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Introduction to Dispersed Systems. FDSC400 09/28/2001. Goals. Scales and Types of Structure in Food Surface Tension Curved Surfaces Surface Active Materials Charged Surfaces. COLLOIDAL SCALE. Dispersed Systems.
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Introduction to Dispersed Systems FDSC400 09/28/2001
Goals • Scales and Types of Structure in Food • Surface Tension • Curved Surfaces • Surface Active Materials • Charged Surfaces
COLLOIDAL SCALE
Dispersed Systems A kinetically stable mixture of one phase in another largely immiscible phase. Usually at least one length scale is in the colloidal range.
Dispersed Systems Dispersed phase Continuous phase Interface
Continuous phase Dispersed phase
Properties of Dispersed Systems • Too small to see • Affected by both gravitational forces and thermal diffusion • Large interfacial area • SURFACE EFFECTS ARE IMPORTANT
Increased Surface Area The same oil is split into 0.1 cm radius droplets, each has a volume of 0.004 cm3 and a surface area 0.125 cm2. As we need about 5000 droplets we would have a total area of 625 cm2 We have 20 cm3 of oil in 1 cm radius droplets. Each has a volume of (4/3.p.r3) 5.5 cm3 and a surface area of (4.p.r2) 12.5 cm2. As we need about 3.6 droplets we would have a total area of 45.5 cm2
For a Fixed COMPOSITION • Decrease size, increase number of particles • Increase AREA of interfacial contact decrease area
LYOPHOBIC Weak interfacial tension Little to be gained by breaking e.g., gums LYOPHILIC Strong interfacial tension Strong energetic pressure to reduce area e.g., emulsions Tendency to break
Surface Tension-bulk scale- Force, g Slope g Interfacial energy Area, A Interfacial area
Curved Surface Highly curved surface Slightly curved surface
Curved Surfaces Molecules at highly deformed surfaces are less well anchored into their phase
Laplace Pressure Surface pressure pulls inwards increasing pressure on dispersed phase pressure Surface tension Increased pressure radius
Curved Surfaces -Consequences- • Dispersed phase structures tend to be round • Small fluid droplets behave as hard spheres • Solubility increases with pressure so… • Large droplets may grow at the expense of small (Ostwald ripening) • Depends on the solubility of the dispersed phase in the continuous
Surface Active Material • Types of surfactant • Surface accumulation • Surface tension lowering
Types of Surfactant-small molecule- Hydrophilic head group (charged or polar) Hydrophobic tail (non-polar)
Types of Surfactant-polymeric- Polymer backbone Sequence of more water soluble subunits Sequence of less water soluble subunits
Surface Binding Equilibrium ENTHALPY COST ENTROPY COST
Surface Binding Isotherm Surface saturation Surface concentration /mg m-2 No binding below a certain concentration ln Bulk concentration
Surface Tension Lowering Bare surface (tension g0) Interface partly “hidden” (tension g) Surface pressure – the ability of a surfactant to lower surface tension p = g-g0