Abstract

The boron trifluoride complex catalyst can effectively facilitate the development of anisotropic structures in FCC decant oil (FCC-DO) through cationic polymerization reaction. However, the fractions of FCC-DO with different boiling points possess different molecular compositions and aromatic nuclei configurations. In this study, FCC-DO is separated into light fraction, middle fraction, and heavy fraction by vacuum distillation. The different carbonization reaction pathways and reactivity were systematically investigated for three narrow fractions with no or 5 wt% addition of boron trifluoride complex catalyst. The results show that the heavy fraction is dominated by 4 and 5 plus ring aromatics with short side chains and methylene-bridged bonds. The catalyst showed excellent catalytic activity for the heavy fraction, the resulting product (MP-HF-5) possessing a softening point of 307 °C and 3.06 wt% methylene-bridged hydrogen at 95.3 wt% mesophase content. However, the catalyst slightly facilitated the development of anisotropic structures in the middle fraction (rich in 3 and 4 rings aromatics with naphthenic structures), which provided mesogen molecules during the FCC-DO carbonization reaction. Finally, the 1 ∼ 3 ring aromatics with long alkyl side chains are mainly present in the light fractions. The catalyst did not show obvious catalytic activity for the light fraction, in contrast, the oxygen-containing functional groups in the catalyst reacted with the aromatic molecule to form a disordered oxidative cross-linked structure, resulting in an almost completely isotropic structure of MP-LF-5.

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