Pt- and Pd-Promoted CeO2–ZrO2 for Passive NOx Adsorber Applications

详细信息    查看全文

• 作者：Yaying Ji ; Dongyan Xu ; Shuli Bai ; Uschi Graham ; Mark CrockerBingbing Chen ; Chuan Shi ; Deb Harris ; Dave Scapens ; John Darab
• 刊名：Industrial & Engineering Chemistry Research
• 出版年：2017
• 出版时间：January 11, 2017
• 年：2017
• 卷：56
• 期：1
• 页码：111-125
• 全文大小：913K
• ISSN：1520-5045

文摘

Pt- and Pd-promoted Ce_xZr_1–xO₂ mixed oxides were characterized and investigated for passive NOx adsorber applications. X-ray diffraction analysis revealed a phase transition from tetragonal to cubic with increasing cerium content in Ce_xZr_1–xO₂, while H₂ and CO chemisorption data in all cases indicated average Pt and Pd particle sizes of close to 2 nm. H₂-temperature programmed reduction (TPD) measurements revealed a shift of the Pt reduction peak to higher temperature with increasing Ce content, consistent with a corresponding increase in the degree of Pt oxidation. According to microreactor data, doping Ce into the ZrO₂ lattice resulted in a significant improvement in low temperature (80–160 °C) NOx storage efficiency. Diffuse reflectance infrared Fourier transform spectroscopy measurements on Pt/Ce_xZr_1–xO₂ showed that as Ce content increased, relatively more nitrite species were generated during NOx storage. However, oxidation of nitrite to nitrate during subsequent NOx-TPD—increasing the concentration of more thermally stable nitrate—also correlated with increased Ce content. The use of Pd as a promoter resulted in decreased NOx storage efficiency compared to Pt, although low-temperature NOx desorption behavior was improved. This is attributed to decreased formation of nitrate during NOx storage compared to that of Pt, as well as the lower activity of Pd for oxidation of nitrite to nitrate during subsequent NOx-TPD. To achieve more balanced NOx storage and desorption behavior, Ce_0.2Zr_0.8O₂ was promoted with both Pt and Pd, resulting in superior overall NOx performance relative to its Pt and Pd analogues. After hydrothermal aging at 750 °C for 16 h, the copromoted sample still maintained excellent NOx adsorption–desorption performance.