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Diffusion of water vapour through stagnant air

Short answer

Molar flux for stagnant diffusion: NA = (DAB P/(RT z)) ln[(P–pA2)/(P–pA1)] = (2.56e-5×101325/(8.314×298×0.15)) ln(101325/98155) = 2.22×10⁻⁴ mol/m²s. Tube area = π(0.01)²/4 = 7.854×10⁻⁵ m². Mass evaporated per hour = NA × area × M × 3600 = 2.22e-4 × 7.854e-5 × 18 × 3600 = 1.13×10⁻³ g/h = 1.13 mg/h.

Water at 25 °C evaporates in a vertical glass tube of internal diameter 10 mm. The water surface is 150 mm below the open top of the tube. Dry air at 1 atm (101 325 Pa) and 25 °C blows across the top so that the vapour concentration there is zero. The saturation pressure of water at 25 °C is 3.17 kPa and the diffusion coefficient of water vapour in air is 0.256 x 10^-4 m^2/s. Treating the air as stagnant, find the molar flux of water vapour and the mass evaporated per hour. (M of water = 18 kg/kmol.)

Model

Water vapour (A) diffuses upward through stagnant air (B). Air does not move, so NB=0N_B = 0 and there is a net bulk flow of the mixture (Stefan flow). For steady state, constant temperature and pressure:

NA=DABPRˉT z ln⁡P−pA2P−pA1N_A = \frac{D_{AB}P}{\bar R T\,z}\,\ln\frac{P-p_{A2}}{P-p_{A1}}

where zz is the diffusion length, pA1p_{A1} the vapour pressure at the water surface and pA2p_{A2} at the top.

Data

  • P=101 325P = 101\,325 Pa, T=298T = 298 K, z=0.15z = 0.15 m
  • pA1=3170p_{A1} = 3170 Pa (saturated at the water surface), pA2=0p_{A2} = 0 (dry air at top)
  • DAB=0.256×10−4D_{AB} = 0.256\times10^{-4} m2^2/s, Rˉ=8.314\bar R = 8.314 J/mol K
  • Ac=π(0.01)2/4=7.854×10−5A_c = \pi(0.01)^2/4 = 7.854\times10^{-5} m2^2

Molar flux

DABPRˉTz=0.256×10−4×101 3258.314×298×0.15=6.98×10−3 mol/m2sln⁡101 325−0101 325−3170=ln⁡(1.0323)=0.03178NA=6.98×10−3×0.03178=2.22×10−4 mol/m2s\begin{aligned} \frac{D_{AB}P}{\bar RTz} &= \frac{0.256\times10^{-4}\times101\,325}{8.314\times298\times0.15} = 6.98\times10^{-3}\ \text{mol/m}^2\text{s}\\ \ln\frac{101\,325-0}{101\,325-3170} &= \ln(1.0323) = 0.03178\\ N_A &= 6.98\times10^{-3}\times0.03178 = 2.22\times10^{-4}\ \text{mol/m}^2\text{s} \end{aligned}

That is 2.22×10−72.22\times10^{-7} kmol/m2^2s.

Evaporation rate

n˙=NAAc=2.2185×10−4×7.854×10−5=1.742×10−8 mol/sm˙=n˙×18 g/mol=3.14×10−7 g/s=3.14×10−7×3600=1.13×10−3 g/h=1.13 mg/h\begin{aligned} \dot n &= N_AA_c = 2.2185\times10^{-4}\times7.854\times10^{-5} = 1.742\times10^{-8}\ \text{mol/s}\\ \dot m &= \dot n\times18\ \text{g/mol} = 3.14\times10^{-7}\ \text{g/s}\\ &= 3.14\times10^{-7}\times3600 = 1.13\times10^{-3}\ \text{g/h} = 1.13\ \text{mg/h} \end{aligned}

Answer: NA≈2.22×10−4 mol/m2N_A \approx 2.22\times10^{-4}\ \text{mol/m}^2s; evaporation rate about 1.131.13 mg per hour.

✓ Answer checked by Claude Sonnet 5.5

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