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Carbon in diesel participate matter: Structure, microwave absorption, and oxidation

Published online by Cambridge University Press:  03 March 2011

V. Suresh Babu
Affiliation:
Department of Physics, P.O. Box 6315, West Virginia University. Morgantown, West Virginia 26506-6315
L. Farinash
Affiliation:
Department of Physics, P.O. Box 6315, West Virginia University. Morgantown, West Virginia 26506-6315
M.S. Seehra
Affiliation:
Department of Physics, P.O. Box 6315, West Virginia University. Morgantown, West Virginia 26506-6315
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Abstract

The structural, microwave absorption, and oxidation characteristics of diesel particulate matter (DPM) collected from a CAT 3304 diesel engine are reported. The x-ray diffraction of DPM yields the characteristic peaks of pregraphitic carbons (cokes and pitches), and its modeling yields d(002) ≍ 3.429 Å and a crystallite size of about 20 Å. The real and imaginary parts of the dielectric constant ∊ = ∊′ + i∊″ are measured at 8.7 GHz using the cavity perturbation technique. The measured values for the DPM are ∊′ = 8.6 ± 1.7 and ∊″ = 7.4 ± 1.5, compared to ∊′ ≍ 1.0 and ∊″ ≍ 6 × 10−5 for the ceramic trap material used for collecting DPM. The oxidation products of the DPM, analyzed by FTIR spectroscopy, are found to contain CO2 and CO with a peak yield occurring around 500 °C. Since microwave power absorption is proportional to ∊″, these results show that selective microwave heating of the DPM in the ceramic traps should be a very efficient process with CO2 and CO as the main oxidation products.

Type
Communication
Copyright
Copyright © Materials Research Society 1995

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References

REFERENCES

1National Institute for Occupational Safety and Health: (NIOSH), Pub. No. 88-116 (NIOSH, Cincinnati, OH, 1988).Google Scholar
2Small, J., Bureau of Mines report (1983).Google Scholar
3Wallace, W., Keane, M., and Tox, X. S., Environ. Health 21, 163166 (1987).Google Scholar
4Garner, C. P. and Dent, J. C., SAE 890174 (1989).Google Scholar
5Garner, C. P. and Dent, J. C., SAE 905116 (1990).Google Scholar
6Nassear, D. L., Gautam, M., Gao, Hong-Guang, M., Wallace, W. E., and Clark, N.N., SAE 921752 (1992).Google Scholar
7Foley, G. M. and Langenberg, D. N., Solid State Commun. 18, 351 (1976).CrossRefGoogle Scholar
8Seehra, M. S. and Pavlovic, A. S., Carbon 31(4), 557564 (1993).CrossRefGoogle Scholar
9Shi, H., Ph.D. Dissertation, Simon Fraser University (September 1993).Google Scholar
10Shi, H., Reimers, J. N., and Dahn, J. R., J. Appl. Crystallogr. 26, 827 (1993).CrossRefGoogle Scholar
11Khanna, S. K., Ehenfreud, E., Garito, A. F., and Heeger, A. J., Phys. Rev. B 10, 2205 (1974).CrossRefGoogle Scholar
12Poole, C. P. Jr., Electron Spin Resonance—A Comprehensive Treatise on Experimental Techniques (Interscience Publications, New York, 1967), p. 71.Google Scholar
13Babu, V. S., Popuri, S., Gautam, M., and Seehra, M. S., in Proc. 4th Symp. Respirable Dust in the Mineral Industries, Pittsburgh, PA, Nov. 8–10, 1994 (unpublished).Google Scholar
14Ismail, I. M. K. and Rodgers, S. L., Carbon 30, 229 (1992).CrossRefGoogle Scholar
15Lang, F. M. and Magnier, P., in Activation of Oxygen and Carbon Dioxide, edited by Walker, P.L. (1981), Vol. 3, pp. 187209.Google Scholar