Abstract

Hydrocracking of hydrotreated Israeli shale oil and its atmospheric residue was studied at 50 atm hydrogen pressure, LHSV 0.5–4.4 h −1, temperature 350°C and V H2 1500 Nl/l in a fixed bed reactor pilot plant with two Ni–Mo–zeolite catalysts based on mono-(HY+Al 2O 3) and bizeolite (HY+H–ZSM–5+Al 2O 3) supports. Desulfurization and denitrogenation conversion of the feedstock was higher than 99.7% (sulfur content 134 ppm, nitrogen content 4.4 ppm) and it comprised 14 vol.% atmospheric residue boiling out at 360°C+. Hydrocracking of the whole hydrotreated shale oil yielded full conversion of atmospheric residue at LHSV=2.75 h −1 with monozeolite catalyst (A) and at LHSV=3.5 h −1 with biozeolite catalyst (B). The yield of liquid fuel at these conditions was 87.6 wt% with catalyst A versus 82.4 wt% with catalyst B. The contents of light naphtha (<100°C), heavy naphtha (<200°C) and jet fuel (160–280°C) in the liquid product were 10–15% higher with catalyst B compared with A. Hydrocracking at full residue conversion produced shifts of the hydrocarbon distributions to lighter molecules inside the hydrocarbon groups, decreased n-paraffins concentrations by isomerization and splitting to C 5-. Hydrocracking of the atmospheric residue with catalyst A yielded full conversion into 360°C-products at LHSV=0.5 h −1. The only liquid product obtained in this case at 72.3% yield was naphtha with distillation patterns corresponding to gasoline specification. The nitrogen content in the liquid hydrocracking products at full conversion of atmospheric residue fraction of the shale oil was <1 ppm and the sulfur content <15 ppm.

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