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钴基金属氧化物上增强的催化碳烟氧化:过渡金属掺杂的影响。

Enhanced Catalytic Soot Oxidation over Co-Based Metal Oxides: Effects of Transition Metal Doping.

作者信息

Luo Jianbin, Zhu Xinbo, Zhong Zhiwei, Chen Geng, Hong Yu, Zhou Zijian

机构信息

Faculty of Maritime and Transportation, Ningbo University, Ningbo 315211, China.

New Materials Institute, University of Nottingham Ningbo China, Ningbo 315100, China.

出版信息

Molecules. 2023 Dec 20;29(1):41. doi: 10.3390/molecules29010041.

Abstract

A series of Co-M (M = Fe, Cr, and Mn) catalysts were synthesized by the sol-gel method for soot oxidation in a loose contact mode. The Co-Fe catalyst exhibited the best catalytic activity among the tested samples, with the characteristic temperatures (T, T, and T) of 470 °C, 557 °C, and 602 °C, respectively, which were 57 °C, 51 °C, and 51 °C lower than those of the CoO catalyst. Catalyst characterizations of N adsorption-desorption, X-ray diffraction (XRD), X-ray photo-electron spectrometry (XPS), and the temperature programmed desorption of O (O-TPD) were performed to gain insights into the relationships between the activity of catalytic soot oxidation and the catalyst properties. The content of Co (68.6%) increased due to the interactions between Co and Fe, while the redox properties and the relative concentration of surface oxygen adsorption (51.7%) were all improved, which could significantly boost the activity of catalytic soot oxidation. The effects of NO and contact mode on soot oxidation were investigated over the Co-Fe catalyst. The addition of 1000 ppm of NO led to significant reductions in T, T, and T by 92 °C, 106 °C, and 104 °C, respectively, compared to the case without the NO addition. In the tight contact mode, the soot oxidation was accelerated over the Co-Fe catalyst, resulting in 46 °C, 50 °C, and 50 °C reductions in T, T, and T compared to the loose contact mode. The comparison between real soot and model Printex-U showed that the T value of real soot (455 °C) was 102 °C lower than the model Printex-U soot.

摘要

采用溶胶-凝胶法合成了一系列Co-M(M = Fe、Cr和Mn)催化剂,用于松散接触模式下的碳烟氧化。在测试的样品中,Co-Fe催化剂表现出最佳的催化活性,其特征温度(T10、T50和T90)分别为470℃、557℃和602℃,比CoO催化剂的特征温度分别低57℃、51℃和51℃。通过N2吸附-脱附、X射线衍射(XRD)、X射线光电子能谱(XPS)以及O2程序升温脱附(O2-TPD)对催化剂进行表征,以深入了解催化碳烟氧化活性与催化剂性能之间的关系。由于Co与Fe之间的相互作用,Co的含量(68.6%)增加,同时氧化还原性能和表面氧吸附的相对浓度(51.7%)均得到改善,这可显著提高催化碳烟氧化的活性。研究了NO和接触模式对Co-Fe催化剂上碳烟氧化的影响。与不添加NO的情况相比,添加1000 ppm的NO可使T10、T50和T90分别显著降低92℃、106℃和104℃。在紧密接触模式下,Co-Fe催化剂上的碳烟氧化加速,与松散接触模式相比,T10、T50和T90分别降低了46℃、50℃和50℃。实际碳烟与模型Printex-U的比较表明,实际碳烟的T50值(455℃)比模型Printex-U碳烟低102℃。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef50/10779816/1db593e5a0f2/molecules-29-00041-g001.jpg

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