Abstract  Much attention has been paid to ozone as a major cause of novel forest decline in Europe. In combination with acidic mist, O(3) has been observed to increase ion leaching. Besides cations lake Mg(2+), Ca(2+), K(+), NH(4)(+), considerable amounts of nitrate were found to be leached by acidic mist from needles of Norway spruce. Controlled fumigation experiments, with 100, 300, and 600 microg O(3)m(-3) over 22 days continuously, have led to a nitrate accumulation of 94.1 +/- 14.8, 119.4 +/- 28.7 and 198.9 +/- 14.9 microg NO(3)(-1) g(-1) FW, respectively, in leaves of Quercus robur. Similar values were found in leaves of Fagus sylvatica and current and previous year needles of Picea abies. Nitrate levels of controls receiving charcoal filtered air were well below 40 microg NO(3)(-) g (-1) FW. Statistically significant elevated nitrate levels were observed after only 48 h of continuous fumigation with 600 microg O(3)m(-3), in all tree species tested, and after 144 h in the 100 microg O(3)m(-3) treatment. In another experiment, trees of Picea abies were kept in two charcoal (C) and two Purafil plus charcoal (P/C) ventilated chambers, and fumigated with O and 500 microg O(3)m(-3) in cabinets of each filter-type in order to eliminate NO(x) from chamber air. After 29 days of continuous ozone fumigation, NO(3)(-) accumulation in needles amounted to 102.0 +/- 37.7 and 137.4 +/- 40.5 microg g(-1) FW in P/C and C-filtered chambers, respectively. Nitrate contents of controls were below 30 microg NO(3)(-)g(-1) FW at the end of the experiment. No significant differences in NO(3)(-) accumulation between filter treatments were observed. Since NO(x) was reduced by more than 95% in the Purafil/charcoal versus the charcoal treatment, NO(3)(-) accumulation in needles can be attributed predominantly to the influence of ozone and not to direct NO(2) uptake of needles by the possible oxidation of NO to NO(2) in the presence of ozone.

Abstract  The addition of positively charged, 30 nm diameter silica nanoparticles to cationic wormlike micellar solutions of cetyltrimethylammonium bromide and sodium nitrate is studied using a combination of rheology, small angle neutron scattering, dynamic light scattering, and cryo-transmission electron microscopy. The mixtures are single phase up to particle volume fractions of 1%. The addition of like-charged particles significantly increases the wormlike micelle (WLM) solution’s zero shear rate viscosity, longest relaxation time, and storage modulus. The changes are hypothesized to originate from a close association of the particles with the micellar mesh. Small angle neutron scattering measurements with contrast matching demonstrate associations between particles mitigated by the WLMs. The effective interparticle interactions measured by SANS can explain the observed phase behavior. Dynamic light scattering measurements confirm the dynamic coupling of the particles to the micellar mesh.

Abstract  Three rare examples of extended inorganic materials possessing a cationic charge on the host have been successfully synthesized hydrothermally. The first structure consists of two-dimensional lead fluoride [Pb9F16]2+ sheets with perchlorate anions occupying the interlayer space. The material is a higher symmetry polytype of our previously reported lead fluoride nitrate Pb3F5·NO3. Two new isoreticular layered metal−organic frameworks have also been discovered with cationic lead fluoride [Pb2F2]2+ layers pillared by 3- and 4-carbon chain alkylenedisulfonate molecules. Each structure was characterized by powder and single-crystal X-ray diffraction and thermogravimetric analysis. The thermal stability increases with the alkylene chain length of the linker molecule. The syntheses require the addition of perchloric acid to the reaction mixture. An improved synthesis for our previously reported lead fluoride polytype pillared by ethanedisulfonate in terms of increased yield and purity was also realized using perchloric acid.

