Page 249 - Introduction to Colloid and Surface Chemistry

238 Colloid stability
effect. However, it is likely that this mechanism is not significant
in practice.
3. The adsorbed layers between the particles may interpenetrate and
so give a local increase in the concentration of polymer segments.
Depending on the balance between polymer-polymer and polymer-
dispersion medium interactions, this may lead to either repulsion
or attraction by an osmotic mechanism. Enthalpic and entropic
changes will be involved. If interpenetration takes place to a
significant extent, elastic repulsion will also operate.

Steric stabilisers are usually block copolymer molecules (e.g. poly
(ethylene oxide) surfactants), with a lyophobic part (the 'anchor'
group) which attaches strongly to the particle surface, and a lyophilic
chain which trails freely in the dispersion medium. The conditions for
stabilisation are similar to those for polymer solubility outlined in the
previous section. If the dispersion medium is a good solvent for the
lyophilic moieties of the adsorbed polymer, interpenetration is not
favoured and interparticle repulsion results; but if, on the other hand,
the dispersion medium is a poor solvent, interpenetration of the
polymer chains is favoured and attraction results. In the latter case,
the polymer chains will interpenetrate to the point where further
interpenetration is prevented by elastic repulsion.
The free energy change which takes place when polymer chains
interpenetrate is influenced by factors such as temperature, pressure
and solvent composition. The point at which this free energy change
is equal to zero is known as the 0 (theta)-point and such a solvent is
called a 0-solvent. More formally, a 0-point is defined as one where
the second virial coefficient of the polymer chains is equal to zero. It
can be determined by light scattering and by osmometry.
The positive AG for polymer chain interpenetration which leads to
steric stabilisation is given in terms of the corresponding enthalpy and
entropy changes by AG = AH - TAS, and therefore, stabilisation
could be the result of a positive A// and/or a negative AS. A positive
AH would reflect the release of bound solvent from the polymer
chains as they interpenetrate and a negative AS would reflect loss of
configurational freedom as the polymer chains interpenetrate. If AH
is positive and AS negative, the dispersion will be sterically stabilised
at all accessible temperatures; however, if AH and AS are both
positive, the dispersion should flocculate on heating above the 6-
temperature (enthalpic stabilisation), whereas if AH and AS are both