Cationic polymerization behavior of β‐methylglycidyl ether derivatives and physical properties of their cationically cured materials |
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| Authors: | Ken‐ichi Tamaso Ryo Ogawa Kozo Matsumoto Takeshi Endo |
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| Affiliation: | 1. ADEKA Corporation, 20 showanuma, Kuki‐shi, Saitama, Japan;2. Department of Biological & Environmental Chemistry, Kinki University, Iizuka, Fukuoka, Japan;3. Molecular Engineering Institute, Kinki University, Iizuka, Fukuoka, Japan |
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| Abstract: | β‐Methylglycidyl ethers have been applied to Electrical and Electronic adhesives. However, there is no report about the detailed polymerization behavior and physical properties of their cured products. Hence, we investigated cationic polymerization behavior of bisphenol A di(β‐methylglycidyl) ether (Me‐BADGE) and physical properties of the cured products containing Me‐BADGE. DSC analysis suggested that Me‐BADGE could be cured completely at lower temperature than bisphenol A diglycidyl ether (BADGE). Physical properties were analyzed by dynamic viscoelastic analysis. Glass transition temperature (Tg) of BADGE homopolymer was 194°C. In contrast, the copolymer of BADGE (50 wt %) with Me‐BADGE (50 wt %) showed Tg at 124°C. According to the data of E’ and tan δ, crosslink density of the cured products decreased with increasing the Me‐BADGE content. The analysis of cationic polymerization of monofunctional β‐methylglycidyl ether suggested that the cationic polymerization proceeded not only through oxonium cation but also through carbocation formed by ring‐opening reaction of oxonium cation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42377. |
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| Keywords: | copolymers mechanical properties thermosets |
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