Filtration

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This article is about Conventional Filtration, for crossflow filtration see Crossflow filtration.

Filtration is a process by which most or all solid particles in a liquid-solid suspension fluid are separated from the fluid by passing the fluid through a porous medium barrier. In conventional filtration (as opposed to crossflow filtration) the incoming fluid, or feed, flows perpendicular to the porous medium. A layer of solids continues to build with time over the surface of the medium, while the flux of the feed through the medium approaches a zero asymptote. In bioprocessing, filtration is an early processing step during the recovery phase. It may be employed, for example, to retrieve a target product in solution from an undesired solid mass of freshly ruptured cells. Filtration is of particular value because it allows for an effect means of volume reduction, a crucial tool in early processing.

The Processes

Design and Operation

Use lots of subsections here as you describe various aspects of the process .[1]

There are four categories of filtration as divided by driving force: gravity, vacuum, pressure and centrifugal force. The last may also be considered a form of centrifugation, and will not be discussed in great detail here.

Gravity filtration

Vacuum filtration

Pressure filtration

Centrifugal force filtration

Materials

Filter media

Filter aid

Principles and theory

In most cases of conventional filtration, a solid suspension fluid, or filtrate, is flowed against a porous medium by application of a pressure gradient across the medium, wherein the solids in the suspension too large to pass through the medium become trapped on one side of the medium, building up in a layer called a cake, of sometimes more specifically filter cake. The flow of the liquid filtrate through the porous medium, which is a bed of solids, may be described by Darcy's Law written in the form:

wherein A is the cross-sectional area of the medium through which the fluid flows, V is the volume of filtrate, t is the time, Δp is the change in pressures across the medium and cake, μo is the is the viscosity of the filtrate, and R is the combined (in series) resistance of the filter medium ("RM") and filter cake ("RC"), which is:

.

The cake resistance may further be described in terms of the specific cake resistance α the the following form:

wherein ρc is the mass of dry cake solids per unit volume of filtrate.

Darcy's Law for the flow of the liquid filtrate through the bed of solids porous filter medium and cake may therefore be rewritten as:

This equation may be integrated with an initial condition of zero filtrate at time zero to yield:

which may also be rewritten in term of the filtrate density ρ, the ratio of the mass of dry cake solids to the mass of feed c, and the ratio of the mass of wet cake to the mass of dry cake w:

History

This section should describe the invention and development of the process. If the section runs long, divide it into chronological subsections, for example:

Invention and early development

This subsection should provide some historical context for the development of your process, describe its invention, and name some early developers and/or applications.[2]

Recent developments

This section should discuss new developments in the field. Don't hesitate to drop in brief mentions of processes or features you don't intend to discuss in depth. By so doing you are planting seeds of articles which will eventually be developed by others.[3]

Applications

This section should discuss how the process is used in practice.[4]

Examples

If you have used a lot of equations in your article, this may be a good place to show an example of how they are used. See the article on the Antoine Equation for an example.

References

  1. First Author and Second Author, "Electro-absorpto-crossflow-sedimento-extractofractionation," Journal of Superspecialized Bioseparation Arcana 36:2 (2010) pp. 86-52.
  2. John Q. Sample, Chromatography, a new analytical tool. City: Publisher, 1885.
  3. "New Directions for Flocculation," American Flocculation Society. 2006. Retrieved July 21, 2009 from http://www.amflocsoc.org/future_devs.html
  4. "Major Success for Bioprocess Fractionation," Anytown Daily News, January 1, 2015, p. A6.