Methane C(sp3)-H bond activation by water microbubbles

被引:1
|
作者
Li, Juan [1 ]
Xu, Jinheng [2 ]
Song, Qingyuan [1 ]
Zhang, Xinxing [3 ]
Xia, Yu [1 ,2 ]
Zare, Richard N. [2 ]
机构
[1] Jianghan Univ, Sch Environm & Hlth, Hubei Key Lab Environm & Hlth Effects Persistent T, Wuhan 430056, Peoples R China
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Nankai Univ, Coll Chem,Minist Educ, Renewable Energy Convers & Storage Ctr,Key Lab Adv, Frontiers Sci Ctr New Organ Matter,Key Lab Biosens, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Compendex;
D O I
10.1039/d4sc05773b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Microbubble-induced oxidation offers an effective approach for activating the C(sp(3))-H bond of methane under mild conditions, achieving a methane activation rate of up to 6.7% per hour under optimized parameters. In this study, microbubbles provided an extensive gas-liquid interface that promoted the formation of hydroxyl (OH center dot) and hydrogen radicals (H-center dot), which facilitated the activation of methane, leading to the generation of methyl radicals (CH3 center dot). These species further participated in free-radical reactions at the interface, resulting in the production of ethane and formic acid. The microbubble system was optimized by adjusting gas-liquid interaction time, water temperature, and bubble size, with the optimal conditions (150 s of water-gas interaction, 15 degrees C, 50 mu m bubble size) yielding a methane conversion rate of 171.5 ppm h(-1), an ethane production rate of 23.5 ppm h(-1), and a formic acid production rate of 2.3 nM h(-1) during 8 h of continuous operation. The stability and efficiency of this process, confirmed through electron spin resonance, high-resolution mass spectrometry, and gas chromatography, suggest that microbubble-based methane activation offers a scalable and energy-efficient pathway for methane utilization.
引用
收藏
页码:17026 / 17031
页数:6
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