Search results for "lcsh:Physical and theoretical chemistry"
showing 6 items of 6 documents
Fast Measurements of Adsorption on Porous Materials Using Jäntti's Method
1999
In 1972, Jäntti et al. formulated a method to shorten the time taken for adsorption measurements. We suggested at the Kiev International Conference on Vacuum Microbalance Techniques (1999) that the applicability of this method could be widened by considering a number of parallel adsorptions. There is, however, a more complicated but perhaps more interesting variant possible when extra mass transport is considered to occur in series. Such an application could involve adsorption within a porous structure where diffusion must be considered as a process occurring in series with adsorption on the surface.
Extension of the Applicability of Jäntti's Method to the Fast Calculation of Desorption Data
2000
The time for sorption measurements may be reduced substantially by measuring several values at short time intervals at the beginning of a kinetic curve and extrapolating them to the equilibrium value. The method used by Jäntti for simple adsorption processes has been extended to complicated processes described by a second-order differential equation. A simulated example is provided.
Some factors affecting the removal of lead(II) ions from aqueous solution by porous hydroxyapatite: relationships between surface and adsorption prop…
2006
A porous hydroxyapatite (p-HAp) was prepared and employed for the removal of lead(II) ions at different concentrations from aqueous solution to determine the adsorption properties of p-HAp and compare them with those of a commercial hydroxyapatite (CAp) sample. The kinetic data obtained indicated that the adsorption performances of the adsorbents depended both on their specific surface area and crystallinity. Complexation of the Pb(II) ion on the adsorbent surface favoured the dissolution of hydroxyapatites characterized by a Ca/Pb molar ratio in the 0.85–1.5 range. The maximum adsorption capacity of p-Hap for Pb(II) ions at 30 ± 2°C was 2.30 mmol/g relative to 1.38 mmol/g for the commercia…
The influence of the solvent's mass on the location of the dividing surface for a model Hamiltonian
2019
The Transition State dividing surface is a key concept, not only for the precise calculation of the rate constant of a reaction, but also for the proper prediction of product ratios. The correct location of this surface is defined by the requirement that reactive trajectories do not recross it. In the case of reactions in solution the solvent plays an important role in the location of the dividing surface. In this paper we show with the aid of a model Hamiltonian that the effective mass of the solvent can dramatically change the location of the dividing surface. Keywords: Dynamical systems, Dividing surface, Reactions in solution, 2019 MSC: 00-01, 99-00
t-Curves for n-Hexane
1992
The adsorption and desorption isotherms of n-hexane on powdered alumina and silica have been studied at 25°C over a wide range of relative pressures. Two t-curves for pore structure analysis are proposed, one for alumina (C = 12) and the second for silica (3 ≤ C ≤ 9). The statistical thickness t of the adsorbed n-hexane layer has been drawn as a function of the relative pressure assuming a maximal thickness of 0.55 nm and a mean thickness of 0.42 nm for the monolayer. The results are discussed in relation to previous published data.
The Jäntti approach to adsorption with increasing gas pressure
2002
Jäntti introduced a method of calculating equilibrium adsorption from measurements where the pressure of the gas was varied in a stepwise manner. His aim was to shorten the time necessary for a given measurement. The method was applied to gas/solid systems in which simple adsorption processes occurred and where the number of adsorption sites was infinite. The present paper discusses the case where no adsorption is possible on an already occupied site (Langmuir isotherm) while the number of positions available for adsorption is considered limited. The advantages of using a gas pressure that increases linearly with time are evident for studies with this limitation. It is shown that such meas…