logo
Language
Bookmarks
Log Out

Journals

Search Sites

Account

© 2022 Steel Science Portal

How to use

Advanced Search

Search Sites

site
site
site
site

Tetsu-to-Hagané Vol. 105 (2019), No. 6

ISIJ International
belloff

Grid List Abstracts
ONLINE ISSN: 1883-2954
PRINT ISSN: 0021-1575
Publisher: The Iron and Steel Institute of Japan

Backnumber

  1. Vol. 110 (2024)

    1. No.6
    2. No.5
    3. No.4
    4. No.3
    5. No.2
    6. No.1

  2. Vol. 109 (2023)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  3. Vol. 108 (2022)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  4. Vol. 107 (2021)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  5. Vol. 106 (2020)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  6. Vol. 105 (2019)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  7. Vol. 104 (2018)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  8. Vol. 103 (2017)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  9. Vol. 102 (2016)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  10. Vol. 101 (2015)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  11. Vol. 100 (2014)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  12. Vol. 99 (2013)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  13. Vol. 98 (2012)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  14. Vol. 97 (2011)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  15. Vol. 96 (2010)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  16. Vol. 95 (2009)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  17. Vol. 94 (2008)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  18. Vol. 93 (2007)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  19. Vol. 92 (2006)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  20. Vol. 91 (2005)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  21. Vol. 90 (2004)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  22. Vol. 89 (2003)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  23. Vol. 88 (2002)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  24. Vol. 87 (2001)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  25. Vol. 86 (2000)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  26. Vol. 85 (1999)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  27. Vol. 84 (1998)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  28. Vol. 83 (1997)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  29. Vol. 82 (1996)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  30. Vol. 81 (1995)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  31. Vol. 80 (1994)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  32. Vol. 79 (1993)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  33. Vol. 78 (1992)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  34. Vol. 77 (1991)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  35. Vol. 76 (1990)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  36. Vol. 75 (1989)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  37. Vol. 74 (1988)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  38. Vol. 73 (1987)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  39. Vol. 72 (1986)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  40. Vol. 71 (1985)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  41. Vol. 70 (1984)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  42. Vol. 69 (1983)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  43. Vol. 68 (1982)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  44. Vol. 67 (1981)

    1. No.16
    2. No.15
    3. No.14
    4. No.13
    5. No.12
    6. No.11
    7. No.10
    8. No.9
    9. No.8
    10. No.7
    11. No.6
    12. No.5
    13. No.4
    14. No.3
    15. No.2
    16. No.1

  45. Vol. 66 (1980)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  46. Vol. 65 (1979)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  47. Vol. 64 (1978)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  48. Vol. 63 (1977)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  49. Vol. 62 (1976)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  50. Vol. 61 (1975)

    1. No.15
    2. No.14
    3. No.13
    4. No.12
    5. No.11
    6. No.10
    7. No.9
    8. No.8
    9. No.7
    10. No.6
    11. No.5
    12. No.4
    13. No.3
    14. No.2
    15. No.1

  51. Vol. 60 (1974)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  52. Vol. 59 (1973)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  53. Vol. 58 (1972)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  54. Vol. 57 (1971)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  55. Vol. 56 (1970)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  56. Vol. 55 (1969)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  57. Vol. 54 (1968)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  58. Vol. 53 (1967)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  59. Vol. 52 (1966)

    1. No.13
    2. No.12
    3. No.11
    4. No.10
    5. No.9
    6. No.8
    7. No.7
    8. No.6
    9. No.5
    10. No.4
    11. No.3
    12. No.2
    13. No.1

  60. Vol. 51 (1965)

    1. No.13
    2. No.12
    3. No.11
    4. No.10
    5. No.9
    6. No.8
    7. No.7
    8. No.6
    9. No.5
    10. No.4
    11. No.3
    12. No.2
    13. No.1

  61. Vol. 50 (1964)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  62. Vol. 49 (1963)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  63. Vol. 48 (1962)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  64. Vol. 47 (1961)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  65. Vol. 46 (1960)

