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Air Concentrations (air + concentration)

Distribution by Scientific Domains

Engineering	45%
Medical Sciences	36%

Selected Abstracts

Epistaxis in a low level hydrogen fluoride exposed industrial staff

AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, Issue 3 2009
Pål Graff
Abstract Objectives To assess the effect of exposure to hydrogen fluoride (HF) on the airway mucosa in an industrial setting. Methods A cross-sectional study encompassing 33 industrial workers in a flame soldering plant and 44 assembly workers unexposed to HF was performed by means of a questionnaire on symptoms and diagnosis regarding upper and lower airways as well as through conduct of a clinical examination of the exposed group. Air concentrations of HF that were monitored in winter amounted to 1.0 mg/m3 and in summer time to 0.15 mg/m3. Results A threefold risk for epistaxis (RR,=,3.6, 95% confidence interval 1.1,11.0) was observed in the exposed group. Time from the start of exposure to HF until debut of a nose bleeding period varied from 1 month to 6 years. Mean induction (latency) time was 42 months. Mean duration of symptoms was 26 months, range 3,72 months, indicating that the exposure level in summer time was sufficient to maintain the propensity of almost daily nose bleeding. Conclusion HF is an irritating vapor, even at relatively low air concentrations. We recommend an 8 hr TLV lower than 1.0 mg/m3. Am. J. Ind. Med. 52:240,245, 2009. © 2008 Wiley-Liss, Inc. [source]

Airborne contact dermatitis from methylchloroisothiazolinone in wall paint.

CONTACT DERMATITIS, Issue 4 2000
Abolition of symptoms by chemical allergen inactivation
Preservatives such as isothiazolinones in paints have been reported to cause airborne contact dermatitis. The patients whom we report experienced acute dermatitis on air-exposed skin and respiratory symptoms after staying in recently painted rooms. Kathon® (methylchloroisothiazolinone/ methylisothiazolinone) added as preservative to the wall paint was identified as causative agent. In one individual symptoms rapidly disappeared after treatment of the painted walls with inorganic sulfur salt, which leads to inactivation of the allergenic properties of methylchloroisothiazolinone/ methylisothiazolinone. We describe the patients, the clinical course and review the literature pertinent to such cases. In addition we report on the chemical analyses of the decorating paints used, and on experiments on emission and air concentration of methylchloroisothiazolinone/methylisothiazolinone from a painted surface before and after inactivation by sodium bisulfite. [source]

Vapor Intrusion in Homes over Gasoline-Contaminated Ground Water in Stafford, New Jersey

GROUND WATER MONITORING & REMEDIATION, Issue 1 2006
Paul F. Sanders
The potential for chemical vapor intrusion from contaminated ground water to the interior of homes was investigated at a site with a leaking underground gasoline storage tank in Stafford Township, New Jersey. This location exhibited conditions favorable to vapor intrusion, with sand soil and a water table depth of 3.3 m. Concentrations of volatile organic chemicals in the ground water were as high as 82 mg/L for total benzene, toluene, ethylbenzene, and xylene (BTEX) and up to 590 mg/L for methyl- t -butyl ether (MTBE). Soil vapor samples at multiple depths were taken adjacent to several homes. Inside the homes, air samples were taken on the main floor, in the basement, and under the foundation slab. Despite high ground water concentrations, only one home had measurable impacts to indoor air quality attributable to some of the ground water contaminants. In this house, the BTEX chemicals were not detected in the basement, indicating a lack of indoor air impacts from the ground water for these chemicals. Oxygen measurements suggested that degradation attenuated these chemicals as they diffused through the vadose zone. However, MTBE, 2,2,4-trimethylpentane (isooctane), and cyclohexane were found in the indoor air. The first two of these chemicals served as gasoline-specific tracers and indicated that vapor intrusion was occurring. Attenuation factors (the ratio of the indoor air concentration to a source soil vapor concentration) for the BTEX chemicals between the ground water and the indoor air were <1 × 10,5, and for MTBE was 1.2 × 10,5. Attenuation factors between the deep-soil vapor and the basement air were as follows: BTEX compounds, <1 × 10,5; MTBE, 2.2 × 10,5; 2,2,4-trimethylpentane, 3.6 × 10,4; and cyclohexane, 1.2 × 10,4. Attenuation factors between the subslab vapor and the basement air were 7 to 8 × 10,3. [source]

Modeling and CFD prediction for diffusion and adsorption within room with various adsorption isotherms

