期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 -, 期 -, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202304244
关键词
Hierarchical Zeolite; LTL; Methylenedianiline; Polyurethane; Solid Acid Catalyst
Researchers report that meso-/microporous hierarchical LTL zeolite shows unprecedentedly high activity, selectivity, and stability. The one-dimensional cage-like micropores promote the bimolecular reaction between intermediates, selectively producing 4,4'-MDA and inhibiting the formation of undesired isomers and oligomers. The secondary mesopores alleviate mass transfer limitations, leading to a 7.8-fold higher MDA formation rate compared to microporous LTL zeolite alone.
In many industrially important reactions, caustic mineral acid catalysts have been successfully replaced with green solid acids such as zeolites. In this context, extensive efforts have been devoted to replacing HCl to produce methylenedianiline (MDA), a key intermediate in polyurethane production. Unfortunately, limited success has been achieved thus far due to low activity, selectivity towards the desired 4,4 & PRIME;-MDA, and rapid catalyst deactivation. Here we report that meso-/microporous hierarchical LTL zeolite exhibits unprecedentedly high activity, selectivity, and stability. The one-dimensional cage-like micropores of LTL promote the bimolecular reaction between two para-aminobenzylaniline intermediates to selectively produce 4,4 & PRIME;-MDA and inhibit the formation of undesired isomers and heavy oligomers. Meanwhile, the secondary mesopores alleviate mass transfer limitations, resulting in a 7.8-fold higher MDA formation rate compared to solely microporous LTL zeolite. Due to suppressed oligomer formation and fast mass transfer, the catalyst exhibits inappreciable deactivation in an industrially relevant continuous flow reactor.
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