Xue Haonan, Xia Haihong, Li Hui, Ge Fei, Xu Wenlin, Yang Xiaohui, Zhou Minghao
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, China.
Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China.
Int J Biol Macromol. 2025 Feb;289:138874. doi: 10.1016/j.ijbiomac.2024.138874. Epub 2024 Dec 17.
The conversion of abundant lignin was of great significance for the utilization of biomass resources. In this study, lignin sulfonate (LS) was selected as a carbon-based support, which was successfully introduced into the NiCo-MOF structure. A series of lignin and MOF hybrid catalysts (NiCo-MOF-LS) with varying metal ratios of Ni and Co were synthesized via the hydrothermal method. Subsequently, the catalytic hydrogenolysis of lignin-derived dimers was conducted over a range of NiCo-MOF-LS, with the impact of calcination temperature and lignin addition in the catalysts taken into account. The selective conversion of benzyl phenyl ether (BPE) and other lignin dimers was achieved over the NiCo-MOF-LS catalyst with isopropanol serving as the hydrogen donor solvent in a nitrogen atmosphere. The Ni/Co metal ratio and calcination temperature were found to have a significant impact on the catalytic performance. Through a comprehensive investigation of various reaction parameters, including temperature, pressure, reaction time, and reaction solvent, it was determined that the catalyst exhibited excellent catalytic activity in the selective hydrogenolysis of BPE to cycloalkane and cyclohexanol. The optimal reaction conditions (240 °C, 4 h, 3 MPa N) were found to be conducive to the effective conversion of BPE into methylcyclohexane and cyclohexanol. The combination of lignin and metal-organic framework represented a novel approach to the utilization of lignin resources and the upgrading of biomass-derived chemicals.
大量木质素的转化对于生物质资源的利用具有重要意义。在本研究中,木质素磺酸盐(LS)被选作碳基载体,并成功引入到NiCo-MOF结构中。通过水热法合成了一系列具有不同Ni和Co金属比例的木质素与MOF混合催化剂(NiCo-MOF-LS)。随后,在一系列NiCo-MOF-LS上进行了木质素衍生二聚体的催化氢解反应,同时考虑了煅烧温度和催化剂中木质素添加量的影响。在氮气气氛中,以异丙醇作为氢供体溶剂,在NiCo-MOF-LS催化剂上实现了苄基苯基醚(BPE)和其他木质素二聚体的选择性转化。发现Ni/Co金属比例和煅烧温度对催化性能有显著影响。通过对温度、压力、反应时间和反应溶剂等各种反应参数的综合研究,确定该催化剂在将BPE选择性氢解为环烷烃和环己醇方面表现出优异的催化活性。发现最佳反应条件(240℃,4 h,3 MPa N)有利于将BPE有效转化为甲基环己烷和环己醇。木质素与金属有机框架的结合代表了一种利用木质素资源和升级生物质衍生化学品的新方法。