Reactions of Nitrate Salts with Ammonia in Supercritical Water
Reactions involving nitrate salts and ammonia were investigated in supercritical water at temperatures from 450 to 530 °C and pressures near 300 bar. Reaction products included nitrite, nitrogen gas, and nitrous oxide. Observed reaction rates and product distributions provided evidence for a free-ra...
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Veröffentlicht in: | Industrial & engineering chemistry research 1997-07, Vol.36 (7), p.2547-2557 |
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creator | Dell'Orco, Philip C Gloyna, Earnest F Buelow, Steven J |
description | Reactions involving nitrate salts and ammonia were investigated in supercritical water at temperatures from 450 to 530 °C and pressures near 300 bar. Reaction products included nitrite, nitrogen gas, and nitrous oxide. Observed reaction rates and product distributions provided evidence for a free-radical reaction mechanism with NO2, NO, and NH2 • as the primary reactive species at supercritical conditions. In the proposed elementary mechanism, the rate-limiting reaction step was determined to be the hydrolysis of MNO3 species, which resulted in the formation of nitric acid and subsequently NO2. A simple second-order reaction model was used to represent the data. In developing an empirical kinetic model, nitrate and nitrite were lumped as an NO x - reactant. Empirical kinetic parameters were developed for four MNO x /NH3 reacting systems, assuming first orders in both NH3 and NO x -. Observed MNO x /NH3 reaction rates and mechanisms suggest immediately a practical significance of these reactions for nitrogen control strategies in supercritical water oxidation processes. |
doi_str_mv | 10.1021/ie9605894 |
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Reaction products included nitrite, nitrogen gas, and nitrous oxide. Observed reaction rates and product distributions provided evidence for a free-radical reaction mechanism with NO2, NO, and NH2 • as the primary reactive species at supercritical conditions. In the proposed elementary mechanism, the rate-limiting reaction step was determined to be the hydrolysis of MNO3 species, which resulted in the formation of nitric acid and subsequently NO2. A simple second-order reaction model was used to represent the data. In developing an empirical kinetic model, nitrate and nitrite were lumped as an NO x - reactant. Empirical kinetic parameters were developed for four MNO x /NH3 reacting systems, assuming first orders in both NH3 and NO x -. Observed MNO x /NH3 reaction rates and mechanisms suggest immediately a practical significance of these reactions for nitrogen control strategies in supercritical water oxidation processes.</description><identifier>ISSN: 0888-5885</identifier><identifier>EISSN: 1520-5045</identifier><identifier>DOI: 10.1021/ie9605894</identifier><identifier>CODEN: IECRED</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>05 NUCLEAR FUELS ; AMMONIA ; Applied sciences ; CHEMICAL REACTION KINETICS ; ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION ; Exact sciences and technology ; HAZARDOUS MATERIALS ; INDUSTRIAL WASTES ; MATHEMATICAL MODELS ; NITRATES ; Other wastes and particular components of wastes ; Pollution ; RADIOACTIVE WASTE PROCESSING ; SUPERCRITICAL GAS EXTRACTION ; Wastes ; WATER</subject><ispartof>Industrial & engineering chemistry research, 1997-07, Vol.36 (7), p.2547-2557</ispartof><rights>Copyright © 1997 American Chemical Society</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a386t-e5db444801ba3fe8c38ba5ddff7fc0ae61b23051f851d911ee302dca228d524c3</citedby><cites>FETCH-LOGICAL-a386t-e5db444801ba3fe8c38ba5ddff7fc0ae61b23051f851d911ee302dca228d524c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ie9605894$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ie9605894$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,881,2751,27055,27903,27904,56716,56766</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2738220$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/529741$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Dell'Orco, Philip C</creatorcontrib><creatorcontrib>Gloyna, Earnest F</creatorcontrib><creatorcontrib>Buelow, Steven J</creatorcontrib><title>Reactions of Nitrate Salts with Ammonia in Supercritical Water</title><title>Industrial & engineering chemistry research</title><addtitle>Ind. Eng. Chem. Res</addtitle><description>Reactions involving nitrate salts and ammonia were investigated in supercritical water at temperatures from 450 to 530 °C and pressures near 300 bar. Reaction products included nitrite, nitrogen gas, and nitrous oxide. Observed reaction rates and product distributions provided evidence for a free-radical reaction mechanism with NO2, NO, and NH2 • as the primary reactive species at supercritical conditions. In the proposed elementary mechanism, the rate-limiting reaction step was determined to be the hydrolysis of MNO3 species, which resulted in the formation of nitric acid and subsequently NO2. A simple second-order reaction model was used to represent the data. In developing an empirical kinetic model, nitrate and nitrite were lumped as an NO x - reactant. Empirical kinetic parameters were developed for four MNO x /NH3 reacting systems, assuming first orders in both NH3 and NO x -. Observed MNO x /NH3 reaction rates and mechanisms suggest immediately a practical significance of these reactions for nitrogen control strategies in supercritical water oxidation processes.