乙酰丙酸
催化作用
选择性
扩散
化学
金属有机骨架
传质
微型多孔材料
吸附
化学工程
基质(水族馆)
无机化学
材料科学
物理化学
有机化学
色谱法
热力学
工程类
地质学
物理
海洋学
作者
Sean R. McIntyre,Paola A. Sáenz-Cavazos,Elwin Hunter‐Sellars,Daryl R. Williams
标识
DOI:10.3389/fchem.2022.1087939
摘要
The diffusion processes between adsorbent and adsorbate naturally play a significant role in the efficiency and selectivity of the heterogenous catalytic process. This paper considers the importance of diffusion processes in the transfer hydrogenation reaction of levulinic acid to γ-valerolactone by MIL-88B, MIL-100, and ZIF8@Pd monolithic catalysts. Over a period of five catalytic cycles, it was shown that the Fe-based catalysts can achieve similar conversions to the ZIF-8 supported Pd, with the only current limitation being the lower aqueous stability of these MOFs. Diffusion constants were calculated using the ZLC method, with micropore diffusion limitation found for ZIF-8 and MIL-100 monolithic frameworks at 2.7 x 10-8 and 4.6 x 10-8 cm2 s-1 respectively. This diffusion limitation was also confirmed by IR spectroscopy with an increasing concentration of C-H bands on the MOF substrate post-reaction. Mass transfer coefficients, also calculated by ZLC, revealed increased mass transport for the hydrophobic ZIF-8 framework, which perhaps aids in the γ-valerolactone selectivity over side products that are produced in the absence of catalytic material, as seen for MIL-88B and MIL-100 after multiple uses.
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