掺加Nd和K改性对Co3O4催化分解N2O活性的影响

Effect of Nd-incorporation and K-modification on catalytic performance of Co3O4 for N2O decomposition

  • 摘要: 用水热法和共沉淀法分别制备了Nd-Co3O4催化剂,催化分解N2O。其中,水热法制备的Nd-Co3O4催化活性较高。在不同组成的Nd-Co3O4中,优化出了较高活性的0.01Nd-Co3O4催化剂,在其表面浸渍K2CO3溶液制备K改性催化剂(K/Nd-Co3O4)。用X射线衍射(XRD)、N2物理吸附、扫描电镜(SEM)、X射线光电子谱(XPS)、程序升温还原(H2-TPR)、O2程序升温脱附(O2-TPD)等技术表征催化剂结构。结果表明,Nd-Co3O4和K改性催化剂均为尖晶石结构;K改性弱化了催化剂表面Co-O键,有利于表面氧的脱除,提高了催化剂活性。有氧有水气氛350 ℃连续反应40 h,K/Nd-Co3O4催化剂上的N2O分解率超过90%,稳定性较好。

     

    Abstract: Nd-Co3O4 catalysts were prepared by hydrothermal and co-precipitation methods to catalyze the decomposition of N2O. The catalysts prepared by hydrothermal method showed higher activity. Among the hydrothermal Nd-Co3O4 catalysts, the catalyst with Nd/Co molar ratio of 0.01 had higher activity. 0.01Nd-Co3O4 catalyst was then impregnated by K2CO3 solution to prepare K-modified catalyst. The catalysts were characterized by means of X-ray diffraction (XRD), nitrogen physisorption, scanning electrons microscopy (SEM), X-ray photoelectron spectroscopy (XPS), hydrogen temperature-programmed reduction (H2-TPR), and oxygen temperature-programmed desorption (O2-TPD). The results show that Nd-Co3O4 and K-modified catalysts exhibit spinel structure. In contrast to bare Nd-Co3O4, the K-modified catalyst with higher activity is due to its weaker strength of Co-O bond and easier desorption of surface oxygen species. In addition, over 90% conversion of N2O can be reached over 0.02K/0.01Nd-Co3O4 at 350 ℃ for 40 h under the co-presence of oxygen and steam in feed gases.

     

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