Polycyclic aromatic hydrocarbons, elemental and organic carbon emissions from tire-wear

Tire-wear is an important source of PAHs, elemental carbon (EC) and organic carbon (OC). The emissions of these pollutants have been studied in an experimental set-up, simulating a realistic road-tire interaction (summer tire-concrete road). The large particle non-exhaust emissions (LPNE; diameter greater than 10 μm) have been evaluated over 14,500 km run of the tire. An increasing linear trend with cumulative km run was observed for emissions of PAHs and carbon. Amongst PAHs in LPNE, pyrene has been observed to be the highest (30 ± 4 mg kg^− 1) followed by benzo[ghi]perylene (17 ± 2 mg kg^− 1). Different fractions of EC-OC for tire-wear have been analyzed, and unlike exhaust emissions, EC1 was observed to be 99% of EC whereas more than 70% of the OC was the high temperature carbon (OC3 and OC4). The overall emission factors (mass tire^− 1 km^− 1) for PAHs, EC and OC from tire-wear are 378 ng tire^− 1 km^− 1, 1.46 mg tire^− 1 km^− 1 and 2.37 mg tire^− 1 km^− 1 for small cars.     

Carbonaceous characteristics of atmospheric particulate matter in Hong Kong

To determine the characteristic of carbonaceous species in atmospheric particles in Hong Kong, PM₁₀ and PM_2.5 samples were collected using high volume (hi-vol.) air samplers from November 2000 to February 2001. The organic carbon (OC) and elemental carbon (EC) were analyzed by the selective thermal manganese dioxide oxidation (TMO) method. The ratios of PM_2.5/PM₁₀ mass ratios were 0.61, 0.78 and 0.53 for particulate matter collected at PolyU station (PolyU, near a major traffic corridor), Kwun Tong station (KT, mixed residential/commercial/industrial) and the Hok Tsui background station (HT), respectively. These results indicate that the PM_2.5 concentrations constitute the majority of the PM₁₀ concentrations, especially in urban and industrial areas of Hong Kong. The average concentrations at the three sites ranged from 73.11 to 83.52 μg/m³ for PM₁₀ and from 42.37 to 57.38 μg/m³ for PM_2.5. The highest daily mass concentrations of PM₁₀ and PM_2.5 were 125.89 μg/m³ and 116.89 μg/m³ at KT, respectively. The correlation between PM₁₀ and PM_2.5 was high at KT and HT (r>0.9, P<0.01). This means that the sources of PM₁₀ and PM_2.5 may be the same at both sites. The highest mean concentration of OC (12.02 μg/m³) and EC (6.86 μg/m³) in PM₁₀ was found at the PolyU among the three sites. For PM_2.5, the highest mean concentration of OC (10.16 μg/m³) was at KT while the highest mean concentration of EC (7.95 μg/m³) was at PolyU. However, the background concentrations at HT were higher than another background area, Kosan, Korea. Transportation of pollutants from the Asian continent may be responsible for the elevations of EC+OC at the remote site. More than 74% of the EC and more than 79% of the OC were found in the PM_2.5 fraction at the three sampling locations. At PolyU station, PM_2.5 consisted of 18.18% OC and 11.16% EC while 17.70% OC and 8.81% EC were found in KT station. Thus OC and EC are major constituents of aerosols in Hong Kong. OC/EC ratios for PM₁₀ and PM_2.5 were less than 2 at PolyU and KT stations while the ratio exceeded 3 at HT background station. This indicates that OC measured in the urban area may be emitted directly as a primary aerosol.     