INDOOR AIR, Issue 2003
S. Murakami
Abstract This paper presents physical models that are used for analyzing numerically the transportation of volatile organic compounds (VOCs) from building materials in a room. The models are based on fundamental physicochemical principles of their diffusion and adsorption/desorption (hereafter simply sorption) both in building materials and in room air. The performance of the proposed physical models is examined numerically in a test room with a technique supported by computational fluid dynamics (CFD). Two building materials are used in this study. One is a VOC emitting material for which the emission rate is mainly controlled by the internal diffusion of the material. The other is an adsorptive material that has no VOC source. It affects the room air concentration of VOCs with its sorption process. The floor is covered with an emission material made of polypropylene styrene,butadiene rubber (SBR). An adsorbent material made of coal-based activated carbon is spread over the sidewalls. The results of numerical prediction show that the physical models and their numerical simulations explain well the mechanism of the transportation of VOCs in a room. [source]

Environmental factors affecting the levels of legacy pesticides in the airshed of Delaware and Chesapeake Bays, USA

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 9 2010
Anubha Goel
Abstract Organochlorine insecticides and their degradation products contribute to toxicity in Chesapeake Bay, USA, sediments and affect the reproductive health of avian species in the region; however, little is known of atmospheric sources or temporal trends in concentrations of these chemicals. Weekly air (n,=,265) and daily rain samples (n,=,494) were collected over 2000 to 2003 from three locations in the Delmarva Peninsula, USA. Pesticides were consistently present in the gas phase with infrequent detection in the particle phase. Hexachlorocyclohexanes (HCHs) and cis - and trans -chlordane were detected most frequently (95,100%), and cis - and trans -nonachlor, oxychlordane, heptachlor, heptachlor epoxide, dieldrin, and 1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene (4,4,-DDE) were also detected frequently. The highest mean air concentrations were for dieldrin (60,84,pg/m3), ,-HCH (37,83,pg/m3), and 4,4,-DDE (16,80,pg/m3). Multiple regression analyses of air concentrations with temperature and wind conditions using modified Clausius-Clapeyron equations explained only 30 to 60% of the variability in concentration for most chemicals. Comparison of the air concentrations and enthalpy of air,surface exchange values at the three sites indicate sources of chlordanes and ,-HCH sources are primarily from long-range transport. However, examination of chlordane isomer ratios indicates some local and regional contributions, and ,-HCH, 4,4,-DDE, dieldrin, heptachlor, heptachlor epoxide, and oxychlordane also have local or regional sources, possibly from contaminated soils. Median rain sample volumes of 1 to 3 L led to infrequent detections in rain; however, average measured concentrations were 2 to 10 times higher than in the Great Lakes. Dissipation half-lives in air were well below 10 years for all chemicals and below published values for the Great Lakes except dieldrin, which did not decline during the sample period. Environ. Toxicol. Chem. 2010;29:1893,1906. © 2010 SETAC [source]

Dichlorodiphenyltrichloroethane in the aquatic ecosystem of the Okavango Delta, Botswana, South Africa

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 1 2003
Bontle Mbongwe
Abstract Concentrations of DDT and its metabolites were measured in water, plants, invertebrates, and fish from lagoons in the Okavango Delta, Botswana (Africa), where DDT has been used for approximately 50 years. The sampling area was sectioned to distinguish spraying for malaria and for African sleeping sickness. Average concentrations of total DDT (sum of DDT and its metabolites) in the Okavango ranged from 0.009 ng/L in water to 18.76 ng/g wet weight in fish. These levels are approximately 1% of those found in piscivorous fish from temperate North America. The dichlorodiphenyl ethylene (DDE) metabolite was the most abundant fraction of total DDT. Although total DDT concentrations were higher in areas treated for malaria than areas treated for sleeping sickness, these concentrations were likely driven by factors other than the historic application of the pesticide. Equilibration with air concentrations is the most likely explanation for these levels. Since the mean annual temperature exceeds the temperature of vaporization of DDT, this research points to the need for reliable transport models. Our results showed that total DDT concentration in fish was best explained by lipid content of the fish and trophic position inferred by ,15N, regardless of DDT application history in those areas. The reservoir above Gaborone Dam, an area downstream of the Okavango but where DDT had not been used, was sampled to compare total DDT levels to the treated areas. The two species (a herbivorous threespot talapia and the omnivorous sharptooth catfish) from Gaborone had levels higher than those found in the Okavango Delta, but these differences can again be explained using trophic position inferred by ,15N rather than by fish size or location. [source]

Age of Irrigation Water in Ground Water from the Eastern Snake River Plain Aquifer, South-Central Idaho

