Evaluation of atmospheric solids analysis probe mass spectrometry for the analysis of coal-related model compounds

被引:37
|
作者
Wang, Shou-Ze [1 ]
Fan, Xing [1 ]
Zheng, Ai-Li [1 ]
Wang, Yu-Gao [1 ]
Dou, You-Quan [1 ]
Wei, Xian-Yong [1 ]
Zhao, Yun-Peng [1 ]
Wang, Rui-Yu [2 ]
Zong, Zhi-Min [1 ]
Zhao, Wei [1 ]
机构
[1] China Univ Min & Technol, Sch Chem Engn, Xuzhou 221116, Jiangsu, Peoples R China
[2] China Univ Min & Technol, Low Carbon Energy Inst, Xuzhou 221116, Jiangsu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Atmospheric solids analysis probe; Ambient ionization; Mass spectrometry; Coal-related model compounds; IDENTIFICATION; PRESSURE;
D O I
10.1016/j.fuel.2013.09.010
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
An atmospheric pressure solids analysis probe (ASAP) was mounted on a commercial atmospheric pressure chemical ionization source with simple modifications. A series of coal-related model compounds (CRMCs) were analyzed using a time-of-flight mass spectrometry equipped with the ASAP ion source. The ionization mechanism and fragmentation pathways for CRMCs were investigated. The temperature of desolvation gas played a crucial role to the response signal, especially for the association behavior of CRMCs. With a fixed desolvation gas temperature, radical cation (M+.) or protonated molecule ([M+H](+)) was the predominant ion generated by corona discharge of ASAP depending on the temperature of drying gas. Fragment ions were produced from bridged bond breaking of the precursor ions, rearrangement reactions and loss of neutral fragments such as H2O, CH2O, CO, CH3OH and CO2. The fragmentation pathways can offer a better understanding of fundamental mechanism of chemical bond breaking for coal derivatives and further explore the application of coal directional conversion. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:556 / 563
页数:8
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