双功能
催化作用
乙二胺四乙酸
镍
煅烧
选择性
化学
纳米颗粒
铝酸盐
无机化学
产量(工程)
尖晶石
己烷
核化学
材料科学
有机化学
螯合作用
纳米技术
冶金
水泥
作者
Ye Yang,Xinmei Liu,Yuchao Lyu,Yuxiang Liu,Weilong Zhan,Zhumo Yu,Lei Fan,Zifeng Yan
标识
DOI:10.1016/j.jcis.2021.07.039
摘要
The nickel based bifunctional catalyst with enhanced hydroisomerization performance was developed using an in-situ solid synthesis method. It was achieved to stabilize smaller Ni active sites on SAPO-5 using ethylenediaminetetraacetic acid (EDTA) ligands. The role of EDTA ligands was clarified by controlling the molar ratio of EDTA to Ni2+ (EDTA/Ni2+) over Ni/SAPO-5 catalysts. EDTA ligands inhibited the formation of nickel aluminate spinel and aggregation of NiO species during calcination, which dispersed Ni nanoparticles in a mean size of 4.7 nm on SAPO-5. The size of Ni nanoparticles could be controlled by regulating EDTA/Ni2+ ratio in [Ni-EDTA]2- complex. The prepared catalyst exhibited high yield of isomers (54.0%) and di-branched isomers selectivity (18.0%) in the n-hexane hydroisomerization, which was approximately 2 times higher than that of the Ni/SAPO-5 catalyst without EDTA ligands at similar conversion. These results are important to propose a facile approach for the preparation of highly dispersed non-noble metal based bifunctional catalysts at a high loading.
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