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991.
992.
Gang Liu Huamin Zhang Hexiang Zhong Jingwei Hu Dongyan Xu 《Electrochimica acta》2006,51(26):5710-5714
A novel Pt4ZrO2/C catalyst was prepared and compared with 20 wt.% Pt/C in terms of the sintering resistance and corrosion resistance. To evaluate their sintering resistance and corrosion resistance properties, an accelerated ageing test (AAT) was performed. The catalysts before and after AAT were characterized by cyclic voltammetry (CV), rotating disk electrode (RDE) and X-ray diffraction (XRD). After AAT, the dissolution rate of Pt and Zr in H3PO4 media (105 wt.%, 204 °C) was characterized by inductively coupled plasma-atomic emission spectroscopy (ICP-AES). The electrochemical area (ECA) changes of thin film electrodes based on Pt4ZrO2/C and Pt/C catalysts were also evaluated using continuous CV sweep technique. All the results showed that Pt4ZrO2/C has higher sintering resistance and corrosion resistance than Pt/C. ‘Anchor effect’ is proposed to explain the enhanced effect of ZrO2 in Pt4ZrO2/C binary catalyst compared with Pt/C that contain platinum alone. 相似文献
993.
994.
Free radical grafting of glycidyl methacrylate (GMA) onto molten polypropylene (PP) was studied in a co-rotating twin screw extruder. Grafting yields of GMA obtained under various experimental conditions along the screw length allowed for a good appreciation of the effects of chemical parameters (the presence of styrene and the concentrations of peroxide and monomers) and those of processing parameters (feed rate, screw speed, and specific throughput). Similar to the results obtained in a batch mixer,1 free radical grafting of GMA carried out in the extruder in the presence or absence of styrene proceeded rapidly, as it was virtually completed half-way down stream of the extruder. Additionally, the presence of styrene as a second monomer increased the GMA grafting yield reatly with reduced PP chain degradation. The ultimate GMA grafting yield increased with increasing concentration of peroxide, 1,3-bis(tert-butylperoxyisopropyl)benzene. This similarity between the batch mixer and the extruder is related to the fact that in both cases it is the concentration of the peroxide and its half lifetime that determine the grafting rate and the ultimate grafting yield. On the othe hand, the GMA grafting yield decreased with increasing screw speed or feed rate. For a particular specific throughput (the ratio of throughput to screw speed), an increase in throughput with a concomitant increase in screw speed brought about a decrease in GMA grafting yield. It was concluded that the GMA grafting yield is affected primarily by the residence time in the zone in which free radicals are not depleted. The effects of screw speed, feed rate, and specific throughput manifest mainly through this local residence time distribution. Specific energy is not a good measure of the performance of the extruder with respect to the free radical rafting of GMA onto PP. © 1995 John Wiley & Sons, Inc. 相似文献
995.
A versatile electrochemical platform for characterizing the adsorption of neutral and positively charged surfactants on hydrophobic surfaces was established using methylene blue (MB) as the probe. As a rigid, planar and electroactive species, MB can intercalate inside the regular self-assembled monolayers (SAMs) of n-hexanethiol and exhibit well-defined electrochemical responses. The adsorption of surfactants on the hydrophobic SAMs through the intercalation interaction between the hydrophobic tails of surfactants and the SAMs might change the density of the SAMs and influence the electrochemical behaviors of MB, providing a simple but effective approach for characterizing surfactant adsorption on hydrophobic surfaces. As an example, the adsorptive behaviors of cetyltrimethylammonium bromide (CTAB), a positively charged surfactant, and Triton X-100, a neutral surfactant, on hydrophobic surfaces were investigated by cyclic voltammetry and electrochemical impedance spectroscopy. The results showed that these surfactants generally experienced three different adsorptive behaviors: the monomer adsorption at low concentrations, the loose monolayer adsorption at intermediate concentrations and the dense monolayer adsorption at high concentrations. In the case of CTAB, a new additional submonolayer adsorptive behavior between the monomer and the loose monolayer adsorption was observed for the first time, due to its rather long hydrophobic tail. 相似文献
996.
