4.7 Article

Ultrasound assisted synthesis of Ca-Al hydrotalcite for U (VI) and Cr (VI) adsorption

期刊

CHEMICAL ENGINEERING JOURNAL
卷 218, 期 -, 页码 295-302

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2012.12.051

关键词

Ca-Al-LDHs; Ultrasonic; Uranium; Chromium; Desorption

资金

  1. Special Innovation Talents of Harbin Science and Technology [2011RFQXG016, 2012RFXXG104]
  2. Fundamental Research Funds of the Central University (HEUCFZ)
  3. Natural Science Foundation of Heilongjiang Province
  4. Program of International S&T Cooperation special Project [S2013ZR0649]
  5. International Science & Technology Cooperation Program of China [2010DFA92460]
  6. National Natural Science Foundation of China [51108112]

向作者/读者索取更多资源

Adsorption of chromium (VI) and uranium (VI) nitrate on Ca-Al hydrotalcite (Ca-Al LDHs) compounds is investigated. The powdered materials are synthesized in a modified co-precipitation method under the ultrasonic treatment with different conditions for Cr (VI) and U (VI) adsorption. Factors that affect the compounds synthesis such as temperature, reaction time, calcination and aging conditions are reported. The effects of various parameters on adsorption process including adsorption/desorption kinetics, isotherms and influencing factors such as contact time, solution pH and effect of competing ions are studied. It is found that Ca-Al LDHs has the largest capacity for both Cr (VI) and U (VI), adsorbing 104.82 +/- 0.02 mg/g and 54.79 +/- 0.02 mg/g, and highest rate of adsorption up to 98.78 +/- 0.02% and 90.28 +/- 0.02% respectively. Cr (VI) and U (VI) adsorption decreased obviously with pH levels outside the range of 7-11. Adsorption/desorption kinetics of Cr (VI) and U (VI) shows that desorption K values of U (VI) are larger than Cr (VI) while adsorption K values U (VI) are smaller than Cr (VI), suggesting that Ca-Al LDHs efficiency for the removal of U (VI) is fast adsorption and slow release compare to Cr (VI). The effect of competing ions such as nitrate radical and chloridion was negligible. (C) 2012 Elsevier B.V. All rights reserved.

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