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S2/TDE85复合材料耐自然库存与加速湿热老化的性能研究 总被引:5,自引:0,他引:5
本文对高强2号玻璃纤维(S2)增强环氧(TDE85-MCD体系)基复合材料单向板经自然库存与加速湿热老化后力学性能的变化进行了研究。研究结果表明,温度和湿度的作用会使单向板的拉伸、弯曲、剪切性能有所降低;温度越高、湿度越大,力学性能变化越大;可用加速湿热试验值来表征自然库存条件下的试验值。 相似文献
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The thermal and hydro‐thermal aging of a hot‐cured epoxy system (diglycidylether of bisphenol A (DGEBA) + dicyandiamide (DDA)) in the glassy state is revisited using DSC and IR attenuated total reflection spectroscopy. Because of the diffusion of DDA from the solid particles into the liquid DGEBA matrix, curing produces a highly crosslinked amorphous matrix that contains low crosslinked amorphous regions. After full curing, the network possesses a relatively low molecular mobility and no residual reactive groups. Thermal and hydro‐thermal loading is performed at 60°C, well below the principal glass transition temperature (Tg1 = 171°C). Both aging regimes cause significant chemical and structural changes to the glassy epoxy. It undergoes a phase separation of relatively mobile segments inside the low mobile matrix, providing a second glass transition that shifts from Tg2 = 86–114°C within 108 days of aging. This phase separation is reversible on heating into the viscoelastic state. Hydro‐thermal aging leads to a reversible and a nonreversible plasticizing effect as well. On thermal aging, no chemical changes are observed but hydro‐thermal aging causes significant chemical modifications in the epoxy system. These modifications are identified as a partial degradation of crosslinks produced by the cyano groups of the DDA and correspond to the nonreversible plasticitation. These changes in the cured epoxy should exert an influence on the mechanical properties of an adhesive bond. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006 相似文献
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In drug delivery systems that use silicone elastomers as a diffusion matrix for the active drug, it is common to crosslink the material by the hydrosilylation reaction. In this platinum‐catalyzed reaction, vinyl groups on a polymer add to the methyl siloxane hydride (MHS) groups on a low molecular mass crosslinker. With an excess of crosslinker, a fast curing is achieved and a fully crosslinked material is formed. Unreacted MHS groups were shown to remain in the elastomer after curing because of the excess crosslinker. In this work, a simple procedure was developed to eliminate the unreacted MHS groups from the final product. We found that storage of the product at +40°C and 75% relative humidity for a few weeks will effectively destroy the residual MHS groups in the elastomer. The effects of varying levels of humidity, oxygen, and temperature on this postcuring procedure were studied. The amount of MHS groups was measured with NMR and IR spectroscopy. We also found that the hardness of the material increased by approximately 25% as a consequence of this postcuring treatment. This increase is probably due to a secondary crosslinking reaction between MHS and silanol groups. Heat treatment at higher temperatures led to an even further increase in the hardness and compression modulus. Because no MHS groups remained in the elastomer when this heat treatment was started, it is apparent that another secondary crosslinking reaction is occurring, probably silanol condensation. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2254–2264, 2002 相似文献
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研究了不同老化方式对沥青低温性能的影响,分3个阶段,对不同老化方式的试验结果进行了比较.阶段1研究表明,沥青在压力老化容器(PAV)中100℃条件下老化20 h后的低温性能与在1.01×105Pa、60℃条件下老化38 d后的低温性能相差无几.阶段2研究表明,可以通过58℃、10 r/s时的高温因子G*/sinδ来修正低温性能分级,从而可以利用短期老化来代替长期老化试验.阶段3研究表明,沥青的低温性能会随着老化时间改变而变化.当老化时间较短时,低温性能分级由劲度指标控制;当老化时间较长时,低温性能分级将转变为由蠕变速率控制. 相似文献
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通过添加各种改性和成型加工助剂,有效地解决粉状聚丙烯在加工和其制品实际使用过程中,可能产生的热氧老化问题。在编织袋应用中,其耐老化性能已达到甚至超过粒状聚丙烯生产的同类制品水平。 相似文献
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X‐ray photoelectron spectroscopy (XPS) was used to study the hydrolytic aging of polypropylene according to the pHs of degrading buffer solutions and the time of aging. The study was concentrated over periods of 3, 6, and 9 months for values of pH close to the real environments of use of the material (pH of 6, 7, and 8). The polypropylene underwent an oxidation of its polymeric matrix, independently of the range of pH values, by the production of C? OH, C?O, and O?C? O groups. These chemical functions were observed in high resolution XPS spectra around C1s and O1s peaks. Beginning with these results and from mechanisms of (photochemical, thermal, and others) aging proposed in the literature, it was then possible to propose mechanisms of hydrolytic ageing of polypropylene. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3830–3838, 2004 相似文献
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钛系催化剂陈化方式和条件对合成高乙烯基聚丁二烯橡胶的影响 总被引:3,自引:1,他引:3
本工艺以Ti(OC4H9)4-Al(i-C4H9)3为催化剂合成乙烯基聚丁二烯,采用催化剂陈化方式,考察了陈化温度和时间等条件对聚合的影响。结果表明,本体系高温陈化后可提高催化活性,降低Al用量;Ti-Bd-Al三元陈化的催化活性高于Ti-Al二元陈化;最佳陈化条件为n(Ti):n(Bd):n(Al)=1:20:20,70℃陈化1h;与未陈化和低温陈化聚合的产物相比,高温陈化产品的分子量和1,2-结构含量较高,凝胶含量较低。 相似文献
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