IF 4.8 Q1 ENVIRONMENTAL SCIENCES
Bin Wang, Henglin Xiao, Guanghui Tao, Wenbin Guo, Lu Li, Hongyu Wang*, Junfeng Su, Zihan Zheng, Dao Zhou, Ling Chen* and Wangye Lu, 
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引用次数: 0

摘要

在这项研究中,镧被原位孵育在磁性壳聚糖微凝胶(LCS)中,用于分离地表水中的磷酸盐。与商用 La(OH)3 及其直接封装到 CS 中相比,在 CS 结构中原位培养镧可使镧效率(ΓLa)比商用 La(OH)3 高 3.3 倍,在镧含量最低的情况下获得最高的磷容量(95.25 mg P/g)。LCS 微凝胶可以很容易地通过磁分离提取,并用 NaOH 再生,从而重复用于循环除磷。与一价阴离子相比,二价 SO42- 能在最初的几个小时内大大加快 LCS 微凝胶对磷的捕获。在批处理模式下对 SO42- 的影响进行了比较分析,然后以实际湖水为进料在搅拌流反应器中进行了验证。在连续运行的情况下,SO42- 的存在可以增加动态 P 容量,有助于将出水 P 抑制到低浓度水平,系统的突破时间几乎延长了一倍。进一步的表征分析阐明了在 SO42- 存在的情况下 LCS 水凝胶网络的特殊膨胀行为,这可以增加磷酸盐扩散和吸收的比表面积和孔径。总之,我们的工作凸显了无机/聚合物复合材料制造的前景,并为水处理提供了有益的启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In Situ Lanthanum Growth in Magnetic Chitosan Microgel for Accelerated Phosphate Separation from Water: Metal Efficiency, Specific Hydrogel Swelling, and Mechanistic Insights

In Situ Lanthanum Growth in Magnetic Chitosan Microgel for Accelerated Phosphate Separation from Water: Metal Efficiency, Specific Hydrogel Swelling, and Mechanistic Insights

In this work, lanthanum was in situ incubated in magnetic chitosan microgel (LCS) for phosphate separation from surface water. Compared to commercial La(OH)3 and its direct encapsulation into CS, in situ La incubation in CS structure could render an La efficiency (ΓLa) 3.3 times higher than that of commercial La(OH)3, harvesting the highest P capacity (95.25 mg P/g) at the lowest La content. LCS microgel can be easily extracted by magnetic separation, regenerated by NaOH, and thus reused for cyclic phosphate removal. Compared to monovalent anions, divalent SO42– could largely accelerate P capture on LCS microgel within the first several hours. The effect of SO42– was comparatively analyzed in batch modes and then verified by stirred-flow reactors using practical lake water as the feed. Under continuous operation, the presence of SO42– could increase the dynamic P capacity and help suppress effluent P to a low concentration level, with the system breakthrough time nearly doubled. Further characterization analysis clarified the specific swelling behavior of LCS hydrogel network in the presence of SO42–, which could increase the specific surface area and pore size for phosphate diffusion and uptake. Overall, our work highlighted a promising option for the fabrication of inorganic/polymer composites and provided useful insights for water treatment.

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