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首页> 外文期刊>Nanotechnology >Synthesis of nanostructured pt/CeO_2-ZrO_2-Al_2O_3 catalysts by a two-step sol-gel method
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Synthesis of nanostructured pt/CeO_2-ZrO_2-Al_2O_3 catalysts by a two-step sol-gel method

机译:两步溶胶-凝胶法合成纳米结构的pt / CeO_2-ZrO_2-Al_2O_3催化剂

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摘要

Porous Pt/CeO_2-ZrO_2-Al_2O_3 catalysts were synthesized by a two-step sol-gel method in which noble metal nanoparticles were first prepared as a dispersed colloid in an aqueous medium, then mixed with aluminum isopropoxide (AIP), Ce(NO_3)_4 and Zr(NO_3)_4, and condensed into a gel. After calcination at 800 deg C for 3 h, these composite catalysts showed large specific surface areas (150-160 m~2 g~(-1)) and a narrow pore size distribution of 10-12 nm as determined from the nitrogen adsorption/desorption isotherms. XPS and TEM scans showed that the active component of the catalyst was well dispersed, with the Pt nanoparticles (particle size 3-5 nm) confined to the pores. It was found that changing the template surfactants from ionic cetyltrimethylammonium bromide (CTAB) to non-ionic polyethylene glycol P-l,l,3,3-tetramethylbutylphenyl ether (TritonX-100) did not change either the specific surface area or the pore structure, but lowered the CO-to-CO_2 reaction temperature by nearly 60 deg C. Measurements of CO conversion proved that the catalyst prepared with TritonX-100 as the template had the highest catalytic activity: the onset of the conversion of CO to CO_2 began at 158 deg C and was complete at 192 deg C. The possible mechanism of the anti-aggregation of nanoparticles and high catalyst activity has been discussed.
机译:通过两步溶胶-凝胶法合成了多孔Pt / CeO_2-ZrO_2-Al_2O_3催化剂,其中首先将贵金属纳米颗粒制备为分散的胶体,然后再与异丙醇铝(AIP),Ce(NO_3)混合。 _4和Zr(NO_3)_4,并浓缩成凝胶。在800摄氏度下煅烧3小时后,这些复合催化剂显示出大的比表面积(150-160 m〜2 g〜(-1))和窄的孔径分布(由氮吸附/吸附法确定)为10-12 nm。解吸等温线。 XPS和TEM扫描表明,催化剂的活性成分分散良好,Pt纳米颗粒(粒径3-5 nm)被限制在孔中。发现将模板表面活性剂从离子型十六烷基三甲基溴化铵(CTAB)更改为非离子型聚乙二醇Pl,1,3,3-四甲基丁基苯基醚(TritonX-100)不会改变比表面积或孔结构,但是将CO-to-CO_2反应温度降低了近60摄氏度。CO转化率的测量证明,以TritonX-100为模板制备的催化剂具有最高的催化活性:CO转化为CO_2的起始时间为158℃。 ℃,并在192℃完成。已经讨论了纳米粒子抗聚集和高催化剂活性的可能机理。

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