Solid-state NMR analyses of the crystalline-noncrystalline structure and its thermal changes for ethylene ionomers

The crystalline–noncrystalline structure and its structural changes from thermal treatments for ethylene ionomers have been investigated with solid‐state 13C and 23Na NMR spectroscopy. 13C spin–lattice relaxation time (T1C) measurements reveal that as‐received ethylene ionomers have much enhanced mo...

Full description

Saved in:
Bibliographic Details
Published in:Journal of polymer science. Part B, Polymer physics Polymer physics, 2002-06, Vol.40 (11), p.1142-1153
Main Authors: Kuwabara, Kazuhiro, Horii, Fumitaka
Format: Article
Language:English
Subjects:
annealing
Applied sciences
crystalline-noncrystalline structure
ethylene ionomers
Exact sciences and technology
Organic polymers
Physicochemistry of polymers
polyethylene (PE)
Properties and characterization
solid-state NMR
Structure, morphology and analysis
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The crystalline–noncrystalline structure and its structural changes from thermal treatments for ethylene ionomers have been investigated with solid‐state 13C and 23Na NMR spectroscopy. 13C spin–lattice relaxation time (T1C) measurements reveal that as‐received ethylene ionomers have much enhanced molecular mobility in the crystalline region in comparison with conventional polyethylene samples. By appropriate annealing, however, polyethylene‐like morphological features reflecting T1C behavior can also be observed. 13C spin–spin relaxation time (T2C) measurements for the noncrystalline region reveal the existence of two components with different T2C values, and these two components have been assigned to the crystalline–amorphous interfacial and rubbery–amorphous components. These results indicate that the structure of the major part of the noncrystalline region in the ethylene ionomers is similar to that of bulk‐crystallized polyethylene samples, regardless of possible ionic aggregates. The origin of the lower temperature endothermic peak in the heating process of the differential scanning calorimetry curve observed for the as‐received sample has also been examined somewhat in detail. As a result, it is proposed that the melting of smaller crystallites produced during storage at room temperature is the origin of the lower temperature peak. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1142–1153, 2002
ISSN:0887-6266
1099-0488
DOI:10.1002/polb.10174