Validation of the new passive monitor without a membrane in indoor air

A series of experiments were conducted to investigate the suitability of activated carbon cloth (ACC) strips for diffusive sampling of volatile organic compounds in air without using a membrane. Experiments were carried out in an environmental chamber and in an indoor air environment. The monitors were analyzed qualitatively by liquid extraction and gas chromatography-mass spectrometry and quantitatively by gas chromatography with a flame ionization detector. It was shown that ACC monitors can provide satisfactory quantitative data for a wide variety of volatile organic compounds in indoor air ranging in concentration from 1 mg/m³ to 0.02 g/m³. It was also observed that the absence of a membrane does not affect the linearity of the sampling rate. In addition, a packaging system has been developed that allows samples to be sent out and returned to the laboratory for analysis by mail. Recycling, a convenient procedure of exposure, delivery, and return by postal service, as well as simple analysis all show that this passive sampler substantially reduces the cost of monitoring, thus demonstrating its benefits in the determination of contamination sources within both large industrial sites or any other building where such an analysis may be required.     

Determination of phthalate ester plasticizers in the aquatic environment of Southwestern Nigeria

Water from the Lagos, Oyo, Osun, Ondo, and Delta states of Nigeria and the cities' water treatment plants had been analized for the presence of ubiquitous phthalate esters using liquid chromatography. Extraction with CH₂Cl₂ and liquid chromatography was used for compound separation. Several phthalate esters, dimethyl- (DMP), diethyl- (DEP), and di-n-butyl- (DBP) were found present at levels of 10 mg L⁻¹ to 1472 mg L⁻¹ in river water and 91 mg L⁻¹ to 1219 mg L⁻¹ in tap water from the cities' water treatment plants. A study of uncontaminated water was done to establish blank levels.     

Chemical and microbiological examination of well and Nile water

The chemical composition and microbiological contamination of well water and Nile River water used for drinking were investigated in localities around Khartoum, Sudan, to present baseline data. The chemical analyses results obtained indicated that public health hazards due to pH, Ca⁺⁺, CO₃^??, HCO₃^?, and NO₃^? are unlikely in all the samples studied, while Na⁺ and Cl^? ions concentrations in well water warrant some attention. Contamination from organic matter and suspended material is also negligible. Microbial contamination with coliform and fecal coliform is high in surface wells and in the Nile River, but negligible in deep bores, tap water, and mineral water. The logarithm of the colony count ranges from zero for mineral water to 6.8 for water from the White Nile. In addition to drawing further attention to the well water and Nile water used for drinking by a wide sector of the population, the microbial count data for water from the Nile disagreed with the generally held belief that the Nile, being one of the largest rivers of the world, carries no detectable fecal contamination. Our data also did not support the belief that the White Nile is more contaminated than the Blue Nile.     

Screening of household products for the emission of volatile organic compounds

10 household products, eight waxes or polishes, and two detergents have been screened by a headspace technique for the emission of volatile organic compounds (VOC). Using Tenax sampling and analysis by combined gas chromatography-mass spectrometry (GC-MS) more than 80 single compounds or groups of isomers have been identified, and semiquantitative data on the initial emission rates (emission rate immediately after application) have been obtained. Products fall into two groups: those containing water as a main (80 to 90%) constituent and those without water. The initial emission rate of the first group ranged from 0.2 to 2 μg cm⁻²min⁻¹, whereas the second group had higher emission rates of up to 430 μg cm⁻²min⁻¹. Products of the second group emit essentially hydrocarbons (alkanes, alkenes, and terpenes), whereas most products of the first group emit oxygenated compounds including terpene alcohols and their acetates, aliphatic alcohols and esters, and alkoxy-alcohols.     

Fractionation of plutonium in environmental and bio-shielding concrete samples using dynamic sequential extraction

Fractionation of plutonium isotopes (²³⁸Pu, ^239,240Pu) in environmental samples (i.e. soil and sediment) and bio-shielding concrete from decommissioning of nuclear reactor were carried out by dynamic sequential extraction using an on-line sequential injection (SI) system combined with a specially designed extraction column. Plutonium in the fractions from the sequential extraction was separated by ion exchange chromatography and measured using alpha spectrometry. The analytical results show a higher mobility of plutonium in bio-shielding concrete, which means attention should be paid to the treatment and disposal of nuclear waste from decommissioning.     

