Occupational exposures to lead-based paint in structural steel demolition and residential renovation work

Occupational exposures to lead are characterised for a number of different lead-based paint abatement techniques in two work settings: residential renovation and structural steel demolition. Exposure levels reported during heavy structural steel demolition work involving acetylene torch cutting, welding, and abrasive blasting can be more than 100 times greater than the permissible exposure limit (PEL) set by the Occupational Safety and Health Administration (OSHA) for construction (200 µg/m³), which was in effect at the time of this study (the PEL was reduced to 50 µg/m³ in 1993). Surveillance data from an OSHA database for those standard industry classification (SIC) codes with a potential for exposure to lead-based paint in construction show that 49% of the air samples collected by OSHA were greater than 200 µg/m³, suggesting widespread non-compliance. New occupational exposure data from lead-based paint abatement work in public and private housing are also presented. In one public housing development, personal exposures to lead particulates measured during open flame burning and uncontained powered sanding were found to be more than 5000 µg/m³. These findings are contrasted with exposures measured during lead-based paint abatement work performed in accordance with the lead-based paint guidelines released by the US Department of Housing and Urban Development, where exposures were all lower than 25 µg/m³. Data from another public housing abatement project, involving work on 400 dwelling units over a 15-month period, show that workers' blood lead levels did not increase by more than 5 µg/dl above the pre-employment baseline. Abatement techniques studied here include interior and exterior building component replacement and exterior paint-stripping using a needle gun equipped with a high efficiency particulate air (HEPA) vacuum dust containment system. The data presented here show that it is feasible to keep airborne lead exposures below 20 µg/m³ in residential lead hazard control work, and to establish medical removal protection at blood lead levels of 25 µg/dl. These findings should be considered as OSHA finalises its interim final rule for lead exposure in construction work.     

Risk assessment of boron in glass wool insulation

Background, aim and scope  Glass wools are man-made vitreous fibres, which consist principally of sodium, calcium and magnesium silicates, but may contain smaller amounts of other elements, including boron. The boron contents originate from the use of borates in the glass melting process as a glass former and a flux agent. During the production and application of glass wool insulation products, workers may legally be exposed to glass fibre up to the occupational limit value, commonly of 1 fibre/cm³. However, in practice, the fibre exposure will be at least ten times lower. Boron is a non-metallic element widely distributed in nature, where it occurs as boric acid, borates and borosilicates. Humans are mainly exposed to boron via vegetarian food and drinking water, mineral supplements and various consumer products. Boron is an essential element for plant growth, but the essentiality for humans is not proven, although intakes of trace amounts of the element seem to be useful for bone health and proper brain function; higher concentrations of boron, however, may be toxic. In relation to the European Union legislation on dangerous substances, an EU Expert Group has recommended classifying boric acid and borates with risk phrases for reproductive toxicity. The aim of this paper is to assess whether the new EU hazard classification of boron compounds should imply that glass wool products used for building insulation in the future should be labelled, “may impair fertility and cause harm to the unborn child”, because of the low boron content. Materials and methods  Boron intakes are estimated in a worst-case occupational situation with human exposure to glass wool fibres at the occupational limit of 1 fibre/cm³ by calculation of the mass of the amount of fibres inhaled during an 8-h work day. Fibres are supposed to be cylinders of glass with a length of 30 μm, an average diameter of 1.5–2 μm and containing either 1.5% or 3.5% boron. As a worst-case scenario, the density of the fibres is set to 2,700 kg/m³. The inhalation rate of the individuals at moderate work load was set to 2 m³/h. A worst-case scenario also corresponds to 100% retention and to 100% solubility of the retained fibres in the lungs. Results  With the normal boron content of 1.5% in glass wool fibres for building insulation, the extra daily occupational boron intake/uptake will be 0.03–0.06 mg B for 5 days a week. For more uncommon glass wool with maximum boron content of 3.5%, the worst-case daily boron intake/uptake will be 0.08–0.16 mg B. The main boron exposure in the general population is from vegetarian food, and the average daily dietary intake with food is estimated to 1.2–1.5 mg B/day. In addition, significant intakes may come with drinking water, especially from mineral water. In some instances, exposure from mineral supplements, cosmetics and other consumer products may be significant. For example, individuals taking mineral supplements, e.g. for bodybuilding, may have an additional intake to that of 1–10 mg/day. During the years, various organisations have recommended safe intake values for boron. Recently, the Scientific Panel on Dietetic Products, Nutrition and Allergies of the European Food Safety Authority (EFSA) has established the ‘Tolerable Upper Intake Level’ (UL) for the intake of boron (boric acid and borates) at 0.16 mg B/kg body weight per day or about 10 mg B/day for an adult. Discussion  The calculated, worst-case exposure scenario during an 8-h work day will result in an extra daily boron intake that only corresponds to about 10% of the average daily adult boron intakes through food and drinks of about 1.5 mg. The inter-individual variations in boron intakes from foods, water and supplements will be much greater than an eventual, very worst-case, additional intake of boron from inhalation of glass wool fibres. In addition, the combined intakes are far lower than the ‘Tolerable Upper Intake Level’ of 10 mg B/day for a person weighing 60 kg, as recommended by the European Food Safety Agency. The potential boron intake from inhalation of glass wool fibres is also much lower than boron intakes by workers in the boron industry, who at the present occupational limit value will be exposed to 50 mg of boron 5 days a week, or 100 times more than the worst case for glass wool fibres. Furthermore, in practice, exposure levels will mostly be ten to 100 times lower than the occupational limit used here as a worst case. Conclusions  The estimated boron intake from inhalation of glass wool fibres in occupational settings will be insignificant and without any health risks, even in the case of non-compliance with the occupational limit value. Any proposal requiring hazard labels on commercial glass wool products for building insulation, because of the boron content, is not supported by the present scientific knowledge. Recommendations and perspectives  The European Commission should ensure that the new EU hazard classification of boron compounds is not applied to commercial glass wool products for building insulation having a low content of boron.     

