Separation of calcium-48 isotope by crown ether chromatography using ethanol/hydrochloric acid mixed solvent. Okumura, S., Umehara, S., Fujii, Y., Nomura, M., Kaneshiki, T., Ozawa, M., & Kishimoto, T. J. Chromatogr. A, 1415:67--72, Elsevier, oct, 2015.
Paper doi abstract bibtex Benzo-18-crown-6 ether resin embedded in porous silica beads was synthesized and used as the packing material for chromatographic separation of (48)Ca isotope. The aim of the present work is to develop efficient isotope enrichment process for double $\beta$ decay nuclide (48)Ca. To this end, ethanol/HCl mixed solvent was selected as the medium for the chromatographic separation. Adsorption of calcium on the resin was studied at different HCl concentrations and different ethanol mixing ratios in batch-wise experiments. A very interesting phenomenon was observed; Ca adsorption is controlled not by the overall HCl concentration of the mixed solvent, but by the initial concentration of added HCl solution. Calcium break-through chromatography experiments were conducted by using 75v/v% ethanol/25v/v% 8M HCl mixed solvent at different flow rates. The isotope separation coefficient between (48)Ca and (40)Ca was determined as 3.8×10(-3), which is larger than that of pure HCl solution system. Discussion is extended to the chromatographic HETP, height equivalent to a theoretical plate.
@article{Okumura2015,
abstract = {Benzo-18-crown-6 ether resin embedded in porous silica beads was synthesized and used as the packing material for chromatographic separation of (48)Ca isotope. The aim of the present work is to develop efficient isotope enrichment process for double $\beta$ decay nuclide (48)Ca. To this end, ethanol/HCl mixed solvent was selected as the medium for the chromatographic separation. Adsorption of calcium on the resin was studied at different HCl concentrations and different ethanol mixing ratios in batch-wise experiments. A very interesting phenomenon was observed; Ca adsorption is controlled not by the overall HCl concentration of the mixed solvent, but by the initial concentration of added HCl solution. Calcium break-through chromatography experiments were conducted by using 75v/v{\%} ethanol/25v/v{\%} 8M HCl mixed solvent at different flow rates. The isotope separation coefficient between (48)Ca and (40)Ca was determined as 3.8×10(-3), which is larger than that of pure HCl solution system. Discussion is extended to the chromatographic HETP, height equivalent to a theoretical plate.},
author = {Okumura, Shin and Umehara, Saori and Fujii, Yasuhiko and Nomura, Masao and Kaneshiki, Toshitaka and Ozawa, Masaki and Kishimoto, Tadafumi},
doi = {10.1016/j.chroma.2015.08.057},
issn = {00219673},
journal = {J. Chromatogr. A},
keywords = {Benzo-18-crown-6 ether,Ca-48,Crown ether,Double beta decay,HETP,Isotope separation},
month = {oct},
pages = {67--72},
publisher = {Elsevier},
title = {{Separation of calcium-48 isotope by crown ether chromatography using ethanol/hydrochloric acid mixed solvent}},
url = {http://linkinghub.elsevier.com/retrieve/pii/S0021967315012388},
volume = {1415},
year = {2015}
}
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To this end, ethanol/HCl mixed solvent was selected as the medium for the chromatographic separation. Adsorption of calcium on the resin was studied at different HCl concentrations and different ethanol mixing ratios in batch-wise experiments. A very interesting phenomenon was observed; Ca adsorption is controlled not by the overall HCl concentration of the mixed solvent, but by the initial concentration of added HCl solution. Calcium break-through chromatography experiments were conducted by using 75v/v% ethanol/25v/v% 8M HCl mixed solvent at different flow rates. The isotope separation coefficient between (48)Ca and (40)Ca was determined as 3.8×10(-3), which is larger than that of pure HCl solution system. 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