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Thermodynamic properties for rare earths and americium in pyropartitioning process solvents
The design of a molten metal‐molten salt based chemical and electrochemical process for separation of actinides from plutonium‐uranium extraction waste requires a consistent set of thermodynamic properties for the actinides and rare earths present in nuclear waste. Standard potential data for Y, La,...
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Published in: | Journal of the Electrochemical Society 1999-07, Vol.146 (7), p.2573-2580 |
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creator | FUSSELMAN, S. P ROY, J. J SAKAMURA, Yoshiharu UOZUMI, Koichi KAWAI, Tsutomu TAKAHASHI, Noriaki GRIMMETT, D. L GRANTHAM, L. F KRUEGER, C. L NABELEK, C. R STORVICK, T. S INOUE, Tadashi HIJIKATA, Takatoshi KINOSHITA, Kensuke |
description | The design of a molten metal‐molten salt based chemical and electrochemical process for separation of actinides from plutonium‐uranium extraction waste requires a consistent set of thermodynamic properties for the actinides and rare earths present in nuclear waste. Standard potential data for Y, La, Ce, Pr, and Gd in molten LiCl‐KCl were obtained. Americium data obtained were standard potentials in molten LiCl‐KCl and activity coefficients for Cd and Bi. Data were obtained between 400 and 500°C. Results for the rare earth chlorides using an improved experimental technique were consistent with theory, with standard free energy of formation values somewhat more negative than those found in the literature. Special attention was given to Am in the LiCl‐KCl/Cd system because it can exist as the +2 and/or +3 ion in this system. Americium ions existed only as the +3 ion in LiCl‐KCl/Bi. Standard electrochemical potentials for
Am
/
Am
+
2
in LiCl‐KCl eutectic at 400, 450, and 500°C were −2.893, −2.853, and −2.838 V, respectively, relative to
Cl
2
/
Cl
−
. Standard electrochemical potentials vs.
Cl
2
/
Cl
−
for
Am
/
Am
+
3
in LiCl‐KCl eutectic were −2.83 V at 450°C and −2.78 V at 500°C. Activity coefficients for Am in molten Cd were
1
×
10
−
5
and
8
×
10
−
5
at 450 and 500°C. Activity coefficients for Am in molten Bi were
2
×
10
−
11
and
2
×
10
−
10
at 450 and 500°C. © 1999 The Electrochemical Society. All rights reserved. |
doi_str_mv | 10.1149/1.1391974 |
format | article |
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Am
/
Am
+
2
in LiCl‐KCl eutectic at 400, 450, and 500°C were −2.893, −2.853, and −2.838 V, respectively, relative to
Cl
2
/
Cl
−
. Standard electrochemical potentials vs.
Cl
2
/
Cl
−
for
Am
/
Am
+
3
in LiCl‐KCl eutectic were −2.83 V at 450°C and −2.78 V at 500°C. Activity coefficients for Am in molten Cd were
1
×
10
−
5
and
8
×
10
−
5
at 450 and 500°C. Activity coefficients for Am in molten Bi were
2
×
10
−
11
and
2
×
10
−
10
at 450 and 500°C. © 1999 The Electrochemical Society. All rights reserved.</description><identifier>ISSN: 0013-4651</identifier><identifier>EISSN: 1945-7111</identifier><identifier>DOI: 10.1149/1.1391974</identifier><identifier>CODEN: JESOAN</identifier><language>eng</language><publisher>Pennington, NJ: Electrochemical Society</publisher><subject>Applied sciences ; Chemical thermodynamics ; Chemistry ; Elements, mineral and organic compounds ; Energy ; Exact sciences and technology ; Fuels ; General and physical chemistry ; Nuclear fuels ; Preparation and processing of nuclear fuels ; Thermodynamic properties</subject><ispartof>Journal of the Electrochemical Society, 1999-07, Vol.146 (7), p.2573-2580</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-d8309b3e8bada2761e64c3d1cad5d97338e38f24e3046717cb27f62e68ec3e263</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1505193$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>FUSSELMAN, S. P</creatorcontrib><creatorcontrib>ROY, J. J</creatorcontrib><creatorcontrib>SAKAMURA, Yoshiharu</creatorcontrib><creatorcontrib>UOZUMI, Koichi</creatorcontrib><creatorcontrib>KAWAI, Tsutomu</creatorcontrib><creatorcontrib>TAKAHASHI, Noriaki</creatorcontrib><creatorcontrib>GRIMMETT, D. L</creatorcontrib><creatorcontrib>GRANTHAM, L. F</creatorcontrib><creatorcontrib>KRUEGER, C. L</creatorcontrib><creatorcontrib>NABELEK, C. R</creatorcontrib><creatorcontrib>STORVICK, T. S</creatorcontrib><creatorcontrib>INOUE, Tadashi</creatorcontrib><creatorcontrib>HIJIKATA, Takatoshi</creatorcontrib><creatorcontrib>KINOSHITA, Kensuke</creatorcontrib><title>Thermodynamic