用户名: 密码: 验证码:
Adsorption of Cesium, Strontium, and Cobalt Ions on Magnetite and a Magnetite-Silica Composite
详细信息    查看全文
  • 作者:Armin D. Ebner ; James A. Ritter ; and James D. Navratil
  • 刊名:Industrial & Engineering Chemistry Research
  • 出版年:2001
  • 出版时间:April 4, 2001
  • 年:2001
  • 卷:40
  • 期:7
  • 页码:1615 - 1623
  • 全文大小:151K
  • 年卷期:v.40,no.7(April 4, 2001)
  • ISSN:1520-5045
文摘
Constant pH adsorption isotherms for nonradioactive Cs+, Sr2+, and Co2+ on pure magnetiteand a 80% (w/w) magnetite-silica composite were measured at 25 C over a wide range of metalion concentrations. The adsorption studies were carried out at four different pH's: 6, 7, 8, and9 for Cs+ and Sr2+ and 5, 6, 7, and 8 for Co2+. All of the constant pH isotherms exhibited typeI behavior with a saturation capacity that was pH-dependent and increased with increasingpH. The corresponding distribution coefficients increased with increasing pH but decreased withincreasing metal ion concentration; they were also 10-1000 times lower than those reported inthe literature for more selective but more expensive adsorbents. These two magnetite-basedadsorbents also exhibited moderate regeneration conditions, with nearly 90-100% regenerationachieved in most cases at pH values between 1 and 3. A Langmuir model with pH-dependentparameters was also fitted successfully to all of the constant pH adsorption isotherms. Thisexperimental data and the corresponding pH-dependent Langmuir correlation should findconsiderable use in the design and development of inexpensive fixed-bed adsorption processesfor the removal of the radioactive isotopes of Cs+, Sr2+, and Co2+ from aqueous solutions thatare produced in nuclear facilities. Magnetite, when encased in silica and placed in a packedcolumn, can also be used as the charging element in high gradient magnetic separation, therebyremoving not only metal ions via surface complexation (adsorption) but also nanoparticles of aparamagnetic nature.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700