Crystallization SB
Crystallization SB
Crystallization SB
Crystallization
It is the spontaneous arrangement of
particles into a repeatitave orderly
array.
In regular geometric patterns.
Applications
Purification
Change micromeritics
Better chemical stability (Amorphous
penicillin G is more stable than
crystalline)
Improved physical stability
Improved bioavailability
Crystal Lattice
Crystal can be defined as solid
particle which is formed by
solidification processes (under
suitable environment)
During this proceses structural units
are arranged by fixed geometric
pattern.
It is orderly internal arrangement of
particles in 3 Dimentional space.
contd...
Units are ions, atoms or molecules.
Units are bond by covalent bond
(dimond) or Van der Walls forces
(Naphthalene)
Smallest geometric portion which
repeat to built up whole structure is a
unit cell.
Crystal bonded by plane surfaces
calles faces.
Contd...
Angle between the perpendicular to
faces is called axial angle.
Distance between centers of two
atom axial length.
Structural units arrangement is
determined by X ray diffraction (XRD)
Crystal form
Cubic
Hexagonal
tetragonal
Orthorhombic
monoclinic
Crystal Habit
Crystal is a polyhedral solid with
number of planer surface.
Angle between given pair of face is
same in all specimens.
It is characterstics irrespective of size.
Size and shape depend on medium
using which crystallization is carried
out.
Ex. Plate, Tubular, Columnar,
Acicular...
Crystal Habit
Columnar
Plate
Columnar
Acicular
Steps of Crystallization
Steps
1.Supersaturation
2.Nucleation
3.Crystal Growth
1.Super saturation
The termsuper saturationrefers to
asolutionthat contains more of the
dissolved material than could be dissolved
by thesolvent under normal
circumstances.
Super saturation can be achieved by
adding more of a substance (to a solution)
than can normally be dissolved. This is a
thermodynamically unstable state
2.Nucleation
Nucleationis the process of forming a
Types of Nucleation
Formation of stable nucleus depends
on number of units (cluster)
assemble together
Spurious nucleation (gives poor
qualitycrystals)
Primary nucleation
Secondary nucleation.
Homogeneous and
hydrogenous nucleation
Nucleation normally occurs atnucleation
siteson surfaces contacting the liquid or vapor.
Suspended particles or minute bubbles also
provide nucleation sites.
This is calledheterogeneous nucleation.
Nucleation without preferential nucleation sites
ishomogeneous nucleation.
Homogeneous nucleation occurs spontaneously
and randomly, but it requiressuperheating or
supercooling of the medium
3.Crystal Growth
Growth & nucleation are competing
processes!
Crystal growth is a diffusion process;
solute molecules reach the growing
surface by diffusion through the liquid
phase and are organized into space
lattice.
Growth rate of most crystals is linear
with super saturation.
Crystal growth
The rate of deposition is proportional to
driving force between
the bulk of the liquor and
wetting the surface of the crystal that is approximately
saturated with respect to crystals of that size.
Oswald Ripening
Oswald Ripening
Solubility of large crystal is less than
that of smaller crystals
It is because of significant surface
energy per unit mass on smaller
crystals.
Smaller crystals are in a state of
unstable equilibrium in a
supersaturated solution.
As a result larger crystals grow until
the small crystals disappear.
Ostwald Ripening
Larger crystals are more stable than smaller
crystals the energy of a system will naturally
trend towards the formation of larger crystals
at the expense of smaller ones
Theory of Crystallization
Miers theory
It is related to Supersaturation.
It postulate definate relation between
concentration and temperature at
which crystal will spontaneously form
in an unseeded solution.
Supersolubility curve represent the
limit at which nucleus formation
begins spontaneously in absence of
any solid particle (seed)
Solubility curve
When equilibrium is attained at final
temperature,mother liquor becomes
saturated in crystallization process
Rate of formation of nucleus is balanced
by the rate of dissolution of nucleus
The equilibrium relationship is the
solubility curve.
It represent maximum conc. of solution
that can be obtained by bringing solute in
eqilibrium of solvent.
Supersaturation is achived by reducing
temp. or evaporation of solvent.
Supersolubility curve
AC normal solubility
curve (Maximum
solubility)
EF supersolubility
curve (nucleus
formation begin)
Region between two
curves is metastable
region.
Crystallization starts
at point E.
Limitation of theory
Crystallization start in region rather
than a point
Crystallization occer below
supersolubility curve after long term
storage.
It is difficult to obtain pure solute
and solvent.
Solubility curves
Solubility curve
It is useful in prediction of
experimental condition for
crystallization.
KNO3 solubility increases with temp.
NaCl Solubility increases with temp.
but with marginal extent.
Na2SO4 solubility increases when it
is in hydrated form. Once compound
turns into unhydrate form its
solubility decreases.
Methods of acieving
Crystallization
Supersaturation can be achieved by
several methods:
Cooling
Evaporation
Solvent addition
Precipitant Addition
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Cooling Method
Concentrated
solution gradually
cooled below
saturation
temperature (5060C) to generate a
supersaturated state
Yields well defined
micron-sized crystals
Shell and tube heat
exchanger is used to
cool solution
Cooling Method
Advantages:
High purity downstream
Disadvantages:
Temperature change does not always have a
positive effect on supersaturation in proteins
Protein stability may be at risk
Solubility can be relatively insensitive to
temperature at high salt concentrations
Cooling will only help reach supersaturation in
systems where solubility and temperature are
directly related
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Evaporation Method
Solute dissolves in solution when heated
to a certain temperature (75C)
Slowly cooled until crystals precipitate
Shell and tube heat exchanger is used to
heat and cool solution
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Evaporation Method
Advantages:
high purity levels downstream
Disadvantages:
Vaporization chamber requires high
pressures
Protein viability very sensitive to high
temperatures
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Solvent Method
Solvents are generally good protein
precipitants
Their low dielectric constants lower the
solvating power of their aqueous
solutions
Requires acidic solvent
For crystallization, an insulin protein falls
out of solution at isoelectric point
pH 5.4-5.7
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Solvent Method
Advantages:
Proteins viability not at risk due to
temperature change
Disadvantages:
Possible protein contamination due to
insufficient downstream solvent
recovery
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Seeding Techniques
Primary nucleation is the first step in
crystallization Growth of a new crystal
Can bypass primary nucleation (creation of
new crystals) by "seeding" the solution
CRYSTALLIZER
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Krystal Crystallizer
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Vacuum Crystallizer
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