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At least 127 records · Page 7Linked to original sources
PubMed2004

Air concentrations of VOCs in portable and traditional classrooms: results of a pilot study in Los Angeles County.

Recent state and federal public school class-size reduction initiatives, increased elementary and pre-K enrollment driven by population growth and immigration, and limited resources for capital projects, modernization, and maintenance at aging schools have increased the prevalence of prefabricated, portable classrooms (portables). At present, approximately one of three California students are taught in portables, whose use is especially prevalent in more populated counties such as Los Angeles, home to the nation's second largest school district. Limited data existed on chemical compound air concentrations, and thus exposures, inside American public schools. Measurements have been limited, usually performed in complaint schools, and varied in sampling protocols and analysis methods. To address a school environment and children's health issue of present concern, an assessment of public school portables was conducted in Los Angeles County. Seven schools in two school districts were recruited, from which 20 classrooms--13 portables, seven in main buildings--were randomly selected. We report indoor air concentrations of 21 target toxic and odorous volatile organic compounds (VOCs), including formaldehyde and acetaldehyde, measured with passive samplers (DNSH PAKS and 3M OVM 3500) in the cooling and heating seasons between June 2000 and June 2001. None of the measured indoor air formaldehyde concentrations exceeded the existing California Air Resources Board guideline (50 ppb, or 60 microg/m(3)). The main sources of aldehydes in classrooms, especially portables, were likely interior finish materials and furnishings made of particleboard without lamination. Indoor air VOC concentrations were generally low in this pilot study. The four most prevalent VOCs measured were toluene, m-/p-xylene, alpha-pinene, and delta-limonene; likely indoor sources were personal, teaching, and cleaning products. Future schools research should attempt larger samples over larger geographical areas.

Acetaldehyde↗
PubMed2000

Development of a calibration system to evaluate VOC losses in a branch enclosure.

Considerable uncertainties are associated with the experimental estimates of emission rates of different volatile organic compound (VOC) species from the biosphere to the atmosphere. Some of this uncertainty derives from the sampling and analytical procedures used in emission rate measurements. A calibration system was developed in order to evaluate possible errors in the measurements of biogenic emission rates using a branch enclosure system. Two types of calibration procedures were tested, a standard additions technique and an internal standard procedure. Both techniques were used to evaluate possible losses while sampling isoprene and monoterpenes, which are the most abundant VOCs of biogenic origin. The losses to Teflon lines and the empty sampling system were tested and losses to the branch enclosure system installed on two VOC emitting plant species were evaluated. A considerable loss of isoprene (approximately 18% of inflow concentration 65 ng l(-1)) to the empty enclosure system and to the system installed on the plant was measured, but no losses of monoterpenes were observed.

Calibration↗
PubMed2003

Determination of VOCs in yellow eel from various inland water bodies in Flanders (Belgium).

Twenty freshwater eels caught in Flanders (Belgium) were analysed by GC-MS for a total of 52 VOCs. The most prominent VOCs are the BTEX and a number of chlorinated compounds such as chloroform and tetrachloroethene. The observed concentrations which, typically, were in the low ng/g wet weight range, could be linked to the major emission sources and the present study gives new evidence that combustion of fossil fuels is a major source of BTEX in the environment. The concentration levels in eels seem to be a reflection of the actual concentrations in their environment. For eels from the same location similar patterns and concentrations were observed, and the concentrations agree with what can be expected from those of the water column. Generally speaking, the observed concentrations do not seem to pose a threat for organisms. More definite statements will, however, require a larger dataset. The study suggests that the yellow eel can possibly be used as a biomonitor or sentinel organism for VOCs.

Animals↗
PubMed2003

SIFT-MS measurement of VOC distribution coefficients in human blood constituents and urine.

The new technique of selected ion flow tube-mass spectrometry (SIFT-MS) has been applied to the measurement of Henry's Law constants for the volatile organic chemicals o-xylene and trichloroethylene that both have low solubility in aqueous solvents. The method is validated by measurements in water at 298 K using the equilibrium partitioning in closed systems (EPICS) methodology in which the equilibrium headspace concentrations for the volatile organic compounds (VOCs) are measured in two sealed bottles containing different liquid volumes of very dilute solutions of the VOC. The range of solvents is then extended to human body fluids at 309 K including urine, saline, whole blood, red cells in saline, and plasma. The dimensionless distribution coefficients for these solvents vary markedly in the different fluids. For o-xylene they range from k(H) = 0.12-0.15 for water, saline, and urine; 0.53 for red cells in saline; 1.9 for whole blood; to 2.4 for plasma. For trichloroethylene the distribution coefficients range from k(H) = 0.070-0.091 for water, saline, and urine; 0.28 for red cells in saline; 0.35 for plasma; to 0.48 in whole blood. The very different solubilities of organic solvents in body fluids influence the uptake of solvents in workers exposed to VOCs. Some implications of these measurements are briefly discussed.

