Factors influencing the increased 90Sr radioisotope migration in highly alkaline groundwater at Chornobyl NPP site.

This paper analyses the formation of high Sr2+ concentration in strong alkaline (pH = 9.5-12.5) groundwater using data of the 27 years of observations around the destroyed Chernobyl NPP Unit 4. It appears that the formation of strong alkaline groundwater in different monitoring wells is consistent with the distribution of 90Sr, pH and main ions. The reason for the increase in 90Sr concentrations is the process of its migration from the sources of contamination - leaks of highly active water localized in certain premises inside the «Shelter ¼ object. These computational experiments showed that for the groundwater in pH range 9.5-12.4, the concentration of strontium in the form of SrOH + increases and in the form of Sr2+ - decreases. In addition, the fraction of 90Sr in the form of a soluble neutral complex compound SrCO30, which is not sorbed, reaches 14-35%. Increased fractions of 90Sr in forms of SrOH+ and SrCO3 are factors which reduce the isotope ability to be sorbed by soils and therefore increase its migration ability. In strongly alkaline groundwater a sharp increase in 90Sr volumetric activity may also be caused by ionic strength (IS) increase above 5 mmol/L. Thus, the factors that influence the increase in 90Sr volumetric activity in strongly alkaline groundwater are the formation of its complex compounds and an increase in ionic strength (IS), which reduces the thickness of the double electric layer and, as a result, reduces the sorption capacity of soils.

Simultaneous removal of caesium and strontium using different removal mechanisms of probiotic bacteria.

When radioactive materials are released into the environment due to nuclear power plant accidents, they may enter into the body, and exposing it to internal radiation for long periods of time. Although several agents have been developed that help excrete radioactive elements from the digestive tract, only one type of radioactive element can be removed using a single agent. Therefore, we considered the simultaneous removal of caesium (Cs) and strontium (Sr) by utilising the multiple metal removal mechanisms of probiotic bacteria. In this study, the Cs and Sr removal capacities of lactobacilli and bifidobacteria were investigated. Observation using an electron probe micro analyser suggested that Cs was accumulated within the bacterial cells. Since Sr was removed non metabolically, it is likely that it was removed by a mechanism different from that of Cs. The amount of Cs and Sr that the cells could simultaneously retain decreased when compared to that for each element alone, but some strains showed only a slight reduction in removal. For example, Bifidobacterium adolescentis JCM1275 could simultaneously retain 55.7 mg-Cs/g-dry cell and 8.1 mg-Sr/g-dry cell. These results demonstrated the potentials of utilizing complex biological system in simultaneous removal of multiple metal species.

Migration mechanisms of 90Sr and 137Cs on terraces.

In order to investigate the impact of environmental conditions on the distribution and migration of 90Sr in the Longji terrace environment, the activity concentrations of 90Sr and 137Cs were determined. The activity concentration ranges of 90Sr and 137Cs in surface soil were 0.15-1.04 Bq/kg and 2.16-6.94 Bq/kg, respectively. These results showed that there was a similar trend between the activity concentration of 90Sr and 137Cs in the surface soil along the runoff path and their activity concentration were influenced by the slope of the terraced terrain. On the other hand, the activity ranges of 90Sr and 137Cs in soil cores were 0.01-2.74 Bq/kg and 0.43-7.19 Bq/kg, respectively. These results indicate that the migration mechanism of 90Sr is different from that of 137Cs. As compared with 137Cs, 90Sr is significantly influenced by the moisture content. In addition, high span of 137Cs/90Sr activity ratios were found in this study, which were attributed to the characteristics of cultivated land and frequent artificial disturbances that intensified the migration of 90Sr.

Processing biological samples from simulated radiological terrorist events using Rapid DNA instruments.

