Synthesis and properties of ultralow dielectric porous polyimide films containing adamantane

被引:49
|
作者
Lv, Pengxia [1 ,2 ]
Dong, Zhixin [1 ]
Dai, Xuemin [1 ]
Wang, Hanfu [1 ]
Qiu, Xuepeng [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Polymer Composites Engn Lab, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
adamantane; dielectric properties; films; in-situ polycondensation; polyimides; porous polyimide films; thermal decomposition; ultralow dielectric constant; PERFORMANCE FUNCTIONAL POLYIMIDES; SIDE-CHAINS; AROMATIC POLYAMIDES; SOLUBLE POLYIMIDES; CONSTANT MATERIALS; POLY(AMIC ACID)S; THIN-FILMS; NANOFOAMS; COPOLYMERS; MOIETIES;
D O I
10.1002/pola.28928
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of novel ultralow dielectric porous polyimide (PI) films containing adamantane groups was prepared via the thermolysis of polyethylene glycol (PEG) oligomers mixed into PI matrix. Scanning electron microscopy results indicated that the porous PI films showed closed pores with an average diameter of 120 +/- 10 nm. Good thermal properties with 5% weight loss temperature of 499 degrees C in air atmosphere and glass transition temperature in excess of 310 degrees C were shown for porous PI films. Notably, the ultralow dielectric constant of porous PI films with 1.85 at 1 MHz was obtained and revealed via broadband dielectric spectroscopy. The effects of the chemical structure of the PI matrix and PEG content on the decomposition behavior of PEG and the performance of porous films were investigated. Wide-angle X-ray diffraction results indicated that the PI matrix with large d-spacing generated weaker interactions between the PEG and PI backbone than those of PI matrix with small d-spacing. As a result, the PEG for the PI matrix with large d-spacing was completely decomposed. As indicated by the broadband dielectric spectroscopy results, lower dielectric porous PI films were prepared when the PEG contents in the PI matrix increased from 0 to 20 wt %. (c) 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 549-559
引用
收藏
页码:549 / 559
页数:11
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