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Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent

[Image: see text] The aim of this work is to develop a biobased functional reactive diluent for thermosetting epoxy resins suitable for high-performance applications. An advanced organosilicon-grafted cardanol novolac epoxy resin (SCNER) was synthesized from cardanol novolac epoxy resin and heptamet...

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Autores principales: Huo, Shuping, Ma, Hongliang, Liu, Guifeng, Jin, Can, Chen, Jian, Wu, Guomin, Kong, Zhenwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644176/
https://www.ncbi.nlm.nih.gov/pubmed/31458276
http://dx.doi.org/10.1021/acsomega.8b02401
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author Huo, Shuping
Ma, Hongliang
Liu, Guifeng
Jin, Can
Chen, Jian
Wu, Guomin
Kong, Zhenwu
author_facet Huo, Shuping
Ma, Hongliang
Liu, Guifeng
Jin, Can
Chen, Jian
Wu, Guomin
Kong, Zhenwu
author_sort Huo, Shuping
collection PubMed
description [Image: see text] The aim of this work is to develop a biobased functional reactive diluent for thermosetting epoxy resins suitable for high-performance applications. An advanced organosilicon-grafted cardanol novolac epoxy resin (SCNER) was synthesized from cardanol novolac epoxy resin and heptamethyltrisiloxane. After the chemical structure of SCNER was identified by Fourier transform infrared, (1)H NMR, and (13)C NMR, it was used to modify the diglycidyl ether of the bisphenol A (DGEBA)/methylhexahydrophthalic anhydride system. The SCNER showed unique advantages, reducing the viscosity of DGEBA and improving the properties of the cured resin. With 10 wt % SCNER, the cured resin exhibited a higher tensile strength (78.84 MPa) and impact strength (32.36 kJ·m(–2)). The single glass transition temperature (T(g)) step proved the homogeneous phase structure of the cured resin. Inevitably, the T(g) of the cured resin decreased for the addition of SCNER. The dynamic mechanical analysis results indicated that the storage modulus of the cured resin decreased with the increasing content of SCNER. The morphology showing the ductile fracture of the cured resin was testified by scanning electron microscopy. The dilution and toughening properties of SCNER paves the way to a wide range of possible “eco-friendly” applications, especially in the fields of coatings, paintings, and adhesives.
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spelling pubmed-66441762019-08-27 Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent Huo, Shuping Ma, Hongliang Liu, Guifeng Jin, Can Chen, Jian Wu, Guomin Kong, Zhenwu ACS Omega [Image: see text] The aim of this work is to develop a biobased functional reactive diluent for thermosetting epoxy resins suitable for high-performance applications. An advanced organosilicon-grafted cardanol novolac epoxy resin (SCNER) was synthesized from cardanol novolac epoxy resin and heptamethyltrisiloxane. After the chemical structure of SCNER was identified by Fourier transform infrared, (1)H NMR, and (13)C NMR, it was used to modify the diglycidyl ether of the bisphenol A (DGEBA)/methylhexahydrophthalic anhydride system. The SCNER showed unique advantages, reducing the viscosity of DGEBA and improving the properties of the cured resin. With 10 wt % SCNER, the cured resin exhibited a higher tensile strength (78.84 MPa) and impact strength (32.36 kJ·m(–2)). The single glass transition temperature (T(g)) step proved the homogeneous phase structure of the cured resin. Inevitably, the T(g) of the cured resin decreased for the addition of SCNER. The dynamic mechanical analysis results indicated that the storage modulus of the cured resin decreased with the increasing content of SCNER. The morphology showing the ductile fracture of the cured resin was testified by scanning electron microscopy. The dilution and toughening properties of SCNER paves the way to a wide range of possible “eco-friendly” applications, especially in the fields of coatings, paintings, and adhesives. American Chemical Society 2018-12-03 /pmc/articles/PMC6644176/ /pubmed/31458276 http://dx.doi.org/10.1021/acsomega.8b02401 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Huo, Shuping
Ma, Hongliang
Liu, Guifeng
Jin, Can
Chen, Jian
Wu, Guomin
Kong, Zhenwu
Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent
title Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent
title_full Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent
title_fullStr Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent
title_full_unstemmed Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent
title_short Synthesis and Properties of Organosilicon-Grafted Cardanol Novolac Epoxy Resin as a Novel Biobased Reactive Diluent and Toughening Agent
title_sort synthesis and properties of organosilicon-grafted cardanol novolac epoxy resin as a novel biobased reactive diluent and toughening agent
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644176/
https://www.ncbi.nlm.nih.gov/pubmed/31458276
http://dx.doi.org/10.1021/acsomega.8b02401
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