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Prediction of colloid detachment in a model porous media: Thermodynamics
Author(s) -
Bergendahl John,
Grasso Domenico
Publication year - 1999
Publication title -
aiche journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.958
H-Index - 167
eISSN - 1547-5905
pISSN - 0001-1541
DOI - 10.1002/aic.690450305
Subject(s) - dlvo theory , colloid , polystyrene , porous medium , ionic strength , porosity , chemical engineering , chemistry , ionic bonding , homogeneous , thermodynamics , chromatography , materials science , aqueous solution , polymer , organic chemistry , physics , ion , engineering
Detachment of polystyrene latex colloids was studied in a model porous media system comprised of a packed column of glass beads. The polystyrene colloids were attached and subsequently detached from the glass beads by varying solution pH and ionic strength. It was found that classical‐DLVO theory could not predict detaching conditions. Extended‐DLVO theory was used to determine the median detaching pH for deionized water, and solutions of 0.01 and 0.1 M NaCl. Although both the colloids and porous media were macroscopically homogeneous, detachment was observed at a variety of pH values. The pH distribution of detachment and the energy distribution of the interaction between the polystyrene latex colloids and the glass beads followed gamma distributions. This work has provided a technique to quantitatively predict the aqueous chemistry changes that induce colloid detachment in porous media.