Duan Haonan, Tian Yajie, Gong Siyuan, Zhang Bofeng, Lu Zongjing, Xia Yinqiang, Shi Yawei, Qiao Congzhen
Henan Province Engineering Research Center of Catalytic Reaction, College of Chemistry and Chemical Engineering, Henan University, Kaifeng 474004, China.
Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China.
Nanomaterials (Basel). 2020 Nov 12;10(11):2246. doi: 10.3390/nano10112246.
Herein, Pt/HZSM-5 zeolite catalysts with different crystallite sizes ranging from nanosheet (2 nm) to bulk crystals (1.5 μm) have been prepared for the hydrodeoxygenation of guaiacol, and their effects on the reaction pathway and product selectivity were explored. HZSM-5 zeolites prepared by seeding (Pt/Z-40: ~40 nm) or templating (Pt/NS-2: ~2 nm) fabricated intra-crystalline mesopores and thus enhanced the reaction rate by promoting the diffusion of various molecules, especially the bulky ones such as guaiacol and 2-methoxycyclohexanol, leading to a higher cyclohexane selectivity of up to 80 wt % (both for Pt/Z-40 and Pt/NS-2) compared to 70 wt % for bulky HZSM-5 (Pt/CZ: ~1.5 μm) at 250 °C and 120 min. Furthermore, decreased crystallite sizes more effectively promoted the dispersion of Pt particles than bulky HZSM-5 (Pt/Z-400: ~400 nm and Pt/CZ). The relatively low distance between Pt and acidic sites on the Pt/Z-40 catalyst enhanced the metal/support interaction and induced the reaction between the guaiacol molecules adsorbed on the acidic sites and the metal-activated hydrogen species, which was found more favorable for deoxygenation than for hydrogenation of oxygen-containing molecules. In addition, Pt/NS-2 catalyst with a highly exposed surface facilitated more diverse reaction pathways such as alkyl transfer and isomerization.
在此,制备了不同微晶尺寸(从纳米片(约2纳米)到块状晶体(约1.5微米))的Pt/HZSM-5沸石催化剂用于愈创木酚的加氢脱氧,并探索了它们对反应途径和产物选择性的影响。通过晶种法(Pt/Z-40:约40纳米)或模板法(Pt/NS-2:约2纳米)制备的HZSM-5沸石形成了晶内介孔,从而通过促进各种分子的扩散,特别是愈创木酚和2-甲氧基环己醇等大分子的扩散来提高反应速率,导致在250℃和120分钟时,与块状HZSM-5(Pt/CZ:约1.5微米)的70重量%相比,环己烷选择性高达80重量%(Pt/Z-40和Pt/NS-2均如此)。此外,与块状HZSM-5(Pt/Z-400:约400纳米和Pt/CZ)相比,减小的微晶尺寸更有效地促进了Pt颗粒的分散。Pt/Z-40催化剂上Pt与酸性位点之间相对较短的距离增强了金属/载体相互作用,并引发了吸附在酸性位点上的愈创木酚分子与金属活化的氢物种之间的反应,发现这种反应对脱氧比对含氧化合物的氢化更有利。此外,具有高度暴露表面的Pt/NS-2催化剂促进了更多样化的反应途径,如烷基转移和异构化。