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To obtain high yields of hydrogen, a series of ZrxPr1–xOy‐supported cobalt catalysts were synthesized by the sol‐gel method and tested in autothermal reforming (ATR) of acetic acid (HAc) derived from bio‐oil. X‐ray diffraction, nitrogen physisorption, H2‐temperature‐programmed reduction, and thermogravimetric analysis were conducted to investigate the factors affecting the activities of the catalysts. Over the Co‐Zr‐Pr‐O catalyst, a ZrxPr1–xOy solid solution was formed after calcination; meanwhile, the active component of Co0 was highly dispersed over the solid solution after reduction in hydrogen for 1 h at 700 °C. As a result, stable reactivity was recorded in the ATR process of HAc: the hydrogen yield reached 2.58 molH2molHAc-1 with near 100 % HAc conversion, while better resistance to coking was observed. [ABSTRACT FROM AUTHOR]

Autothermal reforming (ATR) of acetic acid (HOAc) is a promising and alternative route for hydrogen production from renewable resources, but catalyst deactivation caused by cobalt metal sintering and coking is a major concern in ATR. In this work, perovskite‐like catalysts of the formula SrxTi1–xCoO3±δ (x = 0, 0.2, 0.5, and 0.8) were prepared by evaporation‐induced self‐assembly and then evaluated in ATR for hydrogen production. The SrxTi1–xCoO3±δ catalysts exhibited high activity and stability as well as 100 % conversion of HOAc. Additionally, the Co particles with strong metal‐support interaction of SrTi(Co)O3 inhibited coking and agglomeration, and showed potential for hydrogen production by the ATR process. [ABSTRACT FROM AUTHOR]