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Insights into iron induced fouling of ion-exchange membranes revealed by a quartz crystal microbalance with dissipation monitoring

机译:带有耗散监测的石英晶体微量天平揭示铁离子交换膜结垢的见解

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Understanding the mechanisms of multivalent iron interacting with ion-exchange membranes (IEMs) is crucial for the prediction of membrane fouling as well as the development of control strategies. In this study, the adsorption and desorption behaviors of Fe(III) species on a typical IEM, Nafion, were investigated using a quartz crystal microbalance with dissipation monitoring (QCM-D). The Nafion thin film formed on the crystal sensor surface via a sedimentation method showed a non-rigid structure with a Voigt-based mass concentration of ~500 ng cm?2 at a Nafion solution injection time of 10 min. Adsorption of Fe(III) species was first assessed using a 10 mM Fe(III) solution, followed by rinsing under different conditions to induce the structural transformation and/or release of Fe(III) from the Nafion film. The QCM-D results suggested that there was a rapid deposition of Fe(III) at the initial stage. It has been found that the ongoing adsorption process exhibiting pseudo-first-order kinetics was associated with the interaction between Fe(III) and the surface functional sites (–SO3H) of Nafion, which consequently retarded the proton transfer. Compared to the rinse with an acidic solution (HCl in ultrapure water, pH of 2.37), the QCM-D results of neutral elution (ultrapure water, pH of 6.50) indicated the hydrolysis of Fe(III) and/or structural transformation of the μ-oxo bridged, Fe–O–Fe.
机译:了解多价铁与离子交换膜(IEM)相互作用的机制对于预测膜污染以及控制策略的发展至关重要。在这项研究中,使用具有耗散监测(QCM-D)的石英晶体微天平,研究了典型IEM Nafion上Fe( III )物种的吸附和解吸行为。通过沉淀法在晶体传感器表面形成的Nafion薄膜显示出非刚性结构,基于Voigt的质量浓度约为500 ng cm ?2 。首先使用10 mM Fe( III )溶液评估对Fe( III )物种的吸附,然后在不同条件下冲洗以诱导结构转化和/或释放。 Nafion薄膜中的Fe( III )。 QCM-D结果表明,Fe( III )在初始阶段迅速沉积。已经发现,正在进行的表现出拟一级动力学的吸附过程与Fe( III )和表面官能点(–SO 3 H),从而阻碍了质子转移。与用酸性溶液(超纯水中的HCl,pH为2.37)冲洗相比,中性洗脱(超纯水,pH为6.50)的QCM-D结果表明Fe( III )的水解和-或氧代桥联的Fe–O–Fe的结构转变。

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