Verification of T2VOC using an analytical solution for VOC transport in vadose zone

Energy Technology Data Exchange (ETDEWEB)

Shan, C. [Lawrence Berkeley Laboratory, Berkeley, CA (United States)

1995-03-01

T2VOC represents an adaption of the STMVOC to the TOUGH2 environment. In may contaminated sites, transport of volatile organic chemicals (VOC) is a serious problem which can be simulated by T2VOC. To demonstrate the accuracy and robustness of the code, we chose a practical problem of VOC transport as the test case, conducted T2VOC simulations, and compared the results of T2VOC with those of an analytical solution. The agreements between T2VOC and the analytical solutions are excellent. In addition, the numerical results of T2VOC are less sensitive to grid size and time step to a certain extent.

Natural attenuation processes in landfill leachate plumes at three Danish sites

DEFF Research Database (Denmark)

Bjerg, Poul Løgstrup; Tuxen, Nina; Reitzel, Lotte

2011-01-01

This article provides an overview of comprehensive core and fringe field studies at three Danish landfill sites. The goal of the research activities is to provide a holistic description of core and fringe attenuation processes for xenobiotic organic compounds in landfill leachate plumes. The appr......This article provides an overview of comprehensive core and fringe field studies at three Danish landfill sites. The goal of the research activities is to provide a holistic description of core and fringe attenuation processes for xenobiotic organic compounds in landfill leachate plumes....... The approach used is cross-disciplinary, encompassing integration of field-scale observations at different scales, field injection experiments, laboratory experiments, and reactive solute transport modeling. This is illustrated in examples from the most recently investigated site-the Sjoelund Landfill...... approaches and tools used in the application of MNA. In particular, the use of in situ indicators to document mass removal in landfill leachate plumes is emphasized. In this article, we advocate the application of conceptual and numerical models as tools for the integration of data and testing of hypotheses....

VOCs in Arid soils: Technology summary

International Nuclear Information System (INIS)

1994-02-01

The Volatile Organic Compounds In Arid Soils Integrated Demonstration (VOC-Arid ID) focuses on technologies to clean up volatile organic compounds and associated contaminants in soil and groundwater at arid sites. The initial host site is the 200 West Area at DOE's Hanford site in southeastern Washington state. The primary VOC contaminant is carbon tetrachloride, in association with heavy metals and radionuclides. An estimated 580--920 metric tons of carbon tetrachloride were disposed of between 1955 and 1973, resulting in extensive soil and groundwater contamination. The VOC-Arid ID schedule has been divided into three phases of implementation. The phased approach provides for: rapid transfer of technologies to the Environmental Restoration (EM-40) programs once demonstrated; logical progression in the complexity of demonstrations based on improved understanding of the VOC problem; and leveraging of the host site EM-40 activities to reduce the overall cost of the demonstrations. During FY92 and FY93, the primary technology demonstrations within the ID were leveraged with an ongoing expedited response action at the Hanford 200 West Area, which is directed at vapor extraction of VOCs from the vadose (unsaturated) zone. Demonstration efforts are underway in the areas of subsurface characterization including: drilling and access improvements, off-gas and borehole monitoring of vadose zone VOC concentrations to aid in soil vapor extraction performance evaluation, and treatment of VOC-contaminated off-gas. These current demonstration efforts constitute Phase 1 of the ID and, because of the ongoing vadose zone ERA, can result in immediate transfer of successful technologies to EM-40

Computer-aided mapping of stream channels beneath the Lawrence Livermore National Laboratory Super Fund Site

Energy Technology Data Exchange (ETDEWEB)

Sick, M. [Lawrence Livermore National Lab., CA (United States)

1994-12-01

The Lawrence Livermore National Laboratory (LLNL) site rests upon 300-400 feet of highly heterogeneous braided stream sediments which have been contaminated by a plume of Volatile Organic Compounds (VOCs). The stream channels are filled with highly permeable coarse grained materials that provide quick avenues for contaminant transport. The plume of VOCs has migrated off site in the TFA area, making it the area of greatest concern. I mapped the paleo-stream channels in the TFA area using SLICE an LLNL Auto-CADD routine. SLICE constructed 2D cross sections and sub-horizontal views of chemical, geophysical, and lithologic data sets. I interpreted these 2D views as a braided stream environment, delineating the edges of stream channels. The interpretations were extracted from Auto-CADD and placed into Earth Vision`s 3D modeling and viewing routines. Several 3D correlations have been generated, but no model has yet been chosen as a best fit.

Electrochemical peroxidation of PCBs and VOCs in superfund site water and sediments

Energy Technology Data Exchange (ETDEWEB)

Scrudato, R.J.; Chiarenzelli, J.R. [SUNY, Oswego, NY (United States)

1996-12-31

An electrochemical peroxidation (ECP) process has been developed and used to degrade polychlorinated biphenyls (PCB) and volatile organic compounds (VOC)-contaminated water, sludge, and sediments at a New York State Federal and State Superfund Site. The process involves passing an oscillating low-amperage (<10 amps) current through steel electrodes immersed in an acidified water or sediment slurry into which hydrogen peroxide (<1,000 ppm) is added. The generated free radicals attack organic compounds, including organo-metallic complexes and refractory compounds including PCBs. PCB degradation ranged from about 30% to 80% in experiments involving Federal Superfund Site sediments; total PCBs were reduced by {approximately}97% to 68%, respectively, in water and slurry collected from a State Superfund subsurface storage tank. VOC bench-scale experiments involved chloroethane, 1,1-dichloroethane, dichloromethane, 1,1,1-trichloroethane, and acetone and after a 3-min ECP treatment, degradation ranged from >94% to about 99.9%. Results indicate the ECP is a viable process to degrade organic contaminants in water and sediment suspensions. Because the treated water suspensions are acidified, select trace metal sorbed to the particulates is solubilized and therefore can be segregated from the particulates, offering a process that simultaneously degrades organic contaminants and separates trace metals. 19 refs., 1 fig., 4 tabs.

Volatile Organic Compound (VOC) measurements in the Pearl River Delta (PRD) region, China

Science.gov (United States)

Liu, Ying; Shao, Min; Lu, Sihua; Chang, Chih-Chung; Wang, Jia-Lin; Chen, Gao

2008-03-01

We measured levels of ambient volatile organic compounds (VOCs) at seven sites in the Pearl River Delta (PRD) region of China during the Air Quality Monitoring Campaign spanning 4 October to 3 November 2004. Two of the sites, Guangzhou (GZ) and Xinken (XK), were intensive sites at which we collected multiple daily canister samples. The observations reported here provide a look at the VOC distribution, speciation, and photochemical implications in the PRD region. Alkanes constituted the largest percentage (>40%) in mixing ratios of the quantified VOCs at six sites; the exception was one major industrial site that was dominated by aromatics (about 52%). Highly elevated VOC levels occurred at GZ during two pollution episodes; however, the chemical composition of VOCs did not exhibit noticeable changes during these episodes. We calculated the OH loss rate to estimate the chemical reactivity of all VOCs. Of the anthropogenic VOCs, alkenes played a predominant role in VOC reactivity at GZ, whereas the contributions of reactive aromatics were more important at XK. Our preliminary analysis of the VOC correlations suggests that the ambient VOCs at GZ came directly from local sources (i.e., automobiles); those at XK were influenced by both local emissions and transportation of air mass from upwind areas.

Volatile Organic Compound (VOC measurements in the Pearl River Delta (PRD region, China

Directory of Open Access Journals (Sweden)

Chih-chung Chang

2008-03-01

Full Text Available We measured levels of ambient volatile organic compounds (VOCs at seven sites in the Pearl River Delta (PRD region of China during the Air Quality Monitoring Campaign spanning 4 October to 3 November 2004. Two of the sites, Guangzhou (GZ and Xinken (XK, were intensive sites at which we collected multiple daily canister samples. The observations reported here provide a look at the VOC distribution, speciation, and photochemical implications in the PRD region. Alkanes constituted the largest percentage (>40% in mixing ratios of the quantified VOCs at six sites; the exception was one major industrial site that was dominated by aromatics (about 52%. Highly elevated VOC levels occurred at GZ during two pollution episodes; however, the chemical composition of VOCs did not exhibit noticeable changes during these episodes. We calculated the OH loss rate to estimate the chemical reactivity of all VOCs. Of the anthropogenic VOCs, alkenes played a predominant role in VOC reactivity at GZ, whereas the contributions of reactive aromatics were more important at XK. Our preliminary analysis of the VOC correlations suggests that the ambient VOCs at GZ came directly from local sources (i.e., automobiles; those at XK were influenced by both local emissions and transportation of air mass from upwind areas.

Site characterization and petroleum hydrocarbon plume mapping

Energy Technology Data Exchange (ETDEWEB)

Ravishankar, K. [Harding Lawson Associates, Houston, TX (United States)

1996-12-31

This paper presents a case study of site characterization and hydrocarbon contamination plume mapping/delineation in a gas processing plant in southern Mexico. The paper describes innovative and cost-effective use of passive (non-intrusive) and active (intrusive) techniques, including the use of compound-specific analytical methods for site characterization. The techniques used, on a demonstrative basis, include geophysical, geochemical, and borehole drilling. Geochemical techniques used to delineate the horizontal extent of hydrocarbon contamination at the site include soil gas surveys. The borehole drilling technique used to assess the vertical extent of contamination and confirm geophysical and geochemical data combines conventional hollow-stem auguring with direct push-probe using Geoprobe. Compound-specific analytical methods, such as hydrocarbon fingerprinting and a modified method for gasoline range organics, demonstrate the inherent merit and need for such analyses to properly characterize a site, while revealing the limitations of noncompound-specific total petroleum hydrocarbon analysis. The results indicate that the techniques used in tandem can properly delineate the nature and extent of contamination at a site; often supplement or complement data, while reducing the risk of errors and omissions during the assessment phase; and provide data constructively to focus site-specific remediation efforts. 7 figs.

Contrasting winter and summer VOC mixing ratios at a forest site in the Western Mediterranean Basin: the effect of local biogenic emissions

Science.gov (United States)

Seco, R.; Peñuelas, J.; Filella, I.; Llusià, J.; Molowny-Horas, R.; Schallhart, S.; Metzger, A.; Müller, M.; Hansel, A.

2011-12-01

Atmospheric volatile organic compounds (VOCs) are involved in ozone and aerosol generation, thus having implications for air quality and climate. VOCs and their emissions by vegetation also have important ecological roles as they can protect plants from stresses and act as communication cues between plants and between plants and animals. In spite of these key environmental and biological roles, the reports on seasonal and daily VOC mixing ratios in the literature for Mediterranean natural environments are scarce. We conducted seasonal (winter and summer) measurements of VOC mixing ratios in an elevated (720 m a.s.l.) holm oak Mediterranean forest site near the metropolitan area of Barcelona (NE Iberian Peninsula). Methanol was the most abundant compound among all the VOCs measured in both seasons. While aromatic VOCs showed almost no seasonal variability, short-chain oxygenated VOCs presented higher mixing ratios in summer, presumably due to greater emission by vegetation and increased photochemistry, both enhanced by the high temperatures and solar radiation in summer. Isoprenoid VOCs showed the biggest seasonal change in mixing ratios: they increased by one order of magnitude in summer, as a result of the vegetation's greater physiological activity and emission rates. The maximum diurnal concentrations of ozone increased in summer too, most likely due to more intense photochemical activity and the higher levels of VOCs in the air. The daily variation of VOC mixing ratios was mainly governed by the wind regime of the mountain, as the majority of the VOC species analyzed followed a very similar diel cycle. Mountain and sea breezes that develop after sunrise advect polluted air masses to the mountain. These polluted air masses had previously passed over the urban and industrial areas surrounding the Barcelona metropolitan area, where they were enriched in NOx and in VOCs of biotic and abiotic origin. Moreover, these polluted air masses receive additional biogenic

Contrasting winter and summer VOC mixing ratios at a forest site in the Western Mediterranean Basin: the effect of local biogenic emissions

Directory of Open Access Journals (Sweden)

R. Seco

2011-12-01

Full Text Available Atmospheric volatile organic compounds (VOCs are involved in ozone and aerosol generation, thus having implications for air quality and climate. VOCs and their emissions by vegetation also have important ecological roles as they can protect plants from stresses and act as communication cues between plants and between plants and animals. In spite of these key environmental and biological roles, the reports on seasonal and daily VOC mixing ratios in the literature for Mediterranean natural environments are scarce.

We conducted seasonal (winter and summer measurements of VOC mixing ratios in an elevated (720 m a.s.l. holm oak Mediterranean forest site near the metropolitan area of Barcelona (NE Iberian Peninsula. Methanol was the most abundant compound among all the VOCs measured in both seasons. While aromatic VOCs showed almost no seasonal variability, short-chain oxygenated VOCs presented higher mixing ratios in summer, presumably due to greater emission by vegetation and increased photochemistry, both enhanced by the high temperatures and solar radiation in summer. Isoprenoid VOCs showed the biggest seasonal change in mixing ratios: they increased by one order of magnitude in summer, as a result of the vegetation's greater physiological activity and emission rates. The maximum diurnal concentrations of ozone increased in summer too, most likely due to more intense photochemical activity and the higher levels of VOCs in the air.

The daily variation of VOC mixing ratios was mainly governed by the wind regime of the mountain, as the majority of the VOC species analyzed followed a very similar diel cycle. Mountain and sea breezes that develop after sunrise advect polluted air masses to the mountain. These polluted air masses had previously passed over the urban and industrial areas surrounding the Barcelona metropolitan area, where they were enriched in NO_x and in VOCs of biotic and abiotic origin. Moreover, these

Persistence of uranium groundwater plumes: Contrasting mechanisms at two DOE sites in the groundwater-river interaction zone

Science.gov (United States)

Zachara, John M.; Long, Philip E.; Bargar, John; Davis, James A.; Fox, Patricia; Fredrickson, Jim K.; Freshley, Mark D.; Konopka, Allan E.; Liu, Chongxuan; McKinley, James P.; Rockhold, Mark L.; Williams, Kenneth H.; Yabusaki, Steve B.

2013-04-01

We examine subsurface uranium (U) plumes at two U.S. Department of Energy sites that are located near large river systems and are influenced by groundwater-river hydrologic interaction. Following surface excavation of contaminated materials, both sites were projected to naturally flush remnant uranium contamination to levels below regulatory limits (e.g., 30 μg/L or 0.126 μmol/L; U.S. EPA drinking water standard), with 10 years projected for the Hanford 300 Area (Columbia River) and 12 years for the Rifle site (Colorado River). The rate of observed uranium decrease was much lower than expected at both sites. While uncertainty remains, a comparison of current understanding suggests that the two sites have common, but also different mechanisms controlling plume persistence. At the Hanford 300 A, the persistent source is adsorbed U(VI) in the vadose zone that is released to the aquifer during spring water table excursions. The release of U(VI) from the vadose zone and its transport within the oxic, coarse-textured aquifer sediments is dominated by kinetically-limited surface complexation. Modeling implies that annual plume discharge volumes to the Columbia River are small (oxidation of naturally reduced, contaminant U(IV) in the saturated zone and a continuous influx of U(VI) from natural, up-gradient sources influence plume persistence. Rate-limited mass transfer and surface complexation also control U(VI) migration velocity in the sub-oxic Rifle groundwater. Flux of U(VI) from the vadose zone at the Rifle site may be locally important, but it is not the dominant process that sustains the plume. A wide range in microbiologic functional diversity exists at both sites. Strains of Geobacter and other metal reducing bacteria are present at low natural abundance that are capable of enzymatic U(VI) reduction in localized zones of accumulated detrital organic carbon or after organic carbon amendment. Major differences between the sites include the geochemical nature of

Characteristics of Ambient Volatile Organic Compounds (VOCs Measured in Shanghai, China

Directory of Open Access Journals (Sweden)

Guang-Qiang Zhou

2010-08-01

Full Text Available To better understand the characteristics of ambient abundance of volatile organic compounds (VOCs in Shanghai, one of the biggest metropolis of China, VOCs were measured with a gas chromatography system equipped with a mass-selective detector (GC/MSD from July 2006 to February 2010. An intensive measurement campaign was conducted (eight samples per day with a 3 hour interval during May 2009. The comparison of ambient VOCs collected in different regions of Shanghai shows that the concentrations are slightly higher in the busy commercial area (28.9 ppbv at Xujiaui than in the urban administrative area (24.3 ppbv at Pudong. However, during the intensive measurement period, the concentrations in the large steel industrial area (28.7 ppbv at Baoshan were much higher than in the urban administrative area (18 ppbv at Pudong, especially for alkanes, alkenes, and toluene. The seasonal variations of ambient VOC concentrations measured at the Xujiahui sampling site indicate that the VOC concentrations are significantly affected by meteorological conditions (such as wind direction and precipitation. In addition, although alkanes are the most abundant VOCs at the Xujiahui measurement site, the most important VOCs contributing to ozone formation potential (OFP are aromatics, accounting for 57% of the total OFP. The diurnal variations of VOC concentrations show that VOC concentrations are higher on weekdays than in weekends at the Xujiahui sampling site, suggesting that traffic condition and human activities have important impacts on VOC emissions in Shanghai. The evidence also shows that the major sources of isoprene are mainly resulted from gasoline evaporation at a particular time (06:00–09:00 in the busy commercial area. The results gained from this study provide useful information for better understanding the characteristics of ambient VOCs and the sources of VOCs in Shanghai.

Characteristics of Ambient Volatile Organic Compounds (VOCs) Measured in Shanghai, China

Science.gov (United States)

Cai, Chang-Jie; Geng, Fu-Hai; Tie, Xue-Xi; Yu, Qiong; Peng, Li; Zhou, Guang-Qiang

2010-01-01

To better understand the characteristics of ambient abundance of volatile organic compounds (VOCs) in Shanghai, one of the biggest metropolis of China, VOCs were measured with a gas chromatography system equipped with a mass-selective detector (GC/MSD) from July 2006 to February 2010. An intensive measurement campaign was conducted (eight samples per day with a 3 hour interval) during May 2009. The comparison of ambient VOCs collected in different regions of Shanghai shows that the concentrations are slightly higher in the busy commercial area (28.9 ppbv at Xujiaui) than in the urban administrative area (24.3 ppbv at Pudong). However, during the intensive measurement period, the concentrations in the large steel industrial area (28.7 ppbv at Baoshan) were much higher than in the urban administrative area (18 ppbv at Pudong), especially for alkanes, alkenes, and toluene. The seasonal variations of ambient VOC concentrations measured at the Xujiahui sampling site indicate that the VOC concentrations are significantly affected by meteorological conditions (such as wind direction and precipitation). In addition, although alkanes are the most abundant VOCs at the Xujiahui measurement site, the most important VOCs contributing to ozone formation potential (OFP) are aromatics, accounting for 57% of the total OFP. The diurnal variations of VOC concentrations show that VOC concentrations are higher on weekdays than in weekends at the Xujiahui sampling site, suggesting that traffic condition and human activities have important impacts on VOC emissions in Shanghai. The evidence also shows that the major sources of isoprene are mainly resulted from gasoline evaporation at a particular time (06:00–09:00) in the busy commercial area. The results gained from this study provide useful information for better understanding the characteristics of ambient VOCs and the sources of VOCs in Shanghai. PMID:22163629

Persistence of uranium groundwater plumes: contrasting mechanisms at two DOE sites in the groundwater-river interaction zone.

Science.gov (United States)

Zachara, John M; Long, Philip E; Bargar, John; Davis, James A; Fox, Patricia; Fredrickson, Jim K; Freshley, Mark D; Konopka, Allan E; Liu, Chongxuan; McKinley, James P; Rockhold, Mark L; Williams, Kenneth H; Yabusaki, Steve B

2013-04-01

We examine subsurface uranium (U) plumes at two U.S. Department of Energy sites that are located near large river systems and are influenced by groundwater-river hydrologic interaction. Following surface excavation of contaminated materials, both sites were projected to naturally flush remnant uranium contamination to levels below regulatory limits (e.g., 30 μg/L or 0.126 μmol/L; U.S. EPA drinking water standard), with 10 years projected for the Hanford 300 Area (Columbia River) and 12 years for the Rifle site (Colorado River). The rate of observed uranium decrease was much lower than expected at both sites. While uncertainty remains, a comparison of current understanding suggests that the two sites have common, but also different mechanisms controlling plume persistence. At the Hanford 300 A, the persistent source is adsorbed U(VI) in the vadose zone that is released to the aquifer during spring water table excursions. The release of U(VI) from the vadose zone and its transport within the oxic, coarse-textured aquifer sediments is dominated by kinetically-limited surface complexation. Modeling implies that annual plume discharge volumes to the Columbia River are small (oxidation of naturally reduced, contaminant U(IV) in the saturated zone and a continuous influx of U(VI) from natural, up-gradient sources influence plume persistence. Rate-limited mass transfer and surface complexation also control U(VI) migration velocity in the sub-oxic Rifle groundwater. Flux of U(VI) from the vadose zone at the Rifle site may be locally important, but it is not the dominant process that sustains the plume. A wide range in microbiologic functional diversity exists at both sites. Strains of Geobacter and other metal reducing bacteria are present at low natural abundance that are capable of enzymatic U(VI) reduction in localized zones of accumulated detrital organic carbon or after organic carbon amendment. Major differences between the sites include the geochemical nature of

Volatile organic compounds composition of merged and aged forest fire plumes from Alaska and western Canada

Science.gov (United States)

de Gouw, J. A.; Warneke, C.; Stohl, A.; Wollny, A. G.; Brock, C. A.; Cooper, O. R.; Holloway, J. S.; Trainer, M.; Fehsenfeld, F. C.; Atlas, E. L.; Donnelly, S. G.; Stroud, V.; Lueb, A.

2006-05-01

The NOAA WP-3 aircraft intercepted aged forest fire plumes from Alaska and western Canada during several flights of the NEAQS-ITCT 2k4 mission in 2004. Measurements of acetonitrile (CH3CN) indicated that the air masses had been influenced by biomass burning. The locations of the plume intercepts were well described using emissions estimates and calculations with the transport model FLEXPART. The best description of the data was generally obtained when FLEXPART injected the forest fire emissions to high altitudes in the model. The observed plumes were generally drier than the surrounding air masses at the same altitude, suggesting that the fire plumes had been processed by clouds and that moisture had been removed by precipitation. Different degrees of photochemical processing of the plumes were determined from the measurements of aromatic VOCs. The removal of aromatic VOCs was slow considering the transport times estimated from the FLEXPART model. This suggests that the average OH levels were low during the transport, which may be explained by the low humidity and high concentrations of carbon monoxide and other pollutants. In contrast with previous work, no strong secondary production of acetone, methanol and acetic acid is inferred from the measurements. A clear case of removal of submicron particle volume and acetic acid due to precipitation scavenging was observed.

Installation of reactive metals groundwater collection and treatment systems

International Nuclear Information System (INIS)

Hopkins, J.K.; Primrose, A.L.; Uhland, J.

1998-01-01

Three groundwater plumes contaminated with volatile organic compounds (VOCs) and radionuclides at the Rocky Flats Environmental Technology Site are scheduled for remediation by 1999 based on the Rocky Flats Cleanup Agreement (RFCA) (DOE, 1996). These three plumes are among the top 20 environmental cleanup sites at Rocky Flats. One of these plumes, the Mound Site Plume, is derived from a previous drum storage area, and daylights as seeps near the South Walnut Creek drainage. Final design for remediation of the Mound Site Plume has been completed based on use of reactive metals to treat the contaminated groundwater, and construction is scheduled for early 1998. The two other plumes, the 903 Pad/Ryan's Pit and the East Trenches Plumes, are derived from VOCs either from drums that leaked or that were disposed of in trenches. These two plumes are undergoing characterization and conceptual design in 1998 and construction is scheduled in 1999. The contaminants of concern in these plumes are tetrachloroethene, trichloroethene, carbon tetrachloride and low levels of uranium and americium

Changes in Groundwater Flow and Volatile Organic Compound Concentrations at the Fischer and Porter Superfund Site, Warminster Township, Bucks County, Pennsylvania, 1993-2009

Science.gov (United States)

Sloto, Ronald A.

2010-01-01

The 38-acre Fischer and Porter Company Superfund Site is in Warminster Township, Bucks County, Pa. Historically, as part of the manufacturing process, trichloroethylene (TCE) degreasers were used for parts cleaning. In 1979, the Bucks County Health Department detected TCE and other volatile organic compounds (VOCs) in water from the Fischer and Porter on-site supply wells and nearby public-supply wells. The Fischer and Porter Site was designated as a Superfund Site and placed on the National Priorities List in September 1983. A 1984 Record of Decision for the site required the Fischer and Porter Company to pump and treat groundwater contaminated by VOCs from three on-site wells at a combined rate of 75 gallons per minute to contain groundwater contamination on the property. Additionally, the Record of Decision recognized the need for treatment of the water from two nearby privately owned supply wells operated by the Warminster Heights Home Ownership Association. In 2004, the Warminster Heights Home Ownership Association sold its water distribution system, and both wells were taken out of service. The report describes changes in groundwater levels and contaminant concentrations and migration caused by the shutdown of the Warminster Heights supply wells and presents a delineation of the off-site groundwater-contamination plume. The U.S. Geological Survey (USGS) conducted this study (2006-09) in cooperation with the U.S. Environmental Protection Agency (USEPA). The Fischer and Porter Site and surrounding area are underlain by sedimentary rocks of the Stockton Formation of Late Triassic age. The rocks are chiefly interbedded arkosic sandstone and siltstone. The Stockton aquifer system is comprised of a series of gently dipping lithologic units with different hydraulic properties. A three-dimensional lithostratigraphic model was developed for the site on the basis of rock cores and borehole geophysical logs. The model was simplified by combining individual lithologic

VOCs emission characteristics and priority control analysis based on VOCs emission inventories and ozone formation potentials in Zhoushan

Science.gov (United States)

Wang, Qiaoli; Li, Sujing; Dong, Minli; Li, Wei; Gao, Xiang; Ye, Rongmin; Zhang, Dongxiao

2018-06-01

Zhoushan is an island city with booming tourism and service industry, but also has many developed VOCs and/or NOX emission industries. It is necessary to carry out regional VOCs and O3 pollution control in Zhoushan as the only new area owns the provincial economic and social administration rights. Anthropogenic VOCs emission inventories were built based on emission factor method and main emission sources were identified according to the emission inventories. Then, localized VOCs source profiles were built based on in-site sampling and referring to other studies. Furthermore, ozone formation potentials (OFPs) profiles were built through VOCs source profiles and maximum incremental reactivity (MIR) theory. At last, the priority control analysis results showed that industrial processes, especially surface coating, are the key of VOCs and O3 control. Alkanes were the most emitted group, accounting for 58.67%, while aromatics contributed the most to ozone production accounting for 69.97% in total OFPs. n-butane, m/p-xylene, i-pentane, n-decane, toluene, propane, n-undecane, o-xylene, methyl cyclohexane and ethyl benzene were the top 10 VOC species that should be preferentially controlled for VOCs emission control. However, m/p-xylene, o-xylene, ethylene, n-butane, toluene, propene, 1,2,4-trimethyl benzene, 1,3,5-trimethyl benzene, ethyl benzene and 1,2,3-trimethyl benzene were the top 10 VOC species that required preferential control for O3 pollution control.

Work plan for support to Upper East Fork Poplar Creek east end VOC plumes well installation project at the Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1998-03-01

Under the Resource Conservation and Recovery Act of 1976 guidelines and requirements from the Tennessee Department of Environment and Conservation (TDEC), the Y-12 Plant initiated investigation and monitoring of various sites within its boundaries in the mid-1980s. The entire Oak Ridge Reservation (ORR) was placed on the National Priorities List of the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA) sites in November 1989. Following CERCLA guidelines, sites within the ORR require a remedial investigation (RI) to define the nature and extent of contamination, evaluate the risks to public health and the environment, and determine the goals for a feasibility study (FS) or an engineering evaluation/cost analysis (EE/CA) of potential remedial actions. Data from monitoring wells at the east end of the Y-12 Plant have identified an area of groundwater contamination dominated by the volatile organic compound (VOC) carbon tetrachloride; other VOCs include chloroform, tetrachloroethene, and trichloroethene

Work plan for support to Upper East Fork Poplar Creek east end VOC plumes well installation project at the Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

Energy Technology Data Exchange (ETDEWEB)

NONE

1998-03-01

Under the Resource Conservation and Recovery Act of 1976 guidelines and requirements from the Tennessee Department of Environment and Conservation (TDEC), the Y-12 Plant initiated investigation and monitoring of various sites within its boundaries in the mid-1980s. The entire Oak Ridge Reservation (ORR) was placed on the National Priorities List of the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA) sites in November 1989. Following CERCLA guidelines, sites within the ORR require a remedial investigation (RI) to define the nature and extent of contamination, evaluate the risks to public health and the environment, and determine the goals for a feasibility study (FS) or an engineering evaluation/cost analysis (EE/CA) of potential remedial actions. Data from monitoring wells at the east end of the Y-12 Plant have identified an area of groundwater contamination dominated by the volatile organic compound (VOC) carbon tetrachloride; other VOCs include chloroform, tetrachloroethene, and trichloroethene.

Use of Proton-Transfer-Reaction Mass Spectrometry to Characterize Volatile Organic Compound Sources at the La Porte Super Site During the Texas Air Quality Study 2000

Energy Technology Data Exchange (ETDEWEB)

Karl, Thomas G.; Jobson, B Tom T.; Kuster, W. C.; Williams, Eric; Stutz, Jochen P.; Shetter, Rick; Hall, Samual R.; Goldan, P. D.; Fehsenfeld, Fred C.; Lindinger, Werner

2003-08-19

Proton-transfer-reaction mass spectrometry (PTR-MS) was deployed for continuous real-time monitoring of volatile organic compounds (VOCs) at a site near the Houston Ship Channel during the Texas Air Quality Study 2000. Overall, 28 ions dominated the PTR-MS mass spectra and were assigned as anthropogenic aromatics (e.g., benzene, toluene, xylenes) and hydrocarbons (propene, isoprene), oxygenated compounds (e.g., formaldehyde, acetaldehyde, acetone, methanol, C7 carbonyls), and three nitrogencontaining compounds (e.g., HCN, acetonitrile and acrylonitrile). Biogenic VOCs were minor components at this site. Propene was the most abundant lightweight hydrocarbon detected by this technique with concentrations up to 100+ nmol mol-1, and was highly correlated with its oxidation products, formaldehyde (up to ~40 nmol mol-1) and acetaldehyde (up to ~80 nmol/mol), with typical ratios close to 1 in propene-dominated plumes. In the case of aromatic species the high time resolution of the obtained data set helped in identifying different anthropogenic sources (e.g., industrial from urban emissions) and testing current emission inventories. A comparison with results from complimentary techniques (gas chromatography, differential optical absorption spectroscopy) was used to assess the selectivity of this on-line technique in a complex urban and industrial VOC matrix and give an interpretation of mass scans obtained by ‘‘soft’’ chemical ionization using proton-transfer via H3O+. The method was especially valuable in monitoring rapidly changing VOC plumes which passed over the site, and when coupled with meteorological data it was possible to identify likely sources.

A review and assessment of variable density ground water flow effects on plume formation at UMTRA project sites

International Nuclear Information System (INIS)

1995-01-01

A standard assumption when evaluating the migration of plumes in ground water is that the impacted ground water has the same density as the native ground water. Thus density is assumed to be constant, and does not influence plume migration. This assumption is valid only for water with relatively low total dissolved solids (TDS) or a low difference in TDS between water introduced from milling processes and native ground water. Analyses in the literature suggest that relatively minor density differences can significantly affect plume migration. Density differences as small as 0.3 percent are known to cause noticeable effects on the plume migration path. The primary effect of density on plume migration is deeper migration than would be expected in the arid environments typically present at Uranium Mill Tailings Remedial Action (UMTRA) Project sites, where little or no natural recharge is available to drive the plume into the aquifer. It is also possible that at some UMTRA Project sites, a synergistic affect occurred during milling operations, where the mounding created by tailings drainage (which created a downward vertical gradient) and the density contrast between the process water and native ground water acted together, driving constituents deeper into the aquifer than either process would alone. Numerical experiments were performed with the U.S. Geological Survey saturated unsaturated transport (SUTRA) model. This is a finite-element model capable of simulating the effects of variable fluid density on ground water flow and solute transport. The simulated aquifer parameters generally are representative of the Shiprock, New Mexico, UMTRA Project site where some of the highest TDS water from processing has been observed

Innovative approaches to remediation for VOC sites using recirculating wells

International Nuclear Information System (INIS)

Dawson, G.W.

1996-01-01

In-well air stripping with approaches such as the patented NoVOCs system offer both cost and operational advantages over pump and treat, and in situ air sparging technologies. With in-well stripping, the water is treated in the well and discharged without being brought to the surface. Discharged water is circulated through the saturated zone acting as a carrier to continually flush contaminants from the aquifer matrix and transport them to the well for treatment. With pumping rates up to four times those of comparable extraction wells, large radii of influence can be maintained and remediation is achieved faster and more efficiently. In-well stripping is applicable to any strippable contaminant including chlorinated solvents (i.e., TCE and PCE) and hydrocarbons such as the aromatic components in petroleum fuels. Growing costs associated with water discharge, NPDES permits, water rights and, in some areas, salt water intrusion have provided economic incentives to retrofit existing pump and treat systems with NoVOCs units. A large number of wells are amenable to retrofitting depending on their diameter, location and length of screens, and back fill. Even with the new initiatives for intrinsic remediation for petroleum fuel releases, there is a role for the NoVOCs technology. Free product removal wells based on the NoVOCs design eliminate the need to treat and permit water discharges produced when generating a cone of depression for collecting the floating fuel. Additionally, the stripping action and introduction of dissolved oxygen reduce soluble hydrocarbon concentrations to risk levels that can be easily addressed through intrinsic bioremediation

INDEPENDENT TECHNICAL REVIEW OF THE BUILDING 100 PLUME, FORMER DOE PINELLAS SITE (YOUNG - RAINEY STAR CENTER), LARGO, FLORIDA

Energy Technology Data Exchange (ETDEWEB)

Eddy-Dilek, C.; Rossabi, J.; Amidon, M.; Riha, B.; Kaback, D.

2010-07-30

Contaminated groundwater associated with Building 100 at the Young-Rainey Science, Technology, and Research Center, formerly the DOE Pinellas plant, is the primary remedial challenge that remains to be addressed at the site. Currently, Building 100 is an active industrial facility that is now owned and operated by the Pinellas county government. Groundwater samples collected from monitoring wells recently installed near the southern boundary of the site suggest that contaminated groundwater has migrated off the plant site. In response to the challenges presented by the Building 100 plume, the Office of Legacy Management (LM) requested assistance from the DOE Office of Groundwater and Soil Remediation (EM-32) to provide a review team to make technical recommendations so that they can efficiently and effectively address characterization and remediation of the plume. The review team was unanimous in the conclusion that a dynamic strategy that combines a phased implementation of direct push samplers, sensors, and tools can be used to better delineate the extent of contamination, control plume migration, and rapidly remediate the contaminated groundwater at the site. The initial efforts of the team focused on reviewing the site history and data, organizing the information into a conceptual model, identifying appropriate technologies, and recommending an integrated strategy. The current groundwater data from the site indicate a two-lobed plume extending to the east and south. To the east vinyl chloride is the primary contaminant of concern, to the south, vinyl chloride and cis1, 2-DCE are the primary contaminants. The limited data that are available suggest that reductive dechlorination of the TCE is already occurring but is not sufficient to prevent offsite migration of low concentrations of TCE daughter products. The team recommends that DOE pursue a strategy that builds on the natural cleansing capacity of the subsurface with reductive methods including biostimulation

Organic composition of carbonaceous aerosols in an aged prescribed fire plume

Directory of Open Access Journals (Sweden)

B. Yan

2008-11-01

Full Text Available Aged smoke from a prescribed fire (dominated by conifers impacted Atlanta, GA on 28 February 2007 and dramatically increased hourly ambient concentrations of PM_2.5 and organic carbon (OC up to 140 and 72 μg m⁻³, respectively. It was estimated that over 1 million residents were exposed to the smoky air lasting from the late afternoon to midnight. To better understand the processes impacting the aging of fire plumes, a detailed chemical speciation of carbonaceous aerosols was conducted by gas chromatography/mass spectrometry (GC/MS analysis. Ambient concentrations of many organic species (levoglucosan, resin acids, retene, n-alkanes and n-alkanoic acids associated with wood burning emission were significantly elevated on the event day. Levoglucosan increased by a factor of 10, while hopanes, steranes, cholesterol and major polycyclic aromatic hydrocarbons (PAHs did not show obvious increases. Strong odd over even carbon number predominance was found for n-alkanes versus even over odd predominance for n-alkanoic acids. Alteration of resin acids during transport from burning sites to monitors is suggested by the observations. Our study also suggests that large quantities of biogenic volatile organic compounds (VOCs and semivolatile organic compounds (SVOCs were released both as products of combustion and unburned vegetation heated by the fire. Higher leaf temperature can stimulate biogenic VOC and SVOC emissions, which enhanced formation of secondary organic aerosols (SOA in the atmosphere. This is supported by elevated ambient concentrations of secondary organic tracers (dicarboxylic acids, 2-methyltetrols, pinonic acid and pinic acid. An approximate source profile was built for the aged fire plume to help better understand evolution of wood smoke emission and for use in source impact assessment.

Delineation of contaminant plume for an inorganic contaminated site using electrical resistivity tomography: comparison with direct-push technique.

Science.gov (United States)

Liao, Qing; Deng, Yaping; Shi, Xiaoqing; Sun, Yuanyuan; Duan, Weidong; Wu, Jichun

2018-03-03

Precise delineation of contaminant plume distribution is essential for effective remediation of contaminated sites. Traditional in situ investigation methods like direct-push (DP) sampling are accurate, but are usually intrusive and costly. Electrical resistivity tomography (ERT) method, as a non-invasive geophysical technique to map spatiotemporal changes in resistivity of the subsurface, is becoming increasingly popular in environmental science. However, the resolution of ERT for delineation of contaminant plumes still remains controversial. In this study, ERT and DP technique were both conducted at a real inorganic contaminated site. The reliability of the ERT method was validated by the direct comparisons of their investigation results that the resistivity acquired by ERT method is in accordance with the total dissolved solid concentration in groundwater and the overall variation of the total iron content in soil obtained by DP technique. After testifying the applicability of ERT method for contaminant identification, the extension of contaminant plume at the study site was revealed by supplementary ERT surveys conducted subsequently in the surrounding area of the contaminant source zone.

Natural Remediation at Savannah River Site

International Nuclear Information System (INIS)

Lewis, C. M.; Van Pelt, R.

2002-01-01

Natural remediation is a general term that includes any technology or strategy that takes advantage of natural processes to remediate a contaminated media to a condition that is protective of human health and the environment. Natural remediation techniques are often passive and minimally disruptive to the environment. They are generally implemented in conjunction with traditional remedial solutions for source control (i.e., capping, stabilization, removal, soil vapor extraction, etc.). Natural remediation techniques being employed at Savannah River Site (SRS) include enhanced bio-remediation, monitored natural attenuation, and phytoremediation. Enhanced bio-remediation involves making nutrients available and conditions favorable for microbial growth. With proper precautions and feeding, the naturally existing microbes flourish and consume the contaminants. Case studies of enhanced bio-remediation include surface soils contaminated with PCBs and pesticides, and Volatile Organic Compound (VOC) contamination in both the vadose zone and groundwater. Monitored natural attenuation (MNA) has been selected as the preferred alternative for groundwater clean up at several SRS waste units. Successful implementation of MNA has been based on demonstration that sources have been controlled, groundwater modeling that indicates that plumes will not expand or reach surface water discharge points at levels that exceed regulatory limits, and continued monitoring. Phytoremediation is being successfully utilized at several SRS waste units. Phytoremediation involves using plants and vegetation to uptake, break down, or manage contaminants in groundwater or soils. Case studies at SRS include managing groundwater plumes of tritium and VOCs with pine trees that are native to the area. Significant decreases in tritium discharge to a site stream have been realized in one phytoremediation project. Studies of other vegetation types, methods of application, and other target contaminants are

Guided episodic sampling for capturing and characterizing industrial plumes

Science.gov (United States)

Ou-Yang, Chang-Feng; Liao, Wei-Cheng; Chang, Chih-Chung; Hsieh, Hsin-Cheng; Wang, Jia-Lin

2018-02-01

An integrated sampling technique, dubbed trigger sampling, was developed to capture characteristic industrial emissions or plumes. In the field experiment, a hydrogen sulfide (H2S) analyzer was used as the triggering instrument at the boundary of a refinery plant due to frequent complaints of foul smell from local residents. Ten episodic samples were captured when the H2S level surpassed the prescribed trigger level of 8.5 ppbv over a three-day period. Three non-episodic (blank) samples and 23 road-side samples were also collected for comparison. All the 36 flask samples were analyzed by gas chromatography-mass spectrometry/flame ionization detection (GC-MS/FID) for 108 volatile organic compounds (VOCs). The total VOC abundance of the event samples was exceedingly higher than the non-episodic samples by over 80 times in the extreme case. Alkanes were found to be the dominant constituents in the event samples, amounting to over 90% of the total VOC concentrations vs. only 30-40% for the blank and metropolitan samples. In addition, light alkanes in the event samples were highly correlated with the trigger species H2S (R2 = 0.82), implying their common origin. The matrix of chemical composition vs. sample types permitted easy visualization of the dominance of light alkanes for the event samples compared to other types of samples. Principle component analysis (PCA) identified two major contributors to cover 93% of the total variance arising from the 36 samples, further quantifying the distinction of the triggered episodic samples from the contrast samples. The proposed trigger sampling is a coupling of fast-and-slow measurement techniques. In this example, the fast-response H2S analyzer served to "guide" sampling to capture industrial plumes which were then characterized by a relatively slow method of GC-MS/FID for detailed chemical composition representative of the prominent sources.

Groundwater contaminant plume maps and volumes, 100-K and 100-N Areas, Hanford Site, Washington

Science.gov (United States)

Johnson, Kenneth H.

2016-09-27

This study provides an independent estimate of the areal and volumetric extent of groundwater contaminant plumes which are affected by waste disposal in the 100-K and 100-N Areas (study area) along the Columbia River Corridor of the Hanford Site. The Hanford Natural Resource Trustee Council requested that the U.S. Geological Survey perform this interpolation to assess the accuracy of delineations previously conducted by the U.S. Department of Energy and its contractors, in order to assure that the Natural Resource Damage Assessment could rely on these analyses. This study is based on previously existing chemical (or radionuclide) sampling and analysis data downloaded from publicly available Hanford Site Internet sources, geostatistically selected and interpreted as representative of current (from 2009 through part of 2012) but average conditions for groundwater contamination in the study area. The study is limited in scope to five contaminants—hexavalent chromium, tritium, nitrate, strontium-90, and carbon-14, all detected at concentrations greater than regulatory limits in the past.All recent analytical concentrations (or activities) for each contaminant, adjusted for radioactive decay, non-detections, and co-located wells, were converted to log-normal distributions and these transformed values were averaged for each well location. The log-normally linearized well averages were spatially interpolated on a 50 × 50-meter (m) grid extending across the combined 100-N and 100-K Areas study area but limited to avoid unrepresentative extrapolation, using the minimum curvature geostatistical interpolation method provided by SURFER®data analysis software. Plume extents were interpreted by interpolating the log-normally transformed data, again using SURFER®, along lines of equal contaminant concentration at an appropriate established regulatory concentration . Total areas for each plume were calculated as an indicator of relative environmental damage. These plume

Field demonstration and transition of SCAPS direct push VOC in-situ sensing technologies

International Nuclear Information System (INIS)

Davis, William M.

1999-01-01

This project demonstrated two in-situ volatile organic compound (VOC) samplers in combination with the direct sampling ion trap mass spectrometer (DSITMS). The technologies chosen were the Vadose Sparge and the Membrane Interface Probe (MIP) sensing systems. Tests at two demonstration sites showed the newer VOC technologies capable of providing in situ contaminant measurements at two to four times the rate of the previously demonstrated Hydrosparge sensor. The results of this project provide initial results supporting the utility of these new technologies to provide rapid site characterization of VOC contaminants in the subsurface

Use of an Open-path FTIR sensor to measure VOCs at the Hanford Site

International Nuclear Information System (INIS)

Kagann, R.H.; Fancher, J.D.; Tomich, S.D.

1994-01-01

An Open-path Fourier Transform Infrared (OP-FTIR) instrument was used to measure carbo tetrachloride vapor emitted from contaminated soil and monitoring wells in the 200 West Area of the Hanford Site in southeastern Washington State (see Figure 1). Historical activities at US Department of Energy (DOE) facilities around the United States during World War II, including development of a nuclear deterrent, resulted in the discharge of chemical and radioactive materials to the environment. Beginning in 1955, carbon tetrachloride and other liquid wastes were released to the subsurface along with cocontaminants to three liquid waste disposal facilities. The DOE has now focused a major technical effort on the mitigation of the effects of those discharges through an environmental restoration program. The OP-FTIR was used over the soil surface near the 216-Z-9 Trench (one of the disposal facilities) in the 200 West Area. The Hanford demonstration of the OP-FTIR was conducted as part of the Volatile Organic Compound-Arid Integrated Demonstration (VOC-Arid ID), which is funded by the US Department of Energy, Office of Technology Development. The mission of the VOC-Arid ID is to identify, develop, and demonstrate new and innovative technologies to support environmental restoration

Uranium-Bearing Evaporite Mineralization Influencing Plume Persistence. Literature Review and DOE-LM Site Surveys

International Nuclear Information System (INIS)

2016-01-01

This report on evaporite mineralization was completed as an Ancillary Work Plan for the Applied Studies and Technology program under the U.S. Department of Energy (DOE) Office of Legacy Management (LM). This study reviews all LM sites under Title I and Title II of the Uranium Mill Tailings Radiation Control Act (UMTRCA) and one Decontamination and Decommissioning site to provide (1) a summary of which sites have evaporite deposits, (2) any available quantitative geochemical and mineralogical analyses, and (3) references to relevant reports. In this study, 'evaporite' refers to any secondary mineral precipitate that occurs due to a loss of water through evaporative processes. This includes efflorescent salt crusts, where this term refers to a migration of dissolved constituents to the surface with a resulting salt crust, where 'salt' can refer to any secondary precipitate, regardless of constituents. The potential for the formation of evaporites at LM sites has been identified, and may have relevance to plume persistence issues. Evaporite deposits have the potential to concentrate and store contaminants at LM sites that could later be re-released. These deposits can also provide a temporary storage mechanism for carbonate, chloride, and sulfate salts along with uranium and other contaminants of concern (COCs). Identification of sites with evaporites will be used in a new technical task plan (TTP), Persistent Secondary Contaminant Sources (PeSCS), for any proposed additional sampling and analyses. This additional study is currently under development and will focus on determining if the dissolution of evaporites has the potential to hinder natural flushing strategies and impact plume persistence. This report provides an initial literature review on evaporites followed by details for each site with identified evaporites. The final summary includes a table listing of all relevant LM sites regardless of evaporite identification.

Uranium-Bearing Evaporite Mineralization Influencing Plume Persistence. Literature Review and DOE-LM Site Surveys

Energy Technology Data Exchange (ETDEWEB)

None, None

2016-05-01

This report on evaporite mineralization was completed as an Ancillary Work Plan for the Applied Studies and Technology program under the U.S. Department of Energy (DOE) Office of Legacy Management (LM). This study reviews all LM sites under Title I and Title II of the Uranium Mill Tailings Radiation Control Act (UMTRCA) and one Decontamination and Decommissioning site to provide (1) a summary of which sites have evaporite deposits, (2) any available quantitative geochemical and mineralogical analyses, and (3) references to relevant reports. In this study, “evaporite” refers to any secondary mineral precipitate that occurs due to a loss of water through evaporative processes. This includes efflorescent salt crusts, where this term refers to a migration of dissolved constituents to the surface with a resulting salt crust, where “salt” can refer to any secondary precipitate, regardless of constituents. The potential for the formation of evaporites at LM sites has been identified, and may have relevance to plume persistence issues. Evaporite deposits have the potential to concentrate and store contaminants at LM sites that could later be re-released. These deposits can also provide a temporary storage mechanism for carbonate, chloride, and sulfate salts along with uranium and other contaminants of concern (COCs). Identification of sites with evaporites will be used in a new technical task plan (TTP), Persistent Secondary Contaminant Sources (PeSCS), for any proposed additional sampling and analyses. This additional study is currently under development and will focus on determining if the dissolution of evaporites has the potential to hinder natural flushing strategies and impact plume persistence. This report provides an initial literature review on evaporites followed by details for each site with identified evaporites. The final summary includes a table listing of all relevant LM sites regardless of evaporite identification.

Groundwater contaminant plume ranking

International Nuclear Information System (INIS)

1988-08-01

Containment plumes at Uranium Mill Tailings Remedial Action (UMTRA) Project sites were ranked to assist in Subpart B (i.e., restoration requirements of 40 CFR Part 192) compliance strategies for each site, to prioritize aquifer restoration, and to budget future requests and allocations. The rankings roughly estimate hazards to the environment and human health, and thus assist in determining for which sites cleanup, if appropriate, will provide the greatest benefits for funds available. The rankings are based on the scores that were obtained using the US Department of Energy's (DOE) Modified Hazard Ranking System (MHRS). The MHRS and HRS consider and score three hazard modes for a site: migration, fire and explosion, and direct contact. The migration hazard mode score reflects the potential for harm to humans or the environment from migration of a hazardous substance off a site by groundwater, surface water, and air; it is a composite of separate scores for each of these routes. For ranking the containment plumes at UMTRA Project sites, it was assumed that each site had been remediated in compliance with the EPA standards and that relict contaminant plumes were present. Therefore, only the groundwater route was scored, and the surface water and air routes were not considered. Section 2.0 of this document describes the assumptions and procedures used to score the groundwater route, and Section 3.0 provides the resulting scores for each site. 40 tabs

Measurement of VOC permeability of polymer bags and VOC solubility in polyethylene drum liner

International Nuclear Information System (INIS)

Liekhus, K.J.; Peterson, E.S.

1995-03-01

A test program conducted at the Idaho National Engineering Laboratory (INEL) investigated the use of a transport model to estimate the volatile organic compound (VOC) concentration in the void volume of a waste drum. Unsteady-state VOC transport model equations account for VOC permeation of polymer bags, VOC diffusion across openings in layers of confinement, and VOC solubility in a polyethylene drum liner. In support of this program, the VOC permeability of polymer bags and VOC equilibrium concentration in a polyethylene drum liner were measured for nine VOCs. The VOCs used in experiments were dichloromethane, carbon tetrachloride, cyclohexane, toluene, 1,1,1-trichloroethane, methanol, 1,1,2-trichloro-1,2,2-trifluoroethane (Freon-113), trichloroethylene, and p-xylene. The experimental results of these measurements as well as a method of estimating both parameters in the absence of experimental data are described in this report

What do PANs Tell us about VOC-NOx Photochemistry in the Urban/Rural Interface?

Science.gov (United States)

Roberts, J. M.; Flocke, F. M.; Zheng, W.; Bertman, S.; Marchewka, M.; Williams, E.; Lerner, B.; Kuster, W.; Goldan, P.; Gilman, J.; Sommariva, R.; Trainer, M.; Fehsenfeld, F.

2006-12-01

Peroxycarboxylic Nitric Anhydrides (PANs) are co-products of the VOC-NOx photochemistry that is responsible for O3 and secondary organic aerosol (SOA) formation in the troposphere. The relative abundance of the various PAN type compounds can provide important diagnostic information as to the contribution of different VOC sources to these processes. Anthropogenic, biogenic and petrochemical VOC sources have shown distinct profiles of PAN, PPN, MPAN, PiBN, and APAN, which can be analyzed using simple numerical models and compared to the results of detailed chemical mechanisms. One result of these studies is that the PAN compounds can be used to better define the contribution of isoprene to O3 production in the urban/rural interface. Another result is that high relative concentrations of APAN are characteristic of high petrochemical source impact. In addition, changes in the relative abundance of PPN and PAN can indicate the aging of a continental photochemical plume. This paper will present selected results from five field experiments and modeling studies from the Nashville 1999 Southern Oxidant Study up through the TexAQS 2006 study, in and around Houston, TX.

Review of quantitative surveys of the length and stability of MTBE, TBA, and benzene plumes in groundwater at UST sites.

Science.gov (United States)

Connor, John A; Kamath, Roopa; Walker, Kenneth L; McHugh, Thomas E

2015-01-01

Quantitative information regarding the length and stability condition of groundwater plumes of benzene, methyl tert-butyl ether (MTBE), and tert-butyl alcohol (TBA) has been compiled from thousands of underground storage tank (UST) sites in the United States where gasoline fuel releases have occurred. This paper presents a review and summary of 13 published scientific surveys, of which 10 address benzene and/or MTBE plumes only, and 3 address benzene, MTBE, and TBA plumes. These data show the observed lengths of benzene and MTBE plumes to be relatively consistent among various regions and hydrogeologic settings, with median lengths at a delineation limit of 10 µg/L falling into relatively narrow ranges from 101 to 185 feet for benzene and 110 to 178 feet for MTBE. The observed statistical distributions of MTBE and benzene plumes show the two plume types to be of comparable lengths, with 90th percentile MTBE plume lengths moderately exceeding benzene plume lengths by 16% at a 10-µg/L delineation limit (400 feet vs. 345 feet) and 25% at a 5-µg/L delineation limit (530 feet vs. 425 feet). Stability analyses for benzene and MTBE plumes found 94 and 93% of these plumes, respectively, to be in a nonexpanding condition, and over 91% of individual monitoring wells to exhibit nonincreasing concentration trends. Three published studies addressing TBA found TBA plumes to be of comparable length to MTBE and benzene plumes, with 86% of wells in one study showing nonincreasing concentration trends. © 2014 GSI Environmental Inc. Groundwater published by Wiley Periodicals, Inc. on behalf of National Ground Water Association.

Characterization of VOCs Across Pennsylvania: Assessing Emissions from Rural, Forested, Agricultural and Natural Gas Drilling-Impacted Areas

Science.gov (United States)

Grannas, A. M.; Fuentes, J. D.; Ramos-Garcés, F.; Wang, D. K.; Martins, D. K.

2012-12-01

Volatile organic compounds (VOCs) of both biogenic and anthropogenic origin are important to troposphere chemistry, particularly the formation of photochemical smog and secondary organic aerosol. There is concern that increased natural gas exploration may lead to increased emissions of certain VOCs during well development and due to fugitive emissions from operational well sites and pipelines. For a six-day period in June 2012, a variety of VOCs were measured using canister sampling from a mobile measurement platform. Transects from southwestern to northeastern Pennsylvania were studied, with samples obtained in rural, forested, urban, farm-impacted and gas well-impacted sites. As expected, biogenic VOCs and isoprene oxidation products were enhanced in forested regions, while anthropogenic non-methane hydrocarbons were enhanced in urban areas. BTEX (benzene, toluene, ethylbenzene and xylenes) was enhanced in urban areas, but the concentrations of BTEX measured near developing and existing natural gas sites were similar to rural and forested sites. Halogenated hydrocarbons and Freon compounds were consistent at all site locations. We will discuss the specific concentrations and signatures of these compounds and assess the potential impact of agricultural activities and gas well development on the observed VOC concentrations and variability.

Submarine Alkalic Lavas Around the Hawaiian Hotspot; Plume and Non-Plume Signatures Determined by Noble Gases

Science.gov (United States)

Hanyu, T.; Clague, D. A.; Kaneoka, I.; Dunai, T. J.; Davies, G. R.

2004-12-01

Noble gas isotopic ratios were determined for submarine alkalic volcanic rocks distributed around the Hawaiian islands to constrain the origin of such alkalic volcanism. Samples were collected by dredging or using submersibles from the Kauai Channel between Oahu and Kauai, north of Molokai, northwest of Niihau, Southwest Oahu, South Arch and North Arch volcanic fields. Sites located downstream from the center of the hotspot have 3He/4He ratios close to MORB at about 8 Ra, demonstrating that the magmas erupted at these sites had minimum contribution of volatiles from a mantle plume. In contrast, the South Arch, located upstream of the hotspot on the Hawaiian Arch, has 3He/4He ratios between 17 and 21 Ra, indicating a strong plume influence. Differences in noble gas isotopic characteristics between alkalic volcanism downstream and upstream of the hotspot imply that upstream volcanism contains incipient melts from an upwelling mantle plume, having primitive 3He/4He. In combination with lithophile element isotopic data, we conclude that the most likely source of the upstream magmatism is depleted asthenospheric mantle that has been metasomatised by incipient melt from a mantle plume. After major melt extraction from the mantle plume during production of magmas for the shield stage, the plume material is highly depleted in noble gases and moderately depleted in lithophile elements. Partial melting of the depleted mantle impregnated by melts derived from this volatile depleted plume source may explain the isotopic characteristics of the downstream alkalic magmatism.

VOC-Arid Integrated Demonstration guide to preparation of demonstration documents

International Nuclear Information System (INIS)

Jensen, E.J.; Brouns, T.M.; Koegler, K.J.; McCabe, G.H.; Morris, F.A.

1994-06-01

This guide has been prepared by Demonstration Operations of the Volatile Organic Compound-Arid Integrated Demonstration (VOC-Arid ID). Its purpose is to describe demonstration documents, designate responsibilities for these documents, and guide the Principal Investigator (PI) and others in their preparation. The main emphasis of this guide is to describe the documentation required of the PI. However, it does cover some of the responsibilities of other members of the VOC-Arid ID team. The VOC-Arid ID is one of several US Department of Energy (DOE) integrated demonstrations designed to support the demonstration of emerging environmental management and restoration technologies. The principal objective of the VOC-Arid ID is to identify, develop, and demonstrate new and innovative technologies for environmental restoration at arid or semiarid sites containing volatile organic compounds with or without associated contamination (e.g., radionuclides and metals)

Assessment of subsurface VOCs using a chemical microsensor array

International Nuclear Information System (INIS)

Batterman, S.A.; Zellers, E.T.

1993-06-01

This report describes the results of laboratory investigations of several performance parameters relevant to surface-acoustic-wave (SAW) chemical sensor arrays for the measurement of volatile organic compounds (VOCs) in contaminated soil and groundwater. The small size, low cost, sensitivity and selectivity of such instruments promise improvements in the quality and quantity of data used to guide site assessment and restoration efforts. In this investigation, calibrations were performed for 15 different coated SAW sensors. Each sensor was exposed to six VOCs selected to represent three chemical classes of contaminants that are commonly found at waste sites (i.e., aliphatic, aromatic and chlorinated hydrocarbons). A new pattern recognition method was developed for determining which coated sensors would maximize the selectivity and accuracy of quantitation for a given set of vapor contaminants. Using this method, an optimal subwet of four coated sensors was selected for testing in a prototype microsensor instrument. Additional laboratory experiments were performed with this optimized array to assess the limits of detection and linear response ranges for the representative vapors, as well as the additivity of responses to vapors in binary mixtures, temperature and humidity effects, aging effects, and other performance parameters related to the application of this technology to soil and groundwater VOC monitoring. Results demonstrate that SAW microsensor arrays can identify and quantify specific VOCs at concentrations in the μg/L to mg/L range when present alone or in simple (e.g., binary) mixtures. SAW sensor technology offers a potentially effective alternative to existing field instrumentation for headspace analysis, soil vapor monitoring, and vacuum extraction process monitoring of VOCs in subsurface media

VOCs in Non-Arid Soils Integrated Demonstration: Technology summary

International Nuclear Information System (INIS)

1994-02-01

The Volatile Organic Compounds (VOCs) in Non-Arid Soils Integrated Demonstration (ID) was initiated in 1989. Objectives for the ID were to test the integrated demonstration concept, demonstrate and evaluate innovative technologies/systems for the remediation of VOC contamination in soils and groundwater, and to transfer technologies and systems to internal and external customers for use in fullscale remediation programs. The demonstration brought together technologies from DOE laboratories, other government agencies, and industry for demonstration at a single test bed. The Savannah River Site was chosen as the location for this ID as the result of having soil and groundwater contaminated with VOCS. The primary contaminants, trichlorethylene and tetrachloroethylene, originated from an underground process sewer line servicing a metal fabrication facility at the M-Area. Some of the major technical accomplishments for the ID include the successful demonstration of the following: In situ air stripping coupled with horizontal wells to remediate sites through air injection and vacuum extraction; Crosshole geophysical tomography for mapping moisture content and lithologic properties of the contaminated media; In situ radio frequency and ohmic heating to increase mobility, of the contaminants, thereby speeding recovery and the remedial process; High-energy corona destruction of VOCs in the off-gas of vapor recovery wells; Application of a Brayton cycle heat pump to regenerate carbon adsorption media used to trap VOCs from the offgas of recovery wells; In situ permeable flow sensors and the colloidal borescope to determine groundwater flow; Chemical sensors to rapidly quantify chlorinated solvent contamination in the subsurface; In situ bioremediation through methane/nutrient injection to enhance degradation of contaminants by methanotrophic bateria

Comparison of different real time VOC measurement techniques in a ponderosa pine forest

Directory of Open Access Journals (Sweden)

L. Kaser

2013-03-01

Full Text Available Volatile organic compound (VOC mixing ratios measured by five independent instruments are compared at a forested site dominated by ponderosa pine (Pinus Ponderosa during the BEACHON-ROCS field study in summer 2010. The instruments included a Proton Transfer Reaction Time of Flight Mass Spectrometer (PTR-TOF-MS, a Proton Transfer Reaction Quadrupole Mass Spectrometer (PTR-MS, a Fast Online Gas-Chromatograph coupled to a Mass Spectrometer (GC/MS; TOGA, a Thermal Dissociation Chemical Ionization Mass Spectrometer (PAN-CIMS and a Fiber Laser-Induced Fluorescence Instrument (FILIF. The species discussed in this comparison include the most important biogenic VOCs and a selected suite of oxygenated VOCs that are thought to dominate the VOC reactivity at this particular site as well as typical anthropogenic VOCs that showed low mixing ratios at this site. Good agreement was observed for methanol, the sum of the oxygenated hemiterpene 2-methyl-3-buten-2-ol (MBO and the hemiterpene isoprene, acetaldehyde, the sum of acetone and propanal, benzene and the sum of methyl ethyl ketone (MEK and butanal. Measurements of the above VOCs conducted by different instruments agree within 20%. The ability to differentiate the presence of toluene and cymene by PTR-TOF-MS is tested based on a comparison with GC-MS measurements, suggesting a study-average relative contribution of 74% for toluene and 26% for cymene. Similarly, 2-hydroxy-2-methylpropanal (HMPR is found to interfere with the sum of methyl vinyl ketone and methacrolein (MVK + MAC using PTR-(TOF-MS at this site. A study-average relative contribution of 85% for MVK + MAC and 15% for HMPR was determined. The sum of monoterpenes measured by PTR-MS and PTR-TOF-MS was generally 20–25% higher than the sum of speciated monoterpenes measured by TOGA, which included α-pinene, β-pinene, camphene, carene, myrcene, limonene, cineole as well as other terpenes. However, this difference is consistent throughout the study

In situ bioremediation for the Hanford carbon tetrachloride plume. Innovative technology summary report

International Nuclear Information System (INIS)

1999-04-01

The 200 Area at Hanford (also called the Central Plateau) contains approximately 817 waste sites, 44 facilities to be demolished, and billions of gallons of contaminated groundwater resulting from chemical processing plants and associated waste facilities (e.g., waste tanks). From 1955 to 1973, carbon tetrachloride, nitrate, and other materials were discharged to subsurface liquid waste disposal facilities in the 200 Area. As much as 600,000 kilograms of carbon tetrachloride may have entered the soil column and a portion of this has contaminated the underlying aquifer. In Situ Bioremediation for the Hanford Carbon Tetrachloride Plume (ISB), which is the term used in this report for an in situ treatment process using indigenous micro-organisms with a computer based Accelerated Bioremediation Design Tool (ABDT), remediates groundwater contaminated with volatile organic compounds (VOCs) and nitrates under anaerobic conditions. ISB involves the injection of nutrients into the groundwater and subsequent extraction and re-injection of the groundwater to provide nutrient distribution in the aquifer

Field observations of volatile organic compound (VOC) exchange in red oaks

Science.gov (United States)

Cappellin, Luca; Algarra Alarcon, Alberto; Herdlinger-Blatt, Irina; Sanchez, Juaquin; Biasioli, Franco; Martin, Scot T.; Loreto, Francesco; McKinney, Karena A.

2017-03-01

Volatile organic compounds (VOCs) emitted by forests strongly affect the chemical composition of the atmosphere. While the emission of isoprenoids has been largely characterized, forests also exchange many oxygenated VOCs (oVOCs), including methanol, acetone, methyl ethyl ketone (MEK), and acetaldehyde, which are less well understood. We monitored total branch-level exchange of VOCs of a strong isoprene emitter (Quercus rubra L.) in a mixed forest in New England, where canopy-level fluxes of VOCs had been previously measured. We report daily exchange of several oVOCs and investigated unknown sources and sinks, finding several novel insights. In particular, we found that emission of MEK is linked to uptake of methyl vinyl ketone (MVK), a product of isoprene oxidation. The link was confirmed by corollary experiments proving in vivo detoxification of MVK, which is harmful to plants. Comparison of MEK, MVK, and isoprene fluxes provided an indirect indication of within-plant isoprene oxidation. Furthermore, besides confirming bidirectional exchange of acetaldehyde, we also report for the first time direct evidence of benzaldehyde bidirectional exchange in forest plants. Net emission or deposition of benzaldehyde was found in different periods of measurements, indicating an unknown foliar sink that may influence atmospheric concentrations. Other VOCs, including methanol, acetone, and monoterpenes, showed clear daily emission trends but no deposition. Measured VOC emission and deposition rates were generally consistent with their ecosystem-scale flux measurements at a nearby site.

