Sample records for organic compounds vocs

  1. ACTION CONCENTRATION FOR MIXTURES OF VOLATILE ORGANIC COMPOUNDS (VOC) & METHANE & HYDROGEN

    SciTech Connect (OSTI)

    MARUSICH, R.M.

    2006-07-10T23:59:59.000Z

    Waste containers may contain volatile organic compounds (VOCs), methane, hydrogen and possibly propane. These constituents may occur individually or in mixtures. Determining if a waste container contains a flammable concentration of flammable gases and vapors (from VOCs) is important to the safety of the handling, repackaging and shipping activities. This report provides the basis for determining the flammability of mixtures of flammable gases and vapors. The concentration of a mixture that is at the lowest flammability limit for that mixture is called the action concentration. The action concentration can be determined using total VOC concentrations or actual concentration of each individual VOC. The concentrations of hydrogen and methane are included with the total VOC or individual VOC concentration to determine the action concentration. Concentrations below this point are not flammable. Waste containers with gas/vapor concentrations at or above the action concentration are considered flammable.

  2. NMED COMMENTS ITEM 3 REVISE VOLATILE ORGANIC COMPOUND (VOC) TARGET...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    was not clear if the referenced document is applicable to Resource Conservation and Recovery Act (RCRA) activities. c) Clarify what is meant by the term "original VOC Monitoring...

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

    SciTech Connect (OSTI)

    Center for Human Reliability Studies

    2006-06-01T23:59:59.000Z

    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.

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

    SciTech Connect (OSTI)

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

    1992-07-01T23:59:59.000Z

    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.

  5. TECHNICAL JUSTIFICATION FOR CHOOSING PROPANE AS A CALIBRATION AGENT FOR TOTAL FLAMMABLE VOLATILE ORGANIC COMPOUND (VOC) DETERMINATIONS

    SciTech Connect (OSTI)

    DOUGLAS, J.G.

    2006-07-06T23:59:59.000Z

    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 agent overestimate the value of the VOCs in a sample. By overestimating the VOC content of a sample, we want to minimize false negatives. A false negative is defined as incorrectly estimating the VOC content of the sample to be below programmatic action limits when, in fact, the sample,exceeds the action limits. The disadvantage of overestimating the flammable VOC content of a sample is that additional cost may be incurred because additional sampling and GC-MS analysis may be required to confirm results over programmatic action limits. Therefore, choosing an appropriate calibration standard for the Ar-PDHID is critical to avoid false negatives and to minimize additional analytical costs.

  6. Influence of Atmospheric Pressure and Water Table Fluctuations on Gas Phase Flow and Transport of Volatile Organic Compounds (VOCs) in Unsaturated Zones

    E-Print Network [OSTI]

    You, Kehua

    2013-04-19T23:59:59.000Z

    Understanding the gas phase flow and transport of volatile organic compounds (VOCs) in unsaturated zones is indispensable to develop effective environmental remediation strategies, to create precautions for fresh water protection, and to provide...

  7. ARTIFACT FORMATION IN HIGH VOLUME SAMPLING OF VOC's AND SOLID ORGANIC COMPOUNDS.

    E-Print Network [OSTI]

    Boyer, Edmond

    when sampling polluted air. Purified air containing 180 ppbv ozone seems to destroy PAH according Atmospheriques, Boite 7059, UNIVERSITE PARIS 7, 2, place Jussieu, 75251 PARIS Cedex 05 ABSTRACT Pollutants from well äs solid (SOC's) organic compounds. High volume samplers are commonly used m air quality

  8. Vehicular emission of volatile organic compounds (VOCs) from a tunnel study in Hong Kong

    E-Print Network [OSTI]

    2009-01-01T23:59:59.000Z

    ethene toluene n-butane propane i-pentane i-butane propeneethene, toluene, n-butane, propane and i-pentane. These fiveVOCs emitted. The high propane and n-butane emissions were

  9. Vehicular emission of volatile organic compounds (VOCs) from a tunnel study in Hong Kong

    E-Print Network [OSTI]

    2009-01-01T23:59:59.000Z

    Chemistry and Physics Vehicular emission of volatile organicY. , and Huang, Y. S. : Emission factors and characteristicslight-duty vehicle emissions, Environ. Sci. Technol. , 30,

  10. Methyl tert-butyl ether (MTBE) is a volatile organic com-pound (VOC) derived from natural gas that is added to gas-

    E-Print Network [OSTI]

    Methyl tert-butyl ether (MTBE) is a volatile organic com- pound (VOC) derived from natural gas Water in Urban and Agricultural Areas made from methanol, which is derived primarily from natural gas that is added to gas- oline either seasonally or year round in many parts of the United States to increase

  11. Analysis of volatile organic compounds (VOCs) in A/M Area Crouch Branch (Cretaceous) Aquifer characterization samples: 1993

    SciTech Connect (OSTI)

    Looney, B.B.; Haselow, J.S.; Keenan, M.A.; Van Pelt, R.; Eddy-Dilek, C.A.; Rossabi, J.; Simmons, J.L.

    1993-12-06T23:59:59.000Z

    Samples were collected during the A/M Area Crouch Branch (Cretaceous) Aquifer Characterization (Phase I) Program. The samples were analyzed for chlorinated VOCs by the Savannah River Technology Center (SRTC) and MicroSeeps Ltd. All samples were sealed in the field immediately upon retrieval of the core and subsampling. A total of 113 samples locations were selected for analysis. The Environmental Sciences Section (ESS) of SRTC analyzed all locations in duplicate (226 samples). MicroSeeps Ltd was selected as the quality assurance (QA) check laboratory. MicroSeeps Ltd analyzed 40 locations with 4 duplicates (44 samples). The samples were collected from seven boreholes in A/M Area in the interval from 200 feet deep to the total depth of the boring (360 feet deep nominal); samples were collected every 10 feet within this interval. The sampling zone corresponds approximately to the Crouch Branch Aquifer in A/M Area. The overall A/M Area Crouch Branch Aquifer characterization objectives, a brief description of A/M Area geology and hydrology, and the sample locations, field notes, driller lithologic logs, and required procedural documentation are presented in WSRC (1993).

  12. Volatile organic compound sensor system

    DOE Patents [OSTI]

    Schabron, John F. (Laramie, WY); Rovani, Jr., Joseph F. (Laramie, WY); Bomstad, Theresa M. (Laramie, WY); Sorini-Wong, Susan S. (Laramie, WY)

    2009-02-10T23:59:59.000Z

    Generally, this invention relates to the development of field monitoring methodology for new substances and sensing chemical warfare agents (CWAs) and terrorist substances. It also relates to a portable test kit which may be utilized to measure concentrations of halogenated volatile organic compounds (VOCs) in the field. Specifically it relates to systems for reliably field sensing the potential presence of such items while also distinguishing them from other elements potentially present. It also relates to overall systems and processes for sensing, reacting, and responding to an indicated presence of such substance, including modifications of existing halogenated sensors and arrayed sensing systems and methods.

  13. Volatile organic compound sensor system

    DOE Patents [OSTI]

    Schabron, John F. (Laramie, WY); Rovani, Jr., Joseph F. (Laramie, WY); Bomstad, Theresa M. (Waxahachie, TX); Sorini-Wong, Susan S. (Laramie, WY); Wong, Gregory K. (Laramie, WY)

    2011-03-01T23:59:59.000Z

    Generally, this invention relates to the development of field monitoring methodology for new substances and sensing chemical warfare agents (CWAs) and terrorist substances. It also relates to a portable test kit which may be utilized to measure concentrations of halogenated volatile organic compounds (VOCs) in the field. Specifically it relates to systems for reliably field sensing the potential presence of such items while also distinguishing them from other elements potentially present. It also relates to overall systems and processes for sensing, reacting, and responding to an indicated presence of such substance, including modifications of existing halogenated sensors and arrayed sensing systems and methods.

  14. Adsorption -capacity data for 283 organic compounds

    SciTech Connect (OSTI)

    Yaws, C.L.; Bu, L.; Nijhawan, S. [Lamar Univ., Beaumont, TX (United States)

    1995-05-01T23:59:59.000Z

    Adsorption on activated carbon is a widely used method for removing volatile organic compounds (VOCs) from gases and other exhaust streams. This article presents a compilation of adsorption-capacity data as a function of the VOC concentration in the gas. The results are useful in engineering and environmental studies, and in the design of carbon-based adsorption systems to remove unwanted organic pollutants from gases. For vapor control, carbon-based systems typically combine a carbon-adsorption unit with a secondary control method to reclaim or destroy the vapors desorbed during carbon-bed regeneration. To remove organics dissolved in wastewater, air stripping is typically used to transfer the organics to a vapor stream. Carbon adsorption is then used to separate the organics from the stripper exhaust. Collected vapors can be recovered for reuse or destroyed, depending on their value.

  15. Astatinated organic compounds

    DOE Patents [OSTI]

    Milius, R.A.; Lambrecht, R.M.; Bloomer, W.D.

    1989-05-02T23:59:59.000Z

    Methods and kits for incorporating a radioactive astatine isotope (particularly [sup 211]At) into an organic compound by electrophilic astatodestannylation of organostannanes. 3 figs.

  16. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    C. J. : Effect of petrochemical industrial emis- sions ofVOC) concentrations around a petrochemical com- plex and aatmospheres and around the petrochemical industry in the

  17. Literature review of stabilization/solidification of volatile organic compounds and the implications for Hanford grouts

    SciTech Connect (OSTI)

    Spence, R.D.; Osborne, S.C.

    1993-09-01T23:59:59.000Z

    A literature review was conducted on the stabilization/solidification of volatile organic compounds (VOCs). Based on this literature, it is likely that the limestone-containing grout will not permanently immobilize VOCs and that no presently available additives can guarantee permanent immobilization. The Westinghouse hanford company grout may be fairly effective at retarding aqueous leaching of VOCs, and commercial additives can improve this performance. Significant VOC losses do occur during stabilization/solidification, and the high temperatures of the Westinghouse Hanford Company waste and grout should exacerbate this problem. In fact, these high temperatures raise doubts about the presence of VOCs in the double-shell tanks supernates.

  18. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    methyl tertiary- butyl ether (MTBE) and its effect on plasmaand three VOCs (propyne, furan, MTBE) remained below their 3Ethanol Acetone MEK MAC MVK MTBE Furan CH 3 OH C 2 H 5 OH C

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

    E-Print Network [OSTI]

    Fortner, E. C.

    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 ...

  20. FIELD SCREENING FOR HALOGENATED VOLATILE ORGANIC COMPOUNDS

    SciTech Connect (OSTI)

    John F. Schabron; Joseph F. Rovani, Jr.; Theresa M. Bomstad

    2003-07-01T23:59:59.000Z

    Western Research Institute (WRI) is continuing work toward the development of new screening methodology and a test kit to measure halogenated volatile organic compounds (VOCs) in the field. Heated diode and corona discharge sensors are commonly used to detect leaks of refrigerants from air conditioners, freezers, and refrigerators. They are both selective to the presence of halogens. In prior work, the devices were tested for response to carbon tetrachloride, heptane, toluene, and water vapors. In the current work, sensor response was evaluated with sixteen halogenated VOCs relative to carbon tetrachloride. The results show that the response of the various chlorinated VOCs is within an order of magnitude of the response to carbon tetrachloride for each of the sensors. Thus, for field screening a single response factor can be used. Both types of leak detectors are being further modified to provide an on-board LCD signal readout, which is related to VOC concentration. The units will be fully portable and will operate with 115-V line or battery power. Signal background, noise level, and response data on the Bacharach heated diode detector and the TIF corona discharge detector show that when the response curves are plotted against the log of concentration, the plot is linear to the upper limit for the particular unit, with some curvature at lower levels. When response is plotted directly against concentration, the response is linear at the low end and is curved at the high end. The dynamic ranges for carbon tetrachloride of the two devices from the lower detection limit (S/N=2) to signal saturation are 4-850 vapor parts per million (vppm) for the corona discharge unit and 0.01-70 vppm for the heated diode unit. Additional circuit modifications are being made to lower the detection limit and increase the dynamic response range of the corona discharge unit. The results indicate that both devices show potential utility for future analytical method development work toward the goal of developing a portable test kit for screening halogenated VOCs in the field.

  1. Advanced heat pump for the recovery of volatile organic compounds

    SciTech Connect (OSTI)

    Not Available

    1992-03-01T23:59:59.000Z

    Emissions of Volatile Organic Compounds (VOC) from stationary industrial and commercial sources represent a substantial portion of the total US VOC emissions. The Toxic-Release Inventory'' of The US Environmental Protection Agency estimates this to be at about 3 billion pounds per year (1987 estimates). The majority of these VOC emissions are from coating processes, cleaning processes, polymer production, fuel production and distribution, foam blowing,refrigerant production, and wood products production. The US Department of Energy's (DOE) interest in the recovery of VOC stems from the energy embodied in the recovered solvents and the energy required to dispose of them in an environmentally acceptable manner. This Phase I report documents 3M's work in close working relationship with its subcontractor Nuclear Consulting Services (Nucon) for the preliminary conceptual design of an advanced Brayton cycle heat pump for the recovery of VOC. Nucon designed Brayton cycle heat pump for the recovery of methyl ethyl ketone and toluene from coating operations at 3M Weatherford, OK, was used as a base line for the work under cooperative agreement between 3M and ODE. See appendix A and reference (4) by Kovach of Nucon. This cooperative agreement report evaluates and compares an advanced Brayton cycle heat pump for solvent recovery with other competing technologies for solvent recovery and reuse. This advanced Brayton cycle heat pump is simple (very few components), highly reliable (off the shelf components), energy efficient and economically priced.

  2. Fiber optic micromirror sensor for volatile organic compounds

    SciTech Connect (OSTI)

    Butler, M.A.; Ricco, A.J.; Buss, R. (Sandia National Lab., Albuquerque, NM (US))

    1990-04-01T23:59:59.000Z

    With the growing concern over environmental pollution, there is a need for sensors to locate and measure the distribution of a wide range of pollutants. In this paper the authors report a fiber optic sensor, based on a thin film micromirror, which responds to a wide range of volatile organic compounds (VOCs). This generic class of sensor will be useful for monitoring applications where the pollutant has already been identified.

  3. Modeling VOC sorption of building materials and its impact on indoor air quality

    E-Print Network [OSTI]

    Zhang, Jinsong, 1975-

    2001-01-01T23:59:59.000Z

    Sorption of volatile organic compounds (VOCs) by building materials can have significant effect on the indoor VOC concentration levels and indoor air quality in buildings. The objective of this study was to investigate ...

  4. Airborne and ground based measurements of volatile organic compounds using proton transfer reaction mass spectrometry in Texas and Mexico City

    E-Print Network [OSTI]

    Fortner, Edward Charles

    2009-05-15T23:59:59.000Z

    Measurements of ambient volatile organic compounds (VOCs) by proton transfer reaction mass spectrometry (PTR-MS) are reported from recent airborne and surface based field campaigns. The Southeast Texas Tetroon Study (SETTS) was a project within...

  5. VOCs, Pesticides, Nitrate, and Their Mixtures in Groundwater Used for

    E-Print Network [OSTI]

    areas. For each sample, as many as 60 volatile organic compounds (VOCs), 83 pesticides, and nitrate were of food and water, and dermal contact). Everyone has hundreds of measurable contami- nants in their bodies, especially volatile organic compounds (VOCs), are not known. Defining human exposure to mixtures

  6. Real-time monitoring of volatile organic compounds using chemical ionization mass spectrometry

    DOE Patents [OSTI]

    Mowry, Curtis Dale (Albuquerque, NM); Thornberg, Steven Michael (Peralta, NM)

    1999-01-01T23:59:59.000Z

    A system for on-line quantitative monitoring of volatile organic compounds (VOCs) includes pressure reduction means for carrying a gaseous sample from a first location to a measuring input location maintained at a low pressure, the system utilizing active feedback to keep both the vapor flow and pressure to a chemical ionization mode mass spectrometer constant. A multiple input manifold for VOC and gas distribution permits a combination of calibration gases or samples to be applied to the spectrometer.

  7. Molecular Characterization of Nitrogen Containing Organic Compounds...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Nitrogen Containing Organic Compounds in Biomass Burning Aerosols Using High Resolution Mass Molecular Characterization of Nitrogen Containing Organic Compounds in Biomass Burning...

  8. Energy Saving System to Remove Volatile Organic Compounds (VOCs) from

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOEThe Bonneville Power AdministrationField8, 2000Consumption Survey (CBECS) Data 210EnergyEnergy SaverSavingP

  9. Installation and Operation of Sorbathene Solvent Vapor Recovery Units to Recover and Recycle Volatile Organic Compounds at Operating Sites within the Dow Chemical Company

    E-Print Network [OSTI]

    Hall, T. L.; Larrinaga, L.

    the SORBATHENE vacuum swing adsorption as an economical alternative for the recovery of volatile organic compounds (VOC's) from storage, loading, and process vents streams. This paper discusses the application of the technology on nineteen units to collect...

