石油炼制与化工 ›› 2023, Vol. 54 ›› Issue (8): 67-73.

• 催化剂 • 上一篇    下一篇

Ni-Nb2O5/γ-Al2O3催化1,5-双-(四氢呋喃基)-3-戊酮加氢脱氧制备长链烷烃的研究

闫瑞,赵杰,陶志平,杨鹤,贾丹丹,伏朝林,朱忠朋,郑伟平   

  1. 中石化石油化工科学研究院有限公司
  • 收稿日期:2023-01-06 修回日期:2023-03-13 出版日期:2023-08-12 发布日期:2023-07-27
  • 通讯作者: 闫瑞 E-mail:yanrui.ripp@sinopec.com
  • 基金资助:
    国家重点研发计划

PREPARATION OF LONG-CHAIN ALKANES FROM 1,5-BIS-(TETRAHYDROFURANYL)-3-PENTANONE CATALYZED BY Ni-Nb2O5/γ-Al2O3


  • Received:2023-01-06 Revised:2023-03-13 Online:2023-08-12 Published:2023-07-27
  • Contact: Rui YAN E-mail:yanrui.ripp@sinopec.com
  • Supported by:
    National Key Research and Development Plan

摘要: 设计了以γ-Al2O3为酸性载体、非贵金属Ni和Nb2O5为活性中心的催化剂 x%Ni-y%Nb2O5/γ-Al2O3x%为Ni质量分数,x=1,2,3,4,5;y%为Nb2O5质量分数,y=10,20),考察催化剂中Ni、Nb2O5含量和反应工艺条件对该催化剂催化生物燃料含氧中间体1,5-双-(四氢呋喃基)-3-戊酮加氢脱氧反应的影响。结果表明:在反应温度为260 ℃、H2压力为3 MPa、反应时间为24 h的条件下,4%Ni-20%Nb2O5/γ-Al2O3催化1,5-双-(四氢呋喃基)-3-戊酮加氢脱氧制备长链烷烃的碳摩尔收率总和达89.6%,其中C11烷烃、C12烷烃和C13烷烃的碳摩尔收率分别为3.8%,8.9%,76.9%;同时,4%Ni-20%Nb2O5/γ-Al2O3催化剂具有良好的稳定性,连续催化反应70 h后,C11~C13烷烃的碳摩尔收率总和仍能保持在89.5%。

关键词: 生物质, 加氢脱氧, 催化剂, 长链烷烃

Abstract: A new catalyst x%Ni-y%Nb2O5/γ-Al2O3(x% is the mass fraction of Ni, x=1,2,3,4,5; y% is the mass fraction of Nb2O5, y=10,20) was designed, and the effects of Ni and Nb2O5 content and reaction conditions on the hydrodeoxygenation of 1,5-bis-(tetrahydrofuranyl)-3-pentanone were investigated. The results showed that under the conditions of reaction temperature 260 ℃, pressure 3 MPa and reaction time 24 h, 4%Ni-20%Nb2O5/γ-Al2Ocatalyst for 1,5-bis-(tetrahydrofuryl) -3-pentanone hydrodeoxidization to produce long-chain alkanes had the yields of 89.6%, of which the carbon yields of C11 alkanes, C12 alkanes and C13 alkanes were 3.8%, 8.9% and 76.9%, respectively. Meanwhile, 4%Ni-20%Nb2O5/γ-Al2Ocatalyst had good stability. When the reaction temperature was 260 ℃, the reaction pressure was 3 MPa, the liquid hourly space velocity was 2 h-1, and the volume ratio of hydrogen to oil was 200, the total yield of C11-C13 alkanes could still keep up to 89.5% after 70 h of continuous catalytic reaction.

Key words: biomass, hydrodeoxygenation, catalyst, long-chain alkanes