Abstract
Core-shell catalysts with functional shells could increase the activity and stability of the catalysts in selective catalytic reduction with ammonia (NH3 -SCR) for diesel exhaust NOx treatment. However, the conventional approaches based on the multistep fabrication for core-shell structures encounter persistent restrictions regarding the strict synthesis condition and limited design flexibility. Herein, a facile coaxial 3D printing strategy has been for the first time developed to construct zeolite-based core-shell monolithic catalysts with interconnected honeycomb structures, in which the hydrophilic non-compact silica serves as shell and Cu-SSZ-13 zeolite acts as core. Compared to Cu-SSZ-13 monolith suffered from the interfacial diffusion, the SiO2 shell layer can increase the accessibility of active sites over Cu-SSZ-13@SiO2 , resulting in a 10-20% higher NO conversion at the 200-550 °C under 300,000 cm3 g-1 h-1 . Meanwhile, a thicker SiO2 shell enhances the hydrothermal stability of the aged catalyst by inhibiting the dealumination and the formation of CuOx . Other representative monolithic catalysts with different topological zeolites as shell and diverse metal oxides as core can be also realized by this coaxial 3D printing. This strategy allows multiple porous materials to be directly integrated, which allows for flexible design and fabrication of various core-shell monolithic catalysts with customized functionalities. This article is protected by copyright. All rights reserved.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.