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Synthesis of modulator- driven highly stable zirconium- fumarate frameworks and mechanistic investigations of their arsenite and arsenate adsorption from aqueous solutions plus Phi

机译:调节剂的合成 - 驱动高度稳定的锆富马酸骨框架和机械研究的亚砷酸盐,并从水溶液加上Phi

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摘要

Here, we synthesized a modulator (benzoic acid (BA))-driven zirconium-fumaric acid (Zr-fum) metal-organic framework (MOF) and investigated in detail the adsorption mechanism of arsenic oxyanions (AsO43- and AsO33-) and their stability before and after adsorption from water. Without the support of the modulator, BA, Zr-fum formed an amorphous MOF due to the occurrence of quick precipitation of both zirconium and -fum. Various amounts of BA, 0-10 eq. to ZrCl4, were used to control the surface charge on the MOF nanoparticles, which directly corresponds to the colloid stability of the MOF and helps to obtain a defect-free Zr-fum MOF for high uptakes of AsO43- and AsO33- from water. With the concentration of 3 eq. BA, the adsorption capacities of both arsenic oxyanions on the Zr-fum MOF were found to be higher than those on other MOFs. The CHN analysis indicated that the excess of -fum present does not alter the adsorption densities of AsO43- and AsO33- on MOFs in addition to the negligible amount of BA except for the Zr-fum-10 eq. BA MOF where it is present in higher amounts, as confirmed by NMR studies. The physicochemical properties of the synthesized MOFs with/without the modulator support adsorbents before and after the adsorption of AsO43- and AsO33- were extensively characterized using several advanced instrumental techniques. The maximum uptake performance of AsO43- (1.159 mmol g(-1)) and AsO33- (1.121 mmol g(-1)) was obtained using the Langmuir adsorption isotherm. The adsorption of both AsO43- and AsO33- takes place by electrostatic interaction/complexation and ligand exchange with Zr-fum-5 eq. BA. In addition, the Zr-fum-5 eq. BA was recycled up to four times at a sustained efficiency after washing with 0.1 M NaOH. Owing to their high uptake capacities of AsO43- and AsO33-, the synthesized MOFs are expected to have potential applications as adsorbents for practical applications.
机译:这里,我们合成调节剂(苯甲酸(BA)) - 驱动锆 - 富马酸(Zr-Fum)金属 - 有机骨架(MOF),并详细研究了砷氧基(ASO43和ASO33-)的吸附机理及其从水吸附之前和之后的稳定性。在不支持调节剂,Ba,Zr-Fum的支持,由于锆和umum的快速沉淀出现而形成无定形MOF。各种量的BA,0-10平等。对于ZrCl4,用于控制MOF纳米颗粒上的表面电荷,该纳米颗粒直接对应于MOF的胶体稳定性,并有助于获得ASO43-和ASO33-从水的高上升剂的无缺陷Zr-Fum mof。浓度为3平等。 BA,发现ZR-FUM MOF上的砷氧合的吸附容量高于其他MOF上的吸附容量。 CHN分析表明,除了除ZR-FUM-10平等外,除了可忽略的BA除外,还不会改变ASO43和ASO33-上的吸附密度。 BA MOF,其在较高量的情况下,通过NMR研究证实。在ASO43-和ASO33-吸附之前和之后的合成MOF的合成MOF的物理化学性质被广泛地用几种先进的仪器技术进行了广泛的特征。使用Langmuir吸附等温线获得ASO43-(1.159mmol G(-1))和ASO33-(1.121mmol G(-1))的最大摄取性能。通过静电相互作用/络合和配体交换与ZR-FUM-5当量的静电相互作用和配体交换进行吸附。 BA。此外,ZR-FUM-5 EQ。在用0.1米NaOH洗涤后,BA以持续的效率再循环4次。由于它们的高吸收能力为ASO43和ASO33-,合成的MOF预计将潜在应用作为实际应用的吸附剂。

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  • 来源
    《CrystEngComm》 |2019年第14期|共13页
  • 作者单位

    Kyushu Univ Fac Engn Dept Earth Resources Engn Fukuoka Fukuoka 8190395 Japan;

    Kyushu Univ Fac Engn Dept Earth Resources Engn Fukuoka Fukuoka 8190395 Japan;

    Kyungpook Natl Univ Dept Environm Engn 80 Daehak Ro Daegu 41566 South Korea;

    Kyushu Univ Fac Engn Dept Earth Resources Engn Fukuoka Fukuoka 8190395 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;晶体学;
  • 关键词

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