Synthesis, swelling behavior and surface microstructure of poly(sodium acrylate) gels cross-linked by aluminum ions

被引:21
作者
Harada, T
Hirashima, Y
Suzuki, A
Goto, M
Kawamura, N
Tokita, M
机构
[1] Yokohama Natl Univ, Dept Mat Sci, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
[2] Saitama Daiichi Pharmaceut Co Ltd, Kasukabe, Saitama 3440057, Japan
[3] Kyushu Univ, Dept Phys, Fukuoka 8108560, Japan
关键词
poly(sodium acrylate) gel; chelation; swelling ratio; hydrogen bonding; dehydrated gels; surface structure; AFM; microdomain;
D O I
10.1016/j.eurpolymj.2005.03.017
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report the synthesis and some unique properties of polymer gels cross-linked by metal ions. They are made of poly(sodium acrylate) and aluminum ions. Cylindrical and thin plate gels were synthesized in glass molds by mixing poly(sodium acrylate) with aluminum hydroxide of various concentrations. The swelling ratio of the gels was measured by changing the solvent pH and adding NaCl with different concentrations. Each gel was found to swell at the first stage and shrink thereafter by repeated solvent exchanges; the swelling ratio ultimately returned to the initial one just after gelation. These features could be explained using a qualitative model based on the ion exchange and the formation of hydrogen bonding. A characteristic surface microstructure was observed on the dehydrated gels using an atomic force microscope. The microstructures were analyzed in terms of the autocorrelation function and the root-mean-square roughness. The surface microstructure of this system was characterized by the microdomains, the shape of which was found to depend strongly on the amount of aluminum ions and the gel thickness at gelation. It could be controlled not only by the concentration of the cross-linker but also by the dehydration condition. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2189 / 2198
页数:10
相关论文
共 24 条
[1]  
Abe M., 1997, GELTECHNOLOGY
[2]   ATOMIC FORCE MICROSCOPE [J].
BINNIG, G ;
QUATE, CF ;
GERBER, C .
PHYSICAL REVIEW LETTERS, 1986, 56 (09) :930-933
[3]  
Flory P J., PRINCIPLES POLYM CHE
[4]   Formation of hydrogen bonding in ionized poly(N-isopropylacrylamide) gels by continuous water exchange [J].
Hirashima, Y ;
Tamanishi, H ;
Sato, H ;
Saito, K ;
Naito, A ;
Suzuki, A .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2004, 42 (06) :1090-1098
[5]   Direct observation of internal structures in poly(N-isopropylacrylamide) chemical gels [J].
Hirokawa, Y ;
Jinnai, H ;
Nishikawa, Y ;
Okamoto, T ;
Hashimoto, T .
MACROMOLECULES, 1999, 32 (21) :7093-7099
[6]   VOLUME PHASE-TRANSITION IN A NONIONIC GEL [J].
HIROKAWA, Y ;
TANAKA, T .
JOURNAL OF CHEMICAL PHYSICS, 1984, 81 (12) :6379-6380
[7]   VOLUME-PHASE TRANSITIONS OF IONIZED N-ISOPROPYLACRYLAMIDE GELS [J].
HIROTSU, S ;
HIROKAWA, Y ;
TANAKA, T .
JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (02) :1392-1395
[8]   Osmotic swelling of polyacrylate hydrogels in physiological salt solutions [J].
Horkay, F ;
Tasaki, I ;
Basser, PJ .
BIOMACROMOLECULES, 2000, 1 (01) :84-90
[9]   THE PHOTO-ELASTIC BEHAVIOR AND SMALL-ANGLE X-RAY-SCATTERING OF IONIZED GELS OF CO-POLYMERS OF 2-HYDROXYETHYL METHACRYLATE WITH METHACRYLIC-ACID [J].
ILAVSKY, M ;
PLESTIL, J ;
DUSEK, K .
EUROPEAN POLYMER JOURNAL, 1980, 16 (09) :901-907
[10]   Effect of pH on the volume phase transition of copolymer gels of N-isopropylacrylamide and sodium acrylate [J].
Kawasaki, H ;
Sasaki, S ;
Maeda, H .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (26) :5089-5093