Two commercially available portable Rapid DNA instruments were evaluated for their ability to process 1 µL and 10 µL saliva samples deposited on metal and plastic surfaces and contaminated with surrogates of cesium (Cs)-137, strontium (Sr)-90 and cobalt (Co)-60; radioactive materials potentially released during a nuclear weapon accident or a radiological dispersal device detonation. A comparable success rate was noted for both Rapid DNA instruments when considering the number of complete and balanced DNA profiles, the number of profiles with a minimum of 10 autosomal STR loci (out of 23 [FlexPlex™ 27] or 21 [GlobalFiler™ Express]), and the possibility to search a national DNA database in Canada and the United States. Cobalt had an adverse impact on the quality of the megaplex short tandem repeat (STR) DNA profiles derived on each instrument for two of the three contamination levels tested in this study, i.e., 0.05 M and 0.1 M as reflected by a reduced number of detected alleles and decreased profile peak heights. Strontium exhibited some adverse effect on the Rapid DNA results when used at the highest contamination level (0.1 M) whereas cesium had none. No new artifacts were observed in the Rapid DNA profiles of samples spiked with the non-radiogenic surrogates. Importantly, in the context of a radiological/nuclear (RN) event, the ANDE™ 6C offers the possibility to dispose of all radioactive materials associated with contaminated samples quickly using a chip on which all steps of the Rapid DNA process are performed whereas the RapidHIT™ ID accumulates radioactive materials for many days before disposal. An individual handling 25 samples in a week (5 per day) on the RapidHIT™ ID at a 30.5 cm distance with a 5 min exposure to the radioactive source estimated at every run would exceed the 0.042 µSv/5 min limit with gamma dose rates for Cs at 0.13 mSv and for Co at 3.8 mSv. Beta dose rates calculated for the surrogate isotopes at the three concentrations tested were also above the recommended radiation exposure limit of 1 mSv/yr (0.042 µSv/5 min). Various potential mechanisms of action behind the interference noted for Sr and Co at high concentrations are presented. These elements may play a role in the steps prior to PCR (at the DNA molecule by binding to bases or to phosphate groups), during PCR (at the DNA polymerase as cofactors for catalytic sites), or even during amplified DNA fragment detection (as fluorescence quenchers).

TIME PATTERN OF RADIONUCLIDE EMISSIONS AND DISCHARGES INTO THE NATURAL ENVIRONMENT OF THE PIVDENNOUKRAINSKA NPP SURVEILLANCE ZONE. / ДИНАМІКА ВИКИДІВ ТА СКИДІВ РАДІОНУКЛІДІВ У ПРИРОДНЕ СЕРЕДОВИЩЕ ЗОНИ СПОСТЕРЕЖЕННЯ ПІВДЕННОУКРАЇНСЬКОЇ АЕС.

OBJECTIVE: assessment of impact of operation of the Pivdennoukrainska Nuclear Power Plant (PUNPP) on the environment of surveillance zone (SZ) based on parameters of radiation monitoring within 2015-2021 period. METHODS: socio-hygienic (analysis of the radiation monitoring parameters), analytical, statistical. RESULTS: The environmental radiation impact associated with emissions and discharges of radioactive substances originated in the production cycle of the PUNPP in everyday conditions was found as insignificant. The gas-aerosol atmospheric emissions of inert radioactive gases, long-lived nuclides, and 131I did not exceed the established permissible levels (PL) and amounted to a hundredth of a percent of the emission limit (EL) for the inert radioactive gases and long-lived nuclides, and a thousandth of a percent for radioactive iodine. Total atmospheric emissions of the 51Cr, 54Mn, 59Fe, 58Co, 60Co, 90Sr, 95Zr, 95Nb, 134Cs, 137Cs, and 3Н radionuclides by the PUNPP power units (actual and % of EL) did not exceed the established PL. Maximum average values of atmospheric air concentration of 137Cs in SZ forthe 2015-2021 period ranged from 2.858 µBq/m3 (PUNPP industrial site) to 1.986 µBq/m3 (Riabokoneve village, 33.5 km distance), and maximum average values of the 90Sr air concentration were from 1.310 µBq/m3 to 0.566 µBq/m3, respectively. According to radionuclide monitoring no significant change of the quality of surface water occurred upon the PUNPP discharges to the Pivdennyi Bug River. Specific activity of the 137Сs in agricultural products in the PUNPP SZ was insignificant and not exceeding the PL of the content in food products. Content of 137Cs in the samples from the PUNPP SZ did not exceed 1.0 % of the total activity. CONCLUSION: Average concentration of radionuclides in atmospheric air of the settlements in the PUNPP SZ was several orders of magnitude lower than that established by regulatory documents. The PUNPP discharges to the Pivdennyi Bug River, according to radionuclide parameters that are monitored, have not significantly changed the quality of surface water. The content of 90Sr and 137Cs was uniform in all observation radii of distance from the NPP, confirming the very low level of 90Sr and 137Cs environmental emission by the PUNPP. The content of 137Cs in agricultural products within the PUNPP SZ was significantly lower than PL.

