实验室测量甲烷绝对吸附量的误差研究

    Study on Measurement Error of Absolute Adsorption of Coal-bed Methane in Laboratory

    • 摘要: 为了研究实验室测定煤的吸附量的准确性以及存在的误差,依据实验室测定煤对甲烷吸附量的原理,将实验室测得的吸附量设定为超额吸附量,煤对甲烷的绝对吸附量为真实吸附量,采用了理论分析和实验相结合的方法展开分析。通过对比超额吸附量和绝对吸附量之间的关系及修正后的吸附等温线模型,发现吸附等温线在压力较大时出现分离,超额吸附量对应的等温线明显低于真实吸附量。随着压力的增大,甲烷越接近超临界状态,游离相密度增加的更快,该趋势更加明显。经实验测定的超额吸附量和绝对吸附量进行误差分析发现,压力越大,绝对吸附量和超额吸附量的差值和误差越大。

       

      Abstract: In order to study the measurement accuracy and error of absolute adsorption quantity of coal-bed methane in laboratory, a theoretical analysis and experimental methods were used. Based on the principle of determining the adsorption quantity of coal-bed methane in laboratory, the adsorption capacity that measured in the laboratory is actually the excess adsorption. On the other hand, the true adsorption quantity of coal-bed methane was called the absolute adsorption quantity. The excess adsorption quantity is less than the absolute quantity. By comparing the relationship between the excess adsorption capacity and the absolute adsorption capacity and the modified adsorption isotherm model, it is found that the adsorption isotherms are separated when the pressure becomes larger and the corresponding isotherm is lower than the latter. With the increase of pressure, the methane is close to the supercritical condition, the free phase methane density is bigger, and this trend becomes more obvious. At the same time, by analyzing the error of the excess adsorption quantity and the absolute adsorption quantity, the error between the absolute adsorption quantity and the excess adsorption quantity increases with increasing adsorption equilibrium pressure.

       

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