reaction at the interfaces7 2010 - aalborg...
TRANSCRIPT
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Lecture 7
Contact angle phenomena andContact angle phenomena and wetting
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Young’s equation
• Drop on the surface• complete spreading
• Establishing finite contact angle
cosL S SLγ θ γ γ= −
00S SLγ γ− > partial wetting
0S SLγ γ− < no wetting0S SLγ γ < no wetting
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Young’s equation• Derivation from the equilibrium condition
( ) 0dG dA dAγ γ γ= − + = at 0dV =( ) 0SL S SL L LdG dA dAγ γ γ= − + = at 0dV =
( )2 2LA a hπ= +
( )2 336LV a h hπ
= +
2dA d2SLdA adaπ=
2 2L LL
A AdA da dh ada hdha h
π π∂ ∂= + = +∂ ∂a h∂ ∂
( )2 2 02
L LL
V VdV da dh ahda a h dha h
ππ∂ ∂= + = + + =∂ ∂
2 cosLdA a daπ θ=
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Line tension
• For small drops (<10µm) an additional energy of the wetting line should be taken into account
cosL S SL aκγ θ γ γ= − −
• Estimate:t i l l h 2 b d l ( i i l– at a rim a molecule has 2 bonds less (assuming simple
cubic)– for cyclohexane:for cyclohexane:
113 103
vap Jm
A l
UN a
κ −Δ= = ⋅
3 A molN a
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Complete wetting• If S SL Lγ γ γ> +
Gibbs free energy is decreased by forming a continuousGibbs free energy is decreased by forming a continuous film on the surface
• Spreading coefficient: S SL LS γ γ γ= − −Spreading coefficient: S SL LS γ γ γ
Contact angle• Contact angle decreases with temperature due to pdrop in γL.
• At wetting Stemperature Tw, S=0
and complete wetting is reached.is reached.
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Capillary rise• If capillary is dipped in a liquid, the liquid meniscus
will either rise or lower due to surface tensionwill either rise or lower due to surface tension
2 cosL
c
hr gγ θ
ρ=
c gρ
Indeed:
( ) 22 2C S SL CdG r dh r ghdhπ γ γ π ρ= − ⋅ − +( )C S SL C gγ γ ρ
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Particles at liquid-gas interface• For small particles (i.e. neglecting the gravity) the equilibrium
position at the interface is determined by the surface tensionp y
typically >100µmyp y µ
Works both ways: flotation and stabilization of emulsion by solid particles
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Network of fibers• Network of fibers with final wetting angle will prevent water from passing
through; some pressure has to be applied to let it through
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Measurement of the contact angle• The most common technique is observation of
sessile drop with a microscopesessile drop with a microscope
hθ⎛ ⎞tan2
ha
θ⎛ ⎞ =⎜ ⎟⎝ ⎠
• or by using a Wilhelmy plateo by us g a e y p a e
• Wetting properties of powders can be detrmined fromcan be detrmined from capillary rise
• Note, the contact angle depends strongly on the surface contamination
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Hysteresis in contact angle measurements• If we increase or decrease e.g. droplet volume a hysteresis in
the angle will be observed• Usually:
adv recθ θ>
• Causes for the contact angle hysteresis:f h– surface roughness
– heterogeneity of the surface (resulting in pinning of a droplet)– absorbing dissolved substancesg– mechanical deformation of the surface due to surface tension– adsorption/desorption of liquid molecules at the interface (work required!)
