Immobilization of Uranium in the Al2O3 Matrix
The immobilization of uranium in the Al 2 O 3 matrix was studied. For the modification of Al 2 O 3 precursors containing 10 wt % UO 2 (NO 3 ) 2 three methods were applied: 1) heating the precursor in air for 5 h at temperatures of 573, 973, and 1273 K, 2) treatment of the precursor with a 0.5 M solu...
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Veröffentlicht in: | Radiochemistry (New York, N.Y.) N.Y.), 2021-10, Vol.63 (5), p.651-657 |
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container_title | Radiochemistry (New York, N.Y.) |
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creator | Kulemin, V. V. Krasavina, E. P. Gorbacheva, M. P. Rumer, I. A. Bessonov, A. A. Krapukhin, V. B. Kulyukhin, S. A. |
description | The immobilization of uranium in the Al
2
O
3
matrix was studied. For the modification of Al
2
O
3
precursors containing 10 wt % UO
2
(NO
3
)
2
three methods were applied: 1) heating the precursor in air for 5 h at temperatures of 573, 973, and 1273 K, 2) treatment of the precursor with a 0.5 M solution of hydrazine hydrate (HH) for 2 h, drying to dry air moisture content at 383 K, followed by heating in air for 5 h at temperatures of 573, 973, and 1273 K, and 3) treatment of the precursor with a 2.0 M ammonia solution, followed by drying and heating, as in method (2). X-ray diffraction analysis of the synthesized composites revealed UO
3
hydrates of various compositions after calcination of the materials to
T
~600 K and U
3
O
8
after calcination at
T
> 950 K. After 24 h of contact of the composites with H
2
O at 298 K, the leaching of uranium from the studied samples was ~(10
–2
–10
–3
) g U/(g day) for the samples calcined at 383 and 573 K and ~(10
–4
–10
–5
) g U/(g day) for those calcined at 973 and 1273 K. |
doi_str_mv | 10.1134/S1066362221050143 |
format | Article |
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2
O
3
matrix was studied. For the modification of Al
2
O
3
precursors containing 10 wt % UO
2
(NO
3
)
2
three methods were applied: 1) heating the precursor in air for 5 h at temperatures of 573, 973, and 1273 K, 2) treatment of the precursor with a 0.5 M solution of hydrazine hydrate (HH) for 2 h, drying to dry air moisture content at 383 K, followed by heating in air for 5 h at temperatures of 573, 973, and 1273 K, and 3) treatment of the precursor with a 2.0 M ammonia solution, followed by drying and heating, as in method (2). X-ray diffraction analysis of the synthesized composites revealed UO
3
hydrates of various compositions after calcination of the materials to
T
~600 K and U
3
O
8
after calcination at
T
> 950 K. After 24 h of contact of the composites with H
2
O at 298 K, the leaching of uranium from the studied samples was ~(10
–2
–10
–3
) g U/(g day) for the samples calcined at 383 and 573 K and ~(10
–4
–10
–5
) g U/(g day) for those calcined at 973 and 1273 K.</description><identifier>ISSN: 1066-3622</identifier><identifier>EISSN: 1608-3288</identifier><identifier>DOI: 10.1134/S1066362221050143</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Aluminum oxide ; Ammonia ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Composite materials ; Drying ; Heating ; Hydrates ; Hydrazines ; Immobilization ; Leaching ; Moisture content ; Nuclear Chemistry ; Precursors ; Roasting ; Uranium ; Uranium dioxide</subject><ispartof>Radiochemistry (New York, N.Y.), 2021-10, Vol.63 (5), p.651-657</ispartof><rights>Pleiades Publishing, Ltd. 2021</rights><rights>Pleiades Publishing, Ltd. 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-b95b32f1e592aaca560b29a3d76b63be440b0ee14f314f8f6cd92dc1040a5ce3</citedby><cites>FETCH-LOGICAL-c316t-b95b32f1e592aaca560b29a3d76b63be440b0ee14f314f8f6cd92dc1040a5ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S1066362221050143$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S1066362221050143$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids></links><search><creatorcontrib>Kulemin, V. V.</creatorcontrib><creatorcontrib>Krasavina, E. P.</creatorcontrib><creatorcontrib>Gorbacheva, M. P.</creatorcontrib><creatorcontrib>Rumer, I. A.</creatorcontrib><creatorcontrib>Bessonov, A. A.</creatorcontrib><creatorcontrib>Krapukhin, V. B.</creatorcontrib><creatorcontrib>Kulyukhin, S. A.</creatorcontrib><title>Immobilization of Uranium in the Al2O3 Matrix</title><title>Radiochemistry (New York, N.Y.)</title><addtitle>Radiochemistry</addtitle><description>The immobilization of uranium in the Al
2
O
3
matrix was studied. For the modification of Al
2
O
3
precursors containing 10 wt % UO
2
(NO
3
)
2
three methods were applied: 1) heating the precursor in air for 5 h at temperatures of 573, 973, and 1273 K, 2) treatment of the precursor with a 0.5 M solution of hydrazine hydrate (HH) for 2 h, drying to dry air moisture content at 383 K, followed by heating in air for 5 h at temperatures of 573, 973, and 1273 K, and 3) treatment of the precursor with a 2.0 M ammonia solution, followed by drying and heating, as in method (2). X-ray diffraction analysis of the synthesized composites revealed UO
