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Pervaporation membrane reactors

Y. Zhu, R.G. Minet and T.T. Tsotsis, A Continuous Pervaporation Membrane Reactor for the Study of Esterification Reactions Using a Composite Polymeric/Ceramic Membrane, Chem. Eng. Sci. 51, 4103 (1996). [Pg.391]

Zhu Y, Minet RG, and Tsotsis TT. A continuous pervaporation membrane reactor for the study of esterification reactions using a composite polymeric/ceramic membrane. Chem Eng Sci 1996 5(17) 4103-4113. [Pg.318]

Kiatkittipong W, Assabumrungrat S, Praserthdam P, and Goto S. A pervaporation membrane reactor for liquid phase synthesis of ethyl tert-butyl ether from tert-butyl alcohol and ethanol. J Chem Eng Jpn 2002 35(6) 547-556. [Pg.319]

Marconi, J.G.S. Tsotsis, T.T. Pervaporation membrane reactors. In Catalytic Membranes and Membrane Reactors, Wiley-VCH Weinheim, 2002 Chapter 3, 15-96. [Pg.1586]

Pervaporation membrane reactors (PVMR) are an emerging area of membrane-based reactive separations. An excellent review paper of the broader area of pervaporation-based, hybrid processes has been published recently [3.1]. The brief discussion here is an extract of the more comprehensive discussions presented in that paper, as well as in an earlier paper by Zhu et al [3.2]. Mostly non-biological applications are discussed in this chapter. Some pervaporation membrane bioreactor (PVMBR) applications are also discussed additional information on the topic can be found in a recent publication [3.3], and a number of other examples are also discussed in Chapter 4. [Pg.97]

Pervaporation membrane reactors are not a recent discovery. The use of a PVMR was proposed in a U.S. patent dating back to 1960 [3.6]. Though the technical details on membrane preparation and experimental apparatus were rather sketchy, the basic idea was described there, namely, the use of a water permeable polymeric membrane to drive an esterification reaction to completion. A more detailed description of a PVMR can be found in a later European patent [3.7], which described the use of a flat membrane (commercial PVA or Nafion ) placed in the middle of a reactor consisting of two half-cells. The reaction studied was the acetic acid esterification reaction with ethanol. For an ethanol to acetic acid ratio of 2, liquid hourly space velocities (LHSV) in the range of 2-5, and a temperature of 90 °C complete conversion of the acetic acid was reported. The use of PVMR for this reaction shows promise for process simplification, as indicated schematically in Figure 3.2, which shows a side-by-side comparison of a conventional and a proposed PVMR plant for ethyl acetate production. [Pg.99]

B. Park, Models and Experiments with Pervaporation Membrane Reactors Integrated with a Water Adsorbent System, Ph.D Thesis, University of Southern California, Los Angeles USA, 2001. [Pg.129]

The way membranes (in various forms, i.e., cylindrical, coaxial, flat-sheet, spiral-wound, and hollow fiber, etc.) couple with the bioreactor depends on the role the membrane performs. As with catalytic and pervaporation membrane reactors, the simplest configuration consists of two separate but coupled units, one being the bioreactor the other the membrane module. The biocatalyst (e.g., enzymes, bacteria, yeasts, mammalian cells) could, in this case, be suspended in a solution and continuously circulated through the... [Pg.134]

The first pervaporation membrane reactor model which takes into account solution non-idealities was developed and validated experimentally by Zhu et al [5.90]. Prior studies [5.89, 5.91] also made note of such non-idealities, but offered no unified means for accounting for these phenomena in the description of PVMR. Since the model of Zhu et al. [5.90] appeared, other groups have also utilized similar models [5.92]. A more comprehensive analog of this model was, for example, recently presented and validated experimentally by Park [5.93], and by Lim et al. [5.94]. Zhu et al. [5.90] analyzed a tubular PVMR, in which the homogeneously catalyzed esterification reaction of acetic acid with ethanol to produce ethyl acetate and water took place. The reaction can be expressed generally as ... [Pg.209]


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