摘要
亚铁氰化物是处理含Cs^(+)离子放射性废水的一种重要方法。为了研究亚铁氰化物处理Cs^(+)离子时的置换机理以及基础性质,本文按照M^(2+)/Fe(CN)64-=1.33的比例投加共沉淀剂(其中M^(2+)代表了Ni^(2+)、Cu^(2+)、Co^(2+)、Cd^(2+)),在不同的模拟水样中制备了亚铁氰化物。利用激光粒度分布仪器考察了M(NO_(3))_(2)与亚铁氰化钾形成共沉淀物的粒径分布。利用高氯酸和加热装置对制备的亚铁氰化物进行溶解以分析其组成。结果表明:共沉淀物的粒径几乎全部处于0.1~10μm;Cs^(+)和Mg^(2+)离子主要取代K^(+)和部分取代M^(2+)离子,Na^(+)离子只取代K^(+)离子;对1.00 mg/L Cs^(+)离子的去除率高于99%;对其吸附容量高达310mg/g以上。总之,亚铁氰化物粒径较小,Na^(+)和Mg^(2+)存在不会影响亚铁氰化物对Cs^(+)离子的去除。
Ferrocyanide is an important water treatment method for radioactive Cs^(+)-containing wastewater.To explore the replacement mechanism and the basic properties of ferrocyanide when treating Cs^(+)ions,ferricyanide was produced in different simulated solutions by the addition of a co-precipitant at a ratio of M^(2+)/Fe(CN)_(6)^(4-)=1.33(where M^(2+)is Ni^(2+),Cu^(2+),Co^(2+),or Cd^(2+)).The particle size distribution of the co-precipitates formed by M(NO_(3))_(2)and potassium ferrocyanide was examined using a laser particle size distribution instrument.The obtained ferrocyanides were dissolved in perchloric acid and a heating device to analyze their composition.The results showed that the particle size of the co-precipitate is almost in the range of 0.1~10μm.Cs^(+)and Mg^(2+)ions primarily replaced K^(+)ions and partially replaced M^(2+)ions in the co-precipitate,and Na^(+)ions only replaced K^(+)ions.The re-moval rate of 1.00 mg/L Cs^(+)ions is higher than 99%,and the adsorption capacity is above 310 mg/g.In conclusion,the particle size of ferricyanide is small,and the existence of Na^(+)and Mg^(2+)does not influence the removal of Cs^(+)ions by ferricyanide.
作者
王光辉
王佳林
李耀睿
张萌
高杨
矫彩山
WANG Guanghui;WANG Jialin;LI Yaorui;ZHANG Meng;GAO Yang;JIAO Caishan(College of Nuclear Science and Technology,Harbin Engineering University,Harbin 150001,China)
出处
《哈尔滨工程大学学报》
EI
CAS
CSCD
北大核心
2024年第2期398-405,共8页
Journal of Harbin Engineering University
基金
国家自然科学基金项目(21771045)。
关键词
亚铁氰化物
粒径分布
组成分析
置换机理
去除率
分配系数
吸附容量
模拟海水
ferrocyanide
particle size distribution
composition analysis
replacement mechanism
removal rate
distribution coefficient
adsorption capacity
simulated sea water