Exploring the mechanism of different active species formation in heterogeneous Fenton systems by iron chemical environment regulation

Author(s):  
Yue Yin ◽  
Ruolin Lv ◽  
Weiming Zhang ◽  
Junhe Lu ◽  
Yi Ren ◽  
...  
2017 ◽  
Vol 328 ◽  
pp. 56-62 ◽  
Author(s):  
Yibing Li ◽  
Lianshuang Guo ◽  
Dekang Huang ◽  
Ali Jawad ◽  
Zhuqi Chen ◽  
...  

2019 ◽  
Vol 258 ◽  
pp. 117985 ◽  
Author(s):  
Yang Sun ◽  
Pengfei Tian ◽  
Doudou Ding ◽  
Zixu Yang ◽  
Weizhi Wang ◽  
...  

2013 ◽  
Vol 41 (12) ◽  
pp. 3268-3274 ◽  
Author(s):  
Ruobing Zhang ◽  
Yongrui Zhang ◽  
Xian Fu ◽  
Xian Zhang ◽  
Jie Chen ◽  
...  

Author(s):  
Zhang Kaili ◽  
Yang Yanli ◽  
Xu Miao ◽  
Cheng Tiexin ◽  
Zhou Guangdong

Abstract In this work, Mackinawite (FeSm) was synthesized by the homogeneous precipitation method, which was flower-like nanoparticles formed by the aggregation of nanosheets with a preferred orientation along the (001) plane. The heterogeneous Fenton-like degradation performance of FeSm on Rhodamine B (RhB) was investigated, results illustrated that RhB degradation was the synergistic effect of adsorption, Fenton, and the heterogeneous Fenton-like reaction. In repeated experiments, the reduction of reactivity was attributed to the oxidation of FeSm into lepidocrocite, whereas lepidocrocite has relatively low hydroxyl radicals (•OH) production reactivity. Thus, it showed excellent degradation effects in the long-time degradation of RhB. Photoluminescence (PL) technology and free radical capture experiments demonstrated that •OH produced on the surface of catalyst was the main active species to remove RhB. Meanwhile, the Fe species on the surface of FeSm was the main active center for surface-mediated reactions. The total organic carbon (TOC) test revealed that the degradation was not complete and degradation intermediates were formed. Liquid chromatography-mass spectrometry (LC-MS) technology was used to identify the degradation intermediates. On this basis, possible degradation pathways were proposed.


Geo&Bio ◽  
2019 ◽  
Vol 2019 (17) ◽  
pp. 116-135 ◽  
Author(s):  
Vira V. Protopopova ◽  
◽  
Myroslav Shevera

2018 ◽  
Vol 69 (1) ◽  
pp. 112-115
Author(s):  
Ana Maria Popescu ◽  
Virgil Constantin

The cathodic behavior of Ce3+ ions in LiF-NaF-BaF2, LiF-NaF-NaCl and NaCl-KCl molten salts at 730� C has been studied using different electrochemical techniques. The decomposition potential (Ed) and the cathodic overvoltage were determined by introducing NaCeF4 as electrochemical active species using steady-state potential-current curves recorded under galvanostatic conditions. The values of |Ed| were 1.85 V in LiF-NaF-BaF2, 2.114 V in LiF-NaF-NaCl and 2.538 V in NaCl-KCl, respectively. It was also found that the ohmic drop potential in melt is not dependent on NaCeF4 concentration and it rises as the current intensity increases. The Tafel slopes and other kinetic parameters were calculated on the assumption that the cathodic process consisted of direct discharge of Ce3+, with no solvent-solute interaction. In order to elucidate the mechanisn of cathodic process the cyclic voltammetry technique was finally used. From the evolution of the voltammograms we conclude that the electrochemical reduction of Ce3+ ion is actually a reversible process on the molybdenum electrode and cathodic reduction of Ce3+ takes place in one single step involving three electron exchange. Our study adds to the accumulating data and confirms available results of electrodeposition of metalic cerium from molten salts using NaCeF4 as solute.


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