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Surface Chemistry of Halloysite Nanotubes Controls the Curability of Low Filled Epoxy Nanocomposites Publisher



Akbari V1 ; Najafi F1 ; Vahabi H2, 3 ; Jouyandeh M2, 3 ; Badawi M4 ; Morisset S5 ; Ganjali MR6, 7 ; Saeb MR1
Authors
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Authors Affiliations
  1. 1. Department of Resin and Additives, Institute for Color Science and Technology, P.O. Box 16765-654, Tehran, Iran
  2. 2. Universite de Lorraine, CentraleSupelec, LMOPS, Metz, F-57000, France
  3. 3. Laboratoire Materiaux Optiques, Photoniques et Systemes, CentraleSupelec, Universite Paris-Saclay, Metz, 57070, France
  4. 4. Universite de Lorraine and CNRS, LPCT, UMR 7019, Vandoeuvre-les-Nancy, 54506, France
  5. 5. IC2MP, UMR CNRS 7285, ENSIP, Universite de Poitiers, 1 rue Marcel Dore, Poitiers, 86022, France
  6. 6. Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran, Tehran, Iran
  7. 7. Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Progress in Organic Coatings Published:2019


Abstract

A comparative study was performed on curing potential of low-filled epoxy/amine composites containing pristine halloysite nanotubes (P-HNTs), alkali-activated HNTs (A-HNTs), and silane-functionalized A-HNTs (F-HNTs). A-HNTs was obtained from P-HNTs in NaOH solution, then functionalized with 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane (ETMS) in isopropyl alcohol to obtain F-HNTs. X-ray spectroscopy (XPS) and thermogravimetric analysis (TGA) were employed to receive message from surface and bulk changes in nanoparticles, respectively. TGA results confirmed successful surface functionalization of HNT. In XPS spectra, as expected, Na1s appeared after surface activation. Growth in C1s form F-HNT in comparison with two other nanoparticles further approved successful modification. Harmoniously, oxygen graph was declined due to bonding of hydroxyl groups to the surface. Starting from 1 wt. % of HNTs with substantial aggregated HNTs domains seen in epoxy, we examined 0.5, 0.4, 0.3, 0.2, and then 0.1 wt.% of HNTs in 100 parts by weight of epoxy resin, where 0.2 wt.% loading was below the critical nanoparticle concentration for aggregation. Therefore, nanocomposites containing HNTs, A-HNTs, and F-HNTs were all prepared at such low loading level. Nonisothermal differential scanning calorimetry (DSC) at four different heating rates was performed for qualitative analysis of network formation by the aid of Cure Index dimensionless criterion. It was observed that the presence of low percentage of HNT and F-HNT led to Good cure situation in all heating rates. Whereas in low heating rates A-HNT led to Poor cure, which was compensated for at higher heating rates. © 2019 Elsevier B.V.
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