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Catalytic Dehydration of Isopropanol to Propylene

Journal

CATALYSTS
Volume 12, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/catal12101097

Keywords

isopropanol; propylene; acetone; diisopropyl ether; dehydration; process

Funding

  1. European Union [101037009]

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This article examines the selection criteria for isopropanol dehydration catalysts and analyzes the impact of process conditions and catalyst properties on propylene purity.
Catalytic dehydration of isopropanol to propylene is a common reaction in laboratories to characterize the acid-base properties of catalysts. When acetone is produced, it is the sign of the presence of basic active sites, while propylene is produced on the acid sites. About 2/3rd of the world production of isopropanol is made from propylene, and the other third is made from acetone hydrogenation. Since the surplus acetone available on the market is mainly a coproduct of phenol synthesis, variations in the demand for phenol affect the supply position of acetone and vice versa. High propylene price and low demand for acetone should revive the industrial interest in acetone conversion. In addition, there is an increasing interest in the production of acetone and isopropanol from CO/CO2 via expected more environmentally friendly biochemical conversion routes. To preserve phenol process economics, surplus acetone should be recycled to propylene via the acetone hydrogenation and isopropanol dehydration routes. Some critical impurities present in petrochemical propylene are avoided in the recycling process. In this review, the selection criteria for the isopropanol dehydration catalysts at commercial scale are derived from the patent literature and analyzed with academic literature. The choice of the process conditions, such as pressure, temperature and gas velocity, and the catalysts' properties such as pore size and acid-base behavior, are critical factors influencing the purity of propylene. Dehydration of isopropanol under pressure facilitates the downstream separation of products and the isolation of propylene to yield a high-purity polymer grade. However, it requires to operate at a higher temperature, which is a challenge for the catalyst's lifetime; whereas operation at near atmospheric pressure, and eventually in a diluted stream, is relevant for applications that would tolerate a lower propylene purity (chemical grade).

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