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GIBBS FREE ENERGIES FOR DUAL LANGMUIR-LIKE ADSORPTION ONTO HARD CARBON MATERIALS IN SEDIMENT AND SOILS

机译:沉积物和土壤中对硬质碳材料的双重朗格状吸附的吉布斯自由能

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摘要

Adsorption of organic compounds onto hard carbon constituents of soils and sediments may be described by a dual Langmuir-like equation for adsorption onto high-energy sites and low-energy sites. To describe quantitatively the sorbate—sorbent interactions on these high-energy sites and low-energy sites, Gibbs free energies for adsorption onto several soils and sediments were calculated using suitable experimental sorption data from the literature. A large part of the variation in these Gibbs free energies relative to the pure solid state appeared to be related to differences in sorbate molecular symmetry. Generally, for a broad range of nonpolar organic compounds, from substituted benzenes to five-ring polycyclic aromatic hydrocarbons and hexachlorinated biphenyls, sorbate molecular symmetry-corrected Gibbs free energies for high-energy and low-energy adsorption relative to the pure solid state were within a narrow range or approximately -23 and -11 kJ/mol, respectively. These two average values for the geosorbents were comparable to corresponding values for adsorption onto activated carbon.
机译:有机化合物在土壤和沉积物的硬碳成分上的吸附可以用双重朗缪尔式方程描述,以吸附在高能位点和低能位点上。为了定量描述在这些高能位点和低能位点上的吸附物-吸附剂相互作用,使用来自文献的合适的实验吸附数据,计算了吸附到几种土壤和沉积物上的吉布斯自由能。这些吉布斯自由能相对于纯固态的很大一部分变化似乎与山梨酸酯分子对称性的差异有关。通常,对于广泛的非极性有机化合物,从取代的苯到五环多环芳烃和六氯化联苯,相对于纯固态,用于高能和低能吸附的山梨酸酯分子对称校正的吉布斯自由能都在窄范围或分别约为-23和-11 kJ / mol。地质吸附剂的这两个平均值与吸附在活性炭上的相应值相当。

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