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          <dc:identifier>https://hdl.handle.net/2286/R.I.39444</dc:identifier>
                  <dc:rights>http://rightsstatements.org/vocab/InC/1.0/</dc:rights>
          <dc:rights>All Rights Reserved</dc:rights>
                  <dc:date>2016</dc:date>
                  <dc:format>viii, 53 pages : illustrations (some color)</dc:format>
                  <dc:type>Masters Thesis</dc:type>
          <dc:type>Academic theses</dc:type>
          <dc:type>Text</dc:type>
                  <dc:language>eng</dc:language>
                  <dc:contributor>Williams, Suzanne Jean</dc:contributor>
          <dc:contributor>Lin, Jerry Y.S.</dc:contributor>
          <dc:contributor>Emady, Heather</dc:contributor>
          <dc:contributor>Mu, Bin</dc:contributor>
          <dc:contributor>Arizona State University</dc:contributor>
                  <dc:description>Partial requirement for: M.S., Arizona State University, 2016</dc:description>
          <dc:description>Includes bibliographical references (pages 44-46)</dc:description>
          <dc:description>Field of study: Chemical engineering</dc:description>
          <dc:description>While the solution diffusion model and pore flow model dominate pervaporation transport mechanism modeling, a new model combining the solution diffusion and viscous flow models is validated using membranes with large scale defects exceeding 2 nm in diameter.  A range of membranes was characterized using scanning electron microscopy and x-ray diffraction (XRD) to determine quality and phase characteristics.  MFI zeolite membranes of He/SF6 pure gas permeation ideal selectivities of 25, 15, and 3 for good, medium, and poor quality membranes were subjected to liquid pervaporations with a 5% ethanol in water feed, by weight. Feed pressure was increased from 1 to 5 atm, to validate existence of viscous flow in the defects.  Component molar flux is modeled using the solution diffusion model and the viscous flow model, via J_i=F_i (γ_i x_i P_i^sat )+(ρ )/M_W   ∅/μ_ij  x_i P_h.  A negative coefficient of thermal expansion is observed as permeances drop as a function of temperature in all three membranes, where ϕ=((ϵr_p^2)/τ∆x).  Experimental parameter ϕ increased as a function of temperature, and increased with decreasing membrane quality.  This further proves that zeolitic pores are shrinking in one direction, and pulling intercrystalline voids larger, increasing the (ϵ/τ) ratio.  Permiabilities of the bad, medium, and good quality membrane also decreased over time for both ethanol and water, meaning that fundamental membrane characteristics changed as a function of temperature.  To conclude, the model reasonably fits empirical data reasonably well.</dc:description>
                  <dc:subject>Chemical Engineering</dc:subject>
          <dc:subject>pervaporation</dc:subject>
          <dc:subject>Zeolites</dc:subject>
          <dc:subject>Ethanol</dc:subject>
          <dc:subject>Membranes (Technology)</dc:subject>
                  <dc:title>Experimental and modeling study on pervaporation separation of ethanol and water mixture by polycrystalline MFI zeolite membranes</dc:title></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>
