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Kinetics of Methane Hydrate Replacement with Carbon Dioxide and Nitrogen Gas Mixture Using in Situ NMR Spectroscopy

机译:用原位NMR光谱法测定二氧化碳和氮气混合气体置换甲烷水合物的动力学

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摘要

In this study, the kinetics of methane replacement with carbon dioxide and nitrogen gas in methane gas hydrate prepared in porous silica gel matrices has been studied by in situ ~1H and ~(13)C NMR spectroscopy. The replacement process was monitored by in situ ~1H NMR spectra, where about 42 mol % of the methane in the hydrate cages was replaced in 65 h. Large amounts of free water were not observed during the replacement process, indicating a spontaneous replacement reaction upon exposing methane hydrate to carbon dioxide and nitrogen gas mixture. From in situ ~(13)C NMR spectra, we confirmed that the replacement ratio was slightly higher in small cages, but due to the composition of structure I hydrate, the amount of methane evolved from the large cages was larger than that of the small cages. Compositional analysis of vapor and hydrate phases was also carried out after the replacement reaction ceased. Notably, the composition changes in hydrate phases after the replacement reaction would be affected by the difference in the chemical potential between the vapor phase and hydrate surface rather than a pore size effect. These results suggest that the replacement technique provides methane recovery as well as stabilization of the resulting carbon dioxide hydrate phase without melting.
机译:在这项研究中,通过原位〜1H和〜(13)C NMR光谱研究了在多孔硅胶基质中制备的甲烷水合物中二氧化碳和氮气置换甲烷的动力学。通过原位〜1 H NMR光谱监测置换过程,其中在65小时内置换了水合物笼中约42 mol%的甲烷。在置换过程中未观察到大量的游离水,表明在将甲烷水合物暴露于二氧化碳和氮气的混合物后会发生自发的置换反应。从原位〜(13)C NMR谱图中,我们确认了小笼中的置换率稍高,但由于结构I水合物的组成,从大笼中释放出的甲烷量大于小笼中的甲烷量。笼子。置换反应停止后,还进行了气相和水合物相的组成分析。值得注意的是,置换反应后水合物相的组成变化将受到汽相与水合物表面之间化学势的差异而不是孔径影响的影响。这些结果表明,替代技术提供了甲烷回收以及所生成的二氧化碳水合物相的稳定而不熔化。

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  • 来源
    《Environmental Science & Technology》 |2015年第3期|1964-1971|共8页
  • 作者单位

    Department of Energy and Resources Engineering, Kangwon National University, 1 Kangwondaehak-gil, Chuncheon-si, Gangwon-do 200-701, Republic of Korea;

    Department of Applied Chemistry, Kyungpook National University, 80 Daehak-ro, Buk-gu, Daegu, Gyeongsangbuk-do 702-701, Republic of Korea;

    Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, Chungcheongnam-do 305-701, Republic of Korea;

    National Research Council of Canada, Ottawa, Ontario K1A 0R6, Canada,Max Planck Institute for Solid State Research, Heisenbergstr. 1, 70569 Stuttgart, Germany;

    National Research Council of Canada, Ottawa, Ontario K1A 0R6, Canada;

    Ocean Systems Engineering Division, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, Chungcheongnam-do 305-701, Republic of Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 13:59:37

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