MOF-derived NiMoS hollow sphere for efficient hydrodesulfurization: Effects of composition and morphology of active phase of NiMoS catalysts

IF 7.5 1区 工程技术 Q2 ENERGY & FUELS Fuel Pub Date : 2025-03-21 DOI:10.1016/j.fuel.2025.135121
Dengwei Yan , Fengyue Sun , Yanwei Ju , Haoping Di , Changle Yue , Yanfei Chen , Chongzheng Xu , Yukun Lu
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Abstract

The rational modulation of bimetallic intimately synergistic unsupported catalysts is the essential approach for efficient hydrodesulfurization (HDS). Herein, we have successfully produced NiMoS hollow spheres (H-NiMoS) by the Ni-MOF-engaged strategy using Ni metal–organic framework (Ni-MOF) as a precursor. The Ni-MOF serves as a landing site for vertically oriented MoS2 nanosheets and also acts as a nickel promoter for inducing the formation of the NiMoS active phase. The H-NiMoS catalyst achieves three-dimensional self-assembly of MoS2 nanosheets on hollow spheres, displaying a higher specific surface area (105 m2·g−1) compared to pure MoS2 (52 m2·g−1). The H-NiMoS catalyst produces vertical MoS2 with low stacking number (2–3 layers) and short slab length (2–4 nm), thus providing a large number of “rim” sites for HDS reaction. As expected, the H-NiMoS catalyst exhibits efficient HDS activity with 99.8 % conversion of dibenzothiophene (DBT) and 93.0 % conversion of 4,6-dimethyldibenzothiophene (4,6-DMDBT), as well as HDS selectivity that SHYD/DDS(DBT) = 1.3 and SHYD/DDS(4,6-DMDBT) = 3.2. Consequently, the Ni-MOF-engaged strategy of fabricating MoS2 nanosheets with vertically oriented structures by using Ni-MOF precursors provides significant guidance for improving the activity and HYD selectivity of conventional HDS catalysts by exposing more “rim” sites.

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用于高效加氢脱硫的mof衍生NiMoS空心球:NiMoS催化剂活性相组成和形态的影响
合理调制双金属密切协同无负载催化剂是实现高效加氢脱硫的重要途径。本文以Ni金属有机骨架(Ni- mof)为前驱体,采用Ni- mof接合策略成功制备了Ni- mof空心球(H-NiMoS)。Ni-MOF作为垂直取向MoS2纳米片的着陆点,也作为镍的促进剂诱导NiMoS活性相的形成。H-NiMoS催化剂在空心球上实现了MoS2纳米片的三维自组装,比表面积(105 m2·g−1)高于纯MoS2 (52 m2·g−1)。H-NiMoS催化剂产生的垂直二硫化钼堆积数少(2-3层),板长短(2-4 nm),为HDS反应提供了大量的“边缘”位点。结果表明,H-NiMoS催化剂对二苯并噻吩(DBT)的转化率为99.8%,对4,6-二甲基二苯并噻吩(4,6- dmdbt)的转化率为93.0%,对HDS的选择性为SHYD/DDS(DBT) = 1.3和SHYD/DDS(4,6- dmdbt) = 3.2。因此,利用Ni-MOF前驱体制备具有垂直取向结构的MoS2纳米片的策略为通过暴露更多的“边缘”位点来提高传统HDS催化剂的活性和HYD选择性提供了重要的指导。
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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