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991.
聚甲醛在新型陶瓷注射成型催化脱脂工艺中的应用 总被引:5,自引:0,他引:5
利用聚甲醛对酸性气氛敏感易分解的特性,将其作为主要粘结剂应用于陶瓷注射成型技术中,并采用了新型的催化脱脂技术,使得脱脂速度有了很大提高,实验样品主要粘结剂的脱除量在10h内即达到90%以上,记录了该过程中样品失重的情况,分析了脱脂阶段不同特征及其原因,指出催化脱脂过程速度的控制因素是气态催化剂和气体产物扩散过程,实验观察了脱脂过程不同时刻样品外围与中心区域的微观形貌,证明了脱脂过程由外围逐渐向内部扩散,对物料流变性能的考察表明物料为假塑性,有良好的流动充模性。 相似文献
992.
本文综述了电力绝缘用SF6替代物的开发方法、发展现状和未来趋势。其开发方法包括替代物的设计与确认(物性、安全性评价、环境影响的评价等)、合成、产业化等内容。目前,开发出的SF6替代物包括SF6混合气体、饱和卤代烃、氢氟烯烃、全氟酮和全氟腈,其中七氟异丁腈的绝缘性能优异,是SF6最佳的替代物。同时文中综述了现有七氟异丁腈的合成路线,其中以碳酰氟和六氟丙烯为起始原料催化反应合成七氟异丁腈的路线,具有高效、绿色、环保的优点。以过去发展历程和现在发现现状为基础,展望了SF6替代物的未来发展趋势,提出今后的研究重点在于全面开发七氟异丁腈的应用配套设备,下一代SF6替代物及其绿色、高效的产业化路线。 相似文献
993.
994.
Summary The complex forming poly[(ethylene glycol-co-proplene glycol)-g-acrylamide]: polyacrylic acid interpenetrating polymer network hydrogel is able to bend under electric field stimuli. pH, ionic strength gradients and voltage can influence it's bending degree. So we may improve the sample' responsive speed through manipulating those factor in the further study in order to put it into the biomedical application. 相似文献
995.
为了研究抑制剂对银核和硫化银核的不同作用,本工作考察了1-苯基-5-巯基四氮唑(PMT)和苯并三氮唑(BTA)作为抑制剂在银核和硫化银核上物理显影的阳极抑制和解抑制效应。实验结果表明:1)PMT和BTA对Ag核和银离子过量时制得的硫化银核,Ag2S(Ag),的显影催化活性都有不同程度的抑制作用,而对硫离子过量时制得的硫化银核,Ag2S(S),无明显的抑制作用,这可能是由于过量硫离子在硫化银核上的吸附要强于这两种抑制剂;2)S2O3^2-或I^-离子的存在对BTA在Ag核上有解抑制作用,不仅可恢复甚至提高Ag核的显影催化活性,而对Ag2S核的抑制作用无明显影响;3)与BTA不同,S2O3^2-或I^-离子对PMT在Ag核上没有解抑制作用,对Ag2S(Ag)核的抑制作用还稍有增强,而对Ag2S(S)核稍有减弱;4)银溶胶中的表面增强拉曼谱(SERS)测量证实:BTA在Ag核上的吸附导致Ag核显影催化活性的下降,加入S2O3^2-或I^-离子后致使BTA的SERS信号消失则意味着BTA在银核表面的脱附。以上这些结果说明阳极抑制机理在抑制效应中有重要作用。 相似文献
996.
997.