Abstract  A significant flux of heavy metals, among other toxins, reaches the lungs through smoking. Consequently, contaminated soil is usually avoided for tobacco cultivation. Here we compare the heavy metal concentrations in tobacco from a sample of 47 counterfeit products, representative of the substantial market for these products in the U.K., with their genuine equivalents and find significantly higher concentrations of heavy metals in the counterfeits. Trace element patterns suggest that over-application of fertilizers (phosphate and/or nitrate) is the most likely cause. Nitrogen isotopes showed no significant enrichment in 15N (delta15N range from +1.1 to +4.6 in counterfeits and from +2.5 to +3.3 in genuine tobaccos) as might be expected from a sewage or manure source of nitrate, and a mineral phosphate source is considered the more likely source of metals. Stable carbon isotopes in the same tobaccos have a wide range (delta13C 18.3 to 26.4), indicating the influence of multiple controls during cultivation and possibly post-harvesting. A review of the health effects of heavy metal transfer from tobacco via smoke to the lungs indicates that habitual smokers of counterfeits may be risking additional harm from high levels of cadmium and possibly other metals.

Abstract  During the summer monsoon period in south-east Asia marine airstreams normally prevail at the south China coast. However, when tropical cyclones approach then polluted airmasses from south-eastern China can impart high ionic concentrations and high acidity to rainwater. This is illustrated by two examples and the small-scale horizontal variations in rainwater composition are minor during these episodes. Since long-term quality-assured studies of the composition of rainwater in south-cast Asia are scarce, the results at three sampling sites in Hong Kong during summer monsoon periods are compared with previous data from the same season. The results for the mid- to end- 1990's show a similar trend to those for the ambient concentrations of sulphate and nitrate in aerosol in Hong Kong, which show flattened trends from 1995 to 1999. A marked increase in acidity is found in the summer monsoon period of 2004 which is attributed to the greater proportion of approaching cyclone weather systems in the dataset, reflecting both the increased local emission sources and the burgeoning economic growth of the Pearl River Delta Region. Comparison of the rainwater composition with that at other south-cast Asian cities during the summer monsoon period shows that it is most acidic in Hong Kong. (c) 2007 Elsevier B.V All rights reserved.

Abstract  To understand the influence of aerosol particles and meteorological conditions on visual range in Jinan, the capital of Shandong Province, China, PM(2.5) and PM(10) samples were collected from November 2004 to September 2005. The mass concentrations of PM(2.5) and PM(10), concentrations of water-soluble ions in PM(2.5) and concentrations of black carbon (BC) in the atmosphere were analyzed. The decrease of visual range in Jinan results from the combined influence of PM(2.5), PM(10) and meteorological conditions. For the period studied, the average light extinction coefficient, b(ext), which was estimated from an equation developed by the IMPROVE network was 292 Mm(-1). Ammonium sulfate was the major contributor to visual range impairment, accounting for 41%, while ammonium nitrate, particulate organic matter (POM) and BC made comparable contributions accounting for 20%, 22% and 18%, respectively. This highlights the significance of secondary particles ((NH(4))(2)SO(4), NH(4)NO(3), POM) in visual range impairment in Jinan. The data from this study are also compared with the long-term variations of visual range in Jinan from 1961 to 2005.

Abstract  Soil monoliths from an area exposed to acid precipitation and from an unpolluted area were used in a lysimeter experiment to study effects of different rain qualities on the chemical composition of the leachate from shallow soils rich in organic matter. The vegetation was either dominated by moorgrass [Molinia caerulea (L.) Moench] or heather [Calluna vulgaris (L.) Hull]. The lysimeters received either "acid rain" (pH 4.3) or "normal rain" (pH 5.3). High concentrations of dissolved organic carbon (DOC) were characteristic of the leachate. The different "rain" qualities had no significant influence on the DOC concentration. More DOC was, however, leached from lysimeters with heather vegetation. Roughly 50% of the aluminum (Al) was in complex with organic material and the Al charge was calculated to be between +1.4 and +2.0. Sulfate (SO4(2-)) was the only component that was significantly influenced by the treatment, as more was leached from lysimeters receiving "acid rain." Sulfate was poorly correlated with pH, suggesting that reduced SO4(2-) input would not necessarily lead to reduced acidity. Differences in the pH of the leachate due to the treatments were less than 0.15 pH units. Nitrate (NO3-) was only leached in very low concentrations and of little consequence for the leachate acidity. Some observations do, however, suggest that NO3- may contribute to acidification in episodes with high precipitation. High concentrations of Cl- in the leachate and a significant positive correlation between Cl-, H+, and base cations indicate that sea salt episodes may be important for soil acidification and acidity of the leachate.

