On the Mechanism of Soot Nucleation. III. The Fate and Facility of the E-Bridge.

Rotationally excited dimerization of aromatic moieties is a mechanism proposed recently to explain the initial steps of soot particle inception in combustion and pyrolysis of hydrocarbons. The product of such dimerization, termed E-bridge, is an angled molecular structure composed of two aromatic rings sharing a common bond. The present study explores the immediate fate of the E-bridge.

Transformation of an Embedded Five-Membered Ring in Polycyclic Aromatic Hydrocarbons via the Hydrogen-Abstraction-Acetylene-Addition Mechanism: A Theoretical Study.

Five-membered rings are constituents of many polycyclic aromatic hydrocarbons (PAHs), and their presence on the edges of large PAHs has been repeatedly observed experimentally. However, modern kinetic combustion models often do not consider the growth of PAHs through the transformation of the five-membered rings. In connection with the above, we carried out a theoretical study of the mechanism of hydrogen-abstraction-acetylene-addition (HACA) transformation of an embedded five-membered ring on the armchair PAH edge to a six-membered ring, considering cyclopenta[,,]phenanthrene (4,5-methylenephenanthrene) as a prototype system for this process.

On the mechanism of soot nucleation. II. E-bridge formation at the PAH bay.

A recently proposed mechanism of soot nucleation (M. Frenklach and A. M.

Mechanism and rate constants of the CH + CH CO reactions in triplet and singlet states: A theoretical study.

Ab initio and density functional CCSD(T)-F12/cc-pVQZ-f12//B2PLYPD3/6-311G** calculations have been performed to unravel the reaction mechanism of triplet and singlet methylene CH with ketene CH CO. The computed potential energy diagrams and molecular properties have been then utilized in Rice-Ramsperger-Kassel-Marcus-Master Equation (RRKM-ME) calculations of the reaction rate constants and product branching ratios combined with the use of nonadiabatic transition state theory for spin-forbidden triplet-singlet isomerization. The results indicate that the most important channels of the reaction of ketene with triplet methylene lead to the formation of the HCCO + CH and C H + CO products, where the former channel is preferable at higher temperatures from 1000 K and above.