Lecture 10
Lecture 10
Lecture 10
• Haemodialysis
• Pervaporaion
• Liquid membrane
Liquid membrane
• It consists of a liquid phase (e.g. a thin oil film) existing either in supported or
unsupported form that serves as a membrane barrier between two phases of aqueous
solutions or gas mixtures.
• One of the benefits of using a liquid membrane is that LMs are highly selective, and,
with the use of carriers for the transport mechanism, specific molecular recognition can
be achieved.
• LMs are relatively high in efficiency, and as such, are being looked into for industrial
applications.
Types of LM
• Bulk liquid membrane (BLM) consists of a bulk aqueous feed and receiving phases
separated by a bulk organic which is water-immiscible liquid phase.
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• The phases may be separating by microporous supports which separate the feed and
receiving phases from the LM or module configuration may be without microporous
supports (layered BLM).
• Many of the LM subject reviewers considered only layered BLM and testified its
transport and selectivity inefficiency to be a potential for the practical application.
• In the liquid are the carriers that perform the required separation.
• The ILM takes things from one side of the rigid membrane (the source phase) and carries
it to the other side (the receiving phase) through this liquid phase.
• Liquid impregnated (or immobilized) in the pores of a thin microporous solid support is
defined as a supported liquid membrane (SLM or ILM).
• Flat sheet SLM is useful for research, but the surface area to volume ratio is too low for
industrial applications.
• Spiral-wound and hollow-fiber SLMs have much higher surface areas of the LM modules
(103 and 104 m2/m3, respectively).
• The main problem of SLM technology is the stability: the chemical stability of the
carrier, the mechanical stability of porous support, etc
• In such a system, instability is caused by the removal of carrier or organic liquid in the
pores of that supporting membrane.
• a large pressure differential across the membrane that effectively pushes the fluid out
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•
Applications:
• Metal separation-concentration
• Biotechnological products recovery-separation
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Pervaporation:
• Pervaporation (or pervaporative separation) is a processing method for the separation of
mixtures of liquids by partial vaporization through a non-porous or porous membrane.
• The term pervaporation is derived from the two steps of the process:
(a) permeation through the membrane by the permeate, then
– (b) its evaporation into the vapor phase.
• The membrane acts as a selective barrier between the two phases: the liquid-phase feed
and the vapor-phase permeate.
• It allows the desired component(s) of the liquid feed to transfer through it
by vaporization.
• Separation of components is based on a difference in transport rate of individual
components through the membrane.
• Typically, the upstream side of the membrane is at ambient pressure and the downstream
side is under vacuum to allow the evaporation of the selective component after
permeation through the membrane.
• Driving force for the separation is the difference in the partial pressures of the
components on the two sides and not the volatility difference of the components in the
feed
• The driving force for transport of different components is provided by a chemical
potential difference between the liquid feed/retentate and vapor permeate at each side of
the membrane. The retentate is the remainder of the feed leaving the membrane feed
chamber, which is not permeated through the membrane.
Applications:
• Solvent Dehydration: dehydrating the ethanol/water and isopropanol/water azeotropes
• Continuous ethanol removal from yeast fermenters.
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• Concentration of hydrophobic flavor compounds in aqueous solutions (using
hydrophobic membranes)
Electrodialysis:
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Dialysis:
• In the biochemical practice, dialysis is often used to alter the concentration of salts and/or
small molecules in protein solutions—usually aimed at decreasing the concentration of
these solutes.
• However, the composition of the solution can also be changed in additional ways.
• Dialysis is based on diffusion during which the mobility of solute particles between two liquid
spaces is restricted, mostly according to their size.
•
• Dialyser: The dialysis unit is called as
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• Dialysis: Dialysis is an operation to separate dissolved molecules based on molecular
weight.
• In practice, a biological sample is placed inside a tube of semi permeable membrane, and
placed inside a much bigger container.
• At equilibrium, the concentration of small molecules is the same inside and outside the
membrane.
•
Applications and limitation of Dialysis
• Concentration of macromolecules.
Daily Application:
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Advantage of dialysis
• Dialysis is still in use today for it is very simple and is still the only way to deal
with large-volume samples.
Disadvantage of dialysis
• Slow process several hours for completion, and thus, has been replaced by gel
filtration for most applications. Other forms of dialysis includes flow-dialysis and
pressure-dialysis
Theoretical principle:
Haemodialysis:
• DEFINITION
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– This is accomplished using a machine and a dialyzer, also referred to as an
"artificial kidney
Application:
Construction:
Working principle:
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Applications:
• Stabilisation of wine
• Whey demineralisation
• Pharmaceutical application
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