127
Views
0
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis and Catalytic Graphitization of Silicon Containing Arylacetylenic Resin

, &
Pages 721-729 | Published online: 14 May 2012
 

Abstract

Vinyl(triphenylethynyl)silane ((ph-C≡C)3-Si-C=CH2) (VTPES) was synthesized by Grignard reaction. Its molecular structure was characterized by means of fourier transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance (1H-NMR, 13C-NMR, and 29Si-NMR). Poly(vinyl(triphenylethynyl))silane (PVTPES) was prepared by thermal polymerization and the catalytic graphitization of PVTPES with nickel, and Fe2O3 was also investigated between 900°C and 1600°C under nitrogen atmosphere. The effects of heat-treatment temperature and catalyst concentration on graphitization behavior were analyzed by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM) and Laser Raman spectroscopy (LR). The results show that the presence of the transition metals produced graphitized areas with three-dimensional stacking order, and the Fe2O3 was more effective than nickel for catalytic graphitization. The key factor to affect graphitization behavior of PVTPES was the heat-treatment temperature compared with the catalyst concentration.

Acknowledgments

The authors gratefully acknowledged the support of the National Natural Science Foundation of China (NSFC) (Grant No. 50773017, 50973024).

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.