An investigation on the characteristics of and influence factors for NO2 formation in diesel/methanol dual fuel engine

Fuel ◽  
2019 ◽  
Vol 235 ◽  
pp. 617-626 ◽  
Author(s):  
Han Lu ◽  
Anren Yao ◽  
Chunde Yao ◽  
Chao Chen ◽  
Bin Wang
2019 ◽  
Vol 141 (8) ◽  
Author(s):  
Ehsan Arabian ◽  
Thomas Sattelmayer

A dual fuel engine concept with lean premixed methane–air charge ignited by a diesel pilot flame is highly promising for reducing NOx and soot emissions. One drawback of this combustion method, however, is the high nitric dioxide (NO2) emissions observed at certain operating points. The conditions leading to increased NO2 formation have been investigated using a batch reactor model in cantera. It has been found that the high emission levels of NO2 can be traced back to the mixing of small amounts of quenched CH4 with NO from the hot combustion zones followed by postoxidation in the presence of O2, requiring that the temperatures are within a certain range. NO2 formation in the exhaust duct of a test engine has been modeled and compared to the experimental results. The well-stirred reactor model has been used that calculates the steady-state of a uniform composition for a certain residence time. An appropriate reaction mechanism that considers the effect of NO/NO2 on methane oxidation at low temperature levels has been used. The numerical results of NO–NO2 conversion in the duct at low temperature levels show good agreement with the experimental results. The partial oxidation of CH4 can be predicted well. It can be shown that methane oxidation in the presence of NO/NO2 at low temperature levels is enhanced via the reaction steps CH3+NO2⇌CH3O+NO and CH3O2+NO⇌CH3O+NO2. In addition, the elementary reaction HO2+NO⇌NO2+OH is the important NO oxidizing step.


Author(s):  
Yu Li ◽  
Hailin Li ◽  
Yongzhi Li ◽  
Mingfa Yao ◽  
Hongsheng Guo

The burning of natural gas (NG) in compression ignition dual fuel engines has been highlighted for its fuel flexibility, higher thermal efficiency and reduced particulate matter (PM) emissions. Recent research has reported the significant impact of the introduction of NG to the intake port on nitrogen dioxide (NO2) emissions, particularly at the low loads. However, the research on the mechanism of NO2 formation in dual fuel engines has not been reported. This research simulates the formation and destruction of NO2 in a NG-diesel dual fuel engine using commercial CFD software CONVERGE coupled with a reduced primary reference fuel (PRF) mechanism consisting of 45 species and 142 reactions. The model was validated by comparing the simulated cylinder pressure, heat release rate, and nitrogen oxides (NOx) emissions with experimental data. The validated model was used to simulate the formation and destruction of NO2 in a NG-diesel dual fuel engine. The formation of NO2 and its correlation with the local concentration of nitric oxide (NO), methane, and temperature were examined and discussed. It was revealed that NO2 was mainly formed in the interface region between the hot NO-containing combustion products and the relatively cool unburnt methane-air mixture. NO2 formed at the early combustion stage is usually destructed to NO after the complete oxidation of methane and n-heptane, while NO2 formed during the post-combustion process would survive and exit the engine. This was supported by the distribution of NO and NO2 in the equivalence ratio (ER)-T diagram. A detailed analysis of the chemical reactions occurring in the NO2 containing zone consisting of NO2, NO, O2, methane, etc., was conducted using a quasi-homogeneous constant volume model to identify the key reactions and species dominating NO2 formation and destruction. The HO2 produced during the post combustion process of methane was identified as the primary species dominating the formation of NO2. The simulation revealed the key reaction path for the formation of HO2 noted as CH4->CH3->CH2O->HCO->HO2, with conversion ratios of 98%, 74%, 90%, 98%, accordingly. The backward reaction of OH+NO2 = NO+HO2 consumed 34% of HO2 for the production of NO2. It was concluded that the increased NO2 emissions from NG-diesel dual fuel engines was formed during the post combustion process due to higher concentration of HO2 produced during the oxidation process of the unburned methane at low temperature.


2018 ◽  
Vol 140 (9) ◽  
Author(s):  
Yu Li ◽  
Hailin Li ◽  
Hongsheng Guo ◽  
Yongzhi Li ◽  
Mingfa Yao

This research numerically simulates the formation and destruction of nitrogen dioxide (NO2) in a natural gas (NG)–diesel dual fuel engine using commercial CFD software converge coupled with a reduced primary reference fuel (PRF) mechanism consisting of 45 species and 142 reactions. The model was validated by comparing the simulated cylinder pressure, heat release rate (HRR), and nitrogen oxide (NOx) emissions with experimental data. The validated model was used to simulate the formation and destruction of NO2 in a NG–diesel dual fuel engine. The formation of NO2 and its correlation with the local concentration of nitric oxide (NO), methane, and temperature were examined and discussed. It was revealed that NO2 was mainly formed in the interface region between the hot NO-containing combustion products and the relatively cool unburnt methane–air mixture. The NO2 formed at the early combustion stage is usually destructed to NO after the complete oxidation of methane and n-heptane, while NO2 formed during the postcombustion process survives through the expansion process and exits the engine. The increased NO2 emissions from NG–diesel dual fuel engines was formed during the post combustion process due to higher concentration of HO2 produced during the oxidation process of the unburned methane at low temperature. A detailed analysis of the chemical reactions occurring in the NO2 containing zone consisting of NO2, NO, O2, methane, etc., was conducted using a quasi-homogeneous constant volume (QHCV) model to identify the key reactions and species dominating NO2 formation and destruction. The HO2 produced during the postcombustion process of methane was identified as the primary species dominating the formation of NO2 during the post combustion expansion process. The simulation revealed the key reaction path for the formation of HO2 noted as CH4 → CH3 → CH2O → HCO → HO2, with conversion ratios of 98%, 74%, 90%, 98%, accordingly. The backward reaction of OH + NO2 = NO + HO2 consumed 34% of HO2 for the production of NO2.


Author(s):  
Ehsan Arabian ◽  
Thomas Sattelmayer

A dual fuel engine concept with lean premixed methane-air charge ignited by a diesel pilot flame is highly promising for reducing NOx and soot emissions. One drawback of this combustion method, however, is the high nitric dioxide (NO2) emissions observed at certain operating points. NO2 is a toxic gas, which is identifiable by its yellow color. In this paper the conditions leading to increased NO2 formation have been investigated using a batch reactor model in Cantera. In a first step, it has been found that the high emission levels of NO2 can be traced back to the mixing of small amounts of quenched CH4 with NO from the hot combustion zones followed by post-oxidation in the presence of O2, requiring that the temperatures are within a certain range. In the second step, NO2 formation in the exhaust duct of a test engine has been modeled and compared to the experimental results. For that purpose a well-stirred reactor model has been used that calculates the steady-state of a uniform composition for a certain residence time. An appropriate reaction mechanism that considers the effect of NO/NO2 on methane oxidation at low temperature levels has been used. The numerical results of NO to NO2 conversion in the duct at low temperature and pressure levels show good agreement with the experimental results for various temperatures and concentrations of unburned methane. The partial oxidation of CH4 can be predicted well. It can be shown that methane oxidation in the presence of NO/NO2 at low temperature levels is enhanced via the reaction steps CH3 + NO2 ⇌ CH3O + NO and CH3O2 + NO ⇌ CH3O + NO2. In addition the elementary reaction HO2 + NO ⇌ NO2 + OH is the important NO oxidizing step.


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