Long-term monitoring of water treatment technology designed for radium removal-removal efficiencies and NORM formation.

A drinking water treatment plant in Viimsi, Estonia, was monitored over three years for iron, manganese, radium-226, radium-228, as well as their daughter nuclides, in order to determine the efficiency of the treatment process, gain an insight into the removal mechanisms and interactions between radium, iron, and manganese, and assess the overall longevity and performance of the technology along with the possible build-up of NORM in the treatment process. During the study, samples were collected from raw water, first and second stage filtrate, consumer water, backwash water and filter materials. The results show consistent removal efficiency for iron and manganese, as well as an average of over 85% removal for radium with a slight decline over time. The backwash process has been optimised for maximum radium removal from the filters, while keeping concentrations in the backwash water below exemption levels. However, the accumulation of radium and thorium occurs in the filter material, exceeding exemption levels in the top layer of the filter columns in less than a year. By the end of the observation period, activity concentrations in the top layer of the columns were above 30 000 Bq kg-1 for Ra-226 and Ra-228, and around 15 000 Bq kg-1 for Th-228. Radionuclides are not homogenously distributed in the filter columns. In order to estimate the average activity concentrations in the filter media, the height distribution of radionuclides has to be accounted for. Two years and two months after commissioning the treatment plant, the average activity concentrations of Ra isotopes in the filter columns were in the range 10 000 Bq kg-1, while Th-228 activity concentration was roughly 3500 Bq kg-1.

Long-term monitoring of a water treatment technology designed for radium removal - removal efficiencies and NORM formation.

A drinking water treatment plant in Viimsi, Estonia was monitored over three years for iron, manganese, radium-226, radium-228, and their daughter nuclides in order to determine the efficiency of the treatment process, get an insight of the removal mechanisms and interactions between radium, iron, and manganese, and assess the overall longevity and performance of the technology and possible build-up of NORM from the treatment process. During the study, samples were collected from raw water, first and second stage filtrate, consumer water, backwash water, and filter materials. The results show a consistent removal efficiency for iron and manganese, as well as an average of over 85% removal for radium with a slight decline with time. Backwash process has been optimized for maximum radium removal from the filters, while keeping the radium concentrations in the backwash water below exemption levels. However, accumulation of radium and thorium occurs in the filter material, exceeding exemption levels in the top layer of the filter columns in less than a year. By the end of the observation period, activity concentrations in the top layer of the columns were above 30 000 Bq/kg for Ra-226 and Ra-228, and around 15 000 Bq/kg for Th-228. Radionuclides are not homogenously distributed in the filter columns. In order to estimate the average activity concentrations in the filter media, the height distribution of radionuclides has to be accounted for. Two years and two months after commissioning of the treatment plant average activity concentrations of Ra isotopes in the filter columns were in a range of 10 000 Bq/kg while Th-228 activity concentration was roughly 3500 Bq/kg.

Temporal changes in radiological and chemical composition of Cambrian-Vendian groundwater in conditions of intensive water consumption.

Intensive groundwater uptake is a process at the intersection of the anthroposphere, hydrosphere, and lithosphere. In this study, groundwater uptake on a peninsula where only one aquifer system - the Cambrian-Vendian (CmV) - is available for drinking water uptake is observed for a period of four years for relevant radionuclides and chemical parameters (Cl, Mn, Fe, δ18O). Intensive groundwater uptake from the CmV aquifer system may lead to water inflow either from the sea, through ancient buried valleys or from the under-laying crystalline basement rock which is rich in natural radionuclides. Changes in the geochemical conditions in the aquifer may in turn bring about desorption of Ra from sediment surface. Knowing the hydrogeological background of the wells helps to predict possible changes in water quality which in turn are important for sustainable groundwater management and optimization of water treatment processes. Changes in Cl and Ra concentrations are critical parameters to monitor for sustainable management of the CmV groundwater. Radionuclide activity concentrations in groundwater are often considered rather stable, minimum monitoring frequency of the total indicative dose from drinking water is set at once every ten years. The present study demonstrates that this is not sufficient for ensuring stable drinking water quality in case of aquifer systems as sensitive as the CmV aquifer system. Changes in Cl concentrations can be used as a tool to predict Ra activity concentrations and distribute the production between different wells opening to the same aquifer system.

Polychlorinated biphenyls-containing electrical insulating oil contaminated soil treatment with calcium and magnesium peroxides.

Calcium and magnesium peroxides were applied for the treatment of soil contaminated by polychlorinated biphenyls-containing electrical insulating oil (Aroclor 1016). The removal of PCB-containing electrical insulating oil was achieved with the addition of either calcium peroxide or magnesium peroxide alone and dependent on dosages of the chemical. A 21-d treatment of 60% watered soil with the moderate addition (chemical/oil weight ratio of 0.005/1) of either calcium peroxide or magnesium peroxide resulted in nearly complete (96 ± 2%) oil removal, unsubstantial increase in soil pH and almost no changes in oxygen consumption and dehydrogenase activity, making it suitable for the soil decontamination.

Combined chemical treatment of pharmaceutical effluents from medical ointment production.

Three wastewater samples from a pharmaceutical plant formulating medical ointments were subjected to lab-scale treatment by a Fenton-like system in combination with lime coagulation. All samples were plant pre-treated by adsorption/flocculation/filtration processes with utilization of bentonite, but the quality of effluents did not comply with the regulations for wastewater discharged to local sewerage. The optimization of Fenton-like oxidation demonstrated the highest process efficacy at H(2)O(2)/COD weight ratio of 2:1, H(2)O(2)/Fe(2+) molar ratio of 10:1 and 2h of treatment time. The fast pH decrease to acidic values approximately 3 during first min of oxidation for all effluents suggested that pH adjustment was unnecessary. Combination of Fe(III) precipitation and lime coagulation proved feasible to improve considerably COD and residual iron concentration reduction in pharmaceutical effluents. Additionally, considerable BOD(7) reduction and BOD(7)/COD ratio improvement of pharmaceutical wastewater samples was achieved by combined treatment. The application of Fenton-like oxidation with subsequent iron (III)/lime coagulation did not only enhance the quality of pharmaceutical effluents with different chemical characteristics and help to meet the requirements for wastewater discharged to sewage, but also improve the biodegradability of pharmaceutical effluents.