  10. Use of sonication for in-well softening of semivolatile organic compounds. 1997 annual progress report

    SciTech Connect (OSTI)

    Peters, R.W.; Manning, J. [Argonne National Lab., IL (US); Hoffman, M.R. [California Inst. of Tech., Pasadena, CA (US); Gorelick, S. [Stanford Univ., CA (US)

    1997-01-01T23:59:59.000Z

    'This project investigates the in-situ degradation of semivolatile organic compounds (SVOCs) and volatile organic compounds (VOCs) using in-well sonication, in-well vapor stripping, and bioremediation. Pretreating groundwaters with sonication techniques in-situ would form VOCs that can be effectively removed by in-well vapor stripping and bioremediation. The mechanistic studies focus on the coupling of megasonics and ultrasonics to soften (i.e., partially degrade) the SVOCs; oxidative reaction mechanism studies; surface corrosion studies (on the reactor walls/well); enhancement due to addition of oxidants, quantification of the hydroxyl radical formation; identification/quantification of degradation products; volatility/degradability of the treated waters; development of a computer simulation model to describe combined in-well sonication/in-well vapor stripping/bioremediation; systems analysis/economic analysis; large laboratory-scale experiment verification; and field demonstration of the integrated technology. Benefits of this approach include: (1) Remediation is performed in-situ; (2) The treatment systems complement each other; their combination can drastically reduce or remove SVOCs and VOCs; (3) Ability to convert hard-to-degrade organics into more volatile organic compounds; (4) Ability to remove residual VOCs and softened SVOCs through the combined action of in-well vapor stripping and biodegradation; (5) Does not require handling or disposing of water at the ground surface; and (6) Cost-effective and improved efficiency, resulting in shortened clean-up times to remediate a site.'

  11. Environmental Impact on Applied Technology- Global Warming CFCs & VOCs

    E-Print Network [OSTI]

    Gilbert, J. S.

    Hardly a day goes by that the threats to our environment are not brought to our attention. Whether you are following oil spills, groundwater contamination, global warming, chlorofluorocarbons (CFCs) or volatile organic compounds (VOCs), you must...

  12. Preliminary evaluation of selected in situ remediation technologies for Volatile Organic Compound contamination at Arid sites

    SciTech Connect (OSTI)

    Lenhard, R.J.; Gerber, M.A.; Amonette, J.E.

    1992-10-01T23:59:59.000Z

    To support the Volatile Organic Compounds-Arid Site (VOC-Arid) Integrated Demonstration (ID) in its technical, logistical, institutional, and economical testing of emerging environmental management and restoration technologies. Pacific Northwest Laboratory(a) is evaluating several in situ remediation technologies for possible inclusion in the demonstration. The evaluations are made with respect to the initial focus of the VOC-Arid ID: the carbon tetrachloride contamination at the Hanford Site, where it was disposed to the vadose zone along with other volatile and nonvolatile organic wastes. heavy metals, acids. and radionuclides. The purposes of this report are (1) to identify candidate in situ technologies for inclusion in the program, (2) to evaluate the candidate technologies based on their potential applicability to VOC contamination at arid sites and geologic conditions representative of the ID host site (i.e., Hanford Site), and (3) to prioritize those technologies for future US Department of Energy (DOE) support.

  13. Mobilization and Transport of Organic Compounds from Reservoir Rock and Caprock in Geological Carbon Sequestration Sites

    SciTech Connect (OSTI)

    Zhong, Lirong; Cantrell, Kirk J.; Mitroshkov, Alexandre V.; Shewell, Jesse L.

    2014-05-06T23:59:59.000Z

    Supercritical CO2 (scCO2) is an excellent solvent for organic compounds, including benzene, toluene, ethyl-benzene, and xylene (BTEX), phenols, and polycyclic aromatic hydrocarbons (PAHs). Monitoring results from geological carbon sequestration (GCS) field tests has shown that organic compounds are mobilized following CO2 injection. Such results have raised concerns regarding the potential for groundwater contamination by toxic organic compounds mobilized during GCS. Knowledge of the mobilization mechanism of organic compounds and their transport and fate in the subsurface is essential for assessing risks associated with GCS. Extraction tests using scCO2 and methylene chloride (CH2Cl2) were conducted to study the mobilization of volatile organic compounds (VOCs, including BTEX), the PAH naphthalene, and n-alkanes (n-C20 – n-C30) by scCO2 from representative reservoir rock and caprock obtained from depleted oil reservoirs and coal from an enhanced coal-bed methane recovery site. More VOCs and naphthalene were extractable by scCO2 compared to the CH2Cl2 extractions, while scCO2 extractable alkane concentrations were much lower than concentrations extractable by CH2Cl2. In addition, dry scCO2 was found to extract more VOCs than water saturated scCO2, but water saturated scCO2 mobilized more naphthalene than dry scCO2. In sand column experiments, moisture content was found to have an important influence on the transport of the organic compounds. In dry sand columns the majority of the compounds were retained in the column except benzene and toluene. In wet sand columns the mobility of the BTEX was much higher than that of naphthalene. Based upon results determined for the reservoir rock, caprock, and coal samples studied here, the risk to aquifers from contamination by organic compounds appears to be relatively low; however, further work is necessary to fully evaluate risks from depleted oil reservoirs.

  14. Characteristics of the volatile organic compounds -- Arid Integrated Demonstration Site

    SciTech Connect (OSTI)

    Last, G.V.; Lenhard, R.J.; Bjornstad, B.N.; Evans, J.C.; Roberson, K.R.; Spane, F.A.; Amonette, J.E.; Rockhold, M.L.

    1991-10-01T23:59:59.000Z

    The Volatile Organic Compounds -- Arid Integrated Demonstration Program (VOC-Arid ID) is targeted at demonstration and testing of technologies for the evaluation and cleanup of volatile organic compounds and associated contaminants at arid DOE sites. The initial demonstration site is an area of carbon tetrachloride (CCl{sub 4}) contamination located near the center of the Hanford Site. The movement of CCl{sub 4} and other volatile organic contaminants in the subsurface is very complex. The problem at the Hanford Site is further complicated by the concurrent discharge of other waste constituents including acids, lard oil, organic phosphates, and transuranic radionuclides. In addition, the subsurface environment is very complex, with large spatial variabilities in hydraulic properties. A thorough understanding of the problem is essential to the selection of appropriate containment, retrieval, and/or in situ remedial technologies. The effectiveness of remedial technologies depends on knowing where the contaminants are, how they are held up in a given physical and chemical subsurface environment; and knowing the physical, chemical, and microbiological changes that are induced by the various remedial technologies.

  15. MEMBRANE INTRODUCTION MASS SPECTROMETRY FOR THE ON-LINE ANALYSIS OF VOLATILE ORGANIC COMPOUNDS IN AQUEOUS SOLUTIONS

    E-Print Network [OSTI]

    organic compounds (VOCs) have been detected in urban waters across the United States, including gasoline was partially supported by the NSF-Chemistry CARREER award # CHE-0.34131. #12;v VITA November 4, 1974.S. Pharmaceutical Chemistry, National School of Biological Sciences (Mexico). 2002 ­ 2005

  16. Origins of volatile organic compounds emerging from tank 241-C-106 during sluicing

    SciTech Connect (OSTI)

    STAUFFER, L.A.

    1999-06-02T23:59:59.000Z

    Unexpectedly high concentrations of inorganic gases and volatile organic compounds (VOC) were released from the ventilation stack of tank 241-C-106 during sluicing operations on November 18, 1998. Workers experienced serious discomfort. They reported an obnoxious acrid odor and the 450 ppm VOC in ventilation stack 296-C-006 exceeded the level approved in the air discharge permit. Consequently, the operation was terminated. Subsequent analyses of samples collected opportunistically from the stack indicated many organic compounds including heptenes, heptanones, and normal paraffin hydrocarbons (NPH) and their remnants were present. Subsequently, a process test designed to avoid unnecessary worker exposure and enable collection of analytical samples from the stack, the breathing area, and the receiver tank was conducted on December 16, 1998. The samples obtained during that operation, in which the maximum VOC content of the stack was approximately 35 ppm, have been analyzed by teams at Pacific Northwest National Laboratory and Special Analytic Services (SAS). This report examines the results of these investigations. Future revisions of the report will examine the analytical results obtained for samples collected during sluicing operations in March. This report contains the available evidence about the source term for these emissions. Chapter 2 covers characterization work, including historical information about the layers of waste in the tank, the location of organic compounds in these layers, the total organic carbon (TOC) content and the speciation of organic compounds. Chapter 3 covers the data for the samples from the ventilation stack, which has the highest concentrations of organic compounds. Chapter 4 contains an interpretation of the information connecting the composition of the organic emissions with the composition of the original source term. Chapter 5 summarizes the characterization work, the sample data, and the interpretation of the results.

  17. Distribution of volatile organic compounds in soil vapor in the vicinity of a defense fuel supply point, Hanahan, South Carolina. Water resources investigations report

    SciTech Connect (OSTI)

    Robertson, J.F.; Aelion, C.M.; Vroblesky, D.A.

    1993-12-31T23:59:59.000Z

    The report describes the results of a reconnaissance study to identify areas of potential contamination of the water table aquifer by volatile organic compounds (VOC`s) beneath a Defense Fuel Supply Point and adjacent properties near Hanahan, S.C. Six areas in and around the DFSP facility were investigated with soil-vapor techniques. The northern boundary area has been studied extensively and was, therefore, not included in the investigation.

  18. Organic electronic devices using phthalimide compounds

    DOE Patents [OSTI]

    Hassan, Azad M.; Thompson, Mark E.

    2012-10-23T23:59:59.000Z

    Organic electronic devices comprising a phthalimide compound. The phthalimide compounds disclosed herein are electron transporters with large HOMO-LUMO gaps, high triplet energies, large reduction potentials, and/or thermal and chemical stability. As such, these phthalimide compounds are suitable for use in any of various organic electronic devices, such as OLEDs and solar cells. In an OLED, the phthalimide compounds may serve various functions, such as a host in the emissive layer, as a hole blocking material, or as an electron transport material. In a solar cell, the phthalimide compounds may serve various functions, such as an exciton blocking material. Various examples of phthalimide compounds which may be suitable for use in the present invention are disclosed.

  19. Organic electronic devices using phthalimide compounds

    DOE Patents [OSTI]

    Hassan, Azad M.; Thompson, Mark E.

    2010-09-07T23:59:59.000Z

    Organic electronic devices comprising a phthalimide compound. The phthalimide compounds disclosed herein are electron transporters with large HOMO-LUMO gaps, high triplet energies, large reduction potentials, and/or thermal and chemical stability. As such, these phthalimide compounds are suitable for use in any of various organic electronic devices, such as OLEDs and solar cells. In an OLED, the phthalimide compounds may serve various functions, such as a host in the emissive layer, as a hole blocking material, or as an electron transport material. In a solar cell, the phthalimide compounds may serve various functions, such as an exciton blocking material. Various examples of phthalimide compounds which may be suitable for use in the present invention are disclosed.

  20. Organic electronic devices using phthalimide compounds

    DOE Patents [OSTI]

    Hassan, Azad M.; Thompson, Mark E.

    2013-03-19T23:59:59.000Z

    Organic electronic devices comprising a phthalimide compound. The phthalimide compounds disclosed herein are electron transporters with large HOMO-LUMO gaps, high triplet energies, large reduction potentials, and/or thermal and chemical stability. As such, these phthalimide compounds are suitable for use in any of various organic electronic devices, such as OLEDs and solar cells. In an OLED, the phthalimide compounds may serve various functions, such as a host in the emissive layer, as a hole blocking material, or as an electron transport material. In a solar cell, the phthalimide compounds may serve various functions, such as an exciton blocking material. Various examples of phthalimide compounds which may be suitable for use in the present invention are disclosed.

  1. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

    1993-09-07T23:59:59.000Z

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 figures.

  2. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

    1994-06-14T23:59:59.000Z

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

  3. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, Jr., Lawrence A. (Houston, TX)

    1989-01-01T23:59:59.000Z

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

  4. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

    1993-01-01T23:59:59.000Z

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

  5. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

    1994-01-01T23:59:59.000Z

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

  6. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, L.A. Jr.

    1989-07-18T23:59:59.000Z

    Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

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

    SciTech Connect (OSTI)

    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.

    2010-01-01T23:59:59.000Z

    The volatile organic compound (VOC) distribution in the Mexico City Metropolitan Area (MCMA) and its evolution as it is uplifted and transported out of the MCMA basin was studied during the 2006 MILAGRO/MIRAGE-Mex field campaign. The results show that in the morning hours in the city center, the VOC distribution is dominated by non-methane hydrocarbons (NMHCs) but with a substantial contribution from oxygenated volatile organic compounds (OVOCs), predominantly from primary emissions. Alkanes account for a large part of the NMHC distribution in terms of mixing ratios. In terms of reactivity, NMHCs also dominate overall, especially in the morning hours. However, in the afternoon, as the boundary layer lifts and air is mixed and aged within the basin, the distribution changes as secondary products are formed. The WRF-Chem (Weather Research and Forecasting with Chemistry) model and MOZART (Model for Ozone and Related chemical Tracers) were able to reproduce the general features of the daytime cycle of the VOC OH reactivity distribution showing that NMHCs dominate the distribution except in the afternoon hours and that the VOC OH reactivity peaks in the early morning due to high morning emissions from the city into a shallow boundary layer. The WRF-Chem and MOZART models showed higher reactivity than the experimental data during the nighttime cycle, perhaps indicating problems with the modeled nighttime boundary layer height. In addition, a plume was studied in which air was advected out of the MCMA and intercepted downwind with the DOE G1 on March 18 and the NCAR C130 one day later on March 19. A number of identical species measured aboard each aircraft gave insight into the chemical evolution of the plume as it aged and was transported as far as 1000 km downwind. Ozone and many OVOCs were photochemically produced in the plume. The WRF-Chem and MOZART models were used to examine the spatial and temporal extent of the March 19 plume and to help interpret the OH 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.

  8. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

    1993-01-01T23:59:59.000Z

    Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70.degree. C. and 500.degree. C. and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

  9. Alkylation of organic aromatic compounds

    DOE Patents [OSTI]

    Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

    1993-01-05T23:59:59.000Z

    Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70 C and 500 C and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

  10. VOCs in Arid soils: Technology summary

    SciTech Connect (OSTI)

    Not Available

    1994-02-01T23:59:59.000Z

    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.

  11. Distribution, Magnitudes, Reactivities, Ratios and Diurnal Patterns of Volatile Organic Compounds in the Valley of Mexico During the MCMA 2002 & 2003 Field Campaigns

    SciTech Connect (OSTI)

    Velasco, E.; Lamb, Brian K.; Westberg, Halvor; Allwine, Eugene J.; Sosa, G.; Arriaga-Colina, J. L.; Jobson, B. T.; Alexander, M. Lizabeth; Prazeller, Peter; Knighton, Walter B.; Rogers, T.; Grutter, M.; Herndon, S.; Kolb, C. E.; Zavala, Mary A.; de Foy, B.; Volkamer, Rainer M.; Molina, Luisa; Molina, Mario J.

    2007-01-23T23:59:59.000Z

    A wide array of volatile organic compound (VOC) measurements was conducted in the Valley of Mexico during the MCMA-2002 and 2003 field campaigns. Study sites included locations in the urban core, in a heavily industrial area and at boundary sites in rural landscapes. In addition, a novel mobile-laboratory-based conditional sampling method was used to collect samples dominated by fresh on-road vehicle exhaust to identify those VOCs whose ambient concentrations were primarily due to vehicle emissions. Four distinct analytical techniques were used: whole air canister samples with Gas Chromatography/Flame Ionization Detection (GC-FID), on-line chemical ionization using a Proton Transfer Reaction Mass Spectrometer (PTR-MS), continuous real-time detection of olefins using a Fast Olefin Sensor (FOS), and long path measurements using UV Differential Optical Absorption Spectrometers (DOAS). The simultaneous use of these techniques provided a wide range of individual VOC measurements with different spatial and temporal scales. The VOC data were analyzed to understand concentration and spatial distributions, diurnal patterns, origin and reactivity in the atmosphere of Mexico City. The VOC burden (in ppbC) was dominated by alkanes (60%), followed by aromatics (15%) and olefins (5%). The remaining 20% was a mix of alkynes, halogenated hydrocarbons, oxygenated species (esters, ethers, etc.) and other unidentified VOCs. However, in terms of ozone production, olefins were the most relevant hydrocarbons. Elevated levels of toxic hydrocarbons, such as 1, 3-butadiene, benzene, toluene and xylenes, were also observed. Results from these various analytical techniques showed that vehicle exhaust is the main source of VOCs in Mexico City and that diurnal patterns depend on vehicular traffic in addition to meteorological processes. Finally, examination of the VOC data in terms of lumped modeling VOC classes and its comparison to the VOC lumped emissions reported in other photochemical air quality modeling studies suggests that some alkanes are underestimated in the emissions inventory, while some olefins and aromatics are overestimated.

  12. Measurements of volatile organic compounds at a suburban ground site (T1) in Mexico City during the MILAGRO 2006 campaign: Measurement comparison, emission ratios, and source attribution

    SciTech Connect (OSTI)

    Bon, D.M.; Springston, S.; M.Ulbrich, I.; de Gouw, J. A.; Warneke, C.; Kuster, W. C.; Alexander, M. L.; Baker, A.; Beyersdorf, A. J.; Blake, D.; Fall, R.; Jimenez, J. L., Herndon, S. C.; Huey, L. G.; Knighton, W. B.; Ortega, J.; Vargas, O.

    2011-03-16T23:59:59.000Z

    Volatile organic compound (VOC) mixing ratios were measured with two different instruments at the T1 ground site in Mexico City during the Megacity Initiative: Local and Global Research Observations (MILAGRO) campaign in March of 2006. A gas chromatograph with flame ionization detector (GC-FID) quantified 18 light alkanes, alkenes and acetylene while a proton-transfer-reaction ion-trap mass spectrometer (PIT-MS) quantified 12 VOC species including oxygenated VOCs (OVOCs) and aromatics. A GC separation system was used in conjunction with the PIT-MS (GC-PIT-MS) to evaluate PIT-MS measurements and to aid in the identification of unknown VOCs. The VOC measurements are also compared to simultaneous canister samples and to two independent proton-transfer-reaction mass spectrometers (PTR-MS) deployed on a mobile and an airborne platform during MILAGRO. VOC diurnal cycles demonstrate the large influence of vehicle traffic and liquid propane gas (LPG) emissions during the night and photochemical processing during the afternoon. Emission ratios for VOCs and OVOCs relative to CO are derived from early-morning measurements. Average emission ratios for non-oxygenated species relative to CO are on average a factor of {approx}2 higher than measured for US cities. Emission ratios for OVOCs are estimated and compared to literature values the northeastern US and to tunnel studies in California. Positive matrix factorization analysis (PMF) is used to provide insight into VOC sources and processing. Three PMF factors were distinguished by the analysis including the emissions from vehicles, the use of liquid propane gas and the production of secondary VOCs + long-lived species. Emission ratios to CO calculated from the results of PMF analysis are compared to emission ratios calculated directly from measurements. The total PIT-MS signal is summed to estimate the fraction of identified versus unidentified VOC species.