Humans↗
PubMed2004

Field method comparison between passive air samplers and continuous monitors for Vocs and NO2 in El Paso, Texas.

This study evaluates the performance of Model 3300 Ogawa Passive Nitrogen Dioxide (NO2) Samplers and 3M 3520 Organic Vapor Monitors (OVMs) by comparing integrated passive sampling concentrations to averaged hourly NO2 and volatile organic compound (VOC) measurements at two sites in El Paso, TX. Sampling periods were three time intervals (3-day weekend, 4-day weekday, and 7-day weekly) for three consecutive weeks. OVM concentrations were corrected for ambient pressure to account for higher elevation. Precise results (< 5% relative standard deviation, RSD) were found for NO2 measurements from collocated Ogawa samplers. Reproducibility was lower from duplicate OVMs for BTEX (benzene, toluene, ethylbenzene, and xylene isomers) VOCs (> or = 77% RSD for 2-day samples) with better precision for longer sampling periods. Comparison of Ogawa NO2 samplers with chemiluminescence measurements averaged over the same time period suggested potential calibration problems with the chemiluminescence analyzer. For BTEX species, generally good agreement was obtained between OVMs and automated-gas chromatograph (auto-GC) measurements. The OVMs successfully tracked increasing levels of VOCs recorded by the auto-GCs. However, except for toluene, OVM BTEX measurements generally exceeded their continuous counterparts with a mean bias of 5-10%. Although interpretation of the study results was limited due to small sample sizes, diffusion barrier influences caused by shelters that housed OVMs and differences in sampling heights between OVMs and auto-GC inlet may explain the overestimation.

Air Pollutants↗
PubMed2006

Effect of surface tension reduction on VOC removal during surfactant-enhanced air sparging.

In this study, the effect of decreased surface tension of water on the removal efficiency of a volatile organic compound (VOC) during air sparing was evaluated using a laboratory-scale, two-dimensional physical model packed with sand and water containing dissolved toluene as a representative VOC. Two sets of air sparging experiments were performed: the first at a surface tension of 69 dyne/cm with no surfactant applied, and with a toluene concentration of 110 mg/L; the second at a surface tension of 50 dyne/cm due to 110 mg/L of anionic surfactant, and 99 mg/L of toluene. Under the experimental conditions used in this study, the sparging influence zone estimated at the lower surface tension was about 2.5 times that estimated at the high surface tension. Also the rate of toluene removal by air sparging was found to be much faster at the lower surface tension. The sparging time required for 50% removal of the initial mass of toluene was 16.8 hours at 50 dyne/cm, which was much smaller than 82.5 hours measured at 69 dyne/cm. The final mass recoveries at low and high surface tensions were 92.1% and 56.6%, respectively. Therefore it was concluded that air sparging at reduced surface tension (surfactant-enhanced air sparging) greatly improved the removal efficiency of VOCs from the porous medium compared to conventional air sparging with no applied surfactant.

Air Pollutants↗
PubMed1995

VOC emission rates and emission factors for a sheetfed offset printing shop.

Emission rates were determined during production for a sheetfed offset printing shop by combining the measured concentrations and ventilation rates with mass balance models that characterized the printing space. Air samples were collected simultaneously on charcoal tubes for 12 separate 1-hour periods at 6 locations. Air samples and cleaning solvents were analyzed by gas chromatography for total volatile organic compounds (VOC) and 13 hydrocarbons. The average VOC emission rate was 470 g/hr with a range of 160-1100 g/hr. These values were in good agreement with the amounts of VOC, hexane, toluene, and aromatic C9s determined from estimated solvent usage and measured solvent compositions. Comparison of the emission rates with source activities indicated an emission factor of 30-51 g VOC/press cleaning. Based on the test observations it was estimated that this typical small printing facility was likely to release 1-2 T VOC/year. The methodology also may be useful for the surface coating industry, as emission rates in this study were determined without recourse to a temporary total enclosure and without interfering with worker activities, increasing worker exposure, or increasing safety and explosion hazards.

