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机构地区:[1]东北大学理学院,沈阳110004 [2]辽宁林业职业技术学院,沈阳110101
出 处:《高等学校化学学报》2009年第1期121-124,共4页Chemical Journal of Chinese Universities
基 金:国家“八六三”计划(批准号:2007AA06Z116);国家“九七三”计划(批准号:G2006CB605103);东北大学博士后基金资助
摘 要:利用纳米TiO2的表面吸附活性,以[S2O3]2-为络合剂,应用火焰原子吸收光谱检测方法,高效吸附分离了水中痕量Ag(Ⅰ).系统研究了纳米TiO2的晶体结构、溶液的pH值、吸附时间、Ag(Ⅰ)的起始浓度及常见共存离子对吸附率的影响,确定了最佳吸附条件.FTIR光谱分析结果表明,Ag(Ⅰ)配合物以物理作用吸附在纳米TiO2颗粒表面.纳米TiO2对Ag(Ⅰ)的吸附等温线为S型,表现出多分子层吸附特征.硝酸和硫脲混合溶液可将吸附在TiO2纳米颗粒表面的Ag(Ⅰ)全部洗脱.An efficient separation of coordination compound of Ag( I ) was carried out taking TiO2 nanoparticles as adsorbent, [ S2O3 ] 2-anion as ligand and Flame Atomic Absorption Spectrophometer(FAAS) as detector to determine the concentration of Ag( I ). The effect of the crystalline structure of TiO2 nanoparticles, pH values, adsorption time, initial concentration of Ag( I ), and some coexistent ion on the adsorption rate was systematically studied. The FTIR spectrum show that the coordination compound of Ag( I ) is physically adsorbed on the surface of TiO2 nanoparticles. The adsorption isotherm of Ag ( I ) on nano-TiO2 show "S" type, which can be explained by the multi-molecular layer adsorption. The Ag( I ) adsorbed on TiO2 nanoparticles could be eluted completely by mixed solution of nitric acid( 1 mol/L) and sulfourea(2 g/L). The above experiment results would be valuable for using the nano-adsorbents to separate trace Ag( I ) in waste water.
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