Abstract  A 3-D Lagrangian particle dispersion model including the photochemical reaction has been developed and implemented to the data obtained from the southern oxidants study field campaign to examine the capability of the present model. The model includes parameterizations of the entrainment process and the intermixing process between the superposed Lagrangian particles. It is found that the present model is able to simulate quite well characteristic features of the photochemistry for a plume emitted from the isolated major source of the Cumberland Power Plant in Tennessee, USA including the width of plume and the distribution Of O-3, NOy, and nitrate concentration across the plume. This result suggests that the present model can be used more practically in air quality assessment where photochemical reactions are important. (C) 2003 Elsevier Ltd. All rights reserved.

Abstract  Measurement data from the Pacific 2001 air quality field study was used to evaluate the performance of Models-3/CMAQ for the period of 9-20 August in 2001, for a domain centered about Vancouver and the Lower Fraser Valley in British...

Abstract  The objectives of this study were to identify the sources of the PM2.5 in Indianapolis, Indiana and estimate their contributions to the total PM2.5 mass concentrations by analyzing the data from the samples collected at the EPA Speciation Trends Networks (STN) site in Indianapolis, Indiana. Both positive matrix factorization (PMF2) and an expanded factor analysis model were applied. The two methods obtained essentially identical source profiles and contributions, so the results of the simpler method, PMF, are described in the formal text of this paper in detail while the corresponding results provided by the expanded factor analysis model are presented in the supplemental material for this paper. The seven resolved sources are secondary sulfate (40.2%), secondary nitrate (21.9%), gasoline emission (16.6%), diesel emission (7.9%), airborne soil (5.3%), Fe-related industries (4.4%), and Cu- related industries (2.5%). The comparison between two models suggests that PMF coupled with subsequent data analysis methods (such as CPF, PSCF, seasonal variation analysis, and weekday/weekend variation analysis) yields the results that are comparable to those of the expanded factor analysis. The results suggest that such studies of STN data can be used to assist in the development of State Implementation Plans (SIPs) for PM2.5.

Abstract  In most rural settlements in Nigeria, access to clean and potable water is a great challenge, resulting in water borne diseases. The aim of this study was to assess the levels of some physical, chemical, biochemical and microbial water quality parameters in twelve hand - dug wells in a typical rural area (Igbora) of southwest region of the country. Seasonal variations and proximity to pollution sources (municipal waste dumps and defecation sites) were also examined. Parameters were determined using standard procedures. All parameters were detected up to 200 m from pollution source and most of them increased in concentration during the rainy season over the dry periods, pointing to infiltrations from storm water. Coliform population, Pb, NO3- and Cd in most cases, exceeded the World Health Organization recommended thresholds for potable water. Effect of distance from pollution sources was more pronounced on fecal and total coliform counts, which decreased with increasing distance from waste dumps. The qualities of the well water samples were therefore not suitable for human consumption without adequate treatment. Regular monitoring of groundwater quality, abolishment of unhealthy waste disposal practices and introduction of modern techniques are recommended.

Abstract  Three different diets amended with lead (Pb) nitrate Pb(NO3)2 (7, 77, and 520 microg Pb/g dry weight) and a Pb-free control diet (0.06 microg Pb/g dry weight) were fed to juvenile freshwater rainbow trout for 21 days. Accounting for measured food consumption, the calculated doses per fish were 0.02, 3.7, 39.6, and 221.5 microg/day, for the control, low, intermediate, and high Pb treatments, respectively. The patterns of Pb accumulation over time were determined in various tissues (gills, liver, kidney, intestine, carcass), red blood cells (RBC), and plasma, as well as feeding, growth, hematological, and ionoregulatory parameters. Pb accumulation occurred in a dose-dependent manner in all tissues except the plasma, where accumulation was minimal. Overall, when fed the highest Pb diet, the intestine exhibited the greatest Pb burden (17.8 microg Pb/g tissue wet weight), with high concentrations also found in the kidney (2.4 microg Pb/g tissue wet weight) and liver (1.9 microg Pb/g) at the highest dietary Pb treatment by day 21. The RBCs accumulated a substantial amount of Pb (1.5 microg Pb/g) when compared to the plasma (0.012 microg Pb/g) in the high treatment group. The percentage of Pb retained in the fish decreased with increasing dietary Pb concentrations. Growth, survival, plasma protein, and hematocrit were not significantly affected by dietary Pb. Plasma Ca2+ levels decreased at the beginning of the experiment, whereas Mg2+ levels decreased during the middle of the experiment in both the intermediate and high dietary treatments. Both the Ca2+ and Mg2+ levels stabilized by day 21. Branchial Ca2+ and Na+ influx rates were not affected by dietary Pb, except on day 8 where Na+ influx rates were significantly elevated. The results of this study show that Pb does accumulate internally from the diet when present at levels within the range reported in contaminated benthic invertebrates in nature. We further identify the intestine as a potential target site of chronic toxicity of Pb via the diet, and RBCs as a reservoir of dietary Pb.