Air Pollutants, Occupational↗
PubMed2003

Simultaneous removal of volatile organic compounds (VOCs) and nitrogen: batch test.

A batch test was conducted to investigate the effect of the chemical oxygen demand, (COD)/N ratio, nitrate, nitrite and temperature, on the microbial degradation of volatile organic compounds (VOCs), and the denitrification capability using VOCs-acclimatized and un-acclimatized cultures. The nitrite reduction rates differed with each reactor, as follows: 15.418 NO2-N mg MLVSS g(-1) h(-1) in the benzene and methanol (BM) reactor, 27.463 NO2-N mg MLVSS g(-1) h(-1) in the toluene and methanol (TM) reactor and 44.358 NO2-N mg MLVSS g(-1) h(-1) in the methanol (M) reactor. According to the COD/N ratio, the nitrate reduction rates of the BM and TM reactors acclimatized by VOCs changed in the ranges of 29.4-33.41 NO3-N mg MLVSS g(-1) day(-1) and 56.4-65.9 NO3-N mg MLVSS g(-1) day(-1), respectively. Thus, benzene was not effectively utilized as a carbon source. Conversely, toluene was utilized as a carbon source by the denitrifiers under substrate limited conditions. The specific denitrification rates were also greater in the TM reactor than those for both the substrate limited and unlimited conditions in the BM reactor.

Air Pollution↗
PubMed2004

VOC- and SVOC-emissions from adhesives, floor coverings and complete floor structures.

UNLABELLED: Emissions of volatile organic compounds (VOC) and semivolatile organic compounds (SVOC) from materials for flooring installation (primer, screed, adhesive, floor covering) were measured by means of emission test chambers and cells over a time period of at least 28 days at 23 degrees C, 50% relative humidity and an area specific air flow rate of q = 1.25 m(3)/m(2) h. Single components were tested in comparison to three complete structures (same concrete, primer, screed, adhesive) with different types of floor covering (PVC, carpet, linoleum). Sorption into concrete/screed and different permeability of flooring materials affected the emissions from the complete structures. The complete structures with linoleum and PVC showed the same types of emission and emission rates as the individual floor coverings themselves. Emissions from the carpet-covered structure resulted also from the lower layers. In all cases emissions from the complete structures were lower than the sum of emissions from the single components. For two adhesives the formation of secondary emissions (aldehydes and organic acids) was observed starting after the standard testing time of 28 days. PRACTICAL IMPLICATIONS: This paper gives a survey of possible emissions of VOCs and SVOCs from flooring materials and adhesives. On the example of these materials it is shown that the determination of SVOC-emissions from materials is important because after a few weeks the emission rates for SVOCs might be higher than for VOCs. In the real indoor environment SVOCs will be probably adsorbed to dust but by means of emission test chambers or cells the determination of emission rates from materials is possible. With the knowledge of this "emission potential" it is possible to estimate also the release of SVOCs into the (indoor) environment.

Adhesives↗
PubMed2003

[Measurement of emission rate of formaldehyde and volatile organic compounds(VOCs) from building materials by the small chamber method].

A small chamber for measuring the emission rate of formaldehyde gas and volatile organic compounds(VOCs) from building materials was developed, and formaldehyde and VOCs (toluene and xylene) concentrations emitted from particle boards(PB), medium density fiber-boards(MDF) and wall papers were measured. The emission rates measured by the chamber method were compared with the values by the desiccator method, several modified desiccator methods and the perforator method. The emission rate of formaldehyde increased with time and it became constant after about 20 hours. On the other hand, the emission rate of VOCs decreased with time. A good correlation was obtained on the emission rate of formaldehyde between the chamber method and the conventional desiccator method. The correlation coefficient between the perforator method and the chamber method was also high, but the correlation was low for surface treated materials.

Air Pollution, Indoor↗
PubMed1998

Emission of volatile organic compounds (VOCs) from PVC floor coverings.

In this study 29 PVC floor coverings were tested for emission of vinyl chloride (VC) and other volatile organic compounds (VOCs). A study on the effect of higher temperature on emission of VOCs from newly manufactured PVC flooring was also carried out. The study was conducted in climatic chamber, according to Polish Standard PN-89/Z-04021. GC method was used for analyzing of the compounds emitted. VC was not emitted from any of the floorings tested. Other VOCs were emitted in different concentrations. The influence of temperature on emission was conducted at temperatures of 23 degrees C and 35 degrees C from 2 hrs up to 180 days after introduction of materials in the chamber. The increase of temperature caused increase of total volatile organic compounds (TVOC) emission during 24 hrs of experiment. Then the emission was comparable for both temperatures. After 9 days emission of identified and unidentified compounds (TVOC) showed a rapid decay and stayed on very low level during a few months. The study conducted showed that PVC floorings after 10 days of installation in the room should not be source of indoor air contamination.

