High Pressure Vapor-liquid Equilibria in the System Acetone-methanol-water


Book Description

"In the field of synthetic liquid fuels and organic chemicals there is considerable industrial interest in Fischer-Tropsch-type processes for the production of liquid hydrocarbons and various organic chemicals as by-products. Processes developed primarily for the production of oxygenated organic chemicals by partial oxidation of paraffin hydrocarbons are also in commercial operation. For both processes, recovery and purification of the product constituents by fractional distillation constitute a major problem. Of primary importance to solutions of the problem are the availability of reliable vapor-liquid equilibrium data on the various systems encountered. The need for suitable data is increased by the fact that practically all existing vapor-liquid equilibrium data are for atmospheric pressure only, whereas actual distillation operations are most frequently conducted at pressure above one atmosphere because of favorable economics, design, operations, and control requirements. It is obvious that reliable data at pressure other than one atmosphere and in particular, superatmospheric data are needed. More fundamentally important however, is the need for complete and extended data to evaluate and test the applicability of proposed correlations of the vapor-liquid data. Such extension and correlation involve the change of vapor-liquid equilibria with temperature or pressure, the determination of these data with a minimum of experimental effort, and the extension of binary data into reliable ternary data. Of the numerous oxygenated components produced by the aforementioned processes, acetone, methanol, and water constitute the major portion of the crude products. Binary and ternary systems containing these components have been evaluated and the results reported herein"--Leaves iii-iv



















Determination of Vapor-Liquid Equilibrium Data for the Methanol-Water System


Book Description

Methanol and water, at ordinary temperatures form a two-phase, two-component system, which according to the phase rule, can be completely described by two independent variables. For solutions of varying concentrations, either the boiling points at constant pressure, or the equilibrium-vapor pressures at constant temperature are useful for the study of the system. However, because the relationship of partial and total vapor pressure to composition at constant temperature can be checked theoretically by means of the equations discussed below, this is the criteria most often used for the study.