The adsorption of nonionic surfactants of the alkyl-phenol-poly(ethylene oxide) family and of acrylic latex particles on several anhydrous (but hydrating) or fully hydrated mineral phases of Portland cement was studied. No or negligible adsorption of the surfactant was observed. This was assigned to the ionized character of the surface silanol groups in calcium-silicate-hydrates and to the strongly ionic character of the OH groups in calcium hydroxide and in the calcium-sulfoaluminate-hydrates, which prevents the formation of surface-ethoxy hydrogen bonds. In contrast, provided they are property stabilized by the surfactant, the latex particles form a loose monolayer on the surface Of hydrating tricalcium silicate particles. The attractive interaction between the positive mineral Surface and the negative latex surface appears to be the driving force for adsorption. In line with this, adsorption is reduced by sulfate anions, which adsorb specifically onto the silicate surface. Compared to tricalcium silicate, portlandite and gypsum interact only marginally with the latex particles. Our results show that the stability of the nonionic surfactant/latex/cement systems is essentially controlled by the latex colloidal stability and the latex-cement interactions, the surfactant having little direct interaction, if any, with the mineral surfaces. (C) 2004 Elsevier Inc. All rights reserved.