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51.
Kwang‐Pill Lee Anantha Iyengar Gopalan See‐Hee Lee Ali Md Showkat Young Chang Nho 《应用聚合物科学杂志》2006,102(4):3912-3918
Conducting polydiphenylamine was used to encapsulate silica nanoparticles through the oxidative polymerization of diphenylamine in the presence of ultrasonic irradiation. The polymerization was performed in the presence of sodium lauryl sulfate as a surfactant. Experiments performed in the absence of ultrasound clearly demonstrated that the application of ultrasonication played multiple roles in the preparation of a composite of polydiphenylamine with silica nanoparticles. Ultrasonication dispersed the silica nanoparticles, converted sodium lauryl sulfate to lauryl alcohol, and augmented the dispersion of the silica‐nanoparticle/polydiphenylamine composite in an organic medium. Silica‐nanoparticle/polydiphenylamine composites were also prepared in the absence of ultrasound and/or sodium lauryl sulfate. The silica‐nanoparticle/polydiphenylamine composites were characterized with Fourier trans form infrared spectroscopy, ultraviolet–visible/near‐infrared spectroscopy, and thermogravimetric analysis. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3912–3918, 2006 相似文献
52.
Sara Cavaliere-Jaricot Arnaud Etcheberry Michel Herlem Henri Perez 《Electrochimica acta》2007,52(6):2285-2293
Platinum nanoparticles (n-Pt), over-grafted with 2-thiophenecarbonyl chloride are assembled on gold electrodes, by the Langmuir Blodgett (LB) technique using behenic acid (BHA) as promoting agent. These layers are electrochemically active without any preliminary activation. The [Fe(CN)6]3−/4− redox couple was used as electrochemical probe. This paper reports on the influence of the number of deposited LB layers, and the n-Pt density on the electrochemical response. n-Pt density was modified by the change of the “BHA/n-Pt” ratio. Cyclic voltammograms of “[Fe(CN)6]3−/4−” were observed whatever the coating conditions. As soon as the first layer was deposited the electrochemical response was associated to the n-Pt coverage, its response slightly increased up to a steady state for five or seven layers. As expected, the increase of the Pt density favored the increase of the current density. XPS analysis performed before and after electrochemical cycling showed that 4-mercaptoaniline capped platinum nanoparticles, and their over grafting were chemically and electrochemically stable. Analysis of influence of the number or the n-Pt density of the layers showed that the electrochemically active part of LB electrodes was provided by the last layer plus a part of the underlying one. 相似文献
53.
Zinc oxide (ZnO) nanoparticles assembled in one dimension to give rod‐shaped morphology were synthesized. The effect of these ZnO nanoparticles (average particle size ~ 50 nm) as the curing agent for carboxylated nitrile rubber was studied with special attention to cure characteristics, mechanical properties, dynamic mechanical properties, and swelling. These results were compared with those of the conventional rubber grade ZnO. The study confirmed that the ZnO nanoparticles gave a better state of cure and higher maximum torque with a marginal decrease in optimum cure time and scorch time. The mechanical properties also showed an improvement. There was an increase in tensile strength by ~ 120%, elongation at break by ~ 20%, and modulus at 300% elongation by ~ 30% for the vulcanizate cured with ZnO nanoparticles, as compared with the one containing rubber grade ZnO. Dynamic mechanical analysis revealed that the vulcanizates exhibited two transitions—one occurring at lower temperature due to the Tg of the polymer, while the second at higher temperature corresponding to the hard phase arising due to the ionic structures. The second transition showed a peak broadening because of an increase in the points of interaction of ZnO nanoparticles with the matrix. The tan δ peak showed a shift towards higher Tg in the case of ZnO nanoparticle‐cured vulcanizate, indicating higher crosslinking density. This was further confirmed by volume fraction of rubber in the swollen gel and infrared spectroscopic studies. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 相似文献
54.
55.
玻纤增强聚苯硫醚复合材料的增韧研究 总被引:1,自引:0,他引:1
针对玻纤增强聚苯硫醚材料韧性差的问题,对聚苯硫醚傲璃纤维复合体系的增韧进行了研究,考察了玻纤、改性聚合物、有机超细粒子对复合材料力学性能的影响。采用基体增韧(预增韧)与有机超细粒子增韧技术,在保持复合材料拉伸强度和模量的同时,较大地提高了冲击强度,获得了综合力学性能优异的纤维增强聚苯硫醚材料。 相似文献
56.
Graft copolymerization of acrylic acid (AA) onto polyphenylene sulfide (PPS) nonwoven initiated by low temperature plasma was studied. The effects of various conditions on graft reaction and the grafting rate were investigated. SEM images showed that PPS nonwoven was grafted, and the graft copolymerization only occurred on the surface of PPS. It may be due to the chain transference going with the graft copolymerization. It was found that with the increasing of plasma power, treatment time, space between electrodes, monomer concentration, and temperature of graft polymerization, the grafting rate increased at first, went to the top, and then decreased. The PPS nonwoven surface graft reaction could be optimized by the following processing conditions: 120 s of plasma treatment time, 50 W of plasma power, 1.5 cm of space between electrodes, 30% (w/w) of monomer concentration, and 50°C of temperature of graft polymerization. Measurement of XPS showed that the peak of C1s of graft polyacrylic acid was existed, and the peak area increased with the increase of the grafting rate. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5884–5889, 2006 相似文献
57.
