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arXiv 1407.3198cond-mat.soft
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polymer界面的愈合:界面动力学、缠结和强度

Healing of polymer interfaces: Interfacial dynamics, entanglements, and strength

Ting Ge, Mark O. Robbins, Dvora Perahia, Gary S. Grest

摘要:

聚合物膜的自我修复通常发生在分子扩散穿过损坏区域时,高于其熔化温度。使用分子动力学模拟,我们探测聚合物薄膜的愈合,并与均聚物板的热焊接的结果进行比较。这两种方法在它们的界面结构上不同,因为损伤导致多分散性增加和更短的链。将聚合物样品切割成两个单独的膜,然后将其以熔融状态保持在一起。随着时间的推移,受损膜的恢复和聚合物分子扩散穿过界面。质量摄取和缠结的形成,从原始路径分析,提取和相关的剪切模拟得到的界面强度。我们发现,由于短链的存在,相互扩散是显着更快的损坏的膜相比,焊接。虽然界面缠结增加更迅速的损坏的膜,其中很大一部分是近链端。结果,愈合膜的界面强度比焊接更慢地增加。对于愈合和焊接,界面强度饱和的体积缠结密度恢复整个接口。然而,受损膜的饱和强度低于聚合物样品的体积强度。在饱和时,切割链保持在愈合界面附近。它们的纠缠较少,因此在机械上削弱了界面。当界面强度饱和时,界面缠结的数量与相应的体缠结密度成比例。链刚度增加了缠结的密度,这增加了界面强度。我们的研究结果表明,在界面上的几个缠结足以抵抗界面链拔出,提高机械强度。

英文摘要:

Self-healing of polymer films often takes place as the molecules diffuse across a damaged region, above their melting temperature. Using molecular dynamics simulations we probe the healing of polymer films and compare the results with those for thermal welding of homopolymer slabs. The two processes differ in their interfacial structure since damage leads to increased polydispersity and more short chains. A polymer sample was cut into two separate films that were then held together in the melt state. The recovery of the damaged film was followed as time elapsed and polymer molecules diffused across the interface. The mass uptake and formation of entanglements, as obtained from primitive path analysis, are extracted and correlated with the interfacial strength obtained from shear simulations. We find that the interdiffusion is significantly faster in the damaged film compared to welding because of the presence of short chains. Though interfacial entanglements increase more rapidly for the damaged films, a large fraction of them are near chain ends. As a result, the interfacial strength of the healing film increases more slowly than for welding. For both healing and welding, the interfacial strength saturates as the bulk entanglement density is recovered across the interface. However, the saturation strength of the damaged film is below the bulk strength for the polymer sample. At saturation, cut chains remain near the healing interface. They are less entangled and thus mechanically weaken the interface. When the interfacial strength saturates, the number of interfacial entanglements scales with the corresponding bulk entanglement density. Chain stiffness increases the density of entanglements, which increases the interfacial strength. Our results show that a few entanglements across the interface are sufficient to resist interfacial chain pullout and enhance the mechanical strength.

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