用石膏石灰石对地下水进行除氟

F. Fufa, E. Alemayehu, Bishaw Deboch
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引用次数: 7

摘要

背景:氟中毒是一种慢性环境健康问题,主要是由饮用地下水中过量氟的摄入引起的。因此,在没有水处理设施的氟中毒流行地区,利用当地可获得的低成本材料吸附除氟对于提供安全饮用水非常重要。目的:采用不同氟浓度的天然地下水样品,研究石膏灰岩(GLS)对氟的吸附能力。方法:利用受污染的天然地下水,在室温条件下,通过间歇式吸附装置、空白实验和对照实验,考察不同接触时间、溶液pH、吸附剂剂量和初始浓度对氟的去除规律。结果:搅拌24 h内达到平衡。氟吸附动力学数据符合非线性拟一阶速率方程(R2 ~ 0.99)。氟的吸附在很大程度上取决于地下水的pH值。在pH为3和5的酸性介质上,除氟率高达89%。Langmuir等温线模型很好地描述了平衡氟吸附,吸附量为1.07 mg/g。当吸附剂在200℃下煅烧4 h时,氟的去除率增强。含氟吸附剂经NaOH溶液再生成功。结论:本研究结果为进一步研究GLS在饮用水除氟中的作用提供了基础资料。
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Defluoridation of groundwater using gypsiferous limestone
Background: Fluorosis is a chronic environmental health problem caused by intake of excess fluoride, mainly in the drinking groundwater. Therefore, adsorptive removal of fluoride by locally available low-cost materials is very important for the provision of safe drinking water in the fluorosis endemic regions where there are no water treatment facilities. Aim: The purpose of the study was to investigate fluoride sorption capacity of gypsiferous limestone (GLS) using natural groundwater samples containing different fluoride concentrations. Methods: Sets of batch adsorption setup along with blank and control experiments were conducted at room temperature to examine the pattern of fluoride removal with varying contact time, solution pH, adsorbent dose and initial concentration using contaminated natural groundwater. Results: Equilibrium was achieved within 24 h of agitation time. Kinetics data of fluoride adsorption followed well the non-linear pseudo-first order rate equation (R2 ~ 0.99). Fluoride adsorption was greatly dependent on the pH of the groundwater. High fluoride removal efficiency (~ 89%) was observed over acidic medium at pH 3 and 5. The Langmuir isotherm model well described the equilibrium fluoride adsorption, giving an adsorption capacity of 1.07 mg/g. The removal of fluoride enhanced when the adsorbent was calcined at 200 °C for 4 h. The fluoride loaded adsorbent was successfully regenerated using NaOH solution. Conclusion: The results of the study have provided fundamental information for further investigation of GLS in the defluoridation of drinking water.
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