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作 者:蹇源[1,2] 牟婉君[2] 刘宁[1] 彭述明[1,2]
机构地区:[1]四川大学原子核科学技术研究所,辐射物理及技术教育部重点实验室,成都610064 [2]中国工程物理研究院核物理与化学研究所,四川绵阳621900
出 处:《物理化学学报》2016年第8期2052-2058,共7页Acta Physico-Chimica Sinica
基 金:supported by the National Natural Science Foundation of China(21501159)~~
摘 要:研究Ta掺杂六方相氧化钨(hex-WO_3)材料在吸附Sr^(^(2+))过程中其表面zeta电位的变化情况,并进一步探讨了吸附过程的热力学及吸附机理。结果表明:(1)在实验pH值范围内,Ta掺杂hex-WO_3悬浮液的zeta电位值随溶液中电解质的价态增大而增大;(2)且zeta电位随体系中离子强度的增加而增大;(3)Ta掺杂hexWO_3对Sr^(2+)的吸附容量随着温度降低而增大,随着离子强度的增加而减少;(4)吸附过程的吸附焓为-47 k J?mol^(-1),且Sr^(2+)离子与材料表面之间主要为化学相互作用;(5)Ta掺杂hex-WO_3对Sr^(2+)吸附过程主要为材料表面吸附及材料孔道内离子交换共同作用。The adsorption of Sr^2+ ions onto Ta-doped hex-WO3 nanomaterials was studied by measuring the zeta potentials of the powder nanoparticies and by determining the adsorption isotherm and adsorption mechanism. Five important results were obtained: (1) the zeta potential values of the Ta-doped hex-WO3 suspensions in different electrolyte solutions, within the studied pH ranges, increased with an increase in electrolyte valence; and (2) the zeta potential of the Ta-doped hex-WO3 suspensions increased with an increase in ionic strength. (3) Sr^2+ ion adsorption increased with a decrease in temperature and ionic strength. (4) The adsorption enthalpy was calculated as -47 kJ·mol^-1, and the interaction between the Ta-doped hex-WO3 surface and Sr^2+ ions was concluded to be chemical in nature. (5) The adsorption of Sr^2+ ions onto the Ta-doped hex-WO3 was attributed to surface chemical adsorption and ion exchange (in tunnels).
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