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https://hdl.handle.net/10356/171073
Title: | Degradation and lifetime prediction of epoxy composite insulation materials under high relative humidity | Authors: | Ma, Jielin Yang, Yan Wang, Qi Deng, Yuheng Yap, Malvern Chern, Wen Kwang Oh, Joo Tien Chen, Zhong |
Keywords: | Engineering::Materials Engineering::Electrical and electronic engineering |
Issue Date: | 2023 | Source: | Ma, J., Yang, Y., Wang, Q., Deng, Y., Yap, M., Chern, W. K., Oh, J. T. & Chen, Z. (2023). Degradation and lifetime prediction of epoxy composite insulation materials under high relative humidity. Polymers, 15(12), 2666-. https://dx.doi.org/10.3390/polym15122666 | Project: | EMA-EP010-SNJL-002 | Journal: | Polymers | Abstract: | Insulation failure of composite epoxy insulation materials in distribution switchgear under the stress of heat and humidity is one of the leading causes of damage to switchgear components. This work prepared composite epoxy insulation materials by casting and curing a diglycidyl ether of bisphenol A (DGEBA)/anhydride/wollastonite composite system, and performed material accelerated aging experiments under three conditions: 75 °C and 95% relative humidity (RH), 85 °C and 95% RH, and 95 °C and 95% RH. Material, mechanical, thermal, chemical, and microstructural properties were investigated. Based on the IEC 60216-2 standard and our data, tensile strength and ester carbonyl bond (C=O) absorption in infrared spectra were chosen as failure criteria. At the failure points, the ester C=O absorption decreased to ~28% and the tensile strength decreased to 50%. Accordingly, a lifetime prediction model was established to estimate material lifetime at 25 °C and 95% RH to be 33.16 years. The material degradation mechanism was attributed to the hydrolysis of epoxy resin ester bonds into organic acids and alcohols under heat and humidity stresses. Organic acids reacted with calcium ions (Ca2+) of fillers to form carboxylate, which destroyed the resin-filler interface, resulting in a hydrophilic surface and a decrease in mechanical strength. | URI: | https://hdl.handle.net/10356/171073 | ISSN: | 2073-4360 | DOI: | 10.3390/polym15122666 | Schools: | School of Electrical and Electronic Engineering School of Materials Science and Engineering |
Research Centres: | SP Group–NTU Joint Laboratory | Rights: | © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | EEE Journal Articles |
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polymers-15-02666-v2.pdf | 8.88 MB | Adobe PDF | ![]() View/Open |
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