  13. Advanced heat pump for the recovery of volatile organic compounds. Phase 1, Conceptual design of an advanced Brayton cycle heat pump for the recovery of volatile organic compounds: Final report

    SciTech Connect (OSTI)

    Not Available

    1992-03-01T23:59:59.000Z

    Emissions of Volatile Organic Compounds (VOC) from stationary industrial and commercial sources represent a substantial portion of the total US VOC emissions. The ``Toxic-Release Inventory`` of The US Environmental Protection Agency estimates this to be at about 3 billion pounds per year (1987 estimates). The majority of these VOC emissions are from coating processes, cleaning processes, polymer production, fuel production and distribution, foam blowing,refrigerant production, and wood products production. The US Department of Energy`s (DOE) interest in the recovery of VOC stems from the energy embodied in the recovered solvents and the energy required to dispose of them in an environmentally acceptable manner. This Phase I report documents 3M`s work in close working relationship with its subcontractor Nuclear Consulting Services (Nucon) for the preliminary conceptual design of an advanced Brayton cycle heat pump for the recovery of VOC. Nucon designed Brayton cycle heat pump for the recovery of methyl ethyl ketone and toluene from coating operations at 3M Weatherford, OK, was used as a base line for the work under cooperative agreement between 3M and ODE. See appendix A and reference (4) by Kovach of Nucon. This cooperative agreement report evaluates and compares an advanced Brayton cycle heat pump for solvent recovery with other competing technologies for solvent recovery and reuse. This advanced Brayton cycle heat pump is simple (very few components), highly reliable (off the shelf components), energy efficient and economically priced.

  14. Organic photosensitive devices using subphthalocyanine compounds

    DOE Patents [OSTI]

    Rand, Barry (Princeton, NJ); Forrest, Stephen R. (Ann Arbor, MI); Mutolo, Kristin L. (Hollywood, CA); Mayo, Elizabeth (Alhambra, CA); Thompson, Mark E. (Anaheim Hills, CA)

    2011-07-05T23:59:59.000Z

    An organic photosensitive optoelectronic device, having a donor-acceptor heterojunction of a donor-like material and an acceptor-like material and methods of making such devices is provided. At least one of the donor-like material and the acceptor-like material includes a subphthalocyanine, a subporphyrin, and/or a subporphyrazine compound; and/or the device optionally has at least one of a blocking layer or a charge transport layer, where the blocking layer and/or the charge transport layer includes a subphthalocyanine, a subporphyrin, and/or a subporphyrazine compound.

  15. Groundwater Transport of Organic Compounds in Old Salvage Yard, Oak Ridge, TN - 12089

    SciTech Connect (OSTI)

    Malek-Mohammadi, Siamak [Civil Engineering and Construction Department, Bradley University, Peoria, IL 61625 (United States); Tachiev, Georgio; Roelant, David [Applied Research Center, Florida International University, Miami, FL 33174 (United States); Bostick, Kent; Daniel, Anamary [Pro2Serve Professional Project Services, Inc., Oak Ridge, TN 37830 (United States)

    2012-07-01T23:59:59.000Z

    In 1950's and early 1960's during production of nuclear weapons at the US Department of Energy Y-12 National Security Complex in Oak Ridge TN, volatile organic compounds (VOCs) as well as heavy metals, nitrates, and radionuclides were released to the environment. Field investigations revealed that much of this contamination is still present in soil, bedrock, and groundwater. Operational buildings and old disposal facilities at the site have been identified as major sources of contamination. The Old Salvage Yard (OSY) on the western side of the site has long been characterized as the major source of VOC contamination in soil and groundwater. In order to analyze the fate and transport of VOC contamination- including tetrachloroethene (PCE), 1,2- dichloroethene (1,2-DCE), cis-1,2-dichloroethene (cis-1,2-DCE) and vinyl chloride (VC) - in groundwater and soil at the vicinity of OSY, an integrated surface and subsurface flow and transport model has been developed for the Y-12 NSC using the hydrodynamic and transport numerical package, MIKE-SHE. Hydrogeological characteristics of the site such as hydraulic conductivity, and transport parameters such as partitioning coefficients were varied in an effort to delineate subsurface flow and transport pathways, potential downstream impacts on Upper East Fork Poplar Creek, and the potential risk to industrial workers involved in related Decontamination and Decommissioning (D and D) activities. The simulation results were compared with the analytical modeling results previously performed by McLane Environmental Inc. using SESOIL-AT123D. Specific simulations have been performed to investigate the effect of possible remedial action (removing the contaminated surface soil layers) on the fate and transport of VOCs. The results of the MIKE-SHE reported here can be considered as an upper limit for the predicted concentrations. Based on MIKE-SHE results, PCE, 1,2 DCE, cis-1,2-DCE, and VC are sources in soil with potential to equal or exceed industrial groundwater hazard and risk levels at the vicinity of OSY. VOC contaminants in soil and groundwater will decay below industrial groundwater risk and hazard levels within approximately 20 years. Excavation of surface soil layers at the site will considerably reduce the concentration of VOCs in groundwater and the possibility of migration of VOCs to surface waters. (authors)

  16. Comparison of predicted and derived measures of volatile organic compounds inside four relocatable classrooms due to identified interior finish sources

    SciTech Connect (OSTI)

    Hodgson, Alfred T.; Shendell, Derek G.; Fisk, William J.; Apte, Michael G.

    2003-06-01T23:59:59.000Z

    Indoor exposures to toxic and odorous volatile organic compounds (VOCs) are of general concern. Recently, VOCs in portable or relocatable classrooms (RCs) have received particular attention. However, very little was known about indoor environmental quality (IEQ) and the sources, composition, and indoor concentrations of VOCs in RCs. This project task focused on developing and demonstrating a process for selecting interior finish materials for RCs that have relatively low impacts with respect to their emissions of toxic and odorous VOCs. This task was part of a larger project to demonstrate the potential for simultaneous improvements in IEQ and energy efficiency in four new RCs equipped both with a continuously ventilating advanced heating, ventilating, and air conditioning system (HVAC) and a standard HVAC system. These HVACs were operated on alternate weeks. One RC per pair was constructed with standard interior finish materials, and the other included alternate interior materials identified in our prior laboratory study to have low VOC emissions. The RCs were sited in side-by-side pairs at two elementary schools in distinct northern California climate zones. Classroom VOC emission rates (mg hr{sup -1}) and concentrations were predicted based on VOC emission factors ({micro}g m{sup -2} hr{sup -1}) measured for individual materials in the laboratory, the quantities of installed materials and design ventilation rates. Predicted emission rates were compared to values derived from classroom measurements of VOC concentrations and ventilation rates made at pre-occupancy, eight weeks, and 27 weeks. Predicted concentrations were compared to measured integrated VOC indoor minus outdoor concentrations during school hours in the fall cooling season with the advanced HVAC operated. These measured concentrations also were compared between standard and material-modified RCs. Our combined laboratory and field process proved effective by correctly predicting that IEQ impacts of material VOC emissions would be minor when RCs were ventilated at or above code-minimum requirements. Assuming code-minimum ventilation rates are maintained, the benefits attributable to the use of alternate interior finish materials in RC's constructed by the manufacturer associated with this study are small, implying that it is not imperative to use such alternative finishing materials. However, it is essential to avoid materials that can degrade IEQ, and the results of this study demonstrate that laboratory-based material testing combined with modeling and field validation can help to achieve that aim.

  17. Position for determining gas-phase volatile organic compound concentrations in transuranic waste containers. Revision 2

    SciTech Connect (OSTI)

    Connolly, M.J.; Liekhus, K.J. [Lockheed Martin Idaho Technologies Co., Idaho Falls, ID (United States). Idaho National Engineering and Environmental Lab.] [Lockheed Martin Idaho Technologies Co., Idaho Falls, ID (United States). Idaho National Engineering and Environmental Lab.; Djordjevic, S.M.; Loehr, C.A.; Spangler, L.R. [Benchmark Environmental Corp. (United States)] [Benchmark Environmental Corp. (United States)

    1998-06-01T23:59:59.000Z

    In the conditional no-migration determination (NMD) for the test phase of the Waste Isolation Pilot Plant (WIPP), the US Environmental Protection Agency (EPA) imposed certain conditions on the US Department of Energy (DOE) regarding gas phase volatile organic compound (VOC) concentrations in the void space of transuranic (TRU) waste containers. Specifically, the EPA required the DOE to ensure that each waste container has no layer of confinement that contains flammable mixtures of gases or mixtures of gases that could become flammable when mixed with air. The EPA also required that sampling of the headspace of waste containers outside inner layers of confinement be representative of the entire void space of the container. The EPA stated that all layers of confinement in a container would have to be sampled until DOE can demonstrate to the EPA that sampling of all layers is either unnecessary or can be safely reduced. A test program was conducted at the Idaho National Engineering and Environmental Laboratory (INEEL) to demonstrate that the gas phase VOC concentration in the void space of each layer of confinement in vented drums can be estimated from measured drum headspace using a theoretical transport model and that sampling of each layer of confinement is unnecessary. This report summarizes the studies performed in the INEEL test program and extends them for the purpose of developing a methodology for determining gas phase VOC concentrations in both vented and unvented TRU waste containers. The methodology specifies conditions under which waste drum headspace gases can be said to be representative of drum gases as a whole and describes a method for predicting drum concentrations in situations where the headspace concentration is not representative. The methodology addresses the approach for determining the drum VOC gas content for two purposes: operational period drum handling and operational period no-migration calculations.

  18. Position for determining gas phase volatile organic compound concentrations in transuranic waste containers. Revision 1

    SciTech Connect (OSTI)

    Connolly, M.J.; Liekhus, K.J. [Lockheed Idaho Technologies Co., Idaho Falls, ID (United States); Djordjevic, S.M.; Loehr, C.A.; Spangler, L.R. [Benchmark Environmental Corp., Albuquerque, NM (United States)

    1995-08-01T23:59:59.000Z

    In the conditional no-migration determination (NMD) for the test phase of the Waste Isolation Pilot Plant (WIPP), the US Environmental Protection Agency (EPA) imposed certain conditions on the US Department of Energy (DOE) regarding gas phase volatile organic compound (VOC) concentrations in the void space of transuranic (TRU) waste containers. Specifically, the EPA required the DOE to ensure that each waste container has no layer of confinement that contains flammable mixtures of gases or mixtures of gases that could become flammable when mixed with air. The EPA also required that sampling of the headspace of waste containers outside inner layers of confinement be representative of the entire void space of the container. The EPA stated that all layers of confinement in a container would have to be sampled until DOE can demonstrate to the EPA that sampling of all layers is either unnecessary or can be safely reduced. A test program was conducted at the Idaho National Engineering Laboratory (INEL) to demonstrate that the gas phase VOC concentration in the void space of each layer of confinement in vented drums can be estimated from measured drum headspace using a theoretical transport model and that sampling of each layer of confinement is unnecessary. This report summarizes the studies performed in the INEL test program and extends them for the purpose of developing a methodology for determining gas phase VOC concentrations in both vented and unvented TRU waste containers. The methodology specifies conditions under which waste drum headspace gases can be said to be representative of drum gases as a whole and describes a method for predicting drum concentrations in situations where the headspace concentration is not representative. The methodology addresses the approach for determining the drum VOC gas content for two purposes: operational period drum handling and operational period no-migration calculations.

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

    SciTech Connect (OSTI)

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

    1995-08-01T23:59:59.000Z

    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 ({Sigma}VOC{sub 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{sup {minus}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.

  20. Quantifying VOC emissions for the strategic petroleum reserve.

    SciTech Connect (OSTI)

    Knowlton, Robert G.; Lord, David L.

    2013-06-01T23:59:59.000Z

    A very important aspect of the Department of Energy's (DOE's) Strategic Petroleum Reserve (SPR) program is regulatory compliance. One of the regulatory compliance issues deals with limiting the amount of volatile organic compounds (VOCs) that are emitted into the atmosphere from brine wastes when they are discharged to brine holding ponds. The US Environmental Protection Agency (USEPA) has set limits on the amount of VOCs that can be discharged to the atmosphere. Several attempts have been made to quantify the VOC emissions associated with the brine ponds going back to the late 1970's. There are potential issues associated with each of these quantification efforts. Two efforts were made to quantify VOC emissions by analyzing VOC content of brine samples obtained from wells. Efforts to measure air concentrations were mentioned in historical reports but no data have been located to confirm these assertions. A modeling effort was also performed to quantify the VOC emissions. More recently in 2011- 2013, additional brine sampling has been performed to update the VOC emissions estimate. An analysis of the statistical confidence in these results is presented here. Arguably, there are uncertainties associated with each of these efforts. The analysis herein indicates that the upper confidence limit in VOC emissions based on recent brine sampling is very close to the 0.42 ton/MMB limit used historically on the project. Refining this estimate would require considerable investment in additional sampling, analysis, and monitoring. An analysis of the VOC emissions at each site suggests that additional discharges could be made and stay within current regulatory limits.

  1. Identifying Sources of Volatile Organic Compounds and Aldehydes in a High Performance Building

    SciTech Connect (OSTI)

    Ortiz, Anna C.; Russell, Marion; Lee, Wen-Yee; Apte, Michael; Maddalena, Randy

    2010-09-20T23:59:59.000Z

    The developers of the Paharpur Business Center (PBC) and Software Technology Incubator Park in New Delhi, India offer an environmentally sustainable building with a strong emphasis on energy conservation, waste minimization and superior indoor air quality (IAQ). To achieve the IAQ goal, the building utilizes a series of air cleaning technologies for treating the air entering the building. These technologies include an initial water wash followed by ultraviolet light treatment and biolfiltration using a greenhouse located on the roof and numerous plants distributed throughout the building. Even with the extensive treatment of makeup air and room air in the PBC, a recent study found that the concentrations of common volatile organic compounds and aldehydes appear to rise incrementally as the air passes through the building from the supply to the exhaust. This finding highlights the need to consider the minimization of chemical sources in buildings in combination with the use of advanced air cleaning technologies when seeking to achieve superior IAQ. The goal of this project was to identify potential source materials for indoor chemicals in the PBC. Samples of building materials, including wood paneling (polished and unpolished), drywall, and plastic from a hydroponic drum that was part of the air cleaning system, were collected from the building for testing. All materials were collected from the PBC building and shipped to the Lawrence Berkeley National Laboratory (LBNL) for testing. The materials were pre-conditioned for two different time periods before measuring material and chemical specific emission factors for a range of VOCs and Aldehydes. Of the six materials tested, we found that the highest emitter of formaldehyde was new plywood paneling. Although polish and paint contribute to some VOC emissions, the main influence of the polish was in altering the capacity of the surface to accumulate formaldehyde. Neither the new nor aged polish contributed significantly to formaldehyde emissions. The VOC emission stream (excluding formaldehyde) was composed of up to 18 different chemicals and the total VOC emissions ranged in magnitude from 7 mu g/m2/h (old wood with old polish) to>500 mu g/m2/h (painted drywall). The formaldehyde emissions from drywall and old wood with either new or old polish were ~;;15 mu g/m2/h while the new wood material emitted>100 mu g/m2/h. However, when the projected surface area of each material in the building was considered, the new wood, old wood and painted drywall material all contributed substantially to the indoor formaldehyde loading while the coatings contributed primarily to the VOCs.

  2. A Novel New Approach to VOC and HAP Emission Control

    E-Print Network [OSTI]

    McGinness, M.

    - adsorbent scrubber solution. Water wash paint booth scrubbers can effectively capture PM-IO and PM-2.S particulates as well as VOHAPs. Water wash scrubbers by their very nature represent a reduced fire hazard compared to dry filter booth systems. NFPA...A Novel New Approach to VOC and HAP Emission Control Mike McGinness VP-R&D EcoShield Environmental Systems, Inc. Houston, Texas ABSTRACT HAP (Hazardous Air Pollutant) and VOC (Volatile Organic Compound) thermal emission control devices (ECD...

  3. Second-harmonic generation in transition-metal-organic compounds

    SciTech Connect (OSTI)

    Frazier, C.C.; Harvey, M.A.; Cockerham, M.P.; Hand, H.M.; Chauchard, E.A.; Lee, C.H.

    1986-10-23T23:59:59.000Z

    The second-harmonic generation efficiencies of over 60 transition-metal-organic compounds in powder form were measured, using 1.06 ..mu..m light from a Nd:YAG laser. Most of the studied compounds were either group VI metal carbonyl arene, pyridyl, or chiral phosphine complexes. Four the complexes doubled the laser fundamental as well as or better than ammonium dihydrogen phosphate (ADP). The study shows that the same molecular features (e.g., conjugation and low-lying spectroscopic charge transfer) that contribute to second-order optical nonlinearity in organic compounds also enhance second-order effects in transition-metal-organic compounds.

  4. Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results

    SciTech Connect (OSTI)

    Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

    1990-08-01T23:59:59.000Z

    This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program`s Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

  5. Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results

    SciTech Connect (OSTI)

    Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

    1990-08-01T23:59:59.000Z

    This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program's Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

  6. Southern California Edison's (SCE) Research Program for Industrial Volatile Organic Compound (VOC) Emissions Control

    E-Print Network [OSTI]

    Sung, R. D.; Cascone, R.; Reese, J.

    emission sources, SCE has identified and evaluated a number of alternative solutions and is currently implementing four demonstrations for promising technologies. The SCE program focuses on three major strategies: (1) reformulation, (2) application... is primarily a three-pronged approach, consisting of problem identification, alternatives evaluation, and technology demonstrations. For problem identification, the main thrust was to conduct a comprehensive analysis of the California state and the South...