    1. No.14
    2. No.13
    3. No.12
    4. No.11
    5. No.10
    6. No.9
    7. No.8-supl
    8. No.7
    9. No.6
    10. No.5
    11. No.4
    12. No.3
    13. No.2
    14. No.1

  66. Vol. 45 (1959)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  67. Vol. 44 (1958)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  68. Vol. 43 (1957)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  69. Vol. 42 (1956)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

  70. Vol. 41 (1955)

    1. No.12
    2. No.11
    3. No.10
    4. No.9
    5. No.8
    6. No.7
    7. No.6
    8. No.5
    9. No.4
    10. No.3
    11. No.2
    12. No.1

Keyword Ranking

27 Apr. (Last 30 Days)

Tetsu-to-Hagané Vol. 105 (2019), No. 6

Perspective toward Long-term Global Goal for Carbon Dioxide Mitigation in Steel Industry

Tatsuro Ariyama

pp. 567-586

DOI:

10.2355/tetsutohagane.TETSU-2019-008

Abstract

Global warming has been regarded as a crucial issue in every industry. Since long term global goal was set on the basis of Paris Agreement, a considerable evolution toward CO2 mitigation in 2050 is desired even in steel industry. Until now, many various technology developments were carried out in the ironmaking area; however, the innovative progress beyond the past progressive developments is required to attain the long-term goal in 2050. This review focuses on the current technology development on CO2 mitigation to date and the design of an ambitious ironmaking process for the future. In particular, the directions for low carbon and decarbonization are discussed from the viewpoints of technological aspects and the comprehensive consistency with sustainability in steel industry. Moreover, the perspectives on CCU (CO2 Capture and Utilization) and hydrogen ironmaking process based on the renewable energy aiming for carbon direct avoidance are described.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Perspective toward Long-term Global Goal for Carbon Dioxide Mitigation in Steel Industry

twitter
facebook
mendeley

Bibtex

Ris

Activities of FexO in Molten Slags Coexisting with Solid CaO and Ca2SiO4-Ca3P2O8 Solid Solution

Kohei Miwa, Ryota Matsugi, Masakatsu Hasegawa

pp. 587-594

DOI:

10.2355/tetsutohagane.TETSU-2018-159

Abstract

In steelmaking processes, there are incentives to reduce slag volume and CaO consumption. The key to meet these requirements is the better understanding of CaO dissolution mechanism into molten slag, which relies on the knowledge of the thermochemical properties of slags and fluxes used for dephosphorization. In this study, the liquidus compositions coexisted with solid CaO and Ca2SiO4-Ca3P2O8 solid solution simultaneously were determined in the quaternary system CaO-SiO2-P2O5-FexO at 1573 K. Measurements were also conducted on the FexO activities at temperatures between 1542 K and 1604 K by virtue of an electrochemical technique. By using the present experimental results, phosphorus distribution ratios were estimated.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Activities of FexO in Molten Slags Coexisting with Solid CaO and Ca2SiO4-Ca3P2O8 Solid Solution

twitter
facebook
mendeley

Bibtex

Ris

Experimental Evaluation of Interfacial Free Energies of Solid Iron

Masahito Hanao

pp. 595-600

DOI:

10.2355/tetsutohagane.TETSU-2018-163

Abstract

Interfacial free energy of solid iron was experimentally evaluated for solid/liquid interface and grain boundary of austenite phase in solid Fe/liquid FeO-SiO2 system. Multi-phase equilibrium method was adopted and two kinds of angles such as dihedral angle between solid/liquid interface and grain boundary, and contact angle of sessile drop of molten oxide on solid iron were measured. On the basis of experimental results and literature data of activity of FeO, surface tension of liquid FeO-SiO2 oxide and solid Fe, interfacial tension (interfacial free energy) of solid/liquid interface and grain boundary of γ-Fe were evaluated. Oxygen partial pressure in the experimental atmosphere was evaluated as 1×10–12~10–11 atm. Under this condition, solid/liquid interfacial free energy was evaluated as 1440-1500 mJ/m2 and grain boundary free energy of γ-Fe as 860-940 mJ/m2 at 1350ºC. The evaluated value for the grain boundary was agreed well with the data of previous works.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Experimental Evaluation of Interfacial Free Energies of Solid Iron

twitter
facebook
mendeley

Bibtex

Ris

Structural Analysis of Primary Coal Tar by FD-MS

Yuki Hata, Hideyuki Hayashizaki, Takafumi Takahashi, Koji Kanehashi

pp. 601-609

DOI:

10.2355/tetsutohagane.TETSU-2018-134

Abstract

Understanding chemical structure of primary coal tar is substantially important to promote advanced application and utilization of coal where chemical reaction plays a key role. Mass spectrometry allows us to characterize complex mixture like coal tar pitch, coal extractions, and heavy oil. In the present study, two kinds of primary coal tar A and B were prepared from different types of coal A (bituminous coal) and B (subbituminous coal). The main components such as Hexane Soluble (HS) and Hexane Insoluble-Toluene Soluble (HI-TS) fractions obtained by extraction of each tar were measured by Field Desorption Mass Spectrometry (FD-MS) to determine their constituent chemical structures. 1H NMR spectra of HS and HI-TS were measured to confirm the reliability of proportion of hydrogen types that have been determined by FD-MS. As a result, both of the proportions in HS fractions were found to be almost consistent, while those in HI-TS fractions were not consistent because they have more complex chemical components than HS fractions. Based on the combined analysis of FD-MS and NMR, we concluded that the HS in primary coal tar A mainly consists of polycyclic aromatic hydrocarbons (PAHs) and aliphatic structures including aromatic carbons, while the HS in primary coal tar B mainly consists of aliphatic structures. These results suggest that determining chemical structures and their ratios only from FD-MS spectra is useful to concretely clarify difference between some types of primary coal tar.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Structural Analysis of Primary Coal Tar by FD-MS

twitter
facebook
mendeley

Bibtex

Ris

Effect of Lime Dissolution Rate in Slag on Hot Metal Dephosphorization

Naoki Kikuchi, Akitoshi Matsui, Yu-ichi Uchida

pp. 610-618

DOI:

10.2355/tetsutohagane.TETSU-2018-157

Abstract

In order to clarify the effect of the lime dissolution rate in slag on hot metal dephosphorization, a 150 kg scale hot metal dephosphorization experiment was carried out. The rate of decrease of free CaO and the dephosphorization rate were measured while varying the ratio of the CaO and SiO2 which was denoted as basicity.The dephosphorization rate showed its maximum value at basicity of around 1.0. At basicity higher than 1.0, the dephosphorization rate decreased due to poor dissolution of CaO in the flux.A thermodynamic calculation revealed that crystallization of 2CaO·SiO2 (-3CaO·P2O5) in the liquid slag deteriorated lime dissolution when basicity was higher than 1.5.The mass transfer coefficient of CaO in slag was calculated assuming that the interface between the lime and liquid slag is saturated with CaO. High basicity showed a low mass transfer coefficient.The apparent slag viscosity was calculated in terms of the solid phase, and correlated with the CaO diffusion rate. The CaO diffusion rate in slag decreased with higher values of not only liquid slag viscosity, but also solid-liquid coexistent slag viscosity. These results suggest the existence of an optimum basicity exists for effective CaO dissolution.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Effect of Lime Dissolution Rate in Slag on Hot Metal Dephosphorization

twitter
facebook
mendeley

Bibtex

Ris

Fatigue Strength Improvement by Replacing Welded Joints with Ductile Cast Iron Joints

Tetsuro Hidaka, Nao-Aki Noda, Yoshikazu Sano, Nobuhiro Kai, Hiroyoshi Fujimoto

pp. 619-628

DOI:

10.2355/tetsutohagane.TETSU-2018-158

Abstract

In this study fatigue experiments are conducted for ductile cast iron (DCI) to compare with the fatigue strength of cruciform welded joints. Here, several DCI specimens are prepared to have nearly the same fatigue strength in smooth specimens before welding and to have similar cruciform shapes in the welded joints. It is found that the fatigue strength of DCI specimen is about three times larger than that of the welded joint specimens. The fatigue strength improvement can be explained in terms of the small stress concentration factor, notch insensitivity and compressive residual stress generated by shot blasting for DCI joints.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Fatigue Strength Improvement by Replacing Welded Joints with Ductile Cast Iron Joints

twitter
facebook
mendeley

Bibtex

Ris

Improvement of Rigidity of Super Invar Cast Steel via Austenite Recrystallization Induced by Martensitic Reversion

