On the catalytic nature of nitrided NiMo/γ-Al2O3 catalysts for dry reforming of methane

IF 1.4 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
Jiaqi Wang , Ying Zhang , Qingshan Rong , Yan Shi , Zhiwei Yao
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引用次数: 0

Abstract

Nitrogen and phosphorus are one of the most common Group 15 elements. The chemistry of nitrogen and phosphorus is very important in the field of catalysis. Three types of nitride containing NiMo/γ-Al2O3 catalysts were synthesized using different loading-nitriding sequences and oxide precursor types for dry reforming of methane (DRM). The active components (Ni2Mo3N and Ni/Mo2N) firstly reacted with CO2, transforming into NiO and MoO2. They were then carburized with CH4 to produce Ni/Mo2C during the DRM process. From that point on, a redox cycle, viz. NiO/MoO2 ⇆ Ni/Mo2C, occurred during the DRM reaction. The low activity of nitriding-first NiMo nitride catalyst can be attributed to bulk oxidation. The observed gradual decline in performance of loading-first Ni/Mo nitride catalyst was due to coking. Noticeably, the loading-first NiMo nitride catalyst can demonstrate superiority in both activity and resistance to coking, which was due to its strong metal–Al2O3 interaction and high metal dispersion.
氮化NiMo/γ-Al2O3催化剂对甲烷干重整的催化性能研究
氮和磷是最常见的第15族元素之一。氮和磷的化学性质在催化领域具有重要意义。采用不同的加载-氮化顺序和氧化物前驱体类型,合成了3种含ni /γ-Al2O3氮化物的甲烷干重整催化剂。活性组分Ni2Mo3N和Ni/Mo2N首先与CO2反应,转化为NiO和MoO2。然后在DRM过程中用CH4渗碳生成Ni/Mo2C。从那时起,在DRM反应中发生了一个氧化还原循环,即NiO/MoO2 / Ni/Mo2C。氮化优先的NiMo氮化物催化剂活性较低的原因是本体氧化。观察到负载优先的Ni/Mo氮化物催化剂的性能逐渐下降是由于焦化。值得注意的是,负载优先的氮化镍催化剂具有较强的活性和抗结焦性能,这是由于其具有较强的金属- al2o3相互作用和较高的金属分散性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
7.70%
发文量
103
审稿时长
2.1 months
期刊介绍: Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.
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