Emission factors of gaseous pollutants from recent kerosene space heaters and fuels available in France in 2010

Laboratory measurements of the gaseous emission factors (EF) from two recent kerosene space heaters (wick and injector) with five different fuels have been conducted in an 8-m(3) environmental chamber. The two heaters tested were found to emit mainly CO(2), CO, NO, NO(2), and some volatile organic compounds (VOCs). NO(2) is continuously emitted during use, with an EF of 100-450 μg per g of consumed fuel. CO is normally emitted mainly during the first minutes of use (up to 3 mg/g). Formaldehyde and benzene EFs were quantified at 15 and 16 μg/g, respectively, for the wick heater. Some other VOCs, such as 1,3-butadiene, were detected with lower EFs. We demonstrated the unsuitability of a 'biofuel' containing fatty acid methyl esters for use with the wick heater, and that the accumulation of soot on the same heater, whatever the fuel, leads to a dramatic increase in the CO EF, up to 16 mg/g, which could be responsible for chronic and acute CO intoxications. PRACTICAL IMPLICATIONS: Our results show that in spite of new technologies and emission standards for unvented kerosene space heaters, as well as for the fuels, the use of these heaters in indoor environments still leads to NO(x) levels in excess of current health recommendations. Whereas injection heaters generate more nitrogen oxides than wick heaters, prolonged use of the latter leads to a soot buildup, concomitant with high CO emissions, which could be responsible for acute and chronic intoxications. The use of a biofuel in a wick heater is also of concern. Maintenance of the heaters and adequate ventilation of the room during use of kerosene space heaters are therefore of prime importance to reduce personal exposure.     

A comprehensive assessment of PM emissions from paved roads: Real-world Emission Factors and intense street cleaning trials

Compliance with air quality standards requires control of source emissions: fine exhaust particles are already subject to regulation but vehicle fleets increase whilst the non-exhaust emissions are totally uncontrolled. Emission inventories are scarce despite their suitability for researchers and regulating agencies for managing air quality and PM reduction measures. Only few countries in Europe proposed street cleaning as a possible control measure, but its effectiveness is still far to be determined.This study offers first estimates of Real-world Emission Factors for PM₁₀ and brake-wear elements and the effect on PM₁₀ concentrations induced by intense street cleaning trials.A straightforward campaign was carried out in the city of Barcelona with hourly elemental composition of fine and coarse PM to detect any short-term effect of street cleaning on specific tracers of non-exhaust emissions. Samples were analyzed by Particle Induced X-Ray Emission.Real-world Emission Factor for PM₁₀ averaged for the local fleet resulted to be 97 mg veh^− 1 km^− 1. When compared to other European studies, our EF resulted higher than what found in UK, Germany, Switzerland and Austria but lower than Scandinavian countries. For brake-related elements, total EFs were estimated, accounting for the sum of direct and resuspension emissions, in 7400, 486, 106 and 86 μg veh^− 1 km^− 1, respectively for Fe, Cu, Sn and Sb. In PM_2.5Fe and Cu emission factors were respectively 4884 and 306 μg veh^− 1 km^− 1.Intense street cleaning trials evidenced a PM₁₀ reduction at kerbside of 3 μg m^− 3 (mean daily levels of 54 μg m^− 3), with respect to reference stations. It is important to remark that such benefit could only be detected in small time-integration periods (12:00-18:00) since in daily values this benefit was not noticed. Hourly PM elemental monitoring allowed the identification of mineral and brake-related metallic particles as those responsible of the PM₁₀ reduction.     

Effect of various parameters on the ultraflocculation of fine sorbent particles,used in the wastewater purification from organic contaminants

A sorbent (Organosorb) is used in the wastewater purification from organic contaminants, here simulated by tetradecane. A short hydrodynamic treatment in a rather intense hydrodynamic field (G>10(3)) (called ultraflocculation) is applied to the sorbent suspension to which a flocculant is added. The efficiency of removal of the sorbent is studied. The sorbent concentration, the flocculant concentration, the treatment time, the organic pollutant (which has to be sorbed by the sorbent), the detergent (used for the emulsification of the pollutant), the pH and the calcium concentration of the water all influence the flocculation efficiency (E) of the sorbent particles. For each set of these parameters there exists an optimum intensity of the hydrodynamic treatment at which maximum flocculation efficiency is reached. An increase in the optimum intensity of the hydrodynamic field corresponds to an increased floc break-up, and consequently a lower maximum flocculation efficiency.     

