2016 AIChE Spring Meeting and 12th Global Congress on Process Safety
(63af) Purification of Ibuprofen Enantiomers By a New Technique Combining Distillation and Crystallization
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. A thermodynamic model is developed in this work to simulate the three-phase equilibrium conditions during the SC operation. The experiments show that seeding with ultrasound mixing or magnetic stirring can be efficiently employed to purify S-ibuprofen from ibuprofen enantiomers. The experimental results, including the final enantiomeric purity and recovery ratio of S-ibuprofen, are consistent with the simulation results predicted by the model.
References:
1. Shiau, L. D.*, Wen, C. C. and Lin, B. S. “Separation and purification of p-xylene from the mixture of m-xylene and p-xylene by distillative freezing”, Ind. Eng. Chem. Res, 44(7), p2258-2265, 2005.
2. Shiau, L. D.*, Wen, C. C. and Lin, B. S. “Separation of p-xylene from the multicomponent xylene system by stripping crystallization”, AIChE Journal, 54(1), p337-342, 2008.
3. Shiau, L. D.*; Liu, K. F. ”Investigations into the effects of the cooling rate on stripping crystallization”, Ind. Eng. Chem. Res, 52, p1716-1722, 2013.