2021
DOI: 10.1016/j.polymer.2021.123882
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Exploring the optical and dielectric properties of bifunctional and trifunctional epoxy polymers

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Cited by 9 publications
(10 citation statements)
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References 49 publications
(65 reference statements)
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“…The dipolar segmental relaxations or dipolar group relaxations correspond to β ‐relaxations. The most important mechanisms of β ‐relaxation are movement of dipole side groups about the C‐C chain or a local motion of very short segment of the polymer (such as the twisting of the hydroxyl or carbonyl side groups) 11–13 . Another type of relaxations, known as γ ‐relaxation, is related to faster relaxation processes that occur below glass transition temperature of matrix (e.g., movement of the diphenyl propane group, rotation of the methylene sequence or the hydroxyl‐ether group, etc.).…”
Section: Introductionmentioning
confidence: 99%
“…The dipolar segmental relaxations or dipolar group relaxations correspond to β ‐relaxations. The most important mechanisms of β ‐relaxation are movement of dipole side groups about the C‐C chain or a local motion of very short segment of the polymer (such as the twisting of the hydroxyl or carbonyl side groups) 11–13 . Another type of relaxations, known as γ ‐relaxation, is related to faster relaxation processes that occur below glass transition temperature of matrix (e.g., movement of the diphenyl propane group, rotation of the methylene sequence or the hydroxyl‐ether group, etc.).…”
Section: Introductionmentioning
confidence: 99%
“…4A, the absorption peaks at 3400, 2975 and 734 cm −1 of LMU1-3% were significantly enhanced, it seemed that the enzymatic polymerization had occurred, and the oligomers were formed. The side chains in urushiol and phenolic hydroxyl had converged to be oligomer [28]. And then, the absorption peaks at 1070-1110 cm −1 and 988 cm −1 of LMU1-3% were slightly reduced, which illustrated the structure of the conjugated alkatriene was decreased.…”
Section: Ft-ir Spectra Analysismentioning
confidence: 98%
“…À72 1C and this is due to the g-relaxation. 72,73 The g-relaxation has been attributed to flexible glycidol segments that are formed after oxirane rings open during curing reaction. This relaxation is caused by a crankshaft type rotation of the glycidol group.…”
Section: Dielectric Relaxation Using Dielectric Thermal Analysismentioning
confidence: 99%
“…This relaxation is caused by a crankshaft type rotation of the glycidol group. 72,73 Please note that all the samples exhibit the g-relaxation around the same temperature. However, the changes in the intensity of these samples are somewhat interesting.…”
Section: Dielectric Relaxation Using Dielectric Thermal Analysismentioning
confidence: 99%