2016 AIChE Annual Meeting
(449u) Seeding Effect on the Purification of Enantiomers By a New Technique Combining Distillation and Crystallization
Author
Ibuprofen, also called 2-(isobutylphenyl)-propionic acid, is a non-steroidal anti-inflammatory drug widely used to treat headaches and minor pains. Although it is known that S-ibuprofen is responsible for the anti-inflammatory effects while R-ibuprofen might cause some long-term side effects, ibuprofen is still sold as a racemic mixture in the market due to the complexity involved in the separation of enantiomers. The experiments show that subcooling of the liquid ibuprofen mixture is observed during the temperature-decreasing process. Ultrasound mixing or magnetic stirring only slightly reduces subcooling. However, once crystallization is induced in the subcooled liquid mixture, crystals are formed abruptly, leading to a product with a lower purity. Due to the structure similarity between S-ibuprofen and R-ibuprofen, R-ibuprofen might be incorporated into the S-ibuprofen crystal lattice when S-ibuprofen crystals are formed abruptly. Therefore, the ibuprofen mixture can not be further purified by SC without seeding.
Subcooling can be nearly eliminated by seeding with ultrasound mixing or magnetic stirring during the temperature-decreasing process. Subsequently, crystals are gradually formed preferentially on the seeds, leading to a product with a higher purity. Thus, seeding with ultrasound mixing or magnetic stirring can be applied to further purify the ibuprofen mixture. As magnetic stirring helps to uniformly disperse the seeds, seeding with magnetic stirring leads to a product with a higher purity compared to seeding with ultrasound mixing.
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Keywords: crystallization; vaporization; purification; thermodynamics process; ibuprofen