NMR Water Self- Diffusion and Relaxation Studies on Sodium Polyacrylate Solutions and Gels in Physiologic Ionic Solutions

被引:15
作者
Bai, Ruiliang [1 ,2 ]
Basser, Peter J. [1 ]
Briber, Robert M. [3 ]
Horkay, Ferenc [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Tissue Biophys & Biomimet, Program Pediat Imaging & Tissue Sci, NIH, Bethesda, MD 20892 USA
[2] Univ Maryland, Inst Phys Sci & Technol, Biophys Program, College Pk, MD 20740 USA
[3] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20740 USA
关键词
MOLECULAR-DYNAMICS SIMULATIONS; NUCLEAR-MAGNETIC-RESONANCE; POLYMER SOLVENT SYSTEMS; SPIN-LATTICE RELAXATION; FREE-VOLUME THEORIES; SINGLE-SIDED NMR; HYDRATION WATER; TRANSVERSE RELAXATION; STRUCTURAL-CHANGES; PROTON RELAXATION;
D O I
10.1002/app.40001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Water self-diffusion coefficients and longitudinal relaxation rates in sodium polyacrylate solutions and gels were measured by NMR, as a function of polymer content and structure in a physiological concentration range of monovalent and divalent cations, Ca2+ and Na+. Several physical models describing the self-diffusion of the solvent were applied and compared. A free-volume model was found to be in good agreement with the experimental results over a wide range of polymer concentrations. The longitudinal relaxation rate exhibited linear dependence on polymer concentration below a critical concentration and showed non-linear behavior at higher concentrations. Both the water self-diffusion and relaxation were less influenced by the polymer in the gel state than in the uncrosslinked polymer solutions. The effect of Na+ on the mobility of water molecules was practically undetectable. In contrast, addition of Ca2+ strongly increased the longitudinal relaxation rate while its effect on the self-diffusion coefficient was much less pronounced. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014, 131, 40001. Copyright © 2013 Wiley Periodicals, Inc.
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页数:7
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