Several Mg–Y binary ribbons with Y content up to 17.9 at.% were fabricated by melt-spinning. X-ray diffraction (XRD) revealed that the phase structure changes with increasing Y content from extended solid solution to partially amorphous, and then fully intermetallic Mg24Y5. Anodic potentiodynamic polarization performed in 0.01 M NaCl electrolyte (pH=12) revealed improved anodic passivity behavior compared to pure Mg for all the Mg–Y alloys. X-ray photoelectron spectroscopy (XPS) revealed that the improved passivity of Mg–Y was more related to the elemental oxidation state rather than the concentration of the surface components. To study the effect of Cl− ion on the passivity behavior, anodic potentiodynamic and potentiostatic polarization were performed on Mg–17.9 at.% Y in alkaline (pH=12) NaCl electrolytes containing Cl− ion in the concentration range from 0.00 to 0.50 M. The passive films formed in 0.01 M NaCl electrolyte were similar to the native film, which were composed of MgO and Y2O3. No CO32− and Cl− ions were incorporated into the passive film. The passivity was significantly degraded in the electrolytes containing higher Cl− concentration (0.1 and 0.5 M). Detailed XPS revealed that the surface films under these conditions were composed of much hydrated species Mg(OH)2 and YOOH and/or Y(OH)3 and CO32− was incorporated into the surface film. The incorporation of Y2O3 in the passive film was given as the reason for the enhanced passivity properties of Mg–Y ribbons. The mechanism of Cl− and CO32− ions to the degradation of the passivity was discussed. 相似文献
998.
以TiCl4为原料,采用低温液相水解法制备了纳米TiO2粉体,着重研究了Ti4 的浓度和添加聚乙烯吡咯烷酮(Polyvinylpyrrolidone,PVP)对产物的晶相、颗粒大小和表面形貌的影响.使用XRD,TEM,SEM,激光粒度测试仪对样品进行了表征.结果表明,Ti4 浓度影响TiO2粉体的相转变温度,随着Ti4 浓度的升高金红石相的含量逐渐升高,但粉体分散性变差;添加PVP提高了所得TiO2粉体的分散性,粒径降低为40~50 nm左右,并改善了粉体的形貌. 相似文献
999.
Donggang Yao Pratapkumar Nagarajan Lei Li Allen Y. Yi 《Polymer Engineering and Science》2007,47(4):530-539
An embossing strategy involving a hot station and a cold station for sequentially heating and cooling the embossing tool was investigated to reduce cycle times in hot embossing polymer microstructures. Experimental studies showed that aluminum stamps with a thickness of 1.4 mm can be rapidly heated from room temperature to 200°C in 3 s using contact heating against a hot station at 250°C. Microchannels and microlenses were successfully embossed onto high‐density polyethylene and acrylonitrile–butadiene–styrene substrates using a heating time less than 3 s and a total cycle time around 10 s. The two‐station embossing process for the microlens was also numerically studied. The simulated filling behavior agreed with the experimental observation and the predicted thermal and deformation history of the polymer offered a good explanation on the experimentally observed process characteristics. POLYM. ENG. SCI., 47:530–539, 2007. © 2007 Society of Plastics Engineers. 相似文献
1000.
Photoinitiated crosslinking of EVA in the presence of benzophenone (BP) as photoinitiator and triallyl isocyanurate (TAIC) as crosslinker and characterization of the related properties have been studied by gel determination, heat extension, DSC, DMTA, TGA, and mechanical measurements. The photoinitiated crosslinking efficiency of the EVA‐BP‐TAIC system and various factors affecting the crosslinking process, such as photoinitiator and crosslinker and their concentrations, irradiation temperature, and irradiation atmosphere were studied in detail and optimized by comparison of gel contents. The results show that the EVA samples with a thickness of 1 mm are readily crosslinked to a gel content of above 80% with 5 s UV‐irradiation under optimum conditions. The data from the heat extension and DSC show that the crosslinking density of photocrosslinked EVA increase and their crystallinities decrease with increasing the UV‐irradiation time. At the same time, photocrosslinking of EVA leads to a lowering of the melt temperature and a decrease of heat of fusion. The DMTA results show that photocrosslinking increases the amorphous phase and storage modulus of the crosslinked EVA, but does not change the glass transition temperature. The data from TGA and mechanical tests give evidence that the thermal stability and mechanical properties of photocrosslinked EVA samples are much better than those of the uncrosslinked EVA. POLYM. ENG. SCI., 47:1761–1767, 2007. © 2007 Society of Plastics Engineers 相似文献