4.5 Article

Effect of chemical and physical heterogeneities on colloid-facilitated cesium transport

Journal

JOURNAL OF CONTAMINANT HYDROLOGY
Volume 213, Issue -, Pages 22-27

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jconhyd.2018.03.012

Keywords

Colloid-facilitated transport; Cesium; Physical heterogeneity; Chemical heterogeneity; Colloids

Funding

  1. US Department of Energy Nuclear Energy University Program (NEUP) [DE-NE0000719]
  2. Department of Energy by Battelle Memorial Institute [DE-AC05-76RL01830]
  3. Korea Institute of Energy Technology Evaluation and Planning (KETEP) grant from the Ministry of Trade, Industry& Energy, Republic of Korea [20141720100610]
  4. Office of Biological and Environmental Research

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A set of column experiments was conducted to investigate the chemical and physical heterogeneity effect on colloid facilitated transport under slow pore velocity conditions. Pore velocities were kept below 100 cm d(-1) for all experiments. Glass beads were packed into columns establishing four different conditions: 1) homogeneous, 2) mixed physical heterogeneity, 3) sequentially layered physical heterogeneity, and 4) chemical heterogeneity. The homogeneous column was packed with glass beads (diameter 500-600 mu m), and physical heterogeneities were created by sequential layering or mixing two sizes of glass bead (500-600 mu m and 300-400 mu m). A chemical heterogeneity was created using 25% of the glass beads coated with hydrophobic molecules (1H-1H-2H-2H-perfluorooctyltrichlorosilane) mixed with 75% pristine glass beads (all 500-600 mu m). Input solution with 0.5 mM CsI and 50 mg L-1 colloids (l-mu m diameter SiO2) was pulsed into columns under saturated conditions. The physical heterogeneity in the packed glass beads retarded the transport of colloids compared to homogeneous (R = 25.0), but showed only slight differences between sequentially layered (R = 60.7) and mixed heterogeneity(R = 62.4). The column with the chemical, hydrophobic/hydrophilic, heterogeneity removed most of the colloids from the input solution. All column conditions stripped Cs from colloids onto the column matrix of packed glass beads.

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