</description><subject>05 NUCLEAR FUELS</subject><subject>AMMONIA</subject><subject>Applied sciences</subject><subject>CHEMICAL REACTION KINETICS</subject><subject>ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION</subject><subject>Exact sciences and technology</subject><subject>HAZARDOUS MATERIALS</subject><subject>INDUSTRIAL WASTES</subject><subject>MATHEMATICAL MODELS</subject><subject>NITRATES</subject><subject>Other wastes and particular components of wastes</subject><subject>Pollution</subject><subject>RADIOACTIVE WASTE PROCESSING</subject><subject>SUPERCRITICAL GAS EXTRACTION</subject><subject>Wastes</subject><subject>WATER</subject><issn>0888-5885</issn><issn>1520-5045</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNpt0E1LAzEQBuAgCtbqwX8QQQ8eVvPZzV4ELVaFUj9a0VuYzSY0td0tSYr6711Z6cnTHOaZGeZF6JiSC0oYvfS2GBCpCrGDelQykkki5C7qEaVUJpWS--ggxgUhREoheujqxYJJvqkjbhye-BQgWTyFZYr406c5vl6tmtoD9jWebtY2mOCTN7DEby0Mh2jPwTLao7_aR6-j29nwPhs_3j0Mr8cZcDVImZVVKYRQhJbAnVWGqxJkVTmXO0PADmjJOJHUKUmrglJrOWGVAcZUJZkwvI9Our1NTF5H45M1c9PUtTVJS1bkgrbmvDMmNDEG6_Q6-BWEb02J_g1Hb8Np7Wln1xDbZ1yA2vi4HWA5V4yRlmUd8zHZr20bwoce5DyXevY01c8TOrp5L8Z62PqzzoOJetFsQt2G8s_5H3g-ffw</recordid><startdate>19970701</startdate><enddate>19970701</enddate><creator>Dell'Orco, Philip C</creator><creator>Gloyna, Earnest F</creator><creator>Buelow, Steven J</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19970701</creationdate><title>Reactions of Nitrate Salts with Ammonia in Supercritical Water</title><author>Dell'Orco, Philip C ; Gloyna, Earnest F ; Buelow, Steven J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a386t-e5db444801ba3fe8c38ba5ddff7fc0ae61b23051f851d911ee302dca228d524c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>05 NUCLEAR FUELS</topic><topic>AMMONIA</topic><topic>Applied sciences</topic><topic>CHEMICAL REACTION KINETICS</topic><topic>ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION</topic><topic>Exact sciences and technology</topic><topic>HAZARDOUS MATERIALS</topic><topic>INDUSTRIAL WASTES</topic><topic>MATHEMATICAL MODELS</topic><topic>NITRATES</topic><topic>Other wastes and particular components of wastes</topic><topic>Pollution</topic><topic>RADIOACTIVE WASTE PROCESSING</topic><topic>SUPERCRITICAL GAS EXTRACTION</topic><topic>Wastes</topic><topic>WATER</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dell'Orco, Philip C</creatorcontrib><creatorcontrib>Gloyna, Earnest F</creatorcontrib><creatorcontrib>Buelow, Steven J</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Industrial & engineering chemistry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dell'Orco, Philip C</au><au>Gloyna, Earnest F</au><au>Buelow, Steven J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactions of Nitrate Salts with Ammonia in Supercritical Water</atitle><jtitle>Industrial & engineering chemistry research</jtitle><addtitle>Ind. Eng. Chem. Res</addtitle><date>1997-07-01</date><risdate>1997</risdate><volume>36</volume><issue>7</issue><spage>2547</spage><epage>2557</epage><pages>2547-2557</pages><issn>0888-5885</issn><eissn>1520-5045</eissn><coden>IECRED</coden><abstract>Reactions involving nitrate salts and ammonia were investigated in supercritical water at temperatures from 450 to 530 °C and pressures near 300 bar. Reaction products included nitrite, nitrogen gas, and nitrous oxide. Observed reaction rates and product distributions provided evidence for a free-radical reaction mechanism with NO2, NO, and NH2 • as the primary reactive species at supercritical conditions. In the proposed elementary mechanism, the rate-limiting reaction step was determined to be the hydrolysis of MNO3 species, which resulted in the formation of nitric acid and subsequently NO2. A simple second-order reaction model was used to represent the data. In developing an empirical kinetic model, nitrate and nitrite were lumped as an NO x - reactant. Empirical kinetic parameters were developed for four MNO x /NH3 reacting systems, assuming first orders in both NH3 and NO x -. Observed MNO x /NH3 reaction rates and mechanisms suggest immediately a practical significance of these reactions for nitrogen control strategies in supercritical water oxidation processes.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ie9605894</doi><tpages>11</tpages></addata></record> |
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subjects | 05 NUCLEAR FUELS AMMONIA Applied sciences CHEMICAL REACTION KINETICS ENERGY CONSERVATION, CONSUMPTION, AND UTILIZATION Exact sciences and technology HAZARDOUS MATERIALS INDUSTRIAL WASTES MATHEMATICAL MODELS NITRATES Other wastes and particular components of wastes Pollution RADIOACTIVE WASTE PROCESSING SUPERCRITICAL GAS EXTRACTION Wastes WATER |
title | Reactions of Nitrate Salts with Ammonia in Supercritical Water |
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