Pedro L. Lugo , Tamara B. Benzaquén , Mariano A. Teruel , María B. Blanco
{"title":"氟乙酸乙酯和氟乙酸丁酯氧化:产品产量、机制和环境影响","authors":"Pedro L. Lugo , Tamara B. Benzaquén , Mariano A. Teruel , María B. Blanco","doi":"10.1016/j.atmosenv.2025.121532","DOIUrl":null,"url":null,"abstract":"<div><div>Product studies were developed for the gas-phase reactions of <sup>●</sup>OH radicals with ethyl fluoroacetate (EFA) and butyl fluoroacetate (BFA) at NOx free conditions. The experiments were performed in a 1080 L quartz-glass chamber in synthetic air at (298 ± 2) K and (760 ± 10) torr using long path <em>in situ</em> FTIR spectroscopy to monitor the reactants and products. Fluoroacetic acid (CH<sub>2</sub>FC(O)OH), formyl fluoride (HC(O)F) and formaldehyde (HC(O)H) were positively identified as reaction products. The following molar yields determined were: (52.4 ± 0.5) % of CH<sub>2</sub>FC(O)OH, (32.3 ± 0.3) % of HC(O)H and (86.1 ± 0.8) % of HC(O)F for EFA + OH reaction, while product yields of (28.0 ± 0.1) % of CH<sub>2</sub>FC(O)OH, (11.0 ± 0.3) % of HC(O)F and <5 % of HC(O)H were obtained for the reaction of OH with BFA, respectively.</div><div>Photo-Fenton process was used to degrade a series of fluoracetic acids, CF<sub>3</sub>C(O)OH (TFA), CF<sub>2</sub>HC(O)OH (DFA) and CH<sub>2</sub>FC(O)O (MFA), obtained as products of FES oxidation. Atmospheric implications of the reactions studied are discussed.</div></div>","PeriodicalId":250,"journal":{"name":"Atmospheric Environment","volume":"362 ","pages":"Article 121532"},"PeriodicalIF":3.7000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ethyl fluoroacetate and butyl fluoroacetate oxidation: Products yields, mechanisms and environmental implications\",\"authors\":\"Pedro L. Lugo , Tamara B. Benzaquén , Mariano A. Teruel , María B. Blanco\",\"doi\":\"10.1016/j.atmosenv.2025.121532\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Product studies were developed for the gas-phase reactions of <sup>●</sup>OH radicals with ethyl fluoroacetate (EFA) and butyl fluoroacetate (BFA) at NOx free conditions. The experiments were performed in a 1080 L quartz-glass chamber in synthetic air at (298 ± 2) K and (760 ± 10) torr using long path <em>in situ</em> FTIR spectroscopy to monitor the reactants and products. Fluoroacetic acid (CH<sub>2</sub>FC(O)OH), formyl fluoride (HC(O)F) and formaldehyde (HC(O)H) were positively identified as reaction products. The following molar yields determined were: (52.4 ± 0.5) % of CH<sub>2</sub>FC(O)OH, (32.3 ± 0.3) % of HC(O)H and (86.1 ± 0.8) % of HC(O)F for EFA + OH reaction, while product yields of (28.0 ± 0.1) % of CH<sub>2</sub>FC(O)OH, (11.0 ± 0.3) % of HC(O)F and <5 % of HC(O)H were obtained for the reaction of OH with BFA, respectively.</div><div>Photo-Fenton process was used to degrade a series of fluoracetic acids, CF<sub>3</sub>C(O)OH (TFA), CF<sub>2</sub>HC(O)OH (DFA) and CH<sub>2</sub>FC(O)O (MFA), obtained as products of FES oxidation. Atmospheric implications of the reactions studied are discussed.</div></div>\",\"PeriodicalId\":250,\"journal\":{\"name\":\"Atmospheric Environment\",\"volume\":\"362 \",\"pages\":\"Article 121532\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atmospheric Environment\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1352231025005072\",\"RegionNum\":2,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric Environment","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1352231025005072","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Ethyl fluoroacetate and butyl fluoroacetate oxidation: Products yields, mechanisms and environmental implications
Product studies were developed for the gas-phase reactions of ●OH radicals with ethyl fluoroacetate (EFA) and butyl fluoroacetate (BFA) at NOx free conditions. The experiments were performed in a 1080 L quartz-glass chamber in synthetic air at (298 ± 2) K and (760 ± 10) torr using long path in situ FTIR spectroscopy to monitor the reactants and products. Fluoroacetic acid (CH2FC(O)OH), formyl fluoride (HC(O)F) and formaldehyde (HC(O)H) were positively identified as reaction products. The following molar yields determined were: (52.4 ± 0.5) % of CH2FC(O)OH, (32.3 ± 0.3) % of HC(O)H and (86.1 ± 0.8) % of HC(O)F for EFA + OH reaction, while product yields of (28.0 ± 0.1) % of CH2FC(O)OH, (11.0 ± 0.3) % of HC(O)F and <5 % of HC(O)H were obtained for the reaction of OH with BFA, respectively.
Photo-Fenton process was used to degrade a series of fluoracetic acids, CF3C(O)OH (TFA), CF2HC(O)OH (DFA) and CH2FC(O)O (MFA), obtained as products of FES oxidation. Atmospheric implications of the reactions studied are discussed.
期刊介绍:
Atmospheric Environment has an open access mirror journal Atmospheric Environment: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
Atmospheric Environment is the international journal for scientists in different disciplines related to atmospheric composition and its impacts. The journal publishes scientific articles with atmospheric relevance of emissions and depositions of gaseous and particulate compounds, chemical processes and physical effects in the atmosphere, as well as impacts of the changing atmospheric composition on human health, air quality, climate change, and ecosystems.