Correlation equations for average deposition rate coefficients of nanoparticles in a cylindrical pore

Seetha, N and Hassanizadeh, Majid S and Kumar, Mohan MS and Raoof, Amir (2015) Correlation equations for average deposition rate coefficients of nanoparticles in a cylindrical pore. In: WATER RESOURCES RESEARCH, 51 (10). pp. 8034-8059.

PDF Wat_Res_Res_51-10_8034_2015.pdf - Published Version Restricted to Registered users only Download (1MB) | Request a copy

Abstract

Nanoparticle deposition behavior observed at the Darcy scale represents an average of the processes occurring at the pore scale. Hence, the effect of various pore-scale parameters on nanoparticle deposition can be understood by studying nanoparticle transport at pore scale and upscaling the results to the Darcy scale. In this work, correlation equations for the deposition rate coefficients of nanoparticles in a cylindrical pore are developed as a function of nine pore-scale parameters: the pore radius, nanoparticle radius, mean flow velocity, solution ionic strength, viscosity, temperature, solution dielectric constant, and nanoparticle and collector surface potentials. Based on dominant processes, the pore space is divided into three different regions, namely, bulk, diffusion, and potential regions. Advection-diffusion equations for nanoparticle transport are prescribed for the bulk and diffusion regions, while the interaction between the diffusion and potential regions is included as a boundary condition. This interaction is modeled as a first-order reversible kinetic adsorption. The expressions for the mass transfer rate coefficients between the diffusion and the potential regions are derived in terms of the interaction energy profile. Among other effects, we account for nanoparticle-collector interaction forces on nanoparticle deposition. The resulting equations are solved numerically for a range of values of pore-scale parameters. The nanoparticle concentration profile obtained for the cylindrical pore is averaged over a moving averaging volume within the pore in order to get the 1-D concentration field. The latter is fitted to the 1-D advection-dispersion equation with an equilibrium or kinetic adsorption model to determine the values of the average deposition rate coefficients. In this study, pore-scale simulations are performed for three values of Peclet number, Pe = 0.05, 5, and 50. We find that under unfavorable conditions, the nanoparticle deposition at pore scale is best described by an equilibrium model at low Peclet numbers (Pe = 0.05) and by a kinetic model at high Peclet numbers (Pe = 50). But, at an intermediate Pe (e.g., near Pe = 5), both equilibrium and kinetic models fit the 1-D concentration field. Correlation equations for the pore-averaged nanoparticle deposition rate coefficients under unfavorable conditions are derived by performing a multiple-linear regression analysis between the estimated deposition rate coefficients for a single pore and various pore-scale parameters. The correlation equations, which follow a power law relation with nine pore-scale parameters, are found to be consistent with the column-scale and pore-scale experimental results, and qualitatively agree with the colloid filtration theory. These equations can be incorporated into pore network models to study the effect of pore-scale parameters on nanoparticle deposition at larger length scales such as Darcy scale.

Item Type:	Journal Article
Publication:	WATER RESOURCES RESEARCH
Publisher:	AMER GEOPHYSICAL UNION
Additional Information:	Copy right for this article belongs to the AMER GEOPHYSICAL UNION, 2000 FLORIDA AVE NW, WASHINGTON, DC 20009 USA
Department/Centre:	Division of Mechanical Sciences > Civil Engineering
Date Deposited:	18 Feb 2016 05:21
Last Modified:	18 Feb 2016 05:21
URI:	http://eprints.iisc.ac.in/id/eprint/53290

Actions (login required)

View Item