Radiostrontium determination by combination of automated Sr isolation and "on-column" Cherenkov detection using chromatographic model.

A novel analytical solution of non-linear chromatography in case of parabolic isotherm for frontal analysis was obtained by combination of Cole-Hopf and Laplace transform. It was used for simulation of strontium capturing on chromatographic column with aim to improve quantitative determination of low-level 90Sr activities. From the experimentally determined breakthrough curves, the retention factor and the number of theoretical plates were calculated using the Glueckauf and Wenzel relations and by fitting the breakthrough curves for the linear isotherm using MatLab. These were used to simulate the breakthrough curves using a parabolic isotherm solution where the non-linear term of the isotherm was taken as a small negative deviation of the retention factor. On the base of theoretical prediction and experimental data, procedure for automated capturing of strontium on chromatographic column with specific dimension and off line "on-column" Cherenkov detection on commercial ultra low-level liquid scintillation counter was developed. It was shown that analytical solution for parabolic isotherm in comparison with solution for linear isotherm gives better prediction of mass of captured Sr on column filled with small amount of Sr resin and SuperLig®620 in case of elevated Sr concentration, even when non-linear effect is not obvious. The solution also makes it possible to predict the mass of resin required for strontium isolation at 100% yield under given conditions. Considering the limited dimensions of the column, and consequently small mass of the resin in them, it resulted in the low efficiency of the columns, which, however, did not affect the yield in real conditions of isolation. The results have shown that the yields achieved after isolation on SuperLig®620 from real samples are 100%. In addition, it is shown that captured 90Sr can be detected through 90Y ingrowth, on column filled with strontium specific resin, with Cherenkov detection efficiency of at least 50%. The efficiency may be enhanced to 60%, depending on parameters which can affect detection efficiency change (type of column, resin type, surrounding solution, etc.). The developed procedures enable quantitative determination of 90Sr in natural water samples with MDAC below 12 mBq l-1 and solid (soil and vegetation) samples with MDAC below 6 Bq kg-1 within 2-3 days. The proposed solution may easily be implemented in radiochemical laboratories where this type of analysis is routinely done within environmental monitoring or other purposes.

Strontium-90 levels in seawater southeast of Jeju Island during 2021-2023.

This study introduces an efficient method for determining 90Sr activity levels in seawater, reducing the processing time to <3 h for 50 L of seawater. The key feature of the proposed method is the chemical separation of 90Y when it is in equilibrium with 90Sr, which is achieved by utilizing custom-made sample-loading equipment and an automated radionuclide separation instrument. As a result, the procedure consistently yields a recovery rate > 90 % for 90Y. Investigations of 90Sr levels were conducted in the ocean southeast of Jeju Island from November 2021 to January 2023. Owing to the regional ocean circulation, this region was among the first within the Korean Peninsula to experience the impact of the Fukushima-accident-derived radionuclides. Throughout the investigation period, the observed 90Sr activity concentration ranged from 0.57 to 1.0 Bq m-3. No distinct temporal variation of 90Sr was observed in the selected area during the investigation.

A NEW DOSE DETERMINATION METHOD FOR HP(3) AND DP LENS FOR BETA REFERENCE RADIATION QUALITIES.

