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Selecting polymers for two‐phase partitioning bioreactors ( TPPB s): Consideration of thermodynamic affinity, crystallinity, and glass transition temperature
Author(s) -
Bacon Stuart L.,
Peterson Eric C.,
Daugulis Andrew J.,
Parent J. Scott
Publication year - 2015
Publication title -
biotechnology progress
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.572
H-Index - 129
eISSN - 1520-6033
pISSN - 8756-7938
DOI - 10.1002/btpr.2148
Subject(s) - crystallinity , polymer , amorphous solid , glass transition , dissolution , chemical engineering , partition coefficient , materials science , phase (matter) , thermodynamics , chemistry , organic chemistry , composite material , physics , engineering
Two‐phase partitioning bioreactor technology involves the use of a secondary immiscible phase to lower the concentration of cytotoxic solutes in the fermentation broth to subinhibitory levels. Although polymeric absorbents have attracted recent interest due to their low cost and biocompatibility, material selection requires the consideration of properties beyond those of small molecule absorbents (i.e., immiscible organic solvents). These include a polymer's (1) thermodynamic affinity for the target compound, (2) degree of crystallinity (w c ), and (3) glass transition temperature (T g ). We have examined the capability of three thermodynamic models to predict the partition coefficient (PC) for n‐butyric acid, a fermentation product, in 15 polymers. Whereas PC predictions for amorphous materials had an average absolute deviation (AAD) of ≥16%, predictions for semicrystalline polymers were less accurate (AAD ≥ 30%). Prediction errors were associated with uncertainties in determining the degree of crystallinity within a polymer and the effect of absorbed water on n‐butyric acid partitioning. Further complications were found to arise for semicrystalline polymers, wherein strongly interacting solutes increased the polymer's absorptive capacity by actually dissolving the crystalline fraction. Finally, we determined that diffusion limitations may occur for polymers operating near their T g , and that the T g can be reduced by plasticization by water and/or solute. This study has demonstrated the impact of basic material properties that affects the performance of polymers as sequestering phases in TPPBs, and reflects the additional complexity of polymers that must be taken into account in material selection. © 2015 American Institute of Chemical Engineers Biotechnol. Prog. , 31:1500–1507, 2015