Hostname: page-component-848d4c4894-8kt4b Total loading time: 0 Render date: 2024-07-01T11:01:49.351Z Has data issue: false hasContentIssue false

Materials Development by a Surface Modification for the Sulfuric Acid Decomposer in Iodine-Sulfur(IS)cycle for Nuclear Hydrogen Production System

Published online by Cambridge University Press:  31 January 2011

Jae-Won Park
Affiliation:
pjw@kaeri.re.kr, Korea Atomic Energy Research Institute, Daejon-City, Korea, Republic of
Hyung-Jin Kim
Affiliation:
hjkim1231@kaeri.re.kr, Korea Atomic Energy Research Institute, Daejon-City, Korea, Republic of
Yong-Wan Kim
Affiliation:
ywkim@kaeri.re.kr, Korea Atomic Energy Research Institute, Daejon-City, Korea, Republic of
Get access

Abstract

Efforts have been made to develop long term sustainable materials for use above 900°C in the SO3/SO2 environments utilized in Nuclear Hydrogen Production Systems. In this study, the surface of Hastelloy X was serially modified by evaporative SiC coating, ion beam mixing (IBM), additional coatings, and final ion beam hammering (IBH). Subsequent heating above 900°C results in no peeling-off of the SiC coating layer in spite of the huge difference in their coefficients of thermal expansion (CTE). It was also found that ion beam hammering (irradiation) suppresses the vacuum sublimation of the low density (∼40% of bulk) ceramic film (bulk materials begin to sublime at ∼ 750°C in a vacuum of 1.5×10−5 torr). The sublimation rate is ≤ 30% of the bulk rate after an annealing at 950 for 2 hrs but is decreased to ≤10% of the bulk rate after irradiation with 70 keV ions to a total dose of 1×1017 N ions/cm2. Further irradiation (up to 4×1017 N ions/cm2) does not further decrease the rate. Both an immersion test in 98% sulfuric acid and the potentiodynamic polarization test suggest that the surface modified Hastelloy X has a greatly prolonged life time in the corrosive sulfuric acid atmosphere, suggesting the serial surface modification process is applicable to the thermo-chemical system for the nuclear hydrogen production.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

[1]] Yalcin, S. International journal of hydrogen energy, Vol. 14, No 8(1989) 551 Google Scholar
[2] Ota, Hiroyuki, Kubo, Shinji, Hodotsuka, Masatoshi, Inatomi, Takanari, Kobayashi, Masahiko, Terada, Atuhiko, Kasahara, Seiji, Hino, Ryutaro, Ogura, Kenji, Maruyama, Shigeki, 13th International Conference on Nuclear Engineering, Beijing, China, May 16-20, 2005, ICONE-13-50494Google Scholar
[3] Fujikawa, S. et al. , J. Nucl. Sci. Technol., Vol. 41(2004) 1245 Google Scholar
[4] Riviere, J.-P. Delafond, J. Misaelides, P. Noli, F. Surf. Coat. Technol. 100-101(1998) 243 Google Scholar
[5] Fujikawa, S. Hatashi, H. Nakazawa, T. Kawasaki, K. Iyoku, T. Nakagawa, S. and Sakaba, N.., J. Nucl. Sci. Technol., 41(2004) 1245 Google Scholar
[6] Park, J. Khan, Z. S. Kim, H. Kim, Y. Mater. Res. Symp. Proc., Vol. 1125(2009)65 Google Scholar
[7] Grugel, Richard N. a,, Toutanji, Houssam, Advances in Space Research 41(2008) 103 Google Scholar
[8] CRC hand book of chemistry and physics,(CRC press Inc., 1988) B-60, ISBN 0-8493-0740-6Google Scholar
[9] Park, J. Kim, H. Kim, Y. Submitted for the publication else where(2009)Google Scholar
[10] Ziegler, J. F. Biersack, J. P. Littmark, U.The Stopping Range of Ion in Solids”, Pergamon Press, New York(1985)Google Scholar
[11] Zalar, A. Kovac, J. Pracek, B. Panjan, P. Ceh, M. Applied. Surface Science, Vol. 254, issue 20(2008) 66116618 Google Scholar
[12] Canut, B. Teodorescu, V. Roger, J.A. Blanchin, M.G. Daoudi, K. Sandu, C. Nuclear Instruments and Methods in Physics Research B, 191(2002) 783788 Google Scholar