Abstract
Kinetics of Sr2+sorption from potable water on clinoptilolite tuffs (CLPT) of different deposits (Honguruu (Yakutia), Holinskoe (Transbaikalia) and white Plast (Bulgaria)) is studied in detail. A technique of X-ray fluorescence analysis (XRF) is developed to determine the chemical composition of CLPT from a small sample (0.05 – 0.1 g). The emitters are prepared by pressing 10-mm tablets from the initial material added with polystyrene as a binder in a weight ratio 5:1. Reference standards (reference standards of composition) of rocks close in chemical composition to the CLPT are used for calibration. Using the empirical model of α-correction, the equations are derived to calculate the content of macro components of the sample in the «saturated» layers. To calculate the strontium content in the «intermediate» layers for the CLPT from different deposits the correction equations are derived. It is shown that the correction equation can be the same for all the CLPT used in the experiment. Kinetics of Sr2+sorption on CLPT consists of 3 stages: (a) the intra-diffusion process, described by the coefficient of internal diffusion, (b) deceleration of the sorption process, described by the corresponding kinetic coefficient, and c) secondary increase in Sr2+sorption which terminates when the equilibrium is reached. The results can be used to develop a mathematical model describing the dynamics of the ion-exchange process on CLPT in NH4form from dilute solutions.
Highlights
Kinetics of Sr2+ sorption from potable water on clinoptilolite tuffs (CLPT) of different deposits (Honguruu (Yakutia), Holinskoe (Transbaikalia) and white Plast (Bulgaria)) is studied in detail
Reference standards of rocks close in chemical composition to the CLPT are used for calibration
It is shown that the correction equation can be the same for all the CLPT used in the experiment
Summary
Kinetics of Sr2+ sorption from potable water on clinoptilolite tuffs (CLPT) of different deposits (Honguruu (Yakutia), Holinskoe (Transbaikalia) and white Plast (Bulgaria)) is studied in detail. To calculate the strontium content in the “intermediate” layers for the CLPT from different deposits the correction equations are derived. Ìåòîäîì «òîíêîãî ñëîÿ» [2] ìû èçó÷èëè êèíåòèêó ñîðáöèè Sr2+ èç Ìîñêâîðåöêîé ïèòüåâîé âîäû íà ÊËÏÒ ðàçëè÷íûõ ìåñòîðîæäåíèé: Õîíãóðóó (ßêóòèÿ), Õîëèíñêîå (Çàáàéêàëüå) è Áåëûé Ïëàñò (Áîëãàðèÿ). Äëÿ ðàñøèðåíèÿ äèàïàçîíà îïðåäåëÿåìûõ ñîäåðæàíèé Sr áûëè òàêæå èñïîëüçîâàíû îáðàçöû, ïîëó÷åííûå ïóòåì äîáàâëåíèÿ îêñèäîâ ñòðîíöèÿ â ïðèðîäíûå ÑÎÑ.
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