Colloid particle adsorption at random site (heterogeneous) surfaces.
نویسندگان
چکیده
Irreversible adsorption of colloid particles and globular proteins at heterogeneous surfaces was studied theoretically. The substrate surface was created by covering a uniform surface by coupling sites (active centers) of a desired coverage. In contrast to previous studies concerned with disks, in our simulations the centers were modeled by spheres having a size smaller than that of the adsorbing particles. Adsorption was assumed to occur due to short-ranged attractive interactions if the colloid particle contacted the center. The Monte-Carlo-type simulations enabled one to determine the initial flux, adsorption kinetics, jamming coverage, and the structure of the particle monolayer as a function of the site coverage and the particle/site size ratio, denoted by lambda. It was revealed that the initial flux increased significantly with the site coverage theta(s) and the lambda parameter. This behavior was quantitatively interpreted in terms of the scaled particle theory. It also was demonstrated that particle adsorption kinetics and the jamming coverage increased significantly, at fixed site coverage, when the lambda parameter increased. Practically, for alpha=lambda(2)theta(s)>1 the jamming coverage at the heterogeneous surfaces attained the value pertinent to continuous surfaces. The results obtained prove unequivocally that the spherically shaped sites are much more effective in binding particles than the disk-shaped sites considered previously.
منابع مشابه
Deposition of latex particles at heterogeneous surfaces
Irreversible adsorption (deposition) of colloid particles at heterogeneous surfaces was studied experimentally. The substrate surfaces of desired heterogeneity were produced by covering mica surfaces by positively charged polystyrene latex particles. Then, deposition kinetics of negatively charged latex was studied under diffusion-controlled transport conditions. Particle distributions over sur...
متن کاملStreaming potential studies of colloid, polyelectrolyte and protein deposition.
Recent developments in the electrokinetic determination of particle, protein and polyelectrolyte monolayers at solid/electrolyte interfaces, are reviewed. Illustrative theoretical results characterizing particle transport to interfaces are presented, especially analytical formulae for the limiting flux under various deposition regimes and expressions for diffusion coefficients of various partic...
متن کاملIrreversible adsorption of particles at random-site surfaces.
Irreversible adsorption of negatively charged polystyrene latex particles (averaged diameter 0.9 microm) at heterogeneous surfaces was studied experimentally. The substrate bearing a controlled number of adsorption sites was produced by precovering mica sheets by positively charged polystyrene latex (averaged diameter of 0.45 microm). Positive latex (site) deposition was carried out under diffu...
متن کاملSurfactants with colloids: adsorption or absorption?
HYPOTHESIS The interaction of Aerosol OT (AOT) surfactant with systems of model colloids in nonaqueous solvents (water-in-oil microemulsions, surfactant-stabilized silica organosols, and sterically-stabilized PMMA latexes) is expected to be system specific. Two limiting cases are expected: adsorption, with surfactant located at the particle surfaces, or absorption, with surfactant incorporated ...
متن کاملThe adsorption and reaction of a titanate coupling reagent on the surfaces of different nanoparticles in supercritical CO2.
The adsorption and reaction in supercritical CO2 of the titanate coupling reagent NDZ-201 on the surfaces of seven metal oxide particles, SiO2, Al2O3, ZrO2, TiO2 (anatase), TiO2 (rutile), Fe2O3, and Fe3O4, was investigated. FTIR and TG analysis indicated that the adsorption and reaction were different on different particle surfaces. On SiO2 and Al2O3 particles, there was a chemical reaction of ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Journal of colloid and interface science
دوره 248 1 شماره
صفحات -
تاریخ انتشار 2002