The mechanism of H2O in the superheated steam affecting pyrolysis of the kaolinite-associated kerogen

IF 7.2 2区 工程技术 Q1 CHEMISTRY, APPLIED
Fumin Zhao , Bao Li , Daochang Che , Shengyu Liu
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引用次数: 0

Abstract

In this work, ReaxFF molecular dynamics (MD) simulation was adopted to investigate the effect of superheated steam on the conversion of the kaolinite-associated Barkol kerogen (BLK) and reveal the corresponding mechanism. The ReaxFF simulated weight loss rate (DTG) and release tendency of H2O, H2 and CO2 for BLK and the kaolinite-associated BLK agreed well with the results of Py-MS experiments. H-rich rate, double bond equivalents (DBEs), and hydrocarbon content were adopted to assess the quality of C5-C40, and configurations of C40+ were extracted to investigate the characteristics of residues. And the H2Osteam- and kaolinite-involved (steam refers to the superheated steam) reactions were analyzed. The results indicate that B- and L-acid sites of kaolinite co-catalyzed decomposition of BLK into heavy oil and shale gas in the kaolinite-pyrolysis system, and in steam/kaolinite-pyrolysis system, H2Osteam further promoted decomposition of BLK into higher quality shale oil, especially for C5-C13 components, remaining higher aromatic and porous residues. And this enhanced effect of H2Osteam is attributed to kaolinite and the induced decomposition of H2Osteam molecules and their participation as reactants in reactions in two aspects: i) interaction between kaolinite and H2Osteam, on one hand, inhibited formation of L-acids and facilitated generation of B-acids to catalyze carbocation ion reactions process, further weakened dehydrogenation of organics catalyzed by L-acid sites, and enhanced cracking of residues catalyzed by B-acaid sites, on the other hand, promoted decomposition of H2Osteam molecules to form H-rich environment and further weakened dehydrogenation of organics; ii) attacking Car directly, H2Osteam promoted shedding of alkyl side chains and ring-opening of aromatics to increase the –CH2– content in shale oil. This paper provides theoretical guidance for further understanding mechanism of H2Osteam on pyrolysis of kaolinite-associated kerogen and corresponding catalyst development and preparation.

Abstract Image

过热蒸汽中H2O对高岭石伴生干酪根热解的影响机理
本文采用ReaxFF分子动力学(MD)模拟研究了过热蒸汽对高岭石伴生Barkol干酪根(BLK)转化的影响,并揭示了其机理。ReaxFF模拟BLK和高岭石伴生BLK的失重速率(DTG)和H2O、H2、CO2的释放趋势与Py-MS实验结果吻合较好。采用富氢率、双键当量(DBEs)和碳氢化合物含量评价C5-C40的质量,提取C40+的构型考察残留物的特征。并对h2o2蒸汽和高岭石(蒸汽指过热蒸汽)反应进行了分析。结果表明,在高岭石-热解体系中,高岭石的B-和l -酸位点共同催化了BLK分解为重油和页岩气,而在蒸汽-高岭石-热解体系中,h2o2蒸汽进一步促进了BLK分解为优质页岩油,特别是C5-C13组分,剩余较高的芳香和多孔残留物。而h2o2蒸汽的增强作用主要是由于高岭石及其诱导的h2o2蒸汽分子的分解和作为反应物参与了两个方面的反应:i)高岭石与h2o蒸汽的相互作用一方面抑制l -酸的生成,促进b -酸的生成催化碳正离子反应过程,进一步减弱l -酸位点催化有机物的脱氢反应,增强b -酸位点催化残基的裂解,另一方面促进h2o2蒸汽分子的分解形成富h环境,进一步减弱有机物的脱氢反应;(2) h2o2蒸汽直接攻击Car,促进烷基侧链脱落和芳烃开环,提高页岩油中- ch2 -含量。本文为进一步了解h2o2蒸汽对高岭石伴生干酪根热解机理及相应催化剂的开发与制备提供了理论指导。
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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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