John Nikko V Salvilla, Sasha Yang, Qianqian Liu, Zongli Xie, Zhenyu Chen, Haitao Song, Lian Zhang
{"title":"阐明了在废催化裂化(FCC)催化剂再生过程中,二氧化碳(CO2)在氰化氢(HCN)转化中的作用。","authors":"John Nikko V Salvilla, Sasha Yang, Qianqian Liu, Zongli Xie, Zhenyu Chen, Haitao Song, Lian Zhang","doi":"10.1016/j.jenvman.2025.126165","DOIUrl":null,"url":null,"abstract":"<p><p>The emission of hydrogen cyanide (HCN) from the industrial fluid catalytic cracking (FCC) catalyst regenerator is a concerning pollutant that is highly toxic. Yet, the underpinning rationale particularly the role of carbon dioxide (CO<sub>2</sub>) and its competition with O<sub>2</sub>, remains poorly understood. Through the tests of three industrial spent FCC catalysts via temperature-programmed oxidation and Chemkin simulation, this study revealed a dual role of CO<sub>2</sub> in the transformation of HCN. At high temperatures (e.g. >700<sup>o</sup>C), the presence of CO<sub>2</sub> is in favor of promoting the thermal cracking of coke via the Boudourad reaction, which subsequently accelerates the cracking of the associated N-bearing species for an enhanced formation of HCN. Meanwhile, a high CO<sub>2</sub> partial pressure >10 % was found to benefit the generation of OH<sup>●</sup> and O<sup>●</sup> radicals, which are the chain carriers for the oxidation of HCN into NO<sub>x</sub> and/or N<sub>2</sub>. This is distinct from an environment containing only O<sub>2</sub> in N<sub>2</sub> in which an optimum O<sub>2</sub> partial pressure of ∼1 % maximises the HCN oxidation rate. Higher O<sub>2</sub> partial pressure above 1 % leads to an early release of HCN before its ignition temperature, resulting in significant emission of unreacted HCN in the outlet gas. In an O<sub>2</sub>-CO<sub>2</sub>-N<sub>2</sub> environment, where O<sub>2</sub> and CO<sub>2</sub> coexist, CO<sub>2</sub> can promote additional coke conversion, leading to increased initial HCN formation when the available O<sub>2</sub> is insufficient to fully oxidize the coke. During the subsequent gas-phase oxidation of HCN, CO<sub>2</sub> competes with O<sub>2</sub> for H<sup>●</sup> radicals, reducing the production of OH<sup>●</sup> and O<sup>●</sup> which in turn diminishes the HCN oxidation rates. Additionally, heightened CO formation from the Bouoduard reaction reduced the NO<sub>x</sub> formed into N<sub>2</sub>. From a practical implication perspective, these findings underscore the importance of gas conditions and maintaining temperature uniformity across the regenerator to effectively manage the emissions of HCN and other pollutant gases.</p>","PeriodicalId":356,"journal":{"name":"Journal of Environmental Management","volume":"389 ","pages":"126165"},"PeriodicalIF":8.4000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Elucidating the role of carbon dioxide (CO<sub>2</sub>) in the transformation of hydrogen cyanide (HCN) during the regeneration of spent fluid catalytic cracking (FCC) catalysts.\",\"authors\":\"John Nikko V Salvilla, Sasha Yang, Qianqian Liu, Zongli Xie, Zhenyu Chen, Haitao Song, Lian Zhang\",\"doi\":\"10.1016/j.jenvman.2025.126165\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The emission of hydrogen cyanide (HCN) from the industrial fluid catalytic cracking (FCC) catalyst regenerator is a concerning pollutant that is highly toxic. Yet, the underpinning rationale particularly the role of carbon dioxide (CO<sub>2</sub>) and its competition with O<sub>2</sub>, remains poorly understood. Through the tests of three industrial spent FCC catalysts via temperature-programmed oxidation and Chemkin simulation, this study revealed a dual role of CO<sub>2</sub> in the transformation of HCN. At high temperatures (e.g. >700<sup>o</sup>C), the presence of CO<sub>2</sub> is in favor of promoting the thermal cracking of coke via the Boudourad reaction, which subsequently accelerates the cracking of the associated N-bearing species for an enhanced formation of HCN. Meanwhile, a high CO<sub>2</sub> partial pressure >10 % was found to benefit the generation of OH<sup>●</sup> and O<sup>●</sup> radicals, which are the chain carriers for the oxidation of HCN into NO<sub>x</sub> and/or N<sub>2</sub>. This