Identifying key controls on the behavior of an acidic-U(VI) plume in the Savannah River Site using reactive transport modeling.

Science.gov (United States)

Bea, Sergio A; Wainwright, Haruko; Spycher, Nicolas; Faybishenko, Boris; Hubbard, Susan S; Denham, Miles E

2013-08-01

Acidic low-level waste radioactive waste solutions were discharged to three unlined seepage basins at the F-Area of the Department of Energy (DOE) Savannah River Site (SRS), South Carolina, USA, from 1955 through 1989. Despite many years of active remediation, the groundwater remains acidic and contaminated with significant levels of U(VI) and other radionuclides. Monitored Natural Attenuation (MNA) is a desired closure strategy for the site, based on the premise that regional flow of clean background groundwater will eventually neutralize the groundwater acidity, immobilizing U(VI) through adsorption. An in situ treatment system is currently in place to accelerate this in the downgradient portion of the plume and similar measures could be taken upgradient if necessary. Understanding the long-term pH and U(VI) adsorption behavior at the site is critical to assess feasibility of MNA along with the in-situ remediation treatments. This paper presents a reactive transport (RT) model and uncertainty quantification (UQ) analyses to explore key controls on the U(VI)-plume evolution and long-term mobility at this site. Two-dimensional numerical RT simulations are run including the saturated and unsaturated (vadose) zones, U(VI) and H(+) adsorption (surface complexation) onto sediments, dissolution and precipitation of Al and Fe minerals, and key hydrodynamic processes are considered. UQ techniques are applied using a new open-source tool that is part of the developing ASCEM reactive transport modeling and analysis framework to: (1) identify the complex physical and geochemical processes that control the U(VI) plume migration in the pH range where the plume is highly mobile, (2) evaluate those physical and geochemical parameters that are most controlling, and (3) predict the future plume evolution constrained by historical, chemical and hydrological data. The RT simulation results show a good agreement with the observed historical pH and concentrations of U(VI), nitrates

Surrogate Indicators of Radionuclide Migration at the Amargosa Desert Research Site, Nye County, Nevada

Science.gov (United States)

Stonestrom, D. A.; Andraski, B. J.; Baker, R. J.; Luo, W.; Michel, R. L.

2005-05-01

Contaminant-transport processes are being investigated at the U.S. Geological Survey's Amargosa Desert Research Site (ADRS), adjacent to the Nation's first commercial disposal facility for low-level radioactive waste. Gases containing tritium and radiocarbon are migrating through a 110-m thick unsaturated zone from unlined trenches that received waste from 1962 to 1992. Information on plume dynamics comes from an array of shallow (Radiological analyses require ex-situ wet-chemical techniques, because in-situ sensors for the radionuclides of interest do not exist. As at other LLRW-disposal facilities, radionuclides at the ADRS are mixed with varying amounts of volatile organic compounds (VOCs) and other substances. Halogenated-methanes, -ethanes, and -ethenes dominate the complex mixture of VOCs migrating from the disposal area. These compounds and their degradates provide a distinctive "fingerprint" of contamination originating from low-level radioactive waste. Carbon-dioxide and VOC anomalies provide indicator proxies for radionuclide contamination. Spatial and temporal patterns of co-disposed and byproduct constituents provide field-scale information about physical and biochemical processes involved in transport. Processes include reduction and biorespiration within trenches, and largely non-reactive, barometrically dispersed diffusion away from trenches.

Hydrogeology and historical assessment of a classic sequential-land use landfill site, Illinois, U.S.A.

Science.gov (United States)

Booth, Colin J.; Vagt, Peter J.

1990-05-01

The Blackwell site in northeastern Illinois was a classic sequential-use project combining land reclamation, a sanitary landfill, and a recreational park. This paper adds a recent assessment of leachate generation and groundwater contamination to the site's unfinished record. Hydrogeological studies show that (1) the landfill sits astride an outwash aquifer and a till mound, which are separated from an underlying dolomite aquifer by a thin, silty till; (2) leachate leaks from the landfill at an estimated average rate between 48 and 78 m3/d; (3) the resultant contaminant plume is virtually stagnant in the till but rapidly diluted in the outwash aquifer, so that no off-site contamination is detected; (4) trace VOC levels in the dolomite probably indicate that contaminants have migrated there from the landfill-derived plume in the outwash. Deviations from the original landfill concepts included elimination of a leachate collection system, increased landfill size, local absence of a clay liner, and partial use of nonclay cover. The hydrogeological setting was unsuitable for the landfill as constructed, indicating the importance of detailed geological consideration in landfill and land-use planning.

A simple modeling approach to study the regional impact of a Mediterranean forest isoprene emission on anthropogenic plumes

Directory of Open Access Journals (Sweden)

J. Cortinovis

2005-01-01

Full Text Available Research during the past decades has outlined the importance of biogenic isoprene emission in tropospheric chemistry and regional ozone photo-oxidant pollution. The first part of this article focuses on the development and validation of a simple biogenic emission scheme designed for regional studies. Experimental data sets relative to Boreal, Tropical, Temperate and Mediterranean ecosystems are used to estimate the robustness of the scheme at the canopy scale, and over contrasted climatic and ecological conditions. A good agreement is generally found when comparing field measurements and simulated emission fluxes, encouraging us to consider the model suitable for regional application. Limitations of the scheme are nevertheless outlined as well as further on-going improvements. In the second part of the article, the emission scheme is used on line in the broader context of a meso-scale atmospheric chemistry model. Dynamically idealized simulations are carried out to study the chemical interactions of pollutant plumes with realistic isoprene emissions coming from a Mediterranean oak forest. Two types of anthropogenic sources, respectively representative of the Marseille (urban and Martigues (industrial French Mediterranean sites, and both characterized by different VOC/NOx are considered. For the Marseille scenario, the impact of biogenic emission on ozone production is larger when the forest is situated in a sub-urban configuration (i.e. downwind distance TOWN-FOREST -1. In this case the enhancement of ozone production due to isoprene can reach +37% in term of maximum surface concentrations and +11% in term of total ozone production. The impact of biogenic emission decreases quite rapidly when the TOWN-FOREST distance increases. For the Martigues scenario, the biogenic impact on the plume is significant up to TOWN-FOREST distance of 90km where the ozone maximum surface concentration enhancement can still reach +30%. For both cases, the

Processes Influencing Ozone Levels in Alaskan Forest Fires Plumes during Long-Range Transport over the North Atlantic

Science.gov (United States)

Real, E.; Law, K. S.; Wienzierl, B.; Fiebig, M.; Petzold, A.; Wild, O.; Methven, J.; Arnold, S.; Stohl, A.; Huntrieser, H.;

Measurements of Volatile Organic Compounds Using Proton Transfer Reaction – Mass Spectrometry during the MILAGRO 2006 Campaign

Directory of Open Access Journals (Sweden)

E. C. Fortner

2009-01-01

Full Text Available Volatile organic compounds (VOCs were measured by proton transfer reaction – mass spectrometry (PTR-MS on a rooftop in the urban mixed residential and industrial area North Northeast of downtown Mexico City as part of the Megacity Initiative – Local and Global Research Observations (MILAGRO 2006 field campaign. Thirty eight individual masses were monitored during the campaign and many species were quantified including methanol, acetaldehyde, toluene, the sum of C₂ benzenes, the sum of C₃ benzenes, acetone, isoprene, benzene, and ethyl acetate. The VOC measurements were analyzed to gain a better understanding of the type of VOCs present in the MCMA, their diurnal patterns, and their origins. Diurnal profiles of weekday and weekend/holiday aromatic VOC concentrations showed the influence of vehicular traffic during the morning rush hours and during the afternoon hours. Plumes including elevated toluene as high as 216 parts per billion (ppb and ethyl acetate as high as 183 ppb were frequently observed during the late night and early morning hours, indicating the possibility of significant industrial sources of the two compounds in the region. Wind fields during those peak episodes revealed no specific direction for the majority of the toluene plumes but the ethyl acetate plumes arrived at the site when winds were from the Southwest or West. The PTR-MS measurements combined with other VOC measuring techniques at the field site as well as VOC measurements conducted in other areas of the Mexico City Metropolitan Area (MCMA will help to develop a better understanding of the spatial pattern of VOCs and its variability in the MCMA.

Controls of Plume Dispersal at the Slow Spreading Mid-Atlantic Ridge

Science.gov (United States)

Walter, M.; Mertens, C.; Koehler, J.; Sueltenfuss, J.; Rhein, M.; Keir, R. S.; Schmale, O.; Schneider v. Deimling, J.; German, C. R.; Yoerger, D. R.; Baker, E. T.

2011-12-01

The slow-spreading Mid-Atlantic Ridges hosts a multitude of different types of hydrothermal systems. Here, we compare the fluxes and the plume dispersal at three high temperature sites located in very diverse settings at comparable depths (~3000m): The recently discovered sites Turtle Pits, and Nibelungen on the southern MAR, and the Logatchev field in the North Atlantic. Plume mapping for these sites on cruises between 2004 and 2009 consisted of CTD Towyo-, Yoyo,- and station work, including velocity profiling, as well as water sampling for analysis of trace gases (CH4, H2, 3He/4He) and metals; temperature measurements and fluid sampling at the vent sites were carried out with an ROV. The aim of this work is to gain a better understanding of how the setting of a vent site affects the dispersal of the particle plume, and what means can be used to infer possible locations of vent sites based on the hydrographic properties and plume observations, using high resolution bathymetric mapping and hydrographic information. The ultramafic-hosted Nibelungen site (8°18'S) consists of a single active smoking crater, along with several extinct smokers, which is located off-axis south of a non-transform offset. The setting is characterized by rugged topography, favorable for the generation of internal tides, internal wave breaking, and vertical mixing. Elevated mixing with turbulent diffusivities Kρ up to 0.1 m2 s-1, 3 to 4 orders of magnitude higher than open ocean values, was observed close to the vent site. The mixing as well as the flow field exhibited a strong tidal cycle; the plume dispersal is thus dominated by the fast and intermittent vertical exchange and characterized by small scale spatial and temporal variability. The Turtle Pits vent fields (4°48'S) are located on a sill in a north-south orientated rift valley. The site consists of three (known) high temperature fields: Turtle Pits, Comfortless Cove, and Red Lion. The particle plume is confined to the rift

Borehole induction logging for the Dynamic Underground Stripping Project LLNL gasoline spill site

International Nuclear Information System (INIS)

Boyd, S.; Newmark, R.; Wilt, M.

1994-01-01

Borehole induction logs were acquired for the purpose of characterizing subsurface physical properties and monitoring steam clean up activities at the Lawrence Livermore National Laboratory. This work was part of the Dynamic Underground Stripping Project's demonstrated clean up of a gasoline spin. The site is composed of unconsolidated days, sands and gravels which contain gasoline both above and below the water table. Induction logs were used to characterize lithology, to provide ''ground truth'' resistivity values for electrical resistance tomography (ERT), and to monitor the movement of an underground steam plume used to heat the soil and drive volatile organic compounds (VOCs) to the extraction wells

Volatile Organic Compounds (VOCs) measurements onboard the HALO research aircraft during OMO-ASIA

Science.gov (United States)

Safadi, Layal; Neumaier, Marco; Fischbeck, Garlich; Geiger, Felix; Förster, Eric; Tomsche, Laura; Zahn, Andreas

2017-04-01

The objective of the OMO-Asia campaign that took place in summer 2015 was to study the free-radical chemistry at higher altitudes during the Asian summer monsoon taken over a wide area of Asia. VOC measurements (e.g. acetone, acetonitrile, benzene, and toluene) were conducted using a strongly modified instrument based on a commercial Proton-Transfer-Reaction Mass Spectrometer (PTRMS) from Ionicon. The PTRMS data are generally in good agreement with VOC measurements taken by the GC instrument from Max Planck Institute for Chemistry. In the outflow of the Monsoon plume acetone and acetonitrile volume mixing ratios (VMR) up to 1500 pptV and 180 pptV have been measured, respectively, pointing to a small contribution from biomass burning sources of which acetonitrile is an important tracer. Comparison with VOCs simulated in the atmospheric chemistry model EMAC model exhibits an underestimation (factor of 3 for acetone). The measured data were analyzed with the help of 10 days back trajectories to distinguish air mass origins. For air masses originating from North America (NA) an enhancement of 500 pptV acetone relative to the atmospheric background ( 500 pptV) can be traced back to active biogenic acetone sources in the NA boreal summer. An average enhancement of 400 pptV acetone comes from the Asian summer monsoon. Acetone - CO correlations in the monsoon relative to background air is being analyzed for further characterization and estimation of the sources.

Assessment of subsurface VOCs using a chemical microsensor array. Final report

Energy Technology Data Exchange (ETDEWEB)

Batterman, S.A.; Zellers, E.T. [Michigan Univ., Ann Arbor, MI (United States). School of Public Health

1993-06-01

This report describes the results of laboratory investigations of several performance parameters relevant to surface-acoustic-wave (SAW) chemical sensor arrays for the measurement of volatile organic compounds (VOCs) in contaminated soil and groundwater. The small size, low cost, sensitivity and selectivity of such instruments promise improvements in the quality and quantity of data used to guide site assessment and restoration efforts. In this investigation, calibrations were performed for 15 different coated SAW sensors. Each sensor was exposed to six VOCs selected to represent three chemical classes of contaminants that are commonly found at waste sites (i.e., aliphatic, aromatic and chlorinated hydrocarbons). A new pattern recognition method was developed for determining which coated sensors would maximize the selectivity and accuracy of quantitation for a given set of vapor contaminants. Using this method, an optimal subwet of four coated sensors was selected for testing in a prototype microsensor instrument. Additional laboratory experiments were performed with this optimized array to assess the limits of detection and linear response ranges for the representative vapors, as well as the additivity of responses to vapors in binary mixtures, temperature and humidity effects, aging effects, and other performance parameters related to the application of this technology to soil and groundwater VOC monitoring. Results demonstrate that SAW microsensor arrays can identify and quantify specific VOCs at concentrations in the {mu}g/L to mg/L range when present alone or in simple (e.g., binary) mixtures. SAW sensor technology offers a potentially effective alternative to existing field instrumentation for headspace analysis, soil vapor monitoring, and vacuum extraction process monitoring of VOCs in subsurface media.

Modeling VOC transport in simulated waste drums

International Nuclear Information System (INIS)

Liekhus, K.J.; Gresham, G.L.; Peterson, E.S.; Rae, C.; Hotz, N.J.; Connolly, M.J.

1993-06-01

A volatile organic compound (VOC) transport model has been developed to describe unsteady-state VOC permeation and diffusion within a waste drum. Model equations account for three primary mechanisms for VOC transport from a void volume within the drum. These mechanisms are VOC permeation across a polymer boundary, VOC diffusion across an opening in a volume boundary, and VOC solubilization in a polymer boundary. A series of lab-scale experiments was performed in which the VOC concentration was measured in simulated waste drums under different conditions. A lab-scale simulated waste drum consisted of a sized-down 55-gal metal drum containing a modified rigid polyethylene drum liner. Four polyethylene bags were sealed inside a large polyethylene bag, supported by a wire cage, and placed inside the drum liner. The small bags were filled with VOC-air gas mixture and the VOC concentration was measured throughout the drum over a period of time. Test variables included the type of VOC-air gas mixtures introduced into the small bags, the small bag closure type, and the presence or absence of a variable external heat source. Model results were calculated for those trials where the VOC permeability had been measured. Permeabilities for five VOCs [methylene chloride, 1,1,2-trichloro-1,2,2-trifluoroethane (Freon-113), 1,1,1-trichloroethane, carbon tetrachloride, and trichloroethylene] were measured across a polyethylene bag. Comparison of model and experimental results of VOC concentration as a function of time indicate that model accurately accounts for significant VOC transport mechanisms in a lab-scale waste drum

Evapotranspiration And Geochemical Controls On Groundwater Plumes At Arid Sites: Toward Innovative Alternate End-States For Uranium Processing And Tailings Facilities

International Nuclear Information System (INIS)

Looney, Brian B.; Denham, Miles E.; Eddy-Dilek, Carol A.; Millings, Margaret R.; Kautsky, Mark

2014-01-01

Management of legacy tailings/waste and groundwater contamination are ongoing at the former uranium milling site in Tuba City AZ. The tailings have been consolidated and effectively isolated using an engineered cover system. For the existing groundwater plume, a system of recovery wells extracts contaminated groundwater for treatment using an advanced distillation process. The ten years of pump and treat (P and T) operations have had minimal impact on the contaminant plume - primarily due to geochemical and hydrological limits. A flow net analysis demonstrates that groundwater contamination beneath the former processing site flows in the uppermost portion of the aquifer and exits the groundwater as the plume transits into and beneath a lower terrace in the landscape. The evaluation indicates that contaminated water will not reach Moenkopi Wash, a locally important stream. Instead, shallow groundwater in arid settings such as Tuba City is transferred into the vadose zone and atmosphere via evaporation, transpiration and diffuse seepage. The dissolved constituents are projected to precipitate and accumulate as minerals such as calcite and gypsum in the deep vadose zone (near the capillary fringe), around the roots of phreatophyte plants, and near seeps. The natural hydrologic and geochemical controls common in arid environments such as Tuba City work together to limit the size of the groundwater plume, to naturally attenuate and detoxify groundwater contaminants, and to reduce risks to humans, livestock and the environment. The technical evaluation supports an alternative beneficial reuse (''brownfield'') scenario for Tuba City. This alternative approach would have low risks, similar to the current P and T scenario, but would eliminate the energy and expense associated with the active treatment and convert the former uranium processing site into a resource for future employment of local citizens and ongoing benefit to the Native American Nations

Evapotranspiration And Geochemical Controls On Groundwater Plumes At Arid Sites: Toward Innovative Alternate End-States For Uranium Processing And Tailings Facilities

Energy Technology Data Exchange (ETDEWEB)

Looney, Brian B.; Denham, Miles E.; Eddy-Dilek, Carol A.; Millings, Margaret R.; Kautsky, Mark

2014-01-08

Management of legacy tailings/waste and groundwater contamination are ongoing at the former uranium milling site in Tuba City AZ. The tailings have been consolidated and effectively isolated using an engineered cover system. For the existing groundwater plume, a system of recovery wells extracts contaminated groundwater for treatment using an advanced distillation process. The ten years of pump and treat (P&T) operations have had minimal impact on the contaminant plume – primarily due to geochemical and hydrological limits. A flow net analysis demonstrates that groundwater contamination beneath the former processing site flows in the uppermost portion of the aquifer and exits the groundwater as the plume transits into and beneath a lower terrace in the landscape. The evaluation indicates that contaminated water will not reach Moenkopi Wash, a locally important stream. Instead, shallow groundwater in arid settings such as Tuba City is transferred into the vadose zone and atmosphere via evaporation, transpiration and diffuse seepage. The dissolved constituents are projected to precipitate and accumulate as minerals such as calcite and gypsum in the deep vadose zone (near the capillary fringe), around the roots of phreatophyte plants, and near seeps. The natural hydrologic and geochemical controls common in arid environments such as Tuba City work together to limit the size of the groundwater plume, to naturally attenuate and detoxify groundwater contaminants, and to reduce risks to humans, livestock and the environment. The technical evaluation supports an alternative beneficial reuse (“brownfield”) scenario for Tuba City. This alternative approach would have low risks, similar to the current P&T scenario, but would eliminate the energy and expense associated with the active treatment and convert the former uranium processing site into a resource for future employment of local citizens and ongoing benefit to the Native American Nations.

Apollo Video Photogrammetry Estimation Of Plume Impingement Effects

Science.gov (United States)

Immer, Christopher; Lane, John; Metzger, Philip T.; Clements, Sandra

2008-01-01

The Constellation Project's planned return to the moon requires numerous landings at the same site. Since the top few centimeters are loosely packed regolith, plume impingement from the Lander ejects the granular material at high velocities. Much work is needed to understand the physics of plume impingement during landing in order to protect hardware surrounding the landing sites. While mostly qualitative in nature, the Apollo Lunar Module landing videos can provide a wealth of quantitative information using modem photogrammetry techniques. The authors have used the digitized videos to quantify plume impingement effects of the landing exhaust on the lunar surface. The dust ejection angle from the plume is estimated at 1-3 degrees. The lofted particle density is estimated at 10(exp 8)- 10(exp 13) particles per cubic meter. Additionally, evidence for ejection of large 10-15 cm sized objects and a dependence of ejection angle on thrust are presented. Further work is ongoing to continue quantitative analysis of the landing videos.

VOC amounts in ambient areas of a high-technology science park in Taiwan: their reciprocal correlations and impact on inhabitants.

Science.gov (United States)

Liu, Hsin-Wang; Wu, Bei-Zen; Nian, Hung-Chi; Chen, Hsing-Jung; Lo, Jiunn-Guang; Chiu, Kong-Hwa

2012-02-01

This study presents bihourly, seasonal, and yearly concentration changes in volatile organic compounds (VOCs) in the inlet and effluent water of the wastewater treatment plant (WWTP) of a high-technology science park (HTIP) in Taiwan, with the VOC amounts at different sites correlated geologically. This research adopted a combination of two systems, solid-phase microextraction with a gas chromatography/flame ionization detector and an assembly of purge and trap coupled with gas chromatography/mass spectrometry, to monitor polar and nonpolar VOCs in wastewater. This paper investigated the total VOCs, acetone, isopropyl alcohol (IPA), and dimethylsulfide (DMS) concentrations in real water samples collected in the ambient area of the HTIP. The major contents of VOCs measured in the effluent of the WWTP in the HTIP and the surrounding river region were DMS (14-176 ppb), acetone (5-95 ppb), and IPA (15-316 ppb). In comparison with the total VOCs in the inlet wastewater of the WWTP, no corresponding relationship for total VOC concentration in the wastewater was observed between the inlet water and effluent water of the WWTP. The peak VOC concentrations appeared in the third season, and the correlation of different VOC amounts reflects the production situation of the factories. In addition, VOC concentrations at different sites indicate that the Ke-Ya River is seemingly an effective channel for transporting wastewater to its final destination. The data are good indications for the management of environmental pollution near the HTIP.

Estimation of sources and factors affecting indoor VOC levels using basic numerical methods

Directory of Open Access Journals (Sweden)

Sibel Mentese

2016-11-01

Full Text Available Volatile Organic Compounds (VOCs are a concern due to their adverse health effects and extensive usage. Levels of indoor VOCs were measured in six homes located in three different towns in Çanakkale, Turkey. Monthly indoor VOC samples were collected by passive sampling throughout a year. The highest levels of total volatile organic compounds (TVOC, benzene, toluene, and xylenes occurred in industrial, rural, and urban sites in a descending order. VOC levels were categorized as average values annually, during the heating period, and non-heating period. Several building/environmental factors together with occupants’ habits were scored to obtain a basic indoor air pollution index (IAPi for the homes. Bivariate regression analysis was applied to find the associations between the pollutant levels and home scores. IAPi scores were found to be correlated with average indoor VOC levels. In particular, very strong associations were found for occupants’ habits. Furthermore, observed indoor VOC levels were categorized by using self-organizing map (SOM and two simple scoring approaches, rounded average and maximum value methods, to classify the indoor environments based on their VOC compositions (IAPvoc. Three classes were used for both IAPi and IAPvoc approaches, namely “good”, “moderate”, and “bad”. There is an urgent need for indexing studies to determine the potential sources and/or factors affecting observed VOCs. This study gives a basic but good start for further studies.

Long-term study of VOCs measured with PTR-MS at a rural site in New Hampshire with urban influences

Directory of Open Access Journals (Sweden)

R. Talbot

2009-07-01

Full Text Available A long-term, high time-resolution volatile organic compound (VOC data set from a ground site that experiences urban, rural, and marine influences in the Northeastern United States is presented. A proton-transfer-reaction mass spectrometer (PTR-MS was used to quantify 15 VOCs: a marine tracer dimethyl sulfide (DMS, a biomass burning tracer acetonitrile, biogenic compounds (monoterpenes, isoprene, oxygenated VOCs (OVOCs: methyl vinyl ketone (MVK plus methacrolein (MACR, methanol, acetone, methyl ethyl ketone (MEK, acetaldehyde, and acetic acid, and aromatic compounds (benzene, toluene, C₈ and C₉ aromatics. Time series, overall and seasonal medians, with 10th and 90th percentiles, seasonal mean diurnal profiles, and inter-annual comparisons of mean summer and winter diurnal profiles are shown. Methanol and acetone exhibit the highest overall median mixing ratios 1.44 and 1.02 ppbv, respectively. Comparing the mean diurnal profiles of less well understood compounds (e.g., MEK with better known compounds (e.g., isoprene, monoterpenes, and MVK + MACR that undergo various controls on their atmospheric mixing ratios provides insight into possible sources of the lesser known compounds. The constant diurnal value of ~0.7 for the toluene:benzene ratio in winter, may possibly indicate the influence of wood-based heating systems in this region. Methanol exhibits an initial early morning release in summer unlike any other OVOC (or isoprene and a dramatic late afternoon mixing ratio increase in spring. Although several of the OVOCs appear to have biogenic sources, differences in features observed between isoprene, methanol, acetone, acetaldehyde, and MEK suggest they are produced or emitted in unique ways.

Initial site characterisation of a dissolved hydrocarbon groundwater plume discharging to a surface water environment

International Nuclear Information System (INIS)

Westbrook, S.J.; Commonwealth Scientific and Industrial Research Organisation Land and Water, Wembley, WA; Davis, G.B.; Rayner, J.L.; Fisher, S.J.; Clement, T.P.

2000-01-01

Preliminary characterisation of a dissolved hydrocarbon groundwater plume flowing towards a tidally- and seasonally-forced estuarine system has been completed at a site in Perth, Western Australia. Installation and sampling of multiport boreholes enabled fine scale (0.5-m) vertical definition of hydrocarbon concentrations. Vertical electrical conductivity profiles from multiport and spear probe sampling into the river sediments indicated that two groundwater/river water interfaces or dispersion zones are present: (a) an upper dispersion zone between brackish river water and groundwater, and (b) a lower interface between groundwater and deeper saline water. On-line water level loggers show that near-shore groundwater levels are also strongly influence by tidal oscillation. Results from the initial site characterisation will be used to plan further investigations of contaminated groundwater/surface water interactions and the biodegradation processes occurring at the site

Evaluation of remedial alternatives for the Solar Ponds Plume, Rocky Flats Environmental Technology Site

International Nuclear Information System (INIS)

Hranac, K.C.

1998-01-01

This paper describes the process used to select a remedial alternative for handling contaminated groundwater emanating from the Solar Evaporation Ponds (Solar Ponds) at the Rocky Flats Environmental Technology Site (RFETS) and prevent it from reaching the nearest surface water body, North Walnut Creek. Preliminary results of field investigations conducted to provide additional information for the alternatives analysis are also presented. The contaminated groundwater is referred to as the Solar Ponds Plume (SPP). The primary contaminants in the SPP are nitrate and uranium; however, some metals exceed the site action levels at several locations and volatile organic compounds, originating from other sources, also have been detected. Currently the SPP, local surface water runoff, and infiltrated precipitation are collected by a trench system located downgradient of the Solar Ponds and pumped to three storage tanks. The water (two to three million gallons annually) is then pumped to an on-site treatment plant for evaporation at an approximate cost of $7.57 per liter

Protocol for VOC-Arid ID remediation performance characterization

International Nuclear Information System (INIS)

Tegner, B.J.; Hassig, N.L.; Last, G.V.

1994-09-01

The Volatile Organic Compound-Arid Integrated Demonstration (VOC-Arid ID) is a technology development program sponsored by the US Department of Energy's Office of Technology Development that is targeted to acquire, develop, demonstrate, and deploy new technologies for the remediation of VOC contaminants in the soils and groundwaters of arid DOE sites. Technologies cannot be adequately evaluated unless sufficient site characterization and technology performance data have been collection and analyzed. The responsibility for identifying these data needs has been placed largely on the Principal Investigators (PIs) developing the remediation technology, who usually are not experts in site characterization or in identification of appropriate sampling, analysis, and monitoring techniques to support the field testing. This document provides a protocol for planning the collection of data before, during, and after a test of a new technology. This generic protocol provides the PIs and project managers with a set of steps to follow. The protocol is based on a data collection planning process called the Data Quality Objectives (DQO) process, which was originally developed by the US Environmental Protection Agency and has been expanded by DOE to support site cleanup decisions. The DQO process focuses on the quality and quantity of data required to make decision. Stakeholders to the decisions must negotiate such key inputs to the process as the decision rules that will be used and the acceptable probabilities of making decision errors

Temporal variability and sources of VOCs in urban areas of the eastern Mediterranean

Directory of Open Access Journals (Sweden)

C. Kaltsonoudis

2016-11-01

Full Text Available During the summer of 2012 volatile organic compounds (VOCs were monitored by proton transfer reaction mass spectrometry (PTR-MS in urban sites, in Athens and Patras, two of the largest cities in Greece. Also, during the winter of 2013, PTR-MS measurements were conducted in the center of the city of Athens. Positive matrix factorization (PMF was applied to the VOC measurements to gain insights about their sources. In summer most of the measured VOCs were due to biogenic and traffic emissions. Isoprene, monoterpenes, and several oxygenated VOCs (oVOCs originated mainly from vegetation either directly or as oxidation products. Isoprene average concentrations in Patras and Athens were 1 and 0.7 ppb respectively, while the monoterpene concentrations were 0.3 and 0.9 ppb respectively. Traffic was the main source of aromatic compounds during summer. For Patras and Athens the average concentrations of benzene were 0.1 and 0.2 ppb, of toluene 0.3 and 0.8 ppb, and of the xylenes 0.3 and 0.7 ppb respectively. Winter measurements in Athens revealed that biomass burning used for residential heating was a major VOC source contributing both aromatic VOCs and biogenic compounds such as monoterpenes. Several episodes related to biomass burning were identified and emission ratios (ERs and emission factors (EFs were estimated.

Tropospheric VOC measurements by PTR-MS

International Nuclear Information System (INIS)

Hansel, A.; Wisthaler, A.; Graus, M.; Grabmer, W.

2002-01-01

Full text: O 3 is formed photochemically from the photolysis of NO 2 , and because O 3 reacts rapidly with NO these reactions result in a photoequilibrium between NO, NO 2 with no net formation or loss of O 3 , However, in the presence of volatile organic compounds (VOCs), the degradation reactions of VOCs lead to the formation of intermediate peroxy radicals which react with NO, converting NO to NO 2 , which then photolyze to form O 3 . Thus, in order to understand quantitatively tropospheric ozone chemistry, it is necessary to know the VOC distribution within the troposphere as well as VOC fluxes from individual sources. Examples will be presented how the use of Proton Transfer Reaction Mass Spectrometry (PTR-MS) has enhanced our understanding of anthropogenic VOC emissions, biosphere-atmosphere exchange processes, and photochemical processing of both anthropogenic and biogenic VOCs in the troposphere. (author)

VOC emissions control systems

International Nuclear Information System (INIS)

Spessard, J.E.

1993-01-01

The air pollution control equipment marketplace offers many competing technologies for controlling emissions of volatile organic compounds (VOC) in air. If any technology was economically and technically superior under all conditions, it would be the only one on the market. In fact, each technology used to control VOCs is superior under some set of conditions. The reasons for choosing one control technology over another are situation-specific. Some general guidelines to VOC control technologies and the situations where each may be appropriate are presented in this article. The control technologies and applications are summarized in a table

Characteristics of 1 year of observational data of VOCs, NOx and O3 at a suburban site in Guangzhou, China

Science.gov (United States)

Zou, Y.; Deng, X. J.; Zhu, D.; Gong, D. C.; Wang, H.; Li, F.; Tan, H. B.; Deng, T.; Mai, B. R.; Liu, X. T.; Wang, B. G.

2015-06-01

Guangzhou, one of China's megacities, is beset with frequent occurrence of high-concentration ozone events. In this study, online instruments were used to simultaneously monitor ozone, nitrogen oxides (NOx) and volatile organic compounds (VOCs) at GPACS (the Guangzhou Panyu Atmospheric Composition Station) of the China Meteorological Administration, from June 2011 to May 2012, in order to determine their characteristics, the effect of VOCs on ozone photochemical production and the relationship between VOC / NOx ratio and ozone formation. The results showed that during the observation period, the seasonal variation of ozone concentration was lower in spring and winter compared to summer and autumn, which is opposite that for VOCs and NOx. In terms of VOCs, aromatics had the largest ozone formation potential, among which toluene, xylenes, ethylbenzene, 1,2,4-trimethylbenzene and 1,3,5-trimethylbenzene were the most important species, with a total contribution of about 44%. As the VOC / NOx ratios were very high during high-concentration ozone events that occur all year round, we speculate ozone production was likely to be NOx-limited regime (12:00-16:00 LT) in Guangzhou. Further investigation based on numerical models is needed in the future to obtain more detailed and robust conclusions.

Utilization of a hydraulic barrier to control migration of a uranium plume

International Nuclear Information System (INIS)

Brettschneider, D.J.; Simmons, R.A. Jr.; Kappa, J.D.; Stover, J.A.

1995-01-01

A uranium plume emanating from the U.S. Department of Energy's Fernald Environmental Management Project (FEMP) in Fernald, Ohio had migrated off site and the leading edge of the plume had already mixed with an organic and inorganic plume emanating from two industries south of the FEMP. A method was needed to prevent the further southern migration of the plume, minimize any impacts to the geometry, concentrations, distribution or flow patterns of the organic and inorganic plumes emanating from the off-site industries, while meeting the ultimate cleanup goals for the FEMP. This paper discusses the use of a hydraulic barrier created to meet these goals by pumping a five well recovery system and the problems associated with the disposition of over 2 million gallons per day of water with low concentrations of uranium

Utilisation of VOC in Diesel Engines. Ignition and combustion of VOC released in crude oil tankers

International Nuclear Information System (INIS)

Melhus, Oeyvin

2002-01-01

The emission of VOC (Volatile Organic Compound) is a significant source of hydrocarbon pollution. In Norway, the offshore oil industry represents a major source. This emission represents both an energy loss and an environmental problem. Gas tankers have used boil-off gas from the cargo tanks as fuel for some time. However, for the current VOC project a new fuel injection concept is designed for tankers to take advantage of the energy present in the VOC evaporated from crude oil. The VOC is mixed with inert gas in these tankers, and thus the utilisation of this gas represents new challenges. The VOC project uses the concept of ''Condensate Diesel Process'' with pilot ignition. An experimental study of ignition and combustion of VOC Fuels reported here was initiated by the time it was decided to start a pilot project converting propulsion engines in shuttle tankers to use VOC Fuel. It is an experimental study carried out at the Marine Technology Centre (MTS). The objective was to study ignition and combustion of the chosen process in comparison with an ordinary diesel process. The experimental results have been discussed and compared with theoretical considerations of injection, ignition and combustion. For experiments on combustion, a rapid compression machine ''DyFo'' was redesigned to use VOC Fuel. The DyFo test rig was initially designed to study ignition and early combustion of spark ignited homogeneous gas/air charges. To study the ignition and early combustion of VOC Fuel injected at high pressure and ignited by pilot diesel fuel, a redesign was necessary. An important feature of the DyFo, is the visualisation of the combustion. The advantage of the DyFo test rig over an engine, is its simplicity and controllability. In an engine the visualisation would suffer from combustion deposits disturbing the view through the quartz glasses, making the images more difficult to interpret. The simplicity is on the other side a drawback. Correct thermal conditions inside

Electrical resistance tomography during gas injection at the Savannah River Site

International Nuclear Information System (INIS)

Ramirez, A.L.; Daily, W.D.

1993-05-01

Electrical resistance tomography (ERT) is used to monitor some of the in situ remediation processes being evaluated for removal of volatile organic compounds from subsurface water and soil at the Integrated Demonstration for VOC's in Soils and Groundwater at Non Arid Sites, the Savannah River Site, near Aiken, South Carolina. Air was injected in the saturated zone and the intrained air was tomographically imaged by its effects on the formation electrical resistivity. The authors found that the flow paths are confined to a complex three dimensional network of channels, some of which extend as far as 30 m from the injection well. They conclude, based on these results, that the shape and extent of the air plume are controlled by spatial variations in the local gas permeability. These channels are somewhat unstable over a period of months and new channels appear to form with time

Assessing and evaluating urban VOC emissions in mid-latitude megacities from intensive observations in Paris and Los Angeles

Science.gov (United States)

Borbon, A.; Gilman, J. B.; Kuster, W. C.; McKeen, S. A.; Holloway, J. S.; Gros, V.; Gaimoz, C.; Beekmann, M.; De Gouw, J. A.

2011-12-01

Volatile Organic Compounds (VOC) affect urban air quality and regional climate change by contributing to ozone formation and the build-up of Secondary Organic Aerosols (SOA). Quantification of VOC emissions is a first critical step to predict VOC environmental impacts and to design effective abatement strategies. Indeed, the quality of ozone and SOA forecasts strongly depends on an accurate knowledge of the primary VOC emissions. However, commonly used bottom-up approaches are highly uncertain due to source multiplicity (combustion processes, storage and distribution of fossil fuels, solvent use, etc.) because of numerous controlling factors (driving conditions, fuel type, temperature, radiation, etc.), and their great variability in time and space. Field observations of VOC and other trace gases can provide valuable top-down constraints to evaluate VOC emission inventories at urban scales. In addition, the implementation of emission reduction measures raises the question of the increasing importance of VOC sources other than traffic. Here, we will evaluate VOC emissions of two mid-latitude megacities in the Northern Hemisphere: the Greater Paris area (Europe) and Los Angeles (USA). In 2009 and 2010, three intensive field campaigns took place in Paris and Los Angeles in the framework of the MEGAPOLI (EU FP7) and CalNex-2010 projects, respectively. Very detailed measurements of aerosol composition and properties, and their gaseous VOC precursors were carried out at ground-based sites (urban center and suburban) and on various mobile platforms. This contribution uses a comprehensive suite of VOC measurements collected by GC-MS/FID techniques at ground-based sites in both cities by a source-receptor methodology. First, emission ratios were estimated from the observations (uncertainty of ± 20%) and compared regarding regional characteristics and European vs. Californian control policies. Then, determined emission ratios were used to assess the accuracy of up

Resolving superimposed ground-water contaminant plumes characterized by chromium, nitrate, uranium, and technetium--99

International Nuclear Information System (INIS)

Hall, S.H.

1990-02-01

Leakage from a liquid waste storage and solar evaporation basin at the Hanford Site in southeastern Washington State has resulted in a ground-water contaminant plume characterized by nitrate, hexavalent chromium, uranium, and technetium-99. The plume is superimposed on a larger, pre-existing plume extending from upgradient sites and having the same suite of contaminants. However, the relative abundance of contaminant species is quite different for each plume source. Thus, characteristic concentration ratios, rather than concentrations of individual species, are used as geochemical tracers, with emphasis on graphical analysis. Accordingly, it has been possible to resolve the boundaries of the smaller plume and to estimate the contribution of each plume to the observed contamination downgradient from the storage basin. 11 refs., 7 figs

Solar-Powered Air Stripping at the Rocky Flats Site, Colorado - 12361

Energy Technology Data Exchange (ETDEWEB)

Boylan, John A. [S.M. Stoller Corporation, Rocky Flats Site, 11025 Dover Street, Suite 1000, Westminster, Colorado 80021 (United States)

2012-07-01

The U.S. Department of Energy's Rocky Flats Site (the Site), near Denver, Colorado, is a former nuclear weapons facility that was constructed beginning in 1951. With the end of the Cold War, the Site was cleaned up and closed in 2005. Four gravity-driven groundwater treatment systems were installed during cleanup, and their continued operation was incorporated into the final remedy for the Site. All utilities, including electrical power, were removed as part of this closure, so all Site electrical power needs are now met with small solar-powered systems. The Mound Site Plume Treatment System (MSPTS) was installed in 1998 as an innovative system based on zero-valent iron (ZVI). Groundwater flow from the Mound source area containing elevated concentrations of volatile organic compounds (VOCs), primarily in the tetrachloroethene (PCE)-trichloroethene (TCE) family of chlorinated solvents, is intercepted by a collection trench and routed to twin ZVI treatment cells. Later, in 2005, remediation of VOC-contaminated soils at a second up-gradient source area included adding an electron donor to the backfill to help stimulate biodegradation. This reduced concentrations of primary constituents but caused down-gradient groundwater to contain elevated levels of recalcitrant degradation byproducts, particularly cis-1,2-dichloroethene and vinyl chloride. A gravel drain installed as part of the 2005 remediation directs contaminated groundwater from this second source area to the MSPTS for treatment. This additional contaminant load, coupled with correspondingly reduced residence time within the ZVI media due to the increased flow rate, resulted in reduced treatment effectiveness. Elevated concentrations of VOCs were then detected in MSPTS effluent, as well as in surface water at the downstream performance monitoring location for the MSPTS. Subsequent consultations with the Site regulators led to the decision to add a polishing component to reduce residual VOCs in MSPTS

Coupling of Realistic Rate Estimates with Genomics for Assessing Contaminant Attenuation and Long-Term Plume Containment

International Nuclear Information System (INIS)

Sorenson, Kent S. Jr.

2003-01-01

Natural attenuation of TCE under aerobic conditions at the INEEL Test Area North site was demonstrated largely on the basis of preferential loss of TCE relative to conservative solutes (PCE and H-3) along groundwater flow paths. First order degradation half-lives were calculated from the rate of preferential TCE loss. We are utilizing the same approach at other DOE sites that have aerobic TCE plumes to determine if aerobic natural attenuation of TCE is rapid enough at these sites to be environmentally significant, i.e. if natural attenuation can reduce concentrations to acceptable levels before groundwater reaches potential receptors. The first step in this process was to identify TCE plumes at DOE sites that have the appropriate site conditions and data needed to perform this analysis. The site conditions include the presence of TCE in groundwater at appreciable concentrations in an aerobic aquifer, a co-mingled contaminant that can be used as a conservative tracer (e.g. PCE, H-3, Tc-99), a flow path that represents at least a decade of travel time, and several monitoring wells located along this flow path. Candidate sites were identified through interviews with knowledgeable individuals in the DOE system and by screening the U.S. Dept. of Energy Groundwater Database using the keywords ''TCE'' and ''groundwater''. The initial screening yielded 25 plumes for consideration. These sites had anywhere from one to 37 individual plumes containing TCE. Of the 25 sites, 13 sites were further evaluated because they met the screening criteria or were promising. After contacting DOE personnel from the respective sites, they were divided into three groups: (1) sites that meet all the project criteria, (2) sites that could potentially be used for the project, and (3) DOE sites that did not meet the criteria. The five sites with plumes that met the criteria were: Brookhaven National Laboratory, Lawrence Livermore National Laboratory, Paducah Gaseous Diffusion Plant, Rocky Flats

VOC SAMPLING IN THE WATER TABLE/CAPILLARY FRINGE AREA FOR ASSESSING IMPACT ON VAPOR INTRUSION AND INDOOR AIR QUALITY

Science.gov (United States)

Vapor intrusion has been determined to be a major pathway for increased indoor air contamination from volatile organic contaminants (VOCs) at certain contaminated sites. In order to properly assess vapor intrusion, it is important to adequately evaluate VOC concentrations in the...

Treatability test of a stacked-tray air stripper for VOC in water

Energy Technology Data Exchange (ETDEWEB)

Pico, T., LLNL

1998-04-01

A common strategy for hydraulic containment and mass removal at VOC contaminated sites is `pump and treat (P&T)`. In P&T operations, contaminated ground water is pumped from wells, treated above ground, and discharged. Many P&T remediation systems at VOC sites rely on air stripping technology because VOCs are easily transferred to the vapor phase. In stacked-tray air strippers, contaminated water is aerated while it flows down through a series of trays. System operations at LLNL are strictly regulated by the California and federal Environmental Protection Agencies (Cal/EPA and EPA), the Bay Area Air Quality Management District (BAAQMD), the California Regional Water Quality Control Board (RWQCB) and the Department of Toxic Substances Control (DTSC). These agencies set discharge limits, require performance monitoring, and assess penalties for non-compliance. National laboratories are also subject to scrutiny by the public and other government agencies. This extensive oversight makes it necessary to accurately predict field treatment performance at new extraction locations to ensure compliance with all requirements prior to facility activation. This paper presents treatability test results for a stacked- tray air stripper conducted at LLNL and compares them to the vendor`s modeling software results.

Integrated test plan for crosswell compressional and shear wave seismic tomography for site characterization at the VOC Arid Site

International Nuclear Information System (INIS)

Elbring, G.J.; Narbutovskih, S.M.

1994-01-01

This integrated test plan describes the demonstration of the crosswell acoustic tomography technique as part of the Volatile Organic Compounds-Arid Integrated Demonstration (VOC-Arid ID). The purpose of this demonstration is to image the subsurface seismic velocity structure and to relate the resulting velocity model to lithology and saturation. In fiscal year (FY) 1994 an initial fielding will test three different downhole sources at two different sites at the Hanford US Department of Energy facility to identify which sources will provide the energy required to propagate between existing steel-cased wells at these two sites. Once this has been established, a second fielding will perform a full compressional and shear wave tomographic survey at the most favorable site. Data reduction, analysis, and interpretation of this full data set will be completed by the end of this fiscal year. Data collection for a second survey will be completed by the end of the fiscal year, and data reduction for this data set will be completed in FY 1995. The specific need is detailed subsurface characterization with minimum intrusion. This technique also has applications for long term vadose zone monitoring for both Resource Conservation and Recovery Act (RCRA) waste storage facilities and for remediation monitoring. Images produced are continuous between boreholes. This is a significant improvement over the single point data derived solely from core information. Saturation changes, either naturally occurring (e.g., perched water tables) or remediation induced (e.g., water table mounding from injection wells or during inwell air sparging) could be imaged. These crosswell data allow optimal borehole placement for groundwater remediation, associated monitoring wells and possibly evaluation of the effective influence of a particular remediation technique

Simulation of Mexico City plumes during the MIRAGE-Mex field campaign using the WRF-Chem model

Directory of Open Access Journals (Sweden)

X. Tie

2009-07-01

Full Text Available The quantification of tropospheric O₃ production in the downwind of the Mexico City plume is a major objective of the MIRAGE-Mex field campaign. We used a regional chemistry-transport model (WRF-Chem to predict the distribution of O₃ and its precursors in Mexico City and the surrounding region during March 2006, and compared the model with in-situ aircraft measurements of O₃, CO, VOCs, NO_x, and NO_y concentrations. The comparison shows that the model is capable of capturing the timing and location of the measured city plumes, and the calculated variability along the flights is generally consistent with the measured results, showing a rapid increase in O₃ and its precursors when city plumes are detected. However, there are some notable differences between the calculated and measured values, suggesting that, during transport from the surface of the city to the outflow plume, ozone mixing ratios are underestimated by about 0–25% during different flights. The calculated O₃-NO_x, O₃-CO, and O₃-NO_z correlations generally agree with the measured values, and the analyses of these correlations suggest that photochemical O₃ production continues in the plume downwind of the city (aged plume, adding to the O₃ already produced in the city and exported with the plume. The model is also used to quantify the contributions to OH reactivity from various compounds in the aged plume. This analysis suggests that oxygenated organics (OVOCs have the highest OH reactivity and play important roles for the O₃ production in the aging plume. Furthermore, O₃ production per NO_x molecule consumed (O₃ production efficiency is more efficient in the aged plume than in the young plume near the city. The major contributor to the high O₃ production efficiency in the aged plume is the

Analysis of Sidestream Smoke VOCs and Characterization of their Odor Profiles by VOC Preconcentrator-GC-O Techniques

Directory of Open Access Journals (Sweden)

Higashi N

2014-12-01

Full Text Available Various techniques have been employed in the analysis of volatile organic compounds (VOCs. However, these techniques are insufficient for the precise analysis of tobacco smoke VOCs because of the complexity of the operating system, system instability, or poor sensitivity. To overcome these problems, a combined system of VOC preconcentrator, gas chromatograph, and olfactometer has been developed. The performance of this new system was evaluated in the analysis of VOCs in tobacco smoke and applied to the odor profiling of sidestream smoke (SSS that has not been sufficiently investigated in the past.

Contribution of biogenic and photochemical sources to ambient VOCs during winter to summer transition at a semi-arid urban site in India.

Science.gov (United States)

Sahu, L K; Tripathi, Nidhi; Yadav, Ravi

2017-10-01

This paper presents the sources and characteristics of ambient volatile organic compounds (VOCs) measured using PTR-TOF-MS instrument in a metropolitan city of India during winter to summer transition period. Mixing ratios of VOCs exhibited strong diurnal, day-to-day and episodic variations. Methanol was the most dominant species with monthly mean values of 18-22 pbbv. The emission ratios of VOCs relative to benzene calculated from nighttime data were used to estimate the relative contributions of vehicle exhaust and other sources. The increasing daytime ratios of oxygenated-VOCs (OVOCs)/benzene and isoprene/benzene from February to March indicates increasing contribution of photo-oxidation and biogenic sources. Daytime fractions of acetone (18%), acetaldehyde (15%) and isoprene (4.5%) to the sum of measured VOCs in March were higher than those in February. Variations of VOCs at lower temperatures (biogenic emissions. The emissions of OVOCs from vehicle exhaust were estimated to be smaller (20-40%) than those from other sources. The contributions of biogenic and secondary sources to OVOCs and isoprene increased by 10-15% from winter to summer. This study provides evidence that the winter-to-summer transition has an impact on sources and composition of VOCs in tropical urban areas. Copyright © 2017 Elsevier Ltd. All rights reserved.

Identification and assessment of water pollution as a consequence of a leachate plume migration from a municipal landfill site (Tucumán, Argentina).

Science.gov (United States)

Fernández, Diego S; Puchulu, María E; Georgieff, Sergio M

2014-06-01

Landfills constitute potential sources of different pollutants that could generate human health and environmental problems. While some landfills currently work under the protection of a bottom liner with leachate collection, it was demonstrated that migration could take place even yet with these cautions. The purpose of this paper is to assess the pollution caused by a leachate plume from a municipal landfill that is affecting both groundwater and surface waters. The research was carried out at Pacará Pintado landfill in northwestern Argentina. Analysis of water samples indicates that leachate is affecting groundwater under the landfill area and an abandoned river channel hydraulically connected. In the center of the landfill area, the plume is anoxic and sulfate, nitrate, iron and manganese reduction zones were identified. Leachate plume presented high concentration of organic matter, Fe, Mn, NH(4)(+), Cl(-) and Cr reaching an extension of 900 m. The presence of a leachate plume in a landfill site with a single liner system implies that the use of this groundwater pollution control method alone is not enough especially if permeable sediments are present below.

A mise-a'-la-masse method for landfill contaminant plume evaluation

International Nuclear Information System (INIS)

Rowley, T.H.; Donaldson, P.R.; Osiensky, J.L.; Welham, J.A.

1994-01-01

A mise-a'-la-masse survey was conducted down gradient of the Bannock County Landfill, in Fort Hall Canyon, Idaho in 1993. Data collected during the survey were compared to seismic refraction data also collected at the site. The site at the mouth of Fort Hall Canyon is ideal for use of the mise-a'-la-masse method to characterize a contaminant plume under actual field conditions. A contaminant plume is believed to emanate from the Bannock County Landfill. The plume contains high concentrations of Dense Non-Aqueous Phase Liquids (DNAPLs) plus inorganic groundwater contaminants. These DNAPLs and inorganics have been detected in nearby domestic and municipal water supply wells. The field site is relatively free of cultural interference that would adversely affect electrical-potential fields. 18 refs., 4 figs

VOC reactivity and its effect on ozone production during the HaChi summer campaign

Directory of Open Access Journals (Sweden)

L. Ran

2011-05-01

Full Text Available Measurements of ozone and its precursors conducted within the HaChi (Haze in China project in summer 2009 were analyzed to characterize volatile organic compounds (VOCs and their effects on ozone photochemical production at a suburban site in the North China Plain (NCP. Ozone episodes, during which running 8-h average ozone concentrations exceeding 80 ppbv lasted for more than 4 h, occurred on about two thirds of the observational days during the 5-week field campaign. This suggests continuous ozone exposure risks in this region in the summer. Average concentrations of nitrogen oxides (NO_x and VOCs are about 20 ppbv and 650 ppbC, respectively. On average, total VOC reactivity is dominated by anthropogenic VOCs. The contribution of biogenic VOCs to total ozone-forming potential, however, is also considerable in the daytime. Key species associated with ozone photochemical production are 2-butenes (18 %, isoprene (15 %, trimethylbenzenes (11 %, xylenes (8.5 %, 3-methylhexane (6 %, n-hexane (5 % and toluene (4.5 %. Formation of ozone is found to be NO_x-limited as indicated by measured VOCs/NO_x ratios and further confirmed by a sensitivity study using a photochemical box model NCAR_MM. The Model simulation suggests that ozone production is also sensitive to changes in VOC reactivity under the NO_x-limited regime, although this sensitivity depends strongly on how much NO_x is present.

Plume persistence caused by back diffusion from thin clay layers in a sand aquifer following TCE source-zone hydraulic isolation.

Science.gov (United States)

Parker, Beth L; Chapman, Steven W; Guilbeault, Martin A

2008-11-14

This paper concludes that back diffusion from one or a few thin clayey beds in a sand aquifer can cause contaminant persistence above MCLs in a sand aquifer long after the source zone initially causing the plume is isolated or removed. This conclusion is based on an intensive case study of a TCE contaminated site in Florida, with the processes evaluated using numerical modeling. At this site, the TCE DNAPL zone formed decades ago, and was hydraulically isolated by means of an innovative system performing groundwater extraction, treatment and re-injection. Treated water is re-injected in a row of injection wells situated a short distance downgradient of the extraction wells, creating a clean-water displacement front to efficiently flush the downgradient plume. This scheme avoids the creation of stagnation zones typical of most groundwater pump-and-treat systems, thereby minimizing the time for aquifer flushing and therefore downgradient cleanup. The system began operation in August 2002 and although the performance monitoring shows substantial declines in concentrations, detectable levels of TCE and degradation products persist downgradient of the re-injection wells, long after the TCE should have disappeared based on calculations assuming a nearly homogenous sand aquifer. Three hypotheses were assessed for this plume persistence: 1) incomplete source-zone capture, 2) DNAPL occurrence downgradient of the re-injection wells, and 3) back diffusion from one or more thin clay beds in the aquifer. After careful consideration, the first two hypotheses were eliminated, leaving back diffusion as the only plausible hypothesis, supported by detailed measurements of VOC concentrations within and near the clay beds and also by numerical model simulations that closely represent the field site hydrogeologic conditions. The model was also used to simulate a more generalized, hypothetical situation where more thin clayey beds occur in a sand aquifer with an underlying aquitard

A stable isotope approach for source apportionment of chlorinated ethene plumes at a complex multi-contamination events urban site

Science.gov (United States)

Nijenhuis, Ivonne; Schmidt, Marie; Pellegatti, Eleonora; Paramatti, Enrico; Richnow, Hans Hermann; Gargini, Alessandro

2013-10-01

The stable carbon isotope composition of chlorinated aliphatic compounds such as chlorinated methanes, ethanes and ethenes was examined as an intrinsic fingerprint for apportionment of sources. A complex field site located in Ferrara (Italy), with more than 50 years history of use of chlorinated aliphatic compounds, was investigated in order to assess contamination sources. Several contamination plumes were found in a complex alluvial sandy multi-aquifer system close to the river Po; sources are represented by uncontained former industrial and municipal dump sites as well as by spills at industrial areas. The carbon stable isotope signature allowed distinguishing 2 major sources of contaminants. One source of chlorinated aliphatic contaminants was strongly depleted in 13C (-40‰ which is commonly observed in recent production of chlorinated solvents. The degradation processes in the plumes could be traced interpreting the isotope enrichment and depletion of parent and daughter compounds, respectively. We demonstrate that, under specific production conditions, namely when highly chlorinated ethenes are produced as by-product during chloromethanes production, 13C depleted fingerprinting of contaminants can be obtained and this can be used to track sources and address the responsible party of the pollution in urban areas.

Concentrations and flux measurements of volatile organic compounds (VOC) in boreal forest soil

Science.gov (United States)

Mäki, Mari; Aaltonen, Hermanni; Heinonsalo, Jussi; Hellén, Heidi; Pumpanen, Jukka; Bäck, Jaana

2017-04-01

and August. Organic soil is formed by organic matter which contains energy rich compounds for microbial decomposition and fine root biomass is also highest in soil surface (Helmisaari et al., 2007). With these analyses, we aim at distinguishing the VOC sinks and sources in the soil layers and quantifying the potential role of VOC uptake by soil microbiota. Asensio, D., Yuste, J. C., Mattana, S., Ribas, À., Llusià, J., and Peñuelas, J.: Litter VOCs induce changes in soil microbial biomass C and N and largely increase soil CO2 efflux. Plant and soil, 360(1-2), 163-174, doi:10.1007/s11104-012-1220-9, 2012. Ditengou, F. A., Müller, A., Rosenkranz, M., Felten, J., Lasok, H., van Doorn, M. M., Legue, V., Palme, K., Schnitzler, J.-P., and Polle, A. Volatile signalling by sesquiterpenes from ectomycorrhizal fungi reprogrammes root architecture. Nature communications, 6:6279, doi:10.1038/ncomms7279, 2015. Helmisaari, H. S., Derome, J., Nöjd, P., & Kukkola, M.: Fine root biomass in relation to site and stand characteristics in Norway spruce and Scots pine stands. Tree Physiology, 27(10), 1493-1504, 2007. Hung, R., Lee, S., and Bennett, J. W.: Arabidopsis thaliana as a model system for testing the effect of Trichoderma volatile organic compounds. Fungal Ecology, 6(1), 19-26, doi:10.1016/j.funeco.2012.09.005, 2013.

Emplacement of zero-valent metal for remediation of deep contaminant plumes

International Nuclear Information System (INIS)

Hubble, D.W.; Gillham, R.W.; Cherry, J.A.

1997-01-01

Some groundwater plumes containing chlorinated solvent contaminants are found to be so deep that current in situ remediation technologies cannot be economically applied. Also, source zones are often found to be too deep for removal or inaccessible due to surface features. Plumes emanating from these sources require containment or treatment. Containment technologies are available for shallow sites (< 15 m) and are being developed for greater depths. However, it is important to advance the science of reactive treatment - both for cut off of plumes and to contain and treat source zones. Zero-valent metal technology has been used for remediation of solvent plumes at sites in Canada, the UK and at several industrial and military sites in the USA. To date, all of the plumes treated with zero-valent metal (granular iron) have been at depths less than 15 m. This paper gives preliminary results of research into methods to emplace granular iron at depths in the range of 15 to 60 m. The study included review of available and emerging methods of installing barrier or reactive material and the selection, preliminary design and costing of several methods. The design of a treatment system for a 122 m wide PCE plume that, immediately down gradient from its source, extends from a depth of 24 to 37 m below the ground surface is used as a demonstration site. Both Permeable Reactive Wall and Funnel-and-Gate trademark systems were considered. The emplacement methods selected for preliminary design and costing were slurry wall, driven/vibrated beam, deep soil mixing and hydrofracturing injection. For each of these methods, the iron must be slurried for ease of pumping and placement using biodegradable polymer viscosifiers that leave the iron reactive

Effect of traffic restriction on reducing ambient volatile organic compounds (VOCs): Observation-based evaluation during a traffic restriction drill in Guangzhou, China

Science.gov (United States)

Huang, Xinyu; Zhang, Yanli; Yang, Weiqiang; Huang, Zuzhao; Wang, Yujun; Zhang, Zhou; He, Quanfu; Lü, Sujun; Huang, Zhonghui; Bi, Xinhui; Wang, Xinming

2017-07-01

Traffic restriction (TR) is a widely adopted control measure in case of heavy air pollution particularly in urban areas, yet it is hard to evaluate the effect of TR on reducing VOC emissions based on monitoring data since ambient VOC mixing ratios are influenced not only by source emissions but also by meteorological conditions and atmospheric degradation. Here we collected air samples for analysis of VOCs before, during and after a TR drill carried out in Guangzhou in September 2010 at both a roadside and a rooftop (∼50 m above the ground) site. TR measures mainly included the "odd-even license" rule and banning high-emitting "yellow label" vehicles. The mixing ratios of non-methane hydrocarbons (NMHCs) did not show significant changes at the roadside site with total NMHCs of 39.0 ± 11.8 ppbv during non-TR period and 39.1 ± 14.8 ppbv during TR period, whereas total NMHCs decreased from 30.4 ± 14.3 ppbv during the non-TR period to 22.1 ± 10.6 ppbv during the TR period at rooftop site. However, the ratios of methyl tert-butyl ether (MTBE), benzene and toluene against carbon monoxide (MTBE/CO, T/CO and B/CO) at the both sampling sites dropped significantly. The ratios of toluene to benzene (T/B) instead increased significantly. Changes in these ratios all consistently indicated reduced input from traffic emissions particularly gasoline vehicles. Source attribution by positive matrix factorization (PMF) confirmed that during the TR period gasoline vehicles contributed less VOCs in percentages while industrial sources, biomass burning and LPG shared larger percentages. Assuming that emissions from industrial sources remained unchanged during the TR and non-TR periods, we further used the PMF-retrieved contribution percentages to deduce the reduction rate of traffic-related VOC emissions, and obtained a reduction rate of 31% based on monitoring data at the roadside site and of 34% based on the monitoring data at the rooftop site. Considering VOC emissions from all

2D Electrical Imaging Surveys for Leachate Plume Migration at an Old Dump Site in Ibadan South Western Nigeria: A Case Study

Directory of Open Access Journals (Sweden)

Dare Omolayo

2014-01-01

Full Text Available The site surveyed is along a popular ring road in Ibadan. It is an old dump site which had been closed over a long period of time. Development into industrial and residential house schemes had crowded around the site. This development resulted in the exploitation of groundwater within the thick regolith that characterize the area. The investigation was carried out to ascertain leachate plume generation and migration and its impact on the surrounding soil and the groundwater. 2D electrical resistivity imaging using Wenner array was used to delineate the plume and probable trend of migration. The method involves the injection of low frequency DC current into the subsurface and measuring the potential difference set up by another pair of electrodes called potential electrodes. All the traverses show areas of very low resistivity values ranging between 4 ohm-m and 13.8 ohm-m; in addition to this, the water samples collected from hand dug wells that surround the dump site show high total dissolved solids (TDS with an average value of 2033 mg/L, high conductivity with an average value of 2868 mg/L, and high nitrate value (63 mg/L; these values are above the World Health Organization (WHO permissible values. This poses a health challenge to the residents living around this site.

Analysis of Aquifer Response, Groundwater Flow, and PlumeEvolution at Site OU 1, Former Fort Ord, California

Energy Technology Data Exchange (ETDEWEB)

Jordan, Preston D.; Oldenburg, Curtis M.; Su, Grace W.

2005-02-24

This report presents a continuation from Oldenburg et al. (2002) of analysis of the hydrogeology, In-Situ Permeable Flow Sensor (ISPFS) results, aquifer response, and changes in the trichloroethylene (TCE) groundwater plume at Operational Unit 1 (OU 1) adjacent to the former Fritzsche Army Airfield at the former Fort Ord Army Base, located on Monterey Bay in northern Monterey County. Fuels and solvents were burned on a portion of OU 1 called the Fire Drill Area (FDA) during airport fire suppression training between 1962 and 1985. This activity resulted in soil and groundwater contamination in the unconfined A-aquifer. In the late 1980's, soil excavation and bioremediation were successful in remediating soil contamination at the site. Shortly thereafter, a groundwater pump, treat, and recharge system commenced operation. This system has been largely successful at remediating groundwater contamination at the head of the groundwater plume. However, a trichloroethylene (TCE) groundwater plume extends approximately 3000 ft (900 m) to the northwest away from the FDA. In the analyses presented here, we augment our prior work (Oldenburg et al., 2002) with new information including treatment-system totalizer data, recent water-level and chemistry data, and data collected from new wells to discern trends in contaminant migration and groundwater flow that may be useful for ongoing remediation efforts. Some conclusions from the prior study have been modified based on these new analyses, and these are pointed out clearly in this report.

Suns-VOC characteristics of high performance kesterite solar cells

Science.gov (United States)

Gunawan, Oki; Gokmen, Tayfun; Mitzi, David B.

2014-08-01

Low open circuit voltage (VOC) has been recognized as the number one problem in the current generation of Cu2ZnSn(Se,S)4 (CZTSSe) solar cells. We report high light intensity and low temperature Suns-VOC measurement in high performance CZTSSe devices. The Suns-VOC curves exhibit bending at high light intensity, which points to several prospective VOC limiting mechanisms that could impact the VOC, even at 1 sun for lower performing samples. These VOC limiting mechanisms include low bulk conductivity (because of low hole density or low mobility), bulk or interface defects, including tail states, and a non-ohmic back contact for low carrier density CZTSSe. The non-ohmic back contact problem can be detected by Suns-VOC measurements with different monochromatic illuminations. These limiting factors may also contribute to an artificially lower JSC-VOC diode ideality factor.

