Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, Nanjing Forestry University, No. 159 Longpan Road, Nanjing 210037, China; International Innovation Center for Forest Chemicals and Materials, Nanjing Forestry University, No. 159 Longpan Road, Nanjing 210037, China; Key Laboratory of Pulp and Paper Science & Technology of Ministry of Education/Shandong Province, Qilu University of Technology, No. 3501 Daxue Road, Jinan 250353, China.
Key Laboratory of Pulp and Paper Science & Technology of Ministry of Education/Shandong Province, Qilu University of Technology, No. 3501 Daxue Road, Jinan 250353, China.
J Colloid Interface Sci. 2021 Nov 15;602:146-158. doi: 10.1016/j.jcis.2021.05.161. Epub 2021 May 30.
In this work, a sulfonic acid-functionalized magnetic separable solid acid (FeO@SiO-SOH) was synthesized, characterized, and tested for fructose conversion to 5-hydroxymethylfurfural (HMF). Results indicated that the prepared catalyst had a good efficacy for fructose dehydration to HMF due to its larger specific surface area, appropriate acid amount and homogeneous acid distribution. The maximum HMF yield of this work was 96.1 mol%. It was obtained at 120 °C for 1.5 h with 100 mol% fructose conversion. More importantly, the produced HMF could be further in-situ oxidized into 2,5-diformylfuran (DFF) after the replacing of the FeO@SiO-SOH with a ZnFeRuO catalyst, and the highest DFF yield of 90.2 mol% (based on initial fructose) was obtained after reaction another 8.5 h. The production of DFF from fructose through the above two consecutive steps avoids the intermediate HMF separation, which saves time and energy. In addition, both FeO@SiO-SOH and ZnFeRuO catalysts exhibited satisfied stability in the recycling experiments, which can be reused at least for five times with the HMF and DFF yield loss<5.3% and 3.3%, respectively. Finally, the plausible reaction mechanisms for fructose conversion to HMF or DFF over FeO@SiO-SOH or/and ZnFeRuO catalysts were also proposed in this work.
在这项工作中,合成了一种磺酸功能化的磁性可分离固体酸(FeO@SiO-SOH),并对其进行了表征,用于果糖转化为 5-羟甲基糠醛(HMF)的测试。结果表明,由于具有较大的比表面积、适量的酸量和均匀的酸分布,所制备的催化剂在果糖脱水制 HMF 方面具有良好的效果。该工作的最大 HMF 产率为 96.1 mol%。在 120°C 下反应 1.5 小时,果糖转化率为 100 mol%,可获得最大 HMF 产率。更重要的是,在用 ZnFeRuO 催化剂替代 FeO@SiO-SOH 后,生成的 HMF 可以进一步原位氧化为 2,5-二醛基呋喃(DFF),在反应 8.5 小时后,可获得最高的 90.2 mol%(基于初始果糖)的 DFF 产率。通过上述两个连续步骤从果糖生产 DFF 避免了 HMF 的中间分离,节省了时间和能源。此外,FeO@SiO-SOH 和 ZnFeRuO 催化剂在回收实验中均表现出良好的稳定性,可至少重复使用五次,HMF 和 DFF 的产率损失分别<5.3%和 3.3%。最后,本文还提出了在 FeO@SiO-SOH 或/和 ZnFeRuO 催化剂上果糖转化为 HMF 或 DFF 的可能反应机制。