氢解
化学
催化作用
甘油
选择性
镍
无机化学
有机化学
作者
Chandrashekhar V. Rode,Rajan Pandya,Rasika B. Mane
标识
DOI:10.1002/ajoc.202100704
摘要
Abstract Autogenous glycerol hydrogenolysis to 1,2‐propanediol by aqueous phase reforming (APR) was investigated over supported nickel catalysts. Effect of reduction temperature on physico‐chemical properties of catalysts played a significant role in tuning conversion and product selectivities. The formation of nickel aluminate (NiAl 2 O 4 ) spinel phase during catalyst reduction led to rearrangement of Ni species to obtain small and stable Ni particles. The catalyst activation temperature alters the extent of reduction of multivalent Ni species (Ni 0 , Ni +2/+3 ) which facilitated glycerol dehydration and hydrogenation while suppressing C−C cleavage and thus avoiding undesirable side products. Additionally, presence of moderate BrØnsted/Lewis acid ratio of the catalyst promoted higher 1,2‐PDO selectivity. In‐situ glycerol hydrogenolysis involves glycerol dehydration to acetol with simultaneous reforming to H 2 and CO 2 and this hydrogen converts acetol to 1,2‐PDO.
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