Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 3 de 3
Filtrer
Plus de filtres











Base de données
Gamme d'année
1.
J Environ Radioact ; 244-245: 106829, 2022 Apr.
Article de Anglais | MEDLINE | ID: mdl-35121277

RÉSUMÉ

In this study, two types of biosorbents were used to remove 137Cs and plutonium isotopes from aqueous solutions - moss (Ptilium crista - castrensis) and oak sawdust (Quercus robur), both in the form of natural and modified state. Sorbent modification significantly increases the sorbent surface area (for moss sorbents - from 4.0 to 47.2 m2/g, and for sawdust sorbents - from 1.1 to 26.3 m2/g), pore volume (from 10-3 to 10-2), concentration and amount of basic cations and anions, as well as active functional groups on the sorbent surface. The main functional groups on the surface of natural sorbents modified with iron hydroxide interacting with analytes are carboxyl and hydroxyl groups. For carbonized sawdust and its subsequent activation with concentrated HCl, in addition to carboxyl and hydroxyl groups, acetyl groups also become active. Carbonated sawdust treated with HCl showed the highest average removal efficiency and sorption capacity for radiocesium and plutonium isotopes in laboratory column experiments - for 137Cs ∼78.6% and ∼196.6 Bq/g and for 239+240Pu ∼83% and ∼41.5 Bq/g, respectively. The moss and moss modified with iron hydroxide also showed good properties of adsorbing plutonium isotopes in field (in-situ) experiments. The best results on the sorption of 137Cs in field experiments were shown by carbonated sawdust activated with HCl, and for isotopes of plutonium - the raw moss and moss modified with iron hydroxide. The results of the study showed that sorbents can be used not only for purification of water from plutonium isotopes but allow the operational sampling and more accurate measurement of radiocesium and plutonium isotopes in the fresh water reservoirs by the dynamic flow method.


Sujet(s)
Plutonium , Contrôle des radiations , Polluants radioactifs du sol , Polluants radioactifs de l'eau , Plutonium/analyse , Polluants radioactifs du sol/analyse , Eau , Polluants radioactifs de l'eau/analyse
2.
J Environ Radioact ; 177: 206-217, 2017 Oct.
Article de Anglais | MEDLINE | ID: mdl-28711772

RÉSUMÉ

A laboratory study of the formation of the primary vertical profile of the 137Cs activity concentration in the anaerobic organic matter-rich sediments was carried out. The incubation was performed using sediment baths method (initial thickness of the water layer over the sediments ∼40 cm, initial radiocesium activity concentration in water ∼14.53 Bq·L-1). An exponential profile (R2∼0.999) with the half-height width of ∼0.65 cm was formed after ∼32 days of the incubation. A further course of the experiment (sediments were sampled after 64, 130 and 293 days of the incubation) revealed deviations in the form of the radiocesium activity concentration profile related to the appearance of the additional Gauss factor with the increasing half-height width of ∼1.2, ∼1.3 and ∼3 cm, respectively. In spite of the evident growth of the half-height width, the radiocesium migration rate decreased from 0.02 cm·day-1 for the first 32 days of incubation down to 0.009 cm·day-1 at the end of the incubation experiment. Such a time-dependent decrease in the radiocesium migration is possibly related to the beginning of the second radiocesium migration phase depending on the retardation factor. Besides diffusion, the formation of vertical profiles of radiocesium activity concentrations in sediments was additionally induced by effects of buoyancy of the upper sediment layer due to the seepage of the above lying water into sediments.


Sujet(s)
Radio-isotopes du césium/analyse , Contrôle des radiations , Polluants radioactifs du sol/analyse , Accident nucléaire de Fukushima , Sédiments géologiques/composition chimique , Polluants radioactifs de l'eau/analyse
3.
J Environ Radioact ; 151 Pt 1: 166-173, 2016 Jan.
Article de Anglais | MEDLINE | ID: mdl-26476410

RÉSUMÉ

Fifty five soil samples collected in the Lithuania teritory in 2011 and 2012 were analyzed for (129)I, (137)Cs and Pu isotopes in order to investigate the level and distribution of artificial radioactivity in Lithuania. The activity and atomic ratio of (238)Pu/((239,24)0)Pu, (129)I/(127)I and (131)I/(137)Cs were used to identify the origin of these radionuclides. The (238)Pu/(239+240)Pu and (240)Pu/(239)Pu ratios in the soil samples analyzed varied in the range of 0.02-0.18 and 0.18-0.24, respectively, suggesting the global fallout as the major source of Pu in Lithuania. The values of 10(-9) to 10(-6) for (129)I/(127)I atomic ratio revealed that the source of (129)I in Lithuania is global fallout in most cases though several sampling sites shows a possible impact of reprocessing releases. Estimated (129)I/(131)I ratio in soil samples from the southern part of Lithuania shows negligible input of the Chernobyl fallout. No correlation of the (137)Cs and Pu isotopes with (129)I was observed, indicating their different sources terms. Results demonstrate uneven distribution of these radionuclides in the Lithuanian territory and several sources of contamination i.e. Chernobyl accident, reprocessing releases and global fallout.


Sujet(s)
Radio-isotopes du césium/analyse , Radio-isotopes de l'iode/analyse , Plutonium/analyse , Contrôle des radiations , Polluants radioactifs du sol/analyse , Lituanie
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE