1998
DOI: 10.1002/(sici)1521-3935(19980601)199:6<1107::aid-macp1107>3.0.co;2-d
|View full text |Cite
|
Sign up to set email alerts
|

Crystallization and phase behavior in nylon 6/aromatic polyimide triblock copolymers

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
19
0

Year Published

2000
2000
2020
2020

Publication Types

Select...
6
1

Relationship

3
4

Authors

Journals

citations
Cited by 26 publications
(19 citation statements)
references
References 0 publications
0
19
0
Order By: Relevance
“…The polymer synthesized in DMAc is expected to have more rigidity than that synthesized in NMP because of the presence of the polyimide order. This expectation is based on previous studies of aromatic polyimides suggesting that interactions and structural order generally increase rigidity …”
Section: Resultsmentioning
confidence: 93%
See 1 more Smart Citation
“…The polymer synthesized in DMAc is expected to have more rigidity than that synthesized in NMP because of the presence of the polyimide order. This expectation is based on previous studies of aromatic polyimides suggesting that interactions and structural order generally increase rigidity …”
Section: Resultsmentioning
confidence: 93%
“…The PEG phase is less well understood in the PDODA case due to the structural dominance of the polyimide structural characteristics P asrOO and F lrOO . These features arise from polyimide interaction or alignment on short and long length scales, and are comparable to aromatic features in other aromatic polyimides . The features related to polyimide regularity may be overshadowing any feature corresponding to the PEG on the nanometer scale.…”
Section: Resultsmentioning
confidence: 94%
“…The found difference between the diffraction patterns of all studied samples is the intensity redistribution of these four characteristic components. It is known19–21 that PCA can be routinely obtained as one of the two possible crystalline polymorphs, viz. , monoclinic α or pseudohexagonal γ or generate the amorphous form as well.…”
Section: Resultsmentioning
confidence: 99%
“…The first polyisocyanate‐based rod–coil block copolymer was reported more than 50 years ago . The functional nature of rod blocks makes rod–coil block copolymers promising for numerous applications: organic electronics, biotechnology, and many others . The considerable chemical difference between rod and coil blocks results in microphase separation at a lower molecular weight of each block, and thus, smaller feature size.…”
Section: Rod–coil Systemsmentioning
confidence: 99%