Hydroconversion of methyl laurate on bifunctional Ni2P/AlMCM-41 catalyst prepared via in situ phosphorization using triphenylphosphine

作者：Zhao, Sha; Zhang, Zhena; Zhu, Kongying^*; Chen, Jixiang^*

来源：Applied Surface Science, 2017, 404: 388-397.

DOI：10.1016/j.apsusc.2017.02.016

• Bifunctional Ni2P/AlMCM-41
• in situ phosphorization
• Hydrodeoxygenation
• Hydroisomerization
• Methyl laurate

A series of Ni2P/AlMCM-41-x bifunctional catalysts with different Si/Al ratios (x) were synthesized by in situ phosphorization of Ni/AIMCM-41-x with triphenylphosphine (nominal Ni/P ratio of 0.75) at 300 degrees C on a fixed-bed reactor. For comparison, NiP/AIMCM-41-5-TPR was also prepared by the TPR method from the supported nickel phosphate with the Ni/P ratio of 1.0, during which metallic Ni rather than Ni2P formed. TEM images show that Ni and Ni2P particles uniformly distributed in Ni2P/AIMCM-41-x and NiP/AlMCM-41-5-TPR. The Ni2P/AIMCM-41-x acidity increased with decreasing the Si/Al ratio. In the hydroconversion of methyl laurate, the conversions were close to 100% on all catalysts at 360 degrees C, 3.0 MPa, methyl laurate WHSV of 2 h(-1) and H-2/methyl laurate ratio of 25. As to Ni2P/AlMCM-41-x, with decreasing the Si/Al ratio, the total selectivity to C11 and C12 hydrocarbons decreased, while the total selectivity to isoundecane and isododecane (Si-C11+i-C12) firstly increased and then decreased. Ni2P/AlMCM-41-5 gave the largest Si-C11+i-C12 of 43.2%. While NiP/AIMCM-41-5-TPR gave higher Si-C11+i-C12 than Ni2P/AlMCM-41-5, it was more active for the undesired C-C bond cleavage and methanation. We propose that the in-situ phosphorization adopted here is a promising approach to preparing Ni2P-based bifunctional catalysts.

• 出版日期2017-5-15
• 单位天津大学