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991.
Design of XNBR nanocomposites for underwater acoustic sensor applications: Effect of MWNT on dynamic mechanical properties and morphology 下载免费PDF全文
In this work, application of rubber‐MWNT nanocomposite for underwater acoustic sensors is explored. The nanocomposite is developed by incorporating multiwalled carbon nanotubes (MWNT) into carboxylated nitrile rubber by mechanical mixing. The addition of MWNT up to 10 phr is found to result in about 330% increase in tensile strength, 140% increase in modulus, and 160% increase in tear strength. Transmission electron microscopy and scanning electron microscopy analyses indicate uniform dispersion of nanotubes in the rubber matrix. Dynamic mechanical analysis shows that damping at ambient temperature gradually increases with increasing filler content. This is attributed to the augmented frictional energy loss at the interface. The damping peak position shifts upward with increase in MWNT concentration, which may be gainfully used to tune to the operational frequency range of underwater acoustic sensors. Payne effect is observed at higher filler concentration due to the breakage of aggregates formed by filler–filler interaction. The nanocomposite may find application for damping structural vibrations and thus to improve the performance of underwater acoustic sensors. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40752. 相似文献
992.
Developing toughened aromatic polybenzoxazines using thermoplastic oligomers and telechelics,part 1: Preparation and characterization of the functionalized oligomers 下载免费PDF全文
Ian Hamerton Lisa T. McNamara Brendan J. Howlin Paul A. Smith Paul Cross Steven Ward 《应用聚合物科学杂志》2014,131(19)
The preparation and characterization of three families of thermoplastic oligomers (Mn = 2918–13263 g mol?1) based on polyarylsulfone (PSU) differing in both molecular weight and terminal functionality and one series of polyarylethersulfone (PES) of different molecular weights is reported. Infrared and nuclear magnetic resonance spectroscopy data support the formation of both the hydroxyl terminated oligomers and conversion (67–89% depending on molecular weight) to the telechelic PSU oligomer bearing reactive benzoxazine groups. Differential scanning calorimetry reveals that the onset of homopolymerization in the telechelic PSU oligomer occurs at around 100°C (peak maximum 125°C at 10 K/min) and rescans show values of the glass transition (for the homopolymers) ranging from 124 to 167°C depending on molecular weight. The influence on the oligomer backbone and terminal functionality is examined using thermal analysis. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40875. 相似文献
993.
CO2 Adsorption capacity of activated N‐doping porous carbons prepared from graphite nanofibers/polypyrrole 下载免费PDF全文
In this study, N‐doping porous carbons (NPCs) with a 3D aperiodic hierarchical and layered structure were prepared by the sodium hydride (NaOH) activation of graphite nanofibers (GNFs)/polypyrrole (PPY) composites. The effects of the N groups and structural features on the CO2 adsorption capacity of NPCs were investigated by N2 full isotherms, XRD, SEM, and TEM. The CO2 adsorption capacity was measured by the CO2 isothermal adsorption at 25°C and 1 atm. It was found that GNFs served as a substrate and layered graphitic carbons were formed by the thermal annealing of PPY. The content of N groups and textural properties of NPCs were enhanced with increasing activation temperature, resulting in improved CO2 adsorption capacity. The CO2 adsorption isotherms showed that GPK‐600 exhibited the best CO2 adsorption capacity of 88.8 mg/g when the activation temperature was 600°C. The result indicates that the pore size and its distribution of NPCs lead to feasible contact CO2, and the presence of high N groups on the NPCs could have resulted in further stabilization of the surface effect. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40517. 相似文献
994.
