Radioactivity of cattle fodder and milk after the Chernobyl accident

The radioactivities of⁹⁰Sr,¹³⁷Cs and¹³⁴Cs have been measured in soil, fodder and milk from the south-western region of Slovenia, Yugoslavia after the Chernobyl accident. Maximal concentrations of Sr-isotopes in samples and the rate of their decrease in a period up to two years after the accident are given. The transfer of radionuclides from soil to grass and from fodder to milk is discussed.     

Actinides in the near release from the Chernobyl NPP accident

Actinide elements concentrations in the products of near release from CNPP accident were estimated. The data on uranium,²³⁷Np,²⁴¹Am and plutonium and curium isotopes content in fuel particles are given. Sums of -emitting radionuclides and plutonium isotopes in reactor graphite particles and of uranium,²⁴²Cm,^239+240Pu isotopes in the soil and aerosol samples were also determined. By 1989 soil and dust contamination in near release of the accident is due to long-lived -emitting plutonium isotopes.     

89,90Sr fallout from Chernobyl in the Bucharest-Magurele area

⁸⁹Sr and⁹⁰Sr were determined in the fallout of May 1986. The maximum values of 335 Bq/(m².6 h) and 110 Bq/(m².6 h) were observed on May 2 and 5. Throughout May 1986 a quantity of 860 Bq/m² of⁹⁰Sr, deposited from the fallout in the Bucharest-Mgurele area, was estimated.     

Fallout from Chernobyl in Bologna and its environs: Radioactivity in airborne,rain water and soil

The Chernobyl fallout was estimated in Emilia-Romagna, a Northeastern region of Italy. Nuclide composition of airborne and the time evolution of the radioactivity were investigated. The comparison of the activity ratio of¹⁰³Ru to¹³⁷Cs allows to conclude that Italy was not influenced by the first release. The trend of the total activity and¹³⁷Cs percentage in rain water was very similar to those of air particulates. A calculation model to estimate¹³⁷Cs deposition onto the ground has been developed and validated by comparison of the calculated and experimental values for soil samples. The activity range was 2–40 kBq ·m^–2.     

Long term radioactive uptake by two pasture plants in a field contaminated by the Chernobyl fallout

The radioactive content of alfalfa and rye grass was measured in five consecutive harvests covering a period of one and a half years after the contamination of a field caused by the Chernobyl fallout. The measured long-lived isotopes were¹⁰⁶Ru,¹³⁴Cs and¹³⁷Cs. In the first four harvests alfalfa contained significantly less radioactivity than rye grass, while in the last harvest both plants contained comparable levels of radioactivity. The results from the first harvest, demonstrating the radioactivity obtained in the direct fallout, indicate that the fraction of total initial deposition retained on rye grass is by 55% and 70% greater than alfalfa for Cs and Ru isotopes, respectively. The second, third and fourth harvests demonstrate values of plant to soil concentration ratios /CR/ considerably larger than those observed in the fifth harvest. Only the CR values obtained in the last harvest overlap with commensurate values previously reported in the literature.     

Leaching dynamics of uranium in a contaminated soil site

Samples from a potentially contaminated industrial area were analyzed for uranium using neutron activation analysis (NAA). Uranium concentration values had a typical uncertainty of 2 % and a detection limit of 1 Bq/kg. To investigate the potential leaching dynamics into ground water two techniques were employed. The US EPA Toxicity Characterization Leaching Procedure (TCLP) and the Sequential Extraction Procedure (SEP) were used to determine the concentration of uranium in the leachates. TCLP and SEP showed that very little of the uranium leached into solution under different chemical conditions. Values of uranium leachates ranged from 0.05 to 3.5 Bq/L; a concentration much lower than the results found in the soil concentrations which ranged from 29 to 155 Bq/kg. NAA showed an 8 % uncertainty for leachates with a detection limit of 0.13 Bq/L. To mimic environmental conditions and acid rain, pH 4.3 water was used as the extraction solvent instead of the acetic acid routinely used in TCLP. Results confirmed that very low amounts of uranium leached with values ranging from 0.0002 to 0.0122 Bq/L. These values represent 0.01–1 % of the uranium in the soil samples. The distribution of uranium in soil according to particle size was also investigated to evaluate its potential movement and possible contamination of the water table. Particles below 250 μm in diameter showed a linear increase in uranium concentration whereas those with a larger diameter had constant uranium content.     