Measurements of air–surface exchange rates of volatile organic compounds

Vertical gradients of volatile organic compounds (VOCs) were measured over a maize field and a soybean field in 1995 and 1996, respectively, in the Lower Coastal Plains of North Carolina. The measurements over the maize field were conducted in its early growth period, during May 1995, and the measurements over the soybean field were conducted in its middle and later growth periods during July through August 1996 at the same location. These measurements were combined with micrometeorological flux measurements to determine emission flux measurements for various VOCs. This measurement programme was part of project NOVA (Natural emissions of Oxidant precursors: Validation of techniques and Assessment) to estimate the flux of VOCs. Methanol was identified as the major biogenic compound for both years with the average flux of 3450 ± 1456 µg/m²/hr over maize and 3079 ± 2766 µg/m²/hr over soybean. Acetone is another compound that was identified as a biogenic compound for both years with the average flux of 425 ± 223 µg/m²/hr over maize and 2701 ± 1710 µg/m²/hr over soybean. In addition to biogenic compounds, a large number of aromatic compounds, including styrene and 1,2,4-trimethylbenzene, were also identified as emissions from the ground over the soybean field.     

Natural radiation level in the environment of Tehri Garhwal, Uttaranchal

The natural radiation levels were measured in about 50 residential houses of Tehri Garhwal, Uttaranchal, using an environmental radiation dosimeter in both the indoor and the outdoor atmosphere. The total gamma ray activity was found to vary from 29.74 µR/h to 41.19 µR/h with a mean of 36.5 µR/h for the indoor environment, whereas for outdoors it varied from 28.76 µR/h to 43.46 µR/h with a mean of 30.1 µR/h. The resulting gamma ray dose at 20 traditional rural houses was also measured. The values varied from 38.91 µR/h to 77.68 µR/h with a mean of 66.6 µR/h. Measurements of the diurnal variation of the dose rates showed that they are higher in the rural traditional houses than in modern houses. The variations of dose rate with the type of building material, the mode of construction and the age of houses are also discussed.     

