化学
双金属片
催化作用
粘酸
选择性
己二酸
透射电子显微镜
甲酸
分子
聚合物
多相催化
化学工程
有机化学
化学合成
化学反应
协同催化
绿色化学
组合化学
钯
扫描电子显微镜
高分子化学
光化学
双金属
无机化学
双功能
配体(生物化学)
作者
Ilaria Barlocco,Xiaohui Huang,Di Wang,Francesca Tessore,Sofia Capelli,Carlo Pirola,Laura Prati,Andrea Villa,Marta Stucchi
标识
DOI:10.1002/ejic.202500537
摘要
Biomass‐derived muconic acid (MA) is a promising platform molecule for the sustainable production of a range of value‐added chemicals, including adipic acid (AdA), hexenedioic acids, and muconolactone (Mlac). AdA is a key precursor in the synthesis of nylon 6,6. A renewable route to AdA via MA hydrogenation offers a greener alternative, aligning with the goals of circular and carbon‐neutral chemical manufacturing. In this work, we explore the selective hydrogenation of MA over Pd x Cu y /TiO 2 catalysts, focusing on the tunable production of three distinct compounds of industrial relevance. Pd‐rich catalysts exhibit high activity and selectivity toward full hydrogenation to AdA. With increasing Cu content, a shift in selectivity is observed, favoring the formation of 2‐ and 3‐hexenedioic acids, which are of interest for modifying polymer properties. At high Cu loading, the reaction pathway leads predominantly to Mlac, a versatile intermediate for fine chemical synthesis. Catalyst structure–function relationships were investigated using transmission electron microscopy and high‐angle annular dark‐field scanning transmission electron microscopy, revealing that the nature and distribution of Cu relative to Pd significantly influence the reaction selectivity. These findings demonstrate the potential of catalyst engineering to steer biomass‐derived feedstocks toward multiple high‐value chemical products, offering a flexible and sustainable platform for green chemical synthesis.
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