Ying Quan Mingshan Yang Tongxiang Liang Qin Yan Deshan Liu Riguang Jin 《应用聚合物科学杂志》2007,103(6):3940-3949
Novel composite particles based on nanoscale calcium carbonate (nano‐CaCO3) as the core and polyacrylates as the shell were first synthesized by in situ encapsulating emulsion polymerization in the presence of the fresh slush pulp of calcium carbonate (CaCO3) nanoparticles. Subsequently, these modified nanoparticles were compounded with rigid poly(vinyl chloride) (RPVC) to prepare RPVC/CaCO3 nanocomposites. At the same time, the effects of the reinforcement and toughening of these modified nanoparticles on RPVC were investigated, and the synergistic effect of modified nanoparticles with chlorinated polyethylene (CPE) was also studied. The results showed that in the presence of nano‐CaCO3 particles, the in situ emulsion polymerization of acrylates was carried out smoothly, and polyacrylates successfully encapsulated on the surface of nano‐CaCO3 to prepare the modified nanoparticles, breaking down nano‐CaCO3 particle agglomerates, improving their dispersion in the matrix, and also increasing the particle–matrix interfacial adhesion. Thus, the effects of the reinforcement and toughening of these modified nanoparticles on RPVC were very significant, and the cooperative effect of the nanoparticles with CPE occurred in the united modification system. Scanning electron microscopy analyses indicated that large‐fiber drawing and network morphologies coexisted in the system of joint modification of nanoparticles with CPE. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3940–3949, 2007 相似文献
58.
Changyong Choi Su Young Chae Tai‐Hyoung Kim Jung Keon Kweon Chong Su Cho Mi‐Kyeong Jang Jae‐Woon Nah 《应用聚合物科学杂志》2006,99(6):3520-3527
Diblock copolymers with different poly(ε‐caprolactone) (PCL) block lengths were synthesized by ring‐opening polymerization of ε‐caprolactone in the presence of monomethoxy poly(ethylene glycol) (mPEG‐OH, MW 2000) as initiator. The self‐aggregation behaviors and microscopic characteristics of the diblock copolymer self‐aggregates, prepared by the diafiltration method, were investigated by using 1H NMR, dynamic light scattering (DLS), and fluorescence spectroscopy. The PEG–PCL block copolymers formed the self‐aggregate in an aqueous environment by intra‐ and/or intermolecular association between hydrophobic PCL chains. The critical aggregation concentrations of the block copolymer self‐aggregate became lower with increasing hydrophobic PCL block length. On the other hand, reverse trends of mean hydrodynamic diameters were measured by DLS owing to the increasing bulkiness of the hydrophobic chains and hydrophobic interaction between the PCL microdomains. The partition equilibrium constants (Kv) of pyrene, measured by fluorescence spectroscopy, revealed that the inner core hydrophobicity of the nanoparticles increased with increasing PCL chain length. The aggregation number of PCL chain per one hydrophobic microdomain, investigated by the fluorescence quenching method using cetylpyridinium chloride as a quencher, revealed that 4–20 block copolymer chains were needed to form a hydrophobic microdomain, depending on PCL block length. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3520–3527, 2006 相似文献
59.
A novel macroporous resin was prepared from epoxy resin and triethylenetetramine through a polymerization with phase separation. In this experiment, the polyethylene glycol (PEG‐1000) plays a very important part. It was used as solvent, as phase‐separation reagent in the preparation processes, and as the pore‐forming reagent through removing PEG‐1000 from polymer by water‐cleaning process after completing polymerization. The prepared resin was modified by carbon bisulfide and soaked in 1 mol L?1 NaOH. Its structure was characterized by Fourier transform‐infrared spectra, scanning electron microscopy, and elemental analysis. The adsorption characteristic of the chelating resin was studied by series of experiments. The results show that the chelating resin possesses excellent adsorption characteristic toward trace Hg(II). The recovery can come to 100% when the concentration of Hg(II) is only 0.05 ppm, and the average maximum adsorption capacity of the chelating resin for Hg(II) is 122 mg g?1. The precision (relative standard deviation) for six replicate adsorbent extraction of 0.01 μg mL?1 Hg(II) was 1.1%. The accuracy of the proposed procedure was verified by analyzing a standard reference material. Moreover, the chelating resin was applied to two natural samples and also got satisfactory results. That is to say, the chelating resin modified by carbon bisulfide exhibits a high chelating ability toward Hg(II) and can be used as adsorbent for preconcentration and removal of trace Hg(II) in aqueous solution. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:2372–2378, 2006 相似文献
60.
Polycrystalline (PbS)1.14(TaS2)2, a misfit layer sulfide, was used as cathodic material for lithium secondary battery. One molar LiClO4 in propylene carbonate (PC) was used as electrolyte. The cell could be galvanostatic discharged down to x = 4.6 [Lix(PbS)1.14(TaS2)2] when the current density was 65 μA cm−2 and the cell was cycled more than 100 times between 3.5 and 1.5 V at a current density of 260 μA cm−2. Lattice expansion increased linearly with lithium content and was less than that reported for the Li/TaS2 system. Chemical diffusion coefficients were determined by a modified version of the galvanostatic intermittent titration technique and they were fairly constant in the composition range 0.2 < x < 1, and an average value of 8.1 × 10−11 cm2 s−1 was calculated. Sodium intercalation was also accomplished, but the uptake of this ion resulting in a significant lattice expansion compared with that observed for lithium ions. Moreover, a similar dependence of the sodium chemical diffusion coefficient on the composition was observed with an average value of 1.4 × 10−10 cm2 s−1, somewhat higher than that of lithium ion. We believe that differences in lattice expansion may be responsible for the differences found in the chemical diffusivity values. 相似文献