Energy-dense sustainable aviation fuel-range hydrocarbons from cyclohexanone as a biomass-derived feedstock via sequential catalytic aldol condensation and hydrodeoxygenation

加氢脱氧 环己酮 原材料 催化作用 生物量(生态学) 航空燃料 羟醛缩合 有机化学 喷气燃料 航程(航空) 航空 化学 航空生物燃料 废物管理 材料科学 工程类 航空航天工程 选择性 海洋学 生物柴油 复合材料 地质学
作者
Abarasi Hart,Jude A. Onwudili,Eyüp Yıldırır,Seyed Emad Hashemnezhad
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:509: 161494-161494 被引量:15
标识
DOI:10.1016/j.cej.2025.161494
摘要

• Biomass-derivable cyclohexanone as a feedstock for high-density aviation fuel. • NbOPO 4 catalyst exhibited excellent activity for aldol condensation and alkylation. • Ni/NbOPO 4 catalyst exhibited superior hydrogenation of adducts than Pd/Al 2 O 3. • Similar results from one-pot and two-pot aldol-condensation followed hydrogenation. • Liquid compositions linked to types of coke/char deposits observed on catalyst. Climate change is the main driver for sustainable aviation fuels production as a means of decarbonising/defossilising the sector. In this work, several catalysts have been screened to produce aviation fuel (C 6 -C 16 ) component hydrocarbons from cyclohexanone, a model compound of lignin-derived bio-oils. Using a two-stage two-pot approach, up to 99 % cyclohexanone conversion was achieved in the presence of hydrogen gas. In the first stage, catalytic activities of NbOPO 4 , Al 2 O 3 , SiO 2 , and ZrO 2 -SiO 2 to promote aldol condensation were tested at 160 °C for 3 h. The NbOPO 4 exhibited the highest selectivity towards C-C coupling adducts with mainly C 12 to C 18 . In the second stage, 30 wt% Ni catalysts on three different supports and 5 wt% Pd/Al 2 O 3 were used to catalyse the hydrogenation of the first-stage adducts at 300 °C for 3 h. The 30 wt%Ni/NbOPO 4 was most effective, promoting the formation of bi-cycloalkanes, alkyl aromatic, and partially hydrogenated polyaromatic hydrocarbons. In comparison, a one-pot two-step approach was tested by sequentially reacting cyclohexanone with hydrogen gas over the two temperatures for 3 h each, using 30 wt%Ni/NbOPO 4 as catalyst. Reacting cyclohexanone with 10 wt% bio-oil samples led to significantly reduced first stage conversion, and enhanced yields of single C-C coupled oxygenates and almost no hydrocarbons in the second stage. Overall, combination of catalysts and hydrogen gas over staged reactions has effectively converted pure cyclohexanone into naphthene-rich liquid hydrocarbons and cyclohexanone/bio-oil mixed feedstocks into their oxygenated precursors. These results support potential targeted production of bio-derived sustainable alternative fuels for the defossilisation of aviation industry
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