0000000000082265
AUTHOR
P. Barret
Elucidation of reaction process between solid tricalcium silicate and a lanthanum salt solution in connection with the precipitation pH. Extension to other elements
Abstract Dissolution of tricalcium silicate is strongly accelerated in a La salt solution and releases the amounts of OH, Ca and silicate ions just required to precipitate all of lanthanum at pH 8. It remained to be proved that (1) La silicate hydrate could form at pH 8, and (2) Ca silicate hydrate could not precipitate simultaneously. The plot of silicate hydrate and hydroxide precipitation pH of La, Ca and other elements (Th, Zr) against the dropped volume of K2SiO3 and KOH solution and some physico-chemical characterization methods bring affirmative answers to these questions and allow the immobilization process of La and other elements in the presence of tricalcium silicate to be better…
Importance of the liquid to solid weight ratio in the powdered solid-liquid reactions Example drawn from cement constituent hydration
Abstract It seems justified to wonder if the chemical processes which have been evidenced from diluted stirred suspensions are or are not in accordance with those involved in a stagnant paste. The present paper is aimed at clarifying this question which is in connection with the problem of the so called ‘dormant period’ or ‘induction period’ at the beginning of the hydration of Portland cement.
Heterogeneous kinetics: from solid–gas reaction to solid–liquid dissolution
Abstract The extension of the formal kinetics of solid–gas reactions to solid–liquid dissolution is investigated theoretically. The work is based on modelling the dissolution of a solid in a closed system by a stoichiometrically simple chemical reaction A solid ⇄A liquid proceeding up to either an equilibrium state if the solid phase is initially in excess or exhaustion in the reverse situation. The initial amount of solid compared to the capacity of the liquid phase appears as a major factor of complexity. First, the rate equation is formulated in terms of the intensive variables without any assumption about the mechanism and the rate-limiting step. The resulting equations are compared to …