Activation energy for crystallization of low molecular weight poly(ethylene oxide) and low molecular weight poly(ethylene oxide)/poly(methyl methacrylate) blends determined by DSC and polarized optical microscopy
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Imai, S
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Imai, S
[1
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Shimono, S
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Shimono, S
[1
]
Fukushima, Y
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Fukushima, Y
[1
]
Umezaki, K
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Umezaki, K
[1
]
Okada, M
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Okada, M
[1
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Takahashi, M
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Takahashi, M
[1
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Matsuda, H
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SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPANSHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
Matsuda, H
[1
]
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[1] SHINSHU UNIV,FAC TEXT SCI & TECHNOL,DEPT FINE MAT ENGN,UEDA,NAGANO 386,JAPAN
The crystallization process of poly(ethylene oxide) (PEG) and PEO/poly(methyl methacrylate) (PMMA) blends in the low molecular weight region of PEO was studied by differential scanning calorimetry (DSC) and polarized optical microscopy (POM). The half-time of the crystallization t(1/2), the time at which crystallinity X(t) = 1/2, was inversely proportional to the linear growth rate G of spherulite, i.e. t(1/2)(-1) proportional to G. The value of E characterizes the temperature dependence of the activation energy for the formation of a secondary nucleus on the growing side surface of the crystal lamella and was evaluated from the t(1/2) measured by DSC. The value of E of PEO was not affected by blending PMMA. However, the slightly increasing tendency of E was observed for PEO and PEO/PMMA blends with increasing molecular weight of PEO, M(PEO) This tendency may correspond to the crossover of E from low molecular weight material to polymer.