GROUND WATER, Issue 2 2000
L.N. Plummer
Stable isotope data (2H and 18O) were used in conjunction with chlorofluorocarbon (CFC) and tritium/helium-3 (3H/3He) data to determine the fraction and age of irrigation water in ground water mixtures from farmed parts of the Eastern Snake River Plain (ESRP) Aquifer in south-central Idaho. Two groups of waters were recognized: (1) regional background water, unaffected by irrigation and fertilizer application, and (2) mixtures of irrigation water from the Snake River with regional background water. New data are presented comparing CFC and 3H/3He dating of water recharged through deep fractured basalt, and dating of young fractions in ground water mixtures. The 3H/3He ages of irrigation water in most mixtures ranged from about zero to eight years. The CFC ages of irrigation water in mixtures ranged from values near those based on 3H/3He dating to values biased older than the 3H/3He ages by as much as eight to 10 years. Unsaturated zone air had CFC-12 and CFC-113 concentrations that were 60% to 95%, and 50% to 90%, respectively, of modern air concentrations and were consistently contaminated with CFC-11. Irrigation water diverted from the Snake River was contaminated with CFC-11 but near solubility equilibrium with CFC-12 and CFC-113. The dating indicates ground water velocities of 5 to 8 m/d for water along the top of the ESRP Aquifer near the southwestern boundary of the Idaho National Engineering and Environmental Laboratory (INEEL). Many of the regional background waters contain excess terrigenic helium with a 3He/4He isotope ratio of 7 × 10,6 to 11 × 10,6 (R/Ra= 5 to 8) and could not be dated. Ratios of CFC data indicate that some rangeland water may contain as much as 5% to 30% young water (ages of less than or equal to two to 11.5 years) mixed with old regional background water. The relatively low residence times of ground water in irrigated parts of the ESRP Aquifer and the dilution with low-NO3 irrigation water from the Snake River lower the potential for NO3 contamination in agricultural areas. [source]

Measured concentrations of combustion gases from the use of unvented gas fireplaces

INDOOR AIR, Issue 5 2010
P. W. Francisco
Abstract, Measurements of combustion product concentrations were taken in 30 homes where unvented gas fireplaces were used. Measurements of CO, CO2, NOx, NO2, O2 (depletion), and water vapor were taken at 1-min interval. The analyzers were calibrated with certified calibration gases for each placement and were in operation for 3,4 days at each home. Measured concentrations were compared to published health-based standards and guidelines. The two combustion gases that exceeded published values were NO2 and CO. For NO2, the Health Canada guideline of 250 ppb (1-h average) was exceeded in about 43% of the sample and the World Health Organization (WHO) guideline of 110 ppb (1-h average) was exceeded in 80% of the sample. Carbon monoxide levels exceeded the U.S. EPA 8-h average standard of 9 ppm in 20% of the sample. Moisture problems were not evident in the test homes. An analysis of the distribution of CO showed that the CO is dispersed throughout the home almost immediately upon operation of the fireplace and that the concentrations throughout the home away from the immediate vicinity of the fireplace are 70,80% of the level near the fireplace. Decay analysis of the combustion gases showed that NO was similarly stable to CO and CO2 in the indoor environment but that both NO2 and water vapor were removed from the air at much greater rates. Practical Implications Previous studies on unvented gas fireplaces have made assumptions of how they are operated by users. This article presents the results of field monitoring of 30 unvented gas fireplaces under normal operation, regardless of whether users follow industry recommendations regarding installation, usage patterns, and maintenance. The monitoring found that health-based standards and guidelines were exceeded for CO in 20% of homes and for NO2 in most homes. There were no identified moisture problems in these homes. Nearly, half of the fireplaces were used at least once for longer than 2 h, counter to manufacturers' intended usage as supplemental heating. This demonstrates that given actual usage patterns and compared to current health-based thresholds, these appliances can produce indoor air concentrations considered to be unhealthy to at least sensitive or at-risk individuals. [source]

A critical review of reported air concentrations of organic compounds in aircraft cabins

INDOOR AIR, Issue 3 2003
N. L. Nagda
First page of article [source]

Characterization of a fatal methyl bromide exposure by analysis of the water cooler

AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, Issue 7 2009
David J. Hewitt MD
Abstract Background A suspected inhalation exposure to methyl bromide (MeBr) in the packaging and shipping area of a chemical manufacturer resulted in a worker fatality and several symptomatic cases. However, air testing was negative for MeBr resulting in uncertainty regarding the potential chemical exposure. Methods of quickly confirming the exposure and magnitude were sought. Methods Head space air and water samples were obtained from the breakroom water cooler in the facility and tested for MeBr. Results Increased levels of MeBr were identified in the air and water samples from the cooler and used to calculate the MeBr concentration of air entering the cooler. The MeBr air concentration within the breakroom was estimated as 1,200,2,100,ppm depending on assumptions regarding the amount of water dispensed from the cooler both before and during the incident. Conclusions Estimated MeBr air concentrations in the breakroom were consistent with those known to be associated with reported health effects among the involved workers. The water cooler analysis represented a unique method of retrospectively verifying and quantifying exposure to MeBr. Am. J. Ind. Med. 52:579,586, 2009. © 2009 Wiley-Liss, Inc. [source]