Comparative study of cesium adsorption on dioctahedral and trioctahedral smectites

Bentonites which are characterized by good rheological, mineralogical and chemical stability is considered used as sealing barriers in multibarrier Slovak system of deep geological repository for high-level radioactive waste and spent nuclear fuel. In Slovak Republic there are several significant deposits of bentonite, which are characterized by appropriate adsorption properties and meet the geotechnical requirements for this type of barriers. Study of adsorption properties of bentonites and other smectites is an essential step for developing the migration model long-lived corrosion and activation products, and fission products of uranium. Nuclear wastes contain the most important nuclear fission products, radioisotopes ¹³⁴Cs and ¹³⁷Cs. The present paper investigates and compares the cesium adsorption properties of Slovak and North America bentonites composed mainly of dioctahedral smectite montmorillonite (J, L, SAz-1 and STx-1) and trioctahedral smectites saponite (SapCa-2) and hectorite (SHCa-1).     

Effect of gamma-irradiation on adsorption properties of Slovak bentonites

One of the basic prerequisites for the use of bentonite as engineering barrier in deep geological repositories for radioactive waste and spent nuclear fuel is their stability against ionizing radiation stemming from radionuclides present in radioactive waste and spent nuclear fuel. The aim of this study was to compare the changes in the adsorption properties of selected Slovak bentonites in relation to uranium fission products (¹³⁷Cs and ⁹⁰Sr), prior to and after irradiation of bentonites with a ⁶⁰Co γ-source and specifying the changes in the structure of Slovak bentonites induced by γ-radiation. The changes in irradiated natural forms of Slovak bentonites and the changes in their natrified analogues and fractions with different grain sizes were studied from five Slovak deposits: Jelšovy potok, Kopernica, Lastovce, Lieskovec and Dolná Ves. The EPR spectra of bentonites from deposits Jelšovy potok and Lieskovec with absorbed doses of 10⁴ and 10⁵ Gy γ-rays showed no changes in the structure of the studied Slovak bentonites. The changes, which in terms of structure destabilization can be considered insignificant, occurred only in bentonites with absorbed doses of γ-radiation as much as 1 MGy. The absorbed dose of 1 MGy γ-radiation did not have an effect on the adsorption of cesium on every studied bentonite. Changes that can also be regarded as insignificant occurred only during strontium adsorption, especially on Fe–bentonite from deposit Lieskovec and Ca–Mg–bentonite from deposit Jelšovy potok, when an increase in the adsorption capacity occurred. Attention should be paid in further research of this topic which would require carrying out experiments on bentonite samples with absorbed doses higher by several orders of magnitude.     

Cesium sorption on bentonites and montmorillonite K10

The physical and chemical properties of illitic clay minerals from Slovak deposit suitable for application in engineering barriers for high level radioactive waste repositories and spent nuclear fuels were studied. The isolation of spent nuclear fuels and high level radioactive wastes from the outer environment in a deep repository is gained by means of a system of multiple engineering and natural sealing barriers. Vital segments in a multiple barrier system are clay rocks, of which bentonites represent the most suitable clay material. Cs-adsorption on fine fractions of adsorbents (bentonites from three Slovak deposits: Jelšovy potok J15, Kopernica K15, Lieskovec L15 and montmorillonite K10) has been studied with using batch of radiometric techniques. Adsorption parameters have been determined for adsorbent-cesium solution system as a function of contact time and adsorbate concentration. The influences of pH change, the effect of competitive cations, complex-forming organic chelating agents on the adsorption of Cs have also been studied.     

Utilization of Slovak bentonites in deposition of high-level radioactive waste and spent nuclear fuel

The basic strategic aims in the field of managing high-level radioactive waste and liquidation of nuclear power plants are all contained in the Energy policy of the Slovak Republic. Its aim is to resolve the concept of the backside of the nuclear energetics fuel cycle??long-term deposition of high-level radioactive waste and spent nuclear fuel (SNF). The most important form of high-level radioactive waste and SNF long-term deposition is their deposition in deep geological formations created by natural as well as engineering barriers used to isolate the long-lived radionuclides from the biosphere. The basic components of these barriers are clays, of which bentonite is generally referred to as the most suitable clay material. There are a few significant bentonite deposits in the Slovak Republic: Jel?ový potok, Kopernica, Lastovce, Lieskovec, Dolná Ves. The review article summarizes the information on geotechnical properties of Slovak bentonites published up-to-date, which is inevitable to know for the intention of their use. It highlights the advantages and shows drawbacks of five Slovak deposits. It suggests further research direction, to draw a thorough hydraulical, microbial and radiation profile of Slovak bentonites.     

