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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Encapsulated anion-dominated photocatalytic and adsorption performances for organic dye degradation and oxoanion pollutant capture over cationic Cu(I)-organic framework semiconductors
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Encapsulated anion-dominated photocatalytic and adsorption performances for organic dye degradation and oxoanion pollutant capture over cationic Cu(I)-organic framework semiconductors

机译:用于阳离子Cu(I) - 多糖框架半导体的有机染料降解和氧气污染物捕获的封装的阴离子主导的光催化和吸附性能

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摘要

Decontamination of industrial wastewater containing toxic organic dye molecules and oxoanions is urgently desirable for environmental sustainability and human health. Water-stable porous metal-organic frameworks (MOFs) have emerged as highly efficient photocatalysts and/or adsorbents for water purification through controllable integration of the constitutive requirements. To reveal the inclusion anion effect of microporous MOFs on wastewater treatment, two isostructural MOFs incorporating positive charge and semiconductive characteristics, {[Cu(tpt)]center dot 3H(2)O center dot 0.5SO(4)}(n) (1) and {[Cu(tpt)]center dot 2H(2)O center dot ClO4}(n) (2, tpt = 2,4,6-tris(4-pyridyl)-1,3,5-triazine), have been synthesized and employed as dual-functional materials for both dye photodegradation and oxoanion removal. The two MOFs possess the same 3-fold interpenetrating cationic backbones but are encapsulated by highly disordered sulfate or perchlorate in the open channels. These included anions have significantly tuned the hydrophilicity of the channels, extended the visible-light absorption, optimized the bandgap and decreased the conduction band potential. Under the low-energy irradiation of a 30 W LED lamp, MOF 1 has selectively and efficiently degraded rhodamine B compared to 2 with accelerated kinetics, resulting from the stronger reduction ability and less migration resistance of the photogenerated electrons. Instead, MOF 2 can quickly capture harmful MnO4- and Cr2O72- by exchanging with the entrapped ClO4-, with maximum adsorption amounts of 557 and 168 mg g(-1), respectively, under ambient conditions. The improved decolorization of the aqueous solution over 2 benefits essentially from the shape and charge memory effect and the smaller hydration energy of ClO4- than SO42-. These interesting observations highlight the importance of the included anions inside the porous MOF semiconductors on wastewater treatment.
机译:含有有毒有机染料分子和氧阴离子的工业废水的去污是环境可持续性和人类健康的迫切需要。水稳定的多孔金属有机骨架(MOF)通过可控地整合结构要求,已成为水净化的高效光催化剂和/或吸附剂。为了揭示微孔MOF对废水处理的包合阴离子效应,两种具有正电荷和半导体特性的同构MOF,{[Cu(tpt)]中心点3H(2)O中心点0.5SO(4)}(n)(1)和{[Cu(tpt)]中心点2H(2)O中心点ClO4}(n)(2,tpt=2,4,6-三(4-吡啶基)-1,3,5-三嗪),已经合成并用作染料光降解和氧阴离子去除的双功能材料。两种MOF具有相同的3倍互穿阳离子主链,但在开放通道中被高度无序的硫酸盐或高氯酸盐包裹。这些阴离子显著调节了通道的亲水性,延长了可见光吸收,优化了带隙,降低了导带电位。在30W LED灯的低能辐照下,MOF 1与2相比,选择性且高效地降解罗丹明B,并具有加速动力学,这是因为光生电子的还原能力更强,迁移阻力更小。相反,MOF 2可以通过与截留的ClO4-交换快速捕获有害的MnO4-和Cr2O72-在环境条件下的最大吸附量分别为557和168 mg g(-1)。与SO42-相比,ClO4-的形状和电荷记忆效应以及较小的水化能使水溶液的脱色效果提高了2倍以上。这些有趣的观察结果强调了多孔MOF半导体中所含阴离子对废水处理的重要性。

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    Nankai Univ Dept Chem Collaborat Innovat Ctr Chem Sci &

    Engn Tianjin 300071 Peoples R China;

    Nankai Univ Dept Chem Collaborat Innovat Ctr Chem Sci &

    Engn Tianjin 300071 Peoples R China;

    Tianjin Normal Univ Coll Chem Tianjin Key Lab Struct &

    Performance Funct Mol Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Coll Chem Tianjin Key Lab Struct &

    Performance Funct Mol Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Coll Chem Tianjin Key Lab Struct &

    Performance Funct Mol Tianjin 300387 Peoples R China;

    Tianjin Normal Univ Coll Chem Tianjin Key Lab Struct &

    Performance Funct Mol Tianjin 300387 Peoples R China;

    Nankai Univ Dept Chem Collaborat Innovat Ctr Chem Sci &

    Engn Tianjin 300071 Peoples R China;

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  • 中图分类 化学 ; 无机化学 ;
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