Bifunctional Rh/Al-SBA-15 catalysed cascade hydroformylation and hydroxyalkylation of alkenes to fuel precursors

被引:0
|
作者
Ravi, Krishnan [1 ,2 ,3 ]
Kachgunde, Hanuman [1 ,2 ]
Dasireddy, Venkata D. B. C. [4 ]
Mensah, Jim [4 ]
Lee, Adam F. [4 ]
Biradar, Ankush V. [1 ,2 ]
Wilson, Karen [4 ]
机构
[1] Cent Salt & Marine Chem Res Inst, CSIR, Inorgan Mat & Catalysis Div, GB Marg, Bhavnagar 364002, Gujarat, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[3] RMIT Univ, Sch Sci, 124 La Trobe St, Melbourne, Vic 3000, Australia
[4] Griffith Univ, Sch Environm & Sci, Ctr Catalysis & Clean Energy, Southport, Qld 4222, Australia
基金
澳大利亚研究理事会;
关键词
SINGLE-ATOM CATALYST; HETEROGENEOUS HYDROFORMYLATION; GRAPHENE OXIDE; RANGE ALKANES; RHODIUM OXIDE; FATTY-ACIDS; DIESEL; 2-METHYLFURAN; CARBON; DECARBOXYLATION;
D O I
10.1039/d5cy00171d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Decarbonisation of hard-to-abate liquid transport fuels, notably used in the aviation and shipping sectors, requires new catalytic routes to valorise waste feedstocks. Here we report a bifunctional Rh/Al-SBA-15 catalyst for the one-pot, two step cascade hydroformylation of 1-alkenes with CO/H2 to form linear and branched aldehydes, and their subsequent hydroxyalkylation (HAA) with 2-methylfuran to form oxygenated jet fuel precursors. A strong synergy between Rh and Al-SBA-15 is observed for hydroformylation, with the bifunctional catalyst significantly more active than Rh/SBA-15 for the first step of the cascade. Superior yields of desired HAA products are observed over Rh/Al-SBA-15 relative to a physical mixture of Rh/SBA-15 and Al-SBA-15. Under syngas (CO/H2) at 30 bar and 80 degrees C, alkenes undergo Rh catalysed hydroformylation to aldehydes, and in a subsequent step under N2, HAA of aldehydes over the solid acid sites of Al-SBA-15 gives an overall similar to 60% yield of fuel range precursors.
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页数:8
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