TY - JOUR
T1 - Diffusion-Controlled Recrystallization of Water Sorbed into Poly(meth)acrylates Revealed by Variable-Temperature Mid-Infrared Spectroscopy and Molecular Dynamics Simulation
AU - Yasoshima, Nobuhiro
AU - Fukuoka, Mizuki
AU - Kitano, Hiromi
AU - Kagaya, Shigehiro
AU - Ishiyama, Tatsuya
AU - Gemmei-Ide, Makoto
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/5/18
Y1 - 2017/5/18
N2 - Recrystallization behaviors of water sorbed into four poly(meth)acrylates, poly(2-methoxyethyl acrylate), poly(tetrahydrofurfuryl acrylate), poly(methyl acrylate), and poly(methyl methacrylate), are investigated by variable-temperature mid-infrared (VT-MIR) spectroscopy and molecular dynamics (MD) simulation. VT-MIR spectra demonstrate that recrystallization temperatures of water sorbed into the polymers are positively correlated with their glass-transition temperatures reported previously. The present MD simulation shows that a lower-limit temperature of the diffusion for the sorbed water and the glass-transition temperatures of the polymers also have a positive correlation, indicating that the recrystallization is controlled by diffusion mechanism rather than reorientation mechanism. Detailed molecular processes of not only recrystallization during rewarming but also crystallization during cooling and hydrogen-bonding states of water in the polymers are systematically analyzed and discussed.
AB - Recrystallization behaviors of water sorbed into four poly(meth)acrylates, poly(2-methoxyethyl acrylate), poly(tetrahydrofurfuryl acrylate), poly(methyl acrylate), and poly(methyl methacrylate), are investigated by variable-temperature mid-infrared (VT-MIR) spectroscopy and molecular dynamics (MD) simulation. VT-MIR spectra demonstrate that recrystallization temperatures of water sorbed into the polymers are positively correlated with their glass-transition temperatures reported previously. The present MD simulation shows that a lower-limit temperature of the diffusion for the sorbed water and the glass-transition temperatures of the polymers also have a positive correlation, indicating that the recrystallization is controlled by diffusion mechanism rather than reorientation mechanism. Detailed molecular processes of not only recrystallization during rewarming but also crystallization during cooling and hydrogen-bonding states of water in the polymers are systematically analyzed and discussed.
UR - http://www.scopus.com/inward/record.url?scp=85020635131&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcb.7b01824
DO - 10.1021/acs.jpcb.7b01824
M3 - 学術論文
C2 - 28447461
AN - SCOPUS:85020635131
SN - 1520-6106
VL - 121
SP - 5133
EP - 5141
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 19
ER -