Journal
CARBON
Volume 93, Issue -, Pages 1068-1076Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2015.07.008
Keywords
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Funding
- Argonne, a U.S. Department of Energy Office of Science laboratory [DE-AC02-06CH11357]
- Advanced Engine Combustion Program at the U.S. Department of Energy Office of Vehicle Technologies
- Corning Inc.
- Hyundai motor company
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences
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Oxidizer- and temperature-dependent soot properties were investigated to better understand soot oxidation process. For this work, partially oxidized Printex-U samples as surrogate soot, under three different O-2-NO2 mixtures, were analyzed by using the high resolution-transmission electron microscope, Raman microscope and Fourier transform infrared spectroscopy-attenuated total reflectance. The results show that the maturing process was much dependent on NO2 content in the O-2-NO2 mixture: with no NO2 added, soot oxidized through the internal-burning out process, whereas with increased NO2 in the mixture, soot tended to oxidize through the external burning process. As the NO2 content increased, the preferential oxidation of less-ordered carbon crystallites decreased and as a result the maturing process was delayed. Internal burning-out process by O-2 only was also verified at various temperatures and with actual engine soot such as diesel soot and gasoline direct-injection (GDI) soot by TEM observations. Despite similar internal burning-out process, however, it was shown that oxidation at increased temperature resulted in relatively less-ordered soot, implying that soot maturing process was delayed with temperature. Since soot oxidation rate increased with temperature, the increase in oxidation temperature seems to diminish preference on short-ranged crystallites like more efficient O-2-NO2 cases. (C) 2015 Elsevier Ltd. All rights reserved.
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