加氢脱氧
催化作用
除氧
ZSM-5型
茴香醚
初湿浸渍
沸石
化学
吸附
纳米颗粒
环己烷
金属
无机化学
材料科学
化学工程
有机化学
选择性
纳米技术
工程类
作者
Sen Li,Longhui Guo,Xinyu He,Congzhen Qiao,Yajie Tian
标识
DOI:10.1016/j.renene.2022.05.052
摘要
Bio–oil as the promising renewable resources to replace fossil fuels, requires upgrading into deoxygenated fuel. Zeolite supported base metal catalysts have been deemed highly efficient for the hydrodeoxygenation (HDO) of bio–oil, but facing a degraded activity due to metal aggregation. In this study, uniform Ni nanoparticles (∼4 wt%) encapsulated in ZSM–5 zeolites ([email protected]–5s) were synthesized by a one–pot method for catalytic HDO of phenolic compounds. The Ni dispersion was found to be significantly enhanced in the [email protected]–5s catalysts after encapsulation compared with a catalyst prepared by wetness impregnation (Ni/ZSM–5), which is ascribed to the strong interaction between the Ni and the zeolite surface. The [email protected]–5s catalysts show higher HDO activities for phenolics than the Ni/ZSM–5 catalyst, owing to the enhanced adsorption and spillover of active hydrogen by the highly dispersed Ni species. [email protected]–5–50 (Si/Al of 50) gave cyclohexane yield of 91.6% at 250 °C, through sequenced hydrogenation and deoxygenation of anisole. Moreover, the [email protected]–5–100 (Si/Al of 100) with decreased acidities further gave an enhanced TOF value for the conversion of phenolics. From the FT–IR spectrum obtained for adsorbed anisole, the reduction of acidities is determined to facilitate the desorption of intermediates, which accelerates the initial hydrogenation.
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