Cyclooctane tropospheric degradation initiated by reaction with Cl atoms

Goal, Scope and Background Within the non-methane hydrocarbons, alkanes constitute the largest fraction of the anthropogenic emissions of volatile organic compounds. For the case of cyclic alkanes, tropospheric degradation is expected to be initiated mainly by OH reactions in the gas phase. Nevertheless, Cl atom reaction rate constants are generally one order of magnitude larger than those of OH. In the present work, the reaction of cyclooctane with Cl atoms has been studied within the temperature range of 279–333 K. Methods The kinetic study has been carried out using the fast flow tube technique coupled to mass spectrometry detection. The reaction has been studied under low pressure conditions, p=1 Torr, with helium as the carrier gas. Results The measured room temperature rate constant is very high, k=(2.63±0.54)×10⁻¹⁰ cm³molecule⁻¹s⁻¹, around 20 times larger than that for the corresponding OH reaction. We also report the results of the rate coefficients obtained at different temperatures: k = (3.5±1.2)×10⁻¹⁰ exp[(−79±110)/T] cm³ molecule⁻¹ s⁻¹ within the range of 279–333 K. This reaction shows an activation energy value close to zero. Discussion Quantitative formation of HCl has been observed, confirming the mechanism through H-atom abstraction. The reactivity of cyclic alkanes towards Cl atoms is clearly dependent on the number of CH₂ groups in the molecule, as is shown by the increase in the rate constant when the length of the organic chain increases. This increase is very high for the small cyclic alkanes and it seems that the reactions are approaching the collision-controlled limit for cyclohexane and cyclooctane. Conclusions These results show that gas-phase reaction with Cl in marine or coastal areas is an efficient sink (competing with the gas phase, OH initiated degradation) for the Earth’s emissions of cyclooctane, with a Cl-based lifetime ranging from 11 to 2000 hours, depending on the location and time of day. Recommendations and Perspectives Cl and OH fast reactions with cyclooctane are expected to define the lifetime of cyclooctane emissions to the atmosphere. The degradation of cyclooctane occurs in a short period of time and consequently (under conditions of low atmospheric mass transport), close to the emission sources enabling a significant contribution to local effects, like the formation of photochemical smog. ESS-Submission Editor: Prof. Dr. Gerhard Lammel (lammel@recetox.muni.cz)     

生物磁分离新技术处理含铬废水最佳条件的研究

为了探索新工艺"趋磁细菌-磁分离法"处理含铬废水的最佳条件,首先进行了趋磁细菌对铬离子的去除影响因素试验,研究了pH、温度、时间和微生物量对吸附的影响;其次进行了趋磁细菌的分离试验,考查了磁分离器中悬丝摆放位置和磁场强度对溶液中菌体的去除效果的影响.试验结果表明,体系的pH值对铬离子的去除效率影响最大,pH值的最佳范围为5～11;在室温范围内,温度对吸附的影响不大;随着菌量的增加,菌对Cr(Ⅲ)的去除率略有提高,而单位质量菌的吸附量却有明显下降.在分离趋磁细菌时,磁场强度为100高斯时分离效果很高,而超过100高斯以后,效果不明显;另外,分离器中的金属丝和磁场方向垂直放置要比平行放置效果好,并用扫描电镜放大5 000倍观察了金属丝上被捕集的趋磁细菌的形态和结构.     

Bioaccessibility of polychlorinated biphenyls in different foods using an in vitro digestion method

Bioaccessibility of organic pollutants in food is important for exposure estimation and risk assessment. An in vitro enzyme digestion experiment was carried out to analyze the bioaccessibility of PCBs in different foods including freshwater fish (bighead carp and oriental weather fish) and vegetables (spinach and cabbage). The results indicated that the bioaccessibility of PCBs in freshwater fish (3%) was much lower than that in leafy vegetables (25%). Based on field survey, the daily exposure TEQ value from these two types of food was 17.9 pg/kg bw/day. However, when bioaccessibility was taken into consideration, the value decreased to 0.61 pg/kg bw/day. Therefore, the forms of PCBs existing in food strongly influenced the bioavailability for humans, which may have important implications on dietary exposure. To our knowledge, this is the first paper to illustrate the bioaccessibility of PCBs in different foods using an in vitro digestion method.     

Student’s Exposure to Volatile Organic Compounds While Commuting by Motorcycle and Bus in Taipei City

This study examined student’s exposure to volatile organic compounds (VOCs) while commuting by bus and motorcycle in Taipei, Taiwan in the winter of 1992. A total of 19 target G5-C10 VOCs on three most frequently used commuting routes were collected on Tenax-GC adsorbent tubes. The VOCs were desorbed by thermal desorption method and analyzed by GCMS. The most abundant VOC exposure experienced by commuters was to toluene. Several alkylated benzenes, such as propyl benzenes, ethyl-methyl-benzenes and trimethyl-benzenes, were relatively abundant on the roads in Taipei. The mean benzene concentration measured in buses was 173 µg/m³ and 379.7 µg/m³ on motorcycles. On the average, the commuters in Taipei experienced about three to eight times higher VOC concentrations than the commuters in Los Angeles, California. Higher VOC concentrations were measured on motorcycles than in buses. The VOC concentrations were not significantly different between morning and afternoon commutes, nor among the three commuting routes. VOC concentrations measured in classrooms at three schools in downtown Taipei did not vary significantly on each sampling day. However, at each school the in-classroom VOC concentrations varied significantly over the six consecutive sampling days. The VOC concentrations measured on the roads were about five times higher than those measured in the school classrooms in the city. Moderate to high correlations were found among most of the measurements of the 19 VOCs. The survey questionnaire indicated that daily commuting time ranged from 45 minutes for elementary school students to 95 minutes for vocational school students. The projected upper-bound cancer risks associated with student’s exposure to benzene ranged from 7.5 x 10^-3 to 1.8 x 10^-5 during their commutes in Taipei.     

