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Simultaneous Removal of NO x and SO x from Flue Gases Using ClO2: Process Scaling and Modeling Simulations
The concept of coabsorption of NO2 and SO2 from flue gases, in combination with the enhanced oxidation of NO by ClO2(g), is studied on three scales, 0.2, 100, and 400 N m3/h, all with flue gases of different origins. The results obtained from each setup are presented, together with modeling that was...
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Published in: | Industrial & engineering chemistry research 2021-02, Vol.60 (4), p.1774-1783 |
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creator | Johansson, Jakob Heijnesson Hultén, Anette Normann, Fredrik Andersson, Klas |
description | The concept of coabsorption of NO2 and SO2 from flue gases, in combination with the enhanced oxidation of NO by ClO2(g), is studied on three scales, 0.2, 100, and 400 N m3/h, all with flue gases of different origins. The results obtained from each setup are presented, together with modeling that was applied to assess the scale-up of the concept and to validate the model. The measurements confirm that ClO2 is highly selective toward NO oxidation for temperatures in the range of 70–155 °C. A comparison of the results obtained for each scale reveals that the 0.2 N m3/h setup confers a higher level of NO x absorption than the other setups, although the trends remain similar. Simulations of the results underpredict the level of NO2 absorption in the 0.2 N m3/h setup while capturing the levels of absorption in the 100 N m3/h setup. An important finding is the rapid and complete oxidation of S(IV) in the presence of NO2, which is not represented in the reaction kinetics. |
doi_str_mv | 10.1021/acs.iecr.0c05828 |
format | article |
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The results obtained from each setup are presented, together with modeling that was applied to assess the scale-up of the concept and to validate the model. The measurements confirm that ClO2 is highly selective toward NO oxidation for temperatures in the range of 70–155 °C. A comparison of the results obtained for each scale reveals that the 0.2 N m3/h setup confers a higher level of NO x absorption than the other setups, although the trends remain similar. Simulations of the results underpredict the level of NO2 absorption in the 0.2 N m3/h setup while capturing the levels of absorption in the 100 N m3/h setup. An important finding is the rapid and complete oxidation of S(IV) in the presence of NO2, which is not represented in the reaction kinetics.</description><identifier>ISSN: 0888-5885</identifier><identifier>EISSN: 1520-5045</identifier><identifier>DOI: 10.1021/acs.iecr.0c05828</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>Process Systems Engineering</subject><ispartof>Industrial & engineering chemistry research, 2021-02, Vol.60 (4), p.1774-1783</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-8011-7783 ; 0000-0001-5968-9082</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Johansson, Jakob</creatorcontrib><creatorcontrib>Heijnesson Hultén, Anette</creatorcontrib><creatorcontrib>Normann, Fredrik</creatorcontrib><creatorcontrib>Andersson, Klas</creatorcontrib><title>Simultaneous Removal of NO x and SO x from Flue Gases Using ClO2: Process Scaling and Modeling Simulations</title><title>Industrial & engineering chemistry research</title><addtitle>Ind. Eng. Chem. Res</addtitle><description>The concept of coabsorption of NO2 and SO2 from flue gases, in combination with the enhanced oxidation of NO by ClO2(g), is studied on three scales, 0.2, 100, and 400 N m3/h, all with flue gases of different origins. The results obtained from each setup are presented, together with modeling that was applied to assess the scale-up of the concept and to validate the model. The measurements confirm that ClO2 is highly selective toward NO oxidation for temperatures in the range of 70–155 °C. A comparison of the results obtained for each scale reveals that the 0.2 N m3/h setup confers a higher level of NO x absorption than the other setups, although the trends remain similar. Simulations of the results underpredict the level of NO2 absorption in the 0.2 N m3/h setup while capturing the levels of absorption in the 100 N m3/h setup. 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Eng. Chem. Res</addtitle><date>2021-02-03</date><risdate>2021</risdate><volume>60</volume><issue>4</issue><spage>1774</spage><epage>1783</epage><pages>1774-1783</pages><issn>0888-5885</issn><eissn>1520-5045</eissn><abstract>The concept of coabsorption of NO2 and SO2 from flue gases, in combination with the enhanced oxidation of NO by ClO2(g), is studied on three scales, 0.2, 100, and 400 N m3/h, all with flue gases of different origins. The results obtained from each setup are presented, together with modeling that was applied to assess the scale-up of the concept and to validate the model. The measurements confirm that ClO2 is highly selective toward NO oxidation for temperatures in the range of 70–155 °C. A comparison of the results obtained for each scale reveals that the 0.2 N m3/h setup confers a higher level of NO x absorption than the other setups, although the trends remain similar. Simulations of the results underpredict the level of NO2 absorption in the 0.2 N m3/h setup while capturing the levels of absorption in the 100 N m3/h setup. An important finding is the rapid and complete oxidation of S(IV) in the presence of NO2, which is not represented in the reaction kinetics.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.iecr.0c05828</doi><orcidid>https://orcid.org/0000-0001-8011-7783</orcidid><orcidid>https://orcid.org/0000-0001-5968-9082</orcidid></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Process Systems Engineering |
title | Simultaneous Removal of NO x and SO x from Flue Gases Using ClO2: Process Scaling and Modeling Simulations |
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