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雷尼镍的磷量子点改性及其催化加氢脱硫性能OA北大核心CSTPCD

Modification of Rainey nickel with phosphorus quantum dots and its catalytic hydrodesulfurization performances

中文摘要英文摘要

高硫燃油燃烧产生的排放会对环境造成巨大的破坏,严重影响人类的生存,开发高效的加氢脱硫催化剂至关重要.本文以雷尼镍为前体,首次使用磷量子点和商业红磷对非负载型(雷尼镍)催化剂进行改性,并系统探究了改性条件(改性温度、用量、反应温度)对催化剂加氢脱硫(DBT)性能的影响,采用BET比表面积测试、X射线衍射仪、扫面电子显微镜、透射电子显微镜、能量色散光谱和X射线光电子能谱等技术手段进行表征.结果发现,磷量子点改性催化剂的性能明显提升,改性催化剂孔径增大和磷量子点与镍的强相互作用是催化剂性能提升的主要原因.较大的孔径有利于DBT分子扩散,与磷量子点作用生成的带正电Niδ+物种将有利于DBT的吸附,进而提高催化剂的加氢脱硫性能,并在最佳实验条件下得到了99.1%的DBT转化率.

The emission of high-sulfur fuel combustion will cause great damage to environment and seriously affect the living environment of human beings.It is very important to develop efficient hydrodesulfurization(HDS)catalysts.In this work,Phosphorus quantum dots and commercial red phosphorus were used for the first time to modify the unsupported catalyst(Raney nickel),and the influence of modification conditions(modification temperature,dosage,reaction temperature)on the performance of catalyst hydrodesulfurization(DBT)was systematically explored.The modified catalysts were characterized by BET,XRD,SEM,TEM,EDS and XPS,and their catalytic activity was evaluated for dibenzothiophene(DBT)hydrogenation.The results showed that the HDS performance of Rainey nickel modified with phosphorus quantum dots were greatly improved that could be attributed to the increased pore size of the modified catalyst and the strong interaction between phosphorus quantum dots and nickel.Large pore size was beneficial for the diffusion of DBT molecules,and the positively charged Niδ+ generated by the interaction with phosphorus quantum dots facilitates the adsorption of DBT,thereby improving the hydrodesulfurization performance of the catalyst.DBT conversion rate of 99.1%was achieved under optimal experimental conditions.

谷星朋;马红钦;刘嘉豪

天津大学化工学院,天津 300072天津大学化工学院,天津 300072||天津化工过程安全与装备技术重点实验室,天津 300072

石油、天然气工程

催化剂化学反应磷量子点改性加氢脱硫

catalystchemical reactionphosphorus quantum dotsmodificationhydrodesulfurization

《化工进展》 2024 (003)

1293-1301 / 9

10.16085/j.issn.1000-6613.2023-0359

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