A Monte Carlo simulation method for assessing biotransformation effects on groundwater fuel hydrocarbon plume lengths

International Nuclear Information System (INIS)

McNab, W.W. Jr.

2000-01-01

Biotransformation of dissolved groundwater hydrocarbon plumes emanating from leaking underground fuel tanks should, in principle, result in plume length stabilization over relatively short distances, thus diminishing the environmental risk. However, because the behavior of hydrocarbon plumes is usually poorly constrained at most leaking underground fuel tank sites in terms of release history, groundwater velocity, dispersion, as well as the biotransformation rate, demonstrating such a limitation in plume length is problematic. Biotransformation signatures in the aquifer geochemistry, most notably elevated bicarbonate, may offer a means of constraining the relationship between plume length and the mean biotransformation rate. In this study, modeled plume lengths and spatial bicarbonate differences among a population of synthetic hydrocarbon plumes, generated through Monte Carlo simulation of an analytical solute transport model, are compared to field observations from six underground storage tank (UST) sites at military bases in California. Simulation results indicate that the relationship between plume length and the distribution of bicarbonate is best explained by biotransformation rates that are consistent with ranges commonly reported in the literature. This finding suggests that bicarbonate can indeed provide an independent means for evaluating limitations in hydrocarbon plume length resulting from biotransformation. (Author)

Formation of secondary organic aerosol in the Paris pollution plume and its impact on surrounding regions

Science.gov (United States)

Zhang, Q. J.; Beekmann, M.; Freney, E.; Sellegri, K.; Pichon, J. M.; Schwarzenboeck, A.; Colomb, A.; Bourrianne, T.; Michoud, V.; Borbon, A.

2015-12-01

Secondary pollutants such as ozone, secondary inorganic aerosol, and secondary organic aerosol formed in the plumes of megacities can affect regional air quality. In the framework of the FP7/EU MEGAPOLI (Megacities: Emissions, urban, regional and Global Atmospheric POLlution and climate effects, and Integrated tools for assessment and mitigation) project, an intensive campaign was launched in the greater Paris region in July 2009. The major objective was to quantify different sources of organic aerosol (OA) within a megacity and in its plume. In this study, we use airborne measurements aboard the French ATR-42 aircraft to evaluate the regional chemistry-transport model CHIMERE within and downwind of the Paris region. Two mechanisms of secondary OA (SOA) formation are used, both including SOA formation from oxidation and chemical aging of primary semivolatile and intermediate volatility organic compounds (SI-SOA) in the volatility basis set (VBS) framework. As for SOA formed from traditional VOC (volatile organic compound) precursors (traditional SOA), one applies chemical aging in the VBS framework adopting different SOA yields for high- and low-NOx environments, while another applies a single-step oxidation scheme without chemical aging. Two emission inventories are used for discussion of emission uncertainties. The slopes of the airborne OA levels versus Ox (i.e., O3 + NO2) show SOA formation normalized with respect to photochemical activity and are used for specific evaluation of the OA scheme in the model. The simulated slopes were overestimated slightly by factors of 1.1, 1.7 and 1.3 with respect to those observed for the three airborne measurements, when the most realistic "high-NOx" yields for traditional SOA formation in the VBS scheme are used in the model. In addition, these slopes are relatively stable from one day to another, which suggests that they are characteristic for the given megacity plume environment. The configuration with increased primary

Modeling unsteady-state VOC transport in simulated waste drums

International Nuclear Information System (INIS)

Liekhus, K.J.; Gresham, G.L.; Peterson, E.S.; Rae, C.; Hotz, N.J.; Connolly, M.J.

1994-01-01

This report is a revision of an EG ampersand G Idaho informal report originally titled Modeling VOC Transport in Simulated Waste Drums. A volatile organic compound (VOC) transport model has been developed to describe unsteady-state VOC permeation and diffusion within a waste drum. Model equations account for three primary mechanisms for VOC transport from a void volume within the drum. These mechanisms are VOC permeation across a polymer boundary, VOC diffusion across an opening in a volume boundary, and VOC solubilization in a polymer boundary. A series of lab-scale experiments was performed in which the VOC concentration was measured in simulated waste drums under different conditions. A lab-scale simulated waste drum consisted of a sized-down 55-gal metal drum containing a modified rigid polyethylene drum liner. Four polyethylene bags were sealed inside a large polyethylene bag, supported by a wire cage, and placed inside the drum liner. The small bags were filled with VOC-air gas mixture and the VOC concentration was measured throughout the drum over a period of time. Test variables included the type of VOC-air gas mixtures introduced into the small bags, the small bag closure type, and the presence or absence of a variable external heat source. Model results were calculated for those trials where the permeability had been measured

Seasonal variations in VOC emission rates from gorse (Ulex europaeus)

Science.gov (United States)

Boissard, C.; Cao, X.-L.; Juan, C.-Y.; Hewitt, C. N.; Gallagher, M.

Seasonal variations of biogenic volatile organic compound (VOC) emission rates and standardised emission factors from gorse (Ulex europaeus) have been measured at two sites in the United Kingdom, from October 1994 to September 1995, within temperature and PAR conditions ranging from 3 to 34°C and 10-1300 μmol m-2 s-1, respectively. Isoprene was the dominant emitted compound with a relative composition fluctuating from 7% of the total VOC (winter) to 97% (late summer). The monoterpenes α-pinene, camphene, sabinene, β-pinene, myrcene, limonene, trans-ocimene and γ-terpinene were also emitted, with α-pinene being the dominant monoterpene during most the year. Trans-ocimene represented 33-66% of the total monoterpene during the hottest months from June to September. VOC emissions were found to be accurately predicted using existing algorithms. Standard (normalised) emission factors of VOCs from gorse were calculated using experimental parameters measured during the experiment and found to fluctuate with season, from 13.3±2.1 to 0.1±0.1 μg C (g dwt)-1 h-1 in August 1995 and January 1995, respectively, for isoprene, and from 2.5±0.2 to 0.4±0.2 μg C (g dwt)-1 h-1 in July and November 1995, respectively, for total monoterpenes. No simple clear relation was found to allow prediction of these seasonal variations with respect to temperature and light intensity. The effects of using inappropriate algorithms to derive VOC fluxes from gorse were assessed for isoprene and monoterpenes. Although on an annual basis the discrepancies are not significant, monthly estimation of isoprene were found to be overestimated by more than a factor of 50 during wintertime when the seasonality of emission factors is not considered.

Systematic selection of off-gas treatment at the Savannah River Site

International Nuclear Information System (INIS)

McKillip, S.T.; Rehder, T.E.

1992-01-01

At the Savannah River Site (SRS), from 1958--1985, effluent waste from the reactor fuel and target rod fabrication area (M-Area) was discharged to a settling basin. In 1981, monitoring wells detected groundwater contamination, specifically trichloroethylene and tetrachloroethylene, in the immediate vicinity of the basin. Under the auspices of Resource Conservation and Recovery Act (RCRA) the M-Area contamination must be addressed by a corrective action program until the volatile organic compound (VOC) concentrations reach Drinking Water Standards. This was initiated in 1985 with startup of a full-scale pump-and-treat air stripper system. Recently, remediation efforts have focused on vacuum extraction to treat vadose zone contamination not addressed by the original recovery wells, and additional pump-and-treat systems to achieve hydraulic control of the plume. Regulatory requirements allowed for discharge of VOCs to the atmosphere when the original remediation system was installed; however, 1990 amendments to the Clean Air Act will eventually require treatment of VOC contaminated air prior to discharge. This has ramifications to systems currently being design, as well as the existing systems. In response to the 1990 Clean Air Act amendments, SRS initiated a study to assess commercially available off-gas treatment technologies. These included carbon adsorption, thermal incineration, catalytic oxidation, absorption, condensation, and UV/peroxide destruction, and xenon flashlamp. Criteria used to evaluate the technologies were the thirty (30) year life cycle cost, permitting considerations, and manpower requirements. The study concluded that catalytic oxidation provided the most desirable combination of these elements

Automated recognition and tracking of aerosol threat plumes with an IR camera pod

Science.gov (United States)

Fauth, Ryan; Powell, Christopher; Gruber, Thomas; Clapp, Dan

2012-06-01

Protection of fixed sites from chemical, biological, or radiological aerosol plume attacks depends on early warning so that there is time to take mitigating actions. Early warning requires continuous, autonomous, and rapid coverage of large surrounding areas; however, this must be done at an affordable cost. Once a potential threat plume is detected though, a different type of sensor (e.g., a more expensive, slower sensor) may be cued for identification purposes, but the problem is to quickly identify all of the potential threats around the fixed site of interest. To address this problem of low cost, persistent, wide area surveillance, an IR camera pod and multi-image stitching and processing algorithms have been developed for automatic recognition and tracking of aerosol plumes. A rugged, modular, static pod design, which accommodates as many as four micro-bolometer IR cameras for 45deg to 180deg of azimuth coverage, is presented. Various OpenCV1 based image-processing algorithms, including stitching of multiple adjacent FOVs, recognition of aerosol plume objects, and the tracking of aerosol plumes, are presented using process block diagrams and sample field test results, including chemical and biological simulant plumes. Methods for dealing with the background removal, brightness equalization between images, and focus quality for optimal plume tracking are also discussed.

A stakeholder involvement approach to evaluate and enhance technology acceptance: U.S. Department of Energy Office of Technology Development's Plume Focus Area

International Nuclear Information System (INIS)

McCabe, G.H.; Stein, S.L.; Serie, P.J.

1995-01-01

The US Department of Energy (DOE) faces a major challenge in cleaning up its contaminated sites throughout the United States. One major area of concern is the plumes in soil and ground water which are contaminated with a myriad of different pollutants. DOE recently organized its plume-related problems into the Plume Focus Area. The mission of the Plume Focus Area is to enhance the deployment of innovative technologies for containing and cleaning up contaminant plumes in ground water and soil at all DOE sites. Environmental cleanup priorities for soil and ground water plumes are being defined and technology users have the challenge of matching current and innovative technologies to those priorities. By involving a range of stakeholders in the selection, demonstration, and evaluation of new technologies, the deployment of these technologies can be enhanced. If new plume cleanup technologies are to be deployable, they must improve on today's baseline technologies. The Sites' Coordination Team (SCT) of the Plume Focus Area develops and supports the implementation of methods for stakeholder involvement throughout the multiple steps that define focus area activities. Site-specific teams are being formed to carry out the strategy at each site, and the teams will work through Site Technology Coordination Groups (STCGs) at each location. The SCT is responsible for identifying the site-specific stakeholder involvement teams, training the team members, preparing needed national-level guidance and strategies, helping the teams tailor a strategy for their particular site that meets the overall needs of the focus area, and facilitating inter-site coordination. The results will be used to develop national technology acceptance reports on the innovative technologies being funded and evaluated under the Plume Focus Area

Characterisation and treatment of VOCs in process water from upgrading facilities for compressed biogas (CBG).

Science.gov (United States)

Nilsson Påledal, S; Arrhenius, K; Moestedt, J; Engelbrektsson, J; Stensen, K

2016-02-01

Compression and upgrading of biogas to vehicle fuel generates process water, which to varying degrees contains volatile organic compounds (VOCs) originating from the biogas. The compostion of this process water has not yet been studied and scientifically published and there is currently an uncertainty regarding content of VOCs and how the process water should be managed to minimise the impact on health and the environment. The aim of the study was to give an overview about general levels of VOCs in the process water. Characterisation of process water from amine and water scrubbers at plants digesting waste, sewage sludge or agricultural residues showed that both the average concentration and composition of particular VOCs varied depending on the substrate used at the biogas plant, but the divergence was high and the differences for total concentrations from the different substrate groups were only significant for samples from plants using waste compared to residues from agriculture. The characterisation also showed that the content of VOCs varied greatly between different sampling points for same main substrate and between sampling occasions at the same sampling point, indicating that site-specific conditions are important for the results which also indicates that a number of analyses at different times are required in order to make an more exact characterisation with low uncertainty. Inhibition of VOCs in the anaerobic digestion (AD) process was studied in biomethane potential tests, but no inhibition was observed during addition of synthetic process water at concentrations of 11.6 mg and 238 mg VOC/L. Copyright © 2015 Elsevier Ltd. All rights reserved.

Air sparging for subsurface remediation: Numerical analysis using T2VOC

Energy Technology Data Exchange (ETDEWEB)

McCray, J.E.; Falta, R.W. [Clemson Univ. SC (United States)

1995-03-01

Air sparging is under active investigation as a promising remediation technology for aquifers contaminated with folatile organic dense nonaqueous phase liquids (DNAPLs). A theoretical study for the removal of DNAPLs from the subsurface using this technology is presented. T2VOC is used to conduct multiphase numerical simulations of DNAPL removal utilizing a model aquifer with a radially-symmetric geometry. Both homogeneous and macroscale heterogeneous systems are considered. These simulations suggest that DNAPLs are efficiently removed in a zone of contaminant cleanup at relatively low gas saturations within the injected air plume. The zone of effective removal may be referred to as the radius of influence (ROI). The sparging-induced pressure increase below the water table, which may be measured in the field, is recommended as the best method for determining the ROI. Multiphase numerical simulations are used to support this recommendation, to relate the injected gas ROI to the zone of NAPL cleanup, and to illustrate the transient and steady-state aquifer behavior.

Innovative Strategy For Long Term Monitoring Of Metal And Radionuclide Plumes

International Nuclear Information System (INIS)

Eddy-Dilek, Carol; Millings, Margaret R.; Looney, Brian B.; Denham, Miles E.

2014-01-01

Many government and private industry sites that were once contaminated with radioactive and chemical wastes cannot be cleaned up enough to permit unrestricted human access. The sites will require long term management, in some cases indefinitely, leaving site owners with the challenge of protecting human health and environmental quality at these 'legacy' sites. Long-term monitoring of groundwater contamination is one of the largest projected costs in the life cycle of environmental management at the Savannah River Site, the larger DOE complex, and many large federal and private sites. There is a need to optimize the performance and manage the cost of long term surveillance and monitoring at their sites. Currently, SRNL is initiating a pilot field test using alternative protocols for long term monitoring of metals and radionuclides. A key component of the approach is that monitoring efforts are focused on measurement of low cost metrics related to hydrologic and chemical conditions that control contaminant migration. The strategy combines careful monitoring of hydrologic boundary conditions with measurement of master variables such as chemical surrogates along with a smaller number of standard well analyses. In plumes contaminated with metals, master variables control the chemistry of the groundwater system, and include redox variables (ORP, DO, chemicals), pH, specific conductivity, biological community (breakdown/decay products), and temperature. Significant changes in these variables will result in conditions whereby the plume may not be stable and therefore can be used to predict possible plume migration. Conversely, concentration measurements for all types of contaminants in groundwater are a lagging indicator plume movement - major changes contaminant concentrations indicate that contamination has migrated. An approach based on measurement of master variables and explicit monitoring of hydrologic boundary conditions combined with traditional metrics should lead

Innovative Strategy For Long Term Monitoring Of Metal And Radionuclide Plumes

Energy Technology Data Exchange (ETDEWEB)

Eddy-Dilek, Carol; Millings, Margaret R.; Looney, Brian B.; Denham, Miles E.

2014-01-08

Many government and private industry sites that were once contaminated with radioactive and chemical wastes cannot be cleaned up enough to permit unrestricted human access. The sites will require long term management, in some cases indefinitely, leaving site owners with the challenge of protecting human health and environmental quality at these "legacy" sites. Long-term monitoring of groundwater contamination is one of the largest projected costs in the life cycle of environmental management at the Savannah River Site, the larger DOE complex, and many large federal and private sites. There is a need to optimize the performance and manage the cost of long term surveillance and monitoring at their sites. Currently, SRNL is initiating a pilot field test using alternative protocols for long term monitoring of metals and radionuclides. A key component of the approach is that monitoring efforts are focused on measurement of low cost metrics related to hydrologic and chemical conditions that control contaminant migration. The strategy combines careful monitoring of hydrologic boundary conditions with measurement of master variables such as chemical surrogates along with a smaller number of standard well analyses. In plumes contaminated with metals, master variables control the chemistry of the groundwater system, and include redox variables (ORP, DO, chemicals), pH, specific conductivity, biological community (breakdown/decay products), and temperature. Significant changes in these variables will result in conditions whereby the plume may not be stable and therefore can be used to predict possible plume migration. Conversely, concentration measurements for all types of contaminants in groundwater are a lagging indicator plume movement - major changes contaminant concentrations indicate that contamination has migrated. An approach based on measurement of master variables and explicit monitoring of hydrologic boundary conditions combined with traditional metrics should lead

MEMBRANE BIOTREATMENT OF VOC-LADEN AIR

Science.gov (United States)

The paper discusses membrane biotreatment of air laden with volatile organic compounds (VOCs). Microporous flat-sheet and hollow-fiber membrane contactors were used to support air-liquid mass transfer interfaces. These modules were used in a two-step process to transfer VOCs fr...

[Study on the quantitative estimation method for VOCs emission from petrochemical storage tanks based on tanks 4.0.9d model].

Science.gov (United States)

Li, Jing; Wang, Min-Yan; Zhang, Jian; He, Wan-Qing; Nie, Lei; Shao, Xia

2013-12-01

VOCs emission from petrochemical storage tanks is one of the important emission sources in the petrochemical industry. In order to find out the VOCs emission amount of petrochemical storage tanks, Tanks 4.0.9d model is utilized to calculate the VOCs emission from different kinds of storage tanks. VOCs emissions from a horizontal tank, a vertical fixed roof tank, an internal floating roof tank and an external floating roof tank were calculated as an example. The consideration of the site meteorological information, the sealing information, the tank content information and unit conversion by using Tanks 4.0.9d model in China was also discussed. Tanks 4.0.9d model can be used to estimate VOCs emissions from petrochemical storage tanks in China as a simple and highly accurate method.

Ambient Volatile Organic Compounds (VOCs) pollution in Isolo ...

African Journals Online (AJOL)

The adsorbed VOCs were desorbed with carbondisulphide (CS2) and the solution analysed using Gas Chromatography (GC) fitted with Flame Ionization Detector (FID). The results from analysis of the air samples collected showed that twenty-six (26) VOCs were captured in Isolo Industrial area. The VOCs were classified ...

VOC Control in Kraft Mills; FINAL

International Nuclear Information System (INIS)

Zhu, J.Y.; Chai, X.-S.; Edwards, L.L.; Gu, Y.; Teja, A.S.; Kirkman, A.G.; Pfromm, P.H.; Rezac, M.E.

2001-01-01

The formation of volatile organic compounds (VOCs), such as methanol, in kraft mills has been an environmental concern. Methanol is soluble in water and can increase the biochemical oxygen demand. Furthermore, it can also be released into atmosphere at the process temperatures of kraft mill-streams. The Cluster Rule of the EPA now requires the control of the release of methanol in pulp and paper mills. This research program was conducted to develop a computer simulation tool for mills to predict VOC air emissions. To achieve the objective of the research program, much effort was made in the development of analytical techniques for the analysis of VOC and determination of vapor liquid partitioning coefficient of VOCs in kraft mill-streams using headspace gas chromatography. With the developed analytical tool, methanol formation in alkaline pulping was studied in laboratory to provide benchmark data of the amount of methanol formation in pulping in kraft mills and for the validation of VOC formation and vapor-liquid equilibrium submodels. Several millwide air and liquid samplings were conducted using the analytical tools developed to validate the simulation tool. The VOC predictive simulation model was developed based on the basic chemical engineering concepts, i.e., reaction kinetics, vapor liquid equilibrium, combined with computerized mass and energy balances. Four kraft mill case studies (a continuous digester, two brownstock washing lines, and a pre-evaporator system) are presented and compared with mill measurements. These case studies provide valuable, technical information for issues related to MACT I and MACT II compliance, such as condensate collection and Clean-Condensate-Alternatives (CCA)

Monitoring of volatile organic compounds (VOCs) from an oil and gas station in northwest China for 1 year

Science.gov (United States)

Zheng, Huang; Kong, Shaofei; Xing, Xinli; Mao, Yao; Hu, Tianpeng; Ding, Yang; Li, Gang; Liu, Dantong; Li, Shuanglin; Qi, Shihua

2018-04-01

Oil and natural gas are important for energy supply around the world. The exploring, drilling, transportation and processing in oil and gas regions can release a lot of volatile organic compounds (VOCs). To understand the VOC levels, compositions and sources in such regions, an oil and gas station in northwest China was chosen as the research site and 57 VOCs designated as the photochemical precursors were continuously measured for an entire year (September 2014-August 2015) using an online monitoring system. The average concentration of total VOCs was 297 ± 372 ppbv and the main contributor was alkanes, accounting for 87.5 % of the total VOCs. According to the propylene-equivalent concentration and maximum incremental reactivity methods, alkanes were identified as the most important VOC groups for the ozone formation potential. Positive matrix factorization (PMF) analysis showed that the annual average contributions from natural gas, fuel evaporation, combustion sources, oil refining processes and asphalt (anthropogenic and natural sources) to the total VOCs were 62.6 ± 3.04, 21.5 ± .99, 10.9 ± 1.57, 3.8 ± 0.50 and 1.3 ± 0.69 %, respectively. The five identified VOC sources exhibited various diurnal patterns due to their different emission patterns and the impact of meteorological parameters. Potential source contribution function (PSCF) and concentration-weighted trajectory (CWT) models based on backward trajectory analysis indicated that the five identified sources had similar geographic origins. Raster analysis based on CWT analysis indicated that the local emissions contributed 48.4-74.6 % to the total VOCs. Based on the high-resolution observation data, this study clearly described and analyzed the temporal variation in VOC emission characteristics at a typical oil and gas field, which exhibited different VOC levels, compositions and origins compared with those in urban and industrial areas.

Chlorinated volatile organic compounds (Cl-VOCs) in environment - sources, potential human health impacts, and current remediation technologies.

Science.gov (United States)

Huang, Binbin; Lei, Chao; Wei, Chaohai; Zeng, Guangming

2014-10-01

Chlorinated volatile organic compounds (Cl-VOCs), including polychloromethanes, polychloroethanes and polychloroethylenes, are widely used as solvents, degreasing agents and a variety of commercial products. These compounds belong to a group of ubiquitous contaminants that can be found in contaminated soil, air and any kind of fluvial mediums such as groundwater, rivers and lakes. This review presents a summary of the research concerning the production levels and sources of Cl-VOCs, their potential impacts on human health as well as state-of-the-art remediation technologies. Important sources of Cl-VOCs principally include the emissions from industrial processes, the consumption of Cl-VOC-containing products, the disinfection process, as well as improper storage and disposal methods. Human exposure to Cl-VOCs can occur through different routes, including ingestion, inhalation and dermal contact. The toxicological impacts of these compounds have been carefully assessed, and the results demonstrate the potential associations of cancer incidence with exposure to Cl-VOCs. Most Cl-VOCs thus have been listed as priority pollutants by the Ministry of Environmental Protection (MEP) of China, Environmental Protection Agency of the U.S. (U.S. EPA) and European Commission (EC), and are under close monitor and strict control. Yet, more efforts will be put into the epidemiological studies for the risk of human exposure to Cl-VOCs and the exposure level measurements in contaminated sites in the future. State-of-the-art remediation technologies for Cl-VOCs employ non-destructive methods and destructive methods (e.g. thermal incineration, phytoremediation, biodegradation, advanced oxidation processes (AOPs) and reductive dechlorination), whose advantages, drawbacks and future developments are thoroughly discussed in the later sections. Copyright © 2014 Elsevier Ltd. All rights reserved.

VOC emissions chambers

Data.gov (United States)

Federal Laboratory Consortium — In order to support the development of test methods and reference materials for volatile organic compounds (VOC) emissions from building materials and furnishings,...

The distribution and stabilisation of dissolved Fe in deep-sea hydrothermal plumes

Science.gov (United States)

Bennett, Sarah A.; Achterberg, Eric P.; Connelly, Douglas P.; Statham, Peter J.; Fones, Gary R.; German, Christopher R.

2008-06-01

We have conducted a study of hydrothermal plumes overlying the Mid-Atlantic Ridge near 5° S to investigate whether there is a significant export flux of dissolved Fe from hydrothermal venting to the oceans. Our study combined measurements of plume-height Fe concentrations from a series of 6 CTD stations together with studies of dissolved Fe speciation in a subset of those samples. At 2.5 km down plume from the nearest known vent site dissolved Fe concentrations were ˜ 20 nM. This is much higher than would be predicted from a combination of plume dilution and dissolved Fe(II) oxidation rates, but consistent with stabilisation due to the presence of organic Fe complexes and Fe colloids. Using Competitive Ligand Exchange-Cathodic Stripping Voltammetry (CLE-CSV), stabilised dissolved Fe complexes were detected within the dissolved Fe fraction on the edges of one non-buoyant hydrothermal plume with observed ligand concentrations high enough to account for stabilisation of ˜ 4% of the total Fe emitted from the 5° S vent sites. If these results were representative of all hydrothermal systems, submarine venting could provide 12-22% of the global deep-ocean dissolved Fe budget.

Saharan dust plume charging observed over the UK

Science.gov (United States)

Harrison, R. Giles; Nicoll, Keri A.; Marlton, Graeme J.; Ryder, Claire L.; Bennett, Alec J.

2018-05-01

A plume of Saharan dust and Iberian smoke was carried across the southern UK on 16th October 2017, entrained into an Atlantic cyclone which had originated as Hurricane Ophelia. The dust plume aloft was widely noticed as it was sufficiently dense to redden the visual appearance of the sun. Time series of backscatter from ceilometers at Reading and Chilbolton show two plumes: one carried upwards to 2.5 km, and another below 800 m into the boundary layer, with a clear slot between. Steady descent of particles at about 50 cm s‑1 continued throughout the morning, and coarse mode particles reached the surface. Plumes containing dust are frequently observed to be strongly charged, often through frictional effects. This plume passed over atmospheric electric field sensors at Bristol, Chilbolton and Reading. Consistent measurements at these three sites indicated negative plume charge. The lower edge plume charge density was (‑8.0 ± 3.3) nC m‑2, which is several times greater than that typical for stratiform water clouds, implying an active in situ charge generation mechanism such as turbulent triboelectrification. A meteorological radiosonde measuring temperature and humidity was launched into the plume at 1412 UTC, specially instrumented with charge and turbulence sensors. This detected charge in the boundary layer and in the upper plume region, and strong turbulent mixing was observed throughout the atmosphere’s lowest 4 km. The clear slot region, through which particles sedimented, was anomalously dry compared with modelled values, with water clouds forming intermittently in the air beneath. Electrical aspects of dust should be included in numerical models, particularly the charge-related effects on cloud microphysical properties, to accurately represent particle behaviour and transport.

Plant communication: mediated by individual or blended VOCs?

Science.gov (United States)

Ueda, Hirokazu; Kikuta, Yukio; Matsuda, Kazuhiko

2012-02-01

Plants emit volatile organic compounds (VOCs) as a means to warn other plants of impending danger. Nearby plants exposed to the induced VOCs prepare their own defense weapons in response. Accumulated data supports this assertion, yet much of the evidence has been obtained in laboratories under artificial conditions where, for example, a single VOC might be applied at a concentration that plants do not actually experience in nature. Experiments conducted outdoors suggest that communication occurs only within a limited distance from the damaged plants. Thus, the question remains as to whether VOCs work as a single component or a specific blend, and at which concentrations VOCs elicit insect and pathogen defenses in undamaged plants. We discuss these issues based on available literature and our recent work, and propose future directions in this field.

Evaluations of NOx and highly reactive VOC emission inventories in Texas and their implications for ozone plume simulations during the Texas Air Quality Study 2006

NARCIS (Netherlands)

Kim, S.-W.; McKeen, S.A.; Frost, G.J.; Lee, S.-H.; Trainer, M.; Richter, A.; Angevine, W. M.; Atlas, E.; Bianco, L.; Boersma, K.F.; Brioude, J.; Burrow, J.P.; Gouw, de J.; Fried, A.; Gleason, J.F.; Hilboll, A.; Mellqvist, J.; Peischl, J.; Richter, D.; Rivera, C.; Ryerson, T.; Lintel Hekkert, te L.; Walega, J.; Warneke, C.; Weibring, P.; Williams, E.

2011-01-01

Satellite and aircraft observations made during the 2006 Texas Air Quality Study (TexAQS) detected strong urban, industrial and power plant plumes in Texas. We simulated these plumes using the Weather Research and Forecasting-Chemistry (WRF-Chem) model with input from the US EPA's 2005 National

Comparison of the decomposition VOC profile during winter and summer in a moist, mid-latitude (Cfb climate.

Directory of Open Access Journals (Sweden)

Shari L Forbes

Full Text Available The investigation of volatile organic compounds (VOCs associated with decomposition is an emerging field in forensic taphonomy due to their importance in locating human remains using biological detectors such as insects and canines. A consistent decomposition VOC profile has not yet been elucidated due to the intrinsic impact of the environment on the decomposition process in different climatic zones. The study of decomposition VOCs has typically occurred during the warmer months to enable chemical profiling of all decomposition stages. The present study investigated the decomposition VOC profile in air during both warmer and cooler months in a moist, mid-latitude (Cfb climate as decomposition occurs year-round in this environment. Pig carcasses (Sus scrofa domesticus L. were placed on a soil surface to decompose naturally and their VOC profile was monitored during the winter and summer months. Corresponding control sites were also monitored to determine the natural VOC profile of the surrounding soil and vegetation. VOC samples were collected onto sorbent tubes and analyzed using comprehensive two-dimensional gas chromatography--time-of-flight mass spectrometry (GC × GC-TOFMS. The summer months were characterized by higher temperatures and solar radiation, greater rainfall accumulation, and comparable humidity when compared to the winter months. The rate of decomposition was faster and the number and abundance of VOCs was proportionally higher in summer. However, a similar trend was observed in winter and summer demonstrating a rapid increase in VOC abundance during active decay with a second increase in abundance occurring later in the decomposition process. Sulfur-containing compounds, alcohols and ketones represented the most abundant classes of compounds in both seasons, although almost all 10 compound classes identified contributed to discriminating the stages of decomposition throughout both seasons. The advantages of GC × GC-TOFMS were

Analysis and evaluation of VOC removal technologies demonstrated at Savannah River

International Nuclear Information System (INIS)

Chesnut, D.A.; Wagoner, J.; Nitao, J.J.; Boyd, S.; Shaffer, R.J.; Kansa, E.J.; Buscheck, T.A.; Pruess, K.; Falta, R.W.

1993-09-01

Volatile Organic Compounds, or VOCs, are ubiquitous subsurface contaminants at industrial as well as DOE sites. At the Savannah River Plant, the principles VOCs contaminating the subsurface below A-Area and M-Area are Trichloroethylene (C 2 HCl 3 , or TCE) and Tetrachloroethylene (C 2 Cl 4 , or PCE). These compounds were used extensively as degreasing solvents from 1952 until 1979, and the waste solvent which did not evaporate (on the order of 2x10 6 pounds) was discharged to a process sewer line leading to the M-Area Seepage Basin (Figure I.2). These compounds infiltrated into the soil and underlying sediments from leaks in the sewer line and elsewhere thereby contaminating the vadose zone between the surface and the water table as well as the aquifer

Dilution in Transition Zone between Rising Plumes and Surface Plumes

DEFF Research Database (Denmark)

Larsen, Torben

2004-01-01

The papers presents some physical experiments with the dilution of sea outfall plumes with emphasize on the transition zone where the relative fast flowing vertical plume turns to a horizontal surface plume following the slow sea surface currents. The experiments show that a considerable dilution...

Diurnally resolved particulate and VOC measurements at a rural site: indication of significant biogenic secondary organic aerosol formation

Science.gov (United States)

Sjostedt, S. J.; Slowik, J. G.; Brook, J. R.; Chang, R. Y.-W.; Mihele, C.; Stroud, C. A.; Vlasenko, A.; Abbatt, J. P. D.

2011-06-01

We report simultaneous measurements of volatile organic compound (VOC) mixing ratios including C6 to C8 aromatics, isoprene, monoterpenes, acetone and organic aerosol mass loadings at a rural location in southwestern Ontario, Canada by Proton-Transfer-Reaction Mass Spectrometry (PTR-MS) and Aerosol Mass Spectrometry (AMS), respectively. During the three-week-long Border Air Quality and Meteorology Study in June-July 2007, air was sampled from a range of sources, including aged air from the polluted US Midwest, direct outflow from Detroit 50 km away, and clean air with higher biogenic input. After normalization to the diurnal profile of CO, a long-lived tracer, diurnal analyses show clear photochemical loss of reactive aromatics and production of oxygenated VOCs and secondary organic aerosol (SOA) during the daytime. Biogenic VOC mixing ratios increase during the daytime in accord with their light- and temperature-dependent sources. Long-lived species, such as hydrocarbon-like organic aerosol and benzene show little to no photochemical reactivity on this timescale. From the normalized diurnal profiles of VOCs, an estimate of OH concentrations during the daytime, measured O3 concentrations, and laboratory SOA yields, we calculate integrated local organic aerosol production amounts associated with each measured SOA precursor. Under the assumption that biogenic precursors are uniformly distributed across the southwestern Ontario location, we conclude that such precursors contribute significantly to the total amount of SOA formation, even during the period of Detroit outflow. The importance of aromatic precursors is more difficult to assess given that their sources are likely to be localized and thus of variable impact at the sampling location.

Technology projects for characterization--monitoring of volatile organic compounds (VOCs)

Energy Technology Data Exchange (ETDEWEB)

Junk, G.A.; Haas, W.J. Jr.

1992-07-01

One hundred thirty technology project titles related to the characterization of volatile organic compounds (VOCs) at an arid site are listed alphabetically by first contact person in a master compilation that includes phone numbers, addresses, keywords, and short descriptions. Separate tables are presented for 62 field-demonstrated, 36 laboratory-demonstrated, and 35 developing technology projects. The technology projects in each of these three categories are also prioritized in separate summary tables. Additional tables are presented for a number of other categorizations of the technology projects: In Situ; Fiberoptic; Mass Spectrometer; Optical Spectroscopy; Raman or SERS; Ion Mobility or Acoustic; Associated; and Commercial. Four lists of contact person names are provided so details concerning the projects that deal with sampling, and VOCs in gases, waters, and soils (sediments) can be obtained. Finally, seven wide-ranging conclusions based on observations and experiences during this work are presented.

Technology projects for characterization--monitoring of volatile organic compounds (VOCs)

International Nuclear Information System (INIS)

Junk, G.A.; Haas, W.J. Jr.

1992-07-01

One hundred thirty technology project titles related to the characterization of volatile organic compounds (VOCs) at an arid site are listed alphabetically by first contact person in a master compilation that includes phone numbers, addresses, keywords, and short descriptions. Separate tables are presented for 62 field-demonstrated, 36 laboratory-demonstrated, and 35 developing technology projects. The technology projects in each of these three categories are also prioritized in separate summary tables. Additional tables are presented for a number of other categorizations of the technology projects: In Situ; Fiberoptic; Mass Spectrometer; Optical Spectroscopy; Raman or SERS; Ion Mobility or Acoustic; Associated; and Commercial. Four lists of contact person names are provided so details concerning the projects that deal with sampling, and VOCs in gases, waters, and soils (sediments) can be obtained. Finally, seven wide-ranging conclusions based on observations and experiences during this work are presented

Contrasting VOC Composition in London, UK and Beijing, China

Science.gov (United States)

Dunmore, R.; Hopkins, J. R.; Shaw, M.; Squires, F. A.; Lee, J. D.; Lewis, A. C.; Hamilton, J. F.

2017-12-01

With an increasing fraction of the world's population now living in megacities, urban air quality in those locations has the potential to be one of the largest controllable factors for public health. Both London and Beijing are classified as megacities, with the latter almost twice as densely populated. The key drivers and trajectory of air pollution are unique to each location; London has substantially reduced PM10 concentrations over the past two decades but continues to have high urban NO2. Beijing has had well-reported high levels of PM, is now in a phase of gradual decline, and has proportionately low NO2. Both locations however, continue to emit a mix of gas phase pollutants with the potential to form photochemical ozone. Whilst the abundance of NOx in each city is relatively straightforward to quantify, the VOC mixtures that are present differ between these two cities and this has consequential impacts on the downwind ozone formation potential. This work reports a comprehensive assessment of VOC speciation, reactivity and abundance in the two cities using a common set of inter-comparable measurement approaches. Hourly observations of VOCs over the range C2 - C13+ were made using two gas chromatography (GC) instruments; a PLOT column based GC for the most volatile fraction (C2-C7) and a comprehensive two-dimensional GC (GCxGC) for VOCs with more than 7 carbons. London has atmospheric VOC concentrations that in mass and reactivity terms are dominated by longer chain VOCs from diesel fuel. The VOC mixture in ambient Beijing air is dominated by short chain VOCs, a mix of both alkenes from incomplete combustion sources and alkanes and aromatics from petrochemical sources. The substantial difference in the fleet proportions of gasoline and diesel powered vehicles between the two cities is clearly reflected in ambient VOCs. In summertime, isoprene was a notable contributor to VOC reactivity in both cities despite both being highly urbanised locations. The absolute

Tracking of smokestack and cooling tower plumes using wind measurements at different levels

International Nuclear Information System (INIS)

Miller, R.L.; Patrinos, A.A.N.

1980-08-01

Relationships between cooling tower and smokestack plumes at the Bowen Electric Generating Plant in northwestern Georgia and wind direction measurements at levels from the surface at 850 mb (approx. 1.5 km) are examined. The wind measurements play an important role in estimating plume directions which in turn are utilized to establish control and target (upwind and downwind) areas for a study of plant-induced precipitation modification. Fifty-two plume observations were made during a three week period in December 1979. Results indicate that a windset (4.5 km from the plant) mounted at a level approximating that of the cooling tower plume is a better predictor of plume direction than surface windsets (1.0 km from the plant) or 850 mb level winds. However, an apparent topographical influence on the wind direction measurements at the plume-level windset site somewhat limits its plume tracking capability, at least for ambient winds from the SW quadrant

Modelling pollutants dispersion and plume rise from large hydrocarbon tank fires in neutrally stratified atmosphere

Science.gov (United States)

Argyropoulos, C. D.; Sideris, G. M.; Christolis, M. N.; Nivolianitou, Z.; Markatos, N. C.

2010-02-01

Petrochemical industries normally use storage tanks containing large amounts of flammable and hazardous substances. Therefore, the occurrence of a tank fire, such as the large industrial accident on 11th December 2005 at Buncefield Oil Storage Depots, is possible and usually leads to fire and explosions. Experience has shown that the continuous production of black smoke from these fires due to the toxic gases from the combustion process, presents a potential environmental and health problem that is difficult to assess. The goals of the present effort are to estimate the height of the smoke plume, the ground-level concentrations of the toxic pollutants (smoke, SO 2, CO, PAHs, VOCs) and to characterize risk zones by comparing the ground-level concentrations with existing safety limits. For the application of the numerical procedure developed, an external floating-roof tank has been selected with dimensions of 85 m diameter and 20 m height. Results are presented and discussed. It is concluded that for all scenarios considered, the ground-level concentrations of smoke, SO 2, CO, PAHs and VOCs do not exceed the safety limit of IDLH and there are no "death zones" due to the pollutant concentrations.

Experiments on Plume Spreading by Engineered Injection and Extraction

Science.gov (United States)

Mays, D. C.; Jones, M.; Tigera, R. G.; Neupauer, R.

2014-12-01

The notion that groundwater remediation is transport-limited emphasizes the coupling between physical (i.e., hydrodynamic), geochemical, and microbiological processes in the subsurface. Here we leverage this coupling to promote groundwater remediation using the approach of engineered injection and extraction. In this approach, inspired by the literature on chaotic advection, uncontaminated groundwater is injected and extracted through a manifold of wells surrounding the contaminated plume. The potential of this approach lies in its ability to actively manipulate the velocity field near the contaminated plume, generating plume spreading above and beyond that resulting from aquifer heterogeneity. Plume spreading, in turn, promotes mixing and reaction by chemical and biological processes. Simulations have predicted that engineered injection and extraction generates (1) chaotic advection whose characteristics depend on aquifer heterogeneity, and (2) faster rates and increased extent of groundwater remediation. This presentation focuses on a complimentary effort to experimentally demonstrate these predictions experimentally. In preparation for future work using refractive index matched (RIM) porous media, the experiments reported here use a Hele-Shaw apparatus containing silicone oil. Engineered injection and extraction is used to manipulate the geometry of an initially circular plume of black pigment, and photographs record the plume geometry after each step of injection of extraction. Image analysis, using complimentary Eulerian and Lagrangian approaches, reveals the thickness and variability of the dispersion zone surrounding the deformed plume of black pigment. The size, shape, and evolution of this dispersion zone provides insight into the interplay between engineered injection and extraction, which generates plume structure, and dispersion (here Taylor dispersion), which destroys plume structure. These experiments lay the groundwork for application of engineered

Development of aromatic VOC control technology by electron beam hybrid

International Nuclear Information System (INIS)

Kim, Jo-Chun; Kim, Ki-Joon

2006-01-01

As a fundamental study, the decomposition of volatile organic compounds (VOCs) using electron beam (EB) irradiation has been extensively investigated. EB treatments of VOCs such as toluene and styrene are discussed. The degradation characteristics were intensively investigated under various concentrations and irradiation doses to determine and improve VOC removal efficiencies. This work illustrates that the removal efficiencies of aromatic VOCs generally increase as their concentrations decrease and the irradiation doses increase. Based on these basic studies, it was found that by-products produced from EB irradiation of VOCs would cause a secondary pollution problem. Therefore, a novel hybrid technology has been applied to control aromatic VOC emissions by annexing the catalyst technique with conventional treatment study using EB technology. The experiments were carried out using a bench-scale at first, then a pilot-scale system was followed. Toluene was selected as a typical VOC for EB hybrid control to investigate by-products, effects of ceramic and catalyst, and factors affecting overall efficiency of degradation. It was concluded that VOCs could be destroyed more effectively by a novel hybrid system than single EB irradiation. (author)

Seasonal soil VOC exchange rates in a Mediterranean holm oak forest and their responses to drought conditions

Science.gov (United States)

Asensio, Dolores; Peñuelas, Josep; Ogaya, Romà; Llusià, Joan

Available information on soil volatile organic compound (VOC) exchange, emissions and uptake, is very scarce. We here describe the amounts and seasonality of soil VOC exchange during a year in a natural Mediterranean holm oak forest growing in Southern Catalonia. We investigated changes in soil VOC dynamics in drought conditions by decreasing the soil moisture to 30% of ambient conditions by artificially excluding rainfall and water runoff, and predicted the response of VOC exchange to the drought forecasted in the Mediterranean region for the next decades by GCM and ecophysiological models. The annual average of the total (detected) soil VOC and total monoterpene exchange rates were 3.2±3.2 and -0.4±0.3 μg m -2 h -1, respectively, in control plots. These values represent 0.003% of the total C emitted by soil at the study site as CO 2 whereas the annual mean of soil monoterpene exchange represents 0.0004% of total C. Total soil VOC exchange rates in control plots showed seasonal variations following changes in soil moisture and phenology. Maximum values were found in spring (17±8 μg m -2 h -1). Although there was no significant global effect of drought treatment on the total soil VOC exchange rates, annual average of total VOC exchange rates in drought plots resulted in an uptake rate (-0.5±1.8 μg m -2 h -1) instead of positive net emission rates. Larger soil VOC and monoterpene exchanges were measured in drought plots than in control plots in summer, which might be mostly attributable to autotrophic (roots) metabolism. The results show that the diversity and magnitude of monoterpene and VOC soil emissions are low compared with plant emissions, that they are driven by soil moisture, that they represent a very small part of the soil-released carbon and that they may be strongly reduced or even reversed into net uptakes by the predicted decreases of soil water availability in the next decades. In all cases, it seems that VOC fluxes in soil might have greater

Modeling contaminant plumes in fractured limestone aquifers

DEFF Research Database (Denmark)

Mosthaf, Klaus; Brauns, Bentje; Fjordbøge, Annika Sidelmann

Determining the fate and transport of contaminant plumes from contaminated sites in limestone aquifers is important because they are a major drinking water resource. This is challenging because they are often heavily fractured and contain chert layers and nodules, resulting in a complex transport...... model. The paper concludes with recommendations on how to identify and employ suitable models to advance the conceptual understanding and as decision support tools for risk assessment and the planning of remedial actions....... behavior. Improved conceptual models are needed for this type of site. Here conceptual models are developed by combining numerical models with field data. Several types of fracture flow and transport models are available for the modeling of contaminant transport in fractured media. These include...... the established approaches of the equivalent porous medium, discrete fracture and dual continuum models. However, these modeling concepts are not well tested for contaminant plume migration in limestone geologies. Our goal was to develop and evaluate approaches for modeling the transport of dissolved contaminant...

Generation of dense plume fingers in saturated-unsaturated homogeneous porous media

Science.gov (United States)

Cremer, Clemens J. M.; Graf, Thomas

2015-02-01

Flow under variable-density conditions is widespread, occurring in geothermal reservoirs, at waste disposal sites or due to saltwater intrusion. The migration of dense plumes typically results in the formation of vertical plume fingers which are known to be triggered by material heterogeneity or by variations in source concentration that causes the density variation. Using a numerical groundwater model, six perturbation methods are tested under saturated and unsaturated flow conditions to mimic heterogeneity and concentration variations on the pore scale in order to realistically generate dense fingers. A laboratory-scale sand tank experiment is numerically simulated, and the perturbation methods are evaluated by comparing plume fingers obtained from the laboratory experiment with numerically simulated fingers. Dense plume fingering for saturated flow can best be reproduced with a spatially random, time-constant perturbation of the solute source. For unsaturated flow, a spatially and temporally random noise of solute concentration or a random conductivity field adequately simulate plume fingering.

Advances in chemical sensing technologies for VOCs in breath for security/threat assessment, illicit drug detection, and human trafficking activity.

Science.gov (United States)

Giannoukos, S; Agapiou, A; Taylor, S

2018-01-17

On-site chemical sensing of compounds associated with security and terrorist attacks is of worldwide interest. Other related bio-monitoring topics include identification of individuals posing a threat from illicit drugs, explosive manufacturing, as well as searching for victims of human trafficking and collapsed buildings. The current status of field analytical technologies is directed towards the detection and identification of vapours and volatile organic compounds (VOCs). Some VOCs are associated with exhaled breath, where research is moving from individual breath testing (volatilome) to cell breath (microbiome) and most recently to crowd breath metabolites (exposome). In this paper, an overview of field-deployable chemical screening technologies (both stand-alone and those with portable characteristics) is given with application to early detection and monitoring of human exposome in security operations. On-site systems employed in exhaled breath analysis, i.e. mass spectrometry (MS), optical spectroscopy and chemical sensors are reviewed. Categories of VOCs of interest include (a) VOCs in human breath associated with exposure to threat compounds, and (b) VOCs characteristic of, and associated with, human body odour (e.g. breath, sweat). The latter are relevant to human trafficking scenarios. New technological approaches in miniaturised detection and screening systems are also presented (e.g. non-scanning digital light processing linear ion trap MS (DLP-LIT-MS), nanoparticles, mid-infrared photo-acoustic spectroscopy and hyphenated technologies). Finally, the outlook for rapid and precise, real-time field detection of threat traces in exhaled breath is revealed and discussed.

Influence of adhesive bonding on quantity of emissions VOCs

Directory of Open Access Journals (Sweden)

Petr Čech

2008-01-01

Full Text Available The study deals with the influence of urea-formaldehyde glue and veneered bolstering on technological operation veneering on quantity of emission VOCs (volatile organic compounds.The so-called Volatile Organic Compounds (VOC are among the largest pollution sources of both the internal and external environments.VOC is defined as emission of any organic compound or a mixture thereof, with the exception of methane, whereby the compound exerts the pressure of 0.01 kPa or more at the temperature of 20 °C (293.15 K and reaches the corresponding volatility under the specific conditions of its use and can undergo photochemical reactions with nitrogen oxides when exposed to solar radiation.The effects of VOC upon environment can be described by equation:VOC + NOx + UV radiation + heat = tropospheric ozone (O3.In this work there were tested background working environment in various parts of multi-storeyed press, next was judged emissive charge of veneered device and used glue. We used surface material such as chipboard. We used urea-formaldehyde glue KRONOCOL U300 on technological operation veneering.The VOC emissions from the wooden surfaces with or without finishing were tested in the Equipment for VOC Measuring with a small-space chamber. This equipment was installed in and made available by the Institute of Furniture, Design and Habitation. The small-space chamber is suitable for testing small parts of wood products. The device equipped with small-chamber satisfies all conditions mandated in the standard ENV 13 419 DIN -V-ENV 13 419 ”Determination of the emissions of Volatile organic compounds”.The VOC emissions were collected in columns with sorbent Tenax TA. We analyzed the columns with the VOC emissions by: the gas chromatography in conjunction with mass spectrometer and Direct Thermal Desorption.

Direct measurement of VOC diffusivities in tree tissues

DEFF Research Database (Denmark)

Baduru, K.K.; Trapp, Stefan; Burken, Joel G.

2008-01-01

Recent discoveries in the phytoremediation of volatile organic compounds (VOCs) show that vapor-phase transport into roots leads to VOC removal from the vadose zone and diffusion and volatilization out of plants is an important fate following uptake. Volatilization to the atmosphere constitutes one...... in numerous vegetation−VOC interactions, including the phytoremediation of soil vapors and dissolved aqueous-phase contaminants. The diffusion of VOCs through freshly excised tree tissue was directly measured for common groundwater contaminants, chlorinated compounds such as trichloroethylene, perchloroethene......, and tetrachloroethane and aromatic hydrocarbons such as benzene, toluene, and methyl tert-butyl ether. All compounds tested are currently being treated at full scale with tree-based phytoremediation. Diffusivities were determined by modeling the diffusive transport data with a one-dimensional diffusive flux model...

[Pollution characteristics and health risk assessment of atmospheric VOCs in the downtown area of Guangzhou, China].

Science.gov (United States)

Li, Lei; Li, Hong; Wang, Xue-Zhong; Zhang, Xin-Min; Wen, Chong

2013-12-01

The measurements of 31 kinds of VOCs in the ambient air of a site were carried out in the downtown of Guangzhou by online method from November 5, 2009 to November 9, 2009. The ambient level and composition characteristics, temporal variation characteristics, sources identification, and chemical reactivity of VOCs were studied, and the health risk of VOCs in the ambient air in the study area was assessed by using the international recognized health risk assessment method. Results showed that the mean and the range of the mass concentrations of 31 VOCs were 114.51 microg x m(-3) and 29.42-546.06 microg x m(-3), respectively. The mass concentrations of 31 VOCs, and those of alkanes, alkenes, and aromatics all showed a changing trend of higher in the morning and in the evening, and lower at noontime. Vehicular exhaust, gasoline and liquefied petroleum gas evaporates were the main sources of VOCs with the volatilization of paints and solvents being important emission sources. Toluene, trans-2-butene, m/p-xylene, i-butane, and 1,3,5-trimethylbenzene were the key reactive species among the 31 VOCs. Vehicular exhaust and gasoline evaporation were the main sources of VOCs leading to the formation of ozone. Health risk assessment showed that n-hexane, 1,3-butadiene, benzene, toluene, ethylbenzene, m/p-xylene and o-xylene had no appreciable risk of adverse non-cancer health effect on the exposed population, but 1, 3-butadiene and benzene had potential cancer risk. By comparing the corresponding data about health risk assessment of benzene compounds in some cities in China, it is concluded that benzene can impose relatively high cancer risk to the exposed populations in the ambient air of some cities in China. Therefore, strict countermeasures should be taken to further control the pollution of benzene in the ambient air of cities, and it is imperative to start the related studies and develop the atmospheric environmental health criteria and national ambient air quality

FORMULATING ULTRA-LOW-VOC WOOD FURNITURE COATINGS

Science.gov (United States)

The article discusses the formulation of ultra-low volatile organic compound (VOC) wood furniture coatings. The annual U.S. market for wood coatings is about 240, 000 cu m (63 million gal). In this basis, between 57 and 91 million kg (125 and 200 million lb) of VOCs are emitted i...

Solar Coronal Plumes

Directory of Open Access Journals (Sweden)

Giannina Poletto

2015-12-01

Full Text Available Polar plumes are thin long ray-like structures that project beyond the limb of the Sun polar regions, maintaining their identity over distances of several solar radii. Plumes have been first observed in white-light (WL images of the Sun, but, with the advent of the space era, they have been identified also in X-ray and UV wavelengths (XUV and, possibly, even in in situ data. This review traces the history of plumes, from the time they have been first imaged, to the complex means by which nowadays we attempt to reconstruct their 3-D structure. Spectroscopic techniques allowed us also to infer the physical parameters of plumes and estimate their electron and kinetic temperatures and their densities. However, perhaps the most interesting problem we need to solve is the role they cover in the solar wind origin and acceleration: Does the solar wind emanate from plumes or from the ambient coronal hole wherein they are embedded? Do plumes have a role in solar wind acceleration and mass loading? Answers to these questions are still somewhat ambiguous and theoretical modeling does not provide definite answers either. Recent data, with an unprecedented high spatial and temporal resolution, provide new information on the fine structure of plumes, their temporal evolution and relationship with other transient phenomena that may shed further light on these elusive features.

A gas sensor array for the simultaneous detection of multiple VOCs.

Science.gov (United States)

Zhang, Yumin; Zhao, Jianhong; Du, Tengfei; Zhu, Zhongqi; Zhang, Jin; Liu, Qingju

2017-05-16

Air quality around the globe is declining and public health is seriously threatened by indoor air pollution. Typically, indoor air pollutants are composed of a series of volatile organic compounds (VOCs) that are generally harmful to the human body, especially VOCs with low molecular weights (less than 100 Da). Moreover, in some situations, more than one type of VOC is present; thus, a device that can detect one or more VOCs simultaneously would be most beneficial. Here, we synthesized a sensor array with 4 units to detect 4 VOCs: acetone (unit 1), benzene (unit 2), methanol (unit 3) and formaldehyde (unit 4) simultaneously. All units were simultaneously exposed to 2.5 ppm of all four VOCs. The sensitivity of unit 1 was 14.67 for acetone and less than 2.54 for the other VOCs. The sensitivities of units 2, 3 and 4 to benzene, methanol and formaldehyde were 2 18.64, 20.98 and 17.26, respectively, and less than 4.01 for the other VOCs. These results indicated that the sensor array exhibited good selectivity and could be used for the real-time monitoring of indoor air quality. Thus, this device will be useful in situations requiring the simultaneous detection of multiple VOCs.

Entrainment by turbulent plumes

Science.gov (United States)

Parker, David; Burridge, Henry; Partridge, Jamie; Linden, Paul

2017-11-01

Plumes are of relevance to nature and real consequence to industry. While the Morton, Taylor & Turner (1956) plume model is able to estimate the mean physical flux parameters, the process of entrainment is only parametrised in a time-averaged sense and a deeper understanding is key to understanding how they evolve. Various flow configurations, resulting in different entrainment values, are considered; we perform simultaneous PIV and plume-edge detection on saline plumes in water resulting from a point source, a line source and a line source where a vertical wall is placed immediately adjacent. Of particular interest is the effect the large scale eddies, forming at the edge of the plume and engulfing ambient fluid, have on the entrainment process. By using velocity statistics in a coordinate system based on the instantaneous scalar edge of the plume the significance of this large scale engulfment is quantified. It is found that significant mass is transported outside the plumes, in particular in regions where large scale structures are absent creating regions of relatively high-momentum ambient fluid. This suggests that the large scale processes, whereby ambient fluid is engulfed into the plume, contribute significantly to the entrainment.

Where the oil from surface and subsurface plumes deposited during/after Deepwater Horizon oil spill?

Science.gov (United States)

Yan, B.

2016-02-01

The Deepwater Horizon (DwH) oil spill released an estimated 4.9 million barrels (about 200 million gallons) of crude oil into the Gulf of Mexico between April 20, 2010 and July 15, 2010. Though Valentine et al. has linked the elevated oil components in some sediments with the subsurface plume, the sites with fallout from the ocean surface plume has not been identified. This piece of information is critical not only for a comprehensive scientific understanding of the ecosystem response and fate of spill-related pollutants, but also for litigation purposes and future spill response and restoration planning. In this study we focus on testing the hypothesis that marine snow from the surface plume were deposited on the sea floor over a broad area. To do so, we use publicly available data generated as part of the ongoing Natural Resource Damage Assessment (NRDA) process to assess the spatial distribution of petroleum hydrocarbons in the water column and deep-ocean sediments of the Gulf of Mexico. Sensitive hydrocarbon markers are used to differentiate hydrocarbons from surface plume, deep subsurface plume, and in-situ burning. Preliminary results suggest the overlapping but different falling sites of these plumes and the sedimentation process was controlled by various biological, chemical, and physical factors.

VOCs and odors: key factors in selecting `green` building materials?

Energy Technology Data Exchange (ETDEWEB)

Coombs, C. [Steven Winter Associates Inc., Norwalk, CT and Washington DC (United States)

1998-12-01

The current state of knowledge available for selecting building materials on the basis of emissions of volatile organic compounds (VOCs) and odors is reviewed. The significance of VOCs and odors in building materials is related to their role in influencing indoor air quality. As far as toxicity is concerned, many of the VOCs detected in indoor air are relatively inert when considered singly. They are not however, unimportant because in actual fact they are invariably found in mixtures some of which can be toxic. Although knowledge of VOCs is incomplete, it is important to specify ozone-resistant polymeric building products, i.e. those that are chemically stable and inert to oxidation. In addition to VOCs, attention should also be focused on semi-volatile organic compounds (SVOCs) since they are even more persistent than VOCs and tend to offgas for prolonged periods of time. Similarly, it is reasonable to specify low-odor materials. Inclusion of issues related to complex indoor chemistry, less volatile emissions, in addition to VOCs and odor, should in time result in expanded choices of building materials that promote indoor air quality. 16 refs.,2 tabs.

Origin of VC-only plumes from naturally enhanced dechlorination in a peat-rich hydrogeologic setting

Science.gov (United States)

Filippini, Maria; Amorosi, Alessandro; Campo, Bruno; Herrero-Martìn, Sara; Nijenhuis, Ivonne; Parker, Beth L.; Gargini, Alessandro

2016-09-01

The occurrence of vinyl chloride (VC) is often a main concern at sites contaminated with chlorinated solvents due to its high degree of toxicity and carcinogenicity. VC occurrence in aquifers is most often related to the degradation of higher chlorinated ethenes or ethanes and it is generally detected in plumes along with parent contaminants. However, specific combination of stratigraphic, hydrogeologic and geochemical conditions can enhance the degradation of parents and lead to the formation of plumes almost entirely composed of VC (i.e. VC-only plumes). This paper investigates the causes of VC-only plumes in the aquifers below the city of Ferrara (northern Italy) by combining multiple lines of evidence. The City of Ferrara is located on an alluvial lowland, built by the River Po, and is made up of alternating unconsolidated sandy aquifer and silt-clay aquitard deposits of fluvial origin. This region has been strongly impacted by prior industrial activities, with the occurrence of chlorinated compounds at several sites. VC-only plumes with uncertain source location were found at two contaminated sites. The source zone of a third plume composed of chloroethenes from PCE to VC was investigated for high resolution depositional facies architecture and contaminant distribution (contaminant concentration and Compound Specific Isotope Analysis - CSIA). The investigation suggested that degradation of PCE and TCE takes place during contaminant migration through peat-rich (swamp) layers related to the Holocene transgression, which locally act as a ;reactor; for stimulating degradation with the accumulation of VC in the strongly reducing environment of the peat. Regional-scale stratigraphic architecture showed the ubiquitous occurrence of swamp layers at distinct stratigraphic levels in the investigated system and their apparent linkage to the in situ creation of the VC-only plumes.

Fighting against VOC emissions; Lutter contre les emissions de COV

Energy Technology Data Exchange (ETDEWEB)

Fanlo, J.L. [Ecole des Mines d' Ales, 30 (France); Puech, G. [APAVE, 75 - Paris (France); Patoux, R. [Rhodia Rhoditech (France)] [and others

2001-12-01

This document brings together 15 testimonies of experts about the processes used in the industry for the abatement of volatile organic compound (VOC) emissions. The different points approached concern: the first industrial experiments of fight against VOC emissions, how to audit the facilities, how to make a diagnosis, to hierarchized and to measure continuously VOC emissions, how to anticipate the explosion risks linked with VOC treatment processes, the techniques of VOC abatement at the source implemented by industrialists, the implementation of an emission mastery scheme by Crow Cork and Seal company, the implementation of a solvent management plan by Turbomeca company and of a paints strategy by Renault car-making company, the combination of VOC abatement techniques implemented by industrialists, the classification of destruction and recovery processes: the experience feedback of Sanofi Synthelabo and of Air Liquide companies, the combination of upstream and downstream techniques implemented by Pechiney Rhenalu, Ashland Polyester and Quebecor companies. (J.S.)

Simulation of plume rise: Study the effect of stably stratified turbulence layer on the rise of a buoyant plume from a continuous source by observing the plume centroid

Science.gov (United States)

Bhimireddy, Sudheer Reddy; Bhaganagar, Kiran

2016-11-01

Buoyant plumes are common in atmosphere when there exists a difference in temperature or density between the source and its ambience. In a stratified environment, plume rise happens until the buoyancy variation exists between the plume and ambience. In a calm no wind ambience, this plume rise is purely vertical and the entrainment happens because of the relative motion of the plume with ambience and also ambient turbulence. In this study, a plume centroid is defined as the plume mass center and is calculated from the kinematic equation which relates the rate of change of centroids position to the plume rise velocity. Parameters needed to describe the plume are considered as the plume radius, plumes vertical velocity and local buoyancy of the plume. The plume rise velocity is calculated by the mass, momentum and heat conservation equations in their differential form. Our study focuses on the entrainment velocity, as it depicts the extent of plume growth. This entrainment velocity is made up as sum of fractions of plume's relative velocity and ambient turbulence. From the results, we studied the effect of turbulence on the plume growth by observing the variation in the plume radius at different heights and the centroid height reached before loosing its buoyancy.

Fire analog: a comparison between fire plumes and energy center cooling tower plumes

Energy Technology Data Exchange (ETDEWEB)

Orgill, M.M.

1977-10-01

Thermal plumes or convection columns associated with large fires are compared to thermal plumes from cooling towers and proposed energy centers to evaluate the fire analog concept. Energy release rates of mass fires are generally larger than for single or small groups of cooling towers but are comparable to proposed large energy centers. However, significant physical differences exist between cooling tower plumes and fire plumes. Cooling tower plumes are generally dominated by ambient wind, stability and turbulence conditions. Fire plumes, depending on burning rates and other factors, can transform into convective columns which may cause the fire behavior to become more violent. This transformation can cause strong inflow winds and updrafts, turbulence and concentrated vortices. Intense convective columns may interact with ambient winds to create significant downwind effects such as wakes and Karman vortex streets. These characteristics have not been observed with cooling tower plumes to date. The differences in physical characteristics between cooling tower and fire plumes makes the fire analog concept very questionable even though the approximate energy requirements appear to be satisfied in case of large energy centers. Additional research is suggested in studying the upper-level plume characteristics of small experimental fires so this information can be correlated with similar data from cooling towers. Numerical simulation of fires and proposed multiple cooling tower systems could also provide comparative data.

The use of sparge curtains for contaminant plume control

International Nuclear Information System (INIS)

Molnaa, B.; Dablow, J.

1994-01-01

Contamination by petroleum hydrocarbons and organic solvents represents a major impact to soil and groundwater. Following recent research and development, several technologies have evolved to treat saturated zone adsorbed- and dissolved-phase contaminants in situ. These technologies include bioremediation and air sparging. Funnel and gate approaches have been developed at the Waterloo Center for Groundwater Research to control contaminant plume migration and treat dissolved-phase contaminants before allowing migration downgradient and off site. The process consists of using low hydraulic conductivity cutoff walls to funnel groundwater flow through gates that contain in situ bioreactors. These systems can maintain hydraulic control and treat dissolved-phase contaminants at the downgradient margins of plumes, while minimizing, or in some cases eliminating, the need for groundwater pumping. Sparge curtains can be applied to treat dissolved-phase contaminants and prevent downgradient, off-site migration of contaminated groundwater

Diagnosis of aged prescribed burning plumes impacting an urban area.

