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Phosphate removal from water using freshly formed Fe–Mn binary oxide: Adsorption behaviors and mechanisms

机译:使用刚形成的Fe-Mn二元氧化物从水中去除磷酸盐的吸附行为和机理

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摘要

Freshly formed metal oxide suspensions usually have high reactivity and are easy to achieve in-situ preparation and dosing in water treatment. In this study, a freshly formed Fe–Mn binary oxide (FMBO) suspension was prepared for phosphate removal using simultaneous oxidation and coprecipitation method. FMBO was characterized by SEM, TEM, XRD and zeta potential and compared with the mixture of ferric oxide and manganese oxides (FMMO), hydrous ferric oxide (HFO) and hydrous manganese oxide (HMO). Results indicated that ferric oxide was relatively enriched on the surface of nanostructured binary oxide, resulting in its pHZPC and XRD pattern close to HFO. At pH 3–10, phosphate removals followed trend: FMBO > FMMO > HFO > HMO. The pseudo-second-order kinetics model provided a better fit for phosphate adsorption onto FMBO, indicating that chemisorption may play a dominant role. The maximum adsorption capacity estimated from the Langmuir equation was 0.223 mol-P/mol-Fe at pH 5.0. The competition effects of coexisting substances such as sulfate, bicarbonate, silicate and DOC on phosphate adsorption using FMBO were not significant. Phosphate adsorption onto FMBO could be attributed to electrostatic interaction and replacement of surface hydroxyl groups via formation of monodentate and bidentate complexes.
机译:新鲜形成的金属氧化物悬浮液通常具有高反应活性,并且易于在水处理中实现原位制备和定量添加。在这项研究中,使用同时氧化和共沉淀法制备了新鲜形成的Fe–Mn二元氧化物(FMBO)悬浮液,用于去除磷酸盐。 FMBO的特征在于SEM,TEM,XRD和zeta电位,并与三氧化二铁和锰的氧化物(FMMO),含水三氧化二铁(HFO)和含水的氧化锰(HMO)的混合物进行了比较。结果表明,三氧化二铁在纳米结构二元氧化物的表面相对富集,其pHZPC和XRD图谱接近HFO。在3-10的pH值下,磷酸盐的去除趋势如下:FMBO> FMMO> HFO> HMO。拟二级动力学模型为磷酸盐吸附到FMBO上提供了更好的拟合,表明化学吸附可能起主要作用。根据Langmuir方程估算的最大吸附容量在pH 5.0时为0.223 mol-P / mol-Fe。共存物质如硫酸盐,碳酸氢盐,硅酸盐和DOC对使用FMBO吸附磷酸盐的竞争作用并不显着。磷酸盐吸附到FMBO上可以归因于静电相互作用以及通过单齿和双齿配合物形成表面羟基的置换。

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