Foliary contamination in the area of Bratislava (Czecho-Slovakia) after the Chernobyl accident

The contamination of leaves of some ornamental and fruit-tree plants (18 species), herbs (6) and early leafy vegetable (2) were assessed in the region of Bratislava and its vicinity through the first months after the Chernobyl accident. The levels of contamination showed local and temporal dependence. In October compared to its levels five months earlier, foliar contamination showed a relative 12- to 200-fold decrease of radioactivity. The effective half-life of the mixture of fission products in cumulative fallout on leaves of vegetation changed depending on time after the accident from 4 days (on day 10) to 150 days (after 2 months). The soluble fraction of radioactive contaminants on plant foliage ranged from 0.12 to 0.64.     

Planning for environmental restoration of the contaminated banks near bohunice NPP

The 18 km long banks of the Bohunice NPP waste water recipient are contaminated by¹³⁷Cs as a result of two accidents on the CO₂ cooled NPP-A1 unit in 1976 and 1977. Contamination acceptance limits 6 or 8 Bq¹³⁷Cs/g of soil, depending on contaminated area size, were derived on the basis of developed principles, and approved by the authorities. Removing and safe burial of 1100 m³ of contaminated soil from steep area and 15 cm thick clean soil covering on about 1 ha of flat area of the contaminated banks is planned in frame of the re-considered restoration project implementation in 1995/96.     

Redox site confinement in highly unsymmetric dimanganese complexes

A set of highly preorganized pyrazolate-bridged dimanganese complexes L(Mn)MnX have been prepared and structurally characterized. They can be described as hybrid organometallic/Werner-type systems that consist of a low-spin CpMn(I)(CO)2 subunit (Mn1) and a proximate tripodal tetradentate {N4} binding pocket accommodating a high-spin Mn(II) ion (Mn2), with Mn...Mn distances of approximately 4.3 A and different coligands bound to Mn2. Density functional theory (DFT) calculations (both the hybrid B3LYP and the pure BP86 functionals and the all-electron basis sets 6-311G and 6-311G*) confirm that the valence alpha and beta Kohn-Sham molecular orbitals (MOs) of these mixed-valent Mn(I)Mn(II) compounds have predominant Mn(3d) character and an almost perfectly localized nature: all five unpaired electrons are essentially localized at the Werner-type Mn2, whereas Mn1 possesses an effective closed-shell structure with the MOs of highest energy centered there. One-electron oxidation occurs in a clean process at approximately E(1/2) = -0.6 V (versus ferrocene/ferrocinium), giving the low-spin/high-spin Mn(II)Mn(II) species. UV/vis and IR spectroelectrochemistry as well as a detailed theoretical analysis reveal that the redox process takes place with strict site control at the organometallic subunit, while it does not significantly influence the spin and charge distribution on the Werner-type site. Positions and shifts of the nu(C[triple bond]O) absorptions are largely reproduced by the DFT calculations. These systems thus represent an exceptional example of the effect the unsymmetry of a dinucleating ligand scaffold has on the spin and charge distribution in homobimetallic complexes and might offer interesting prospects for the study of the cooperative effects of bimetallic arrays.     