Science.gov (United States)

Lee, Sangil; Kim, Hyeon K; Yan, Bo; Cobb, Charles E; Hennigan, Chris; Nichols, Sara; Chamber, Michael; Edgerton, Eric S; Jansen, John J; Hu, Yongtao; Zheng, Mei; Weber, Rodney J; Russell, Armistead G

2008-03-01

An unanticipated wind shift led to the advection of plumes from two prescribed burning sites that impacted Atlanta, GA, producing a heavy smoke event late in the afternoon on February 28, 2007. Observed PM2.5 concentrations increased to over 140 microg/m3 and O3 concentrations up to 30 ppb in a couple of hours, despite the late hour in February when photochemistry is less vigorous. A detailed investigation of PM2.5 chemical composition and source apportionment analysis showed that the increase in PM2.5 mass was driven mainly by organic carbon (OC). However, both results from source apportionment and an observed nonlinear relationship between OC and PM2.5 potassium (K) indicate that the increased OC was not due solely to primary emissions. Most of the OC was water-soluble organic carbon (WSOC) and was dominated by hydrophobic compounds. The data are consistent with large enhancements in isoprenoid (isoprene and monoterpenes) and other volatile organic compounds emitted from prescribed burning that led to both significant O3 and secondary organic aerosol (SOA) production. Formation of oligomers from oxidation products of isoprenoid compounds or condensation of volatile organic compounds (VOCs) with multiple functional groups emitted during prescribed burning appears to be a major component of the secondary organic contributor of the SOA. The results from this study imply that enhanced emissions due to the fire itself and elevated temperature in the burning region should be considered in air quality models (e.g., receptor and emission-based models) to assess impacts of prescribed burning emissions on ambient air quality.

Pulsed Corona Plasma Technology for Treating VOC Emissions from Pulp Mills

International Nuclear Information System (INIS)

Fridman, Alexander A.; Gutsol, Alexander; Kennedy, Lawrence A.; Saveliev, Alexei V.; Korobtsev, Sergey V.; Shiryaevsky, Valery L.; Medvedev, Dmitry

2004-01-01

Under the DOE Office of Industrial Technologies Forest Products program various plasma technologies were evaluated under project FWP 49885 ''Experimental Assessment of Low-Temperature Plasma Technologies for Treating Volatile Organic Compound Emissions from Pulp Mills and Wood Products Plants''. The heterogeneous pulsed corona discharge was chosen as the best non-equilibrium plasma technology for control of the vent emissions from HVLC Brownstock Washers. The technology for removal of Volatile Organic Compounds (VOCs) from gas emissions with conditions typical of the exhausts of the paper industry by means of pulsed corona plasma techniques presented in this work. For the compounds of interest in this study (methanol, acetone, dimethyl sulfide and ? -pinene), high removal efficiencies were obtained with power levels competitive with the present technologies for the VOCs removal. Laboratory experiments were made using installation with the average power up to 20 W. Pilot plant prepared for on-site test has average plasma power up to 6.4 kW. The model of the Pilot Plant operation is presented

Indoor air quality (IAQ) assessment in a multistorey shopping mall by high-spatial-resolution monitoring of volatile organic compounds (VOC).

Science.gov (United States)

Amodio, M; Dambruoso, P R; de Gennaro, Gianluigi; de Gennaro, L; Loiotile, A Demarinis; Marzocca, A; Stasi, F; Trizio, L; Tutino, M

2014-12-01

In order to assess indoor air quality (IAQ), two 1-week monitoring campaigns of volatile organic compounds (VOC) were performed in different areas of a multistorey shopping mall. High-spatial-resolution monitoring was conducted at 32 indoor sites located in two storehouses and in different departments of a supermarket. At the same time, VOC concentrations were monitored in the mall and parking lot area as well as outdoors. VOC were sampled at 48-h periods using diffusive samplers suitable for thermal desorption. The samples were then analyzed with gas chromatography-mass spectrometry (GC-MS). The data analysis and chromatic maps indicated that the two storehouses had the highest VOC concentrations consisting principally of terpenes. These higher TVOC concentrations could be a result of the low efficiency of the air exchange and intake systems, as well as the large quantity of articles stored in these small spaces. Instead, inside the supermarket, the food department was the most critical area for VOC concentrations. To identify potential emission sources in this department, a continuous VOC analyzer was used. The findings indicated that the highest total VOC concentrations were present during cleaning activities and that these activities were carried out frequently in the food department. The study highlights the importance of conducting both high-spatial-resolution monitoring and high-temporal-resolution monitoring. The former was able to identify critical issues in environments with a complex emission scenario while the latter was useful in interpreting the dynamics of each emission source.

Plume Mitigation for Mars Terminal Landing: Soil Stabilization Project

Science.gov (United States)

Hintze, Paul E.

2014-01-01

Kennedy Space Center (KSC) has led the efforts for lunar and Martian landing site preparation, including excavation, soil stabilization, and plume damage prediction. There has been much discussion of sintering but until our team recently demonstrated it for the lunar case there was little understanding of the serious challenges. Simplistic sintering creates a crumbly, brittle, weak surface unsuitable for a rocket exhaust plume. The goal of this project is to solve those problems and make it possible to land a human class lander on Mars, making terminal landing of humans on Mars possible for the first time.

Modeling the uncertainty of several VOC and its impact on simulated VOC and ozone in Houston, Texas

Science.gov (United States)

Pan, Shuai; Choi, Yunsoo; Roy, Anirban; Li, Xiangshang; Jeon, Wonbae; Souri, Amir Hossein

2015-11-01

A WRF-SMOKE-CMAQ modeling system was used to study Volatile Organic Compound (VOC) emissions and their impact on surface VOC and ozone concentrations in southeast Texas during September 2013. The model was evaluated against the ground-level Automated Gas Chromatograph (Auto-GC) measurement data from the Texas Commission on Environmental Quality (TCEQ). The comparisons indicated that the model over-predicted benzene, ethylene, toluene and xylene, while under-predicting isoprene and ethane. The mean biases between simulated and observed values of each VOC species showed clear daytime, nighttime, weekday and weekend variations. Adjusting the VOC emissions using simulated/observed ratios improved model performance of each VOC species, especially mitigating the mean bias substantially. Simulated monthly mean ozone showed a minor change: a 0.4 ppb or 1.2% increase; while a change of more than 5 ppb was seen in hourly ozone data on high ozone days, this change moved model predictions closer to observations. The CMAQ model run with the adjusted emissions better reproduced the variability in the National Aeronautics and Space Administration (NASA)'s Ozone Monitoring Instrument (OMI) formaldehyde (HCHO) columns. The adjusted model scenario also slightly better reproduced the aircraft HCHO concentrations from NASA's DISCOVER-AQ campaign conducted during the simulation episode period; Correlation, Mean Bias and RMSE improved from 0.34, 1.38 ppb and 2.15 ppb to 0.38, 1.33 ppb and 2.08 ppb respectively. A process analysis conducted for both industrial/urban and rural areas suggested that chemistry was the main process contributing to ozone production in both areas, while the impact of chemistry was smaller in rural areas than in industrial and urban areas. For both areas, the positive chemistry contribution increased in the sensitivity simulation largely due to the increase in emissions. Nudging VOC emissions to match the observed concentrations shifted the ozone hotspots

Photochemical processing of organic aerosol at nearby continental sites: contrast between urban plumes and regional aerosol

Science.gov (United States)

Slowik, J. G.; Brook, J.; Chang, R. Y.-W.; Evans, G. J.; Hayden, K.; Jeong, C.-H.; Li, S.-M.; Liggio, J.; Liu, P. S. K.; McGuire, M.; Mihele, C.; Sjostedt, S.; Vlasenko, A.; Abbatt, J. P. D.

2011-03-01

As part of the BAQS-Met 2007 field campaign, Aerodyne time-of-flight aerosol mass spectrometers (ToF-AMS) were deployed at two sites in southwestern Ontario from 17 June to 11 July 2007. One instrument was located at Harrow, ON, a rural, agriculture-dominated area approximately 40 km southeast of the Detroit/Windsor/Windsor urban area and 5 km north of Lake Erie. The second instrument was located at Bear Creek, ON, a rural site approximately 70 km northeast of the Harrow site and 50 km east of Detroit/Windsor. Positive matrix factorization analysis of the combined organic mass spectral dataset yields factors related to secondary organic aerosol (SOA), direct emissions, and a factor tentatively attributed to the reactive uptake of isoprene and/or condensation of its early generation reaction products. This is the first application of PMF to simultaneous AMS measurements at different sites, an approach which allows for self-consistent, direct comparison of the datasets. Case studies are utilized to investigate processing of SOA from (1) fresh emissions from Detroit/Windsor and (2) regional aerosol during periods of inter-site flow. A strong correlation is observed between SOA/excess CO and photochemical age as represented by the NOx/NOy ratio for Detroit/Windsor outflow. Although this correlation is not evident for more aged air, measurements at the two sites during inter-site transport nevertheless show evidence of continued atmospheric processing by SOA production. However, the rate of SOA production decreases with airmass age from an initial value of ~10.1 μg m-3 ppmvCO-1 h-1 for the first ~10 h of plume processing to near-zero in an aged airmass (i.e. after several days). The initial SOA production rate is comparable to the observed rate in Mexico City over similar timescales.

In situ treatment of VOCs by recirculation technologies

International Nuclear Information System (INIS)

Siegrist, R.L.; Webb, O.F.; Ally, M.R.; Sanford, W.E.; Kearl, P.M.; Zutman, J.L.

1993-06-01

The project described herein was conducted by Oak Ridge National Laboratory (ORNL) to identify processes and technologies developed in Germany that appeared to have near-term potential for enhancing the cleanup of volatile organic compound (VOC) contaminated soil and groundwater at DOE sites. Members of the ORNL research team identified and evaluated selected German technologies developed at or in association with the University of Karlsruhe (UoK) for in situ treatment of VOC contaminated soils and groundwater. Project activities included contacts with researchers within three departments of the UoK (i.e., Applied Geology, Hydromechanics, and Soil and Foundation Engineering) during fall 1991 and subsequent visits to UoK and private industry collaborators during February 1992. Subsequent analyses consisted of engineering computations, groundwater flow modeling, and treatment process modeling. As a result of these project efforts, two processes were identified as having near-term potential for DOE: (1) the vacuum vaporizer well/groundwater recirculation well and (2) the porous pipe/horizontal well. This document was prepared to summarize the methods and results of the assessment activities completed during the initial year of the project. The project is still ongoing, so not all facets of the effort are completely described in this document. Recommendations for laboratory and field experiments are provided

In situ treatment of VOCs by recirculation technologies

Energy Technology Data Exchange (ETDEWEB)

Siegrist, R.L.; Webb, O.F.; Ally, M.R.; Sanford, W.E. [Oak Ridge National Lab., TN (US); Kearl, P.M.; Zutman, J.L. [Oak Ridge National Lab., Grand Junction, CO (US)

1993-06-01

The project described herein was conducted by Oak Ridge National Laboratory (ORNL) to identify processes and technologies developed in Germany that appeared to have near-term potential for enhancing the cleanup of volatile organic compound (VOC) contaminated soil and groundwater at DOE sites. Members of the ORNL research team identified and evaluated selected German technologies developed at or in association with the University of Karlsruhe (UoK) for in situ treatment of VOC contaminated soils and groundwater. Project activities included contacts with researchers within three departments of the UoK (i.e., Applied Geology, Hydromechanics, and Soil and Foundation Engineering) during fall 1991 and subsequent visits to UoK and private industry collaborators during February 1992. Subsequent analyses consisted of engineering computations, groundwater flow modeling, and treatment process modeling. As a result of these project efforts, two processes were identified as having near-term potential for DOE: (1) the vacuum vaporizer well/groundwater recirculation well and (2) the porous pipe/horizontal well. This document was prepared to summarize the methods and results of the assessment activities completed during the initial year of the project. The project is still ongoing, so not all facets of the effort are completely described in this document. Recommendations for laboratory and field experiments are provided.

Reducing VOC Press Emission from OSB Manufacturing

Energy Technology Data Exchange (ETDEWEB)

Dr. Gary D. McGinnis; Laura S. WIlliams; Amy E. Monte; Jagdish Rughani: Brett A. Niemi; Thomas M. Flicker

2001-12-31

Current regulations require industry to meet air emission standards with regard to particulates, volatile organic compounds (VOCs), hazardous air pollutants (HAPs) and other gases. One of many industries that will be affected by the new regulations is the wood composites industry. This industry generates VOCs, HAPs, and particulates mainly during the drying and pressing of wood. Current air treatment technologies for the industry are expensive to install and operate. As regulations become more stringent, treatment technologies will need to become more efficient and cost effective. The overall objective of this study is to evaluate the use of process conditions and chemical additives to reduce VOC/HAPs in air emitted from presses and dryers during the production of oriented strand board.

Chemical evolution of volatile organic compounds in the outflow of the Mexico City Metropolitan area

Energy Technology Data Exchange (ETDEWEB)

Apel, Eric; Emmons, L.; Karl, Thomas G.; Flocke, Frank M.; Hills, A. J.; Madronich, Sasha; Lee-Taylor, J.; Fried, Alan; Weibring, P.; Walega, J.; Richter, Dirk; Tie, X.; Mauldin, L.; Campos, Teresa; Weinheimer, Andrew J.; Knapp, David; Sive, B.; Kleinman, Lawrence I.; Springston, S.; Zaveri, Rahul A.; Ortega, John V.; Voss, Paul B.; Blake, D. R.; Baker, Angela K.; Warneke, Carsten; Welsh-Bon, Daniel; de Gouw, Joost A.; Zheng, J.; Zhang, Renyi; Rudolph, Jochen; Junkermann, W.; Riemer, D.

2010-01-01

reactivity in the downwind plume. The model results generally showed good agreement with experimental results for the total VOC OH reactivity downwind and gave insight into the distributions of VOC chemical classes downwind. A box model with detailed gas phase chemistry (NCAR Master Mechanism), initialized with concentrations observed at one of the ground sites in the MCMA, was used to examine the expected evolution of specific VOCs over a 1-2 day period. The models clearly supported the experimental evidence for NMHC oxidation leading to the formation of OVOCs downwind, which then become the primary fuel for ozone production far away from the MCMA.

Chemical evolution of volatile organic compounds in the outflow of the Mexico City Metropolitan area

Energy Technology Data Exchange (ETDEWEB)

Apel, E.; Springston, S.; Karl, T.; Emmons, L.; Flocke, F.; Hills, A. J.; Madronich, S.; Lee-Taylor, J.; Fried, A.; Weibring, P.; Walega, J.; Richter, D., Tie, X.; Mauldin, L.; Campos, T.; Sive, B.; Kleinman, L.; Springston, S., Zaveri, R.; deGouw, J.; Zheng, J.; Zhang, R.; Rudolph, J.; Junkermann, W.; Riemer, D. D.

2009-11-01

reactivity in the downwind plume. The model results generally showed good agreement with experimental results for the total VOC OH reactivity downwind and gave insight into the distributions of VOC chemical classes downwind. A box model with detailed gas phase chemistry (NCAR Master Mechanism), initialized with concentrations observed at one of the ground sites in the MCMA, was used to examine the expected evolution of specific VOCs over a 1-2 day period. The models clearly supported the experimental evidence for NMHC oxidation leading to the formation of OVOCs downwind, which then become the primary fuel for ozone production far away from the MCMA.

PTR-MS in environmental research: biogenic VOCs

International Nuclear Information System (INIS)

Beauchamp, J.; Grabmer, W.; Graus, M.; Wisthaler, A.; Hansel, A.

2004-01-01

Proton-transfer-reaction mass spectrometry (PTR-MS) is a chemical ionization mass spectrometry technique that allows for on-line measurements of volatile organic compounds (VOCs) at pptV levels. This well established analytical tool has been used in a broad variety of research, including the investigation of VOCs in various foods (e.g. for quality control or food degradation studies), as well as being used as a tool for non-invasive medical diagnostics (e.g. human breath analysis). In addition to these fields of study, PTR-MS has been widely used in environmental research, from trace gas analysis in the troposphere to VOC emissions from plants. Participation in two field campaigns (BEWA and ECHO - both part of the German AFO 2000 program) by the Institute of Ion Physics involved a variety of investigations for monitoring biogenic emissions. These included the technique of disjunct eddy covariance for flux measurements above a forest canopy, C-13 carbon labelling experiments to follow carbon use in a plant, and stress-induced VOC emission investigations to gain understanding of how plants react to stress (e.g. ozone exposure). A selection of results from these investigations will be discussed in this presentation. (author)

Modelling tools for integrating geological, geophysical and contamination data for characterization of groundwater plumes

DEFF Research Database (Denmark)

Balbarini, Nicola

the contaminant plume in a shallow and a deep plume. These plumes have different chemical characteristics and different migration paths to the stream. This has implications for the risk assessment of the stream and groundwater in the area. The difficulty of determining groundwater flow paths means that it is also...... receptors, including streams. Key risk assessment parameters, such as contaminant mass discharge estimates, and tools are then used to evaluate the risk. The cost of drilling often makes investigations of large and/or deep contaminant plumes unfeasible. For this reason, it is important to develop cost...... organic compounds, including pharmaceutical compounds and chlorinated ethenes. The correlation between DCIP and organic compounds is indirect and depends on the chemical composition of the contaminant plume and the transport processes. Thus, the correlations are site specific and may change between...

Application of ion chemistry to tropospheric VOC measurements

International Nuclear Information System (INIS)

Hansel, A.; Wisthaler, A.; Graus, M.; Grabmer, W.

2002-01-01

The main interest in tropospheric volatile organic compounds (VOCs) originating from biogenic sources such as forests and anthropogenic sources such as cities is because these reactive trace gases can have a significant impact on levels of oxidants such as ozone (O 3 ) and the hydroxyl radical (OH). The proton-transfer-reaction mass-spectrometry (PTR-MS) technique developed by Werner Lindingers Laboratory, utilizes positive ion chemistry to measure trace neutral concentrations in air. It has been applied in food research, medicine and environmental studies to gain gas phase information about VOCs at parts per trillion (pptv) levels.The real-time method relies on proton transfer reactions between H 3 O + primary ions and VOCs which have a higher proton affinity than water molecules. Organic trace gases such as hydrocarbons, carbonyls, alcohols, acetonitrile, and others can be monitored on-line.Results on tropospheric VOCs measurements in tropical regions and in cities are discussed. (nevyjel)

Monitoring and forecasting Etna volcanic plumes

Directory of Open Access Journals (Sweden)

S. Scollo

2009-09-01

Full Text Available In this paper we describe the results of a project ongoing at the Istituto Nazionale di Geofisica e Vulcanologia (INGV. The objective is to develop and implement a system for monitoring and forecasting volcanic plumes of Etna. Monitoring is based at present by multispectral infrared measurements from the Spin Enhanced Visible and Infrared Imager on board the Meteosat Second Generation geosynchronous satellite, visual and thermal cameras, and three radar disdrometers able to detect ash dispersal and fallout. Forecasting is performed by using automatic procedures for: i downloading weather forecast data from meteorological mesoscale models; ii running models of tephra dispersal, iii plotting hazard maps of volcanic ash dispersal and deposition for certain scenarios and, iv publishing the results on a web-site dedicated to the Italian Civil Protection. Simulations are based on eruptive scenarios obtained by analysing field data collected after the end of recent Etna eruptions. Forecasting is, hence, supported by plume observations carried out by the monitoring system. The system was tested on some explosive events occurred during 2006 and 2007 successfully. The potentiality use of monitoring and forecasting Etna volcanic plumes, in a way to prevent threats to aviation from volcanic ash, is finally discussed.

Sulfate Reduction Remediation of a Metals Plume Through Organic Injection

International Nuclear Information System (INIS)

Phifer, M.A.

2003-01-01

Laboratory testing and a field-scale demonstration for the sulfate reduction remediation of an acidic/metals/sulfate groundwater plume at the Savannah River Site has been conducted. The laboratory testing consisted of the use of anaerobic microcosms to test the viability of three organic substrates to promote microbially mediated sulfate reduction. Based upon the laboratory testing, soybean oil and sodium lactate were selected for injection during the subsequent field-scale demonstration. The field-scale demonstration is currently ongoing. Approximately 825 gallons (3,123 L) of soybean oil and 225 gallons (852 L) of 60 percent sodium lactate have been injected into an existing well system within the plume. Since the injections, sulfate concentrations in the injection zone have significantly decreased, sulfate-reducing bacteria concentrations have significantly increased, the pH has increased, the Eh has decreased, and the concentrations of many metals have decreased. Microbially mediated sulfate reduction has been successfully promoted for the remediation of the acidic/metals/sulfate plume by the injection of soybean oil and sodium lactate within the plume

Measurements of VOC adsorption/desorption characteristics of typical interior building materials

Energy Technology Data Exchange (ETDEWEB)

An, Y.; Zhang, J.S.; Shaw, C.Y.

2000-07-01

The adsorption/desorption of volatile organic compounds (VOCs) on interior building material surfaces (i.e., the sink effect) can affect the VOC concentrations in a building, and thus need to be accounted for an indoor air quality (IAQ) prediction model. In this study, the VOC adsorption/desorption characteristics (sink effect) were measured for four typical interior building materials including carpet, vinyl floor tile, painted drywall, and ceiling tile. The VOCs tested were ethylbenzene, cyclohexanone, 1,4-dichlorobenzene, benzaldehyde, and dodecane. These five VOCs were selected because they are representative of hydrocarbons, aromatics, ketones, aldehydes, and chlorine substituted compounds. The first order reversible adsorption/desorption model was based on the Langmuir isotherm was used to analyze the data and to determine the equilibrium constant of each VOC-material combination. It was found that the adsorption/desorption equilibrium constant, which is a measure of the sink capacity, increased linearly with the inverse of the VOC vapor pressure. For each compound, the adsorption/desorption equilibrium constant, and the adsorption rate constant differed significantly among the four materials tested. A detailed characterization of the material structure in the micro-scale would improve the understanding and modeling of the sink effect in the future. The results of this study can be used to estimate the impact of sink effect on the VOC concentrations in buildings.

Seismic Imaging of Mantle Plumes

Science.gov (United States)

Nataf, Henri-Claude

The mantle plume hypothesis was proposed thirty years ago by Jason Morgan to explain hotspot volcanoes such as Hawaii. A thermal diapir (or plume) rises from the thermal boundary layer at the base of the mantle and produces a chain of volcanoes as a plate moves on top of it. The idea is very attractive, but direct evidence for actual plumes is weak, and many questions remain unanswered. With the great improvement of seismic imagery in the past ten years, new prospects have arisen. Mantle plumes are expected to be rather narrow, and their detection by seismic techniques requires specific developments as well as dedicated field experiments. Regional travel-time tomography has provided good evidence for plumes in the upper mantle beneath a few hotspots (Yellowstone, Massif Central, Iceland). Beneath Hawaii and Iceland, the plume can be detected in the transition zone because it deflects the seismic discontinuities at 410 and 660 km depths. In the lower mantle, plumes are very difficult to detect, so specific methods have been worked out for this purpose. There are hints of a plume beneath the weak Bowie hotspot, as well as intriguing observations for Hawaii. Beneath Iceland, high-resolution tomography has just revealed a wide and meandering plume-like structure extending from the core-mantle boundary up to the surface. Among the many phenomena that seem to take place in the lowermost mantle (or D''), there are also signs there of the presence of plumes. In this article I review the main results obtained so far from these studies and discuss their implications for plume dynamics. Seismic imaging of mantle plumes is still in its infancy but should soon become a turbulent teenager.

Tree Sampling as a Method to Assess Vapor Intrusion Potential at a Site Characterized by VOC-Contaminated Groundwater and Soil.

Science.gov (United States)

Wilson, Jordan L; Limmer, Matthew A; Samaranayake, V A; Schumacher, John G; Burken, Joel G

2017-09-19

Vapor intrusion (VI) by volatile organic compounds (VOCs) in the built environment presents a threat to human health. Traditional VI assessments are often time-, cost-, and labor-intensive; whereas traditional subsurface methods sample a relatively small volume in the subsurface and are difficult to collect within and near structures. Trees could provide a similar subsurface sample where roots act as the "sampler' and are already onsite. Regression models were developed to assess the relation between PCE concentrations in over 500 tree-core samples with PCE concentrations in over 50 groundwater and 1000 soil samples collected from a tetrachloroethylene- (PCE-) contaminated Superfund site and analyzed using gas chromatography. Results indicate that in planta concentrations are significantly and positively related to PCE concentrations in groundwater samples collected at depths less than 20 m (adjusted R 2 values greater than 0.80) and in soil samples (adjusted R 2 values greater than 0.90). Results indicate that a 30 cm diameter tree characterizes soil concentrations at depths less than 6 m over an area of 700-1600 m 2 , the volume of a typical basement. These findings indicate that tree sampling may be an appropriate method to detect contamination at shallow depths at sites with VI.

Tree sampling as a method to assess vapor intrusion potential at a site characterized by VOC-contaminated groundwater and soil

Science.gov (United States)

Wilson, Jordan L.; Limmer, Matthew A.; Samaranayake, V. A.; Schumacher, John G.; Burken, Joel G.

2017-01-01

Vapor intrusion (VI) by volatile organic compounds (VOCs) in the built environment presents a threat to human health. Traditional VI assessments are often time-, cost-, and labor-intensive; whereas traditional subsurface methods sample a relatively small volume in the subsurface and are difficult to collect within and near structures. Trees could provide a similar subsurface sample where roots act as the “sampler’ and are already onsite. Regression models were developed to assess the relation between PCE concentrations in over 500 tree-core samples with PCE concentrations in over 50 groundwater and 1000 soil samples collected from a tetrachloroethylene- (PCE-) contaminated Superfund site and analyzed using gas chromatography. Results indicate that in planta concentrations are significantly and positively related to PCE concentrations in groundwater samples collected at depths less than 20 m (adjusted R2 values greater than 0.80) and in soil samples (adjusted R2 values greater than 0.90). Results indicate that a 30 cm diameter tree characterizes soil concentrations at depths less than 6 m over an area of 700–1600 m2, the volume of a typical basement. These findings indicate that tree sampling may be an appropriate method to detect contamination at shallow depths at sites with VI.

Plume Mitigation: Soil Erosion and Lunar Prospecting Sensor Project

Science.gov (United States)

Metzger, Philip T.

2014-01-01

Demonstrate feasibility of the simplest, lowest-mass method of measuring density of a cloud of lunar soil ejected by rocket exhaust, using new math techniques with a small baseline laser/camera system. Focus is on exploring the erosion process that occurs when the exhaust plume of a lunar rocket impacts the regolith. Also, predicting the behavior of the lunar soil that would be blasted from a lunar landing/launch site shall assist in better design and protection of any future lunar settlement from scouring of structures and equipment. NASA is gathering experimental data to improve soil erosion models and understand how lunar particles enter the plume flow.

Investigation of Contaminated Groundwater at Solid Waste Management Unit 12, Naval Weapons Station Charleston, North Charleston, South Carolina, 2008

Science.gov (United States)

Vroblesky, Don A.; Petkewich, Matthew D.

2009-01-01

The U.S. Geological Survey and the Naval Facilities Engineering Command Southeast investigated natural and engineered remediation of chlorinated volatile organic compound (VOC) groundwater contamination at Solid Waste Management Unit 12 at the Naval Weapons Station Charleston, North Charleston, South Carolina, beginning in 2000. The primary contaminants of interest in the study are tetrachloroethene, 1,1,1-trichloroethane, trichloroethene, cis-1,2-dichloroethene, vinyl chloride, 1,1-dichloroethane, and 1,1-dichloroethene. Engineered remediation aspects at the site consist of a zero-valent-iron permeable reactive barrier (PRB) installed in December 2002 intercepting the contamination plume and a phytoremediation test stand of loblolly pine trees planted in the source area in May 2003. The U.S. Geological Survey planted an additional phytoremediation test stand of loblolly pine trees on the upgradient side of the southern end of the PRB in February 2008. At least once during the summer, however, the trees were inadvertently mowed during lawn cutting activity. The PRB along the main axis of the contaminant plume appears to be actively removing contamination. In contrast to the central area of the PRB, the data from the southern end of the PRB indicate that contaminants are moving around the PRB. Concentrations in wells upgradient from the PRB showed a general decrease in VOC concentrations. VOC concentrations in some wells in the forest downgradient from the PRB showed a sharp increase in 2005, followed by a decrease in 2006. Farther downgradient in the forest, the VOC concentrations began to increase in 2007 and continued to increase into 2008. The VOC-concentration changes in groundwater beneath the forest appear to indicate movement of a groundwater-contaminant pulse through the forest. It also is possible that the data may represent lateral shifting of the plume in response to changes in groundwater-flow direction.

Model Intercomparison Study to Investigate a Dense Contaminant Plume in a Complex Hydrogeologic System

International Nuclear Information System (INIS)

Williams, Mark D.; Cole, Charles R.; Foley, Michael G.; Zinina, Galina A.; Zinin, Alexander I.; Vasil'Kova, Nelly A.; Samsonova, Lilia M.

2001-01-01

A joint Russian and U.S. model intercomparison study was undertaken for developing more realistic contaminant transport models of the Mayak Site, Southern Urals. The test problems were developed by the Russian Team based on their experience modeling contaminant migration near Lake Karachai. The intercomparison problems were designed to address lake and contaminant plume interactions, as well as river interactions and plume density effects. Different numerical codes were used. Overall there is good agreement between the results of both models. Features shown by both models include (1) the sinking of the plume below the lake, (2) the raising of the water table in the fresh water adjacent to the lake in response to the increased pressure from the dense plume, and (3) the formation of a second sinking plume in an area where evapotranspiration exceeded infiltration, thus increasing the solute concentrations above the source (i.e., lake) values

Ionic liquid technology to recover volatile organic compounds (VOCs).

Science.gov (United States)

Salar-García, M J; Ortiz-Martínez, V M; Hernández-Fernández, F J; de Los Ríos, A P; Quesada-Medina, J

2017-01-05

Volatile organic compounds (VOCs) comprise a wide variety of carbon-based materials which are volatile at relatively low temperatures. Most of VOCs pose a hazard to both human health and the environment. For this reason, in the last years, big efforts have been made to develop efficient techniques for the recovery of VOCs produced from industry. The use of ionic liquids (ILs) is among the most promising separation technologies in this field. This article offers a critical overview on the use of ionic liquids for the separation of VOCs both in bulk and in immobilized form. It covers the most relevant works within this field and provides a global outlook on the limitations and future prospects of this technology. The extraction processes of VOCs by using different IL-based assemblies are described in detail and compared with conventional methods This review also underlines the advantages and limitations posed by ionic liquids according to the nature of the cation and the anions present in their structure and the stability of the membrane configurations in which ILs are used as liquid phase. Copyright © 2016 Elsevier B.V. All rights reserved.

A buoyant plume adjacent to a headland-Observations of the Elwha River plume

Science.gov (United States)

Warrick, J.A.; Stevens, A.W.

2011-01-01

Small rivers commonly discharge into coastal settings with topographic complexities - such as headlands and islands - but these settings are underrepresented in river plume studies compared to more simplified, straight coasts. The Elwha River provides a unique opportunity to study the effects of coastal topography on a buoyant plume, because it discharges into the Strait of Juan de Fuca on the western side of its deltaic headland. Here we show that this headland induces flow separation and transient eddies in the tidally dominated currents (O(100. cm/s)), consistent with other headlands in oscillatory flow. These flow conditions are observed to strongly influence the buoyant river plume, as predicted by the "small-scale" or "narrow" dynamical classification using Garvine's (1995) system. Because of the transient eddies and the location of the river mouth on the headland, flow immediately offshore of the river mouth is directed eastward twice as frequently as it is westward. This results in a buoyant plume that is much more frequently "bent over" toward the east than the west. During bent over plume conditions, the plume was attached to the eastern shoreline while having a distinct, cuspate front along its westernmost boundary. The location of the front was found to be related to the magnitude and direction of local flow during the preceding O(1. h), and increases in alongshore flow resulted in deeper freshwater mixing, stronger baroclinic anomalies, and stronger hugging of the coast. During bent over plume conditions, we observed significant convergence of river plume water toward the frontal boundary within 1. km of the river mouth. These results show how coastal topography can strongly influence buoyant plume behavior, and they should assist with understanding of initial coastal sediment dispersal pathways from the Elwha River during a pending dam removal project. ?? 2010.

Geochemical evolution of highly alkaline and saline tank waste plumes during seepage through vadose zone sediments

International Nuclear Information System (INIS)

Wan, Jiamin; Tokunaga, Tetsu K.; Larsen, Joern T.; Serne, R. JEFFREY

2004-01-01

Leakage of highly saline and alkaline radioactive waste from storage tanks into underlying sediments is a serious environmental problem at the Hanford Site in Washington State. This study focuses on geochemical evolution of tank waste plumes resulting from interactions between the waste solution and sediment. A synthetic tank waste solution was infused into unsaturated Hanford sediment columns (0.2, 0.6, and 2 m) maintained at 70C to simulate the field contamination process. Spatially and temporally resolved geochemical profiles of the waste plume were obtained. Thorough OH neutralization (from an initial pH 14 down to 6.3) was observed. Three broad zones of pore solutions were identified to categorize the dominant geochemical reactions: the silicate dissolution zone (pH > 10), pH-neutralized zone (pH 10 to 6.5), and displaced native sediment pore water (pH 6.5 to 8). Elevated concentrations of Si, Fe, and K in plume fluids and their depleted concentrations in plume sediments reflected dissolution of primary minerals within the silicate dissolution zone. The very high Na concentrations in the waste solution resulted in rapid and complete cation exchange, reflected in high concentrations of Ca and Mg at the plume front. The plume-sediment profiles also showed deposition of hydrated solids and carbonates. Fair correspondence was obtained between these results and analyses of field borehole samples from a waste plume at the Hanford Site. Results of this study provide a well-defined framework for understanding waste plumes in the more complex field setting and for understanding geochemical factors controlling transport of contaminant species carried in waste solutions that leaked from single-shell storage tanks in the past

Flux measurement of methanol, acetaldehyde and other oxygenated VOCs from crop harvesting using proton-transfer-reaction mass spectrometry and surface layer gradient method

International Nuclear Information System (INIS)

Lindinger, C.; Jordan, A.; Karl, T.; Guenther, A.; Tschiersch, J.; Ruckerbauer, F.; Paretzke, H.

2002-01-01

PTR-MS technique was used to measure fluxes of various VOC's including oxygenates using surface layer gradient method. The VOC concentrations and temperature were measured at heights of about 0.5 m and 3.9 m above ground at field site in St. Johann in Tirol during and after grass cutting (24th and 25th of May 2000) in order to calculate fluxes. The sensible heat flux was obtained by a sonic anemometer with turbulence data analyzer. The major crop in this part of Austria are perennial grasses used for livestock farming. We observed VOC emission fluxes including methanol and acetaldehyde as the major volatile, C 5 and C 6 leaf wound compounds with lesser amounts and traces of acetone and butanone. This composition of VOC's is very similar to that released from slashed pasture grass. At the same time, VOC fluxes were measured with PTR-MS and eddy covariance method. Comparing the flux data of methanol and acetaldehyde of both days have shown very similar results. (author)

Characteristics of bubble plumes, bubble-plume bubbles and waves from wind-steepened wave breaking

NARCIS (Netherlands)

Leifer, I.; Caulliez, G.; Leeuw, G. de

2007-01-01

Observations of breaking waves, associated bubble plumes and bubble-plume size distributions were used to explore the coupled evolution of wave-breaking, wave properties and bubble-plume characteristics. Experiments were made in a large, freshwater, wind-wave channel with mechanical wind-steepened

Measurements at cooling tower plumes. Part 3. Three-dimensional measurements at cooling tower plumes

International Nuclear Information System (INIS)

Fortak, H.

An extended field experiment is described in which cooling tower plumes were studied by means of three-dimensional in situ measurements. The goal was to obtain input data for numerical models of cooling tower plumes. Of special interest were data for testing or developing assumptions for sub-grid parametrizations. Utilizing modern systems for high-resolution aerology and small aircraft, four measuring campaigns were conducted: two campaigns (1974) at the cooling towers of the RWE power station Neurath and also two (1975) at the single cooling tower of the RWE power station Meppen. Because of the broad spectrum of weather situations it can be assumed that the results are representative with regard to the interrelationship between structure of cooling tower plume and large-scale meteorological situation. A large number of flights with a powered glider crossing the plumes on orthogonal tracks was performed. All flights showed that the plume could be identified up to large downwind distances by discontinuous jumps of temperature and vapor pressure. Therefore, a definite geometry of the plume could always be defined. In all cross sections a vertical circulation could be observed. At the boundary, which could be defined by the mentioned jumps of temperature and vapor pressure, a maximum of downward vertical motion could be observed in most cases. Entrainment along the boundary of a cross section seems to be very small, except at the lower part of the plume. There, the mass entrainment is maximum and is responsible for plume rise as well as for enlargement of the cross section. The visible part of the plume (cloud) was only a small fraction of the whole plume. High-resolution aerology is necessary in order to explain the structure and behavior of such plumes. This is especially the case in investigations regarding the dynamic break-through of temperature inversions. Such cases were observed frequently under various meteorological conditions and are described

ASSESSING AEROBIC NATURAL ATTENUATION OF TRICHLOROETHENE AT FOUR DOE SITES

International Nuclear Information System (INIS)

Koelsch, Michael C.; Starr, Robert C.; Sorenson, Kent S. Jr.

2005-01-01

A 3-year Department of Energy Environmental Science Management Program (EMSP) project is currently investigating natural attenuation of trichloroethane (TCE) in aerobic groundwater. This presentation summarizes the results of a screening process to identify TCE plumes at DOE facilities that are suitable for assessing the rate of TCE cometabolism under aerobic conditions. In order to estimate aerobic degradation rates, plumes had to meet the following criteria: TCE must be present in aerobic groundwater, a conservative co-contaminant must be present and have approximately the same source as TCE, and the groundwater velocity must be known. A total of 127 TCE plumes were considered across 24 DOE sites. The four sites retained for the assessment were: (1) Brookhaven National Laboratory, OU III; (2) Paducah Gaseous Diffusion Plant, Northwest Plume; (3) Rocky Flats Environmental Technology Site, Industrialized Area--Southwest Plume and 903 Pad South Plume; and (4) Savannah River Site, A/M Area Plume. For each of these sites, a co-contaminant derived from the same source area as TCE was used as a nonbiodegrading tracer. The tracer determined the extent to which concentration decreases in the plume can be accounted for solely by abiotic processes such as dispersion and dilution. Any concentration decreases not accounted for by these processes must be explained by some other natural attenuation mechanism. Thus, ''half-lives'' presented herein are in addition to attenuation that occurs due to hydrologic mechanisms. This ''tracer-corrected method'' has previously been used at the DOE's Idaho National Engineering and Environmental Laboratory in conjunction with other techniques to document the occurrence of intrinsic aerobic cometabolism. Application of this method to other DOE sites is the first step to determining whether this might be a significant natural attenuation mechanism on a broader scale. Application of the tracer-corrected method to data from the Brookhaven

Ozone, OH and NO3 sink terms at a coniferous forest site in Central Germany: Role of biogenic VOCs

Science.gov (United States)

Bonn, B.; Bourtsoukidis, S.; Haunold, W.; Sitals, R.; Jacobi, S.

2012-04-01

Oxidation capacities of ecosystems are important to facilitate an ecosystem feedback on oxidation stress and in order to survive. We have conducted seasonal ambient measurements of a series of biogenic VOCs using a plant enclosure technique and determined the ambient levels of ozone, NOx as well as basic meteorological parameters at a managed spruce forest site in Central Germany (Mt. Kleiner Feldberg). The site is 810 m a.s.l. and faces distinct anthropogenic contributions from the Rhine-Main-area including the airport and major traffic routes in from the southeast. The opposite direction is moderately polluted and can be classified as Central German background condition. Since atmospheric chemistry and pollutants become very important especially for this site, which is the most polluted one in Germany with respect to ozone we approximated the sink terms for the atmospheric oxidation agents of interest at this site, i.e ozone, OH and NO3 using the measurements and box model steady state calculations for intermediate species not measured directly between the first of April and the start of November 2011. BVOC measurements were obtained with PTR-MS every 36 s and averaged for 30 min intervals afterwards to facilitate the inclusion of the monitoring data of the Hessian Agency for the Environment and Geology (HLUG) in Wiesbaden, Germany: temperature, humidity, global radiation, ozone and NOx. Analysis was performed with Matlab (Mathworks Inc.) and included the gas-phase chemistry set-up described by the Master Chemical Mechanism (MCM, v3, [1]). This resulted in the following outcome for sinks of oxidants: Ozone: Significant contributions were found for mono- and sesquiterpenes as well as for NOx. The individual contributions vary notably with the time of the day and the year and the emission strength of biogenic VOCs. Especially for the early season in April sesquiterpene reactions dominated the sink by up to 80% during nighttime, while NOx reactions dominated the

On predicting mantle mushroom plumes

Directory of Open Access Journals (Sweden)

Ka-Kheng Tan

2011-04-01

Top cooling may produce plunging plumes of diameter of 585 km and at least 195 Myr old. The number of cold plumes is estimated to be 569, which has not been observed by seismic tomography or as cold spots. The cold plunging plumes may overwhelm and entrap some of the hot rising plumes from CMB, so that together they may settle in the transition zone.

Air exchange rates and migration of VOCs in basements and residences.

Science.gov (United States)

Du, L; Batterman, S; Godwin, C; Rowe, Z; Chin, J-Y

2015-12-01

Basements can influence indoor air quality by affecting air exchange rates (AERs) and by the presence of emission sources of volatile organic compounds (VOCs) and other pollutants. We characterized VOC levels, AERs, and interzonal flows between basements and occupied spaces in 74 residences in Detroit, Michigan. Flows were measured using a steady-state multitracer system, and 7-day VOC measurements were collected using passive samplers in both living areas and basements. A walk-through survey/inspection was conducted in each residence. AERs in residences and basements averaged 0.51 and 1.52/h, respectively, and had strong and opposite seasonal trends, for example, AERs were highest in residences during the summer, and highest in basements during the winter. Airflows from basements to occupied spaces also varied seasonally. VOC concentration distributions were right-skewed, for example, 90th percentile benzene, toluene, naphthalene, and limonene concentrations were 4.0, 19.1, 20.3, and 51.0 μg/m(3), respectively; maximum concentrations were 54, 888, 1117, and 134 μg/m(3). Identified VOC sources in basements included solvents, household cleaners, air fresheners, smoking, and gasoline-powered equipment. The number and type of potential VOC sources found in basements are significant and problematic, and may warrant advisories regarding the storage and use of potentially strong VOCs sources in basements. Few IAQ studies have examined basements. A sizable volume of air can flow between the basement and living area, and AERs in these two zones can differ considerably. In many residences, the basement contains significant emission sources and contributes a large fraction of VOC concentrations found in the living area. Exposures can be lowered by removing VOC sources from the basement; other exposure management options, such as local ventilation or isolation, are unlikely to be practical. © 2014 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

[Development of biogenic VOC emissions inventory with high temporal and spatial resolution].

Science.gov (United States)

Hu, Y; Zhang, Y; Xie, S; Zeng, L

2001-11-01

A new method was developed to estimate biogenic VOC emissions with high temporal and spatial resolution by use of Mesoscale Meteorology Modeling System Version5 (MM5). In this method, the isoprene and monoterpene standard emission factors for some types of tree in China were given and the standard VOC emission factors and seasonally average densities of leaf biomass for all types of vegetation were determined. A biogenic VOC emissions inventory in South China was established which could meet the requirement of regional air quality modeling. Total biogenic VOC emissions in a typical summer day were estimated to be 1.12 x 10(4) metric tons in an area of 729 km x 729 km of South China. The results showed the temporal and spatial distributions of biogenic VOC emission rates in this area. The results also showed that the geographical distribution of biogenic VOC emission rates depended on vegetation types and their distributions and the diurnal variation mainly depended on the solar radiation and temperature. The uncertainties of estimating biogenic VOC emissions were also discussed.

Biogenic VOC Emissions from Tropical Landscapes

Science.gov (United States)

Guenther, A.; Greenberg, J.; Harley, P.; Otter, L.; Vanni Gatti, L.; Baker, B.

2003-04-01

Biogenic VOC have an important role in determining the chemical composition of atmosphere. As a result, these compounds are important for visibility, biogeochemical cycling, climate and radiative forcing, and the health of the biosphere. Tropical landscapes are estimated to release about 80% of total global biogenic VOC emissions but have been investigated to lesser extent than temperate regions. Tropical VOC emissions are particularly important due to the strong vertical transport and the rapid landuse change that is occurring there. This presentation will provide an overview of field measurements of biogenic VOC emissions from tropical landscapes in Amazonia (Large-scale Biosphere-atmosphere experiment in Amazonia, LBA) Central (EXPRESSO) and Southern (SAFARI 2000) Africa, Asia and Central America. Flux measurement methods include leaf-scale (enclosure measurements), canopy-scale (above canopy tower measurements), landscape-scale (tethered balloon), and regional-scale (aircraft measurements) observations. Typical midday isoprene emission rates for different landscapes vary by more than a factor of 20 with the lowest emissions observed from degraded forests. Emissions of alpha-pinene vary by a similar amount with the highest emissions associated with landscapes dominated by light dependent monoterpene emitting plants. Isoprene emissions tend to be higher for neotropical forests (Amazon and Costa Rica) in comparison to Africa and Asian tropical forests but considerable differences are observed within regions. Strong seasonal variations were observed in both the Congo and the Amazon rainforests with peak emissions during the dry seasons. Substantial emissions of light dependent monoterpenes, methanol and acetone are characteristic of at least some tropical landscapes.

Indoor Air Quality Assessment and Study of Different VOC Contributions within a School in Taranto City, South of Italy

Directory of Open Access Journals (Sweden)

Annalisa Marzocca

2017-03-01

Full Text Available Children spend a large amount of time in school environments and when Indoor Air Quality (IAQ is poor, comfort, productivity and learning performances may be affected. The aim of the present study is to characterize IAQ in a primary school located in Taranto city (south of Italy. Because of the proximity of a large industrial complex to the urban settlement, this district is one of the areas identified as being at high environmental risk in Italy. The study carried out simultaneous monitoring of indoor and outdoor Volatile Organic Compounds (VOC concentrations and assessed different pollutants’ contributions on the IAQ of the investigated site. A screening study of VOC and determination of Benzene, Toluene, Ethylbenzene, Xylenes (BTEX, sampled with Radiello® diffusive samplers suitable for thermal desorption, were carried out in three classrooms, in the corridor and in the yard of the school building. Simultaneously, Total VOC (TVOC concentration was measured by means of real-time monitoring, in order to study the activation of sources during the monitored days. The analysis results showed a prevalent indoor contribution for all VOC except for BTEX which presented similar concentrations in indoor and outdoor air. Among the determined VOC, Terpenes and 2-butohxyethanol were shown to be an indoor source, the latter being the indoor pollutant with the highest concentration.

The 2016 Case for Mantle Plumes and a Plume-Fed Asthenosphere (Augustus Love Medal Lecture)

Science.gov (United States)

Morgan, Jason P.

2016-04-01

The process of science always returns to weighing evidence and arguments for and against a given hypothesis. As hypotheses can only be falsified, never universally proved, doubt and skepticism remain essential elements of the scientific method. In the past decade, even the hypothesis that mantle plumes exist as upwelling currents in the convecting mantle has been subject to intense scrutiny; from geochemists and geochronologists concerned that idealized plume models could not fit many details of their observations, and from seismologists concerned that mantle plumes can sometimes not be 'seen' in their increasingly high-resolution tomographic images of the mantle. In the place of mantle plumes, various locally specific and largely non-predictive hypotheses have been proposed to explain the origins of non-plate boundary volcanism at Hawaii, Samoa, etc. In my opinion, this debate has now passed from what was initially an extremely useful restorative from simply 'believing' in the idealized conventional mantle plume/hotspot scenario to becoming an active impediment to our community's ability to better understand the dynamics of the solid Earth. Having no working hypothesis at all is usually worse for making progress than having an imperfect and incomplete but partially correct one. There continues to be strong arguments and strong emerging evidence for deep mantle plumes. Furthermore, deep thermal plumes should exist in a mantle that is heated at its base, and the existence of Earth's (convective) geodynamo clearly indicates that heat flows from the core to heat the mantle's base. Here I review recent seismic evidence by French, Romanowicz, and coworkers that I feel lends strong new observational support for the existence of deep mantle plumes. I also review recent evidence consistent with the idea that secular core cooling replenishes half the mantle's heat loss through its top surface, e.g. that the present-day mantle is strongly bottom heated. Causes for

Thermal plumes in ventilated rooms

DEFF Research Database (Denmark)

Kofoed, Peter; Nielsen, Peter V.

1990-01-01

The design of a displacement ventilation system involves determination of the flow rate in the thermal plumes. The flow rate in the plumes and the vertical temperature gradient influence each other, and they are influenced by many factors. This paper shows some descriptions of these effects. Free...... above a point heat source cannot be used. This is caused either by the way of generating the plume including a long intermediate region or by the environmental conditions where vertical temperature gradients are present. The flow has a larger angle of spread and the entrainment factor is greather than...... turbulent plumes from different heated bodies are investigated. The measurements have taken place in a full-scale test room where the vertical temperature gradient have been changed. The velocity and the temperature distribution in the plume are measured. Large scale plume axis wandering is taken...

Photochemical processing of organic aerosol at nearby continental sites: contrast between urban plumes and regional aerosol

Directory of Open Access Journals (Sweden)

J. G. Slowik

2011-03-01

Full Text Available As part of the BAQS-Met 2007 field campaign, Aerodyne time-of-flight aerosol mass spectrometers (ToF-AMS were deployed at two sites in southwestern Ontario from 17 June to 11 July 2007. One instrument was located at Harrow, ON, a rural, agriculture-dominated area approximately 40 km southeast of the Detroit/Windsor/Windsor urban area and 5 km north of Lake Erie. The second instrument was located at Bear Creek, ON, a rural site approximately 70 km northeast of the Harrow site and 50 km east of Detroit/Windsor. Positive matrix factorization analysis of the combined organic mass spectral dataset yields factors related to secondary organic aerosol (SOA, direct emissions, and a factor tentatively attributed to the reactive uptake of isoprene and/or condensation of its early generation reaction products. This is the first application of PMF to simultaneous AMS measurements at different sites, an approach which allows for self-consistent, direct comparison of the datasets. Case studies are utilized to investigate processing of SOA from (1 fresh emissions from Detroit/Windsor and (2 regional aerosol during periods of inter-site flow. A strong correlation is observed between SOA/excess CO and photochemical age as represented by the NO_x/NO_y ratio for Detroit/Windsor outflow. Although this correlation is not evident for more aged air, measurements at the two sites during inter-site transport nevertheless show evidence of continued atmospheric processing by SOA production. However, the rate of SOA production decreases with airmass age from an initial value of ~10.1 μg m⁻³ ppmv_CO⁻¹ h⁻¹ for the first ~10 h of plume processing to near-zero in an aged airmass (i.e. after several days. The initial SOA production rate is comparable to the observed rate in Mexico City over similar timescales.

PHYTOREMEDIATION POTENTIAL OF A CHLORINATED SOLVENTS PLUME IN CENTRAL FLORIDA

Science.gov (United States)

The potential for phytoremediation of a shallow chlorinated solvent plume was assessed by application of ground water flow and evapotranspiration (ET) models for a site in Orlando, Florida. The focus of the work was on the hydrologic and hydraulic factors that influence phytoreme...

Cost-effective management of hydrocarbon plumes using monitored natural attenuation: case studies

International Nuclear Information System (INIS)

Borg, G.A.

2000-01-01

Engineered remediation of hydrocarbon plumes in groundwater at operating service station sites is expensive, disruptive, does not improve the management of risks to receptors, and does not provide certainty of outcome. When plumes are delineated, potential receptors identified and primary sources removed, monitored natural attenuation (MINA) is a cost-effective remediation option. If available, hydrocarbon concentration data from successive groundwater monitoring events showing that a plume is stable or reducing will provide enough primary evidence that natural attenuation is occurring. Where potential receptors will not be impacted in the short to medium term, MNA provides the same level of risk management as engineered remediation with much less cost, no disruption to the service station business, and with a certainty of meeting the objectives of the remediation

Life Cycle of Mantle Plumes: A perspective from the Galapagos Plume (Invited)

Science.gov (United States)

Gazel, E.; Herzberg, C. T.

2009-12-01

Hotspots are localized sources of heat and magmatism considered as modern-day evidence of mantle plumes. Some hotspots are related to massive magmatic production that generated Large Igneous Provinces (LIPS), an initial-peak phase of plume activity with a mantle source hotter and more magmatically productive than present-day hotspots. Geological mapping and geochronological studies have shown much lower eruption rates for OIB compared to lavas from Large Igneous Provinces LIPS such as oceanic plateaus and continental flood provinces. Our study is the first quantitative petrological comparison of mantle source temperatures and extent of melting for OIB and LIP sources. The wide range of primary magma compositions and inferred mantle potential temperatures for each LIP and OIB occurrence suggest that this rocks originated form a hotspot, a spatially localized source of heat and magmatism restricted in time. Extensive outcrops of basalt, picrite, and sometimes komatiite with circa 65-95 Ma ages occupy portions of the pacific shore of Central and South America included in the Caribbean Large Igneous Province (CLIP). There is general consensus of a Pacific-origin of CLIP and most studies suggest that it was produced by melting in the Galapagos mantle plume. The Galapagos connection is consistent with isotopic and geochemical similarities with lavas from the present-day Galapagos hotspot. A Galapagos link for rocks in South American oceanic complexes (eg. the island of Gorgona) is more controversial and requires future work. The MgO and FeO contents of lavas from the Galapagos related lavas and their primary magmas have decreased since the Cretaceous. From petrological modeling we infer that these changes reflect a cooling of the Galapagos mantle plume from a potential temperature of 1560-1620 C in the Cretaceous to 1500 C at the present time. These temperatures are higher than 1350 C for ambient mantle associated with oceanic ridges, and provide support for the mantle

Volatile organic compound (VOC) determination in working atmospheres; Determinacion de compuestos organicos volatiles (VOC) en ambiente laboral

Energy Technology Data Exchange (ETDEWEB)

Blass A, Georgina; Panama T, Luz A; Corrales C, Deyanira [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico)

2003-07-01

The present work describes, in a synthesized way, the implementation and application of procedures based on the normativity related to the subject of the volatile organic compounds (Volatile Organic Compounds VOC), that allow to sample, quantify and evaluate the present contamination in the working atmosphere of a refinery due to the fugitive emissions of VOC and other substances. In accordance with the corresponding normativity, more than 189 organic compounds denominated dangerous air polluting agents (Hazardous Air Pollutants, HAP) can be found in a working atmosphere, but they are the 11 main HAP that can be found in a refinery. In the present article the work made for the sampling and quantification of 5 of the 11 dangerous polluting agents of the air: benzene, toluene, xylene, iso-octane and naphthalene. [Spanish] El presente trabajo describe, de manera sintetizada, la implementacion y aplicacion de procedimientos basados en la normatividad relacionada al tema de los compuestos organicos volatiles (Volatil Organic Compounds, VOC), que permiten muestrear, cuantificar y evaluar la contaminacion presente en el ambiente laboral de una refineria debido a las emisiones fugitivas de VOC y otras sustancias. De acuerdo con la normatividad correspondiente, mas de 189 compuestos organicos denominados contaminantes peligrosos del aire (Hazardous Air Pollutants, HAP), pueden ser encontrados en un ambiente laboral, pero son 11 los principales HAP que pueden ser hallados en una refineria. En el presente articulo se informa el trabajo realizado para el muestreo y cuantificacion de 5 de los 11 contaminantes peligrosos del aire: benceno, tolueno, xileno, iso-octano y naftaleno.

Reducing VOC Press Emission from OSB Manufacturing; FINAL

International Nuclear Information System (INIS)

Gary D, McGinnis; Laura S, WIlliams; Amy E, Monte; Jagdish Rughani; Brett A, Niemi; Thomas M, Flicker

2001-01-01

Current regulations require industry to meet air emission standards with regard to particulates, volatile organic compounds (VOCs), hazardous air pollutants (HAPs) and other gases. One of many industries that will be affected by the new regulations is the wood composites industry. This industry generates VOCs, HAPs, and particulates mainly during the drying and pressing of wood. Current air treatment technologies for the industry are expensive to install and operate. As regulations become more stringent, treatment technologies will need to become more efficient and cost effective. The overall objective of this study is to evaluate the use of process conditions and chemical additives to reduce VOC/HAPs in air emitted from presses and dryers during the production of oriented strand board

Biofiltration of airborne VOCs with green wall systems-Microbial and chemical dynamics.

Science.gov (United States)

Mikkonen, A; Li, T; Vesala, M; Saarenheimo, J; Ahonen, V; Kärenlampi, S; Blande, J D; Tiirola, M; Tervahauta, A

2018-05-06

Botanical air filtration is a promising technology for reducing indoor air contaminants, but the underlying mechanisms need better understanding. Here, we made a set of chamber fumigation experiments of up to 16 weeks of duration, to study the filtration efficiencies for seven volatile organic compounds (VOCs; decane, toluene, 2-ethylhexanol, α-pinene, octane, benzene, and xylene) and to monitor microbial dynamics in simulated green wall systems. Biofiltration functioned on sub-ppm VOC levels without concentration-dependence. Airflow through the growth medium was needed for efficient removal of chemically diverse VOCs, and the use of optimized commercial growth medium further improved the efficiency compared with soil and Leca granules. Experimental green wall simulations using these components were immediately effective, indicating that initial VOC removal was largely abiotic. Golden pothos plants had a small additional positive impact on VOC filtration and bacterial diversity in the green wall system. Proteobacteria dominated the microbiota of rhizosphere and irrigation water. Airborne VOCs shaped the microbial communities, enriching potential VOC-utilizing bacteria (especially Nevskiaceae and Patulibacteraceae) in the irrigation water, where much of the VOC degradation capacity of the biofiltration systems resided. These results clearly show the benefits of active air circulation and optimized growth media in modern green wall systems. © 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

[Emission Characteristics of VOCs from Typical Restaurants in Beijing].

Science.gov (United States)

Cui, Tong; Cheng, Jing-chen; He, Wan-qing; Ren, Pei-fang; Nie, Lei; Xu, Dong-yao; Pan, Tao

2015-05-01

Using the EPA method, emission of volatile organic compounds (VOCs) , sampled from barbecue, Chinese and Western fast-food, Sichuan cuisine and Zhejiang cuisine restaurants in Beijing was investigated. VOCs concentrations and components from different cuisines were studied. The results indicated that based on the calibrated baseline ventilation volume, the VOCs emission level from barbecue was the highest, reaching 12.22 mg · m(-3), while those from fast-food of either Chinese or Western, Sichuan cuisine and Zhejiang cuisine were about 4 mg · m(-3). The components of VOCs from barbecue were different from those in the other cuisines, which were mainly propylene, 1-butene, n-butane, etc. The non-barbecue cuisines consisted of high concentration of alcohols, and Western fast-food contained relatively high proportion of aldehydes and ketones organic compounds. According to emission concentration of baseline ventilation volume, barbecue released more pollutants than the non-barbecue cuisines at the same scale. So, barbecue should be supervised and controlled with the top priority.

Scaling for turbulent viscosity of buoyant plumes in stratified fluids: PIV measurement with implications for submarine hydrothermal plume turbulence

Science.gov (United States)

Zhang, Wei; He, Zhiguo; Jiang, Houshuo

2017-11-01

Time-resolved particle image velocimetry (PIV) has been used to measure instantaneous two-dimensional velocity vector fields of laboratory-generated turbulent buoyant plumes in linearly stratified saltwater over extended periods of time. From PIV-measured time-series flow data, characteristics of plume mean flow and turbulence have been quantified. To be specific, maximum plume penetration scaling and entrainment coefficient determined from the mean flow agree well with the theory based on the entrainment hypothesis for buoyant plumes in stratified fluids. Besides the well-known persistent entrainment along the plume stem (i.e., the 'plume-stem' entrainment), the mean plume velocity field shows persistent entrainment along the outer edge of the plume cap (i.e., the 'plume-cap' entrainment), thereby confirming predictions from previous numerical simulation studies. To our knowledge, the present PIV investigation provides the first measured flow field data in the plume cap region. As to measured plume turbulence, both the turbulent kinetic energy field and the turbulence dissipation rate field attain their maximum close to the source, while the turbulent viscosity field reaches its maximum within the plume cap region; the results also show that maximum turbulent viscosity scales as νt,max = 0.030(B/N)1/2, where B is source buoyancy flux and N is ambient buoyancy frequency. These PIV data combined with previously published numerical simulation results have implications for understanding the roles of hydrothermal plume turbulence, i.e. plume turbulence within the cap region causes the 'plume-cap' entrainment that plays an equally important role as the 'plume-stem' entrainment in supplying the final volume flux at the plume spreading level.

In-situ treatment of a mixed hydrocarbon plume through a permeable reactive barrier and enhanced bio-remediation

International Nuclear Information System (INIS)

Aglietto, I.; Bretti, L.L.

2005-01-01

Groundwater is frequently polluted with mixtures of contaminants that are amenable to different types of remediation. One example is the combination of petroleum hydrocarbons (mostly BTEX) and chlorinated solvents (chlorinated ethenes and propanes), as it occurs in the groundwater beneath the industrial site that is the objective of the present case study. The site is located in Italy near a main river (Arno), which is supposed to be the final recipient of the contamination and where a possible exposure might take place. The aim of the treatment is the plume containment within the site boundaries in order to avoid further migration of the contaminants towards the river. The design of the remediation system was based on an extensive site characterization that included - but was not limited to - the following information: geological and geochemical, microbiological and hydrological data, together with analytical data (i.e. contaminant concentrations). Pilot tests were also implemented in order to collect the necessary parameters for the full-scale treatment design and calibration. The site was contaminated by a mixed plume of more than 30 different contaminants, ranging from BTEX, to MTBE, to PAH, to chlorinated solvents. The concentration peaks were in the order of 1-100 mg/l for each contaminant. Petroleum hydrocarbons are quickly degradable through oxidative mechanisms (especially aerobic biodegradation), whereas fully-chlorinated compounds are only degradable via reductive pathways. A mixed plume of both types of contaminants therefore requires a combined approach with the application of different treatment technologies. The remediation strategy elaborated combines a permeable reactive barrier (PRB) in a funnel and gate configuration for the down-gradient plume containment, with the enhanced bio-remediation of the contaminants for the control of the plume boundaries and for the abatement of the concentration peaks. Pilot tests were carried out in order to assess

Predicted and observed cooling tower plume rise and visible plume length at the John E. Amos power plant

Energy Technology Data Exchange (ETDEWEB)

Hanna, S R

1976-01-01

A one-dimensional numerical cloud growth model and several empirical models for plume rise and cloud growth are compared with twenty-seven sets of observations of cooling tower plumes from the 2900 MW John E. Amos power plant in West Virginia. The three natural draft cooling towers are 200 m apart. In a cross wind, the plumes begin to merge at a distance of about 500 m downwind. In calm conditions, with reduced entrainment, the plumes often do not merge until heights of 1000 m. The average plume rise, 750 m, is predicted well by the models, but day-to-day variations are simulated with a correlation coefficient of about 0.5. Model predictions of visible plume length agree, on the average, with observations for visible plumes of short to moderate length (less than about 1 km). The prediction of longer plumes is hampered by our lack of knowledge of plume spreading after the plumes level off. Cloud water concentrations predicted by the numerical model agree with those measured in natural cumulus clouds (about 0.1 to 1 g kg/sup -1/).

Turbulent buoyant jets and plumes

CERN Document Server

Rodi, Wolfgang

The Science & Applications of Heat and Mass Transfer: Reports, Reviews, & Computer Programs, Volume 6: Turbulent Buoyant Jets and Plumes focuses on the formation, properties, characteristics, and reactions of turbulent jets and plumes. The selection first offers information on the mechanics of turbulent buoyant jets and plumes and turbulent buoyant jets in shallow fluid layers. Discussions focus on submerged buoyant jets into shallow fluid, horizontal surface or interface jets into shallow layers, fundamental considerations, and turbulent buoyant jets (forced plumes). The manuscript then exami

The VOC-Ozone connection: a grassland case study

Science.gov (United States)

Wohlfahrt, G.; Hoertnagl, L.; Bamberger, I.; Schnitzhofer, R.; Dunkel, J.; Hammerle, A.; Graus, M.; Hansel, A.

2009-04-01

Trophospheric ozone (O3) is formed in the presence of sunlight through the interaction of volatile organic compounds (VOCs) and NOx (NO, NO2). O3 damages plants in several ways, most importantly by reducing net photosynthesis and growth. The extent of this damage depends on the time-integrated absorbed O3 flux (i.e. the dose), which is a function of leaf stomatal conductance and ambient O3 concentration, and further influenced by plant species specific defence mechanisms. VOCs are produced by plants through a variety of pathways and in response to a large number of different driving forces. A large variety of VOCs are emitted by plants in response to stress conditions, including the foliar uptake of O3. Here we present preliminary data from an ongoing study where concurrent measurements of the fluxes of VOCs and O3 are made above a managed mountain grassland in Tyrol/Austria. Fluxes of several different VOCs and O3 are measured by means of the eddy covariance method and a proton transfer reaction mass spectrometer (PTR-MS) and an ozone analyser, respectively. Our findings show that the Methanol (MeOH) flux is correlated with the daily time-integrated O3 uptake by vegetation (integrated daily from sunrise - a surrogate for the O3 dose absorbed and the oxidative stress experienced by plants) - MeOH deposition and emission prevailing at low and high time-integrated O3 uptake rates, respectively. Fluxes of other VOCs were not related to the time-integrated O3 uptake. Integrated over longer time scales (several weeks) no correlation between the O3 uptake and MeOH emissions were found. Our study thus confirms earlier leaf-level studies, who found that MeOH emission increase with O3 dose, at the ecosystems scale. As the reaction with the hydroxyl radical (OH), which is responsible for the destruction of the greenhouse gas methane (CH4), is the major sink of atmospheric MeOH, this process provides a potentially important indirect radiative forcing.