3
hydrates of various compositions after calcination of the materials to
T
~600 K and U
3
O
8
after calcination at
T
> 950 K. After 24 h of contact of the composites with H
2
O at 298 K, the leaching of uranium from the studied samples was ~(10
–2
–10
–3
) g U/(g day) for the samples calcined at 383 and 573 K and ~(10
–4
–10
–5
) g U/(g day) for those calcined at 973 and 1273 K.</description><subject>Aluminum oxide</subject><subject>Ammonia</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Composite materials</subject><subject>Drying</subject><subject>Heating</subject><subject>Hydrates</subject><subject>Hydrazines</subject><subject>Immobilization</subject><subject>Leaching</subject><subject>Moisture content</subject><subject>Nuclear Chemistry</subject><subject>Precursors</subject><subject>Roasting</subject><subject>Uranium</subject><subject>Uranium dioxide</subject><issn>1066-3622</issn><issn>1608-3288</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE9LxDAQxYMouK5-AG8Fz9GZJE3T47Kou7CyB9dzSdpUs_TPmrSgfnqzVPAgHoYZeL_3Bh4h1wi3iFzcPSNIySVjDCEFFPyEzFCCopwpdRrvKNOjfk4uQtgDgEKpZoSu27Y3rnFfenB9l_R18uJ158Y2cV0yvNlk0bAtT5704N3HJTmrdRPs1c-ek93D_W65opvt43q52NCSoxyoyVPDWY02zZnWpU4lGJZrXmXSSG6sEGDAWhQ1j6NqWVY5q0oEATotLZ-Tmyn24Pv30Yah2Pej7-LHgqVKZCLPchkpnKjS9yF4WxcH71rtPwuE4lhK8aeU6GGTJ0S2e7X-N_l_0zc5lWE_</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Kulemin, V. V.</creator><creator>Krasavina, E. P.</creator><creator>Gorbacheva, M. P.</creator><creator>Rumer, I. A.</creator><creator>Bessonov, A. A.</creator><creator>Krapukhin, V. B.</creator><creator>Kulyukhin, S. A.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20211001</creationdate><title>Immobilization of Uranium in the Al2O3 Matrix</title><author>Kulemin, V. V. ; Krasavina, E. P. ; Gorbacheva, M. P. ; Rumer, I. A. ; Bessonov, A. A. ; Krapukhin, V. B. ; Kulyukhin, S. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-b95b32f1e592aaca560b29a3d76b63be440b0ee14f314f8f6cd92dc1040a5ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aluminum oxide</topic><topic>Ammonia</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Composite materials</topic><topic>Drying</topic><topic>Heating</topic><topic>Hydrates</topic><topic>Hydrazines</topic><topic>Immobilization</topic><topic>Leaching</topic><topic>Moisture content</topic><topic>Nuclear Chemistry</topic><topic>Precursors</topic><topic>Roasting</topic><topic>Uranium</topic><topic>Uranium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kulemin, V. V.</creatorcontrib><creatorcontrib>Krasavina, E. P.</creatorcontrib><creatorcontrib>Gorbacheva, M. P.</creatorcontrib><creatorcontrib>Rumer, I. A.</creatorcontrib><creatorcontrib>Bessonov, A. A.</creatorcontrib><creatorcontrib>Krapukhin, V. B.</creatorcontrib><creatorcontrib>Kulyukhin, S. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Radiochemistry (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kulemin, V. V.</au><au>Krasavina, E. P.</au><au>Gorbacheva, M. P.</au><au>Rumer, I. A.</au><au>Bessonov, A. A.</au><au>Krapukhin, V. B.</au><au>Kulyukhin, S. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immobilization of Uranium in the Al2O3 Matrix</atitle><jtitle>Radiochemistry (New York, N.Y.)</jtitle><stitle>Radiochemistry</stitle><date>2021-10-01</date><risdate>2021</risdate><volume>63</volume><issue>5</issue><spage>651</spage><epage>657</epage><pages>651-657</pages><issn>1066-3622</issn><eissn>1608-3288</eissn><abstract>The immobilization of uranium in the Al
2
O
3
matrix was studied. For the modification of Al
2
O
3
precursors containing 10 wt % UO
2
(NO
3
)
2
three methods were applied: 1) heating the precursor in air for 5 h at temperatures of 573, 973, and 1273 K, 2) treatment of the precursor with a 0.5 M solution of hydrazine hydrate (HH) for 2 h, drying to dry air moisture content at 383 K, followed by heating in air for 5 h at temperatures of 573, 973, and 1273 K, and 3) treatment of the precursor with a 2.0 M ammonia solution, followed by drying and heating, as in method (2). X-ray diffraction analysis of the synthesized composites revealed UO
3
hydrates of various compositions after calcination of the materials to
T
~600 K and U
3
O
8
after calcination at
T
> 950 K. After 24 h of contact of the composites with H
2
O at 298 K, the leaching of uranium from the studied samples was ~(10
–2
–10
–3
) g U/(g day) for the samples calcined at 383 and 573 K and ~(10
–4
–10
–5
) g U/(g day) for those calcined at 973 and 1273 K.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1066362221050143</doi><tpages>7</tpages></addata></record> |
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source | SpringerLink Journals - AutoHoldings |
subjects | Aluminum oxide Ammonia Chemistry Chemistry and Materials Science Chemistry/Food Science Composite materials Drying Heating Hydrates Hydrazines Immobilization Leaching Moisture content Nuclear Chemistry Precursors Roasting Uranium Uranium dioxide |
title | Immobilization of Uranium in the Al2O3 Matrix |
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