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Mild hydrogenation pretreatment of FCC slurry oil for high-value-added utilization: Exploitable high-boiling components and carbonization discrepancy

碳化 蒸馏 沸腾 化学工程 热解 产量(工程) 泥浆 燃烧热 有机化学 连续蒸馏 化学 材料科学 碳纤维 碳氢化合物 减压蒸馏 蒸汽蒸馏 燃烧 冶金 复合材料 吸附 工程类 复合数
作者
Shouhui Jiao,Zeliang Li,Hu Jingxin,Bernard Wiafe Biney,Feng Wang,He Liu,Kun Chen,Aijun Guo,Lanyi Sun,Zongxian Wang
出处
期刊:Journal of Analytical and Applied Pyrolysis [Elsevier BV]
卷期号:161: 105411-105411 被引量:4
标识
DOI:10.1016/j.jaap.2021.105411
摘要

In response to the enormous market demand for high-value-added carbonaceous materials and the urgent requirement of energy conservation and emission reduction, FCC slurry oil (SO) has drawn widespread attention in the preparation of these kinds of carbonaceous materials due to its abundant aromatic hydrocarbon contents. Distillation can be utilized as a pretreatment to efficiently remove the quinoline insoluble and other undesirable components in SO before carbonization. However, the distillate depth and yield are greatly restricted by the conspicuous coking phenomenon during thermal effect in the distillation. Mild hydrogenation coupled with distillation were adopted as the pretreatments before carbonization and effects of the hydrogenation on the distillation process were studied. Besides, transform patterns for the properties of sub-fractions in specimen before and after hydrogenation and resulted variations in carbonization performances were then systematically analyzed. Through hydrogenation, the distillation depth of hydrotreated SO (HSO) could be greatly improved to 530 °C with no significant coking phenomenon and the distillation yield was increased dramatically (from 38.4 wt% to 68.1 wt%). Especially, partial super high-boiling (above 530 °C) components in SO could be transformed into naphthenoaromatic structures by hydrogenation and acquired through distillation for further utilizations. Using anthracene as chemical probe, the hydrogen-donating abilities (HDAs) of specimens were detected, and results indicated the amounts of transferable hydrogen in HSO low-boiling and high-boiling sub-fractions were greatly increased compared with that of SO, which would provide the specimen with stronger stability in the thermal treatment and restrain the rapid coking. The carbonization performance varied with the properties of sub-fractions and a section of high-boiling components in SO was discovered to be exploitable through hydrogenation and demonstrated to be beneficial in the preparation of needle coke.
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