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Thermal dry reforming of methane over La2O3 co-supported Ni/MgAl2O4 catalyst for hydrogen-rich syngas production

机译:La2O3共负载Ni / MgAl2O4氢化Ni / MgAl2O4催化剂的热干重整

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摘要

The excess emission of greenhouse gases (GHGs) such as CO2 and CH4 is posing an acute threat to the environment, and efficient ways are being sought to utilize GHGs to produce syngas (H-2, CO) and lighter hydrocarbons (HCs). In this study, the dry reforming of methane (DRM) has been carried out at 700 degrees C using La2O3 co-supported Ni/MgAl2O4 nano-catalyst in a fixed bed thermal reactor. The catalyst is characterized using various techniques such as XRD, FESEM, EDX-mapping, CO2-TPD, H-2-TPR and TGA. The modified MgAl2O4 shows the flake type structure after the addition of La2O3. The TPR and TPD analysis shows the highly dispersed metal and strong basic nature of the catalyst consequently enhances the conversion of CO2 and CH4. The highest conversion for CH4 is 87.3% while CO2 conversion is nearly 89.5% in 20 h of operation time. The selectivity of H-2 and CO approached 50% making the H-2/CO ratio above unity. In the longer time-on-stream (TOS) test, the catalyst shows elevated potential for longer runs showcasing better catalytic activity. The stability of the catalyst is indicated via a proposed reaction mechanism for DRM in operating conditions. Moreover, TGA indicates the lower weight loss of spent catalyst which ascribed the lower formation of carbon during TOS 20 h.
机译:多余的温室气体(GHG)的排放等CO2和CH4对环境的急性威胁造成严重威胁,并且正在寻求有效的方式利用GHG生产合成气(H-2,CO)和更轻的烃(HCS)。在该研究中,在固定床热反应器中使用La2O3共负载的Ni / MgAl2O4纳米催化剂在700℃下在700℃下进行甲烷(DRM)的干燥重整。催化剂的特征在于使用各种技术,例如XRD,FESEM,EDX映射,CO2-TPD,H-2-TPR和TGA。改性的MgAl2O4显示加入La2O3后的薄片型结构。 TPR和TPD分析显示了高度分散的金属和催化剂的强基本性质,因此增强了CO 2和CH4的转化。 CH4的最高转化率为87.3%,而二氧化碳转化率为20小时的近89.5%。 H-2和Co的选择性接近50%,使H-2 / Co比率高于Unity。在较长的流时间(TOS)试验中,催化剂显示出升高的电位,延长均匀的催化活性。催化剂的稳定性通过在操作条件下的DRM的提出的反应机理表明。此外,TGA表示在TOS 20h期间均匀碳的碳的较低形成的废催化剂的较低重量损失。

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