Parallelism and differences of pervaporation and vacuum membrane distillation in the removal of VOCs from aqueous streams (original) (raw)
2001, Separation and Purification Technology
Abstract
In this work two gas-liquid separation processes, pervaporation (PV) and vacuum membrane distillation (VMD), have been compared in their application to the separation of chloroform-water mixtures. After selection of the adequate separation membrane the comparison of the PV and VMD should be based on the kinetics and selectivity towards the desired compound. The kinetic models and parameters previously reported by the authors (A.M. Urtiaga,
Figures (15)
Fig. 1. Flow diagram of the membrane process for the treat- ment of contaminated water and the recovery of chloroform.
Fig. 2. Mechanisms of mass transfer in: (a) PV and (b) VMD. In both membrane systems the feed liquid mixture to be separated is placed in contact with one side of the membrane, producing an enriched vapor permeate on the other side, that is conducted to a condenser (Fig. 1). However, significant differ- ences can be found between pervaporation and vacuum membrane distillation (Fig. 2). In PV the separation is determined by the selective sorption and diffusion of the components of the mixture, chloroform and water, through a dense membrane [3]. The availability of commercial membranes is one of the most important constraints for the development and application of PV technology. In VMD the aqueous feed is brought into contact with one side of a hydrophobic, microporous membrane. The hydrophobic nature of the mem- brane prevents the penetration of the aqueous solution into the pores, resulting in a vapor-—liq- uid interface at each pore entrance. Water and chloroform evaporate from the interface, diffuse
3.1. PV Characteristics of the PV and VMD modules Table 1
Fig. 3. PV results. Influence of the flowrate of the feed. T = 40°C. The solid lines are simulated results.
Fig. 5. VMD results. Influence of the flowrate of the feed. T = 25°C. The solid lines are simulated results. The effect of varying the flowrate of the aqueous feed in the laminar regime is given in Fig. 5. The solid lines in Figs. 5 and 6 are simulated courses of concentration, using Eqs. (1)—(9) of his paper. Increasing the flowrate resulted in a faster removal of chloroform from the feed phase. It was found that only at the highest flowrates in he turbulent regime the resistance of the mem- brane starts to be of relative importance since under these conditions the kinetics of the chloro- form separation are only slightly influenced by the flowrate of the feed phase [5]. Regarding the influence of temperature, Fig. 6 presents some representative experimental data reported in a
Fig. 4. PV results. Influence of the temperature of the feed. (@) Re = 606, (Ml) Re = 623, (A) Re = 580. The solid lines are simulated results.
* Data obtained from Ref. [12]. The kinetic model is completed with the mass balance to the tank of the feed aqueous phase considered as ideal stirred vessel, as given by Eq. (5):
membranes have hollow fiber geometry and the aqueous feed is circulating through the inside of the fibers. Thus, the evolution of the chloroform concentration in the feed within the hollow fiber membranes can be described by the continuity equation and the associated boundary conditions, being the diffusion coefficient of chloroform in the aqueous phase the design parameter: The left-hand side of Eq. (4) gives the flux of chloroform arriving at the liquid—membrane in- terface from the fluid circulating through the in- side of the fiber. The right-hand side of Eq. (4) accounts for the transport of chloroform through the membrane. Although the system is operated in batch mode the pseudo-steady state assumption given by Eq. (1) is a good approximation since under the operating conditions the variation of concentration at the module entrance is much less
Fig. 6. VMD results. Influence of the temperature of the feed. (@) Re = 1117, (MI) Re = 907, (A) Re = 708, (@) Re = 557, (©) Re = 418. The solid lines are simulated results.
Fig. 7. Simulated concentration of chloroform in the feed tank of the PV system (dotted line) and VMD system (solid line). Re = 150.
Conditions of simulation Table 3 Another parameter that can be used to com- pare the VMD and the PV systems is the selectiv- ity of the separation between chloroform and water. The selectivity is related to the ability of concentrating the chloroform in the permeate phase starting from the dilute aqueous feed. number as the constant parameter for the com- parison, instead of a given flowrate of the feed, since the large difference in the geometrical char- acteristics of the PV and VMD membrane mod- ules makes it difficult to obtain similar fluodynamic conditions at a given flowrate of the feed phase. The equivalency between flowrate, temperature and Reynolds number is given in Table 3.
Fig. 8. Simulated concentration of chloroform in the feed tank of the PV system (dotted line) and VMD system (solid line). Re = 700. In Eq. (12) the flux of chloroform was calcu- lated using Eq. (10) and the values of water flux were taken from the data in Table 2. In the VMD
Fig. 9. Simulated evolution of the flux of chloroform in the PV and VMD systems. T= 25°C.
Fig. 10. Selectivity of the VMD of chloroform—water mix- tures. Experimental results obtained at T=25°C. Feed flowrate = 0.68 1 min~!. Commercial PDMS membranes for the PV pro- cess and microporous polypropylene membranes for the VMD process are both easily available. Thus in the separation of dilute chloroform—wa- ter mixtures the selection of the appropriate mem- brane system should be based on the objectives of the separation process. In the separation of chlo-
Selectivity of the separation in the PV and VMD systems Table 4 mass transfer flux and selectivity in both separa- tion processes. roform the two systems under study provide the same rate of remova and, thus, an equivalent membrane area for a given separation require- ment would be needed , whenever the geometrical characteristics of the hollow fiber membrane mod- ules are the same. If solvent is required a recycling of the recovered high selectivity is desirable and, thus, the PDMS the best option. pervaporation membrane is
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