Radionuclide contamination of foods imported into Iraq following the Chernobyl nuclear reactor accident

Since early 1986, a monitoring program for radionuclides in imported foods has been carried out by the Iraqi Atomic Energy Commission. After the Chernobyl nuclear reactor accident in the Soviet Union, the program was expanded; our laboratory was officially designated by the Iraqi Government to measure radionuclide activity concentrations in foodstuff imported from countries known to be severely contaminated by Chernobyl radioactive fallout. Gamma-spectrometric analysis was used. Food items such as powdered milk, lamb meat, poultry, cereals and grains imported into Iraq before the Chernobyl accident did not contain any detectable fission products. However, all lamb meat, 81% of the lentil, 44% of the powdered milk and chick-pea, and 17% of the roast beef samples were contaminated with 137Cs or 134Cs and 137Cs. The highest 137Cs contamination levels found were 82, 147, 420, 6 and 4 Bq kg-1, respectively. Contamination by 134Cs was approximately 50% of the values given above.     

Predictions of nitrate diffusion in sediment using horizontal attenuated total reflection (HATR) by Fourier transform infrared (FTIR) spectrometry

Using a novel and simple method based on horizontal attenuated total reflection (HATR) by Fourier transform infrared (FTIR) spectrometry, the effective diffusion coefficient, De, of nitrate in a contaminated anthropogenic sediment was estimated as 7.34 x 10(-6)cm2 s(-1). This method, which requires as little as 1 mL of sediment sample, was able to measure the De of a chemical species with a reproducibility of +/-3% in about 5h. Based on this De and a pre-determined nitrate reduction rate, the profiles of nitrate concentration in two sediment columns were satisfactorily predicted from a mathematical model. Results showed that the profile in this aged sediment depended mainly on the diffusion of nitrate and, only to a much lesser degree, the rate of nitrate reduction. Measurements in 55 anthropogenic sediment samples collected from five locations and various depths of a contaminated site further showed that the De of nitrate increased linearly with the water content of the sediment, but decreased with the sediment density. The technique demonstrated in this study shall be applicable for the risk assessment of toxic pollutants in contaminated sediments, and for planning the spatial and time intervals of nitrate injection strategy in bioremediation.     

Congratulations to Valerii Viktorovich Mikheev

Anniversaries and Memorable Dates

Congratulations to Valerii Viktorovich Mikheev Candidate of Technical Sciences, honorable builder of the Russian Federation, and recipient of the prize awarded by the Council of Ministers of the USSR     

Comparative study of dark patinas on granitic outcrops and buildings

Formation of dark patinas on rocky surfaces is mainly related to the deposition of gases and particles and to sulphation mechanisms. In the present study, samples of dark patinas taken from granitic outcrops and from granitic buildings were examined in an attempt to understand the mechanisms of their formation. The outcrops are located in non-polluted areas and are characterized by the absence of any extraneous material that provides calcium, such as e.g. mortar. The buildings are located in areas with low levels of pollution. The climate in the study area favours proliferation of microorganisms. Important differences between the patinas sampled from outcrops and from buildings were observed, as the former are of biological origin and the latter of anthropogenic origin. Although the levels of pollution are low in the sampling area, sulphur was present in all of the samples from urban buildings. Sulphur was not present in patinas from outcrops or in patinas from monuments that are assumed to behave as outcrops (dolmens), although the latter are also of anthropogenic origin. Finally, the patinas were found to be formed by elements accumulated on the surface and not from elements contained within the rock itself.     

Effect of surfactants on the determination of aluminium in waters

Eleven surfactants representing pure cationic, anionic and nonionic detergents, four commercial detergents, sodium pyrophosphate, sodium tripolyphosphate, a soap and nitrilotriacetic acid (NTA) were investigated for their effect on the determination of aluminium in water using the eriochrome cyanine R, ferron-orthophenanthroline and chrome azurol S methods. Cationic, anionic and nonionic detergents at concentrations up to 2, 100 and 1000 mg l⁻¹, respectively, did not interfere. Sodium tripolyphosphate interfered badly above 1.0 mg l⁻¹, and therefore the interference by formulated detergents containing tripolyphosphate was serious. Concentrations of NTA, soap and sodium pyrophosphate had to be below 0.5, 10 and 20 mg l⁻¹, respectively, to limit the error to 5%.     

