Jagadeesan Dinesh, Eswaramoorthy Muthusamy, Rao C N R
Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore, India.
ChemSusChem. 2009;2(9):878-82. doi: 10.1002/cssc.200900152.
Inorganic carbonates, which occur abundantly on earth, constitute an inexpensive natural source of carbon. Therefore, the direct conversion of these carbonates into methane is of considerable importance. Thermal decomposition of transition metal carbonates with the composition MCa(CO(3))(2) (where M=Co, Ni, or Fe, and M/Ca is 1:1) and M(1)M(2)Ca(CO(3))(3) (where M(1)M(2)=CoNi, NiFe, or FeCo, and M(1)/M(2)/Ca is 1:1:2) shows that the reduced transition metals in combination with metal oxide nanoparticles (e.g., Co/CoO/CaO) act as catalysts for the conversion of CO(2) (produced from the carbonates) into methane. The favorable decomposition conditions include heating at 550 degrees C in an H(2) atmosphere for 5-6 h. These catalysts are found to be excellent for the methanation of CaCO(3), exhibiting high efficiency in the utilization of H(2) with 100 % conversion and 100 % selectivity. The best catalyst for conversion of CaCO(3) into CH(4) is Co/CoO/CaO. There are also indications that similar catalysts based on Fe may yield higher hydrocarbons.
无机碳酸盐在地球上储量丰富,是一种廉价的天然碳源。因此,将这些碳酸盐直接转化为甲烷具有相当重要的意义。对组成为MCa(CO₃)₂(其中M = Co、Ni或Fe,且M/Ca为1:1)和M₁M₂Ca(CO₃)₃(其中M₁M₂ = CoNi、NiFe或FeCo,且M₁/M₂/Ca为1:1:2)的过渡金属碳酸盐进行热分解表明,还原态的过渡金属与金属氧化物纳米颗粒(如Co/CoO/CaO)结合可作为将(由碳酸盐产生的)CO₂转化为甲烷的催化剂。有利的分解条件包括在H₂气氛中于550℃加热5 - 6小时。这些催化剂被发现对CaCO₃的甲烷化反应非常有效,在H₂的利用方面表现出高效率,转化率和选择性均为100%。将CaCO₃转化为CH₄的最佳催化剂是Co/CoO/CaO。也有迹象表明,基于Fe的类似催化剂可能会生成更高碳数的烃类。