For the purpose of obtaining the smaller uncertainties for Hp(3) and Dp lens in 90Sr/90Y beta reference fields, a new dose determination method based on the Monte-Carlo simulation was proposed. The conversion coefficients from the absorbed dose in air, at the reference point of the extrapolation ionisation chamber, Dair, det to Hp(3; α) and the conversion factors from Dair, det to Dp lens(α) were calculated with EGSnrc, respectively, for the irradiation angles from 0° to 60°. Compared with the dose determination method in International Organization for Standardization (ISO) 6980 standard, the uncertainty reductions of 7.7-52.8% for Hp(3; α) and 7.9-55.0% for Dp lens(α) were achieved, respectively. In addition, for the conversion coefficients from the reference absorbed dose DR to Hp(3; α), the calculations were performed for more irradiation conditions, which are not included in the current ISO 6980 standard. For the calculations of the conversion factors from DR to Dp lens(α), the eye and head phantoms with Chinese characteristics were utilised, which makes the conversion factors more suitable for use in China.

Fish otoliths as biological dosimeter: internal dose calculation.

Otoliths are organs used by fish for hearing and keeping balance. They consist of biogenic crystals of hydroxyapatite and do not contain any living cells. Upon exposure to ionizing radiation, otolith hydroxyapatite accumulates radiation-induced stable CO2- radicals whose amount is proportional to absorbed dose. In electron paramagnetic resonance (EPR) dosimetry, carbonate ions are registered and, hence, the total accumulated dose in the fish otolith can be quantified. Therefore, otoliths can be used as individual fish dosimeters to support radiobiological and radioecological studies. An important aspect of otolith-based EPR dosimetry on fish from contaminated water bodies is the potential presence of bone-seeking 90Sr. Consequently, cumulative absorbed doses measured with EPR in otoliths may reflect the superposition of internal exposure to 90Sr/90Y and external exposure due to radionuclides circulating in soft tissue of the fish as well as due to environmental contamination. The objective of the present study was to develop a method that allows for an assessment of the contribution of 90Sr to the total dose in otolith. The method has been tested using otoliths from seven fish taken from reservoirs located in the Southern Urals contaminated with radionuclides including 90Sr. It has been shown that dose to otoliths is largely determined by 90Sr in the hydroxyapatite. The internal dose component can be calculated using activity concentration-to-dose conversion factors, which vary slightly in the range of 2.0-2.8 × 10-3 Gy year-1 per Bq g-1 depending on fish species and age. Internal doses to fish from water bodies with different levels of 90Sr contamination were calculated in the range from 2 mGy to ~ 200 Gy. External dose contribution was derived for two fish only to be about 100 and 40 Gy. It is concluded that EPR dosimetry on fish otoliths is a promising tool when external exposure prevails or is comparable to internal exposure due to 90Sr.

Clean feed as countermeasure to reduce the 90Sr and 137Cs levels in fish from contaminated lakes.

Glubokoye Lake situated within the Chernobyl Exclusion Zone is highly contaminated with respect to radioactive caesium and strontium isotopes, which also is reflected in the contaminated fish. To utilize the fish resources in contaminated lakes, the present work presents for the first time the effectiveness of using clean feed to counteract contamination of radionuclides in fish. The study is based on a series of repeated experiments with Prussian carp (Carassius gibelio (Bloch, 1782)) kept in cages in the contaminated Glubokoye Lake during summer 2018-2021. By the addition of clean feed, the activity concentration of 137Cs in fish muscle tissues was lowered with a factor of 2-5 due to biodilution. Surprisingly, additional clean feed did not lead to further decrease in the uptake of 137Cs in fish. In contrast to 137Cs, the addition of clean feed increased the 90Sr activity concentration in fish by a factor of 2-4 compared to fish fed with naturally occurring feed items. Radioactive strontium accumulated mainly in the fish bones and the muscle tissue level was 2 orders of magnitude lower, similar to the distribution observed for stable Sr. By utilizing a new kinetic model describing the dynamics of strontium isotopes in bone tissues of fish, predictions fitted well with site-specific data, taking growth rates and aging into account. Results showed that clean feeding can be used to counteract high activity concentration of 137Cs in fish due to biodilution, but cannot counteract bioaccumulation of 90Sr. Findings highlighted that it is essential to understand underlying factors influencing the uptake pathways for contaminants, as access to clean feed could increase the growth and thereby reduce the body activity concentration of dietary associated radionuclides such as 137Cs (biodilution), as well as increase the transfer of dissolved compounds such as 90Sr directly from water to fish.

