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首页> 外文期刊>Journal of the air & waste management association >Improving the activity of Mn/TiO_2 catalysts through control of the pH and valence state of Mn during their preparation
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Improving the activity of Mn/TiO_2 catalysts through control of the pH and valence state of Mn during their preparation

机译:通过控制制备过程中Mn的pH和价态来提高Mn / TiO_2催化剂的活性

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In this study, the authors investigated the influence of the valence state of Mn on the efficacy of selective catalytic reduction using a Mn-based catalyst. The nitrogen oxides (NO_x) conversion rate of the catalyst was found to be dependent on the type of TiO_2 support employed and on the temperature, as the catalyst showed an excellent conversion of> 80% at a space velocity of 60,000 hr~(-1) when the temperature was above 200℃. Brunauer-Emmett-Teller, X-ray diffraction, and X-ray photoelectron spectroscopy analyses confirmed that catalyst displaying the highest activity contained the Mn~(4+) species and that its valence state was highly dependent on the pH during the catalyst preparation. Implications: Recently, various Mn catalysts have been evaluated as selective catalyst reduction (SCR) catalysts. However, in these previous studies, only the reaction characteristics and catalytic activity on the NH_3 SCR over Mn catalysts were evaluated. There have been no studies on the effect of pH during catalyst preparation. Therefore, in this study, the effect of pH during the catalyst preparation process was examined and a new application of the Mn catalysts was proposed based on the current findings.
机译:在这项研究中,作者研究了Mn的价态对使用Mn基催化剂进行选择性催化还原的功效的影响。发现催化剂的氮氧化物(NO_x)转化率取决于所用TiO_2载体的类型和温度,因为该催化剂在60,000 hr〜(-1)的空速下表现出优异的转化率> 80% )温度高于200℃时。 Brunauer-Emmett-Teller,X射线衍射和X射线光电子能谱分析证实,显示出最高活性的催化剂含有Mn〜(4+)物种,并且其价态高度依赖于催化剂制备过程中的pH值。启示:最近,各种锰催化剂已被评估为选择性催化剂还原(SCR)催化剂。然而,在这些先前的研究中,仅评价了在Mn催化剂上在NH_3 SCR上的反应特性和催化活性。尚未对催化剂制备过程中pH值的影响进行研究。因此,在这项研究中,研究了pH在催化剂制备过程中的影响,并基于目前的发现提出了锰催化剂的新应用。

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  • 来源
    《Journal of the air & waste management association 》 |2012年第3期| p.362-369| 共8页
  • 作者

    Sung Su Kim; Sung Chang Hong;

  • 作者单位

    Department of Environmental Energy Systems Engineering, Kyonggi University, 94 San,lui-dong, Youngtong-ku, Suwon-si, Gyeonggi-do, 442-760, Korea;

    Department of Environmental Energy Systems Engineering, Kyonggi University, 94 San,lui-dong, Youngtong-ku, Suwon-si, Gyeonggi-do, 442-760, Korea;

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