Emissions of mercury and other trace elements from coal-fired power plants in Japan

To evaluate trace element emissions from modern coal-fired power plants into the atmospheric environment in Japan, trace elements in the coal used in electric utility boilers, stack concentrations, emission rates and emission ratios of coal-fired power plants, and proportions of trace elements in coal-fired power plants were studied. The elements were As, B, Be, Cd, Co, Cr, F, Hg, Mn, Ni, Pb, Sb, Se and V, which are designated in the Law of Pollutant Release and Transfer Register. The particulate trace elements were collected in an electrostatic precipitator and a wet desulfurization scrubber. Emissions into the atmosphere were lower than 1% of the quantity in coal, but the volatile trace elements showed somewhat higher emission ratios. For mercury, the mean concentration in coal was 0.045 ppm, the mean emission rate was 4.4 microg/kW h, and the mean emission ratio was 27%, the highest ratio among all elements in this study. The total annual emission of mercury from coal-fired power plants of the electric power industry in Japan was estimated to be 0.63 t/y. On the basis of these data, the atmospheric environment loads from a coal-fired power station were investigated. The calculation of stack gas dispersion showed that maximum annual mean ground level concentrations were in the order of 10(-2) to 10(-5) of the background concentrations, and that the adverse effect of the emissions from the coal-fired power station was small.     

Stable isotopes of bulk organic matter to trace carbon and nitrogen dynamics in an estuarine ecosystem in Babitonga Bay (Santa Catarina, Brazil)

The biogeochemical processes affecting the transport and cycling of terrestrial organic carbon in coastal and transition areas are still not fully understood. One means of distinguishing between the sources of organic materials contributing to particulate organic matter (POM) in Babitonga Bay waters and sediments is by the direct measurement of δ¹³C of dissolved inorganic carbon (DIC) and δ¹³C and δ¹⁵N in the organic constituents. An isotopic survey was taken from samples collected in the Bay in late spring of 2004. The results indicate that the δ¹³C and δ¹⁵N compositions of OM varied from − 21.7‰ to − 26.2‰ and from + 9.2‰ to − 0.1‰, respectively. δ¹³C from DIC ranges from + 0.04‰ to − 12.7‰. The difference in the isotope compositions enables the determination of three distinct end-members: terrestrial, marine and urban. Moreover, the evaluation of source contribution to the particulate organic matter (POM) in the Bay, enables assessment of the anthropogenic impact. Comparing the depleted values of δ¹³C_DIC and δ¹³C_POC it is possible to further understand the carbon dynamic within Babitonga Bay.     

Respiratory effects of indoor particles in young children are size dependent

Background

Extensive epidemiological studies have provided evidence of an association between elevated outdoor particulate air pollution and adverse health effects. However, while people typically spend majority of time indoors, there is limited knowledge on airborne indoor particles and on the correlation between the concentrations of indoor particles and health effects. Even insights into the influence of differently sized indoor particles on human health are still rare.

Objective

The association between differentially sized indoor air particles and the development of respiratory diseases was studied for three year aged children.

Methods

Short-term measurements of particle mass and number concentrations were carried out in children's rooms. Information on possible particle sources (smoking habits, type of heating, and traffic) and respiratory outcomes were obtained from questionnaires. Measured indoor particle concentrations were correlated with possible sources of indoor particles and with respiratory health impacts.

Results

Daily smoking, smoking more than 5 cigarettes per day at home and traffic density in front of the window of children's room were found to be related to indoor exposure by particles of different diameters. High indoor particle exposures were associated with an increased risk for the development of obstructive bronchitis and in some extent of non-obstructive bronchitis. The strongest impact was observed for the mass concentration of particles < 1 μm and the number concentration of particles > 0.5 μm. The risk increases still remain significant if tested for stability changing the number of adjustment variables or omitting randomly selected cases, respectively.

Conclusion

Our results show significant associations between indoor particle concentrations and the risks for respiratory diseases in young children. The applied short-term measurements can help to assess the health risks of indoor particles with different sizes within epidemiological studies.     

