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As, Se, and Re Sorption by Mg-Al Layered Double Hydroxides

机译:镁铝层状双氢氧化物对砷,硒和and的吸附

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Layered double hydroxides (LDHs) have high anion exchange capacities and are easily synthesized in the laboratory, giving them considerable potential as adsorbents for anionic contaminants in the environment. In this study, sorption of arsenate, selenate, and perrhenate by uncalcined Mg-Al LDH (Mg:Al ratio 2.4:1) was evaluated. To investigate sorption mechanisms, the substrate was added to the solution both as a pre-wetted slurry (allowing 24 hours for rehydration), and as a dry powder. Sorption results varied for different anionic complexes. For selenate and perrhenate, an incubation time was required for the dry material to achieve the same K_d value as the pre-wetted material. For arsenate, however, both wetted and dry materials initially had high K_ds, which decreased with time. These behaviors are attributed to the structural reconstruction of the calcined LDH material in solution. Se and Re are not highly sorbed by the phases present in the calcined material, but are incorporated as interlayer anions in the LDH structure upon hydration and reconstruction, while As may be sorbing onto the dehydration products, and being partially released during rehydration.
机译:层状双氢氧化物(LDHs)具有很高的阴离子交换能力,并且在实验室中易于合成,因此它们有很大的潜力作为环境中阴离子污染物的吸附剂。在这项研究中,评估了未煅烧的Mg-Al LDH(Mg:Al比为2.4:1)对砷酸盐,硒酸盐和高r酸盐的吸附。为了研究吸附机理,将底物以预先润湿的浆液形式(允许24小时补液)和干粉形式添加到溶液中。吸附结果因不同的阴离子络合物而异。对于硒酸盐和高r酸盐,干燥材料要达到与预润湿材料相同的K_d值,需要一个孵育时间。但是,对于砷酸盐,湿物料和干物料最初都具有较高的K_ds,其随时间降低。这些行为归因于在溶液中煅烧的LDH材料的结构重建。 Se和Re未被煅烧材料中存在的相高度吸收,但在水合和重构时作为​​层间阴离子掺入LDH结构中,而As可能吸附在脱水产物上,并在再水化过程中部分释放。

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