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研究金属表面处理工艺对金属/天然橡胶(NR)热硫化粘接剥离强度的影响。结果表明:对金属进行脱脂、磷化和硅烷化处理能够有效增大金属/NR热硫化粘接剥离强度,3种处理工艺中对金属进行2次环保水溶性无铬密封剂GardoleneD6890浸渍可增大金属/NR热硫化粘接剥离强度;合理调控金属磷化时间、GardoleneD6890质量分数及其浸渍温度和浸渍后金属烘干温度能增大金属/NR热硫化粘接剥离强度;金属磷化时间为90 s、Gardolene D6890质量分数为5%及其浸渍温度为55℃时金属/NR热硫化粘接剥离强度最大,而提高GardoleneD6890浸渍后金属烘干温度能进一步增大金属/NR热硫化粘接剥离强度。 相似文献
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提出一个观点:在橡胶中填料之间相互作用的强弱可直观地用填料粒子间作用距离的不同来表示,同一种填料体系中,颗粒间存在着由强到弱的多级相互作用,这种多级相互作用距离服从正态分布,橡胶在外力作用下的应力-应变行为和动态性能均与填料颗粒间作用距离在外界应力作用下的变化有关。以此观点为基础,可细致分析并很好地解释应力-应变曲线中应力上翘现象、不同粒径的填料对橡胶材料模量的影响、填充橡胶的伸长率比纯胶大的现象、橡胶材料的疲劳生热问题、周期应力作用下滚动阻力测试中的温升现象以及炭黑补强橡胶的Payne效应。 相似文献
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Eu(OA)3(TTA) (OA=cis-9-octadecenoic acid, TTA=4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione) complexes (Eu- complexes) containing the ligand OA with long molecular chains were synthesized. The Eu(OA)3(TTA) complexes and peroxide were added into nitrile-butadiene rubber (NBR) by mechanical shearing to get the uncured composites. The cured composites were obtained by vulcanizing the uncured composites at high temperature. The in-situ reaction including polymerization and grafting of Eu-complex took place at the curing process, which was verified by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) observations showed the fine dispersion of Eu(OA)3(TTA) complex (Eu-complex) in the cured composites compared with the uncured ones. Fluorescent spectra and Judd-Ofelt parameters analysis revealed that the fluorescent intensity increased approximate linearly with the content of Eu- complex increasing due to the in-situ reaction and long molecular chains of OA. The fluorescent lifetime of composites was longer than that of original Eu-complexes. 相似文献
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A simple europium complex,Eu(TTA)3 AA(TTA=4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedione,AA=acrylic acid) was synthesized by a simple solution method.Then,two kinds of rubber matrix,nitrile-butadiene rubber(NBR) and silicone rubber(SiR) were used as the substrate for Eu(TTA)3 AA to prepare fluorescence composites.The neat Eu(TTA)3 AA complex showed the ability of self-polymerization when it was heated at 145 °C.It was found that the fluorescence intensity of the neat Eu(TTA)3 AA decreased over 70% when the polymerization time was over 25 min at 145 °C.The results also revealed that the polymerizated Eu(TTA)3 AA could be dispersed in nano-scale in two matrices and the luminescent intensities decreased 52% in NBR matrix,and 95% in SiR matrix compared with two relative compounds without crosslinking.To optimize the luminescence intensity of the composites,the Eu(TTA)3 AA polymerization kinetic process in matrix was investigated in detail by controlling the temperature,the crosslinking agent,etc.The results showed that the peroxide could accelerate Eu(TTA)3 AA self-polymerization in the rubber matrix,and therefore improved the dispersion,but not be helpful for the luminescence intensity enhancement.In addition,the relatively higher luminescence intensity in Eu(TTA)3 AA/NBR in comparison to that of Eu(TTA)3 AA/SiR might contribute to the interaction between nitrile group(–CN) in NBR and Eu-complexes,suggesting that the luminescence intensity of the composites also depended on the matrix characteristics. 相似文献
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