A fumed hydrophilic nano‐silica‐filled polypropylene (PP) composite was blended with a liquid‐crystalline polymer (LCP; Rodrun LC5000). The preblended polymer blend was extruded through a capillary die; this was followed by a series of rheological and morphological characterizations. The viscosity of the PP matrix increased with the addition of the hydrophilic nano‐silica. At shear rates between 50 and 200 s?1, the composite displays marked shear‐thinning characteristics. However, the incorporation of LC5000 in the PP composite eliminated the shear‐thinning characteristic, which suggests that LC5000 destroyed the agglomerated nano‐silica network in the PP matrix. Although the viscosity ratio of LCP/PP was reduced after the addition of nano‐silica fillers, the LCP phases existed as droplets and ellipsoids. The nano‐silicas were concentrated in the LC5000 phase, which hindered the formation of LCP fibers when processed at high shear deformation. We carried out surface modification of the hydrophilic nano‐silica to investigate the effect of modified nano‐silica (M‐silica) on the morphology of the PP/LC5000 blend system. Ethanol was successfully grafted onto the nano‐silica surface with a controlled grafting ratio. The viscosity was reduced for PP filled with ethanol‐M‐silica when compared to the system filled with untreated hydrophilic nano‐silica. The LC5000 in the (PP/M‐silica)/LC5000 blend existed mainly in the form of fibrils. At high shear rates (e.g., 3000 s?1), the LC5000 fibril network was formed at the skin region of the extrudates. The exclusion of nano‐silica in the LC5000 phase and the increased viscosity of the matrix were responsible for the morphological changes of the LCP phase. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1484–1492, 2003 相似文献
997.
Wei Hu Baijun Liu Dong Wang Yanhua Yang Chunhai Chen Zhenhua Jiang Wanjin Zhang Zhongwen Wu 《应用聚合物科学杂志》2003,89(5):1347-1350
Novel aromatic poly(ether ketones) containing bulky lateral groups were synthesized via nucleophilic substitution reactions of 4,4′‐biphenol and (4‐chloro‐3‐trifluoromethyl)phenylhydroquinone (CF‐PH) with 1,4‐bis(p‐fluorobenzoyl)benzene. The copolymers were characterized by differential scanning calorimetry (DSC), wide‐angle X‐ray diffraction, and polarized light microscopy observation. Thermotropic liquid‐crystalline behavior was observed in the copolymers containing 40, 50, 60, and 70 mol % CF‐PH. The crystalline–liquid‐crystalline transition [melting temperature (Tm)] and the liquid‐crystalline–isotropic phase transition appeared in the DSC thermograms, whereas the biphenol‐based homopolymer had only a melting transition. The novel poly(aryl ether ketones) had glass‐transition temperatures that ranged from 143 to 151°C and lower Tm's that ranged from 279 to 291°C, due to the copolymerization. The polymers showed high thermal stability, and some exhibited a large range in mesophase stability. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1347–1350, 2003 相似文献
998.
999.
木粉/低密度聚乙烯复合材料的发泡研究 总被引:1,自引:1,他引:1
用模压法制备木粉/低密度聚乙烯发泡材料。通过差示量热扫描分析,考察了纯偶氮二甲酰胺(AC)及与 ZnO共混物、纯NaHCO3及与柠檬酸(L)共混物的热分解特性,探讨了发泡剂AC、NaHCO3、柠檬酸、交联剂过氧化二异丙苯等对材料力学性能的影响,并在扫描电镜下观察了材料断面的微观形态。结果表明:采用放热发泡剂和复合发泡剂都能使复合材料密度下降20%左右,发泡后材料的冲击性能为发泡前体系的1.5倍左右;复合发泡剂的发泡效果优于单放热发泡剂的效果。 相似文献
1000.