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Products and yields for the NO3 radical initiated atmospheric degradation of 2-methylfuran (2-MF, CH3–C4H3O)
https://orcid.org/0000-0002-5643-5148
https://orcid.org/0000-0002-5669-0165
https://orcid.org/0000-0003-4411-2904
https://orcid.org/0000-0002-8299-4306
https://orcid.org/0000-0002-0125-581X
https://orcid.org/0000-0002-9049-0319
Abstract Furans represent a group of oxygenated, heterocyclic, organic compounds that are emitted during biomass burning (BB). Notably, these compounds undergo rapid oxidation, a process observed both during the day and at night. Methylated furanoids comprise a large fraction of total furan emissions. Recent kinetic studies suggest that the NO3 initiated degradation of methylated furans is the dominant reaction pathway during nighttime, and with significant contribution on daytime. The aim of this study is to investigate the degradation products and the reaction mechanism of 2-methylfuran (2-MF) reaction with NO3 radicals using two atmospheric simulation chambers: CHARME (Chamber for the Atmospheric Reactivity and the Metrology of the Environment, Dunkerque, France) and THALAMOS (Thermally Regulated Atmospheric Simulation Chamber, Douai, France). All experiments were carried out at ambient temperature, (294 ± 2) K and atmospheric pressure (760 Torr, zero air). Oxidation products were qualitatively and quantitatively characterized using multiple, complementary detection techniques. Gas phase major and minor products were detected via offline GC-EI-MS (Gas chromatography - Electronic Impact - Mass Spectrometry) after trapping the gas-phase mixture on different adsorption media. PTR-ToF-MS (Proton Transfer Mass Reaction – Time of Flight – Mass Spectrometer, CHARME) and SIFT-MS (Selected Ion Flow Tube Mass Spectrometry, THALAMOS) were used on-line to monitor reactants and major products and to determine the end-product yields. 4-Oxo-2-pentenal (H(O)CCHCHC(O)CH3), and 2(5H)-furanone, 5-methyl, 5-nitrooxy ((CH3)C(ONO2)(C4H2O2)) were detected as major products with yields (62 ± 15) % and (26 ± 3) %, respectively. In-situ FTIR (Fourier Transform Infrared Spectroscopy) along with quantum mechanical molecular calculations revealed that organic nitrates and dinitrates were also formed. Secondary organic aerosols (SOA) formation, in the presence of ammonium sulfate seed, was also monitored using SMPS-CPC (Scanning Mobility Particle Sizer-Condensation Particle Counter). The size distribution and the mass concentration of the particles were determined for 2-MF concentration between 80 and 531 ppbv leading to SOA yields 1.03–2.23 %. Finally, SOA formed were chemically characterized using ESI-LC-QToF-MS/MS (Electrospray Ionization Liquid Chromatography – Quadrupole - Time of Flight - Tandem Mass Spectrometer) revealing that oligomers, e.g. highly oxygenated molecules (HOMs) were also formed. Based on our experimental observations, a reaction mechanism is proposed. NO3 radical is predominately added to the C2/C5 double bond of 2-MF, while the H atom abstraction channel, is estimated to be of minor importance. Results from this work provide detailed information about the NO3 radical initiated oxidation of 2-MF that can be used in chemical transport models to simulate the ageing processes occurring in biomass burning plumes.
Highlights 4-oxo-2-pentanal was the major product formed from NO3 addition to 2-MF with a yield of 61.5 ± 14.7 %. The H atom abstraction pathway leading to furfural formation was of minor importance, <1%. The yield of organic nitrates and dinitrates formed was 26% supported by experiments and quantum mechanical calculations. The formation of highly oxygenated molecules (HOMs) were observed in the particulate phase. The yield of secondary organic aerosols formed was below 2%.
