A mathematical model for a copolymer in an emulsion

作者：den Hollander F^*; Petrelis N

来源：Journal of Mathematical Chemistry, 2010, 48(1): 83-94.

DOI：10.1007/s10910-009-9564-y

• Random copolymer
• Random emulsion
• Localization
• Delocalization
• Phase transition
• Percolation

In this paper we review some recent results, obtained jointly with Stu Whittington, for a mathematical model describing a copolymer in an emulsion. The copolymer consists of hydrophobic and hydrophilic monomers, concatenated randomly with equal density. The emulsion consists of large blocks of oil and water, arranged in a percolation-type fashion. To make the model mathematically tractable, the copolymer is allowed to enter and exit a neighboring pair of blocks only at diagonally opposite corners. The energy of the copolymer in the emulsion is minus alpha times the number of hydrophobic monomers in oil minus beta times the number of hydrophilic monomers in water. Without loss of generality we may assume that the interaction parameters are restricted to the cone {(alpha, beta) is an element of R-2 : vertical bar beta vertical bar <= alpha}. We show that the phase diagram has two regimes: (1) in the supercritical regime where the oil blocks percolate, there is a single critical curve in the cone separating a localized and a delocalized phase; (2) in the subcritical regime where the oil blocks do not percolate, there are three critical curves in the cone separating two localized phases and two delocalized phases, and meeting at two tricritical points. The different phases are characterized by different behavior of the copolymer inside the four neighboring pairs of blocks.

• 出版日期2010-7