1994
DOI: 10.1016/0014-3057(94)90192-9
|View full text |Cite
|
Sign up to set email alerts
|

Membranes par melange de polymeres—I. Morphologie

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

2
2
0

Year Published

2002
2002
2019
2019

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 10 publications
(4 citation statements)
references
References 9 publications
2
2
0
Order By: Relevance
“…It is noteworthy that EVOH/PVOH7 and EVOH/PVOH15 showed quite the same size distribution profile despite a slightly higher average mean domain size value for EVOH/PVOH15. The large domain size distribution observed for EVOH/PVOH30 was consistent with the trend commonly reported in the literature for blend composition approaching the phase inversion …”
Section: Resultssupporting
confidence: 91%
See 1 more Smart Citation
“…It is noteworthy that EVOH/PVOH7 and EVOH/PVOH15 showed quite the same size distribution profile despite a slightly higher average mean domain size value for EVOH/PVOH15. The large domain size distribution observed for EVOH/PVOH30 was consistent with the trend commonly reported in the literature for blend composition approaching the phase inversion …”
Section: Resultssupporting
confidence: 91%
“…The large domain size distribution observed for EVOH/PVOH30 was consistent with the trend commonly reported in the literature for blend composition approaching the phase inversion. [16][17][18][19][20][21][22] Microstructure Table 1 summarizes the values of the characteristic transitions observed for the neat EVOH and neat PVOH films during cooling from 250 C at 20 C min −1 and subsequent heating scan at 20 C min −1 .…”
Section: Resultsmentioning
confidence: 99%
“…More hydroxyl groups are then available as hydrogen bond‐donors to develop more interchain interactions with the sulfonate acceptor group in PSSNa; and thus, the presence of a moderate amount of acetate groups in PVA appears to be important to obtain PVA/PSSNa compatibility. This result confirms the early hypothesis which assumed that the compatibility of PVA and PSSNa is due to the formation of hydrogen bonds between the hydroxyl groups of PVA and the sulfonate groups of PSSNa 27…”
Section: Resultssupporting
confidence: 91%
“…The PVA-PSSNa compatibility would be driven by the decrease in the hydrolysis degree of PVA. 38 The higher the number of distributed acetate groups that remain randomly on the chains after incomplete hydrolysis, the weaker the interactions among OH groups, and the lower the crystallinity.…”
mentioning
confidence: 99%