Pervaporation, in its simplest form, is an energy efficient combination of membrane permeation and evaporation.It's considered an attractive alternative to other separation methods for a variety of processes.For example, with the low temperatures and pressures involved in pervaporation, it often has cost and performance advantages for the separation of constant-boiling azeotropes. Pervaporation is also used for the dehydration of organic solvents and the removal of organics from aqueous streams.Additionally, pervaporation has emerged as a good choice for separation heat sensitive products.
Pervaporation involves the separation of two or more components across a membrane by differing rates of diffusion through a thin polymer and an evaporative phase change comparable to a simple flash step. A concentrate and vapor pressure gradient is used to allow one component to preferentially permeate across the membrane.A vacuum applied to the permeate side is coupled with the immediate condensation of the permeated vapors.Pervaporation is typically suited to separating a minor component of a liquid mixture, thus high selectivity through the membrane is essential.
Pervaporation can used for breaking azeotropes, dehydration of solvents and other volatile organics,organic/organic separations such as ethanol or methanol removal, and wastewater purification.
Characteristics of the pervaporation process include:
1.Low energy consumption
2.No entrainer required, no contamination
3.Permeate must be volatile at operating conditions
4.Functions independent of vapor/liquid equilibrium
Types of Pervaporation Process
Batch pervaporation is a simple system with great
flexibility, however a buffer tank is required for batch
operation. Continuous pervaporation consumes very
little energy, operates best with low impurities in the
feed, and is best for larger capacities. Vapor phase
permeation is preferred for direct feeds from distillation columns or for streams with dissolved solids.
Pervaporation for Separation
Liquid transport in pervaporation is described by various solution-diffusion models1. The steps included are the
sorption of the permeate at the interface of the solution feed and the membrane, diffusion across the membrane
due to concentration gradients (rate determining steps), and finally desorption into a vapor phase at the
permeate side of the membrane. The first two steps are primarily responsible for the permselectivity1. As
material passes through the membrane a "swelling" effect makes the membrane more permeable, but less
selective, until a point of unacceptable selectivity is reached and the membrane must be regenerated.
The other driving force for separation is the difference in partial pressures across the membrane. By reducing
the pressure on the permeate side of the membrane, a driving force is created. Another method of inducing a
partial pressure gradient is to sweep an inert gas over the permeate side of the membrane. These methods are
described as vacuum and sweep gas pervaporation respectively.
Basics of the Pervaporation System
Figure 3 shows a typical pervaporation system. The feed is allowed to flow along one side of the membrane and a
fraction of the feed (permeate) passes through the membrane and leaves in the vapor phase on the opposite side
of the membrane. The "vapor phase" side of the membrane is either kept under a vacuum or it is purged with a
stream of inert carrier gas. The permeate is finally collected in the liquid state after condensation. The liquid
product is rich in the more rapidly permeating component of feed mixture. The retentate is made up of the feed
materials that cannot pass through the membrane.
Membranes
The membranes used in pervaporation processes are classified according to the nature of the separation being
performed. Hydrophilic membranes are used to remove water from organic solutions. These types of
membranes are typical made of polymers with glass transition temperatures above room temperatures. Polyvinyl
alcohol is an example of a hydrophilic membrane material. Organophilic membranes are used to recover
organics from solutions. These membranes are typically made up of elastomer materials (polymers with glass
transition temperatures below room temperature). The flexible nature of these polymers make them ideal for
allowing organic to pass through. Examples include nitrile, butadiene rubber, and styrene butadiene rubber.
Factors Affecting Membrane Performance
According to the solution-diffusion model, higher fluxes can be obtained with an increased thermal motion of
the polymer chains and the diffusing species. Properties of the polymers that affect diffusion include the
"backbone" material, degree of cross-linking, and porosity. Molecular-level interactions between membranes
and diffusing species is expressed via a permeability constant used in the Arrhenius relationship:
Where,
Ep = Activation energy
Po = Permeability constant
R = Gas constant
T = Temperature
Pervaporation Characteristics
1. Molecular Flux
Molecular flux is the amount of a component permeated per unit area per unit time for a given membrane.
Where,
Ji = Flux of component "i" (moles/h cm2)
Qi = Moles of component "i" permeated in time "t"
A = Effective membrane surface area (cm2)
2. Permselectivity
The performance of a given membrane can be expressed in terms of a parameter called permselectivity:
(3)
Assuming the density of the components in the feed is the same, then:
Where,
X = Weight fraction
V = Volume fraction
p = Density
Superscripts "p" and "f" denote "permeate" and "feed" respectively while "i" and "j" represent individual
components.
