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.
引用
收藏
页码:26700 / 26709
页数:10
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