Freek Karaçoban, Yara Bonne, Tomas van Haasterecht, Johannes H. Bitter
{"title":"碳纳米纤维负载的Ru和K2CO3协同作用对CO2的直接空气捕获和转化","authors":"Freek Karaçoban, Yara Bonne, Tomas van Haasterecht, Johannes H. Bitter","doi":"10.1016/j.jcou.2025.103122","DOIUrl":null,"url":null,"abstract":"<div><div>Dual functional materials for CO<sub>2</sub> capture (DFMs) combine a CO<sub>2</sub> sorbent and hydrogenation catalyst on the same support material. Here, we present a DFM specifically designed for direct air capture of CO<sub>2</sub> and subsequent conversion of the captured CO<sub>2</sub>. The DFM consists of K<sub>2</sub>CO<sub>3</sub> (sorbent) and ruthenium (catalyst) on a carbon nanofiber support. We will show that synergy between the sorbent and catalyst exists and we will explore the nature of this synergy. DFMs were tested in cycles of direct air capture and subsequent conversion of CO<sub>2</sub> in H<sub>2</sub>. By comparing a physical mixture of sorbent and catalyst to the DFM it was found that conversion over the DFM was higher by more than threefold. This indicates that a synergy due to the physical interaction between sorbent and catalyst is present. Examination of the evolved gasses during the conversion phase showed that CO<sub>2</sub> that desorbed from the sorbent under H<sub>2</sub> re-adsorbed on the DFM. The amount of these re-adsorption sites, and therefore the conversion, increased with Ru loading. By varying the sorption time, K<sub>2</sub>CO<sub>3</sub> loading (2.5–15 wt%), and Ru loading (0.8–3.1 wt%) it will be shown that 100 % of captured CO<sub>2</sub> can be converted at temperatures below 225 °C, as long as the amount of CO<sub>2</sub> does not exceed the number of re-adsorption sites.</div></div>","PeriodicalId":350,"journal":{"name":"Journal of CO2 Utilization","volume":"97 ","pages":"Article 103122"},"PeriodicalIF":7.2000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"On the synergy between Ru and K2CO3 supported on carbon nanofibers for the direct air capture and conversion of CO2\",\"authors\":\"Freek Karaçoban, Yara Bonne, Tomas van Haasterecht, Johannes H. Bitter\",\"doi\":\"10.1016/j.jcou.2025.103122\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Dual functional materials for CO<sub>2</sub> capture (DFMs) combine a CO<sub>2</sub> sorbent and hydrogenation catalyst on the same support material. Here, we present a DFM specifically designed for direct air capture of CO<sub>2</sub> and subsequent conversion of the captured CO<sub>2</sub>. The DFM consists of K<sub>2</sub>CO<sub>3</sub> (sorbent) and ruthenium (catalyst) on a carbon nanofiber support. We will show that synergy between the sorbent and catalyst exists and we will explore the nature of this synergy. DFMs were tested in cycles of direct air capture and subsequent conversion of CO<sub>2</sub> in H<sub>2</sub>. By comparing a physical mixture of sorbent and catalyst to the DFM it was found that conversion over the DFM was higher by more than threefold. This indicates that a synergy due to the physical interaction between sorbent and catalyst is present. Examination of the evolved gasses during the conversion phase showed that CO<sub>2</sub> that desorbed from the sorbent under H<sub>2</sub> re-adsorbed on the DFM. The amount of these re-adsorption sites, and therefore the conversion, increased with Ru loading. By varying the sorption time, K<sub>2</sub>CO<sub>3</sub> loading (2.5–15 wt%), and Ru loading (0.8–3.1 wt%) it will be shown that 100 % of captured CO<sub>2</sub> can be converted at temperatures below 225 °C, as long as the amount of CO<sub>2</sub> does not exceed the number of re-adsorption sites.</div></div>\",\"PeriodicalId\":350,\"journal\":{\"name\":\"Journal of CO2 Utilization\",\"volume\":\"97 \",\"pages\":\"Article 103122\"},\"PeriodicalIF\":7.2000,\"publicationDate\":\"2025-05-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of CO2 Utilization\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2212982025001064\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of CO2 Utilization","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2212982025001064","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
On the synergy between Ru and K2CO3 supported on carbon nanofibers for the direct air capture and conversion of CO2
Dual functional materials for CO2 capture (DFMs) combine a CO2 sorbent and hydrogenation catalyst on the same support material. Here, we present a DFM specifically designed for direct air capture of CO2 and subsequent conversion of the captured CO2. The DFM consists of K2CO3 (sorbent) and ruthenium (catalyst) on a carbon nanofiber support. We will show that synergy between the sorbent and catalyst exists and we will explore the nature of this synergy. DFMs were tested in cycles of direct air capture and subsequent conversion of CO2 in H2. By comparing a physical mixture of sorbent and catalyst to the DFM it was found that conversion over the DFM was higher by more than threefold. This indicates that a synergy due to the physical interaction between sorbent and catalyst is present. Examination of the evolved gasses during the conversion phase showed that CO2 that desorbed from the sorbent under H2 re-adsorbed on the DFM. The amount of these re-adsorption sites, and therefore the conversion, increased with Ru loading. By varying the sorption time, K2CO3 loading (2.5–15 wt%), and Ru loading (0.8–3.1 wt%) it will be shown that 100 % of captured CO2 can be converted at temperatures below 225 °C, as long as the amount of CO2 does not exceed the number of re-adsorption sites.
期刊介绍:
The Journal of CO2 Utilization offers a single, multi-disciplinary, scholarly platform for the exchange of novel research in the field of CO2 re-use for scientists and engineers in chemicals, fuels and materials.
The emphasis is on the dissemination of leading-edge research from basic science to the development of new processes, technologies and applications.
The Journal of CO2 Utilization publishes original peer-reviewed research papers, reviews, and short communications, including experimental and theoretical work, and analytical models and simulations.