Key Laboratory of Applied Surface and Colloid Chemistry (SNNU), MOE, School of Chemistry and Chemical Engineering , Shaanxi Normal University , Xi'an 710062 , P. R. China.
ACS Appl Mater Interfaces. 2019 Apr 3;11(13):12481-12491. doi: 10.1021/acsami.8b22183. Epub 2019 Mar 22.
A carbon-based solid acid, which functionalized with p-toluenesulfonic acid (TsOH), an encapsulated non-noble CuCo multifunctional heterogeneous catalyst was for the first time developed and used to catalyze the one-pot direct conversion of fructose into 2,5-dimethylfuran (2,5-DMF) without purification of 5-hydroxymethylfurfural (5-HMF) from the reaction solutions. Fructose was first transformed into intermediate 5-HMF over the outer shell carbon-based solid acid sites via dehydration, and subsequently 5-HMF was further converted to produce 2,5-DMF over the non-noble metal active sites in the core. As high as 71.1 mol % yield of 2,5-DMF was achieved in tetrahydrofuran at 220 °C and 3 MPa H for 10 h, which is higher than the yield reported for the direct conversion of fructose to 2,5-DMF. Besides, the carbon-based solid acid-coated CuCo catalyst could be reused up to five times.
一种基于碳的固体酸,功能化了对甲苯磺酸(TsOH),被封装的非贵金属 CuCo 多功能多相催化剂首次被开发出来,并用于在无需从反应溶液中纯化 5-羟甲基糠醛(5-HMF)的情况下,一锅法直接将果糖转化为 2,5-二甲基呋喃(2,5-DMF)。果糖首先在外壳碳基固体酸位上通过脱水转化为中间产物 5-HMF,然后在核中的非贵金属活性位上进一步转化生成 2,5-DMF。在四氢呋喃中,在 220°C 和 3 MPa H 的条件下反应 10 小时,2,5-DMF 的产率高达 71.1 mol%,高于直接将果糖转化为 2,5-DMF 的产率。此外,碳基固体酸包覆的 CuCo 催化剂可以重复使用多达 5 次。