Bernardo A. Souto, Justice Asomaning, David C. Bressler
{"title":"链长和饱和度对羧酸热解机理的影响","authors":"Bernardo A. Souto, Justice Asomaning, David C. Bressler","doi":"10.1016/j.fuproc.2025.108336","DOIUrl":null,"url":null,"abstract":"<div><div>This study investigates radical-driven deoxygenation mechanisms during the non-catalytic pyrolysis of saturated and unsaturated carboxylic acids. Pyrolysis experiments were conducted at 410 °C, between 0.5 and 2 h, using carboxylic acids of varying carbon chain lengths (C6 to C18) and saturation levels, along with ketones. Feedstock conversion and deoxygenation products were quantified using GC–MS/FID for liquids and GC-TCD/FID for gases. Results demonstrated that carboxylic acid chain length significantly influences pyrolysis behavior, with significant differences in deoxygenation pathway linked to acid chain length and saturation level. Decarboxylation was the predominant pathway for short-chain carboxylic acids, whereas long-chain acids showed increased tendency towards decarbonylation. Short-chain saturated carboxylic acids favoured ketonic decarboxylation during the initial stages of pyrolysis, resulting in notable amounts of ketones and carbon dioxide. Subsequent decarbonylation of these ketones contributed to further deoxygenation, generating hydrocarbons and shorter-chain ketones via radical-driven mechanisms. In contrast unsaturated carboxylic acids underwent extensive cracking, which suppressed ketonic decarboxylation and led to reduced overall hydrocarbon yields. Additionally, mixed carboxylic acid feedstocks showed decreased conversion efficiencies, primarily due to limited intermolecular interactions necessary for effective ketonic decarboxylation. This work explores radical-driven, non-catalytic pyrolysis of fatty acids, providing a detailed mechanistic understanding of how chain length and saturation influence reaction pathway. The findings highlight key determinants of product selectivity and deoxygenation efficiency, providing valuable insights for optimizing feedstock compositions in pyrolysis-based sustainable biofuel production.</div></div>","PeriodicalId":326,"journal":{"name":"Fuel Processing Technology","volume":"278 ","pages":"Article 108336"},"PeriodicalIF":7.7000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Influence of chain length and saturation on carboxylic acid pyrolysis mechanisms\",\"authors\":\"Bernardo A. Souto, Justice Asomaning, David C. Bressler\",\"doi\":\"10.1016/j.fuproc.2025.108336\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study investigates radical-driven deoxygenation mechanisms during the non-catalytic pyrolysis of saturated and unsaturated carboxylic acids. Pyrolysis experiments were conducted at 410 °C, between 0.5 and 2 h, using carboxylic acids of varying carbon chain lengths (C6 to C18) and saturation levels, along with ketones. Feedstock conversion and deoxygenation products were quantified using GC–MS/FID for liquids and GC-TCD/FID for gases. Results demonstrated that carboxylic acid chain length significantly influences pyrolysis behavior, with significant differences in deoxygenation pathway linked to acid chain length and saturation level. Decarboxylation was the predominant pathway for short-chain carboxylic acids, whereas long-chain acids showed increased tendency towards decarbonylation. Short-chain saturated carboxylic acids favoured ketonic decarboxylation during the initial stages of pyrolysis, resulting in notable amounts of ketones and carbon dioxide. Subsequent decarbonylation of these ketones contributed to further deoxygenation, generating hydrocarbons and shorter-chain ketones via radical-driven mechanisms. In contrast unsaturated carboxylic acids underwent extensive cracking, which suppressed ketonic decarboxylation and led to reduced overall hydrocarbon yields. Additionally, mixed carboxylic acid feedstocks showed decreased conversion efficiencies, primarily due to limited intermolecular interactions necessary for effective ketonic decarboxylation. This work explores radical-driven, non-catalytic pyrolysis of fatty acids, providing a detailed mechanistic understanding of how chain length and saturation influence reaction pathway. The findings highlight key determinants of product selectivity and deoxygenation efficiency, providing valuable insights for optimizing feedstock compositions in pyrolysis-based sustainable biofuel production.</div></div>\",\"PeriodicalId\":326,\"journal\":{\"name\":\"Fuel Processing Technology\",\"volume\":\"278 \",\"pages\":\"Article 108336\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fuel Processing Technology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378382025001602\",\"RegionNum\":2,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Processing Technology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378382025001602","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Influence of chain length and saturation on carboxylic acid pyrolysis mechanisms
This study investigates radical-driven deoxygenation mechanisms during the non-catalytic pyrolysis of saturated and unsaturated carboxylic acids. Pyrolysis experiments were conducted at 410 °C, between 0.5 and 2 h, using carboxylic acids of varying carbon chain lengths (C6 to C18) and saturation levels, along with ketones. Feedstock conversion and deoxygenation products were quantified using GC–MS/FID for liquids and GC-TCD/FID for gases. Results demonstrated that carboxylic acid chain length significantly influences pyrolysis behavior, with significant differences in deoxygenation pathway linked to acid chain length and saturation level. Decarboxylation was the predominant pathway for short-chain carboxylic acids, whereas long-chain acids showed increased tendency towards decarbonylation. Short-chain saturated carboxylic acids favoured ketonic decarboxylation during the initial stages of pyrolysis, resulting in notable amounts of ketones and carbon dioxide. Subsequent decarbonylation of these ketones contributed to further deoxygenation, generating hydrocarbons and shorter-chain ketones via radical-driven mechanisms. In contrast unsaturated carboxylic acids underwent extensive cracking, which suppressed ketonic decarboxylation and led to reduced overall hydrocarbon yields. Additionally, mixed carboxylic acid feedstocks showed decreased conversion efficiencies, primarily due to limited intermolecular interactions necessary for effective ketonic decarboxylation. This work explores radical-driven, non-catalytic pyrolysis of fatty acids, providing a detailed mechanistic understanding of how chain length and saturation influence reaction pathway. The findings highlight key determinants of product selectivity and deoxygenation efficiency, providing valuable insights for optimizing feedstock compositions in pyrolysis-based sustainable biofuel production.
期刊介绍:
Fuel Processing Technology (FPT) deals with the scientific and technological aspects of converting fossil and renewable resources to clean fuels, value-added chemicals, fuel-related advanced carbon materials and by-products. In addition to the traditional non-nuclear fossil fuels, biomass and wastes, papers on the integration of renewables such as solar and wind energy and energy storage into the fuel processing processes, as well as papers on the production and conversion of non-carbon-containing fuels such as hydrogen and ammonia, are also welcome. While chemical conversion is emphasized, papers on advanced physical conversion processes are also considered for publication in FPT. Papers on the fundamental aspects of fuel structure and properties will also be considered.