Dielectric characterization of poly(methyl methacrylate) geometrically confined into mesoporous SiO2 glasses

被引:21
作者
Kalogeras, IM [1 ]
Vassilikou-Dova, A
Neagu, ER
机构
[1] Univ Athens, Dept Phys, Solid State Phys Sect, Zografos 15784, Greece
[2] Tech Univ Iasi, Dept Phys, Iasi 6600, Romania
关键词
polymeric-inorganic hybrids; poly(methyl methacrylate); hydrogen bond; glass transition; thermally stimulated depolarization; isothermal discharge; dielectric relaxation;
D O I
10.1007/s100190000111
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Characteristics of the dielectric relaxation mechanisms (gamma, beta, beta ', alpha and rho) in poly(methyl methacrylate) (PMMA) and hybrids of PMMA polymerized into 5 nm SiO2 pore matrices were studied by means of the thermally stimulated depolarization currents (TSD) technique, applied in the range 10-460 K. Low frequency relaxations (10 mu Hz-10 mHz) were investigated by measuring the isothermal discharging current, with the loss factor epsilon"(f) determined using a new development of the Hamon method. Compared to pure PMMA, the hybrids presented a 14 to 18 degrees reduction of the TSD beta -relaxation maximum (T-beta) and a drastic high temperature shift of the prominent syndiotactic alpha -peak. The average energy barrier for dipole (re)orientation (W) slightly decreases for both the alpha and beta relaxations. The latter observations, as well as the time evolution of the TSD spectra, are discussed in terms of the variation of the initiator (azobisisobutyronitrile) content and the effects of polymerization in spatial confinements (e.g. reduced monomer-to-polymer conversion at high initiator loadings and interaction effects). The shifts reflect the presence of several antagonistic mechanisms controlling the molecular dynamics of the polymeric phase. The extent of the polymer-SiO2 hydrogen bonding interaction induces an increase of the energy barrier for the activation of the motions of the carboxymethyl lateral groups (beta -process) and parts of the main chain (alpha -process). On the other hand, the reduction of the chain entanglements (due to the pore-directed propagation of polymerization) loosens several steric hindrances on the rotational motion of the side group, explaining the accompanying decrease of W.
引用
收藏
页码:322 / 333
页数:12
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