is distinct from an environment containing only O<sub>2</sub> in N<sub>2</sub> in which an optimum O<sub>2</sub> partial pressure of ∼1 % maximises the HCN oxidation rate. Higher O<sub>2</sub> partial pressure above 1 % leads to an early release of HCN before its ignition temperature, resulting in significant emission of unreacted HCN in the outlet gas. In an O<sub>2</sub>-CO<sub>2</sub>-N<sub>2</sub> environment, where O<sub>2</sub> and CO<sub>2</sub> coexist, CO<sub>2</sub> can promote additional coke conversion, leading to increased initial HCN formation when the available O<sub>2</sub> is insufficient to fully oxidize the coke. During the subsequent gas-phase oxidation of HCN, CO<sub>2</sub> competes with O<sub>2</sub> for H<sup>●</sup> radicals, reducing the production of OH<sup>●</sup> and O<sup>●</sup> which in turn diminishes the HCN oxidation rates. Additionally, heightened CO formation from the Bouoduard reaction reduced the NO<sub>x</sub> formed into N<sub>2</sub>. From a practical implication perspective, these findings underscore the importance of gas conditions and maintaining temperature uniformity across the regenerator to effectively manage the emissions of HCN and other pollutant gases.</p>\",\"PeriodicalId\":356,\"journal\":{\"name\":\"Journal of Environmental Management\",\"volume\":\"389 \",\"pages\":\"126165\"},\"PeriodicalIF\":8.4000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Environmental Management\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jenvman.2025.126165\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Environmental Management","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.jenvman.2025.126165","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/14 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Elucidating the role of carbon dioxide (CO2) in the transformation of hydrogen cyanide (HCN) during the regeneration of spent fluid catalytic cracking (FCC) catalysts.
The emission of hydrogen cyanide (HCN) from the industrial fluid catalytic cracking (FCC) catalyst regenerator is a concerning pollutant that is highly toxic. Yet, the underpinning rationale particularly the role of carbon dioxide (CO2) and its competition with O2, remains poorly understood. Through the tests of three industrial spent FCC catalysts via temperature-programmed oxidation and Chemkin simulation, this study revealed a dual role of CO2 in the transformation of HCN. At high temperatures (e.g. >700oC), the presence of CO2 is in favor of promoting the thermal cracking of coke via the Boudourad reaction, which subsequently accelerates the cracking of the associated N-bearing species for an enhanced formation of HCN. Meanwhile, a high CO2 partial pressure >10 % was found to benefit the generation of OH● and O● radicals, which are the chain carriers for the oxidation of HCN into NOx and/or N2. This is distinct from an environment containing only O2 in N2 in which an optimum O2 partial pressure of ∼1 % maximises the HCN oxidation rate. Higher O2 partial pressure above 1 % leads to an early release of HCN before its ignition temperature, resulting in significant emission of unreacted HCN in the outlet gas. In an O2-CO2-N2 environment, where O2 and CO2 coexist, CO2 can promote additional coke conversion, leading to increased initial HCN formation when the available O2 is insufficient to fully oxidize the coke. During the subsequent gas-phase oxidation of HCN, CO2 competes with O2 for H● radicals, reducing the production of OH● and O● which in turn diminishes the HCN oxidation rates. Additionally, heightened CO formation from the Bouoduard reaction reduced the NOx formed into N2. From a practical implication perspective, these findings underscore the importance of gas conditions and maintaining temperature uniformity across the regenerator to effectively manage the emissions of HCN and other pollutant gases.
期刊介绍:
The Journal of Environmental Management is a journal for the publication of peer reviewed, original research for all aspects of management and the managed use of the environment, both natural and man-made.Critical review articles are also welcome; submission of these is strongly encouraged.