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Bridging Strength and Ductility in Crosslinked Epoxy Networks AITranslate

U.S. DEVCOM Army Research Laboratory; National Institute of Standards and Technology; U.S. DEVCOM Army Research Laboratory; U.S. DEVCOM Army Research Laboratory; U.S. DEVCOM Army Research Laboratory; U.S. DEVCOM Army Research Laboratory; U.S. DEVCOM Army Research Laboratory
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Publisher: ACS
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Abstract AITranslate

By introducing a monofunctional epoxy compound in epoxy-amine structural adhesives, a series of polymer glasses are studied which systematically varies the apparent molecular weight between crosslinks (Mc,a) from 500 to 1800 g/mol while maintaining a glass transition temperature (Tg) above 110 °C. Young’s modulus and yield strength, measured in uniaxial tension, increased with increasing Mc,a breaking from common trends in highly crosslinked polymers. Positron annihilation spectroscopy elucidated a local densification of the relative free volume with increasing monofunctional epoxy content, providing a plausible origin to the increase in tensile properties. While fracture toughness (KIC) remained relatively constant across the series, the high-rate impact performance increased as a function of tensile strength achieving a 10% improvement in impact resistance. Overall, this study highlights the sensitivity of macroscale, mechanical performance on polymer topology, and local density within the polymer glass.

KeyWords AITranslate

highrate impact mitigation toughened polymer glass structural adhesives positron annihilation lifetime spectroscopy Show More
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.3c00586

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Citation Information:

By introducing a monofunctional epoxy compound in epoxy-amine structural adhesives, a series of polymer glasses are studied which systematically varies the apparent molecular weight between crosslinks (Mc,a) from 500 to 1800 g/mol while maintaining a glass transition temperature (Tg) above 110 °C. Young’s modulus and yield strength, measured in uniaxial tension, increased with increasing Mc,a breaking from common trends in highly crosslinked polymers. Positron annihilation spectroscopy elucidated a local densification of the relative free volume with increasing monofunctional epoxy content, providing a plausible origin to the increase in tensile properties. While fracture toughness (KIC) remained relatively constant across the series, the high-rate impact performance increased as a function of tensile strength achieving a 10% improvement in impact resistance. Overall, this study highlights the sensitivity of macroscale, mechanical performance on polymer topology, and local density within the polymer glass.

quote

GB/T 7714-2015 [1] Joseph M. Dennis, Ajay Krishnamurthy, Timothy W. Sirk, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.3c00586.
MLA [1] Joseph M. Dennis, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.3c00586.
APA [1] Joseph M. Dennis, Ajay Krishnamurthy, Timothy W. Sirk, Brendan A. Patterson, Casey E. Busch, Joseph L. Lenhart, & Daniel B. Knorr, Jr. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.3c00586
IEEE [1] Joseph M. Dennis, Ajay Krishnamurthy, Timothy W. Sirk, Brendan A. Patterson, Casey E. Busch, Joseph L. Lenhart, and Daniel B. Knorr, Jr, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.3c00586. keywords: {highrate impact mitigation;toughened polymer glass;structural adhesives;positron annihilation lifetime spectroscopy;Show More}