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First demonstration of direct hydrocarbon fuel production from water and carbon dioxide by solar-driven thermochemical cycles using rhodium-ceria

机译:首次展示了使用铑-二氧化铈通过太阳能驱动的热化学循环从水和二氧化碳中直接生产烃类燃料的演示

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摘要

Solar-driven thermochemical cycles (STCs) are one of the direct pathways to store solar energy in the chemical bonds of energy-rich molecules. By utilizing a redox material like ceria (CeO2) as reactive medium, STCs can produce the chemical fuels hydrogen and carbon monoxide from water and carbon dioxide. The produced syngas, a mixture of hydrogen and carbon monoxide, can be upgraded to hydrocarbon fuels by the Fischer-Tropsch process. Here, we explore a new concept of producing hydrocarbon fuels directly from water and carbon dioxide by incorporating a catalytic process into STCs. To achieve this, a starting material of ceria doped with a catalyst is used as reactive medium. The primary role of the catalyst is to catalyze the formation of hydrocarbon molecules during the reoxidation of ceria by water and carbon dioxide. In this study, nickel-doped ceria and rhodium-doped ceria were investigated for their methane formation activity after being activated by chemical or thermal reduction. Both materials, after being reduced by hydrogen at 600 degrees C, are active in producing methane during their reoxidation by water and carbon dioxide at 500 degrees C. After being thermally reduced at extreme temperatures of 1400 degrees C and 1500 degrees C, metallic rhodium is formed in rhodium-doped ceria. The activated rhodium-ceria produces methane directly from water and carbon dioxide during reoxidation. The long-term methane formation activity of rhodium-ceria for 59 cycles with thermal reduction is reported. With rhodium-ceria, this study demonstrates for the first time the concept of producing hydrocarbon fuels, i.e. methane, directly from water and carbon dioxide by realistic STCs. In contrast, nickel-doped ceria is not active in producing methane after thermal activation, owing to rapid sintering and loss of nickel at high temperatures. This underlines the importance of evaluating the effect of thermal reduction on the redox material used. The material's physicochemical properties could be rapidly and significantly altered at the extreme temperatures required for the thermal reduction of ceria. Such changes may render a material that is active and stable at low temperatures inactive when used under realistic conditions of STCs.
机译:太阳能驱动的热化学循环(STC)是将太阳能存储在能量丰富的分子的化学键中的直接途径之一。通过利用氧化铈(CeO2)等氧化还原材料作为反应性介质,STC可以从水和二氧化碳中产生氢气和一氧化碳。产生的合成气是氢气和一氧化碳的混合物,可以通过费-托工艺升级为烃类燃料。在这里,我们探索通过将催化过程纳入STC来直接从水和二氧化碳生产碳氢燃料的新概念。为此,将掺杂有催化剂的二氧化铈的原料用作反应介质。催化剂的主要作用是在二氧化铈被水和二氧化碳再氧化期间,催化碳氢化合物分子的形成。在这项研究中,研究了镍掺杂的二氧化铈和铑掺杂的二氧化铈在通过化学或热还原活化后的甲烷形成活性。两种材料均在600℃下被氢气还原后,在水和500℃下被二氧化碳再氧化的过程中,在生成甲烷方面具有活性。金属铑在1400℃和1500℃的极端温度下被热还原后,在掺铑二氧化铈中形成。活化的铑-二氧化铈在再氧化过程中直接从水和二氧化碳中产生甲烷。据报道铑二氧化铈在59个循环中具有热还原作用的长期甲烷形成活性。这项研究使用铑-二氧化铈首次展示了通过现实的STC直接从水和二氧化碳中生产碳氢化合物燃料(即甲烷)的概念。相反,由于快速烧结和在高温下镍的损失,掺杂镍的二氧化铈在热活化后不能产生甲烷。这强调了评估热还原对所用氧化还原材料的影响的重要性。在二氧化铈热还原所需的极端温度下,该材料的物理化学性质可能会迅速而显着改变。当在STC的实际条件下使用时,这种变化可能会使在低温下具有活性和稳定性的材料失去活性。

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  • 来源
    《Energy & environmental science》 |2016年第7期|2400-2409|共10页
  • 作者单位

    Paul Scherrer Inst, Solar Technol Lab, CH-5232 Villigen, Switzerland;

    Paul Scherrer Inst, Lab Catalysis & Sustainable Chem, CH-5232 Villigen, Switzerland|ETH, Inst Chem & Bioengn, Vladimir Prelog Weg 2, CH-8093 Zurich, Switzerland;

    Paul Scherrer Inst, Solar Technol Lab, CH-5232 Villigen, Switzerland;

    Paul Scherrer Inst, Lab Catalysis & Sustainable Chem, CH-5232 Villigen, Switzerland|ETH, Inst Chem & Bioengn, Vladimir Prelog Weg 2, CH-8093 Zurich, Switzerland;

    Paul Scherrer Inst, Gen Energy Res Dept, CH-5232 Villigen, Switzerland;

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