Distribution of the solvent-extractable organic compounds in fine (PM1) and coarse (PM1-10) particles in urban, industrial and forest atmospheres of Northern Algeria

The distribution of the solvent-extractable organic components in the fine (PM₁) and coarse (PM_1-10) fractions of airborne particulate was studied for the first time in Algeria. That was done during October 2006 concurrently in a big industrial district, a busy urban area, and a forest national park located in Algiers, Boumerdes, Blida, respectively, which are the three biggest provinces of Northern Algeria. Most of the organic matter identified in both particle size ranges consisted of n-alkanes and n-alkanoic acids, with minor contributions coming from polycyclic aromatic hydrocarbons (PAHs), nitrated polycyclic aromatic hydrocarbons (NPAHs), oxygenated PAHs, and other polar compounds (e.g., caffeine and nicotine). The potential emission sources of airborne contaminants were reconciled by combining the values of n-alkane carbon preference index (CPI) and selected diagnostic ratios of PAHs, calculated in both size ranges. The mean cumulative concentrations of PAHs reached 3.032 ng m^− 3 at the Boumerdes site, urban, 80% of which (i.e. 2.246 ng m^− 3) in the PM₁ fraction, 6.462 ng m^− 3 at Rouiba-Réghaia, industrial district, (5.135 ng m^− 3 or 80% in PM₁), and 0.512 ng m^− 3 at Chréa, forested mountains (0.370 ng m^− 3 or 72% in PM₁). Similar patterns were shown by all organic groups, which resulted overall enriched in the fine particles at the three sites. Carcinogenic and mutagenic potencies associated to PAHs were evaluated by multiplying the concentrations of “toxic” compounds times the corresponding potency factors normalized vs. benzo(a)pyrene (BaP), and were found to be both acceptable.     

Predictions of Benefits and Costs Derived from Improving Indoor Air Quality in Telephone Switching Offices

Airborne pollutants can cause failures in switching and computing equipment. This paper focuses on a subset of such pollutants - airborne fine panicles (< 2.5 μm diameter). It begins by examining the extent to which different improvements in heating, ventilating and air conditioning (HVAC) systems reduce indoor concentrations of fine particles. For each modification, the consequent reduction in soiling rate is derived. The concomitant increase in operating costs is also calculated. These costs are then compared with the costs of failures in telephone switching offices, leading to estimates of failure rate reductions that would make improvements cost-effective. Finally, the reduction in failures required to offset the costs of the improvements are compared with documented differences in failure rates between unimproved and improved environments. This study suggests that, in many telephone switching offices, the added operating costs associated with more efficient building filters and continuous fan operation are more than offset by reductions in failure rates.     

Emission of N2O and CH4 from a constructed wetland in southeastern Norway

The Skjønhaug constructed wetland (CW) is a free surface water (FSW) wetland polishing chemically treated municipal wastewater in southeastern Norway and consists of three ponds as well as trickling, unsaturated filters with light weight aggregates (LWA). Fluxes of nitrous oxide (N₂O) and methane (CH₄) have been measured during the autumn, winter and summer from all three ponds as well as from the unsaturated filters. Physicochemical parameters of the water have been measured at the same localities. The large temporal and spatial variation of N₂O fluxes was found to cover a range of − 0.49 to 110 mg N₂O–N m^− 2 day⁻¹, while the fluxes of CH₄ was found to cover a range of − 1.2 to 1900 mg m^− 2 day^− 1. Thus, both emission and consumption occurred. Regarding fluxes of N₂O there was a significant difference between the summer, winter and autumn, with the highest emissions occurring during the autumn. The fluxes of CH₄ were, on the other hand, not significantly different with regard to seasons. Both the emissions of N₂O and CH₄ were positively influenced by the amount of total organic carbon (TOC). The measured fluxes of N₂O and CH₄ are in the same range as those reported from other CWs treating wastewater. There was an approximately equal contribution to the global warming potential from N₂O and CH₄.     

