Qiao Huang , Ruomiao Yang , Junheng Liu , Tianfang Xie , Jinlong Liu
{"title":"研究从纯柴油发动机过渡到甲醇/柴油双燃料发动机时二氧化氮排放量激增的机理","authors":"Qiao Huang , Ruomiao Yang , Junheng Liu , Tianfang Xie , Jinlong Liu","doi":"10.1016/j.fuproc.2024.108131","DOIUrl":null,"url":null,"abstract":"<div><div>In diesel engines, nitrogen monoxide (NO) is the predominant component of nitrogen oxides (NOx) emissions. However, when transitioning to methanol/diesel dual-fuel operation, even with a small percentage of methanol replacing diesel energy (e.g. 10 %), the concentration of nitrogen dioxide (NO<sub>2</sub>) increases significantly, becoming comparable to that of NO. This study employs multi-dimensional computational fluid dynamics (CFD) modeling to reproduce this NO<sub>2</sub>/NOx surge ratio phenomenon and investigates the underlying mechanism driving the surge in NO<sub>2</sub> emissions, an area insufficiently explored in existing literature. By comparing CFD simulations with and without the NO+HO<sub>2</sub>↔NO<sub>2</sub> + OH reaction in the chemical mechanism, the results reveal that the surge in NO<sub>2</sub> concentration disappears when this reaction is invalidated, while engine efficiency, combustion phasing, and overall NOx emissions remain largely unchanged. This indicates that the NO+HO<sub>2</sub>↔NO<sub>2</sub> + OH reaction is the primary contributor to the sudden increase in the NO<sub>2</sub>/NOx ratio. Further analysis during the main combustion stage shows that the diesel spray splits into two distinct regions after impinging on the bowl boundary, with one region deep within the bowl and the other near the squish region. During the late oxidation stage, the diffusion flame directed towards the deep bowl area remains a high-temperature zone with a high concentration of NO, whereas the flame near the squish region evolves into a low-temperature zone due to effective mixing with the low-temperature methanol/air mixture. In these low-temperature regions, almost all NO formed during the main combustion stage is converted to NO<sub>2</sub> during the late oxidation stage, leading to the observed NO<sub>2</sub>/NOx ratio surge. Methanol oxidation contributes HO<sub>2</sub> radicals, which facilitate the NO-to-NO<sub>2</sub> conversion. Consequently, the low-temperature oxidation of methanol outside the high-temperature region does not lead to thermal ignition but is instead responsible for the rare occurrence of the NO<sub>2</sub> surge.</div></div>","PeriodicalId":326,"journal":{"name":"Fuel Processing Technology","volume":"264 ","pages":"Article 108131"},"PeriodicalIF":7.2000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0378382024001012/pdfft?md5=c3715bc5aacc519a78369d93364876b5&pid=1-s2.0-S0378382024001012-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Investigation of the mechanism behind the surge in nitrogen dioxide emissions in engines transitioning from pure diesel operation to methanol/diesel dual-fuel operation\",\"authors\":\"Qiao Huang , Ruomiao Yang , Junheng Liu , Tianfang Xie , Jinlong Liu\",\"doi\":\"10.1016/j.fuproc.2024.108131\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In diesel engines, nitrogen monoxide (NO) is the predominant component of nitrogen oxides (NOx) emissions. However, when transitioning to methanol/diesel dual-fuel operation, even with a small percentage of methanol replacing diesel energy (e.g. 10 %), the concentration of nitrogen dioxide (NO<sub>2</sub>) increases significantly, becoming comparable to that of NO. This study employs multi-dimensional computational fluid dynamics (CFD) modeling to reproduce this NO<sub>2</sub>/NOx surge ratio phenomenon and investigates the underlying mechanism driving the surge in NO<sub>2</sub> emissions, an area insufficiently explored in existing literature. By comparing CFD simulations with and without the NO+HO<sub>2</sub>↔NO<sub>2</sub> + OH reaction in the chemical mechanism, the results reveal that the surge in NO<sub>2</sub> concentration disappears when this reaction is invalidated, while engine efficiency, combustion phasing, and overall NOx emissions remain largely unchanged. This indicates that the NO+HO<sub>2</sub>↔NO<sub>2</sub> + OH reaction is the primary contributor to the sudden increase in the NO<sub>2</sub>/NOx ratio. Further analysis during the main combustion stage shows that the diesel spray splits into two distinct regions after impinging on the bowl boundary, with one region deep within the bowl and the other near the squish region. During the late oxidation stage, the diffusion flame directed towards the deep bowl area remains a high-temperature zone with a high concentration of NO, whereas the flame near the squish region evolves into a low-temperature zone due to effective mixing with the low-temperature methanol/air mixture. In these low-temperature regions, almost all NO formed during the main combustion stage is converted to NO<sub>2</sub> during the late oxidation stage, leading to the observed NO<sub>2</sub>/NOx ratio surge. Methanol oxidation contributes HO<sub>2</sub> radicals, which facilitate the NO-to-NO<sub>2</sub> conversion. Consequently, the low-temperature oxidation of methanol outside the high-temperature region does not lead to thermal ignition but is instead responsible for the rare occurrence of the NO<sub>2</sub> surge.</div></div>\",\"PeriodicalId\":326,\"journal\":{\"name\":\"Fuel Processing Technology\",\"volume\":\"264 \",\"pages\":\"Article 108131\"},\"PeriodicalIF\":7.2000,\"publicationDate\":\"2024-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0378382024001012/pdfft?md5=c3715bc5aacc519a78369d93364876b5&pid=1-s2.0-S0378382024001012-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fuel Processing Technology\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378382024001012\",\"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/S0378382024001012","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}
Investigation of the mechanism behind the surge in nitrogen dioxide emissions in engines transitioning from pure diesel operation to methanol/diesel dual-fuel operation
In diesel engines, nitrogen monoxide (NO) is the predominant component of nitrogen oxides (NOx) emissions. However, when transitioning to methanol/diesel dual-fuel operation, even with a small percentage of methanol replacing diesel energy (e.g. 10 %), the concentration of nitrogen dioxide (NO2) increases significantly, becoming comparable to that of NO. This study employs multi-dimensional computational fluid dynamics (CFD) modeling to reproduce this NO2/NOx surge ratio phenomenon and investigates the underlying mechanism driving the surge in NO2 emissions, an area insufficiently explored in existing literature. By comparing CFD simulations with and without the NO+HO2↔NO2 + OH reaction in the chemical mechanism, the results reveal that the surge in NO2 concentration disappears when this reaction is invalidated, while engine efficiency, combustion phasing, and overall NOx emissions remain largely unchanged. This indicates that the NO+HO2↔NO2 + OH reaction is the primary contributor to the sudden increase in the NO2/NOx ratio. Further analysis during the main combustion stage shows that the diesel spray splits into two distinct regions after impinging on the bowl boundary, with one region deep within the bowl and the other near the squish region. During the late oxidation stage, the diffusion flame directed towards the deep bowl area remains a high-temperature zone with a high concentration of NO, whereas the flame near the squish region evolves into a low-temperature zone due to effective mixing with the low-temperature methanol/air mixture. In these low-temperature regions, almost all NO formed during the main combustion stage is converted to NO2 during the late oxidation stage, leading to the observed NO2/NOx ratio surge. Methanol oxidation contributes HO2 radicals, which facilitate the NO-to-NO2 conversion. Consequently, the low-temperature oxidation of methanol outside the high-temperature region does not lead to thermal ignition but is instead responsible for the rare occurrence of the NO2 surge.
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.