Insight into the interdependence of Ni and Al in bifunctional Ni/ZSM-5 catalysts at the nanoscale

被引:8
作者
Vu, Hue-Tong [1 ]
Arcon, Iztok [2 ,3 ]
de Souza, Danilo Oliveira [4 ]
Pollastri, Simone [4 ]
Drazic, Goran [1 ]
Volavsek, Janez [1 ]
Mali, Gregor [1 ]
Logar, Natasa Zabukovec [1 ,2 ]
Tusar, Natasa Novak [1 ,2 ]
机构
[1] Natl Inst Chem, Hajdrihova 19, Ljubljana 1000, Slovenia
[2] Univ Nova Gorica, Vipavska 13, Nova Garica 5000, Slovenia
[3] Jozef Stefan Inst, Jamova Cesta 39, Ljubljana 1000, Slovenia
[4] Elettra Sincrotrone Trieste, Ss 14,Km 163-5, I-34149 Trieste, Italy
来源
NANOSCALE ADVANCES | 2022年 / 4卷 / 10期
关键词
SUPPORTED METAL-CATALYSTS; ZSM-5; ZEOLITE; CHEMISTRY; BEHAVIOR; HYDRODEOXYGENATION; HYDROGENATION; OXIDES; ACID;
D O I
10.1039/d2na00102k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalyst design is crucial for improving catalytic activity and product selectivity. In a bifunctional Ni/ZSM-5 zeolite type catalyst, catalytic properties are usually tuned via varying Al and Ni contents. While changes in acid properties associated with Al sites are usually closely investigated, Ni phases, however, receive inadequate attention. Herein, we present a systematic structural study of Ni in the Ni/ZSM-5 materials by using Ni K-edge XANES and EXAFS analyses, complemented by XRD and TEM, to resolve the changes in the local environment of Ni species induced by the different Al contents of the parent ZSM-5 prepared by a "green", template free technique. Ni species in Ni/ZSM-5 exist as NiO crystals (3-50 nm) and as charge compensating Ni2+ cations. The Ni K-edge XANES and EXAFS results enabled the quantification of Ni-containing species. At a low Al to Si ratio (n(Al)/n(Si) <= 0.04), the NiO nanoparticles predominate in the samples and account for over 65% of Ni phases. However, NiO is outnumbered by Ni2+ cations attached to the zeolite framework in ZSM-5 with a high Al to Si ratio (n(Al)/n(Si) = 0.05) due to a higher number of framework negative charges imparted by Al. The obtained results show that the number of highly reducible and active NiO crystals is strongly correlated with the framework Al sites present in ZSM-5 zeolites, which depend greatly on the synthesis conditions. Therefore, this kind of study is beneficial for any further investigation of the catalytic activities of Ni/ZSM-5 and other metal-modified bifunctional catalysts.
引用
收藏
页码:2321 / 2331
页数:11
相关论文
共 48 条
[11]   Chemistry 2030: A Roadmap for a New Decade [J].
Garcia-Martinez, Javier .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2021, 60 (10) :4956-4960
[12]   Catalytic decomposition of ammonia to COx-free hydrogen over Ni/ZSM-5 catalysts: A comparative study of the preparation methods [J].
Hu, Zhong-Pan ;
Weng, Chen-Chen ;
Chen, Chong ;
Yuan, Zhong-Yong .
APPLIED CATALYSIS A-GENERAL, 2018, 562 :49-57
[13]  
IHM SK, 1994, STUD SURF SCI CATAL, V84, P1765
[14]  
Jacobs P., 1987, Synthesis of ZSM-5 Zeolites in the Presence of Tetrapropylammonium Ions, P47
[15]   Characterization of metallic species on Ni- and Co-containing ZSM-5 catalysts - Reduction behavior and catalytic properties [J].
Jentys, A ;
Lugstein, A ;
Vinek, H .
ZEOLITES, 1997, 18 (5-6) :391-397
[16]   Methane activation by ZSM-5-supported transition metal centers [J].
Kiani, Daniyal ;
Sourav, Sagar ;
Tang, Yadan ;
Baltrusaitis, Jonas ;
Wachs, Israel E. .
CHEMICAL SOCIETY REVIEWS, 2021, 50 (02) :1251-1268
[17]   Catalytic hydrogenation, hydrocracking and isomerization reactions of biomass tar model compound mixture over Ni-modified zeolite catalysts in packed bed reactor [J].
Kostyniuk, Andrii ;
Bajec, David ;
Likozar, Blaz .
RENEWABLE ENERGY, 2021, 167 :409-424
[18]   Rethinking chemistry for a circular economy [J].
Kuemmerer, Klaus ;
Clark, James H. ;
Zuin, Vania G. .
SCIENCE, 2020, 367 (6476) :369-370
[19]   EXAFS and XANES analysis of oxides at the nanoscale [J].
Kuzmin, Alexei ;
Chaboy, Jesus .
IUCRJ, 2014, 1 :571-589
[20]   Valence and spin state of Co and Ni ions and their relation to metallicity and ferromagnetism in LaCo0.5Ni0.5O3 -: art. no. 104416 [J].
Kyômen, T ;
Yamazaki, R ;
Itoh, M .
PHYSICAL REVIEW B, 2003, 68 (10)