Question 30.6: The “bubbleless” shell-and-tube membrane aeration system sho......

The “bubbleless” shell-and-tube membrane aeration system shown in Figure 30.13 is used to transfer oxygen gas (O_{2}) to liquid water. Water containing no dissolved oxygen is added to the tube side at the entrance at a bulk velocity of 50 cm/s. The inner diameter of the tube is 1.0 cm, and the tube wall thickness is 1.0 mm (0.10 cm). The tube wall is made of silicone, a polymer that is highly permeable to O2 gas but not to water vapor. Pure oxygen gas (100% O_{2}) is maintained at a constant pressure of 1.50 atm in the annular space surrounding the tube. The O_{2} gas partitions into silicone polymer, and then diffuses through the tube wall to reach the flowing water, as shown in Figure 30.13.

As the fluid flows down the length of the tube, the absorption of oxygen will increase the concentration of the dissolved oxygen. Determine the length of tubing necessary for the dissolved oxygen concentration to reach 30% of saturation with respect to the O_{2} gas. The process is maintained at 25 C. At 25 C, the Henry’s law constant for O_{2} gas dissolved in water is H = 0.78 atm m³/gmole, the molecular diffusion coefficient for dissolved O2 (A) in water (B) is D_{A B}=2.1\times10^{-5}\mathrm{~cm}^{2}/s, and the kinematic viscosity of water is \nu_{B}=9.12\times10^{-3}\;\mathrm{cm}^{2}/s. The solubility constant of O_{2} gas in the silicone polymer is S_{m} = 0.029\ atm ⋅ m^{3}-silicone/gmole, which is defined by the equilibrium relationship P_{A}=S_{m}/C_{A}^{\prime}. The effective diffusion coefficient of O_{2} in the silicone polymer is { D}_{A e}=5.0\times10^{-6}\mathrm{~cm}^{2}/s.^{27}

Figure 30.13
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The process analysis and solution strategy will require determination of the overall mass-transfer coefficient K_{L}, and the development of a model to predict the dissolved O_{2} concentration in the flowing water down the length of the tube. The flux of O_{2} from gas to the bulk flowing water is determined by two mass-transfer resistances in series, the diffusion of  O_{2} through the silicone tube wall, and the convective mass transfer of O_{2} to the flowing water inside the tube. If the overall mass-transfer flux is defined based on the liquid phase, then

N_{A}=K_{L}(c_{A L}^{*}-c_{A L})

where c_{A L}^{*}=P_{A}/H,\;\mathrm{and}\;K_{L} is the overall mass-transfer coefficient based on the liquid-phase driving force, defined by

{\frac{1}{K_{L}}}={\frac{1}{k_{L}}}+{\frac{1}{k_{m}}}        (30-40)

with

k_{m}={\frac{H\,D_{A\epsilon}}{S_{m}\,l_{m}}}      (30-41)

In equations (30-40) and (30-41), k_{L} is the convective mass-transfer coefficient for O_{2} mass transfer into the water flowing through the tube, and k_{m} is the membrane permeation coefficient, which describes the diffusion of O_{2} through the silicone tube wall of thickness \ell_{\mathrm{m}}, and includes solubility constant for partitioning of O_{2} gas into the silicone polymer (S_{m}), the effective diffusion coefficient of O_{2}  in the silicone polymer (D_{Ae}), and solubility constant for partitioning of O_{2} gas into the fluid (H). The derivation of equations (30-40) and (30-41), which ignore the radius of curvature of the tube, is left as an exercise for the reader.

To determine k_{L}, the Reynolds number (R_{e}) and Schmidt number (S_{c}) for flow inside the tube must first be estimated. The Reynolds number is

\mathrm{Re}={\frac{\mathrm{v}_{\mathrm{\infty }}\,D}{\nu_{L}}}={\frac{(50\,\mathrm{cm}/s)(1.0\,\mathrm{cm})}{(9.12\times10^{-3}\,\mathrm{cm}^{2}/s)}}=5482

and the Schmidt number (Sc) is

\mathrm{Sc}={\frac{\nu_{L}}{D_{A B}}}={\frac{9.12\times10^{-3}\,\mathrm{cm}^{2}/s}{2.1\times10^{-5}\,\mathrm{cm}^{2}/s}}=434

The process is considered to be in turbulent flow, since {\mathrm{Re}}\gt 2100. Therefore, it is necessary to use the Linton–Sherwood correlation for turbulent flow of liquid flowing inside of a tube, given by equation (30-18):

\mathrm{Sh}={\frac{k_{L}D}{D_{A B}}}=0.023\,\mathrm{Re}^{0.83}\mathrm{Sc}^{1/3}        (30-18)

\mathrm{Sh}=0.023\,\mathrm{Re}^{0.83}\,\mathrm{Sc}^{1/3}=0.023(5482)^{0.83}(434)^{1/3}=221

The convective mass transfer coefficient k_{L} is backed out from the Sherwood number

k_{L}=\frac{\mathrm{Sh}}{D}D_{A B}=\frac{221}{1.0\,\mathrm{cm}}2.1\times10^{-5}\,\mathrm{cm}^{2}/s=4.64\times10^{-3}\,\mathrm{cm}/\mathrm{s}

The membrane permeation constant is

k_{m}={\frac{H D_{A e}}{S_{m}l_{m}}}={\frac{(0.78\,\mathrm{atm}\cdot{\mathrm{m}}^{3}/\mathrm{gmole})(5.0\times10^{-6}\,{\mathrm{cm}}^{2}/{\mathrm{s}})}{(0.029\,\mathrm{atm}\cdot{\mathrm{m}}^{3}/\mathrm{gmole})(0.1\,{\mathrm{cm}})}}=1.35\times10^{-3}\,{\mathrm{cm}}/{\mathrm{s}}

