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981.
介绍季戊四醇的超分子化学,包括超分子网状结构、螺环冠醚、非常规液晶、富勒烯衍生物、固相光催化反应、Janus树枝状分子等等。  相似文献   
982.
The wetting properties of polystyrene‐based ionomers treated with plasma source ion implantation (PSII) were investigated by the measurement of water contact angles. When sulfonated ionomers were aged for a few days, the hydrophobic recovery for the ionomers became much slower than that for the nonionic polymers. However, when the samples were aged over 20 days, the water contact angle of the ionomers converged with that of the nonionic polymer. Thus, it was concluded that the ionic interaction between the ionic groups and the presence of ionic groups together resulted in the slow hydrophobic recovery and that the aging effect was significant for the ionomers. For the methacrylate ionomer of low ion content, on the other hand, it was found that the PSII treatment produced only a small change in hydrophobic recovery behavior. Thus, it was suggested that the low ionic content coupled with the small size of the ionic unit might cause changes only of a very insignificant degree in hydrophobic recovery behavior. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2500–2504, 2002  相似文献   
983.
不同结合系统刚玉-方镁石-尖晶石浇注料的性能   总被引:4,自引:2,他引:4  
对比研究了水泥结合和水合氧化铝结合的刚玉 -方镁石 -尖晶石浇注料的性能。结果表明 :二者相比 ,水合氧化铝结合浇注料的需水量较大 ,流动性较差 ,烧结致密化温度高 ,在 1 5 5 0℃下烧结后的强度和致密度低 ,但其抗热震性能及抗渣性能较好。  相似文献   
984.
二氧化碳激光熔铸技术在氨压缩机曲轴修复中的应用   总被引:3,自引:0,他引:3  
邢辉  张晓萍 《化工科技》2002,10(5):39-40
用连续输出功率在千瓦级的二氧化碳激光器 ,激光功率密度达到 (10 4~ 10 5)W·cm-2 时 ,对铁基材料表面进行熔铸 ,讨论了激光熔铸修复工艺 ,论述了对修复件强度、表面硬度和抗磨性能、残余应力的影响。  相似文献   
985.
膜分离技术在丙烯尾气回收中的应用   总被引:2,自引:0,他引:2  
分析了聚丙烯生产过程中压缩 /冷凝法丙烯尾气回收的不足 ,介绍了压缩 /冷凝 /有机蒸汽膜法在丙烯尾气回收中的应用  相似文献   
986.
The effects of pH, ferrous ion and hydrogen peroxide dosage on the decolorisation and mineralisation of CI Reactive Black 8 by the Fenton process with/without ultrasonic irradiation were investigated. It was verified that the presence of ultrasonic irradiation did not enhance the decolorisation of CI Reactive Black 8 significantly by Fenton's reagents, but it enhanced the chemical oxygen demand removal efficiency. The enhancement was more pronounced for lower (<0.89 mm) or higher (>1.78 mm) ferrous ion dosage. The optimal pH for chemical oxygen demand removal was 3.0. Chemical oxygen demand removal efficiency increased with the increasing H2O2 dosage and reached the highest level at 5.88 mm, but further increase in H2O2 dosage would not increase removal efficiency significantly.  相似文献   
987.
Poly(amide imide)–epoxysilane (coupling agent) composites were reacted with silica, a condensation product of tetraethylorthosilicate (TEOS), by a sol–gel process and were then cast into films. After this procedure, the chemical characteristics and mechanical and thermal properties were measured. Fourier transform infrared showed that silica existed in the poly(amide imide) matrix. When a proper amount of silica was added to the poly(amide imide) matrix, the tensile strength, elongation, and toughness increased greatly. A poly(amide imide)/30 wt % epoxysilane composite with 20 wt % TEOS had the best mechanical properties. Thermogravimetric analysis under nitrogen and oxygen atmospheres indicated that the char contents increased with the amount of silica. The glass‐transition temperatures of the poly(amide imide)–silica nanocomposites were observed around 170–180°C with differential scanning calorimetry. This approach may be a new method for the low‐temperature thermal curing of poly(amide imide). © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1780–1788, 2004  相似文献   
988.
For this study, we first prepared a fluorocarbon polymer and its hybrid materials. We found that fluorocarbon copolymers can produce hydrogen bonds with SiO2 to form hybrid materials. We also used thermogravimetric analyzer and tested the thermostabilities of the four products, which were ranked as follows: fluorocarbon copolymer/SiO2 hybrid material > fluorocarbon polymer/SiO2 hybrid material > fluorocarbon copolymer > fluorocarbon polymer. In addition, we found that, due to the inorganic SiO2 used, the number of pores and the specific surface areas of the hybrid materials both increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1140–1145, 2007  相似文献   
989.
The purpose of this investigation was to study the origin of the differences in paper‐to‐paper friction of linerboards based on old corrugated containers (OCC). The sheets were subjected to two extraction stages and analyzed with respect to, surface roughness, and their content of low‐molecular‐mass lipophilic compounds (LLC). Friction was measured using a friction tester based on the horizontal plane principle. The surface roughness was measured using a Perthometer profiler and the low molecular mass lipophilic constituent of the paper sheets was determined by gas chromatography‐mass spectroscopy. The sheets were imaged using environmental scanning electron microscopy (ESEM), and the relative compositions of inorganic ions on the paper surfaces were determined by energy dispersive X‐ray spectroscopy (EDS). The results showed that a high amount of LLC in the sheets lead to low friction, due to lubrication. It was also observed that large CaCO3 particles on the surface had a friction‐increasing effect, and that there was no relationship between the surface roughness and the friction. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1511–1520, 2002  相似文献   
990.
The relative viscosity (RV) of polyvinylpyrrolidone (PVP) with different molecular weights was measured with a glass capillary viscometer and with a differential dual‐capillary viscometer in water at different concentrations. For the differential dual‐capillary viscometer, RV increases with a decreasing flow rate, especially for high molecular weight PVP at a 1% concentration. A good agreement in the RV between the two methods can be obtained for PVP with different molecular weights and at various concentrations if an appropriate flow rate is selected for the differential dual‐capillary viscometer. Special precaution is needed when using the differential dual‐capillary viscometer to measure the viscosity of a pure solvent. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1312–1315, 2002  相似文献   
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