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Title: Density Changes in the Optimized CSSX Solvent System

Technical Report ·
DOI:https://doi.org/10.2172/885674· OSTI ID:885674

Density increases in caustic-side solvent extraction (CSSX) solvent have been observed in separate experimental programs performed by different groups of researchers. Such changes indicate a change in chemical composition. Increased density adversely affects separation of solvent from denser aqueous solutions present in the CSSX process. Identification and control of factors affecting solvent density are essential for design and operation of the centrifugal contactors. The goals of this research were to identify the factors affecting solvent density (composition) and to develop correlations between easily measured solvent properties (density and viscosity) and the chemical composition of the solvent, which will permit real-time determination and adjustment of the solvent composition. In evaporation experiments, virgin solvent was subjected to evaporation under quiescent conditions at 25, 35, and 45 C with continuously flowing dry air passing over the surface of the solvent. Density and viscosity were measured periodically, and chemical analysis was performed on the solvent samples. Chemical interaction tests were completed to determine if any chemical reaction takes place over extended contact time that changes the composition and/or physical properties. Solvent and simulant, solvent and strip solution, and solvent and wash solution were contacted continuously in agitated flasks. They were periodically sampled and the density measured (viscosity was also measured on some samples) and then submitted to the Chemical Sciences Division of Oak Ridge National Laboratory for analysis by nuclear magnetic resonance (NMR) spectrometry and high-performance liquid chromatography (HPLC) using the virgin solvent as the baseline. Chemical interaction tests showed that solvent densities and viscosities did not change appreciably during contact with simulant, strip, or wash solution. No effects on density and viscosity and no chemical changes in the solvent were noted within experimental limits. Evaporation test results showed that all solvents were evaporated to densities of greater than 0.90 g/cm{sup 3}. Viscosities increased from 3.5 to >6.5 cP as the densities increased. NMR and HPLC data indicate that diluent loss is the primary reason for density increase and that the ratio of BOBCalixC6 (referred to as calix) to Cs-7SB remained almost constant. Density and viscosity vary linearly with the loss of diluent and the increase in Cs-7SB concentration. Solvent viscosity and density are both sensitive indicators of the loss of diluent, especially when such loss is greater than 10%. However, density is more reliable at low values for diluent loss. The ratio of Cs-7SB to calix appears relatively constant during evaporation to losses of more than 50% of the diluent. A simple density model accurately predicts the composition of the solvent when density is known. Density and viscosity increases can affect the throughput in the centrifugal contactors and, at the extreme, can cause complete loss of flow. The distribution coefficient can also increase, especially in the strip stage, causing the loss of the ability to strip extracted cesium from the solvent. These effects can be addressed by internal changes to the contactor and by adding additional stripping stages in processing. However, these changes are extremely difficult under remote operation and maintenance restrictions.

Research Organization:
Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
DE-AC05-00OR22725
OSTI ID:
885674
Report Number(s):
ORNL/TM-2002/204; TRN: US200617%%127
Country of Publication:
United States
Language:
English