Ternary Thermosetting Blends of Epoxy Resin, Poly(ethylene oxide) and Poly(ε‐caprolactone)

Macromolecular Chemistry and Physics - Tập 206 Số 9 - Trang 929-937 - 2005
Yin Ming-hua1, Sixun Zheng2
1Department of Polymer Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China
2Department of Polymer Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, P. R. China. Fax: +86‐21‐54741297

Tóm tắt

AbstractSummary:The ternary thermosetting blends composed of epoxy resin, poly(ethylene oxide) (PEO) and poly(ε‐caprolactone) (PCL) were prepared via in situ polymerization of epoxy monomers in the presence of the two crystalline polymers, PEO and PCL. DSC results showed that the binary blends of epoxy with PEO (and/or PCL) are fully miscible in the entire composition in the amorphous state. FTIR indicates that there were interchain specific interactions between the crosslinked epoxy and the linear polymers in the binary blends and the hydrogen bonding interactions between epoxy and PCL are much weaker than those between epoxy and PEO. The difference in the strength of interchain specific interactions gives rise to the competitive hydrogen bonding interactions in the ternary blends of epoxy, PEO and PCL, which were evidenced by the results of FTIR. The results of optical microscopy and DSC showed that in the ternary blends PCL component separated out with inclusion of PEO. The formation of the specific phase structures is ascribed to the competitive interchain specific interactions among the crosslinked epoxy, PEO and PCL.Phase boundary diagram of epoxy, PEO and PCL ternary blends.imagePhase boundary diagram of epoxy, PEO and PCL ternary blends.

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Tài liệu tham khảo

Pascault J. P., 2000, Polymer Blends, 379

Guo Q., 1999, Polymer Blends and Alloys, 155ff

10.1016/S0032-3861(00)00813-2

10.1016/S0032-3861(01)00093-3

10.1016/S0032-3861(01)00348-2

10.1002/(SICI)1099-0518(19971115)35:15<3161::AID-POLA9>3.0.CO;2-Z

10.1002/(SICI)1099-0518(19971115)35:15<3169::AID-POLA10>3.0.CO;2-9

10.1007/s00396-003-0870-9

10.1002/polb.10435

10.1002/polb.10436

10.1002/polb.20119

Lu H., 2004, Polymer, 44, 4683

10.1002/macp.200400054

10.1021/ma981819o

10.1016/S0032-3861(02)00928-X

10.1002/pen.760342204

10.1016/S0032-3861(98)00302-4

10.1016/S0032-3861(98)00454-6

10.1021/ma000429a

10.1002/pol.1974.170120318

10.1002/app.1984.070291115

10.1016/0032-3861(91)90033-F

10.1016/0032-3861(94)90389-1

10.1016/0032-3861(95)92037-F

10.1002/1521-3935(20010401)202:7<1077::AID-MACP1077>3.0.CO;2-5

10.1016/0032-3861(83)90258-6

10.1103/PhysRevA.39.783

Fox T. G., 1956, Bull. Am. Phys. Soc., 1, 123

Gordon M., 1952, J. Appl. Chem., 2, 496, 10.1002/jctb.5010020901

10.1021/ma60066a018

10.1002/pol.1982.180200203

10.1016/0032-3861(82)90407-4

10.1002/pol.1984.130220603

10.1021/ma00171a055

10.1021/ma00200a052

10.1016/0032-3861(93)90275-F

Jungnickel B.‐J., 1997, Curr. Trends Polym. Sci., 2, 157

10.1002/(SICI)1099-0488(20000501)38:9<1250::AID-POLB16>3.0.CO;2-M

10.1002/app.1984.070290606

10.1007/BF00657443

10.1016/S0032-3861(03)00167-8

Purcell K. F., 1968, J. Am. Chem. Soc., 24, 251

10.1021/ma00043a027

10.1080/05704928408060422

10.1016/j.polymer.2004.02.050

10.1002/macp.200300164

10.1021/bk-1989-0395

Coleman M. M., 1991, Specific Interactions and the Miscibility of Polymer Blends

10.1002/(SICI)1521-3935(20000301)201:6<705::AID-MACP705>3.0.CO;2-9