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首页> 外文期刊>The journal of physics and chemistry of solids >Promotional effect of H2O2 modification on the cerium-tungsten-titanium mixed oxide catalyst for selective catalytic reduction of NO with NH3
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Promotional effect of H2O2 modification on the cerium-tungsten-titanium mixed oxide catalyst for selective catalytic reduction of NO with NH3

机译:H2O2改性对铈 - 钨钛混合氧化物催化剂的促进作用,用于选择性催化还原NO

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摘要

Several cerium-tungsten-titanium mixed oxide catalysts were prepared through the hydrothermal precipitation method, and the influence of H2O2 modification on the NH3-SCR activity of Ce20W10Ti100Oz was investigated. The samples were characterized by XRD, N-2 adsorption-desorption, XPS and NH3-TPD to reveal the effect of H2O2 modification on its structure properties and redox properties. In addition, the NH3-SCR mechanisms at 200 degrees C for Ce20W10Ti100Oz catalyst modified by 2 ml H2O2 (1 mol/L) was also studied by in situ DRIFTS. The NH3-SCR activity of Ce20W10Ti100Oz was improved by H2O2 modification, and the suitable volume of H2O2 (1 mol/L) is 2 ml. The introduction of H2O2 refined the pore size of Ce20W10Ti100Oz and enlarged its BET surface area. In addition, H2O2 modification improved the molar ratio of Ce3+/Ce4+ on the surface of catalyst and made large amount of active oxygen belonging to surface hydroxyl formed on its surface with the total concentration of the active absorbed oxygen (O alpha + O'(alpha)) enhanced. They all contributed to enhance the NOx conversion over Ce20W10Ti100Oz catalyst. The intensity of acid sites for Ce20W10Ti100Oz was also improved by H2O2 modification, especially the Bronsted acid sites. Ionic NH4+ adsorbed on the Bronsted acid sites was mainly the active adsorbed NH3 species in the NH3-SCR reaction at 200 degrees C, and the reaction between active adsorbed NH3 species and gaseous NOx mainly occurred on Ce20W10Ti100Oz-2 at 200 degrees C following the E-R mechanism.
机译:通过水热沉淀法制制备几种铈 - 钨钛混合氧化物催化剂,研究了H2O2改性对Ce20w10Ti100oz的NH3-SCR活性的影响。样品的特征在于XRD,N-2吸附 - 解吸,XPS和NH 3-TPD,以揭示H 2 O 2改性对其结构性质和氧化还原性能的影响。另外,通过原位漂移研究了由2mL H 2 O 2(1mol / L)改性的CE20W10TI100OZ催化剂的NH 3-SCR机制。通过H 2 O 2改性改善Ce20w10Ti100oz的NH 3-SCR活性,合适的H 2 O 2(1mol / L)为2mL。 H2O2的引入精制CE20W10Ti100oz的孔径并扩大了其BET表面积。此外,H 2 O 2改性改善了Ce3 + / Ce4 +在催化剂表面上的摩尔比,并使属于其表面上形成的表面羟基的大量活性氧,具有活性吸收的氧(Oα+ O'(α)的总浓度(α ))增强。它们都有助于增强CE20W10TI100OZ催化剂上的NOx转换。通过H 2 O 2改性,尤其是伪造酸位点,还改善了Ce20w10Ti100oz的酸部位的强度。吸附在桥接酸部位上的离子NH 4 +主要是NH3-SCR反应中的活性吸附的NH 3种,在200℃下,活性吸附的NH 3物种与气态NOx之间的反应主要在ER后的200摄氏度下发生在CE20W10TI100oZ-2上机制。

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