链长和饱和度对羧酸热解机理的影响

IF 7.7 2区 工程技术 Q1 CHEMISTRY, APPLIED
Bernardo A. Souto, Justice Asomaning, David C. Bressler
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引用次数: 0

摘要

本研究探讨了饱和和不饱和羧酸非催化热解过程中自由基驱动的脱氧机制。热解实验在410°C, 0.5 ~ 2 h之间进行,使用不同碳链长度(C6 ~ C18)和饱和度的羧酸以及酮类。用GC-MS /FID和GC-TCD/FID分别对液体和气体的原料转化和脱氧产物进行定量。结果表明,羧酸链长度对热解行为有显著影响,羧酸链长度和饱和水平对脱氧途径有显著影响。短链羧酸的主要途径是脱羧,而长链羧酸的脱羧倾向增加。短链饱和羧酸在热解初期有利于酮脱羧,产生大量的酮和二氧化碳。随后这些酮类的脱碳作用促进了进一步脱氧,通过自由基驱动机制生成碳氢化合物和短链酮类。相反,不饱和羧酸发生了广泛的裂解,这抑制了酮脱羧,导致总烃收率降低。此外,混合羧酸原料的转化效率下降,主要是由于有效酮脱羧所必需的分子间相互作用有限。这项工作探索了自由基驱动的脂肪酸非催化热解,提供了链长和饱和度如何影响反应途径的详细机制理解。这些发现突出了产品选择性和脱氧效率的关键决定因素,为优化基于热解的可持续生物燃料生产中的原料组成提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.
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来源期刊
Fuel Processing Technology
Fuel Processing Technology 工程技术-工程:化工
CiteScore
13.20
自引率
9.30%
发文量
398
审稿时长
26 days
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.
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