Adsorption of cesium on domestic bentonites

Bentonite is a natural clay and one of the most promising candidates for use as a buffer material in the geological disposal systems for spent nuclear fuel and high-level nuclear waste. It is intended to isolate metal canisters with highly radioactive waste products from the surrounding rocks because of its ability to retard the movement of radionuclides by adsorption. Slovak Republic avails of many significant deposits of bentonites. Adsorption of Cs on five Slovak bentonites of deposits (Jelšovy potok, Kopernica, Lieskovec, Lastovce and Dolná Ves) has been studied with the use of batch technique. In the case of Dolná Ves deposit, the mixed-layer illite–smectite has been identified as the main clay component. Natural and irradiated samples, in two different kinds of grain size: 45 and 250 μm have been used in the experiments. The adsorptions of Cs on bentonite under various experimental conditions, such as contact time, adsorbent and adsorbate concentrations have been studied. The Cation Exchange Capacity values for particular deposits drop in the following order: Jelšovy potok > Kopernica > Lieskovec > Lastovce > Dolná Ves. Bentonites irradiated samples with 390 kGy have shown higher specific surface and higher values of the adsorption capacity. Distribution coefficients have been determined for bentonite-cesium solution system as a function of contact time and adsorbate and adsorbent concentration. The data have been interpreted in terms of Langmuir isotherm. The uptake of Cs has been rapid and the adsorption of cesium has increased with increasing metal concentrations. The adsorption percentage has decreased with increasing of metal concentrations. Adsorption of Cs has been suppressed by presence of Ca²⁺ more than Na⁺ cation. Sorption experiments carried out show that the most suitable materials intended for use as barriers surrounding a canister of spent nuclear fuel are bentonites of the Jelšovy potok and Kopernica deposits.     

First shrinkage parameters of Slovak bentonites considered for engineered barriers in the deep geological repository of high-level radioactive waste and spent nuclear fuel

The high potential of bentonites to volume changes depending on the water content is considered as their advantage for the engineered barriers in the deep geological repository of high-level radioactive waste and spent nuclear fuel because of swelling and self-healing of cracks in contact with water. On the other hand, drying may lead to opening of cracks and spaces between the bentonite blocks. This would increase the permeability and contamination risk around the hot container with high-level radioactive waste and spent nuclear fuel, especially if the host rock mass is dry. First shrinkage tests on four Slovak bentonites studied for engineered barriers were carried out. The water content at the shrinkage limit and the relative linear shrinkage are the first available shrinkage parameters received for the bentonite paste. The shrinkage hazard is higher in the best bentonites with high swelling potential—from Kopernica and Jel?ový potok. The results indicated the necessity of further shrinkage tests to determine the relative linear and volume shrinkage of bentonite elements pressed of the loose bentonite powder of low water content.     

Adsorption equilibrium and kinetic studies of strontium on Mg-bentonite, Fe-bentonite and illite/smectite

Radionuclide adsorption on clay rocks has in recent years been studied mainly in connection with their use as sealing barriers in nuclear waste and spent nuclear fuel repositories. In Slovakia we find deposits of bentonites which should be used for the above mentioned purpose. The usability of adsorbents in practical applications depends on the speed of the adsorption process of the adsorbate on the adsorbent surface and distribution ratio. The work objective was the study of the kinetics of Sr adsorption on clay adsorbents with different geological origin. The geological origin of bentonite significantly influences its mineralogical and chemical composition and therein its adsorption properties. The adsorption process of strontium was fast. Adsorption equilibrium was reached for all three samples studied within 1 min from the beginning of the contact between solid and liquid phases. After the adsorption equilibrium was reached there were no more changes in the values of distribution coefficients and the adsorption percentage, and comparable values were reached in the contact-phase time span studied within 10 days. The values of adsorbed strontium were decreasing in the following order: J250 > L250 > DV45. The pseudo second-order kinetic models was used to describe model the kinetic data and provided excellent kinetic data fitting (R ² > 0.999).     

Uncertainty of decay heat calculations originating from errors in the nuclear data and the yields of individual fission products

The calculation of the abundance pattern of the fission products with due account taken of feeding from the fission of²³⁵U,²³⁸U, and²³⁹Pu, from the decay of parent nuclei, from neutron capture, and from delayed-neutron emission is described. By means of the abundances and the average beta and gamma energies the decay heat in nuclear fuel is evaluated along with its error derived from the uncertainties of fission yields and nuclear properties of the individual fission products.     

Migration of radionuclides in the enviroment

The mechanisms of transport and retaidation processes, chemistry and migration behaviour of radionuclides of fission products and actinides in engineered barriers, especially bentonites, have been summarised. A “critical group of radionuclides” is proposed for thorough investigation of their retardation properties in natural sorbents. The evaluation of accessible data of retardation and transport parameters relevant for the conditions of underground deep repository to be projected is carried out from point of view their possible inclusion into a data-bank. The effect of solubilities and dissolution reactions, diffusion and sorption/desorption, complexation and variations in the aqueous phase composition, pH-value and oxidation-reduction properties and other phenomena on Kd values is discussed. Attention is devoted to thermodynamic modelling and its validation for evaluation of various phenomena in the buffer/backfill-ground water systems.     

