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Synthesis of different crystallographic FeOOH catalysts for peroxymonosulfate activation towards organic matter degradation

机译:不同晶体FeOOH催化剂的合成过氧键硫酸盐对有机质降解的活化

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摘要

In this study, different crystalline structures of FeOOH have been prepared. alpha-FeOOH was synthesized through a hydrothermal method, whereas beta-FeOOH was synthesized via a direct hydrolysis method. Moreover, gamma- and delta-FeOOH were prepared by precipitation methods through slow and quick oxidation, respectively. On this basis, their crystal structure, morphology, and surface area were measured. Then, all the synthesized materials were applied to activate peroxymonosulfate (PMS) to generate sulfate radicals (SO4-center dot) for acid orange 7(AO7) degradation. Compared with alpha-FeOOH, beta-FeOOH, and gamma-FeOOH, delta-FeOOH showed more efficient decolorization of AO7 in the catalytic system because of its abundant surface area and crystalline structure. The effects of several parameters in the delta-FeOOH/PMS/AO7 system were investigated. The results show that the initial pH, which is related to the features of surface hydroxyl groups, is the decisive factor, and excellent catalytic activity is maintained in the pH range 5-8. The increase of catalyst dosage and appropriate increase of PMS concentration contributed to promote the degradation effect. However, self-quenching was observed in a high PMS concentration system. Moreover, delta-FeOOH was stable after six consecutive cycles, and the leaching of iron ions was negligible. According to the quenching test and electron spin resonance analysis, both SO4-center dot and (OH)-O-center dot were the dominant radicals for AO7 degradation.
机译:在这项研究中,已经制备了FeOOH的不同晶体结构。通过水热法合成α-FeO​​OH,而通过直接水解方法合成β-FeOHH。此外,通过缓慢和快速氧化来通过缓慢和快速氧化来制备γ-和Delta-FeOOH。在此基础上,测量它们的晶体结构,形态和表面积。然后,施加所有合成材料以激活过氧氧键(PMS)以产生酸橙7(AO7)降解的硫酸盐基团(SO 4中心点)。与Alpha-FeOOH,Beta-FeOH和Gamma-Feoh相比,Delta-FeOh,由于其表面积丰富和晶体结构,Δ-FeOOH在催化系统中显示出更有效的AO7脱色。研究了若干参数在Delta-FeoH / PMS / AO7系统中的影响。结果表明,与表面羟基的特征有关的初始pH是决定性因子,优异的催化活性保持在pH范围5-8中。催化剂剂量的增加和PMS浓度的适当增加有助于促进降解效果。然而,在高pms浓度系统中观察到自熄。此外,在连续六个循环后,Delta-FeOOH稳定,铁离子的浸出可忽略不计。根据淬火试验和电子自旋共振分析,SO4中心点和(OH)-O中心点是AO7降解的主要自由基。

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  • 来源
    《RSC Advances》 |2018年第13期|共11页
  • 作者单位

    Army Logist Univ Dept Mil Facil Chongqing 401311 Peoples R China;

    Chongqing Univ State Minist Educ Key Lab Gorges Reservoir Reg Ecoenvironm 3 Chongqing 400045 Peoples R China;

    Army Logist Univ Dept Mil Facil Chongqing 401311 Peoples R China;

    Army Logist Univ Dept Mil Facil Chongqing 401311 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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