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

被引:12
作者
Chen, Mei [1 ]
Ma, Jinxing [2 ]
Wang, Zhiwei [1 ]
Zhang, Xingran [1 ]
Wu, Zhichao [1 ]
机构
[1] Tongji Univ, Coll Environm Sci & Engn, State Key Lab Pollut Control & Resources Reuse, Shanghai 200092, Peoples R China
[2] Univ New South Wales, Sch Civil & Environm Engn, Sydney, NSW 2052, Australia
来源
RSC ADVANCES | 2017年 / 7卷 / 58期
基金
中国国家自然科学基金;
关键词
MICROBIAL FUEL-CELLS; IONOMER MEMBRANES; CAPACITIVE DEIONIZATION; FLOW ELECTRODES; WATER-SORPTION; PERFORMANCE; ADSORPTION; NAFION; BIOREACTORS; NANOPARTICLES;
D O I
10.1039/c7ra05510b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 similar to 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 mu-oxo bridged, Fe-O-Fe.
引用
收藏
页码:36555 / 36561
页数:7
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