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Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites

The graphene oxide (GO) and polyethylene terephthalate (PET) molecular chains are connected together by the two amino groups of the crosslinking agent p-phenylenediamine (PPD). The presence of macromolecular chains could make GO uniformly dispersed in the polymer matrix, improving the antistatic per...

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Autores principales: Meng, Zhaorui, Lu, Shichao, Zhang, Dianbo, Liu, Qun, Chen, Xiangdong, Liu, Wei, Guo, Cheng, Liu, Zongfa, Zhong, Weihua, Ke, Yangchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679732/
https://www.ncbi.nlm.nih.gov/pubmed/36425195
http://dx.doi.org/10.1039/d2ra06725k
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author Meng, Zhaorui
Lu, Shichao
Zhang, Dianbo
Liu, Qun
Chen, Xiangdong
Liu, Wei
Guo, Cheng
Liu, Zongfa
Zhong, Weihua
Ke, Yangchuan
author_facet Meng, Zhaorui
Lu, Shichao
Zhang, Dianbo
Liu, Qun
Chen, Xiangdong
Liu, Wei
Guo, Cheng
Liu, Zongfa
Zhong, Weihua
Ke, Yangchuan
author_sort Meng, Zhaorui
collection PubMed
description The graphene oxide (GO) and polyethylene terephthalate (PET) molecular chains are connected together by the two amino groups of the crosslinking agent p-phenylenediamine (PPD). The presence of macromolecular chains could make GO uniformly dispersed in the polymer matrix, improving the antistatic performance and thermal stability of the nanocomposite. In this paper, GO was prepared by the improved Hummers, method. In the first step, an amine group of PPD undergoes a nucleophilic ring-opening reaction with an epoxy group on GO. Multiple characterization methods indicate that PPD is successfully grafted to the surface of GO sheets and GO is partially reduced simultaneously. The graphene layer spacing increased from 0.81 nm for GO to 1.49 nm for grafted graphene oxide (g-GO). The number of oxygen-containing functional groups in GO is also reduced. The conductivity of g-GO at room temperature is 1.8 S cm(−1), which is much higher than that of GO. In addition, the thermal stability of g-GO has also been improved. In the second step, the other unreacted terminal amino group of PPD is grafted to PET molecular chains through hydrogen bonding or amidation reactions. Antistatic and thermally stable nanocomposites were then obtained by hot pressing. Different ratios of graphene/polyester nanocomposites were obtained. At the same time, the g-GO is further thermally reduced. The thermal stability of PET/g-GO nanocomposite has been greatly improved, while the thermal stability of PET/GO nanocomposite is basically the same as that of pure PET. For the PET/g-GO nanocomposite, the residue rate has increased by nearly 10%, and the maximum thermal decomposition temperature has also increased by 11 °C. When the content of g-GO is 1.0 vol%, the bulk conductivity of PET/g-GO nanocomposite is increased by 8 orders of magnitude. However, when the content of GO is 1.0 vol%, the bulk conductivity of the PET/GO nanocomposite is only improved by 3 orders of magnitude. PET/g-GO nanocomposites exhibit good antistatic properties. The PET/g-GO nanocomposite's conductive percolation threshold is 0.61 vol%, while that of the PET/GO nanocomposite is 1.64 vol%. The electrical conductivity of the nanocomposite increases with the increase of graphene content. And the well-dispersed modified graphene can improve the electrical conductivity of the nanocomposite.
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spelling pubmed-96797322022-11-23 Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites Meng, Zhaorui Lu, Shichao Zhang, Dianbo Liu, Qun Chen, Xiangdong Liu, Wei Guo, Cheng Liu, Zongfa Zhong, Weihua Ke, Yangchuan RSC Adv Chemistry The graphene oxide (GO) and polyethylene terephthalate (PET) molecular chains are connected together by the two amino groups of the crosslinking agent p-phenylenediamine (PPD). The presence of macromolecular chains could make GO uniformly dispersed in the polymer matrix, improving the antistatic performance and thermal stability of the nanocomposite. In this paper, GO was prepared by the improved Hummers, method. In the first step, an amine group of PPD undergoes a nucleophilic ring-opening reaction with an epoxy group on GO. Multiple characterization methods indicate that PPD is successfully grafted to the surface of GO sheets and GO is partially reduced simultaneously. The graphene layer spacing increased from 0.81 nm for GO to 1.49 nm for grafted graphene oxide (g-GO). The number of oxygen-containing functional groups in GO is also reduced. The conductivity of g-GO at room temperature is 1.8 S cm(−1), which is much higher than that of GO. In addition, the thermal stability of g-GO has also been improved. In the second step, the other unreacted terminal amino group of PPD is grafted to PET molecular chains through hydrogen bonding or amidation reactions. Antistatic and thermally stable nanocomposites were then obtained by hot pressing. Different ratios of graphene/polyester nanocomposites were obtained. At the same time, the g-GO is further thermally reduced. The thermal stability of PET/g-GO nanocomposite has been greatly improved, while the thermal stability of PET/GO nanocomposite is basically the same as that of pure PET. For the PET/g-GO nanocomposite, the residue rate has increased by nearly 10%, and the maximum thermal decomposition temperature has also increased by 11 °C. When the content of g-GO is 1.0 vol%, the bulk conductivity of PET/g-GO nanocomposite is increased by 8 orders of magnitude. However, when the content of GO is 1.0 vol%, the bulk conductivity of the PET/GO nanocomposite is only improved by 3 orders of magnitude. PET/g-GO nanocomposites exhibit good antistatic properties. The PET/g-GO nanocomposite's conductive percolation threshold is 0.61 vol%, while that of the PET/GO nanocomposite is 1.64 vol%. The electrical conductivity of the nanocomposite increases with the increase of graphene content. And the well-dispersed modified graphene can improve the electrical conductivity of the nanocomposite. The Royal Society of Chemistry 2022-11-22 /pmc/articles/PMC9679732/ /pubmed/36425195 http://dx.doi.org/10.1039/d2ra06725k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Meng, Zhaorui
Lu, Shichao
Zhang, Dianbo
Liu, Qun
Chen, Xiangdong
Liu, Wei
Guo, Cheng
Liu, Zongfa
Zhong, Weihua
Ke, Yangchuan
Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
title Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
title_full Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
title_fullStr Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
title_full_unstemmed Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
title_short Grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
title_sort grafting macromolecular chains on the surface of graphene oxide through crosslinker for antistatic and thermally stable polyethylene terephthalate nanocomposites
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9679732/
https://www.ncbi.nlm.nih.gov/pubmed/36425195
http://dx.doi.org/10.1039/d2ra06725k
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