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Chabazite: Stable Cation-Exchanger in Hyper Alkaline Concrete Pore Water

机译:菱沸石:高碱性混凝土孔隙水中的稳定阳离子交换剂

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摘要

To avoid impact on the environment, facilities for permanent disposal of hazardous waste adopt multibarrier design schemes. As the primary barrier very often consists of cement-based materials, two distinct aspects are essential for the selection of suitable complementary barriers: (1) selective sorption of the contaminants in the repository and (2) long-term chemical stability in hyperalkaline concrete-derived media. A multidisciplinary approach combining experimental strategies from environmental chemistry and materials science is therefore essential to provide a reliable assessment of potential candidate materials. Chabazite is typically synthesized in 1 M KOH solutions but also crystallizes in simulated young cement pore water, a pH 13 aqueous solution mainly containing K~+ and Na~+ cations. Its formation and stability in this medium was evaluated as a function of temperature (60 and 85 ℃) over a timeframe of more than 2 years and was also asessed from a mechanistic point of view. Chabazite demonstrates excellent cation-exchange properties in simulated young cement pore water. Comparison of its Cs~+ cation exchange properties at pH 8 and pH 13 unexpectedly demonstrated an increase of the K_D with increasing pH. The combined results identify chabazite as a valid candidate for inclusion in engineered barriers for concrete-based waste disposal.
机译:为避免对环境造成影响,永久性处置危险废物的设施采用多屏障设计方案。由于主要的屏障通常由水泥基材料组成,因此选择合适的互补屏障必不可少的两个方面:(1)选择性吸附储存库中的污染物;(2)高碱性混凝土的长期化学稳定性-派生媒体。因此,将来自环境化学和材料科学的实验策略相结合的多学科方法对于提供对潜在候选材料的可靠评估至关重要。菱沸石通常在1 M KOH溶液中合成,但也会在模拟的年轻水泥孔隙水中(主要包含K +和Na +阳离子的pH 13水溶液)中结晶。在2年以上的时间范围内,根据温度(60和85℃)对它在该介质中的形成和稳定性进行了评估,并从机理的角度对其进行了评估。菱沸石在模拟的年轻水泥孔隙水中表现出优异的阳离子交换性能。比较其在pH 8和pH 13下的Cs〜+阳离子交换性能,出乎意料地表明,随着pH的升高,K_D升高。综合结果确定菱沸石是用于混凝土废物处置的工程屏障的有效候选者。

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  • 来源
    《Environmental Science & Technology》 |2015年第4期|2358-2365|共8页
  • 作者单位

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

    Electron Microscopy for Materials Science (EMAT), University of Antwerp, Groenenborgerlaan 171, 2020 Antwerp, Belgium;

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

    Electron Microscopy for Materials Science (EMAT), University of Antwerp, Groenenborgerlaan 171, 2020 Antwerp, Belgium;

    Electron Microscopy for Materials Science (EMAT), University of Antwerp, Groenenborgerlaan 171, 2020 Antwerp, Belgium;

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

    Centre for Surface Chemistry and Catalysis, KU Leuven, Kasteelpark Arenberg 23 - box 2461, 3001 Heverlee, Belgium;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-17 13:59:37

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