Systematic investigation of the effects of temperature and pressure on gas transport through polyurethane/poly(methylmethacrylate) phase-separated blends

• Published in: Journal of membrane science 2008-03, Vol.310 (1), p.129-140
• Main Authors: de Sales, J.A., Patrício, P.S.O., Machado, J.C., Silva, G.G., Windmöller, D.
• Format: Article
• Language: English
• Subjects: Gas separation; Polymer blend; Positron; Pressure; Temperature
• ISSN: 0376-7388; 1873-3123
• DOI: 10.1016/j.memsci.2007.10.045

Polyurethane (PU) and polyurethane–poly(methylmethacrylate) (PMMA) blend membranes were used in gas separation studies. The effects of blend composition, temperature, and pressure on the permeability, diffusivity, and solubility of CO 2, H 2, O 2, CH 4, and N 2 were investigated. The separation factors of some gas pairs were also evaluated. Positron annihilation lifetime spectroscopy was applied to assess free volume changes as a function of blend composition and temperature. Free volume size increases by approximately 30% with increasing temperature from 10 to 40 °C for all blends studied. The permeability of all gases decreases by approximately 55% with the addition of 30 wt% of PMMA. The permeation process is governed by diffusion, except that of CO 2. In relation to the behavior of gas transport as a function of temperature, some important observations are (i) CO 2 presents the lowest permeation activation energy value (28 kJ/mol), and (ii) gas pair selectivity increases at low temperatures and is high for gas pairs that present differences in permeation activation energies as high as 15 kJ/mol for the CO 2/CH 4 gas pair. Furthermore, the study with pressure variations shows that: (i) at elevated pressure, the PU and the blend membrane permeability to CO 2 and H 2 increases by approximately 35%, and (ii) oxygen-to-nitrogen selectivity increases with pressure as a consequence of the decrease in the permeability to nitrogen in the case of the 30%-PMMA blend.