Abstract
The rate coefficients and mechanisms of the reaction of Cl-atoms with a series of unsaturated hydrocarbons under atmospheric conditions were studied. It was observed the product yielded from both trans-2-butene and 1-butene were found to be oxygen dependent. The results showed that the variation of the product yielded with O2 in the case of 1-butene resulted from competitive reaction pathways for the two β-chlorobutoxy radicals involved in the oxidation.
| Original language | English |
|---|---|
| Pages (from-to) | 334-353 |
| Number of pages | 20 |
| Journal | International Journal of Chemical Kinetics |
| Volume | 35 |
| Issue number | 8 |
| DOIs | |
| State | Published - Aug 2003 |