“…They not only control the colloidal stability of the particles in the latex, but the type and architecture of the used surfactant also have a large influence on the physical and rheological properties of the latex and thus on the final application. − In most cases, surfactants are not covalently bound to the colloidal particles; therefore, surfactants can desorb over time. Furthermore, during film formation, surfactants can migrate from the colloidal particles toward the film surface and have a negative effect on film properties such as adhesion strength, peel strength, water resistance, gloss, and blocking. − To circumvent these negative effects, reactive surfactants that are chemically bound to the polymer particles can be used. − An ideal reactive surfactant should not be too reactive at the start of the emulsion polymerization, in order to avoid the chemically bound surfactant molecules from being buried inside the latex particles, but at the end of the emulsion polymerization, all surfactants should have reacted to obtain a stable latex. − Reactive surfactants containing a propenyl end-group are promising candidates displaying the right reactivity, and methacrylic oligomers containing these end-groups (called macromonomers in the remainder of this paper) are readily prepared via catalytic chain transfer polymerization (CCTP), , and their subsequent copolymerization behavior has been subscribed previously. − In earlier studies, amphiphilic macromonomers were synthesized and subsequently used as stabilizers in an emulsion polymerization. − In our earlier work, methacrylic acid (MAA) macromonomers were synthesized via CCTP and were used directly in an emulsion polymerization to form in situ amphiphilic copolymers, in a mechanism similar to what is commonly known as polymerization-induced self-assembly. − Only in the cases where the MAA macromonomers were sufficiently fast converted into amphiphilic copolymers, stable latexes could be produced. In another study, a two-step copolymerization of MAA macromonomers with methyl methacrylate (MMA) or butyl acrylate (BA) gave amphiphilic stabilizers suitable for the emulsion polymerization with MMA, albeit the rheology and physical properties of the systems were rather different .…”