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首页> 外文期刊>Iranian polymer journal >Fe3O4 nanoparticles coated by new functionalized tetraaza-2,3 dialdehyde micro-crystalline cellulose: synthesis, characterization, and catalytic application for degradation of Acid Yellow 17
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Fe3O4 nanoparticles coated by new functionalized tetraaza-2,3 dialdehyde micro-crystalline cellulose: synthesis, characterization, and catalytic application for degradation of Acid Yellow 17

机译:新型功能化四氮杂-2,3二醛微晶纤维素包覆的Fe3O4纳米颗粒:酸性黄17的合成,表征和催化应用

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摘要

In this study, we developed an original approach for preparing cellulose-coated magnetite nanoparticles (NPs). Two novel Schiff bases (PDA-g-DAC) and [Bz-(PDA-g-DAC)] were synthesized via condensation reactions of periodate oxidized micro-crystalline cellulose (DAC) with o-phenylene diamine (PDA) to obtain its azomethine derivative with 85% yield. Subsequently, the functionalization of (PDA-g-DAC) with benzil (Bz) yields the tetraaza macrocycle [Bz-(PDA-g-DAC)]. The physicochemical characterization of the condensation products was performed using (CNMR)-C-13, FTIR, ATG, DSC, and X-ray diffraction techniques. Magnetic nanomaterial-based Schiff base cellulose was successfully prepared using in situ chemical co-precipitation of coordinated ferric and ferrous ions in cellulose Schiff base matrix under optimized conditions, and then, its magnetic properties were characterized. The results demonstrated that the Fe3O4 NPs coated with [Bz-(PDA-g-DAC)] were homogeneously coated in the matrix under ultrasonic irradiation with the saturation magnetization of 69.50 emu g(-1). In addition, XRD line broadening analysis showed that the average particle size of the NPs was 37.3 nm. Furthermore, FTIR spectra demonstrated that [Bz-(PDA-g-DAC)] concavity was anchored to magnetite Fe3O4 NPs through azomethine groups. Vibrating sample magnetometry (VSM) of[Bz-(PDA-g-DAC)@ Fe3O4] magnetic nanocomposite samples showed the typical behavior of ferromagnetism. This study provided a green and facile method to inhibit magnetic nanoparticle aggregation. Activity results revealed that the prepared [Bz-(PDA-g-DAC)@ Fe3O4] catalyst shows the maximum activity for degradation of Acid Yellow 17 (AY17) compared to other prepared catalysts. After degradation reaction, the [Bz-(PDA-g-DAC)@ Fe3O4] catalyst was recovered from the reaction mixture via an external magnet and used for further five consecutive cycles with excellent catalytic activity, successively, which was comparable to the fresh catalyst. The catalyst degradation efficiency and its easy separation exhibited that [Bz-(PDA-g-DAC)@ Fe3O4] catalyst is a promising material for the removal of AY17 from aqueous solutions in green chemistry perspectives.
机译:在这项研究中,我们开发了一种制备纤维素包覆的磁铁矿纳米颗粒(NPs)的原始方法。通过高碘酸盐氧化微晶纤维素(DAC)与邻苯二胺(PDA)的缩合反应合成了两个新型Schiff碱(PDA-g-DAC)和[Bz-(PDA-g-DAC)],以获得其甲亚胺衍生物,产率为85%。随后,将(PDA-g-DAC)与苄基(Bz)官能化,生成四氮杂大环[Bz-(PDA-g-DAC)]。使用(CNMR)-C-13,FTIR,ATG,DSC和X射线衍射技术进行缩合产物的物理化学表征。通过在优化条件下原位化学共沉淀纤维素希夫碱基体中的三价铁离子和亚铁离子,成功制备了磁性纳米材料希夫碱基纤维素,然后对其磁性进行了表征。结果表明,在超声辐照下,饱和磁化强度为69.50 emu g(-1)的情况下,[Bz-(PDA-g-DAC)]包覆的Fe3O4 NPs被均匀地包覆在基质中。另外,XRD线展宽分析表明NP的平均粒径为37.3nm。此外,FTIR光谱表明,[Bz-(PDA-g-DAC)]凹度通过偶氮甲碱基团固定在磁铁矿Fe3O4 NP上。 [Bz-(PDA-g-DAC)@ Fe3O4]磁性纳米复合材料样品的振动样品磁力法(VSM)显示出铁磁性的典型行为。这项研究提供了一种抑制磁性纳米粒子聚集的绿色简便方法。活性结果表明,与其他制备的催化剂相比,制备的[Bz-(PDA-g-DAC)@ Fe3O4]催化剂具有最大的降解酸性黄17(AY17)的活性。降解反应后,通过外部磁体从反应混合物中回收[Bz-(PDA-g-DAC)@ Fe3O4]催化剂,并连续连续五个连续循环使用,具有优异的催化活性,与新鲜催化剂相当。 。催化剂的降解效率及其易分离性表明,[Bz-(PDA-g-DAC)@ Fe3O4]催化剂从绿色化学的角度来看是一种有望从水溶液中去除AY17的材料。

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