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Surface roughness and heterogeneity
• Roughness increases the actual surface area and thereforesurface area and therefore decreases the apparent wetting angle for hydrophilic surface and increases it for a hydrophobicincreases it for a hydrophobic surface (Wenzel law)
cos cosapp roughRθ θ= ⋅
• Heterogeneous surfaces:• Heterogeneous surfaces: Cassie equation
f fθ θ θ1 1 2 2cos cos cosapp f fθ θ θ= ⋅ + ⋅
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Theory aspects• Surface tension at solid-air and solid-liquid interfaces strongly depend on the
surface preparation (e.g. deformation) • Experimentally only advancing and receding angles can be determined• Macroscopic (Young’s) contact angle is different from a microscopic one
(caused by van der Waals and DL-forces, at distances <100nm)
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Theory aspects• Surface tension at solid-liquid is the most difficult to be accessed by the
experiment• Though it can be estimated based on the properties of clean interfaces
(Gi if l G d d F k d l)(Girifalco, Good and Fowkes model)
1 2 12w γ γ γ= + −
A AA 11 22122 20 012 12
A AAwD Dπ π
= ≈1 3 2 3
1 3 2 3
34HA kT ε ε ε ε
ε ε ε ε⎛ ⎞⎛ ⎞− −
= +⎜ ⎟⎜ ⎟+ +⎝ ⎠⎝ ⎠
11 1111 112 2
0 0
and24 24
A AD D
γ γπ π
= = ( ) ( )( ) ( )
( ) ( )( ) ( )
1 3 2 3
1 3 2 3
1 3 2 31
34 v
iv iv iv ivh dviv iv iv iv
ε ε ε επ ε ε ε ε
∞
⎝ ⎠⎝ ⎠⎛ ⎞⎛ ⎞− −
+ ⎜ ⎟⎜ ⎟⎜ ⎟⎜ ⎟+ +⎝ ⎠⎝ ⎠∫
2γ γ γ γ γ= + −12 1 2 1 22γ γ γ γ γ= +
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Dynamics of wetting• Typical measurement geometries
• Typical measurement geometries
• Apparent contact angle depends also on the speed and viscosity, that can be combined into a
• Capillary number:p y
L
vCa ηγ
=
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Dynamic of wetting and dewetting
• Apparent contact angle vs. speed
Apparent ad ancing angle s capillar n mber for t o• Apparent advancing angle vs. capillary number for two mixtures of glycerol/water
Despite 7 times difference in viscosity, capillary number is a viscosity, capillary number is a good parameter for both liquids
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Dynamics of wetting• Liquid spreading on a solid surface
movement of the drop. Heat is dissipated byHeat is dissipated by eddies
Thin <0.1µm precursor film
binding of molecules at the front of thethe front of the precursor film
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Dynamics of wetting: examples• Spreading of PDMS drops on Si surface
Ellipsometerprofile 19h after
AFM image of PDMS drops
profile, 19h after deposition:
on Si surface
• Fabrication of polymer nanotubes using precursor film
Brief dipping of the alumina filter in a polystyrol melt
SEM image of the nanotubes(scale 1µm)p y y ( µ )
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Dynamics wetting: mechanism• The wetting kinetics is determined by absorption of
the precursor film molecules e g finding the bindingthe precursor film molecules e.g. finding the binding sites and displacing the gas molecules
• Maximum wetting speed and minimum dewettingspeed can be predicted based on the modelling (e.g. f 10 /for water vmax=5-10 m/s
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Polymer deposition and DewettingM fil t t bl t bl b• Many films are metastable or stable above certain thickness
• polymers are typically deposited either by dip or spin coating y p p g
• if wetting angle θ=0, the film is thermodynamically stable
• if wetting angle θ>0, the film is g g ,metastable and the holes will be formed spontaneously above the glass transition temperature
spontaneous formation of holes
dewetting of a 28nm polystyrene film on Si at 121 ºC
holes
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Flotation• Flotation is a method to separate solid particles from
each other based on their wetting properties
Technology• crushing into smallcrushing into small
particles (<0.1mm) and mixing with water (pulp)
• bubbling air through• the higher the wetting
angle the betterangle the better particles attach to a bubble
• specifically adsorbed surfactants (”collectors”) can be used to improvecan be used to improve efficiency
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Detergency• Detergency: theory and praxis of removing
foreign material from solids by surface-active substrates
Mechanism:Mechanism:• Dirt-Solid interface
is replaced by Dirt-Water and Water-Solid interfaces after addition ofafter addition of detergent
• Dirt particles are suspended in water preventing aggregation and ( ) 0DW SW SDG A γ γ γΔ = + − ≤aggregation and flocculation (e.g. electrostatically)
( ) 0DW SW SDG γ γ γ
SD DW SWγ γ γ≤ +
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Adjustable wetting
• Electrowettingec o e g2
00cos cos
2U
hεεθ θ
γ= +
• Photoswitching of hydrophobic/hydrophilic state (e g a oben ene)
2 Lhγ
state (e.g. azobenzene)
• Electrical field controlled conformation of SAMElectrical field controlled conformation of SAM layer
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Problems
• ch.7.1End of chapter problems:
c• ch.7.2• ch.7.3