Influence of kenaf form and loading on the properties of kenaf‐filled polypropylene/waste tire dust composites: A comparison study 下载免费PDF全文
Kenaf (KNF)‐filled polypropylene/waste tire dust (PP/WTD) composites containing different KNF loadings (0, 5, 10, 15, and 20 parts per hundred parts of resin (phr)) were prepared using a Thermo Haake Polydrive internal mixer. The influence of the KNF form (KNF short fiber (KNFs) and KNF powder (KNFp)) at different KNF loadings on properties of the composites was studied. Results showed that with increasing KNF loading, the stabilization torque, tensile modulus, water absorption, and thermal properties increased for both KNFp‐ and KNFs‐filled PP/WTD composites. However, the tensile strength and elongation at break decreased by 29.2% and 53.9%, respectively, for KNFp‐filled PP/WTD composites, whereas KNFs‐filled PP/WTD composites showed a decrement of 24.5% and 63.5%, respectively. The stabilization torque, tensile strength, and tensile modulus increased by 22.4%, 6.7%, and 2.6%, respectively, for KNFs‐filled PP/WTD composites at 20 phr KNF loading. The scanning electron microscopy morphological studies on the tensile fractured surfaces revealed poor adhesion between KNFp and PP/WTD matrices as compared to KNFs and PP/WTD matrices. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40877. 相似文献
995.
Investigation on the morphology and tensile behavior of β‐nucleated isotactic polypropylene with different stereo‐defect distribution 下载免费PDF全文
Hongmei Peng Bin Wang Jinggang Gai Jinyao Chen Feng Yang Ya Cao Huilin Li Jian Kang Ming Xiang 《应用聚合物科学杂志》2014,131(6)
Large amount of work has been published on the tacticity‐properties relationship of isotactic polypropylene (iPP). However, the stereo‐defect distribution dependence of morphology and mechanical properties of β‐nucleated iPP (β‐iPP) is still not clear. In this study, two different iPP resins (PP‐A and PP‐B) with similar average isotacticity but different uniformities of stereo‐defect distribution were selected, their β‐iPP injection molding specimens were prepared, and the morphology evolution and tensile behaviors were studied by means of differential scanning calorimetry (DSC), 2D wide‐angle X‐ray diffraction (2D‐WAXD) and scanning electron microscope (SEM). DSC results showed that with the same concentration of β‐nucleating agent (0.3 wt % WBG‐II), PP‐B with more uniform stereo‐defect distribution exhibited more amount of β‐phase than that of PP‐A with less uniform stereo‐defect distribution, indicating that PP‐B is more favorable for the formation of β‐phase. SEM results showed that PP‐B formed more amount of β‐crystals with relatively high structural perfection, while in PP‐A a mixed morphology of α‐ and β‐phase with obviously higher amount of structural imperfection emerges. The results of room‐temperature tensile test indicated that the yield peak width of PP‐B was obviously wider, and the elongation at break of PP‐B was higher than that of PP‐A, showing a better ductile of PP‐B. The morphology evolution results of SEM, 2D‐WAXD and DSC suggest that, a combination of lamellar deformation and amorphous deformation occurred in PP‐A, while only amorphous deformation mainly took place in PP‐B, which was thought to be the reason for the different tensile behaviors of the samples. In the production of β‐PP products via injection molding, the uniformity of stereo‐defect distribution was found to be an important factor. PP with more uniform distribution of stereo‐defect favors the formation of large amount of β‐phase with high perfection, which exhibit superior ductile property. The related mechanism was discussed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 40027. 相似文献
996.
Preparation and dielectric properties of sulfonated poly(aryl ether ketone)/acidified graphite nanosheet composites 下载免费PDF全文
Percolative dielectric composites of sulfonated poly(aryl ether ketone) (SPAEK) and acidified graphite nanosheets (AGSs) were fabricated by a solution method. The dielectric constant of the as‐prepared composite with 4.01 vol % AGSs was found to be 330 at 1000 Hz; this was a significant increase compared to that of pure SPAEK. Through the calculation, a low percolation threshold of the AGS/SPAEK composite was confirmed at 3.18 vol % (0.0318 volume fraction) AGSs; this was attributed to the large surface area and high conductivity of the AGSs. Additionally, our percolative dielectric composites also exhibited good mechanical performances and good thermostability, with a tensile strength of 71.7 MPa, a tensile modulus of 1.91 GPa, a breaking elongation of 16.4%, and a mass loss temperature at 5% of 336°C. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 40028. 相似文献
997.