Radioactivity in coffee

This research was dedicated to the study of the background levels of ²¹⁰Po and natural gamma emitters as ⁴⁰K, ²¹⁴Pb, ²¹⁴Bi, ²²⁸Ac, ²¹²Pb and ²¹²Bi in coffee powder and in coffee beverage; also the artificial ¹³⁷Cs was determined. In the coffee powder the mean ²¹⁰Po activity resulted 7.25 ± 2.25 × 10^?2 Bq kg^?1. ⁴⁰K showed a mean activity of 907.4 ± 115.6 Bq kg^?1. The mean activity concentration of ²¹⁴Pb and ²¹⁴Bi, indicators of ²²⁶Ra, given as mean value of the two radionuclides, resulted 10.61 ± 4.02 Bq kg^?1. ²²⁸Ac, ²²⁸Ra indicator, showed a mean activity concentration of 13.73 ± 3.20 Bq kg^?1. The mean activity concentration of ²¹²Pb, ²²⁴Ra indicator, was 8.28 ± 2.88 Bq kg^?1. ²⁰⁸Tl, ²²⁴Ra indicator, presented a mean activity concentration of 11.03 ± 4.34 Bq kg^?1. In all samples, the artifical ¹³⁷Cs resulted below the detection limit (2.0 Bq kg^?1). The arithmetical mean value of percentage of ²¹⁰Po extraction in coffee beverage resulted 20.5 ± 6.9. The percentage of transfer of gamma emitters,⁴⁰K, ²¹⁴Pb, ²¹⁴Bi, ²²⁸Ac, ²¹²Pb, ²⁰⁸Tl resulted of 80.0, 33.5, 24.7, 30.0, 35.1 and 53.5 % for ⁴⁰K, ²¹⁴Pb, ²¹⁴Bi, ²²⁸Ac, ²¹²Pb and ²⁰⁸Tl respectively.     

Development of radiochemical analysis of uranium isotopes in highly contaminated soil samples

An accurate and reliable analytical technique of uranium isotopes in highly contaminated soil samples was developed and applied to the IAEA reference samples. The conventional TBP method of uranium isotopes is insufficient to completely purify uranium from actinides such as plutonium and americium isotopes in highly contaminated soil samples. For overcoming the demerits of the conventional TBP extraction method, sample materials were decomposed with HNO₃ and HF, and uranium isotopes were purified by TBP extraction and anion exchange columns and extraction chromatography. Among the purifying methods of uranium, with a TRU Spec resin column after TBP solvent extraction, uranium was completely separated from the radionuclides in a highly contaminated samples. With the modified TBP extraction method, it was found that the concentrations of uranium isotopes were consistent with the reference values reported by the IAEA.     

Radioactivity in deuterated compounds

Commercially available D₂O and deuterated toluene have been measured with a liquid scintillation spectrometer and were found to contain 2.71–6.15 Bq of tritium in 1 ml of D₂O, and 1.10 Bq of tritium in 1 ml of deuterated toluene.     

Use of a pentachlorophenol degrading bacterium to bioremediate highly contaminated soil

ASphingomonas species that mineralizes high concentrations of pentachlorophenol (PCP) was isolated from a PCP-contaminated EPA Superfund site. This bacterium, identified asSphingomonas sp. strain RA2, is able to degrade PCP at concentrations of up to 300 μg/mL in liquid culture. This organism was tested for its ability to degrade high concentrations of PCP in a soil that did not contain organisms capable of degrading high concentrations of PCP. When inoculated into contaminated soil,Sphingomonas sp. RA2 mineralized PCP at concentrations of 300, 600, 900, and 1200 μg PCP/g of soil, but was unable to mineralize 1500 μg PCP/g of soil. Only very minimal loss of PCP was seen in uninoculated soils. The results of this study demonstrate thatSphingomonas sp. RA2 may be a useful organism for remediation of sites contaminated with high concentrations of PCP.     

宝兴大理石矿的放射性检测

宝兴县境内的大理石资源以其白度高、储量丰、品质优、易开采而享誉中外。对四川省宝兴县陇东镇大理石矿区进行了放射性环境地质调查,通过对取回的大理石样品中226Ra、232Th、40K这3种核素的比活度的测定,根据比活度换算出这几种核素的外照射指数和内照射指数,把所得结果和中华人民共和国国家标准《建筑材料放射性核素限量》中规定的建筑性材料分类标准作对比后发现其内照射指数与外照射指数都符合《建筑材料放射性核素限量》中A类建筑材料和装饰材料的要求,它的产销与适用范围不受限制。     

Determination of137Cs and134Cs in air samples collected near Belgrade /Yugoslavia/ following the Chernobyl accident

This paper presents the results of measurements of¹³⁷Cs and¹³⁴Cs content in air sampled during May 1986. Maximum concentrations:¹³⁷Cs 2.94±0.01 Bq m^–3 and¹³⁴Cs 1.38±0.01 Bq m^–3 were registered on May 3. Several other long lived radionuclides having -energies in the region 33 keV to 1365 keV were registered in the same samples two years later. The results of measurements of the total -activity in air for the same period are also presented.     

