Catalytic pyrolysis performance of alkanes to light olefins over bifunctional ZSM-5 zeolites

被引:13
作者
Liu, Meijia [1 ]
Wang, Gang [1 ]
Zhang, Zhongdong [2 ]
Li, Zhengyu [1 ]
Xu, Shunnian [1 ]
Wang, Ruipu [2 ]
He, Shengbao [2 ]
机构
[1] China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] PetroChina, Petrochem Res Inst, Beijing 102206, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkane; Catalytic pyrolysis; Light olefins; ZSM-5; Transition metals; REACTION PATHWAYS; PENTANE CRACKING; NAPHTHA CRACKING; FCC UNIT; DEHYDROGENATION; AROMATICS; MECHANISMS; REDUCTION; STABILITY; OXIDATION;
D O I
10.1016/j.jaap.2023.105924
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Light alkanes in naphtha are difficult to crack into light olefins due to high energy chemical bonds. Here, we proposed a method to improve the conversion of light alkanes by promoting C-H bonds breakage. According to the results of thermodynamic analysis, it was discovered that light olefins yield generated by dehydrogenation cracking of alkanes was about 15% higher than that by protonation cracking, indicating that light olefins yield could be enhanced by promoting C-H bonds cleavage of alkanes. After that, bifunctional ZSM-5 zeolites were modified with phosphorus and transition metals to enhance the dehydrogenation and cracking of alkanes. It showed that Ag-P-ZSM-5 zeolite could improve C5-C7 alkanes conversion by 3.88%-36.09%, and light olefins yield by 1.60%-14.81%, compared with P-ZSM-5 zeolite. The characterization results showed that silver modification could increase Lewis acid sites on zeolite, and promote C-H bonds breakage of alkanes. Further- more, Ag+ and Agnd+ species were active centers that promote C-H bonds cleavage. This work could provide a good foundation to the preparation of catalysts for naphtha catalytic pyrolysis.
引用
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页数:10
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