logo
Language
Bookmarks
Log Out

Journals

Search Sites

Account

© 2022 Steel Science Portal

How to use

Advanced Search

Search Sites

site
site
site
site

Journal of the Japan Institute of Energy Vol. 83 (2004), No. 2

ISIJ International
belloff
ONLINE ISSN: 1882-6121
PRINT ISSN: 0916-8753
Publisher: The Japan Institute of Energy

Backnumber

  1. Vol. 103 (2024)

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

  2. Vol. 102 (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. 101 (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. 100 (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. 99 (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. 98 (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. 97 (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. 96 (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. 95 (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. 94 (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. 93 (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. 92 (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. 91 (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. 90 (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. 89 (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. 88 (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. 87 (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. 86 (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. 85 (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. 84 (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. 83 (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. 82 (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. 81 (2002)

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

  24. Vol. 80 (2001)

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

  25. Vol. 79 (2000)

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

  26. Vol. 78 (1999)

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

  27. Vol. 77 (1998)

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

  28. Vol. 76 (1997)

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

  29. Vol. 75 (1996)

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

  30. Vol. 74 (1995)

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

  31. Vol. 73 (1994)

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

  32. Vol. 72 (1993)

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

  33. Vol. 71 (1992)

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

Keyword Ranking

21 Nov. (Last 30 Days)

Journal of the Japan Institute of Energy Vol. 83 (2004), No. 2

Active Carbon Supported Rhodium Catalyst in the Hydroformylation of 1-Hexene

Baitao LI, Xiaohong LI, Kenji ASAMI, Kaoru F UJIMOTO

pp. 130-136

DOI:

10.3775/jie.83.130

Abstract

Hydroformylation performance of 1-hexene over rhodium solid catalyst was studied under mild reac-tion condition (H2/CO=1/1, Pressure=3.0MPa, T=403K). Its hydroformylation activities were examined systematically in various solvents. Effects of operating variables on the CO conversion, yields of products and stability of the catalysts also have been discussed in detail. It was found that the rhodium catalyst exhibited the excellent activity in the n-octane solvent, while poor activity in the alcoholic and H2O solvent. Rh/active carbon (Rh/C) catalyst presented superior catalytic performances over Rh/SiO2 catalyst in the activity, selectivity and stability. As the most important, Rh/C catalyst showed stable activity in the continuous (olefin and synthesis gas) feeding system even in the low metal loading, giving the total turn over number (TON) of 500 during 14 hs reaction.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Active Carbon Supported Rhodium Catalyst in the Hydroformylation of 1-Hexene

twitter
facebook
mendeley

Bibtex

Ris

Chlorine Behavior During Low-Temperature Pyrolysis Process at the First Stage of the Two-Stage Fluidized-Bed Waste Incinerator

Hidetoshi YAMAMOTO, Masamichi ASANO, Tatsuya IKEDA, Tomomasa TAGUCHI, Takao HARA

pp. 137-148

DOI:

10.3775/jie.83.137

Abstract

The aim of this study is to research the mechanism of dechlorination for low-temperature pyrolysis process not only by establishing the material and calorific balance at the first stage of the two-stage fluid-ized-bed waste incinerator but also by revealing the behavior of chlorine towards products formed in the pyrolysis. The pyrolysis experiments have been performed using wood chips containing poly (vinyl chloride) in a 5: 1 weight ratio as a model refuse-feed. The feed is pyrolyzed with and without catalyst (disposable iron sulfide catalyst), as well as under the presence of low oxygen concentration (5.7vol%) at 360-420°C. The acidic and acid-free fractions separated by the treatment with an anion exchange resin from tar component are characterized by means of spectroscopic techniques (FT-i.r., 1H-NMR and 13C-NMR) and ultimate analysis, comparing to those from tar components formed by the pyrolysis of six different kinds of hydrocarbons and poly (vinyl chloride).
The results show that; (1) Calorific value of char retains more than 40% of the starting feed, which exceeds the process target for calorific balance between the first and second stage of the total incineration process.(2) More than 95% of chlorine involved in the feed is removed during pyrolysis and the dechlori-nated char component (Cl content: 0.4-0.8wt%) could be transferred into the second stage for the total system.(3) The presence of the catalyst in the pyrolysis plays an important role in the reduction of chlorophenols formed in the low-temperature pyrolysis process.

Readers Who Read This Article Also Read

mendeley

Bookmark

Detail

PDF Download

Share it with SNS

Article Title

Chlorine Behavior During Low-Temperature Pyrolysis Process at the First Stage of the Two-Stage Fluidized-Bed Waste Incinerator

twitter
facebook
mendeley

Bibtex

Ris

Article Access Ranking

21 Nov. (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.