Products and yields for the NO3 radical initiated atmospheric degradation of 2-methylfuran (2-MF, CH3–C4H3O)
https://orcid.org/0000-0002-5643-5148
https://orcid.org/0000-0002-5669-0165
https://orcid.org/0000-0003-4411-2904
https://orcid.org/0000-0002-8299-4306
https://orcid.org/0000-0002-0125-581X
https://orcid.org/0000-0002-9049-0319
Abstract Furans represent a group of oxygenated, heterocyclic, organic compounds that are emitted during biomass burning (BB). Notably, these compounds undergo rapid oxidation, a process observed both during the day and at night. Methylated furanoids comprise a large fraction of total furan emissions. Recent kinetic studies suggest that the NO3 initiated degradation of methylated furans is the dominant reaction pathway during nighttime, and with significant contribution on daytime. The aim of this study is to investigate the degradation products and the reaction mechanism of 2-methylfuran (2-MF) reaction with NO3 radicals using two atmospheric simulation chambers: CHARME (Chamber for the Atmospheric Reactivity and the Metrology of the Environment, Dunkerque, France) and THALAMOS (Thermally Regulated Atmospheric Simulation Chamber, Douai, France). All experiments were carried out at ambient temperature, (294 ± 2) K and atmospheric pressure (760 Torr, zero air). Oxidation products were qualitatively and quantitatively characterized using multiple, complementary detection techniques. Gas phase major and minor products were detected via offline GC-EI-MS (Gas chromatography - Electronic Impact - Mass Spectrometry) after trapping the gas-phase mixture on different adsorption media. PTR-ToF-MS (Proton Transfer Mass Reaction – Time of Flight – Mass Spectrometer, CHARME) and SIFT-MS (Selected Ion Flow Tube Mass Spectrometry, THALAMOS) were used on-line to monitor reactants and major products and to determine the end-product yields. 4-Oxo-2-pentenal (H(O)CCHCHC(O)CH3), and 2(5H)-furanone, 5-methyl, 5-nitrooxy ((CH3)C(ONO2)(C4H2O2)) were detected as major products with yields (62 ± 15) % and (26 ± 3) %, respectively. In-situ FTIR (Fourier Transform Infrared Spectroscopy) along with quantum mechanical molecular calculations revealed that organic nitrates and dinitrates were also formed. Secondary organic aerosols (SOA) formation, in the presence of ammonium sulfate seed, was also monitored using SMPS-CPC (Scanning Mobility Particle Sizer-Condensation Particle Counter). The size distribution and the mass concentration of the particles were determined for 2-MF concentration between 80 and 531 ppbv leading to SOA yields 1.03–2.23 %. Finally, SOA formed were chemically characterized using ESI-LC-QToF-MS/MS (Electrospray Ionization Liquid Chromatography – Quadrupole - Time of Flight - Tandem Mass Spectrometer) revealing that oligomers, e.g. highly oxygenated molecules (HOMs) were also formed. Based on our experimental observations, a reaction mechanism is proposed. NO3 radical is predominately added to the C2/C5 double bond of 2-MF, while the H atom abstraction channel, is estimated to be of minor importance. Results from this work provide detailed information about the NO3 radical initiated oxidation of 2-MF that can be used in chemical transport models to simulate the ageing processes occurring in biomass burning plumes.
Highlights 4-oxo-2-pentanal was the major product formed from NO3 addition to 2-MF with a yield of 61.5 ± 14.7 %. The H atom abstraction pathway leading to furfural formation was of minor importance, <1%. The yield of organic nitrates and dinitrates formed was 26% supported by experiments and quantum mechanical calculations. The formation of highly oxygenated molecules (HOMs) were observed in the particulate phase. The yield of secondary organic aerosols formed was below 2%.
