期刊
FUEL PROCESSING TECHNOLOGY
卷 224, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.fuproc.2021.107025
关键词
Sulfur-containing compounds; Residual oils; FT-ICR mass spectrometry; Sulfur removal
The study revealed that volatile PASHs are present in lower quantities in the products of residue hydrotreating process, while the major refractory sulfur compounds are identified as S1 class compounds. Furthermore, collision-induced dissociation experiments showed that the key refractory PASHs have a structure of alkyl (C2)-substituted DBT.
Molecular-level structures and distribution of refractory polycyclic aromatic sulfur heterocycles (PASHs) during residue hydrotreating process (RHT) are investigated. A prior atmospheric pressure photoionization (APPI) FT-ICR MS was used to obtain the distribution of refractory PASHs. Then the key refractory PASHs were further dissociated by collision-induced dissociation (CID) to identify the isomers and gain their fragment ions. During deep hydrodesulfurization (HDS), S1 class compounds detected in the RHT products was identified as the major refractory sulfur compounds. Moreover, an increase in the aromatic structure of S1 class species is present during RHT. The key refractory PASHs are these with DBE = 9-12, which also determine HDS depth during RHT process. From the CID experiments, as indicated by an increase of abundance of fragmentation of alkyl(C1-C4)-substituted DBT, alkyl(C2)-substituted DBT in particular, these key refractory PASHs have a structure of alkyl (C2)-substituted DBT, such as 4,6-DMDBT. In addition, the molecular chemical formula and molecular struc-ture for these key refractory PASHs were proposed, shedding a light on the development of industrial HDS catalysts and optimization of RHT process
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