Naoki Sakaguchi, Kotaro Ona, Rui Bao, Nobuo Nakada

pp. 629-635

DOI:

10.2355/tetsutohagane.TETSU-2019-001

Abstract

Super invar cast steel, 32 mass%Ni-5 mass%Co, with an excellent low thermal expansion coefficient exhibits very low Young’s modulus due to a course solidified columnar structure with <100> austenite texture. For the improvement of the low Young’s modulus, a novel heat treatment consisted of subzero treatment and subsequent annealing was applied to stimulate microstructure evolution accompanied with texture variation. Lenticular martensite preferentially formed along a dendrite structure with lower Ni concentration after subzero treatment at liquid nitrogen temperature and then reversed into austenite again by the subsequent annealing above 873 K via diffusionless shear mechanism, that is, martensitic reversion took place. Since the martensitic reversion realizes a crystallographic reversibility, the course columnar structure at initial state was reconstructed after the completion of reversion. Furthermore, the course structure formed via martensitic reversion recrystallized to equiaxed fine-grained structure when the annealing temperature became higher, because high density dislocations in martensitic reversed austenite caused by the invariant lattice deformation on two directional martensitic transformations drives the austenite recrystallization. The recrystallization leads to the formation of fine-grained austenitic structure with random orientation, and as a result, Young’s modulus of super invar cast steel was improved to be as high as the forged one without any plastic deformation process.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Improvement of Rigidity of Super Invar Cast Steel via Austenite Recrystallization Induced by Martensitic Reversion

twitter
facebook
mendeley

Bibtex

Ris

Competition between Fatigue Crack Growth and Wear under Rolling – Sliding Contact Condition

Makoto Akama, Mamoru Murahashi

pp. 636-647

DOI:

10.2355/tetsutohagane.TETSU-2018-138

Abstract

A numerical model was developed to simulate the competition between crack initiation and growth by rolling contact fatigue (RCF) and wear in a railhead. The simulation model assumes that the materials are polycrystalline ferrite and pearlite and that RCF crack initiation is determined by the total accumulated plastic shear strain. The growth of short cracks is calculated using the Hobson model and the Archard model is used to calculate wear. In order to validate the developed model, twin disc rolling-sliding contact fatigue tests were performed. In the tests, rail material and slip ratio were changed and the crack initiation, crack growth and wear trace on the contact surfaces were investigated by SEM, EPMA and shape measuring instrument. Under these test conditions, simulations were performed using the developed model and compared the results. It was confirmed that the crack occurred at the nonmetallic inclusion/ferrite and ferrite/pearlite boundary at almost the same locations, therefore, the assumption of the model for the initiation was validated. It was also found that cracks of almost the same length and the direction existed in the vicinity of the contact surface at the same rolling cycles. Regarding wear, it was found that accurate analyses can be performed by considering the change of the contact pressure distribution and selecting an appropriate wear coefficient.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Competition between Fatigue Crack Growth and Wear under Rolling – Sliding Contact Condition

twitter
facebook
mendeley

Bibtex

Ris

Correlation in the Parameters Obtained by Direct-Fitting Method and Modified Williamson-Hall Method for Cold Worked Iron

Setsuo Takaki, Takuro Masumura, Toshihiro Tsuchiyama

pp. 648-654

DOI:

