4.7 Article

Molecular origins of Epoxy-Amine/Iron oxide interphase formation

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 613, 期 -, 页码 415-425

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ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.01.016

关键词

Iron-oxide; Epoxy-amine; Interphase; AFM-IR; ATR-FTIR; Molecular dynamics simulation

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The hypothesis of this study is that interphase properties in composites, adhesives, and protective coatings can be predicted based on the interfacial interactions between polymeric precursor molecules and the inorganic surface during network formation. The researchers applied conventional analysis techniques, atomic force microscopy coupled with infrared (AFM-IR), and molecular dynamics simulations to investigate the molecular interactions and properties of nanocomposite specimens. The findings revealed the presence of under-cured interphase regions and the excess of epoxy functionality near the particle surfaces, and demonstrated the driving force for molecular orientation and raised Tg values in the goethite composite samples.
Hypothesis: Interphase properties in composites, adhesives and protective coatings can be predicted on the basis of interfacial interactions between polymeric precursor molecules and the inorganic surface during network formation. The strength of molecular interactions is expected to determine local segmen-tal mobility (polymer glass transition temperature, Tg) and cure degree. Experiments: Conventional analysis techniques and atomic force microscopy coupled with infrared (AFM-IR) are applied to nanocomposite specimens to precisely characterise the epoxy-amine/iron oxide inter-phase, whilst molecular dynamics simulations are applied to identify the molecular interactions under-pinning its formation. Findings: Attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and high-resolution AFM-IR mapping confirm the presence of nanoscale under-cured interphase regions. Interfacial segregation of the molecular triethylenetetraamine (TETA) cross-linker results in an excess of epoxy functionality near synthetic hematite, (Fe2O3) magnetite (Fe3O4) and goethite (Fe(O)OH) particle surfaces. This occurs independently of the variable surface binding energies, as a result of entropic seg-regation during the cure. Thermal analysis and molecular dynamics simulations demonstrate that restricted segmental motion is imparted by strong interfacial binding between surface Fe sites in goethite, where the position of surface hydroxyl protons enables synergistic hydrogen bonding and elec-trostatic binding to Fe atoms at specific sites. This provides a strong driving force for molecular orienta-tion resulting in significantly raised Tg values for the goethite composite samples. (C) 2022 Elsevier Inc. All rights reserved.

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