Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism
The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully unde...
Ausführliche Beschreibung
Autor*in: |
Long, Yangke [verfasserIn] Huang, Shixin [verfasserIn] Zhao, Shiyin [verfasserIn] Xiao, Guicong [verfasserIn] Sun, Jianlin [verfasserIn] Peng, Dan [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: Separation and purification technology - Amsterdam [u.a.] : Elsevier Science, 1997, 317 |
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Übergeordnetes Werk: |
volume:317 |
DOI / URN: |
10.1016/j.seppur.2023.123945 |
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Katalog-ID: |
ELV062763075 |
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245 | 1 | 0 | |a Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism |
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520 | |a The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. | ||
650 | 4 | |a Wastewater treatment | |
650 | 4 | |a Advanced oxidation technology | |
650 | 4 | |a Zero-valent iron | |
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650 | 4 | |a Nonradical oxidation | |
700 | 1 | |a Huang, Shixin |e verfasserin |4 aut | |
700 | 1 | |a Zhao, Shiyin |e verfasserin |4 aut | |
700 | 1 | |a Xiao, Guicong |e verfasserin |4 aut | |
700 | 1 | |a Sun, Jianlin |e verfasserin |4 aut | |
700 | 1 | |a Peng, Dan |e verfasserin |4 aut | |
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10.1016/j.seppur.2023.123945 doi (DE-627)ELV062763075 (ELSEVIER)S1383-5866(23)00853-5 DE-627 ger DE-627 rda eng 540 VZ 58.11 bkl 58.13 bkl Long, Yangke verfasserin aut Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. Wastewater treatment Advanced oxidation technology Zero-valent iron Fe–N Nonradical oxidation Huang, Shixin verfasserin aut Zhao, Shiyin verfasserin aut Xiao, Guicong verfasserin aut Sun, Jianlin verfasserin aut Peng, Dan verfasserin aut Enthalten in Separation and purification technology Amsterdam [u.a.] : Elsevier Science, 1997 317 Online-Ressource (DE-627)320620123 (DE-600)2022535-0 (DE-576)259485349 nnns volume:317 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_101 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_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_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 58.11 Mechanische Verfahrenstechnik VZ 58.13 Thermische Verfahrenstechnik VZ AR 317 |
spelling |
10.1016/j.seppur.2023.123945 doi (DE-627)ELV062763075 (ELSEVIER)S1383-5866(23)00853-5 DE-627 ger DE-627 rda eng 540 VZ 58.11 bkl 58.13 bkl Long, Yangke verfasserin aut Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. Wastewater treatment Advanced oxidation technology Zero-valent iron Fe–N Nonradical oxidation Huang, Shixin verfasserin aut Zhao, Shiyin verfasserin aut Xiao, Guicong verfasserin aut Sun, Jianlin verfasserin aut Peng, Dan verfasserin aut Enthalten in Separation and purification technology Amsterdam [u.a.] : Elsevier Science, 1997 317 Online-Ressource (DE-627)320620123 (DE-600)2022535-0 (DE-576)259485349 nnns volume:317 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_101 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_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_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 58.11 Mechanische Verfahrenstechnik VZ 58.13 Thermische Verfahrenstechnik VZ AR 317 |
allfields_unstemmed |
10.1016/j.seppur.2023.123945 doi (DE-627)ELV062763075 (ELSEVIER)S1383-5866(23)00853-5 DE-627 ger DE-627 rda eng 540 VZ 58.11 bkl 58.13 bkl Long, Yangke verfasserin aut Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. Wastewater treatment Advanced oxidation technology Zero-valent iron Fe–N Nonradical oxidation Huang, Shixin verfasserin aut Zhao, Shiyin verfasserin aut Xiao, Guicong verfasserin aut Sun, Jianlin verfasserin aut Peng, Dan verfasserin aut Enthalten in Separation and purification technology Amsterdam [u.a.] : Elsevier Science, 1997 317 Online-Ressource (DE-627)320620123 (DE-600)2022535-0 (DE-576)259485349 nnns volume:317 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_101 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_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_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 58.11 Mechanische Verfahrenstechnik VZ 58.13 Thermische Verfahrenstechnik VZ AR 317 |
allfieldsGer |
10.1016/j.seppur.2023.123945 doi (DE-627)ELV062763075 (ELSEVIER)S1383-5866(23)00853-5 DE-627 ger DE-627 rda eng 540 VZ 58.11 bkl 58.13 bkl Long, Yangke verfasserin aut Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. Wastewater treatment Advanced oxidation technology Zero-valent iron Fe–N Nonradical oxidation Huang, Shixin verfasserin aut Zhao, Shiyin verfasserin aut Xiao, Guicong verfasserin aut Sun, Jianlin verfasserin aut Peng, Dan verfasserin aut Enthalten in Separation and purification technology Amsterdam [u.a.] : Elsevier Science, 1997 317 Online-Ressource (DE-627)320620123 (DE-600)2022535-0 (DE-576)259485349 nnns volume:317 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_101 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_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_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 58.11 Mechanische Verfahrenstechnik VZ 58.13 Thermische Verfahrenstechnik VZ AR 317 |
