Sulfur compounds in deep hydrodesulfurization
(HDS)-derived diesels
were effectively separated into thiophenic and sulfidic fractions
using the methylation/demethylation method and characterized by gas
chromatography–mass spectrometry (GC–MS) and GC–sulfur
chemiluminescence detector (SCD). Sulfidic fractions account for over
15 wt % of total residual sulfur, in which a series of refractory
cyclic sulfidic compounds, 1,1-dimethylhexahydrodibenzothiophenes
(1,1-DMH<sub>6</sub>DBTs) and 1,9b-dimethylhexahydrodibenzothiophenes
(1,9b-DMH<sub>6</sub>DBTs), were found in the diesels, and larger
molecular weight homologues were identified. Some homologue series
of C<sub>1</sub>–C<sub>4</sub> alkyl-substituted thiaadamantanes
were detected in the HDS diesel. These cyclic sulfidic components
are refractory to deep HDS, which require more prudent catalysis and
reaction systems to achieve ultralow-sulfur diesel (ULSD) production