首页> 外文期刊>Radiochimica Acta: International Journal for Chemical Aspects of Nuclear Science and Technology >Sequestration of uranium on fabricated aluminum co-precipitated with goethite (Al-FeOOH)
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Sequestration of uranium on fabricated aluminum co-precipitated with goethite (Al-FeOOH)

机译:与针铁矿(Al-FeOOH)共沉淀的铝上的铀固存

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Aluminum co-precipitated with goethites (Al-FeOOHs) are ubiquitous within (sub)-surface environments, which are considered one of the most important sinks for radionuclide pollution management. Accordingly, variousmole ratios Al-FeOOH were synthesized and characterized by XRD, FT-IR, TEM, specific surface area and potentiometric acid-base titration. According to XRD and TEM images, the morphology of Al-FeOOH was transformed from acicular-like goethite to cotton-like gibbsite with increasing Al content. The adsorption and sequential desorption of U(VI) on Al-FeOOHs were conducted by batch techniques under N_2 conditions. The batch adsorption results showed that the adsorption of U(VI) on Al-FeOOHs slightly increased at pH<4.0, then the significant increase of U(VI) adsorption was observed at pH from 4.0 to 7.0, whereas the suppressed adsorption at pH>8.0 was due to the electrostatic repulsion between negative charge surface and negative carbonato-complexes. The adsorption of U(VI) on Al-FeOOHs was independent of ionic strength at pH>5.0, indicating that the inner-sphere surface complexation predominated their adsorption behaviors, whereas U(VI) adsorption on Al-FeOOH could be theouter-spheresurface/cationexchange reaction.Thesequential extraction texts showed that the desorption of U(VI) from Al-FeOOHs decreased with increasing Al content. These findings highlighted the effect of Al content on the sequestration and immobilization of U(VI) onto Al-FeOOHs from (sub)-surface environments in pollution management.
机译:与针铁矿(Al-FeOOHs)共沉淀的铝在(次)表面环境中无处不在,被认为是放射性核素污染管理的最重要汇。因此,合成了各种摩尔比的Al-FeOOH,并通过XRD,FT-IR,TEM,比表面积和电位酸碱滴定来表征。根据XRD和TEM图像,随着Al含量的增加,Al-FeOOH的形态从针状针铁矿转变为棉状菱铁矿。 U(VI)在Al-FeOOHs上的吸附和顺序解吸是通过分批技术在N_2条件下进行的。批吸附结果表明,在pH <4.​​0时,U(VI)在Al-FeOOHs上的吸附略有增加,然后在pH从4.0到7.0时,U(VI)的吸附显着增加,而在pH> 4.0时,吸附被抑制。 8.0是由于负电荷表面和负碳酸盐络合物之间的静电排斥。在pH> 5.0时,U(VI)在Al-FeOOHs上的吸附与离子强度无关,表明内球表面络合作用占主导地位,而U(VI)在Al-FeOOH上的吸附可能是外球面/顺序萃取结果表明,随着Al含量的增加,U-VI从Al-FeOOHs中的解吸量降低。这些发现突显了铝含量对污染管理中(亚)表面环境中U(VI)螯合和固定在Al-FeOOHs上的影响。

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