Formation of alkylated aromatic acids in groundwater by anaerobic degradation of alkylbenzenes

Evidence for the presence of previously unreported alkylated aromatic acids in anaerobic groundwater samples from a jet fuel-contaminated site is presented. The redox conditions are dominated by sulfate reduction. A gas chromatography/mass spectrometry screening showed a composition of aromatic hydrocarbons ranging from BTEX (C(0)-C(2)-substituted benzenes) up to C(7)-benzenes. Known metabolites like methylbenzoates (C(1)-BA), C(2)-BA, C(3)-BA as well as methylbenzylsuccinates (C(1)-BSA) were detected. Additionally, previously unreported metabolites of higher alkylated benzenes have been identified in the extracts: those are C(2)-BSA to C(5)-BSA as well as C(4)-BA to C(6)-BA, which were detected in the microg/l-concentration range. The formation of C(1)- and C(2)-BSA as well as the C(1)- and C(2)-BA can be linked to structurally corresponding parent contaminants like the xylene isomers and the trimethylbenzene isomers. The C(3)-BSA and C(3)-BA represent metabolites of C(4)-benzenes. The occurrence of C(4)-C(5)-BSA and C(4)-C(6)-BA is attributed to C(5)-C(7)-benzenes acting as parent compounds. The concentration of total aromatic contaminants decreased along the plume centre line. In contrast, benzoates and benzylsuccinates (BA and BSA) showed constant concentrations over a distance of 84 m. BA concentrations were up to 162 times higher compared to BSA, as indicated by the ratio f(BA/BSA). A pronounced transient behaviour of BSA or an overall persistent behaviour of BA can explain this. Hence, along the plume centre line, f(BA/BSA) was constant over a distance of 128 m. The degradation products detected in a monitoring well are not necessarily tied to contaminants detected in that well. Therefore, the metabolite plume is partly located in front of the contaminant plume, but does not significantly migrate downstream the plume toe.     

Radon and 'King Solomon's Miners': Faynan Orefield, Jordanian Desert

Concentrations of 222Rn were measured in ancient copper mines which exploited the Faynan Orefield in the South-Western Jordanian Desert. The concentrations of radon gas detected indicate that the ancient metal workers would have been exposed to a significant health risk and indicate that any future attempt to exploit the copper ores must deal with the hazard identified. Seasonal variations in radon concentrations are noted and these are linked to the ventilation of the mines. These modern data are used to explore the differential exposure to radon and the health of ancient mining communities.     

The impact of preoxidation of SAS on biosorption efficiency on activated carbon

We have studied the process of a prolonged dynamic filtration on activated carbon in two biosorption systems — without preoxidation treatment of the initial matter and after ozonization. It has been shown that given the uniform load on activated carbon terms of the organic matter the efficiency of the biosorption process after preozonization is 2.3 times as small compared with that that without pretreatment, which correlates with the change of adsorption free energy.     

Impact of the River Maine Drainage Scheme on Hydro-Power Generation

A comparison is made between pre- and post-drainage scheme river flows recorded on the River Maine, Co. Antrim. A method of using five-year reference periods has been applied to the mean daily flows to smooth and eliminate, as far as possible, variations due to climatic changes.
Any loss of energy production which might have been due to changes in river flow was examined for turbine installations at a factory at Cullybackey. The quantities of usable water, and hence potential energy production, were calculated for each of the post-scheme five-year periods and compared with a pre-scheme five-year reference period. Any potential loss was then represented by a depreciation factor. It was found that no measurable loss of potential energy production has occurred on the River Maine in the post-scheme period.