Drugs of abuse and benzodiazepines in the Madrid Region (Central Spain): Seasonal variation in river waters,occurrence in tap water and potential environmental and human risk

This work analyzes the seasonal variation (winter and summer) of ten drugs of abuse, six metabolites and three benzodiazepines in surface waters from the Jarama and Manzanares Rivers in the Madrid Region, the most densely populated area in Spain. The occurrence of these compounds in tap water in this region is also investigated and a preliminary human health risk characterization performed for those substances found in tap water. Finally, a screening level risk assessment that combines the measured environmental concentrations (MECs) with dose–response data to estimate Hazard Quotients (HQs) for the compounds studied is also presented.The results of this study show the presence of fourteen out of the nineteen compounds analyzed in winter and twelve of them in summer. The most ubiquitous compounds, with a frequency of detection of 100% in both seasons, were the cocaine metabolite benzoylecgonine (BE), the amphetamine-type stimulant (ATS) ephedrine (EPH), the opioid methadone (METH), the METH metabolite 2-ethylene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP), and the three benzodiazepines investigated, namely alprazolam (ALP), diazepam (DIA) and lorazepam (LOR). The highest concentrations observed corresponded to EPH (1020 ng L^− 1 in winter and 250 ng L^− 1 in summer). The only compounds not detected in both seasons were heroin (HER) and its metabolite 6-acetylmorphine (6ACM), lysergic acid diethylamide (LSD) and its metabolite 2-oxo-3-hydroxy-LSD (O-H-LSD), and Δ⁹-tetrahydrocannabinol (THC). In terms of overall concentration, all sampling points presented higher concentrations in winter than in summer. Statistical analyses performed to gather evidence concerning occasional seasonal differences in the concentrations of individual substances between summer and winter showed statistically significantly higher concentrations (p < 0.05) of BE, EPH and the opioid morphine (MOR) in winter than in summer. Two out of the nineteen compounds studied, namely cocaine (CO) and EPH, were detected in tap water from one sampling point at concentrations of 1.61 and 0.29 ng L^− 1, respectively. The preliminary human health risk characterization showed that no toxic effects could be expected at the detected concentration level in tap water.The screening level risk assessment showed that MOR, EDDP and the THC metabolite 11-nor-9-carboxy-Δ⁹-tetrahydrocannabinol (THC-COOH) were present in at least one of the sampling sites in a concentration leading to a Hazard Quotient (HQ) value between 1.0 and 10.0, thus indicating some possible adverse effects. The cumulative HQ or Toxic units (TUs) calculated for each of the groups studied showed that opioids and cannabinoids were present at concentrations high enough to potentially generate some adverse effects on at least one sampling point.     

Association of organic matter, iron and inorganic phosphorus in lake waters

Gel permeation chromatography was used to fractionate ³²PO₄³⁻ labelled components by molecular size in filtered, destabilized lake foam, concentrated lake water, and lake sediment extracts. Evidence is presented for the abiotic formation of organic matter iron inorganic P complexes in lake foam, water and sediments. ³²PO₄^staggered was found to excahnge with low molecular weight, dissolved P fraction, probably an organic matter -Fe- inorganic P complex, but not with a high molecular weight, non-inorganic dissolved reactive P pool, hypothesized to be similar to the dimer. Our experiments suggest that inorganic P binding by high molecular weight organic matter may play a significant role in the P cycle. If the bound P is unavailable to algae and bacteria, the complexes could explain Rigler's (1968) hypothesis that the molybdenum blue technique may overestimate the free orthophosphate concentration by 10–100 times.     

CO2 dispersion around two PWR nuclear power plants in Brazil

Atmospheric air samples were taken within 3 km from power plants encompassing five different distances and wind directions. Samples were taken between 2002 and 2005 aiming to evaluate the environmental ¹⁴C enrichment due to the operation of Brazilian nuclear power plants. The sampling system consisted of a pump connected to a trapping column filled with a 3 M NaOH solution. The trapped CO₂ was analyzed for ¹⁴C by using a single stage accelerator mass spectrometry (SSAMS).     

