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Bioresource technology · 2026

Tandem beds catalysis for aviation fuel from aqueous phase bio-oil: synergistic ketonization-HDO toward high-density cycloalkanes.

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Liu Guangxuan, Bai Xiaowei, Tursun Yalkunjan, Zhao Yunpeng, Li Jian, Dai Zhenghua

Аннотация

The decarbonization of aviation urgently demands efficient pathways to produce renewable jet fuels meeting stringent ASTM D7566 specifications. Current hydrodeoxygenation (HDO) of aqueous phase bio-oil (APBO) suffers from low carbon efficiency (<40%) and undesired short-chain hydrocarbons, due to its high acidity, water content, and low-carbon oxygenates. Herein, we propose a tandem catalytic strategy using a dual-bed system to achieve precise fraction-based conversion of APBO into jet-range hydrocarbons. The first bed, 10Ni/CeZrOx, leverages synergistic Lewis acid-base pairs and highly dispersed Ni sites to catalyze carboxylic acid ketonization, completely converting acetic acid and furans into C8+ ketones at 280°C and WHSV = 1h-1 while suppressing decarboxylation (gas yield ≤ 13.5%). The second bed, PtNiCo/β, facilitates deep hydrodeoxygenation via Pt-Ni-Co alloy-enabled H2 dissociation and Brønsted acid-mediated deoxygenation, attaining > 89.7% conversion of cyclopentanone and guaiacol under 280°C and WHSV = 2h-1. Notably, the integrated systemdemonstrates remarkable synergy: conversion of refractory oxygenates exceeds 90% (a 23-25% gain over single catalysts), C8-C16 hydrocarbon yield reaches 70.2% with > 85% carbon efficiency, and cycloalkanes selectivity attains 80.8%-ideal for high-density jet fuel-while aromatics are suppressed to 4.0%. Gas byproducts are minimized to 1.6% (>80% reduction), and coke formation is markedly lowered (5.1% weight loss shifted to 400-700°C). Operated under mild conditions (280°C, 3 MPa H2), this approach offers a scalable and carbon-conserving route to sustainable aviation fuel (SAF), overcoming key limitations of conventional APBO upgrading.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты