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101.
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Micron‐sized polymer particles were coated with layers of nickel compounds by plating electrolessly in the presence of aqueous solutions of nickel chloride, sodium hypophosphite, sodium citrate, and ammonium chloride at elevated temperature. The uniform functional polymer particle could be obtained by seeded polymerization. To investigate the effect of surface functionality on the conditions for nickel deposition, the polymer particle was functionalized with the thiol group. From morphological observation, it was found that the mode of nickel deposition was greatly dependent on the surface functionality of the polymer particle. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 420–424, 2003 相似文献
104.
用透射电镜和高分辨电镜观察研究了PTC型BaTiO_3陶瓷的孪晶和孪晶界结构,并提出了可能的{111}孪晶及孪晶界的原子结构模型。结果表明,{111}孪晶形成氧八面体共面的共格倾斜孪晶界,在孪晶界处可能存在一定量的A空位且原子密度要低于孪晶体内。同时还发现两种其它特征的孪晶现象。 相似文献
105.
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
106.
107.
Yuxin Yin Zhengguo Jin Feng Hou Xu Wang 《Journal of the American Ceramic Society》2007,90(8):2384-2389
Titanium dioxide (TiO2 ) nanotube arrays were prepared by electrochemical anodization of titanium sheets in the glycerol 176 mL/H2 O 44 mL/NH4 F 0.5 wt% electrolytes modified with H2 SO4 and NaAc addition. The surface morphologies, average inner diameter, and the length of the nanotube arrays changed with the solution pH in the range from 5.6 to 4.0 by adding H2 SO4 . A uniform surface morphology of the nanotubes with average inner diameter of ∼80 nm and a length of ∼1000 nm was obtained when the solution pH was 5.0. The growth rates of the nanotubes were remarkably enhanced by NaAc addition in the range of 0.04–0.14 M . With NaAc addition of 0.10 M , the length of the nanotube arrays reached 4.16 μm after an 8-h anodization, increasing 3.23 μm compared with no NaAc addition. The relationship between solution pH and growth of TiO2 nanotubes was analyzed by current–time curves, solution electrical conductivities, and scanning electron microscopy (SEM), and the role of NaAc was also discussed based on SEM and solution electrical conductivities. 相似文献
108.
CeO2 particles confined within the pores of an SBA-15 mesoporous silica host were prepared by incipient wetness impregnation (IMP)
and deposition precipitation (DP) methods. The materials were characterized by XRD, N2-adsorption and temperature programmed reduction (TPR) to evaluate the structure, texture, and redox properties. The preparation
procedure had significant impact on the assembling mode of CeO2 inside the SBA-15 mesopores. A high dispersion of CeO2 particles was achieved via DP, whereas the dispersion of CeO2 prepared by IMP was found to be inhomogeneous and CeO2 partially blocked the pores. The CO conversion in the water-gas-shift reaction was enhanced over 1 wt% Pt supported on CeO2-modified SBA-15 obtained by DP. 相似文献
109.
110.
The glass transition temperatures (Tg's) of several polystyrenes and styrene–alkyl methacrylate copolymers and terpolymers were measured using thermomechanical analysis (TMA) and differential scanning calorimetry (DSC). The polymers studied had number-average molecular weights from 3000 to 250,000 g/mole. The results indicate that the composition dependence of the Tg's for the copolymers and terpolymers can be satisfactorily described by a general Fox equation. In general, the measured Tg's of the copolymer and terpolymer samples depend more on the steric effects of the constituent pendent groups than on their molecular weights. The chain flexibility rather than the size of the pendent group is the determining factor in the glass transition properties of the styrene polymers. 相似文献