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Application of fly ash-based geopolymer for removal of cesium, strontium and arsenate from aqueous solutions: kinetic, equilibrium and mechanism analysis

机译:粉煤灰基地质聚合物从水溶液中去除铯,锶和砷化物中的应用:动力学,平衡和机理分析

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摘要

Geopolymerization is a developing reaction process for the utilization of solid wastes. In the present study, fly ash-based geopolymer and its derivative (Fe(II)-modified geopolymer) were synthesized and characterized using XRD, SEM, FTIR, BET, UV-Vis DRS as well as TG-DTA, and adopted as adsorbents for removal of Cs+ and Sr2+, and AsO43- from solutions. Each sorption kinetic was well fitted to the pseudo-second-order model. The sorption of Cs+ and Sr2+ onto original geopolymer were better fitted to the Langmuir model. However, the Freundlich model is more befitting for sorption of AsO43- onto Fe(II)-modified geopolymer. The free energies calculated from the D-R isotherm indicated that the sorption for Cs+ and Sr2+ were dominantly ion exchanges. Ring size plays a decisive role in ion exchanges for both Cs+ and Sr2+. Furthermore, the arrangement of SiO4 and AlO4 tetrahedrons has significant impacts on the ion exchange of Sr2+. XPS results indicated that a part of Fe2+ in Fe (II)-modified geopolymer had been oxidized to Fe3+ after sorption. Precipitation of FeAsO4 could partially contribute to the arsenate removal from solution. AsO43- sorption has also occurred through the formation of inner-sphere complexes via ion exchange reaction, which could be predominantly attached by bidentate linkages.
机译:地质聚合物是用于利用固体废物的开发反应过程。在本研究中,使用XRD,SEM,FTIR,BET,UV-VIS和TG-DTA合成粉煤灰基地质聚合物及其衍生物(Fe(II)制态地质聚合物)并表征,并用作吸附剂用于去除CS +和SR2 +,以及来自溶液的ASO43。每个吸附动力学都适合伪二阶模型。将Cs +和Sr2 +的吸附在原始地质聚合物上更好地安装在Langmuir模型中。然而,Freundlich模型更加坚持为ASO43-进入Fe(II)制定的地质聚合物的吸附。从D-R等温线计算的自由能表明CS +和SR2 +的吸附是主要的离子交换。环尺寸在CS +和SR2 +两种离子交换中起着决定性作用。此外,SiO 4和AlO4四边体的布置对SR2 +的离子交换产生显着影响。 XPS结果表明,在吸附后,Fe2 +在Fe(II)的Fe2 +中的一部分已被氧化至Fe3 +。 FEASO4的沉淀可以部分有助于来自溶液的砷化物除去。通过离子交换反应形成内部球形复合物,也可以通过离子交换反应形成α43,这可以主要通过双齿键连接。

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