Eleni Heracleous , Flora Papadopoulou , Angelos A. Lappas
{"title":"半间歇连续反应器中钼基分散催化剂对真空气相油的浆相加氢处理","authors":"Eleni Heracleous , Flora Papadopoulou , Angelos A. Lappas","doi":"10.1016/j.fuproc.2025.108271","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, we investigate the use of Mo-based dispersed catalyst, using oleo-soluble Mo-octoate as precursor, for the slurry hydrocracking of VGO as model feedstock in both semi-batch and continuous slurry reactors. The <em>in-situ</em> formation of the catalyst from the corresponding precursor investigated under reaction conditions with Light Cycle Oil (LCO) as feed demonstrates that Mo sulfidation occurs rapidly between 300 and 350 °C, leading to the formation of MoS<sub>2</sub> nanoparticles of hexagonal structure with laminar morphology. Thermal and catalytic semi-batch tests at varying Mo concentration and reaction time indicate that the hydrodesulfurization reactions are catalytically-driven, while cracking follows the thermal free-radical reaction mechanism. At Mo concentrations ≤ 2000 wppm, the active hydrogen formed by the catalyst quenches the free radicals thereby restricting the cracking reactions, while at loadings > 2000 wppm Mo, MoS<sub>2</sub> partially contributes to cracking <em>via</em> C<img>C bond hydrogenolysis. Continuous pilot-scale tests for over 60 h showed no operability issues, achieving high liquid yields (> 98 wt.%). Variation of the sulfur removal and cracking extent with time-on-stream suggests partial catalyst accumulation in the slurry reactor during operation.</div></div>","PeriodicalId":326,"journal":{"name":"Fuel Processing Technology","volume":"276 ","pages":"Article 108271"},"PeriodicalIF":7.7000,"publicationDate":"2025-06-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Slurry-phase hydrotreating of vacuum gas oil with Mo-based dispersed catalyst in semi-batch and continuous reactors\",\"authors\":\"Eleni Heracleous , Flora Papadopoulou , Angelos A. Lappas\",\"doi\":\"10.1016/j.fuproc.2025.108271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this study, we investigate the use of Mo-based dispersed catalyst, using oleo-soluble Mo-octoate as precursor, for the slurry hydrocracking of VGO as model feedstock in both semi-batch and continuous slurry reactors. The <em>in-situ</em> formation of the catalyst from the corresponding precursor investigated under reaction conditions with Light Cycle Oil (LCO) as feed demonstrates that Mo sulfidation occurs rapidly between 300 and 350 °C, leading to the formation of MoS<sub>2</sub> nanoparticles of hexagonal structure with laminar morphology. Thermal and catalytic semi-batch tests at varying Mo concentration and reaction time indicate that the hydrodesulfurization reactions are catalytically-driven, while cracking follows the thermal free-radical reaction mechanism. At Mo concentrations ≤ 2000 wppm, the active hydrogen formed by the catalyst quenches the free radicals thereby restricting the cracking reactions, while at loadings > 2000 wppm Mo, MoS<sub>2</sub> partially contributes to cracking <em>via</em> C<img>C bond hydrogenolysis. Continuous pilot-scale tests for over 60 h showed no operability issues, achieving high liquid yields (> 98 wt.%). Variation of the sulfur removal and cracking extent with time-on-stream suggests partial catalyst accumulation in the slurry reactor during operation.</div></div>\",\"PeriodicalId\":326,\"journal\":{\"name\":\"Fuel Processing Technology\",\"volume\":\"276 \",\"pages\":\"Article 108271\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-06-19\",\"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/S0378382025000955\",\"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/S0378382025000955","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}
Slurry-phase hydrotreating of vacuum gas oil with Mo-based dispersed catalyst in semi-batch and continuous reactors
In this study, we investigate the use of Mo-based dispersed catalyst, using oleo-soluble Mo-octoate as precursor, for the slurry hydrocracking of VGO as model feedstock in both semi-batch and continuous slurry reactors. The in-situ formation of the catalyst from the corresponding precursor investigated under reaction conditions with Light Cycle Oil (LCO) as feed demonstrates that Mo sulfidation occurs rapidly between 300 and 350 °C, leading to the formation of MoS2 nanoparticles of hexagonal structure with laminar morphology. Thermal and catalytic semi-batch tests at varying Mo concentration and reaction time indicate that the hydrodesulfurization reactions are catalytically-driven, while cracking follows the thermal free-radical reaction mechanism. At Mo concentrations ≤ 2000 wppm, the active hydrogen formed by the catalyst quenches the free radicals thereby restricting the cracking reactions, while at loadings > 2000 wppm Mo, MoS2 partially contributes to cracking via CC bond hydrogenolysis. Continuous pilot-scale tests for over 60 h showed no operability issues, achieving high liquid yields (> 98 wt.%). Variation of the sulfur removal and cracking extent with time-on-stream suggests partial catalyst accumulation in the slurry reactor during operation.
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.