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Structural Evolution of Iron-Loaded Metal-Organic Framework Catalysts for Continuous Gas-Phase Oxidation of Methane to Methanol
被引:15
|作者:
Rungtaweevoranit, Bunyarat
[1
]
Abdel-Mageed, Ali M. M.
[4
,7
,8
]
Khemthong, Pongtanawat
[1
]
Eaimsumang, Srisin
[1
]
Chakarawet, Khetpakorn
[2
,3
]
Butburee, Teera
[1
]
Kunkel, Benny
[4
]
Wohlrab, Sebastian
[4
]
Chainok, Kittipong
[5
]
Phanthasri, Jakkapop
[1
]
Wannapaiboon, Suttipong
[6
]
Youngjan, Saran
[1
]
Seehamongkol, Theerada
[1
]
Impeng, Sarawoot
[1
]
Faungnawakij, Kajornsak
[1
]
机构:
[1] Natl Sci & Technol Dev Agcy NSTDA, Natl Nanotechnol Ctr NANOTEC, Pathum Thani 12120, Thailand
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Mahidol Univ, Fac Sci, Dept Chem, Bangkok 10400, Thailand
[4] Leibniz Inst Katalyse eV LIKAT Rostock, D-18059 Rostock, Germany
[5] Thammasat Univ, Res Unit Multifunct Crystalline Mat & Applicat TU, Fac Sci & Technol, Pathum Thani 12121, Thailand
[6] Synchrotron Light Res Inst Publ Org, Nakhon Ratchasima 30000, Thailand
[7] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt
[8] Ulm Univ, Inst Surface Chem & Catalysis, D-89069 Ulm, Germany
关键词:
partial methane oxidation;
methanol;
metal-organicframework;
heterogeneous catalysis;
iron catalyst;
ACTIVE-SITE STRUCTURE;
SELECTIVE OXIDATION;
EXCHANGED ZEOLITES;
DIRECT CONVERSION;
SURFACE;
NANOPARTICLES;
OXIDE;
SPECTROSCOPY;
ADSORPTION;
REACTIVITY;
D O I:
10.1021/acsami.3c03310
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Catalytic partial oxidation of methane presents a promisingrouteto convert the abundant but environmentally undesired methane gasto liquid methanol with applications as an energy carrier and a platformchemical. However, an outstanding challenge for this process remainsin developing a catalyst that can oxidize methane selectively to methanolwith good activity under continuous flow conditions in the gas phaseusing O-2 as an oxidant. Here, we report a Fe catalyst supportedby a metal-organic framework (MOF), Fe/UiO-66, for the selectiveand on-stream partial oxidation of methane to methanol. Kinetic studiesindicate the continuous production of methanol at a superior reactionrate of 5.9 x 10(-2) mu mol(MeOH) g(Fe) (-1) s(-1) at 180 degrees C and high selectivity toward methanol, with the catalytic turnoververified by transient methane isotopic measurements. Through an arrayof spectroscopic characterizations, electron-deficient Fe speciesrendered by the MOF support is identified as the probable active sitefor the reaction.
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页码:26700 / 26709
页数:10
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