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Towards acid MOFs - catalytic performance of sulfonic acid functionalized architectures

机译:朝着酸MOF-磺酸功能化建筑的催化性能

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摘要

In this work, the inclusion of free sulfonic acid groups in highly stable MOFs is explored. The synthesized catalysts have been applied in a model esterification reaction. Two metal organic frameworks bearing sulfonic acid moieties are investigated: HSO3-MIL-101(Cr) synthesized following different approaches and a new structure based on HSO3-bdc and Zr. The acidic properties, catalytic performance, deactivation and stability of the different structures are critically evaluated. In the case of MIL-101(Cr), deactivation of the sulfonic groups via formation of butanol sulfonic esters has been observed. Due to the strong interaction between -SO3~ and the Cr open metal site where usually fluorine (F~-) is located in the structure, the HSO3-MIL-101(Cr) catalysts are not stable under acidic regeneration conditions. When using Zr as a metal node, a new and stable sulfonic acid containing porous structure was synthesized. This structure showed high activity and full re-usability in the esterification of n-butanol with acetic acid. In this case, deactivation of the catalyst due to sulfonic ester formation could be reversed by reactivation under acidic conditions.
机译:在这项工作中,探索了在高度稳定的MOF中包含游离磺酸基团。合成的催化剂已应用于模型酯化反应中。研究了两个带有磺酸部分的金属有机框架:按照不同的方法合成HSO3-MIL-101(CR),并基于HSO3-BDC和ZR合成。严格评估了不同结构的酸性特性,催化性能,失活和稳定性。在MIL-101(CR)的情况下,已经观察到通过形成丁醇硫酸酯通过形成硫基团。由于-SO3〜与CR开放金属位点之间的强烈相互作用,该位点通常位于结构中,因此HSO3-MIL-101(CR)催化剂在酸性再生条件下不稳定。当使用ZR作为金属节点时,合成了含有多孔结构的新的稳定磺酸。这种结构在用乙酸对N-丁醇的酯化中表现出很高的活性和充分的可重复性。在这种情况下,由于酸性条件下的重新激活可以逆转由于硫酯形成而导致的催化剂。

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