Modelling of Organophilic and Hydrophilic Pervaporations for Separation of Ethyl Acetate – water Mixture

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Abstract

Pervaporation is a separation method that is considered as green technology because of its low energy consumption. The mechanism of component separation in a liquid mixture by pervaporation is complex but it can be explained with the solution-diffusion mechanism. The work is motivated by an industrial separation problem, that is, ethyl acetate removal from aqueous mixture. To complete this goal hybrid organophilic/hydrophilic pervaporation of ethyl acetate/water mixture through commercially available Sulzer PERVAP™ 4060 and 1510 membranes are investigated to obtain information about the removal of ethyl acetate. Our experimental data are evaluated with the pervaporation model of our improvement (Valentínyi et al., 2013) and it is found that the model can be applied also for both cases. The hybrid separation process is rigorously modelled in professional flowsheet environment, and optimized with the dynamic programming optimization method. The objective function is product purity of 99.0, 99.5 m/m% in water and ethyl acetate content and the total annual cost is also determined. It can be determined, this hybrid separation should be become the alternative of distillation if the energy prices are too high.

Introduction

Pervaporation (PV) is a chemical unit operation where the liquid mixture to be separated is vaporized at low pressure on the downstream/permeate side of the membranes and the separation of the mixtures takes place by preferential sorption and diffusion of the desired component through the membrane (Valentínyi et al., 2013). A solution to achieve the difference in the partial pressures is to maintain a low vapour pressure using a vacuum pump on the permeate side (Van Baelen et al., 2005). Pervaporation shows good features such as special separation effect, no-extra material addition and energy-saving which are difficult to obtain by other conventional methods (Szabados et al., 2018). Depending on the permeating component two main areas of pervaporation can be identified: hydrophilic (HPV) and organophilic pervaporation (OPV) (Heintz and Stephan, 1994a, Heintz and Stephan, 1994b).

The aim of this work is to examine the ethyl acetate (EtAc) - water separation with pervaporation. The organophilic-hydrophilic pervaporation process is modelled and optimized for the separation of a binary mixture. EtAc forms heteroazeotrope with water (Gmehling et al., 1978), therefore this mixture cannot be separated with conventional distillation (Waltermann et al., 2017). Basically, the problem and the aims must be defined, that is, 5 m/m% ethyl acetate-water mixture with a feed flow of 1000 kg/h should be separated. The product purity of 99.0 and 99.5 m/m% should be achieved both for water and ethyl acetate.

Section snippets

Material and methods

Modelling of pervaporation has the following main steps (Toth et al., 2015):

  • 1.

    System identification,

  • 2.

    Model parameters estimation for pervaporation model,

  • 3.

    Model verification/validation and

  • 4.

    Optimization.

For the modelling of pervaporation, our model is selected and applied (Haaz and Toth, 2018). The parameters of the model are determined on the basis of experiments using the parameter estimation process (Valentinyi et al., 2013). The pervaporation model with the determined parameters is verified with

Results and discussion

A comparison of the measured and calculated partial fluxes are presented in Figure 3 and Figure 4.

The minimized objective functions are shown in Table 1.

Generally, it can be concluded that the pervaporation model with the concentration dependency of the transport coefficient fit for the pervaporation experiments in a wide concentration range of the feed flow, particularly in the case of water fluxes. Table 2 shows the necessary total membrane surface areas in the function of product purities.

Conclusions

The experiments and simulations suggest that the pervaporation is able to remove the ethyl acetate from an aqueous mixture. Organophilic and hydrophilic pervaporations are modelled with our verified and adequate model in professional flowsheeting environment that enables verified rigorous modelling, optimization and cost estimation. The results show that the capital cost of the pervaporation unit is the highest part of the total annual cost.

Acknowledgments

This publication was supported by the Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences, ÚNKP-19-4-BME-416 New National Excellence Program of the Ministry for Innovation and Technology, OTKA 112699, 128543 and 131586. This research was supported by the European Union and the Hungarian State, co-financed by the European Regional Development Fund in the framework of the GINOP-2.3.4-15-2016-00004 project, aimed to promote the cooperation between the higher education and the

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