Functional Condensation Polymers 2002
DOI: 10.1007/0-306-47563-4_8
|View full text |Cite
|
Sign up to set email alerts
|

Preparation and Properties of Sulfonated or Phosphonated Polybenzimidazoles and Polybenzoxazoles

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
15
0

Year Published

2004
2004
2015
2015

Publication Types

Select...
6
1
1

Relationship

0
8

Authors

Journals

citations
Cited by 15 publications
(16 citation statements)
references
References 16 publications
0
15
0
Order By: Relevance
“…The most common PEMs are perfluorosulfonate ionomers,47 but considerable contemporary ionomer research has focused on the development of sulfonated hydrocarbon polymers as substitutes for the relatively expensive perfluorosulfonates 48–51. Phosphonate ionomers have also been studied for PEM applications,52–59 but that represents only a relatively small part of the materials development for PEMs conducted over the past decade. In the present study, the styrene–phosphonate ionomers were evaluated for their applicability as PEMs.…”
Section: Resultsmentioning
confidence: 99%
“…The most common PEMs are perfluorosulfonate ionomers,47 but considerable contemporary ionomer research has focused on the development of sulfonated hydrocarbon polymers as substitutes for the relatively expensive perfluorosulfonates 48–51. Phosphonate ionomers have also been studied for PEM applications,52–59 but that represents only a relatively small part of the materials development for PEMs conducted over the past decade. In the present study, the styrene–phosphonate ionomers were evaluated for their applicability as PEMs.…”
Section: Resultsmentioning
confidence: 99%
“…13,[29][30][31][32][33][34][35][36][37][38][39][40][41][42][43][44][45][46][47][48] Three common approaches are typically employed for functionalizing PBI: (1) direct sulfonation of the backbone, 29,47,49 (2)chemical grafting of functionalized monomers, 31,35 or (3) polycondensation of a sulfonated aromatic diacid with an aromatic tetraamine. 30,50 The last method provides advantages over the first two, such as limitation of side reactions and control over the degree of sulfonation. Previously published work has focused on modification of the m-PBI backbone structure.…”
Section: Introductionmentioning
confidence: 99%
“…Sulfonated polybenzoxazoles were prepared from 5-sulfoisophthalic or 2-sulfoterephthalic acids and different bis-(o-aminophenols) [159].…”
Section: Scheme 18mentioning
confidence: 99%