Colloids and Surfaces A: Physicochem. Eng. Aspects 298 (2007) 34–41
The effect of mixing on stability and break-up of aggregates
formed from aluminum sulfate hydrolysis products
Irina Solomentseva
a,∗
, S´ andor B´ ar´ any
b
, John Gregory
c
a
Institute of Colloid and Water Chemistry, 42 Vernadsky Blvd., 03680 Kiev, Ukraine
b
Institute of Chemistry, University of Miskolc, 3515 Miskolc-Egyetemvaros, Hungary
c
Department of Civil and Environmental Engineering, University College London, Gower Street, London WC1E 6BT, UK
Available online 15 December 2006
Abstract
The structure of aggregates formed from aluminum sulfate hydrolysis product particles (HPP), their stability, break-up and re-growth, under the
action of shear (stirring the dispersion at different rates) have been studied. The effect of main variables such as the hydrolyzing salt dose, pH,
alkalinity and ionic strength of the water on the growth, breakage and re-growth of HPP aggregates has been investigated. It has been shown that the
aluminum sulfate hydrolysis product particles formed in a model water with parameters that facilitate appearance of small particles with relatively
high charge and -potential values, low degree of hydration and interaction of particles predominantly in the primary minimum, are stronger and
more easily reformed after their breakage by intense stirring, than aggregates built of particles with lower charge, higher initial particle size and
hydration, aggregating in the secondary minimum.
© 2006 Elsevier B.V. All rights reserved.
Keywords: Aluminum sulfate; Hydrolysis products; Aggregates; Stability; Break-up; Re-growth; Shear; Salt dose; pH; Alkalinity; Ionic strength
1. Introduction
Aggregation of dispersed particles plays a key role dur-
ing phase separation processes, in particular in the course of
water conditioning and treatment [1]. Typically, these processes
are initiated or enhanced by adding hydrolyzing salts or high-
molecular polymeric flocculants to dispersion or water to be
treated. Depending on the balance of main variables operating in
the system, the size of aggregates formed, their packing density
as well as the changes of these parameters during the aggregation
process can be varied in a broad interval [2–4].
There is special interest concerning the laws and kinetics of
aggregate formation from the aluminum salts hydrolysis prod-
uct particles (HPP) widely used in water treatment [4–8]. It
has been shown that the HPP aggregation occurs in a step-
wise manner and the “discreteness” of the process increases in
series: basic aluminum chloride (BAC) > basic aluminum sulfate
(BAS) > aluminum sulfate (AS). The course of these processes
as well as the size and density of aggregates depend not only on
the coagulant nature but also on the system variables like pH,
∗
Corresponding author.
E-mail address: irinasol@i.com.ua (I. Solomentseva).
ionic strength and alkalinity. By changing these parameters, the
colloid-chemical properties of the hydrolysis product primary
particles, the size and density of aggregates formed and their
strength, can be regulated.
Recently several papers have been published on the problem
of breakage and re-growth of aggregates formed under the action
of coagulants or polymeric flocculants [9–13]. Different ideas
about the mechanisms of these processes have been proposed
but without satisfactory experimental confirmation.
Mixing conditions can have a very significant effect on the
performance of coagulants and flocculants. The first require-
ment is for the additive to be distributed uniformly throughout
the suspension and this should be achieved by some form of
rapid mixing. The particles then need to collide in order to form
aggregates and this process can be assisted by some form of
agitation.
With hydrolyzing metal salts, the formation of hydrolysis
products occurs very rapidly and competing processes, such as
adsorption and precipitation, could depend on mixing conditions
[1]. After coagulant dosing and mixing, flocs grow initially at
a rate that is determined mainly by the applied shear, the parti-
cle concentration and the collision efficiency. As flocs become
larger, further growth is restricted by the applied shear for essen-
tially two reasons. Existing flocs may be broken as a result of
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doi:10.1016/j.colsurfa.2006.12.016