journal article·2005-10

Electron-beam curing of epoxy resins: Effect of alcohols on cationic polymerization

N. N. Ghosh, G. R. Palmese

Bulletin of Materials Science· Volume 28· Issue 6
Publisher page

Abstract

Electron-beam (e-beam) induced polymerization of epoxy resins proceeds via cationic mechanism in presence of suitable photoinitiator. Despite good thermal properties and significant processing advantages, epoxy-based composites manufactured using e-beam curing suffer from low compressive strength, poor interlaminar shear strength, and low fracture toughness. A detailed understanding of the reaction mechanism involving e-beam induced polymerization is required to properly address the shortcomings associated with e-beam curable resin systems. This work investigated the effect of hydroxyl containing materials on the reaction mechanism of e-beam induced cationic polymerization of phenyl glycidyl ether (PGE). The alcohols were found to play important roles in polymerization. Compared to hydroxyl group of aliphatic alcohol, phenolic hydroxyl group is significantly less reactive with the oxonium active centre, generated during e-beam induced polymerization of epoxy resin system.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Photopolymerization techniques and applications · Dental materials and restorations

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

References (15)

Show source-provided references
1. Bednarek M, Kubisa P and Penczek S 1989Macromol. Chem. Chem. Suppl. 15 4910.1002/macp.1989.020151989106 ↗
2. Bednarek M, Biedron T, Szymanski R, Kubisa P and Penczek S 1991Macromol. Chem. 42/43 47510.1002/masy.19910420139 ↗
3. Benziers D and Capdepuy B 1990Proceedings of SAMPE international symposium (USA: SAMPE)35 p. 1220
4. Bouillon N, Pascault J P and Tighzert L 1990Macromol. Chem. 191 1403, 143510.1002/macp.1990.021910619 ↗
5. Chabanne P, Tighzert L and Pascault J P 1994J. Appl. Polym. Sci. 53 769, 78710.1002/app.1994.070530607 ↗
6. Crivello C J and Lam J H W 1977Macromolecules 10 130710.1021/ma60060a028 ↗
7. Fouassir J P, Burr D and Crivello J V 1994JMS-Pure Appl. Chem. A31 677
8. Goodman D L, Birx D L, Palmese G R and Chen A 1996Proceedings of 41st SAMPE international symposium (USA: SAMPE)41 p. 207
9. Janke C J, Havens S J, Dorsay G F and Lopata V J 1996Proceedings of 41st international SAMPE symposium (USA: SAMPE)41 p. 196
10. Janke C J, Norris R E, Yarborough K, Havens S J and Lopata V J 1997Proceedings of 42nd international SAMPE symposium (USA: SAMPE)42 p. 477
11. Lopata V J, Chung M, Janke C J and Havens S J 1996Proceedings of 28th international SAMPE technical conference (USA: SAMPE)28 p. 901
12. Matejka L, Chabanne P, Tighzert L and Pascault J P 1994J. Polym. Chem. Chem. Ed. 32 144710.1002/pola.1994.080320806 ↗
13. Matejka L, Chabanne P, Tighzert L and Pascault J P 1997J. Polym. Chem. Chem. Ed. 35 651, 66510.1002/(SICI)1099-0518(199703)35:4<651::AID-POLA7>3.0.CO;2-S ↗
14. Saunders C B, Lopata V J, Kremers W, McDougall T E, Tateishi M and Sing A 1993Proceedings of 38th international SAMPE symposium (USA: SAMPE)38 p. 1681
15. Saunders C B, Lopata V J, Kremers W, Chung M and Barnard J W 1995Proceedings of 40th SAMPE international symposium (USA: SAMPE)40 p. 112