Rice James W, Fu Jinxia, Suuberg Eric M
Brown University School of Engineering, 182 Hope Street Box D, Providence, RI USA 02912.
Ind Eng Chem Res. 2011 Mar 16;50(6):3613-3620. doi: 10.1021/ie102325d.
This study explores the solid/liquid phase behavior of mixtures of polycyclic aromatic hydrocarbons (PAHs), exploring the transition from non-ideal solid mixtures to a relatively ideal liquid behavior characteristic of "tars". PAH mixtures have been studied using differential scanning calorimetry, melting point analysis and Knudsen effusion. Mixtures of anthracene, pyrene and fluoranthene show behavior that is consistent with other binary PAH mixtures; that is, the initially solid mixture exhibits a significant melting point depression, relative to the pure components, and in a certain range of composition, solid azeotrope behavior on vaporization. As the number of distinct PAH species is increased (by adding in benzo[a]pyrene, phenanthrene, fluorene and chrysene) this behavior gradually gives way to liquid phase character at even room temperature, and the vaporization behavior approaches that crudely predictable from ideal mixture theory.
本研究探索了多环芳烃(PAHs)混合物的固/液相行为,研究了从非理想固体混合物到具有“焦油”特征的相对理想液体行为的转变。使用差示扫描量热法、熔点分析和克努森 effusion 法对 PAH 混合物进行了研究。蒽、芘和荧蒽的混合物表现出与其他二元 PAH 混合物一致的行为;也就是说,相对于纯组分,初始固体混合物表现出显著的熔点降低,并且在一定组成范围内,汽化时具有固体共沸物行为。随着不同 PAH 种类数量的增加(通过添加苯并[a]芘、菲、芴和 Chrysene),这种行为在室温下甚至逐渐让位于液相特征,并且汽化行为接近理想混合物理论粗略预测的行为。