Abstract
The intrinsic kinetics of liquid phase catalytic dehydration of methanol to dimethyl ether over a macroporous sulphonic acid ion exchange resin was determined in a fixed-bed micro-reactor in the temperature range of 391–423 K and pressures up to 2.0 MPa. The kinetic model based on Eley–Rideal mechanism, as well as the power-rate law model, was adopted for fitting the experimental data. However, the Langmuir–Hinshelwood mechanism is not feasible for describing the dehydration reaction of methanol, as deduced from the macroscopic kinetic data and/or no dependence of methanol conversion on initial methanol concentration in the absence of water at the inlet using acetone as inert solvent. Moreover, an improved process consisting of the combination of a fixed-bed reactor and a catalytic distillation column for the synthesis of DME (Process A) was proposed, and a mathematical model was established, into which the intrinsic kinetics obtained in this work was incorporated. The comparison of operating performance among the improved process, Process B consisting of a fixed-bed reactor and two ordinary distillation columns, and Process C consisting of a catalytic distillation column and an ordinary distillation column was also made. It was found that the improved process is more promising than others in energy consumption, production capacity and column number under the same product purity, and is easy to be implemented based on Process B that is currently used in the actual industrial plants with a long catalyst lifetime.
Published Version
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