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Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications
Water-tree resistances of styrene block copolymer/polypropylene (SEBS/PP) composites are investigated by characterizing crystallization structures in correlation with the dynamic mechanical properties to elucidate the micro-structure mechanism of improving insulation performances, in which the accel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463533/ https://www.ncbi.nlm.nih.gov/pubmed/32806568 http://dx.doi.org/10.3390/molecules25163669 |
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author | Chen, Jun-Qi Wang, Xuan Sun, Wei-Feng Zhao, Hong |
author_facet | Chen, Jun-Qi Wang, Xuan Sun, Wei-Feng Zhao, Hong |
author_sort | Chen, Jun-Qi |
collection | PubMed |
description | Water-tree resistances of styrene block copolymer/polypropylene (SEBS/PP) composites are investigated by characterizing crystallization structures in correlation with the dynamic mechanical properties to elucidate the micro-structure mechanism of improving insulation performances, in which the accelerated aging experiments of water trees are performed with water-knife electrodes. The water-tree morphology in spherulites, melt-crystallization characteristics and lamella structures of the composite materials are observed and analyzed by polarizing microscopy (PLM), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM), respectively. Dynamic relaxation and stress-strain characteristics are specifically studied by means of a dynamic thermomechanical analyzer (DMA) and electronic tension machine, respectively. No water-tree aging occurs in both the highly crystalline PP and the noncrystalline SEBS elastomer, while the water trees arising in SEBS/PP composites still has a significantly lower size than that in low-density polyethylene (LDPE). Compared with LDPE, the PP matrix of the SEBS/PP composite represent a higher crystallinity with a larger crystallization size in consistence with its higher mechanical strength and lower dynamic relaxation loss. SEBS molecules agglomerate as a “island” phase, and PP molecules crystallize into thin and short lamellae in composites, leading to the blurred spherulite boundary and the appreciable slips between lamellae under external force. The high crystallinity of the PP matrix and the strong resistance to slips between lamellae in the SEBS/PP composite essentially account for the remarkable inhibition on water-tree growth. |
format | Online Article Text |
id | pubmed-7463533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74635332020-09-02 Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications Chen, Jun-Qi Wang, Xuan Sun, Wei-Feng Zhao, Hong Molecules Article Water-tree resistances of styrene block copolymer/polypropylene (SEBS/PP) composites are investigated by characterizing crystallization structures in correlation with the dynamic mechanical properties to elucidate the micro-structure mechanism of improving insulation performances, in which the accelerated aging experiments of water trees are performed with water-knife electrodes. The water-tree morphology in spherulites, melt-crystallization characteristics and lamella structures of the composite materials are observed and analyzed by polarizing microscopy (PLM), differential scanning calorimetry (DSC) and scanning electron microscopy (SEM), respectively. Dynamic relaxation and stress-strain characteristics are specifically studied by means of a dynamic thermomechanical analyzer (DMA) and electronic tension machine, respectively. No water-tree aging occurs in both the highly crystalline PP and the noncrystalline SEBS elastomer, while the water trees arising in SEBS/PP composites still has a significantly lower size than that in low-density polyethylene (LDPE). Compared with LDPE, the PP matrix of the SEBS/PP composite represent a higher crystallinity with a larger crystallization size in consistence with its higher mechanical strength and lower dynamic relaxation loss. SEBS molecules agglomerate as a “island” phase, and PP molecules crystallize into thin and short lamellae in composites, leading to the blurred spherulite boundary and the appreciable slips between lamellae under external force. The high crystallinity of the PP matrix and the strong resistance to slips between lamellae in the SEBS/PP composite essentially account for the remarkable inhibition on water-tree growth. MDPI 2020-08-12 /pmc/articles/PMC7463533/ /pubmed/32806568 http://dx.doi.org/10.3390/molecules25163669 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chen, Jun-Qi Wang, Xuan Sun, Wei-Feng Zhao, Hong Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications |
title | Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications |
title_full | Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications |
title_fullStr | Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications |
title_full_unstemmed | Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications |
title_short | Improved Water-Tree Resistances of SEBS/PP Semi-Crystalline Composites under Crystallization Modifications |
title_sort | improved water-tree resistances of sebs/pp semi-crystalline composites under crystallization modifications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463533/ https://www.ncbi.nlm.nih.gov/pubmed/32806568 http://dx.doi.org/10.3390/molecules25163669 |
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