Characterization of Solid-Phase Microextraction and Gas Chromatography for the Analysis of Gasoline Tracers in Different Microenvironments

Abstract

Gasoline tracers were collected on solid-phase microextraction (SPME) fibers and analyzed by capillary gas chromatography with photoionization detector (GC/PID). This was part of a larger study to quantify personal exposure to motor vehicle gasoline evaporative and combustive emissions in high-end exposure microenvironments (MEs). The SPME fiber selected for this application was a 75-µm carboxen/polydimethylsiloxane. Sequential 10-min samples were collected for measurement of benzene, toluene, ethylbenzene, and ortho-, meta-, and para-xylene in different MEs in Atlanta, GA, in summer 2002 and Reno, NV, in spring 2003. Field calibrations were performed with certified gas standards in 1-L Tedlar bags for varying concentrations and exposure times. SPME detection limits were ～0.2 ppbv with a precision of 3–17% and accuracy of 30%. A dynamic system was designed for temperature and relative humidity calibrations, with corrections for the effects of these variables performed when necessary. SPME data compared satisfactorily with integrated canister samples, continuous PID, and field portable mass spectrometer data.     

Rates of particulate pollution deposition onto leaf surfaces: Temporal and inter-species magnetic analyses

Evaluation of health impacts arising from inhalation of pollutant particles <10 μm (PM₁₀) is an active research area. However, lack of exposure data at high spatial resolution impedes identification of causal associations between exposure and illness. Biomagnetic monitoring of PM₁₀ deposited on tree leaves may provide a means of obtaining exposure data at high spatial resolution. To calculate ambient PM₁₀ concentrations from leaf magnetic values, the relationship between the magnetic signal and total PM₁₀ mass must be quantified, and the exposure time (via magnetic deposition velocity (MV_d) calculations) known. Birches display higher MV_d (∼5 cm⁻¹) than lime trees (∼2 cm⁻¹). Leaf saturation remanence values reached ‘equilibrium’ with ambient PM₁₀ concentrations after ∼6 ‘dry’ days (<3 mm/day rainfall). Other co-located species displayed within-species consistency in MV_d; robust inter-calibration can thus be achieved, enabling magnetic PM₁₀ biomonitoring at unprecedented spatial resolution.     

DEARS particulate matter relationships for personal,indoor, outdoor,and central site settings for a general population

This analysis provides the initial summary of PM_2.5 mass concentrations relationships for all seasons and participants for a general population in the Detroit Exposure and Aerosol Research Study (DEARS). The summary presented highlights the utility of the new methodologies applied, in addition to summarizing the particulate matter (PM) data.Results include the requirement to adjust the exposure data for monitor wearing compliance and measured environmental tobacco smoke (ETS) levels, even though the study design specified a non-smoking household. A 40% wearing compliance acceptance level was suggested as necessary to balance minimizing exposure misclassification (from poor compliance) and having sufficient data to conduct robust statistical analyses. An ETS threshold level equivalent to adding more than 1.5 μg m^?3 to the collected sample was found to be necessary to detect changes in the personal exposure factor (F_pex). It is not completely clear why such a large threshold level was necessary.Statistically significant spatial PM_2.5 gradients were identified in three of the six DEARS neighborhoods in Wayne County. These were expected, given the number of strong, localized PM sources in the Detroit (Michigan) metro area. Some residential outdoor bias levels compared with the central site at Allen Park exceeded 15%. After adjusting for ETS biases, the outdoor contributions to the personal exposure were typically larger by factors from 1.75 to 2.2 compared with those of the non-outdoor sources. The outdoor contribution was larger in the summer than in the winter, which is consistent with the fractions of time spent outdoors in the summer vs. the winter (6.7% vs. 1.1% of the time).Mean personal PM_2.5 cloud levels for the general population DEARS cohort ranged from 1.5 to 3.8 (after ETS adjustment) and were comparable to those reported previously. The personal exposure collections indoors were typically at least 13 times greater than those contributed outdoors.     

