Skip to content
Licensed Unlicensed Requires Authentication Published by De Gruyter August 21, 2014

Development and characterization of homo, co and terpolyimides based on BPDA, BTDA, 6FDA and ODA with low dielectric constant

  • Revathi Purushothaman EMAIL logo and I. Mohammed Bilal

Abstract

Polyimides are a sophisticated family of materials, which cover an exhaustive range of high performance polymers and find applications from aerospace to microelectronics. Microelectronic applications demand low dielectric constant and high performance. Aromatic terpolyimides were synthesized by reacting 3,3′,4,4′-biphenyl tetracarboxylic dianhydride (BPDA), 3,3′,4,4′-benzophenone tetracarboxylic dianhydride (BTDA) and 4,4′-(hexafluoroisopropylidene) diphthalic anhydride (6FDA) with 4,4′-oxydianiline (ODA) by thermal imidization with the view to decrease their dielectric constant without compromising thermal properties and mechanical properties compared to their homo and copolyimides. They were characterized by Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-ray diffraction (XRD). Their FTIR spectra established formation of polyimide by the characteristic vibrations at 1375 cm-1 (C-N stretch) and 1113 cm-1 (imide ring deformation). The TGA results showed decomposition of imides at about 515°C. The glass transition temperature (Tg) of the polymers varied from 261°C to 281°C. The XRD spectrum of BPDA/BTDA/6FDA-ODA, which contained 50% of 6FDA, showed a broadened envelope with a peak at 16.8° (2θ), illustrating a semicrystalline nature. Incorporation of 6FDA, with a bulky bridging group into the backbone of BPDA/6FDA-ODA and BPDA/BTDA/6FDA-ODA (0.25:0.25:0.5::1) caused a decrease in the dielectric constant (2.13 and 2.38, respectively). Such polyimides can find application in microelectronics such as flexible printed circuits and tape automated bonding applications.


Corresponding author: Revathi Purushothaman, B.S. Abdur Rahman University, G.S.T. Road, Vandalur, Chennai 600 048, India, e-mail:

Acknowledgments

The authors are grateful to B.S. Abdur Rahman University for financial support. The technical support of Mr. Selvam, Anjan Chemicals, for FTIR, Dr. S. Rajendran and Dr. M. S. Pandian, Pondicherry University for XRD, Mr. Rohan Bosale, Hemetek Technologies for tensile properties, Dr. R. Vasanthakumari, B.S. Abdur Rahman University for DSC and TGA, and Dr. V. Geethaguru, Dr. M. Murugan, Mr. K. Gunasekar, Mr. T. Kannakaraj and Mr. R. Tamilselvan, B.S. Abdur Rahman University for their support in fabricating the solution casting machine and thickness measurements are greatly appreciated. Ms. H. Sofia is kindly acknowledged for correcting the English.

References

[1] Ho CW, Chance DA, Bajorek CH, Acosta RE. IBMJ. Res. Dev. 1982, 26, 286–296.Search in Google Scholar

[2] Chao CC, Scholz KD, Leibovitz J, Cobarruiaz M, Chung CC. IEEE T. Compon. Hybr. 1989, 12, 180–184.Search in Google Scholar

[3] Ramos MMD. Vacuum 2002, 64, 255–260.10.1016/S0042-207X(01)00332-3Search in Google Scholar

[4] Kim MH, Lee KW. Met. Mater. Int. 2006, 12, 425–433.Search in Google Scholar

[5] Barlow F, Lostetter A, Elshabini A. Microelectron. Reliab. 2002, 42, 1091–1099.Search in Google Scholar

[6] Kamiya S, Furuta H, Omiya M. Surf. Coat. Technol. 2007, 202, 1084–1088.Search in Google Scholar

[7] Noh BI, Yoon JW, Choi JH, Jung SB. Microelectron. Eng. 2011, 88, 718–723.Search in Google Scholar

[8] Park J, Mukherjee B, Cho H, Kim S, Pyo S. Synth. Met. 2011, 161, 143–147.Search in Google Scholar

[9] Lee C, Shul Y, Han H. J. Polym. Sci. B Polym. Phys. 2002, 40, 2190–2198.Search in Google Scholar

[10] Yang CY, Hsu SLC, Chen JS. J. Appl. Polym. Sci. 2005, 98, 2064–2069.Search in Google Scholar

[11] Zuo M, Xiang Q, Takeichi T. Polymer 1998, 39, 6883–6889.10.1016/S0032-3861(98)00179-7Search in Google Scholar

[12] Tsai FY, Harding DR, Chen SH, Blanton TN. Polymer 2003, 44, 995–100.10.1016/S0032-3861(02)00787-5Search in Google Scholar

[13] Purushothaman R, Bilal IM, Palanichamy M. J. Polym. Res. 2011, 18, 1597–1604.Search in Google Scholar

[14] Purushothaman R. Ph.D thesis, Anna University, Chennai, India, 2011.Search in Google Scholar

[15] Harris FW. In Polyimides, Wilson D, Stenzenberger HD, Hergenrother PM, Eds., Blackie & Son Ltd.: Glasgow and London, 1990.Search in Google Scholar

[16] Wang X, Li YF, Zhang S, Ma T, Shao Y. Eur. Polym. J. 2006, 42, 1229–1239.Search in Google Scholar

[17] Clair SAK, Clair STL, Winfree WP. Polym. Mater. Sci. Eng. 1988, 59, 28–33.Search in Google Scholar

[18] Pan H, Pu H, Wan D, Jin M, Chang Z. J. Power Sources 2010, 195, 3077–3083.10.1016/j.jpowsour.2009.11.116Search in Google Scholar

[19] Xie K, Zhang SY, Liu JG, He MH, Yang SY. J. Polym. Sci., Part A: Polym. Chem. 2001, 39, 2581–2590.Search in Google Scholar

[20] Yen CT, Chen WC, Liaw DJ, Lu HY. Polymer 2000, 344, 7079–7087.Search in Google Scholar

[21] Hougham G, Tesoro G, Shaw J. Macromolecules 1994, 27, 3642–3649.10.1021/ma00091a028Search in Google Scholar

[22] Misra AC, Tesoro G, Hougham G, Pendharkar SM. Polymer 1992, 33, 1078–1082.10.1016/0032-3861(92)90025-RSearch in Google Scholar

[23] Leu TS, Wang CS. Polymer 2002, 43, 7069–7074.10.1016/S0032-3861(02)00530-XSearch in Google Scholar

[24] Brink MH, Brandom DK, Wilkes GL, McGrath JE. Polymer 1994, 35, 5018–5023.10.1016/0032-3861(94)90658-0Search in Google Scholar

[25] Rogers ME, Brink MH, McGratht JE, Brennan A. Polymer 1993, 34, 849–855.10.1016/0032-3861(93)90373-ISearch in Google Scholar

Received: 2013-8-14
Accepted: 2014-7-6
Published Online: 2014-8-21
Published in Print: 2014-12-1

©2014 by De Gruyter

Downloaded on 31.5.2024 from https://www.degruyter.com/document/doi/10.1515/polyeng-2013-0167/html
Scroll to top button