The use of plastic scintillation microspheres in flow scintillation analysis.

This manuscript deals with the possible utilization of plastic microspheres for radiation detection. The aim was to determine the suitability of microspheres for this application, factors that affect detection efficiency, and based on the evaluation of current state technology to design and test a constructional solution suitable for this use. Three detection cell variations and their configurations, which utilize plastic microspheres, were tested for their response to selected militarily important radionuclides during a series of static measurements. Based on the results of static measurements, the most structurally suitable cell variation was subsequently tested for flow scintillation analysis. Among the cells designed for flow scintillation counting in 2π geometry, the highest achieved detection efficiency for 241Am was 13.1 ± 0.7% using Cell #5, for 90Sr/Y was 71.2 ± 3.9% using Cell #10 and for 3H was 3.9 ± 0.2% using Cell #5 respectively. Cell #10 was evaluated to perform universally the best despite achieving slightly lower detection efficiencies for 241Am and 3H than Cell #5, as the results were easily replicable and due to the cell constructional simplicity, its application was problem-free.

DETERMINING THE TRANSFER FACTORS FOR ESTIMATES OF THE RADIATION CONTAMINATION OF AGRICULTURAL CROPS.

The study aims to provide a basis for measures reducing the consequences of a nuclear accident in its late phase, when plant contamination occurs mainly through the root system. Samples of the above-ground biomass of crops and soil were taken in 2020 in the vicinity of the Temelín and Dukovany nuclear power plants (Czech Republic). The 137Cs activities were determined using gamma spectrometry, and the 90Sr activities were measured through beta radiation. From the obtained values, the radionuclide transfer factors (TFs) from soil to crop biomass were calculated. The average area activity of 137Cs in the soil around Dukovany and Temelín was 1700 and 2400 Bq m-2, respectively. The average area activity of 90Sr around Dukovany and Temelín was 211 and 184 Bq m-2, respectively. The TF 137Cs ranged from < 6.3 × 10-6 to 7.9 × 10-3, with a mean of 3.5 × 10-4 m2 kg-1, and the TF 90Sr ranged from 2.7 × 10-4 to 6 × 10-2, with a mean of 1.7 × 10-2 m2 kg-1.

Novel approach for strontium preconcentration from seawater and rapid determination of 89,90Sr in emergency situations.

A novel approach for rapid 89,90Sr determination in seawater samples is developed. For the first time in the radioanalytical application, the features of the synthetic zeolite Z4A and a highly selective material for Sr separation were synergically employed. Seawater composition significantly reduces Sr yield on highly selective solid-phase extraction materials, making the preconcentration step essentially important but laborious and time-consuming. To address this issue, the ability of zeolite 4A to concentrate the Sr from the seawater matrix was employed. With the proposed method, two important goals were achieved: (i) simple preconcentration of Sr that can be conducted directly at the sampling site, enabling a rapid procedure for 89,90Sr determination in emergencies, and (ii) high and stable Sr recoveries (89 ± 4%) necessary for lowering detection limits. Strontium is effectively separated from 1 L of seawater in less than 1.5 h, which is especially important in emergency situations, such as the Fukushima Daiichi Nuclear Power Plant accident. Minimum detectable activities achieved for 89Sr:90Sr activity ratio ∼10:1 were 0.74 Bq/L for 89Sr, and 1.47 Bq/L for 90Sr, detected by Cherenkov counting, 36-38 h after separation, and 30 min counting time.

Novel 90Sr analysis of environmental samples by Ion-Laser InterAction Mass Spectrometry.

