Sorption-catalytic steam conversion of CO on a mechanical mixture of Pt/Ce0.75Zr0.25O2 catalyst and NaNO3/MgO sorbent

A. Gorlova, I. E. Karmadonova, V. S. Derevshchikov, V. Rogozhnikov, P. Snytnikov, D. Potemkin
{"title":"Sorption-catalytic steam conversion of CO on a mechanical mixture of Pt/Ce0.75Zr0.25O2 catalyst and NaNO3/MgO sorbent","authors":"A. Gorlova, I. E. Karmadonova, V. S. Derevshchikov, V. Rogozhnikov, P. Snytnikov, D. Potemkin","doi":"10.18412/1816-0387-2022-4-28-35","DOIUrl":null,"url":null,"abstract":"The sorption-catalytic steam conversion of CO using a mechanical mixture of 5 wt.% Pt/Ce0.75Zr0.25O2 catalyst grains and 10 mol.% NaNO3/MgO sorbent was studied. It was shown under the model conditions that initially MgO adsorbs СО2 only slightly, whereas its promotion with NaNO3 leads to a considerable growth of the adsorption dynamic capacity in the temperature range of 300–350 °С with a maximum at 320 °С. High activity and selectivity of the catalyst in steam conversion of CO were demonstrated for a model mixture with the composition (vol.%) 11.6 CO, 61 H2 and 27.4 H2O: the concentration of СО at the reactor outlet did not exceed 1 vol.% in the temperature range of 220– 400 °С (the minimum value of 0.3 vol.% was observed at 240 °С), and СН4 – at temperatures below 320 °С (0.61 vol.% at this point). The use of the sorbent in a mixture with the catalyst in the sorption-catalytic steam conversion of CO at 320 °С led to a considerable decrease in its sorption capacity; this may be related to the conversion of all NaNO3 into Na2CO3, which decomposed incompletely during regeneration. Nevertheless, this made it possible to decrease twofold the outlet concentrations of СО and СН4 as compared to the values observed at the indicated temperature in the experiment without a sorbent: particularly, in the middle of the first adsorption cycle they were equal to 6.1·10–4 and 8.2·10–2 vol.%, respectively, on a dry gas basis. Thus, the indicated approach to the sorption-catalytic conversion of CO was shown to be promising; further studies are needed to increase the capacity and stability of the presented type of sorbents.","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kataliz v promyshlennosti","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18412/1816-0387-2022-4-28-35","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

The sorption-catalytic steam conversion of CO using a mechanical mixture of 5 wt.% Pt/Ce0.75Zr0.25O2 catalyst grains and 10 mol.% NaNO3/MgO sorbent was studied. It was shown under the model conditions that initially MgO adsorbs СО2 only slightly, whereas its promotion with NaNO3 leads to a considerable growth of the adsorption dynamic capacity in the temperature range of 300–350 °С with a maximum at 320 °С. High activity and selectivity of the catalyst in steam conversion of CO were demonstrated for a model mixture with the composition (vol.%) 11.6 CO, 61 H2 and 27.4 H2O: the concentration of СО at the reactor outlet did not exceed 1 vol.% in the temperature range of 220– 400 °С (the minimum value of 0.3 vol.% was observed at 240 °С), and СН4 – at temperatures below 320 °С (0.61 vol.% at this point). The use of the sorbent in a mixture with the catalyst in the sorption-catalytic steam conversion of CO at 320 °С led to a considerable decrease in its sorption capacity; this may be related to the conversion of all NaNO3 into Na2CO3, which decomposed incompletely during regeneration. Nevertheless, this made it possible to decrease twofold the outlet concentrations of СО and СН4 as compared to the values observed at the indicated temperature in the experiment without a sorbent: particularly, in the middle of the first adsorption cycle they were equal to 6.1·10–4 and 8.2·10–2 vol.%, respectively, on a dry gas basis. Thus, the indicated approach to the sorption-catalytic conversion of CO was shown to be promising; further studies are needed to increase the capacity and stability of the presented type of sorbents.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Pt/Ce0.75Zr0.25O2催化剂和NaNO3/MgO吸附剂的机械混合吸附-催化蒸汽转化CO
采用5 wt.% Pt/Ce0.75Zr0.25O2催化剂颗粒和10 mol.% NaNO3/MgO吸附剂的机械混合物,研究了CO的吸附-催化蒸汽转化。结果表明,在模型条件下,MgO最初对СО2的吸附作用较弱,而NaNO3对MgO的促进作用使其在300-350°С温度范围内的吸附动态容量显著增加,在320°С温度范围内达到最大值。该催化剂在CO蒸汽转化过程中具有较高的活性和选择性,其组成为(vol.%) 11.6 CO, 61 H2和27.4 H2O的模型混合物:反应器出口的СО浓度在220 - 400°С温度范围内不超过1 vol.%(最小值为0.3 vol.%),在240°С温度范围内,СН4 -温度低于320°С(此时为0.61 vol.%)。在320°С下CO的吸附-催化蒸汽转化过程中,将吸附剂与催化剂混合使用导致其吸附能力明显下降;这可能与所有的NaNO3都转化为Na2CO3有关,而Na2CO3在再生过程中分解不完全。尽管如此,与没有吸附剂的实验中在指定温度下观察到的值相比,这使得СО和СН4的出口浓度降低了两倍:特别是,在第一个吸附循环的中间,它们在干气基础上分别等于6.1·10-4和8.2·10-2 vol.%。因此,所指出的吸附催化转化CO的方法是有前途的;需要进一步的研究来提高所提出的吸附剂的容量和稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Improvement of mathematical model for catalytic reforming process with a stationary catalyst layer Block catalysts, based on Ce and Mn oxides and cordierite ceramics, for ozone decomposition Influence of the Fe/Cr ratio on the catalytic activity of FeCr/C catalysts in the process of oxidative dehydrogenation of ethane Kinetic model for selective trimerization of ethylene to hexene-1 on chromium-pyrrole catalyst Heterogeneous hydrogenation and isomerization of carbocyclic compounds of the norbornene series (review)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1