Soot Oxidation in Flames

1981 ◽  
pp. 261-282 ◽  
Author(s):  
K. G. Neoh ◽  
J. B. Howard ◽  
A. F. Sarofim
Keyword(s):  
2021 ◽  
Vol 415 ◽  
pp. 128959
Author(s):  
M. Pilar Orihuela ◽  
Paolo Miceli ◽  
Joaquín Ramírez-Rico ◽  
Debora Fino ◽  
Ricardo Chacartegui

2021 ◽  
Vol 285 ◽  
pp. 119850
Author(s):  
Meng Wang ◽  
Yan Zhang ◽  
Yunbo Yu ◽  
Wenpo Shan ◽  
Hong He
Keyword(s):  

2021 ◽  
pp. 125523
Author(s):  
Jaesung Lee ◽  
Min Woo Lee ◽  
Min June Kim ◽  
Jae Hwan Lee ◽  
Eun Jun Lee ◽  
...  

2014 ◽  
Vol 14 (9) ◽  
pp. 7087-7096 ◽  
Author(s):  
Zhongpeng Wang ◽  
Liguo Wang ◽  
Fang He ◽  
Zheng Jiang ◽  
Tiancun Xiao ◽  
...  

2020 ◽  
Vol 273 ◽  
pp. 119058 ◽  
Author(s):  
Baofang Jin ◽  
Baohuai Zhao ◽  
Shuang Liu ◽  
Zhenguo Li ◽  
Kaixiang Li ◽  
...  
Keyword(s):  

2005 ◽  
Vol 61 (3-4) ◽  
pp. 334-345 ◽  
Author(s):  
D. Uner ◽  
M.K. Demirkol ◽  
B. Dernaika

2016 ◽  
Vol 188 ◽  
pp. 235-244 ◽  
Author(s):  
Jakob M. Christensen ◽  
Jan-Dierk Grunwaldt ◽  
Anker D. Jensen

2021 ◽  
Vol 316 ◽  
pp. 105-109
Author(s):  
Evgeny A. Kirichenko ◽  
Pavel G. Chigrin ◽  
Anton A. Gnidenko

YFeO3-δ (δ = 0.26) and LaFeO3-δ (δ = 0.5) perovskites with a high specific surface and oxygen non-stoichiometry was firstly synthesized by pyrolysis of polymer-salt compositions. It was shown that the catalytic oxidation of carbon in the presence of these complex oxide systems proceeds in the range of 400 - 700 °С, with a maximum temperature at 556 °С for YFeO3-δ; and 380 - 620 °С ,with a maximum temperature at 501 °С for LaFeO3-δ, in one-stage mode for both. By means of thermal analysis and diffractometry, it was shown that there is no contribution to the soot oxidation mechanism by cyclic perovskite surface transformations, due to the reduction of metal oxides by the soot and their subsequent reoxidation. It has been established that the basis of the catalytic reaction mechanism for both perovskites is the presence of oxygen vacancies on the surface of complex oxides.


2018 ◽  
Vol 20 (8-9) ◽  
pp. 953-966 ◽  
Author(s):  
Madhu Singh ◽  
Mek Srilomsak ◽  
Yujun Wang ◽  
Katsunori Hanamura ◽  
Randy Vander Wal

Development of the regeneration process on diesel particulate filters requires a better understanding of soot oxidation phenomena, especially its relation to soot nanostructure. Nitrogen dioxide (NO2) is known to play an essential role in passive regeneration by oxidizing soot at low temperatures, especially in the presence of oxygen (O2) in the exhaust. However, change in soot nanostructure due to oxidation by NO2–O2 mixtures has not received much attention. This work focuses on nanostructure evolution during passive regeneration of the diesel particulate filter by oxidation of soot at normal exhaust gas temperatures (300°C–400°C). High-resolution transmission electron microscopy of partially oxidized model carbons (R250, M1300, arc-generated soot) and diesel soot under NO2–O2 mixtures is used to investigate physical changes in nanostructure correlating with the material’s behavior during oxidation. Microscopy reveals the changing nanostructure of model carbons during oxidation while fringe analysis of the images points to the differences in the structural metrics of fringe length and tortuosity of the resultant structures. The variation in oxidation rates highlights the inter-dependence of the material’s reactivity with its structure. NO2 preferentially oxidizes edge-site carbon, promotes surface oxidation by altering the particle’s burning mode with increased overall reactivity of NO2+O2 resulting in inhibition of internal burning, typically observed by O2 at exhaust gas temperatures.


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