The sensitive analysis of 90Sr with accelerator mass spectrometry (AMS) was developed to advance environmental radiology. One advantage of AMS is the ability to analyze environmental samples with 90Sr/88Sr atomic ratios of 10-14 in following a simple chemical separation. Three different IAEA samples with known 90Sr concentrations (moss-soil, animal bone, Syrian soil: 1 g each) were analyzed to assess the validity of the chemical separation and the AMS measurement. The 90Sr measurements were conducted on the AMS system VERA combined with the Ion Laser InterAction Mass Spectrometry (ILIAMS) setup at the University of Vienna, which has excellent isobaric separation performance. The isobaric interference of 90Zr in the 90Sr AMS was first largely removed by chemical separation. The separation factor of Zr in two-step column chromatography with Sr resin and anion exchange resin was 106. The 90Zr remaining in the sample was effectively suppressed by ILIAMS. This procedure achieved a limit of detection <0.1 mBq in the 90Sr AMS, which is lower than typical ß-ray detection. The agreement between AMS measurements and nominal values for the 90Sr concentrations of IAEA samples indicated that the new highly-sensitive 90Sr analysis in the environmental samples with AMS is reliable.

Measurement of 90Sr in Marine Biological Samples.

Strontium-90 (90Sr) is one of the most hazardous radionuclides, and it contributes to radiation exposure by ingestion. The routine determination of 90Sr in marine biological samples is highly desirable given the development of the nuclear power industry. A fast, simple, and low-detection-limit method was developed for the measurement of 90Sr in marine biological samples based on determining 90Y by means of coprecipitation and solvent extraction with bis-2-ethylhexyl-phosphoric acid (HDEHP) in n-heptane. The interfering 210Bi is removed using Bi2S3 precipitation. The separation and purification of eight samples per day can be accomplished through this method. The detection limit of 90Sr for this method is 0.10 Bq/kg (ash weight). The radiochemical procedure was validated by fitting the decay curve of the sample source and by the determination of 90Sr standards.

Determination of strontium radioisotopes in routine and emergency samples.

We present the radioanalytical strategies used for the determination of strontium radioisotopes in routine and emergency samples. While in routine monitoring, the main goal is to achieve limits of detection as low as possible. In emergency, priority is given to the rapid procurement of data about a contamination. The parameters accuracy, precision and detection limit of the radiochemical methods are shown. We present the results obtained over the past 22 years in proficiency tests and in the analysis of reference materials.

Speciation of 137Cs, 90Sr, 241Am, and 239+240Pu artificial radionuclides in soils at the Semipalatinsk test site.

This paper reports the speciation of 137Cs, 241Am, 90Sr and 239+240Pu in the soil samples of the Experimental Field (EF). The EF is a testing ground of the Semipalatinsk nuclear weapons test site used for surface and atmospheric tests. The study revealed low mobility of artificial radionuclides in the EF site soils. The revealed high radionuclide concentrations in soil mainly exist in tightly bound form. On average, the content of the tightly bound form of 137Cs was revealed to be below 98%, that of 90Sr - 94%, 241Am - 89%, and 239+240Pu - 98%. The radionuclides occurrence forms were analyzed in correlation with the physicochemical parameters of soils. Reliable relationships have been established between the content of carbonates and the content of the exchangeable, acid-soluble and strongly bound 90Sr forms in soils, as well as the content of the water-soluble salts and the content of the strongly bound 239+240Pu form in the soil. Similarly, we compared the distributions of the radionuclides speciation and their stable isotopes with their analogous elements in the soil. Unlike 137Cs and 90Sr, which are in a tightly bound form in the soils of the Experimental Field site, the main content of soil "competitors" of the 137Cs radionuclide - K and Cs is observed in an exchange form, less significantly in an acid-soluble form. The alkaline earth metals (analogous elements for 90Sr) are mainly observed as a composition of the exchangeable and acid-soluble forms. The results allow to conclude that there is no equilibrium distribution of the physicochemical forms of radionuclides introduced into the soil and the natural presence forms of their stable analogs in the soil. Such equilibrium distribution can only be achieved at a complete isotopic exchange in phases and soil components, which under the conditions of the Experimental Field is not possible in the near future. It can be concluded that the behavior of the studied radionuclides in soils is stipulated by the initial form delivered by the fallouts from tests at the EF site.

Accumulation of 90SR by Betula pendula within the East Ural Radioactive Trace zone.

