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91.
Si及变质处理对Mg2Si/Mg复合材料的影响 总被引:1,自引:1,他引:1
分析了Mg-Si二元合金直接原位形成Mg2Si/Mg复合材料的过程,研究了Si含量以及变质处理对复合材料组织和性能的影响。试验结果表明,随着合金中Si含量的增加,合金的流动性降低,复合材料中原位Mg2Si的数量增多,树枝晶形态更为发达;对优化的Mg-8Si合金,进行混合稀土(MM)和Sb变质处理,可明显改善Mg2Si的形态和分布,但Sb变质的效果要好于MM。合金经质量分数为1.2%的Sb变质处理后,Mg2Si以颗粒状均匀分布在Mg基体中,从而使复合材料具有较好的耐磨性。 相似文献
92.
CdZnTeCrystalGrowthbyVerticalGradientFreezingMethodHouQingrun;WangJinyi;DengJincheng;DuBing,(侯清润)(王金义)(邓金诚)(杜冰);LiMeirongandC... 相似文献
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Coloring study in organic hybrid of polyamide (PA6) and N,N′‐ethylene‐bis(tetrabromophthalimide) (EPT), where the chromophore was self‐assembled by hydrogen bonding formed between PA6 molecular chains and EPT compound, have been characterized by several techniques. CS930 double wavelength lamella scanner was employed to measure the change of color. The existence of hydrogen bonding in PA6/N‐N′‐ethylene‐bis (tetrabromophthalimide) (PA6EPT) was investigated with Fourier transform infrared (FTIR), the results of which were compared with that of PA6 with the same thermal history. FTIR spectra at room temperature revealed that there is essentially hydrogen bonding between PA6 and EPT. The crystallization behavior of PA6EPT affected by hydrogen bonding was studied by using FTIR. The temperature‐dependent behavior of both PA6 and PA6EPT was studied by temperature‐FTIR spectroscopy and differential scanning calorimetry (DSC). With temperature increasing, changes in sensitive, high‐resolution absorbance spectra are observed as dissolve‐volatilizing thin film. Temperature‐FTIR results showed that the hydrogen bonding in PA6EPT attenuated and dissociated considerably at a smaller rate than PA6, that is to say, hydrogen bonding in PA6EPT is more stable than that in PA6. DSC showed that the melting temperature of PA6EPT and PA6 are similar. However, the crystalline degree and crystalline temperature and melting enthalpy of PA6 and PA6EPT are different. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 594–600, 2007 相似文献
97.
Wei Xie Rebecca Heltsley Xinhua Cai Fuquan Deng Jiemin Liu Charles Lee Wei‐Ping Pan 《应用聚合物科学杂志》2002,83(6):1219-1227
The oxidative stability of the carbon fiber‐reinforced composite of polyimide was examined, in real time, using the evolved gas analysis techniques. Off‐gas degradation products suggested the onset temperature for chain scissions to be fairly low at about 190–220°C. Based on the off‐gas products present and the trend of their release, the composite degradation mechanism appeared to be similar between 190 and 371°C, thereby marking 371°C to be the highest accelerated aging temperature for its long‐term lifetime prediction. Beyond 371°C, different degradation mechanisms would apply. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 1219–1227, 2002 相似文献
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在用药用明胶为主要原料生产药用空心胶囊的生产中,由于明胶中的过氧化物对胶囊中各种色素的颜色具有氧化褪色作用,胶囊产品放置时间过长,其颜色就会发生变化,加上药品自身安全性的要求等原因,故国内引进的外国胶囊生产线对明胶原料中的过氧化物含量的要求特别严格,要求明胶中不得检出过氧化物成分.尽管目前我国药典和轻工行业对药用明胶标准未作过氧化物含量的规定,相信很多生产药用空心胶囊的厂家对此项目都有内控标准,如本胶囊公司就规定,凡对购进的明胶均不得检出过氧化物成分,否则一律退货.笔者相信,不久的将业,药用明胶的标准修订肯定会增加过氧化物含量的规定.为此,明胶生产企业就必须在明胶生产中严格控制过氧化物的含量,使其达到客户的要求. 相似文献
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The photografting copolymerization of a low‐density polyethylene/vinyl acetate (VAC)–maleic anhydride (MAH) binary monomer system was studied from the perspective of dynamics. The total conversion percentage (CP) and grafting conversion percentage (CG) were measured by gravimetry. On the basis of plots of CP and CG as functions of the polymerization time, the total polymerization rate (RP) and grafting polymerization rate (RG) were calculated. In addition, the apparent activation energy (Ea) and the reaction orders of the photografting polymerization under different reaction conditions, such as the total monomer concentration and the concentration of benzophenone (BP), were determined also. The results showed that, in comparison with the photografting polymerization of the two single monomers (VAC and MAH), RP and RG noticeably increased for the VAC–MAH binary monomer system. When the total monomer concentration was kept at 4M, the apparent Ea's of the three photografting polymerization systems were as follows: for VAC ([MAH]/[VAC] = 0/4), Ea's for the total polymerization and grafting polymerization were 41.00 and 43.90 kJ/mol, respectively; for MAH ([MAH]/[VAC] = 4/0, Ea's were 39.65 and 43.23 kJ/mol, respectively; and for the VAC–MAH binary monomer system, Ea's were 34.35 and 40.32 kJ/mol, respectively. These results suggested that the polymerization of the binary system occurred more readily than the other two. The reaction orders of RP with respect to the total monomer concentration of the monomers and the concentration of BP were 1.34 and 0.81, respectively. According to these investigations, it could be inferred that in the binary monomer system, both the free monomers and charge‐transfer complex took part in the polymerization; to the termination of the propagating chains, two possible pathways, unimolecular termination and bimolecular termination, coexisted in this binary monomer system. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 910–915, 2005 相似文献