journal article·2004-08

Molecular mobility and fragility in n-ethylene glycol dimethacrylate monomers

M.T. Viciosa, M. Dionı́sio

Journal of Non-Crystalline Solids· Volume 341· Issue 1-3
Publisher page

Abstract

Di-, tri- and tetra-ethylene glycol dimethacrylate monomers were investigated by dielectric relaxation spectroscopy in the frequency range from 20 Hz to 1 MHz and in the temperature region comprised between −120 and +25 °C. A rather intense relaxation process associated with the glass transition is found for all the monomers in the temperature region between −80 and −50 °C. The mobility of the cooperative process decreases with the molecular weight increase. The temperature dependence of the relaxation times reveals some curvature, which increases with the size of the ethylene glycol moiety (di≅tri<tetra). In spite of this behavior the di- and tri-ethylene monomers could be treated as Arrhenius type, presenting similar activation energies . The fragility indexes estimated by both dielectric relaxation spectroscopy and differential scanning calorimetry techniques agree for the di- and tri-ethylene monomers only when Arrhenius behavior is assumed. Despite the different values estimated, the fragility is comparable to a quite strong glass former as glycerol.
Source: expertdata · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Material Dynamics and Properties · Liquid Crystal Research Advancements · Photochemistry and Electron Transfer Studies

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

References (34)

Show source-provided references
1. Disorder Effects on Relaxational Processes
2. Laughlin · J. Phys. Chem. · 1972 · 76 · 231710.1021/j100660a023 ↗
3. Ngai · J. Non-Cryst. Solids · 2000 · 275 · 710.1016/S0022-3093(00)00238-6 ↗
4. Angell · 1985 · 1
5. Angell · J. Non-Cryst. Solids · 1991 · 131–133 · 1310.1016/0022-3093(91)90266-9 ↗
6. Bohmer · J. Chem. Phys. · 1993 · 99 · 420110.1063/1.466117 ↗
7. Angell · Science · 1995 · 267 · 192410.1126/science.267.5206.1924 ↗
8. Debenedetti · 1997
9. Angell · J. Res. Nat. Inst. Stand. Technol. · 1997 · 102 · 17110.6028/jres.102.013 ↗
10. Ngai · IEEE Trans. Dielectr. Electr. Insul. · 2001 · 8 · 32910.1109/94.933340 ↗
11. Ngai · J. Non-Cryst. Solids · 2000 · 275 · 710.1016/S0022-3093(00)00238-6 ↗
12. Park · J. Phys. Soc. Japan · 1998 · 67 · 413110.1143/JPSJ.67.4131 ↗
13. Döß · J. Chem. Phys. · 2002 · 117 · 658210.1063/1.1506147 ↗
14. Dietz · Polymer · 1997 · 38 · 376710.1016/S0032-3861(96)00902-0 ↗
15. Anseth · Adv. Polym. Sci. · 1995 · 122 · 17710.1007/3540587888_16 ↗
16. 1993
17. Kannurpatti · Macromolecules · 1998 · 31 · 331110.1021/ma970721r ↗
18. Ramos · J. Therm. Anal. Calorim. · 2003 · 71 · 65910.1023/A:1022884716750 ↗
19. Havriliak · Polymer · 1967 · 8 · 16110.1016/0032-3861(67)90021-3 ↗
20. Vogel · Phys. Z. · 1921 · 22 · 645
21. Fulcher · J. Am. Chem. Soc. · 1925 · 8 · 339
22. Tammann · Z. Anorg. Allg. Chem. · 1926 · 156 · 24510.1002/zaac.19261560121 ↗
23. Morgan · Biomaterials · 2000 · 21 · 189710.1016/S0142-9612(00)00067-3 ↗
24. Moynihan · J. Phys. Chem. · 1974 · 78 · 267310.1021/j100619a008 ↗
25. Moynihan · Thermochim. Acta · 1996 · 280/281 · 15310.1016/0040-6031(95)02781-5 ↗
26. Davidson · J. Chem. Phys. · 1950 · 18 · 141710.1063/1.1747496 ↗
27. McCrum · 1967
28. Ngai · J. Phys.: Condens. Matter · 2003 · 15 · S1107
29. Nagi · J. Chem. Phys. · 2004 · 120 · 875
30. Brand · Phys. Rev. B · 2000 · 62 · 887810.1103/PhysRevB.62.8878 ↗
31. Schneider · Phys. Rev. Lett. · 2000 · 84 · 556010.1103/PhysRevLett.84.5560 ↗
32. Aliotta · J. Phys.:Condens. Matter · 1998 · 10 · 545
33. Crowley · Thermochim. Acta · 2001 · 380 · 7910.1016/S0040-6031(01)00662-1 ↗
34. Correia · J. Chem. Phys. · 2000 · 113 · 320410.1063/1.1286959 ↗