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A Comparative Study on Cure Kinetics of Layered Double Hydroxide (Ldh)/Epoxy Nanocomposites Publisher



Karami Z1 ; Paran SMR1 ; Poornima VP2 ; Ganjali MR1, 3 ; Jouyandeh M1 ; Esmaeili A4 ; Habibzadeh S5 ; Stadler FJ6 ; Saeb MR1
Authors
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Authors Affiliations
  1. 1. Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran, Tehran, 11155-4563, Iran
  2. 2. Department of Chemistry, Sree Narayana College for Women (affiliated to University of Kerala), Kollam, Kerala, 691001, India
  3. 3. Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, 14535, Iran
  4. 4. Department of Chemical Engineering, School of Engineering Technology and Industrial Trades, College of the North Atlantic—Qatar, Arab League St, Doha, 24449, Qatar
  5. 5. Department of Chemical Engineering, Amirkabir University of Technology (Tehran Polytechnic), Tehran, 1591639675, Iran
  6. 6. College of Materials Science and Engineering, Shenzhen Key Laboratory of Polymer Science and Technology, Guangdong Research Center for Interfacial Engineering of Functional Materials, Nanshan District Key Lab for Biopolymers and Safety Evaluation, Shenzhen University, Shenzhen, 518055, China

Source: Journal of Composites Science Published:2020


Abstract

Layered double hydroxide (LDH) minerals are promising candidates for developing polymer nanocomposites and the exchange of intercalating anions and metal ions in the LDH structure considerably affects their ultimate properties. Despite the fact that the synthesis of various kinds of LDHs has been the subject of numerous studies, the cure kinetics of LDH-based thermoset polymer composites has rarely been investigated. Herein, binary and ternary structures, including [Mg0.75 Al0.25 (OH)2]0.25+ [(CO2−3 )0.25/2·m H2O]0.25−, [Mg0.75 Al0.25 (OH)2]0.25+ [(NO−3 )0.25·m H2O]0.25− and [Mg0.64 Zn0.11 Al0.25 (OH)2]0.25+ [(CO2−3 )0.25/2·m H2O]0.25−, have been incorporated into epoxy to study the cure kinetics of the resulting nanocomposites by differential scanning calorimetry (DSC). Both integral and differential isoconversional methods serve to study the non-isothermal curing reactions of epoxy nanocomposites. The effects of carbonate and nitrate ions as intercalating agents on the cure kinetics are also discussed. The activation energy of cure (Eα) was calculated based on the Friedman and Kissinger–Akahira–Sunose (KAS) methods for epoxy/LDH nanocomposites. The order of autocatalytic reaction (m) for the epoxy/Mg-Al-NO3 (0.30 and 0.254 calculated by the Friedman and KAS methods, respectively) was smaller than that of the neat epoxy, which suggested a shift of the curing mechanism from an autocatalytic to noncatalytic reaction. Moreover, a higher frequency factor for the aforementioned nanocomposite suggests that the incorporation of Mg-Al-NO3 in the epoxy composite improved the curability of the epoxy. The results elucidate that the intercalating anions and the metal constituent of LDH significantly govern the cure kinetics of epoxy by the participation of nitrate anions in the epoxide ring-opening reaction. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
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