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Chapter 10 Interface (Surface) Phenomenon. Phase. Homogeneous system one phase. Heterogeneous system two or more phase. 10.1 Interface. Interface, surface. Volume surface. Mass surface. Result in the tendency
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Chapter 10 Interface (Surface) Phenomenon Phase Homogeneous system one phase Heterogeneous system two or more phase 10.1 Interface Interface, surface
Volume surface Mass surface • Result in the tendency • Liquid surface is to become as small as possible • Physical and Chemical adsorption Dispersity
10.2 Surface Tension 10.2.1. Surface Tension Surface work Wr = dAs unit J·m-2=N·m·m-2=N·m-1, -- surface tension
dl L F (a) dl dl L L F (b) (c)
L dl
10.2.2 Surface Energy of Dispersion System dU = TdS - pdV +dAs + BdnB dH = TdS + Vdp +dAs + BdnB dA =-SdT - pdV +dAs + BdnB dG =-SdT + Vdp +dAs + BdnB Unit surface free energy
10.2.3 Temperature Dependence of Surface Tension T , — p
10.3 Curved Surface 10.3.1 Excess Pressure of Curved Surface
x +dx y+dy dz y x dz r2 r1 O2 O1 r: curvature radius Young -Laplace equation r1 = r2 = r,
convex: r>0, p >0, p1>pg concave:r<0 p <0, p1< pg plane: r=0 p =0, p1= pg
Kelvin equation 10.3.2 Saturated Vapor Pressure of Curved Surface pr*——Saturated vapor pressure of curved liquid surface p* ——Saturated vapor pressure of plane, MB——molar mass ; B——volume mass σ——surface tension; r——curvature radius convex(droplet): r>0, ln(pr*/p*)>0, pr*>p*; concave(bubbles): r<0, ln(pr*/p*)<0, pr*<p*。
• • • • • P(r>0) • • • g • • • • • • p(r=0) • • • p(r<0) g • • • • l • • • g • • • • • l l pr*(convex)>pr*(plane)>pr*(concave) F (convex)<F( plane)<F( concave)
3 2 {Pr} 1 10-1 100 101 102 103 Saturated vapor pressure of curved liquid surface r /nm 298.15 K convex plane concave
10.3.3 Metastable State Supersaturated vapor Supersaturated solution Superheated liquid Superhcooled liquid dG=-SdT+Vdp+dAs dGT,P=dAs>0 v ∝r2exp(-Br2)
10.3.4 Wetting (a) adhesion wetting
(c) spreading wetting Spreading coefficient
< 90—wetting; > 90—unwetting; Contact angle Young’s equation
<90( >90) >90( <90) =180-θ
r R h 10.3.5 Capillary Phenomenon
Ⅰ {} Ⅱ Ⅲ {c} 10.4 Surface adsorption of solution 10.4.1 Surface tension of solution
h h 体相 V h1 h1 h0 Surface phase S1 h0 h0 界面层S Surface layer S2 AS h2 h2 V (a) practice system (b) c ~ h (c) Gibbs model 10.4.2 Surface adsorption of solution Positive adsorption,negative adsorption Surface excess B
Ⅰ {} Ⅱ {c} (I),B<0,negative adsorption; (II、III),则B >0, positive adsorption 。 10.4.3 Gibbs equation Gibbs equation
hydrophile lipophile COO- CH3(CH2)7=CH(CH2)7 H+ Structure characteristic of a surfactant 4. Surfactants
Surface film of unimolecular layer Associated colloid(micell)
Critical micell concentration Increase dissolution
anionic surfactants e.g.soap RCOONa cationic surfactants Ionic surfactants C18H37NH3+Cl- Amphoteric surfactants Surfactants R-NH-CH2COOH Nonionic surfactants e.g. R[CH2OCH2]nCH2OH
Wetting action Emulsification , dispersed action Foaming action , do away with foam Washing action
kink terrace impurity adsorbed atom step dislocation 10.5 The extent of adsorption 10.5.1 Solid surface adsorption, adsorbate, adsorbent
H H H b b H a Cu Cu Cu X Cu Cu Cu {E} D Ea a 0 Hc= -33.5kJ 55.4kJ Hp H H C Cu Cu Cu H H Cu Cu H H Cu Cu {r}
Adsorption quantityΓ m——mass of solid ; V——volume of adsorbed gas at T.p T fixed, Γ = f (p) Adsorption isotherm p fixed, Γ = f (T) Adsorption isobar pΓ fixed, p = f (T) Adsorption isostere {Γ} {p} (a) (b) (c) (d) (e) 10.4.3 Adsorption curve
A(g) + M(surface) A ka M kd 10.4.4 Langmuir isotherm Langmuir assumption (i) Adsorption cannot proceed beyond monolayer coverage. (ii)All site are equivalent and the surface is uniform ( that is , the surface is perfectly flat on a microscopic scale) . (iii)The ability of a molecule to adsorb at a given site is independent of the occupation of neighboring sites. (iv)At equilibrium, the rates of adsorption and desorption of molecules from the surface are equal. ka :rate coefficient of adsorption kd :rate coefficient of desorption
equilibrium constant of adsorption Langmuir isotherm Coverage of surfaceθ υa= ka (1-θ)p υd= kd θ at equilibrium,υa=υd, ka (1-θ)p =kdθ
{Γ} (a) (i)bp<<1, θ=bp (ii)bp>>1, θ=1 V——volume of adsorbate adsorbed by solid at T,p V∞——volume of adsorbate corresponding to complete monolayer coverage
Mixed adsorption A、B Dissociation adsorption A2 + 2* 2(A – *)
10.4.5 The BET isotherm BET isotherm