Air Pollution, Indoor↗
PubMed2000

Performance characteristics of a regenerative catalytic oxidizer for treating VOC-contaminated airstreams.

A pilot apparatus of a regenerative catalytic oxidizer (RCO) equipped with two electrical heaters and two 20-cm i.d. x 200-cm height regenerative beds was used to treat methyl ethyl ketone (MEK) and toluene, respectively, in an airstream. The regenerative beds were packed with gravel (approximate particle size 1.25 cm, specific area 205 m2/m3, and specific heat capacity 840 J/kg degree C) as a solid regenerative material and K-type thermal couples for measuring solid and gas temperatures, respectively. The catalyst bed temperature was kept around 400 degrees C and the gas superficial velocity was operated at 0.234 m/sec. This investigation measured and analyzed distributions of solid and gas temperatures with operating time and variations of volatile organic compound (VOC) concentrations in the regenerative beds. The overall VOC removal efficiency exceeded 98% for MEK and 95% for toluene. Degradation of VOCs will exist for MEK on the surface of solid material (gravel) in the temperature range of 330-400 degrees C, but toluene does not exhibit this phenomenon.

Air Movements↗
PubMed2003

VOC removal from contaminated groundwater through membrane pervaporation. (I): Water-1,1,1-trichloroethane system.

1,1,1-trichloroethane (TCA), a common chlorinated organic solvent and volatile organic compound (VOC), was removed from contaminated groundwater by using a bench-scale membrane pervaporation unit. The effects of TCA concentration, temperature, and flow rate on permeation flux and selectivity (a value) of the process were evaluated. In general, higher temperature leads to higher VOC flux but lower selectivity; higher flow rate of TCA feed stream results in higher VOC flux and selectivity, an indication of the effect of concentration polarization; higher TCA feed concentration produces higher TCA permeation, however, the selectivity was virtually unchanged.

Chromatography, Gas↗
PubMed2003

VOC removal from contaminated groundwater through membrane pervaporation. (II): 1,1,1-trichloroethane-SDS surfactant solution system.

The conventional "pump-and-treat" technology for subsurface remediation of groundwater contaminated with volatile organic compounds (VOCs) such as 1,1,1-trichloroethane (TCA), a common chlorinated organic solvent, has limitation of prohibitively long treatment time due to extremely low water solubility of the VOCs. Surfactant-based soil remediation has emerged as the effective technology that substantially reduces the treatment time. In order to make the whole process economical, the surfactant used in soil washing has to be recovered and reused. This study examined the recovery of anionic surfactant, sodium dodecyl sulfate (SDS), from soil remediation fluids containing TCA, using a bench-scale membrane pervaporation unit. The effects of high TCA concentration, surfactant dosage, and flow rate on permeation flux and selectivity (alpha value) of the process were evaluated. In general, higher surfactant concentration yielded lower TCA flux and constant water flux, resulting in declining a values; higher flow rate of TCA feed stream results in higher VOC flux and selectivity, an indication of the effect of concentration polarization; higher TCA feed concentration produces higher TCA permeation across the membrane, however, the selectivity was virtually unchanged unless the total TCA concentration exceeded 2000 ppm.

Chromatography, Gas↗
PubMed1991

Sources of air pollutants indoors: VOC and fine particulate species.

The average concentrations of a large number of fine particle aerosol and VOC species measured in ten Boise, Idaho, residences in wintertime have been apportioned according to their contributions from all inside sources and all outside sources, regarded as two composite source categories. Air change rates for the residences were in the range 0.2-0.8 hr-1. None of the residences had obvious major indoor sources (smokers, woodburning appliances, etc.). The two category apportionment was accomplished through use of the single chamber mass balance indoor air quality model given by Dockery and Spengler. The method depends on the availability of average concentrations measured outside each residence during the same sampling periods used for the inside measurements, and on the ability to identify one or more species that have negligible indoor sources. Calculated infiltration factors (the indoor/outdoor ratio in the absence of indoor sources) for fine particle species averaged 0.5, and varied in a reasonably way with measured air change rates, essentially independent of species. Infiltration factors for the VOCs were indistinguishable from unity. The relative importance of indoor and outdoor sources to measured indoor concentrations showed great variation between species and between residences. In most homes the indoor source contribution was dominant for fine particle Si, Ca, and Fe, while the infiltration contribution was dominant for S, K, Pb, Zn, mass, and extractable organic matter. Indoor contributions to individual VOCs were frequently very large at a few residences and negligible at the others.

