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Dispersions are classified in a number of different ways, including how large the particles are in relation to the particles of the continuous phase, whether or not precipitation occurs, and the presence of Brownian motion. In general, dispersions of particles sufficiently large for sedimentation are called suspensions, while those of smaller particles are called colloids and solutions.
Structure and propertiesEdit
Dispersions do not display any structure; i.e., the particles (or in case of emulsions: droplets) dispersed in the liquid or solid matrix (the "dispersion medium") are assumed to be statistically distributed. Therefore, for dispersions, usually percolation theory is assumed to appropriately describe their properties.
However, percolation theory can be applied only if the system it should describe is in or close to thermodynamic equilibrium. There are only very few studies about the structure of dispersions (emulsions), although they are plentiful in type and in use all over the world in innumerable applications (see below).
In the following, only such dispersions with a dispersed phase diameter of less than 1 µm will be discussed. To understand the formation and properties of such dispersions (incl emulsions), it must be considered that the dispersed phase exhibits a "surface", which is covered ("wet") by a different "surface" that, hence, are forming an interface (chemistry). Both surfaces have to be created (which requires a huge amount of energy), and the interfacial tension (difference of surface tension) is not compensating the energy input, if at all.
Experimental evidence suggests dispersions have a structure very much different from any kind of statistical distribution (which would be characteristics for a system in thermodynamic equilibrium), but in contrast display structures similar to self-organisation, which can be described by non-equilibrium thermodynamics. This is the reason why some liquid dispersions turn to become gels or even solid at a concentration of a dispersed phase above a critical concentration (which is dependent on particle size and interfacial tension). Also, the sudden appearance of conductivity in a system of a dispersed conductive phase in an insulating matrix has been explained.
Process of dispersionEdit
Dispersion is a process by which (in the case of solid dispersing in a liquid) agglomerated particles are separated from each other and a new interface between the inner surface of the liquid dispersion medium and the surface of the dispersed particles is generated. This process is facilitated by molecular diffusion and convection.
With respect to molecular diffusion, dispersion occurs as a result of an unequal concentration of the introduced material throughout the bulk medium. When the dispersed material is first introduced into the bulk medium, the region at which it is introduced then has a higher concentration of that material than any other point in the bulk. This unequal distribution results in a concentration gradient that drives the dispersion of particles in the medium so that the concentration is constant across the entire bulk. With respect to convection, variations in velocity between flow paths in the bulk facilitate the distribution of the dispersed material into the medium.
Although both transport phenomena contribute to the dispersion of a material into the bulk, the mechanism of dispersion is primarily driven by convection in cases where there is significant turbulent flow in the bulk. Diffusion is the dominant mechanism in the process of dispersion in cases of little to no turbulence in the bulk, where molecular diffusion is able to facilitate dispersion over a long period of time. These phenomena are reflected in common real-world events. The molecules in a drop of food coloring added to water will eventually disperse throughout the entire medium, where the effects of molecular diffusion are more evident. However, stirring the mixture with a spoon will create turbulent flows in the water that accelerate the process of dispersion through convection-dominated dispersion.
Degree of dispersionEdit
The term dispersion also refers to the physical property of the degree to which particles clump together into agglomerates or aggregates. While the two terms are often used interchangeably, according to ISO nanotechnology definitions, an agglomerate is a reversible collection of particles weakly bound, for example by van der Waals forces or physical entanglement, whereas an aggregate is composed of irreversibly bonded or fused particles, for example through covalent bonds. A full quantification of dispersion would involve the size, shape, and number of particles in each agglomerate or aggregate, the strength of the interparticle forces, their overall structure, and their distribution within the system. However, the complexity is usually reduced by comparing the measured size distribution of "primary" particles to that of the agglomerates or aggregates.
Types of dispersionsEdit
A solution describes a homogeneous mixture of one material dispersed into another. The dispersed particles will not settle if the solution is left undisturbed for a prolonged period of time.
