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生物炭负载钌催化剂对 5-羟甲基糠醛选择性加氢制备 1-羟基-2,5-己二酮。

Selective Hydrogenation of 5-Hydroxymethylfurfural to 1-Hydroxy-2,5-hexanedione by Biochar-Supported Ru Catalysts.

机构信息

CATMAT Lab, Department of Molecular Sciences and Nanosystems, Ca' Foscari University of Venice and INSTM RUVe, via Torino 155, 30172, Venezia Mestre, Italy.

Department of Physics and Geology, University of Perugia, Via Pascoli, 06123, Perugia, Italy.

出版信息

ChemSusChem. 2022 Jul 7;15(13):e202200437. doi: 10.1002/cssc.202200437. Epub 2022 May 18.

Abstract

The development of sustainable and efficient catalysts -namely Ru supported on activated biochars- is carried out for the selective hydrogenation of 5-hydroxymethylfurfural (HMF) to 1-hydroxy-2,5-hexanedione (HHD). Activated biochars obtained from pyrolysis and steam-based physical activation of two different biomasses from animal (leather tannery waste; A ) and vegetal (hazelnut shells; A ) origins show completely different chemical, textural, and morphological properties. Compared to A , after impregnation with 0.5 wt % Ru, A , with inner micro-mesochannels and cavities and higher layer stacking disorder, leads to better trapping and anchoring of Ru nanoparticles on the catalyst and a suitable Ru single crystal dispersion. This leads to a highly active Ru/A catalyst in the proposed reaction, giving more than 80 % selectivity to HHD and full HMF conversion at 100 °C with 30 bar H for 3 h. Ru/A also shows promising performance compared to a commercial Ru/C catalyst.

摘要

针对 5-羟甲基糠醛(HMF)选择性加氢制备 1-羟基-2,5-己二酮(HHD),开发了可持续且高效的催化剂——负载在活化生物炭上的 Ru。通过热解和蒸汽物理活化两种不同生物质(动物来源的制革废料;A )和植物来源的榛子壳;A )得到的活化生物炭具有完全不同的化学、结构和形态特性。与 A 相比,在浸渍 0.5wt%Ru 后,A 具有内微孔道和空腔以及更高的层堆积无序性,这有利于 Ru 纳米颗粒在催化剂上的捕获和锚定,并实现合适的 Ru 单晶体分散。这使得 Ru/A 催化剂在该反应中具有很高的活性,在 100°C、30 bar H 2 下反应 3 h 时,HHD 的选择性超过 80%,HMF 转化率达到 100%。与商业 Ru/C 催化剂相比,Ru/A 也表现出了良好的性能。

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