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High-pressure CO2 dissociation with nanosecond pulsed discharges
Herein we investigate the conversion of CO2 into CO and O2 with nanosecond repetitively pulsed (NRP) discharges in a high-pressure batch reactor. Stable discharges are obtained at up to 12 bar. By-products are measured with gas chromatography. The energy efficiency is determined for a range of proce...
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Published in: | Plasma sources science & technology 2023-11, Vol.32 (11) |
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creator | Yong, Taemin Zhong, Hongtao Pannier, Erwan Laux, Christophe Cappelli, Mark A |
description | Herein we investigate the conversion of CO2 into CO and O2 with nanosecond repetitively pulsed (NRP) discharges in a high-pressure batch reactor. Stable discharges are obtained at up to 12 bar. By-products are measured with gas chromatography. The energy efficiency is determined for a range of processing times, pulse energy, and fill pressures. It is only weakly sensitive to the plasma operating parameters, i.e the extent of CO2 conversion is almost linearly-dependent on the specific energy invested. A conversion rate as high as 14% is achieved with an energy efficiency of 23%. For long processing times, saturation in the yield and a drop in efficiency are observed, due to the increasing role of three-body recombination reactions, as described by zero-dimensional detailed kinetic modeling. The modeling reveals the presence of three-stage kinetics between NRP pulses, controlled by electron-impact CO2 dissociation, vibrational relaxation, and neutral elementary kinetics. Transport effects are shown to be important for CO2 conversion at high pressures. For fill pressures beyond 10 bar, CO2 may locally transit into supercritical states. The supercritical plasma kinetics may bypass atomic oxygen pathways and directly convert CO2 into O2. This work provides a detailed analysis of plasma-based high-pressure CO2 conversion, which is of great relevance to future large-scale sustainable carbon capture, utilization, and storage. |
doi_str_mv | 10.1088/1361-6595/ad066e |
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Stable discharges are obtained at up to 12 bar. By-products are measured with gas chromatography. The energy efficiency is determined for a range of processing times, pulse energy, and fill pressures. It is only weakly sensitive to the plasma operating parameters, i.e the extent of CO2 conversion is almost linearly-dependent on the specific energy invested. A conversion rate as high as 14% is achieved with an energy efficiency of 23%. For long processing times, saturation in the yield and a drop in efficiency are observed, due to the increasing role of three-body recombination reactions, as described by zero-dimensional detailed kinetic modeling. The modeling reveals the presence of three-stage kinetics between NRP pulses, controlled by electron-impact CO2 dissociation, vibrational relaxation, and neutral elementary kinetics. Transport effects are shown to be important for CO2 conversion at high pressures. For fill pressures beyond 10 bar, CO2 may locally transit into supercritical states. The supercritical plasma kinetics may bypass atomic oxygen pathways and directly convert CO2 into O2. 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Technol</addtitle><description>Herein we investigate the conversion of CO2 into CO and O2 with nanosecond repetitively pulsed (NRP) discharges in a high-pressure batch reactor. Stable discharges are obtained at up to 12 bar. By-products are measured with gas chromatography. The energy efficiency is determined for a range of processing times, pulse energy, and fill pressures. It is only weakly sensitive to the plasma operating parameters, i.e the extent of CO2 conversion is almost linearly-dependent on the specific energy invested. A conversion rate as high as 14% is achieved with an energy efficiency of 23%. For long processing times, saturation in the yield and a drop in efficiency are observed, due to the increasing role of three-body recombination reactions, as described by zero-dimensional detailed kinetic modeling. The modeling reveals the presence of three-stage kinetics between NRP pulses, controlled by electron-impact CO2 dissociation, vibrational relaxation, and neutral elementary kinetics. Transport effects are shown to be important for CO2 conversion at high pressures. For fill pressures beyond 10 bar, CO2 may locally transit into supercritical states. The supercritical plasma kinetics may bypass atomic oxygen pathways and directly convert CO2 into O2. This work provides a detailed analysis of plasma-based high-pressure CO2 conversion, which is of great relevance to future large-scale sustainable carbon capture, utilization, and storage.