Quality assessment of hydrosphere in the vicinity of Czech nuclear power plants by radioanalytical methods

Summary The paper deals with the impact of nuclear plants and radioactive waste disposal on surface and ground water quality in their vicinity using various radiometric and radioanalytical methods. The impact of nuclear power plant Temelin on activation concentrations and fission products in hydrosphere, including tritium, was detected. The annual average tritium concentrations in Vltava River correspond to the previously calculated estimates for average and minimal quaranteed flow rates. The concentrations histories of ⁹⁰Sr and ¹³⁷Cs in surface water show a decreasing trend. This trend was not influenced by the nuclear power plant pilot operation. In the case of tritium, a concentration increase trend has been already observed since the startup of pilot operation. An attempt has made interpreting the sorption and diffusion data for radionuclides of cesium, strontium and tritium and technetium as representatives of multivalent elements. Sorption and diffusion data of ¹³⁷Cs and ⁹⁰Sr in contact with natural sorbent bentonite lead to the conclusion that both diffusion and batch sorption experiments can be simulated by an exchange model. Sorption of technetium on various bentonites plus additives materials is described. Retention of technetium on these solid phases is driven by sorption of reduced form of technetium Tc(IV).     

Dating the age of a recent nuclear event by gamma-spectrometry

Summary The age of a recent, i.e., fresh, nuclear event can be determined by measuring the activity of short-lived parent and daughter fission products. The event studied was a short irradiation, of a small sample of uranium, in a nuclear reactor. Two clocks were investigated, ⁹²Sr-⁹²Y and ¹³⁵I-¹³⁵Xe. Measurements of the source by gamma-spectrometry yielded very good agreement between true and measured ages. The upper and lower age limits of applicability for the clocks in question were defined. The half-life of ⁹²Sr was found 2.635±0.008 hours and of ¹³⁵I 6.65±0.04 hours.     

The separation of99Tc from mixed fission products and its determination by neutron activation

Technetium is separated from the bulk of fission products and other elements in dissolved nuclear fuel by a ferric hydroxide precipitation followed by filtration and loading of the filtrate on an anion exchange resin. The technetium remains on the resin presumably as pertechnate ion. The resin is exposed to a neutron flux in a nuclear reactor activating⁹⁹Tc to¹⁰⁰Tc which decays with the emission of a 539keV gamma-ray with a 15.8 second half-life. This gamma-ray is conveniently counted with conventional solid state techniques.Work performed under contract to the U. S. Department of Energy under contract number DE-ACO7-76IDO1570.     

Adsorption of cesium and strontium on natrified bentonites

The influence of chemical activation–natrification of bentonites on adsorption of Cs and Sr was studied with regards to utilization of bentonites for depositing high-level radioactive waste and spent nuclear fuel. Bentonite samples from three Slovak deposits in three different grain-size (15, 45 and 250 μm), natural and natrified forms (Na-bentonites); under various experimental conditions, such as contact time, adsorbent and adsorbate concentration have been studied. When comparing the Na-bentonites and their natural analogues, the highest adsorbed Cs and Sr amounts were reached on the natrified samples. After the Sr adsorption a drop in the pH equilibrium value was observed together with the increase of the initial Sr concentration. A disadvantage of the natrified bentonite forms is formation of colloid particles. After 2 h of phase mixing a gentle turbidity was observed as well as formation of a gel-like form. The above findings were confirmed by observing the particle distribution in dry and wet dispersion and centrifugation at two different speeds. Natrification as a technological process of bentonite quality improvement cannot be applied when constructing a long-term repository for high-level radioactive waste and spent nuclear fuel. The main problem of natrification is a technological process which leads to a significant pH increase. Alkaline environment in combination with the K presence and increased temperature in the vicinity of radio-active waste can lead to a rapid illitization of smectite and loss of the original adsorption qualities. Moreover, sodium additions are a significant point of uncertainty since it is not possible to state what amount of Na enters the interlayer space and what amount stays in the inter-partition space.     

Nuclear decay studies of rare-earth fission-product nuclides using fast radiochemical separation techniques

A facility for the rapid radiochemical separation of individual rare-earth fission product nuclides from mixed fission products has been developed at the Idaho National Engineering Laboratory (INEL). This facility, called the INEL ESOL (elemental separation on-line) facility, includes an electroplated spontaneously fissioning²⁵²Cf source, a He jet transport system to deliver short half-life fission products from the²⁵²Cf hot cell to the radiochemistry laboratory, and a high pressure liquid chromatograph for the individual separation of rare-earth radioelemental fractions. The fission product collection and separation instrumentation is interfaced to a microprocessor that controls valves, motors and other devices and monitoring instrumentation. The data acquistion instrumentation can be controlled from a signal originating from the microprocessor or initiated manually. The results of some recent decay scheme studies on¹⁵³Pm and¹⁵⁴Pm are reported.     

