Laboratory of Advanced Materials, Department of Materials Science and Engineering, Tsinghua University, Beijing 100084, China.
J Environ Sci (China). 2011;23(7):1205-10. doi: 10.1016/s1001-0742(10)60533-5.
Manganese oxide-loaded and -doped ceria as well as the corresponding barium-modified oxide catalysts were prepared for soot oxidation in the presence of NO(x), and were characterized by using X-ray diffraction, Brunauer-Emmett-Teller and NO temperature-programmed oxidation measurements. The activity of catalyst depended strongly on the NO2 production capacity, and the importance of surface nitrates was weakened without heat transfer limitations. The formation of perovskite-type oxides after the high-temperature calcination caused the loss of NO(x) storage capacity for the Ba-modified catalysts, but did not seem to affect the NO oxidation activity obviously. The addition of barium did not prevent the phase separation of MnO(x)-CeO2 solid solutions, whereas it inhibited the sintering of oxide crystallites effectively. This, as well as the relatively high surface area, resulted in a small increase in soot oxidation temperature for the thermally aged Ba/Mn-Ce catalyst.
负载和掺杂氧化锰的氧化铈以及相应的钡改性氧化物催化剂被制备用于在存在 NO(x) 的情况下氧化烟尘,并用 X 射线衍射、Brunauer-Emmett-Teller 和 NO 程序升温氧化测量进行了表征。催化剂的活性强烈依赖于 NO2 生成能力,而在没有传热限制的情况下,表面硝酸盐的重要性会减弱。高温煅烧后形成的钙钛矿型氧化物导致钡改性催化剂失去了 NO(x)存储能力,但似乎对 NO 氧化活性没有明显影响。钡的添加并没有阻止 MnO(x)-CeO2 固溶体的相分离,而是有效地抑制了氧化物晶粒的烧结。这以及相对较高的表面积,导致热老化的 Ba/Mn-Ce 催化剂的烟尘氧化温度略有升高。