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Structural transition range of methane-ethane gas hydrates during decomposition below ice point

机译:冰点以下分解过程中甲烷-乙烷气体水合物的结构转变范围

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摘要

The structural transition of methane-ethane gas hydrates is generally observed during the forming process; however, it has seldom been reported during the dissociation process. Study on the dissociation behavior of methane-ethane hydrate below ice point has important implications on gas storage and transportation. It was also be helpful for the natural gas hydrate production by depressurization in permafrost zones. The dissociation of a series of methane-ethane hydrate samples at atmospheric pressure and temperatures below ice point (272.15-269.15 K) was performed, and the influence of gas composition and temperature on the structural transition was examined using in situ Raman spectroscopy. The hydrate structures were found to transition from structure I to structure II over a methane composition range of 50-68 mol%. The hydrates remained as sI or sII type compounds, and no structural transition occurred during the dissociation when the methane content in methane-ethane gas mixture was decreased to a certain amount ( 50 mol%) or increased to a higher value (= 70 mol%). Further investigation showed that the occurrence time of structural transition reduced with an increase in the methane concentration under the same decomposition temperature. Furthermore, hydrate dissociation was retarded upon decreasing the temperature in this temperature range (272.15-269.15 K). The mechanism of the structural transition occurring in gas hydrate decomposition was proposed.
机译:甲烷-乙烷气体水合物的结构转变通常在成型过程中观察到。但是,在解离过程中很少有报道。研究冰点以下甲烷-乙烷水合物的解离行为对气体的储运具有重要意义。通过永久冻土带的减压生产天然气水合物也很有帮助。在大气压力和低于冰点(272.15-269.15 K)的温度下进行了一系列甲烷-乙烷水合物样品的离解,并使用原位拉曼光谱法研究了气体组成和温度对结构转变的影响。发现水合物结构在50-68mol%的甲烷组成范围内从结构I转变为结构II。水合物保留为sI或sII型化合物,当甲烷-乙烷气体混合物中的甲烷含量降低至一定量(<50 mol%)或增加至更高的值(> = 70)时,在解离过程中未发生结构转变mol%)。进一步的研究表明,在相同分解温度下,随着甲烷浓度的增加,结构转变的发生时间减少。此外,在该温度范围(272.15-269.15 K)下降低温度后,水合物的离解被延迟。提出了天然气水合物分解过程中发生结构转变的机理。

著录项

  • 来源
    《Applied Energy》 |2019年第1期|873-881|共9页
  • 作者单位

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    Beijing Oriental Yuhong Waterproof Technol Co Ltd, State Key Lab Special Funct Waterproof Mat, Beijing 101309, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Univ Petr, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China;

    China Natl Offshore Oil Corp Res Ctr, Beijing 100027, Peoples R China;

    China Natl Offshore Oil Corp Res Ctr, Beijing 100027, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Methane-ethane hydrate; Dissociation mechanism; Structural transition; Raman spectra; Kinetics;

    机译:甲烷 - 乙烷水合物;解离机制;结构转变;拉曼光谱;动力学;

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