  7. Vehicular emission of volatile organic compounds (VOCs) from a tunnel study in Hong Kong

    E-Print Network [OSTI]

    2009-01-01T23:59:59.000Z

    2004. Haszpra, L. and Szilagyi, I. : Non-methane hydrocarbonet al. , 1990; Haszpra and Szilagyi, 1994; Gertler et al. ,

  8. NMED COMMENTS ITEM 3 REVISE VOLATILE ORGANIC COMPOUND (VOC) TARGET ANALYTE LIST

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Saleshttp://www.fnal.gov/directorate/nalcal/nalcal02_07_05_files/nalcal.gif Directorate1, Issue 23 NETL NEVIS- NIF|7, 2015 NMED3 NMED

  9. Process for reducing organic compounds with calcium, amine, and alcohol

    DOE Patents [OSTI]

    Benkeser, R.A.; Laugal, J.A.; Rappa, A.

    1985-08-06T23:59:59.000Z

    Olefins are produced by contacting an organic compound having at least one benzene ring with calcium metal, ethylenediamine, a low molecular weight aliphatic alcohol, and optionally a low molecular weight aliphatic primary amine, and/or an inert, abrasive particulate substance. The reduction is conducted at temperatures ranging from about [minus]10 C to about 30 C or somewhat higher. Substantially all of the organic compounds are converted to corresponding cyclic olefins, primarily diolefins.

  10. The Effect of Organic Compounds in Pot Experiments.

    E-Print Network [OSTI]

    Fraps, G. S.

    1915-01-01T23:59:59.000Z

    TEXAS AGRICULTURAL EXPERIMENT STATION BULLETIN NO. 174 APRIL, 1915 DIVISION OF CHEMISTRY The Effect of Organic Compounds in Pot Experiments POSTOFFICE: COLLEGE STATION, BRAZOS COUNTY, TEXAS VON BOECK~UNN-JON&S CO ?? PRINTERS, AUSTIN, TEXAS... 19 15 BLANK PAGE IN ORIGINAL A116-715-10m TEXAS AGRICULTURAL EXPERIMENT STATION BULLETIN NO. 174 APRIL,. 1915 DIVISION OF CHEMISTRY The Effect of Organic Compounds In Pot Experiments BY G. S. FRAPS, Chemist in Charge; State Chemist...

  11. Process for reducing organic compounds with calcium, amine, and alcohol

    DOE Patents [OSTI]

    Benkeser, Robert A. (West Lafayette, IN); Laugal, James A. (Lostant, IL); Rappa, Angela (Baltimore, MD)

    1985-01-01T23:59:59.000Z

    Olefins are produced by contacting an organic compound having at least one benzene ring with calcium metal, ethylenediamine, a low molecular weight aliphatic alcohol, and optionally a low molecular weight aliphatic primary amine, and/or an inert, abrasive particulate substance. The reduction is conducted at temperatures ranging from about -10.degree. C. to about 30.degree. C. or somewhat higher. Substantially all of the organic compounds are converted to corresponding cyclic olefins, primarily diolefins.

  12. Oxidation of Organic Compounds in the Soil.

    E-Print Network [OSTI]

    Fraps, G. S. (George Stronach)

    1915-01-01T23:59:59.000Z

    oxidized to nitrates. The direct study of the changes in organic matter or carbon in the soil is more satisfactory than any assumption. A considerable amount of work upon the oxidation of organic matter in the soil has been clone hy Wollny... cflpo8city, so the re1ati~-e power of the soil to support oxidizing organisms ma!r he termed its oxidafion cnpaciiy. The nitrif-ing capac- it" the oxidatioa capacity 'and the capacit~ of the soil to convert am- monia into nitrates and ammonia are to a...

  13. Installation and certification of continuous VOC emissions monitoring systems for a steel mill sinter plant

    SciTech Connect (OSTI)

    Taylor, K.L.; Macak, J.J. III; Cioffi, J.

    1999-07-01T23:59:59.000Z

    The counties of Lake, Porter, and LaPorte in Northwest Indiana are classified as severe non-attainment for the ozone National Ambient Air Quality Standard (NAAQS). In response to the non-attainment problem, the Indiana Department of Environmental Management (IDEM) promulgated a number of regulations over the last several years. One of these rules requires steel mills with sinter plants to control and continuously monitor volatile organic compound (VOC) emissions from the facilities. One of the accepted compliance methods is to install and certify Continuous Emission Monitoring Systems (CEMS) to monitor VOC emissions and volumetric flow rate in order to generate a VOC emission number in units of pounds per hour. Compliance with the regulation also requires that the sinter plants accurately monitor sinter production in order to determine compliance during the winter months, when the limits are based on pounds of VOC emissions per ton of sinter produced.

  14. Determination of VOC emissions from French wood products Christophe YRIEIX *, Franois MAUPETIT **, Olivier RAMALHO **

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    wood manufacturers to determine IAQ performances of their products and to confront them with other quality (IAQ). Indeed, building products are significant sources of Volatile Organic Compounds (VOCs. This is particularly important for French wood manufacturers to determine IAQ performances of their products

  15. CAN SORBENT-BASED GAS PHASE AIR CLEANING FOR VOCS SUBSTITUTE FOR VENTILATION IN COMMERCIAL BUILDINGS?

    SciTech Connect (OSTI)

    Fisk, William; Fisk, William J.

    2007-08-01T23:59:59.000Z

    This paper reviews current knowledge about the suitability of sorbent-based air cleaning for removing volatile organic compounds (VOCs) from the air in commercial buildings, as needed to enable reductions in ventilation rates and associated energy savings. The principles of sorbent air cleaning are introduced, criteria are suggested for sorbent systems that can counteract indoor VOC concentration increases from reduced ventilation, major findings from research on sorbent performance for this application are summarized, and related priority research needs are identified. Major conclusions include: sorbent systems can remove a broad range of VOCs with moderate to high efficiency, sorbent technologies perform effectively when challenged with VOCs at the low concentrations present indoors, and there is a large uncertainty about the lifetime and associated costs of sorbent air cleaning systems when used in commercial buildings for indoor VOC control. Suggested priority research includes: experiments to determine sorbent system VOC removal efficiencies and lifetimes considering the broad range and low concentration of VOCs indoors; evaluations of in-situ regeneration of sorbents; and an updated analysis of the cost of sorbent air cleaning relative to the cost of ventilation.

  16. Sorbent-Based Gas Phase Air Cleaning for VOCs in CommercialBuildings

    SciTech Connect (OSTI)

    Fisk, William J.

    2006-05-01T23:59:59.000Z

    This paper provides a review of current knowledge about the suitability of sorbent-based air cleaning for removing volatile organic compounds (VOCs) from the air in commercial buildings as needed to enable reductions in ventilation rates and associated energy savings. The fundamental principles of sorbent air cleaning are introduced, criteria are suggested for sorbent systems that can counteract indoor VOC concentration increases from reduced ventilation, major findings from research on sorbent performance for this application are summarized, novel sorbent technologies are described, and related priority research needs are identified. Major conclusions include: sorbent systems can remove a broad range of VOCs with moderate to high efficiency, sorbent technologies perform effectively when challenged with VOCs at the low concentrations present indoors, and there is a large uncertainty about the lifetime and associated costs of sorbent air cleaning systems when used in commercial buildings for indoor VOC control. Suggested priority research includes: experiments to determine sorbent system VOC removal efficiencies and lifetimes considering the broad range and low concentration of VOCs indoors; evaluations of in-situ regeneration of sorbents; and an updated analysis of the cost of sorbent air cleaning relative to the cost of ventilation.

  17. Evaluation of Ultra-Violet Photocatalytic Oxidation (UVPCO) forIndoor Air Applications: Conversion of Volatile Organic Compounds at LowPart-per-Billion Concentrations

    SciTech Connect (OSTI)

    Hodgson, Alfred T.; Sullivan, Douglas P.; Fisk, William J.

    2005-09-30T23:59:59.000Z

    Efficient removal of indoor generated airborne particles and volatile organic compounds (VOCs) in office buildings and other large buildings may allow for a reduction in outdoor air supply rates with concomitant energy savings while still maintaining acceptable indoor air quality in these buildings. Ultra-Violet Photocatalytic Oxidation (UVPCO) air cleaners have the potential to achieve the necessary reductions in indoor VOC concentrations at relatively low cost. In this study, laboratory experiments were conducted with a scaled, prototype UVPCO device designed for use in a duct system. The experimental UVPCO contained two 30 by 30-cm honeycomb monoliths coated with titanium dioxide and 3% by weight tungsten oxide. The monoliths were irradiated with 12 UVC lamps arranged in four banks. The UVPCO was challenged with four mixtures of VOCs typical of mixtures encountered in indoor air. A synthetic office mixture contained 27 VOCs commonly measured in office buildings. A cleaning product mixture contained three cleaning products with high market shares. A building product mixture was created by combining sources including painted wallboard, composite wood products, carpet systems, and vinyl flooring. A fourth mixture contained formaldehyde and acetaldehyde. Steady-state concentrations were produced in a classroom laboratory or a 20-m{sup 3} environmental chamber. Air was drawn through the UVPCO, and single pass conversion efficiencies were measured from replicate air samples collected upstream and downstream of the reactor section. Concentrations of the mixtures were manipulated, with concentrations of individual VOCs mostly maintained below 10 ppb. Device flow rates were varied between 165 and 580 m{sup 3}/h. Production of formaldehyde, acetaldehyde, acetone, formic acid, and acetic acid as reaction products was investigated. Conversion efficiency data were generated for 48 individual VOCs or groups of closely related compounds. Alcohols and glycol ethers were the most reactive chemical classes with conversion efficiencies often near or above 70% at the low flow rate and near 40% at the high flow rate. Ketones and terpene hydrocarbons were somewhat less reactive. The relative VOC conversion rates are generally favorable for treatment of indoor air since many contemporary products used in buildings employ oxygenated solvents. A commercial UVPCO device likely would be installed in the supply air stream of a building and operated to treat both outdoor and recirculated air. Assuming a recirculation rate comparable to three times the normal outdoor air supply rate, simple mass-balance modeling suggests that a device with similar characteristics to the study unit has sufficient conversion efficiencies for most VOCs to compensate for a 50% reduction in outdoor air supply without substantially impacting indoor VOC concentrations. Formaldehyde, acetaldehyde, acetone, formic acid, and acetic acid were produced in these experiments as reaction byproducts. No other significant byproducts were observed. A coupled steady-state mass balance model is presented and applied to VOC data from a study of a single office building. For the operating assumptions described above, the model estimated a three-fold increase in indoor formaldehyde and acetaldehyde concentrations. The outcome of this limited assessment suggests that evaluation of the potential effects of the operation of a UVPCO device on indoor concentrations of these contaminants is warranted. Other suggested studies include determining VOC conversion efficiencies in actual buildings and evaluating changes in VOC conversion efficiency as monoliths age with long-term operation.

  18. Final Report on Testing of Off-Gas Treatment Technologies for Abatement of Atmospheric Emissions of Chlorinated Volatile Organic Compounds

    SciTech Connect (OSTI)

    Jarosch, T.R.; Haselow, J.S.; Rossabi, J.; Burdick, S.A.; Raymond, R.; Young, J.E.; Lombard, K.H.

    1995-01-23T23:59:59.000Z

    The purpose of this report is to summarize the results of the program for off-gas treatment of atmospheric emissions of chlorinated volatile organic compounds (CVOCs), in particular trichloroethylene (TCE) and perchloroethylene (PCE). This program was funded through the Department of Energy Office of Technology Development`s VOC`s in Non-Arid Soils Integrated Demonstration (VNID). The off-gas treatment program was initiated after testing of in-situ air stripping with horizontal wells was completed (Looney et al., 1991). That successful test expectedly produced atmospheric emissions of CVOCs that were unabated. It was decided after that test that an off-gas treatment is an integral portion of remediation of CVOC contamination in groundwater and soil but also because several technologies were being developed across the United States to mitigate CVOC emissions. A single platform for testing off-gas treatment technologies would facilitate cost effective evaluation of the emerging technologies. Another motivation for the program is that many CVOCs will be regulated under the Clean Air Act Amendments of 1990 and are already regulated by many state regulatory programs. Additionally, compounds such as TCE and PCE are pervasive subsurface environmental contaminants, and, as a result, a small improvement in terms of abatement efficiency or cost will significantly reduce CVOC discharges to the environment as well as costs to United States government and industry.

  19. Evaluation of emplacement sensors for detecting radiation and volatile organic compounds and for long-term monitoring access tubes for the BWCS

    SciTech Connect (OSTI)

    Lord, D.L.; Averill, R.H.

    1997-10-01T23:59:59.000Z

    This document evaluates sensors for detecting contaminants in the excavated waste generated by the Buried Waste Containment System (BWCS). The Barrier Placement Machine (BPM) removes spoils from under a landfill or plume and places it on a conveyor belt on the left and right sides of the BPM. The spoils will travel down the conveyor belts past assay monitors and be deposited on top of the site being worked. The belts are 5 ft wide and transport approximately 15 ft3 /minute of spoils. This corresponds to a 10 ft per hour BPM advance rate. With a 2 in. spoils height the belt speed would be 3.6 in. per second. The spoils being removed are expected to be {open_quotes}clean{close_quotes} (no radiation or volatile organics above background levels). To ensure that the equipment is not digging through a contaminated area, assay equipment will monitor the spoils for mg radiation and volatile organic compounds (VOCs). The radiation monitors will check for gross radiation indication. Upon detection of radiation levels above a predetermined setpoint, further evaluation will be performed to determine the isotopes present and their quantity. This will require hand held monitors and a remote monitoring station. Simultaneously, VOC monitors will monitor for predetermined volatile/semi-volatile organic compounds. A Fourier-Transform Infrared Spectrometer (FTIR) monitor is recommended for this operation. Specific site requirements and regulations will determine setpoints and operation scenarios. If VOCs are detected, the data will be collected and recorded. A flat panel display will be mounted in the BPM operator`s cab showing the radio nuclide and VOC monitoring data. As the BPM advances, a 3-in. diameter PVC tube will be placed on the bottom of the barrier slot in front of the 12 to 16-in. containment barrier being emplaced.

  20. Dosimeter for monitoring vapors and aerosols of organic compounds

    DOE Patents [OSTI]

    Vo-Dinh, Tuan (625 Gulfwood Rd., Knoxville, TN 37923)

    1987-01-01T23:59:59.000Z

    A dosimeter is provided for collecting and detecting vapors and aerosols of organic compounds. The dosimeter comprises a lightweight, passive device that can be conveniently worn by a person as a badge or placed at a stationary location. The dosimeter includes a sample collector comprising a porous web treated with a chemical for inducing molecular displacement and enhancing phosphorescence. Compounds are collected onto the web by molecular diffusion. The web also serves as the sample medium for detecting the compounds by a room temperature phosphorescence technique.

  1. Dosimeter for monitoring vapors and aerosols of organic compounds

    DOE Patents [OSTI]

    Vo-Dinh, T.

    1987-07-14T23:59:59.000Z

    A dosimeter is provided for collecting and detecting vapors and aerosols of organic compounds. The dosimeter comprises a lightweight, passive device that can be conveniently worn by a person as a badge or placed at a stationary location. The dosimeter includes a sample collector comprising a porous web treated with a chemical for inducing molecular displacement and enhancing phosphorescence. Compounds are collected onto the web by molecular diffusion. The web also serves as the sample medium for detecting the compounds by a room temperature phosphorescence technique. 7 figs.

  2. 5, 90979126, 2005 VOC emissions from

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    ACPD 5, 9097­9126, 2005 VOC emissions from vegetation pyrolysis J. P. Greenberg et al. Title Page Discussions Volatile organic emissions from the distillation and pyrolysis of vegetation J. P. Greenberg, H is licensed under a Creative Commons License. 9097 #12;ACPD 5, 9097­9126, 2005 VOC emissions from vegetation

  3. Hybrid inorganic-organic, organic charge transfer, and radical based compounds with chalcofulvalene donors and organic acceptors

    E-Print Network [OSTI]

    Reinheimer, Eric Wade

    2009-05-15T23:59:59.000Z

    HYBRID INORGANIC-ORGANIC, ORGANIC CHARGE TRANSFER, AND RADICAL BASED COMPOUNDS WITH CHALCOFULVALENE DONORS AND ORGANIC ACCEPTORS A Dissertation by ERIC WADE REINHEIMER Submitted to the Office of Graduate Studies... COMPOUNDS WITH CHALCOFULVALENE DONORS AND ORGANIC ACCEPTORS A Dissertation by ERIC WADE REINHEIMER Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree...

  4. Volatile Organic Compounds in Untreated Ambient Groundwater of

    E-Print Network [OSTI]

    Volatile Organic Compounds in Untreated Ambient Groundwater of the United States, 1985-1995 P A U L, ambient groundwater of the conterminous United States was conducted based on samples collected from 2948-chloropropane, which had a reporting level of 1.0 µg/L. Because ambient groundwater was targeted, areas of known

  5. Potential VOC Deflagrations in a Vented TRU Drum

    SciTech Connect (OSTI)

    Mukesh, GUPTA

    2005-04-07T23:59:59.000Z

    The objective of the analysis is to examine the potential for lid ejection from a vented transuranic (TRU) waste drum due to pressure buildup caused by the deflagration of hydrogen and volatile organic compounds (VOCs) inside the drum. In this analysis, the AICC pressure for a stoichiometric mixture of VOCs is calculated and then compared against the experimental peak pressure of stoichiometric combustion of propane and hexane in a combustion chamber. The experimental peak pressures of propane and hexane are about 12 percent lower than the calculated AICC pressure. Additional losses in the drum are calculated due to venting of the gases, drum bulging, waste compaction, and heat losses from the presence of waste in the drum. After accounting for these losses, the final pressures are compared to the minimum observed pressure that ejects the lid from a TRU drum. The ejection pressure of 105 psig is derived from data that was recorded for a series of tests where hydrogen-air mixtures were ignited inside sealed TRU drums. Since the calculated pressures are below the minimum lid ejection pressure, none of the VOCs and the hydrogen (up to 4 percent) mixtures present in the TRU waste drum is expected to cause lid ejection if ignited. The analysis of potential VOC deflagrations in a vented TRU drum can be applied across the DOE-Complex since TRU waste is stored in drums throughout the complex.

  6. Mass yields of secondary organic aerosols from the oxidation of alpha-pinene and real plant emissions

    E-Print Network [OSTI]

    Kroll, Jesse

    Biogenic volatile organic compounds (VOCs) are a significant source of global secondary organic aerosol (SOA); however, quantifying their aerosol forming potential remains a challenge. This study presents smog chamber ...

  7. Evaluation of three analytical techniques used to determine high levels of volatile organic compounds in type IV sludge from Rocky Flats Plant

    SciTech Connect (OSTI)

    Parish, K.J.; Applegate, D.V.; Tsai, Y. [and others

    1996-01-01T23:59:59.000Z

    Before disposal, radioactive sludge (Type IV) from Rocky Flats Plant (RFP) must be evaluated for volatile organic compound (VOC) content. The Type IV sludge consists of organic solvents, degreasers, cutting oils, and transuranic (TRU) waste mixed with calcium silicate (MicroCel E{reg_sign}) and Oil Dri{reg_sign} to form a grease or paste-like material. For laboratory testing, a simulated Type IV RFP sludge (nonradioactive) was prepared at Argonne National Laboratory-East. This sludge has a composition similar to that expected from field samples. On the basis of historical information, a typical Type IV sludge is expected to contain approximately 1-10 percent of three target VOCs. The objective of this work is to evaluate three proposed methods for the determination of high levels of these three VOCs in Type IV sludge. The three methods are (1) static headspace gas analysis, (2) methanol extraction, and (3) ethylene glycol extraction. All three methods employ gas chromatography/mass spectrometry (GC/MS). They were evaluated regarding general method performance criteria, ease of operation, and amounts of secondary mixed waste generated.

  8. NICS report links VOCs to respiratory problems

    SciTech Connect (OSTI)

    Kirschner, E.

    1992-04-22T23:59:59.000Z

    Children who live near the chemical plants of Kanawha Valley, WV, suffer more acute and chronic respiratory aliments than those farther away, says a Harvard University School of Public Health report. In the $1-million, five-year study commissioned by the National Institute for Chemical Studies (NICS:Charleston, WV) and funded by the Environmental Protection Agency, proximity to chemical plants that emit volatile organic compounds (VOCs) was linked to higher incidence of asthma, acute eye irritation, shortness of breath, and chronic cough. The researchers say they adjusted for most other factors, such as parental smoking and petroleum. {open_quotes}The research hypothesis was whether children in the valley had more symptoms,{close_quotes} says NICS president Paul Hill. {open_quotes}Yes, there is a difference.{close_quotes} The study showed that some ailments were up to 28% more prevalent in children in the valley than in other Kanawha County children.

  9. VOCs in Non-Arid Soils Integrated Demonstration: Technology summary

    SciTech Connect (OSTI)

    Not Available

    1994-02-01T23:59:59.000Z

    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.

  10. Analysis and evaluation of VOC removal technologies demonstrated at Savannah River

    SciTech Connect (OSTI)

    Chesnut, D.A.; Wagoner, J.; Nitao, J.J.; Boyd, S.; Shaffer, R.J.; Kansa, E.J.; Buscheck, T.A. [Lawrence Livermore National Lab., CA (United States); Pruess, K. [Lawrence Berkeley Lab., CA (United States); Falta, R.W. [Clemson Univ., SC (United States)

    1993-09-01T23:59:59.000Z

    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{sub 2}HCl{sub 3}, or TCE) and Tetrachloroethylene (C{sub 2}Cl{sub 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 2{times}10{sup 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.

  11. Process for removing an organic compound from water

    DOE Patents [OSTI]

    Baker, Richard W. (Palo Alto, CA); Kaschemekat, Jurgen (Palo Alto, CA); Wijmans, Johannes G. (Menlo Park, CA); Kamaruddin, Henky D. (San Francisco, CA)

    1993-12-28T23:59:59.000Z

    A process for removing organic compounds from water is disclosed. The process involves gas stripping followed by membrane separation treatment of the stripping gas. The stripping step can be carried out using one or multiple gas strippers and using air or any other gas as stripping gas. The membrane separation step can be carried out using a single-stage membrane unit or a multistage unit. Apparatus for carrying out the process is also disclosed. The process is particularly suited for treatment of contaminated groundwater or industrial wastewater.

  12. Biogeochemical processes governing exposure and uptake of organic pollutant compounds in aquatic organisms. Environmental Health Perspectives

    E-Print Network [OSTI]

    John W. Farrington

    1991-01-01T23:59:59.000Z

    This paper reviews current knowledge of biogeochemical cycles of pollutant organic chemicals in aquatic ecosystems with a focus on coastal ecosystems. There is a bias toward discussng chemkal and geochemical aspects ofbiogeochemical cycles and an emphasis on hydrophobic organic compounds such as polynuckar aromatic hydrocarbons, polychlorinated biphenyls, and chlorinated organic compounds used as pesticides. The complexity of mixtures of pollutant organic compounds, their various modes of entering ecosystems, and their physical chemical forms are discussed. Important factors that influence bioavailability and disposition (e.g., organism-water partitioning, uptake via food, food meb transfer) are reviewed. These factors include solubilities of chemicals; partitioning of chemicals between solid surfaces, colloids, and soluble phases; variables rates of sorption, desorption; and physiological status of organism. It appears that more emphasis on considering food as a source of uptake and bioaccumulation is important in benthic and epibenthic ecosystems when sediment-associated pollutants are a nt source of input to an aquatic ecosystem. Progress with mathematical models for exposure and uptake of contaminant chemicals is discussed briefly.

  13. VOC and HAP recovery using ionic liquids

    SciTech Connect (OSTI)

    Michael R. Milota : Kaichang Li

    2007-05-29T23:59:59.000Z

    During the manufacture of wood composites, paper, and to a lesser extent, lumber, large amounts of volatile organic compounds (VOCs) such as terpenes, formaldehyde, and methanol are emitted to air. Some of these compounds are hazardous air pollutants (HAPs). The air pollutants produced in the forest products industry are difficult to manage because the concentrations are very low. Presently, regenerative thermal oxidizers (RTOs and RCOs) are commonly used for the destruction of VOCs and HAPs. RTOs consume large amounts of natural gas to heat air and moisture. The combustion of natural gas generates increased CO2 and NOx, which have negative implications for global warming and air quality. The aforementioned problems are addressed by an absorption system containing a room-temperature ionic liquid (RTIL) as an absorbent. RTILs are salts, but are in liquid states at room temperature. RTILs, an emerging technology, are receiving much attention as replacements for organic solvents in industrial processes with significant cost and environmental benefits. Some of these processes include organic synthesis, extraction, and metal deposition. RTILs would be excellent absorbents for exhausts from wood products facilities because of their unique properties: no measurable vapor pressure, high solubility of wide range of organic compounds, thermal stability to 200°C (almost 400°F), and immisciblity with water. Room temperature ionic liquids were tested as possible absorbents. Four were imidizolium-based and were eight phosphonium-based. The imidizolium-based ionic liquids proved to be unstable at the conditions tested and in the presence of water. The phosphonium-based ionic liquids were stable. Most were good absorbents; however, cleaning the contaminates from the ionic liquids was problematic. This was overcome with a higher temperature (120°C) than originally proposed and a very low pressure (1 kPa. Absorption trials were conducted with tetradecy(trihexyl)phosphonium dicyanamide as the RTIL. It was determined that it has good absorption properties for methanol and ?-pinene, is thermally stable, and is relatively easy to synthesize. It has a density of 0.89 g/mL at 20°C and a molecular weight of 549.9 g/mol. Trials were conducted with a small absorption system and a larger absorption system. Methanol, formaldehyde, and other HAPs were absorbed well, nearly 100%. Acetaldehyde was difficult to capture. Total VOC capture, while satisfactory on methanol and ?-pinene in a lab system, was less than expected in the field, 60-80%. The inability to capture the broad spectrum of total organics is likely due to difficulties in cleaning them from the ionic liquid rather than the ability of the ionic liquid to absorb. It’s likely that a commercial system could be constructed to remove 90 to 100% of the gas contaminates. Selecting the correct ionic liquid would be key to this. Absorption may not be the main selection criterion, but rather how easily the ionic liquid can be cleaned is very important. The ionic liquid absorption system might work very well in a system with a limited spectrum of pollutants, such as a paint spray line, where there are not very high molecular weight, non volatile, compounds in the exhaust.

  14. Prediction of short-term and long-term VOC emissions from SBR bitumen-backed carpet under different temperatures

    SciTech Connect (OSTI)

    Yang, S.; Chen, Q. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Building Technology Program; Bluyssen, P.M. [TNO Building and Construction Research, Delft (Netherlands)

    1998-12-31T23:59:59.000Z

    This paper presents two models for volatile organic compound (VOC) emissions from carpet. One is a numerical model using the computational fluid dynamics (CFD) technique for short-term predictions, the other an analytical model for long-term predictions. The numerical model can (1) deal with carpets that are not new, (2) calculate the time-dependent VOC distributions in a test chamber or room, and (3) consider the temperature effect on VOC emissions. Based on small-scale chamber data, both models were used to examine the VOC emissions under different temperatures from polypropene styrene-butadiene rubber (SBR) bitumen-backed carpet. The short-term predictions show that the VOC emissions under different temperatures can be modeled solely by changing the carpet diffusion coefficients. A formulation of the Arrhenius relation was used to correlate the dependence of carpet diffusion coefficient with temperature. The long-term predictions show that it would take several years to bake out the VOCs, and temperature would have a major impact on the bake-out time.

  15. Method of estimating maximum VOC concentration in void volume of vented waste drums using limited sampling data: Application in transuranic waste drums

    SciTech Connect (OSTI)

    Liekhus, K.J.; Connolly, M.J.

    1995-12-01T23:59:59.000Z

    A test program has been conducted at the Idaho National Engineering Laboratory to demonstrate that the concentration of volatile organic compounds (VOCs) within the innermost layer of confinement in a vented waste drum can be estimated using a model incorporating diffusion and permeation transport principles as well as limited waste drum sampling data. The model consists of a series of material balance equations describing steady-state VOC transport from each distinct void volume in the drum. The primary model input is the measured drum headspace VOC concentration. Model parameters are determined or estimated based on available process knowledge. The model effectiveness in estimating VOC concentration in the headspace of the innermost layer of confinement was examined for vented waste drums containing different waste types and configurations. This paper summarizes the experimental measurements and model predictions in vented transuranic waste drums containing solidified sludges and solid waste.

  16. Environmental chamber studies of atmospheric reactivities of volatile organic compounds: Effects of varying chamber and light source

    SciTech Connect (OSTI)

    Carter, W.; Luo, D.; Malkina, I.; Pierce, J. [California Univ., Riverside, CA (United States)

    1995-05-01T23:59:59.000Z

    Photochemical oxidant models are essential tools for assessing effects of emissions changes on ground-level ozone formation. Such models are needed for predicting the ozone impacts of increased alternative fuel use. The gas-phase photochemical mechanism is an important component of these models because ozone is not emitted directly, but is formed from the gas-phase photochemical reactions of the emitted volatile organic compounds (VOCs) and oxides of nitrogen (NO{sub x}) in air. The chemistry of ground level ozone formation is complex; hundreds of types of VOCs being emitted into the atmosphere, and most of their atmospheric reactions are not completely understood. Because of this, no chemical model can be relied upon to give even approximately accurate predictions unless it has been evaluated by comparing its predictions with experimental data. Therefore an experimental and modeling study was conducted to assess how chemical mechanism evaluations using environmental chamber data are affected by the light source and other chamber characteristics. Xenon arc lights appear to give the best artificial representation of sunlight currently available, and experiments were conducted in a new Teflon chamber constructed using such a light source. Experiments were also conducted in an outdoor Teflon Chamber using new procedures to improve the light characterization, and in Teflon chambers using blacklights. These results, and results of previous runs other chambers, were compared with model predictions using an updated detailed chemical mechanism. The magnitude of the chamber radical source assumed when modeling the previous runs were found to be too high; this has implications in previous mechanism evaluations. Temperature dependencies of chamber effects can explain temperature dependencies in chamber experiments when Ta-300{degree}K, but not at temperatures below that.

  17. Field-usable portable analyzer for chlorinated organic compounds

    SciTech Connect (OSTI)

    Buttner, W.J.; Penrose, W.R.; Stetter, J.R.; Williams, R.D.

    1996-12-31T23:59:59.000Z

    In 1992, a chemical sensor was developed which showed almost perfect selectivity to vapors of chlorinated solvents. When interfaced to an instrument, a chemical analyzer will be produced that has near- absolute selectivity to vapors of volatile chlorinated organic compounds. TRI has just completed the second of a 2-phase program to develop this new instrument system, which is called the RCL MONITOR. In Phase II, this instrument was deployed in 5 EM40 operations. Phase II applications covered clean-up process monitoring, environmental modeling, routine monitoring, health and safety, and technology validation. Vapor levels between 0 and 100 ppM can be determined in 90 s with a lower detection limit of 0.5 ppM using the hand-portable instrument. Based on the favorable performance of the RCL MONITOR, the commercial instrument was released for commercial sales on Sept. 20, 1996.

  18. Detection of volatile organic compounds using surface enhanced Raman scattering

    SciTech Connect (OSTI)

    Chang, A S; Maiti, A; Ileri, N; Bora, M; Larson, C C; Britten, J A; Bond, T C

    2012-03-22T23:59:59.000Z

    The authors present the detection of volatile organic compounds directly in their vapor phase by surface-enhanced Raman scattering (SERS) substrates based on lithographically-defined two-dimensional rectangular array of nanopillars. The type of nanopillars is known as the tapered pillars. For the tapered pillars, SERS enhancement arises from the nanofocusing effect due to the sharp tip on top. SERS experiments were carried out on these substrates using various concentrations of toluene vapor. The results show that SERS signal from a toluene vapor concentration of ppm level can be achieved, and the toluene vapor can be detected within minutes of exposing the SERS substrate to the vapor. A simple adsorption model is developed which gives results matching the experimental data. The results also show promising potential for the use of these substrates in environmental monitoring of gases and vapors.

  19. Tetratopic phenyl compounds, related metal-organic framework materials and post-assembly elaboration

    DOE Patents [OSTI]

    Farha, Omar K; Hupp, Joseph T

    2013-06-25T23:59:59.000Z

    Disclosed are tetratopic carboxylic acid phenyl for use in metal-organic framework compounds. These compounds are useful in catalysis, gas storage, sensing, biological imaging, drug delivery and gas adsorption separation.

  20. Tetratopic phenyl compounds, related metal-organic framework materials and post-assembly elaboration

    DOE Patents [OSTI]

    Farha, Omar K.; Hupp, Joseph T.

    2012-09-11T23:59:59.000Z

    Disclosed are tetratopic carboxylic acid phenyl for use in metal-organic framework compounds. These compounds are useful in catalysis, gas storage, sensing, biological imaging, drug delivery and gas adsorption separation.

  1. Comparisons of diffusive and advective fluxes of gas phase volatile organic compounds (VOCs) in unsaturated zones under natural conditions

    E-Print Network [OSTI]

    Zhan, Hongbin

    ) in unsaturated zones under natural conditions Kehua You a , Hongbin Zhan a,b, a Department of Geology

  2. Precipitate hydrolysis process for the removal of organic compounds from nuclear waste slurries

    DOE Patents [OSTI]

    Doherty, J.P.; Marek, J.C.

    1987-02-25T23:59:59.000Z

    A process for removing organic compounds from a nuclear waste slurry comprising reacting a mixture of radioactive waste precipitate slurry and an acid in the presence of a catalytically effective amount of a copper(II) catalyst whereby the organic compounds in the precipitate slurry are hydrolyzed to form volatile organic compounds which are separated from the reacting mixture. The resulting waste slurry, containing less than 10 percent of the original organic compounds, is subsequently blended with high level radioactive sludge land transferred to a vitrification facility for processing into borosilicate glass for long-term storage. 2 figs., 3 tabs.

  3. Precipitate hydrolysis process for the removal of organic compounds from nuclear waste slurries

    DOE Patents [OSTI]

    Doherty, Joseph P. (Elkton, MD); Marek, James C. (Augusta, GA)

    1989-01-01T23:59:59.000Z

    A process for removing organic compounds from a nuclear waste slurry comprising reacting a mixture of radioactive waste precipitate slurry and an acid in the presence of a catalytically effective amount of a copper (II) catalyst whereby the organic compounds in the precipitate slurry are hydrolyzed to form volatile organic compounds which are separated from the reacting mixture. The resulting waste slurry, containing less than 10 percent of the orginal organic compounds, is subsequently blended with high level radioactive sludge and transferred to a virtrification facility for processing into borosilicate glass for long-term storage.

  4. Arid sites stakeholder participation in evaluating innovative technologies: VOC-Arid Site Integrated Demonstration

    SciTech Connect (OSTI)

    Peterson, T.S.; McCabe, G.H.; Brockbank, B.R. [and others

    1995-05-01T23:59:59.000Z

    Developing and deploying innovative environmental cleanup technologies is an important goal for the U.S. Department of Energy (DOE), which faces challenging remediation problems at contaminated sites throughout the United States. Achieving meaningful, constructive stakeholder involvement in cleanup programs, with the aim of ultimate acceptance of remediation decisions, is critical to meeting those challenges. DOE`s Office of Technology Development sponsors research and demonstration of new technologies, including, in the past, the Volatile Organic Compounds Arid Site Integrated Demonstration (VOC-Arid ID), hosted at the Hanford Site in Washington State. The purpose of the VOC-Arid ID has been to develop and demonstrate new technologies for remediating carbon tetrachloride and other VOC contamination in soils and ground water. In October 1994 the VOC-Arid ID became a part of the Contaminant Plume Containment and Remediation Focus Area (Plume Focus Area). The VOC Arid ID`s purpose of involving stakeholders in evaluating innovative technologies will now be carried on in the Plume Focus Area in cooperation with Site Technology Coordination Groups and Site Specific Advisory Boards. DOE`s goal is to demonstrate promising technologies once and deploy those that are successful across the DOE complex. Achieving that goal requires that the technologies be acceptable to the groups and individuals with a stake in DOE facility cleanup. Such stakeholders include groups and individuals with an interest in cleanup, including regulatory agencies, Native American tribes, environmental and civic interest groups, public officials, environmental technology users, and private citizens. This report documents the results of the stakeholder involvement program, which is an integral part of the VOC-Arid ID.

  5. Refined conceptual model for the Volatile Organic Compounds-Arid Integrated Demonstration and 200 West Area Carbon Tetrachloride Expedited Response Action

    SciTech Connect (OSTI)

    Last, G.V. [Pacific Northwest Lab., Richland, WA (United States); Rohay, V.J. [Westinghouse Hanford Co., Richland, WA (United States)

    1993-03-01T23:59:59.000Z

    This report presents a refined geohydrologic and geochemical conceptual model of the host site (Hanford Reservation) for the Volatile Organic Compounds -- Arid Integrated Demonstration (VOC-Arid ID) and 200 West Area Carbon Tetrachloride (CCl{sub 4}) Expedited Response Action (ERA), based on the results from fiscal year 1992 site characterization activities. The ERA was initiated in December 1990 to minimize or stabilize CCl{sub 4} migration within the unsaturated (vadose) zone in the vicinity of three CCl{sub 4} disposal sites in the 200 West Area (216-Z-1A tile field, 216-Z-9 trench, and 216-Z-18 crib). Implementation of this ERA was based on concerns that CCl{sub 4} residing in the soils was continuing to spread to the groundwater and, if left unchecked, would significantly increase the area of groundwater contamination. A soil-vapor-extraction system began operating at the site in February 1992.

  6. LOW TEMPERATURE VOC COMBUSTION OVER MANGANESE, COBALT AND ZINC ALPO4 MOLECULAR SIEVES

    SciTech Connect (OSTI)

    Rosemarie Szostak

    2003-03-06T23:59:59.000Z

    The objective of this project was to prepare microporous aluminophosphates containing magnesium, manganese, cobalt and zinc (MeAPOs) and to evaluate their performance as oxidation catalysts for the removal of low levels of volatile organic compounds (VOCs) from gas streams. The tasks to be accomplished were as follows: (1) To develop reliable synthesis methods for metal aluminophosphates containing manganese, cobalt and zinc in their framework; (2) To characterize these materials for crystallinity, phase purity, the location and nature of the incorporated metal in the framework; and (3) To evaluate the materials for their catalytic activities in the oxidation of volatile organic environmental pollutants.

  7. Volatile Organic Compound Emissions from Dairy Cows and

    E-Print Network [OSTI]

    Goldstein, Allen

    , acetone + propanal, dimethylsulfide, and m/z 109 (likely 4-methyl-phenol). The compounds with highest. Agricultural pro- cesses, notably animal operations, are no longer exempt from emission controls as a result with a pro

  8. Methods and systems for chemoautotrophic production of organic compounds

    DOE Patents [OSTI]

    Fischer, Curt R.; Che, Austin J.; Shetty, Reshma P.; Kelly, Jason R.

    2013-01-08T23:59:59.000Z

    The present disclosure identifies pathways, mechanisms, systems and methods to confer chemoautotrophic production of carbon-based products of interest, such as sugars, alcohols, chemicals, amino acids, polymers, fatty acids and their derivatives, hydrocarbons, isoprenoids, and intermediates thereof, in organisms such that these organisms efficiently convert inorganic carbon to organic carbon-based products of interest using inorganic energy, such as formate, and in particular the use of organisms for the commercial production of various carbon-based products of interest.

  9. 1. PRECONCENTRATION, THERMAL DESORPTION & ANALYSIS OF VOLATILE ORGANIC COMPOUNDS

    E-Print Network [OSTI]

    Boyer, Edmond

    : peltier, liq. N?.. Heated transfer line 2) Desorption & transfer by fastheatlng Cooled & heated trap jas trap. The trap is then quickly heated, under a low flow of hélium, to desorb and inject thé compounds. This highly concentrated plug of sample is transferred via a heated transfer line, to a capillary

  10. In situ treatment of VOCs by recirculation technologies

    SciTech Connect (OSTI)

    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)

    1993-06-01T23:59:59.000Z

    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.

  11. Weathered Diesel oil as a sorptive phase for hydrophobic organic compounds in aquifer materials

    E-Print Network [OSTI]

    Hudson, Rondall James

    1994-01-01T23:59:59.000Z

    The sorptive properties of weathered diesel oil were investigated by conducting miscible displacement experiments with three hydrophobic organic compounds (HOCs), acenapthene, fluorene, and dibenzothiophene, as tracers in columns containing aquifer...

  12. Weathered Diesel oil as a sorptive phase for hydrophobic organic compounds in aquifer materials 

    E-Print Network [OSTI]

    Hudson, Rondall James

    1994-01-01T23:59:59.000Z

    The sorptive properties of weathered diesel oil were investigated by conducting miscible displacement experiments with three hydrophobic organic compounds (HOCs), acenapthene, fluorene, and dibenzothiophene, as tracers in columns containing aquifer...

  13. Progress in Understanding Low-Temperature Organic Compound Oxidation Using a Jet-Stirred Reactor

    E-Print Network [OSTI]

    1 Progress in Understanding Low-Temperature Organic Compound Oxidation Using a Jet-Stirred Reactor Lorraine, CNRS, ENSIC, BP 20451, 1 rue Grandville, 54000 Nancy, France Abstract The jet-stirred reactor compounds: rapid compression machines, shock tubes, and heated continuous flow reactors, such as flow tubes

  14. Low-Level Detections of Halogenated Volatile Organic Compounds in Groundwater

    E-Print Network [OSTI]

    compounds; Groundwater management; Drinking water. Introduction Approximately one-half of the U and Hitt 2006 , or more complex process-based analyses utilizing groundwater models Eberts et al. 2005Low-Level Detections of Halogenated Volatile Organic Compounds in Groundwater: Use in Vulnerability

  15. Concentration of light organic compounds from dilute aqueous solutions by adsorption on bound silicalite

    E-Print Network [OSTI]

    Flores, Kathryn Louise

    1989-01-01T23:59:59.000Z

    CONCENTRATION OF LIGHT ORGANIC COMPOUNDS FROM DILUTE AQUEOUS SOLUTIONS BY ADSORPTION ON BOUND SILICALITE A Thesis KATHRYN LOUISE FLORES Submitted to the Office of Graduate Studies of Texas ARM University in partial fulfillment... of the requirements for the degree of MASTER OF SCIENCE May 1989 Major Subject: Chemical Engineering CONCENTRATION OF LIGHT ORGANIC COMPOUNDS FROM DILUTE AQUEOUS SOLUTIONS BY ADSORPTION ON BOUND SILICALITE A Thesis by KATHRYN LOUISE FLORES Approved...

  16. Subtask 1.15-Passive Diffusion Sample Bags Made from Expanded Polytetrafluorethylene (ePTFE) to Measure VOC Concentrations in Groundwater

    SciTech Connect (OSTI)

    Barry W. Botnen

    2006-08-01T23:59:59.000Z

    With laboratory testing of expanded polytetrafluoroethylene (ePTFE) membranes complete, collected data support that volatile organic compound (VOC) molecules will readily diffuse across ePTFE membranes. Membrane samples, supplied by BHA Technologies (GE Osmonics), were tested to determine diffusion rates for VOCs in groundwater. Tests were conducted using membranes with two different pore sizes, with and without thermally laminated spun bond backing, and multiple concentrations of contaminated groundwater. Results suggest that typical residence times associated with traditional samplers constructed of polyethylene (2 weeks) can be reduced by 1 week using ePTFE membranes (reducing project costs) and that VOCs will diffuse more readily at lower temperatures (2.2-3.3 C) across ePTFE materials.

  17. Clean process to destroy arsenic-containing organic compounds with recovery of arsenic

    DOE Patents [OSTI]

    Upadhye, R.S.; Wang, F.T.

    1996-08-13T23:59:59.000Z

    A reduction method is provided for the treatment of arsenic-containing organic compounds with simultaneous recovery of pure arsenic. Arsenic-containing organic compounds include pesticides, herbicides, and chemical warfare agents such as Lewisite. The arsenic-containing compound is decomposed using a reducing agent. Arsine gas may be formed directly by using a hydrogen-rich reducing agent, or a metal arsenide may be formed using a pure metal reducing agent. In the latter case, the arsenide is reacted with an acid to form arsine gas. In either case, the arsine gas is then reduced to elemental arsenic. 1 fig.

  18. Deuterium enrichment by selective photo-induced dissociation of an organic carbonyl compound

    DOE Patents [OSTI]

    Marling, John B. (Livermore, CA)

    1981-01-01T23:59:59.000Z

    A method for producing a deuterium enriched material by photoinduced dissociation which uses as the working material a gas phase photolytically dissociable organic carbonyl compound containing at least one hydrogen atom bonded to an atom which is adjacent to a carbonyl group and consisting of molecules wherein said hydrogen atom is present as deuterium and molecules wherein said hydrogen atom is present as another isotope of hydrogen. The organic carbonyl compound is subjected to intense infrared radiation at a preselected wavelength to selectively excite and thereby induce dissociation of the deuterium containing species to yield a deuterium enriched stable molecular product. Undissociated carbonyl compound, depleted in deuterium, is preferably redeuterated for reuse.

  19. Dual cure low-VOC coating process. Final technical report, Phase 3

    SciTech Connect (OSTI)

    Kinzer, K.E.

    1993-12-01T23:59:59.000Z

    US EPA is implementing increasingly stringent environmental regulations on the emissions of volatile organic compounds (VOCs), which amount to about 7 {times} 10{sup 9} lb/year, largely from paints and other coating systems in industry. Objective of this project is to develop Dual Cure Photocatalyst coating technology for aerospace topcoats (urethane/acrylate), aerospace primers (epoxy/acrylate), and solventless tape backings. Some problems (moisture etc.) were encountered in the primer area. Cost, economic, and energy analyses were conducted. The dual cure technology has already been commercialized in 3M`s flexible diamond resin products. Tabs.

  20. A Tree's Response to Herbivory: Quantification of Biogenic Volatile Organic Compound Emissions

    E-Print Network [OSTI]

    Collins, Gary S.

    A Tree's Response to Herbivory: Quantification of Biogenic Volatile Organic Compound Emissions an abundant source of Secondary Organic Aerosols (SOA). These emissions are known to vary in quantity and composition due to both biogenic and anthropogenic stressors. In this study, BVOC emissions from bristlecone

  1. Composites for removing metals and volatile organic compounds and method thereof

    DOE Patents [OSTI]

    Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Reynolds, John G. (San Ramon, CA)

    2006-12-12T23:59:59.000Z

    Functionalized hydrophobic aerogel/solid support structure composites have been developed to remove metals and organic compounds from aqueous and vapor media. The targeted metals and organics are removed by passing the aqueous or vapor phase through the composite which can be in molded, granular, or powder form. The composites adsorb the metals and the organics leaving a purified aqueous or vapor stream. The species-specific adsorption occurs through specific functionalization of the aerogels tailored towards specific metals and/or organics. After adsorption, the composites can be disposed of or the targeted metals and/or organics can be reclaimed or removed and the composites recycled.

  2. Sources of organic aerosol investigated using organic compounds as tracers measured during CalNex in Bakersfield

    E-Print Network [OSTI]

    Cohen, Ronald C.

    to be mainly through gas-to-particle condensation of gas-phase oxidation products during the day. Our results) and provide insights into secondary organic aerosol (SOA) formation, positive matrix factorization analysis in the afternoon. Although contributions to SOA from oxidation of biogenic gas-phase compounds were less

  3. Removal of hydrophobic Volatile Organic Compounds1 in an integrated process coupling Absorption and2

    E-Print Network [OSTI]

    Boyer, Edmond

    is an interesting method, owing to the low pressure drop generated and68 the low maintenance needed, contrarily to membrane processes that require high working pressures to69 treat low gas flow rates (Fig. 1). An emerging of the process, hydrophobic VOC27 absorption in a gas-liquid contactor, and biodegradation in the TPPB. VOC

  4. Absorption of organic compounds and organometallics on ceramic substrates for wear reduction

    SciTech Connect (OSTI)

    Kennedy, P.J.; Agarwala, V.S. [Naval Air Warfare Center, Patuxent River, MD (United States)

    1996-12-31T23:59:59.000Z

    The concept of employing thermally stable compounds (that is, metal oxides) as high temperature vapor phase ceramic lubricants was investigated. A major part of this study was devoted to the development of various calorimetric and tribological techniques that could be used to determine interfacial reactions between thermally stable compounds and ceramic substrates such as zirconia and alumina. This interaction is pivotal in understanding the mechanism of high temperature lubricity. The approach consisted of selecting low sublimation temperature materials and measuring their thermodynamic interactions as vapors with the ceramic substrates. The materials studied included two easily sublimable organic compounds (that is, naphthalene and salicylic acid) and several organometallics (for example, copper phthalocyanine). Thermodynamic data such as heat of adsorption, packing density, and reversibility of the adsorption were obtained on some of these compounds and were related to wear characteristics. All of these compounds provided effective lubrication at room temperature. Copper phthalocyanine was an effective lubricant at temperatures up to 400 C.

  5. Natural attenuation assessment of multiple VOCs in a deep vadose zone

    SciTech Connect (OSTI)

    PETERSON,DAVID M.; SINGLETARY,MICHAEL A.; STUDER,JAMES E.; MILLER,DAVID R.

    2000-03-08T23:59:59.000Z

    The fate of six volatile organic compounds (VOC) in a 150-meter deep vadose zone was examined in support of a RCRA Corrective Measures Study of the Chemical Waste Landfill at Sandia National Laboratories, Albuquerque, New Mexico. The study focused on the modeling of potential future transport of the VOCs to exposure media upon the completion of two separate voluntary corrective measures--soil vapor extraction and landfill excavation--designed to significantly reduce contaminant levels in subsurface soils. modeling was performed with R-UNSAT, a finite-difference simulator that was developed by the U.S. Geological Survey. R-UNSAT facilitated a relatively unique and comprehensive assessment of vapor transport because it (1) simulated the simultaneous movement of all six VOCs, taking into account each constituent's diffusion coefficient as affected by its mole fraction within a mixture of chemicals, and (2) permitted simultaneous assessment of risk to human health via volatilization (air) and drinking water (groundwater) pathways. Modeling results suggested that monitored natural attenuation would represent a viable remedial alternative at the landfill after both voluntary corrective measures were completed.

  6. Thermal engine driven heat pump for recovery of volatile organic compounds

    DOE Patents [OSTI]

    Drake, Richard L. (Schenectady, NY)

    1991-01-01T23:59:59.000Z

    The present invention relates to a method and apparatus for separating volatile organic compounds from a stream of process gas. An internal combustion engine drives a plurality of refrigeration systems, an electrical generator and an air compressor. The exhaust of the internal combustion engine drives an inert gas subsystem and a heater for the gas. A water jacket captures waste heat from the internal combustion engine and drives a second heater for the gas and possibly an additional refrigeration system for the supply of chilled water. The refrigeration systems mechanically driven by the internal combustion engine effect the precipitation of volatile organic compounds from the stream of gas.

  7. Deuterium enrichment by selective photoinduced dissociation of a multihalogenated organic compound

    DOE Patents [OSTI]

    Marling, John B. (Livermore, CA); Herman, Irving P. (Oakland, CA)

    1981-01-01T23:59:59.000Z

    A method for deuterium enrichment by photoinduced dissociation which uses as the deuterium source a multihalogenated organic compound selected from the group consisting of a dihalomethane, a trihalomethane, a 1,2-dihaloethene, a trihaloethene, a tetrahaloethane and a pentahaloethane. The multihalogenated organic compound is subjected to intense infrared radiation at a preselected wavelength to selectively excite and thereby induce dissociation of substantially only those molecules containing deuterium to provide a deuterium enriched dissociation product. The deuterium enriched product may be combusted with oxygen to provide deuterium enriched water. The deuterium depleted undissociated molecules may be redeuterated by treatment with a deuterium source such as water.

  8. The solubilities of significant organic compounds in HLW tank supernate solutions -- FY 1995 progress report

    SciTech Connect (OSTI)

    Barney, G.S.