Abstract  The degradation of alachlor by direct ozonation and advanced oxidation process O(3)/H(2)O(2) was investigated in this study with focus on identification of degradation byproducts. The second-order reaction rate constant between ozone and alachlor was determined to be 2.5+/-0.1M(-1)s(-1) at pH 7.0 and 20 degrees C. Twelve and eight high-molecular-weight byproducts (with the benzene ring intact) from alachlor degradation were identified during direct ozonation and O(3)/H(2)O(2), respectively. The common degradation byproducts included N-(2,6-diethylphenyl)-methyleneamine, 8-ethyl-3,4-dihydro-quinoline, 8-ethyl-quinoline, 1-chloroacetyl-2-hydro-3-ketone-7-acetyl-indole, 2-chloro-2',6'-diacetyl-N-(methoxymethyl)acetanilide, 2-chloro-2'-acetyl-6'-ethyl-N-(methoxymethyl)-acetanilide, and two hydroxylated alachlor isomers. In direct ozonation, four more byproducts were also identified including 1-chloroacetyl-2,3-dihydro-7-ethyl-indole, 2-chloro-2',6'-ethyl-acetanilide, 2-chloro-2',6'-acetyl-acetanilide and 2-chloro-2'-ethyl-6'-acetyl-N-(methoxymethyl)-acetanilide. Degradation of alachlor by O(3) and O(3)/H(2)O(2) also led to the formation of low-molecular-weight byproducts including formic, acetic, propionic, monochloroacetic and oxalic acids as well as chloride ion (only detected in O(3)/H(2)O(2)). Nitrite and nitrate formation was negligible. Alachlor degradation occurred via oxidation of the arylethyl group, N-dealkylation, cyclization and cleavage of benzene ring. After O(3) or O(3)/H(2)O(2) treatment, the toxicity of alachlor solution examined by the Daphnia magna bioassay was slightly reduced.

Abstract  Regional simulations of sulfate, nitrate and ammonium aerosols were performed by a nested application of the online-coupled three-dimensional Eulerian model system COSMO-MUSCAT. This was done in a domain covering the northern part of Germany and surrounding regions for the full month of May and a 6-week period in August/September 2006 with the primary focus on secondary inorganic aerosol levels caused by ammonia emissions from domesticated animals and agricultural operations. The results show that in situations with westerly winds ammonium nitrate dominates with concentrations of about 5 to 10 [mu]g/m3 whereas the ammonium sulfate concentrations are about 5 [mu]g/m3. In situations with winds mainly from the East characterized by warmer and dryer air the ammonium sulfate concentrations have their maximum at about 10 [mu]g/m3 whereas at the same time no ammonium nitrate is present. A reduction of agricultural NH3 emissions by 50% in a regional scale reduces the ammonium nitrate concentrations to a maximum of 30%, while the ammonium sulfate concentrations are unchanged. The reduction of NH3 emissions in a more limited area (here in the Federal state of Germany Niedersachsen) does have no noticeable effect neither on ammonium sulfate nor on ammonium nitrate.