Implementation of Enhanced Attenuation at the DOE Mound Site OU-1 Landfill: Accelerating Progress and Reducing Costs

Energy Technology Data Exchange (ETDEWEB)

Hooten, Gwendolyn [U.S. Department of Energy, Office of Legacy Management; Cato, Rebecca [Navarro Research and Engineering; Looney, Brian [Savannah River National Laboratory, Aiken, SC

2016-03-06

At the US Department of Energy (DOE), Office of Legacy Management, Mound, Ohio, Site, chlorinated organic contaminants (cVOCs) originating from the former solid-waste landfill have impacted groundwater in Operable Unit 1 (OU-1). The baseline groundwater remedy was groundwater pump and treat (P&T). Since the source materials have been removed from the landfill, the Mound core team, which consists of DOE, US Environmental Protection Agency (US EPA), Ohio EPA, and other stakeholders, is assessing the feasibility of switching from the active P&T remedy to a passive attenuation-based remedy. Toward this end, an enhanced attenuation (EA) strategy based on the creation of structured geochemical zones was developed. This EA strategy addresses the residual areas of elevated cVOCs in soil and groundwater while minimizing the rebound of groundwater concentrations above regulatory targets (e.g., maximum contaminant levels [MCLs]) and avoiding plume expansion while the P&T system is turned off. The EA strategy has improved confidence and reduced risk on the OU-1 groundwater transition path to monitored natural attenuation (MNA). To better evaluate the EA strategy, DOE is conducting a field demonstration to evaluate the use of edible oils to enhance the natural attenuation processes. The field demonstration is designed to determine whether structured geochemical zones can be established that expedite the attenuation of cVOCs in the OU-1 groundwater. The EA approach at OU-1 was designed based on “structured geochemical zones” and relies on groundwater flow through a succession of anaerobic and aerobic zones. The anaerobic zones stimulate relatively rapid degradation of the original solvent source compounds (e.g., cVOCs such as tetrachloroethene [PCE] and trichloroethene [TCE]). The surrounding aerobic areas encourage relatively rapid degradation of daughter products (such as dichloroethene [DCE] and vinyl chloride [VC]) as well as enhanced cometabolism of TCE resulting from

Removal of VOCs from groundwater using membrane-assisted solvent extraction

International Nuclear Information System (INIS)

Hutter, J.C.; Vandegrift, G.F.; Nunez, L.; Redfield, D.H.

1992-01-01

A membrane-assisted solvent extraction (MASX) system coupled to a membrane-assisted distillation stripping (MADS) system for use in decontaminating groundwater is discussed. Volatile organic compounds (VOCs) are extracted in the MASX using a sunflower oil solvent. In the MADS, VOCs are stripped from the sunflower oil, and the oil is recycled to the MASX. Thermodynamic data for the sunflower oil-water-VOCs system were experimentally collected. Published membrane-mass transfer results along with these data were used to design the MASX and MADS modules

Investigation of VOC emissions from indoor and outdoor painting processes in shipyards

Science.gov (United States)

Celebi, Ugur Bugra; Vardar, Nurten

Volatile organic compounds (VOCs) from painting solvents are one of the most important sources of pollutant outputs for the shipbuilding and ship repair industry. Two ships of equal tonnage with the same painted area as each other, which were built in Turkish shipyards, are compared in terms of VOCs produced during painting and coating. Total area of all painted surfaces and total paint consumption of a 3500 deadweight tonne (DWT) oil/chemical tanker and a general cargo ship are calculated. An improved model for calculating the surface emissions of VOCs from painting and coating processes is utilized. Material balance emission estimation approach is employed to calculate the amount of VOCs, since it is used most often where a relatively large amount of material is emitted during use, and/or all air emissions are uncaptured. For both ships calculated VOCs are presented in figures. For the years 2005 and 2006 the total deadweight tonnage of ships delivered in Tuzla region, where 42 shipyards are located, is known. Therefore, a linear estimation is made to guess the total annual VOC emissions caused by painting operations. Finally, this information is used to project the total amount of VOCs emitted to the atmosphere for the year 2010.

Comparison of decomposition characteristics between aromatic and aliphatic VOCs using electron beam

International Nuclear Information System (INIS)

Kim, Jo-Chun

2011-01-01

The removal efficiency of n-decane (C 10 H 22 ) by electron beam was the highest among aliphatic VOCs of concern, and that of n-hexane (C 6 H 14 ), n-butane (C 4 H 10 ), and methane (CH 4 ) followed. On the other hand, in terms of aromatic VOC decomposition efficiencies, benzene (C 6 H 6 ) decomposition was the lowest and that of toluene (C 7 H 8 ), ethylbenzene (C 8 H 10 ), and p-xylene (C 8 H 10 ) were similar. It was also found that there was increase in by-product (untreated VOC, CO, CO 2 , O 3 , and other compounds) formation as well as all VOC removal efficiencies. It was demonstrated that the removal efficiency of VOC increased as its concentration decreased and the irradiation dose increased. In addition, low removal efficiency was observed because helium was relatively stable compared to the other gases, and nothing but electrons produced by electron accelerator reacted with VOC. It was also found that relative humidity had some effects on the decomposition rates of VOC. The removal efficiency at the 100% RH condition was slightly higher than that at 7.4% RH (dry condition) due to OH radical formation. (author)

Volatile Organic Compound (VOC) Air Monitoring Program design for the Waste Isolation Pilot Plant

International Nuclear Information System (INIS)

Frank, L.

1991-01-01

The Waste Isolation Pilot Plant (WIPP) Volatile Organic Compound (VOC) Monitoring Program has been developed as part of the Department of Energy's (DOE's) No-Migration Variance petition submitted to the Environmental Protection Agency (EPA). The program is designed to demonstrate that there will be no migration of hazardous chemicals past the unit boundary in concentrations which exceed any health-based standards. The monitoring program will use EPA compendium Method TO-14. Both air and carbon sorption media samples will be collected as part of the program. Eleven separate monitoring sites have been selected where both 24-hour integrated and 1-hour grab samples will be collected and analyzed for five target compounds. The bin-scale experimental test rooms will be configured with a gas collection manifold and an activated carbon sorption bed to remove VOCs before they can be emitted into the WIPP underground atmosphere. 10 refs., 4 figs., 7 tabs

Volatile organic compounds (VOCs) source profiles of on-road vehicle emissions in China.

Science.gov (United States)

Hong-Li, Wang; Sheng-Ao, Jing; Sheng-Rong, Lou; Qing-Yao, Hu; Li, Li; Shi-Kang, Tao; Cheng, Huang; Li-Ping, Qiao; Chang-Hong, Chen

2017-12-31

Volatile Organic Compounds (VOCs) source profiles of on-road vehicles were widely studied as their critical roles in VOCs source apportionment and abatement measures in megacities. Studies of VOCs source profiles from on-road motor vehicles from 2001 to 2016 were summarized in this study, with a focus on the comparisons among different studies and the potential impact of different factors. Generally, non-methane hydrocarbons dominated the source profile of on-road vehicle emissions. Carbonyls, potential important components of vehicle emission, were seldom considered in VOCs emissions of vehicles in the past and should be paid more attention to in further study. VOCs source profiles showed some variations among different studies, and 6 factors were extracted and studied due to their impact to VOCs source profile of on-road vehicles. Vehicle types, being dependent on engine types, and fuel types were two dominant factors impacting VOCs sources profiles of vehicles. In comparison, impacts of ignitions, driving conditions and accumulated mileage were mainly due to their influence on the combustion efficiency. An opening and interactive database of VOCs from vehicle emissions was critically essential in future, and mechanisms of sharing and inputting relative research results should be formed to encourage researchers join the database establishment. Correspondingly, detailed quality assurance and quality control procedures were also very important, which included the information of test vehicles and test methods as detailed as possible. Based on the community above, a better uncertainty analysis could be carried out for the VOCs emissions profiles, which was critically important to understand the VOCs emission characteristics of the vehicle emissions. Copyright © 2017 Elsevier B.V. All rights reserved.

Characterization of the geology, geochemistry, and microbiology of the radio frequency heating demonstration site at the Savannah River Site

International Nuclear Information System (INIS)

Eddy Dilek, C.A.; Jarosch, T.R.; Fliermans, C.B.; Looney, B.B.; Parker, W.H.

1993-08-01

The overall objective of the Integrated Demonstration Project for the Remediation of Organics at Nonarid Sites at the Savannah River Site (SRS) is to evaluate innovative remediation, characterization, and monitoring systems to facilitate restoration of contaminated sites. The first phase of the demonstration focused on the application and development of in situ air stripping technologies to remediate sediments and groundwater contaminated with volatile organic compounds (VOCs). The second phase focused on the enhancement of the in situ air stripping process by adding selected nutrients to stimulate naturally occurring microorganisms that degrade VOCs. The purpose of the third phase was to evaluate the use of heating technologies [radio frequency (rf) and ohmic heating] to enhance the removal of contamination from clay layers where mass transfer is limited. The objective of this report is to document pretest and post-test data collected in support of the rf heating demonstration. The following data are discussed in this report: (1) a general description of the site including piezometers and sensors installed to monitor the remedial process; (2) stratigraphy, lithology, and a detailed geologic cross section of the study site; (3) tabulations of pretest and post-test moisture and VOC content of the sediments; (4) sampling and analysis procedures for sediment samples; (5) microbial abundance and diversity; (6) three-dimensional images of pretest and post-test contaminant distribution; (7) volumetric calculations

A WRF-Chem model study of the impact of VOCs emission of a huge petro-chemical industrial zone on the summertime ozone in Beijing, China

Science.gov (United States)

Wei, Wei; Lv, Zhao Feng; Li, Yue; Wang, Li Tao; Cheng, Shuiyuan; Liu, Huan

2018-02-01

In China, petro-chemical manufacturing plants generally gather in the particular industrial zone defined as PIZ in some cities, and distinctly influence the air quality of these cities for their massive VOCs emissions. This study aims to quantify the local and regional impacts of PIZ VOCs emission and its relevant reduction policy on the surface ozone based on WRF-Chem model, through the case study of Beijing. Firstly, the model simulation under the actual precursors' emissions over Beijing region for July 2010 is conducted and evaluated, which meteorological and chemical predictions both within the thresholds for satisfactory model performance. Then, according to simulated H2O2/HNO3 ratio, the nature of photochemical ozone formation over Beijing is decided, the VOCs-sensitive regime over the urban areas, NOx-sensitive regime over the northern and western rural areas, and both VOCssbnd and NOx-mixed sensitive regime over the southern and eastern rural areas. Finally, a 30% VOCs reduction scenario (RS) and a 100% VOCs reduction scenario (ZS) for Beijing PIZ are additional simulated by WRF-Chem. The sensitivity simulations imply that the current 30% reduction policy would bring about an O3 increase in the southern and western areas (by +4.7 ppb at PIZ site and +2.1 ppb at LLH station), and an O3 decrease in the urban center (by -1.7 ppb at GY station and -2.5 ppb at DS station) and in the northern and eastern areas (by -1.2 ppb at MYX station), mainly through interfering with the circulation of atmospheric HOx radicals. While the contribution of the total VOCs emission of PIZ to ozone is greatly prominent in the PIZ and its surrounding areas along south-north direction (12.7% at PIZ site on average), but slight in the other areas of Beijing (<3% in other four stations on average).

POLLUTION PREVENTION CASE STUDIES: LOW-VOC/HAP WOOD FURNITURE COATINGS

Science.gov (United States)

This article provides a brief profile of the wood furniture industry, discusses pollution prevention activities typically implemented, describes the four low-VOC/HAP coating technologies studied. and summarizes one case study for each of the low-VOC/HAP coating yechnologies inves...

Vertical characteristics of VOCs in the lower troposphere over the North China Plain during pollution periods.

Science.gov (United States)

Sun, Jie; Wang, Yuesi; Wu, Fangkun; Tang, Guiqian; Wang, Lili; Wang, Yinghong; Yang, Yuan

2018-05-01

In recent years, photochemical smog and gray haze-fog have frequently appeared over northern China. To determine the spatial distribution of volatile organic compounds (VOC) during a pollution period, tethered balloon flights were conducted over a suburban site on the North China Plain. Statistical analysis showed that the VOCs concentrations peaked at the surface, and decreased with altitude. A rapid decrease appeared from the surface to 400 m, with concnetrations of alkanes, alkenes, aromatics and halocarbons decreasing by 48.0%, 53.3%, 43.3% and 51.1%, respectively. At heights in the range of 500-1000 m, alkenes concnetrations decline by 40.2%; alkanes and halocarbons concnetrations only decreased by 24.8% and 6.4%, respectively; and aromatics increased slightly by 5.5%. High concentrations VOCs covered a higher range of height (400 m) on heavy pollution days due to lacking of diffusion power. The VOCs concentrations decreased by 50% at 200 m on light pollution days. The transport of air mass affected the composition and concentration of high-altitude VOCs, especially on lightly polluted days. These air masses originated in areas with abundant traffic and combustion sources. Reactive aromatics (k OH >20,000 ppm -1  min -1 and k OH <20,000 ppm -1  min -1 ) were the main contributor to the ozone formation, accounting for 37%, on the surface on light pollution days. The contribution increased to 52% with pollution aggravated, and increased to 64% with height. The contributions of reactive aromatics were influenced by the degree of air mass aging. Under the umbrella of aging air mass, the contribution of reactive aromatics increased with height. Copyright © 2017. Published by Elsevier Ltd.

Mobile membrane introduction tandem mass spectrometry for on-the-fly measurements and adaptive sampling of VOCs around oil and gas projects in Alberta, Canada

Science.gov (United States)

Krogh, E.; Gill, C.; Bell, R.; Davey, N.; Martinsen, M.; Thompson, A.; Simpson, I. J.; Blake, D. R.

2012-12-01

The release of hydrocarbons into the environment can have significant environmental and economic consequences. The evolution of smaller, more portable mass spectrometers to the field can provide spatially and temporally resolved information for rapid detection, adaptive sampling and decision support. We have deployed a mobile platform membrane introduction mass spectrometer (MIMS) for the in-field simultaneous measurement of volatile and semi-volatile organic compounds. In this work, we report instrument and data handling advances that produce geographically referenced data in real-time and preliminary data where these improvements have been combined with high precision ultra-trace VOCs analysis to adaptively sample air plumes near oil and gas operations in Alberta, Canada. We have modified a commercially available ion-trap mass spectrometer (Griffin ICX 400) with an in-house temperature controlled capillary hollow fibre polydimethylsiloxane (PDMS) polymer membrane interface and in-line permeation tube flow cell for a continuously infused internal standard. The system is powered by 24 VDC for remote operations in a moving vehicle. Software modifications include the ability to run continuous, interlaced tandem mass spectrometry (MS/MS) experiments for multiple contaminants/internal standards. All data are time and location stamped with on-board GPS and meteorological data to facilitate spatial and temporal data mapping. Tandem MS/MS scans were employed to simultaneously monitor ten volatile and semi-volatile analytes, including benzene, toluene, ethylbenzene and xylene (BTEX), reduced sulfur compounds, halogenated organics and naphthalene. Quantification was achieved by calibrating against a continuously infused deuterated internal standard (toluene-d8). Time referenced MS/MS data were correlated with positional data and processed using Labview and Matlab to produce calibrated, geographical Google Earth data-visualizations that enable adaptive sampling protocols

Magnetotelluric Detection Thresholds as a Function of Leakage Plume Depth, TDS and Volume

Energy Technology Data Exchange (ETDEWEB)

Yang, X. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Buscheck, T. A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Mansoor, K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Carroll, S. A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2017-04-21

We conducted a synthetic magnetotelluric (MT) data analysis to establish a set of specific thresholds of plume depth, TDS concentration and volume for detection of brine and CO₂ leakage from legacy wells into shallow aquifers in support of Strategic Monitoring Subtask 4.1 of the US DOE National Risk Assessment Partnership (NRAP Phase II), which is to develop geophysical forward modeling tools. 900 synthetic MT data sets span 9 plume depths, 10 TDS concentrations and 10 plume volumes. The monitoring protocol consisted of 10 MT stations in a 2×5 grid laid out along the flow direction. We model the MT response in the audio frequency range of 1 Hz to 10 kHz with a 50 Ωm baseline resistivity and the maximum depth up to 2000 m. Scatter plots show the MT detection thresholds for a trio of plume depth, TDS concentration and volume. Plumes with a large volume and high TDS located at a shallow depth produce a strong MT signal. We demonstrate that the MT method with surface based sensors can detect a brine and CO₂ plume so long as the plume depth, TDS concentration and volume are above the thresholds. However, it is unlikely to detect a plume at a depth larger than 1000 m with the change of TDS concentration smaller than 10%. Simulated aquifer impact data based on the Kimberlina site provides a more realistic view of the leakage plume distribution than rectangular synthetic plumes in this sensitivity study, and it will be used to estimate MT responses over simulated brine and CO₂ plumes and to evaluate the leakage detectability. Integration of the simulated aquifer impact data and the MT method into the NRAP DREAM tool may provide an optimized MT survey configuration for MT data collection. This study presents a viable approach for sensitivity study of geophysical monitoring methods for leakage detection. The results come in handy for rapid assessment of leakage detectability.

The Ensemble Kalman Filter for Groundwater Plume Characterization: A Case Study.

Science.gov (United States)

Ross, James L; Andersen, Peter F

2018-04-17

The Kalman filter is an efficient data assimilation tool to refine an estimate of a state variable using measured data and the variable's correlations in space and/or time. The ensemble Kalman filter (EnKF) (Evensen, 2004, 2009) is a Kalman filter variant that employs Monte Carlo analysis to define the correlations that help to refine the updated state. While use of EnKF in hydrology is somewhat limited, it has been successfully applied in other fields of engineering (e.g. oil reservoir modeling, weather forecasting). Here, EnKF is used to refine a simulated groundwater TCE plume that underlies the Tooele Army Depot-North (TEAD-N) in Utah, based on observations of TCE in the aquifer. The resulting EnKF-based assimilated plume is simulated forward in time to predict future plume migration. The correlations that underpin EnKF updating implicitly contain information about how the plume developed over time under the influence of complex site hydrology and variable source history, as they are predicated on multiple realizations of a well-calibrated numerical groundwater flow and transport model. The EnKF methodology is compared to an ordinary kriging-based assimilation method with respect to the accurate representation of plume concentrations in order to determine the relative efficacy of EnKF for water quality data assimilation. This article is protected by copyright. All rights reserved.

Report from Workshop on VOCs in diving chambers

International Nuclear Information System (INIS)

Crosbie, A.; Simpson, M.

2000-05-01

This report of the 'Setting the Standards' workshop on the problems of volatile organic compounds (VOCs) in diving in offshore operations, sponsored jointly by the UK Health and Safety Executive Offshore Safety Division and the Stolt Rockwater Joint Venture, gives details of the papers presented covering the chemical contamination of diver's atmosphere, sampling protocols and methods, analytical procedures used for VOCs in hyperbaric chambers, and contamination in buildings. The setting of exposure limits in the UK, the derivation of threshold limiting values (TVLs), the selection of Tenax tubes for atmospheric sampling, organic contaminant monitoring, and NASA's approach to contamination in the space environment are examined, and dealing with contamination problems in a submarine atmosphere, and the simulation of a condensate spillage in a diving bell are discussed. Guidelines for the measurement of VOCs in hyperbaric chambers are given in the appendices

Rapid detection of pathogenic bacteria by volatile organic compound (VOC) analysis

Science.gov (United States)

Senecal, Andre G.; Magnone, Joshua; Yeomans, Walter; Powers, Edmund M.

2002-02-01

Developments in rapid detection technologies have made countless improvements over the years. However, because of the limited sample that these technologies can process in a single run, the chance of capturing and identifying a small amount of pathogens is difficult. The problem is further magnified by the natural random distribution of pathogens in foods. Methods to simplify pathogenic detection through the identification of bacteria specific VOC were studied. E. coli O157:H7 and Salmonella typhimurium were grown on selected agar medium to model protein, and carbohydrate based foods. Pathogenic and common spoilage bacteria (Pseudomonas and Morexella) were screened for unique VOC production. Bacteria were grown on agar slants in closed vials. Headspace sampling was performed at intervals up to 24 hours using Solid Phase Micro-Extraction (SPME) techniques followed by GC/MS analysis. Development of unique volatiles was followed to establish sensitivity of detection. E. coli produced VOC not found in either Trypticase Soy Yeast (TSY) agar blanks or spoilage organism samples were - indole, 1-decanol, and 2-nonanone. Salmonella specific VOC grown on TSY were 3-methyl-1-butanol, dimethyl sulfide, 2-undecanol, 2-pentadecanol and 1-octanol. Trials on potato dextrose agar (PDA) slants indicated VOC specific for E. coli and Salmonella when compared to PDA blanks and Pseudomonas samples. However, these VOC peaks were similar for both pathogens. Morexella did not grow on PDA slants. Work will continue with model growth mediums at various temperatures, and mixed flora inoculums. As well as, VOC production based on the dynamics of bacterial growth.

Total OH reactivity study from VOC photochemical oxidation in the SAPHIR chamber

Science.gov (United States)

Yu, Z.; Tillmann, R.; Hohaus, T.; Fuchs, H.; Novelli, A.; Wegener, R.; Kaminski, M.; Schmitt, S. H.; Wahner, A.; Kiendler-Scharr, A.

2015-12-01

It is well known that hydroxyl radicals (OH) act as a dominant reactive species in the degradation of VOCs in the atmosphere. In recent field studies, directly measured total OH reactivity often showed poor agreement with OH reactivity calculated from VOC measurements (e.g. Nölscher et al., 2013; Lu et al., 2012a). This "missing OH reactivity" is attributed to unaccounted biogenic VOC emissions and/or oxidation products. The comparison of total OH reactivity being directly measured and calculated from single component measurements of VOCs and their oxidation products gives us a further understanding on the source of unmeasured reactive species in the atmosphere. This allows also the determination of the magnitude of the contribution of primary VOC emissions and their oxidation products to the missing OH reactivity. A series of experiments was carried out in the atmosphere simulation chamber SAPHIR in Jülich, Germany, to explore in detail the photochemical degradation of VOCs (isoprene, ß-pinene, limonene, and D6-benzene) by OH. The total OH reactivity was determined from the measurement of VOCs and their oxidation products by a Proton Transfer Reaction Time of Flight Mass Spectrometer (PTR-TOF-MS) with a GC/MS/FID system, and directly measured by a laser-induced fluorescence (LIF) at the same time. The comparison between these two total OH reactivity measurements showed an increase of missing OH reactivity in the presence of oxidation products of VOCs, indicating a strong contribution to missing OH reactivity from uncharacterized oxidation products.

Emission characteristics of VOCs emitted from consumer and commercial products and their ozone formation potential.

Science.gov (United States)

Dinh, Trieu-Vuong; Kim, Su-Yeon; Son, Youn-Suk; Choi, In-Young; Park, Seong-Ryong; Sunwoo, Young; Kim, Jo-Chun

2015-06-01

The characteristics of volatile organic compounds (VOCs) emitted from several consumer and commercial products (body wash, dishwashing detergent, air freshener, windshield washer fluid, lubricant, hair spray, and insecticide) were studied and compared. The spray products were found to emit the highest amount of VOCs (~96 wt%). In contrast, the body wash products showed the lowest VOC contents (~1.6 wt%). In the spray products, 21.6-96.4 % of the VOCs were propane, iso-butane, and n-butane, which are the components of liquefied petroleum gas. Monoterpene (C10H16) was the dominant component of the VOCs in the non-spray products (e.g., body wash, 53-88 %). In particular, methanol was present with the highest amount of VOCs in windshield washer fluid products. In terms of the number of carbon, the windshield washer fluids, lubricants, insecticides, and hair sprays comprised >95 % of the VOCs in the range C2-C5. The VOCs in the range C6-C10 were predominantly found in the body wash products. The dishwashing detergents and air fresheners contained diverse VOCs from C2 to C11. Besides comprising hazardous VOCs, VOCs from consumer products were also ozone precursors. The ozone formation potential of the consumer and commercial spray products was estimated to be higher than those of liquid and gel materials. In particular, the hair sprays showed the highest ozone formation potential.

Plume rise from multiple sources

International Nuclear Information System (INIS)

Briggs, G.A.

1975-01-01

A simple enhancement factor for plume rise from multiple sources is proposed and tested against plume-rise observations. For bent-over buoyant plumes, this results in the recommendation that multiple-source rise be calculated as [(N + S)/(1 + S)]/sup 1/3/ times the single-source rise, Δh 1 , where N is the number of sources and S = 6 (total width of source configuration/N/sup 1/3/ Δh 1 )/sup 3/2/. For calm conditions a crude but simple method is suggested for predicting the height of plume merger and subsequent behavior which is based on the geometry and velocity variations of a single buoyant plume. Finally, it is suggested that large clusters of buoyant sources might occasionally give rise to concentrated vortices either within the source configuration or just downwind of it

Environmental restoration at the Lawrence Livermore National Laboratory Livermore Site

International Nuclear Information System (INIS)

Ziagos, J.P.; Bainer, R.W.; Dresen, M.D.; Hoffman, J.D.

1992-04-01

Ground water beneath Lawrence Livermore National Laboratory (LLNL) near Livermore California, contains 19 compounds in concentrations exceeding regulatory standards. These include volatile organic compounds (VOCs), dissolved fuel hydrocarbons, free product gasoline, cadmium, chromium, lead, and tritium. VOCs are the most widespread hazardous materials in the ground water, covering an area of about 1.4 square miles. The other compounds occur sporadically around the site. The LLNL site was added to the National Priorities (Superfund) List in 1987. This paper describes the technology developed at LLNL to remediate soil and ground water contamination. Included in this paper are methods in which site characterization has been aided by using a drilling technique developed at LLNL to evaluate the vertical distribution of VOCs in multiple water-bearing zones in single borehole. The paper also describes the development and implementation of a comprehensive three-step program to investigate and evaluate potential sources of hazardous materials in soil and ground water

Volatile Organic Compound (VOC) Emissions from Dairy Cows and Their Waste

Science.gov (United States)

Shaw, S.; Holzinger, R.; Mitloehner, F.; Goldstein, A.

2005-12-01

Biogenic VOCs are typically defined as those directly emitted from plants, but approximately 6% of global net primary production is consumed by cattle that carry out enteric fermentation and then emit VOCs that could also be considered biogenic. Current regulatory estimates suggest that dairy cattle in central California emit VOCs at rates comparable to those from passenger vehicles in the region, and thus contribute significantly to the extreme non-attainment of ozone standards there. We report PTR-MS measurements of ammonia and VOCs, and cavity-enhanced-absorption gas analyzer (Los Gatos Research, Inc.) measurements of CH4, emitted from dairy cattle in various stages of pregnancy/lactation and their waste. Experiments were conducted in chambers at UC Davis that simulate freestall cow housing conditions. CH4 fluxes ranged from 125-374 lb/cow/year. The compounds with the highest fluxes from '3 cows+waste' treatments were: ammonia (1-18), methanol (0-2.3), acetone+propanal (0.2-0.7), dimethylsulfide (0-0.4), and mass 109 (likely ID = p-cresol; 0-0.3) in lb/cow/year. Mass 60 (likely ID = trimethylamine) and acetic acid were also abundant. There were 10s of additional compounds with detectable, but small, emissions. A few compounds that were likely emitted (i.e. ethanol, formaldehyde, and dimethylamine) were not quantified by the PTR-MS. The total flux for all measured organic gases (TOG = CH4 + PTR-MS VOCs(including acetone+propanal)) averaged 246±45 lb/cow/year for '3 cows+waste' treatments, and was dominated by methane (>98%). TOG flux for 'waste only' treatments averaged 1.1±0.1 lb/cow/year, and was instead dominated by VOC (>84%). The PTR-MS VOCs as a percent of TOG (0.6±0.2%) emitted from '3 cows+waste' treatments in chamber conditions was a factor of 10 smaller than that currently estimated by the California Air Resources Board. In addition, the ozone forming potentials of the most abundant VOCs are only about 10% those of typical combustion or plant

Comparison of decomposition characteristics between aromatic and aliphatic VOCs using electron beam

Energy Technology Data Exchange (ETDEWEB)

Kim, Jo-Chun [Department of Environmental Engineering, Konkuk University, Seoul (Korea, Republic of)

2011-07-01

The removal efficiency of n-decane (C{sub 10}H{sub 22}) by electron beam was the highest among aliphatic VOCs of concern, and that of n-hexane (C{sub 6}H{sub 14}), n-butane (C{sub 4}H{sub 10}), and methane (CH{sub 4}) followed. On the other hand, in terms of aromatic VOC decomposition efficiencies, benzene (C{sub 6}H{sub 6}) decomposition was the lowest and that of toluene (C{sub 7}H{sub 8}), ethylbenzene (C{sub 8}H{sub 10}), and p-xylene (C{sub 8}H{sub 10}) were similar. It was also found that there was increase in by-product (untreated VOC, CO, CO{sub 2}, O{sub 3}, and other compounds) formation as well as all VOC removal efficiencies. It was demonstrated that the removal efficiency of VOC increased as its concentration decreased and the irradiation dose increased. In addition, low removal efficiency was observed because helium was relatively stable compared to the other gases, and nothing but electrons produced by electron accelerator reacted with VOC. It was also found that relative humidity had some effects on the decomposition rates of VOC. The removal efficiency at the 100% RH condition was slightly higher than that at 7.4% RH (dry condition) due to OH radical formation. (author)

Origin of 2-ethylhexanol as a VOC

International Nuclear Information System (INIS)

Nalli, Sandro; Horn, Owen J.; Grochowalski, Adam R.; Cooper, David G.; Nicell, Jim A.

2006-01-01

2-Ethylhexanol has been identified as a volatile organic compound (VOC) that contributes to the deterioration of indoor air quality. Plasticizers are common components of dust and building materials and are shown to be degraded by a variety of bacteria and fungi to produce 2-ethyhexanol and other metabolites. Of these, the 2-ethylhexanol has significant volatility and was observed in appreciable quantities. The degree to which 2-ethylhexanol is observed as a VOC in air samples would be limited by the fact that many of the microorganisms that are capable of producing this compound are also able to oxidize it to 2-ethylhexanoic acid, which is much less volatile. It is argued that an abiotic degradation mechanism of plasticizers that results in the generation of 2-ethylhexanol is unlikely and, if this did occur, other metabolites should have been observed. Thus, the microbial degradation of plasticizers is the most likely source of 2-ethylhexanol in indoor air. - A link has been observed between the partial biodegradation of plasticizers by microorganisms and VOCs associated with poor indoor air quality

Major reactive species of ambient volatile organic compounds (VOCs) and their sources in Beijing

Institute of Scientific and Technical Information of China (English)

SHAO; Min; FU; Linlin; LIU; Ying; LU; Sihua; ZHANG; Yuanhan

2005-01-01

Volatile organic compounds (VOCs) are important precursors of atmospheric chemical processes. As a whole mixture, the ambient VOCs show very strong chemical reactivity. Based on OH radical loss rates in the air, the chemical reactivity of VOCs in Beijing was calculated. The results revealed that alkenes, accounting for only about 15% in the mixing ratio of VOCs, provide nearly 75% of the reactivity of ambient VOCs and the C4 to C5 alkenes were the major reactive species among the alkenes. The study of emission characteristics of various VOCs sources indicated that these alkenes are mainly from vehicle exhaust and gasoline evaporation. The reduction of alkene species in these two sources will be effective in photochemical pollution control in Beijing.

Removal of VOCs by hybrid electron beam reactor with catalyst bed

International Nuclear Information System (INIS)

Kim, Jinkyu; Han, Bumsoo; Kim, Yuri; Lee, J.H.; Park, C.R.; Kim, J.C.; Kim, J.C.; Kim, K.J.

2004-01-01

Electron beam decomposition of volatile organic compounds (VOCs) was studied in order to obtain information for developing effective treatment method of off-gases from industries. We have examined the combination of electron beam and catalyst honeycomb which is either 1% platinum based or ceramic honeycomb- based aluminum oxide, using a hybrid reactor in order to improve removal efficiency and CO 2 formation; and to suppress undesirable by-product formation e.g. O 3 , aerosol, H x C y. , and tar. The experiments were conducted using a pilot-scale treatment system (maximum capacity; 1800 N m 3 /h) that fitted the field size to scale up from the traditional laboratory scale system for VOC removal with electron beam irradiation. Toluene was selected as a typical VOC that was irradiated to investigate product formation, effect of ceramic and catalyst, and factors effecting overall efficiency of degradation. Styrene was selected as the most odorous compound among the VOCs of interest. It was found that VOCs could be destroyed more effectively using a hybrid system with catalyst bed than with electron beam irradiation only

[CoCuMnOx Photocatalyzed Oxidation of Multi-component VOCs and Kinetic Analysis].

Science.gov (United States)

Meng, Hai-long; Bo, Long-li; Liu, Jia-dong; Gao, Bo; Feng, Qi-qi; Tan, Na; Xie, Shuai

2016-05-15

Solar energy absorption coating CoCuMnOx was prepared by co-precipitation method and applied to photodegrade multi- component VOCs including toluene, ethyl acetate and acetone under visible light irradiation. The photocatalytic oxidation performance of toluene, ethyl acetate and acetone was analyzed and reaction kinetics of VOCs were investigated synchronously. The research indicated that removal rates of single-component toluene, ethyl acetate and acetone were 57%, 62% and 58% respectively under conditions of 400 mg · m⁻³ initial concentration, 120 mm illumination distance, 1 g/350 cm² dosage of CoCuMnOx and 6 h of irradiation time by 100 W tungsten halogen lamp. Due to the competition among different VOCs, removal efficiencies in three-component mixture were reduced by 5%-26% as compared with single VOC. Degradation processes of single-component VOC and three-component VOCs both fitted pseudo first order reaction kinetics, and kinetic constants of toluene, ethyl acetate and acetone were 0.002, 0.002 8 and 0.002 33 min⁻¹ respectively under single-component condition. Reaction rates of VOCs in three-component mixture were 0.49-0.88 times of single components.

Six-phase soil heating accelerates VOC extraction from clay soil

International Nuclear Information System (INIS)

Gauglitz, P.A.; Roberts, J.S.; Bergsman, T.M.; Caley, S.M.; Heath, W.O.; Miller, M.C.; Moss, R.W.; Schalla, R.; Jarosch, T.R.; Eddy-Dilek, C.A.

1994-08-01

Six-Phase Soil Heating (SPSH) was demonstrated as a viable technology for heating low permeability soils containing volatile organic contaminants. Testing was performed as part of the Volatile Organic Compounds in Non-Arid Soils Integrated Demonstration (VOC Non-Arid ID) at the Savannah River Site. The soil at the integrated demonstration site is contaminated with perchloroethylene (PCE) and trichloroethylene (TCE); the highest soil contamination occurs in clay-rich zones that are ineffectively treated by conventional soil vapor extraction due to the very low permeability of the clay. The SPSH demonstration sought to heat the clay zone and enhance the performance of conventional soil vapor extraction. Thermocouples at thirty locations quantified the areal and vertical heating within the treated zone. Soil samples were collected before and after heating to quantify the efficacy of heat-enhanced vapor extraction of PCE and TCE from the clay soil. Samples were taken (essentially every foot) from six wells prior to heating and adjacent to these wells after heating. Results show that contaminant removal from the clay zone was 99.7% (median) within the electrode array. Outside the array where the soil was heated, but to only 50 degrees C, the removal efficiency was 93%, showing that heating accelerated the removal of VOCs from the clay soil. The accelerated remediation resulted from effective heating of the contaminated clay zone by SPSH. The temperature of the clay zone increased to 100 degrees C after 8 days of heating and was maintained near 100 degrees C for 17 days. Electrical heating removed 19,000 gal of water from the soil as steam, with peak removal rate of 1,500 gpd of condensed steam

Containment and recovery of a light non-aqueous phase liquid plume at a woodtreating facility

International Nuclear Information System (INIS)

Crouse, D.; Powell, G.; Hawthorn, S.; Weinstock, S.

1997-01-01

A woodtreating site in Montana used a formulation (product) of 5 percent pentachlorophenol and 95 percent diesel fuel as a carrier liquid to pressure treat lumber. Through years of operations approximately 378,500 liters of this light non-aqueous phase liquid (LNAPL) product spilled onto the ground and soaked into the groundwater. A plume of this LNAPL product flowed in a northerly direction toward a stream located approximately 410 meters from the pressure treatment building. A 271-meter long high density polyethylene (HDPE) containment cutoff barrier wall was installed 15 meters from the stream to capture, contain, and prevent the product from migrating off site. This barrier was extended to a depth of 3.7 meters below ground surface and allowed the groundwater to flow beneath it. Ten product recovery wells, each with a dual-phase pumping system, were installed within the plume, and a groundwater model was completed to indicate how the plume would be contained by generating a cone of influence at each recovery well. The model indicated that the recovery wells and cutoff barrier wall would contain the plume and prevent further migration. To date, nearly 3 1/2 year's later, approximately 106,000 liters of product have been recovered

Dynamic relationship between the VOC emissions from a Scots pine stem and the tree water relations

Science.gov (United States)

Vanhatalo, Anni; Chan, Tommy; Aalto, Juho; Kolari, Pasi; Rissanen, Kaisa; Hakola, Hannele; Hölttä, Teemu; Bäck, Jaana

2013-04-01

The stems of coniferous trees contain huge storages of oleoresin. The composition of oleoresin depends on e.g. tree species, age, provenance, health status, and environmental conditions. Oleoresin is under pressure in the extensive network of resin ducts in wood and needles. It flows out from a mechanically damaged site to protect the tree by sealing the wounded site. Once in contact with air, volatile parts of oleoresin evaporate, and the residual compounds harden to make a solid protective seal over damaged tissues. The hardening time of the resin depends on evaporation rate of the volatiles which in turn depends on temperature. The storage is also toxic to herbivores and attracts predators that restrict the herbivore damage. Despite abundant knowledge on emissions of volatile isoprenoids from foliage, very little is known about their emissions from woody plant parts. We set up an experiment to measure emissions of isoprene and monoterpenes as well as two oxygenated VOCs, methanol and acetone, from a Scots pine (Pinus sylvestris) stem and branches. The measurements were started in early April and continued until mid-June, 2012. Simultaneously, we measured the dynamics of whole stem and xylem diameter changes, stem sap flow rate and foliage transpiration rate. These measurements were used to estimate A) pressure changes inside the living stem tissue and the water conducting xylem, B) the refilling of stem water stores after winter dehydration (the ratio of sap flow at the stem base to water loss by foliage), and C) the increase in tree water transport capacity (the ratio of maximum daily sap flow rate to the diurnal variation in xylem pressure) during spring due to winter embolism refilling and/or the temperature dependent root water uptake capacity. The results show that already very early in spring, significant VOC emissions from pine stem can be detected, and that they exhibit a diurnal cycle similar to that of ambient temperature. During the highest emission

Satellite and Ground Based Monitoring of Aerosol Plumes

International Nuclear Information System (INIS)

Doyle, Martin; Dorling, Stephen

2002-01-01

Plumes of atmospheric aerosol have been studied using a range of satellite and ground-based techniques. The Sea-viewing WideField-of-view Sensor (SeaWiFS) has been used to observe plumes of sulphate aerosol and Saharan dust around the coast of the United Kingdom. Aerosol Optical Thickness (AOT) was retrieved from SeaWiFS for two events; a plume of Saharan dust transported over the United Kingdom from Western Africa and a period of elevated sulphate experienced over the Easternregion of the UK. Patterns of AOT are discussed and related to the synoptic and mesoscale weather conditions. Further observation of the sulphate aerosol event was undertaken using the Advanced Very High Resolution Radiometer instrument(AVHRR). Atmospheric back trajectories and weather conditions were studied in order to identify the meteorological conditions which led to this event. Co-located ground-based measurements of PM 10 and PM 2.5 were obtained for 4sites within the UK and PM 2.5/10 ratios were calculated in order to identify any unusually high or low ratios(indicating the dominant size fraction within the plume)during either of these events. Calculated percentiles ofPM 2.5/10 ratios during the 2 events examined show that these events were notable within the record, but were in noway unique or unusual in the context of a 3 yr monitoring record. Visibility measurements for both episodes have been examined and show that visibility degradation occurred during both the sulphate aerosol and Saharan dust episodes

Production of Peroxy Nitrates in Boreal Biomass Burning Plumes over Canada During the BORTAS Campaign

Science.gov (United States)

Busilacchio, Marcella; Di Carlo, Piero; Aruffo, Eleonora; Biancofiore, Fabio; Salisburgo, Cesare Dari; Giammaria, Franco; Bauguitte, Stephane; Lee, James; Moller, Sarah; Hopkins, James;

Production of peroxy nitrates in boreal biomass burning plumes over Canada during the BORTAS campaign

Directory of Open Access Journals (Sweden)

M. Busilacchio

2016-03-01

Full Text Available The observations collected during the BOReal forest fires on Tropospheric oxidants over the Atlantic using Aircraft and Satellites (BORTAS campaign in summer 2011 over Canada are analysed to study the impact of forest fire emissions on the formation of ozone (O3 and total peroxy nitrates ∑PNs, ∑ROONO2. The suite of measurements on board the BAe-146 aircraft, deployed in this campaign, allows us to calculate the production of O3 and of  ∑PNs, a long-lived NOx reservoir whose concentration is supposed to be impacted by biomass burning emissions. In fire plumes, profiles of carbon monoxide (CO, which is a well-established tracer of pyrogenic emission, show concentration enhancements that are in strong correspondence with a significant increase of concentrations of ∑PNs, whereas minimal increase of the concentrations of O3 and NO2 is observed. The ∑PN and O3 productions have been calculated using the rate constants of the first- and second-order reactions of volatile organic compound (VOC oxidation. The ∑PN and O3 productions have also been quantified by 0-D model simulation based on the Master Chemical Mechanism. Both methods show that in fire plumes the average production of ∑PNs and O3 are greater than in the background plumes, but the increase of ∑PN production is more pronounced than the O3 production. The average ∑PN production in fire plumes is from 7 to 12 times greater than in the background, whereas the average O3 production in fire plumes is from 2 to 5 times greater than in the background. These results suggest that, at least for boreal forest fires and for the measurements recorded during the BORTAS campaign, fire emissions impact both the oxidized NOy and O3,  but (1 ∑PN production is amplified significantly more than O3 production and (2 in the forest fire plumes the ratio between the O3 production and the ∑PN production is lower than the ratio evaluated in the background air masses, thus confirming that the

Spatial and temporal migration of a landfill leachate plume in alluvium

Science.gov (United States)

Masoner, Jason R.; Cozzarelli, Isabelle M.

2015-01-01

conditions provides increased understanding of plume behavior and migration potential and may be applied at less monitored landfill sites to evaluate potential risks of contamination to downgradient receptors.

An updated emission inventory of vehicular VOCs and IVOCs in China

Science.gov (United States)

Liu, Huan; Man, Hanyang; Cui, Hongyang; Wang, Yanjun; Deng, Fanyuan; Wang, Yue; Yang, Xiaofan; Xiao, Qian; Zhang, Qiang; Ding, Yan; He, Kebin

2017-10-01

Currently, the emission inventory of vehicular volatile organic compounds (VOCs) is one of those with the largest errors and uncertainties due to suboptimal estimation methods and the lack of first-hand basic data. In this study, an updated speciated emission inventory of VOCs and an estimation of intermediate-volatility organic compounds (IVOCs) from vehicles in China at the provincial level for the year of 2015 are developed based on a set of state-of-the-art methods and an abundance of local measurement data. Activity data for light-duty vehicles are derived from trajectories of more than 70 000 cars for 1 year. The annual mileage of trucks are calculated from reported data by more than 2 million trucks in China. The emission profiles are updated using measurement data. Vehicular tailpipe emissions (VTEs) and four types of vehicular evaporation emissions (VEEs), including refueling, hot soak, diurnal and running loss, are taken into account. Results show that the total vehicular VOC emissions in China are 4.21 Tg (with a 95 % confidence interval range from 2.90 to 6.54 Tg) and the IVOC emissions are 200.37 Gg in 2015. VTEs are still the predominant contributor, while VEEs are responsible for 39.20 % of VOC emissions. The control of VEEs is yet to be optimized in China. Among VTEs, passenger vehicles emissions have the largest share (49.86 %), followed by trucks (28.15 %) and motorcycles (21.99 %). Among VEEs, running loss is the largest contributor (81.05 %). For both VTEs and VEEs, Guangdong, Shandong and Jiangsu province are three of the highest, with a respective contribution of 10.66, 8.85 and 6.54 % to the total amounts of VOCs from vehicles. 97 VOC species are analyzed in this VOC emission inventory. i-Pentane, toluene and formaldehyde are found to be the most abundant species in China's vehicular VOC emissions. The estimated IVOCs are another inconvenient truth, concluding that precursor emissions for secondary organic aerosol (SOA) from vehicles are much

Evaluation of impact factors on VOC emissions and concentrations from wooden flooring based on chamber tests

Energy Technology Data Exchange (ETDEWEB)

Lin, Chi-Chi [Department of Civil and Environmental Engineering, National University of Kaohsiung, No. 700, Kaohsiung University Rd., Kaohsiung (China); Yu, Kuo-Pin [Institute of Environmental and Occupational Health Sciences, National Yang-Ming University, No.155, Sec.2, Linong Street, Taipei (China); Zhao, Ping [Filtration Group Inc., 912 E. Washington Street, Joliet, IL 60433 (United States); Whei-May Lee, Grace [Graduate Institute of Environmental Engineering, National Taiwan University, 71, Chou-Shan Rd., Taipei (China)

2009-03-15

In this study, the impact factors of temperature, relative humidity (RH), air exchange rate, and volatile organic compound (VOC) properties on the VOC (toluene, n-butyl acetate, ethylbenzene, and m,p-xylene) specific emission rates (SERs) and concentrations from wooden flooring were investigated by chamber test for 8 days. The tested wood in this study is not common solid wood, but composite wood made of combined wood fibers. The experiments were conducted in a stainless-steel environmental test chamber coated with Teflon. The experimental results within 8 days of testing showed that, when the temperature increased from 15 to 30 C, the VOC SERs and concentrations increased 1.5-129 times. When the RH increased from 50% to 80%, the VOC concentrations and SERs increased 1-32 times. When the air change rate increased from 1 to 2 h{sup -1}, the VOC concentrations decreased 9-40%, while the VOC SERs increased 6-98%. The relations between the boiling points of the VOCs and each of the normalized VOC SERs and concentrations were linear with negative slopes. The relations between the vapor pressures of the VOCs and each of the normalized VOC SERs and concentrations were linear with positive slopes. At 15 C, RH50%, the relations between the diffusivities of VOCs and each of the normalized VOC equilibrium SERs and concentrations were linear with a positive slope. (author)

Building materials. VOC emissions, diffusion behaviour and implications from their use.

Science.gov (United States)

Katsoyiannis, Athanasios; Leva, Paolo; Barrero-Moreno, Josefa; Kotzias, Dimitrios

2012-10-01

Five cement- and five lime-based building materials were examined in an environmental chamber for their emissions of Volatile Organic Compounds (VOCs). Typical VOCs were below detection limits, whereas not routinely analysed VOCs, like neopentyl glycol (NPG), dominated the cement-based products emissions, where, after 72 h, it was found to occur, in levels as high as 1400 μg m(-3), accounting for up to 93% of total VOCs. The concentrations of NPG were not considerably changed between the 24 and 72 h of sampling. The permeability of building materials was assessed through experiments with a dual environmental chamber; it was shown that building materials facilitate the diffusion of chemicals through their pores, reaching equilibrium relatively fast (6 h). Copyright © 2012 Elsevier Ltd. All rights reserved.

Active Iron Sites of Disordered Mesoporous Silica Catalyst FeKIL-2 in the Oxidation of Volatile Organic Compounds (VOC

Directory of Open Access Journals (Sweden)

Mojca Rangus

2014-05-01

Full Text Available Iron-functionalized disordered mesoporous silica (FeKIL-2 is a promising, environmentally friendly, cost-effective and highly efficient catalyst for the elimination of volatile organic compounds (VOCs from polluted air via catalytic oxidation. In this study, we investigated the type of catalytically active iron sites for different iron concentrations in FeKIL-2 catalysts using advanced characterization of the local environment of iron atoms by a combination of X-ray Absorption Spectroscopy Techniques (XANES, EXAFS and Atomic-Resolution Scanning Transmission Electron Microscopy (AR STEM. We found that the molar ratio Fe/Si ≤ 0.01 leads to the formation of stable, mostly isolated Fe3+ sites in the silica matrix, while higher iron content Fe/Si > 0.01 leads to the formation of oligonuclear iron clusters. STEM imaging and EELS techniques confirmed the existence of these clusters. Their size ranges from one to a few nanometers, and they are unevenly distributed throughout the material. The size of the clusters was also found to be similar, regardless of the nominal concentration of iron (Fe/Si = 0.02 and Fe/Si = 0.05. From the results obtained from sample characterization and model catalytic tests, we established that the enhanced activity of FeKIL-2 with the optimal Fe/Si = 0.01 ratio can be attributed to: (1 the optimal concentration of stable isolated Fe3+ in the silica support; and (2 accelerated diffusion of the reactants in disordered mesoporous silica (FeKIL-2 when compared to ordered mesoporous silica materials (FeSBA-15, FeMCM-41.

Using ASCEM Modeling and Visualization to Inform Stakeholders of Contaminant Plume Evolution and Remediation Efficacy at F-Basin Savannah River, SC – 15156

Energy Technology Data Exchange (ETDEWEB)

Flach, G. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Wainwright, H. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Molins, S. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Davis, J. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Arora, B. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Faybishenko, B. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Krishnan, H. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Hubbard, S. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Flach, G. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Denham, M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Eddy-Dilek, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Moulton, D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Lipnikov, K. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Gable, C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Miller, T. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Freshley, M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2015-01-28

Communication with stakeholders, regulatory agencies, and the public is an essential part of implementing different remediation and monitoring activities, and developing site closure strategies at contaminated sites. Modeling of contaminant plume evolution plays a critical role in estimating the benefit, cost, and risk of particular options. At the same time, effective visualization of monitoring data and modeling results are particularly important for conveying the significance of the results and observations. In this paper, we present the results of the Advanced Simulation Capability for Environmental Management (ASCEM) project, including the discussion of the capabilities of newly developed ASCEM software package, along with its application to the F-Area Seepage Basins located in the U.S. Department of Energy Savannah River Site (SRS). ASCEM software includes state-of-the-art numerical methods for simulating complex flow and reactive transport, as well as various toolsets such as a graphical user interface (GUI), visualization, data management, uncertainty quantification, and parameter estimation. Using this software, we have developed an advanced visualization of tritium plume migration coupled with a data management system, and simulated a three-dimensional model of flow and plume evolution on a high-performance computing platform. We evaluated the effect of engineered flow barriers on a nonreactive tritium plume, through advanced plume visualization and modeling of tritium plume migration. In addition, we developed a geochemical reaction network to describe complex geochemical processes at the site, and evaluated the impact of coupled hydrological and geochemical heterogeneity. These results are expected to support SRS’s monitoring activities and operational decisions.

Rebound of a coal tar creosote plume following partial source zone treatment with permanganate.

Science.gov (United States)

Thomson, N R; Fraser, M J; Lamarche, C; Barker, J F; Forsey, S P

2008-11-14

The long-term management of dissolved plumes originating from a coal tar creosote source is a technical challenge. For some sites stabilization of the source may be the best practical solution to decrease the contaminant mass loading to the plume and associated off-site migration. At the bench-scale, the deposition of manganese oxides, a permanganate reaction byproduct, has been shown to cause pore plugging and the formation of a manganese oxide layer adjacent to the non-aqueous phase liquid creosote which reduces post-treatment mass transfer and hence mass loading from the source. The objective of this study was to investigate the potential of partial permanganate treatment to reduce the ability of a coal tar creosote source zone to generate a multi-component plume at the pilot-scale over both the short-term (weeks to months) and the long-term (years) at a site where there is >10 years of comprehensive synoptic plume baseline data available. A series of preliminary bench-scale experiments were conducted to support this pilot-scale investigation. The results from the bench-scale experiments indicated that if sufficient mass removal of the reactive compounds is achieved then the effective solubility, aqueous concentration and rate of mass removal of the more abundant non-reactive coal tar creosote compounds such as biphenyl and dibenzofuran can be increased. Manganese oxide formation and deposition caused an order-of-magnitude decrease in hydraulic conductivity. Approximately 125 kg of permanganate were delivered into the pilot-scale source zone over 35 days, and based on mass balance estimates 35% reduction for all monitored compounds except for biphenyl, dibenzofuran and fluoranthene 150 days after treatment, which is consistent with the bench-scale experimental results. Pre- and post-treatment soil core data indicated a highly variable and random spatial distribution of mass within the source zone and provided no insight into the mass removed of any of the

Draft no-migration variance petition. Volume 7, Appendices: SUM, SURV, VOC, WAP

International Nuclear Information System (INIS)

1995-01-01

The Department of Energy is responsible for the disposition of transuranic (TRU) waste generated by national defense-related activities. Approximately 2,6 million cubic feet of these waste have been generated and are stored at various facilities across the country. The Waste Isolation Pilot Plant (WIPP), was sited and constructed to meet stringent disposal requirements. In order to permanently dispose of TRU waste, the DOE has elected to petition the US EPA for a variance from the Land Disposal Restrictions of RCRA. This document fulfills the reporting requirements for the petition. This report is volume 7 of the petition which presents details about the waste analysis plan for WIPP. VOC screening methodologies; and a summary of the site characterization studies conducted from 1983 through 1987 at WIPP

Evaluation of plume potential and plume abatement of evaporative cooling towers in a subtropical region

International Nuclear Information System (INIS)

Xu Xinhua; Wang Shengwei; Ma Zhenjun

2008-01-01

Hong Kong is a typical subtropical region with frequently high humidity in late spring and summer seasons. Plume from evaporative cooling towers, which service air-conditioning systems of civil buildings, has aroused public concerns since 2000 when the fresh water evaporative cooling towers were allowed to be used for high energy efficiency and environmental issues. This paper presents the evaluation of the plume potential and its effect on the sizing of the plume abatement system in a large commercial office building in Hong Kong for practical application. This evaluation was conducted based on a dynamic simulation platform using the typical meteorological year of Hong Kong since the occurrence of the plume heavily depends on the state conditions of the exhaust air from cooling towers and the ambient air, while the state condition of the exhaust air is determined by the total building cooling load and the control strategies of cooling towers employed mainly for improving energy efficiency. The results show that the control strategies have a significant effect on the plume potential and further affect the system design and sizing of the plume abatement system

Methane Emission Estimates from Landfills Obtained with Dynamic Plume Measurements

International Nuclear Information System (INIS)

Hensen, A.; Scharff, H.

2001-01-01

Methane emissions from 3 different landfills in the Netherlands were estimated using a mobile Tuneable Diode Laser system (TDL). The methane concentration in the cross section of the plume is measured downwind of the source on a transect perpendicular to the wind direction. A gaussian plume model was used to simulate the concentration levels at the transect. The emission from the source is calculated from the measured and modelled concentration levels.Calibration of the plume dispersion model is done using a tracer (N 2 O) that is released from the landfill and measured simultaneously with the TDL system. The emission estimates for the different locations ranged from 3.6 to 16 m 3 ha -1 hr -1 for the different sites. The emission levels were compared to emission estimates based on the landfill gas production models. This comparison suggests oxidation rates that are up to 50% in spring and negligible in November. At one of the three sites measurements were performed in campaigns in 3 consecutive years. Comparison of the emission levels in the first and second year showed a reduction of the methane emission of about 50% due to implementation of a gas extraction system. From the second to the third year emissions increased by a factor of 4 due to new land filling. Furthermore measurements were performed in winter when oxidation efficiency was reduced. This paper describes the measurement technique used, and discusses the results of the experimental sessions that were performed

Belowground communication: impacts of volatile organic compounds (VOCs) from soil fungi on other soil-inhabiting organisms.

Science.gov (United States)

Werner, Stephanie; Polle, Andrea; Brinkmann, Nicole

2016-10-01

We reviewed the impact of fungal volatile organic compounds (VOCs) on soil-inhabiting organisms and their physiological and molecular consequences for their targets. Because fungi can only move by growth to distinct directions, a main mechanism to protect themselves from enemies or to manipulate their surroundings is the secretion of exudates or VOCs. The importance of VOCs in this regard has been significantly underestimated. VOCs not only can be means of communication, but also signals that are able to specifically manipulate the recipient. VOCs can reprogram root architecture of symbiotic partner plants or increase plant growth leading to enlarged colonization surfaces. VOCs are also able to enhance plant resistance against pathogens by activating phytohormone-dependent signaling pathways. In some cases, they were phytotoxic. Because the response was specific to distinct species, fungal VOCs may contribute to regulate the competition of plant communities. Additionally, VOCs are used by the producing fungus to attack rivaling fungi or bacteria, thereby protecting the emitter or its nutrient sources. In addition, animals, like springtails, nematodes, and earthworms, which are important components of the soil food web, respond to fungal VOCs. Some VOCs are effective repellents for nematodes and, therefore, have applications as biocontrol agents. In conclusion, this review shows that fungal VOCs have a huge impact on soil fauna and flora, but the underlying mechanisms, how VOCs are perceived by the recipients, how they manipulate their targets and the resulting ecological consequences of VOCs in inter-kingdom signaling is only partly understood. These knowledge gaps are left to be filled by future studies.

Variability of indoor and outdoor VOC measurements: An analysis using variance components

International Nuclear Information System (INIS)

Jia, Chunrong; Batterman, Stuart A.; Relyea, George E.

2012-01-01

This study examines concentrations of volatile organic compounds (VOCs) measured inside and outside of 162 residences in southeast Michigan, U.S.A. Nested analyses apportioned four sources of variation: city, residence, season, and measurement uncertainty. Indoor measurements were dominated by seasonal and residence effects, accounting for 50 and 31%, respectively, of the total variance. Contributions from measurement uncertainty (<20%) and city effects (<10%) were small. For outdoor measurements, season, city and measurement variation accounted for 43, 29 and 27% of variance, respectively, while residence location had negligible impact (<2%). These results show that, to obtain representative estimates of indoor concentrations, measurements in multiple seasons are required. In contrast, outdoor VOC concentrations can use multi-seasonal measurements at centralized locations. Error models showed that uncertainties at low concentrations might obscure effects of other factors. Variance component analyses can be used to interpret existing measurements, design effective exposure studies, and determine whether the instrumentation and protocols are satisfactory. - Highlights: ► The variability of VOC measurements was partitioned using nested analysis. ► Indoor VOCs were primarily controlled by seasonal and residence effects. ► Outdoor VOC levels were homogeneous within neighborhoods. ► Measurement uncertainty was high for many outdoor VOCs. ► Variance component analysis is useful for designing effective sampling programs. - Indoor VOC concentrations were primarily controlled by seasonal and residence effects; and outdoor concentrations were homogeneous within neighborhoods. Variance component analysis is a useful tool for designing effective sampling programs.

Chemistry in aircraft plumes

Energy Technology Data Exchange (ETDEWEB)

Kraabol, A.G.; Stordal, F.; Knudsen, S. [Norwegian Inst. for Air Research, Kjeller (Norway); Konopka, P. [Deutsche Forschungsanstalt fuer Luft- und Raumfahrt e.V. (DLR), Wessling (Germany). Inst. fuer Physik der Atmosphaere

1997-12-31

An expanding plume model with chemistry has been used to study the chemical conversion of NO{sub x} to reservoir species in aircraft plumes. The heterogeneous conversion of N{sub 2}O{sub 5} to HNO{sub 3}(s) has been investigated when the emissions take place during night-time. The plume from an B747 has been simulated. During a ten-hour calculation the most important reservoir species was HNO{sub 3} for emissions at noon. The heterogeneous reactions had little impact on the chemical loss of NO{sub x} to reservoir species for emissions at night. (author) 4 refs.

Chemistry in aircraft plumes

Energy Technology Data Exchange (ETDEWEB)

Kraabol, A G; Stordal, F; Knudsen, S [Norwegian Inst. for Air Research, Kjeller (Norway); Konopka, P [Deutsche Forschungsanstalt fuer Luft- und Raumfahrt e.V. (DLR), Wessling (Germany). Inst. fuer Physik der Atmosphaere

1998-12-31

An expanding plume model with chemistry has been used to study the chemical conversion of NO{sub x} to reservoir species in aircraft plumes. The heterogeneous conversion of N{sub 2}O{sub 5} to HNO{sub 3}(s) has been investigated when the emissions take place during night-time. The plume from an B747 has been simulated. During a ten-hour calculation the most important reservoir species was HNO{sub 3} for emissions at noon. The heterogeneous reactions had little impact on the chemical loss of NO{sub x} to reservoir species for emissions at night. (author) 4 refs.

Barometric pumping with a twist: VOC containment and remediation without boreholes. Phase I

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-08-01

The majority of the planned remediation sites within the DOE complex are contaminated with volatile organic compounds (VOCs). In many instances the contamination has not reached the water table, does not pose an immediate threat, and is not considered a high priority problem. These sites will ultimately require remediation of some type, either by active vapor extraction, bioremediation, or excavation and ex-situ soil treatment. The cost of remediating these sites can range from $50 K to more than $150 K, depending on site characteristics, contaminants, and remediation method. Additionally, for many remediated sites, residual contamination exists which could not practically be removed by the applied remediation technology. These circumstances result in modest sites with contamination of limited risk, but by regulation they must still be controlled. A remediation solution being developed by Science and Engineering Associates, Inc. (SEA) for the Department of Energy serves as an in-situ containment and extraction methodology for sites where most or all of the contamination resides in the vadose zone soil. The approach capitalizes on the advective soil gas movement resulting from barometric pressure oscillations.

VOCs and OVOCs distribution and control policy implications in Pearl River Delta region, China

Science.gov (United States)

Louie, Peter K. K.; Ho, Josephine W. K.; Tsang, Roy C. W.; Blake, Donald R.; Lau, Alexis K. H.; Yu, Jian Zhen; Yuan, Zibing; Wang, Xinming; Shao, Min; Zhong, Liuju

2013-09-01

Ambient air measurements of volatile organic compounds (VOCs) and oxygenated volatile organic compounds (OVOCs) were conducted and characterised during a two-year grid study in the Pearl River Delta (PRD) region of southern China. The present grid study pioneered the systematic investigation of the nature and characteristics of complex VOC and OVOC sources at a regional scale. The largest contributing VOCs, accounting over 80% of the total VOCs mixing ratio, were toluene, ethane, ethyne, propane, ethene, butane, benzene, pentane, ethylbenzene, and xylenes. Sub-regional VOC spatial characteristics were identified, namely: i) relatively fresh pollutants, consistent with elevated vehicular and industrial activities, around the PRD estuary; and ii) a concentration gradient with higher mixing ratios of VOCs in the west as compared with the eastern part of PRD. Based on alkyl nitrate aging determination, a high hydroxyl radical (OH) concentration favoured fast hydrocarbon reactions and formation of locally produced ozone. The photochemical reactivity analysis showed aromatic hydrocarbons and alkenes together consisted of around 80% of the ozone formation potential (OFP) among the key VOCs. We also found that the OFP from OVOCs should not be neglected since their OFP contribution was more than one-third of that from VOCs alone. These findings support the choice of current air pollution control policy which focuses on vehicular sources but warrants further controls. Industrial emissions and VOCs emitted by solvents should be the next targets for ground-level ozone abatement.

The Alberta smoke plume observation study

Directory of Open Access Journals (Sweden)

K. Anderson

2018-02-01

Full Text Available A field project was conducted to observe and measure smoke plumes from wildland fires in Alberta. This study used handheld inclinometer measurements and photos taken at lookout towers in the province. Observations of 222 plumes were collected from 21 lookout towers over a 6-year period from 2010 to 2015. Observers reported the equilibrium and maximum plume heights based on the plumes' final levelling heights and the maximum lofting heights, respectively. Observations were tabulated at the end of each year and matched to reported fires. Fire sizes at assessment times and forest fuel types were reported by the province. Fire weather conditions were obtained from the Canadian Wildland Fire Information System (CWFIS. Assessed fire sizes were adjusted to the appropriate size at plume observation time using elliptical fire-growth projections. Though a logical method to collect plume observations in principle, many unanticipated issues were uncovered as the project developed. Instrument limitations and environmental conditions presented challenges to the investigators, whereas human error and the subjectivity of observations affected data quality. Despite these problems, the data set showed that responses to fire behaviour conditions were consistent with the physical processes leading to plume rise. The Alberta smoke plume observation study data can be found on the Canadian Wildland Fire Information System datamart (Natural Resources Canada, 2018 at http://cwfis.cfs.nrcan.gc.ca/datamart.

