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Computational modeling of biodegradable starch based polymer composites.

机译:可生物降解淀粉基聚合物复合材料的计算模型。

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摘要

Purpose. The goal of this study is to improve the favorable molecular interactions between starch and PPC by addition of grafting monomers MA and ROM as compatibilizers, which would advance the mechanical properties of starch/PPC composites.Methodology. DFT and semi-empirical methods based calculations were performed on three systems: (a) starch/PPC, (b) starch/PPC-MA, and (c) starch-ROM/PPC. Theoretical computations involved the determination of optimal geometries, binding-energies and vibrational frequencies of the blended polymers.Findings. Calculations performed on five starch/PPC composites revealed hydrogen bond formation as the driving force behind stable composite formation, also confirmed by the negative relative energies of the composites indicating the existence of binding forces between the constituent co-polymers. The interaction between starch and PPC is also confirmed by the computed decrease in stretching CO and OH group frequencies participating in hydrogen bond formation, which agree qualitatively with the experimental values.A three-step mechanism of grafting MA on PPC was proposed to improve the compatibility of PPC with starch. Nine types of 'blends' produced by covalent bond formation between starch and MA-grafted PPC were found to be energetically stable, with blends involving MA grafted at the 'B' and 'C' positions of PPC indicating a binding-energy increase of 6.8 and 6.2 kcal/mol, respectively, as compared to the non-grafted starch/PPC composites. A similar increase in binding-energies was also observed for three types of 'composites' formed by hydrogen bond formation between starch and MA-grafted PPC.Next, grafting of ROM on starch and subsequent blend formation with PPC was studied. All four types of blends formed by the reaction of ROM-grafted starch with PPC were found to be more energetically stable as compared to the starch/PPC composite and starch/PPC-MA composites and blends. A blend of PPC and ROM grafted at the ' a&d12 ' position on amylose exhibited a maximal increase of 17.1 kcal/mol as compared with the starch/PPC-MA blend.Conclusions. ROM was found to be a more effective compatibilizer in improving the favorable interactions between starch and PPC as compared to MA. The ' a&d12 ' position was found to be the most favorable attachment point of ROM to amylose for stable blend formation with PPC.
机译:目的。这项研究的目的是通过添加接枝单体MA和ROM作为增容剂来改善淀粉和PPC之间的良好分子相互作用,这将改善淀粉/ PPC复合材料的机械性能。基于DFT和半经验方法的计算在以下三个系统上进行:(a)淀粉/ PPC,(b)淀粉/ PPC-MA,以及(c)淀粉-ROM / PPC。理论计算涉及确定共混聚合物的最佳几何构型,结合能和振动频率。对五种淀粉/ PPC复合材料进行的计算显示,氢键的形成是稳定复合材料形成的驱动力,这也被复合材料的负相对能量所证实,表明组成共聚物之间存在结合力。淀粉和PPC之间的相互作用也通过计算得出的参与氢键形成的CO和OH基团拉伸频率的降低而得到证实,这与实验值基本吻合。提出了将MA接枝到PPC上的三步机理含淀粉的PPC。发现淀粉和MA接枝的PPC之间通过共价键形成产生的9种类型的“共混物”在能量上稳定,涉及MA接枝在PPC的“ B”和“ C”位置的共混物表明结合能提高6.8与未接枝的淀粉/ PPC复合材料相比,其粘度分别为6.2 kcal / mol和6.2 kcal / mol。淀粉和MA接枝的PPC之间通过氢键形成形成的三种``复合物''的结合能也有类似的增加。接下来,研究了ROM在淀粉上的接枝以及随后与PPC形成共混物的过程。发现与淀粉/ PPC复合物和淀粉/ PPC-MA复合物和共混物相比,由ROM接枝的淀粉与PPC反应形成的所有四种共混物在能量上更稳定。与淀粉/ PPC-MA混合物相比,在直链淀粉的“ a&d12”位置接枝的PPC和ROM混合物显示出最大的17.1 kcal / mol的增加。与MA相比,发现ROM在改善淀粉和PPC之间的有利相互作用方面是更有效的相容剂。发现“ a&d12”位置是ROM与直链淀粉最有利的连接点,可与PPC形成稳定的混合物。

著录项

  • 作者

    Joshi, Sachin Sudhakar.;

  • 作者单位

    Florida International University.;

  • 授予单位 Florida International University.;
  • 学科 Chemistry Polymer.Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 116 p.
  • 总页数 116
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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