Mehri Mahdieh, Fallah Narges, Nasernejad Bahram
Department of Chemical Engineering, Amirkabir University of Technology, Tehran, Iran.
Environ Sci Pollut Res Int. 2022 Apr;29(16):23619-23638. doi: 10.1007/s11356-021-17253-4. Epub 2021 Nov 23.
The focus of the present study was to explore how and to what extent ultrahigh salinity affects the adsorption of cadmium and hydrocarbon pollutants onto aluminum hydroxide adsorbents formed in an electrocoagulation process. The changes in the nature and structure of the electro-generated aluminum particles and the possible removal mechanisms due to high salt content were investigated by using FE-SEM/EDS, FTIR, BET, and XRD analyses. The pseudo-second order and Freundlich models proved to fit the data for cadmium adsorption onto the aluminum hydroxides best. It was demonstrated that the adsorption capacities were significantly affected by the high salinity. With the rise of the salinity from 2 to 170 g/L, the cadmium and COD removal yields dropped from 81 to 60% and from 90 to 72%. The increase of the oil content led to the enhanced cadmium adsorption capacity due to surface complexation and ion exchange mechanisms. It was proved that Lagergren pseudo-first-order kinetic model could justify COD abatement trends. FTIR spectra depicted that the negative impact of high salinities on the adsorption was due to causing the formation of less stable adsorbents. According to BET analysis, the occurrence of much wider pore size distribution and smaller specific surface area in high salinity case was the main reason for the decreased adsorption capacity. Based on XRD analysis, the higher crystallinity of the produced aluminum hydroxide particles and their consequential smaller surface areas resulted in the lower adsorption capacity in the hypersaline environment. It was concluded that adsorption via inner-sphere and outer-sphere complexation and sweep flocculation were the possible removal mechanisms. Total treatment cost of 8.75 and 3.49 €/m were estimated for low and ultrahigh salinity conditions.
本研究的重点是探讨超高盐度如何以及在何种程度上影响镉和碳氢化合物污染物在电凝聚过程中形成的氢氧化铝吸附剂上的吸附。通过使用场发射扫描电子显微镜/能谱仪(FE-SEM/EDS)、傅里叶变换红外光谱仪(FTIR)、比表面积分析仪(BET)和X射线衍射仪(XRD)分析,研究了电生成铝颗粒的性质和结构变化以及高盐含量导致的可能去除机制。伪二级动力学模型和弗伦德利希模型被证明最适合镉在氢氧化铝上的吸附数据。结果表明,高盐度对吸附容量有显著影响。随着盐度从2 g/L升至170 g/L,镉和化学需氧量(COD)的去除率分别从81%降至60%,从90%降至72%。油含量的增加由于表面络合和离子交换机制导致镉吸附容量增强。结果证明,拉格朗日伪一级动力学模型可以解释COD的去除趋势。傅里叶变换红外光谱图表明,高盐度对吸附的负面影响是由于导致形成不太稳定的吸附剂。根据比表面积分析,在高盐度情况下出现更宽的孔径分布和更小的比表面积是吸附容量降低的主要原因。基于X射线衍射分析,所制备的氢氧化铝颗粒的较高结晶度及其相应较小表面积导致在高盐环境中吸附容量较低。得出的结论是,通过内球和外球络合以及扫絮凝进行吸附是可能的去除机制。估计在低盐度和超高盐度条件下的总处理成本分别为8.75欧元/立方米和3.49欧元/立方米。