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Membrane and Desalination Technologies - TCE Moodle Website

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292 J. Paul Chen et al.<br />

Considering the membrane process as a binary system, the transport of solvent (e.g. water)<br />

<strong>and</strong> solute is involved. Designating solute <strong>and</strong> solvent by subscripts A <strong>and</strong> B, Eq. (5) can be<br />

written for solvent B as<br />

rm B ¼ RTr ln aBm þ vBrp: (6)<br />

Assuming vB is constant, integration over the membrane thickness yields<br />

Dm B ¼ vB<br />

RT<br />

D ln aBm þ Dp : (7)<br />

vB<br />

(D is defined here as “permeate side–feed side”.)<br />

Assuming further that thermodynamic equilibrium is established at the membrane–<br />

solution boundaries, aBm = aB, where aB is the activity of solvent (mol/m 3 ) outside of the<br />

membrane. This relationship should be valid on both sides of the membrane. Since the<br />

osmotic pressure, P (Pa), is defined as<br />

P ¼ RT<br />

ln aB; (8)<br />

Eq. (7) can be written as<br />

vB<br />

Dm B ¼ vBðDp DPÞ: (9)<br />

For practical purposes, the osmotic pressure of a feed may be estimated by van’t Hoff’s<br />

equation<br />

or for NaCl,<br />

P ¼ RðT þ 273Þ X Mi<br />

(10a)<br />

P ¼ 7;720ðT þ 273Þ X Mi; (10b)<br />

where T is the temperature ( C) <strong>and</strong> P Mi is the sum of molalities or molarities of ions <strong>and</strong><br />

non-ionic compounds (mol/kg or mol/L).<br />

As for solute A, we shall further assume that the activity coefficient remains constant, then<br />

Eq. (5) becomes<br />

rmA ¼ RTr ln aAm þ vArp<br />

¼ RTr ln cAm þ vArp;<br />

where aAm is the activity of solute in the membrane (mol/m 3 ), cAm is the concentration of<br />

solute in the membrane (mol/m 3 ) <strong>and</strong> v A is the molar volume of solute (m 3 /mol).<br />

Integration over the membrane thickness yields<br />

(11)<br />

Dm A ¼ RTD ln cAm þ vADp: (12)

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