Abstract  Two regional-scale photochemical modeling systems, RAMS/UAM-V and MM5/MAQSIP, are used to simulate precursor concentrations for 4 June--31 August 1995 period. The time series of simulated and observed precursor concentrations are spectrally decomposed into intra-day, diurnal, synoptic, and longer-term (baseline) forcings and compared on each time scale. The results reveal that the observed and modeled precursor concentrations are uncorrelated on the intra-day time scale for both modeling systems while correlations are higher on longer time scales. In observations, the variability in NO, concentrations is dominated by the diurnal and synoptic-scale processes, while NOy is found to vary most on the synoptic time scale. In observations of volatile organic compounds (VOCs), the variability is dominated by the diurnal and synoptic processes for both biogenic and anthropogenic hydrocarbons. The pattern seen in the observations, in terms of the relative contribution of different temporal components to the total variance, is better captured by the two modeling systems for NO, than for NO, and VOCs. There are differences between model predictions and observations in terms of the actual magnitudes of variances of each temporal component. These results suggest the need to cover longer time periods in modeling simulations to resolve longer-term processes, because they seem to play a dominant role in dictating the precursor variability. (C) 2001 Elsevier Science Ltd. All rights reserved.

Abstract  BACKGROUND: In the sub-urban areas of Kampala city, springs are a major source of water for domestic use. Though spring water is considered to be aesthetically acceptable for domestic use, presence of poorly designed pit latrines, poor solid waste management as well as poor and inadequate spring protection, may lead to contamination of spring water with pathogenic bacteria. OBJECTIVES: The objectives of the study were to examine the bacteriological quality of water from ten springs in Katwe and Kisenyi parishes of Kampala, and to identify and quantify risks for spring water contamination with faecal bacteria. METHODS: A cross-sectional sanitary risk assessment using a standardised format was carried out in ten randomly selected springs in the parishes of Katwe and Kisenyi parishes in Kampala. A total of 80 samples of water from these springs were collected from December 2001 to March 2002. The samples were analysed for indicators of faecal contamination: total coliforms, faecal coliforms and faecal streptococci. Physico-chemical parameters were measured. RESULTS: Aggregate qualitative sanitary risk scores ranged from medium to high. The total coliform counts in 90% of the samples exceeded the WHO guideline for drinking water. All the samples had faecal coliform counts above the WHO guideline. A strong correlation (r2= 887) was observed between the median faecal coliform counts and the sanitary risk score. Sixty percent of the samples had nitrate levels above the WHO recommended limit. There was no correlation between the levels of chlorides and nitrates and levels of indicators of faecal bacterial contamination. CONCLUSIONS: The sanitary risk assessment score is a reliable tool for predicting the likely levels of bacterial contamination of spring water. Water from the ten protected springs studied is unsuitable for drinking without treatment.

Abstract  A methodology using ordinal logistic regression is proposed to predict the probability of occurrence of heavy metals in ground water. The predicted probabilities are defined with reference to the background concentration and the maximum contaminant level. The model is able to predict the occurrence due to different influencing variables such as the land use, soil hydrologic group (SHG), and surface elevation. The methodology was applied to the Sumas-Blaine Aquifer located in Washington State to predict the occurrence of five heavy metals. The influencing variables considered were (1) SHG; (2) land use; (3) elevation; (4) clay content; (5) hydraulic conductivity; and (6) well depth. The predicted probabilities were in agreement with the observed probabilities under existing conditions. The results showed that aquifer vulnerability to each heavy metal was related to different sets of influencing variables. However, all heavy metals had a strong influence from land use and SHG. The model results also provided good insight into the influence of various hydrogeochemical factors and land uses on the presence of each heavy metal. A simple economic analysis was proposed and demonstrated to evaluate the cost effects of changing the land use on heavy metal occurrence.

Abstract  An intensive sampling campaign was performed in Fresno, CA during December 2003 measuring fine particulate matter including both the semi-volatile and nonvolatile fractions of the aerosol. Both the newly developed R&P FDMS Monitor and a PC-BOSS have been shown to measure total PM2.5 concentrations including semi-volatile nitrate and organic material. Good agreement was observed between the PC-BOSS and the R&P FDMS Monitor in this study with linear regression analysis resulting in a zerointercept slope of 1.00 ± 0.02 and an R2 = 0.93. Several real-time measuring systems including the R&P Differential TEOM, the Met One BAMS, and a GRIMM Monitor were also employed and comparisons of total PM2.5 mass were made with the R&P FDMS Monitor. Agreement among these various monitors was generally good. However, differences were sometimes seen. Reasons for observed differences in the real-time mass measurement systems are explained by the composition and complexity of the measured aerosol, most importantly the composition of semi-volatile material. A newly automated ion chromatographic system developed by Dionex was also field tested and compared to both R&P 8400N Nitrate and integrated PC-BOSS inorganic species measurements. Sulfate and nitrate determined by the Dionex and PC-BOSS systems agreed. However, nitrate measured by the 8400N was low during fog events compared to the other two systems.