Elemental analysis of biological tissues of Dmdmdx/J and C57BL/6J mice strains investigated by neutron activation analysis

Radioactivity measurement of short-lived nuclides is the basis of decay data measurement, which requires rapid separation and purification of the interested nuclides from complicated fission products. A rapid separation system based on SISAK and extraction chromatography technique was established to isolate ⁹⁵Y, which half-life is 10.3 min. With the best conditions studied in this paper, ⁹⁵Y was separated successfully from complicated fission products under the mini-reactor in the China Institute of Atomic Energy. Decontamination factors to other nuclides except ⁹⁴Y are higher than 2 × 10³.     

Determination of the 238U spontaneous fission decay constant without neutron irradiation

We have developed a methodology for measuring the decay constant of the spontaneous fission of ²³⁸U, l_f, using nuclear particle track detectors where thermal neutron irradiation is unnecessary. This methodology is based on the fact that the radiation damage caused by spontaneous fission of trans-uranium elements bearing a mass number close to 238 are similar to ²³⁸U spontaneous-fission ones. Loading a thick source of uranium (thickness greater than the fission fragment range) with a small amount of a suitable trans-uranium element (for instance, ²⁴²Pu, which presents a spontaneous fission half-life of 6.75^.10¹⁰ y), it is possible to determine the observation efficiency of a particle-track detector for fission fragments. Procedures concerning our thick source manufacture and uniformity tests of the trans-uranium distribution are also presented. These results make it possible for the exposure of thick uranium sources (without trans-uranium element) to lead to a l_f value.     

Adsorption of fission products onto soils using a fission multitracer

The adsorption behavior of fission products to various soils was studied using a multitracer. The multitracer was prepared by neutron irradiation of ²³⁵U. Distribution coefficients of fission products were obtained for seventeen kinds of Japanese soils. It was found that zirconium, niobium, and rare earth elements show high distribution coefficients for all soil samples, however, elements like alkali metals show varied values.     

Adsorption of fission products on a metal surface in nitric acid solutions: Radiochemical study using a multitracer

Adsorption behavior of fission products in nitric acid solution on various alloys and metals was studied by using a multitracer produced by neutron irradiation of UO₂. The adsorption behavior of the fission products ⁹⁹Mo, ¹³¹I, ¹³²Te, ¹⁴⁰La, and ¹⁴³Ce, and ²³⁹Np was simultaneously studied. Some chemical decontamination tests were also examined. Clear adsorption of ⁹⁹Mo, ¹³¹I, and ¹³²Te was observed, whereas adsorption of ¹⁴⁰La, ¹⁴³Ce, and ²³⁹Np was not. The adsorption characteristics were discussed by considering anion-exchange reaction and surface complexation.     

Xe-135 production from Cf-252

The presence of ¹³⁵Xe is often used as an indicator that fission has occurred, and is used to help enforce the Comprehensive Test Ban Treaty. There are no known commercial suppliers, though it can be acquired. Readily available standards of this isotope are very useful. ¹³⁵Xe can be produced through fission, or by neutron capture on ¹³⁴Xe. At the INL, scientists have previously transported fission products from an electroplated ²⁵²Cf thin source for the measurement of nuclear data of short-lived fission products using a technique called He-Jet collection. A similar system has been applied to the collection of gaseous ¹³⁵Xe, and ¹³³Xe, in order to produce standards of these isotopes.     

The role of NAA in nuclear chemistry education

One of the missions of our Institute is the promotion of basic nuclear teaching for students as well as professional teaching for workers in nuclear industry and research. For nuclear chemistry education, we present here a one day teaching course on radioactive decay and nuclear reactions, and a two or three days course based on reactor irradiation of uranium oxide, instrumental and radiochemical analysis of fission products. In the first experiment, the neutron capture is presented as an example of nuclear reaction; the neutron activation of a silver coin with a Am-Be neutron source, followed by γ-ray spectrometry, is used to identify three radionuclides of silver and to calculate their half-lives. In the second experiment, our teaching reactor is used as a neutron source with a flux about 10¹⁰ n·cm⁻²·s⁻¹ at a low thermal power (10 kW). This low flux allows us to irradiate a small uranium sample which is usable for spectrometry after a short cooling time of about two hours. The first day is reserved for instrumental analysis of the fission products and a second day for the radiochemical separation of a fission radionuclides. With these experimental results, the students have to calculate the number of fissions in the irradiated sample. On optional third day for postgraduate students is devoted to the presentation of NAA and some applications as uranium determination by the fission product spectrometry.