Characterization of polychlorinated dibenzo-p-dioxin/dibenzofuran emissions from joss paper burned in a furnace with air pollution control devices

Burning joss paper, a common practice in temples in some Asian countries, can release toxic pollutants. This study investigated polychlorinated dibenzo-p-dioxin/dibenzofuran (PCDD/F) emissions and profiles from burning joss paper in a temple furnace connected to two wet scrubbers. The mean total PCDD/F content and corresponding toxic equivalent quantity (TEQ) in joss paper were 193 ng kg^− 1 and 0.645 ng I-TEQ kg^− 1, respectively, whereas those in bottom ash from burned joss paper were 18.5 ng kg^− 1 and 1.92 ng I-TEQ kg^− 1, respectively. The wet scrubbers decreased individual PCDD/F emissions by 26.7-71.0% and those of total PCDD/Fs and I-TEQ by 47.2% and 66.0%, respectively. The total PCDD/F TEQ emission factors before and after the wet scrubbers were 8.14 and 3.42 µg I-TEQ ton-feedstock^− 1, respectively. The estimated total PCDD/F and corresponding TEQ emissions were 5.29 g year^− 1 and 0.462 g I-TEQ year^− 1, respectively, in Taiwan. Burning joss paper in temple furnaces is a significant source of PCDD/F emissions.     

A screening level fate model of organic contaminants from advanced water treatment in a potable water supply reservoir

Augmentation of potable water sources by planned indirect potable reuse of wastewater is being widely considered to address growing water shortages. Environmental buffers such as lakes and dams may act as one of a series of barriers to potable water contamination stemming from micropollutants in wastewater. In South-East Queensland, Australia, current government policy is to begin indirect potable reuse of water from reverse osmosis equipped advanced water treatment plants (AWTPs) when the combined capacity of its major storages is at 40% capacity. A total of 15 organic contaminants including NDMA and bisphenol A have been publically reported as detected in recycled water from one of South-East Queensland’s AWTPs, while another 98 chemicals were analysed for, but found to be below their detection limit. To assess the natural attenuation in Lake Wivenhoe, a Level III fugacity based evaluative fate model was constructed using the maximum concentrations of these contaminants detected as input data. A parallel aquivalence based model was constructed for those contaminants, such as dichloroacetic acid, dalapon and triclopyr, which are ionised in the environment of Lake Wivenhoe. A total of 247 organic chemicals of interest, including disinfection by-products, pesticides, pharmaceuticals and personal care products, xenoestrogens and industrial chemicals, were evaluated with the model to assess their potential for natural attenuation. Out of the 15 detected chemicals, trihalomethanes are expected to volatilise with concentrations in the outflow from the dam approximately 400 times lower than influent from the AWTPs. Transformation processes in water are likely to be more significant for NDMA and pharmaceuticals such as salicylic acid and paracetamol as well as for caffeine and the herbicides dalapon and triclopyr. For hydrophobic contaminants such as cholesterol and phenolic xenoestrogens such as 4-nonylphenol, 4-t-octylphenol and bisphenol A, equilibrium between water and sediments will not be attained and hence fate processes such as removal in outflow are predicted to become relatively important.     

Effects of ozone and ozone/peroxide on trace organic contaminants and NDMA in drinking water and water reuse applications

An ozone and ozone/peroxide oxidation process was evaluated at pilot scale for trace organic contaminant (TOrC) mitigation and NDMA formation in both drinking water and water reuse applications. A reverse osmosis (RO) pilot was also evaluated as part of the water reuse treatment train. Ozone/peroxide showed lower electrical energy per order of removal (EEO) values for TOrCs in surface water treatment, but the addition of hydrogen peroxide increased EEO values during wastewater treatment. TOrC oxidation was correlated to changes in UV₂₅₄ absorbance and fluorescence offering a surrogate model for predicting contaminant removal. A decrease in N-nitrosodimethylamine (NDMA) formation potential (after chloramination) was observed after treatment with ozone and ozone/peroxide. However, during spiking experiments with surface water, ozone/peroxide achieved limited destruction of NDMA, while in wastewaters net direct formation of NDMA of 6-33 ng/L was observed after either ozone or ozone/peroxide treatment. Once formed during ozonation, NDMA passed through the subsequent RO membranes, which highlights the significance of the potential for direct NDMA formation during oxidation in reuse applications.     

