Thermodynamic interactions in double-network hydrogels

被引:80
|
作者
Tominaga, Taiki [1 ,2 ]
Tirumala, Vijay R. [1 ,3 ]
Lee, Sanghun [1 ]
Lin, Eric K. [1 ]
Gong, Jian Ping [2 ]
Wu, Wen-Li [1 ]
机构
[1] Natl Inst Stand & Technol, Div Polymers, Gaithersburg, MD 20899 USA
[2] Hokkaido Univ, Grad Sch Sci, Sapporo, Hokkaido, Japan
[3] Univ Massachusetts, Amherst, MA 01003 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2008年 / 112卷 / 13期
关键词
D O I
10.1021/jp710284e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Double-network hydrogels (DN-gels) prepared from the combination of a moderately cross-linked anionic polyelectrolyte (PE) and an uncross-linked linear polymer solution (NP) exhibit mechanical properties such as fracture toughness that are intriguingly superior to that of their individual constituents. The scheme of double-network preparation, however, is. not equally successful for all polyelectrolyte/neutral polymer pairs. A successful example is the combination of poly(2-acrylamido-2-methyl-1-propane sulfortic acid) (PAMPS) cross-linked network and linear polyacrylamide (PAAm), which results in DN-gels with fracture strength under compression approaching that of articular cartilage (, 20 MPa). Small-angle neutron scattering was used to determine the thermodynamic interaction parameters for PAMPS and PAAm in water as a first step to elucidate the molecular origin responsible for this superior property. Measurements on PAMPS/PAAm DN-gels and their solution blend counterparts indicate that the two polymers interact favorably with each other while in water. This favorable PAMPS/PAAm interaction given by the condition chi(PE-NP) << chi(PE-water) <chi(NP-water), where chi is the Flory-Huggins interaction parameter, is consistent with some of the salient features of the DN structure revealed by SANS, and it may also contribute to the ultimate mechanical properties of DN-gels.
引用
收藏
页码:3903 / 3909
页数:7
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