Chemical Industry and Engineering Progress ›› 2025, Vol. 44 ›› Issue (7): 3917-3927.DOI: 10.16085/j.issn.1000-6613.2024-0935

• Industrial catalysis • Previous Articles    

Effect of alumina support crystal structure of Ru-based catalysts on polyethylene hydrogenolysis performance

GAO Jiaojiao1(), YAN Shiyu1, YANG Taishun1, XIE Shangzhi1, YANG Yanjuan1, XU Jing1,2()   

  1. 1.Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, Guangxi, China
    2.State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China
  • Received:2024-06-07 Revised:2024-08-06 Online:2025-08-04 Published:2025-07-25
  • Contact: XU Jing

不同晶型Al2O3负载Ru催化剂对聚乙烯氢解的影响

高姣姣1(), 颜诗宇1, 杨太顺1, 谢尚志1, 杨艳娟1, 徐晶1,2()   

  1. 1.广西大学化学化工学院广西石化资源加工与过程强化技术重点实验室,广西 南宁 530004
    2.华东理工大学绿色化工与工业催化全国重点实验室,化工学院,上海 200237
  • 通讯作者: 徐晶
  • 作者简介:高姣姣(1998—),女,硕士研究生,研究方向为工业催化。E-mail:gaojiaojiao0625@163.com
  • 基金资助:
    广西科技重大专项(桂科AA23062018);广西科技基地和人才专项(桂科AD23026311)

Abstract:

The production of fuel from polyethylene (PE) by catalytic hydrogen hydrolysis is an important approach to realize green recycle of PE. In this work, the effect of crystal structure of Al2O3 on the performance of Ru-based catalyst for PE hydrogenolysis was investigated. Four kinds of Ru/Al2O3 catalysts were prepared by impregnation method, and characterized by TEM, H2-TPR and XPS to reveal the interaction between active metal Ru and Al2O3 support. The experimental results of PE hydrolysis showed that the difference in Al2O3 crystal structure led to a significant effect on the catalytic performance. Under the same reaction conditions, the total yield of products by Ru/(δ+α)-Al2O3 catalyst was less than 10%, and the methane yield was less than 5%, while the total yield for the other three catalysts was all higher than 90%. Among them, Ru/(θ+α)-Al2O3 exhibited the highest methane yield and selectivity, with methane yield higher than 90% and methane selectivity over 95%. By adjusting the hydrogen pressure, it was found that the different coverage of *H led to different reaction behaviors. With the combination of H2-TPD and CO-DRIFTS characterization methods, it was found that the excess adsorption of *H at the active site Ru0 of Ru/γ-Al2O3 could result in hydrogen poisoning. For Ru/(θ+α)-Al2O3, the adsorption of *H at the active site Ru0 and the C—C intermediate could reach adsorption equilibrium. On Ru/(δ+α)-Al2O3 catalyst, no *H adsorption on the active site Ru0 was detected, hence the total product yield for Ru/(δ+α)-Al2O3 was below 10%.

Key words: Ru/Al2O3 catalyst, hydrogenation, methane, alumina, adsorption

摘要:

废聚乙烯(PE)通过催化氢解制取燃料产品是实现塑料绿色循环的重要途径之一。本文探究了Al2O3晶型对负载型Ru基催化剂在PE催化氢解中反应性能的影响。通过浸渍法制备4种不同晶型的Ru/Al2O3催化剂,采用TEM、H2-TPR和XPS对Ru/Al2O3催化剂进行表征,以揭示活性金属Ru与Al2O3载体之间的相互作用差异。PE氢解实验的结果表明,Al2O3晶型的差异对Ru/Al2O3催化剂催化氢解性能产生显著影响。在相同条件下进行PE氢解反应时,Ru/(δ+α)-Al2O3上产物总产率低于10%,甲烷的产率低于5%;而其他3种催化剂的产物总产率均高于90%,其中Ru/(θ+α)-Al2O3的甲烷产率(>90%)和选择性(>95%)最高。调控氢气反应压力,发现不同的*H覆盖率导致Ru/Al2O3催化剂上不同的反应行为。采用H2-TPD和CO-DRIFTS对Ru/Al2O3催化剂进行表征,发现Ru/γ-Al2O3上活性位点Ru0上的*H的过量吸附,导致了氢中毒;在Ru/(θ+α)-Al2O3上,活性位点Ru0上的*H吸附和C-C长链吸附达到了平衡;在Ru/(δ+α)-Al2O3上,由于Ru n+的含量过高,导致*H在金属Ru上的吸附较弱,从而Ru/(δ+α)-Al2O3上产物总产率低于10%。

关键词: Ru/Al2O3催化剂, 加氢, 甲烷, 氧化铝, 吸附

CLC Number: 

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