首页> 外文期刊>Desalination and water treatment >Ruthenium hydroxide supported on activated alumina for catalytic permanganate oxidation of aniline
【24h】

Ruthenium hydroxide supported on activated alumina for catalytic permanganate oxidation of aniline

机译:活性氧化铝上负载的氢氧化钌对苯胺的高锰酸盐催化氧化

获取原文
获取原文并翻译 | 示例
       

摘要

Ruthenium loaded on CeO2 or TiO2 has been proved to be effective catalysts in permanganate oxidation, but the small size of supports led to a difficult separation of catalysts from the aqueous solution. Therefore, ruthenium hydroxide supported on activated alumina (diameter 3-4 mm), i.e. Ru-AA, was synthesized and employed as catalyst in permanganate oxidation of aniline at circumneutral pH for the first time. The characterization for Ru-AA by SEM-EDAX proved the existence of Ru on the surface of AA, but XRD patterns for AA were not affected by the impregnation of ruthenium hydroxide, due to its low concentration, low crystallinity, and good dispersion. Acting as an electron shuttle, Ru-AA significantly improved the apparent second-order rate constant (k(app)) of aniline oxidation from 10.3 to 18.9 M-1 s(-1) with its concentration increasing from 0.55 to 2.2 g L-1. Aniline degradation in catalytic oxidation was markedly influenced by pH, and the k(app) decreased from 314.3 to 3.3 M-1 s(-1) with increasing pH from 4.0 to 9.0. The intermediates of aniline in the catalytic permanganate oxidation were determined by LC-MS/MS analysis. Ru-AA displayed an excellent stability in first 10 consecutive runs, and the regenerated Ru-AA showed a better performance than the spent one after 15 runs, but less catalytic capability than the virgin one due to the leaching of Ru. The schematic mechanism for Ru-AA-catalyzed permanganate oxidation of aniline was proposed finally.
机译:负载在CeO2或TiO2上的钌已被证明是高锰酸盐氧化的有效催化剂,但是载体的小尺寸导致催化剂难以从水溶液中分离出来。因此,首次合成了负载在活性氧化铝(直径3-4 mm)上的氢氧化钌,即Ru-AA,并首次在环境pH值下用作苯胺高锰酸盐氧化的催化剂。 SEM-EDAX对Ru-AA的表征证明了AA表面上存在Ru,但是由于其低浓度,低结晶度和良好的分散性,AA的XRD图案不受氢氧化钌浸渍的影响。作为电子穿梭,Ru-AA可以将苯胺氧化的表观二级速率常数(k(app))从10.3提高到18.9 M-1 s(-1),其浓度从0.55增加到2.2 g L- 1。 pH显着影响苯胺在催化氧化中的降解,并且随着pH从4.0增加到9.0,k(app)从314.3降低到3.3 M-1 s(-1)。通过LC-MS / MS分析确定高锰酸催化氧化中苯胺的中间体。 Ru-AA在连续的前10次运行中表现出出色的稳定性,再生的Ru-AA在15次运行后表现出比废旧的更好的催化性能,但由于Ru的浸出,其催化能力比未使用的Ru-AA弱。最后提出了Ru-AA催化苯胺高锰酸盐氧化的机理。

著录项

  • 来源
    《Desalination and water treatment》 |2016年第37期|17355-17366|共12页
  • 作者单位

    Hohai Univ, Coll Environm, Key Lab Integrated Regulat & Resource Dev Shallow, Minist Educ, Nanjing 210098, Jiangsu, Peoples R China;

    Hohai Univ, Coll Environm, Key Lab Integrated Regulat & Resource Dev Shallow, Minist Educ, Nanjing 210098, Jiangsu, Peoples R China;

    Hohai Univ, Coll Environm, Key Lab Integrated Regulat & Resource Dev Shallow, Minist Educ, Nanjing 210098, Jiangsu, Peoples R China|Hohai Univ, Coll Mech & Elect Engn, Changzhou 213022, Peoples R China;

    CSCEC AECOM Consultants Co Ltd, Beijing 100044, Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Aniline; Kinetics; Catalysis; Byproduct; Pathway;

    机译:苯胺;动力学;催化;副产物;途径;
  • 入库时间 2022-08-18 02:01:03

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号