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HERO ID
2588263
Reference Type
Journal Article
Title
Polyimide Multilayer Thin Films Prepared via Spin Coating from Poly(amic acid) and Poly(amic acid) Ammonium Salt
Author(s)
Ha, Y; Choi, MC; Jo, N; Kim, Il; Ha, CSik; Han, D; Han, S; Han, M
Year
2008
Is Peer Reviewed?
1
Journal
Macromolecular Research
ISSN:
1598-5032
Volume
16
Issue
8
Page Numbers
725-733
Web of Science Id
WOS:000262275000010
Abstract
Polyimide (PI) multilayer thin films were prepared by spin-coating from a poly(amic acid) (PAA) and poly(amic acid) ammonium salt (PAAS). PI was prepared from pyromellitic dianhydride (PMDA) and 4,4'-oxydianiline (ODA) PAA. Different compositions of PAAS were prepared by incorporating triethylamine (TEA) into PMDA-ODA PAA in dimethylacetamide. PI multilayer thin films were spin-coated from PMDA-ODA PAA and PAAS. The PAAS comprising cationic and anionic moieties were spherical with a particle size of 20-40 nm. Some particles showed layers with ammonium salts, despite poor ordering. Too much salt obstructed the interaction between the polymer chains and caused phase separation. A small amount of salt did not affect the interactions of the interlayer structure but did interrupt the stacking between chains. Thermogravimetric analysis (TGA) showed that the average decomposition temperature of the thin films was 611 degrees C. All the films showed almost single-step, thermal decomposition behavior. The nanostructure of the multilayer thin films was confirmed by X-ray reflectivity (XRR). The LF 43 film, which was prepared with a 4:3 molar ratio of PM DA and ODA, was comprised of uniformly spherical PAAS particles that influenced the nanostructure of the interlayer by increasing the interaction forces. This result was supported by the atomic force microscopy (AFM) data. It was concluded that the relationship between the uniformity of the PAAS particle shapes and the interaction between the layers affected the optical and thermal properties of PI layered films.
Keywords
polyimide; multilayer films; spin coating; ammonium salt; nanostructure
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