The inÑuence of latex morphology, composition and drying conditions on Ðlm formation and Ðlm properties is investigated for heterogeneous poly(acrylate) latex model systems. For blends of small latex particles water evaporation is the rate limiting process of Ðlm formation and the critical hard phase content reaches theoretical predictions. Upon increasing the size of the particles, their deformation becomes rate limiting which results in lower critical hard phase content, which signiÐcantly depends on Ðlm thickness. Film forming properties of blends are compared with that of heterogeneous lattices possessing di †erent morphology. According to conventional measurements of the minimum Ðlm forming temperature, core-shell lattices with a glassy (high shell are non-Ðlm forming. A more thorough investigation reveals signiÐcant di †erences T g ) depending on latex composition and even Ðlm formation. It is demonstrated that this Ðlm formation is rate limited by particle deformation. Electron microscopy, turbidity measurements, electromechanical testing and interferometrical thickness determination are used to investigate Ðlm densiÐcation and particle deformation. Solid state NMR spin di †usion measurements are applied to characterize morphological changes during Ðlm formation and interdi †usion.