Back to Search Start Over

Improving impact toughness of polylactide/poly(ether)urethane blends via designing the phase morphology assisted by hydrophilic silica nanoparticles.

Authors :
Xiu, Hao
Huang, Chunmei
Bai, Hongwei
Jiang, Jia
Chen, Feng
Deng, Hua
Wang, Ke
Zhang, Qin
Fu, Qiang
Source :
Polymer. Mar2014, Vol. 55 Issue 6, p1593-1600. 8p.
Publication Year :
2014

Abstract

Abstract: Obtaining network-like morphology (rubber particles are unevenly distributed in the matrix, forming a discontinuous rubber network structure) has been considered to be an effective strategy to optimize the toughness of rubber-toughened polymers. However, it is very difficult to achieve using conventional processing method. In this work, taking elastomer-toughened polylactide (PLA) as an example, we attempt to use hydrophilic silica (SiO2) nanoparticles with self-networking capability to control the phase morphology and the mechanical properties of PLA/poly(ether)urethane (PU) (85/15) blend. It is interesting to find that the selective localization of SiO2 nanoparticles in the PU phase and at the phase interface induces the morphological change from a common sea-island structure to a unique network-like structure constructed by discrete PU particles with irregular shapes, thus giving rise to a remarkable improvement in the impact toughness of the blend with strength and modulus unaffected. The formation of the network-like structure is attributed to the synergistic effect between the self-networking of the interface-localized SiO2 and the enhanced elasticity of the SiO2-localized PU phase. This inspiring result proves the introduction of nanoparticles with self-networking capability into polymers blends to be a universal platform to design their performance via tuning the phase structure. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00323861
Volume :
55
Issue :
6
Database :
Academic Search Index
Journal :
Polymer
Publication Type :
Academic Journal
Accession number :
94897206
Full Text :
https://doi.org/10.1016/j.polymer.2014.01.057