Butadiyne (diacetylene, HC4H) is produced during combustions, and has been quantified in different flames as well as a biomass burning emission. Its reaction with the hydroxyl radical, HO(2 Π3/2), under combustion conditions, was investigated in a thorough RRKM study by J. P. Senosiain, S. J. Klippenstein, and J. A. Miller (Proc. Combust. Inst. 2007, 31, 185−192). The present density functional theory (DFT) study focuses on the mechanism of further oxidation by O 2(3Σ− g ). The DFT(M06-2X)/cc-pVTZ reaction energy hypersurface for the system C4H2/HO /O2 is studied to define a variety of reaction pathways, and the relevant thermochemistry for temperatures ranging from 200 to 2500 K is assessed, thus encompassing combustive, postcombustive, and tropospheric conditions. Energies are then recomputed at the coupled cluster level [CCSD(T)/cc-pVTZ], and combined with the DFT thermochemistry. Finally, the role of the different reaction channels is assessed by RRKM-ME simulations in the same temperature range for P = 1 atm, to comprise the situation of emission in the troposphere and those pertaining to different flames. This shows that, when considering HO addition to the triple bond, dioxygen takes part in C4H2 oxidation with higher efficiency at lower temperatures, whereas, as T rises, the O2 adducts are inclined to redissociate: for instance, a 50% redissociation is estimated at T = 1800 K. For 200 < T < 1100 K, two polycarbonyl products (CHO.CO.CCHand CHO.CO.CHCO) and two fragmentation products (HCOOH plus OC−CCH) are the main species predicted as products from the addition channel (fragmentation is entropy-favored by higher T values). However, at higher temperatures, an initial H abstraction by HO can give the butadiynyl radical (HC4 ) as the starting point for subsequent dioxygen intervention. Then, new pathways opened by O 2 addition become accessible and bring about fragmentations mainly to HC3 + CO2 and also to HC3O + CO.
Combustive, Postcombustive, and Tropospheric Butadiyne Oxidation by O2, Following Initial HO Attack. Theoretical Study
MARANZANA, Andrea;GHIGO, Giovanni;TONACHINI, Glauco
2015-01-01
Abstract
Butadiyne (diacetylene, HC4H) is produced during combustions, and has been quantified in different flames as well as a biomass burning emission. Its reaction with the hydroxyl radical, HO(2 Π3/2), under combustion conditions, was investigated in a thorough RRKM study by J. P. Senosiain, S. J. Klippenstein, and J. A. Miller (Proc. Combust. Inst. 2007, 31, 185−192). The present density functional theory (DFT) study focuses on the mechanism of further oxidation by O 2(3Σ− g ). The DFT(M06-2X)/cc-pVTZ reaction energy hypersurface for the system C4H2/HO /O2 is studied to define a variety of reaction pathways, and the relevant thermochemistry for temperatures ranging from 200 to 2500 K is assessed, thus encompassing combustive, postcombustive, and tropospheric conditions. Energies are then recomputed at the coupled cluster level [CCSD(T)/cc-pVTZ], and combined with the DFT thermochemistry. Finally, the role of the different reaction channels is assessed by RRKM-ME simulations in the same temperature range for P = 1 atm, to comprise the situation of emission in the troposphere and those pertaining to different flames. This shows that, when considering HO addition to the triple bond, dioxygen takes part in C4H2 oxidation with higher efficiency at lower temperatures, whereas, as T rises, the O2 adducts are inclined to redissociate: for instance, a 50% redissociation is estimated at T = 1800 K. For 200 < T < 1100 K, two polycarbonyl products (CHO.CO.CCHand CHO.CO.CHCO) and two fragmentation products (HCOOH plus OC−CCH) are the main species predicted as products from the addition channel (fragmentation is entropy-favored by higher T values). However, at higher temperatures, an initial H abstraction by HO can give the butadiynyl radical (HC4 ) as the starting point for subsequent dioxygen intervention. Then, new pathways opened by O 2 addition become accessible and bring about fragmentations mainly to HC3 + CO2 and also to HC3O + CO.File | Dimensione | Formato | |
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