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Enhanced catalytic oxidation of formaldehyde over dual-site supported catalysts at ambient temperature

机译:在环境温度下通过双中心负载型催化剂增强甲醛的催化氧化

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In the study highly active dual-site TiO2 supported Pt catalysts were prepared for catalytic oxidation of formaldehyde (HCHO) at ambient temperature. We used (3-aminopropyl)triethoxysilane to modify the TiO2 supported Pt catalysts, resulting in amino groups grafted on their surfaces and thus dual sites on supports. Characterization of the dual-site catalysts and the corresponding catalytic activity for HCHO decomposition were analyzed and evaluated. The TiO2 supported Pt catalysts featuring amino groups showed significant enhancement on the catalytic activity for HCHO removal. Compared to the supported catalyst with Pt active sites only, the presence of amino groups on the surface of the TiO2 supported Pt catalyst enhanced the catalytic oxidation of HCHO by a factor of 2.8 times at 5-ppm inlet HCHO concentration. The optimal enhancement occurred on the moderate gas hourly space velocity and low HCHO concentration. We speculate that the enhancement may result from the synergistic effect of Pt active sites and amino groups. The affinity of amino groups as capture sites to HCHO or formate molecules leads to higher localized HCHO concentration in the vicinity of Pt active sites, thereby resulting in a higher catalytic activity for the dual-site catalysts.
机译:在这项研究中,制备了高活性的双中心TiO2负载的Pt催化剂,用于在环境温度下催化氧化甲醛(HCHO)。我们使用(3-氨基丙基)三乙氧基硅烷对TiO2负载的Pt催化剂进行了改性,从而在其表面接枝了氨基,从而在载体上形成了两个位点。分析和评估了双中心催化剂的表征和相应的HCHO分解催化活性。带有氨基的TiO2负载的Pt催化剂在去除HCHO的催化活性上有显着提高。与仅具有Pt活性位点的负载型催化剂相比,TiO2负载型Pt催化剂表面氨基的存在在5 ppm入口HCHO浓度下将HCHO的催化氧化作用提高了2.8倍。最佳的增强发生在适度的气体时空速度和低HCHO浓度上。我们推测这种增强可能是由于Pt活性位点和氨基的协同作用所致。氨基作为捕获位点对HCHO或甲酸分子的亲和力导致Pt活性位点附近更高的局部HCHO浓度,从而导致双位点催化剂具有更高的催化活性。

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