACT FROM AUTHOR]

In strain-hardening cement-based composites (SHCC), polypropylene (PP) fibers are often used to provide ductility through micro crack-bridging, in particular when subjected to high loading rates. For the purposeful material design of SHCC, fundamental research is required to understand the failure mechanisms depending on the mechanical properties of the fibers and the fiber–matrix interaction. Hence, PP fibers with diameters between 10 and 30 µm, differing tensile strength levels and Young's moduli, but also circular and trilobal cross-sections were produced using melt-spinning equipment. The structural changes induced by the drawing parameters during the spinning process and surface modification by sizing were assessed in single-fiber tensile experiments and differential scanning calorimetry (DSC) of the fiber material. Scanning electron microscopy (SEM), atomic force microscopy (AFM) and contact angle measurements were applied to determine the topographical and wetting properties of the fiber surface. The fiber–matrix interaction under quasi-static and dynamic loading was studied in single-fiber pull-out experiments (SFPO). The main findings of microscale characterization showed that increased fiber tensile strength in combination with enhanced mechanical interlocking caused by high surface roughness led to improved energy absorption under dynamic loading. Further enhancement could be observed in the change from a circular to a trilobal fiber cross-section. [ABSTRACT FROM AUTHOR]

In this paper, we report on the use of amorphous lignin, a waste by-product of the paper industry, for the production of high performance carbon fibers (CF) as precursor with improved thermal stability and thermo-mechanical properties. The precursor was prepared by blending of lignin with polyacrylonitrile (PAN), which was previously dissolved in an ionic liquid. The fibers thus produced offered very high thermal stability as compared with the fiber consisting of pure PAN. The molecular compatibility, miscibility, and thermal stability of the system were studied by means of shear rheological measurements. The achieved mechanical properties were found to be related to the temperature-dependent relaxation time (consistence parameter) of the spinning dope and the diffusion kinetics of the ionic liquids from the fibers into the coagulation bath. Furthermore, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical tests (DMA) were utilized to understand in-depth the thermal and the stabilization kinetics of the developed fibers and the impact of lignin on the stabilization process of the fibers. Low molecular weight lignin increased the thermally induced physical shrinkage, suggesting disturbing effects on the semi-crystalline domains of the PAN matrix, and suppressed the chemically induced shrinkage of the fibers. The knowledge gained throughout the present paper allows summarizing a novel avenue to develop lignin-based CF designed with adjusted thermal stability. [ABSTRACT FROM AUTHOR]