Laboratory for Catalysis and Sustainable Chemistry, Paul Scherrer Institut, 5232 Villigen, Switzerland.
Institute for Chemistry and Bioengineering, ETH Zurich, Vladimir-Prelog-Weg 1, 8093 Zürich, Switzerland.
Science. 2017 May 5;356(6337):523-527. doi: 10.1126/science.aam9035.
Direct functionalization of methane in natural gas remains a key challenge. We present a direct stepwise method for converting methane into methanol with high selectivity (~97%) over a copper-containing zeolite, based on partial oxidation with water. The activation in helium at 673 kelvin (K), followed by consecutive catalyst exposures to 7 bars of methane and then water at 473 K, consistently produced 0.204 mole of CHOH per mole of copper in zeolite. Isotopic labeling confirmed water as the source of oxygen to regenerate the zeolite active centers and renders methanol desorption energetically favorable. On the basis of in situ x-ray absorption spectroscopy, infrared spectroscopy, and density functional theory calculations, we propose a mechanism involving methane oxidation at Cu oxide active centers, followed by Cu reoxidation by water with concurrent formation of hydrogen.
直接将天然气中的甲烷转化为甲醇仍然是一个关键挑战。我们提出了一种在含铜沸石上通过部分氧化水将甲烷高选择性(~97%)直接转化为甲醇的分步方法。在氦气中于 673 开尔文(K)下进行活化,然后连续将催化剂暴露于 7 巴的甲烷和 473 K 的水,在沸石中铜的摩尔数始终产生 0.204 摩尔的 CHOH。同位素标记证实水是再生沸石活性中心的氧源,并使甲醇解吸具有能量优势。根据原位 X 射线吸收光谱、红外光谱和密度泛函理论计算,我们提出了一种涉及 Cu 氧化物活性中心氧化甲烷的机制,然后水对 Cu 进行再氧化,同时形成氢气。