A colloid is a heterogeneous mixture of one phase in another, where the dispersed particles are usually. Like solutions, dispersed particles will not settle if the solution is left undisturbed for a prolonged period of time.
A suspension is a heterogeneous dispersion of larger particles in a medium. Unlike solutions and suspensions, if left undisturbed for a prolonged period of time, the suspended particles will settle out of the mixture.
Although suspensions are relatively simple to distinguish from solutions and colloids, it may be difficult to distinguish solutions from colloids since the particles dispersed in the medium may be too small to distinguish by the human eye. Instead, the Tyndall effect is used to distinguish solutions and colloids. Due to the various reported definitions of solutions, colloids, and suspensions provided in literature, it is difficult to label each classification with a specific particle size range.
In addition to classification by particle size, dispersions can also be labeled by the combination of the dispersed phase and the medium phase that the particles are suspended in. Aerosols are liquids dispersed in gas, sols are solids in liquids, emulsions are liquids dispersed in liquids (more specifically a dispersion of two immiscible liquids), and gels are liquids dispersed in solids.
|Dissolved or dispersed phase||Continuous medium||
Solution: Homogeneous mixture
|Colloid: Heterogeneous mixture (smaller particles)||Suspension: Heterogeneous mixture (larger particles)|
|Gas||Gas||Gas mixture: air (oxygen and other gases in nitrogen)|
|Liquid||Gas||Aerosol: fog, mist, vapor, hair sprays||Aerosol|
|Solid||Gas||Solid aerosol: smoke, cloud, air particulates||Solid aerosol: dust|
|Gas||Liquid||Oxygen in water||Foam: whipped cream, shaving cream||Foam|
|Liquid||Liquid||Alcoholic beverages||Emulsion: miniemulsion, microemulsion, milk, mayonnaise, hand cream|
|Solid||Liquid||Sugar in water||Sol: pigmented ink, blood||Mud (soil, clay or silt particles are suspended in water), chalk powder suspended in water|
|Gas||Solid||Hydrogen in metals||Solid foam: aerogel, styrofoam, pumice|
|Liquid||Solid||Amalgam (mercury in gold), hexane in paraffin wax||Gel: agar, gelatin, silicagel, opal|
|Solid||Solid||Alloys, plasticizers in plastics||Solid sol: cranberry glass|
Examples of dispersionsEdit
Milk is a commonly cited example of an emulsion, a specific type of dispersion of one liquid into another liquid where to two liquids are immiscible. The fat molecules suspended in milk provide a mode of delivery of important fat-soluble vitamins and nutrients from the mother to newborn. The mechanical, thermal, or enzymatic treatment of milk manipulates the integrity of these fat globules and results in a wide variety of dairy products.
Oxide dispersion-strengthened alloy (ODS) is an example of oxide particle dispersion into a metal medium, which improves the high temperature tolerance of the material. Therefore these alloys have several applications in the nuclear energy industry, where materials must withstand extremely high temperatures to maintain operation.
The degradation of coastal aquifers is a direct result of seawater intrusion into the and dispersion into the aquifer following excessive use of the aquifer. When an aquifer is depleted for human use, it is naturally replenished by groundwater moving in from other areas. In the case of coastal aquifers, the water supply is replenished both from the land boundary on one side and the sea boundary on the other side. After excessive discharge, saline water from the sea boundary will enter the aquifer and disperse in the freshwater medium, threatening the viability of the aquifer for human use. Several different solutions to seawater intrusion in coastal aquifers have been proposed, including engineering methods of artificial recharge and implementing physical barriers at the sea boundary.
Chemical dispersants are used in oil spills to mitigate the effects of the spill and promote the degradation of oil particles. The dispersants effectively isolate pools on oil sitting on the surface of the water into smaller droplets that disperse into the water, which lowers the overall concentration of oil in the water to prevent any further contamination or impact on marine biology and coastal wildlife.
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