On investigating the generation of microcellular polyurethane foam via reaction in carbon dioxide, we have observed that common polyurethane precursors are CO 2 miscible, whereas typically fluorinated compounds or specially designed surfactants are needed to solubilize polymers in CO 2 . Both isocyanates and polyols are CO 2 ‐miscible at workable pressures and temperatures and in useful concentrations to allow generation of polyurethane foams in CO 2 . By characterizing the phase behavior of several series of propylene oxide and ethylene oxide polyols, we have observed that the combined effects of molecular weight and hydroxyl number fix the location of the phase separation pressures. In general, lower molecular weights and lower hydroxyl mole fractions produce phase boundaries at relatively lower pressures in carbon dioxide. It also has been shown that CO 2 ‐soluble compounds may have a com̀patibilizing effect on less CO 2 ‐soluble materials.
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Parks et al. (1996) studied this question.
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