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Geogenic arsenic removal through core-shell based functionalized nanoparticles: Groundwater in-situ treatment perspective in the post-COVID anthropocene

机译:基于核 - 壳体官能化纳米颗粒的造环砷中除去:在核心糖后拟人的地下水原位治疗透视

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Groundwater, one of the significant potable water resources of the geological epoch is certainly contaminated with class I human carcinogenic metalloid of pnictogen family which delimiting its usability for human con-sumption. Hence, this study concerns with the elimination of arsenate (As(V)) from groundwater using bilayer-oleic coated iron-oxide nanoparticles (bilayer-OA@FeO NPs). The functionalized (with high-affinity carboxyl groups) adsorbent was characterized using the state-of-the-art techniques in order to understand the structural arrangement. The major emphasis was to examine the effects of pH (5.0-13), contact times (0-120 min), initial concentrations (10-150 mu g L-1), adsorbent dosages (0.1-3 g L-1), and co-existing anions in order to understand the optimal experimental conditions for the effective removal process. The adsorbent had better adsorption efficiency (32.8 mu g g(-1), after 2 h) for As(V) at neutral pH. Adsorption process mainly followed pseudo-second-order kinetics and Freundlich isotherm models (R-2-0.90) and was facilitated by coulombic, charge-dipole and surface complexation interactions. The regeneration (upto five cycles with 0.1 M NaOH) and competition studies (with binary and cocktail mixture of co-anions) supported the potential field application of the proposed adsorbent.
机译:地下水,地质时代的显着饮用水资源之一肯定污染了肺炎系列的I类人致癌物质,这界定了其对人类概念的可用性。因此,该研究涉及使用双层 - 油酸涂层的铁氧化物纳米粒子(双层-OA @ Feo NPS)从地下水中消除砷酸盐(AS(V))。使用最先进的技术表征官能化(具有高亲和力羧基)吸附剂以理解结构排列。主要重点是检查pH(5.0-13),接触时间(0-120分钟),初始浓度(10-150μg1-1),吸附剂量(0.1-3g l-1)的影响,和共存阴离子,以了解有效去除过程的最佳实验条件。吸附剂在中性pH下具有更好的吸附效率(32.8μg(-1),2小时后,2小时后)(v)。吸附过程主要跟随伪二阶动力学和Freundlich等温机型(R-2-0.90),并通过库仑,电荷 - 偶极和表面络合相互作用促进。再生(高达五个循环,0.1米NaOH)和竞争研究(具有二元和共阴离子的混合物)支持所提出的吸附剂的潜在场施加。

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