properties for rare earths and americium in pyropartitioning process solvents</title><title>Journal of the Electrochemical Society</title><description>The design of a molten metal‐molten salt based chemical and electrochemical process for separation of actinides from plutonium‐uranium extraction waste requires a consistent set of thermodynamic properties for the actinides and rare earths present in nuclear waste. Standard potential data for Y, La, Ce, Pr, and Gd in molten LiCl‐KCl were obtained. Americium data obtained were standard potentials in molten LiCl‐KCl and activity coefficients for Cd and Bi. Data were obtained between 400 and 500°C. Results for the rare earth chlorides using an improved experimental technique were consistent with theory, with standard free energy of formation values somewhat more negative than those found in the literature. Special attention was given to Am in the LiCl‐KCl/Cd system because it can exist as the +2 and/or +3 ion in this system. Americium ions existed only as the +3 ion in LiCl‐KCl/Bi. Standard electrochemical potentials for
Am
/
Am
+
2
in LiCl‐KCl eutectic at 400, 450, and 500°C were −2.893, −2.853, and −2.838 V, respectively, relative to
Cl
2
/
Cl
−
. Standard electrochemical potentials vs.
Cl
2
/
Cl
−
for
Am
/
Am
+
3
in LiCl‐KCl eutectic were −2.83 V at 450°C and −2.78 V at 500°C. Activity coefficients for Am in molten Cd were
1
×
10
−
5
and
8
×
10
−
5
at 450 and 500°C. Activity coefficients for Am in molten Bi were
2
×
10
−
11
and
2
×
10
−
10
at 450 and 500°C. © 1999 The Electrochemical Society. All rights reserved.</description><subject>Applied sciences</subject><subject>Chemical thermodynamics</subject><subject>Chemistry</subject><subject>Elements, mineral and organic compounds</subject><subject>Energy</subject><subject>Exact sciences and technology</subject><subject>Fuels</subject><subject>General and physical chemistry</subject><subject>Nuclear fuels</subject><subject>Preparation and processing of nuclear fuels</subject><subject>Thermodynamic properties</subject><issn>0013-4651</issn><issn>1945-7111</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpFkEtrwzAQhEVpoenj0H-gQyn04FRryZJ1LKEvCPSSnnowirxuVGzZ1TqF_Ps6JNDTsMw3wzKM3YCYAyj7AHOQFqxRJ2wGVhWZAYBTNhMCZKZ0Aefsguh7OqFUZsY-VxtMXV_vouuC50PqB0xjQOJNn3hyCTm6NG6Iu1hz12EKPmw7HiIfdhM8eWEMfQzxax_2SMSpb38xjnTFzhrXEl4f9ZJ9PD-tFq_Z8v3lbfG4zLw0dszqUgq7lliuXe1yowG18rIG7-qitkbKEmXZ5AqlUNqA8evcNDpHXaKXmGt5ye4OvdMDP1ukseoCeWxbF7HfUpUbsMLqcgLvD6BPPVHCphpS6FzaVSCq_XwVVMf5Jvb2WOrIu7ZJLvpA_4FCFGCl_AN7MHBr</recordid><startdate>19990701</startdate><enddate>19990701</enddate><creator>FUSSELMAN, S. P</creator><creator>ROY, J. J</creator><creator>SAKAMURA, Yoshiharu</creator><creator>UOZUMI, Koichi</creator><creator>KAWAI, Tsutomu</creator><creator>TAKAHASHI, Noriaki</creator><creator>GRIMMETT, D. L</creator><creator>GRANTHAM, L. F</creator><creator>KRUEGER, C. L</creator><creator>NABELEK, C. R</creator><creator>STORVICK, T. S</creator><creator>INOUE, Tadashi</creator><creator>HIJIKATA, Takatoshi</creator><creator>KINOSHITA, Kensuke</creator><general>Electrochemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>19990701</creationdate><title>Thermodynamic properties for rare earths and americium in pyropartitioning process solvents</title><author>FUSSELMAN, S. P ; ROY, J. J ; SAKAMURA, Yoshiharu ; UOZUMI, Koichi ; KAWAI, Tsutomu ; TAKAHASHI, Noriaki ; GRIMMETT, D. L ; GRANTHAM, L. F ; KRUEGER, C. L ; NABELEK, C. R ; STORVICK, T. S ; INOUE, Tadashi ; HIJIKATA, Takatoshi ; KINOSHITA, Kensuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-d8309b3e8bada2761e64c3d1cad5d97338e38f24e3046717cb27f62e68ec3e263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Applied sciences</topic><topic>Chemical