colloid stability ?
DESCRIPTION
Colloid Stability ?. Colloidal systems. A state of subdivision in which the particles, droplets, or bubbles dispersed in another phase have at least one dimension between 1 and 1000 nm all combinations are possible between : gas, liquid, and solid W. Ostwald. - PowerPoint PPT PresentationTRANSCRIPT
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Colloid Stability ?
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• A state of subdivision in which the particles, droplets, or bubbles dispersed in another phase have at least one dimension between 1 and 1000 nm
• all combinations are possible between :
gas, liquid, and solid W. Ostwald
Colloidal systems
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Surface area of colloidal systems
• Cube (1cm; 1cm; 1cm) after size reduction to an edge length of 500 nm: surface area of 60 m2
• Spinning dope (1 cm3) after spinning to a fibre with diameter of 1000 nm:
fiber length of 1273 km
• 1 liter of a 0.1 M surfactant solution: interfacial area of 40000 m2
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Surface atoms [in %] in dependence on the particle size [in nm]
0102030405060708090
100
20 10 5 2 1
part of surfaceatoms in %%
nm
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Colloidal systems
• have large surface areas
• surface atoms become dominant
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Colloid stability
• Colloidal gold: stabilized against coagulation !
• Creme: stabilized against coagulation !
• Milk: stabilized against coagulation !
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Particle – Particle interactions
• Interaction Energy ( Vtot) – Distance of Separation (d) Relationship
d
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Vtot(d) = Vattr(d) + Vrep(d)
- Van der Waals attraction - Electrostatic repulsion
- Steric repulsion
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DLVO - Theory
• 1940 – Derjaguin; Landau; Verwey; Overbeek
• Long range attractive van der Waals forces
• Long range repulsive electrostatic forces
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DLVO – TheoryVan der Waals attractive energy
a) between two plates:
b) between two spheres:
2.
12 d
AV attr
WaalsderVan
d
aAV attr
WaalsderVan 12.
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Double layer models
• Helmholtz
• Gouy Chapman
• Stern
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Gouy Chapman model
• planar double layer
• Ions as point charges
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Electrolyte theory
kT
xez
iii
i
enezxd
xd
0
2
2 4
I distribution of ions in the diffuse double layer (Boltzmann equation)
II equation for the room charge density
III Poisson relation
Aus I, II und III folgt:
Poisson – Boltzmann - relation
kT
xezenxn i
ii
xnezx iii
02
2 4 x
xd
xd
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Solution of the P-B equation
xekx
xxd
xd
0
22
2
For small potentials (< 25 mV) :
Integrable form
kT
xez
iii
i
enezdx
xd
0
2
2 4
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DLVO – TheoryElectrostatic repulsive energy
Resulting repulsive overlap energy
a) Between two plates:
c° – volume concentration of the z – valent electrolyte
b) Between two spheres
drepelektrost e
kTcV
64
.
2
2
2
220
22
.
1
18
kT
ze
kT
ze
drepelektrost
e
ee
ze
TkV
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Vtot(d) = Vattr(d) + Vrep(d)
Vvan der Waals = - A a / 12 d Velectrost. = k e-d
A – Hamaker constant
a – particle radius
d – distance between the particles
1/ - thickness of the double-layer
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Electrostatic stabilization
stabilized against coagulation
Kinetically stable state
energetic metastable state in the secondary minimum with an energy barrier
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Critical coagulation concentration (CCC)
• The energy barrier disappears by adding a critical amount of low molecular salts
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DLVO – Theory
(CCC)
Vtot / dd = 0 Vtot = 0
for two spheres:
2
266
30
3553
2
2
2
21
220
22
1
1
4
1039,3
121
18
kT
ze
kT
ze
kT
ze
kT
ze
e
e
Aze
Tkccc
d
aA
e
ee
ze
Tk
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DLVO – Theory
(CCC)
• For two spheres the ccc should be related to the valency (1 : 2 : 3) of the counterions as:
1000 : 16 : 1,3
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CCC of a colloidal dispersion as a function of the salt concentration
AlCl3
CaCl2
MgCl2
KCl
NaCl
electrolyte
1,79,3 10-5
136,5 10-4
137,2 10-4
10005,0 10-2
10005,1 10-2
Schulze-Hardy-ratioCCC of a
Arsensulfid -Dispersion
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Steric stabilization
• What will be happen when we add polymers to a colloidal dispersion ?
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Particle – Particle interactions
Polymer adsorption layer
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Particle – Particle interactions
Overlap of the polymer adsorption layer
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Overlap of the adsorption layer
• Osmotic repulsion
• Entropic repulsion
• Enthalpic repulsion
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Sterically stabilized systems can be controlled by
• The thickness of the adsorption layer
• The density of the adsorption layer
• The temperature
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Stabilization and destabilization in dependence on the molecular weight of the added polymer
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Stabilization and destabilization in dependence on the
polymer-concentration