Effects of recreational activities on the soil and water components of a deciduous forest ecosystem in Turkey

Impacts of recreational activities on some hydrological properties of a deciduous forest ecosystem related to water production have been evaluated with an inclusive soil study, coupled with a two‐year water quality monitoring program. Spatial variations of water quality parameters did not indicate a statistically significant deterioration caused by the recreational activities in the stream water, but the effects of trampling on physical soil properties were clear. The bulk density of the soils increased with the intensity of recreation from 1.18 to 1.29 g cm^?3, while the percentage of clay fraction decreased, as an indicator of erosion. The soils of the stream banks in the recreation area had reasonable saturated hydraulic conductivity values, and were affected sharply by the intensity of recreational use. The low inclination (0.5%) and the coarse texture of the soils were possibly the main factors diminishing or concealing the trampling effects not observed on the water quality of the stream passing through the recreation area.     

Characterisation of organic matter in IX and PACl treated wastewater in relation to the fouling of a hydrophobic polypropylene membrane

Extensive organic characterisation of a wastewater using liquid chromatography with a photodiode array and fluorescence spectroscopy (Method A), and UV₂₅₄ and organic carbon detector (Method B) was undertaken, as well as with fluorescence excitation emission spectroscopy (EEM). Characterisation was performed on the wastewater before and after ion exchange (IX) treatment and polyaluminium chlorohydrate (PACl) coagulation, and following microfiltration of the wastewater and pre-treated wastewaters. Characterisation by EEM was unable to detect biopolymers within the humic rich wastewaters and was not subsequently used to characterise the MF permeates. IX treatment preferentially removed low molecular weight (MW) organic acids and neutrals, and moderate amounts of biopolymers in contrast to a previous report of no biopolymer removal with IX. PACl preferentially removed moderate MW humic and fulvic acids, and large amounts of biopolymers. PACl showed a great preference for removal of proteins from the biopolymer component in comparison to IX. An increase in the fluorescence response of tryptophan-like compounds in the biopolymer fraction following IX treatment suggests that low MW neutrals may influence the structure and/or inhibit aggregation of organic compounds. Fouling rates for IX and PACl treated wastewaters had high initial fouling rates that reduced to lower fouling rates with time, while the untreated Eastern Treatment Plant (ETP) wastewater displayed a consistent, high rate of fouling. The results for the IX and PACl treated wastewaters were consistent with the long-term fouling rate being determined by cake filtration while both pore constriction and cake filtration contributed to the higher initial fouling rates. Higher rejection of biopolymers was observed for PACl and IX waters compared to the untreated ETP water, suggesting increased adhesion of biopolymers to the membrane or cake layer may lead to the higher rejection.     

Relationship of indoor and outdoor air pollutants in a naturally ventilated historical building envelope

Concentrations of NO₂, O₃, SO₂, acetic and formic acids, HNO₃ and NH₃ were measured inside and outside a historical building, the Baroque Library Hall (BLH) in the National Library in Prague (Czech Republic). The naturally ventilated system of the building, the restriction of personnel access, reduced groups of visitors and absence of activities which could influence indoor pollutant concentrations are characteristics that make the Baroque Library Hall a suitable location to study the influence of outdoor environment on the indoor air quality. The relationship between indoor and outdoor (I/O) concentration was investigated to assess the infiltration of outdoor generated pollutants. Outdoor and indoor pollution sources were determined and, infiltration of ammonium nitrate and a shift of the equilibrium to the gas phase were the reason for the high concentration of ammonia measured inside the BLH. A significant seasonal variation was observed and interpreted as a consequence of different infiltration regime associated with indoor–outdoor temperature differences, which in addition drives dilution processes of indoor generated pollutants. Based on the indoor air quality assessment performed in the BLH with regard to human and material exposure, there is reason for concern about material preservation and in particular paper at the BLH.     

