TY - JOUR
T1 - Extensive Theoretical Study of the Thermochemical Properties of Unsaturated Hydrocarbons and Allylic and Super-Allylic Radicals: The Development and Optimization of Group Additivity Values
AU - Li, Yang
AU - Curran, Henry J.
N1 - Generated from Scopus record by KAUST IRTS on 2023-10-22
PY - 2018/5/24
Y1 - 2018/5/24
N2 - In this study, the thermochemistry of C2-C7 unsaturated hydrocarbons (22 alkene and 6 diene molecules) and 16 allylic and 5 super-allylic radicals is determined using high-accuracy quantum chemistry calculations. In addition, the group additivity values (GAVs) of a total of 19 relevant groups are systematically optimized on the basis of the calculated thermochemistry of species clusters. The M06-2X method using the 6-311++G(d,p) basis set is used for the geometry optimizations, vibrational frequency calculations, and internal rotation scans for lower-frequency modes. The composite compound methods, CBS-APNO, G3, and G4, are utilized to derive the average atomization formation enthalpies. The entropy and temperature-dependent heat capacity values of all species are calculated using statistical thermodynamics in MultiWell. These results are in good agreement with literature data. A GAVs optimization is performed on the basis of a statistical analysis: a Bland-Altman plot, which is employed to visualize the agreement between the results from the quantum chemical calculations and the GA method. It is found that the 298 K entropies of the CD/C2, C/CD2/H2, C/C/CD2/H, and C/CD3/H groups disagree by more than 5 cal K-1 mol-1 compared to existing values, while the values for the ALLYLS and ALLYLT radical groups also differ by ∼2.4 and 4.1 cal K-1 mol-1, respectively. The 298 K formation enthalpies of the C/CD2/H2, C/C/CD2/H, C/CD3/H, and ALLYLT groups are modified by more than 1 kcal mol-1, compared to existing values. The updated GAVs can be used with increased confidence to estimate the thermochemical properties of combustion-relevant unsaturated hydrocarbon molecules and their radicals which are critical for the development of accurate chemical kinetic models describing the pyrolysis and oxidation of hydrocarbon and oxygenated hydrocarbon fuels.
AB - In this study, the thermochemistry of C2-C7 unsaturated hydrocarbons (22 alkene and 6 diene molecules) and 16 allylic and 5 super-allylic radicals is determined using high-accuracy quantum chemistry calculations. In addition, the group additivity values (GAVs) of a total of 19 relevant groups are systematically optimized on the basis of the calculated thermochemistry of species clusters. The M06-2X method using the 6-311++G(d,p) basis set is used for the geometry optimizations, vibrational frequency calculations, and internal rotation scans for lower-frequency modes. The composite compound methods, CBS-APNO, G3, and G4, are utilized to derive the average atomization formation enthalpies. The entropy and temperature-dependent heat capacity values of all species are calculated using statistical thermodynamics in MultiWell. These results are in good agreement with literature data. A GAVs optimization is performed on the basis of a statistical analysis: a Bland-Altman plot, which is employed to visualize the agreement between the results from the quantum chemical calculations and the GA method. It is found that the 298 K entropies of the CD/C2, C/CD2/H2, C/C/CD2/H, and C/CD3/H groups disagree by more than 5 cal K-1 mol-1 compared to existing values, while the values for the ALLYLS and ALLYLT radical groups also differ by ∼2.4 and 4.1 cal K-1 mol-1, respectively. The 298 K formation enthalpies of the C/CD2/H2, C/C/CD2/H, C/CD3/H, and ALLYLT groups are modified by more than 1 kcal mol-1, compared to existing values. The updated GAVs can be used with increased confidence to estimate the thermochemical properties of combustion-relevant unsaturated hydrocarbon molecules and their radicals which are critical for the development of accurate chemical kinetic models describing the pyrolysis and oxidation of hydrocarbon and oxygenated hydrocarbon fuels.
UR - https://pubs.acs.org/doi/10.1021/acs.jpca.8b02912
UR - http://www.scopus.com/inward/record.url?scp=85046958794&partnerID=8YFLogxK
U2 - 10.1021/acs.jpca.8b02912
DO - 10.1021/acs.jpca.8b02912
M3 - Article
SN - 1520-5215
VL - 122
SP - 4736
EP - 4749
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 20
ER -