And so, finally, K_{L} is

K_{L}=\frac{k_{L}k_{m}}{k_{L}+k_{m}}=\frac{\left(4.64\times10^{-3}\,\mathrm{cm/s}\right)\left(1.35\times10^{-3}\,\mathrm{cm/s}\right)}{\left(4.64\times10^{-3}\,\mathrm{cm/s}\right)+\left(1.35\times10^{-3}\,\mathrm{cm/s}\right)}=1.04\times10^{-3}\,\mathrm{cm/s}

As an aside, note that as km increases, K_{L} approaches k_{L} and the mass-transfer resistance offered by the membrane becomes small. Increasing k_{m} can be accomplished by decreasing the membrane thickness \ell_{m} or by using a membrane material with a lower S_{m}—i.e., a material that is more soluble for O_{2}.

A model to predict dissolved oxygen profile down the length of the tube requires a material balance for O_{2} on a differential volume element of the tube, as shown in Figure 30.13 and as stated below:

\left(\begin{array}{lccc} \text{rate of}\ O_{2}\ \text{carried by fluid} \\ \text{into control volume (IN)} \end{array} \right) +\left(\begin{array}{lccc} \text{mass transfer of}\ O_{2}\ \\ \text{into control volume (IN)} \end{array} \right) – \left(\begin{array}{lccc} \text{rate of}\ O_{2}\ \text{carried by fluid} \\ \text{into control volume (OUT)} \end{array} \right) + \left(\begin{array}{lccc} \text{rate of}\ O_{2}\ \text{generation within} \\ \text{volume element (GEN)} \end{array} \right) = \left(\begin{array}{lccc} \text{rate of}\ O_{2}\ \text{accumulation within} \\ \text{volume element (ACC)} \end{array} \right)

All terms are in units of moles O_{2}/time. The source for O_{2} mass transfer is the O_{2} gas, and the sink is the flowing water. The model development requires three primary assumptions: (1) the process is at steady state, (2) the concentration profile of interest is along the z-direction only and represents the local bulk concentration and fluid properties, (3) there is no reaction of O_{2} in the water, and (4) the process is dilute with respect to dissolved O_{2}. Under these assumptions, the differential material balance is

\frac{\pi D^{2}}{4}\mathrm{v}_{\infty }\ c_{A L}\bigg|_{z}+N_{A}\,\pi\,D\,\Delta z-\frac{\pi D^{2}}{4}\mathrm{v}_{\infty }\ c_{A L}\bigg|_{z+\Delta z}+0=0

Rearrangement yields

-\frac{\pi{D}^{2}}{4}{ v}_{\infty}\left(\frac{c_{A L}|_{z+\Delta z}-c_{A L}|_{z}}{\Delta z}\right)+K_{L}\,\pi\,{D}\left(c_{A L}^{*}-c_{A L}\right)=0

When Δz  → 0,

-\frac{dc_{AL}}{dz}+\frac{4K_L}{D_{v∞}}(c^*_{AL}\ -\ c_{AL}) = 0

At constant p_{A},\,c_{A L}^{*} is also constant, and so separation of dependent variable c_{AL} from independent variable z, followed by integration gives

\int_{c_{AL,o}}^{c_{A L}}\frac{-d c_{A L}}{c_{A L}^{*}-c_{A L}}=-\frac{4K_{L}}{v_{\infty }D}\int_{0}^{L}d{z}

or

\mathrm{ln}\biggl(\frac{c_{A L}^{*}-c_{A L,o}}{c_{A L}^{*}-c_{A L}}\biggr)=-\frac{4K_{L}L}{{\mathrm v_{\infty }}D}      (30-42)

\mathrm{For}\,p_{A}=1.5\;\mathrm{atm},

c_{A L}^{*}={\frac{p_{A}}{H}}={\frac{1.5\;\mathrm{atm}}{0.78\;\mathrm{atm}\cdot{\mathrm{m}}^{3}/\mathrm{gmole}}}=1.92\;\mathrm{gmole}\;\mathrm{O}_{2}/\mathrm{m}^{3}

and so at 30% of saturation c_{A L} at z=L is 0.3c_{A L}^{*}, or 0.577\ \mathrm{gmole}\ O_{2}/\mathrm{m^{3}}. Therefore, the required length L is

L={\frac{\mathrm{v_{\infty }}D}{4K_{L}}}\ln\left({\frac{c_{A L}^{*}-c_{A L,o}}{c_{A L}^{*}-c_{A L}}}\right)={\frac{(50\operatorname{cm/s})(1.0\operatorname{cm})}{4\cdot{\big(}1.04\times10^{-3}\operatorname{cm/s}\big)}}{\mathrm{ln}}\left({\frac{(1.92-0)\operatorname{gmole}/{\mathrm{m}}^{3}}{(1.92-0.577)\operatorname{gmole}/{\mathrm{m}}^{3}}}\right) = 4296\ cm

or 43 m. Rearrangement of equation (30-42) for the concentration profile gives

c_{A L}(z)=c_{A L}^{*}-\left(c_{A L}^{*}-c_{A L,o}\right)\mathrm{exp}\left(-{\frac{4K_{L Z}}{\mathrm{v}_{\infty D}}}\right)

Two plots of c_{A L}(z) are provided in Figure 30.14, one ending at 50 m, and the second ending at 500 m, to reveal the approach of c_{A L}(z)\ \mathrm{to}\ C_{A L}^{*}.

Figure 30.14

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