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download pdf version of PhD book - Universiteit Utrecht

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pore-scale solute transport processes by accounting for limitations in mixing<br />

as a result <strong>of</strong> reduced water content. The numerically computed dispersivities<br />

could successfully explain the results obtained through experimental studies,<br />

and shows the underplaying pore scale processes contributing to dispersion under<br />

unsaturated conditions. Results <strong>of</strong> Chapter 6 show that, under partially<br />

saturated conditions, dispersivity coefficient is strongly depended on saturation.<br />

The relation could be non-monotonic, with the maximum dispersivity<br />

(α max ) corresponding to a specific saturation, which we refer to it as the critical<br />

saturation (S cr ). We could explain the α − S w relation by investigating<br />

pore-scale properties such as fraction <strong>of</strong> percolating saturated pores and coefficient<br />

<strong>of</strong> variation <strong>of</strong> pore velocities under different saturations. These pore<br />

scale observations could clearly explain the relation between solute dispersivity<br />

and saturation under partially saturated conditions. We have shown that<br />

saturation-relative permeability (k r − S w ) curve may be utilized to get insight<br />

into the behavior <strong>of</strong> α − S w curve and to approximate the critical saturation<br />

at which the maximum dispersivity (α max ) occurs.<br />

Chapter 7 is specified to transport <strong>of</strong> adsorptive solute under partially<br />

saturated conditions. Under partially saturated conditions, the system contains<br />

three phases: air, water, and solid. The principal interactions usually<br />

occur at the solid-water interfaces (SW) and air-water interfaces (AW), thus<br />

greatly influenced by water content. All <strong>of</strong> the modeling capabilities which<br />

were implemented through last chapters are also included in this chapter. In<br />

addition, we have formulated various types <strong>of</strong> adsorption such as i) two site<br />

(SW and AW interfaces) kinetic, ii) two site equilibrium, and iii) one site (SW<br />

or AW interfaces) kinetic and one site equilibrium. For the macro scale representation<br />

<strong>of</strong> equilibrium adsorptive transport, we have chosen two models:<br />

Advection-Dispersion Equation (ADE) with equilibrium adsorption term and<br />

Mobile-Immobile Model (MIM) which models the non-equilibrium transport.<br />

Comparing the results from analytical solutions <strong>of</strong> these two macro-scale models<br />

with the results obtained from pore network model show that the Mobile-<br />

Immobile Model (MIM) provides a better fit to the results <strong>of</strong> the pore network<br />

modeling. Applying equilibrium macro-scale model (ADE), we need to apply<br />

higher values <strong>of</strong> dispersivity which in addition to saturation will depend on<br />

the value <strong>of</strong> pore scale adsorption coefficient. However, using MIM we could<br />

use the dispersion coefficients which were independently determined through<br />

tracer simulations to simulate adsorptive transport. The results <strong>of</strong> this chapter<br />

show that, even if there is equilibrium adsorption at the solid-water (SW) and<br />

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