Author/Authors :
Wang، نويسنده , , Yu-Gao and Wei، نويسنده , , Xian-Yong and Liu، نويسنده , , Jing and Li، نويسنده , , Zhan-Ku and Wang، نويسنده , , Shou-Ze and Wang، نويسنده , , Ying-Hua and Kang، نويسنده , , Guo-Jun and Fan، نويسنده , , Xing and Zong، نويسنده , , Zhi-Min، نويسنده ,
Abstract :
A series of coal-related model compounds (CRMCs) were analyzed with an atmospheric solids analysis probe/time of flight-mass spectrometer (ASAP/TOF-MS). Pyrene, anthracene, and phenanthrene were ionized to generate stable radical molecular cation (M+•) and protonated molecular cation ([M+H]+). The ratio of [M+H]+ to M+• is positively related to the superdelocalizability of the condensed arenes (CAs), indicating that the CA ionizations rely on the intrinsic reactivities of the CA to a certain extent. Fragmental ions were formed via cleavage and/or rearrangement of [M+H]+/M+• from bridged bond-containing CRMCs during ASAP/TOF-MS analysis. Their formation is related to drying gas temperature and the stabilities of fragmental species. Using ASAP/TOF-MS, a reaction mixture from di(1-naphthyl)methane hydrocracking was directly and rapidly analyzed, and as coal derivates succinic acid and polymethyl benzenepolycarboxylates were identified in the water-soluble portions from a coal and char oxidation within short time, respectively. The fact suggests that ASAP/TOF-MS could be used for real-time monitoring organic mixtures during the reactions of CRMCs and coal conversion.
Keywords :
Atmospheric solids analysis probe , Coal-related model compounds , Coal derivates , Bridged bonds , Ionization pathway