Fe Nanocatalysts Supported on Dealuminated ZSM‐5 for Efficient Decomposition of Ammonia to CO x ‐Free Hydrogen | Zendy

Hu ZhongPan | Zendy; Chen Lei | Zendy; Weng ChenChen | Zendy; Yuan ZhongYong | Zendy

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Fe Nanocatalysts Supported on Dealuminated ZSM‐5 for Efficient Decomposition of Ammonia to CO x ‐Free Hydrogen

Author(s) -

Hu ZhongPan,

Chen Lei,

Weng ChenChen,

Yuan ZhongYong

Publication year - 2018

Publication title -

chemistryselect

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 34

ISSN - 2365-6549

DOI - 10.1002/slct.201800785

Subject(s) - catalysis , nanomaterial based catalyst , decomposition , zeolite , sorption , inorganic chemistry , zsm 5 , ferric , hydrogen , chemistry , selective catalytic reduction , ion exchange , ammonia , materials science , adsorption , ion , organic chemistry

A series of dealuminated ZSM‐5 zeolite (deAlZSM‐5) supported Fe‐based catalysts are prepared by a modified solid‐state ion exchange method, in which the HZSM‐5 zeolite is dealuminated by concentrated HNO 3 and subsequently ground with ferric nitrate. The physicochemical properties of the resultant Fe/deAlZSM‐5 catalysts are characterized by XRD, N 2 sorption, TEM, H 2 ‐TPR and NH 3 ‐TPD techniques. It is revealed that the Fe species are highly dispersed in the deAlZSM‐5, and would be transformed into elemental Fe nanoparticles after reduction by H 2 . Due to the confinement effect of ZSM‐5 zeolite, the Fe/deAlZSM‐5 catalysts exhibit high catalytic activity and excellent stability for NH 3 decomposition. At 650 o C, about 100% NH 3 conversion can be achieved over the 9%Fe/deAlZSM‐5 catalysts for 50 h time‐on‐stream, demonstrating a very promising catalyst system in NH 3 decomposition.

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