Hybrid reactor for priority pollutant-trichloroethylene removal

The present study was initiated to explore the potential of a hybrid biological reactor, combining trickling filter (TF) and activated sludge process (ASP), to treat wastewater containing trichloroethylene (TCE) at ambient temperature at different hydraulic retention time (HRT). The biofilm acclimation was achieved in 55-60 days with gradual increase in TCE concentration from 1 mg/l to 100 mg/l with a parallel increase in the concentration of substrate sodium acetate and other nutrients. COD and TCE concentration were taken as prime parameters for monitoring the growth of biofilm. During acclimation COD removal varied between 54.6-97.5% while TCE was removed 72.6-99.9%. HRT study was performed after acclimation. The removal efficiency increased with decreasing flow rate with maximum TCE removal (99.99%) at 6 l/d corresponding to an HRT of 28 h (TF 18 h + ASP 10 h). This was followed by a C:N:P ratio study. A ratio of 100:20:1 led to the sustenance of maximum TCE removal. Maximum TCE removal (99.99%) was observed at a substrate:cosubstrate ratio of 100:1. A pH of 7.4 +/- 0.2 was found to be optimum for degradation. Finally, volatilization losses were estimated to be 18.5%. A mass balance gave an efficiency of 81.51% for biological removal of TCE.     

Sulfolane biodegradation potential in aquifer sediments at sour natural gas plant sites

Sulfolane is used in the treatment of sour natural gas. It is a highly water soluble compound that has been introduced into soils and groundwaters at a number of sour gas processing plant sites. Aquifer sediments from contaminated locations at three sites in western Canada were assessed for microbial activity and their ability to degrade sulfolane under aerobic and five anaerobic (nitrate-, Mn(IV)-, Fe(III)-, sulfate- and CO₂-reducing) conditions. The microcosms were supplemented with 200 mg/L sulfolane and adequate supplies of N, P, and the appropriate terminal electron acceptor. Microcosms containing contaminated aquifer sediments from each of the three sites were able to degrade sulfolane aerobically at 8°C and 28°C, and the biodegradation followed zero-order kinetics. The lag times before the onset of sulfolane biodegradation were shorter when sulfolane-contaminated sediments were used as inocula than when uncontaminated soils were used. No anaerobic sulfolane biodegradation was observed at 28°C, nor was sulfolane biodegradation observed at 8°C under Fe(III)-, sulfate- and CO₂-reducing conditions. At 8°C, anaerobic degradation of sulfolane coupled to Mn(IV) reduction was observed in microcosms from two sites, and degradation coupled to nitrate reduction was seen in a microcosm from one of the contaminated sites.     

The manual determination of ammonia in fresh waters using an ammonia-sensitive membrane-electrode

The use of a commercially-available ammonia-sensitive membrane-electrode for the manual determination of ammonia in discrete samples of fresh water has been investigated and the analytical procedure is described. The electrode is simple and convenient to use, and a sample can be analyzed in a few minutes. For normal routine analysis, the lower limit of determination is approximately 0·1 mg N 1⁻¹ though smaller concentrations can be measured. The relative standard deviation of analytical results varied from approximately 10 to 3 per cent as ammonia concentration increased from 0·1 to 4 mg N 1⁻¹. Results for samples of river water agreed well with those obtained by absorptiometric methods of analysis; the electrode responds to amines but otherwise appears to be essentially specific for ammonia. Use of the electrode will be advantageous in a number of applications, and it also has good potential for the on-line analysis of fresh waters.     

Treatment of poultry manure wastewater using a rotating biological contactor

A pilot scale, six stage rotating biological contactor was used to evaluate the feasibility of this process for the stabilization of liquid animal manures. Total disc surface area was approx. 16.7 m². Treatment efficiencies were determined at various waste strengths and influent flow rates.With loading rates of 14.7–322 g m⁻² day⁻¹, the average COD reduction was 61%. With loading rates of 4.88-24.4 g m⁻² day⁻¹, the average BOD₅ reduction was 87%. Total nitrogen removal averaged approximately 30% for the entire study. Mixed liquor oxygen uptake rates were generally in excess of 80 mg 1⁻¹ h⁻¹.Clarified effluent was non-odorous and suitable to be reused for manure flushing or spray irrigation. Treatment was not sufficient to permit effluent discharge to surface waters.     

Assessment of environmental tobacco smoke exposure: urinary cotinine concentrations in children are strongly associated with the house dust concentrations of nicotine at home

In the present study the possibility of using nicotine in house dust as an index of environmental tobacco smoke (ETS) exposure was evaluated in an environmental investigation of 23 children with asthma. A standardized procedure for house dust sampling of nicotine with a filter holder connected to a vacuum cleaner, for a defined time and area was developed (F-nicotine). Also, house dust sampling was carried out from the vacuum cleaner bags of the homes (VC-nicotine). There was a larger variation in VC-nicotine (13-655, median 66 microg/g) compared with F-nicotine (15-393 median 156 microg/g). There were statistically significant associations between an inquiry data based ETS exposure index on the one hand, and urinary cotinine concentrations in children (U-cotinine), F-nicotine and VC-nicotine of their homes, on the other. The strong correlation between U-cotinine and F-nicotine (rs = 0.93; P < 0.0001) indicates that the new standardized house dust sampling method should be useful in ETS exposure assessment. However, further validation by a larger sample size with repeated measurements in the same homes is needed.     

