Time Dependence of Adsorption at Solid Liquid Interfaces*

نویسنده

  • Ivica Ružić
چکیده

In this paper the time dependence of adsorption at solid-Iiquid interface is discussed for both the mass-transport and intrinsic kinetic control of the adsorption process. It has been shown that the time dependence of adsorption of the mass-transport control' of the adsorption process is mostly dependent on the strength of adsorption (natur al diffusion) and sametimes on the mass-transport coefficient (dispersion coefficient in the case of eddies), which appear in natural environments). For the intrinsic kinetic control of adsorption several rate laws, are reviewed. Methods for the interpretation of adsorption experiments available in the literature are discussed. The possibility of distinguishing the mass-transport and kinetic control is mentioned. Simple models of a two-step adsorption process are described assuming the first step to be a very fast attachment of adsorbate from the homogeneous phase to the interface. It is concluded that for a correct interpretation of adsorption experiments the impression that adsorption is under equilibrium conditions should always be supported by the right shape of the adsorption isotherm. Otherwise additional experiments should be performed in a wider range of adsorption times.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Adsorption of Polylysine, Poly(glutamic) acid and their Block Copolymers on Polystyrene and on Carbon Nanotubes

A better understanding of protein behavior at solid-liquid interfaces is important to improve our knowledge of various natural and synthetic processes. A few examples where protein adsorption at a solid-liquid interface may play an important role are found in: blood coagulation, artificial kidney failure, biomedical microdevices, self-assembling microelectromechanical systems (MEMS), protein ba...

متن کامل

Atomic-Scale Simulation Study of Equilibrium Solute Adsorption at Alloy Solid-Liquid Interfaces

Equilibrium structural properties of solid-liquid interfaces in Cu-Ni alloys are studied by Monte-Carlo simulations employing interatomic potentials based on the embedded-atom method. We describe a thermodynamicintegration approach used to derive bulk concentrations and densities for solid and liquid phases in two-phase thermodynamic equilibrium. These results are used as a basis for constructi...

متن کامل

Irreversible adsorption of macromolecules at a liquid-solid interface: Theoretical studies of the effects of conformational change

The effects of particle conformational changes on the kinetics and saturation coverage of irreversible macromolecular adsorption at liquid-solid interfaces are investigated by computer simulation of a modified random sequential adsorption model. In this model, macromolecules (modeled as disks of diameter a,) adsorb onto a surface at a rate k, . Once adsorbed, the particles spread symmetrically ...

متن کامل

Adsorption of Nonspherical Particles at Solid/Liquid Interfaces

Localized adsorption of nonspherical particles at solid/liquid interfaces was analyzed theoretically. Aproximate models for calculating interactions between particles and interfaces as well as between particles were discussed. It was demonstrated that for convex particles the Derjaguin model can be used for small separations, whereas for larger separations the equivalent sphere approach proved ...

متن کامل

A theoretical approach for modeling reactivity at solid–liquid interfaces

We present a new general methodology capable of modeling chemical reactions at solid–liquid interfaces called CECILIA ~combined embedded cluster at the interface with liquid approach!. The main idea is to combine the embedded cluster molecular orbital or density functional methods for describing interactions at the surface of a solid with the dielectric continuum approach for modeling a liquid....

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2017