    1996-04-26T23:59:59.000Z

    At the Hanford Site organic compounds were measured in tank supernate simulant solutions during FY 1995. This solubility information will be used to determine if these organic salts could exist in solid phases (saltcake or sludges) in the waste where they might react violently with the nitrate or nitrite salts present in the tanks. Solubilities of sodium glycolate, succinate, and caproate salts; iron and aluminum and butylphosphate salts; and aluminum oxalate were measured in simulated waste supernate solutions at 25 {degree}C, 30 {degree}C, 40 {degree}C, and 50 {degree}C. The organic compounds were selected because they are expected to exist in relatively high concentrations in the tanks. The solubilities of sodium glycolate, succinate, caproate, and butylphosphate in HLW tank supernate solutions were high over the temperature and sodium hydroxide concentration ranges expected in the tanks. High solubilities will prevent solid sodium salts of these organic acids from precipitating from tank supernate solutions. The total organic carbon concentrations (YOC) of actual tank supernates are generally much lower than the TOC ranges for simulated supernate solutions saturated (at the solubility limit) with the organic salts. This is so even if all the dissolved carbon in a given tank and supernate is due to only one of these eight soluble compounds (an unlikely situation). Metal ion complexes of and butylphosphate and oxalate in supernate solutions were not stable in the presence of the hydroxide concentrations expected in most tanks. Iron and aluminum dibutylphosphate compounds reacted with hydroxide to form soluble sodium dibutylphosphate and precipitated iron and aluminum hydroxides. Aluminum oxalate complexes were also not stable in the basic simulated supernate solutions. Solubilities of all the organic salts decrease with increasing sodium hydroxide concentration because of the common ion effect of Na+. Increasing temperatures raised the solubilities of the organic salts, especially the succinate and caproate salts.

  9. Rejection and fate of trace organic compounds (TrOCs) during membrane distillation

    E-Print Network [OSTI]

    Rejection and fate of trace organic compounds (TrOCs) during membrane distillation Kaushalya COCs) Direct contact membrane distillation (DCMD) Volatility Fate and transport Hydrophobicity/hydrophilicity a b s t r a c t In this study, we examined the feasibility of membrane distillation (MD) for removing

  10. Field Test to Demonstrate Real-Time In-Situ Detection of Volatile Organic Compounds

    E-Print Network [OSTI]

    Ho, Cliff

    1 Field Test to Demonstrate Real-Time In-Situ Detection of Volatile Organic Compounds Hazmat Spill Center, Nevada Test Site September 19-25, 2001 Clifford K. Ho Sandia National Laboratories Albuquerque-filled 55- gallon drum at the Hazmat Spill Center at the Nevada Test Site. Background and Objectives Tens

  11. Supporting Information1 Condensational Uptake of Semivolatile Organic Compounds in Gasoline3

    E-Print Network [OSTI]

    Meskhidze, Nicholas

    Supporting Information1 2 Condensational Uptake of Semivolatile Organic Compounds in Gasoline31A 0H3 Canada (now at Department of Chemistry,13 University of Christchurch, Canterbury 8041, New Zealand)14 15 For submission to Atmospheric Chemistry and Physics16 17 Revised Version: May 31, 201118 19

  12. Study of the VOC emissions from a municipal solid waste storage pilot-scale cell: Comparison with biogases from municipal waste landfill site

    SciTech Connect (OSTI)

    Chiriac, R., E-mail: rodica.chiriac@univ-lyon1.fr [Universite de Lyon, Universite Lyon 1, CNRS, UMR 5615, Laboratoire des Multimateriaux et Interfaces, 43 boulevard du 11 Novembre 1918, F-69622 Villeurbanne (France); De Araujos Morais, J. [Universite Federal de Paraiba, Campus I Departamento de Engenharia Civil e Ambiental, Joao Pessoa, Paraiba (Brazil); Carre, J. [Universite de Lyon, Universite Lyon 1, CNRS, UMR 5256, Institut de Recherche sur la Catalyse et l'Environnement, 43 boulevard du 11 Novembre 1918, F-69622 Villeurbanne (France); Bayard, R. [Universite de Lyon, INSA de Lyon, Laboratoire de Genie Civil et d'Ingenierie environnementale (LGCIE), F-69622 Villeurbanne (France); Chovelon, J.M. [Universite de Lyon, Universite Lyon 1, CNRS, UMR 5256, Institut de Recherche sur la Catalyse et l'Environnement, 43 boulevard du 11 Novembre 1918, F-69622 Villeurbanne (France); Gourdon, R. [Universite de Lyon, INSA de Lyon, Laboratoire de Genie Civil et d'Ingenierie environnementale (LGCIE), F-69622 Villeurbanne (France)

    2011-11-15T23:59:59.000Z

    Highlights: > Follow-up of the emission of VOCs in a municipal waste pilot-scale cell during the acidogenesis and acetogenesis phases. > Study from the very start of waste storage leading to a better understanding of the decomposition/degradation of waste. > Comparison of the results obtained on the pilot-scale cell with those from 3 biogases coming from the same landfill site. > A methodology of characterization for the progression of the stabilization/maturation of waste is finally proposed. - Abstract: The emission of volatile organic compounds (VOCs) from municipal solid waste stored in a pilot-scale cell containing 6.4 tonnes of waste (storage facility which is left open during the first period (40 days) and then closed with recirculation of leachates during a second period (100 days)) was followed by dynamic sampling on activated carbon and analysed by GC-MS after solvent extraction. This was done in order to know the VOC emissions before the installation of a methanogenesis process for the entire waste mass. The results, expressed in reference to toluene, were exploited during the whole study on all the analyzable VOCs: alcohols, ketones and esters, alkanes, benzenic and cyclic compounds, chlorinated compounds, terpene, and organic sulphides. The results of this study on the pilot-scale cell are then compared with those concerning three biogases from a municipal waste landfill: biogas (1) coming from waste cells being filled or recently closed, biogas (2) from all the waste storage cells on site, and biogas (3) which is a residual gas from old storage cells without aspiration of the gas. The analysis of the results obtained revealed: (i) a high emission of VOCs, principally alcohols, ketones and esters during the acidogenesis; (ii) a decrease in the alkane content and an increase in the terpene content were observed in the VOCs emitted during the production of methane; (iii) the production of heavier alkanes and an increase in the average number of carbon atoms per molecule of alkane with the progression of the stabilisation/maturation process were also observed. Previous studies have concentrated almost on the analysis of biogases from landfills. Our research aimed at gaining a more complete understanding of the decomposition/degradation of municipal solid waste by measuring the VOCs emitted from the very start of the landfill process i.e. during the acidogenesis and acetogenesis phases.

  13. Detection and Differentiation of Neutral Organic Compounds by [superscript 19]F NMR with a Tungsten Calix[4]arene Imido Complex

    E-Print Network [OSTI]

    Zhao, Yanchuan

    Fluorinated tungsten calix[4]arene imido complexes were synthesized and used as receptors to detect and differentiate neutral organic compounds. It was found that the binding of specific neutral organic molecules to the ...

  14. COMPOSITING WATER SAMPLES FOR ANALYSIS OF VOLATILE ORGANIC COMPOUNDS Thomas J. Lopes1

    E-Print Network [OSTI]

    in conjunction with chemical analysis by a conventional laboratory, field-portable equipment, or a mobile, 1998). However, automatic VOC samplers are expensive, sometimes have uncertain reliability, and may

  15. Laboratory and field investigation of the adsorption of gaseous organic compounds onto quartz filters

    SciTech Connect (OSTI)

    Kirchstetter, Thomas W.; Corrigan, Craig E.; Novakov, T.

    2000-07-01T23:59:59.000Z

    A common method for measuring the mass of organic carbon in airborne particulate matter involves collection on a quartz filter and subsequent thermal analysis. If unaccounted for, the adsorption of organic gases onto quartz filters will lead to the overestimation of aerosol organic carbon concentrations (positive artifact). A recommended method of correction for the positive artifact involves sampling with a backup filter. Placed behind either the primary quartz filter, or behind a Teflon filter and collected in parallel with the primary quartz filter, the carbon content of the quartz backup filter is a measure of the adsorbed organic material on the primary quartz filter. In this paper, we illustrate the application of this technique to samples collected in Berkeley, California. While the tandem quartz filter method can be successfully applied to correct for the positive artifact, we discuss two cases when this method will fail. We have found that the capacity for adsorption of organic gases is not uniform for all filters. Instead, filters manufactured by the same company, but having different lot numbers, exhibit variable adsorption capacity. Thus, a filter pair composed of filters from different lots may lead to significant under- or overestimation of particulate organic carbon concentration. Additionally, we have observed that the tandem filter method under-corrects for the positive artifact if the sampling time is short (few hours). Laboratory experiments with vapors of single organic compounds corroborate results based on ambient samples. The evolution of adsorbed organic gases, particularly polar compounds, during thermal analysis indicates that a single compound may experience two distinct adsorbent-adsorbate binding energies. Adsorbed gases may co-evolve with particles at temperatures in excess of 250-degree C.

  16. Process for the solvent extraction for the radiolysis and dehalogenation of halogenated organic compounds in soils, sludges, sediments and slurries

    DOE Patents [OSTI]

    Golden, Jeffry

    2007-02-13T23:59:59.000Z

    A process of extracting halogenated organic compounds, and particularly PCBs, from soil, sediment, slurry, sludge and dehalogenating the compounds contacts a contaminated soil sample with an extraction medium of a mixture of an alkane and a water miscible alcohol. The organic compounds dissolve in the extraction medium which is separated from the soil by passing water upwardly through the soil. The extraction medium floats to the surface of the water and is separated. Thereafter, the extraction medium containing the halogenated organic contaminants is subjected to ionizing radiation to radiolytically dehalogenate the compounds.

  17. Process for the solvent extraction for the radiolysis and dehalogenation of halogenated organic compounds in soils, sludges, sediments and slurries

    DOE Patents [OSTI]

    Mincher, Bruce J. (3705 Creekside Dr., Idaho Falls, ID 83404); Curry, Randy Dale (1104 Merrill Ct., Columbia, MO 65203); Clevenger, Thomas E. (2512 Bluff Blvd., Columbia, MO 65201); Golden, Jeffry (12612 Cedarbrook La., Laurel, MD 20708)

    2000-01-01T23:59:59.000Z

    A process of extracting halogenated organic compounds, and particularly PCBs, from soil, sediment, slurry, sludge and dehalogenating the compounds contacting a contaminated soil sample with an extraction medium of a mixture of an alkane and a water miscible alcohol. The organic compounds dissolve in the extraction medium which is separated from the soil by passing water upwardly through the soil. The extraction medium floats to the surface of the water and is separated. Thereafter, the extraction medium containing the halogenated organic contaminants is subjected to ionizing radiation to radiolytically dehalogenate the compounds.

  18. Process for the solvent extraction for the radiolysis and dehalogenation of halogenated organic compounds in soils, sludges, sediments and slurries

    DOE Patents [OSTI]

    Mincher, Bruce J.; Curry, Randy Dale; Clevenger, Thomas E.; Golden, Jeffry

    2003-05-27T23:59:59.000Z

    A process of extracting halogenated organic compounds, and particularly PCBs, from soil, sediment, slurry, sludge and dehalogenating the compounds contacts a contaminated soil sample with an extraction medium of a mixture of an alkane and a water miscible alcohol. The organic compounds dissolve in the extraction medium which is separated from the soil by passing water upwardly through the soil. The extraction medium floats to the surface of the water and is separated. Thereafter, the extraction medium containing the halogenated organic contaminants is subjected to ionizing radiation to radiolytically dehalogenate the compounds.

  19. Cancer risks from soil emissions of volatile organic compounds at the Lawrence Livermore National Laboratory

    SciTech Connect (OSTI)

    Dibley, V. R., LLNL

    1998-02-01T23:59:59.000Z

    The emission isolation flux chamber (EIFC) methodology was applied to Superfund investigations at the Lawrence Livermore National Laboratory Site 300 to determine if on-site workers were exposed to VOCs volatilizing from the subsurface and what, if any, health risks could be attributed to the inhalation of the VOCs volatilizing from the subsurface. During July and August of 1996, twenty, eighteen, and twenty six VOC soil vapor flux samples were collected in the Building 830, 832, and 854 areas, respectively using EIFCS. The VOC concentrations in the vapor samples were used to calculate soil flux rates which were used as input into an air dispersion model to calculate ambient air exposure-point concentrations. The exposure-point concentrations were compared to EPA Region IX Preliminary Remediation Goals (PRGs). Buildings 830 and 832 exposure-point concentrations were less then the PRGs therefore no cancer risks were calculated. The cancer risks for Building 854 ranged from 1.6 x 10{sup -7} to 2.1 x 10{sup -6}. The resultant inhalation cancer risks were all within the acceptable range, implying that on-site workers were not exposed to VOC vapors volatilizing from the subsurface soil that could have significant cancer risks. Therefore remediation in these areas would not be necessary.

  20. Integrated production of fuel gas and oxygenated organic compounds from synthesis gas

    DOE Patents [OSTI]

    Moore, Robert B. (Allentown, PA); Hegarty, William P. (State College, PA); Studer, David W. (Wescosville, PA); Tirados, Edward J. (Easton, PA)

    1995-01-01T23:59:59.000Z

    An oxygenated organic liquid product and a fuel gas are produced from a portion of synthesis gas comprising hydrogen, carbon monoxide, carbon dioxide, and sulfur-containing compounds in a integrated feed treatment and catalytic reaction system. To prevent catalyst poisoning, the sulfur-containing compounds in the reactor feed are absorbed in a liquid comprising the reactor product, and the resulting sulfur-containing liquid is regenerated by stripping with untreated synthesis gas from the reactor. Stripping offgas is combined with the remaining synthesis gas to provide a fuel gas product. A portion of the regenerated liquid is used as makeup to the absorber and the remainder is withdrawn as a liquid product. The method is particularly useful for integration with a combined cycle coal gasification system utilizing a gas turbine for electric power generation.

  1. Photochemical aging of volatile organic compounds in the Los Angeles basin: Weekday-weekend effect

    E-Print Network [OSTI]

    Cohen, Ronald C.

    in ozone, caused by lower NOx emissions due to reduced diesel truck traffic in the weekends, has been previously observed in Los Angeles and other cities. Measurements in the Caldecott tunnel show that emission nonattainment area. [3] In the LA basin the main emission sources for the ozone precursors VOCs and NOx (NO + NO

  2. Thermodynamics and kinetics of hydrophobic organic compound sorption in natural sorbents and quantification of black carbon by electron microscopy

    E-Print Network [OSTI]

    Kuo, Dave Ta Fu, 1978-

    2010-01-01T23:59:59.000Z

    The sorption behaviors of hydrophobic organic compounds (HOCs) in sediments were investigated using pyrene. Native pyrene desorbed slowly, taking from weeks to months to equilibrate. The end-point data suggested that, at ...

  3. Online measurements of the emissions of intermediate-volatility and semi-volatile organic compounds from aircraft

    E-Print Network [OSTI]

    Herndon, S. C.

    A detailed understanding of the climate and air quality impacts of aviation requires measurements of the emissions of intermediate-volatility and semi-volatile organic compounds (I/SVOCs) from aircraft. Currently both the ...

  4. 4, 66916718, 2004 VOC emissions of

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    ACPD 4, 6691­6718, 2004 VOC emissions of Scots pine V. Tarvainen et al. Title Page Abstract Discussions Temperature and light dependence of the VOC emissions of Scots pine V. Tarvainen 1 , H. Hakola 1.tarvainen@fmi.fi) 6691 #12;ACPD 4, 6691­6718, 2004 VOC emissions of Scots pine V. Tarvainen et al. Title Page Abstract

  5. The development of a sensitive method to study volatile organic compounds in gaseous emissions of lung cancer cell lines

    E-Print Network [OSTI]

    Maroly, Anupam

    2005-08-29T23:59:59.000Z

    THE DEVELOPMENT OF A SENSITIVE METHOD TO STUDY VOLATILE ORGANIC COMPOUNDS IN GASEOUS EMISSIONS OF LUNG CANCER CELL LINES A Thesis by ANUPAM MAROLY Submitted to the Office of Graduate Studies of Texas A&M University in partial... fulfillment of the requirements for the degree of MASTER OF SCIENCE May 2005 Major Subject: Biomedical Engineering THE DEVELOPMENT OF A SENSITIVE METHOD TO STUDY VOLATILE ORGANIC COMPOUNDS IN GASEOUS EMISSIONS OF LUNG CANCER CELL...

  6. Supercritical CO2 extraction of organic compounds from soil-water slurries

    E-Print Network [OSTI]

    Carter, Brian Dean

    1993-01-01T23:59:59.000Z

    , the characteristics of SCFs may This thesis is presented in the style and fromat of the A1ChE Journal. be altered to fit a specific need. Solvent regeneration can be achieved in one of two ways. One method is to flow the saturated SCF over an adsorbent bed... the contaminants were physically adsorbed onto soil or if there was a possibility that chemical adsorption was prominent. Isotherms for organic compounds on soil are often linear. In which case, the partition coefficients are simply the slope of the isotherms...

  7. Electrocatalytic Materials and Techniques for the Anodic Oxidation of Various Organic Compounds

    SciTech Connect (OSTI)

    Stephen Everett Treimer

    2002-06-27T23:59:59.000Z

    The focus of this thesis was first to characterize and improve the applicability of Fe(III) and Bi(V) doped PbO{sub 2} film electrodes for use in anodic O-transfer reactions of toxic and waste organic compounds, e.g. phenol, aniline, benzene, and naphthalene. Further, they investigated the use of alternative solution/electrode interfacial excitation techniques to enhance the performance of these electrodes for remediation and electrosynthetic applications. Finally, they have attempted to identify a less toxic metal oxide film that may hold promise for future studies in the electrocatalysis and photoelectrocatalysis of O-transfer reactions using metal oxide film electrodes.

