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Copolymers of acrylamide and styrene with two distinct structures were synthesized to study the effect of polymer structure on protein partitioning in two-phase aqueous systems. Micellar copolymerization was used to prepare a multiblock copolymer, while homogeneous copolymerization was used to prepare a random copolymer, both with the same composition and molecular weight. Phase behavior studies of the copolymers with poly(ethylene glycol) in water showed little difference in the phase boundaries. However, the partitioning of bovine serum albumin between the two aqueous phases was sensitive to the polymer structure. A molecular picture is proposed for the interactions between the protein and block copolymers. The effect of pH on the protein partition is analyzed in terms of the hydrophobic interactions, and the polymer and protein partitioning was correlated using a model based on the Flory-Huggins theory.

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Diffusion and reactions in a porous pellet are treated as transient, nonisothermal, nonisobaric processes. Continuity and energy balance equations are solved simultaneously for temperature and concentration profiles in the pellet. Conductive, convective as well as radiative heat transfer are included. The ‘dusty gas’ flux model is used to describe the transport of diffusing gases. Viscous, bulk and concentration gradient terms have been included. Structural changes with reaction are accounted by considering the effect of changing grain radius on porosity and pore diameter. The model predictions match conversion trends for carbon gasification over a temperature range of 800 to 1100°C investigated experimentally.