</description><subject>70 PLASMA PHYSICS AND FUSION TECHNOLOGY</subject><subject>carbon conversion</subject><subject>chemistry</subject><subject>CO2 dissociation</subject><subject>dissociation</subject><subject>high pressure</subject><subject>nanosecond repetitively pulsed discharge</subject><subject>plasma-based CO</subject><subject>plasma-based CO2 chemistry</subject><issn>0963-0252</issn><issn>1361-6595</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNo9kE1LxDAURYMoWEf3Lotr6-Tlq8lOGdQRBmaj65Amr9MM0pSmg3_flhFXFy6Hy-UQcg_0CajWa-AKKiWNXLtAlcILUvxXl6SgRvGKMsmuyU3OR0oBNKsL8ryNh64aRsz5NGK52bMyxJyTj26KqS9_4tSVvetTRp_6UA6n74xhYXznxgPmW3LVurm7-8sV-Xp7_dxsq93-_WPzsqsiAzNVxkvRUGO4F47XtTcBAWsNMtRK1KwJEBoUTdsyIRvKhEdBgWvvUKPkAfiKPJx3U56izT5O6Lv5Uo9-sowrw6ieocczFNNgj-k09vMlC9Quiuziwy4-7FkR_wVxh1mQ</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Yong, Taemin</creator><creator>Zhong, Hongtao</creator><creator>Pannier, Erwan</creator><creator>Laux, Christophe</creator><creator>Cappelli, Mark A</creator><general>IOP Publishing</general><scope>OIOZB</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-9129-1186</orcidid><orcidid>https://orcid.org/0000-0003-4064-6298</orcidid><orcidid>https://orcid.org/0000-0003-3093-3357</orcidid><orcidid>https://orcid.org/0000000291291186</orcidid><orcidid>https://orcid.org/0000000340646298</orcidid><orcidid>https://orcid.org/0000000330933357</orcidid></search><sort><creationdate>20231101</creationdate><title>High-pressure CO2 dissociation with nanosecond pulsed discharges</title><author>Yong, Taemin ; Zhong, Hongtao ; Pannier, Erwan ; Laux, Christophe ; Cappelli, Mark A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i219t-9c54b0993c4a377c9de1e7815d76472bd1dbe4bff245b024ce40138cae8e53d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>70 PLASMA PHYSICS AND FUSION TECHNOLOGY</topic><topic>carbon conversion</topic><topic>chemistry</topic><topic>CO2 dissociation</topic><topic>dissociation</topic><topic>high pressure</topic><topic>nanosecond repetitively pulsed discharge</topic><topic>plasma-based CO</topic><topic>plasma-based CO2 chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yong, Taemin</creatorcontrib><creatorcontrib>Zhong, Hongtao</creatorcontrib><creatorcontrib>Pannier, Erwan</creatorcontrib><creatorcontrib>Laux, Christophe</creatorcontrib><creatorcontrib>Cappelli, Mark A</creatorcontrib><creatorcontrib>Stanford Univ., CA (United States)</creatorcontrib><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Plasma sources science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yong, Taemin</au><au>Zhong, Hongtao</au><au>Pannier, Erwan</au><au>Laux, Christophe</au><au>Cappelli, Mark A</au><aucorp>Stanford Univ., CA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-pressure CO2 dissociation with nanosecond pulsed discharges</atitle><jtitle>Plasma sources science & technology</jtitle><stitle>PSST</stitle><addtitle>Plasma Sources Sci. Technol</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>32</volume><issue>11</issue><issn>0963-0252</issn><eissn>1361-6595</eissn><coden>PSTEEU</coden><abstract>Herein we investigate the conversion of CO2 into CO and O2 with nanosecond repetitively pulsed (NRP) discharges in a high-pressure batch reactor. Stable discharges are obtained at up to 12 bar. By-products are measured with gas chromatography. The energy efficiency is determined for a range of processing times, pulse energy, and fill pressures. It is only weakly sensitive to the plasma operating parameters, i.e the extent of CO2 conversion is almost linearly-dependent on the specific energy invested. A conversion rate as high as 14% is achieved with an energy efficiency of 23%. For long processing times, saturation in the yield and a drop in efficiency are observed, due to the increasing role of three-body recombination reactions, as described by zero-dimensional detailed kinetic modeling. The modeling reveals the presence of three-stage kinetics between NRP pulses, controlled by electron-impact CO2 dissociation, vibrational relaxation, and neutral elementary kinetics. Transport effects are shown to be important for CO2 conversion at high pressures. For fill pressures beyond 10 bar, CO2 may locally transit into supercritical states. The supercritical plasma kinetics may bypass atomic oxygen pathways and directly convert CO2 into O2. 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subjects | 70 PLASMA PHYSICS AND FUSION TECHNOLOGY carbon conversion chemistry CO2 dissociation dissociation high pressure nanosecond repetitively pulsed discharge plasma-based CO plasma-based CO2 chemistry |
title | High-pressure CO2 dissociation with nanosecond pulsed discharges |
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