4.2 Article

Reductive immobilization of perrhenate in soil and groundwater using starch-stabilized ZVI nanoparticles

期刊

CHINESE SCIENCE BULLETIN
卷 58, 期 2, 页码 275-281

出版社

SCIENCE PRESS
DOI: 10.1007/s11434-012-5425-3

关键词

heavy metals; nanoparticles; perrhenate; pertechnetate; radionuclides; reductive immobilization; zero valent iron

资金

  1. National Natural Science Foundation of China [41072265, 40810152]
  2. Science-Technology Research of Colleges in Shanxi Province [20091022]
  3. Shanxi Provincial 100 Talents Program, China
  4. Auburn University VPR's

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Perrhenate (ReO (4) (-) ) was used as nonradioactive surrogate for the radionuclide pertechnetate ((TcO)-Tc-99 (4) (-) ) to investigate the potential of using starch-stabilized zero valent iron (ZVI) nanoparticles for reductive immobilization of pertechnetate in soil and groundwater. Batch kinetic tests indicated that the starch-stabilized ZVI nanoparticles were able to reductively remove 96% of perrhenate (10 mg/L) from water within 8 h. XRD analyses confirmed that ReO2 was the reduction product. A pseudo-first-order kinetic model was able to interpret the kinetic data, which gave a pseudo first order rate constant (k (obs)) value of 0.43 h(-1) at pH 6.9 and room temperature (25A degrees C). Increasing solution pH up to 8 progressively increased the reaction rate. However, highly alkaline pH (10) resulted in much inhibited reaction rate. Consequently, the optimal pH range was identified to be from 7 to 8. Increasing solution temperature from 15 to 45A degrees C increased k (obs) from 0.38 to 0.53 h(-1). The classical Arrhenius equation was able to interpret the temperature effect, which gave a low activation energy value of 7.61 kJ/mol. When the ReO (4) (-) -loaded loess was treated with the stabilized nanoparticles suspension ([Fe]=560 mg/L), the water leachable ReO (4) (-) was reduced by 57% and nearly all eluted Re was in the form of ReO2. This finding indicates that starch-stabilized ZVI nanoparticles are promising for facilitating in situ immobilization of ReO (4) (-) in soil and groundwater.

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