Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Preparation and characterization of polyimide nanocomposites with different organo-montmorillonites

Authors
Chang, JHPark, KMCho, DHYang, HSIhn, KJ
Issue Date
Sep-2001
Publisher
SOC PLASTICS ENG INC
Citation
POLYMER ENGINEERING AND SCIENCE, v.41, no.9, pp 1514 - 1520
Pages
7
Journal Title
POLYMER ENGINEERING AND SCIENCE
Volume
41
Number
9
Start Page
1514
End Page
1520
URI
https://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/27052
DOI
10.1002/pen.10850
ISSN
0032-3888
1548-2634
Abstract
Poly(amic acid) nanocomposites were synthesized from a dimethylacetamide (DMA) solution with two organophilic montmorillonites (organo-MMTs). It was then heated at various temperatures under vacuum, yielding 15-20 um thick films of polyimide/organo-MMT hybrid with different clay contents (1-8 wt%). Dodecylamine (C-12-) and hexadecylamine (C-16-) were used as aliphatic alkylamines in organo MMT The ultimate strength monotonically increased with increasing clay content in the polymer matrix. Maximum enhancement in the Initial modulus was observed for the blends containing 2 wt% clay with two kinds of organo-clays, and values did not alter significantly with further Increases in clay content. Additions of only 2 wt% C-12- and C-16-MMT to the polyimide were shown to cause 94%-95% reduction in oxygen gas permeability. This is caused by the barrier properties of the clay layers dispersed in the composite. In general, C-16-MMT is more effective than C-12-MMT in increasing both the tensile property and the gas barrier in a polyimide matrix Intercalations of the polymer chains in clay were examined through wide-angle X-ray diffraction (XRD) and electron microscopies (SEM and TEM).
Files in This Item
There are no files associated with this item.
Appears in
Collections
ETC > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE