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Arsenate Removal by Nanostructured ZrO_2 Spheres

机译:纳米ZrO_2球去除砷。

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摘要

A new zirconium oxide-based media for arsenate removal from water was fabricated and evaluated in batch and continuous flow experiments. Highly porous (∈p ≈ 0.9) nanostructured zirconium oxide spheres were fabricated by the impregnation of macroporous ion-exchange media (CalRes 2103, Calgon) with zirconium sa the media was then ashed at T > 750 ± 50 ℃ to remove the organic polymer resin and obtain ZrO_2 spheres. The spheres generally ranged from 200 to 800 μm in diameter, and consisted of ZrO_2 nanoastructures generally ranging between 20 and 100 nm. They also exhibited monoclinic and tetragonal crystalline structures, and had an isoelectric point of 5.6. Equilibrium batch experiments were conducted in 10 mM NaHCO_3 buffered nanopure water at three pH values (6.4,7.3, and 8.3) with 120 μg/L As(V). Data were fit with the Freundlich isotherm equation (q_e - K × C_E~(1) ), resulting in an intensity parameter (1) of ~ 0.33 and capacity parameters (K) ranging from 115 to 400 (μg As(V) g~(-1) dry media)(L μg~(-1))~(1). The pore diffusion coefficient and toruosity were estimated to be 6.4 × 10~(-6) cm~2 s~(-1) and 1.3, respectively. For a packed bed adsorbent operating at a loading rate of 11.5 m~3 m~(-20 hr~(-1) in a realistic continuous flow experiment the external mass transport coefficient was estimated to be k_f 6.3 × 10~(-3) cm s~(-1). The pore diffusion coefficient and the external mass transport coefficient were used with the pore surface diffusion model (PSDM) to predict the arsenate breakthrough curve. A short bed adsorbent (SBA) test was conducted under the same conditions to validate the model. In this study, surface diffusion was ignored because the particles have a very high porosity. The validated model was used to predict arsenate breakthrough in a simulated full-scale system. The overall combined use of modeling, material characterization, equilibria, and kinetics tests determined the suitability of the media for arsenate treatment cheaper, easier, faster, and with less media than a long duration pilot test would have. Although the fabricated zirconium oxide spheres exhibited adsorption capacity comparable to some commercially available media such as iron based (hydr)oxides, the high cost of fabrication may render the media not feasible for wide use in commercial applications. However, the very high porosity of this media provides for improved pore diffusion and faster overall mass transport, which may be critical for applications where mass transport is the limiting factor.
机译:制造了一种新的基于氧化锆的介质,用于从水中去除砷酸盐,并在分批和连续流动实验中进行了评估。通过用锆盐浸渍大孔离子交换介质(CalRes 2103,Calgon)来制造高度多孔(∈p≈0.9)的纳米结构的氧化锆球。然后在> 750±50℃的温度下灰化介质,以除去有机聚合物树脂并获得ZrO_2球。球体的直径通常为200至800μm,由ZrO_2纳米结构组成,通常在20至100 nm之间。它们还显示出单斜晶体和四方晶体结构,等电点为5.6。在含120μg/ L As(V)的三个pH值(6.4、7.3和8.3)的10 mM NaHCO_3缓冲的纳米纯水中进行了平衡批处理实验。数据符合Freundlich等温方程(q_e-K×C_E〜(1 / n)),强度参数(1 / n)为〜0.33,容量参数(K)为115至400(μgAs( V)g〜(-1)干燥介质)(Lμg〜(-1))〜(1 / n)。孔扩散系数和曲折度分别估计为6.4×10〜(-6)cm〜2 s〜(-1)和1.3。对于在实际连续流实验中以11.5 m〜3 m〜(-20 hr〜(-1)的加载速率运行的填充床吸附剂,外部传质系数估计为k_f 6.3×10〜(-3) cm s〜(-1)。结合孔扩散系数和外部传质系数与孔表面扩散模型(PSDM)预测砷的穿透曲线,在相同条件下进行了短床吸附剂(SBA)测试在本研究中,由于颗粒具有很高的孔隙率,因此忽略了表面扩散;使用了经过验证的模型来预测模拟全尺寸系统中的砷突破;结合了建模,材料表征和平衡的整体用途,并且动力学测试确定了介质的适合砷酸盐处理的费用比长期的中试测试更便宜,更容易,更快速且使用的介质更少,尽管制成的氧化锆球具有吸附能力c与某些商用介质(如铁基(氢)氧化物)相比,其制造成本高,可能会使该介质无法在商业应用中广泛使用。但是,这种介质的高孔隙率可改善孔的扩散并加快整体质量传输,这对于质量传输是限制因素的应用可能至关重要。

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