Aerosols↗
PubMed2005

Production of volatile organic compounds (VOCs) by yeasts isolated from the ascocarps of black (Tuber melanosporum Vitt.) and white (Tuber magnatum Pico) truffles.

Twenty-nine yeast strains were isolated from the ascocarps of black and white truffles (Tuber melanosporum Vitt. and Tuber magnatum Pico, respectively), and identified using a polyphasic approach. According to the conventional taxonomic methods, MSP-PCR fingerprinting and sequencing of the D1/D2 domain of 26S rDNA, the strains were identified as Candida saitoana, Debaryomyces hansenii, Cryptococcus sp., Rhodotorula mucilaginosa, and Trichosporon moniliiforme. All isolates assimilated L: -methionine as a sole nitrogen source and produced the volatile organic compounds (VOCs), 2-methyl butanol, 3-methyl butanol, methanethiol, S-methyl thioacetate, dimethyl sulfide, dimethyl disulfide, dimethyl trisulfide, dihydro-2-methyl-3(2H)-thiophenone and 3-(methylthio)-1-propanol (MTP). ANOVA analysis of data showed significant (P<0.01) differences in VOCs produced by different yeasts, with MTP as the major component (produced at concentrations ranging from 19.8 to 225.6 mg/l). In addition, since some molecules produced by the isolates of this study are also characteristic of truffle complex aroma, it is possible to hypothesize a complementary role of yeasts associated with this ecosystem in contributing to final Tuber spp. aroma through the independent synthesis of yeast-specific volatile constituents.

Ascomycota↗
PubMed2004

An automated monitoring system for VOC ozone precursors in ambient air: development, implementation and data analysis.

An automated system for the monitoring of volatile organic compound (VOC) ozone precursors in ambient air is described. The measuring technique consists of subambient preconcentration on a cooled trap followed by thermal desorption and GC/FID analysis. First, the technical development, which permits detection limits below 0.05 ppbv to be reached, proceeded in two steps: (1). the determination of optimum sampling parameters (trap composition and conditioning, outlet split, desorption temperature); (2). the development of a reliable calibration method based on a highly accurate standard. Then, a 4-year field application of the hourly measuring chain was carried out at two urban sites. On the one hand, quality control procedures provided the best VOC identification (peak assignment) and quantification (reproducibility, blank system control). On the other hand, the success and performances of the routine experience (88% of the measurements covered more than 40 target compounds) indicated the high quality and suitability of the instrumentation which is actually applied in several French air quality monitoring networks. Finally, an example of data analysis is presented. Data handling identified important organic compound sources other than vehicle exhaust.

Journal Article↗
PubMed2004

Effects of cross-substrate interaction on biotrickling filtration for the control of VOC emissions.

The effects of cross-substrate interaction to the performance of a gas-phase biotrickling filter for treating a mixture of volatile organic compounds (VOCs), including three structural heterologous in acetone, toluene, and trichloroethylene, were investigated. The biotrickling filter was inoculated with microbial consortium containing at least seven bacterial species utilizing either acetone or toluene, or both, as their carbon sources. In the performance study, the column operating under variable conditions typifying the waste gas emission from the microelectronics fabrication processes achieved a total hydrocarbon (THC) removal efficiency in excess of 85% and a mineralization capacity over 50% for THC mass loading as high as 36.2 g-CH4 m-3h-1. The cross-substrate effects were examined by correlating the relative changes in the mass removal of each substrate with the biodegradative capability of the microbial consortium. The degradation of trichloroethylene was primarily due to co-metabolism by the toluene-oxidizing enzymes, but the results also indicated that trichloroethylene partially induced its own degradation. Concentration increases in acetone appeared to cause a diauxie effect that suppressed degradation of toluene and trichloroethylene, and shifted the microbial population toward the selective acetone-degraders. No irrecoverable toxicity or inhibitory effects were observed throughout the experiments. These results suggest that the relative VOC concentration in the waste gas mixture is a factor as important as the biodegradative function of the microbial consortium, and thus should be carefully evaluated to satisfy the treatment objectives.

Acetone↗