AbstractFilms of polystyrene–polybutadiene–polystyrene (PS/PB/PS) triblock copolymer and polystyrene‐poly(ethylene/propylene) (PS/PEP) diblock copolymer were cast from toluene solutions subjected to hydrodynamic flow at room temperature using a device based on a novel casting method we term ‘roll‐casting.’ Polymer solutions were rolled between two corotating eccentric cylinders while at the same time the solvent was removed at a controlled rate. As the solvent evaporated, the block copolymers microphase separated into globallyorientedstructures. A discussion of the flow field that develops during roll‐casting is presented and specific attention is given to the importance of the shear and elongation rates present. For the triblock and diblock, respectively, the processed structures consisted of polystyrene cylinders assembled on a hexagonal lattice in a polybutadiene matrix, and unidirectional lamellae of alternating polystyrene and polyethylene/propylene. Small‐angle x‐ray scattering (SAXS) and transmission electron microscopy (TEM) indicated the near single‐crystal structure both types of films. SAXS also showed the styrene cylinders and the alternating lamellae to be packed closer together in roll‐cast films than in simple quiescently cast films. A molecular orientation mechanism is proposed to describe both these results as well as the changes in packing and in macroscopic sample dimensions measured after complete solvent evaporation and after sample annealing. © 199