Noh Young Su, Yang Eun-Hyeok, Lim Sung Soo, Lee Kwan-Young, Kim Sang Woo, Moon Dong Ju
J Nanosci Nanotechnol. 2017 Apr;17(4):2545-549. doi: 10.1166/jnn.2017.13364.
Ni catalysts supported on ordered mesoporous alumina (OMA) were prepared by EISA method and calcined under air and Ar atmospheres. Both catalysts showed stable performance for the dry reforming of methane for 24 h, however the catalytic activity of Ar calcined catalyst was relatively lower than that in the air calcined one. It was found that the carbon (C β ) layer around nickel particles was observed for the Ar calcined catalyst after dry reforming of methane. The encapsulating carbon species in the Ar calcined catalyst lowering the mass transfer rate of feeds led to lower performance, but no whisker carbon was observed. In the case of the air calcined catalyst, whisker carbon (C(v)) which is inactive during dry reforming was accumulated on the catalyst, and it resulted in catalyst breakdown and pressure drop during the reaction.
采用蒸发诱导自组装(EISA)法制备了负载在有序介孔氧化铝(OMA)上的镍催化剂,并在空气和氩气气氛下进行煅烧。两种催化剂在甲烷干重整反应中均表现出24小时的稳定性能,然而,氩气煅烧催化剂的催化活性相对低于空气煅烧的催化剂。研究发现,在甲烷干重整反应后,氩气煅烧的催化剂在镍颗粒周围观察到碳(Cβ)层。氩气煅烧催化剂中包裹的碳物种降低了进料的传质速率,导致性能较低,但未观察到晶须状碳。在空气煅烧催化剂的情况下,在干重整过程中无活性的晶须状碳(C(v))在催化剂上积累,导致反应过程中催化剂破裂和压力降。