Selective Methane Oxidation to Acetic Acid Using Molecular Oxygen over a Mono-Copper Hydroxyl Catalyst

被引:41
作者
Antil, Neha [1 ]
Chauhan, Manav [1 ]
Akhtar, Naved [1 ]
Kalita, Rahul [1 ]
Manna, Kuntal [1 ]
机构
[1] Indian Inst Technol Delhi, Dept Chem, New Delhi 110016, India
关键词
METAL-ORGANIC FRAMEWORKS; DENSITY-FUNCTIONAL THEORY; H BOND ACTIVATION; HIGHLY EFFICIENT; DIRECT CONVERSION; CARBONYLATION; VANADIUM; CH4; CO; SITES;
D O I
10.1021/jacs.2c12042
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Acetic acid is an industrially important chemical, produced mainly via carbonylation of methanol using precious metal-based homogeneous catalysts. As a low-cost feedstock, methane is commercially transformed to acetic acid via a multistep process involving energy-intensive methane steam reforming, methanol synthesis, and, subsequently, methanol carbonylation. Here, we report a direct single-step conversion of methane to acetic acid using molecular oxygen (O-2) as the oxidant under mild conditions over a mono-copper hydroxyl site confined in a porous cerium metal-organic framework (MOF), Ce-UiO-Cu(OH). The Ce-UiO MOF-supported single-site copper hydroxyl catalyst gave exceptionally high acetic acid productivity of 335 mmolg(cat)(-1) in 96% selectivity with a Cu TON up to 400 at 115 degrees C in water. Our spectroscopic and theoretical studies and controlled experiments reveal that the conversion of methane to acetic acid occurs via oxidative carbonylation, where methane is first activated at the copper hydroxyl site via sigma-bond metathesis to afford Cu-methyl species, followed by carbonylation with in situ-generated carbon monoxide and subsequent hydrolysis by water. This work may guide the rational design of heterogeneous abundant metal catalysts for the activation and conversion of methane to acetic acid and other valuable chemicals under mild and environmentally friendly reaction conditions.
引用
收藏
页码:6156 / 6165
页数:10
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