4.7 Article

Development of a cost-effective CO2 adsorbent from petroleum coke via KOH activation

Journal

APPLIED SURFACE SCIENCE
Volume 429, Issue -, Pages 62-71

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2017.08.075

Keywords

CO2 adsorption; Porous carbon; Petroleum coke; KOH activation; Narrow micropore

Funding

  1. Basic Science Research Program [2015R1A1A1A05001363]
  2. Super Ultra Low Energy and Emission Vehicle Engineering Research Center of the National Research Foundation of Korea (NRF) - Korean Government (Ministry of Science, ICT and Future Planning) [NRF-2016R1A5A1009592]

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The capture of CO2 via adsorption is considered an effective technology for decreasing global warming issues; hence, adsorbents for CO2 capture have been actively developed. Taking into account cost-effectiveness and environmental concerns, the development of CO2 adsorbents from waste materials is attracting considerable attention. In this study, petroleum coke (PC), which is the carbon residue remaining after heavy oil upgrading, was used to produce high-value-added porous carbon for CO2 capture. Porous carbon materials were prepared by KOH activation using different weight ratios of KOH/PC (1:1, 2:1, 3:1, and 4:1) and activation temperatures (600, 700, and 800 degrees C). The specific surface area and total pore volume of resulting porous carbon materials increased with KOH amount, reaching up to 2433 m(2)/g and 1.11 cm(3)/g, respectively. The sample prepared under moderate conditions with a KOH/PC weight ratio of 2:1 and activation temperature of 700 degrees C exhibited the highest CO2 adsorption uptake of 3.68 mmol/g at 25 degrees C and 1 bar. Interestingly, CO2 adsorption uptake was linearly correlated with the volume of micropores less than 0.8 nm, indicating that narrow micropore volume is crucial for CO2 adsorption. The prepared porous carbon materials also exhibited good selectivity for CO2 over N-2, rapid adsorption, facile regeneration, and stable adsorption-desorption cyclic performance, demonstrating potential as a candidate for CO2 capture. (C) 2017 Elsevier B.V. All rights reserved.

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