This study was conducted in 2010-2020 at the head of the East Ural Radioactive Trace (EURT), which was formed in 1957 as a result of the Kyshtym accident at the Mayak Production Association. The main contaminant in this zone is the long-lived radionuclide Strontium-90 (90Sr). Secondary forests dominated by silver birch (Betula pendula) occupy 45% of the EURT area. Concentration of 90Sr in birch leaves and small branches was higher than that in the trunks. The 90Sr content in birch sapwood varied slightly in the radial direction and did not depend on tree age. This was due to the dynamic equilibrium of the migration processes responsible for the accumulation and horizontal transfer of 90Sr. The 90Sr concentration increases in false heartwood, which is formed as a result of the secondary metabolism of dying parenchyma in the inner part of sapwood and is characterised by a high content of ash elements. The concentration of radionuclides in the aboveground organs of birch increased and the aggregated transfer factors (Tag) decreased with an increase in the soil contamination density, in accordance with the power function. The reasons for these patterns are also discussed.

Online solid-phase extraction-inductively coupled plasma-quadrupole mass spectrometric quantification of 90Sr using 88Sr/86Sr isotope dilution method.

Due to the lack of a correlation with the natural Strontium (Sr) isotopes, it is difficult to apply the isotope dilution (ID) method to an artificial radioactive mononuclide Strontium-90 (90Sr), in inductively coupled plasma-quadrupole mass spectrometry (ICP-QMS). Meanwhile, online solid-phase extraction (SPE)-ICP-QMS (SPE-ICP-QMS) serves as an automatic sequential analytical technique for measuring the ultra-trace amounts of radionuclides; however, apparent assay values obtained using this method are often negatively affected by differences in the sample matrix composition between standard and actual samples. In this study, the pg L-1 level of 90Sr was successfully measured by combining online SPE-ICP-QMS and the ID method with 88Sr/86Sr ratios in one sample injection, without the radioactive standard. Although naturally occurring abundant isobaric 90Zr significantly influences 90Sr quantification during mass spectrometry, consecutive separations between automated SPE and dynamic reaction cell (DRC) oxidation enable 90Sr quantification, even in the presence of isobaric 90Zr (acceptable down to 5.7 × 10-9 of 90Sr/Zr in sample solution), using this method. Through this method, both radioactive 90Sr and naturally occurring Sr were simultaneously quantified using 88Sr-to-86Sr and 88Sr-to-90Sr ratios without radioactive 90Sr standard solutions. This simultaneous quantification of stable Sr and 90Sr was achieved within 15 min with good recovery rates. The limit of detection of 90Sr was 1.1 pg L-1 (equivalent to radioactivity 5.6 Bq L-1) for a 10 mL injection. Finally, water collected from an actual contaminated water storage tank at the Fukushima Daiichi Nuclear Power Plant (Fukushima, Japan) was analyzed using the proposed method, and the obtained results agreed well with those obtained using conventional analytical methods.

Analytical Methods for the Determination of 90Sr and 239,240Pu in Environmental Samples.

Artificial long-lived radionuclides such as 90Sr and 239,240Pu have been long released into the environment by human nuclear activities, which have a profound impact on the ecological environment. It is of great significance to monitor the concentration of these radionuclides for environmental safety. This paper summarizes and critically discusses the separation and measurement methods for ultra-trace determination of 90Sr, 239Pu, and 240Pu in the environment. After selecting the measurement method, it is necessary to consider the decontamination of the interference from matrix elements and the key elements, and this involves the choice of the separation method. Measurement methods include both radiometric methods and non-radiometric methods. Radiometric methods, including alpha spectroscopy, liquid scintillation spectrometry, etc., are commonly used methods for measuring 239+240Pu and 90Sr. Mass spectrometry, as the representative of non-radiometric measurement methods, has been regarded as the most promising analytical method due to its high absolute sensitivity, low detection limit, and relatively short sample-analysis time. Through the comparison of various measurement methods, the future development trend of radionuclide measurement is prospected in this review. The fully automatic and rapid analysis method is a highlight. The new mass spectrometer with ultra-high sensitivity shows strong analytical capabilities for extremely low concentrations of 90Sr, 239Pu, and 240Pu, and it is expected to develop determination methods with higher sensitivity and lower detection limit.