Abstract  Rainwater collected on the island of Bermuda between January 2000 and January 2001 shows pronounced seasonal variation in the nitrogen and oxygen isotopic composition of nitrate. Higher 15N/14N and lower 18O/16O ratios are observed in the warm season (April–September) in comparison to the cool season (October–March): The mean δ15N of nitrate for the warm and cool seasons is −2.1‰ and −5.9‰ (versus air N2), respectively, while the mean δ18O is 68.6‰ and 76.9‰ (versus Vienna Standard Mean Ocean Water). The few cool season rain events that had high 15N/14N and low 18O/16O exhibited trajectory paths originating from the south, similar to those of warm season samples. Accordingly, the region from which air is transported to the island determines the 15N/14N and 18O/16O of the nitrate. The source region provides precursor nitrogen oxides (NO x ), influencing the 15N/14N of nitrate, and contributes to the chemistry that produces nitrate from NO x , which determines the 18O/16O of nitrate. While the range in nitrate 15N/14N observed during the cool season is consistent with anthropogenic emissions from North America, the higher warm season 15N/14N suggests that lightning is a significant source of nitrate to Bermuda. The isotopic evidence for a significant southern source of nitrate to Bermuda helps to explain the previous observation of unexpectedly high nitrate concentrations in warm season rain. The 18O/16O of nitrate in rain at Bermuda is high throughout the year (δ18O = 60.3 to 86.5‰) as a result of interactions of precursor NO x with ozone, which has a high 18O/16O ratio. The lower nitrate 18O/16O in the warm season and in cool season air masses from the south is consistent with elevated concentrations of hydroxyl radical (OH), which dilutes the isotopic signal of ozone. Our limited data set suggests that the relative importance of the OH sink for NO x during the cool season varies spatially over as large a range as is observed between the warm and cool seasons.

Abstract  BACKGROUND: Epidemiological evidence has implicated fine particulate air pollution, particularly particles less than 10 microns in diameter (PM10), in the development of exacerbations of asthma and chronic obstructive pulmonary disease (COPD) although the mechanism is unknown. The hypothesis that PM10 particles induce oxidant stress, causing inflammation and injury to airway epithelium, was tested. METHODS: The effects of intratracheal instillation of PM10 was assessed in rat lungs (three per group). Inflammatory cell influx was measured by bronchoalveolar lavage (BAL) and air space epithelial permeability was assessed as the total protein in BAL fluid in vivo. The oxidant properties of PM10 particles were determined by their ability to cause damage to plasmid DNA and by changes in reduced (GSH) and oxidised (GSSG) glutathione. The effects of PM10 particles were compared in some experiments with those of fine (CB) and ultrafine (ufCB) carbon black particles. RESULTS: Six hours after intratracheal instillation of PM10 there was an influx of neutrophils (up to 15% of total cells in BAL fluid) into the alveolar space, increased epithelial permeability, the mean (SE) total protein in the BAL fluid increasing from 0.39 (0.01) to 0.62 (0.01) mg/ml, and increased lactate dehydrogenase (LDH) concentrations in the BAL fluid. An even greater inflammatory response was seen following intratracheal instillation of ufCB but not following CB instillation. PM10 particles had free radical activity in vivo, as shown by a decrease in GSH levels in the BAL fluid from 0.36 (0.05) to 0.25 (0.01) nmol/ml following instillation. The free radical activity of PM10 was confirmed in vitro by its ability to deplete supercoiled plasmid DNA, an effect which could be reversed by mannitol, a specific hydroxyl radical scavenger. BAL fluid leucocytes from rats treated with PM10 produced greater amounts of nitric oxide (NO), measured as nitrite (control 3.07 (0.33), treated 4.45 (0.23) microM/1 x 10(6) cells), and tumour necrosis factor alpha (control 21.0 (3.1), treated 179.2 (29.4) units/l x 10(6) cells) in culture than those obtained from control animals. Since the PM10 preparation was contaminated with small amounts of filter fibres due to the extraction process, the effects of instillation of filter fibres alone was assessed. These studies showed that filter fibres did not account for the proinflammatory and injurious effects of the PM10 suspension. CONCLUSIONS: These findings provide evidence that PM10 has free radical activity and causes lung inflammation and epithelial injury. These data support the proposed hypothesis for the mechanism by which particulate air pollution causes adverse effects in patients with airways diseases.

