Abstract
The potential for the metal organic framework (MOF) Cu-BTC to selectively adsorb and separate CO2 is considered. Isotherms for CO2, CH4, and N2 were measured from 0 to 15 bar and at temperatures between 25 and 105 °C. The isotherms suggest a much higher working capacity (×4) for CO2 adsorption on Cu-BTC relative to the benchmark zeolite 13X over the same pressure range. Higher CO2/N2 and CO2/CH4 selectivities in the higher pressure range (1−15 bar) and with lower heats of adsorption were also demonstrated. Cu-BTC was observed to be stable in O2 at 25 °C, but its crystallinity was reduced in humid environments. The CO2 adsorption capacity was progressively reduced upon cyclic exposure to water vapor at low relative humidity (<30%), but leveled out at 75% of its original value after several water adsorption/desorption cycles.
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