Antimony distribution in soils and plants near an abandoned mining site

A study about antimony distribution and mobility in soils located in the surroundings of an abandoned mining site is carried out. The mineralogical composition of the soils is obtained, and the samples classified into three groups attempting to correlate antimony level and behavior with the main mineral phases present. The total antimony concentrations are measured (5-40 mg kg⁻¹), and mobility of the metalloid is assessed by using selective extractants. Maximum mobility is obtained when extracting with a reducing-complexing medium which, taking into account the characteristics of the zone, means antimony availability to plants should be low. This is verified by analyzing both roots and leaves of vegetation growing in the area. The maximum level present in the leaves is 1.5 mg kg⁻¹ dry matter, but most of the samples show antimony concentrations below 0.5 mg kg⁻¹. The results indicate that plants represent an effective barrier to antimony that is incorporated only in small proportions, and so the risk posed to biota is low.     

Assessing toxicity and mobilisation of impregnation salts at a contaminated site

Severe soil contamination is often encountered at wood-impregnation plants due to spills, dripping and deposition of sludge associated with dissolved salts of copper, chromium and arsenic (CCA). Soil samples from a CCA-plant in southern Norway were analysed via a factorial extraction design to investigate mobilisation of contaminated soils. Various concentrations of organic acids, sea-salts, and pH showed that contaminants were not stable, and could be mobilised to the aqueous phase. To further investigate mobilisation of impregnation salts, soil solution collectors were installed at various depths at the site. Concentrations varied considerably. Hydrological changes revealed elevated levels of dissolved salts, which agree with the factorial experiment. Soil chemical processes (not total solid-phase concentrations) dominated the mobilisation and subsequent leaching. Soil solutions were tested for changes in toxicity by chemical analysis and degree of inhibition of luminescence in Vibrio fisheri (Microtox). Changes in toxicity corresponded to changes in soil solution.     

The use of expert systems for determining sampling strategies in contaminated site investigations

Sampling in site investigations is mostly done on the basis of hit or miss probing. Several mathematical and (geo)statistical methods are available for improving the reliability of sampling procedures. Combining these tools with the knowledge of experts in a so-called soft-knowledge based computer program is an excellent way of rationalizing sampling strategies.     

Assessing toxicity and mobilisation of impregnation salts at a contaminated site

Severe soil contamination is often encountered at wood-impregnation plants due to spills, dripping and deposition of sludge associated with dissolved salts of copper, chromium and arsenic (CCA). Soil samples from a CCA-plant in southern Norway were analysed via a factorial extraction design to investigate mobilisation of contaminated soils. Various concentrations of organic acids, sea-salts, and pH showed that contaminants were not stable, and could be mobilised to the aqueous phase. To further investigate mobilisation of impregnation salts, soil solution collectors were installed at various depths at the site. Concentrations varied considerably. Hydrological changes revealed elevated levels of dissolved salts, which agree with the factorial experiment. Soil chemical processes (not total solid-phase concentrations) dominated the mobilisation and subsequent leaching. Soil solutions were tested for changes in toxicity by chemical analysis and degree of inhibition of luminescence in Vibrio fisheri (Microtox). Changes in toxicity corresponded to changes in soil solution.     

90Sr and137Cs in fallout from Chernobyl in the Bucharest-Măgurele area during 1986–1987

This work shows the variation of⁹⁰Sr and¹³⁷Cs in atmospheric fallout in the Bucharest-Mgurele area during 1986–1987. The amount of⁹⁰Sr in the fallout was estimated to be about 900 Bq.m^–2 in 1986 and about 9.2 Bq.m^–2 in 1987. The amount of¹³⁷Cs was estimated to be 13300 and 615 Bq.m^–2 in 1986 and 1987, respectively.