Title :
Investigation on the morphology and properties of PI/SiO2-Al2O3 composite films
Author :
Lizhu Liu ; Yang, Liqian ; Weng, Ling ; Lin, Jiaqi
Author_Institution :
Coll. of Mater. Sci. & Eng., Harbin Univ. of Sci. & Technol., Harbin, China
Abstract :
Polyimides (PI) are widely used in microelectronic industries because of their outstanding characteristics such as good mechanical, thermal and dielectric properties. In this paper, a novel PI/SiO2-Al2O3 co-doped composite film was prepared. The inorganic phases of SiO2 were added to PAA solution by sol-gel method with TEOS as precursor, while the Al2O3 phase was added as particles by ultrasonic-mechanical method. The structure and morphology of polyimide/SiO2-Al2O3 composite films were characterized by FTIR and SEM. FTIR results indicated that after SiO2 and Al2O3 addition, the Si-O-Si band drafted from 1100cm-1 to 1154cm-1, possibly indicated the new structure formation. Moreover, all the mechanical properties of PI/SiO2-Al2O3 co-doped films are higher than that of the pure PI. When the Si/Al weight ratio was 4:1 and total inorganic phases content reached 2wt.%, the electric breakdown strength of PI/SiO2-Al2O3 composite films was the highest among the samples and reached 204kV/mm, which was 24% higher than pure PI.
Keywords :
Fourier transform spectra; alumina; electric breakdown; filled polymers; infrared spectra; nanocomposites; nanofabrication; nanoparticles; polymer films; silicon compounds; sol-gel processing; FTIR spectra; SEM; SiO2-Al2O3; electric breakdown strength; inorganic phases; mechanical properties; nanocomposite films; polyimide; sol-gel method; ultrasonic-mechanical method; Atmospheric measurements; Films; Heating; Lead; Particle measurements; Polyimides; Silicon; Polyimide composite films; electric breakdown strength; mechanical properties; morphology; thermal stability;
Conference_Titel :
Strategic Technology (IFOST), 2010 International Forum on
Conference_Location :
Ulsan
Print_ISBN :
978-1-4244-9038-7
Electronic_ISBN :
978-1-4244-9036-3
DOI :
10.1109/IFOST.2010.5668000