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作 者:陈华柏 谢水波[1] 刘金香[1] 肖拾红 李仕友[1] 吴宇琦[1]
机构地区:[1]南华大学污染控制与资源化技术湖南省重点实验室,衡阳421001
出 处:《环境工程学报》2015年第3期1141-1147,共7页Chinese Journal of Environmental Engineering
基 金:国家自然科学基金资助项目(11175081);高等学校博士点基金项目(20134324110003);湖南省自然科学基金项目(13JJ3078);湖南省高校创新平台项目(13K085)
摘 要:以生活污水处理厂剩余活性污泥为原料,制备粉末活性污泥(PAS)作为生物吸附剂,考察p H值,PAS投加量,U(Ⅵ)初始浓度和吸附时间对PAS吸附U(Ⅵ)的影响,探讨了PAS吸附U(Ⅵ)的作用机理。实验结果表明,在U(Ⅵ)初始浓度为10 mg/L时,其最佳吸附p H值为3,去除率97.77%,吸附平衡时间120 min;吸附过程较好地拟合了准二级动力学模型(R2≈1)和Freundlich等温模型(R2≈1);X射线能谱和离子交换实验分析表明,离子交换为其主要吸附方式,参与交换的主要离子为Ca2+;红外光谱分析表明,PAS吸附U(Ⅵ)后自身结构未发生改变。以0.1 mol/L的HCl溶液作为解吸液,初次解吸率达92.83%,循环利用3次仍具有较好的吸附效果。The residual activated sludge from an urban sewage treatment plant was used to prepare powdered activated sludge( PAS) as a novel biological adsorbent. Different experimental parameters such as solution p H,adsorbent dose,initial concentration and contact time were examined to investigate their effects on adsorption of uranium by PAS. Changes of FT-IR spectra,scanning electron microscope and energy-dispersive spectrometry of PAS before and after adsorption were also studied. The results showed that the maximum adsorption occured at p H of 3,the adsorption reaches equilibrium within 120 min and the removal rate was up to 97. 77%for initial U( Ⅵ) ions concentration of 10 mg / L. The equilibrium data fit well with the pseudo-second-order model( R2≈1) and Freundlich model( R2≈1). Ion exchange experiments and EDS analysis verified that ion exchange was the main adsorption mechanism with Ca2 +as the main exchange ion. FTIR spectra before and after PAS adsorbed uranium indicated that its structure did not change. The used PAS can be desorbed by 0. 1 mol / L HCl( the first desorption rate is up to 92. 83%) and became reusable. PAS is nontoxic and eco-friendly,which has a good prospect in the treatment of uranium-containing wastewater.
分 类 号:X771[环境科学与工程—环境工程] X703
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