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Flow microcalorimetry: Experimental development and application to adsorption of heavy metal cations on silica

机译:流动微量量热法:重金属阳离子在二氧化硅上吸附的实验开发与应用

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Sorption of metal ions at the oxide mineral-water interfaces is a complex process involving many various contributions that can be explained using thermodynamics. The aim of this study is to obtain experimental thermodynamic data on adsorption of two heavy metal ions (Cd(Ⅱ) and Pb(Ⅱ)) on macroporous silica. Thermal signals of adsorption are studied by flow microcalorimetry which has been preferred because physico-chemicals conditions (pH, equilibrium concentration,...) can be controlled (the routine configuration was optimized in order to get a very stable pressure baseline and avoid important fluctuations in the determination of heat). Mechanisms driving the adsorption have been explained. The calculation of the effective charge of ions determined from the speciation diagrams and of the surface charges shows that the interactions between the two metals and the silica surface are mainly electrostatic. The differential enthalpies of adsorption Δ_(ads)H have been experimentally measured. The heat of cadmium adsorption is low, endothermic and quantitatively equivalent to that of desorption. In the case of lead, the adsorption is athermal. Free energies and entropic effects related to cation adsorption have then been deduced according to the Gibbs'law. The entropy is positive during the adsorption process and at this temperature (298 K) is quite equivalent to free energy. This entropy is due to modification of hydration shell of the ions during their insertion into the interfacial region.
机译:金属离子在氧化物矿物质-水的界面处的吸附是一个复杂的过程,涉及许多不同的贡献,可以用热力学来解释。本研究的目的是获得大孔二氧化硅吸附两种重金属离子(Cd(Ⅱ)和Pb(Ⅱ))的实验热力学数据。吸附的热信号通过流动微量量热法进行研究,这是优选的方法,因为可以控制物理化学条件(pH,平衡浓度等)(优化常规配置以获得非常稳定的压力基线并避免重要的波动)在确定热量)。已经解释了驱动吸附的机理。由形态图确定的离子有效电荷和表面电荷的计算表明,两种金属与二氧化硅表面之间的相互作用主要为静电。已经通过实验测量了吸附差Δ_(ads)H。镉吸附的热量低,吸热且在数量上等同于解吸热量。在铅的情况下,吸附是无热的。然后根据吉布斯定律推导了与阳离子吸附有关的自由能和熵效应。熵在吸附过程中为正,在此温度下(298 K)相当等于自由能。该熵归因于离子在插入界面区域期间的水合壳的改性。

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