Exposure to perfluorooctane sulfonic acid (PFOS) adversely affects the life-cycle of the damselfly Enallagma cyathigerum

We evaluated whether life-time exposure to PFOS affects egg development, hatching, larval development, survival, metamorphosis and body mass of Enallagma cyathigerum (Insecta: Odonata). Eggs and larvae were exposed to five concentrations ranging from 0 to 10 000 μg/L. Our results show reduced egg hatching success, slower larval development, greater larval mortality, and decreased metamorphosis success with increasing PFOS concentration. PFOS had no effect on egg developmental time and hatching or on mass of adults. Eggs were the least sensitive stage (NOEC = 10 000 μg/L). Larval NOEC values were 1000 times smaller (10 μg/L). Successful metamorphosis was the most sensitive response trait studied (NOEC < 10 μg/L). The NOEC value suggests that E. cyathigerum is amongst the most sensitive freshwater organisms tested. NOEC for metamorphosis is less than 10-times greater than the ordinary reported environmental concentrations in freshwater, but is more than 200-times smaller than the greatest concentrations measured after accidental releases.     

Observation based analysis for the determination of equilibrium time constant between ammonia, acid gases, and fine particles

Experimental measurements of ammonia, acid gases, and the inorganic components of atmospheric aerosols were made at a commercial hog farm in eastern North Carolina from May 1998 to June 1999 by an annular denuder system (ADS). The ADS consisted of a cyclone separator, one diffusion denuder coated with sodium carbonate, another diffusion denuder with citric acid, and a filter pack containing Teflon and nylon filters in series. The equilibrium time constant for transfer between ammonia, acid gases, and aerosol phase of ammonium nitrate and ammonium chloride was determined based on kinetic rate constants (k_N as the rate constant of ammonium nitrate aerosol: 2.04 × 10^-4 m³/µmole/sec; k_Cl as the rate constant of ammonium chloride aerosol: 3.44 × 10^-4 m³/µmole/sec) and the observed inorganic components of atmospheric aerosols. The equilibrium time constant was determined based on kinetic rate constants and the observed inorganic components of atmospheric aerosols. The equilibrium time constant has a wide range of values, with an average value of 15.26 (±10.94) minutes for ambient equilibrium time between ammonia, nitric acid gas and ammonium nitrate aerosol; and 8.22 (±6.81) minutes for ammonia, hydrochloric acid, and ammonium chloride. Significant correlations were determined between comparisons of equilibrium time constant estimates with meteorological parameters, such as ambient temperature and relative humidity. The predicted chemical compositions in the particle by EQUISOLV II Model are in good agreement with the observed chemical composition at the experimental site.     

The effect of dimethoate and cypermethrin on soil-dwelling beetles under semi-field conditions

The effect of cypermethrin and dimethoate exposure on soil-dwelling beetles, in spring barley at different growth stages, of doses of up to eight times maximum field application rate has been investigated. Doses up to eight times maximum field application rate of cypermethrin did not have any acute effects on larger beetles, such as P. melanarius and C. erratus. Small beetles (A. bilineata, A. dorsale, B. lanpros, B. obtusum) were not harmed by doses up to two times maximum field application rate. T. hypnorum was affected at maximum field rate. Dimethoate at maximum field application rate harmed all species, but in particular the smaller species. When dimethoate was applied in high foliage density fields in the summer, very severe acute effects on spring breeding beetles were found. In the autumn, when only a low crop cover existed, this very high effect was not observed. The severe effect in the summer may be explained by the mode of action of dimethoate on 'old beetles'. The observed high toxic effect of dimethoate on spring breeders in the summer is expected only to have limited effect on the population, because the spring breeders at this time of the year have finished their egg depositing in the soil.     

