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NiO-dispersed small-sized Pt/Mg2Al4Si5O18 as a high-performance and robust catalyst for formaldehyde purification
Fen Wang1, Dajun Wu2, Zhongao Zhang3
1Anhui Provincial International Joint Research Center of Modern Environmental Engineering, Anhui University of Science and Technology, Huainan 232001, China; School of Chemical and Blasting Engineering, Anhui University of Science and Technology, Huainan 232001, China; Engineering Technology Research Center of Coal Resources Comprehensive Utilization, Anhui Province, Anhui University of Science and Technology, Huainan 232001, China; State Key Laboratory for Safe Mining of Deep Coal Resources and Environment Protection, Huainan 232000, China.
None:
Commercial Mg2Al4Si5O18 cordierite materials are extensively employed in catalytic reactions due to their outstanding high-temperature stability and low thermal expansion coefficient. Nevertheless, the limited specific surface area of these materials presents a significant challenge for the preparation of small-sized Pt nanoparticles. In this work, we achieved the preparation of ∼3 nm Pt nanoparticles on commercial Mg2Al4Si5O18 cordierite with an ultralow specific surface area via NiO modification. The research results indicate that appropriate amounts of NiO modification can notably enhance the activity and stability of the Pt/Mg2Al4Si5O18 catalyst. During a 20 h long-term stability test at 60 °C under a weight hourly space velocity (WHSV) of 30,000 mL/(g⋅h) and relative humidity (RH) of 25 %, the 6NiO-1Pt/Mg2Al4Si5O18 and 9NiO-1Pt/Mg2Al4Si5O18 catalysts (with ∼3 nm Pt nanoparticles) achieve stable HCHO conversions of 91.5 %-96.7 % and 93.4 %-100 %, respectively. Comprehensive characterization studies disclose that there is a distinct interaction between Pt and NiO, which increases the dispersion of Pt. This interaction also greatly improves the adsorption and activation of O2 and HCHO, enhances the mobility of O2, and strengthens the adsorption of dioxymethylene (DOM) intermediate species. These factors are the key reasons for the significant enhancement of the catalytic performance of Pt/Mg2Al4Si5O18 catalysts after NiO modification. Additionally, we propose a possible reaction process where formaldehyde reacts with OH and oxygen species, and is then gradually oxidized to CO2 via dioxymethylene (DOM), formate species, and CO on 9NiO-1Pt/Mg2Al4Si5O18 catalyst.
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