Enlargement process: smaller particles are put together to form larger masses but the original particles can still be identified. Example of applications: pharmaceutical formulation - defined active ingredient, catalyst support - control surface to volume ratio. Bonding due to moisture moisture retention in powder = f(nature of the solids, ambient humidity, temperature, pressure)
Enlargement process: smaller particles are put together to form larger masses but the original particles can still be identified. Example of applications: pharmaceutical formulation - defined active ingredient, catalyst support - control surface to volume ratio. Bonding due to moisture moisture retention in powder = f(nature of the solids, ambient humidity, temperature, pressure)
Enlargement process: smaller particles are put together to form larger masses but the original particles can still be identified. Example of applications: pharmaceutical formulation - defined active ingredient, catalyst support - control surface to volume ratio. Bonding due to moisture moisture retention in powder = f(nature of the solids, ambient humidity, temperature, pressure)
enlargement process (granulation, agglomeration, tabletting), fine particle processes (fluidization, particle transport).
Size enlargement process: smaller particles are put
together to form larger masses but the original particles can still be identified.
Why increase the mean size: to reduce dust hazard,
reduce caking and lumping formation, improve flow properties etc.
Example of applications: pharmaceutical formulation
defined active ingredient, catalyst support control surface to volume ratio.
4.2 Interparticle bonding.
The most important forces causing the structuring of a
mixture are: o due to moisture o due to electrostatic charge o due to Van der Waal forces
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4.2.1 Bonding due to moisture
Moisture retention in powder = f(nature of the solids,
ambient humidity, temperature, pressure)
Moisture will be present as :
(i) adsorbed vapour if the humidity is below a critical value (ii) liquid bridges for higher humidities.
The binding force = f(actual humidity) for both cases.
4.2.1.1
Adsorbed layer bonding
The bonding is caused by the overlapping of the
adsorbed layers of neighbouring particles and its strength is proportional to tensile strength of the adsorbed film and the area of contact.
In a simple case of two dissimilar spheres, the contact
area and the bond strength can be calculated. y
R2
R1
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y m
S = 4 R2
2 m + 1
Boding surface between a flat surface and a sphere
would be twice as large as that between two equi-sized spheres.
Important variable of bonding: particle shape and surface
roughness.
In most cases, the surfaces of the contacting particles
will not be perfectly smooth and surface roughness will reduce the area of contact and hence the bond strength.
4.2.1.2
Liquid bridge bonding
When the relative humidity reaches a critical point, liquid
bridges form between particles and this is a nature of cohesive particles.
A liquid bridge will only be stable if its tendency to
evaporate equals the tendency of water vapour to condense on it.
As humidity increases, the area of particle surface
covered by the bridge increases and the independence of neighbouring liquid bridges becomes a function of porosity and of absolute particle size.
4.2.2 Electrostatic bonding
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Two solids in rubbing contact will charge each other
electrostatically.
Electrons are transferred until at equilibrium, a contact
potential difference is established.
Depending on the sign of the charge particles will tend to
bond to the mixer wall or to other dissimilar particles.
Generally, electrostatic effects are unwelcome as they
are not only unpredictable but they could give the potential for a dangerous electrostatic charge.
4.2.3 Van der Waal force bonding
Attractive forces exist between neutral atoms or
molecules which are separated by a distance which is large compared to their own dimension.
These force known as Van der Waal forces and they
decrease with the distance apart according to a power law.
The extension of Van der Waals theory of attractive force
for bulk powder was carried out by Lifshitz (1955)
Particles do not have to touch in order that attraction
occurs but it can be seen from equation 4.1 and 4.2 that the magnitude of the force decreases with the square of the distance between the surfaces. 64
For attraction force between flat surface and a sphere,
Fvdw
hw = R 2 8Z o
(4.1)
Equation (4.1) was then modified for the attraction force
two sphericals:
Fvdw
hw = 8Z o2
R1 R2
R1 + R2
(4.2)
where hw = Lifshitz VDW constant
Zo = distance between two solids R = radius of sphere
4.3
The range of attraction is smaller than for electrostatic
bonding and for a similar packing density, the effective area of contact will also be smaller. Interaction of the bonding forces In powder mixing, the humidity of the atmosphere plays a crucial role in determining the relative importance of the forces.
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Adsorbed and liquid bridge bonding forces can dominate
other possible bonding forces and also influence their magnitude.
On theoretical basis, Rumpf (1962) plotted the
theoretical tensile strength of agglomerates as a function of particle size (Fig. 11.2 pg 271 from handout).
The effect of adsorbed moisture on the Van der Waals
forces is to increase their value as the adsorbed layers may be considered as part of particle and a decrease in the interparticulate distance will occur.
Rumpf suggests that the effect of such adsorbed layers
can increase the contribution of Van der Waals forces to the cohesive strength of bulk powders by a factor of 100.
Electrostatic forces will decay rapidly as humidity causes
air to be more conductive and therefore favour discharge from the particles.
Adsorbed moisture also reduces the magnitude of
mechanical forces such as friction and interlocking, as the adsorbed film act as lubricant, decrease friction and reduces the chances of stable interlocking.
As the particle size of fine component decreases to the
sub-micron range, the relative importance of the bonding forces will change again.