Contrasting cesium dynamics in neighboring deep and shallow warm-water reservoirs

To measure the long term retention and seasonal dynamics of an initial 4 kg addition of ¹³³Cs into an 11.4-ha, 157,000 m³ reservoir (Pond 4, near Aiken, South Carolina, USA), the concentrations and inventories of ¹³³Cs in the water column were measured at periodical intervals for 522 days following the 1 August, 1999 release. After rapid declines in concentrations and inventories during the first 90 days, the ¹³³Cs concentrations in the water column declined at an average proportional rate of 0.004 d⁻¹. However, there were periods of less rapid and more rapid rates of declines, and these were correlated with periods of increasing and decreasing K concentrations in the water column. The decline rates were less and the K concentrations greater in the winter than in the summer. In the deeper, neighboring monomictic reservoirs of Par Pond and Pond B, a yearly cycle of increasing and decreasing ¹³⁷Cs concentrations in the water column is driven by anoxic remobilization of Cs from the sediments into a persistent summer hypolimnion. In Pond 4, whose mean depth of 1.6 m is too shallow to support a persistent anoxic hypolimnion, the pattern of yearly dynamics for K and Cs appear to be related to the accumulation and release of these elements from the extensive, seasonal macrophyte communities. The contrasting results between Pond 4 and Pond B suggest that a full appreciation of the relative importance of 1) anoxic remobilization and 2) accumulation and release by macrophytes in these systems remains to be established.     

Foliar uptake of Cs from the water column by aquatic macrophytes

A transplant experiment was performed to determine the relative importances of root uptake from the sediments and foliar uptake from the water column in determining the accumulation of ¹³⁷Cs by aquatic macrophytes. Uncontaminated individuals of three species, Brasenia schreberi, Nymphaea odorata and Nymphoides cordata, were transplanted into pots containing either contaminated sediments (i.e. 1.2 Bq ¹³⁷Cs g⁻¹ dry mass) or uncontaminated sediments (i.e. < 0.1 Bq g⁻¹ dry mass) and immersed in Pond B, a former reactor cooling pond where ¹³⁷Cs concentrations in surface waters range from 0.4 to 0.8 Bq liter⁻¹. The plants in uncontaminated sediments rapidly accumulated ¹³⁷Cs from the water column and after 35 days of immersion had ¹³⁷Cs concentrations in leaves that were: (1) not statistically significantly different from those for plants in contaminated sediments; and (2) similar to those for the same species growing naturally in Pond B. The similarity in ¹³⁷Cs concentrations between naturally-occurring plants and those in pots with uncontaminated sediments suggests that foliar uptake from the water column is the principal mode of Cs accumulation by these species in Pond B.     

Cesium accumulation by fish following acute input to lakes: a comparison of experimental and Chernobyl-impacted systems

An uptake parameter u (L kg⁻¹ d⁻¹) and a loss rate parameter k (d⁻¹) were estimated for the patterns of accumulation and loss of ¹³³Cs by three fish species following an experimental ¹³³Cs addition into a pond in South Carolina, USA. These u and k parameters were compared to similar estimates for fish from other experimental ponds and from lakes that received ¹³⁷Cs deposition from Chernobyl. Estimates of u from ponds and lakes declined with increasing potassium concentrations in the water column. Although loss rates were greater in the experimental ponds, the times required to reach maximum Cs concentrations in fish were similar between ponds and lakes, because ponds and lakes had similar retentions of Cs in the water column. The maximum Cs concentrations in fish were largely determined by initial Cs concentrations in the water column. These maximum concentrations in fish and the times required to reach these maxima are potentially useful indicators for assessments of risks to humans from fish consumption.     

The influence of ventilation on indoor/outdoor air contaminants in an office building

The air quality in a newly built preschool was investigated in a longitudinal study. Typical air contaminants emanating from building materials were determined, their variation over time (0–18 months) was measured, and the influence of the ventilation system (81%–91% recirculation of return air) on contaminant concentrations was studied. Volatile organic compounds were sampled by adsorption on porous polymer, analysed by a GC/FID system, and identified by MS. A spatial build-up in concentration (ppb or μg/m³ levels) is evident for all the organic compounds, as well as for CO₂, from the outdoor air, through the ventilation system, and through the rooms to the exhaust air. The longitudinal comparison over time shows that all the organic compounds decline in concentration mainly within the first 6 months of occupancy: 1-butanol 4–14 times, toluene and pentanal + hexanal 2–4 times, while formaldehyde remained at a constant low level of 90 ppb (110 μg/m³). It is difficult to believe that the problems of poor air quality in 100 preschools in Stockholm are caused by the organic compounds alone unless interactions occur. A preschool building needs to be gassed off during the first 6 months after its construction with no recirculation of return air allowed (outdoor air rate approx 4–5 ach). During at least 1–2 additional years, it is desired that the recirculation rate of return air is restricted, perhaps to 50%.     

