Mild oxidation of methane to methanol or acetic acid on supported isolated rhodium catalysts

催化作用 甲醇 化学 醋酸 羰基化 甲烷 氧合物 合成气 无机化学 一氧化碳 有机化学
作者
Junjun Shan,Mengwei Li,Lawrence F. Allard,Sungsik Lee,Maria Flytzani‐Stephanopoulos
出处
期刊:Nature [Nature Portfolio]
卷期号:551 (7682): 605-608 被引量:763
标识
DOI:10.1038/nature24640
摘要

An efficient and direct method of catalytic conversion of methane to liquid methanol and other oxygenates would be of considerable practical value. However, it remains an unsolved problem in catalysis, as typically it involves expensive or corrosive oxidants or reaction media that are not amenable to commercialization. Although methane can be directly converted to methanol using molecular oxygen under mild conditions in the gas phase, the process is either stoichiometric (and therefore requires a water extraction step) or is too slow and low-yielding to be practical. Methane could, in principle, also be transformed through direct oxidative carbonylation to acetic acid, which is commercially obtained through methane steam reforming, methanol synthesis, and subsequent methanol carbonylation on homogeneous catalysts. However, an effective catalyst for the direct carbonylation of methane to acetic acid, which might enable the economical small-scale utilization of natural gas that is currently flared or stranded, has not yet been reported. Here we show that mononuclear rhodium species, anchored on a zeolite or titanium dioxide support suspended in aqueous solution, catalyse the direct conversion of methane to methanol and acetic acid, using oxygen and carbon monoxide under mild conditions. We find that the two products form through independent pathways, which allows us to tune the conversion: three-hour-long batch-reactor tests conducted at 150 degrees Celsius, using either the zeolite-supported or the titanium-dioxide-supported catalyst, yield around 22,000 micromoles of acetic acid per gram of catalyst, or around 230 micromoles of methanol per gram of catalyst, respectively, with selectivities of 60-100 per cent. We anticipate that these unusually high activities, despite still being too low for commercial application, may guide the development of optimized catalysts and practical processes for the direct conversion of methane to methanol, acetic acid and other useful chemicals.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
emnjkl完成签到,获得积分10
刚刚
大个应助song采纳,获得10
刚刚
大个应助李奥采纳,获得10
刚刚
一一发布了新的文献求助10
1秒前
khjia发布了新的文献求助10
1秒前
jay完成签到,获得积分10
1秒前
小贝完成签到,获得积分10
1秒前
vampire完成签到 ,获得积分10
2秒前
小飞完成签到,获得积分10
2秒前
2秒前
吴五五完成签到,获得积分10
2秒前
罗丹明完成签到,获得积分10
2秒前
科目三应助赛特新思采纳,获得10
2秒前
小费发布了新的文献求助30
2秒前
今后应助阳光小虾米采纳,获得10
3秒前
Will发布了新的文献求助10
3秒前
FashionBoy应助cr2025采纳,获得10
3秒前
慕青应助qinglinglie采纳,获得10
3秒前
Tenacity发布了新的文献求助10
3秒前
Drtaoao完成签到 ,获得积分10
3秒前
英姑应助Regina采纳,获得10
3秒前
sdwdw发布了新的文献求助10
3秒前
hetao286完成签到,获得积分10
3秒前
Suxxin完成签到,获得积分10
4秒前
Green发布了新的文献求助10
4秒前
Hello应助抗体药物偶联采纳,获得10
4秒前
emnjkl发布了新的文献求助10
4秒前
lilixia完成签到,获得积分10
5秒前
科研通AI6.4应助立冬采纳,获得20
5秒前
麦子发布了新的文献求助10
6秒前
木桔发布了新的文献求助10
6秒前
怡然宛应助curry采纳,获得10
6秒前
6秒前
无名花生完成签到 ,获得积分10
6秒前
7秒前
7秒前
很难过发布了新的文献求助10
8秒前
葱白应助钊子采纳,获得20
8秒前
khjia完成签到,获得积分10
8秒前
8秒前
高分求助中
Overcoming Stigma and Bias in Obesity Management 800
Malcolm Fraser : a biography 700
Signals, Systems, and Signal Processing 610
Materials selection in mechanical design 500
Bounds for Statistical Estimation in Semiparametric Models 500
Climate change and sports: Statistics report on climate change and sports 500
Forced degradation and stability indicating LC method for Letrozole: A stress testing guide 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6477843
求助须知:如何正确求助?哪些是违规求助? 8279558
关于积分的说明 17657947
捐赠科研通 5560067
什么是DOI,文献DOI怎么找? 2910942
邀请新用户注册赠送积分活动 1887930
关于科研通互助平台的介绍 1741499