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Removal of chromate from aqueous solution by reduction with nanoscale Fe-Al layered double hydroxide

机译:通过用纳米级Fe-Al层层双氢氧化物还原从水溶液中除去铬酸盐

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摘要

Nanoscale layered double hydroxides of Fe-II and Al-III (Fe-Al LDH) have been applied for removal of chromate (Cr-VI) from aqueous solution. Given the reaction stoichiometry, Cr-VI was completely reduced to Cr-III and coprecipitated with Fe-III and Al-III oxyhydroxides. The extent of Cr-VI removal decreased with increasing initial pH and decreasing molar ratio of Cr-VI/structural Fe-II in the LDH. The chromate reduction rate at different initial concentrations of Cr-VI was well described by the pseudo-second-order model with reaction rate constant ranging from 197.4 to 13.53 (mmol min)(-1). Initial pH and substitution of various amounts of Fe-III in the LDH structure had little effect on the reaction rate. Backtransformation of Cr-III to Cr-VI by birnessite Mn oxide (delta-MnO2) after 40 days of reaction was less than 1% of the initial Cr (as Cr-III solid), indicating high stability of the final reaction products and high efficiency of nanoscale Fe-Al LDHs for removal of chromate from aqueous solution.
机译:纳米级分层双氢氧氧化物的Fe-II和Al-III(Fe-Al LDH)已被应用于从水溶液中除去铬酸盐(Cr-VI)。考虑到反应化学计量,Cr-VI完全减少至Cr-III并用Fe-III和Al-III羟基氧化物共沉淀。随着初始pH的初始pH和降低LDH中的CR-VI /结构Fe-II的初始pH和降低摩尔比的CR-VI去除程度降低。伪二阶模型的不同初始浓度Cr-VI的铬酸盐还原速率通过197.4至13.53(Mmol Min)( - 1)的反应速率恒定。 LDH结构中各种Fe-III的初始pH和取代对反应速率影响不大。在40天反应后,通过Birneryite Mn氧化物(Delta-MnO 2)的Cr-III对Cr-VI的反向变化小于初始Cr的1%(作为Cr-III固体),表明最终反应产物的高稳定性和高纳米级Fe-Al LDH的效率从水溶液中除去铬酸盐。

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