10.2355/tetsutohagane.TETSU-2018-167

Abstract

In the dislocation characterization using radiation diffraction, the modified Williamson-Hall method gives the parameter α, φ and S, in which the information about crystallite size, dislocation density and screw component of dislocation are contained respectively. On the other hand, the direct-fitting method gives the parameter α, micro-strain ε and the correction parameter ωh00. In this study, the correlation in these parameters was investigated in cold rolled ferritic steel (Fe-0.0056%C). Results obtained are as follows: Almost same values were obtained for the parameter α in both methods. The value of parameter ε increases as the S-value becomes small even under the same dislocation density. At the constant S-value, however, linear relationship was found between ε and φ. Between the parameter S and ωh00, there is an identical relationship expressed by the equation; S=1.16+1.46ωh00–3.71ωh002 regardless of dislocation density. In addition, it was confirmed that there is no large effect of texture on the dislocation characterization by the direct-fitting method and the modified Williamson-Hall method.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Correlation in the Parameters Obtained by Direct-Fitting Method and Modified Williamson-Hall Method for Cold Worked Iron

twitter
facebook
mendeley

Bibtex

Ris

Effects of Drawn Strain and Aging Temperature on Critical Diffusible Hydrogen Content and Absorbed Hydrogen Content in Pearlitic Steel Wires

Tetsushi Chida, Makoto Kosaka, Manabu Kubota, Toshimi Tarui, Tomohiko Omura

pp. 655-663

DOI:

10.2355/tetsutohagane.TETSU-2019-002

Abstract

It is well-known that pearlitic steel wires have a higher resistance to hydrogen embrittlement than tempered martensitic steels. It is significant to clarify the effect of various mechanisms of the hardening on hydrogen embrittlement for the compatibility between high strength and resistance to hydrogen embrittlement. In this study, effects of drawing strain and aging temperature in pearlitic steel wires on hydrogen embrittlement properties were investigated. Absorbed hydrogen content after cyclic corrosion test (HE) was increased with added drawn strain and saturated with large amounts of drawn strain. Furthermore, the higher the aging temperature, the smaller HE is obtained. The critical diffusible hydrogen content (HC) in pearlitic steel wires aged at 450°C is higher than that aged at 250°C and as-drawn pearlitic steel wires. The reasons are considered to be a decrease in the dislocation density and suppression of crack propagation due to the short length of ferrite-cementite interface. Consequently, the pearlitic steel wires aged at 450°C are excellent in resistance to hydrogen embrittlement because HC is much higher than HE, although the tensile strength of pearlitic steel wires is decreased by aging at 450°C and above.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Effects of Drawn Strain and Aging Temperature on Critical Diffusible Hydrogen Content and Absorbed Hydrogen Content in Pearlitic Steel Wires

twitter
facebook
mendeley

Bibtex

Ris

Dissolution Behavior of Fe from CaO-SiO2-FeOx Glassy Phase

Shohei Koizumi, Gao Xu, Shigeru Ueda, Shin-ya Kitamura

pp. 664-673

DOI:

10.2355/tetsutohagane.TETSU-2018-120

Abstract

To recover the degraded paddy field, the efficient supply of Fe, Ca, and Si to the soil water is important. Steelmaking slag was confirmed as a useful fertilizer for paddy growth to supply Ca and Si. In addition, to suppress the H2S generation in paddy soil, supplement of Fe from fertilizer made of slag has been expected.By our previous research, it was found that Fe was supplied mainly from the CaO-SiO2-FeO glassy phase in slag. However, to design the fertilizer made of slag, the optimum composition of the glassy phase has to be clarified.In this research, the glassy phases with difference iron valence, basicity, and FeO content were synthesized to investigate the dissolution behavior of Fe in paddy water. The experiment was conducted by the addition of grounded power of the synthesized phase into water which kept pH at 5 by adding HNO3 to simulate the initial stage after irrigation of paddy fields. The dissolved amount of each element in water was analyzed by ICP-AES. The result showed that the dissolution ratio of Fe increased by increasing the ratio of Fe2+/T-Fe and the FeO content in the glassy oxides, and showed local maximum by the increase in CaO/SiO2 ratio at 0.67.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Dissolution Behavior of Fe from CaO-SiO2-FeOx Glassy Phase

twitter
facebook
mendeley

Bibtex

Ris

Article Access Ranking

27 Apr. (Last 30 Days)

You can use this feature after you logged into the site.
Please click the button below.

Advanced Search

Article Title

Author

Abstract

Journal Title

Year

Please enter the publication date
with Christian era
(4 digits).

Please enter your search criteria.