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1.
醇镁还原法一步制取对氯苯胺是一种新的方法 ,研究发现最佳反应温度为 80℃~ 85℃ ,反应时间为4h ,对氯硝基苯与镁粉的用量 (物质的量比 )为 1∶3,产率为 80 %。 相似文献
2.
Peichun Li Amar Zerroukhi Jianding Chen Yvan Chalamet Thomas Jeanmaire Zhean Xia 《应用聚合物科学杂志》2008,110(6):3990-3998
Chemical shrinkage was used for the in situ measurement of the progressing chemical stabilization reactions and the influence of ozone during the stabilization of polyacrylonitrile. A method for evaluating the activation energy through the sensitivity temperature is presented. The calculated results show that the activation energies were 161.57 kJ/mol in air and 181.23 kJ/mol in ozone-enriched air. Therefore, the chemical reactions were postponed during stabilization in ozone-enriched air. Ozone seemed to act in three ways: first, ozone promoted the formation of the serious skin–core structure. Second, ozone accelerated the chemical reactions and shortened the stabilization time at lower heating rates. Third, ozone postponed the chemical reactions. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008 相似文献
3.
掺杂改性对聚苯乙烯性能影响的研究 总被引:3,自引:0,他引:3
文章阐述了掺杂烷氧金属的聚苯乙烯的制备以及用红外光谱、扫描电镜和热分析分析其微观结构和热性能的部分研究结果。 相似文献
4.
Yoshihiro Hirata Kazuyoshi Sakeda Yumi Matsushita Kinji Shimada Yoshimi Ishihara 《Journal of the American Ceramic Society》1989,72(6):995-1002
Submicrometer SiO2 -Al2 O3 powders with compositions of 46.5 to 76.6 wt% Al2 O3 were prepared by hydrolysis of mixed alkoxides. Phase change, mullite composition, and particle size of powders with heating were analyzed by DTA, XRD, IR, BET, and TEM. As-produced amorphous powders partially transformed to mullite and Al-Si spinel at around 980°C. The compositions of mullite produced at 1400° and 1550°C were richer in Al2 O3 than the compositions of stable mullite solid solutions predicted from the phase diagram of the SiO2 -Al2 O3 system. Particle size decreased with increasing Al2 O3 content. The sintered densities depended upon the amount of SiO2 -rich glassy phase formed during sintering and the green density expressed as a function of particle size. 相似文献
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Polymerization of β-butyrolactone has been studied in toluene with Al(OiPr)3 as an initiator. The ring-opening polyaddition proceeds through a coordination–insertion mechanism at a very low rate. Well defined α-isopropylester, ω-hydroxy poly(β-butyrolactone)s (PBL) are formed with a narrow molecular weight distribution at low monomer-to-initiator molar ratios, When this ratio is higher (ca. 170), a competition occurs between propagation and side reactions, i.e. elimination, inter- and intra-molecular transesterifications and thermal degradation, which is responsible for a loss of control of the PBL molecular charcteristics. The addition of a Lewis base (1 equivalent of nicotine/Al) to the Al-alkoxide initiator has no significant effect on the polymerization rate, although the chain microstructure is deeply affected since predominantly syndiotactic PBL chains are formed (63% syndio-diads) in contrast to a completely atactic polymer in the absence of nicotine. 相似文献
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醇化合物法合成钙磷酸盐 总被引:8,自引:0,他引:8
用乙二醇钙和P2O5的n-丁醇溶液为先驱体,用较为简便的方法分别合成出β-Ca2P2O7、β-磷酸三钙和羟基磷灰石。研究结果表明:醋酸的引入可以有产控制先驱体间反应,避免两先驱体直接混合时沉淀的产生。当醋酸与下的摩尔比(HOAC/Ca)为4时,两先驱体分别以Ca/P比为1.00,1.50和1.67混合,均可以获得稳定混合溶液。将混合溶液蒸发溶剂后得到的干胶状粉末在1000℃煅烧,对应不同的Ca/P 相似文献
9.
Monodispersed spherical β-SiC powder was synthesized by heating spherical gel powder derived from the hydrolysis of a mixture of phenyltriethoxysilane and tetraethyl orthosilicate. The solution was prepared in a beaker and hydrolyzed by NH4 OH without stirring. The monodispersed spherical gel powder of submicrometer size was obtained when the added amount of NH4 OH was greater than 16 moles per mole of silane plus alkoxide, and it became monodispersed spherical β-SiC powder by heat-treating at 1500°C for 4 h in an Ar atmosphere. The SiC content of the powder was 92.6 wt%. 相似文献
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