• The Effects of CO2 Released from Deep Geological Formations on the Dissolution Process of Galena in Shallow Subsurface Environments
  • Nam, Jieun;Wang, Sookyun;
  • Department of Energy Resources Engineering, Pukyong National University;Department of Energy Resources Engineering, Pukyong National University;
  • 지중저장 이산화탄소의 누출이 천부환경에서 방연석의 용해 과정에 미치는 영향
  • 남지은;왕수균;
  • 부경대학교 에너지자원공학과;부경대학교 에너지자원공학과;
Abstract
If $CO_2$ stored for geological sequestration escapes from deep formations and is introduced to shallow aquifers, it dissolves into groundwater, creates acidic environments, and enhance mineral dissolution from rocks and soils. Among these minerals, dissolution and spread of hazardous trace metals can cause environmental problems with detrimental impacts on groundwater quality. This study aims to investigate geochemical effects of $CO_2$ in groundwater on dissolution of galena, the main mineral controlling the mobility of lead. A series of batch experiments are performed with granulated galena in $CO_2$ solutions under various experimental conditions for $CO_2$ concentration and reaction temperature. Results show that dissolution of galena is significantly enhanced under acidic environments so that both of equilibrium concentrations and dissolution rates of lead increase. For thermodynamic analysis on galena dissolution, the apparent rate constants and the activation energy for galena dissolution are calculated by applying rate law to experimental results. The apparent rate constants are $6.71{\times}10^{-8}mol/l{\cdot}sec$ at $15^{\circ}C$, $1.77{\times}10^{-7}mol/l{\cdot}sec$ at $25^{\circ}C$, $3.97{\times}10^{-7}mol/l{\cdot}sec$ at $35^{\circ}C$ and the activation energy is 63.68 kJ/mol. The galena dissolution is suggested to be a chemically controlled surface reaction, and the rate determining step is the dissociation of Pb-S bond of surface complex.

Keywords: $CO_2$;Galena;Lead;Dissolution;Activation Energy;

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This Article

  • 2015; 20(1): 19-27

    Published on Feb 28, 2015

  • 10.7857/JSGE.2015.20.1.019
  • Received on Nov 25, 2014
  • Revised on Feb 25, 2015
  • Accepted on Feb 25, 2015