2020
DOI: 10.1007/s12221-020-1260-3
|View full text |Cite
|
Sign up to set email alerts
|

Effect of Blending Modifications for Phenylethynyl-terminated Polyimides

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
3
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 26 publications
0
3
0
Order By: Relevance
“…Symmetric or asymmetric stretching vibration peaks of CO appeared at 1775 cm −1 and 1712 cm −1 , indicating the generation of the imide ring. 26 Moreover, the symmetric or asymmetric stretching vibration peaks of CN, C–O, and C–F appeared at 1596 cm −1 , 1272 cm −1 , and 1134 cm −1 , respectively; 27,28 skeletal vibration absorption peaks of the benzene ring and characteristic absorption peaks of the methyl group also appeared at 1509 cm −1 and 1362 cm −1 , which indicated that both PBAB6F and BPADA were successfully introduced into the polymer. 12 Combined with 1 H NMR (Fig.…”
Section: Resultsmentioning
confidence: 93%
“…Symmetric or asymmetric stretching vibration peaks of CO appeared at 1775 cm −1 and 1712 cm −1 , indicating the generation of the imide ring. 26 Moreover, the symmetric or asymmetric stretching vibration peaks of CN, C–O, and C–F appeared at 1596 cm −1 , 1272 cm −1 , and 1134 cm −1 , respectively; 27,28 skeletal vibration absorption peaks of the benzene ring and characteristic absorption peaks of the methyl group also appeared at 1509 cm −1 and 1362 cm −1 , which indicated that both PBAB6F and BPADA were successfully introduced into the polymer. 12 Combined with 1 H NMR (Fig.…”
Section: Resultsmentioning
confidence: 93%
“…And the characteristic absorptions of the imide ring structure at 1780, 1720 and 1370, 740 cm −1 appeared, due to the C=O asymmetric and symmetric stretching vibrations and the C-N stretching and bending vibrations, and their intensities were increased with the increasing treatment temperature of the blend resins. In addition, the absorptions at 2210 cm −1 , attributed to the carbon-carbon stretching vibrations in phenylethynyl groups (-C≡C-), were not disappeared even after being thermally treated at 260 °C, implying that no obvious thermal curing reaction occurred [ 39 ]. The characteristic peaks of isoimide around 1800 cm −1 and 905 cm −1 were not detected, implying that the imidization process didn’t produce the corresponding isoimide groups [ 40 ].…”
Section: Resultsmentioning
confidence: 99%
“…The results indicated that the thermosetting blend resins followed the first-order kinetics of phenylethynyl-terminated resins [ 42 ]. A two-staged kinetic/diffusion model could be used to explain the curing process of the thermosetting blend resins, which possess more dynamic endcaps and more rigid molecular chains [ 39 ]. The dominating reactions during thermal cure are ethynyl to ethynyl addition.…”
Section: Resultsmentioning
confidence: 99%