Issue 59, 2017, Issue in Progress

A study on the crystallization behavior and mechanical properties of poly(ethylene terephthalate) induced by chemical degradation nucleation

Abstract

In order to overcome the low crystallization rate of poly(ethylene terephthalate) (PET), bicyclo[2.2.1]heptane-2,3-dicarboxylic acid disodium salt (HPN-68L), a highly active organic nucleating agent for polypropylene, was selected to replace the special nucleating agent of PET to improve PET crystallization due to its carboxylate anion structure, which usually shows a high induced nucleation ability for PET. The crystallization and properties of the composites were systematically investigated. It was found that HPN-68L had a significant nucleation effect on PET. The crystallization temperature and the nucleation efficiency of PET was increased by approximately 14 °C and 68.4%, respectively at a very low content of 0.6 wt% HPN-68L. Moreover, the half-time of crystallization and isothermal crystallization activation energy decreased upon the addition of HPN-68L. The long period of PET decreased and the number of spherulites increased after adding HPN-68L, while the crystal form of PET did not change. In addition, the nucleation mechanism of HPN-68L induced PET crystallization was studied and a chemical degradation nucleation mechanism was proposed. The flexural strength and modulus of PET were improved, whereas the impact strength decreased to a certain extent upon the addition of HPN-68L.

Graphical abstract: A study on the crystallization behavior and mechanical properties of poly(ethylene terephthalate) induced by chemical degradation nucleation

Article information

Article type
Paper
Submitted
19 Jun 2017
Accepted
13 Jul 2017
First published
26 Jul 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 37139-37147

A study on the crystallization behavior and mechanical properties of poly(ethylene terephthalate) induced by chemical degradation nucleation

D. Wang, F. Luo, Z. Shen, X. Wu and Y. Qi, RSC Adv., 2017, 7, 37139 DOI: 10.1039/C7RA06823A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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