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- (425f) Process Intensification of a Non-Phosgene Route for Isocyanate Manufacture
McGhee et al have previously worked on a route to manufacture isocyanates from primary amine, carbon dioxide, a nitrogenous base and an electrophilic dehydrating agent. However, due to the generation of huge amount of salt of the dehydrating agent and the base and due to the absence of an appropriate recycling strategy this route could not be commercialized.
We present a modification to this route by eliminating the use of the nitrogenous base and hence reducing the salt formed. A recycling strategy is proposed with the goal of making the process commercially viable. A primary amine in presence of low concentrations of carbon dioxide is converted to their corresponding carbamate salt. In presence of a strong dehydrating agent like trifluoroacetic anhydride, the carbamate is converted to isocyanate and salt of the primary amine and trifluoroacetic acid. In excess of carbon dioxide, the zwitterion intermediate of the primary amine is formed which on reaction with a dehydrating agent forms isocyanate without any salt as byproduct. The theoretical isocyanate to amine ratio is 1:2 with the carbamate route and is 1:1 with the zwitterion route. Solubility of CO2 is high in polar solvents at very low temperatures and atmospheric pressure as well as at moderately high pressures and atmospheric temperatures. We have studied the effect of different solvents, dehydrating agents and varying temperature and pressures on the overall yield of isocyanates with the aim of maximizing the isocyanate content in the product mixture.
McGhee, W.D., Paster M.D., Riley D.P., Ruettimann K.W., Solodar J.A, Waldman T.E, U.S. Patent # 5,451,697, 1995