Degradation of organic matter from black shales and charcoal by the wood-rotting fungus Schizophyllum commune and release of DOC and heavy metals in the aqueous phase

We investigated the degradation of refractory organic matter (OM) by the basidiomycete fungus Schizophyllum commune to understand the release of dissolved organic compounds, heavy metals and sulfur. The investigated OM consisted of: charcoal, the short time end product of high temperature wood alteration in the absence of oxygen and composed mainly of pure OM; and black shales composed of clay minerals, quartz, sulfides and OM formed geogenically in an abiotic long-term process. In both cases, the OM fraction contains mainly polyaromatic hydrocarbons. We investigated the degradation of these fractions by a wood-rotting basidiomycete, which is able to produce exoenzymes like peroxidases and laccases. These enzymes can perform radical reactions to oxidize OM (like lignin) and therefore hypothetically are able to degrade OM from charcoal and/or low grade metamorphic black shales. Release of new components into dissolved organic carbon (DOC) could be detected in both cases. The attack on OM in the case of black shales coincided with the release of the heavy metals Fe, Mn and Ni. By following sulfur concentrations throughout the experiment, it was shown that heavy metal release is not due to pyrite oxidation. Ground black shale and charcoal samples were inoculated with S. commune in a diluted minimal medium containing aspartic acid and glucose. The aqueous and solid phases were sampled after 1, 7, 28 and 84 days. DOC was measured as non purgeable carbon and characterized by size exclusion chromatography and UV detection. Carbon concentrations of the solid phase were determined by element analyses. After initial decrease of the DOC concentrations due to the degradation of the carbon source provided with the medium, DOC increased up to 80 mg/l after 84 days. Carbon decreased in the solid fraction confirming that this carbon was released as DOC by the fungus. The newly generated DOC formed larger agglomerations than the DOC of the growth medium. The investigation proved that the degradation of persistent carbon sources, such as charcoal and black shale, is accelerated by fungal activity. Consequently, the associated release of heavy metals is also accelerated by the fungus. Main products of the biological degradation processes were organic heavy metal complexes which can enter the environment.     

Time and space patterns of volatile organic compounds in a sewage treatment plant

47 regulated and non-regulated volatile organic compounds (VOCs) were characterised by closed-loop stripping analysis (CLSA) and high resolution gas chromatography coupled to mass spectrometry (HRGC/MS) in 28 aqueous samples from 4 sampling points along a sewage treatment plant in Manresa, Catalonia, Spain. A 4 x 2(2) factorial design (16 samples) was first prepared for the sampling, and reinforced with 12 additional samples at the plant influent. The total analyte weighted mean concentration was 232 microg x l(-1) at the plant influent, with a mass flow of 2231 kg x yr(-1). Petroleum solvents and terpenic compounds accounted for 79% of the influent analyte concentration. VOC concentration in influent was clearly higher for most VOCs from 12 to 22 h (high organic load hours), and lower from 24 to 10 h (lower organic load). Differences between time bands were confirmed through t tests. Differences between weekdays and the weekend were not so clear, and could not be confirmed through t tests. VOC concentrations along the plant are discussed. Overall analyte removal in the plant was 89%.     

Simulation of smoke from a burning vehicle and pollution levels caused by traffic jam in a road tunnel

Detailed analyses of smoke movement from a burning vehicle in a road tunnel have been carried out for the westbound Melbourne City Link tunnel. The time-averaged equations for velocity, pressure, temperature, and mass fraction of emissions were solved for transient condition using the CFD software FLUENT 6.0. For the analysis, a burning bus was assumed to release an equivalent energy of burning 500 l of diesel in 6 min, with vehicles upstream of the fire at a standstill. On the other hand, the vehicles downstream of the fire had enough time to escape from the tunnel through the exit portal. Due to the action of jet fans, most of the smoke was pushed downstream of the fire. The smoke had also dispersed about 55 m upstream of the fire, putting the passengers in this region at great risk. The emissions released from the vehicles in the jam, with their engines running, also posed a threat to human health. Within 8 min after the fire had started, the mass concentrations of O₂, CO₂ and CO were in the ranges of 0.12–0.15, 0.08–0.11 and 0.0006–0.0014, respectively. Therefore, quick evacuation of the passengers is essential in the event of a fire in the tunnel.