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Concentration and temperature dependence on diffusivities of CO2 and N2 for poly(dimethyl, methylphenyl siloxane)

✍ Scribed by Praveen Jha; J. Douglas Way


Publisher
American Institute of Chemical Engineers
Year
2007
Tongue
English
Weight
323 KB
Volume
54
Category
Article
ISSN
0001-1541

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✦ Synopsis


Abstract

Experimental determination of solubility and diffusion coefficients of CO~2~ and N~2~ in poly(dimethyl, methylphenyl siloxane) (PMPS) for the pressure range 0–150 kPa and the temperature range of βˆ’10Β°C to 45Β°C is discussed. The absorption isotherms were measured by pressure decay equilibrium. Diffusion coefficients were determined by modeling the transient absorption data by Fickian diffusion. The value of solubility coefficient for CO~2~ at 35Β°C was 1.21 Β± 0.02 cm^3^ CO~2~ (STP)/(cm^3^ polymer.atm) and it increased to 2.07 Β± 0.01 cm^3^ CO~2~ (STP)/(cm^3^ polymer.atm) at 1Β°C. The absorption isotherms of CO~2~ obtained were linear for the pressure range 0–200 kPa and the enthalpy of sorption value was βˆ’10.82 kJ/mole for CO~2~. However, the diffusion coefficients of CO~2~ changed with feed pressure. The diffusion coefficient of CO~2~ in PMPS at 22Β°C and 128.6 kPa equilibrium pressure was 7.22 Γ— 10^βˆ’6^ cm^2^/s and thus the permeability value at these conditions was 1392 Barrers. The diffusion coefficients of CO~2~ at 0Β°C and equilibrium pressures of 125.8 kPa and 10.5 kPa were 5.72 Γ— 10^βˆ’6^ cm^2^/s and 4.31 Γ— 10^βˆ’6^ cm^2^/s, respectively. Consequently, the CO~2~ permeability in PMPS decreases by about 20% when the pressure is reduced from 125.8 to 10.5 kPa at 0Β°C. Β© 2007 American Institute of Chemical Engineers AIChE J, 2008


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