A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition
Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we propose...
Ausführliche Beschreibung
Autor*in: |
Cui, Dongxu [verfasserIn] Wu, Shiliang [verfasserIn] Li, Tao [verfasserIn] Zhang, Yuxin [verfasserIn] Jun Yoon, Sang [verfasserIn] Bae, Youn-Sang [verfasserIn] Park, Bugae [verfasserIn] Wu, Yinlong [verfasserIn] Xiao, Rui [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: The chemical engineering journal - Amsterdam : Elsevier, 1997, 466 |
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Übergeordnetes Werk: |
volume:466 |
DOI / URN: |
10.1016/j.cej.2023.143123 |
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Katalog-ID: |
ELV009862803 |
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520 | |a Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. | ||
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700 | 1 | |a Xiao, Rui |e verfasserin |4 aut | |
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10.1016/j.cej.2023.143123 doi (DE-627)ELV009862803 (ELSEVIER)S1385-8947(23)01854-5 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Cui, Dongxu verfasserin aut A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. SOFC reactor Fluidized bed electrode N Mass transfer Wu, Shiliang verfasserin aut Li, Tao verfasserin aut Zhang, Yuxin verfasserin aut Jun Yoon, Sang verfasserin aut Bae, Youn-Sang verfasserin aut Park, Bugae verfasserin aut Wu, Yinlong verfasserin aut Xiao, Rui verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 466 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:466 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 466 |
spelling |
10.1016/j.cej.2023.143123 doi (DE-627)ELV009862803 (ELSEVIER)S1385-8947(23)01854-5 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Cui, Dongxu verfasserin aut A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. SOFC reactor Fluidized bed electrode N Mass transfer Wu, Shiliang verfasserin aut Li, Tao verfasserin aut Zhang, Yuxin verfasserin aut Jun Yoon, Sang verfasserin aut Bae, Youn-Sang verfasserin aut Park, Bugae verfasserin aut Wu, Yinlong verfasserin aut Xiao, Rui verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 466 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:466 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 466 |
allfields_unstemmed |
10.1016/j.cej.2023.143123 doi (DE-627)ELV009862803 (ELSEVIER)S1385-8947(23)01854-5 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Cui, Dongxu verfasserin aut A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. SOFC reactor Fluidized bed electrode N Mass transfer Wu, Shiliang verfasserin aut Li, Tao verfasserin aut Zhang, Yuxin verfasserin aut Jun Yoon, Sang verfasserin aut Bae, Youn-Sang verfasserin aut Park, Bugae verfasserin aut Wu, Yinlong verfasserin aut Xiao, Rui verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 466 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:466 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 466 |
allfieldsGer |
10.1016/j.cej.2023.143123 doi (DE-627)ELV009862803 (ELSEVIER)S1385-8947(23)01854-5 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Cui, Dongxu verfasserin aut A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. SOFC reactor Fluidized bed electrode N Mass transfer Wu, Shiliang verfasserin aut Li, Tao verfasserin aut Zhang, Yuxin verfasserin aut Jun Yoon, Sang verfasserin aut Bae, Youn-Sang verfasserin aut Park, Bugae verfasserin aut Wu, Yinlong verfasserin aut Xiao, Rui verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 466 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:466 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 466 |
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10.1016/j.cej.2023.143123 doi (DE-627)ELV009862803 (ELSEVIER)S1385-8947(23)01854-5 DE-627 ger DE-627 rda eng 660 VZ 660 VZ 58.10 bkl Cui, Dongxu verfasserin aut A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. SOFC reactor Fluidized bed electrode N Mass transfer Wu, Shiliang verfasserin aut Li, Tao verfasserin aut Zhang, Yuxin verfasserin aut Jun Yoon, Sang verfasserin aut Bae, Youn-Sang verfasserin aut Park, Bugae verfasserin aut Wu, Yinlong verfasserin aut Xiao, Rui verfasserin aut Enthalten in The chemical engineering journal Amsterdam : Elsevier, 1997 466 Online-Ressource (DE-627)320500322 (DE-600)2012137-4 (DE-576)098330152 1873-3212 nnns volume:466 GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_150 GBV_ILN_151 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 58.10 Verfahrenstechnik: Allgemeines VZ AR 466 |
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Cui, Dongxu @@aut@@ Wu, Shiliang @@aut@@ Li, Tao @@aut@@ Zhang, Yuxin @@aut@@ Jun Yoon, Sang @@aut@@ Bae, Youn-Sang @@aut@@ Park, Bugae @@aut@@ Wu, Yinlong @@aut@@ Xiao, Rui @@aut@@ |
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660 VZ 58.10 bkl A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition SOFC reactor Fluidized bed electrode N Mass transfer |
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a novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for n 2 o catalytic decomposition |
title_auth |
A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition |
abstract |
Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. |
abstractGer |
Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. |
abstract_unstemmed |
Global warming potential (GWP) of N2O is 310 times that of CO2. However, conventional solid oxide fuel cell (SOFC) cathode catalytic N2O decomposition has been observed to have a low conversion rate, leading to uneven temperature distribution on the cathode surface. To address this issue, we proposed a novel gas–solid phase fluidized bed catalytic electrode for N2O decomposition in a SOFC system. The fluidized bed material was prepared using cerium oxide particles coated with lanthanum, strontium, and iron (CeO2-LSF). The N2O conversion rate was 99.78% at 720 °C. By assisting particle fluidization with argon, compared to the case of fixed bed electrode, the peak power density improved by a maximum of 39.86% at 670 °C. This improvement was due to mass transfer enhancement by particle fluidization, thereby reducing the concentration polarization of the SOFC. Furthermore, the maximum temperature difference inside the reactor decreased significantly from 92 °C to 42 °C when the cathode particles were fluidized. The reactor can achieve high-efficiency decomposition of N2O while simultaneously improving fuel cell power density and operational reliability. |
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A novel fluidized-bed-electrode solid-oxide-fuel-cell reactor for N 2 O catalytic decomposition |
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Wu, Shiliang Li, Tao Zhang, Yuxin Jun Yoon, Sang Bae, Youn-Sang Park, Bugae Wu, Yinlong Xiao, Rui |
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|
score |
7.403063 |