Effect of 226Ra purity as a target for 225Ac production using a fast reactor
Researchers are seeking alternative 225 Ac production methods because of the scarcity of 225 Ac for targeted alpha therapy. Although 226 Ra from waste sources has been considered, obtaining 226 Ra is challenging. Therefore, the authors focused on the contamination of minerals with 232 Th-derived 228...
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Veröffentlicht in: | Journal of radioanalytical and nuclear chemistry 2024-11, Vol.333 (11), p.5987-5996 |
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container_issue | 11 |
container_start_page | 5987 |
container_title | Journal of radioanalytical and nuclear chemistry |
container_volume | 333 |
creator | Sasaki, Yuto Maeda, Shigetaka |
description | Researchers are seeking alternative
225
Ac production methods because of the scarcity of
225
Ac for targeted alpha therapy. Although
226
Ra from waste sources has been considered, obtaining
226
Ra is challenging. Therefore, the authors focused on the contamination of minerals with
232
Th-derived
228
Ra while investigating methods to recover
226
Ra from uranium ores. The effect of
228
Ra contamination on
225
Ac production by
226
Ra transmutation using fast reactors was evaluated. Consequently, toxic
228
Ac contaminates
225
Ac. However, using the different half-lives of
225
Ac and
228
Ac, pure
225
Ac can be obtained from the chemical separation of actinium after cooling for 5–8 days. |
doi_str_mv | 10.1007/s10967-024-09397-7 |
format | Article |
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225
Ac production methods because of the scarcity of
225
Ac for targeted alpha therapy. Although
226
Ra from waste sources has been considered, obtaining
226
Ra is challenging. Therefore, the authors focused on the contamination of minerals with
232
Th-derived
228
Ra while investigating methods to recover
226
Ra from uranium ores. The effect of
228
Ra contamination on
225
Ac production by
226
Ra transmutation using fast reactors was evaluated. Consequently, toxic
228
Ac contaminates
225
Ac. However, using the different half-lives of
225
Ac and
228
Ac, pure
225
Ac can be obtained from the chemical separation of actinium after cooling for 5–8 days.</description><identifier>ISSN: 0236-5731</identifier><identifier>EISSN: 1588-2780</identifier><identifier>DOI: 10.1007/s10967-024-09397-7</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Actinium ; Chemical separation ; Chemistry ; Chemistry and Materials Science ; Contamination ; Diagnostic Radiology ; Fast nuclear reactors ; Hadrons ; Heavy Ions ; Inorganic Chemistry ; Nuclear Chemistry ; Nuclear Physics ; Physical Chemistry ; Production methods ; Radium 226 ; Transmutation ; Uranium ores</subject><ispartof>Journal of radioanalytical and nuclear chemistry, 2024-11, Vol.333 (11), p.5987-5996</ispartof><rights>Akadémiai Kiadó, Budapest, Hungary 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c200t-6bb6cc430d58da86016871d3beacd6613977e2e3fb58862a3b388587ea8903023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10967-024-09397-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10967-024-09397-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Sasaki, Yuto</creatorcontrib><creatorcontrib>Maeda, Shigetaka</creatorcontrib><title>Effect of 226Ra purity as a target for 225Ac production using a fast reactor</title><title>Journal of radioanalytical and nuclear chemistry</title><addtitle>J Radioanal Nucl Chem</addtitle><description>Researchers are seeking alternative
225
Ac production methods because of the scarcity of
225
Ac for targeted alpha therapy. Although
226
Ra from waste sources has been considered, obtaining
226
Ra is challenging. Therefore, the authors focused on the contamination of minerals with
232
Th-derived
228
Ra while investigating methods to recover
226
Ra from uranium ores. The effect of
228
Ra contamination on
225
Ac production by
226
Ra transmutation using fast reactors was evaluated. Consequently, toxic
228
Ac contaminates
225
Ac. However, using the different half-lives of
225
Ac and
228
Ac, pure
