首页> 外文会议>Southeast regional meeting of the American Chemical Society >MOLECULAR SIMULATION AND MODELING OF THE STRUCTURE AND PROPERTIES OF POLYMER NANO-PARTICLES
【24h】

MOLECULAR SIMULATION AND MODELING OF THE STRUCTURE AND PROPERTIES OF POLYMER NANO-PARTICLES

机译:聚合物纳米粒子结构与性能的分子模拟及建模

获取原文

摘要

In this study of polymer nano-particles using molecular dynamics simulations we have analyzed the thermal and mechanical properties of the particles generated with up to 60,000 Two groups of atoms were singled out for analysis: those in the central and adjacent fluid slices at the beginning of the simulation. The fraction of kinetic energy in the z direction was followed in each group of atoms. Typical results are shown in Fig. 2. The fraction of z kinetic energy steadily decreases in the central region atoms, averaging about the thermal equilibrium value, 1/3, within less than 5 ps. The adjacent region atoms suddenly gain z kinetic energy within about the first 0.1 ps and then a decreasing trend similar to that for the central region atoms. No coherent transfer of z kinetic energy is observed. In short, the motion very rapidly thermalizes, which is consistent with the results of visualization. In several simulations, positions of every fluid atom were saved every 0.05 ps. The movies showed that within 2 ps, the atoms in the initial plug essentially interspersed themselves within the adjacent fluid volume and then randomly dispersed. This behavior was observed at each nanotube radius, atoms. It is found that surface effects provide interesting properties that are different from those of the bulk polymer system. In particular, the melting point and glass transition temperature were found to be dramatically dependent on the size of the polymer particles. This study also demonstrated that the nano-scale PE particles have dynamical flexibility and behave like an elastomer. The result is quantified by the fractal dimension and compressive modulus. We are currently extending this model and methodology to larger size particles and other types of polymer systems to study the interfacial tension between incompatible polymers, shear flow effects, and thermal properties of blended polymer particles. The molecular dynamics simulations used here should provide useful insights to explain and predict the properties and behavior of ultra fine polymer particles to be used in future new materials and devices.
机译:在使用分子动力学模拟的聚合物纳米颗粒的研究中,我们分析了多达60,000组原子产生的颗粒的热和力学性能进行分析:中央和相邻流体切片的那些模拟。在每组原子中遵循Z方向上的动能的级分。典型结果如图2所示。Z动能的分数稳定地减小中心区域原子,概述围绕热平衡值,1/3,小于5ps。相邻区域原子突然在围绕前0.1 ps内突出z动能,然后与中心区域原子类似的趋势。观察到Z动能的不相干转移。简而言之,运动非常迅速热化,这与可视化结果一致。在几种模拟中,每0.05 ps省去每个流体原子的位置。电影表明,在2 p中,初始插头中的原子基本上穿插在相邻的流体体积内,然后随机分散。在每个纳米管半径,原子下观察到这种行为。结果发现表面效应提供了与散装聚合物系统不同的有趣性质。特别地,发现熔点和玻璃化转变温度显着依赖于聚合物颗粒的尺寸。该研究还证明纳米级PE颗粒具有动态的柔性,并表现得像弹性体。结果由分形尺寸和压缩模量量化。我们目前将该模型和方法扩展到更大尺寸的颗粒和其他类型的聚合物系统,以研究混合聚合物颗粒的不相容聚合物,剪切流动效应和热性质之间的界面张力。这里使用的分子动力学模拟应该提供有用的见解来解释和预测超细聚合物颗粒的性质和行为,以便在未来的新材料和设备中使用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号