3. Permeability Coefficient
The molecular flux for pervaporation across a membrane can be related to the permeability coefficient by:
or
Here, and , therefore
Equation 6 becomes,
Industrial Applications
Established industrial applications of pervaporation include:
The treatment of wastewater contaminated with organics4
Pollution control applications4
Recovery of valuable organic compounds from process side streams5
Separation of 99.5% pure ethanol-water solutions6
Harvesting of organic substances from fermented broth7
Other products separated or purified by pervaporation include:
Alcohols
Ketones
Methanol
Acetone
Ethanol
Butanone
Propanol (both isomers)
Methyl isobutyl ketone (MIBK)
Butanol (all isomers)
Amines
Pentanol (all isomers)
Triethylamine
Cyclohexanol
Pyridine
Benzyl alcohol
Aniline
Aromatics
Aliphatics
Benzene
Chlorinated hydrocarbons (various)
Toluene
Dichloro methane
Phenol
Perchloroethylene
Ester
Ethers
Methyl acetate
Methyl tert-butyl ether (MTBE)
Ethyl acetate
Ethyl tert-butyl ether (ETBE)
Butyl acetate
Di-isopropyl ether (DIPE)
Organic Acid
Tetrahydro furan (THF)
Acetic acid
Dioxane
Continuing Research on Pervaporation
Pervaporation of Apple Juice
Pervaporation is used to recover any lost juice solution during evaporation. The vapor from the evaporation
process is further processed using pervaporation. The recovered, concentrated apple juice can be combined with
the product solution to help the apple juice retain it's aromatic and taste qualities.
Pervaporation in the Production of Fuel Ethanol
To establish a continuous fermentation process, the ethanol concentration within the fermentation vessel must
be kept at 5% by weight or lower. Pervaporation has been used to maintain the necessary ethanol concentration
in the broth. The advantages of using pervaporation in such a system include the ease of processing the clean,
nearly pure ethanol extracted from the fermentation vessel and a significantly higher fermentation capacity or
the reduction in fermentor size and costs.
Summary
Pervaporation continues to evolve as a feasible separation technology for many different applications. As a
proven method of separation as low temperatures and pressure, further application development for food
processing is likely. Using pervaporation to clean wastewater streams by removing a variety of organic
compounds also holds much promise.
References
1. Yong Soo Kang, Sang Wook Lee, Un Young Kim and Jyong sup shim, Pervaporation of water - Ethanol
mixtures through
cross - linked and surface modified poly (vinyl alcohol) membrane, J. Member. Sc., Elsevier Science
Publishers B.V., Amsterdam, 51, 215, 1990.
2. K.W. Boddeker and G. Bengston, Pervaporation membranes separation processes, Ed. By R.Y M. Hang.
Elsevier, Amsterdam 437 - 460, 1991.
3. G.H. Koops and C.A. Smolders Pervaporation membrane separation process, Ed. by R.Y.M Haung, Elsevier,
Amsterdam 249 - 273, 1991.
4. C. Lipski and P. cote, the use of Pervaporation for removal of organic containment from water,
Environmental program, 9, 254 - 261, 1990.
5. J. Kashemekat, J.G. Wiljmans and R.W Baker, Removal of organic solvent containments from industrial
effluent streams by
Pervaporation, Ed. By R. Bakish, Proc. 4th int. Conf. On Pervaporation, process in chemical industry, Bakish
materials
Corporation, Englewood, NJ, 321, 1981.
6. B.K. Dutta and S.K Sridhar, separation of azeotropic organic liquid mixtures by Pervaporation, AIChE
journal, vol.37, No.4, 581 - 588, 1991.
7. M.E.F. Garcia, A.C. Habert, R. Nobrega and L.A. Piers, Use of PDMS and EVA membranes to remove
ethanol during
fermentation, Ed, by R. Bakish Proc. 5th Int. Conf. on Pervaporation process in the chemical industry, Bakish
Materials
corporation, Englewood, NJ, 319 - 330, 1991.
8. Aptel, P., N. Challard, J. Cuny, and J. Neel, " Application of the Pervaporation Process to Separate
Azeotropic Mixtures," J.
Membrane Science., 1, 271 (1976).
9. Dutta, B.K., D. Randolph, and S.K. Sikdar, " Separation of Amino Acids Using Composite Ion Exchange
Membranes,"
Biochemical Engineering VI, new York Academy of science, 589, 203,1990