Numerical modelling on rate-limited dissolution mass transfer of entrapped petroleum hydrocarbons in a saturated sub-surface system

被引:0
|
作者
Vasudevan M. [1 ]
Suresh Kumar G. [2 ]
Nambi I.M. [1 ]
机构
[1] Environmental and Water Resources Engineering Division, Department of Civil Engineering, Indian Institute of Technology Madras, Chennai
[2] Petroleum Engineering Programme, Department of Ocean Engineering, Indian Institute of Technology Madras, Chennai
关键词
diffusion; dissolution; dual-domain; rate-limited mass transfer;
D O I
10.1080/09715010.2015.1043596
中图分类号
学科分类号
摘要
Petroleum hydrocarbons generally referred to as light non-aqueous phase liquid (LNAPL) entrapped within a saturated subsurface geological formation can result in longer duration of contamination due to mass transfer limitations associated with heterogeneity of the system. Considering a part of the total pore volume as immobile is significant in capturing the behaviour of extended tailing by solute breakthrough profiles. In this context, the present numerical model investigates dissolution characteristics of residual petroleum hydrocarbons (LNAPL) resulting from both mobile and immobile domains under varying conditions of rate-limited diffusive mass transfer, longitudinal dispersivity and mean mobile fluid velocity in a saturated groundwater system. The numerical results suggest that the influence of residual LNAPL saturation on dissolution mass transfer coefficient is critical in comparison with mobile flow velocity and dispersivity. In addition, the rate-limited effect becomes predominant with significant increase in advective velocity and reduction in residual LNAPL saturation for structured porous media. It is concluded from this study that the transport of dissolved contaminant is dominated by advection at the mobile pores, while the diffusive equilibrium at the immobile volume is significant in characterizing the extended tailing and subsequently determines the overall mass transfer resistance. © 2015 Indian Society for Hydraulics.
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页码:3 / 15
页数:12
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