Products and yields for the NO3 radical initiated atmospheric degradation of 2-methylfuran (2-MF, CH3–C4H3O)
https://orcid.org/0000-0002-5643-5148
https://orcid.org/0000-0002-5669-0165
https://orcid.org/0000-0003-4411-2904
https://orcid.org/0000-0002-8299-4306
https://orcid.org/0000-0002-0125-581X
https://orcid.org/0000-0002-9049-0319
Abstract Furans represent a group of oxygenated, heterocyclic, organic compounds that are emitted during biomass burning (BB). Notably, these compounds undergo rapid oxidation, a process observed both during the day and at night. Methylated furanoids comprise a large fraction of total furan emissions. Recent kinetic studies suggest that the NO3 initiated degradation of methylated furans is the dominant reaction pathway during nighttime, and with significant contribution on daytime. The aim of this study is to investigate the degradation products and the reaction mechanism of 2-methylfuran (2-MF) reaction with NO3 radicals using two atmospheric simulation chambers: CHARME (Chamber for the Atmospheric Reactivity and the Metrology of the Environment, Dunkerque, France) and THALAMOS (Thermally Regulated Atmospheric Simulation Chamber, Douai, France). All experiments were carried out at ambient temperature, (294 ± 2) K and atmospheric pressure (760 Torr, zero air). Oxidation products were qualitatively and quantitatively characterized using multiple, complementary detection techniques. Gas phase major and minor products were detected via offline GC-EI-MS (Gas chromatography - Electronic Impact - Mass Spectrometry) after trapping the gas-phase mixture on different adsorption media. PTR-ToF-MS (Proton Transfer Mass Reaction – Time of Flight – Mass Spectrometer, CHARME) and SIFT-MS (Selected Ion Flow Tube Mass Spectrometry, THALAMOS) were used on-line to monitor reactants and major products and to determine the end-product yields. 4-Oxo-2-pentenal (H(O)CCHCHC(O)CH3), and 2(5H)-furanone, 5-methyl, 5-nitrooxy ((CH3)C(ONO2)(C4H2O2)) were detected as major products with yields (62 ± 15) % and (26 ± 3) %, respectively. In-situ FTIR (Fourier Transform Infrared Spectroscopy) along with quantum mechanical molecular calculations revealed that organic nitrates and dinitrates were also formed. Secondary organic aerosols (SOA) formation, in the presence of ammonium sulfate seed, was also monitored using SMPS-CPC (Scanning Mobility Particle Sizer-Condensation Particle Counter). The size distribution and the mass concentration of the particles were determined for 2-MF concentration between 80 and 531 ppbv leading to SOA yields 1.03–2.23 %. Finally, SOA formed were chemically characterized using ESI-LC-QToF-MS/MS (Electrospray Ionization Liquid Chromatography – Quadrupole - Time of Flight - Tandem Mass Spectrometer) revealing that oligomers, e.g. highly oxygenated molecules (HOMs) were also formed. Based on our experimental observations, a reaction mechanism is proposed. NO3 radical is predominately added to the C2/C5 double bond of 2-MF, while the H atom abstraction channel, is estimated to be of minor importance. Results from this work provide detailed information about the NO3 radical initiated oxidation of 2-MF that can be used in chemical transport models to simulate the ageing processes occurring in biomass burning plumes.
Highlights 4-oxo-2-pentanal was the major product formed from NO3 addition to 2-MF with a yield of 61.5 ± 14.7 %. The H atom abstraction pathway leading to furfural formation was of minor importance, <1%. The yield of organic nitrates and dinitrates formed was 26% supported by experiments and quantum mechanical calculations. The formation of highly oxygenated molecules (HOMs) were observed in the particulate phase. The yield of secondary organic aerosols formed was below 2%.
Products and yields for the NO3 radical initiated atmospheric degradation of 2-methylfuran (2-MF, CH3–C4H3O)
Al Ali, Fatima (author) / Cœur, Cécile (author) / Houzel, Nicolas (author) / Genevray, Paul (author) / Cazier, Fabrice (author) / Cuisset, Arnaud (author) / Papadimitriou, Vassileios C. (author) / Tomas, Alexandre (author) / Romanias, Manolis N. (author)
Atmospheric Environment ; 319
2023-12-02
Article (Journal)
Electronic Resource
English