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首页> 外文期刊>Beilstein Journal of Nanotechnology >Nanocrystalline ZrO2 and Pt-doped ZrO2 catalysts for low-temperature CO oxidation
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Nanocrystalline ZrO2 and Pt-doped ZrO2 catalysts for low-temperature CO oxidation

机译:用于低温CO氧化的纳米ZrO2和Pt掺杂ZrO2纳米催化剂

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摘要

Zirconia (ZrO2) nanoparticles were synthesized by solution combustion using urea as an organic fuel. Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), transmission electron microscopy (TEM), UV–vis and Fourier transform infrared (FTIR) measurements were performed in order to characterize the catalyst. The calculated crystallite size of ZrO2, calculated with the help of the Scherrer equation, was around 30.3 nm. The synthesized ZrO2 was scrutinized regarding its role as catalyst in the oxidation of carbon monoxide (CO). It showed 100% CO conversion at 240 °C, which is the highest conversion rate reported for ZrO2 in literature to date. It is found that through solution combustion, Pt2+ ions replace Zr4+ ions in the ZrO2 lattice and because of this, oxygen vacancies are formed due to charge imbalance and lattice distortion in ZrO2. 1% Pt was doped into ZrO2 and yielded excellent CO oxidation. The working temperature was lowered by 150 °C in comparison to pure ZrO2. Further, it is highly stable for the CO reaction (time-on-stream ≈ 40 h). This is because of a synergic effect between Pt and Zr components, which results in an increase of the oxygen mobility and oxygen vacancies and improves the activity and stability of the catalyst. The effects of gas hourly space velocity (GHSV) and initial CO concentration on the CO oxidation over Pt(1%)-ZrO2 were studied.
机译:使用尿素作为有机燃料通过溶液燃烧合成了氧化锆(ZrO2)纳米粒子。为了表征催化剂,进行了Brunauer-Emmett-Teller(BET),X射线衍射(XRD),热重分析(TGA),透射电子显微镜(TEM),UV-vis和傅立叶变换红外(FTIR)测量。借助Scherrer方程计算得出的ZrO2的微晶尺寸约为30.3 nm。仔细检查合成的ZrO2在一氧化碳(CO)氧​​化中的催化剂作用。它显示了240°C时100%的CO转化率,这是迄今为止文献中ZrO2报道的最高转化率。发现通过固溶燃烧,Pt2 +离子替代了ZrO2晶格中的Zr4 +离子,因此,由于ZrO2中的电荷不平衡和晶格畸变而形成了氧空位。将1%Pt掺杂到ZrO2中,并产生出色的CO氧化。与纯ZrO2相比,工作温度降低了150°C。此外,它对于CO反应非常稳定(运行时间≈40小时)。这是由于Pt和Zr组分之间的协同作用,这导致氧迁移率和氧空位的增加并提高了催化剂的活性和稳定性。研究了气体时空速度(GHSV)和初始CO浓度对Pt(1%)-ZrO2上CO氧化的影响。

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