The Alberta smoke plume observation study

Science.gov (United States)

Anderson, Kerry; Pankratz, Al; Mooney, Curtis; Fleetham, Kelly

2018-02-01

A field project was conducted to observe and measure smoke plumes from wildland fires in Alberta. This study used handheld inclinometer measurements and photos taken at lookout towers in the province. Observations of 222 plumes were collected from 21 lookout towers over a 6-year period from 2010 to 2015. Observers reported the equilibrium and maximum plume heights based on the plumes' final levelling heights and the maximum lofting heights, respectively. Observations were tabulated at the end of each year and matched to reported fires. Fire sizes at assessment times and forest fuel types were reported by the province. Fire weather conditions were obtained from the Canadian Wildland Fire Information System (CWFIS). Assessed fire sizes were adjusted to the appropriate size at plume observation time using elliptical fire-growth projections. Though a logical method to collect plume observations in principle, many unanticipated issues were uncovered as the project developed. Instrument limitations and environmental conditions presented challenges to the investigators, whereas human error and the subjectivity of observations affected data quality. Despite these problems, the data set showed that responses to fire behaviour conditions were consistent with the physical processes leading to plume rise. The Alberta smoke plume observation study data can be found on the Canadian Wildland Fire Information System datamart (Natural Resources Canada, 2018) at http://cwfis.cfs.nrcan.gc.ca/datamart.

Volatile Organic Compound Concentrations and Emission Rates in New Manufactured and Site-Built Houses

Energy Technology Data Exchange (ETDEWEB)

Armin Rudd

2008-10-30

This study was conducted with the primary objective of characterizing and comparing the airborne concentrations and the emission rates of total VOCs and selected individual VOCs, including formaldehyde, among a limited number of new manufactured and site-built houses.

Selection of Sustainable Technology for VOC Abatement in an Industry: An Integrated AHP-QFD Approach

Science.gov (United States)

Gupta, Alok Kumar; Modi, Bharat A.

2018-04-01

Volatile organic compounds (VOCs) are universally present in global atmospheric pollutants. These VOCs are responsible for photo chemical reaction in atmosphere leading to serious harmful effects on human health and environment. VOCs are produced from both natural and man-made sources and may have good commercial value if it can be utilized as alternate fuel. As per data from US EPA, 15% of total VOC emissions are generated from surface coating industry but VOC concentration and exhaust air volume varies to a great extent and is dependent on processes used by industry. Various technologies are available for abatement of VOCs. Physical, Chemical and Biological technologies are available to remove VOCs by either recovery or destruction with many advantages and limitations. With growing environmental awareness and considering the resource limitations of medium and small scale industries, requirement of a tool for selecting appropriate techno economically viable solution for removal of VOCs from industrial process exhaust is envisaged. The aim of the present study is to provide management a tool to determine the overall effect of implementation of VOC abatement technology on business performance and VOC emissions. The primary purpose of this work is to outline a methodology to rate various VOC abatement technologies with respect to the constraint of meeting current and foreseeable future regulatory requirements, operational flexibility and Over All Economics Parameters considering conservation of energy. In this paper an integrated approach has been proposed to select most appropriate abatement technology strategically. Analytical hierarchy process and Quality function deployment have been integrated for Techno-commercial evaluation. A case study on selection of VOC abatement technology for a leading aluminium foil surface coating, lamination and printing facility using this methodology is presented in this study.

Content and Formation Cause of VOCs in Medical Waste Non-incineration Treatment Project

Science.gov (United States)

Dengchao, Jin; Hongjun, Teng; Zhenbo, Bao; Yang, Li

2018-02-01

When medical waste is treated by non-incineration technology, volatile organic compounds in the waste will be volatile out and form odor pollution. This paper studied VOCs productions in medical waste steam treatment project, microwave treatment project and chemical dinifection project. Sampling and analysis were carried out on the waste gas from treatment equipment and the gas in treatment workshop. The contents of nine VOCs were determined. It was found that the VOCs content in the exhaust gas at the outlet of steam treatment unit was much higher than that of microwave and chemical treatment unit, while the content of VOCs in the chemical treatment workshop was higher than that in the steam and microwave treatment workshop. The formation causes of VOCs were also analyzed and discussed in this paper.

688 AMBIENT VOLATILE ORGANIC COMPOUNDS (VOCS ...

African Journals Online (AJOL)

Osondu

using Gas Chromatography (GC) fitted with Flame Ionization Detector (FID). ... and Industrial emission were identified as sources of VOCs in the studied .... Wax, IIasamaja Market, Chesebrough way, ... A validation processes for diffusive.

Membrane Biotreatment of VOC-Laden Air

National Research Council Canada - National Science Library

Peretti, Stephen

2000-01-01

...%, depending primarily on air contact time. Octanol was used as the stripping fluid because of its low vapor pressure and water solubility, its high partitioning of VOCs from air, and its compatibility...

Building materials. VOC emissions, diffusion behaviour and implications from their use

International Nuclear Information System (INIS)

Katsoyiannis, Athanasios; Leva, Paolo; Barrero-Moreno, Josefa; Kotzias, Dimitrios

2012-01-01

Five cement- and five lime-based building materials were examined in an environmental chamber for their emissions of Volatile Organic Compounds (VOCs). Typical VOCs were below detection limits, whereas not routinely analysed VOCs, like neopentyl glycol (NPG), dominated the cement-based products emissions, where, after 72 h, it was found to occur, in levels as high as 1400 μg m −3 , accounting for up to 93% of total VOCs. The concentrations of NPG were not considerably changed between the 24 and 72 h of sampling. The permeability of building materials was assessed through experiments with a dual environmental chamber; it was shown that building materials facilitate the diffusion of chemicals through their pores, reaching equilibrium relatively fast (6 h). - Highlights: ► Neopentyl glycol is reported in emissions from building materials for the first time. ► Neopentyl glycol dominates the VOC emissions from cement-based building materials. ► A dual chamber was developed to control diffusion through building materials. ► Building materials facilitate diffusion of indoor air pollutants through their pores. - Neopentyl glycol was detected in high concentrations in emissions from building materials.

FEV manoeuvre induced changes in breath VOC compositions: an unconventional view on lung function tests

Science.gov (United States)

Sukul, Pritam; Schubert, Jochen K.; Oertel, Peter; Kamysek, Svend; Taunk, Khushman; Trefz, Phillip; Miekisch, Wolfram

2016-06-01

Breath volatile organic compound (VOC) analysis can open a non-invasive window onto pathological and metabolic processes in the body. Decades of clinical breath-gas analysis have revealed that changes in exhaled VOC concentrations are important rather than disease specific biomarkers. As physiological parameters, such as respiratory rate or cardiac output, have profound effects on exhaled VOCs, here we investigated VOC exhalation under respiratory manoeuvres. Breath VOCs were monitored by means of real-time mass-spectrometry during conventional FEV manoeuvres in 50 healthy humans. Simultaneously, we measured respiratory and hemodynamic parameters noninvasively. Tidal volume and minute ventilation increased by 292 and 171% during the manoeuvre. FEV manoeuvre induced substance specific changes in VOC concentrations. pET-CO2 and alveolar isoprene increased by 6 and 21% during maximum exhalation. Then they decreased by 18 and 37% at forced expiration mirroring cardiac output. Acetone concentrations rose by 4.5% despite increasing minute ventilation. Blood-borne furan and dimethyl-sulphide mimicked isoprene profile. Exogenous acetonitrile, sulphides, and most aliphatic and aromatic VOCs changed minimally. Reliable breath tests must avoid forced breathing. As isoprene exhalations mirrored FEV performances, endogenous VOCs might assure quality of lung function tests. Analysis of exhaled VOC concentrations can provide additional information on physiology of respiration and gas exchange.

Use of biofilters and suspended-growth reactors to treat VOC's

Energy Technology Data Exchange (ETDEWEB)

Neal, A.B.; Loehr, R.C.

2000-07-01

The greater limits placed on volatile organic compound (VOC) emissions by the Clean Air Act Amendments have stimulated evaluation of various VOC treatment methods. Two applicable gas phase treatment technologies are biofiltration and suspended growth reactors. Biofiltration removes contaminants from gas streams that are passed through a bed of biologically active solids. An aerobic suspended-growth reactor (SGR) removes VOCs by biologically treating contaminated air bubbled through an aqueous suspension of active microorganisms. This research compared the performance of a typical compost biofilter to a SGR for the removal of a common VOC (toluene) from gas streams. The objective was to evaluate the impact of mass loading on process performance. Major performance parameters investigated were (1) mass emitted and elimination capacity, (2) off-gas concentrations exiting each type of reactor for various mass loadings, and (3) removal efficiencies obtained by each type of reactor. The results indicated that SGRs can effectively treat gases containing VOCs. For mass loadings ranging from 5 to 30 mg/l-h, the biofilters and SGRs achieved similar VOC removals, in the range of 96--99.7%. Drying of the biofilter medium occurred a high mass loadings. In the SGRs, at mass loadings greater than 17 mg/l-h, process performance decreased when an unknown colored substance was present.

Radionuclide inventories for the F- and H-area seepage basin groundwater plumes

Energy Technology Data Exchange (ETDEWEB)

Hiergesell, Robert A [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Kubilius, Walter P. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2016-05-01

Within the General Separations Areas (GSA) at the Savannah River Site (SRS), significant inventories of radionuclides exist within two major groundwater contamination plumes that are emanating from the F- and H-Area seepage basins. These radionuclides are moving slowly with groundwater migration, albeit more slowly due to interaction with the soil and aquifer matrix material. The purpose of this investigation is to quantify the activity of radionuclides associated with the pore water component of the groundwater plumes. The scope of this effort included evaluation of all groundwater sample analyses obtained from the wells that have been established by the Environmental Compliance & Area Completion Projects (EC&ACP) Department at SRS to monitor groundwater contamination emanating from the F- and H-Area Seepage Basins. Using this data, generalized groundwater plume maps for the radionuclides that occur in elevated concentrations (Am-241, Cm-243/244, Cs-137, I-129, Ni-63, Ra-226/228, Sr-90, Tc-99, U-233/234, U-235 and U-238) were generated and utilized to calculate both the volume of contaminated groundwater and the representative concentration of each radionuclide associated with different plume concentration zones.

Liquid Booster Module (LBM) plume flowfield model

Science.gov (United States)

Smith, S. D.

1981-01-01

A complete definition of the LBM plume is important for many Shuttle design criteria. The exhaust plume shape has a significant effect on the vehicle base pressure. The LBM definition is also important to the Shuttle base heating, aerodynamics and the influence of the exhaust plume on the launch stand and environment. For these reasons a knowledge of the LBM plume characteristics is necessary. A definition of the sea level LBM plume as well as at several points along the Shuttle trajectory to LBM, burnout is presented.

Measurements on cooling tower plumes. Pt. 3

International Nuclear Information System (INIS)

Fortak, H.

1975-11-01

In this paper an extended field experiment is described in which cooling tower plumes were investigated by means of three-dimensional in situ measurements. The goal of this program was to obtain input data for numerical models of cooling tower plumes. Data for testing or developing assumptions for sub-grid parametrizations were of special interest. Utilizing modern systems for high-resolution aerology and small aircraft, four measuring campaigns were conducted: two campaigns (1974) at the cooling towers of the RWE power station at Neurath and also two (1975) at the single cooling tower of the RWE power station at Meppen. Because of the broad spectrum of weather situations, it can be assumed that the results are representative with regard to the interrelationship between the structure of cooling tower plumes and the large-scale meteorological situation. A large number of flights with a powered glider ASK 16 (more than 100 flight hours) crossing the plumes on orthogonal tracks was performed. All flights showed that the plume could be identified up to large downwind distances by discontinuous jumps of temperature and vapour pressure. Therefore a definite geometry of the plume could always be defined. In all cross sections a vertical circulation could be observed. At the plumes boundaries, which could be defined by the mentioned jumps of temperature and vapour pressure, a maximum of downward vertical motion was observed in most cases. Entrainment along the boundary of a cross section seems to be very small, except at the lower part of the plume. There, the mass entrainment is maximum and is responsible for plume rise as well as for enlargement of the cross section. The visible part of the plume (cloud) was only a small fraction of the whole plume. The discontinuities of temperature and vapour pressure show that the plume fills the space below the visible plume down to the ground. However, all effects decrease rapidly towards the ground. It turned out that high

A comparative study of fungal and bacterial biofiltration treating a VOC mixture

International Nuclear Information System (INIS)

Estrada, José M.; Hernández, Sergio; Muñoz, Raúl; Revah, Sergio

2013-01-01

Highlights: ► Bacterial biofilter showed better EC and ΔP than fungal biofilter. ► The preferential biodegradation order was: propanal > hexanol > MIBK > toluene. ► Propanal partially inhibited the biodegradation of the rest of VOCs. ► The two-stage biofilter showed a higher stability than the individual units. -- Abstract: Bacterial biofilters usually exhibit a high microbial diversity and robustness, while fungal biofilters have been claimed to better withstand low moisture contents and pH values, and to be more efficient coping with hydrophobic volatile organic compounds (VOCs). However, there are only few systematic evaluations of both biofiltration technologies. The present study compared fungal and bacterial biofiltration for the treatment of a VOC mixture (propanal, methyl isobutyl ketone-MIBK, toluene and hexanol) under the same operating conditions. Overall, fungal biofiltration supported lower elimination capacities than its bacterial counterpart (27.7 ± 8.9 vs 40.2 ± 5.4 g C m −3 reactor h −1 ), which exhibited a final pressure drop 60% higher than that of the bacterial biofilter due to mycelial growth. The VOC mineralization ratio was also higher in the bacterial bed (≈63% vs ≈43%). However, the substrate biodegradation preference order was similar for both biofilters (propanal > hexanol > MIBK > toluene) with propanal partially inhibiting the consumption of the rest of the VOCs. Both systems supported an excellent robustness versus 24 h VOC starvation episodes. The implementation of a fungal/bacterial coupled system did not significantly improve the VOC removal performance compared to the individual biofilter performances

A comparative study of fungal and bacterial biofiltration treating a VOC mixture

Energy Technology Data Exchange (ETDEWEB)

Estrada, José M. [Departamento de Procesos y Tecnología, Universidad Autónoma Metropolitana-Cuajimalpa, Artificios 40, Col. Miguel Hidalgo, Delegación Álvaro Obregón (Mexico); Departamento de Ingeniería Química y Tecnología del Medio Ambiente – Universidad de Valladolid, Valladolid (Spain); Hernández, Sergio [Departmento de Procesos e Hidráulica – Universidad Autónoma Metropolitana – Iztapalapa Mexico D.F. Mexico (Mexico); Muñoz, Raúl [Departamento de Ingeniería Química y Tecnología del Medio Ambiente – Universidad de Valladolid, Valladolid (Spain); Revah, Sergio, E-mail: srevah@xanum.uam.mx [Departamento de Procesos y Tecnología, Universidad Autónoma Metropolitana-Cuajimalpa, Artificios 40, Col. Miguel Hidalgo, Delegación Álvaro Obregón (Mexico)

2013-04-15

Highlights: ► Bacterial biofilter showed better EC and ΔP than fungal biofilter. ► The preferential biodegradation order was: propanal > hexanol > MIBK > toluene. ► Propanal partially inhibited the biodegradation of the rest of VOCs. ► The two-stage biofilter showed a higher stability than the individual units. -- Abstract: Bacterial biofilters usually exhibit a high microbial diversity and robustness, while fungal biofilters have been claimed to better withstand low moisture contents and pH values, and to be more efficient coping with hydrophobic volatile organic compounds (VOCs). However, there are only few systematic evaluations of both biofiltration technologies. The present study compared fungal and bacterial biofiltration for the treatment of a VOC mixture (propanal, methyl isobutyl ketone-MIBK, toluene and hexanol) under the same operating conditions. Overall, fungal biofiltration supported lower elimination capacities than its bacterial counterpart (27.7 ± 8.9 vs 40.2 ± 5.4 g C m{sup −3} reactor h{sup −1}), which exhibited a final pressure drop 60% higher than that of the bacterial biofilter due to mycelial growth. The VOC mineralization ratio was also higher in the bacterial bed (≈63% vs ≈43%). However, the substrate biodegradation preference order was similar for both biofilters (propanal > hexanol > MIBK > toluene) with propanal partially inhibiting the consumption of the rest of the VOCs. Both systems supported an excellent robustness versus 24 h VOC starvation episodes. The implementation of a fungal/bacterial coupled system did not significantly improve the VOC removal performance compared to the individual biofilter performances.

Radioactive Plumes Monitoring Simulator

International Nuclear Information System (INIS)

Kapelushnik, I.; Sheinfeld, M.; Avida, R.; Kadmon, Y.; Ellenbogen, M.; Tirosh, D.

1999-01-01

The Airborne Radiation Monitoring System (ARMS) monitors air or ground radioactive contamination. The contamination source can be a radioactive plume or an area contaminated with radionuclides. The system is based on two major parts, an airborne unit carried by a helicopter and a ground station carried by a truck. The system enables real time measurement and analysis of radioactive plumes as well as post flight processing. The Radioactive Plumes Monitoring Simulator purpose is to create a virtual space where the trained operators experience full radiation field conditions, without real radiation hazard. The ARMS is based on a flying platform and hence the simulator allows a significant reduction of flight time costs

Seasonal variability and source apportionment of volatile organic compounds (VOCs in the Paris megacity (France

Directory of Open Access Journals (Sweden)

A. Baudic

2016-09-01

Full Text Available Within the framework of air quality studies at the megacity scale, highly time-resolved volatile organic compound (C2–C8 measurements were performed in downtown Paris (urban background sites from January to November 2010. This unique dataset included non-methane hydrocarbons (NMHCs and aromatic/oxygenated species (OVOCs measured by a GC-FID (gas chromatograph with a flame ionization detector and a PTR-MS (proton transfer reaction – mass spectrometer, respectively. This study presents the seasonal variability of atmospheric VOCs being monitored in the French megacity and their various associated emission sources. Clear seasonal and diurnal patterns differed from one VOC to another as the result of their different origins and the influence of environmental parameters (solar radiation, temperature. Source apportionment (SA was comprehensively conducted using a multivariate mathematical receptor modeling. The United States Environmental Protection Agency's positive matrix factorization tool (US EPA, PMF was used to apportion and quantify ambient VOC concentrations into six different sources. The modeled source profiles were identified from near-field observations (measurements from three distinct emission sources: inside a highway tunnel, at a fireplace and from a domestic gas flue, hence with a specific focus on road traffic, wood-burning activities and natural gas emissions and hydrocarbon profiles reported in the literature. The reconstructed VOC sources were cross validated using independent tracers such as inorganic gases (NO, NO2, CO, black carbon (BC and meteorological data (temperature. The largest contributors to the predicted VOC concentrations were traffic-related activities (including motor vehicle exhaust, 15 % of the total mass on the annual average, and evaporative sources, 10 %, with the remaining emissions from natural gas and background (23 %, solvent use (20 %, wood-burning (18 % and a biogenic source (15 %. An

Non-thermal plasmas for non-catalytic and catalytic VOC abatement

International Nuclear Information System (INIS)

Vandenbroucke, Arne M.; Morent, Rino; De Geyter, Nathalie; Leys, Christophe

2011-01-01

Highlights: → We review the current status of catalytic and non-catalytic VOC abatement based on a vast number of research papers. → The underlying mechanisms of plasma-catalysis for VOC abatement are discussed. → Critical process parameters that determine the influent are discussed and compared. - Abstract: This paper reviews recent achievements and the current status of non-thermal plasma (NTP) technology for the abatement of volatile organic compounds (VOCs). Many reactor configurations have been developed to generate a NTP at atmospheric pressure. Therefore in this review article, the principles of generating NTPs are outlined. Further on, this paper is divided in two equally important parts: plasma-alone and plasma-catalytic systems. Combination of NTP with heterogeneous catalysis has attracted increased attention in order to overcome the weaknesses of plasma-alone systems. An overview is given of the present understanding of the mechanisms involved in plasma-catalytic processes. In both parts (plasma-alone systems and plasma-catalysis), literature on the abatement of VOCs is reviewed in close detail. Special attention is given to the influence of critical process parameters on the removal process.

Investigation of Balcony Plume Entrainment

OpenAIRE

Liu, F.; Nielsen, Peter V.; Heiselberg, Per; Brohus, Henrik; Li, B. Z.

2009-01-01

An investigation on the scenarios of the spill plume and its equation was presented in this paper. The study includes two aspects, i.e., the small-scale experiment and the numerical simulation. Two balcony spill plume models are assessed by comparing with the FDS (Fire Dynamic Simulation) and small scale model experiment results. Besides validating the spill model by experiments, the effect of different fire location on balcony plume is also discussed.The results show that the balcony equatio...

Smartphone-based sensing system using ZnO and graphene modified electrodes for VOCs detection.

Science.gov (United States)

Liu, Lei; Zhang, Diming; Zhang, Qian; Chen, Xing; Xu, Gang; Lu, Yanli; Liu, Qingjun

2017-07-15

Volatile organic compounds (VOCs) detection is in high demand for clinic treatment, environment monitoring, and food quality control. Especially, VOCs from human exhaled breath can serve as significant biomarkers of some diseases, such as lung cancer and diabetes. In this study, a smartphone-based sensing system was developed for real-time VOCs monitoring using alternative current (AC) impedance measurement. The interdigital electrodes modified with zinc oxide (ZnO), graphene, and nitrocellulose were used as sensors to produce impedance responses to VOCs. The responses could be detected by a hand-held device, sent out to a smartphone by Bluetooth, and reported with concentration on an android program of the smartphone. The smartphone-based system was demonstrated to detect acetone at concentrations as low as 1.56ppm, while AC impedance spectroscopy was used to distinguish acetone from other VOCs. Finally, measurements of the exhalations from human being were carried out to obtain the concentration of acetone in exhaled breath before and after exercise. The results proved that the smartphone-based system could be applied on the detection of VOCs in real settings for healthcare diagnosis. Thus, the smartphone-based system for VOCs detection provided a convenient, portable and efficient approach to monitor VOCs in exhaled breath and possibly allowed for early diagnosis of some diseases. Copyright © 2016 Elsevier B.V. All rights reserved.

An updated emission inventory of vehicular VOCs and IVOCs in China

Directory of Open Access Journals (Sweden)

H. Liu

2017-10-01

Full Text Available Currently, the emission inventory of vehicular volatile organic compounds (VOCs is one of those with the largest errors and uncertainties due to suboptimal estimation methods and the lack of first-hand basic data. In this study, an updated speciated emission inventory of VOCs and an estimation of intermediate-volatility organic compounds (IVOCs from vehicles in China at the provincial level for the year of 2015 are developed based on a set of state-of-the-art methods and an abundance of local measurement data. Activity data for light-duty vehicles are derived from trajectories of more than 70 000 cars for 1 year. The annual mileage of trucks are calculated from reported data by more than 2 million trucks in China. The emission profiles are updated using measurement data. Vehicular tailpipe emissions (VTEs and four types of vehicular evaporation emissions (VEEs, including refueling, hot soak, diurnal and running loss, are taken into account. Results show that the total vehicular VOC emissions in China are 4.21 Tg (with a 95 % confidence interval range from 2.90 to 6.54 Tg and the IVOC emissions are 200.37 Gg in 2015. VTEs are still the predominant contributor, while VEEs are responsible for 39.20 % of VOC emissions. The control of VEEs is yet to be optimized in China. Among VTEs, passenger vehicles emissions have the largest share (49.86 %, followed by trucks (28.15 % and motorcycles (21.99 %. Among VEEs, running loss is the largest contributor (81.05 %. For both VTEs and VEEs, Guangdong, Shandong and Jiangsu province are three of the highest, with a respective contribution of 10.66, 8.85 and 6.54 % to the total amounts of VOCs from vehicles. 97 VOC species are analyzed in this VOC emission inventory. i-Pentane, toluene and formaldehyde are found to be the most abundant species in China's vehicular VOC emissions. The estimated IVOCs are another inconvenient truth, concluding that precursor emissions for secondary organic

Increasing competitiveness of wine producers in strategic alliances VOC

Directory of Open Access Journals (Sweden)

Martin Prokeš

2012-01-01

Full Text Available The paper describes the main reasons for the formation of new regional association of wineries, based on a different origin for wines in the wine region of Moravia in the southeast part of the Czech Republic. This research aim is to create a plan for new development of such strategic alliances on the basis of results of localization factors. There coefficient of localization is used for identification of cluster. Results are compared with already operating on associations for the appellation in Austria DAC. They were traced changes in consumer preferences in the Czech wine market. Consumers are placing more emphasis on the selection of wine on its descent from a particular area, growing community and the individual grower. This paper specifically introduces new associations for appellation system VOC. This alliance is described in the context of the establishment, operation, development and expansion, respectively the possibility of involvement of additional organizations suppliers and research institutions. The application of the results of research was a plan for the establishment of new alliance VOC Modré Hory, where are associated 30 wine producers of wine in 5 villages around the center Velké Pavlovice. Based on the experience of newly emerging VOC system of appellations was setting up a plan of formation association with the proposed methodological approach. Open cooperation between associations VOC appellation and other entities involving suppliers, customers, research institutions and universities has the possibility of creating an institutionalized wine cluster. The plan to create a wine cluster was proposed to establish cooperation between the newly emerging associations of VOC at three sub-regions of South Moravia, in order to achieve competitive advantage.

Are splash plumes the origin of minor hotspots?

Science.gov (United States)

Davies, J. H.; Bunge, H.-P.

2006-05-01

It has been claimed that focused hot cylindrical upwelling plumes cause many of the surface volcanic hotspots on Earth. It has also been argued that they must originate from thermal boundary layers. In this paper, we present spherical simulations of mantle circulation at close to Earth-like vigor with significant internal heating. These show, in addition to thermal boundary layer plumes, a new class of plumes that are not rooted in thermal boundary layers. These plumes develop as instabilities from the edge of bowls of hot mantle, which are produced by cold downwelling material deforming hot sheets of mantle. The resulting bowl and plume structure can look a bit like the “splash” of a water droplet. These splash plumes might provide an explanation for some hotspots that are not underlain by thermal boundary layer sourced plumes and not initiated by large igneous provinces. We suggest that in Earth's mantle, lithospheric instabilities or small pieces of subducting slab could play the role of the model downwelling material in initiating splash plumes. Splash plumes would have implications for interpreting ocean-island basalt geochemistry, plume fixity, excess plume temperature, and estimating core heat flux. Improved seismic imaging will ultimately test this hypothesis.

Numerical model simulation of atmospheric coolant plumes

International Nuclear Information System (INIS)

Gaillard, P.

1980-01-01

The effect of humid atmospheric coolants on the atmosphere is simulated by means of a three-dimensional numerical model. The atmosphere is defined by its natural vertical profiles of horizontal velocity, temperature, pressure and relative humidity. Effluent discharge is characterised by its vertical velocity and the temperature of air satured with water vapour. The subject of investigation is the area in the vicinity of the point of discharge, with due allowance for the wake effect of the tower and buildings and, where application, wind veer with altitude. The model equations express the conservation relationships for mometum, energy, total mass and water mass, for an incompressible fluid behaving in accordance with the Boussinesq assumptions. Condensation is represented by a simple thermodynamic model, and turbulent fluxes are simulated by introduction of turbulent viscosity and diffusivity data based on in-situ and experimental water model measurements. The three-dimensional problem expressed in terms of the primitive variables (u, v, w, p) is governed by an elliptic equation system which is solved numerically by application of an explicit time-marching algorithm in order to predict the steady-flow velocity distribution, temperature, water vapour concentration and the liquid-water concentration defining the visible plume. Windstill conditions are simulated by a program processing the elliptic equations in an axisymmetrical revolution coordinate system. The calculated visible plumes are compared with plumes observed on site with a view to validate the models [fr

Biomass burning contribution to ambient volatile organic compounds (VOCs) in the Chengdu-Chongqing Region (CCR), China

Science.gov (United States)

Li, Lingyu; Chen, Yuan; Zeng, Limin; Shao, Min; Xie, Shaodong; Chen, Wentai; Lu, Sihua; Wu, Yusheng; Cao, Wei

2014-12-01

Ambient volatile organic compounds (VOCs) were measured intensively using an online gas chromatography-mass spectrometry/flame ionization detector (GC-MS/FID) at Ziyang in the Chengdu-Chongqing Region (CCR) from 6 December 2012 to 4 January 2013. Alkanes contributed the most (59%) to mixing ratios of measured non-methane hydrocarbons (NMHCs), while aromatics contributed the least (7%). Methanol was the most abundant oxygenated VOC (OVOC), contributing 42% to the total amount of OVOCs. Significantly elevated VOC levels occurred during three pollution events, but the chemical composition of VOCs did not differ between polluted and clean days. The OH loss rates of VOCs were calculated to estimate their chemical reactivity. Alkenes played a predominant role in VOC reactivity, among which ethylene and propene were the largest contributors; the contributions of formaldehyde and acetaldehyde were also considerable. Biomass burning had a significant influence on ambient VOCs during our study. We chose acetonitrile as a tracer and used enhancement ratio to estimate the contribution of biomass burning to ambient VOCs. Biomass burning contributed 9.4%-36.8% to the mixing ratios of selected VOC species, and contributed most (>30% each) to aromatics, formaldehyde, and acetaldehyde.

Is the 'Fast Halo' around Hawaii as imaged in the PLUME experiment direct evidence for buoyant plume-fed asthenosphere?

Science.gov (United States)

Morgan, J. P.; Shi, C.; Hasenclever, J.

2010-12-01

An intriguing spatial pattern of variations in shear-wave arrival times has been mapped in the PLUME ocean bottom experiment (Wolfe et al., 2009) around Hawaii. The pattern consists of a halo of fast travel times surrounding a disk of slow arrivals from waves traveling up though the plume. We think it is directly sensing the pattern of dynamic uplift of the base of a buoyant asthenosphere - the buoyancy of the plume conduit lifting a 'rim' of the cooler, denser mantle that the plume rises through. The PLUME analysis inverted for lateral shear velocity variations beneath the lithosphere, after removing the assumed 1-D model velocity structure IASP91. They found that a slow plume-conduit extends to at least 1200 km below the Hawaiian hotspot. In this inversion the slow plume conduit is — quite surprisingly - surrounded by a fast wavespeed halo. A fast halo is impossible to explain as a thermal halo around the plume; this should lead to a slow wavespeed halo, not a fast one. Plume-related shearwave anisotropy also cannot simply explain this pattern — simple vertical strain around the plume conduit would result in an anisotropic slow shear-wavespeed halo, not a fast one. (Note the PLUME experiment’s uniform ‘fast-halo’ structure from 50-400km is likely to have strong vertical streaking in the seismic image; Pacific Plate-driven shear across a low-viscosity asthenosphere would be expected to disrupt and distort any cold sheet of vertical downwelling structure between 50-400km depths so that it would no longer be vertical as it is in the 2009 PLUME image with its extremely poor vertical depth control.) If the asthenosphere is plume-fed, hence more buoyant than underlying mantle, then there can be a simple explanation for this pattern. The anomaly would be due to faster traveltimes resulting from dynamic relief at the asthenosphere-mesosphere interface; uplift of the denser mesosphere by the buoyancy of the rising plume increases the distance a wave travels

Occurrence and Concentrations of Toxic VOCs in the Ambient Air of Gumi, an Electronics-Industrial City in Korea

Directory of Open Access Journals (Sweden)

Sung-Ok Baek

2015-08-01

Full Text Available This study was carried out to characterize the occurrence and concentrations of a variety of volatile organic compounds (VOCs including aliphatic, aromatic, halogenated, nitrogenous, and carbonyl compounds, in the ambient air of Gumi City, where a large number of electronics industries are found. Two field monitoring campaigns were conducted for a one year period in 2003/2004 and 2010/2011 at several sampling sites in the city, representing industrial, residential and commercial areas. More than 80 individual compounds were determined in this study, and important compounds were then identified according to their abundance, ubiquity and toxicity. The monitoring data revealed toluene, trichloroethylene and acetaldehyde to be the most significant air toxics in the city, and their major sources were mainly industrial activities. On the other hand, there was no clear evidence of an industrial impact on the concentrations of benzene and formaldehyde in the ambient air of the city. Overall, seasonal variations were not as distinct as locational variations in the VOCs concentrations, whereas the within-day variations showed a typical pattern of urban air pollution, i.e., increase in the morning, decrease in the afternoon, and an increase again in the evening. Considerable decreases in the concentrations of VOCs from 2003 to 2011 were observed. The reductions in the ambient concentrations were confirmed further by the Korean PRTR data in industrial emissions within the city. Significant decreases in the concentrations of benzene and acetaldehyde were also noted, whereas formaldehyde appeared to be almost constant between the both campaigns. The decreased trends in the ambient levels were attributed not only to the stricter regulations for VOCs in Korea, but also to the voluntary agreement of major companies to reduce the use of organic solvents. In addition, a site planning project for an eco-friendly industrial complex is believed to play a contributory

Development of a novel biofilter for aerobic biodegradation of volatile organic compounds (VOCs)

International Nuclear Information System (INIS)

Govind, R.; Utgikar, V.; Shan, Y.; Zhao, Wang; Sayles, G.D.; Bishop, D.F.; Safferman, S.I.

1992-01-01

In recent years, the emission into the atmosphere of volatile organic compounds (VOCs) has undergone increased regulation by EPA, OSHA and other government agencies due to potential human health hazards. The sources of these VOCs include releases during industrial production and use, from contaminated wastewaters in collection systems and treatment plants, and from hazardous wastes in landfills and contaminated ground water. Conventional methods for treating VOC emissions include adsorption on solids, absorption in solvents, incineration and catalytic oxidation. One alternative to these conventional treatment methods is the biological destruction of the VOCs in gas phase biofilters. This method has the advantage of pollution destruction (as compared to transfer to another medium) at lower operation and maintenance costs. The biofilter method also can be combined with various stripping or vapor extraction separation processes which effectively transfer VOCs from liquid or solid matrices into the gas phase entering biofilters

Pollution characteristic of VOCs of ambient air in winter and spring in Shijiazhuang City

Directory of Open Access Journals (Sweden)

Qing CHANG

2015-06-01

Full Text Available In order to further explore the pollution characteristics of volatile organic compounds in ambient air in winter and spring in Shijiazhuang City, the pollution characteristics of 62 volatile organic compounds (VOCs, monthly and quarterly variation, the correlation between VOCs and PM2.5, and the main sources of VOCs are investigated by using EPA TO-15 method. It shows that 40 organic compounds of the 64 VOCs have been quantitatively determined in winter and spring in the city, which are mainly acetone, benzene, carbon tetrachloride, dichloromethane, toluene, ethyl acetate, etc.. In the no-quantitatively determined components, higher ethanol, butyl acetate, butane etc. are detected. The VOCs concentration has positive correlation with the PM2.5 concentration during haze days.

Hanford Site Groundwater Monitoring for Fiscal Year 2005

Energy Technology Data Exchange (ETDEWEB)

Hartman, Mary J.; Morasch, Launa F.; Webber, William D.

2006-02-28

This report is one of the major products and deliverables of the Groundwater Remediation and Closure Assessment Projects detailed work plan for FY 2006, and reflects the requirements of The Groundwater Performance Assessment Project Quality Assurance Plan (PNNL-15014). This report presents the results of groundwater and vadose zone monitoring and remediation for fiscal year 2005 on the U.S. Department of Energy's Hanford Site, Washington. The most extensive contaminant plumes in groundwater are tritium, iodine-129, and nitrate, which all had multiple sources and are very mobile in groundwater. The largest portions of these plumes are migrating from the central Hanford Site to the southeast, toward the Columbia River. Carbon tetrachloride and associated organic constituents form a relatively large plume beneath the west-central part of the Hanford Site. Hexavalent chromium is present in plumes beneath the reactor areas along the river and beneath the central part of the site. Strontium-90 exceeds standards beneath all but one of the reactor areas. Technetium-99 and uranium plumes exceeding standards are present in the 200 Areas. A uranium plume underlies the 300 Area. Minor contaminant plumes with concentrations greater than standards include carbon-14, cesium-137, cis-1,2-dichloroethene, cyanide, fluoride, plutonium, and trichloroethene. Monitoring for the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 is conducted in 11 groundwater operable units. The purpose of this monitoring is to define and track plumes and to monitor the effectiveness of interim remedial actions. Interim groundwater remediation in the 100 Areas continued with the goal of reducing the amount of chromium (100-K, 100-D, and 100-H) and strontium-90 (100-N) reaching the Columbia River. The objective of two interim remediation systems in the 200 West Area is to prevent the spread of carbon tetrachloride and technetium-99/uranium plumes. Resource Conservation and

VOCs Air Pollutant Cleaning with Polyacrylonitrile/Fly Ash Nanocomposite Electrospun Nanofibrous Membranes

Science.gov (United States)

Cong Ge, Jun; Wang, Zi Jian; Kim, Min Soo; Choi, Nag Jung

2018-01-01

Volatile organic compounds (VOCs) as an environmental pollution, which have many kinds of chemical structures, and many of them are very toxic. Therefore, controlling and reducing the presence of VOCs has become a hot topic among researchers for many years. In this study, the VOCs adsorption capacity of polyacrylonitrile/fly ash (PAN/FA) nanocomposite electrospun nanofibrous membranes were investigated. The results indicated that the PAN with different contents of FA powder (20%, 40%, 60%, 80%, and 100% compared with PAN by weight) could be spun well by electrospinning. The diameter of the fiber was very fine and its arrangement was irregular. The PAN nanofibrous membrane containing 60 wt% FA powder had the highest VOCs absorption capacity compared with other nanofibrous membranes due to its large specific surface area.

317/319 phytoremediation site monitoring report - 2003 growing season.

Energy Technology Data Exchange (ETDEWEB)

Negri, M. C.; Gopalakrishnan, G.; Hamilton, C.; Energy Systems

2004-02-20

In 1999, Argonne National Laboratory-East (ANL-E) designed and installed a series of engineered plantings consisting of a vegetative cover system and approximately 800 hybrid poplars and willows rooting at various predetermined depths. The plants were installed using various methods including Applied Natural Science's TreeWell{reg_sign} system. The goal of the installation was to protect downgradient surface and groundwater by hydraulic control of the contaminated plume by intercepting the contaminated groundwater with the tree roots, removing moisture from the upgradient soil area, reducing water infiltration, preventing soil erosion, degrading and/or transpiring the residual volatile organic compounds (VOCs), and removing tritium from the subsoil and groundwater. This report presents the results of the monitoring activities conducted by Argonne's Energy Systems Division (ES) in the growing season of 2003. ES was tasked with the biomonitoring of the plantation to determine contaminant uptake and groundwater contact. VOCs were found in plant tissue both at the French Drain and the Hydraulic Control locations in varying concentrations, and tritium levels in transpirate was found to continue a trend of higher concentrations compared to the background in the ANL-E area.

Implementation of VOC source reduction practices in a manufactured house and in school classrooms

International Nuclear Information System (INIS)

Hodgson, A.T.; Apte, M.G.; Shendell, D.G.; Beal, D.; McIlvaine, J.E.R.

2002-01-01

Detailed studies of a new manufactured house and four new industrialized relocatable school classrooms were conducted to determine the emission sources of formaldehyde and other VOCs and to identify and implement source reduction practices. Procedures were developed to generate VOC emission factors that allowed reasonably accurate predictions of indoor air VOC concentrations. Based on the identified sources of formaldehyde and other aldehydes, practices were developed to reduce the concentrations of these compounds in new house construction. An alternate ceiling panel reduced formaldehyde concentrations in the classrooms. Overall, the classrooms had relatively low VOC concentrations

Photocatalysts: ambient temperature destruction of VOCs

Energy Technology Data Exchange (ETDEWEB)

Miller, R [IT Corp., Oak Ridge, TN (United States)

1994-12-31

Photocatalysis was a failure as a solar energy driven organic synthesis technique, but as this study indicates, it has undergone a renaissance as a promising treatment method for volatile organic compounds (VOCs) in air streams. Photocatalytic oxidation (PCO) relies upon the ability of certain semiconductors to be stimulated by UV radiation. UV light excites valence band electrons in the semiconductor catalyst to jump to a conductance band leaving holes in the valence band. The electrons and holes can react with compounds such as organic contaminants present in an air stream. Hallmarks of the technology include rapid destruction kinetics for many VOCs at ambient temperature and efficient use energy in the form of UV-A photons. Studies clearly indicate that PCO is competitive on capital cost and offers significant operating cost savings on selected applications. 6 refs., 3 tabs., 2 figs.

Photocatalysts: ambient temperature destruction of VOCs

International Nuclear Information System (INIS)

Miller, R.

1994-01-01

Photocatalysis was a failure as a solar energy driven organic synthesis technique, but as this study indicates, it has undergone a renaissance as a promising treatment method for volatile organic compounds (VOCs) in air streams. Photocatalytic oxidation (PCO) relies upon the ability of certain semiconductors to be stimulated by UV radiation. UV light excites valence band electrons in the semiconductor catalyst to jump to a conductance band leaving holes in the valence band. The electrons and holes can react with compounds such as organic contaminants present in an air stream. Hallmarks of the technology include rapid destruction kinetics for many VOCs at ambient temperature and efficient use energy in the form of UV-A photons. Studies clearly indicate that PCO is competitive on capital cost and offers significant operating cost savings on selected applications. 6 refs., 3 tabs., 2 figs

Theoretical study of simultaneous water and VOCs adsorption and desorption in a silica gel rotor

DEFF Research Database (Denmark)

Zhang, G.; Zhang, Y.F.; Fang, Lei

2008-01-01

One-dimensional partial differential equations were used to model the simultaneous water and VOC (Volatile Organic Compound) adsorption and desorption in a silica gel rotor which was recommended for indoor air cleaning. The interaction among VOCs and moisture in the adsorption and desorption...... process was neglected in the model as the concentrations of VOC pollutants in typical indoor environment were much lower than that of moisture and the adsorbed VOCs occupied only a minor portion of adsorption capacity of the rotor. Consequently VOC transfer was coupled with heat and moisture transfer only...... by the temperatures of the rotor and the air stream. The VOC transfer equations were solved by discretizing them into explicit up-wind finite differential equations. The model was validated with experimental data. The calculated results suggested that the regeneration time designed for dehumidification may...

Remediating Contaminant Plumes in Groundwater with Shallow Excavations Containing Coarse Reactive Media.

Science.gov (United States)

Hudak, Paul F

2018-02-01

A groundwater flow and mass transport model tested the capability of shallow excavations filled with coarse, reactive media to remediate a hypothetical unconfined aquifer with a maximum saturated thickness of 5 m. Modeled as contaminant sinks, the rectangular excavations were 10 m downgradient of an initial contaminant plume originating from a source at the top of the aquifer. The initial plume was approximately 259 m long, 23 m wide, and 5 m thick, with a downgradient tip located approximately 100 m upgradient of the site boundary. The smallest trench capable of preventing offsite migration was 11 m long (measured perpendicular to groundwater flow), 4 m wide (measured parallel to groundwater flow), and 3 m deep. Results of this study suggest that shallow trenches filled with coarse filter media that partially penetrate unconfined aquifers may be a viable alternative for remediating contaminated groundwater at some sites.

Lithosphere erosion atop mantle plumes

Science.gov (United States)

Agrusta, R.; Arcay, D.; Tommasi, A.

2012-12-01

Mantle plumes are traditionally proposed to play an important role in lithosphere erosion. Seismic images beneath Hawaii and Cape Verde show a lithosphere-asthenosphere-boundary (LAB) up to 50 km shallower than the surroundings. However, numerical models show that unless the plate is stationary the thermo-mechanical erosion of the lithosphere does not exceed 30 km. We use 2D petrological-thermo-mechanical numerical models based on a finite-difference method on a staggered grid and marker in cell method to study the role of partial melting on the plume-lithosphere interaction. A homogeneous peridotite composition with a Newtonian temperature- and pressure-dependent viscosity is used to simulate both the plate and the convective mantle. A constant velocity, ranging from 5 to 12.5 cm/yr, is imposed at the top of the plate. Plumes are created by imposing a thermal anomaly of 150 to 350 K on a 50 km wide domain at the base of the model (700 km depth); the plate right above the thermal anomaly is 40 Myr old. Partial melting is modeled using batch-melting solidus and liquidus in anhydrous conditions. We model the progressive depletion of peridotite and its effect on partial melting by assuming that the melting degree only strictly increases through time. Melt is accumulated until a porosity threshold is reached and the melt in excess is then extracted. The rheology of the partially molten peridotite is determined using viscous constitutive relationship based on a contiguity model, which enables to take into account the effects of grain-scale melt distribution. Above a threshold of 1%, melt is instantaneously extracted. The density varies as a function of partial melting degree and extraction. Besides, we analyze the kinematics of the plume as it impacts a moving plate, the dynamics of time-dependent small-scale convection (SSC) instabilities developing in the low-viscosity layer formed by spreading of hot plume material at the lithosphere base, and the resulting thermal

Occurrence of Indoor VOCs in Nursery School - Case Study

Science.gov (United States)

Juhasova Senitkova, Ingrid

2017-10-01

Children’s exposure to air pollutants is an important public health challenge. Particular attention should be paid to preschools because younger children are more vulnerable to air pollution than higher grade children and spend more time indoors. The concentrations of volatile organic compounds (VOCs) as well as carbon dioxide (CO2) concentrations in younger and older children’s classrooms during the winter season were studied. An electronic nose based on gas chromatography was used for the analysis of individual VOCs and a photoionization detector with a UV lamp was used for the determination of total volatile organic compounds (TVOC) concentration. Continuous measurements of CO2 concentrations both inside classrooms and outside each building were performed using automatic portable monitors. Improving ventilation, decreasing the occupancy per room and completing cleaning activities following occupancy periods can contribute to alleviating high CO2 and VOCs occurrence levels.

Mathematical modelling of thermal-plume interaction at Waterford Nuclear Power Station

International Nuclear Information System (INIS)

Tsai, S.Y.H.

1981-01-01

The Waldrop plume model was used to analyze the mixing and interaction of thermal effluents in the Mississippi River resulting from heated-water discharges from the Waterford Nuclear Power Station Unit 3 and from two nearby fossil-fueled power stations. The computer program of the model was modified and expanded to accommodate the multiple intake and discharge boundary conditions at the Waterford site. Numerical results of thermal-plume temperatures for individual and combined operation of the three power stations were obtained for typical low river flow (200,000 cfs) and maximum station operating conditions. The predicted temperature distributions indicated that the surface jet discharge from Waterford Unit 3 would interact with the thermal plumes produced by the two fossil-fueled stations. The results also showed that heat recirculation between the discharge of an upstream fossil-fueled plant and the intake of Waterford Unit 3 is to be expected. However, the resulting combined temperature distributions were found to be well within the thermal standards established by the state of Louisiana

Extended Research on Detection of Deception Using Volatile Organic Compound (VOC) Emissions

Energy Technology Data Exchange (ETDEWEB)

Center for Human Reliability Studies

2006-06-01

A system that captures and analyzes volatile organic compound (VOC) emissions from skin surfaces may offer a viable alternative method to the polygraph instrument currently in use for detecting deception in U.S. government settings. Like the involuntary autonomic central nervous system response data gathered during polygraph testing, VOC emissions from the skin may provide data that can be used to detect stress caused by deception. Detecting VOCs, then, may present a noninvasive, non-intrusive method for observing, recording, and quantifying evidence of stress or emotional change.

Turbulent forces within river plumes affect spread

Science.gov (United States)

Bhattacharya, Atreyee

2012-08-01

When rivers drain into oceans through narrow mouths, hydraulic forces squeeze the river water into buoyant plumes that are clearly visible in satellite images. Worldwide, river plumes not only disperse freshwater, sediments, and nutrients but also spread pollutants and organisms from estuaries into the open ocean. In the United States, the Columbia River—the largest river by volume draining into the Pacific Ocean from North America—generates a plume at its mouth that transports juvenile salmon and other fish into the ocean. Clearly, the behavior and spread of river plumes, such as the Columbia River plume, affect the nation's fishing industry as well as the global economy.

Plume rise measurements at Turbigo

Energy Technology Data Exchange (ETDEWEB)

Anfossi, D

1982-01-01

This paper presents analyses of plume measurements obtained during that campaign by the ENEL ground-based Lidar. The five stacks of Turbigo Power Plant have different heights and emission parameters and their plumes usually combine, so a model for multiple sources was used to predict the plume rises. These predictions are compared with the observations. Measurements of sigma/sub v/ and sigma/sub z/ over the first 1000 m are compared with the curves derived from other observations in the Po Valley, using the no-lift balloon technique over the same range of downwind distance. Skewness and kurtosis distributions are shown, both along the vertical and the horizontal directions. In order to show the plume structure in more detail, we present two examples of Lidar-derived cross sections and the corresponding vertically and horizontally integrated concentration profiles.

Crude oil metabolites in groundwater at two spill sites

Science.gov (United States)

Bekins, Barbara A.; Cozzarelli, Isabelle M.; Erickson, Melinda L.; Steenson, Ross; Thorn, Kevin A.

2016-01-01

Two groundwater plumes in north central Minnesota with residual crude oil sources have 20 to 50 mg/L of nonvolatile dissolved organic carbon (NVDOC). These values are over 10 times higher than benzene and two to three times higher than Diesel Range Organics in the same wells. On the basis of previous work, most of the NVDOC consists of partial transformation products from the crude oil. Monitoring data from 1988 to 2015 at one of the sites located near Bemidji, MN show that the plume of metabolites is expanding toward a lakeshore located 335 m from the source zone. Other mass balance studies of the site have demonstrated that the plume expansion is driven by the combined effect of continued presence of the residual crude oil source and depletion of the electron accepting capacity of solid phase iron oxide and hydroxides on the aquifer sediments. These plumes of metabolites are not covered by regulatory monitoring and reporting requirements in Minnesota and other states. Yet, a review of toxicology studies indicates that polar metabolites of crude oil may pose a risk to aquatic and mammalian species. Together the results suggest that at sites where residual sources are present, monitoring of NVDOC may be warranted to evaluate the fates of plumes of hydrocarbon transformation products.

Plume meander and dispersion in a stable boundary layer

Science.gov (United States)

Hiscox, April L.; Miller, David R.; Nappo, Carmen J.

2010-11-01

Continuous lidar measurements of elevated plume dispersion and corresponding micrometeorology data are analyzed to establish the relationship between plume behavior and nocturnal boundary layer dynamics. Contrasting nights of data from the JORNADA field campaign in the New Mexico desert are analyzed. The aerosol lidar measurements were used to separate the plume diffusion (plume spread) from plume meander (displacement). Mutiresolution decomposition was used to separate the turbulence scale (90 s). Durations of turbulent kinetic energy stationarity and the wind steadiness were used to characterize the local scale and submesoscale turbulence. Plume meander, driven by submesoscale wind motions, was responsible for most of the total horizontal plume dispersion in weak and variable winds and strong stability. This proportion was reduced in high winds (i.e., >4 m s-1), weakly stable conditions but remained the dominant dispersion mechanism. The remainder of the plume dispersion in all cases was accounted for by internal spread of the plume, which is a small eddy diffusion process driven by turbulence. Turbulence stationarity and the wind steadiness are demonstrated to be closely related to plume diffusion and plume meander, respectively.

Impact of intentionally introduced sources on indoor VOC levels

Energy Technology Data Exchange (ETDEWEB)

Davis, C.S. [BOVAR Environmental, Downsview, Ontario (Canada); Otson, R. [Health Canada, Ottawa, Ontario (Canada). Environmental Health Centre

1997-12-31

The concentrations of 33 target volatile organic compounds (VOC) were measured in outdoor air and in indoor air before and after the introduction of dry-cleaned clothes, and consumer products into two suburban homes. Emissions from the household products (air fresheners, furniture polishes, mothballs, and dry-cleaned clothes), showering, and two paints were analyzed to obtain source profiles. There were measurable increases in the 24 h average concentrations for 10 compounds in one house and 8 compounds in the second house after introduction of the sources. A contribution by showering to indoor VOC was not evident although the impact of the other sources and outdoor air could be discerned, based on results for the major constituents of source emissions. Also, contributions by paints, applied three to six weeks prior to the monitoring, to indoor VOC concentrations were evident. The pattern of concentrations indicated that sink effects need to be considered in explaining the indoor concentrations that result when sources are introduced into homes. Quantitative estimates of the relative contributions of the sources to indoor VOC levels were not feasible through the use of chemical mass balance since the number of tracer species detected (up to 6) and that could be used for source apportionment was similar to the number of sources to be apportioned (up to 7).

Measurements of VOCs in Mexico City during the MILAGRO Campaign

Science.gov (United States)

Baker, A. K.; Beyersdorf, A. J.; Blake, N. J.; Meinardi, S.; Atlas, E.; Rowland, F.; Blake, D. R.

2006-12-01

During March of 2006 we participated in MILAGRO (Megacities Initiative: Local and Global Research Observations), a multi-platform campaign to measure pollutants in and in outflow from the Mexico City metropolitan area. As part of MILAGRO we collected whole air canister samples at two Mexico City ground sites: the Instituto Mexicano del Petroleo, located in the city, northeast of the center, and the Universidad Technologica de Tecamac, a suburban site approximately 50 km northeast of the city center. Samples were also collected in various other locations throughout Mexico City. Over 300 whole air samples were collected and analyzed for a wide range of volatile organic compounds (VOCs) including methane, carbon monoxide, nonmethane hydrocarbons (NMHCs) and halocarbons. Propane was the most abundant NMHC at both the urban and suburban locations, with mixing ratios frequently in excess of 10 parts per billion at both locations. This is likely the result of the widespread use of liquefied petroleum gas (LPG) of which propane is the major component. For most species, median mixing ratios at the urban sites were significantly greater than at the suburban site. Here we compare results from both urban and suburban locations and also examine the influence of transport on the composition of outflow from Mexico City.

Experimental investigation of bubble plume structure instability

Energy Technology Data Exchange (ETDEWEB)

Marco Simiano; Robert Zboray; Francois de Cachard [Thermal-Hydraulics Laboratory, Paul Scherrer Institut, 5232 Villigen PSI (Switzerland); Djamel Lakehal; George Yadigaroglu [Institute of Energy Technology, Swiss Federal Institute of Technology, ETH-Zentrum/CLT, 8092 Zurich (Switzerland)

2005-07-01

Full text of publication follows: The hydrodynamic properties of a 3D bubble plume in a large water pool are investigated experimentally. Bubble plumes are present in various industrial processes, including chemical plants, stirred reactors, and nuclear power plants, e.g. in BWR suppression pools. In these applications, the main issue is to predict the currents induced by the bubbles in the liquid phase, and to determine the consequent mixing. Bubble plumes, especially large and unconfined ones, present strong 3D effects and a superposition of different characteristic length scales. Thus, they represent relevant test cases for assessment and verification of 3D models in thermal-hydraulic codes. Bubble plumes are often unsteady, with fluctuations in size and shape of the bubble swarm, and global movements of the plume. In this case, local time-averaged data are not sufficient to characterize the flow. Additional information regarding changes in plume shape and position is required. The effect of scale on the 3D flow structure and stability being complex, there was a need to conduct studies in a fairly large facility, closer to industrial applications. Air bubble plumes, up to 30 cm in base diameter and 2 m in height were extensively studied in a 2 m diameter water pool. Homogeneously sized bubbles were obtained using a particular injector. The main hydrodynamic parameters. i.e., gas and liquid velocities, void fraction, bubble shape and size, plume shape and position, were determined experimentally. Photographic and image processing techniques were used to characterize the bubble shape, and double-tip optical probes to measure bubble size and void fraction. Electromagnetic probes measured the recirculation velocity in the pool. Simultaneous two-phase flow particle image velocimetry (STPFPIV) in a vertical plane containing the vessel axis provided instantaneous velocity fields for both phases and therefore the relative velocity field. Video recording using two CCD

Source profiles of volatile organic compounds (VOCs) measured in China: Part I

Science.gov (United States)

Liu, Ying; Shao, Min; Fu, Linlin; Lu, Sihua; Zeng, Limin; Tang, Dagang

The profiles of major volatile organic compound (VOC) sources in China, including vehicle exhaust, gasoline vapor, paint, asphalt, industrial and residential coal burning, biomass burning, and the petrochemical industry, were experimentally determined. Source samples were taken using a dilution chamber for mobile and stationary sources, biomass burning in an actual Chinese farmer's house, and ambient air in a petrochemical industrial area. The concentrations of 92 VOC species were quantified using canister sampling and a gas chromatography-flame ionization detection/mass spectrometry system, and VOC source profiles were developed for source apportionment of VOCs in the Pearl River Delta region. Based on the measurement of source profiles, possible tracers for various emission sources were identified; e.g., 2-methylpentane and 1,3-butadiene could be used as tracers for vehicle exhaust; the characteristic compounds of architectural coating were aromatics such as toluene and m, p-xylene; the light hydrocarbons, namely n-butane, trans-2-butene, and n-pentane, dominated the composition of gasoline vapor; and n-nonane, n-decane, and n-undecane were found to be typical of diesel vapor and asphalt application processes. As different emission sources are characterized by overlapping VOC species, the ratio of possible VOC tracers could be used to assess the contribution of various sources. The ratios between n-butane and isobutane, 1,3-butadiene and isoprene, and the ratios of aromatics (e.g., toluene to benzene and ethylbenzene to m, p-xylene) in the measured sources were compared.

Chesapeake Bay plume dynamics from LANDSAT

Science.gov (United States)

Munday, J. C., Jr.; Fedosh, M. S.

1981-01-01

LANDSAT images with enhancement and density slicing show that the Chesapeake Bay plume usually frequents the Virginia coast south of the Bay mouth. Southwestern (compared to northern) winds spread the plume easterly over a large area. Ebb tide images (compared to flood tide images) show a more dispersed plume. Flooding waters produce high turbidity levels over the shallow northern portion of the Bay mouth.

PLUME-MoM 1.0: A new integral model of volcanic plumes based on the method of moments

Science.gov (United States)

de'Michieli Vitturi, M.; Neri, A.; Barsotti, S.

2015-08-01

In this paper a new integral mathematical model for volcanic plumes, named PLUME-MoM, is presented. The model describes the steady-state dynamics of a plume in a 3-D coordinate system, accounting for continuous variability in particle size distribution of the pyroclastic mixture ejected at the vent. Volcanic plumes are composed of pyroclastic particles of many different sizes ranging from a few microns up to several centimeters and more. A proper description of such a multi-particle nature is crucial when quantifying changes in grain-size distribution along the plume and, therefore, for better characterization of source conditions of ash dispersal models. The new model is based on the method of moments, which allows for a description of the pyroclastic mixture dynamics not only in the spatial domain but also in the space of parameters of the continuous size distribution of the particles. This is achieved by formulation of fundamental transport equations for the multi-particle mixture with respect to the different moments of the grain-size distribution. Different formulations, in terms of the distribution of the particle number, as well as of the mass distribution expressed in terms of the Krumbein log scale, are also derived. Comparison between the new moments-based formulation and the classical approach, based on the discretization of the mixture in N discrete phases, shows that the new model allows for the same results to be obtained with a significantly lower computational cost (particularly when a large number of discrete phases is adopted). Application of the new model, coupled with uncertainty quantification and global sensitivity analyses, enables the investigation of the response of four key output variables (mean and standard deviation of the grain-size distribution at the top of the plume, plume height and amount of mass lost by the plume during the ascent) to changes in the main input parameters (mean and standard deviation) characterizing the

Fossil plume head beneath the Arabian lithosphere?

Science.gov (United States)

Stein, Mordechai; Hofmann, Albrecht W.

1992-12-01

Phanerozoic alkali basalts from Israel, which have erupted over the past 200 Ma, have isotopic compositions similar to PREMA ("prevalent mantle") with narrow ranges of initial ɛ Nd(T) = +3.9-+5.9; 87Sr/ 86Sr(T)= 0.70292-0.70334; 206Pb/ 204Pb(T)= 18.88-19.99; 207Pb/ 204Pb(T)= 15.58-15.70; and 208Pb/ 204Pb(T)= 38.42-39.57. Their Nb/U(43 ± 9) and Ce/Pb(26 ± 6) ratios are identical to those of normal oceanic basalts, demonstrating that the basalts are essentially free of crustal contamination. Overall, the basalts are chemically and isotopically indistinguishable from many ordinary plume basalts, but no plume track can be identified. We propose that these and other, similar, magmas from the Arabian plate originated from a "fossilized" head of a mantle plume, which was unable to penetrate the continental lithosphere and was therefore trapped and stored beneath it. The plume head was emplaced some time between the late Proterozoic crust formation and the initiation of the Phanerozoic magmatic cycles. Basalts from rift environments in other continental localities show similar geochemistry to that of the Arabian basalts and their sources may also represent fossil plume heads trapped below the continents. We suggest that plume heads are, in general, characterized by the PREMA isotopic mantle signature, because the original plume sources (which may have HIMU or EM-type composition) have been diluted by overlying mantle material, which has been entrained by the plume heads during ascent. On the Arabian plate, rifting and thinning of the lithosphere caused partial melting of the stored plume, which led to periodic volcanism. In the late Cenozoic, the lithosphere broke up and the Red Sea opened. N-MORB tholeiites are now erupting in the central trough of the Red Sea, where the lithosphere has moved apart and the fossil plume has been exhausted, whereas E-MORBs are erupting in the northern and southern troughs, still tapping the plume reservoir. Fossil plumes, which are

Buoyant plume calculations

International Nuclear Information System (INIS)

Penner, J.E.; Haselman, L.C.; Edwards, L.L.

1985-01-01

Smoke from raging fires produced in the aftermath of a major nuclear exchange has been predicted to cause large decreases in surface temperatures. However, the extent of the decrease and even the sign of the temperature change, depend on how the smoke is distributed with altitude. We present a model capable of evaluating the initial distribution of lofted smoke above a massive fire. Calculations are shown for a two-dimensional slab version of the model and a full three-dimensional version. The model has been evaluated by simulating smoke heights for the Hamburg firestorm of 1943 and a smaller scale oil fire which occurred in Long Beach in 1958. Our plume heights for these fires are compared to those predicted by the classical Morton-Taylor-Turner theory for weakly buoyant plumes. We consider the effect of the added buoyancy caused by condensation of water-laden ground level air being carried to high altitude with the convection column as well as the effects of background wind on the calculated smoke plume heights for several fire intensities. We find that the rise height of the plume depends on the assumed background atmospheric conditions as well as the fire intensity. Little smoke is injected into the stratosphere unless the fire is unusually intense, or atmospheric conditions are more unstable than we have assumed. For intense fires significant amounts of water vapor are condensed raising the possibility of early scavenging of smoke particles by precipitation. 26 references, 11 figures

ANALYSIS OF REMEDIATION PROCESS OF THE GROUDWATER COTAMINATION IN AN ILLEGAL DUMPING SITE

Science.gov (United States)

Nishida, Norikazu; Furuichi, Toru; Ishii, Kazuei

Among on-site remediation technologies applied to illegal dumping sites, a technology to remedy contaminated groundwater without removal of the dumped waste is expected to provide a great opportunity to fulfill a societal need due to its economic advantage compared to removal of all waste. However heterogeneously-distributed waste makes the remedial process difficult. In this study, an in situflushing technology was applied to an illegal dumping site in Kuwana city, Mie, in order to remedy groundwater contaminated with several volatile organic compounds (VOCs) within five years. The key to successfully achieve the target was to conduct a series of advanced remediation processes; introducing a new indicator by which multiple VOCs can be estimated integratelly, monitoring the progress of remediation with a contour map of VOC concentration as well as the weighted averages of the concentration derived from the indicator, pinpointing residual contaminants area, reexamining the plan, and taking additional steps that promote further remediation.

PLUME and research sotware

Science.gov (United States)

Baudin, Veronique; Gomez-Diaz, Teresa

2013-04-01

The PLUME open platform (https://www.projet-plume.org) has as first goal to share competences and to value the knowledge of software experts within the French higher education and research communities. The project proposes in its platform the access to more than 380 index cards describing useful and economic software for this community, with open access to everybody. The second goal of PLUME focuses on to improve the visibility of software produced by research laboratories within the higher education and research communities. The "development-ESR" index cards briefly describe the main features of the software, including references to research publications associated to it. The platform counts more than 300 cards describing research software, where 89 cards have an English version. In this talk we describe the theme classification and the taxonomy of the index cards and the evolution with new themes added to the project. We will also focus on the organisation of PLUME as an open project and its interests in the promotion of free/open source software from and for research, contributing to the creation of a community of shared knowledge.

Characterization of redox conditions in pollution plumes

DEFF Research Database (Denmark)

Christensen, Thomas Højlund; Bjerg, Poul Løgstrup; Banwart, Steven A.

2000-01-01

Evalution of redox conditions in groundwater pollution plumes is often a prerequisite for understanding the behviour of the pollutants in the plume and for selecting remediation approaches. Measuring of redox conditions in pollution plumes is, however, a fairly recent issue and yet relative few...

Io Pele plume

Science.gov (United States)

2000-01-01

Voyager 1 took this narrow-angle camera image on 5 March 1979 from a distance of 450,000 kilometers. At this geometry, the camera looks straight down through a volcanic plume at one of Io's most active volcanos, Pele. The large heart-shaped feature is the region where Pele's plume falls to the surface. At the center of the 'heart' is the small dark fissure that is the source of the eruption. The Voyager Project is managed by the Jet Propulsion Laboratory for NASA's Office of Space Science.

Io's Active Eruption Plumes: Insights from HST

Science.gov (United States)

Jessup, K. L.; Spencer, J. R.

