Thermochemistry of ion exchange and particle interaction in clay suspensions

1982 ◽  
Vol 60 (4) ◽  
pp. 486-494 ◽  
Author(s):  
Laurier L. Schramm ◽  
Jan C. T. Kwak

The measurement of enthalpies of ion exchange for a number of homovalent and heterovalent exchange pairs by titration calorimetry is described. A self-consistent addition to previous measurements on such systems is reported. In addition to the enthalpies of ion exchange the heats of tactoid formation and breakdown were observed. The apparent heat of tactoid formation for the Na–Ca exchange pair is estimated to be −4.9 kJ per equivalent of ion exchange.


1992 ◽  
Vol 47 (2) ◽  
pp. 235-248 ◽  
Author(s):  
V. L. Krasovsky

The propagation of a Langmuir wave with a small group of trapped particles in a weakly non-uniform plasma along a density gradient is considered. The dynamics of trapped electrons accelerated by the wave is investigated in the adiabatic approximation, including the relativistic case. The set of equations describing the self-consistent spatial evolution of the wave—trapped-particles system is obtained and analysed. It is shown that the possibility exists of wave transmission through a classically forbidden barrier as a consequence of the reversibility of the wave—particle interaction. The conditions of validity of the theory developed are also discussed.





1981 ◽  
Vol 59 (20) ◽  
pp. 2927-2933 ◽  
Author(s):  
Gavin J. Ewin ◽  
Brian P. Erno ◽  
Loren G. Hepler

We have built a titration calorimeter that is suitable for measurements on colloidal suspensions as well as more conventional chemical reactions in solution. This calorimeter has been used for investigation of a number of ion exchange reactions involving kaolinite and montmorillonite clays. Results of these measurements have led to cation exchange capacities, to enthalpies of ion exchange reactions, and also to equilibrium constants for some of these same reactions. These calorimetrically determined cation exchange capacities and equilibrium constants agree well with corresponding quantities obtained by way of conventional methods based on chemical analyses. It has been demonstrated that titration calorimetry is a useful and convenient method for investigation of ion exchange in clays.



2021 ◽  
Vol 333 ◽  
pp. 15001
Author(s):  
Joao Simoes-Cardoso ◽  
Nanako Hoshino ◽  
Noriko Yoshimoto ◽  
Shuichi Yamamoto

Ion exchange chromatography is a widely used method for purification of all types of biomolecules in current biotechnological downstream processes. Knowledge on the binding behavior of proteins provides valuable insight for understanding the molecular mechanisms of protein interactions in a biological context. However, thermodynamic parameters such as enthalpy and entropy changes that characterize protein adsorption are still unknown. Isothermal titration calorimetry applications in biosciences has gained its merit to study binding of soluble molecules, protein inhibition, conformational changes, reaction kinetics, and protein adsorption. However, in the case of protein adsorption, a lot of complications arise since the usual models used to study protein interactions in solution are no longer valid. This work explains a detailed methodology for the obtention of adsorption enthalpy, entropy and Gibbs energy of protein adsorption, by using ITC together with equilibrium adsorption isotherms.



1998 ◽  
Vol 111 (1-3) ◽  
pp. 133-149 ◽  
Author(s):  
S.D. Pinches ◽  
L.C. Appel ◽  
J. Candy ◽  
S.E. Sharapov ◽  
H.L. Berk ◽  
...  


2010 ◽  
Vol 25 (21n23) ◽  
pp. 2012-2013
Author(s):  
FUTOSHI MINATO ◽  
CHUNLIN BAI

β-decay half-lives around 78 Ni and 132 Sn are studied with proton-neutron Quasiparticle Random Phase Approximation on the basis of Skyrme-Hartree-Fock (SHF) method. We take into account tensor force correlation in calculating the ground and excited states and find it improves the half-life of 132 Sn . However, the Q value is still underestimated. We also discuss that half-lives do not strongly depend on type of particle-particle interaction in isospin T = 0 channel.



Soil Science ◽  
1967 ◽  
Vol 104 (2) ◽  
pp. 134-137 ◽  
Author(s):  
ROBERT VAN BLADEL ◽  
HENRI LAUDELOUT


Sign in / Sign up

Export Citation Format

Share Document