225
Ac can be obtained from the chemical separation of actinium after cooling for 5–8 days.</description><subject>Actinium</subject><subject>Chemical separation</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Contamination</subject><subject>Diagnostic Radiology</subject><subject>Fast nuclear reactors</subject><subject>Hadrons</subject><subject>Heavy Ions</subject><subject>Inorganic Chemistry</subject><subject>Nuclear Chemistry</subject><subject>Nuclear Physics</subject><subject>Physical Chemistry</subject><subject>Production methods</subject><subject>Radium 226</subject><subject>Transmutation</subject><subject>Uranium ores</subject><issn>0236-5731</issn><issn>1588-2780</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kEFLAzEQhYMouFb_gKeA5-gk6SbZYynVCgVB9Byy2aRs0c2aZA_996au4M3THOa9N_M-hG4p3FMA-ZAoNEISYEsCDW8kkWeoorVShEkF56gCxgWpJaeX6CqlAwA0SvEK7TbeO5tx8Jgx8WrwOMU-H7FJ2OBs4t5l7EMsy3pl8RhDN9nchwFPqR_2ReNNyjg6Y3OI1-jCm4_kbn7nAr0_bt7WW7J7eXper3bEMoBMRNsKa5cculp1RgmgQkna8bakdELQ8r90zHHflgKCGd5ypWolnVEN8NJkge7m3PLP1-RS1ocwxaGc1JwyygQVzUnFZpWNIaXovB5j_2niUVPQJ2p6pqYLNf1DTcti4rMpFfGwd_Ev-h_XN1RfbQE</recordid><startdate>20241101</startdate><enddate>20241101</enddate><creator>Sasaki, Yuto</creator><creator>Maeda, Shigetaka</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20241101</creationdate><title>Effect of 226Ra purity as a target for 225Ac production using a fast reactor</title><author>Sasaki, Yuto ; Maeda, Shigetaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c200t-6bb6cc430d58da86016871d3beacd6613977e2e3fb58862a3b388587ea8903023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Actinium</topic><topic>Chemical separation</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Contamination</topic><topic>Diagnostic Radiology</topic><topic>Fast nuclear reactors</topic><topic>Hadrons</topic><topic>Heavy Ions</topic><topic>Inorganic Chemistry</topic><topic>Nuclear Chemistry</topic><topic>Nuclear Physics</topic><topic>Physical Chemistry</topic><topic>Production methods</topic><topic>Radium 226</topic><topic>Transmutation</topic><topic>Uranium ores</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasaki, Yuto</creatorcontrib><creatorcontrib>Maeda, Shigetaka</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of radioanalytical and nuclear chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasaki, Yuto</au><au>Maeda, Shigetaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of 226Ra purity as a target for 225Ac production using a fast reactor</atitle><jtitle>Journal of radioanalytical and nuclear chemistry</jtitle><stitle>J Radioanal Nucl Chem</stitle><date>2024-11-01</date><risdate>2024</risdate><volume>333</volume><issue>11</issue><spage>5987</spage><epage>5996</epage><pages>5987-5996</pages><issn>0236-5731</issn><eissn>1588-2780</eissn><abstract>Researchers are seeking alternative
225
Ac production methods because of the scarcity of
225
Ac for targeted alpha therapy. Although
226
Ra from waste sources has been considered, obtaining
226
Ra is challenging. Therefore, the authors focused on the contamination of minerals with
232
Th-derived
228
Ra while investigating methods to recover
226
Ra from uranium ores. The effect of
228
Ra contamination on
225
Ac production by
226
Ra transmutation using fast reactors was evaluated. Consequently, toxic
228
Ac contaminates
225
Ac. However, using the different half-lives of
225
Ac and
228
Ac, pure
225
Ac can be obtained from the chemical separation of actinium after cooling for 5–8 days.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s10967-024-09397-7</doi><tpages>10</tpages></addata></record> |
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subjects | Actinium Chemical separation Chemistry Chemistry and Materials Science Contamination Diagnostic Radiology Fast nuclear reactors Hadrons Heavy Ions Inorganic Chemistry Nuclear Chemistry Nuclear Physics Physical Chemistry Production methods Radium 226 Transmutation Uranium ores |
title | Effect of 226Ra purity as a target for 225Ac production using a fast reactor |
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