2011-10-01

Taking advantage of the available data, we recently [10] completed a detailed analysis of the spectral signature of Io's Pele-type Tvashtar plume as imaged by the HST Wide Field and Planetary Camera 2 (HST/WFPC2) via absorption during Jupiter transit and via reflected sunlight in 2007, as well as HST/WFPC2 observations of the 1997 eruption of Io's Prometheus-type Pillan plume (Fig. 1). These observations were obtained in the 0.24-0.42 μm range, where the plumes gas absorption and aerosol scattering properties are most conspicuous. By completing a detailed analysis of these observations, several key aspects of the reflectance and the absorption properties of the two plumes have been revealed. Additionally, by considering the analysis of the HST imaging data in light of previously published spectral analysis of Io's Prometheus and Pele-type plumes several trends in the plume properties have been determined, allowing us to define the relative significance of each plume on the rate of re-surfacing occurring on Io and providing the measurements needed to better assess the role the volcanoes play in the stability of Io's tenuous atmosphere.

Influence of way of finishing furniture segments on amount emissions VOCs

Directory of Open Access Journals (Sweden)

Petr Čech

2010-01-01

Full Text Available The study deals with the influence of way of finishing furniture segments on amount emissions VOCs (volatile organic compounds. The so-called Volatile Organic Compounds (VOC are among the largest pollution sources of both the internal and external environments.VOC is defined as emission of any organic compound or a mixture thereof, with the exception of methane, whereby the compound exerts the pressure of 0.01 kPa or more at the temperature of 20 °C (293.15 K and reaches the corresponding volatility under the specific conditions of its use and can undergo photochemical reactions with nitrogen oxides when exposed to solar radiation. The effects of VOC upon environment can be described by equation: VOC + NOx + UV radiation + heat = tropospheric ozone (O3In this work there were tested MDF (medium density fibreboard coated by resin impregnated paper was used for the furniture components’ production. Next were tested compressed wood, which was used as a second material of furniture components. These both chosen materials was covered by resin impregnated paper and than sequentially finished by regular coat of finish.An attention of this study is especially put on mentioned factors and on quantity of instant and long-term VOCs emissions emitted from furniture components.The amount of emissions from furniture components, in different phases of the preparation including the resin impregnated paper coating finish, was monitored within the time intervals of 24 hours and 720 hours starting after the time of the finish preparation.The MDF (medium density fibreboard coated by resin impregnated paper was used for the furniture components´ production.A compressed wood was used as a second material of furniture components. This alternative material was covered by resin impregnated paper and than sequentially finished by regular coat of finish.

Small rocket exhaust plume data

Science.gov (United States)

Chirivella, J. E.; Moynihan, P. I.; Simon, W.

1972-01-01

During recent cryodeposit tests with an 0.18-N thruster, the mass flux in the plume back field was measured for the first time for nitrogen, carbon dioxide, and a mixture of nitrogen, hydrogen, and ammonia at various inlet pressures. This mixture simulated gases that would be generated by a hydrazine plenum attitude propulsion system. The measurements furnish a base upon which to build a mathematical model of plume back flow that will be used in predicting the mass distribution in the boundary region of other plumes. The results are analyzed and compared with existing analytical predictions.

VOCs and formaldehyde emissions from cleaning products and air fresheners

OpenAIRE

Solal , Cécilia; Rousselle , Christophe; Mandin , Corinne; Manel , Jacques; Maupetit , François

2008-01-01

International audience; Human indoor exposure to Volatile Organic Compounds (VOCs) may be associated with the use of household products. However little is known about their emissions and to what extent they contribute to indoor air pollution. The French Agency for Environmental and Occupational Health Safety (Afsset) conducted tests in order to characterize VOCs emissions from 32 consumer products: air fresheners, glass cleaners, furniture polishes, toilet products, carpet and floor cleaning ...

Investigations of VOCs in and around buildings close to service stations

Science.gov (United States)

Hicklin, William; Farrugia, Pierre S.; Sinagra, Emmanuel

2018-01-01

Gas service stations are one of the major sources of volatile organic compounds in urban environments. Their emissions are expected not only to affect the ambient air quality but also that in any nearby buildings. This is particularly the case in Malta where most service stations have been built within residential zones. For this reason, it is important to understand the dispersion of volatile organic compounds (VOCs) from service stations and their infiltration into nearby residences. Two models were considered; one to predict the dispersion of VOCs in the outdoor environment in the vicinity of the service station and another one to predict the filtration of the compounds indoors. The two models can be used in tandem to predict the concentration of indoor VOCs that originate from a service station in the vicinity. Outdoor and indoor concentrations of VOCs around a service station located in a street canyon were measured, and the results used to validate the models. Predictions made using the models were found to be in general agreement with the measured concentrations of the pollutants.

[Concentration and change of VOCs in summer and autumn in Tangshan].

Science.gov (United States)

Sun, Jie; Wang, Yue-si; Wu, Fang-kun; Qiu, Jun

2010-07-01

In order to study the potential impact of volatile organic compounds (VOCs) in summer and autumn on region ozone, ambient concentrations and changes of VOCs were analyzed at Tangshan from June to September 2007 and 2008, by using the method of two-step-concentration-gas spectrometry/mass (CCD-GC/MS). The average concentration in Tangshan was 163.5 x 10(-9) C. The major components were alkanes, aromatics, alkenes and halogen hydrocarbons which accounted for 45.9%, 29.9%, 5.9% and 18.9% respectively. The average concentration decreased 51.9% compare with 2007 (340.4 x 10(-9) C), confine gas stations is the main reason of the decline of alkyl, the large decline is aromatic hydrocarbons, 67%, which has the most potential impact of ozone formation, and dichlorobenzene in industrial emissions has increased. The concentrations of VOCs in Tangshan were lower 8% than that of Beijing during the same period in 2008. The changes of VOCs during 2008 Beijing Olympic show that in addition to traffic source industrial emissions is also an important source of atmospheric pollution.

Origin and variability in volatile organic compounds observed at an Eastern Mediterranean background site (Cyprus)

Science.gov (United States)

Debevec, Cécile; Sauvage, Stéphane; Gros, Valérie; Sciare, Jean; Pikridas, Michael; Stavroulas, Iasonas; Salameh, Thérèse; Leonardis, Thierry; Gaudion, Vincent; Depelchin, Laurence; Fronval, Isabelle; Sarda-Esteve, Roland; Baisnée, Dominique; Bonsang, Bernard; Savvides, Chrysanthos; Vrekoussis, Mihalis; Locoge, Nadine

2017-09-01

More than 7000 atmospheric measurements of over 60 C2 - C16 volatile organic compounds (VOCs) were conducted at a background site in Cyprus during a 1-month intensive field campaign held in March 2015. This exhaustive dataset consisted of primary anthropogenic and biogenic VOCs, including a wide range of source-specific tracers, and oxygenated VOCs (with various origins) that were measured online by flame ionization detection-gas chromatography and proton transfer mass spectrometry. Online submicron aerosol chemical composition was performed in parallel using an aerosol mass spectrometer. This study presents the high temporal variability in VOCs and their associated sources. A preliminary analysis of their time series was performed on the basis of independent tracers (NO, CO, black carbon), meteorological data and the clustering of air mass trajectories. Biogenic compounds were mainly attributed to a local origin and showed compound-specific diurnal cycles such as a daily maximum for isoprene and a nighttime maximum for monoterpenes. Anthropogenic VOCs as well as oxygenated VOCs displayed higher mixing ratios under the influence of continental air masses (i.e., western Asia), indicating that long-range transport significantly contributed to the VOC levels in the area. Source apportionment was then conducted on a database of 20 VOCs (or grouped VOCs) using a source receptor model. The positive matrix factorization and concentration field analyses were hence conducted to identify and characterize covariation factors of VOCs that were representative of primary emissions as well as chemical transformation processes. A six-factor PMF solution was selected, namely two primary biogenic factors (relative contribution of 43 % to the total mass of VOCs) for different types of emitting vegetation; three anthropogenic factors (short-lived combustion source, evaporative sources, industrial and evaporative sources; 21 % all together), identified as being either of local origin

Origin and variability in volatile organic compounds observed at an Eastern Mediterranean background site (Cyprus

Directory of Open Access Journals (Sweden)

C. Debevec

2017-09-01

Full Text Available More than 7000 atmospheric measurements of over 60 C2 − C16 volatile organic compounds (VOCs were conducted at a background site in Cyprus during a 1-month intensive field campaign held in March 2015. This exhaustive dataset consisted of primary anthropogenic and biogenic VOCs, including a wide range of source-specific tracers, and oxygenated VOCs (with various origins that were measured online by flame ionization detection–gas chromatography and proton transfer mass spectrometry. Online submicron aerosol chemical composition was performed in parallel using an aerosol mass spectrometer. This study presents the high temporal variability in VOCs and their associated sources. A preliminary analysis of their time series was performed on the basis of independent tracers (NO, CO, black carbon, meteorological data and the clustering of air mass trajectories. Biogenic compounds were mainly attributed to a local origin and showed compound-specific diurnal cycles such as a daily maximum for isoprene and a nighttime maximum for monoterpenes. Anthropogenic VOCs as well as oxygenated VOCs displayed higher mixing ratios under the influence of continental air masses (i.e., western Asia, indicating that long-range transport significantly contributed to the VOC levels in the area. Source apportionment was then conducted on a database of 20 VOCs (or grouped VOCs using a source receptor model. The positive matrix factorization and concentration field analyses were hence conducted to identify and characterize covariation factors of VOCs that were representative of primary emissions as well as chemical transformation processes. A six-factor PMF solution was selected, namely two primary biogenic factors (relative contribution of 43 % to the total mass of VOCs for different types of emitting vegetation; three anthropogenic factors (short-lived combustion source, evaporative sources, industrial and evaporative sources; 21 % all together, identified

Concentrations and fluxes of isoprene and oxygenated VOCs at a French Mediterranean oak forest

International Nuclear Information System (INIS)

Kalogridis, C.; Gros, V.; Sarda-Esteve, R.; Bonsang, B.; Bonnaire, N.; Boissard, C.; Baisnee, D.; Lathiere, J.

2014-01-01

The CANOPEE project aims to better understand the biosphere-atmosphere exchanges of biogenic volatile organic compounds (BVOCs) in the case of Mediterranean ecosystems and the impact of in-canopy processes on the atmospheric chemical composition above the canopy. Based on an intensive field campaign, the objective of our work was to determine the chemical composition of the air inside a canopy as well as the net fluxes of reactive species between the canopy and the boundary layer. Measurements were carried out during spring 2012 at the field site of the Oak Observatory of the Observatoire de Haute Provence (O3HP) located in the southeast of France. The site is a forest ecosystem dominated by downy oak, Quercus pubescens Willd., a typical Mediterranean species which features large isoprene emission rates. Mixing ratios of isoprene, its degradation products methylvinylketone (MVK) and methacrolein (MACR) and several other oxygenated VOC (OxVOC) were measured above the canopy using an online proton transfer reaction mass spectrometer (PTR-MS), and fluxes were calculated by the disjunct eddy covariance approach. The O3HP site was found to be a very significant source of isoprene emissions, with daily maximum ambient concentrations ranging between 2-16 ppbv inside and 2-5 ppbv just above the top of the forest canopy. Significant isoprene fluxes were observed only during daytime, following diurnal cycles with midday net emission fluxes from the canopy ranging between 2.0 and 9.7 mgm -2 h -1 . Net isoprene normalized flux (at 30 C, 1000 μmol quantam -2 s -1 ) was estimated at 7.4 mgm -2 h -1 . Evidence of direct emission of methanol was also found exhibiting maximum daytime fluxes ranging between 0.2 and 0.6 mgm -2 h -1 , whereas flux values for monoterpenes and others OxVOC such as acetone and acetaldehyde were below the detection limit. The MVK+MACR-to-isoprene ratio provided useful information on the oxidation of isoprene, and is in agreement with recent findings

Volatile Organic Compound (VOC Removal by Vapor Permeation at Low VOC Concentrations: Laboratory Scale Results and Modeling for Scale Up

Directory of Open Access Journals (Sweden)

Philippe Moulin

2011-03-01

Full Text Available Petroleum transformation industries have applied membrane processes for solvent and hydrocarbon recovery as an economic alternative to reduce their emissions and reuse evaporated components. Separation of the volatile organic compounds (VOCs (toluene-propylene-butadiene from air was performed using a poly dimethyl siloxane (PDMS/α-alumina membrane. The experimental set-up followed the constant pressure/variable flow set-up and was operated at ~21 °C. The membrane is held in a stainless steel module and has a separation area of 55 × 10−4 m². Feed stream was set to atmospheric pressure and permeate side to vacuum between 3 and 5 mbar. To determine the performance of the module, the removed fraction of VOC was analyzed by Gas Chromatography/Flame Ionization Detector (GC/FID. The separation of the binary, ternary and quaternary hydrocarbon mixtures from air was performed at different flow rates and more especially at low concentrations. The permeate flux, permeance, enrichment factor, separation efficiency and the recovery extent of the membrane were determined as a function of these operating conditions. The permeability coefficients and the permeate flux through the composite PDMS-alumina membrane follow the order given by the Hildebrand parameter: toluene > 1,3-butadiene > propylene. The simulated data for the binary VOC/air mixtures showed fairly good agreement with the experimental results in the case of 1,3-butadiene and propylene. The discrepancies observed for toluene permeation could be minimized by taking into account the effects of the porous support and an influence of the concentration polarization. Finally, the installation of a 0.02 m2 membrane module would reduce 95% of the VOC content introduced at real concentration conditions used in the oil industry.

Thermal Plumes in Ventilated Rooms

DEFF Research Database (Denmark)

Kofoed, Peter; Nielsen, Peter V.

The design of a displacement ventilation system involves determination of the flow rate in the thermal plumes. The flow rate in the plumes and the vertical temperature gradient influence each other, and they are influenced by many factors. This paper shows some descriptions of these effects....

[Estimation of VOC emission from forests in China based on the volume of tree species].

Science.gov (United States)

Zhang, Gang-feng; Xie, Shao-dong

2009-10-15

Applying the volume data of dominant trees from statistics on the national forest resources, volatile organic compounds (VOC) emissions of each main tree species in China were estimated based on the light-temperature model put forward by Guenther. China's VOC emission inventory for forest was established, and the space-time and age-class distributions of VOC emission were analyzed. The results show that the total VOC emissions from forests in China are 8565.76 Gg, of which isoprene is 5689.38 Gg (66.42%), monoterpenes is 1343.95 Gg (15.69%), and other VOC is 1532.43 Gg (17.89%). VOC emissions have significant species variation. Quercus is the main species responsible for emission, contributing 45.22% of the total, followed by Picea and Pinus massoniana with 6.34% and 5.22%, respectively. Southwest and Northeast China are the major emission regions. In specific, Yunnan, Sichuan, Heilongjiang, Jilin and Shaanxi are the top five provinces producing the most VOC emissions from forests, and their contributions to the total are 15.09%, 12.58%, 10.35%, 7.49% and 7.37%, respectively. Emissions from these five provinces occupy more than half (52.88%) of the national emissions. Besides, VOC emissions show remarkable seasonal variation. Emissions in summer are the largest, accounting for 56.66% of the annual. Forests of different ages have different emission contribution. Half-mature forests play a key role and contribute 38.84% of the total emission from forests.

VOC emissions from residential combustion of Southern and mid-European woods

Science.gov (United States)

Evtyugina, Margarita; Alves, Célia; Calvo, Ana; Nunes, Teresa; Tarelho, Luís; Duarte, Márcio; Prozil, Sónia O.; Evtuguin, Dmitry V.; Pio, Casimiro

2014-02-01

Emissions of trace gases (carbon dioxide (CO2), carbon monoxide (CO), total hydrocarbons (THC)), and volatile organic compounds (VOCs) from combustion of European beech, Pyrenean oak and black poplar in a domestic woodstove and fireplace were studied. These woods are widely used as biofuel in residential combustion in Southern and mid-European countries. VOCs in the flue gases were collected in Tedlar bags, concentrated in sorbent tubes and analysed by thermal desorption-gas chromatography-flame ionisation detection (GC-FID). CO2 emissions ranged from 1415 ± 136 to 1879 ± 29 g kg-1 (dry basis). The highest emission factors for CO and THC, 115.8 ± 11.7 and 95.6 24.7 ± 6.3 g kg-1 (dry basis), respectively, were obtained during the combustion of black poplar in the fireplace. European beech presented the lowest CO and THC emission factors for both burning appliances. Significant differences in emissions of VOCs were observed among wood species burnt and combustion devices. In general the highest emission factors were obtained from the combustion of Pyrenean oak in the woodstove. Among the VOCs identified, benzene and related compounds were always the most abundant group, followed by oxygenated compounds and aliphatic hydrocarbons. The amount and the composition of emitted VOCs were strongly affected by the wood composition, the type of burning device and operating conditions. Emission data obtained in this work are useful for modelling the impact of residential wood combustion on air quality and tropospheric ozone formation.

The Vapor Plume at Material Disposal Are C in Relation to Pajarito Corridor Facilities

Energy Technology Data Exchange (ETDEWEB)

Masse, William B. [Los Alamos National Laboratory

2012-04-02

A vapor plume made up of volatile organic compounds is present beneath Material Disposal Area C (MDA C) at Los Alamos National Laboratory (LANL). The location and concentrations within the vapor plume are discussed in relation to existing and planned facilities and construction activities along Pajarito Road (the 'Pajarito Corridor') and in terms of worker health and safety. This document provides information that indicates that the vapor plume does not pose a threat to the health of LANL workers nor will it pose a threat to workers during construction of proposed facilities along Pajarito Road. The Los Alamos National Laboratory (LANL or the Laboratory) monitors emissions, effluents, and environmental media to meet environmental compliance requirements, determine actions to protect the environment, and monitor the long-term health of the local environment. LANL also studies and characterizes 'legacy' waste from past Laboratory operations to make informed decisions regarding eventual corrective actions and the disposition of that waste. Starting in 1969, these activities have been annually reported in the LANL Environmental Report (formerly Environmental Surveillance Report), and are detailed in publicly accessible technical reports meeting environmental compliance requirements. Included among the legacy sites being investigated are several formerly used material disposal areas (MDAs) set aside by the Laboratory for the general on-site disposal of waste from mission-related activities. One such area is MDA C located in Technical Area 50 (TA-50), which was used for waste disposal between 1948 and 1974. The location of TA-50 is depicted in Figure 1. The present paper uses a series of maps and cross sections to address the public concerns raised about the vapor plume at MDA C. As illustrated here, extensive sampling and data interpretation indicate that the vapor plume at MDA C does not pose a threat to the health of LANL workers nor will it pose a

Dig-face monitoring during excavation of a radioactive plume at Mound Laboratory, Ohio

International Nuclear Information System (INIS)

Josten, N.E.; Gehrke, R.J.; Carpenter, M.V.

1995-12-01

A dig-face monitoring system consists of onsite hardware for collecting information on changing chemical, radiological, and physical conditions in the subsurface soil during the hazardous site excavation. A prototype dig-face system was take to Mount Laboratory for a first trial. Mound Area 7 was the site of historical disposals of 232 Th, 227 Ac, and assorted debris. The system was used to monitor a deep excavation aimed at removing 227 Ac-contaminated soils. Radiological, geophysical, and topographic sensors were used to scan across the excavation dig-face at four successive depths as soil was removed. A 3-D image of the contamination plumes was developed; the radiation sensor data indicated that only a small portion of the excavated soil volume was contaminated. The spatial information produced by the dig-face system was used to direct the excavation activities into the area containing the 227 Ac and to evaluate options for handling the separate 232 Th plume

Galileo observations of volcanic plumes on Io

Science.gov (United States)

Geissler, P.E.; McMillan, M.T.

2008-01-01

Io's volcanic plumes erupt in a dazzling variety of sizes, shapes, colors and opacities. In general, the plumes fall into two classes, representing distinct source gas temperatures. Most of the Galileo imaging observations were of the smaller, more numerous Prometheus-type plumes that are produced when hot flows of silicate lava impinge on volatile surface ices of SO2. Few detections were made of the giant, Pele-type plumes that vent high temperature, sulfur-rich gases from the interior of Io; this was partly because of the insensitivity of Galileo's camera to ultraviolet wavelengths. Both gas and dust spout from plumes of each class. Favorably located gas plumes were detected during eclipse, when Io was in Jupiter's shadow. Dense dust columns were imaged in daylight above several Prometheus-type eruptions, reaching heights typically less than 100 km. Comparisons between eclipse observations, sunlit images, and the record of surface changes show that these optically thick dust columns are much smaller in stature than the corresponding gas plumes but are adequate to produce the observed surface deposits. Mie scattering calculations suggest that these conspicuous dust plumes are made up of coarse grained “ash” particles with radii on the order of 100 nm, and total masses on the order of 106 kg per plume. Long exposure images of Thor in sunlight show a faint outer envelope apparently populated by particles small enough to be carried along with the gas flow, perhaps formed by condensation of sulfurous “snowflakes” as suggested by the plasma instrumentation aboard Galileo as it flew through Thor's plume [Frank, L.A., Paterson, W.R., 2002. J. Geophys. Res. (Space Phys.) 107, doi:10.1029/2002JA009240. 31-1]. If so, the total mass of these fine, nearly invisible particles may be comparable to the mass of the gas, and could account for much of Io's rapid resurfacing.

Three-dimensional analysis of future groundwater flow conditions and contaminant plume transport in the Hanford Site unconfined aquifer system: FY 1996 and 1997 status report

Energy Technology Data Exchange (ETDEWEB)

Cole, C.R.; Wurstner, S.K.; Williams, M.D.; Thorne, P.D.; Bergeron, M.P.

1997-12-01

A three-dimensional numerical model of groundwater flow and transport, based on the Coupled Fluid Energy, and Solute Transport (CFEST) code, was developed for the Hanford Site to support the Hanford Groundwater Project (HGWP), managed by Pacific Northwest National Laboratory. The model was developed to increase the understanding and better forecast the migration of several contaminant plumes being monitored by the HGWP, and to support the Hanford Site Composite Analysis for low-level waste disposal in the 200-Area Plateau. Recent modeling efforts have focused on continued refinement of an initial version of the three-dimensional model developed in 1995 and its application to simulate future transport of selected contaminant plumes in the aquifer system. This version of the model was updated using a more current version of the CFEST code called CFEST96. Prior to conducting simulations of contaminant transport with the three-dimensional model, a previous steady-state, two-dimensional model of the unconfined aquifer system was recalibrated to 1979 water-table conditions with a statistical inverse method implemented in the CFEST-INV computer code. The results of the recalibration were used to refine the three-dimensional conceptual model and to calibrate it with a conceptualization that preserves the two-dimensional hydraulic properties and knowledge of the aquifer`s three-dimensional properties for the same 1979 water-table conditions. The transient behavior of the three-dimensional flow model was also calibrated by adjusting model storage properties (specific yield) until transient water-table predictions approximated observed water-table elevations between 1979 and 1996.

Three-dimensional analysis of future groundwater flow conditions and contaminant plume transport in the Hanford Site unconfined aquifer system: FY 1996 and 1997 status report

International Nuclear Information System (INIS)

Cole, C.R.; Wurstner, S.K.; Williams, M.D.; Thorne, P.D.; Bergeron, M.P.

1997-12-01

A three-dimensional numerical model of groundwater flow and transport, based on the Coupled Fluid Energy, and Solute Transport (CFEST) code, was developed for the Hanford Site to support the Hanford Groundwater Project (HGWP), managed by Pacific Northwest National Laboratory. The model was developed to increase the understanding and better forecast the migration of several contaminant plumes being monitored by the HGWP, and to support the Hanford Site Composite Analysis for low-level waste disposal in the 200-Area Plateau. Recent modeling efforts have focused on continued refinement of an initial version of the three-dimensional model developed in 1995 and its application to simulate future transport of selected contaminant plumes in the aquifer system. This version of the model was updated using a more current version of the CFEST code called CFEST96. Prior to conducting simulations of contaminant transport with the three-dimensional model, a previous steady-state, two-dimensional model of the unconfined aquifer system was recalibrated to 1979 water-table conditions with a statistical inverse method implemented in the CFEST-INV computer code. The results of the recalibration were used to refine the three-dimensional conceptual model and to calibrate it with a conceptualization that preserves the two-dimensional hydraulic properties and knowledge of the aquifer's three-dimensional properties for the same 1979 water-table conditions. The transient behavior of the three-dimensional flow model was also calibrated by adjusting model storage properties (specific yield) until transient water-table predictions approximated observed water-table elevations between 1979 and 1996

Rise of a cold plume

International Nuclear Information System (INIS)

Kakuta, Michio

1977-06-01

The rise of smoke from the stacks of two research reactors in normal operation was measured by photogrametric method. The temperature of effluent gas is less than 20 0 C higher than that of the ambient air (heat emission of the order 10 4 cal s -1 ), and the efflux velocity divided by the wind speed is between 0.5 and 2.8 in all 16 smoke runs. The field data obtained within downwind distance of 150m are compared with those by plume rise formulas presently available. Considering the shape of bending-over plume, the Briggs' formula for 'jet' gives a reasonable explanation of the observed plume rise. (auth.)

PLUME-MoM 1.0: a new 1-D model of volcanic plumes based on the method of moments

Science.gov (United States)

de'Michieli Vitturi, M.; Neri, A.; Barsotti, S.

2015-05-01

In this paper a new mathematical model for volcanic plumes, named PlumeMoM, is presented. The model describes the steady-state 1-D dynamics of the plume in a 3-D coordinate system, accounting for continuous variability in particle distribution of the pyroclastic mixture ejected at the vent. Volcanic plumes are composed of pyroclastic particles of many different sizes ranging from a few microns up to several centimeters and more. Proper description of such a multiparticle nature is crucial when quantifying changes in grain-size distribution along the plume and, therefore, for better characterization of source conditions of ash dispersal models. The new model is based on the method of moments, which allows description of the pyroclastic mixture dynamics not only in the spatial domain but also in the space of properties of the continuous size-distribution of the particles. This is achieved by formulation of fundamental transport equations for the multiparticle mixture with respect to the different moments of the grain-size distribution. Different formulations, in terms of the distribution of the particle number, as well as of the mass distribution expressed in terms of the Krumbein log scale, are also derived. Comparison between the new moments-based formulation and the classical approach, based on the discretization of the mixture in N discrete phases, shows that the new model allows the same results to be obtained with a significantly lower computational cost (particularly when a large number of discrete phases is adopted). Application of the new model, coupled with uncertainty quantification and global sensitivity analyses, enables investigation of the response of four key output variables (mean and standard deviation (SD) of the grain-size distribution at the top of the plume, plume height and amount of mass lost by the plume during the ascent) to changes in the main input parameters (mean and SD) characterizing the pyroclastic mixture at the base of the plume

Development of new VOC exposure metrics and their relationship to ''Sick Building Syndrome'' symptoms

Energy Technology Data Exchange (ETDEWEB)

Ten Brinke, JoAnn [Univ. of California, Berkeley, CA (United States); Lawrence Berkeley National Lab., Berkeley, CA (United States)

1995-08-01

Volatile organic compounds (VOCs) are suspected to contribute significantly to ''Sick Building Syndrome'' (SBS), a complex of subchronic symptoms that occurs during and in general decreases away from occupancy of the building in question. A new approach takes into account individual VOC potencies, as well as the highly correlated nature of the complex VOC mixtures found indoors. The new VOC metrics are statistically significant predictors of symptom outcomes from the California Healthy Buildings Study data. Multivariate logistic regression analyses were used to test the hypothesis that a summary measure of the VOC mixture, other risk factors, and covariates for each worker will lead to better prediction of symptom outcome. VOC metrics based on animal irritancy measures and principal component analysis had the most influence in the prediction of eye, dermal, and nasal symptoms. After adjustment, a water-based paints and solvents source was found to be associated with dermal and eye irritation. The more typical VOC exposure metrics used in prior analyses were not useful in symptom prediction in the adjusted model (total VOC (TVOC), or sum of individually identified VOCs (ΣVOC_i)). Also not useful were three other VOC metrics that took into account potency, but did not adjust for the highly correlated nature of the data set, or the presence of VOCs that were not measured. High TVOC values (2--7 mg m^-3) due to the presence of liquid-process photocopiers observed in several study spaces significantly influenced symptoms. Analyses without the high TVOC values reduced, but did not eliminate the ability of the VOC exposure metric based on irritancy and principal component analysis to explain symptom outcome.

Characterization of void volume VOC concentration in vented TRU waste drums - an interim report

International Nuclear Information System (INIS)

Liekhus, K.J.

1994-09-01

A test program is underway at the Idaho National Engineering Laboratory to determine if the concentration of volatile organic compounds (VOCs) in the drum headspace is representative of the VOC concentration in the entire drum void space and to demonstrate that the VOC concentration in the void space of each layer of confinement can be estimated using a model incorporating diffusion and permeation transport principles and limited waste drum sampling data. An experimental test plan was developed requiring gas sampling of 66 transuranic (TRU) waste drums. This interim report summarizes the experimental measurements and model predictions of VOC concentration in the innermost layer of confinement from waste drums sampled and analyzed in FY 1994

Detection of new VOC compounds with iCRDS

Science.gov (United States)

Huang, H.; Leen, J. B.; Gardner, A.; Gupta, M.; Baer, D. S.

2015-12-01

The instrument at Los Gatos Research (a member of ABB Inc.) which is based on incoherent cavity ringdown spectroscopy (iCRDS) that operates in the mid-infrared (bands from 860-1060 cm-1 or 970-1280 cm-1) is capable of detecting a broad range of VOCs, in situ, continuously and autonomously, for example, BTEX compounds (benzene, toluene, ethylbenzene, xylene), including differentiation of xylene isomers. Previously, we have demonstrated the measurement of trichloroethylene (TCE) in zero air with a precision of 0.17 ppb (1σ in 4 minutes), and the measurement of tetrachloroethylene (PCE) with a precision of 0.15 ppb (1σ in 4 minutes). Both of these measured precisions exceed the EPA's commercial building action limit, which for TCE is 0.92 ppb (5 µg/m3) and for PCE is 0.29 ppb (2 µg/m3). This ability has been fully demonstrated by the deployment of the instrument to the Superfund site at Moffett Naval Air Station in Mountain View, California where contaminated ground water results in vapor intrusion of TCE and PCE. For two weeks, the instrument operated continuously and autonomously, successfully measuring TCE and PCE concentrations in both the breathing zone and steam tunnel air, in excellent agreement with previous TO-15 data. In this poster, we present laboratory performance data targeting new toxic molecules with the same instrument. We have demonstrated the measurement of trichlorofluolomethane (Freon 11) in zero air with a precision of 1 ppb (3σ at 1075cm-1), and hexafluoropropene in zero air with a precision of about 0.3 ppb (3σ per spectrum). The iCRDS instrument has shown the ability to continuously and autonomously measure sub-ppb levels of toxic VOCs in the lab/field, offering an unprecedented picture of the short term dynamics associated with vapor intrusion and ground water pollution.

An Analysis of Air Pollution Control Technologies for Shipyard Emitted Volatile Organic Compounds (VOCS)

National Research Council Canada - National Science Library

Snider, Thomas J

1993-01-01

...) emissions from industrial operations. One approach to VOC reduction is through air pollution control technology to remove the contaminants from the exhaust airstream of VOC generating processes...

Aromatic VOCs global influence in the ozone production

Science.gov (United States)

Cabrera-Perez, David; Pozzer, Andrea

2016-04-01

Aromatic hydrocarbons are a subgroup of Volatile Organic Compounds (VOCs) of special interest in the atmosphere of urban and semi-urban areas. Aromatics form a high fraction of VOCs, are highly reactive and upon oxidation they are an important source of ozone. These group of VOCs are released to the atmosphere by processes related to biomass burning and fossil fuel consumption, while they are removed from the atmosphere primarily by OH reaction and by dry deposition. In addition, a branch of aromatics (ortho-nitrophenols) produce HONO upon photolysis, which is responsible of certain amount of the OH recycling. Despite their importance in the atmosphere in anthropogenic polluted areas, the influence of aromatics in the ozone production remains largely unknown. This is of particular relevance, being ozone a pollutant with severe side effects on air quality, health and climate. In this work the atmospheric impacts at global scale of the most emitted aromatic VOCs in the gas phase (benzene, toluene, xylenes, ethylbenzene, styrene, phenol, benzaldehyde and trimethylbenzenes) are analysed and assessed. Specifically, the impact on ozone due to aromatic oxidation is estimated, as this is of great interest in large urban areas and can be helpful for developing air pollution control strategies. Further targets are the quantification of the NOx loss and the OH recycling due to aromatic oxidation. In order to investigate these processes, two simulations were performed with the numerical chemistry and climate simulation ECHAM/MESSy Atmospheric Chemistry (EMAC) model. The simulations compare two cases, one with ozone concentrations when aromatics are present or the second one when they are missing. Finally, model simulated ozone is compared against a global set of observations in order to better constrain the model accuracy.

Volatile organic compounds (VOCs) emission characteristics and control strategies for a petrochemical industrial area in middle Taiwan.

Science.gov (United States)

Yen, Chia-Hsien; Horng, Jao-Jia

2009-11-01

This study investigated VOC emissions from the largest petrochemical industrial district in Taiwan and recommended some control measures to reduce VOC emissions. In addition to the petrochemical industry, the district encompasses a chemical and fiber industry, a plastics industry and a harbor, which together produce more than 95% of the VOC emissions in the area. The sequence of VOC emission was as follows: components (e.g., valves, flanges, and pumps) (47%) > tanks (29%) > stacks (15%) > wastewater treatment facility (6%) > loading (2%) > flares (1%). Other plants producing high-density polyethylene (HDPE), styrene, ethylene glycol (EG), gas oil, and iso-nonyl-alchol (INA) were measured to determine the VOC leaching in the district. The VOC emissions of these 35 plants (90% of all plants) were less than 100 tons/year. About 74% of the tanks were fixed-roof tanks that leached more VOCs than the other types of tanks. To reduce leaching, the components should be checked periodically, and companies should be required to follow the Taiwan EPA regulations. A VOC emission management system was developed in state implementation plans (SIPs) to inspect and reduce emissions in the industrial district.

Assessment of Exposure to VOCs among Pregnant Women in the National Children's Study.

Science.gov (United States)

Boyle, Elizabeth Barksdale; Viet, Susan M; Wright, David J; Merrill, Lori S; Alwis, K Udeni; Blount, Benjamin C; Mortensen, Mary E; Moye, John; Dellarco, Michael

2016-03-29

Epidemiologic studies can measure exposure to volatile organic compounds (VOCs) using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children's Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS) method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS). We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking) and by observations by a trained data collector (presence of scented products in homes). We found several significant (p < 0.01) relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite N

The effect of wet film thickness on VOC emissions from a finishing varnish.

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Lee, Shun-Cheng; Kwok, Ngai-Hong; Guo, Hai; Hung, Wing-Tat

2003-01-20

Finishing varnishes, a typical type of oil-based varnishes, are widely used to shine metal, wood trim and cabinet surfaces in Hong Kong. The influence of wet film thickness on volatile organic compound (VOC) emissions from a finishing varnish was studied in an environmental test chamber. The varnish was applied on an aluminium foil with three different wet film thickness (35.2, 69.9 and 107.3 microm). The experimental conditions were 25.0 degrees C, 50.0% relative humidity (RH) with an air exchange rate of 0.5 h(-1). The concentrations of the major VOCs were monitored for the first 10 h. The air samples were collected by canisters and analysed by gas chromatography/mass selective detector (GC/MSD). Six major VOCs including toluene, chlorobenzene, ethylbenzene, m,p-xylene, o-xylene and 1,3,5-trimethylbenzene were identified and quantified. Marked differences were observed for three different film thicknesses. VOC concentrations increased rapidly during the first few hours and then decreased as the emission rates declined. The thicker the wet film, the higher the VOC emissions. A model expression included an exponentially decreasing emission rate of varnish film. The concentration and time data measured in the chamber were used to determine the parameters of empirical emission rate model. The present work confirmed that the film thickness of varnish influenced markedly the concentrations and emissions of VOCs. Copyright 2002 Elsevier Science B.V.

Genome-resolved metagenomics reveals that sulfur metabolism dominates the microbial ecology of rising hydrothermal plumes

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Anantharaman, K.; Breier, J. A., Jr.; Jain, S.; Reed, D. C.; Dick, G.

2015-12-01

Deep-sea hydrothermal plumes occur when hot fluids from hydrothermal vents replete with chemically reduced elements and compounds like sulfide, methane, hydrogen, ammonia, iron and manganese mix with cold, oxic seawater. Chemosynthetic microbes use these reduced chemicals to power primary production and are pervasive throughout the deep sea, even at sites far removed from hydrothermal vents. Although neutrally-buoyant hydrothermal plumes have been well-studied, rising hydrothermal plumes have received little attention even though they represent an important interface in the deep-sea where microbial metabolism and particle formation processes control the transformation of important elements and impact global biogeochemical cycles. In this study, we used genome-resolved metagenomic analyses and thermodynamic-bioenergetic modeling to study the microbial ecology of rising hydrothermal plumes at five different hydrothermal vents spanning a range of geochemical gradients at the Eastern Lau Spreading Center (ELSC) in the Western Pacific Ocean. Our analyses show that differences in the geochemistry of hydrothermal vents do not manifest in microbial diversity and community composition, both of which display only minor variance across ELSC hydrothermal plumes. Microbial metabolism is dominated by oxidation of reduced sulfur species and supports a diversity of bacteria, archaea and viruses that provide intriguing insights into metabolic plasticity and virus-mediated horizontal gene transfer in the microbial community. The manifestation of sulfur oxidation genes in hydrogen and methane oxidizing organisms hints at metabolic opportunism in deep-sea microbes that would enable them to respond to varying redox conditions in hydrothermal plumes. Finally, we infer that the abundance, diversity and metabolic versatility of microbes associated with sulfur oxidation impart functional redundancy that could allow it to persist in the dynamic settings of hydrothermal plumes.

Optimized Field Sampling and Monitoring of Airborne Hazardous Transport Plumes; A Geostatistical Simulation Approach

International Nuclear Information System (INIS)

Chen, DI-WEN

2001-01-01

Airborne hazardous plumes inadvertently released during nuclear/chemical/biological incidents are mostly of unknown composition and concentration until measurements are taken of post-accident ground concentrations from plume-ground deposition of constituents. Unfortunately, measurements often are days post-incident and rely on hazardous manned air-vehicle measurements. Before this happens, computational plume migration models are the only source of information on the plume characteristics, constituents, concentrations, directions of travel, ground deposition, etc. A mobile ''lighter than air'' (LTA) system is being developed at Oak Ridge National Laboratory that will be part of the first response in emergency conditions. These interactive and remote unmanned air vehicles will carry light-weight detectors and weather instrumentation to measure the conditions during and after plume release. This requires a cooperative computationally organized, GPS-controlled set of LTA's that self-coordinate around the objectives in an emergency situation in restricted time frames. A critical step before an optimum and cost-effective field sampling and monitoring program proceeds is the collection of data that provides statistically significant information, collected in a reliable and expeditious manner. Efficient aerial arrangements of the detectors taking the data (for active airborne release conditions) are necessary for plume identification, computational 3-dimensional reconstruction, and source distribution functions. This report describes the application of stochastic or geostatistical simulations to delineate the plume for guiding subsequent sampling and monitoring designs. A case study is presented of building digital plume images, based on existing ''hard'' experimental data and ''soft'' preliminary transport modeling results of Prairie Grass Trials Site. Markov Bayes Simulation, a coupled Bayesian/geostatistical methodology, quantitatively combines soft information

A numerical study of the Magellan Plume

Science.gov (United States)

Palma, Elbio D.; Matano, Ricardo P.

2012-05-01

In this modeling study we investigate the dynamical mechanisms controlling the spreading of the Magellan Plume, which is a low-salinity tongue that extends along the Patagonian Shelf. Our results indicate that the overall characteristics of the plume (width, depth, spreading rate, etc.) are primarily influenced by tidal forcing, which manifests through tidal mixing and tidal residual currents. Tidal forcing produces a homogenization of the plume's waters and an offshore displacement of its salinity front. The interaction between tidal and wind-forcing reinforces the downstream and upstream buoyancy transports of the plume. The influence of the Malvinas Current on the Magellan Plume is more dominant north of 50°S, where it increases the along-shelf velocities and generates intrusions of saltier waters from the outer shelf, thus causing a reduction of the downstream buoyancy transport. Our experiments also indicate that the northern limit of the Magellan Plume is set by a high salinity discharge from the San Matias Gulf. Sensitivity experiments show that increments of the wind stress cause a decrease of the downstream buoyancy transport and an increase of the upstream buoyancy transport. Variations of the magnitude of the discharge produce substantial modifications in the downstream penetration of the plume and buoyancy transport. The Magellan discharge generates a northeastward current in the middle shelf, a recirculation gyre south of the inlet and a region of weak currents father north.

Remediation of the Wells G & H Superfund Site, Woburn, Massachusetts.

Science.gov (United States)

Bair, E Scott; Metheny, Maura A

2002-01-01

Remediation of ground water and soil contamination at the Wells G & H Superfund Site, Woburn, Massachusetts, uses technologies that reflect differences in hydrogeologic settings, concentrations of volatile organic compounds (VOCs), and costs of treatment. The poorly permeable glacial materials that overlie fractured bedrock at the W.R. Grace property necessitate use of closely spaced recovery wells. Contaminated ground water is treated with hydrogen peroxide and ultraviolet (UV) oxidation. At UniFirst, a deep well completed in fractured bedrock removes contaminated ground water, which is treated by hydrogen peroxide, UV oxidation, and granular activated carbon (GAC). The remediation system at Wildwood integrates air sparging, soil-vapor extraction, and ground water pumping. Air stripping and GAC are used to treat contaminated water; GAC is used to treat contaminated air. New England Plastics (NEP) uses air sparging and soil-vapor extraction to remove VOCs from the unsaturated zone and shallow ground water. Contaminated air and water are treated using separate GAC systems. After nine years of operation at W.R. Grace and UniFirst, 30 and 786 kg, respectively, of VOCs have been removed. In three years of operation, 866 kg of VOCs have been removed at Wildwood. In 15 months of operation, 36 kg of VOCs were removed at NEP. Characterization work continues at the Olympia Nominee Trust, Whitney Barrel, Murphy Waste Oil, and Aberjona Auto Parts properties. Risk assessments are being finalized that address heavy metals in the floodplain sediments along the Aberjona River that are mobilized from the Industri-Plex Superfund Site located a few miles upstream.

PARAMETRIC EVALUATION OF VOC CONVERSION VIA CATALYTIC INCINERATION

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Kaskantzis Neto G.

1997-01-01

Full Text Available Abstract - A pilot-scale catalytic incineration system was used to investigate the effectiveness of catalytic incineration as a means of reducing volatile organic compound (VOC air pollutants. The objectives of the study were: 1 to investigate the effects of operating and design variables on the reduction efficiency of VOCs; and 2 to evaluate reduction efficiencies for specific compounds in different chemical classes. The study results verified that the following factors affect the catalyst performance: inlet temperature, space velocity, compound type, and compound inlet concentration. Tests showed that reduction efficiencies exceeding 98% were possible, given sufficiently high inlet gas temperatures for the following classes of compounds: alcohols, acetates, ketones, hydrocarbons, and aromatics

Ocean outfall plume characterization using an Autonomous Underwater Vehicle.

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Rogowski, Peter; Terrill, Eric; Otero, Mark; Hazard, Lisa; Middleton, William

2013-01-01

A monitoring mission to map and characterize the Point Loma Ocean Outfall (PLOO) wastewater plume using an Autonomous Underwater Vehicle (AUV) was performed on 3 March 2011. The mobility of an AUV provides a significant advantage in surveying discharge plumes over traditional cast-based methods, and when combined with optical and oceanographic sensors, provides a capability for both detecting plumes and assessing their mixing in the near and far-fields. Unique to this study is the measurement of Colored Dissolved Organic Matter (CDOM) in the discharge plume and its application for quantitative estimates of the plume's dilution. AUV mission planning methodologies for discharge plume sampling, plume characterization using onboard optical sensors, and comparison of observational data to model results are presented. The results suggest that even under variable oceanic conditions, properly planned missions for AUVs equipped with an optical CDOM sensor in addition to traditional oceanographic sensors, can accurately characterize and track ocean outfall plumes at higher resolutions than cast-based techniques.

Volatile Organic Compounds (VOCs in Conventional and High Performance School Buildings in the U.S.

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Lexuan Zhong

2017-01-01

Full Text Available Exposure to volatile organic compounds (VOCs has been an indoor environmental quality (IEQ concern in schools and other buildings for many years. Newer designs, construction practices and building materials for “green” buildings and the use of “environmentally friendly” products have the promise of lowering chemical exposure. This study examines VOCs and IEQ parameters in 144 classrooms in 37 conventional and high performance elementary schools in the U.S. with the objectives of providing a comprehensive analysis and updating the literature. Tested schools were built or renovated in the past 15 years, and included comparable numbers of conventional, Energy Star, and Leadership in Energy and Environmental Design (LEED-certified buildings. Indoor and outdoor VOC samples were collected and analyzed by thermal desorption, gas chromatography and mass spectroscopy for 94 compounds. Aromatics, alkanes and terpenes were the major compound groups detected. Most VOCs had mean concentrations below 5 µg/m3, and most indoor/outdoor concentration ratios ranged from one to 10. For 16 VOCs, the within-school variance of concentrations exceeded that between schools and, overall, no major differences in VOC concentrations were found between conventional and high performance buildings. While VOC concentrations have declined from levels measured in earlier decades, opportunities remain to improve indoor air quality (IAQ by limiting emissions from building-related sources and by increasing ventilation rates.

Volatile Organic Compounds (VOCs) in Conventional and High Performance School Buildings in the U.S.

Science.gov (United States)

Zhong, Lexuan; Su, Feng-Chiao; Batterman, Stuart

2017-01-21

Exposure to volatile organic compounds (VOCs) has been an indoor environmental quality (IEQ) concern in schools and other buildings for many years. Newer designs, construction practices and building materials for "green" buildings and the use of "environmentally friendly" products have the promise of lowering chemical exposure. This study examines VOCs and IEQ parameters in 144 classrooms in 37 conventional and high performance elementary schools in the U.S. with the objectives of providing a comprehensive analysis and updating the literature. Tested schools were built or renovated in the past 15 years, and included comparable numbers of conventional, Energy Star, and Leadership in Energy and Environmental Design (LEED)-certified buildings. Indoor and outdoor VOC samples were collected and analyzed by thermal desorption, gas chromatography and mass spectroscopy for 94 compounds. Aromatics, alkanes and terpenes were the major compound groups detected. Most VOCs had mean concentrations below 5 µg/m³, and most indoor/outdoor concentration ratios ranged from one to 10. For 16 VOCs, the within-school variance of concentrations exceeded that between schools and, overall, no major differences in VOC concentrations were found between conventional and high performance buildings. While VOC concentrations have declined from levels measured in earlier decades, opportunities remain to improve indoor air quality (IAQ) by limiting emissions from building-related sources and by increasing ventilation rates.

The evolution of photochemical smog in a power plant plume

Science.gov (United States)

Luria, Menachem; Valente, Ralph J.; Tanner, Roger L.; Gillani, Noor V.; Imhoff, Robert E.; Mueller, Stephen F.; Olszyna, Kenneth J.; Meagher, James F. Present address: Aeronomy Laboratory, NOAA, 325 Broadway, Boulder CO 80303, USA.)

The evolution of photochemical smog in a plant plume was investigated with the aid of an instrumented helicopter. Air samples were taken in the plume of the Cumberland Power Plant, located in central Tennessee, during the afternoon of 16 July 1995 as part of the Southern Oxidants Study - Nashville Middle Tennessee Ozone Study. Twelve cross-wind air sampling traverses were made at six distance groups from 35 to 116 km from the source. During the sampling period the winds were from the west-northwest and the plume drifted towards the city of Nashville TN. Ten of the traverses were made upwind of the city, where the power plant plume was isolated, and two traverses downwind of the city when the plumes were possibly mixed. The results revealed that even six hours after the release, excess ozone production was limited to the edges of the plume. Only when the plume was sufficiently dispersed, but still upwind of Nashville, was excess ozone (up to 109 ppbv, 50-60 ppbv above background levels) produced in the center of the plume. The concentrations image of the plume and a Lagrangian particle model suggests that portions of the power plant plume mixed with the urban plume. The mixed urban power plant plume began to regenerate O 3 that peaked at 120 ppbv at a short distance (15-25 km) downwind of Nashville. Ozone productivity (the ratio of excess O 3 to NO y and NO z) in the isolated plume was significantly lower compared with that found in the city plume. The production of nitrate, a chain termination product, was significantly higher in the power plant plume compared to the mixed plume, indicating shorter chain length of the photochemical smog chain reaction mechanism.

The evolution of photochemical smog in a power plant plume

International Nuclear Information System (INIS)

Luria, M.; The Hebrew University, Jerusalem; Valente, R.J.; Tanner, R.L.; Imhoff, R.E.; Mueller, S.F.; Olszyna, K.J.; Meagher, J.F.; Gillani, N.V.; University of Alabama, Huntsville, AL

1999-01-01

The evolution of photochemical smog in a plant plume was investigated with the aid of an instrumented helicopter. Air samples were taken in the plume of the Cumberland Power Plant, located in central Tennessee, during the afternoon of 16 July 1995 as part of the Southern Oxidants Study - Nashville Middle Tennessee Ozone Study. Twelve cross-wind air sampling traverses were made at six distance groups from 35 to 116 km from the source. During the sampling period the winds were from the west-northwest and the plume drifted towards the city of Nashville TN. Ten of the traverses were made upwind of the city, where the power plant plume was isolated, and two traverses downwind of the city when the plumes were possibly mixed. The results revealed that even six hours after the release, excess ozone production was limited to the edges of the plume. Only when the plume was sufficiently dispersed, but still upwind of Nashville, was excess ozone (up to 109 ppbv, 50-60 ppbv above background levels) produced in the center of the plume. The concentrations image of the plume and a Lagrangian particle model suggests that portions of the power plant plume mixed with the urban plume. The mixed urban power plant plume began to regenerate O 3 that peaked at 120 ppbv at a short distance (15-25 km) downwind of Nashville. Ozone productivity (the ratio of excess O 3 to NO y and NO z ) in the isolated plume was significantly lower compared with that found in the city plume. The production of nitrate, a chain termination product, was significantly higher in the power plant plume compared to the mixed plume, indicating shorter chain length of the photochemical smog chain reaction mechanism. (author)

Plume structure in high-Rayleigh-number convection

Science.gov (United States)

Puthenveettil, Baburaj A.; Arakeri, Jaywant H.

2005-10-01

Near-wall structures in turbulent natural convection at Rayleigh numbers of 10^{10} to 10^{11} at A Schmidt number of 602 are visualized by a new method of driving the convection across a fine membrane using concentration differences of sodium chloride. The visualizations show the near-wall flow to consist of sheet plumes. A wide variety of large-scale flow cells, scaling with the cross-section dimension, are observed. Multiple large-scale flow cells are seen at aspect ratio (AR)= 0.65, while only a single circulation cell is detected at AR= 0.435. The cells (or the mean wind) are driven by plumes coming together to form columns of rising lighter fluid. The wind in turn aligns the sheet plumes along the direction of shear. the mean wind direction is seen to change with time. The near-wall dynamics show plumes initiated at points, which elongate to form sheets and then merge. Increase in rayleigh number results in a larger number of closely and regularly spaced plumes. The plume spacings show a common log normal probability distribution function, independent of the rayleigh number and the aspect ratio. We propose that the near-wall structure is made of laminar natural-convection boundary layers, which become unstable to give rise to sheet plumes, and show that the predictions of a model constructed on this hypothesis match the experiments. Based on these findings, we conclude that in the presence of a mean wind, the local near-wall boundary layers associated with each sheet plume in high-rayleigh-number turbulent natural convection are likely to be laminar mixed convection type.

Modeling explicit tropospheric oxidation through identifying volatile organic compound (VOC) sources, their impact on air quality and their signatures in South China

Science.gov (United States)

Cheng, Hairong

Photochemical smog, characterized by high concentrations of ozone (O 3) and fine particles, is of great concern in the urban areas like the Pearl River Delta (PRD). Ambient O3 and its precursors were simultaneously measured for the first time at a site within the inland PRD region (WQS) and a site in Hong Kong (TC) from 22 October to 01 December 2007, in order to improve our understanding of the interplay of O3 pollution between Hong Kong and the inland PRD region, to explore the relationships between O3 and its precursors, and to identify the key volatile organic compound (VOC) species and emission source categories contributing to the O3 formation. Ratio analyses for trace gases and VOCs and back trajectory calculation revealed that the air masses arriving at WQS were more aged due to regional influence, whereas the air masses at TC were mainly affected by local emissions and/or regional transport. An observation-Based Model (OBM) was employed to determine the O 3-precursor relationship. At both sites, O3 production was found to be VOC-limited. Anthropogenic hydrocarbons played a key role in O 3 production, while reducing NO emissions aided the build up of O 3 concentrations. The contribution of carbonyls to O3 formation was firstly input in the OBM by using measured data, the results showed that the net O3 production derived from the OBM agreed better with the observed O3 increment after hourly carbonyl concentrations were included. A photochemical trajectory model was developed and used for the first time to simulate the formation of photochemical pollutants at WQS, Guangzhou during photochemical pollution episodes between 12 and 17 November, 2007. Calculated photochemical ozone creation potential (POCP) indices indicated that alkanes and oxygenated organic compounds had relatively low reactivity, while alkenes and aromatics presented high reactivity. Analysis of the emission inventory found that the sum of 60 of the 139 VOC species accounted for 91% of the

Nematicidal effect of volatile organic compounds (VOCs on the plant-parasitic nematode Meloidogyne javanica

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Mauricio Batista Fialho

2012-06-01

Full Text Available Previous studies have demonstrated that volatile organic compounds (VOCs, produced by the yeast Saccharomyces cerevisiae, were able to inhibit the development of phytopathogenic fungi. In this context, the nematicidal potential of the synthetic mixture of VOCs, constituted of alcohols and esters, was evaluated for the control of the root-knot nematode Meloidogyne javanica, which causes losses to crops of high economic value. The fumigation of substrate containing second-stage juveniles with VOCs exhibited nematicidal effect higher than 30% for the lowest concentration tested (33.3 µL g-1 substrate, whereas at 66.6 and 133.3 µL g-1 substrate, the nematode mortality was 100%. The present results stimulate other studies on VOCs for nematode management.

Characterization of DNAPL Source Zone Architecture and Prediction of Associated Plume Response: Progress and Perspectives

Science.gov (United States)

Abriola, L. M.; Pennell, K. D.; Ramsburg, C. A.; Miller, E. L.; Christ, J.; Capiro, N. L.; Mendoza-Sanchez, I.; Boroumand, A.; Ervin, R. E.; Walker, D. I.; Zhang, H.

2012-12-01

It is now widely recognized that the distribution of contaminant mass will control both the evolution of aqueous phase plumes and the effectiveness of many source zone remediation technologies at sites contaminated by dense nonaqueous phase liquids (DNAPLs). Advances in the management of sites containing DNAPL source zones, however, are currently hampered by the difficulty associated with characterizing subsurface DNAPL 'architecture'. This presentation provides an overview of recent research, integrating experimental and mathematical modeling studies, designed to improve our ability to characterize DNAPL distributions and predict associated plume response. Here emphasis is placed on estimation of the most information-rich DNAPL architecture metrics, through a combination of localized in situ tests and more readily available plume transect concentration observations. Estimated metrics will then serve as inputs to an upscaled screening model for prediction of long term plume response. Machine learning techniques were developed and refined to identify a variety of source zone metrics and associated confidence intervals through the processing of down gradient concentration data. Estimated metrics include the volumes and volume percentages of DNAPL in pools and ganglia, as well as their ratio (pool fraction). Multiphase flow and transport simulations provided training data for model development and assessment that are representative of field-scale DNAPL source zones and their evolving plumes. Here, a variety of release and site heterogeneity (sequential Gaussian permeability) conditions were investigated. Push-pull tracer tests were also explored as a means to provide localized in situ observations to refine these metric estimates. Here, two-dimensional aquifer cell experiments and mathematical modeling were used to quantify upscaled interphase mass transfer rates and the interplay between injection and extraction rates, local source zone architecture, and tracer

DSMC Simulations of Io's Pele Plume

Science.gov (United States)

McDoniel, William; Goldstein, D.; Varghese, P.; Trafton, L.

2012-10-01

Io’s Pele plume rises over 300km in altitude and leaves a deposition ring 1200km across on the surface of the moon. Material emerges from an irregularly-shaped vent, and this geometry gives rise to complex 3D flow features. The Direct Simulation Monte Carlo method is used to model the gas flow in the rarefied plume, demonstrating how the geometry of the source region is responsible for the asymmetric structure of the deposition ring and illustrating the importance of very small-scale vent geometry in explaining large observed features of interest. Simulations of small particles in the plume and comparisons to the black “butterfly wings” seen at Pele are used to constrain particle sizes and entrainment mechanisms. Preliminary results for the effects of plasma energy and momentum transfer to the plume will also be presented.

Status and Needs Research for On-line Monitoring of VOCs Emissions from Stationary Sources

Science.gov (United States)

Zhou, Gang; Wang, Qiang; Zhong, Qi; Zhao, Jinbao; Yang, Kai

2018-01-01

Based on atmospheric volatile organic compounds (VOCs) pollution control requirements during the twelfth-five year plan and the current status of monitoring and management at home and abroad, instrumental architecture and technical characteristics of continuous emission monitoring systems (CEMS) for VOCs emission from stationary sources are investigated and researched. Technological development needs of VOCs emission on-line monitoring techniques for stationary sources in china are proposed from the system sampling pretreatment technology and analytical measurement techniques.

Simulating Fine-Scale Marine Pollution Plumes for Autonomous Robotic Environmental Monitoring

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Muhammad Fahad

2018-05-01

Full Text Available Marine plumes exhibit characteristics such as intermittency, sinuous structure, shape and flow field coherency, and a time varying concentration profile. Due to the lack of experimental quantification of these characteristics for marine plumes, existing work often assumes marine plumes exhibit behavior similar to aerial plumes and are commonly modeled by filament based Lagrangian models. Our previous field experiments with Rhodamine dye plumes at Makai Research Pier at Oahu, Hawaii revealed that marine plumes show similar characteristics to aerial plumes qualitatively, but quantitatively they are disparate. Based on the field data collected, this paper presents a calibrated Eulerian plume model that exhibits the qualitative and quantitative characteristics exhibited by experimentally generated marine plumes. We propose a modified model with an intermittent source, and implement it in a Robot Operating System (ROS based simulator. Concentration time series of stationary sampling points and dynamic sampling points across cross-sections and plume fronts are collected and analyzed for statistical parameters of the simulated plume. These parameters are then compared with statistical parameters from experimentally generated plumes. The comparison validates that the simulated plumes exhibit fine-scale qualitative and quantitative characteristics similar to experimental plumes. The ROS plume simulator facilitates future evaluations of environmental monitoring strategies by marine robots, and is made available for community use.

Quantitative assessment of industrial VOC emissions in China: Historical trend, spatial distribution, uncertainties, and projection

Science.gov (United States)

Zheng, Chenghang; Shen, Jiali; Zhang, Yongxin; Huang, Weiwei; Zhu, Xinbo; Wu, Xuecheng; Chen, Linghong; Gao, Xiang; Cen, Kefa

2017-02-01

The temporal trends of industrial volatile organic compound (VOC) emissions was comprehensively summarized for the 2011 to 2013 period, and the projections for 2020 to 2050 for China were set. The results demonstrate that industrial VOC emissions in China increased from 15.3 Tg in 2011 to 29.4 Tg in 2013 at an annual average growth rate of 38.3%. Guangdong (3.45 Tg), Shandong (2.85 Tg), and Jiangsu (2.62 Tg) were the three largest contributors collectively accounting for 30.4% of the national total emissions in 2013. The top three average industrial VOC emissions per square kilometer were Shanghai (247.2 ton/km2), Tianjin (62.8 ton/km2), and Beijing (38.4 ton/km2), which were 12-80 times of the average level in China. The data from the inventory indicate that the use of VOC-containing products, as well as the production and use of VOCs as raw materials, as well as for storage and transportation contributed 75.4%, 10.3%, 9.1%, and 5.2% of the total emissions, respectively. ArcGIS was used to display the remarkable spatial distribution variation by allocating the emission into 1 km × 1 km grid cells with a population as surrogate indexes. Combined with future economic development and population change, as well as implementation of policy and upgrade of control technologies, three scenarios (scenarios A, B, and C) were set to project industrial VOC emissions for the years 2020, 2030, and 2050, which present the industrial VOC emissions in different scenarios and the potential of reducing emissions. Finally, the result shows that the collaborative control policies considerably influenced industrial VOC emissions.

VOC emission into the atmosphere by trees and leaf litter in Polish forests

Science.gov (United States)

Isidorov, V.; Smolewska, M.; Tyszkiewicz, Z.

2009-04-01

It is generally recognized at present that the vegetation of continents is the principal source of reactive volatile organic compounds (VOC) of the atmosphere. The upper limit of the evaluation of global phytogenic VOC is 1100-1500 Tg/yr (Isidorov, 1990; Guenther et al., 1995). Although these global evaluations showing the place of phytogenic emission among of other VOC sources are important, evaluations for individual countries are also very important. This poster represents the results of the estimation of VOC emission from Polish forests. Calculations took into account the composition and age of forests. According to our estimation, the total VOC emission by the arboreal vegetation differs from 190 to 750 kt/yr, depending of weather conditions in different years. There are only few studies conducted on decaying plant material as a source of atmospheric VOCs, but still they are able to give evidence of the importance of this source. For Polish forests, the litter mass is estimated to be (16-19)106 t/yr. These organic materials undergo decomposition by mesofauna and microorganisms. In these processes volatile organic compounds (VOC) stored in the litter and secondary metabolites of litter-destroying fungi are emitted into the atmosphere. The scale of the phenomenon makes leaf litter an important VOC source in the atmosphere. The filling of numerous gaps in researches of VOC emissions from decomposing leaf litter demands carrying out of long term field experiments in various climatic conditions. In this communication we report also the results of 3.5-year experiment on qualitative and quantitative GC-MS investigations of VOC emitted into the gas phase from leaves litter of some species of deciduous and coniferous trees of Polish forests. Apart from terpenes and their oxygenated derivatives, which are usual in plant tissues, leaf litter intensively emits vast amounts of lower alcohols and carbonyl compounds. We suppose that these volatile substances are products

Preliminary measurements of aromatic VOCs in public transportation modes in Guangzhou, China.

Science.gov (United States)

Chan, L Y; Lau, W L; Wang, X M; Tang, J H

2003-07-01

This study examined the exposure level of aromatic volatile organic compounds (VOCs) in public transportation modes in Guangzhou, China. A total of 40 VOC samples were conducted in four popular public commuting modes (subway, taxis, non-air-conditioned buses and air-conditioned buses) while traversing in urban areas of Guangzhou. Traffic-related VOCs (benzene, toluene, ethylbenzene, m/p-xylene and o-xylene) were collected on adsorbent tubes and analyzed by thermal desorption (TD) and gas chromatography/mass-selective detector (GC/MSD) technique. The results indicate that commuter exposure to VOCs is greatly influenced by the choice of public transport. For the benzene measured, the mean exposure level in taxis (33.6 microg/m(3)) was the highest and was followed by air-conditioned buses (13.5 microg/m(3)) and non-air-conditioned buses (11.3 microg/m(3)). The exposure level in the subway (7.6 microg/m(3)) is clearly lower than that in roadway transports. The inter-microenvironment variations of other target compounds were similar to that of benzene. The target VOCs were well correlated to each other in all the measured transports. The concentration profile of the measured transport was also investigated and was found to be similar to each other. Based on the experiment results, the average B/T/E/X found in this study was about (1.0/4.3/0.7/1.4). In this study, the VOC levels measured in evening peak hours were only slightly higher than those in afternoon non-peak hours. This is due to the insignificant change of traffic volume on the measured routes between these two set times. The out-dated vehicle emission controls and slow-moving traffic conditions may be the major reasons leading elevated in-vehicle exposure level in some public commuting journeys.

On the dating of você, ocê and senhorita

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Odete Pereira da Silva Menon

2009-11-01

Full Text Available Knowing the date when a word first appeared in the language is not only helpful for linguistic dating purposes. This information is important because it can guide studies about the actuation problem and evaluation stages (WEINREICH; LABOV; HERZOG, 1968 of linguistic changes. The present study is an attempt to locate, historically and socially, the behavior of forms to address the interlocutor, using more grammaticalized variants of the pronoun (honorific form vossa mercê, first in Portugal (você — you, en English then in Brazil (você and ocê/cê — contracted forms of você , correcting, updating and fixing the appearance dates of these occurrences. By referring to literature authors born between the 17th Century and the beginning of the 20th Century it was also possible to anticipate by half a century the dating of the noun senhorita (Eng. mistress, maybe an indicator of a new statute for women.

Understanding CO2 Plume Behavior and Basin-Scale Pressure Changes during Sequestration Projects through the use of Reservoir Fluid Modeling

Science.gov (United States)

Leetaru, H.E.; Frailey, S.M.; Damico, J.; Mehnert, E.; Birkholzer, J.; Zhou, Q.; Jordan, P.D.

