首页> 外文期刊>Radiochimica Acta: International Journal for Chemical Aspects of Nuclear Science and Technology >Investigation of humic acid complexation behavior with uranyl ions using modified synthetic and natural humic acids
【24h】

Investigation of humic acid complexation behavior with uranyl ions using modified synthetic and natural humic acids

机译:用改良的合成和天然腐殖酸研究腐殖酸与铀酰离子的络合行为

获取原文
获取原文并翻译 | 示例
           

摘要

We investigated the influence of phenolic OH groups on the complexation behavior of humic acid (HA) with UO22+ ions at pH 4. Starting from synthetic HA type M1, natural HA Aldrich, and natural HA Kranichsee, we synthesized modified HAs with blocked phenolic OH groups by derivatization with diazomethane. The partial blocking of phenolic OH groups was confirmed by a radiometric method which quantitatively determined the functional groups and by FTIR spectroscopy. The complexation behavior of the chemically modified and unmodified HAs with UO22+ ions was investigated by time-resolved laser-induced fluorescence spectroscopy. The experimental data were evaluated with the metal ion charge neutralization model. We determined comparable complexation constants for all HAs. Two modified HAs (type M1 and Aldrich) had significantly lower loading capacities for UO22+ ions (10.5 +/- 0.9% and 9.7 +/- 1.6%, respectively) than the corresponding unmodified HAs (18.0 +/- 2.0% and 17.5 +/- 1.6%, respectively). This indicates that the blocking of the phenolic OH groups changes the complexation behavior of HAs. [References: 24]
机译:我们研究了酚羟基在pH 4下对腐殖酸(HA)与UO22 +离子络合行为的影响。从合成的HA型M1,天然HA Aldrich和天然HA Kranichsee开始,我们合成了具有封闭酚OH基的改性HA。用重氮甲烷衍生化。酚OH基团的部分封端通过定量确定官能团的放射法和FTIR光谱法确认。通过时间分辨激光诱导荧光光谱研究了化学修饰的和未修饰的HAs与UO22 +离子的络合行为。用金属离子电荷中和模型评估了实验数据。我们确定了所有HA的可比络合常数。与相应的未修饰HAs(18.0 +/- 2.0%和17.5 + /)相比,两种修饰的HAs(M1和Aldrich型)对UO22 +离子的负载能力明显较低(分别为10.5 +/- 0.9%和9.7 +/- 1.6%)。 -分别为1.6%)。这表明酚OH基团的封闭改变了HA的络合行为。 [参考:24]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号