Uptake and elimination of perchlorate in eastern mosquitofish

The purpose of this study was to investigate the uptake and elimination of perchlorate in eastern mosquitofish (Gambusia holbrooki). Fish were exposed to 0.1-1000 mg/l sodium perchlorate for 12h, 1, 2, 5, 10, and 30 days, and perchlorate was determined in whole body extracts. Perchlorate was not detected in mosquitofish exposed to the low concentrations of perchlorate (0, 0.1, and 1mg/l sodium perchlorate), regardless of the exposure time, whereas it was detected when fish were exposed to 10, 100, and 1000 mg/l. The tissue concentrations were approximately 10 times less than that in the water. There was no difference in the uptake of perchlorate depending upon the exposure time, however, a difference in perchlorate uptake depending upon the concentration of the exposure dose (P<0.001) was observed. Uptake (K(u)) and elimination (K(e)) rate constants were 0.09 l/mg day and 0.70 day(-1), respectively. The half-life (T1/2) of perchlorate was 0.99 day. Thus, it appears that perchlorate is rapidly taken up and eliminated in eastern mosquitofish. These results are critical and may be used to develop models of fate, effects, and transport of perchlorate in natural systems, as well as to assess ecological risk in affected ecosystems.     

Environmental conditions enhance toxicant effects in larvae of the ground beetle Pterostichus oblongopunctatus (Coleoptera: Carabidae)

The wide geographical distribution of ground beetles Pterostichus oblongopunctatus makes them very likely to be exposed to several environmental stressors at the same time. These could include both climatic stress and exposure to chemicals. Our previous studies demonstrated that the combined effect of nickel (Ni) and chlorpyrifos (CHP) was temperature (T)-dependent in adult P. oblongopunctatus. Frequently the different developmental stages of an organism are differently sensitive to single stressors, and for a number of reasons, such as differences in exposure routes, their interactions may also take different forms. Because of this, we studied the effects of the same factors on the beetle larvae. The results showed that all factors, as well as their interactions, influenced larvae survival. The synergistic effect of Ni and CPF was temperature-dependent and the effect of Ni × T interaction on the proportion of emerged imagines indicated stronger toxicity of Ni at 25 °C than at 10 °C.     

Applications of GPS-tracked personal and fixed-location PM2.5 continuous exposure monitoring

Continued development of personal air pollution monitors is rapidly improving government and research capabilities for data collection. In this study, we tested the feasibility of using GPS-enabled personal exposure monitors to collect personal exposure readings and short-term daily PM_2.5 measures at 15 fixed locations throughout a community. The goals were to determine the accuracy of fixed-location monitoring for approximating individual exposures compared to a centralized outdoor air pollution monitor, and to test the utility of two different personal monitors, the RTI MicroPEM V3.2 and TSI SidePak AM510. For personal samples, 24-hr mean PM_2.5 concentrations were 6.93 μg/m³ (stderr = 0.15) and 8.47 μg/m³ (stderr = 0.10) for the MicroPEM and SidePak, respectively. Based on time–activity patterns from participant journals, exposures were highest while participants were outdoors (MicroPEM = 7.61 µg/m³, stderr = 1.08, SidePak = 11.85 µg/m³, stderr = 0.83) or in restaurants (MicroPEM = 7.48 µg/m³, stderr = 0.39, SidePak = 24.93 µg/m³, stderr = 0.82), and lowest when participants were exercising indoors (MicroPEM = 4.78 µg/m³, stderr = 0.23, SidePak = 5.63 µg/m³, stderr = 0.08). Mean PM_2.5 at the 15 fixed locations, as measured by the SidePak, ranged from 4.71 µg/m³ (stderr = 0.23) to 12.38 µg/m³ (stderr = 0.45). By comparison, mean 24-h PM_2.5 measured at the centralized outdoor monitor ranged from 2.7 to 6.7 µg/m³ during the study period. The range of average PM_2.5 exposure levels estimated for each participant using the interpolated fixed-location data was 2.83 to 19.26 µg/m³ (mean = 8.3, stderr = 1.4). These estimated levels were compared with average exposure from personal samples. The fixed-location monitoring strategy was useful in identifying high air pollution microclimates throughout the county. For 7 of 10 subjects, the fixed-location monitoring strategy more closely approximated individuals’ 24-hr breathing zone exposures than did the centralized outdoor monitor. Highlights are: Individual PM_2.5 exposure levels vary extensively by activity, location and time of day; fixed-location sampling more closely approximated individual exposures than a centralized outdoor monitor; and small, personal exposure monitors provide added utility for individuals, researchers, and public health professionals seeking to more accurately identify air pollution microclimates.

