(3-Aminopropyl)trimethoxysilane-Assisted Co-assembly to Monolithic Pd@SiO2/Al2O3/Al Catalysts for Low Concentration CH4 Combustion: Effect of Preparation Conditions

Herein, an affordable strategy was developed to form Pd@SiO2 nanostructure assembled onto monolithic AlOOH/Al nanoarrays from nano- to macro-scale by a one-step reaction process. (3-Aminopropyl)trimethoxysilane (APTMS) was employed as a dual-role reagent for the bidirectional bridging between Pd2+ and AlOOH/Al, as well as the formation of SiO2 matrix and mesopores. The effects of one-step organization conditions on the preparation process, catalyst structure, and catalytic performance were all studied. High hydroxyl contents in Al-based nanoarrays promoted the silanization reaction of APTMS deposition, resulting in a well-formed SiO2 shell and abundant mesopores during the thermal decomposition of APTMS. APTMS amount was not only related to SiO2 loading and encapsulation effect of the core-shell structure, but also affected Pd accessibility. Such proposed APTMS-assisted protocol for the in-situ organization of monolithic Pd@SiO2 catalysts can effectively prevent the growth and aggregation of Pd NPs, thereby favoring low-temperature activity and stability for CH4 combustion. [GRAPHICS]