Hydrogen reduction of low-surface area uranium trioxide
The kinetics of the hydrogen reduction of uranium trioxide of surface area below 1.2m/sup 2//g were investigated. An increase in surface area and pore volume occurred during the reaction and an intermediate compound (composition, UO/ sub 2.6/ to UO/sub 2.7/) was formed. The initial rate of reductio...
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Veröffentlicht in: | Transactions of the Faraday Society 1961, Vol.57, p.1400 |
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creator | Morrow, Sheila A. Graves, S. Tomlinson, L. |
description | The kinetics of the hydrogen reduction of uranium trioxide of surface area below 1.2m/sup 2//g were investigated. An increase in surface area and pore volume occurred during the reaction and an intermediate compound (composition, UO/ sub 2.6/ to UO/sub 2.7/) was formed. The initial rate of reductio n was found to be directly proportional to the surface area of the UO/sub 3/ and to (hydrogen partial pressure)/sup 0.7//sup 8/. The shape of the rate curve obtained was dependent on the nature of the UO/sub 3/ and the apparent activation energy for the reaction varied between 25 and 32 kcal/mole. The observed kinetics were best interpreted in terms of hydrogen chemisorption on the solid surface as the rate-controlling step. Hydration or the addition of sulfate ions to the trioxide greatly increased its surface area. (auth) |
doi_str_mv | 10.1039/tf9615701400 |
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An increase in surface area and pore volume occurred during the reaction and an intermediate compound (composition, UO/ sub 2.6/ to UO/sub 2.7/) was formed. The initial rate of reductio n was found to be directly proportional to the surface area of the UO/sub 3/ and to (hydrogen partial pressure)/sup 0.7//sup 8/. The shape of the rate curve obtained was dependent on the nature of the UO/sub 3/ and the apparent activation energy for the reaction varied between 25 and 32 kcal/mole. The observed kinetics were best interpreted in terms of hydrogen chemisorption on the solid surface as the rate-controlling step. Hydration or the addition of sulfate ions to the trioxide greatly increased its surface area. (auth)</description><identifier>ISSN: 0014-7672</identifier><identifier>DOI: 10.1039/tf9615701400</identifier><language>eng</language><subject>ADSORPTION ; CHEMISTRY ; HYDROGEN ; IONS ; POROSITY ; PRESSURE ; REACTION KINETICS ; REDUCTION ; SOLIDS ; SULFATES ; SURFACES ; URANIUM TRIOXIDE ; USES ; VOLUME</subject><ispartof>Transactions of the Faraday Society, 1961, Vol.57, p.1400</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c199t-7cf73e5080e3b90e59511c8e5ff93e325582ede31024e51dd930f7c51802ca103</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,883,2820,4012,27906,27907,27908</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/4842048$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Morrow, Sheila A.</creatorcontrib><creatorcontrib>Graves, S.</creatorcontrib><creatorcontrib>Tomlinson, L.</creatorcontrib><creatorcontrib>United Kingdom Atomic Energy Authority, Springfields, Lancs, Eng</creatorcontrib><title>Hydrogen reduction of low-surface area uranium trioxide</title><title>Transactions of the Faraday Society</title><description>The kinetics of the hydrogen reduction of uranium trioxide of surface area below 1.2m/sup 2//g were investigated. An increase in surface area and pore volume occurred during the reaction and an intermediate compound (composition, UO/ sub 2.6/ to UO/sub 2.7/) was formed. The initial rate of reductio n was found to be directly proportional to the surface area of the UO/sub 3/ and to (hydrogen partial pressure)/sup 0.7//sup 8/. The shape of the rate curve obtained was dependent on the nature of the UO/sub 3/ and the apparent activation energy for the reaction varied between 25 and 32 kcal/mole. The observed kinetics were best interpreted in terms of hydrogen chemisorption