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机构地区:[1]中南大学化学化工学院,长沙410083 [2]深圳大学应用化学系,深圳518060
出 处:《中国有色金属学报》2005年第9期1465-1470,共6页The Chinese Journal of Nonferrous Metals
基 金:国家高技术研究发展计划资助项目(2001AA218041);国家自然科学基金资助项目(20475065)
摘 要:采用石英晶体微天平现场技术研究了Hg(Ⅱ)离子在纳米TiO2表面的吸附及光化学还原过程。结果表明:Hg(Ⅱ)离子借助于纳米TiO2表面羟基发生吸附,吸附平衡常数约为3.9×105L/mol,且Hg(Ⅱ)离子的吸附量受溶液的pH值、浓度和共存阴离子的影响;在pH值为4的HgCl2溶液中,Hg(Ⅱ)离子在纳米TiO2上的饱和吸附量约为0.85 mmol/g;在UV光照射下,初始阶段TiO2表面水光解产生的质子可使吸附的Hg(Ⅱ)离子从TiO2表面脱附下来,而且Hg(Ⅱ)浓度和pH值越大,脱附现象越明显;随后Hg(Ⅱ)光还原沉积逐渐占主导地位,且光沉积速率受Hg(Ⅱ)浓度、溶液pH值和有机物加入的影响。In-situ technique of quartz crystal microbalance (QCM) was used to investigate the adsorption and the photochemical reduction process of Hg( Ⅱ ) at the surface of nanocrystalline TiO2. The results show the Hg( Ⅱ ) is adsorbed onto the surface of nanocrystalline TiO2 by hydroxyl groups, and the adsorption equilibrium constant is about 3.9 ×10^5 L/mol based on the pseudo-first-order kinetic model. The adsorption amount of Hg( Ⅱ ) at the surface of TiO2 is affected by pH value, concentration of Hg( Ⅱ ) and coexisting anions, and the saturated adsorption amount of Hg( Ⅱ ) is approximately 0. 85 mmol/g at pH of 4. During the initial stage of UV illumination, the protons produced in photodegradative reactions of water can cause the desorption of adsorbed Hg( Ⅱ ) from the surface of TiO2. The degree of desorption increases with the increase of both the concentration of Hg( Ⅱ ) and pH value of solution. Then, the photochemical deposit reaction of Hg from the solution strengths and the rate of Hg photodeposition are influenced by the concentration of Hg( Ⅱ ), pH value and added organics.
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