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41.
Chen Hou Chunnuan Ji Chunhua Wang Rongjun Qu 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):226-231
The reverse atom‐transfer radical polymerization (RATRP) technique using CuCl2/2,2′‐bipyridine (bipy) complex as a catalyst was applied to the living radical polymerization of acrylonitrile (AN). A hexasubstituted ethane thermal iniferter, diethyl 2,3‐dicyano‐2,3‐diphenylsuccinate (DCDPS), was firstly used as the initiator in this copper‐based RATRP initiation system. A CuCl2 to bipy ratio of 0.5 not only gives the best control of molecular weight and its distribution, but also provides rather rapid reaction rate. The rate of polymerization increases with increasing the polymerization temperature, and the apparent activation energy was calculated to be 57.4 kJ mol?1. Because the polymers obtained were end‐functionalized by chlorine atoms, they were used as macroinitiators to proceed the chain extension polymerization in the presence of CuCl/bipy catalyst system via a conventional ATRP process. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 226–231, 2006 相似文献
42.
Chen Hou Rongjun Qu Chunnuan Ji Chunhua Wang Chengguo Wang 《Journal of polymer science. Part A, Polymer chemistry》2006,44(1):219-225
FeCl3 coordinated by isophthalic acid was first used as a catalyst in the azobisisobutyronitrile‐initiated reverse atom transfer radical polymerization of acrylonitrile. N,N‐Dimethylformamide was used as a solvent to improve the solubility of the ligand. An FeCl3‐to‐isophthalic acid ratio of 0.5 not only gave the best control of the molecular weight and its distribution but also provided rather a rapid reaction rate. The effects of different solvents on the polymerization of acrylonitrile were also investigated. The rate of the polymerization in N,N‐dimethylformamide was faster than that in propylene carbonate and toluene. The molecular weight of polyacrylonitrile agreed reasonably well with the theoretical molecular weight in N,N‐dimethylformamide. The rate of polymerization increased with increasing polymerization temperature, and the apparent activation energy was calculated to be 59.9 kJ mol?1. Reverse atom transfer radical polymerization was first used to successfully synthesize acrylonitrile polymers with a molecular weight higher than 80,000 and a narrow polydispersity as low as 1.22. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 219–225, 2006 相似文献
43.
Yabin Zhou Shifeng Wang Yinxi Zhang Yong Zhang 《Journal of Polymer Science.Polymer Physics》2006,44(8):1226-1236
Methacrylic acid (MAA) was used as in situ surface modifier to improve the interface interaction between nano‐CaCO3 particle and ethylene–propylene–diene monomer (EPDM) matrix, and hence the mechanical properties of nano‐CaCO3‐filled EPDM vulcanizates. The results showed that the incorporation of MAA improved the filler–matrix interaction, which was proved by Fourier transformation infrared spectrometer (FTIR), Kraus equation, crosslink density determination, and scanning electron microscope (SEM). The formation of carboxylate and the participation of MAA in the crosslinking of EPDM indicated the strong filler–matrix interaction from the aspect of chemical reaction. The results of Kraus equation showed that the presence of MAA enhanced the reinforcement extent of nano‐CaCO3 on EPDM vulcanizates. Crosslink density determination proved the formation of the ionic crosslinks in EPDM vulcanizates with the existence of MAA. The filler particles on tensile fracture were embedded in the matrix and could not be observed obviously, indicating that a strong interfacial interaction between the filler and the matrix had been achieved with the incorporation of MAA. Meanwhile, the presence of MAA remarkably increased the modulus and tensile strength of the vulcanizates, without negative effect on the high elongation at break. Furthermore, the ionic bond was thought to be formed only on filler surface because of the absolute deficiency of MAA, which resulted in the possible structure where filler particles were considered as crosslink points. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1226–1236, 2006 相似文献
44.
This paper reviews our recent experimental and simulation results regarding the electromagnetic wave transmission through
three configurations of sandwiching structures of metamaterials: a metallic mesh sandwiched between two identical layers composed
of split rings, metallic fractals, and fractal slits, respectively. We observed the enhanced transmission of the waves through
these three types of sandwiching composites with respect to the opaque metallic mesh. The locations of the transmission peaks
in the spectrum are associated closely with the band characteristics of the sandwiching layer by appearing either on the left-
or the right-hand side of its band.
PACS 41.20.Jb; 42.70.Qs; 78.20.-e; 42.25.Bs; 47.53.+n 相似文献
45.
本文介绍了一种新的自动调焦方法准直小孔法.对自动调焦的原理和后继电路处理方法作了详细的分析.它具有响应时间短、灵敏度高,能够很好的在激光直接写入系统中克服物镜工作台运动中导轨的不平和轴向窜动所造成的离焦。 相似文献
46.
Chemically modified electrodes prepared by treating the cobalt tetraphenylporphyrin modified glassy-carbon electrode at 750 degrees (HCME) are shown to catalyze the electrooxidation of hydrazine. The oxidation occurred at +0.63 V vs. Ag/AgCl (saturated potassium chloride) in pH 2.5 media. The catalytic response is evaluated with respect to solution pH, potential scan-rate, concentration dependence and flow-rate. The catalytic stability of the HCME is compared with that of the cobalt tetraphenylporphyrin adsorbed glassy-carbon electrode. The stability of the HCME was excellent in acidic solution and even in solutions containing organic solvent (50% CH(3)OH). When used as the sensing electrode in amperometric detection in flow-injection analysis, the HCME permitted sensitive detection of hydrazine at 0.5 V. The limit of detection was 0.1 ng. The linear range was from 50 ng to 2.4 mug. The method is very sensitive and selective. 相似文献
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50.
DongJunWANG QunLUO DanDanJIA XiaoDongLI XinQiouWANG YongHuang ZhenZHEN XinHouLIU 《中国化学快报》2003,14(12):1306-1308
The hydrolysis of tetraethoxysilane (TEOS) occurred on the surface of poly(methyl methacrylate) (PMMA) microshperes immediately after these microshperes were prepared in TEOS. Micron-sized hollow SiO2 spheres were obtained by calcination of the coated PMMA microshperes. It was found that the final hollow spheres were constituted by small SiO2 particles. 相似文献