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Experimental study of multilayer adsorption on fractal surfaces in porous media

机译:多孔介质中分形表面多层吸附的实验研究

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We report a nitrogen adsorption isotherm study on three shale samples that have been previously characterized by small-angle neutron scattering (SANS). The scattering data establish that the pore surfaces in these porous materials are self-similar fractals over a range of length scales between 5 and 500 Angstrom, and the fractal dimension D varies between 2.59 and 2.83. For isothermal adsorption of multilayer liquid film on fractal surfaces, the theoretical predictions are (i) the number of adsorbed molecules N increases with the vapor pressure P as N similar to[ln(P-0/P)](D-3) and (ii) the area of the liquid-vapor interface S-I decreases as S-I similar to[ln(P-0/P)](D-2). We find that fitting our data to these predictions results in D values that are significantly lower than the SANS results. More careful examination of the data reveals systematic deviations from the predicted power-law behaviors. We discuss the assumptions and approximations made in the theories that could have caused this discrepancy. [References: 35]
机译:我们报告了先前已通过小角中子散射(SANS)表征的三个页岩样品的氮吸附等温线研究。散射数据表明,这些多孔材料中的孔表面在5到500埃的长度尺度范围内是自相似的分形,而分形维数D在2.59和2.83之间变化。对于等温吸附在分形表面上的多层液膜,理论预测是:(i)吸附分子的数量N随着蒸气压P的增加而增加,类似于[ln(P-0 / P)](D-3),并且(ii)与[ln(P-0 / P)](D-2)相似,液-气界面SI的面积随着SI而减小。我们发现,将我们的数据拟合到这些预测结果中的D值大大低于SANS结果。更仔细地检查数据可以发现与预测的幂律行为的系统偏差。我们讨论了可能导致这种差异的理论中的假设和近似。 [参考:35]

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