Implications: Personal air pollution monitoring technology is advancing rapidly. Currently, personal monitors are primarily used in research settings, but could they also support government networks of centralized outdoor monitors? In this study, we found differences in performance and practicality for two personal monitors in different monitoring scenarios. We also found that personal monitors used to collect outdoor area samples were effective at finding pollution microclimates, and more closely approximated actual individual exposure than a central monitor. Though more research is needed, there is strong potential that personal exposure monitors can improve existing monitoring networks.     

Effect of Long Retention Time in the Settler on Phosphorus Removal from Communal Wastewater (4 pp)

- Goals. The objective of the paper is to illustrate the solution of a chronic problem occurring in a wastewater treatment facility with a capacity of 12,000 inhabitant equivalent. A drastic phosphorus concentration increase (two or three times higher than the Hungarian limit of 1 mg/l) was observed in the wastewater treatment facility for a long time (12–24 h) with changing time periods indicating malfunctioning in the operation of the facility. Methods Computer-aided simulation technique was used to develop a solution for the treatment of the problem using a software developed by the Department of Environmental and Chemical Engineering, University of Veszprém, Hungary. Results and Discussion The simulation studies show that if the nightly inflow is less than 200 m3/h at least for two hours, the system doesn't then receive enough fresh nutrients which can cause a deficiency in the nutrient uptake of the PAOs in the anaerobic zones. This can result in the fact that the PAOs accumulate less phosphorus into the aerobic zones. Conclusion Long retention time (10 h) is the reason for the problem, namely – under special conditions – the phosphorus in the sludge of the settling tank of the wastewater treatment plant. The problem was caused by phosphorus dissolution from the sludge of the settling tank during the undesirably long retention time.     

Consultant Guide/1978

Abstract

Biomarkers of methyl tertiary butyl ether (MTBE) exposure and the partitioning of inhaled MTBE into the body were investigated in a human chamber study. Two subjects were exposed to an environmentally relevant nominal 5,011 µg/m³ (1.39 ppm) MTBE for 1 hour, followed by clean–air exposure for 7 hours. Breath and blood were simultaneously sampled, while total urine was collected at prescribed times before, during, and after the exposure. Mass–balance and toxicokinetic analyses were conducted based upon the time series measurement of multiple body–burden endpoints, including MTBE in alveolar breath, and MTBE and tertiary butyl alcohol (TBA) in venous blood and urine.

The decay of MTBE in the blood was assessed by fitting the post–exposure data to a 2– or 3–exponential model that yielded residence times (τ) of 2–3 min, 15–50 min, and 3–13 h as measured by alveolar breath, and 5 min, 60 min, and 32 h as evaluated from venous blood measurements. Based on observations of lower than expected blood and breath MTBE during uptake and a decreasing blood–to–breath ratio during the post–exposure decay period, we hypothesize that the respiratory mucous membranes were serving as a reservoir for the retention of MTBE. The decay data suggest that 6–9% of the MTBE intake may be retained by this non–blood reservoir. The compartmental modeling was further used to estimate important parameters that define the uptake of inhaled MTBE. The first of these parameters is f, the fraction of C_air exhaled at equilibrium, estimated as 0.60 and 0.46 for the female and male subject, respectively. The second parameter is the blood–to–breath partition coefficient (P) estimated as ～18. The product of these parameters provides an estimate of the blood concentration at equilibrium as 8–11 times the air concentration. Blood TBA lagged MTBE levels and decayed more slowly (τ = 1.5–3 h), providing a more stable indication of longer term integrated exposure.

The concentration ranges of MTBE and TBA in urine were similar to that of the blood, ranging from 0.37 to 15 µg/L and 2 to 15 µg/L, respectively. In urine, MTBE and TBA by themselves bore little relationship to the exposure. However, the MTBE:TBA ratio followed the pattern of exposure, with peak values occurring at the end of the exposure (20– and 60–fold greater than pre–exposure values) before decaying back to pre–exposure levels by the end of the 7–h decay period. Urinary elimination accounted for a very small fraction of total MTBE elimination (<1%).     

Electrofluidized Beds in the Filtration Of a Submicron Aerosol

A plug-flow model is developed showing the way in which efficiency depends on unfluidized bed height, bed particle size, participate mobility, gas flow rate and applied electric field intensity. This model is successfully correlated with tests in which flow rate, bed particle size, and unfluidized bed height are varied. It is shown that efficiencies better than 90% can be achieved in collecting 0.4 µm DOP with a gas residence time less than 50 msec and a pressure drop of about 10 cm of water.