journal article·2025-06-20

Preparation of hollow mesoporous silica/polyimide composite films and study of their properties

Xin Li, Qi‐wen Ma, Guang‐ning Yu, Ji Shi, Hai‐yang Chang, Rong‐rong Zheng, San‐jun Fan, Cheng Wang

Polymer Composites· Volume 46· Issue 9
Publisher page

Abstract

Abstract Constructing high‐performance polyimide (PI) films with low dielectric constant, excellent mechanical properties, hydrophobicity, and thermal stability is of great significance, but remains a great challenge. Herein, five PI films (labeled as P1, P2, P3, P4, and P5, respectively) were successfully synthesized by a conventional two‐step method using 1,4‐bis(4‐amino‐2‐trifluoromethylphenoxy)benzene as the sole diamine monomer and pyromellitic dianhydride, 2,3,6,7‐Naphthalenetetracarboxylic 2,3:6,7‐Dianhydride, 3,3′,4,4′‐biphenyltetracarboxylic dianhydride, o‐4,4′‐oxydiphthalic anhydride, and 3,3′,4,4′‐benzophenonetetracarboxylic dianhydride as dianhydride monomers, respectively. Particularly, a hollow mesoporous silica (HMSMs)/PI film with excellent comprehensive properties was successfully synthesized by introducing HMSMs into P4 film based on a polymerization strategy. The results showed that doping HMSMs contributed to reducing the dielectric constant, improving the mechanical properties and hydrophobicity, and maintaining the excellent thermal stability in comparison to the conventional P4 film. When the HMSMs content was 1.5 wt.%, the thermal decomposition temperature, tensile strength, water contact angle, and dielectric constant of the HMSMs/PI composite films were measured at 489°C, 162 MPa, 86.45°, and 2.40, respectively. This study presents a new approach for preparing advanced PI composite films. Highlights High‐performance HMSMs/PI composite films were synthesized. Doping HMSMs into PI enhances the overall performance of film. A lower dielectric constant (2.40) was achieved.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Synthesis and properties of polymers · Silicone and Siloxane Chemistry · Mesoporous Materials and Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Petrochemical Engineering Shenyang University of Technology Liaoyang People's Republic of China

School of Chemical Engineering and Light Industry Guangdong University of Technology Guangzhou People's Republic of China

Guangdong Provincial Laboratory of Chemistry and Fine Chemical Engineering Jieyang Center Jieyang People's Republic of China

Department of Chemistry and Biochemistry The Ohio State University Columbus Ohio USA

Funding

National Natural Science Foundation of China

References (46)

Show source-provided references
1. 10.1016/j.coco.2024.10212910.1016/j.coco.2024.102129 ↗
2. 10.1016/j.porgcoat.2024.10870810.1016/j.porgcoat.2024.108708 ↗
3. 10.1016/j.tsf.2005.12.21610.1016/j.tsf.2005.12.216 ↗
4. 10.1016/j.matlet.2023.13441710.1016/j.matlet.2023.134417 ↗
5. 10.1016/j.eurpolymj.2024.11358010.1016/j.eurpolymj.2024.113580 ↗
6. 10.1016/j.jallcom.2024.17591210.1016/j.jallcom.2024.175912 ↗
7. 10.1016/j.eurpolymj.2024.11296910.1016/j.eurpolymj.2024.112969 ↗
8. 10.1016/j.mtadv.2024.10051410.1016/j.mtadv.2024.100514 ↗
9. 10.1016/j.eurpolymj.2024.11309910.1016/j.eurpolymj.2024.113099 ↗
10. 10.1016/j.ceramint.2024.03.02210.1016/j.ceramint.2024.03.022 ↗
11. 10.3390/polym1607098410.3390/polym16070984 ↗
12. 10.1016/j.eurpolymj.2022.11166710.1016/j.eurpolymj.2022.111667 ↗
13. 10.1016/j.est.2024.11338110.1016/j.est.2024.113381 ↗
14. 10.1016/j.polymer.2023.12636110.1016/j.polymer.2023.126361 ↗
15. 10.1016/j.mtcomm.2024.11018910.1016/j.mtcomm.2024.110189 ↗
16. 10.1016/j.compscitech.2019.10770010.1016/j.compscitech.2019.107700 ↗
17. 10.1016/j.jcis.2013.04.01410.1016/j.jcis.2013.04.014 ↗
18. 10.1016/j.eurpolymj.2023.11232710.1016/j.eurpolymj.2023.112327 ↗
19. 10.1016/j.eurpolymj.2023.11219510.1016/j.eurpolymj.2023.112195 ↗
20. 10.1016/j.polymer.2020.12311510.1016/j.polymer.2020.123115 ↗
21. 10.1016/j.cej.2024.15082410.1016/j.cej.2024.150824 ↗
22. 10.1016/j.triboint.2020.10618410.1016/j.triboint.2020.106184 ↗
23. 10.1016/j.compscitech.2018.07.02110.1016/j.compscitech.2018.07.021 ↗
24. 10.1016/j.polymer.2024.12769410.1016/j.polymer.2024.127694 ↗
25. 10.1016/j.recm.2022.08.00110.1016/j.recm.2022.08.001 ↗
26. 10.1002/app.5060010.1002/app.50600 ↗
27. 10.1002/pc.2791210.1002/pc.27912 ↗
28. 10.1016/j.partic.2023.06.01110.1016/j.partic.2023.06.011 ↗
29. 10.1016/j.msec.2016.10.08110.1016/j.msec.2016.10.081 ↗
30. 10.1016/j.micromeso.2009.06.02810.1016/j.micromeso.2009.06.028 ↗
31. 10.1016/j.matlet.2017.06.04510.1016/j.matlet.2017.06.045 ↗
32. 10.1016/j.colsurfa.2022.12959610.1016/j.colsurfa.2022.129596 ↗
33. 10.1016/j.micromeso.2010.09.03610.1016/j.micromeso.2010.09.036 ↗
34. 10.1016/j.jddst.2024.10560410.1016/j.jddst.2024.105604 ↗
35. 10.1016/j.cej.2024.15161310.1016/j.cej.2024.151613 ↗
36. 10.1016/j.colsurfa.2024.13383110.1016/j.colsurfa.2024.133831 ↗
37. 10.1016/j.ejps.2023.10664110.1016/j.ejps.2023.106641 ↗
38. 10.1007/s10118‐021‐2514‐210.1007/s10118‐021‐2514‐2 ↗
39. 10.1039/C8TC00998H10.1039/C8TC00998H ↗
40. 10.1039/D2PY00550F10.1039/D2PY00550F ↗
41. 10.1016/j.mtphys.2024.10142510.1016/j.mtphys.2024.101425 ↗
42. 10.1016/j.jiec.2022.07.03410.1016/j.jiec.2022.07.034 ↗
43. 10.1016/j.compositesb.2019.10691710.1016/j.compositesb.2019.106917 ↗
44. 10.1039/d4ra01389a10.1039/d4ra01389a ↗
45. 10.1016/j.polymer.2022.12538210.1016/j.polymer.2022.125382 ↗
46. 10.1016/j.surfin.2024.10409910.1016/j.surfin.2024.104099 ↗