Institut de Combustion, Aérothermique, Réactivité et Environnement (ICARE), CNRS, 45071 Orléans Cedex 2, France.
J Phys Chem A. 2010 Jan 21;114(2):942-8. doi: 10.1021/jp908862c.
The kinetics of the thermal desorption of a set of three- to five-ring polycyclic aromatic hydrocarbons (PAHs) from a laboratory-generated kerosene soot surface was studied over the temperature range 250-355 K in a low-pressure flow reactor combined with an electron-impact mass spectrometer. Two methods were used to measure the desorption rate constants: monitoring of the surface-bound PAH decays due to desorption using off-line HPLC measurements of their concentrations in soot samples and monitoring of the desorbed molecules (anthracene and phenanthtrene) in the gas phase using in situ mass spectrometric detection. The Arrhenius parameters (A factors and activation energies) for the desorption rate constants of 10 soot-bound PAHs were determined. The PAH-soot binding energies were found to be similar for PAHs with the same number of carbon atoms and to increase with increasing number of PAH carbon atoms. The experimental data are discussed in the frame of the existing theoretical gas to particle partitioning model.
在低压流动反应器中结合电子冲击质谱仪,研究了在 250-355 K 温度范围内,一组三到五环多环芳烃(PAHs)从实验室生成的煤油烟尘表面的热解吸动力学。使用两种方法测量解吸率常数:使用离线 HPLC 测量烟尘样品中 PAH 浓度,监测由于解吸而导致的表面结合 PAH 的衰减,以及使用原位质谱检测监测气相中解吸的分子(蒽和菲)。确定了 10 种烟尘结合 PAH 的解吸率常数的 Arrhenius 参数(A 因子和活化能)。发现 PAH-烟尘结合能对于具有相同碳原子数的 PAH 是相似的,并随 PAH 碳原子数的增加而增加。实验数据在现有的理论气固分配模型的框架内进行了讨论。