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Insight into the Microscopic Structure of Module-Assembled Thermoresponsive Conetwork Hydrogels
被引:12
|作者:
Nakagawa, Shintaro
[1
]
Li, Xiang
[1
]
Shibayama, Mitsuhiro
[1
]
Kamata, Hiroyuki
[2
]
Sakai, Takamasa
[2
]
Gilbert, Elliot Paul
[3
]
机构:
[1] Univ Tokyo, Inst Solid State Phys, 5-1-5 Kashiwanoha, Kashiwa, Chiba 2778581, Japan
[2] Univ Tokyo, Sch Engn, Dept Bioengn, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[3] Australian Nucl Sci & Technol Org, Australian Ctr Neutron Scattering, Locked Bag 2001, Kirrawee Dc, NSW 2232, Australia
关键词:
ANGLE NEUTRON-SCATTERING;
MOLECULAR THERMODYNAMIC THEORY;
AMPHIPHILIC MODEL NETWORKS;
X-RAY-SCATTERING;
BLOCK-COPOLYMERS;
MICROPHASE SEPARATION;
GELS;
MACROMONOMERS;
COMPRESSION;
WATER;
D O I:
10.1021/acs.macromol.8b00868
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
The microscopic structure of module-assembled thermoresponsive was systematically investigated as a function of both temperature T and the mole fraction of the thermoresponsive modules r using small-angle neutron scattering (SANS). The were prepared by end-linking of hydrophilic modules and LCST-type thermoresponsive modules in water by the molar ratio of (1 - r):r. When the hydrogels with 0.02 <= r <= 0.10 were heated above certain T, nanometer-scale spherical domains were formed by aggregation of several prepolymer modules, whereas for the hydrogel with r = 0.01 such domain formation was not detected in the T range investigated. The size of spherical domains increased with increasing r and T. The observed r dependence of the domain size was theoretically explained by considering the free energy of domain formation, from which we concluded that the equilibrium domain size was determined mainly by the balance between two free energy contributions: the interfacial free energy of domain-matrix interface Delta G(interf) and the conformational free energy of the matrix network Delta Gconf(.)
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页码:6645 / 6652
页数:8
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