Analysis of precipitates from reactions of hyperalkaline solutions with soluble silica

被引:25
作者
Mashal, K
Harsh, JB
Flury, M [1 ]
Felmy, AR
机构
[1] Washington State Univ, Dept Crop & Soil Sci, Ctr Multiphase Environm Res, Pullman, WA 99164 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/j.apgeochem.2005.01.015
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Cancrinite, sodalite, and zeolite A have been found to form upon contacting hyperalkaline simulated tank waste (STW) with vadose zone sediments from the Hanford Reservation. Here, soluble silica and STW are used to study mineral formation and transformation. Two Hanford sediment fractions (diameters < 50 and > 50 mu m instead of soluble silica) are also used as silica sources for comparison. A series of batch experiments at 50 degrees C and 25 days duration were conducted by reacting 0.026 mol/kg soluble Si with 6 different STW solutions. The STW solutions differed in NaOH and Al concentrations. Cancrinite, sodalite, and zeolite A formed when soluble Si was used as the Si source. The minerals were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and Al-27 and Si-29 magic-angle spinning nuclear magnetic resonance (MAS-NMR). Larger NaOH and Al concentrations favored formation of the more compact structures of cancrinite and sodalite. At larger NaOH concentration more Al for Si substitution occurred in the tetrahedral sites. A greater Al(4)/Al(6) ratio in the solids was found for the higher Si/Al ratio solutions based on NMR results. Mixtures of cancrinite and sodalite were characterized by particles with lepispheric morphology. At low Al concentration, increasing NaOH resulted in distinct hexagonal, prismatic particles common to crystalline cancrinite. At low Al/Si ratio, the characteristic cubic morphology of zeolite was observed in addition to cancrinite and socialite. (c) 2005 Elsevier Ltd. All rights reserved.
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页码:1357 / 1367
页数:11
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