Jump to main content
Jump to site search

Issue 16, 2017, Issue in Progress
Previous Article Next Article

Performance assessment of activated carbon supported catalyst during catalytic wet oxidation of simulated pulping effluents generated from wood and bagasse based pulp and paper mills

Author affiliations

Abstract

In the present study, the performance of catalytic wet oxidation (CWO) was investigated for the treatment of two simulated pulping effluents (with chemical oxygen demand (COD) = 15 000 and 17 000 mg L−1, respectively) from large and small scale pulp and paper mills. CWO was performed in a 0.7 L capacity high pressure reactor at 190 °C temperature and 0.9 MPa oxygen partial pressure for 3 h duration with activated carbon (AC) supported Cu–Ce catalyst. More than 70% reduction in chemical oxygen demand (COD) and 90% color removal from the wastewaters were achieved during CWO. The biodegradability ratio of wastewater samples was improved to 0.52 from the initial values of 0.26 and 0.31, respectively. The conversion of lignin after CWO was confirmed by nuclear magnetic resonance analysis. Homo-catalytic oxidation equally contributed to organics degradation during the hetero-catalytic reaction. The detailed results on metal leaching, hydrothermal treatment without oxygen and catalyst reuse are also presented.

Graphical abstract: Performance assessment of activated carbon supported catalyst during catalytic wet oxidation of simulated pulping effluents generated from wood and bagasse based pulp and paper mills

Back to tab navigation

Publication details

The article was received on 23 Oct 2016, accepted on 17 Jan 2017 and first published on 03 Feb 2017


Article type: Paper
DOI: 10.1039/C6RA25695C
Citation: RSC Adv., 2017,7, 9754-9763
  • Open access: Creative Commons BY license
  •   Request permissions

    Performance assessment of activated carbon supported catalyst during catalytic wet oxidation of simulated pulping effluents generated from wood and bagasse based pulp and paper mills

    B. R. Yadav and A. Garg, RSC Adv., 2017, 7, 9754
    DOI: 10.1039/C6RA25695C

    This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. Material from this article can be used in other publications provided that the correct acknowledgement is given with the reproduced material.

    Reproduced material should be attributed as follows:

    • For reproduction of material from NJC:
      [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the Centre National de la Recherche Scientifique (CNRS) and the RSC.
    • For reproduction of material from PCCP:
      [Original citation] - Published by the PCCP Owner Societies.
    • For reproduction of material from PPS:
      [Original citation] - Published by The Royal Society of Chemistry (RSC) on behalf of the European Society for Photobiology, the European Photochemistry Association, and RSC.
    • For reproduction of material from all other RSC journals:
      [Original citation] - Published by The Royal Society of Chemistry.

    Information about reproducing material from RSC articles with different licences is available on our Permission Requests page.

Search articles by author

Spotlight

Advertisements