on the solid surface as the rate-controlling step. Hydration or the addition of sulfate ions to the trioxide greatly increased its surface area. (auth)</description><subject>ADSORPTION</subject><subject>CHEMISTRY</subject><subject>HYDROGEN</subject><subject>IONS</subject><subject>POROSITY</subject><subject>PRESSURE</subject><subject>REACTION KINETICS</subject><subject>REDUCTION</subject><subject>SOLIDS</subject><subject>SULFATES</subject><subject>SURFACES</subject><subject>URANIUM TRIOXIDE</subject><subject>USES</subject><subject>VOLUME</subject><issn>0014-7672</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1961</creationdate><recordtype>article</recordtype><recordid>eNpNUM1OAyEY5KCJtfbmAxDPrn7AUuBoGrUmTbzYM0H4UEy7GGCjfXvX1IOnmcNk_gi5ZHDDQJjbFs2SSQWsBzghM5hIp5aKn5HzWj8AuJSgZ0StD6HkNxxowTD6lvJAc6S7_NXVsUTnkbqCjo7FDWnc01ZS_k4BL8hpdLuKiz-ck-3D_ctq3W2eH59Wd5vOM2Nap3xUAqckQPFqAKWRjHmNMkYjUEwlNMeAggHvUbIQjICovGQauHfTkDm5Ovrm2pKtPjX07z4PA_pme91z6PUkuj6KfMm1Foz2s6S9KwfLwP6-Yf-_IX4AV6RTJA</recordid><startdate>1961</startdate><enddate>1961</enddate><creator>Morrow, Sheila A.</creator><creator>Graves, S.</creator><creator>Tomlinson, L.</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>1961</creationdate><title>Hydrogen reduction of low-surface area uranium trioxide</title><author>Morrow, Sheila A. ; Graves, S. ; Tomlinson, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c199t-7cf73e5080e3b90e59511c8e5ff93e325582ede31024e51dd930f7c51802ca103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1961</creationdate><topic>ADSORPTION</topic><topic>CHEMISTRY</topic><topic>HYDROGEN</topic><topic>IONS</topic><topic>POROSITY</topic><topic>PRESSURE</topic><topic>REACTION KINETICS</topic><topic>REDUCTION</topic><topic>SOLIDS</topic><topic>SULFATES</topic><topic>SURFACES</topic><topic>URANIUM TRIOXIDE</topic><topic>USES</topic><topic>VOLUME</topic><toplevel>online_resources</toplevel><creatorcontrib>Morrow, Sheila A.</creatorcontrib><creatorcontrib>Graves, S.</creatorcontrib><creatorcontrib>Tomlinson, L.</creatorcontrib><creatorcontrib>United Kingdom Atomic Energy Authority, Springfields, Lancs, Eng</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Transactions of the Faraday Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morrow, Sheila A.</au><au>Graves, S.</au><au>Tomlinson, L.</au><aucorp>United Kingdom Atomic Energy Authority, Springfields, Lancs, Eng</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrogen reduction of low-surface area uranium trioxide</atitle><jtitle>Transactions of the Faraday Society</jtitle><date>1961</date><risdate>1961</risdate><volume>57</volume><spage>1400</spage><pages>1400-</pages><issn>0014-7672</issn><abstract>The kinetics of the hydrogen reduction of uranium trioxide of surface area below 1.2m/sup 2//g were investigated. An increase in surface area and pore volume occurred during the reaction and an intermediate compound (composition, UO/ sub 2.6/ to UO/sub 2.7/) was formed. The initial rate of reductio n was found to be directly proportional to the surface area of the UO/sub 3/ and to (hydrogen partial pressure)/sup 0.7//sup 8/. The shape of the rate curve obtained was dependent on the nature of the UO/sub 3/ and the apparent activation energy for the reaction varied between 25 and 32 kcal/mole. The observed kinetics were best interpreted in terms of hydrogen chemisorption on the solid surface as the rate-controlling step. Hydration or the addition of sulfate ions to the trioxide greatly increased its surface area. (auth)</abstract><doi>10.1039/tf9615701400</doi></addata></record> |
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source | Royal Society of Chemistry Journals Archive (1841-2007) |
subjects | ADSORPTION CHEMISTRY HYDROGEN IONS POROSITY PRESSURE REACTION KINETICS REDUCTION SOLIDS SULFATES SURFACES URANIUM TRIOXIDE USES VOLUME |
title | Hydrogen reduction of low-surface area uranium trioxide |
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