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CO hydrogenation combined with water-gas-shift reaction for synthetic natural gas production: a thermodynamic and experimental study

机译:一氧化碳加氢结合水煤气变换反应生产合成天然气的热力学和实验研究

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摘要

The hydrogenation of CO to synthetic natural gas (SNG) needs a high molar ratio of H2/CO (usually large than 3.0 in industry),which consumes a large abundant of hydrogen.The reverse dry reforming reaction (RDR,2H2 + 2CO (→) CH4 + CO2),combining CO methanation with water-gas-shift reaction,can significantly decrease the H2/CO molar ratio to 1 for SNG production.A detailed thermodynamic analysis of RDR reaction was carried out based on the Gibbs free energy minimization method.The effect of temperature,pressure,H2/CO ratio and the addition of H2O,CH4,CO2,O2 and C2H4 into the feed gas on CO conversion,CH4 and CO2 selectivity,as well as CH4 and carbon yield,are discussed.Experimental results obtained on homemade impregnated Ni/Al2O3 catalyst are compared with the calculations.The results demonstrate that low temperature (200-500 ℃),high pressure (1-5 MPa) and high H2/CO ratio (at least 1) promote CO conversion and CH4 selectivity and decrease carbon yield.Steam and CO2 in the feed gas decrease the CH4 selectivity and carbon yield,and enhance the CO2 content.Extra CH4 elevates the CH4 content in the products,but leads to more carbon formation at high temperatures.O2 significantly decreases the CH4 selectivity and C2H4 results in the generation of carbon.
机译:将CO加氢为合成天然气(SNG)需要高的H2 / CO摩尔比(工业上通常大于3.0),消耗大量的氢气。反向干重整反应(RDR,2H2 + 2CO(→ CH4 + CO2),结合CO甲烷化与水煤气变换反应,可将S2 / SNG生产中的H2 / CO摩尔比大大降低至1.基于Gibbs自由能最小化方法对RDR反应进行了详细的热力学分析讨论了温度,压力,H2 / CO比以及在进料气中添加H2O,CH4,CO2,O2和C2H4对CO转化率,CH4和CO2选择性以及CH4和碳收率的影响。将自制的Ni / Al2O3浸渍催化剂的计算结果与计算结果进行了比较。结果表明,低温(200-500℃),高压(1-5 MPa)和高H2 / CO比(至少1)可促进CO转化和CH4选择性并降低碳收率。原料气中的蒸汽和CO2降低额外的CH4会增加产品中的CH4含量,但导致高温下更多的碳形成。O2会显着降低CH4的选择性,而C2H4会导致碳的生成​​。

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  • 来源
    《国际煤炭科学技术学报(英文)》 |2018年第004期|439-451|共13页
  • 作者单位

    Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Institute of Coal Chemical Engineering, Taiyuan University of Technology, No.79 West Yingze Street, Taiyuan 030024, Shanxi, China;

    Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Institute of Coal Chemical Engineering, Taiyuan University of Technology, No.79 West Yingze Street, Taiyuan 030024, Shanxi, China;

    Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Institute of Coal Chemical Engineering, Taiyuan University of Technology, No.79 West Yingze Street, Taiyuan 030024, Shanxi, China;

    Key Laboratory of Coal Science and Technology of Ministry of Education and Shanxi Province, Institute of Coal Chemical Engineering, Taiyuan University of Technology, No.79 West Yingze Street, Taiyuan 030024, Shanxi, China;

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