A mathematical model has been developed to describe the behavior of the nitroxide-mediated miniemulsion polymerization (NMMP) of styrene initiated by alkoxyamine initiators. The model includes mechanisms describing reactions in the aqueous and organic phases, particle nucleation, the entry and exit of oligomerie radicals, and the partitioning of nitroxide and styrene between the aqueous and organic phases. The influence of nitroxide partitioning on the polymerization kinetics was examined by modeling systems initiated by the alkoxyamines BST and hydroxyl-BST; BST and hydroxyl-BST are benzoylstyryl radicals terminated by the nitroxides TEMPO and 4-hydroxyl-TEMPO, respectively. Predicted monomer conversions, number average molecular weights and polydispersities were in agreement with experimentally measured values. Simulations and mathematical analysis showed that the rate of styrene NMMP is, not strongly influenced by the partitioning properties of TEMPO and 4-hydroxyl-TEMPO because of the complex interaction between reaction equilibrium, phase equilibrium, termination and thermal initiation. However, in the absence of styrene thermal initiation, nitroxide partitioning was found to have a significant influence on the polymerization kinetics. The model was also used to make quantitative estimates of. the population of active and dormant polymer radicals derived from both alkoxyamine initiators and thermal initiation; the population of dead polymer chains; and the number molecular weight distributions of living and dead polymer chains. (C) 2003 Elsevier Science Ltd. All rights reserved.