摘要
Mo/C、Ni/C和Ni-Mo/C催化剂吡啶加氢脱氮研究表明,Mo/C催化剂在Mo含量小于3.65%时,随着Mo含量的增加,脱氮活性增加,其后趋于稳定。Ni/C催化剂也具有加氢脱氮活性,在Ni含量为5%左右达到最大值。Ni-Mo/C催化剂只有在M和Mo相互匹配时才具有较高的活性。XPS的研究表明,硫化后Ni-Mo/C催化剂中Mo主要是以MoS_2的形态存在的;Ni是以NiS和Ni_3S_2的混合态存在的;硫主要是以S ̄(2-)的形态存在的,也含有一些(S-S) ̄(2-)的形态。SEM的研究表明,Mo/C催化剂中的活性组分MoS_2在载体上呈大小不等的三维微晶,微晶的总体分布均匀;Ni在Ni/C催化剂载体上的分布不均匀;Ni-Mo/C催化剂中的活性组分在载体上的总体分布均匀,微晶上存在许多纤维状的形态,它和Mo/C、Ni/C催化剂有明显的差别。
A series of Ni , Mo and Ni-Mo hydrodenitrogen(HDN ) catalysts supported on activated carbon were prepared by using incipient wetness impregnation method. The HDN activity of Ni/C, Mo/Cand Ni-Mo/C catalysts after sulfidation was measured. TheHDN activity of Mo/C catalyst increases with the increasing of the Mo content when Mocontent is lower than 3. 65 wt%, After that it maintains constant. The Ni/Ccatalyst aloneexhibits HDN activity, but it is lower than that of Mo/Cand Ni-Mo/Ccatalysts。 The Ni-Mo/Ccatalyst exhibits very high HDN activity when Ni and Mo are compatible. XPS analy-sis whows that Ni-Mo/C contains principally MoS_2and NiS-Ni_3S_2 on the surface after sul-fidation, and the low-valence-state sulphur,e.g.,(S-S) ̄(2-)in it. SEM analysis showsthat the crystalline size of the MoS_2 in Mo/C catalyst covers a wide range but are well-dis-persed on the average. Ni sulfide particles in Ni/C catalyst are not homogeneously distribu-ed. Ni and Mo active phase in Ni-Mo/C catalyst is also well-dispersed on the average, butit has many fiber-like structures, this is different from Mo/Cand Ni/Ccatalysts.
出处
《燃料化学学报》
EI
CAS
CSCD
北大核心
1995年第2期138-143,共6页
Journal of Fuel Chemistry and Technology