1987
DOI: 10.1021/ma00178a028
|View full text |Cite
|
Sign up to set email alerts
|

Observation of cluster formation in an ionomer

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
56
0

Year Published

1990
1990
2008
2008

Publication Types

Select...
6

Relationship

1
5

Authors

Journals

citations
Cited by 70 publications
(57 citation statements)
references
References 5 publications
1
56
0
Order By: Relevance
“…In this context, sample preparation method usually involves some method of solvent casting; and it is not at all clear (without using elevated temperatures) that room temperature drying, even under vacuum, removes all solvent, especially for a glassy polymer. With this reservation, studies have shown that solution casting and/or precipitation from solution can lead to a sample with no SAXS peak [55][56][57]. No SAXS peak has often been interpreted as indicating no ionic aggregates.…”
Section: Ionomer Synthesismentioning
confidence: 99%
See 1 more Smart Citation
“…In this context, sample preparation method usually involves some method of solvent casting; and it is not at all clear (without using elevated temperatures) that room temperature drying, even under vacuum, removes all solvent, especially for a glassy polymer. With this reservation, studies have shown that solution casting and/or precipitation from solution can lead to a sample with no SAXS peak [55][56][57]. No SAXS peak has often been interpreted as indicating no ionic aggregates.…”
Section: Ionomer Synthesismentioning
confidence: 99%
“…Showing this type of behavior is sodium-neutralized SPS with 5.5 mol% acid groups [97,98], manganese-neutralized SPS with 2.6% and 7.6 mol% acid groups [55,56]. A zinc-neutralized PTMO-based polyurethane [84] and a sodium-neutralized EMAA [81] showed a decrease in both scattering angle and peak height with increasing temperature, suggesting that some aggregates (presumably small ones) were breaking apart; however, an alternate interpretation is that both aggregate size and spatial distribution are becoming more disordered.…”
Section: Ionomer Synthesismentioning
confidence: 99%
“…That notion may be supported by the dynamic mechanical results of Agarwal et al, 12 who attributed a melt relaxation to motion in the ionic domains. The results of Galambos et al 8 for sulfonated polystyrene ionomers suggest that the intensity of the low-angle scattering upturn shown in Figure 1 should increase as the ionic peak disappears, that is, as the ionic groups are dispersed into the polymer continuous phase. The SAXS data for temperatures from 140 to 294°C show a monotonic increase in the zero-angle scattering as temperature increases.…”
mentioning
confidence: 94%
“…Although the origin of this scattering upturn is uncertain, in the past it has been attributed to a heterogeneous distribution of the ionic species in the polymer. 8,9 Agarwal and Prestridge 10 observed large ionic domains, ϳ500 to 1000 nm, by transmission electron microscopy (TEM) studies of Zn-SEPDM, which could contribute to the intense zero-angle scattering seen in Figure 1. However, TEM evaluation of Zn-SEPDM ionomers by Handlin et al 11 only detected ionic domains with diameters of 2 to 3 nm.…”
mentioning
confidence: 98%
“…8 Since partly crystalline ionomers have a wide range of application, extensive studies have been devoted to their morphology. [1][2][3]8 The morphology of polystyrene 7,[9][10][11][12][13][14][15][16][17][18][19][20][21][22] ionomers was also investigated widely using the SAXS technique.…”
Section: Introductionmentioning
confidence: 99%