Environmental significance of nitrogenous organic compounds in aquatic sources

The presence of nitrogenous organic compounds in raw water sources for municipal supplies is of environmental concern because many of them exert significant chlorine demand, while some produce complex stable mutagenic products upon chlorination or are precursors to haloform formation. Seven N-organic compounds have been identified in municipal water concentrates (adenine, 5-chlorouracil, cytosine, guanine, purine, thymine, and uracil) at concentrations ranging from 20 to 860 μg/L. Eight compounds (adenine, cytosine, purine, pyrrole, thymine, tryptophan, tyrosine, and uracil) have been found in filtrates from cultures of either Anabaena flos aquae or Oscillatoria tenuis. Calculated CHCl₃ levels which might have formed at pH 7 in the water supplies were well below the maximum contaminant level (MCL) of 0.1 mg/L proposed by the U.S. Environmental Protection Agency (USEPA) for total trihalogenated methanes. Calculated levels of CHCl₃ which might have been formed under more alkaline conditions, however, were more than 10% of the MCL and were therefore significant. Calculated levels of combined forms of chlorine yielding falsely positive tests for free chlorine in some samples were slightly less or exceeded the 0.5 mg/L free chlorine residual generally taken as an acceptable level of disinfection. The demonstration of a parallel increase in organic nitrogen content with population density in two laboratory grown blue-green algal cultures, and the finding of elevated organic nitrogen values in a water supply sample collected during the occurrence of a blue-green algal bloom, suggested that summer algal bloom occurrence can add considerably to the organic nitrogen content and the trihalomethane potential of water supplies.     

Sulfide production during anaerobic lagoon treatment of tapioca wastewater

Laboratory-scale experiments on anaerobic lagoon treatment of tapioca wastewater were conducted under ambient, tropical conditions. The objectives of this study were to investigate factors that affect hydrogen sulfide production and to propose means to control the formation of hydrogen sulfide in lagoon effluents. The concentrations of sulfides were found to increase with increasing organic loading from 2.76 to 5.77 kg COD/m³.d, decreasing hydraulic retention time; and increasing pH from 3 to 7. The maximum total sulfide concentration of 18.8 mg/L occurred at the organic loading of 5.77 kg COD/ m³.d and neutral pH. the maximum H₂S concentration was calculated to be 13.3 mg/L which occurred in the laggoon operated at an organic loading of 5.77 kg COD/m³.d and a pH of 5. The control of odour problems due to the H₂S formation should be possible by raising pH of the lagoon water to be more than 8 or operating the lagoon at low organic loadings.     

Deposition of gamma emitters from Chernobyl accident and their transfer in lichen–soil columns

Lichen–soil column samples were taken from several locations in the Southern Finland between 1986 and 2006. Columns were divided into three parts, upper lichen, lower lichen and underlying soil, and their gamma emitting radionuclides, ¹³⁴Cs, ¹³⁷Cs, ¹⁰³Ru, ⁹⁵Zr, ¹⁰⁶Ru, ^110mAg, ¹²⁵Sb and ¹⁴⁴Ce, were measured with gamma spectrometry. Deposition values were calculated as Bq/m² for each sampling site. Distribution of various radionuclides in the three compartments as a function of time was determined. Both effective and ecological half-lives of all radionuclides were calculated for upper lichen, whole lichen and whole lichen–soil column. A linear relation was derived between the physical half-lives and effective half-lives for whole lichen and for whole lichen–soil column. Reindeer meat activity concentrations of various radionuclides and ensuing radiation doses to reindeer-herding people were also estimated for a hypothetical case where a similar high radioactive pollution, as was taken place in the Southern Finland, would have occurred in the reindeer-herding areas in the Finnish Lapland.     

Pu/Cs ratios in the water column of the North Pacific: a proxy of biogeochemical processes

Anthropogenic radionuclides in seawater have been used as transient tracers of processes in the marine environment. Especially, plutonium in seawater is considered to be a valuable tracer of biogeochemical processes due to its particle-reactive properties. However, its behavior in the ocean is also affected by physical processes such as advection, mixing and diffusion. Here we introduce Pu/¹³⁷Cs ratio as a proxy of biogeochemical processes and discuss its trends in the water column of the North Pacific Ocean. We observed that the ^239,240Pu/¹³⁷Cs ratio in seawater exponentially increased with increasing depth (depth range: 100–1000 m). This finding suggests that the profiles of the ^239,240Pu/¹³⁷Cs ratios in shallower waters directly reflect biogeochemical processes in the water column. A half-regeneration depth deduced from the curve fitting the observed data, showed latitudinal and longitudinal distributions, also related to biogeochemical processes in the water column.     

