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    ǰ¶Îʱ¼äÎÒÔÚInternational Journal of Coal GeologyÉÏͶÁËÆªÎÄÕ£¨ÎÄÕºËÐÄÄÚÈÝÊÇ·ÖÎöÎü¸½Æ½ºâѹÁ¦¶Ô¿é״úÑùÍß˹½âÎüƽºâʱ¼äµÄÓ°Ïì¹æÂÉ£©£¬Éó¸åÈ˶ÔÎÒµÄÊý¾Ý½øÐÐÁË·ÖÎö£¬·¢ÏÖúÑùÖеIJÐÓàÎü¸½Íß˹£¨ÔÚ0.1MPaϽâÎüƽºâºóÊ£ÓàµÄÆøÌå£©ËæÎü¸½Æ½ºâѹÁ¦·¢Éú±ä»¯£¬¾ßÌåÒâ¼ûÈçÏ£º
    1. Comment: The amount of gas remaining adsorbed at atmospheric pressure (calculated as the difference between the "adsorption capacity" from Table 1 and the fitted "ultimate desorption capacity" from Table 2 is about 28 L at initial adsorption pressures of 1 and 2 MPa, and about 19-23 L at initial adsorption pressures of 3 and 4 MPa. Why should these final equilibrium residual amounts depend on initial pressure (with the change occurring between 2 and 3 MPa)? Is there any justification for this dependence? Would this effect persist every time upon repeating the whole pressure cycle (from 1 to 4 MPa?)
       2. Comment: Would obtaining equilibrium adsorption/desorption isotherms and verifying their repeatability with respect to adsorption/desorption cycles at varying pressures help elucidate the issues above?
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