Abstract  In this paper, we explore the efficacy of (1) reducing the iodine value of soy-derived biodiesel fuels through increasing the methyl oleate (methyl ester of oleic acid) content and (2) addition of cetane improvers, as strategies to combat the biodiesel NOx effect: the increase in NOx emissions observed in most studies of biodiesel and biodiesel blends. This is accomplished by spiking a conventional soy-derived biodiesel fuel with methyl oleate or with cetane improver. The impact on bulk modulus of compressibility, fuel injection timing, cetane number, combustion, and emissions were examined. The conventional B20 blend produced a NOx increase of 3-5% relative to petroleum diesel, depending on injection timing. However, by using a B20 blend where the biodiesel portion contained 76% methyl oleate, the biodiesel NOx effect was eliminated and a NOx neutral blend was produced. The bulk modulus of petroleum diesel was measured to be 2% lower than 1320, yielding a shift in fuel injection timing of 0.1-0.3 crank angle. The bulk modulus of the high methyl oleate B20 blend was measured to be 0.5% lower than 1320, not enough to have a measurable impact on fuel injection timing. Increasing the methyl oleate portion of the biodiesel to 76% also had the effect of increasing the cetane number from 48.2 for conventional B20 to 50.4, but this effect is small compared to the increase to 53.5 achieved by adding 1000 ppm of 2-ethylhexyl nitrate (EHN) to B20. For the particular engine tested, NOx emissions were found to be insensitive to ignition delay, maximum cylinder temperature, and maximum rate of heat release. The dominant effect on NOx emissions was the timing of the combustion process, initiated by the start of injection, and propagated through the timing of maximum heat release rate and maximum temperature. (c) 2004 Elsevier B.V. All rights reserved.

Abstract  Several samples of airborne particulate matter (PM), collected from 6th November to 6th December 2003 at a coastal site in the south-east of Italy, have been analyzed by different techniques to characterize elemental composition and morphological properties of the inorganic PM fraction and obtain preliminary results on anthropogenic contributions. Al, Cr, Cu, Fe, Mn, V, Pb, Ti, Ca and Zn mass concentrations, evaluated by an inductively coupled plasma atomic emission spectrometer, account for up to l% of the bulk PM mass in the investigated samples. According to geochemical calculations, Ca, Al, Fe and Mn are predominantly of crustal origin, while Cr, Cu, Pb, V, Ti and Zn heavy metals are of anthropogenic origin. Ion chromatography analyses have identified sulfate (SO(4)(2-)) nitrate (NO(3)(-)), sodium (Na(+)), and ammonium (NH(4)(+)) as the main ionic components accounting for up to 38% of the total PM mass and up to 90% of the total ionic mass. Besides ion chromatography, X-ray energy dispersive (EDX) microanalyses have revealed the high variability of Cl: its weight concentration varies from about 24% to below the detection limit (>or=0.5%) in the investigated samples. The marked anti-correlation between the excess of S and the Cl/Na ratio has allowed inferring that reactions between sea salt particles and acidic sulfates, which liberate HCl gas to the atmosphere leaving particles enriched in non-sea-salt sulfates, have significantly contributed to chloride depletion. Morphological analyses by scanning electron microscopy have shown that about 90% of the total sampled particles have a diameter

Abstract  This paper presents the development and evaluation of ambient fine particle concentrators for conducting animal and human exposure studies. These systems utilize the technology of virtual impactors to concentrate particles in the range 0.15-2.5 Ám. Ambient particles are first drawn at 5000 l m-1 through a preselective inlet that removes particles above 2.5 Ám. Subsequently, the remaining aerosol is drawn through a series of virtual impactors, which increase particle concentration by a factor of about 10 and 30, for human and animal exposures, respectively. Results from the experimental characterization of the concentrators showed that the concentration enrichment process occurs without any distortion in the size distribution and chemical composition of the sampled ambient aerosols. Furthermore, labile constituents of fine particles, such as volatile ammonium nitrate are preserved during this process.