应用化学 ›› 2019, Vol. 36 ›› Issue (6): 698-703.DOI: 10.11944/j.issn.1000-0518.2019.06.180328

• 研究论文 • 上一篇    下一篇

NiO/Mn3O4整体式催化剂催化分解臭氧的性能

余会发a,陈崇来b,王月娟a,罗孟飞a*()   

  1. a浙江师范大学物理化学研究所,先进催化材料教育部重点实验室 浙江 金华 321004
    b金华职业技术学院 浙江 金华 321004
  • 收稿日期:2018-10-12 接受日期:2019-01-23 出版日期:2019-06-01 发布日期:2019-06-03
  • 通讯作者: 罗孟飞

Ozone Decomposition over NiO/Mn3O4 Monolithic Catalysts

YU Huifaa,CHEN Chonglaib,WANG Yuejuana,LUO Mengfeia*()   

  1. aKey Laboratory of Advanced Catalytic Materials,Ministry of Education, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua, Zhejiang 321004, China
    bJinhua Vocational and Technical College, Jinhua, Zhejiang 321004, China
  • Received:2018-10-12 Accepted:2019-01-23 Published:2019-06-01 Online:2019-06-03
  • Contact: LUO Mengfei

摘要:

将原料Ni(NO3)2·6H2O、Mn3O4粉末和拟薄水铝石用球磨机球磨,以所得的浆料浸渍堇青石,经过焙烧,得到不同比例的NiO/Mn3O4催化剂。 通过催化分解臭氧活性测试发现,在空速为20000 h-1时, 30NiO/Mn3O4(NiO占总质量的30%)催化剂的活性最高,臭氧分解率达到98%,催化剂活性稳定。 当提高空速为40000 h-1,50NiO/Mn3O4(NiO占总质量的50%)催化剂的活性最高,臭氧分解率在90%左右,并且出现失活现象。 通过X射线衍射(XRD)、程序升温(TPR)、X射线光电子能谱分析(XPS)、BET比表面积法等表征,发现Mn3O4和NiO复合催化剂的比表面积大于单一金属氧化物催化剂的比表面积并且在Mn3O4和NiO复合催化剂中Mn3O4与NiO发生电子相互作用。 催化剂中的Mn3O4与NiO的协同催化作用。 使得Mn3O4与NiO混合物催化剂的还原温度降低,分解臭氧(O3)活性提高。

关键词: Mn3O4, NiO, 催化剂, 臭氧分解, 活性位

Abstract:

A series of NiO/Mn3O4 monolithic catalysts with different NiO contents was prepared by ball-milling of Ni(NO3)2·6H2O, Mn3O4 and pseudo boehmite precusors via subsequent impregnation with cordierite, followed by calcination. These catalysts were tested for ozone decomposition. It was found that the 30NiO/Mn3O4(mass fraction of NiO in total mass is 30%) catalyst has the highest activity at a space velocity of 20000 h-1, and leads to 98% conversion of ozone, while the catalyst remains stable. When the space velocity is increased to 40000 h-1, the 50NiO/Mn3O4(mass fraction of NiO in total mass is 50%) catalyst gives the highest activity, with a ozone conversion at about 90%. But the catalyst suffers deactivation. Characterizations by X-ray diffraction(XRD), TPR, XPS and BET reveal that the presence of Mn3O4 in the NiO increases the specific surface area of the catalyst, and electronic interaction between Mn3O4 and NiO. Meanwhile, the co-presence of Mn3O4 and NiO in the catalyst results in facile reduction of these oxides. This synergy is believed to be responsible for the enhanced catalytic performance.

Key words: Mn3O4, NiO, catalyst, Ozone decomposition, active site