Association of plutonium with sediments from the Ob and Yenisey Rivers and Estuaries

The present study applied sequential extraction techniques to investigate the binding and mobility of plutonium (Pu) in sediments from the rivers and estuaries of the Ob and Yenisey. As a study site, the Ob and Yenisey are particularly interesting as both rivers have weapons-grade Pu sources in their catchment areas, including the Russian Pu production and reprocessing plants at Mayak, Tomsk-7 and Krashnoyarsk, and the Semipalantinsk nuclear weapons testing site in Kazakhstan. Plutonium activity and ²⁴⁰Pu/²³⁹Pu ratios were determined using accelerator mass spectrometry (AMS). Sequential extractions showed that between 47 and 80% of the Pu in Yenisey River sediments and 35–53% of the Pu in soils around the Techa River are mobilized with weak oxidising agents, which can indicate that Pu is bound to organic material. In contrast, Pu in Ob and Yenisey Estuarine sediments was more strongly bound, with 60–100% being found in the HNO₃-extractable fraction. This change in speciation could reflect either that Pu bound to organic material in the Techa and Yenisey River sediments becomes more fixed to the sediments with time, or that organic-bound Pu is mobilized and released to the water when the sediments encounter the more saline water of the Ob and Yenisey estuaries. In general, ²⁴⁰Pu/²³⁹Pu ratios were relatively consistent between different extraction fractions, although, in whole sediments, an increase in ratio was observed with distance from the source. This reflects the increased influence of weapon fallout from catchment runoff within the river systems, as compared to the weapons-grade sources close to the production and reprocessing plants. Knowledge of Pu speciation in the Ob and Yenisey Rivers, and the processes controlling its behaviour in estuarine systems, can improve predictions of its transfer and subsequent environmental impact to Arctic Seas.     

Determination of U, Pu and Am isotopes in Irish Sea sediment by a combination of AMS and radiometric methods

Samples from a marine sediment core from the Irish Sea (54.416 N, 3.563 W) were analyzed for the isotopic composition of uranium, plutonium and americium by a combination of radiometric methods and AMS. The radiochemical procedure consisted of a Pu separation step by anion exchange, subsequent U separation by extraction chromatography using UTEVA^® and finally Am separation with TRU^® Resin.Additionally to radiometric determination of these isotopes by alpha spectrometry, the separated samples were also used for the determination of ²³⁶U/²³⁸U and plutonium isotope ratios by Accelerator Mass Spectrometry (AMS) at the VERA facility.     

Towards green membranes: preparation of cellulose acetate ultrafiltration membranes using methyl lactate as a biosolvent

Ultrafiltration membranes were prepared using cellulose acetate (CA) as a polymer, LiCl and CaCl₂ as porogens and methyl-(S)-lactate as a solvent. CA, methyl lactate and the porogens used in this work are obtained from renewable resources; they are biodegradable, non-toxic and non-volatile organic compounds. Flat sheet ultrafiltration membranes were prepared by the phase inversion technique. A molecular weight cut-off between 15 and 35 kDa (polyethylene glycol) and pure water permeability between 13 and 177 litres h^? 1m^? 2 bar^? 1 were obtained. These parameters are in the ideal range for water treatment industry. Improvement of pollutant degree and ecotoxicity of the process was evaluated by ‘green’ metrics by the P (pollutants, persistent and bioaccumulative) and E (ecotoxicity) parameters. Both of these variables were recorded as zero using our method. This study represents a step ahead towards the production of ultrafiltration polymeric membranes by a ‘greener’ process than current methods.     

Indoor air pollution due to organic gases and vapours of solvents in building materials

The emission of organic gases and vapours of solvent type from 42 commonly used building materials was measured under standard atmospheric conditions. An average of 22 compounds was found in the air around each building material, and the total concentration of gases and vapours was from 0.01 to 1410 mg/m³. The average arithmetic emission rate was 9.5 mg/m² h, and 52 different compounds were identified. A mathematical model was established for the indoor air concentrations of pollutants originating from building materials. The model was tested on three model rooms constructed from the materials investigated. The calculated total air concentrations of gases and vapours in the three rooms ranged from 1.6 to 23.6 mg/m³, and the number of compounds in the air from 23 to 32. These concentrations and number of compounds did not differ from those found in actual rooms similar in size and construction to the model rooms. The risks of health effects due to the compounds identified from the building materials were investigated, and criteria for future air quality standards are discussed. It is concluded that the possibility of negative health effects cannot be neglected, especially not for the more sensitive minority of the general population.