2009-01-01

Large scale geologic sequestration tests are in the planning stages around the world. The liability and safety issues of the migration of CO2 away from the primary injection site and/or reservoir are of significant concerns for these sequestration tests. Reservoir models for simulating single or multi-phase fluid flow are used to understand the migration of CO2 in the subsurface. These models can also help evaluate concerns related to brine migration and basin-scale pressure increases that occur due to the injection of additional fluid volumes into the subsurface. The current paper presents different modeling examples addressing these issues, ranging from simple geometric models to more complex reservoir fluid models with single-site and basin-scale applications. Simple geometric models assuming a homogeneous geologic reservoir and piston-like displacement have been used for understanding pressure changes and fluid migration around each CO2 storage site. These geometric models are useful only as broad approximations because they do not account for the variation in porosity, permeability, asymmetry of the reservoir, and dip of the beds. In addition, these simple models are not capable of predicting the interference between different injection sites within the same reservoir. A more realistic model of CO2 plume behavior can be produced using reservoir fluid models. Reservoir simulation of natural gas storage reservoirs in the Illinois Basin Cambrian-age Mt. Simon Sandstone suggest that reservoir heterogeneity will be an important factor for evaluating storage capacity. The Mt. Simon Sandstone is a thick sandstone that underlies many significant coal fired power plants (emitting at least 1 million tonnes per year) in the midwestern United States including the states of Illinois, Indiana, Kentucky, Michigan, and Ohio. The initial commercial sequestration sites are expected to inject 1 to 2 million tonnes of CO2 per year. Depending on the geologic structure and

Low VOC Barrier Coating for Industrial Maintenance

Science.gov (United States)

2012-09-01

VOC Total Solids (wt) Total Solids (volume) Percent Pigment Stormer Viscosity Brookfield Viscosity Pot Life Sag Resistance Theoretical...Percent Pigment – Stormer Viscosity – Brookfield Viscosity – Pot Life – Sag Resistance – Theoretical Coverage – Drying Times – Mixing Ratio

Sesquiterpene volatile organic compounds (VOCs are markers of elicitation by sulfated laminarine in grapevine

Directory of Open Access Journals (Sweden)

Malik eChalal

2015-05-01

Full Text Available Inducing resistance in plants by application of elicitors of defense reactions is an attractive plant protection strategy, especially for grapevine (Vitis vinifera which is susceptible to severe fungal diseases. Though induced resistance (IR can be successful in controlled conditions, under outdoor conditions IR is in most cases not effective enough for practical disease control. Progress in the application of IR requires a better understanding of grapevine defense mechanisms and the ability to monitor defense markers in order to identify factors (physiological, environmental… that can impact IR in the vineyard.Volatile organic compounds (VOCs are well-known plant defenses compounds that have only received little or no attention in the case of grape-pathogen interactions to date. This prompted us to investigate whether an elicitor, the sulfated laminarin (PS3, actually induces the production of VOCs in grapevine. Online analysis (PTR-QMS of VOC emissions in dynamic cuvettes and passive sampling in gas tight bags with solid phase micro extraction (SPME-GC-MS under greenhouse conditions showed that PS3 elicited emission of VOCs. Some of them (as (E,E-α-farnesene might be good candidates as biomarkers of elicitor-IR whereas methyl salicylate appears to be rather a biomarker of downy mildew infection. A negative correlation between VOC emission and disease severity suggests a positive role of VOCs in grape defense against diseases.

A Review of Photocatalysts Prepared by Sol-Gel Method for VOCs Removal

Directory of Open Access Journals (Sweden)

Ting Ke Tseng

2010-05-01

Full Text Available The sol-gel process is a wet-chemical technique (chemical solution deposition, which has been widely used in the fields of materials science, ceramic engineering, and especially in the preparation of photocatalysts. Volatile organic compounds (VOCs are prevalent components of indoor air pollution. Among the approaches to remove VOCs from indoor air, photocatalytic oxidation (PCO is regarded as a promising method. This paper is a review of the status of research on the sol-gel method for photocatalyst preparation and for the PCO purification of VOCs. The review and discussion will focus on the preparation and coating of various photocatalysts, operational parameters, and will provide an overview of general PCO models described in the literature.

Modelling thermal plume impacts - Kalpakkam approach

International Nuclear Information System (INIS)

Rao, T.S.; Anup Kumar, B.; Narasimhan, S.V.

2002-01-01

A good understanding of temperature patterns in the receiving waters is essential to know the heat dissipation from thermal plumes originating from coastal power plants. The seasonal temperature profiles of the Kalpakkam coast near Madras Atomic Power Station (MAPS) thermal out fall site are determined and analysed. It is observed that the seasonal current reversal in the near shore zone is one of the major mechanisms for the transport of effluents away from the point of mixing. To further refine our understanding of the mixing and dilution processes, it is necessary to numerically simulate the coastal ocean processes by parameterising the key factors concerned. In this paper, we outline the experimental approach to achieve this objective. (author)

Volatile organic compounds (VOCs) in air from Nisyros Island (Dodecanese Archipelago, Greece): Natural versus anthropogenic sources

International Nuclear Information System (INIS)

Tassi, F.; Capecchiacci, F.; Giannini, L.; Vougioukalakis, G.E.; Vaselli, O.

2013-01-01

This study presents the chemical composition of VOCs in air and gas discharges collected at Nisyros Island (Dodecanese Archipelago, Greece). The main goals are i) to discriminate between natural and anthropogenic VOC sources and ii) to evaluate their impact on local air quality. Up to 63 different VOCs were recognized and quantitatively determined in 6 fumaroles and 19 air samples collected in the Lakki caldera, where fumarolic emissions are located, and the outer ring of the island, including the Mandraki village and the main harbor. Air samples from the crater area show significant concentrations of alkanes, alkenes, cyclic, aromatics, and S- and O-bearing heterocycles directly deriving from the hydrothermal system, as well as secondary O-bearing compounds from oxidation of primary VOCs. At Mandraki village, C 6 H 6 /Σ(methylated aromatics) and Σ(linear)/Σ(branched) alkanes ratios 2 O–CO 2 –H 2 S rich and discharge a large variety of VOC species. •Benzene/toluene ratios identify anthropogenic and natural sources of VOCs in air. •Aldehydes in air are produced by oxidation of alkanes and alkenes. •Geogenic furans and hydrogenated halocarbons in air are recalcitrant. -- Anthropogenic and natural VOCs in air are distinguished on the basis of aromatic, O-substituted, S-substituted and halogenated compounds

Ambient volatile organic compounds (VOCs) in Calgary, Alberta: Sources and screening health risk assessment.

Science.gov (United States)

Bari, Md Aynul; Kindzierski, Warren B

2018-08-01

Exposure to ambient volatile organic compound (VOCs) in urban areas is of interest because of their potential chronic and acute adverse effects to public health. Limited information is available about VOC sources in urban areas in Canada. An investigation of ambient VOCs levels, their potential sources and associated risks to public health was undertaken for the urban core of Alberta's largest city (downtown Calgary) for the period 2010-2015. Twenty-four hour arithmetic and geometric mean concentrations of total VOCs were 42μg/m 3 and 39μg/m 3 , respectively and ranged from 16 to 160μg/m 3 , with winter levels about two-fold higher than summer. Alkanes (58%) were the most dominant compounds followed by halogenated VOCs (22%) and aromatics (11%). Mean and maximum 24h ambient concentrations of selected VOCs of public health concern were below chronic and acute health risk screening criteria of the United States regulatory agencies and a cancer screening benchmark used in Alberta equivalent to 1 in 100,000 lifetime risk. The Positive matrix factorization (PMF) model revealed nine VOC sources at downtown Calgary, where oil/natural gas extraction/combustion (26%), fuel combustion (20%), traffic sources including gasoline exhaust, diesel exhaust, mixed fugitive emissions (10-15%), and industrial coatings/solvents (12%) were predominant. Other sources included dry cleaning (3.3%), biogenic (3.5%) and a background source (18%). Source-specific health risk values were also estimated. Estimated cancer risks for all sources were below the Alberta cancer screening benchmark, and estimated non-cancer risks for all sources were well below a safe level. Copyright © 2018 Elsevier B.V. All rights reserved.

Cone penetrometer testing at the Hanford Site: Final performance evaluation report

International Nuclear Information System (INIS)

Richterich, L.R.; Cassem, B.R.

1994-08-01

The Volatile Organic Compounds-Arid Integrated Demonstration (VOC-Arid ID) is one of several US Department of Energy (DOE) integrated demonstrations designed to support the testing of emerging environmental characterization and remediation technologies in support of the Environmental Restoration (ER) and Waste Management (WM) Programs. The primary objective of the VOC Arid ID at the Hanford Site is to characterize, remediate, and monitor arid and semi-arid sites containing volatile organic compounds with or without associated contamination. The main objective of the Arid Drilling Technology Technical Task Plan is to demonstrate promising subsurface access technologies; this includes using the cone penetrometer (CPT) system for source detection, characterization, monitoring, and remediation in support of environmental activities. The utility of the CPT for performing site characterization work has been the subject of much discussion and speculation at the Hanford Site and other arid sites because of the preponderance of thick units of coarse cobbles and gravel in the subsurface

Paducah Gaseous Diffusion Plant Northwest Plume interceptor system evaluation

International Nuclear Information System (INIS)

Laase, A.D.; Clausen, J.L.

1998-01-01

The Paducah Gaseous Diffusion Plant (PGDP) recently installed an interceptor system consisting of four wells, evenly divided between two well fields, to contain the Northwest Plume. As stated in the Northwest Plume Record of Decision (ROD), groundwater will be pumped at a rate to reduce further contamination and initiate control of the northwest contaminant plume. The objective of this evaluation was to determine the optimum (minimal) well field pumping rates required for plume hotspot containment. Plume hotspot, as defined in the Northwest Plume ROD and throughout this report, is that portion of the plume with trichloroethene (TCE) concentrations greater than 1,000 microg/L. An existing 3-dimensional groundwater model was modified and used to perform capture zone analyses of the north and south interceptor system well fields. Model results suggest that the plume hotspot is not contained at the system design pumping rate of 100 gallons per minute (gal/min) per well field. Rather, the modeling determined that north and south well field pumping rates of 400 and 150 gal/min, respectively, are necessary for plume hotspot containment. The difference between the design and optimal pumping rates required for containment can be attributed to the discovery of a highly transmissive zone in the vicinity of the two well fields

Follow the plume: the habitability of Enceladus.

Science.gov (United States)

McKay, Christopher P; Anbar, Ariel D; Porco, Carolyn; Tsou, Peter

2014-04-01

The astrobiological exploration of other worlds in our Solar System is moving from initial exploration to more focused astrobiology missions. In this context, we present the case that the plume of Enceladus currently represents the best astrobiology target in the Solar System. Analysis of the plume by the Cassini mission indicates that the steady plume derives from a subsurface liquid water reservoir that contains organic carbon, biologically available nitrogen, redox energy sources, and inorganic salts. Furthermore, samples from the plume jetting out into space are accessible to a low-cost flyby mission. No other world has such well-studied indications of habitable conditions. Thus, the science goals that would motivate an Enceladus mission are more advanced than for any other Solar System body. The goals of such a mission must go beyond further geophysical characterization, extending to the search for biomolecular evidence of life in the organic-rich plume. This will require improved in situ investigations and a sample return.

Volatile organic compounds in Tijuana during the Cal-Mex 2010 campaign: Measurements and source apportionment

Science.gov (United States)

Zheng, Jun; Garzón, Jessica P.; Huertas, María E.; Zhang, Renyi; Levy, Misti; Ma, Yan; Huertas, José I.; Jardón, Ricardo T.; Ruíz, Luis G.; Tan, Haobo; Molina, Luisa T.

2013-05-01

As part of the Cal-Mex 2010 air quality study, a proton transfer reaction-mass spectrometer (PTR-MS) was deployed at the San Diego-Tijuana border area to measure volatile organic compounds (VOCs) from 15 May to 30 June 2010. The major VOCs identified during the study included oxygenated VOCs (e.g., methanol, acetaldehyde, acetone, and methyl ethyl ketone) and aromatics (e.g., benzene, toluene, C8- and C9-aromatics). Biogenic VOCs (e.g., isoprene) were scarce in this region because of the lack of vegetation in this arid area. Using an U.S. EPA positive matrix factorization model, VOCs together with other trace gases (NOx, NOz and SO2) observed in this border region were attributed to four types of sources, i.e., local industrial solvent usage (58% in ppbC), gasoline vehicle exhaust (19% in ppbC), diesel vehicle exhaust (14% in ppbC), and aged plume (9% in ppbC) due to regional background and/or long-range transport. Diesel vehicle emission contributed to 87% of SO2 and 75% of NOx, and aged plume contributed to 92% of NOz. An independent conditional probability function analysis of VOCs, wind direction, and wind speed indicated that the industrial source did not show a significant tendency with wind direction. Both gasoline and diesel engine emissions were associated with air masses passing through two busy cross-border ports. Aged plumes were strongly associated with NW wind, which likely brought in aged air masses from the populated San Diego area.

A compact PTR-ToF-MS instrument for airborne measurements of volatile organic compounds at high spatiotemporal resolution

Directory of Open Access Journals (Sweden)

M. Müller

2014-11-01

Full Text Available Herein, we report on the development of a compact proton-transfer-reaction time-of-flight mass spectrometer (PTR-ToF-MS for airborne measurements of volatile organic compounds (VOCs. The new instrument resolves isobaric ions with a mass resolving power (m/Δm of ~1000, provides accurate m/z measurements (Δm < 3 mDa, records full mass spectra at 1 Hz and thus overcomes some of the major analytical deficiencies of quadrupole-MS-based airborne instruments. 1 Hz detection limits for biogenic VOCs (isoprene, α total monoterpenes, aromatic VOCs (benzene, toluene, xylenes and ketones (acetone, methyl ethyl ketone range from 0.05 to 0.12 ppbV, making the instrument well-suited for fast measurements of abundant VOCs in the continental boundary layer. The instrument detects and quantifies VOCs in locally confined plumes (< 1 km, which improves our capability of characterizing emission sources and atmospheric processing within plumes. A deployment during the NASA 2013 DISCOVER-AQ mission generated high vertical- and horizontal-resolution in situ data of VOCs and ammonia for the validation of satellite retrievals and chemistry transport models.

TECHNICAL JUSTIFICATION FOR CHOOSING PROPANE AS A CALIBRATION AGENT FOR TOTAL FLAMMABLE VOLATILE ORGANIC COMPOUND (VOC) DETERMINATIONS

International Nuclear Information System (INIS)

DOUGLAS, J.G.

2006-01-01

This document presents the technical justification for choosing and using propane as a calibration standard for estimating total flammable volatile organic compounds (VOCs) in an air matrix. A propane-in-nitrogen standard was selected based on a number of criteria: (1) has an analytical response similar to the VOCs of interest, (2) can be made with known accuracy and traceability, (3) is available with good purity, (4) has a matrix similar to the sample matrix, (5) is stable during storage and use, (6) is relatively non-hazardous, and (7) is a recognized standard for similar analytical applications. The Waste Retrieval Project (WRP) desires a fast, reliable, and inexpensive method for screening the flammable VOC content in the vapor-phase headspace of waste containers. Table 1 lists the flammable VOCs of interest to the WRP. The current method used to determine the VOC content of a container is to sample the container's headspace and submit the sample for gas chromatography--mass spectrometry (GC-MS) analysis. The driver for the VOC measurement requirement is safety: potentially flammable atmospheres in the waste containers must be allowed to diffuse prior to processing the container. The proposed flammable VOC screening method is to inject an aliquot of the headspace sample into an argon-doped pulsed-discharge helium ionization detector (Ar-PDHID) contained within a gas chromatograph. No actual chromatography is performed; the sample is transferred directly from a sample loop to the detector through a short, inert transfer line. The peak area resulting from the injected sample is proportional to the flammable VOC content of the sample. However, because the Ar-PDHID has different response factors for different flammable VOCs, a fundamental assumption must be made that the agent used to calibrate the detector is representative of the flammable VOCs of interest that may be in the headspace samples. At worst, we desire that calibration with the selected calibrating

Determination of Summertime VOC Emission Rates from Produced Water Ponds in the Uintah Basin

Science.gov (United States)

Martin, R. S.; Woods, C.; Lyman, S.

2013-12-01

The observance of excess ozone concentrations in Utah's Uintah Basin over past several years has prompted several investigations into the extent and causes of the elevated ozone. Among these is the assessment of potential emissions of reactive VOCs. Evaporation ponds, used a remediation technique for treatment of contaminated production and other waters, are one potential source of significant VOC emissions and is estimated that there are around 160 such ponds within the Uintah Basin's oil and gas production areas. In June 2012 VOC emission rates for several reactive VOCs were derived for an evaporation facility consisting of a small inlet pond (≈0.03 acres) and two larger, serial ponds (≈4.3 acres each). The emission rates were determined over three sampling periods using an inverse modeling approach. Under this methodology, ambient VOC concentrations are determined at several downwind locations through whole-air collection into SUMMA canisters, followed by GC/MS quantification and compared with predicted concentrations using an EPA-approved dispersion model, AERMOD. The presumed emission rates used within the model were then adjusted until the modeled concentrations approach the observed concentrations. The derived emission rates for the individual VOCs were on the order of 10-3 g/s/m2 from the inlet pond and 10-6 g/s/m2 from the larger ponds. The emissions from the 1st pond in series after the inlet pond were about 3-4x the emissions from the 2nd pond. These combined emission rates are about an order of magnitude those reported for a single study in Colorado (Thoma, 2009). It should be noted, however, that the variability about each of the VOC emission rates was significant (often ×100% at the 95% confidence interval). Extrapolating these emission rates to the estimated total areas of all the evaporation ponds within Basin resulted in calculated Basin-wide VOC emissions 292,835 tons/yr. However, Bar-Ilan et al. (2009) estimated 2012 VOC oil and gas related

An intercomparison of airborne VOC measurements

International Nuclear Information System (INIS)

Wisthaler, A.; Hansel, A.; Fall, R.

2002-01-01

Full text: During the Texas Air Quality Study (TexAQS) 2000 ambient air samples were analyzed on-board the NSF/NCAR ELECTRA research aircraft by two VOC measurement techniques: 1) an in-situ gas chromatograph named TACOH (Tropospheric Airborne Chromatograph for Oxy-hydrocarbons and Hydrocarbons), operated by NOAA' Aeronomy Laboratory, and 2) a chemical ionization mass spectrometer named PTR-MS (Proton-Transfer-Reaction Mass Spectrometer) and operated by the University of Innsbruck. The sample protocols were quite different for the two methods: the TACOH system collected air samples for 15-60 sec (depending upon altitude) every 15 min, the PTR-MS system monitored selected VOCs on a time-shared basis for 2 sec respectively, once every 4-20 sec, depending upon the number of monitored species. Simultaneous measurements of acetaldehyde, isoprene, the sum* of acetone and propanal, the sum* of methyl vinyl ketone and methacrolein (* PTR-MS does not distinguish between isobaric species) and toluene show good agreement despite being performed in the complex and highly polluted Houston air matrix. (author)

Wave Glider Monitoring of Sediment Transport and Dredge Plumes in a Shallow Marine Sandbank Environment.

Science.gov (United States)

Van Lancker, Vera; Baeye, Matthias

2015-01-01

As human pressure on the marine environment increases, safeguarding healthy and productive seas increasingly necessitates integrated, time- and cost-effective environmental monitoring. Employment of a Wave Glider proved very useful for the study of sediment transport in a shallow sandbank area in the Belgian part of the North Sea. During 22 days, data on surface and water-column currents and turbidity were recorded along 39 loops around an aggregate-extraction site. Correlation with wave and tidal-amplitude data allowed the quantification of current- and wave-induced advection and resuspension, important background information to assess dredging impacts. Important anomalies in suspended particulate matter concentrations in the water column suggested dredging-induced overflow of sediments in the near field (i.e., dynamic plume), and settling of finer-grained material in the far field (i.e., passive plume). Capturing the latter is a successful outcome to this experiment, since the location of dispersion and settling of a passive plume is highly dependent on the ruling hydro-meteorological conditions and thus difficult to predict. Deposition of the observed sediment plumes may cause habitat changes in the long-term.

Wave Glider Monitoring of Sediment Transport and Dredge Plumes in a Shallow Marine Sandbank Environment.

Directory of Open Access Journals (Sweden)

Vera Van Lancker

Full Text Available As human pressure on the marine environment increases, safeguarding healthy and productive seas increasingly necessitates integrated, time- and cost-effective environmental monitoring. Employment of a Wave Glider proved very useful for the study of sediment transport in a shallow sandbank area in the Belgian part of the North Sea. During 22 days, data on surface and water-column currents and turbidity were recorded along 39 loops around an aggregate-extraction site. Correlation with wave and tidal-amplitude data allowed the quantification of current- and wave-induced advection and resuspension, important background information to assess dredging impacts. Important anomalies in suspended particulate matter concentrations in the water column suggested dredging-induced overflow of sediments in the near field (i.e., dynamic plume, and settling of finer-grained material in the far field (i.e., passive plume. Capturing the latter is a successful outcome to this experiment, since the location of dispersion and settling of a passive plume is highly dependent on the ruling hydro-meteorological conditions and thus difficult to predict. Deposition of the observed sediment plumes may cause habitat changes in the long-term.

Birth, life, and death of a solar coronal plume

Energy Technology Data Exchange (ETDEWEB)

Pucci, Stefano; Romoli, Marco [Department of Physics and Astronomy, University of Firenze, Largo Enrico Fermi 5, I-50125 Firenze (Italy); Poletto, Giannina [INAF-Arcetri Astrophysical Observatory, Largo Enrico Fermi 5, I-50125 Firenze (Italy); Sterling, Alphonse C., E-mail: stpucci@arcetri.astro.it [Space Science Office, NASA/MSFC, Huntsville, AL 35812 (United States)

2014-10-01

We analyze a solar polar-coronal-hole (CH) plume over its entire ≈40 hr lifetime, using high-resolution Solar Dynamic Observatory Atmospheric Imaging Assembly (AIA) data. We examine (1) the plume's relationship to a bright point (BP) that persists at its base, (2) plume outflows and their possible contribution to the solar wind mass supply, and (3) the physical properties of the plume. We find that the plume started ≈2 hr after the BP first appeared and became undetectable ≈1 hr after the BP disappeared. We detected radially moving radiance variations from both the plume and from interplume regions, corresponding to apparent outflow speeds ranging over ≈(30-300) km s{sup –1} with outflow velocities being higher in the 'cooler' AIA 171 Å channel than in the 'hotter' 193 Å and 211 Å channels, which is inconsistent with wave motions; therefore, we conclude that the observed radiance variations represent material outflows. If they persist into the heliosphere and plumes cover ≈10% of a typical CH area, these flows could account for ≈50% of the solar wind mass. From a differential emission measure analysis of the AIA images, we find that the average electron temperature of the plume remained approximately constant over its lifetime, at T {sub e} ≈ 8.5 × 10{sup 5} K. Its density, however, decreased with the age of the plume, being about a factor of three lower when the plume faded compared to when it was born. We conclude that the plume died due to a density reduction rather than to a temperature decrease.

Characterization of Volatile Organic Compound (VOC) Emissions at Sites of Oil Sands Extraction and Upgrading in northern Alberta

Science.gov (United States)

Marrero, J.; Simpson, I. J.; Meinardi, S.; Blake, D. R.

2011-12-01

The crude oil reserves in Canada's oil sands are second only to Saudi Arabia, holding roughly 173 billion barrels of oil in the form of bitumen, an unconventional crude oil which does not flow and cannot be pumped without heating or dilution. Oil sands deposits are ultimately used to make the same petroleum products as conventional forms of crude oil, though more processing is required. Hydrocarbons are the basis of oil, coal and natural gas and are an important class of gases emitted into the atmosphere during oil production, particularly because of their effects on air quality and human health. However, they have only recently begun to be independently assessed in the oil sands regions. As part of the 2008 ARCTAS airborne mission, whole air samples were collected in the boundary layer above the surface mining operations of northern Alberta. Gas chromatography analysis revealed enhanced concentrations of 53 VOCs (C2 to C10) over the mining region. When compared to local background levels, the measured concentrations were enhanced up to 1.1-400 times for these compounds. To more fully characterize emissions, ground-based studies were conducted in summer 2010 and winter 2011 in the oil sands mining and upgrading areas. The data from the 200 ground-based samples revealed enhancements in the concentration of 65 VOCs. These compounds were elevated up to 1.1-3000 times above background concentrations and include C2-C8 alkanes, C1-C5 alkyl nitrates, C2-C4 alkenes and potentially toxic aromatic compounds such as benzene, toluene, and xylenes.

Bioinjection Performance Review for the Building 100 Area and 4.5 Acre Site at the Pinellas County, Florida, Site

Energy Technology Data Exchange (ETDEWEB)

Survochak, Scott [US Department of Energy, Washington, DC (United States). Office of Legacy Management; Daniel, Joe [Navarro Research and Engineering, Oak Ridge, TN (United States)

2016-05-01

This document provides a summary of a review of the performance of bioinjection activities at the Building 100 Area and the 4.5 Acre Site at the Pinellas County, Florida, Site since 2010, determines how best to optimize future injection events, and identifies the approach for the bioinjection event in 2016 at (1) the 4.5 Acre Site and (2) the Essentra property at the Building 100 Area. Because this document describes the next bioinjection event at the 4.5 Acre Site, it also serves as an addendum to the Interim Remedial Action Plan for Emulsified Edible Oil Injection at the 4.5 Acre Site (DOE 2013). In addition, this document revises the injection layout and injection intervals for the Essentra property that were originally described in the Interim Corrective Measure Work Plan for Source and Plume Treatment at the Building 100 Area (DOE 2014), and is a de facto update of that document. Bioinjection consists of injection of emulsified vegetable oil (EVO) and the microorganism Dehalococcoides mccartyi (DHM; formerly known as Dehalococcoides ethenogenes) into the subsurface to enhance biodegradation of trichloroethene (TCE), dichloroethene (DCE), and vinyl chloride (VC). VC is the only contaminant that exceeds its maximum contaminant level (10 micrograms per liter onsite and 1 microgram per liter onsite) on the 4.5 Acre Site and the Essentra property. Bioinjection was conducted at the 4.5 Acre Site in 2010 and 2013. Approximately 49,900 gallons of EVO and DHM were injected at 95 injection points in February 2010, and approximately 22,900 gallons of EVO and DHM were injected at 46 injection points in July 2013. The injection locations are shown on Figure 1. The goal of bioinjection at the 4.5 Acre Site is to decrease contaminant concentrations to maximum contaminant levels along the west and southwest property boundaries (to meet risk–based corrective action requirements) and to minimize the extent of the contaminant plume in the interior of the site. Bioinjection was

Optimization of an Innovative Biofiltration System as a VOC Control Technology for Aircraft Painting Facilities

Science.gov (United States)

2004-04-20

plants. Since the 1980s, however, biofiltration has also been used to eliminate VOCs in gases emitted from a wide range of processes (van Groenestijn...process for the VOC-laden waste gases exiting paint spray booths at DoD maintenance facilities. Conceptually, the biofiltration process can be divided...recently, biofiltration applications have been expanded to treat VOC-laden waste gases emitted by industry (Ottengraf, 1986, van Groenestijn, 1994; Swanson

[Study on atmospheric VOCs in Gongga Mountain base station].

Science.gov (United States)

Zhang, Jun-Ke; Wang, Yue-Si; Wu, Fang-Kun; Sun, Jie

2012-12-01

Volatile organic compounds (VOCs) play important roles in the atmosphere as precursors of secondary air pollutants. The regional background concentrations and variation characteristics of VOCs in the atmosphere of southwestern China were studied. Meanwhile, a receptor model based on principal component analysis (PCA) was used to identify the major sources of VOCs. Weekly samples were collected in 2007 in the Gongga Mountain base station and analyzed with a three-stage preconcentration method coupled with GC-MS. The annual mean concentration of TVOCs and NMHCs were 9.40 x 10(-9) +/- 4.55 x 10(-9) and 7.73 x 10(-9) +/- 4.43 x 10(-9), respectively. Aromatic hydrocarbons provided the largest contribution to TVOCs (37.3%), follow by alkanes (30.0%) and halogenated hydrocarbons (19.8%), the smallest contribution was from alkenes (12.9%). Three major sources were resolved by the receptor model, traffic sources, biogenic sources and combustion sources. The seasonal variation of TVOCs in this area was obviously, and the order was autumn > winter > spring > summer. TVOCs concentration in autumn was very significantly higher than that in summer (P station emission characteristic.

Is the IP response related to geology or contaminants in a leachate plume at the Grindsted Landfill, Denmark?

DEFF Research Database (Denmark)

Møller, Ingelise; Maurya, Pradip Kumar; Balbarini, Nicola

Contaminants in leachate plumes from landfills and other contaminated sites are a threat to the environment. Efficient site characterization methods are needed. The perspectives of the IP method are investigated in combination with geological sampling and chemical analyses of water samples. Along...... a leachate plume from a landfill hosting both household and chemical waste, borehole IP data, geological samples, grain size, and contaminant concentrations in water samples are examined for correlations related to geology and concentrations of contaminants. Results relating the Cole-Cole parameters...... with sediment types and pore water resistivity representing the concentrations of the contaminants show that the formation resistivity primarily is controlled by the contaminant concentrations while the IP parameters primarily are related to the clay content and grain size distribution of sandy sediments...

Is the IP response related to geology or contaminants in a leachate plume at the Grindsted Landfill, Denmark?

DEFF Research Database (Denmark)

Møller, Ingelise; Maurya, Pradip Kumar; Balbarini, Nicola

a leachate plume from a landfill hosting both household and chemical waste, borehole IP data, geological samples, grain size, and contaminant concentrations in water samples are examined for correlations related to geology and concentrations of contaminants. Results relating the Cole-Cole parameters...... with sediment types and pore water resistivity representing the concentrations of the contaminants show that the formation resistivity primarily is controlled by the contaminant concentrations while the IP parameters primarily are related to the clay content and grain size distribution of sandy sediments......Contaminants in leachate plumes from landfills and other contaminated sites are a threat to the environment. Efficient site characterization methods are needed. The perspectives of the IP method are investigated in combination with geological sampling and chemical analyses of water samples. Along...

Smoke plumes: Emissions and effects

Science.gov (United States)

Susan O' Neill; Shawn Urbanski; Scott Goodrick; Sim Larkin

2017-01-01

Smoke can manifest itself as a towering plume rising against the clear blue sky-or as a vast swath of thick haze, with fingers that settle into valleys overnight. It comes in many forms and colors, from fluffy and white to thick and black. Smoke plumes can rise high into the atmosphere and travel great distances across oceans and continents. Or smoke can remain close...

Plume Splitting in a Two-layer Stratified Ambient Fluid

Science.gov (United States)

Ma, Yongxing; Flynn, Morris; Sutherland, Bruce

2017-11-01

A line-source plume descending into a two-layer stratified ambient fluid in a finite sized tank is studied experimentally. Although the total volume of ambient fluid is fixed, lower- and upper-layer fluids are respectively removed and added at a constant rate mimicking marine outfall through diffusers and natural and hybrid ventilated buildings. The influence of the plume on the ambient depends on the value of λ, defined as the ratio of the plume buoyancy to the buoyancy loss of the plume as it crosses the ambient interface. Similar to classical filling-box experiments, the plume can always reach the bottom of the tank if λ > 1 . By contrast, if λ < 1 , an intermediate layer eventually forms as a result of plume splitting. Eventually all of the plume fluid spreads within the intermediate layer. The starting time, tv, and the ending time, tt, of the transition process measured from experiments correlate with the value of λ. A three-layer ambient fluid is observed after transition, and the mean value of the measured densities of the intermediate layer fluid is well predicted using plume theory. Acknowledgments: Funding for this study was provided by NSERC.

Teaching the Mantle Plumes Debate

Science.gov (United States)

Foulger, G. R.

2010-12-01

There is an ongoing debate regarding whether or not mantle plumes exist. This debate has highlighted a number of issues regarding how Earth science is currently practised, and how this feeds into approaches toward teaching students. The plume model is an hypothesis, not a proven fact. And yet many researchers assume a priori that plumes exist. This assumption feeds into teaching. That the plume model is unproven, and that many practising researchers are skeptical, may be at best only mentioned in passing to students, with most teachers assuming that plumes are proven to exist. There is typically little emphasis, in particular in undergraduate teaching, that the origin of melting anomalies is currently uncertain and that scientists do not know all the answers. Little encouragement is given to students to become involved in the debate and to consider the pros and cons for themselves. Typically teachers take the approach that “an answer” (or even “the answer”) must be taught to students. Such a pedagogic approach misses an excellent opportunity to allow students to participate in an important ongoing debate in Earth sciences. It also misses the opportunity to illustrate to students several critical aspects regarding correct application of the scientific method. The scientific method involves attempting to disprove hypotheses, not to prove them. A priori assumptions should be kept uppermost in mind and reconsidered at all stages. Multiple working hypotheses should be entertained. The predictions of a hypothesis should be tested, and unpredicted observations taken as weakening the original hypothesis. Hypotheses should not be endlessly adapted to fit unexpected observations. The difficulty with pedagogic treatment of the mantle plumes debate highlights a general uncertainty about how to teach issues in Earth science that are not yet resolved with certainty. It also represents a missed opportunity to let students experience how scientific theories evolve, warts

New device for time-averaged measurement of volatile organic compounds (VOCs)

Energy Technology Data Exchange (ETDEWEB)

Santiago Sánchez, Noemí; Tejada Alarcón, Sergio; Tortajada Santonja, Rafael; Llorca-Pórcel, Julio, E-mail: julio.llorca@aqualogy.net

2014-07-01

Contamination by volatile organic compounds (VOCs) in the environment is an increasing concern since these compounds are harmful to ecosystems and even to human health. Actually, many of them are considered toxic and/or carcinogenic. The main sources of pollution come from very diffuse focal points such as industrial discharges, urban water and accidental spills as these compounds may be present in many products and processes (i.e., paints, fuels, petroleum products, raw materials, solvents, etc.) making their control difficult. The presence of these compounds in groundwater, influenced by discharges, leachate or effluents of WWTPs is especially problematic. In recent years, law has been increasingly restrictive with the emissions of these compounds. From an environmental point of view, the European Water Framework Directive (2000/60/EC) sets out some VOCs as priority substances. This binding directive sets guidelines to control compounds such as benzene, chloroform, and carbon tetrachloride to be at a very low level of concentration and with a very high frequency of analysis. The presence of VOCs in the various effluents is often highly variable and discontinuous since it depends on the variability of the sources of contamination. Therefore, in order to have complete information of the presence of these contaminants and to effectively take preventive measures, it is important to continuously control, requiring the development of new devices which obtain average concentrations over time. As of today, due to technical limitations, there are no devices on the market that allow continuous sampling of these compounds in an efficient way and to facilitate sufficient detection limits to meet the legal requirements which are capable of detecting very sporadic and of short duration discharges. LABAQUA has developed a device which consists of a small peristaltic pump controlled by an electronic board that governs its operation by pre-programming. A constant flow passes

Airborne VOC measurements on board the Zeppelin NT during the PEGASOS campaigns in 2012 deploying the improvement Fast-GC-MSD system

Energy Technology Data Exchange (ETDEWEB)

Jaeger, Julia Elisabeth

2014-04-01

Volatile organic compounds (VOCs) comprise a large number of different species, estimated to 10{sup 4}-10{sup 6}. They are emitted on the Earth's surface from a variety of biogenic and anthropogenic sources. VOCs are removed by multiple pathways from the atmosphere, by oxidation and finally by dry or wet deposition. Most primary emitted VOCs are non-polar and therefore have a low solubility in water. Oxidation facilitates efficient VOC removal by wet deposition. In the atmosphere the main photochemical VOC oxidation agent is the OH radical. As a consequence the polarity of the VOCs is increased and they can be removed faster. The oxidation of VOCs proceeds in several steps until the VOCs are deposited or are eventually oxidized to carbon dioxide. A downside of the VOCs oxidation process lies in the production of significant amounts ozone if nitrogen oxide is present which is a serious health hazard. Most of the VOC oxidation takes place in lower part of the atmosphere between the altitudes of 100 to 1000 m, which is only sparsely analyzed. Therefore, fast VOCs measurements by GC-MSD on board the Zeppelin NT offered new important insights in the distribution of VOCs. The measurements were performed within the PEAGSOS campaigns in the Netherlands and in Italy in 2012. For the implementation of the GC-MSD system (HCG) on board the Zeppelin it was reconstructed to enhance its performance and to meet aviation requirements. The system was optimized to measure VOCs ranging from C4 to C10 as well as oxygenated VOCs (OVOCs) with a detection limit below 10 ppt. The analyzed VOCs for both parts of the campaigns showed low mean concentration below 5 ppb for all VOCs. Especially, the mixing ratios of the primary emitted VOCs were very low with mean values lower than 200 ppt. Higher concentrations could be observed for the OVOCs with mean concentrations up to 5 ppb. The most abundant OVOCs apart from formaldehyde were methanol, ethanol, acetone and acetaldehyde.

Airborne VOC measurements on board the Zeppelin NT during the PEGASOS campaigns in 2012 deploying the improvement Fast-GC-MSD system

Energy Technology Data Exchange (ETDEWEB)

Jaeger, Julia Elisabeth

2014-04-01

Volatile organic compounds (VOCs) comprise a large number of different species, estimated to 10{sup 4}-10{sup 6}. They are emitted on the Earth's surface from a variety of biogenic and anthropogenic sources. VOCs are removed by multiple pathways from the atmosphere, by oxidation and finally by dry or wet deposition. Most primary emitted VOCs are non-polar and therefore have a low solubility in water. Oxidation facilitates efficient VOC removal by wet deposition. In the atmosphere the main photochemical VOC oxidation agent is the OH radical. As a consequence the polarity of the VOCs is increased and they can be removed faster. The oxidation of VOCs proceeds in several steps until the VOCs are deposited or are eventually oxidized to carbon dioxide. A downside of the VOCs oxidation process lies in the production of significant amounts ozone if nitrogen oxide is present which is a serious health hazard. Most of the VOC oxidation takes place in lower part of the atmosphere between the altitudes of 100 to 1000 m, which is only sparsely analyzed. Therefore, fast VOCs measurements by GC-MSD on board the Zeppelin NT offered new important insights in the distribution of VOCs. The measurements were performed within the PEAGSOS campaigns in the Netherlands and in Italy in 2012. For the implementation of the GC-MSD system (HCG) on board the Zeppelin it was reconstructed to enhance its performance and to meet aviation requirements. The system was optimized to measure VOCs ranging from C4 to C10 as well as oxygenated VOCs (OVOCs) with a detection limit below 10 ppt. The analyzed VOCs for both parts of the campaigns showed low mean concentration below 5 ppb for all VOCs. Especially, the mixing ratios of the primary emitted VOCs were very low with mean values lower than 200 ppt. Higher concentrations could be observed for the OVOCs with mean concentrations up to 5 ppb. The most abundant OVOCs apart from formaldehyde were methanol, ethanol, acetone and acetaldehyde.

Airborne VOC measurements on board the Zeppelin NT during the PEGASOS campaigns in 2012 deploying the improvement Fast-GC-MSD system

International Nuclear Information System (INIS)

Jaeger, Julia Elisabeth

2014-01-01

Volatile organic compounds (VOCs) comprise a large number of different species, estimated to 10 4 -10 6 . They are emitted on the Earth's surface from a variety of biogenic and anthropogenic sources. VOCs are removed by multiple pathways from the atmosphere, by oxidation and finally by dry or wet deposition. Most primary emitted VOCs are non-polar and therefore have a low solubility in water. Oxidation facilitates efficient VOC removal by wet deposition. In the atmosphere the main photochemical VOC oxidation agent is the OH radical. As a consequence the polarity of the VOCs is increased and they can be removed faster. The oxidation of VOCs proceeds in several steps until the VOCs are deposited or are eventually oxidized to carbon dioxide. A downside of the VOCs oxidation process lies in the production of significant amounts ozone if nitrogen oxide is present which is a serious health hazard. Most of the VOC oxidation takes place in lower part of the atmosphere between the altitudes of 100 to 1000 m, which is only sparsely analyzed. Therefore, fast VOCs measurements by GC-MSD on board the Zeppelin NT offered new important insights in the distribution of VOCs. The measurements were performed within the PEAGSOS campaigns in the Netherlands and in Italy in 2012. For the implementation of the GC-MSD system (HCG) on board the Zeppelin it was reconstructed to enhance its performance and to meet aviation requirements. The system was optimized to measure VOCs ranging from C4 to C10 as well as oxygenated VOCs (OVOCs) with a detection limit below 10 ppt. The analyzed VOCs for both parts of the campaigns showed low mean concentration below 5 ppb for all VOCs. Especially, the mixing ratios of the primary emitted VOCs were very low with mean values lower than 200 ppt. Higher concentrations could be observed for the OVOCs with mean concentrations up to 5 ppb. The most abundant OVOCs apart from formaldehyde were methanol, ethanol, acetone and acetaldehyde.

Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study

Directory of Open Access Journals (Sweden)

Elizabeth Barksdale Boyle

2016-03-01

Full Text Available Epidemiologic studies can measure exposure to volatile organic compounds (VOCs using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children’s Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS. We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking and by observations by a trained data collector (presence of scented products in homes. We found several significant (p < 0.01 relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite

Assessment of Exposure to VOCs among Pregnant Women in the National Children’s Study

Science.gov (United States)

Boyle, Elizabeth Barksdale; Viet, Susan M.; Wright, David J.; Merrill, Lori S.; Alwis, K. Udeni; Blount, Benjamin C.; Mortensen, Mary E.; Moye, John; Dellarco, Michael

2016-01-01

Epidemiologic studies can measure exposure to volatile organic compounds (VOCs) using environmental samples, biomarkers, questionnaires, or observations. These different exposure assessment approaches each have advantages and disadvantages; thus, evaluating relationships is an important consideration. In the National Children’s Vanguard Study from 2009 to 2010, participants completed questionnaires and data collectors observed VOC exposure sources and collected urine samples from 488 third trimester pregnant women at in-person study visits. From urine, we simultaneously quantified 28 VOC metabolites of exposure to acrolein, acrylamide, acrylonitrile, benzene, 1-bromopropane, 1,3-butadiene, carbon disulfide, crotonaldehyde, cyanide, N,N-dimethylformamide, ethylbenzene, ethylene oxide, propylene oxide, styrene, tetrachloroethylene, toluene, trichloroethylene, vinyl chloride, and xylene exposures using ultra high performance liquid chromatography coupled with an electrospray ionization tandem mass spectrometry (UPLC-ESI/MSMS) method. Urinary thiocyanate was measured using an ion chromatography coupled with an electrospray ionization tandem mass spectrometry method (IC-ESI/MSMS). We modeled the relationship between urinary VOC metabolite concentrations and sources of VOC exposure. Sources of exposure were assessed by participant report via questionnaire (use of air fresheners, aerosols, paint or varnish, organic solvents, and passive/active smoking) and by observations by a trained data collector (presence of scented products in homes). We found several significant (p < 0.01) relationships between the urinary metabolites of VOCs and sources of VOC exposure. Smoking was positively associated with metabolites of the tobacco constituents acrolein, acrylamide, acrylonitrile, 1,3-butadiene, crotonaldehyde, cyanide, ethylene oxide, N,N-dimethylformamide, propylene oxide, styrene, and xylene. Study location was negatively associated with the toluene metabolite N

[Characteristics of volatile organic compounds (VOCs) emission from electronic products processing and manufacturing factory].

Science.gov (United States)

Cui, Ru; Ma, Yong-Liang

2013-12-01

Based on the EPA method T0-11 and 14/15 for measurement of toxic organics in air samples, fast VOCs detector, Summa canister and DNPH absorbent were used to determine the VOCs concentrations and the compositions in the ambient air of the workshops for different processes as well as the emission concentration in the exhaust gas. In all processes that involved VOCs release, concentrations of total VOCs in the workshops were 0.1-0.5 mg x m(-3), 1.5-2.5 mg x m(-3) and 20-200 mg x m(-3) for casting, cutting and painting respectively. Main compositions of VOCs in those workshops were alkanes, eneynes, aromatics, ketones, esters and ethers, totally over 20 different species. The main compositions in painting workshop were aromatics and ketones, among which the concentration of benzene was 0.02-0.34 mg x m(-3), toluene was 0.24-3.35 mg x m(-3), ethyl benzene was 0.04-1.33 mg x m(-3), p-xylene was 0.13-0.96 mg x m(-3), m-xylene was 0.02-1.18 mg x m(-3), acetone was 0.29-15.77 mg x m(-3), 2-butanone was 0.06-22.88 mg x m(-3), cyclohexene was 0.02-25.79 mg x m(-3), and methyl isobutyl ketone was 0-21.29 mg x m(-3). The VOCs emission from painting process was about 14 t x a(-1) for one single manufacturing line, and 840 t x a(-1) for the whole factory. According to the work flows and product processes, the solvent used during painting process was the main source of VOCs emission, and the exhaust gas was the main emission point.

Lidar sounding of volcanic plumes

Science.gov (United States)

Fiorani, Luca; Aiuppa, Alessandro; Angelini, Federico; Borelli, Rodolfo; Del Franco, Mario; Murra, Daniele; Pistilli, Marco; Puiu, Adriana; Santoro, Simone

2013-10-01

Accurate knowledge of gas composition in volcanic plumes has high scientific and societal value. On the one hand, it gives information on the geophysical processes taking place inside volcanos; on the other hand, it provides alert on possible eruptions. For this reasons, it has been suggested to monitor volcanic plumes by lidar. In particular, one of the aims of the FP7 ERC project BRIDGE is the measurement of CO2 concentration in volcanic gases by differential absorption lidar. This is a very challenging task due to the harsh environment, the narrowness and weakness of the CO2 absorption lines and the difficulty to procure a suitable laser source. This paper, after a review on remote sensing of volcanic plumes, reports on the current progress of the lidar system.

Plume collimation for laser ablation electrospray ionization mass spectrometry

Science.gov (United States)

Vertes, Akos; Stolee, Jessica A.

2014-09-09

In various embodiments, a device may generally comprise a capillary having a first end and a second end; a laser to emit energy at a sample in the capillary to ablate the sample and generate an ablation plume in the capillary; an electrospray apparatus to generate an electrospray plume to intercept the ablation plume to produce ions; and a mass spectrometer having an ion transfer inlet to capture the ions. The ablation plume may comprise a collimated ablation plume. The device may comprise a flow cytometer. Methods of making and using the same are also described.

Hanford Site Groundwater Monitoring for Fiscal Year 2000

Energy Technology Data Exchange (ETDEWEB)

Hartman, Mary J.; Morasch, Launa F.; Webber, William D.

2001-03-01

This report presents the results of groundwater and vadose zone monitoring and remediation for fiscal year 2000 on the U.S. Department of Energy's Hanford Site, Washington. The most extensive contaminant plumes are tritium, iodine-129, and nitrate, which all had multiple sources and are very mobile in groundwater. Carbon tetrachloride and associated organic constituents form a relatively large plume beneath the central part of the Site. Hexavalent chromium is present in smaller plumes beneath the reactor areas along the river and beneath the central part of the site. Strontium-90 exceeds standards beneath each of the reactor areas, and technetium-99 and uranium are present in the 200 Areas. RCRA groundwater monitoring continued during fiscal year 2000. Vadose zone monitoring, characterization, remediation, and several technical demonstrations were conducted in fiscal year 2000. Soil gas monitoring at the 618-11 burial ground provided a preliminary indication of the location of tritium in the vadose zone and in groundwater. Groundwater modeling efforts focused on 1) identifying and characterizing major uncertainties in the current conceptual model and 2) performing a transient inverse calibration of the existing site-wide model. Specific model applications were conducted in support of the Hanford Site carbon tetrachloride Innovative Treatment Remediation Technology; to support the performance assessment of the Immobilized Low-Activity Waste Disposal Facility; and in development of the System Assessment Capability, which is intended to predict cumulative site-wide effects from all significant Hanford Site contaminants.

40 CFR Table 1 to Subpart C - VOC Content Limits by Product Category

Science.gov (United States)

2010-07-01

... (weight-percent VOC) Air fresheners: Single-phase 70 Double-phase 30 Liquids/pump sprays 18 Solids/gels 3... 40 Protection of Environment 5 2010-07-01 2010-07-01 false VOC Content Limits by Product Category 1 Table 1 to Subpart C Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR...

Effect of catalyst for the decomposition of VOCs in a NTP reactor

International Nuclear Information System (INIS)

Mohanty, Suchitra; Das, Smrutiprava; Paikaray, Rita; Sahoo, Gourishankar; Samantaray, Subrata

2015-01-01

Air pollution has become a major cause of human distress both directly and indirectly. VOCs are becoming the major air pollutants. So the decomposition of VOCs is present need of our society. Non-thermal plasma reactor (NTP) is proven to be effective for low concentration VOCs decomposition. For safe and effective application of DBD, optimization of treatment process requires different plasma parameter characterization. So electron temperature and electron density parameters of VOCs show the decomposition path ways. In this piece of work by taking the emission spectra and comparing the line intensity ratios, the electron temperature and density were determined. Also the decomposition rate in terms of the deposited products on the dielectric surface was studied. Decomposition rate increases in presence of catalyst as compared to the pure compound in presence of a carrier gas. Decomposition process was studied by UV-VIS, FTIR, OES Spectroscopic methods and by GCMS. Deposited products are analyzed by UV-VIS and FTIR spectroscopy. Plasma parameters like electron temperature, density are studied with OES. And gaseous products are studied by GCMS showing the peaks for the by products. (author)

Proceedings of plumes, plates and mineralisation symposium: an introduction

CSIR Research Space (South Africa)

Hatton, CJ

1997-12-01

Full Text Available of plume-theory. Mechanisms of magma formation are identified and plume positions and distances to their surface expression considered. Mantle plumes are considered as a heat and fluid source for the Witwatersrand gold deposits....

Simplified scheme or radioactive plume calculations

International Nuclear Information System (INIS)

Gibson, T.A.; Montan, D.N.

1976-01-01

A simplified mathematical scheme to estimate external whole-body γ radiation exposure rates from gaseous radioactive plumes was developed for the Rio Blanco Gas Field Nuclear Stimulation Experiment. The method enables one to calculate swiftly, in the field, downwind exposure rates knowing the meteorological conditions and γ radiation exposure rates measured by detectors positioned near the plume source. The method is straightforward and easy to use under field conditions without the help of mini-computers. It is applicable to a wide range of radioactive plume situations. It should be noted that the Rio Blanco experiment was detonated on May 17, 1973, and no seep or release of radioactive material occurred

Biogenic volatile organic compound (VOC) emissions from forests in Finland

International Nuclear Information System (INIS)

Lindfors, V.; Laurila, T.

2000-01-01

We present model estimates of biogenic volatile organic compound (VOC) emissions from the forests in Finland. The emissions were calculated for the years 1995-1997 using the measured isoprene and monoterpene emission factors of boreal tree species together with detailed satellite land cover information and meteorological data. The three-year average emission is 319 kilotonnes per annum, which is significantly higher than the estimated annual anthropogenic VOC emissions of 193 kilotonnes. The biogenic emissions of the Finnish forests are dominated by monoterpenes, which contribute approximately 45% of the annual total. The main isoprene emitter is the Norway spruce (Picea abies) due to its high foliar biomass density. Compared to the monoterpenes, however, the total isoprene emissions are very low, contributing only about 7% of the annual forest VOC emissions. The isoprene emissions are more sensitive to the meteorological conditions than the monoterpene emissions, but the progress of the thermal growing season is clearly reflected in all biogenic emission fluxes. The biogenic emission densities in northern Finland are approximately half of the emissions in the southern parts of the country. (orig.)

[VOCs tax policy on China's economy development].

Science.gov (United States)

Liu, Chang-Xin; Wang, Yu-Fei; Wang, Hai-Lin; Hao, Zheng-Ping; Wang, Zheng

2011-12-01

In this paper, environmental tax was designed to control volatile organic compounds (VOCs) emissions. Computable general equilibrium (CGE) model was used to explore the impacts of environmental tax (in forms of indirect tax) on the macro-economy development at both national and sector levels. Different levels of tax were simulated to find out the proper tax rate. It is found out that imposing environmental tax on high emission sectors can cause the emission decreased immediately and can lead to negative impacts on macro-economy indicators, such as GDP (gross domestic products), total investment, total product and the whole consumption etc. However, only the government income increased. In addition, the higher the tax rate is, the more pollutants can be reduced and the worse economic effects can be caused. Consequently, it is suggested that, the main controlling policies of VOCs abatement should be mandatory orders, and low environmental tax can be implemented as a supplementary.

Emission of VOC's from modified rendering process

International Nuclear Information System (INIS)

Bhatti, Z.A.; Raja, I.A.; Saddique, M.; Langenhove, H.V.

2005-01-01

Rendering technique for processing of dead animal and slaughterhouse wastes into valuable products. It involves cooking of raw material and later Sterilization was added to reduce the Bovine Spongiform Encephalopathy (BSE). Studies have been carried out on rendering emission, with the normal cooking process. Our study shows, that the sterilization step in rendering process increases the emission of volatile organic compounds (VOC's). Gas samples, containing VOC's, were analyzed by the GC/MS (Gas Chromatograph and Mass Spectrometry). The most important groups of compounds- alcohols and cyclic hydrocarbons were identified. In the group of alcohol; 1-butanol, l-pentanol and l-hexanol compounds were found while in the group of cyclic hydrocarbon; methyl cyclopentane and cyclohexane compounds were detected. Other groups like aldehyde, sulphur containing compounds, ketone and furan were also found. Some compounds, like l-pentanol, 2-methyl propanal, dimethyl disulfide and dimethyl trisulfide, which belong to these groups, cause malodor. It is important to know these compounds to treat odorous gasses. (author)

Smartphone-Based VOC Sensor Using Colorimetric Polydiacetylenes.

Science.gov (United States)

Park, Dong-Hoon; Heo, Jung-Moo; Jeong, Woomin; Yoo, Young Hyuk; Park, Bum Jun; Kim, Jong-Man

2018-02-07

Owing to a unique colorimetric (typically blue-to-red) feature upon environmental stimulation, polydiacetylenes (PDAs) have been actively employed in chemosensor systems. We developed a highly accurate and simple volatile organic compound (VOC) sensor system that can be operated using a conventional smartphone. The procedure begins with forming an array of four different PDAs on conventional paper using inkjet printing of four corresponding diacetylenes followed by photopolymerization. A database of color changes (i.e., red and hue values) is then constructed on the basis of different solvatochromic responses of the 4 PDAs to 11 organic solvents. Exposure of the PDA array to an unknown solvent promotes color changes, which are imaged using a smartphone camera and analyzed using the app. A comparison of the color changes to the database promoted by the 11 solvents enables the smartphone app to identify the unknown solvent with 100% accuracy. Additionally, it was demonstrated that the PDA array sensor was sufficiently sensitive to accurately detect the 11 VOC gases.

Allelopatic Potential of Dittrichia viscosa (L. W. Greuter Mediated by VOCs: A Physiological and Metabolomic Approach.

Directory of Open Access Journals (Sweden)

Fabrizio Araniti

Full Text Available Dittrichia viscosa (L. W. Greuter is a pioneer species belonging to the Compositae family. It is widespread in the Mediterranean basin, where it is considered invasive. It is a source of secondary metabolites, playing an important ecological role. D. viscosa plant extracts showed a phytotoxic activity on several physiological processes of different species. In the current study, the allelopathic potential of D. viscosa VOCs, released by its foliage, was evaluated on seed germination and root growth of lettuce. The VOCs effect was also studied on lettuce adult plants in microcosm systems, which better mimicked the open field conditions. D. viscosa VOCs inhibited both seed germination and root growth of lettuce. The VOCs composition revealed a large presence of terpenoids, responsible of the effects observed. Moreover, D. viscosa VOCs caused an alteration on plant water status accompanied by oxidative damages and photoinhibition on lettuce adult plants.

In-vehicle VOCs composition of unconditioned, newly produced cars.

Science.gov (United States)

Brodzik, Krzysztof; Faber, Joanna; Łomankiewicz, Damian; Gołda-Kopek, Anna

2014-05-01

The in-vehicle volatile organic compounds (VOCs) concentrations gains the attention of both car producers and users. In the present study, an attempt was made to determine if analysis of air samples collected from an unconditioned car cabin can be used as a quality control measure. The VOCs composition of in-vehicle air was analyzed by means of active sampling on Carbograph 1TD and Tenax TA sorbents, followed by thermal desorption and simultaneous analysis on flame ionization and mass detector (TD-GC/FID-MS). Nine newly produced cars of the same brand and model were chosen for this study. Within these, four of the vehicles were equipped with identical interior materials and five others differed in terms of upholstery and the presence of a sunroof; one car was convertible. The sampling event took place outside of the car assembly plant and the cars tested left the assembly line no later than 24 hr before the sampling took place. More than 250 compounds were present in the samples collected; the identification of more than 160 was confirmed by comparative mass spectra analysis and 80 were confirmed by both comparison with single/multiple compounds standards and mass spectra analysis. In general, aliphatic hydrocarbons represented more than 60% of the total VOCs (TVOC) determined. Depending on the vehicle, the concentration of aromatic hydrocarbons varied from 12% to 27% of total VOCs. The very short period between car production and sampling of the in-vehicle air permits the assumption that the entire TVOC originates from off-gassing of interior materials. The results of this study expand the knowledge of in-vehicle pollution by presenting information about car cabin air quality immediately after car production. Copyright © 2014 The Research Centre for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

Hubble Captures Volcanic Eruption Plume From Io

Science.gov (United States)

1997-01-01

The Hubble Space Telescope has snapped a picture of a 400-km-high (250-mile-high) plume of gas and dust from a volcanic eruption on Io, Jupiter's large innermost moon.Io was passing in front of Jupiter when this image was taken by the Wide Field and Planetary Camera 2 in July 1996. The plume appears as an orange patch just off the edge of Io in the eight o'clock position, against the blue background of Jupiter's clouds. Io's volcanic eruptions blasts material hundreds of kilometers into space in giant plumes of gas and dust. In this image, material must have been blown out of the volcano at more than 2,000 mph to form a plume of this size, which is the largest yet seen on Io.Until now, these plumes have only been seen by spacecraft near Jupiter, and their detection from the Earth-orbiting Hubble Space Telescope opens up new opportunities for long-term studies of these remarkable phenomena.The plume seen here is from Pele, one of Io's most powerful volcanos. Pele's eruptions have been seen before. In March 1979, the Voyager 1 spacecraft recorded a 300-km-high eruption cloud from Pele. But the volcano was inactive when the Voyager 2 spacecraft flew by Jupiter in July 1979. This Hubble observation is the first glimpse of a Pele eruption plume since the Voyager expeditions.Io's volcanic plumes are much taller than those produced by terrestrial volcanos because of a combination of factors. The moon's thin atmosphere offers no resistance to the expanding volcanic gases; its weak gravity (one-sixth that of Earth) allows material to climb higher before falling; and its biggest volcanos are more powerful than most of Earth's volcanos.This image is a contrast-enhanced composite of an ultraviolet image (2600 Angstrom wavelength), shown in blue, and a violet image (4100 Angstrom wavelength), shown in orange. The orange color probably occurs because of the absorption and/or scattering of ultraviolet light in the plume. This light from Jupiter passes through the plume and is

Distribution of artificial radionuclides in particle-size fractions of soil on fallout plumes of nuclear explosions.

Science.gov (United States)

Kabdyrakova, A M; Lukashenko, S N; Mendubaev, A T; Kunduzbayeva, A Ye; Panitskiy, A V; Larionova, N V

2018-06-01

In this paper are analyzed the artificial radionuclide distributions ( 137 Cs, 90 Sr, 241 Am, 239+240 Pu) in particle-size fractions of soils from two radioactive fallout plumes at the Semipalatinsk Test Site. These plumes were generated by a low-yield surface nuclear test and a surface non-nuclear experiment with insignificant nuclear energy release, respectively, and their lengths are approximately 3 and 0,65 km. In contrast with the great majority of similar studies performed in areas affected mainly by global fallout where adsorbing radionuclides such as Pu are mainly associated with the finest soil fractions, in this study it was observed that along both analyzed plumes the highest activity concentrations are concentrated in the coarse soil fractions. At the plume generated by the surface nuclear test, the radionuclides are concentrated mainly in the 1000-500 μm soil fraction (enrichment factor values ranging from 1.2 to 3.8), while at the plume corresponding to the surface non-nuclear test is the 500-250 μm soil fraction the enriched one by technogenic radionuclides (enrichment factor values ranging from 1.1 to 5.1). In addition, the activity concentration distributions among the different soil size fractions are similar for all radionuclides in both plumes. All the obtained data are in agreement with the hypothesis indicating that enrichment observed in the coarse fractions is caused by the presence of radioactive particles resulted from the indicated nuclear tests. Copyright © 2017 Elsevier Ltd. All rights reserved.

Biogeochemistry of landfill leachate plumes

DEFF Research Database (Denmark)

Christensen, Thomas Højlund; Kjeldsen, Peter; Bjerg, Poul Løgstrup

2001-01-01

are relatively narrow and do not in terms of width exceed the width of the landfill. The concept of redox zones being present in the plume has been confirmed by the reported composition of the leachate contaminated groundwater at several landfills and constitutes an important framework for understanding...... the behavior of the contaminants in the plume as the leachate migrates away from the landfill. Diverse microbial communities have been identified in leachate plumes and are believed to be responsible for the redox processes. Dissolved organic C in the leachate, although it appears to be only slowly degradable...... to be subject to anaerobic oxidation, but the mechanisms are not yet understood. Heavy metals do not seem to constitute a significant pollution problem at landfills, partly because the heavy metal concentrations in the leachate often are low, and partly because of strong attenuation by sorption...

Experimental and statistical characterization of Volatile Organic Compounds (VOC) within the ile-de-France region

International Nuclear Information System (INIS)

Baudic, Alexia

2016-01-01

Volatile organic compounds (VOCs) play a key role within the atmospheric system acting as precursors of ground-level ozone and secondary organic aerosols (causing health and climatic impacts); hence the growing interest of better characterizing them. Significant uncertainties are still associated with compounds speciation, quantification and respective contributions from the different emission sources. This thesis proposes, through several laboratory and intensive field campaigns, a detailed characterization of VOCs and their main emissions sources within the Ile-de-France region. We used methods based on the determination of speciation profiles indicative of road traffic, wood burning and natural gas sources obtained from near-field investigations (inside a tunnel, at a fireplace and from a domestic gas flue). These different source profiles were used as chemical fingerprints for the identification of the main VOC emission sources, which respective contributions were estimated using the Positive Matrix Factorization (PMF) source-receptor model applied to one-year VOCs (including NMHC+OVOC) measurements in Paris. This thesis allowed, for the first time, to evaluate the seasonal variability of VOCs and their main emission sources. Road traffic-related emissions are major VOC local/regional sources in Paris (contributing to a quarter of total annual emissions). The important impact of wood burning in winter (50 % of the VOC total mass) was observed. Results obtained from this approach were compared with the regional emissions inventory provided by the air quality monitoring network Airparif. Finally, a good agreement was found between our observations and the inventory for road traffic and wood burning-related sources. This independent assessment of inventories is of great interest because they are currently used as input data within air quality prediction models. (author) [fr

Trends of VOC exposures among a nationally representative sample: Analysis of the NHANES 1988 through 2004 data sets

Science.gov (United States)

Su, Feng-Chiao; Mukherjee, Bhramar; Batterman, Stuart

2011-09-01

Exposures to volatile organic compounds (VOCs) are ubiquitous due to emissions from personal, commercial and industrial products, but quantitative and representative information regarding long term exposure trends is lacking. This study characterizes trends from 1988 to 2004 for the 15 VOCs measured in blood in five cohorts of the National Health and Nutrition Examination Survey (NHANES), a large and representative sample of U.S. adults. Trends were evaluated at various percentiles using linear quantile regression (QR) models, which were adjusted for solvent-related occupations and cotinine levels. Most VOCs showed decreasing trends at all quantiles, e.g., median exposures declined by 2.5 (m,p-xylene) to 6.4 (tetrachloroethene) percent per year over the 15 year period. Trends varied by VOC and quantile, and were grouped into three patterns: similar decreases at all quantiles (including benzene, toluene); most rapid decreases at upper quantiles (ethylbenzene, m,p-xylene, o-xylene, styrene, chloroform, tetrachloroethene); and fastest declines at central quantiles (1,4-dichlorobenzene). These patterns reflect changes in exposure sources, e.g., upper-percentile exposures may result mostly from occupational exposure, while lower percentile exposures arise from general environmental sources. Both VOC emissions aggregated at the national level and VOC concentrations measured in ambient air also have declined substantially over the study period and are supportive of the exposure trends, although the NHANES data suggest the importance of indoor sources and personal activities on VOC exposures. While piecewise QR models suggest that exposures of several VOCs decreased little or any during the 1990's, followed by more rapid decreases from 1999 to 2004, questions are raised concerning the reliability of VOC data in several of the NHANES cohorts and its applicability as an exposure indicator, as demonstrated by the modest correlation between VOC levels in blood and personal air