Microbial activity and distribution during enhanced contaminant dissolution from a NAPL source zone

Laboratory experiments were conducted to assess microbial reductive dechlorination in one-dimensional sand columns containing a 10 cm long source zone of uniformly distributed residual tetrachloroethene (PCE) nonaqueous phase liquid (NAPL), a 10 cm long transition zone directly down-gradient of the source zone containing some nonuniformly distributed NAPL ganglia, and a 40 cm long plume region down-gradient of the transition zone. The activity and distribution of Sulfurospirillum multivorans, a PCE-to-1,2-cis-dichloroethene (cis-DCE) dechlorinating bacterium, was evaluated in columns containing either a mixed-NAPL (0.25 mol/mol PCE in hexadecane) or pure PCE-NAPL. Significant dechlorination of PCE to cis-DCE was observed in the mixed-NAPL column, resulting in 53% PCE-NAPL mass recovery in the effluent with PCE-NAPL dissolution enhanced by up to 13.6-fold (maximum) and 4.6-fold (cumulative) relative to abiotic dissolution. Quantitative real-time PCR targeting pceA, the PCE reductive dehalogenase gene of S. multivorans, revealed that S. multivorans cells were present in the NAPL source zone, and increased in numbers (i.e., grew) throughout the source and transition zones. In contrast, minimal reductive dechlorination and microbial growth were observed in the column containing pure PCE-NAPL, where aqueous-phase PCE concentrations reached saturation. These results demonstrate that microbial growth within NAPL source zones is possible, provided that contaminant concentrations remain below levels toxic to the dechlorinating organisms, and that microbial growth can result in significant bioenhanced NAPL dissolution.     

Haloacetic acids and trihalomethanes in finished drinking waters from heterogeneous sources

Trihalomethanes (THM) and haloacetic acids (HAA) are the most frequent chlorination by-products (CBP) in finished drinking waters. Traditionally, THM have been used as surrogates for CBP although the quantitative association between THM and other CBP is not well established. This problem is addressed in the present study from the analysis of THM and HAA in drinking water samples from four Spanish regions, representing areas with very different CBP composition, e.g. between 86 and 8.0 microg/l of THM and 50-3.0 microg/l of HAA.The resulting dataset exhibit a statistically significant correlation between total THM and HAA (Pearson's correlation coefficient, r(p)=0.815,p<0.0005). Furthermore, specific HAA are highly correlated with specific THM or their combinations. Accordingly, multivariate linear regression analysis of the concentrations observed show that the levels in total and specific HAA can be predicted from the THM content. These results are relevant for epidemiological studies on health effects from CBP exposure since they usually involve comparison of populations consuming waters of very distinct quality.     

The acute effect of bunker C oil and an oil dispersant on: 1 Serum glucose, serum sodium and gill morphology in both freshwater and seawater acclimated rainbow trout (Salmo gairdneri)

Bunker C oil and an oil dispersant were tested for physiological stress on both freshwater and saltwater acclimated rainbow trout. Both compounds tended to reduce serum glucose levels with Bunker C causing the more significant decrease (P < 0.08), indicating a possible dysfunction of the kidney. The freshwater treatment group showed a significant decrease in sodium levels (P < 0.01) when treated with a dispersant, while under similar conditions, saltwater acclimated fish show a very marked increase in serum sodium concentrations (P < 0.025). Those fluctuations in sodium levels are resultant from direct interference with the energy activated sodium transport systems of the gills. Microphotographs of gill filaments and lamellae show severe damage caused by the dispersant and dispersant/oil mixture with less impairment resultant from Bunker C exposure.     

Organochlorine insecticides and PCB'S in sediments of Lake St. Claire (1970 and 1974) and Lake Erie (1971).

Sediments were collected on a grid from Lake St. Clair in 1970 and 1974 and from Lake Erie in 1971 and analysed for organochlorine insecticides and PCBs. Suspended solids were centrifuged from pumped water in the Detroit River in 1974. Residues of DDE, TDE and DDT were highest in sediment from the Western Basin (70.3 ppb) Lake Erie and lowest in sediment from Lake St. Clair (6.6 ppb in 1970 and 2.6 ppb in 1974). The Central and Eastern Basins of Lake Erie contained residues that fell about mid-way between these means. TDE was the predominant component of ΣDDT and was followed by DDE at approximately half this residue. While DDT represented the lowest component in lake sediments, it was the highest component in suspended solids from the Detroit River.HEOD was present in the entire lake system but at only a fraction of the level of ΣDDT. The mean residue in Lake St. Clair was only 0.1 ppb while Lake Erie sediments contained 1–2 ppb. The highest mean residue (3.6 ppb) was in suspended solids in the Detroit River. Other organochlorine insecticides were only occasionally identified.PCB residues in sediment were approximately 3 times higher than the total organochlorine insecticide residue, being highest in the Western Basin (252 ppb) and lowest in Lake St. Clair (19 ppb in 1970 and 10 ppb in 1974). The Detroit River and Central and Eastern Basins of Lake Erie had intermediate residues.Residues in Lake St. Clair indicated a decline in ΣDDT, HEOD, and PCB residues between 1970 and 1974, and this coincided with the restrictions on the materials. A core sample from the Western Basin of Lake Erie indicated that ΣDDT, HEOD and PCB began to accumulate in sediments in 1958, 1953, and 1956, respectively. This appeared to indicate a lag period of 2–5 years after wide-spread use occurred.