In this article, a novel boron‐doped silicone resin (BSR) was synthesized by hydrolysis‐polycondensation method, with propyl‐triethoxysilane (PTES), dimethyl‐diethoxysilane (DMDES), and boric acid (BA) as starting materials, using absolute ethyl alcohol as solvent and hydrochloric acid as catalyst. The structures of the BSR were characterized by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), X‐ray photoelectron spectroscopy (XPS), and gel permeation chromatography (GPC). FTIR spectra showed characteristic B? O? Si and Si? O? Si stretching modes. XPS and NMR results confirmed further that boron element was doped successfully into the main chains of the silicone resin as Si? O? B bond motifs, and hydroxyl groups from BA were condensed properly with Si? OH or Si? OR to form cross‐linked structure of BSR with narrowed molecular weight distributions in optimum experimental condition. The thermal stability of the BSR was studied by thermogravimetry analysis and derivative thermogravimetry. The thermal degradation temperature of the silicone resin improved greatly after doping element boron into the main chain, and the thermal stability of the BSR was influenced by the content of boron. The thermal degradation mechanism of this BSR was also discussed. The degradation process can be divided into two stages, the weight loss in the first stages may be corresponding to the loss of the small groups and weaker bonds in the chains, such as ? CH3, and ? C3H7, the weight loss in the second stage may be corresponding to the loss of the group as ? OC2H5. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40934. 相似文献
998.
Char barrier effect of graphene nanoplatelets on the flame retardancy and thermal stability of high‐density polyethylene flame‐retarded by brominated polystyrene 下载免费PDF全文
Graphene nanoplatelets (GNPs) with the char barrier effect were combined with brominated polystyrene (BPS) and antimony trioxide (Sb2O3) to improve the flame retardancy and thermal stability of high‐density polyethylene. Thermogravimetric analysis, limited oxygen index (LOI) testing, and vertical burning testing (UL‐94) showed that the presence of GNPs led to enhanced thermal oxidation stability and significantly reduced the flammability. The addition of 1 wt % GNPs to polyethylene/BPS–Sb (mass ratio = 92/6/2) led to UL‐94 grades from NG (first burning time > 30 s) to V‐2 (total burning time = 14 s), and the LOI value increased from 23.4 to 24.1%. The results of the pyrolysis products provided evidence that the GNPs restricted volatilization. The morphology of the chars also proved the formation of the char layer, which could act as a barrier to isolate the material from the flame and retard the vaporization of flammable gases via a tortuous pathway. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40520. 相似文献
999.
The development of the plastic and viscoelastic properties and the corresponding failure limits of the acetal homopolymer polyoxymethylene were studied in unidirectional cyclic fatigue. Samples with molecular weights (MWs) ranging from 90 to 142 kg/kmol were tested in displacement‐controlled conditions, resulting in maximum stress amplitudes between 30 and 59 MPa and strain amplitudes between 35.8 and 92.6 με. The zero‐hour material properties and the cycle‐dependent property development were predominantly dictated by deformations in the crystalline regions and showed a negligible dependence on MW. However, the final failure limits were found to be primarily dependent on the length of the amorphous tie chains that connect the crystallites. As such, fatigue life analysis showed a strong dependence on MW. Results are interpreted in light of the primary mechanical failure mechanisms and the corresponding molecular deformations. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40762. 相似文献
1000.
Curing characteristics,morphology, thermal stability,mechanical properties,and irradiation resistance of methylethylsilicone/methylphenylsilicone rubber blends 下载免费PDF全文
Methylethylsilicone rubber (MESR)/methylphenylsilicone rubber (MPSR) blends were cured with 2,5‐dimethyl‐2,5‐di(tert‐butylperoxy)hexane. The curing characteristics, morphology, thermal behaviors, mechanical properties at different temperatures, radiation resistance, and thermal aging resistance of the MESR/MPSR blends were investigated. The results show that a high MPSR content could decrease the optimum curing time and improve the scorch safety. Dynamic mechanical analysis revealed that the glass‐transition temperature of the blends increased slightly with the addition of MPSR. Scanning electron microscopy showed that MESR and MPSR had good compatibility in the blends. Thermogravimetric analysis indicated that the thermal stability of the blends increased with increasing quantity of MPSR. The blends had excellent mechanical properties at low temperatures. However, these properties were significantly reduced when the temperature was increased. Moreover, changes in the mechanical properties decreased with increasing MPSR content at high temperatures, especially at temperatures higher than 100°C. In addition, the radiation resistance and thermal aging resistance of the blends increased with increasing MPSR content. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40529. 相似文献