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首页> 外文期刊>Colloids and Surfaces, A. Physicochemical and Engineering Aspects >Removal mechanism of polymeric borate by calcined layered double hydroxides containing different divalent metals
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Removal mechanism of polymeric borate by calcined layered double hydroxides containing different divalent metals

机译:含不同二价金属的煅烧层状双氢氧化物去除聚合物硼酸盐的机理

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The removal mechanism of polymeric borate by calcined layered double hydroxides is not clear. In this work, layered double hydroxides containing different divalent metals were synthesized and calcined to produce calcined layered double hydroxides (Zn-, Mg-, and Ca-CLDH). Then, Zn-, Mg-, and Ca-CLDH were applied to remove polymeric borate. Zn-CLDH showed better performance for the removal of borate than Ca-CLDH, and hardly any borate was removed by Mg-CLDH. Based on the characterization results, the detailed removal process of polymeric borate by different calcined layered double hydroxides is discussed. Because there is little H3BO3 that can act as a trigger, and ligand promoted dissolution of the complex H3BO3 and MgO is prevented. Therefore, Mg-CLDH could not transform to the layered structure to immobilize the borate. For the Zn-CLDH, Zn-CLDH transformed into Zn-LDH, and polymeric borate was absorbed into the interlayer of layered double hydroxides, which is the dominant mechanism of borate removal by Zn-CLDH. Reconstruction of the Ca-LDH from the Ca-CLDH was more rapid than the other calcined layered double hydroxides. However, formation of borate-containing ettringite was the main removal mechanism in the first stage. With increasing reaction time, the reaction between CO32- and Ca2+ released from ettringite, and the regeneration of Ca-LDH to form CaCO3 were the main reasons for borate removal in the second stage. (C) 2015 Elsevier B.V. All rights reserved.
机译:煅烧的层状双氢氧化物对聚合物硼酸盐的去除机理尚不清楚。在这项工作中,合成并煅烧了包含不同二价金属的层状双氢氧化物,并煅烧生成了煅烧的层状双氢氧化物(Zn-,Mg-和Ca-CLDH)。然后,使用Zn-,Mg-和Ca-CLDH去除聚合硼酸盐。 Zn-CLDH在去除硼酸盐方面表现出比Ca-CLDH更好的性能,并且几乎没有硼酸盐被Mg-CLDH去除。根据表征结果,讨论了不同煅烧的层状双氢氧化物去除聚合物硼酸盐的详细过程。因为几乎没有H3BO3可以作为触发物,并且阻止了配体促进的复合H3BO3和MgO的溶解。因此,Mg-CLDH不能转变成层状结构来固定硼酸盐。对于Zn-CLDH,Zn-CLDH转化为Zn-LDH,聚合物硼酸盐被吸收到层状双氢氧化物的中间层中,这是Zn-CLDH去除硼酸盐的主要机理。从Ca-CLDH重建Ca-LDH比其他煅烧的层状双氢氧化物更快。然而,在第一阶段,形成含硼酸盐的钙矾石是主要的去除机理。随着反应时间的增加,钙矾石释放出的CO32-与Ca2 +之间的反应以及Ca-LDH的再生生成CaCO3是第二阶段去除硼酸盐的主要原因。 (C)2015 Elsevier B.V.保留所有权利。

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