当前位置: X-MOL 学术Kinet. Catal. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Activity of 5% CuO/Ce 1 – x Pr x O y Catalysts in the Reaction of Carbon Monoxide Oxidation with Oxygen in an Excess of Hydrogen
Kinetics and Catalysis ( IF 1.3 ) Pub Date : 2021-03-03 , DOI: 10.1134/s0023158421010031
A. N. Il’ichev , M. Ya. Bykhovsky , Z. T. Fattakhova , D. P. Shashkin , V. N. Korchak

Abstract

The 5% CuO/Ce1 – xPrxOy catalysts were synthesized on the basis of CeO2 and PrO2 oxides and Ce1 – xPrxOy solid solutions with x = 0.2, 0.5, and 0.8. Highly dispersed copper oxide was present in the 5%CuO/Ce1 – xPrxOy catalysts. Upon interaction with the support, it formed active oxygen, which participated in CO chemisorption and a low-temperature reaction of CO oxidation in the presence of hydrogen. The highest conversion of CO in an excess of H2mах(Т)), which was close to 100%, was obtained at temperatures of 120–160°C on a 5% CuO/CeO2 catalyst. Upon the modification of CeO2 with Pr cations, 5% Ce0.2Pr0.8Oy sample, it decreased to 65% at 220°C due to an increase in the bond strength of oxygen in copper-containing centers. A maximum conversion of CO (93%) on a sample of 5% CuO/PrOy was detected at 200°C. Upon the modification of PrO2 with Ce cations, the activity of 5% CuO/Ce0.5Pr0.5Oy and 5% CuO/Ce0.2Pr0.8Oy catalysts did not exceed that of 5% CuO/PrOy. The forms of CO and CO2 adsorption on 5% CuO/Ce1 – xPrxOy samples were studied using the TPD method. In a range of 170–500°C, the desorption of oxygen from the supports of 5% CuO/Ce0.5Pr0.5Oy and 5% CuO/PrOy samples was observed. The occurrence of the reaction on 5% CuO/Ce1 – xPrxOy catalysts was discussed. With consideration for the properties of CO complexes formed on copper-containing oxidation and adsorption centers, their participation in the reaction of low-temperature oxidation in hydrogen was examined.



中文翻译:

5%CuO / Ce 1 – x Pr x O y催化剂在氢气过量的情况下一氧化碳氧化与氧气反应中的活性

摘要

在CeO 2和PrO 2氧化物和Ce 1- x Pr x O y固溶体(x = 0.2、0.5和0.8)的基础上,合成了5%CuO / Ce 1-  x Pr x O y催化剂。高度分散的氧化铜存在于5%CuO / Ce 1 – x Pr x O y催化剂中。与载体相互作用后,它形成了活性氧,该活性氧参与了CO的化学吸附和在氢存在下的CO氧化的低温反应。H 2γmах)中的最高CO转化率  Т))接近120%,是在5%CuO / CeO 2催化剂上于120–160°C的温度下获得的。在用Pr阳离子(5%Ce 0.2 Pr 0.8 O y样品)对CeO 2进行改性后,由于含铜中心中氧的键合强度增加,在220°C下它降至65%。在200°C下检测到5%CuO / PrO y样品上CO的最大转化率(93%)。通过用Ce阳离子修饰PrO 2,活性为5%CuO / Ce 0.5 Pr 0 5 O y和5%CuO / Ce 0.2 Pr 0.8 O y催化剂不超过5%CuO / PrO y。使用TPD方法研究了5%CuO / Ce 1 – x Pr x O y样品上CO和CO 2的吸附形式。在170-500°C的温度范围内,观察到氧气从5%CuO / Ce 0.5 Pr 0.5 O y和5%CuO / PrO y样品的载体上解吸。在5%CuO / Ce 1 – x Pr x O y上发生反应 讨论了催化剂。考虑到在含铜的氧化和吸附中心上形成的CO配合物的性质,研究了它们在氢中低温氧化反应中的参与。

更新日期:2021-03-04
down
wechat
bug