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Recovery of radioactive cesium using nickel hexacyanoferrate as an electrically switched ion exchanger

机译:使用六氰合铁酸镍作为电开关离子交换剂回收放射性铯

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A combination of conventional ion exchange and electrochemical processes was conducted in production of electrically switched nickel hexacyanoferrate ion exchanger, specially used for ~(134)Cs recovery. The deposited films were physically characterized by energy dispersive X-ray spectroscopy and X-ray diffraction techniques. ~(134)Cs uptake was controlled by modulation of the ion exchanger potential in batch and flow systems. The deposited nickel hexacyanoferrate ion exchange film was found hydromechanically stable up to 130 bed volume/h. The ion uptake was about more than 90% achieved after 15 h of equilibrium. The reduced film state showed higher performance than the oxidized one in presence and absence of Na~+ ions with different concentrations. The breakthrough of the electrically switched ion exchange (ESIX) process was also conducted in different stacking of electrodes cells. Three and six stacked electrodes assemblies showed longer breakthroughs than single electrode assembly at the same operating conditions. In vertical cell, representing larger scale tests, higher concentrations (60ppm Cs~+) could be successfully treated.
机译:在生产专用于〜(134)Cs回收的电开关六氰合铁酸镍离子交换剂的生产过程中,将常规离子交换和电化学工艺相结合。通过能量色散X射线光谱和X射线衍射技术对沉积的膜进行物理表征。 〜(134)Cs的吸收是通过调节间歇和流动系统中离子交换剂电势来控制的。发现沉积的六氰合高铁酸镍离子交换膜在高达130床体积/小时的条件下具有流体力学稳定性。平衡15小时后,离子吸收达到约90%以上。在存在和不存在不同浓度的Na +离子的情况下,还原后的膜态表现出比氧化态更高的性能。电开关离子交换(ESIX)工艺的突破也通过电极电池的不同堆叠进行。在相同的工作条件下,三个和六个堆叠式电极组件的穿透力比单个电极组件更长。在代表较大规模测试的垂直电池中,可以成功处理更高的浓度(60ppm Cs〜+)。

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