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Heterogeneous catalytic ozonation of phenacetin in water using magnetic spinel ferrite as catalyst : comparison of surface property and efficiency

机译:磁性尖晶石铁氧体为催化剂的非那西丁在水中的非均相催化臭氧化反应:表面性质和效率的比较

摘要

In this study, a systematic investigation on the degradation of phenacetin (PNT) by magnetic spinel ferrite (including MnFe2O4 and NiFe2O4) via catalytic ozonation was carried out. The structural and surface property of the catalyst, the performance and mineralization during PNT degradation, and center dot OH/H2O2 identification were studied. The precursors of the catalyst, i.e. MnFe2(OH)(8) and NiFe2(OH)(8), showed certain magnetic properties and a superior catalytic activity for ozonation enhancement than spinel ferrites. Spinel ferrites containing manganese initiate an ozone mass transfer into the solution, where the critical intermediate (H2O2) is generated. The manganese ferrite spinel triggers H2O2 decomposition in the presence of ozone and generates center dot OH for the mineralization of PNT and its intermediates. Spinel ferrites involved nickel catalyzed ozone decomposition and generate H2O2 and center dot OH. All catalysts showed a weak heavy metal leaching, which suggests that the heterogeneous reaction dominates the catalytic reaction and the resultant effluent is safe for the aqueous environment. The magnetic variation of catalysts involving nickel is insignificant, suggesting that the catalyst can be reused many times. The fate of the intermediates on spinel oxides surface influenced for the catalytic ozonation process differently.
机译:在这项研究中,系统研究了磁性尖晶石铁氧体(包括MnFe2O4和NiFe2O4)通过催化臭氧氧化降解非那西丁(PNT)。研究了催化剂的结构和表面性质,PNT降解过程中的性能和矿化以及中心点OH / H2O2的鉴定。催化剂的前体MnFe2(OH)(8)和NiFe2(OH)(8)具有一定的磁性,并具有比尖晶石型铁氧体更强的臭氧氧化催化活性。包含锰的尖晶石铁氧体会引发臭氧质量转移到溶液中,在溶液中生成关键中间体(H2O2)。锰铁氧体尖晶石在存在臭氧的情况下触发H2O2分解,并生成中心点OH,用于PNT及其中间体的矿化。尖晶石铁氧体涉及镍催化的臭氧分解,并生成H2O2和中心点OH。所有催化剂均显示出较弱的重金属浸出,这表明非均相反应在催化反应中占主导地位,所产生的流出物对于水性环境是安全的。涉及镍的催化剂的磁变化不明显,表明该催化剂可多次重复使用。尖晶石氧化物表面上中间体的命运对催化臭氧化过程的影响不同。

著录项

  • 作者

    Qi F; Xu BB; Chu W;

  • 作者单位
  • 年度 2015
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
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