27Al Pulsed Field Gradient, Diffusion-NMR Spectroscopy of Solvation Dynamics and Ion Pairing in Alkaline Aluminate Solutions

被引:19
作者
Graham, Trent R. [1 ,3 ]
Han, Kee Sung [1 ]
Dembowski, Mateusz [1 ]
Krzysko, Anthony J. [2 ]
Zhang, Xin [1 ]
Hu, Jianzhi [1 ]
Clark, Sue B. [1 ,2 ]
Clark, Aurora E. [2 ]
Schenter, Gregory K. [1 ]
Pearce, Carolyn, I [1 ]
Rosso, Kevin M. [1 ]
机构
[1] Pacific Northwest Natl Lab, Richland, WA 99354 USA
[2] Washington State Univ, Dept Chem, Pullman, WA 99164 USA
[3] Washington State Univ, Voiland Sch Chem & Biol Engn, Pullman, WA 99164 USA
关键词
NUCLEAR-MAGNETIC-RESONANCE; DENSITY-FUNCTIONAL THEORY; HIGH-TEMPERATURE; SPIN-ECHO; SODIUM; AGGREGATION; VISCOSITY;
D O I
10.1021/acs.jpcb.8b10145
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
Pulsed field gradient nuclear magnetic resonance (PFG-NMR) measurements were successfully applied to the Al-27 (I = 5/2) nucleus in concentrated electrolytes to investigate the diffusion of aluminate ions [Al(OH)(4)(-)] in simulant high-level nuclear waste (3 M NaOH) between 25 and 85 degrees C. The temperature-dependent diffusion coefficients obtained from H-1, Na-23, and Al-27 PFG-NMR were well fit by a Vogel-Fulcher-Tammann model and a power law equation. Comparison of Al-27 diffusion coefficients of 0.1 M Al(OH)(4)(-) in similar to 3 M MOH (where M = Na+, K+, (CH3)(4)N+) at room temperature varied in agreement with the expected changes in solution viscosity via Stokes-Einstein relationship, confirming that the dominant Al species at these conditions are Al(OH)(4)(-) monomers. This Al-27 PFG-NMR study extends an established methodology to a previously unexplored nucleus enabling this experimental technique to be leverage for exploring ion transport, speciation, and solution structure in concentrated electrolytes.
引用
收藏
页码:10907 / 10912
页数:6
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