School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory /Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology, Liaocheng University, Liaocheng 252000, China.
School of Chemistry and Chemical Engineering, Shandong Provincial Key Laboratory /Collaborative Innovation Center of Chemical Energy Storage & Novel Cell Technology, Liaocheng University, Liaocheng 252000, China.
J Colloid Interface Sci. 2023 Oct;647:188-200. doi: 10.1016/j.jcis.2023.05.139. Epub 2023 May 24.
Reasonable construction of bi-function catalysts with well dispersed hydrogenation active sites and acidic sites are crucial for the hydrodeoxygenation (HDO) of biomass-derived compounds but still a huge challenge. Herein, a 3D Mo functionalized Ni-based bimetallic embedded catalyst with fine metal nanoparticles size (<6 nm) was prepared for the first time using dendritic mesoporous silica as a sacrificial template by one-pot hydrothermal synthesis and adopted in the HDO process of vanillin (VAN) upgrade to 2-methoxy-4-methylphenol (MMP). The characterization results illustrated that Mo species regulated the acidity of the catalyst and promoted the formation of Ni-Mo alloy sites. Density functional theory (DFT) calculations further unveiled that Ni-Mo alloy sites promoted the activation and dissociation of CO bond in VAN, enhanced the ability of protonation hydrogenolysis. Benefitting from the synergistic effect of the highly uniformly dispersed hydrogenation metal sites and acidic sites, nearly 100% yield of MMP could obtained over the designed catalyst under mild conditions (130 °C, 1.5 MPa H, 3 h, 10 wt% catalyst dosage). Additionally, the NiMo@MSN catalyst displayed robust activity for no less than 8 recycles and excellent universality for the HDO of a variety of lignin derivatives and biomass platform molecules, which provide a feasible strategy for the construction of 3D confined catalysts for the high-efficiency HDO of biomass derivatives.
合理构建具有良好分散加氢活性位和酸性位的双功能催化剂对于生物质衍生化合物的加氢脱氧(HDO)至关重要,但仍然是一个巨大的挑战。本文首次采用树枝状介孔硅作为牺牲模板,通过一步水热合成法制备了三维 Mo 功能化 Ni 基双金属嵌入式催化剂,该催化剂具有细小的金属纳米颗粒尺寸(<6nm),并在香草醛(VAN)升级为 2-甲氧基-4-甲基苯酚(MMP)的 HDO 过程中得到了应用。表征结果表明,Mo 物种调节了催化剂的酸度,并促进了 Ni-Mo 合金位的形成。密度泛函理论(DFT)计算进一步揭示了 Ni-Mo 合金位促进了 VAN 中 CO 键的活化和解离,增强了质子化氢解的能力。得益于高度均匀分散的加氢金属位和酸性位的协同作用,在温和条件(130°C、1.5 MPa H、3 h、10 wt%催化剂用量)下,设计的催化剂可获得近 100%的 MMP 产率。此外,NiMo@MSN 催化剂在不少于 8 次循环中的活性稳定,对各种木质素衍生物和生物质平台分子的 HDO 具有优异的通用性,为高效生物质衍生物 HDO 的三维受限催化剂的构建提供了一种可行的策略。