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10.1016/j.seppur.2023.123945 doi (DE-627)ELV062763075 (ELSEVIER)S1383-5866(23)00853-5 DE-627 ger DE-627 rda eng 540 VZ 58.11 bkl 58.13 bkl Long, Yangke verfasserin aut Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism 2023 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. Wastewater treatment Advanced oxidation technology Zero-valent iron Fe–N Nonradical oxidation Huang, Shixin verfasserin aut Zhao, Shiyin verfasserin aut Xiao, Guicong verfasserin aut Sun, Jianlin verfasserin aut Peng, Dan verfasserin aut Enthalten in Separation and purification technology Amsterdam [u.a.] : Elsevier Science, 1997 317 Online-Ressource (DE-627)320620123 (DE-600)2022535-0 (DE-576)259485349 nnns volume:317 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_101 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_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_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 58.11 Mechanische Verfahrenstechnik VZ 58.13 Thermische Verfahrenstechnik VZ AR 317 |
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Long, Yangke @@aut@@ Huang, Shixin @@aut@@ Zhao, Shiyin @@aut@@ Xiao, Guicong @@aut@@ Sun, Jianlin @@aut@@ Peng, Dan @@aut@@ |
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Long, Yangke |
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Long, Yangke ddc 540 bkl 58.11 bkl 58.13 misc Wastewater treatment misc Advanced oxidation technology misc Zero-valent iron misc Fe–N misc Nonradical oxidation Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism |
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540 VZ 58.11 bkl 58.13 bkl Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism Wastewater treatment Advanced oxidation technology Zero-valent iron Fe–N Nonradical oxidation |
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ddc 540 bkl 58.11 bkl 58.13 misc Wastewater treatment misc Advanced oxidation technology misc Zero-valent iron misc Fe–N misc Nonradical oxidation |
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ddc 540 bkl 58.11 bkl 58.13 misc Wastewater treatment misc Advanced oxidation technology misc Zero-valent iron misc Fe–N misc Nonradical oxidation |
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ddc 540 bkl 58.11 bkl 58.13 misc Wastewater treatment misc Advanced oxidation technology misc Zero-valent iron misc Fe–N misc Nonradical oxidation |
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title |
Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism |
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Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism |
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Long, Yangke |
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Long, Yangke Huang, Shixin Zhao, Shiyin Xiao, Guicong Sun, Jianlin Peng, Dan |
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10.1016/j.seppur.2023.123945 |
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pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: active site and degradation mechanism |
title_auth |
Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism |
abstract |
The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. |
abstractGer |
The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. |
abstract_unstemmed |
The practical application of periodate-based advanced oxidation technologies (PI-AOTs) for wastewater treatment requires efficient and cost-effective activators. Pyrolyzed Fe–N/C materials are potential candidates, however, their actual active sites and activation mechanisms are yet to be fully understood. Herein, a series of Fe–N/C samples (denoted as FeNC-X) with differing structures and iron components were delicately synthesized. Experimental studies on the structure–activity relationship and density functional theory (DFT) computations revealed that Fe–Nx species serve as the dominant active site for periodate activation, while the inactive iron-based particles (i.e., Fe0 and Fe3C) optimized the binding affinity of surrounding carbon layers with periodate, resulting in enhanced activity. In-depth exploration of the oxidative mechanism revealed that Fe@NC-X activated periodate through an electron transfer regime. Our results also showed that the optimal Fe@NC-0.2/periodate system was highly effective in catalyzing the oxidation of 4-CP, outperforming many reported activators. These findings provide an indispensable foundation for the rational development of advanced Fe–N/C activators and offer vital insights into the mechanism underlying pollutant destruction through PI-AOTs. |
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title_short |
Pyrolyzed iron–nitrogen–carbon hybrids for efficient contaminant decomposition via periodate activation: Active site and degradation mechanism |
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Huang, Shixin Zhao, Shiyin Xiao, Guicong Sun, Jianlin Peng, Dan |
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