thermodynamics</topic><topic>Chemistry</topic><topic>Elements, mineral and organic compounds</topic><topic>Energy</topic><topic>Exact sciences and technology</topic><topic>Fuels</topic><topic>General and physical chemistry</topic><topic>Nuclear fuels</topic><topic>Preparation and processing of nuclear fuels</topic><topic>Thermodynamic properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>FUSSELMAN, S. P</creatorcontrib><creatorcontrib>ROY, J. J</creatorcontrib><creatorcontrib>SAKAMURA, Yoshiharu</creatorcontrib><creatorcontrib>UOZUMI, Koichi</creatorcontrib><creatorcontrib>KAWAI, Tsutomu</creatorcontrib><creatorcontrib>TAKAHASHI, Noriaki</creatorcontrib><creatorcontrib>GRIMMETT, D. L</creatorcontrib><creatorcontrib>GRANTHAM, L. F</creatorcontrib><creatorcontrib>KRUEGER, C. L</creatorcontrib><creatorcontrib>NABELEK, C. R</creatorcontrib><creatorcontrib>STORVICK, T. S</creatorcontrib><creatorcontrib>INOUE, Tadashi</creatorcontrib><creatorcontrib>HIJIKATA, Takatoshi</creatorcontrib><creatorcontrib>KINOSHITA, Kensuke</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of the Electrochemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>FUSSELMAN, S. P</au><au>ROY, J. J</au><au>SAKAMURA, Yoshiharu</au><au>UOZUMI, Koichi</au><au>KAWAI, Tsutomu</au><au>TAKAHASHI, Noriaki</au><au>GRIMMETT, D. L</au><au>GRANTHAM, L. F</au><au>KRUEGER, C. L</au><au>NABELEK, C. R</au><au>STORVICK, T. S</au><au>INOUE, Tadashi</au><au>HIJIKATA, Takatoshi</au><au>KINOSHITA, Kensuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermodynamic properties for rare earths and americium in pyropartitioning process solvents</atitle><jtitle>Journal of the Electrochemical Society</jtitle><date>1999-07-01</date><risdate>1999</risdate><volume>146</volume><issue>7</issue><spage>2573</spage><epage>2580</epage><pages>2573-2580</pages><issn>0013-4651</issn><eissn>1945-7111</eissn><coden>JESOAN</coden><abstract>The design of a molten metal‐molten salt based chemical and electrochemical process for separation of actinides from plutonium‐uranium extraction waste requires a consistent set of thermodynamic properties for the actinides and rare earths present in nuclear waste. Standard potential data for Y, La, Ce, Pr, and Gd in molten LiCl‐KCl were obtained. Americium data obtained were standard potentials in molten LiCl‐KCl and activity coefficients for Cd and Bi. Data were obtained between 400 and 500°C. Results for the rare earth chlorides using an improved experimental technique were consistent with theory, with standard free energy of formation values somewhat more negative than those found in the literature. Special attention was given to Am in the LiCl‐KCl/Cd system because it can exist as the +2 and/or +3 ion in this system. Americium ions existed only as the +3 ion in LiCl‐KCl/Bi. Standard electrochemical potentials for
Am
/
Am
+
2
in LiCl‐KCl eutectic at 400, 450, and 500°C were −2.893, −2.853, and −2.838 V, respectively, relative to
Cl
2
/
Cl
−
. Standard electrochemical potentials vs.
Cl
2
/
Cl
−
for
Am
/
Am
+
3
in LiCl‐KCl eutectic were −2.83 V at 450°C and −2.78 V at 500°C. Activity coefficients for Am in molten Cd were
1
×
10
−
5
and
8
×
10
−
5
at 450 and 500°C. Activity coefficients for Am in molten Bi were
2
×
10
−
11
and
2
×
10
−
10
at 450 and 500°C. © 1999 The Electrochemical Society. All rights reserved.</abstract><cop>Pennington, NJ</cop><pub>Electrochemical Society</pub><doi>10.1149/1.1391974</doi><tpages>8</tpages></addata></record> |
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language | eng |
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source | Institute of Physics:Jisc Collections:IOP Publishing Read and Publish 2024-2025 (Reading List) |
subjects | Applied sciences Chemical thermodynamics Chemistry Elements, mineral and organic compounds Energy Exact sciences and technology Fuels General and physical chemistry Nuclear fuels Preparation and processing of nuclear fuels Thermodynamic properties |
title | Thermodynamic properties for rare earths and americium in pyropartitioning process solvents |
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