  8. Pilot scale test of a produced water-treatment system for initial removal of organic compounds

    SciTech Connect (OSTI)

    Sullivan, Enid J [Los Alamos National Laboratory; Kwon, Soondong [UT-AUSTIN; Katz, Lynn [UT-AUSTIN; Kinney, Kerry [UT-AUSTIN

    2008-01-01T23:59:59.000Z

    A pilot-scale test to remove polar and non-polar organics from produced water was performed at a disposal facility in Farmington NM. We used surfactant-modified zeolite (SMZ) adsorbent beds and a membrane bioreactor (MBR) in combination to reduce the organic carbon content of produced water prior to reverse osmosis (RO). Reduction of total influent organic carbon (TOC) to 5 mg/L or less is desirable for efficient RO system operation. Most water disposed at the facility is from coal-bed gas production, with oil production waters intermixed. Up to 20 gal/d of produced water was cycled through two SMZ adsorbent units to remove volatile organic compounds (BTEX, acetone) and semivolatile organic compounds (e.g., napthalene). Output water from the SMZ units was sent to the MBR for removal of the organic acid component of TOC. Removal of inorganic (Mn and Fe oxide) particulates by the SMZ system was observed. The SMZ columns removed up to 40% of the influent TOC (600 mg/L). BTEX concentrations were reduced from the initial input of 70 mg/L to 5 mg/L by the SMZ and to an average of 2 mg/L after the MBR. Removal rates of acetate (input 120-170 mg/L) and TOC (input up to 45 mg/L) were up to 100% and 92%, respectively. The water pH rose from 8.5 to 8.8 following organic acid removal in the MBR; this relatively high pH was likely responsible for observed scaling of the MBR internal membrane. Additional laboratory studies showed the scaling can be reduced by metered addition of acid to reduce the pH. Significantly, organic removal in the MBR was accomplished with a very low biomass concentration of 1 g/L throughout the field trial. An earlier engineering evaluation shows produced water treatment by the SMZ/MBR/RO system would cost from $0.13 to $0.20 per bbl at up to 40 gpm. Current estimated disposal costs for produced water are $1.75 to $4.91 per bbl when transportation costs are included, with even higher rates in some regions. Our results suggest that treatment by an SMZ/MBR/RO system may be a feasible alternative to current methods for produced water treatment and disposal.

  9. Determination of iodine in organic compounds using low-temperature ammoniacal plasma of high-frequency discharge

    SciTech Connect (OSTI)

    Volodina, M.A.; Kutseva, N.K.

    1986-09-01T23:59:59.000Z

    This paper presents a method for the determination of iodine in organic compounds, based on the use of a low-temperature ammonial plasma of an electrodeless high frequency discharge. The method was tested on a large number of compounds, and is distinguished by simplicity of operation, rapidity, accuracy and applicability for simultaneous determination of iodine and palladium. The results of the simultaneous determination of iodine and palladium in organic compounds are shown. The relative standard deviation does not exceed 0.011. The duration of each determination is 15-20 min.

  10. Chemical oxidation of volatile and semi-volatile organic compounds in soil

    SciTech Connect (OSTI)

    Gates, D.D.; Siegrist, R.L.; Cline, S.R.

    1995-06-01T23:59:59.000Z

    Subsurface contamination with fuel hydrocarbons or chlorinated hydrocarbons is prevalent throughout the Department of Energy (DOE) complex and in many sites managed by the Environmental Protection Agency (EPA) Superfund program. The most commonly reported chlorinated hydrocarbons (occurring > 50% of DOE contaminated sites) were trichloroethylene (TCE), 1, 1, 1,-trichloroethane (TCA), and tetrachloroethylene (PCE) with concentrations in the range of 0.2 {mu}g/kg to 12,000 mg/kg. The fuel hydrocarbons most frequently reported as being present at DOE sites include aromatic compounds and polyaromatic compounds such as phenanthrene, pyrene, and naphthalene. The primary sources of these semi-volatile organic compounds (SVOCs) are coal waste from coal fired electric power plants used at many of these facilities in the past and gasoline spills and leaks. Dense non-aqueous phase liquids (DNAPLs) can migrate within the subsurface for long periods of time along a variety of pathways including fractures, macropores, and micropores. Diffusion of contaminants in the non-aqueous, aqueous, and vapor phase can occur from the fractures and macropores into the matrix of fine-textured media. As a result of these contamination processes, removal of contaminants from the subsurface and the delivery of treatment agents into and throughout contaminated regions are often hindered, making rapid and extensive remediation difficult.

  11. Geobacter strains that use alternate organic compounds, methods of making, and methods of use thereof

    DOE Patents [OSTI]

    Lovley, Derek R; Summers, Zarath Morgan; Haveman, Shelley Annette; Izallalen, Mounir

    2013-12-03T23:59:59.000Z

    In preferred embodiments, the present invention provides new isolated strains of Geobacter species that are capable of using a carbon source that is selected from C.sub.3 to C.sub.12 organic compounds selected from pyruvate or metabolic precursors of pyruvate as an electron donor in metabolism and in subsequent energy production. In other aspects, other preferred embodiments of the present invention include methods of making such strains and methods of using such strains. In general, the wild type strain of the microorganisms has been shown to be unable to use these C.sub.3 to C.sub.12 organic compounds as electron donors in metabolic steps such as the reduction of metallic ions. The inventive strains of microorganisms are useful improving bioremediation applications, including in situ bioremediation (including uranium bioremediation and halogenated solvent bioremediation), microbial fuel cells, power generation from small and large-scale waste facilities (e.g., biomass waste from dairy, agriculture, food processing, brewery, or vintner industries, etc.) using microbial fuel cells, and other applications of microbial fuel cells, including, but not limited to, improved electrical power supplies for environmental sensors, electronic sensors, and electric vehicles.

  12. Capillary electrophoresis separation of neutral organic compounds, pharmaceutical drugs, proteins and peptides, enantiomers, and anions

    SciTech Connect (OSTI)

    Ding, W.L.

    1999-02-12T23:59:59.000Z

    Addition of a novel anionic surfactant, namely lauryl polyoxyethylene sulfate, to an aqueous-acetonitrile electrolyte makes it possible to separate nonionic organic compounds by capillary electrophoresis. Separation is based on differences in the association between analytes and the surfactant. Highly hydrophobic compounds such as polyaromatic hydrocarbons are well separated by this new surfactant. Migration times of analytes can be readily changed over an unusually large range by varying the additive concentration and the proportion of acetonitrile in the electrolyte. Several examples are given, including the separation of four methylbenz[a]anthracene isomers and the separation of normal and deuterated acetophenone. The effect of adding this new surfactant to the acidic electrolyte was also investigated. Incorporation of cetyltrimethylammonium bromide in the electrolyte is shown to dynamically coat the capillary and reverse electroosmotic flow. Chiral recognition mechanism is studied using novel synthetic surfactants as chiral selectors, which are made from amino acids reacting with alkyl chloroformates. A satisfactory separation of both inorganic and organic anions is obtained using electrolyte solutions as high as 5 M sodium chloride using direct photometric detection. The effect of various salts on electrophoretic and electroosmotic mobility is further discussed. Several examples are given under high-salt conditions.

  13. Plasmas and Polymers, Vol. 5, Nos. 3/4, 2000 Synthesis of Organic Compounds from Mixtures of

    E-Print Network [OSTI]

    Greifswald, Ernst-Moritz-Arndt-Universität

    Plasmas and Polymers, Vol. 5, Nos. 3/4, 2000 Synthesis of Organic Compounds from Mixtures operation, due to surface modification processes (polymer film deposition, its oxidation or reduction gases; polymer films; dielectric-barrier discharge; organic synthesis. 1. INTRODUCTION The first

  14. Skin: Major target organ of allergic reactions to small molecular weight compounds

    SciTech Connect (OSTI)

    Merk, Hans F. [Department of Dermatology and Allergology, Univ.-Hospital, RWTH Aachen, Pauwelsstr. 30, D-52074 Aachen (Germany)], E-mail: hans.merk@post.rwth-aachen.de; Baron, Jens M.; Neis, Mark M.; Obrigkeit, Daniela Hoeller [Department of Dermatology and Allergology, Univ.-Hospital, RWTH Aachen, Pauwelsstr. 30, D-52074 Aachen (Germany); Karlberg, Ann-Therese [Dermatochemistry and Skin Allergy, Department of Chemistry, Goeteborg University, SE-412 96 Goeteborg (Sweden)

    2007-11-01T23:59:59.000Z

    Skin is a major target organ for allergic reactions to small molecular weight compounds. Drug allergic reactions may be life-threatening such as in the case of anaphylactic reactions or bullous drug reactions and occur in about 5% of all hospitalized patients. Allergic contact dermatitis has an enormous influence on the social life of the patient because it is the most frequent reason for occupational skin diseases and the treatment and prevention of this disease cost approximately Euro 3 billion per year in Germany. The different proposed pathophysiological pathways leading to a drug eruption are discussed in this paper. All major enzymes which are involved in the metabolism of xenobiotica were shown to be present in skin. Evidence supporting the role of metabolism in the development of drug allergy and allergic contact dermatitis is demonstrated in the example of sulphonamides and fragrances.

  15. Levels of nonpolar organic compounds in the Columbia Generating Station cooling pond. Technical completion report

    SciTech Connect (OSTI)

    Andren, A.W.; Erickson, R.

    1983-01-01T23:59:59.000Z

    In 1970, plans to build a coal-fired generating station near Portage, Wisconsin and an interest by involved utilities in carrying out a preconstruction analysis of potential environmental changes created a unique opportunity for broadly based research on the impacts of coal-fired steam plants. Of particular concern to aquatic scientists are the potential problems associated with the 192-ha manmade cooling pond. The research presented in this report describes a survey of the types and levels of nonpolar xenobiotic organic compounds in sediments and fish from the cooling pond. Sediment and fish samples were analyzed for PCBs, Sigma DDT, and hexachlorobenzene using techniques developed at the Water Chemistry Laboratory, University of Wisconsin-Madison. It was hypothesized that polyaromatic hydrocarbons and chlorinated hydrocarbons would accumulate; however, results indicate that the microcontaminants do not concentrate in the cooling pond. Reasons for why there is no microcontaminant problem are presented.

  16. Technology status report: Off-gas treatment technologies for chlorinated volatile organic compound air emissions

    SciTech Connect (OSTI)

    Rossabi, J.; Haselow, J.S.

    1992-04-15T23:59:59.000Z

    The purpose of this document is to review technologies for treatment of air streams that contain chlorinated volatile organic compounds (CVOCS) and to describe a Department of Energy Office of Technology Development program that is planned to demonstrate innovative technologies for the abatement of CVOC emissions. This report describes the first phase of testing of off-gas treatment technologies. At least one more phase of testing is planned. Guidance for the preparation of this document was provided by a predecisional draft outline issued by the Department of Energy's Office of Technology Development. The report is intended to evaluate the technical and regulatory aspects, public acceptance, and estimated costs of technologies selected for development and testing. These technologies are compared to currently practiced or baseline methods for treatment of CVOC-laden airstreams. A brief overview is provided rather than detailed cost and data comparisons because many of these technologies have not yet been field tested. A description of other promising technologies for the treatment of CVOC emissions is also included. Trichloroethylene (TCE) and perchloroethylene (PCE) were used for industrial cleaning and solvent applications for several decades. These chemicals can be classified as CVOCS. As a result of past standard disposal practices, these types of compounds are persistent groundwater and soil contaminants throughout the United States and the Department of Energy Complex.

  17. Technology status report: Off-gas treatment technologies for chlorinated volatile organic compound air emissions

    SciTech Connect (OSTI)

    Rossabi, J.; Haselow, J.S.

    1992-04-15T23:59:59.000Z

    The purpose of this document is to review technologies for treatment of air streams that contain chlorinated volatile organic compounds (CVOCS) and to describe a Department of Energy Office of Technology Development program that is planned to demonstrate innovative technologies for the abatement of CVOC emissions. This report describes the first phase of testing of off-gas treatment technologies. At least one more phase of testing is planned. Guidance for the preparation of this document was provided by a predecisional draft outline issued by the Department of Energy`s Office of Technology Development. The report is intended to evaluate the technical and regulatory aspects, public acceptance, and estimated costs of technologies selected for development and testing. These technologies are compared to currently practiced or baseline methods for treatment of CVOC-laden airstreams. A brief overview is provided rather than detailed cost and data comparisons because many of these technologies have not yet been field tested. A description of other promising technologies for the treatment of CVOC emissions is also included. Trichloroethylene (TCE) and perchloroethylene (PCE) were used for industrial cleaning and solvent applications for several decades. These chemicals can be classified as CVOCS. As a result of past standard disposal practices, these types of compounds are persistent groundwater and soil contaminants throughout the United States and the Department of Energy Complex.

  18. Recent VOC Control Test Data for a Reactive VOC Converter- Scrubber System for Non-Thermal Control of VOCs

    E-Print Network [OSTI]

    McGinness, M.

    by their very nature represent a reduced fire hazard compared to dry filter booth systems. NFPA (National Fire Protection Agency) fire safety codes require the use of fire suppression automatic sprinklers on dry filter booths but not on water wash booths...Recent VOC Control Test Data for a Reactive VOC Converter Scrubber System for Non-Thermal Control of VOCs Mike McGinness VP-R&D EcoShield Environmental Systems, Inc. Houston, Texas ABSTRACT HAP (Hazardous Air Pollutant) and VOC (Volatile...

  19. A Pilot Study of the Effectiveness of Indoor Plants for Removal of Volatile Organic Compounds in Indoor Air in a Seven-Story Office Building

    SciTech Connect (OSTI)

    Apte, Michael G.; Apte, Joshua S.

    2010-04-27T23:59:59.000Z

    The Paharpur Business Centre and Software Technology Incubator Park (PBC) is a 7 story, 50,400 ft{sup 2} office building located near Nehru Place in New Delhi India. The occupancy of the building at full normal operations is about 500 people. The building management philosophy embodies innovation in energy efficiency while providing full service and a comfortable, safe, healthy environment to the occupants. Provision of excellent Indoor Air Quality (IAQ) is an expressed goal of the facility, and the management has gone to great lengths to achieve it. This is particularly challenging in New Delhi, where ambient urban pollution levels rank among the worst on the planet. The approach to provide good IAQ in the building includes a range of technical elements: air washing and filtration of ventilation intake air from rooftop air handler, the use of an enclosed rooftop greenhouse with a high density of potted plants as a bio-filtration system, dedicated secondary HVAC/air handling units on each floor with re-circulating high efficiency filtration and UVC treatment of the heat exchanger coils, additional potted plants for bio-filtration on each floor, and a final exhaust via the restrooms located at each floor. The conditioned building exhaust air is passed through an energy recovery wheel and chemisorbent cartridge, transferring some heat to the incoming air to increase the HVAC energy efficiency. The management uses 'green' cleaning products exclusively in the building. Flooring is a combination of stone, tile and 'zero VOC' carpeting. Wood trim and finish appears to be primarily of solid sawn materials, with very little evidence of composite wood products. Furniture is likewise in large proportion constructed from solid wood materials. The overall impression is that of a very clean and well-kept facility. Surfaces are polished to a high sheen, probably with wax products. There was an odor of urinal cake in the restrooms. Smoking is not allowed in the building. The plants used in the rooftop greenhouse and on the floors were made up of a number of species selected for the following functions: daytime metabolic carbon dioxide (CO{sub 2}) absorption, nighttime metabolic CO{sub 2} absorption, and volatile organic compound (VOC) and inorganic gas absorption/removal for air cleaning. The building contains a reported 910 indoor plants. Daytime metabolic species reported by the PBC include Areca Palm, Oxycardium, Rubber Plant, and Ficus alii totaling 188 plants (21%). The single nighttime metabolic species is the Sansevieria with a total of 28 plants (3%). The 'air cleaning' plant species reported by the PBC include the Money Plant, Aglaonema, Dracaena Warneckii, Bamboo Palm, and Raphis Palm with a total of 694 plants (76%). The plants in the greenhouse (Areca Palm, Rubber Plant, Ficus alii, Bamboo Palm, and Raphis Palm) numbering 161 (18%) of those in the building are grown hydroponically, with the room air blown by fan across the plant root zones. The plants on the building floors are grown in pots and are located on floors 1-6. We conducted a one-day monitoring session in the PBC on January 1, 2010. The date of the study was based on availability of the measurement equipment that the researchers had shipped from Lawrence Berkeley National Lab in the U.S.A. The study date was not optimal because a large proportion of the regular building occupants were not present being New Year's Day. An estimated 40 people were present in the building all day during January 1. This being said, the building systems were in normal operations, including the air handlers and other HVAC components. The study was focused primarily on measurements in the Greenhouse and 3rd and 5th floor environments as well as rooftop outdoors. Measurements included a set of volatile organic compounds (VOCs) and aldehydes, with a more limited set of observations of indoor and outdoor particulate and carbon dioxide concentrations. Continuous measurements of Temperature (T) and relative humidity (RH) were made selected indoor and outdoor locations.

  20. Field evaluation of ground water sampling devices for volatile organic compounds

    SciTech Connect (OSTI)

    Muska, C F; Colven, W P; Jones, V D; Scogin, J T; Looney, B B; Price, V Jr

    1986-01-01T23:59:59.000Z

    Previous studies conducted under laboratory conditions demonstrated that the type of device used to sample ground water contaminated with volatile organic compounds can significantly influence and analytical results. The purpose of this study was to evaluate, under field conditions, both commercial and developmental ground water sampling devices as part of an ongoing ground water contamination investigation and remediation program at the Savannah River Plant (SRP). Ground water samples were collected using six types of sampling devices in monitoring wells of different depths and concentrations of volatile organic contaminants (primarily trichloroethylene and tetrachloroethylene). The study matrix was designed to statistically compare the reuslts of each sampling device under the test conditions. Quantitative and qualitative evaluation criteria were used to determine the relative performance of each device. Two categories of sampling devices were evaluated in this field study, positive displacement pumps and grab samplers. The positive displacement pumps consisted of a centrifugal (mechanical) pump and a bladder pump. The grab samples tested were a syringe sampler, a dual-check valve bailer, a surface bomb sampler, and a pressurized bailer. Preliminary studies were conducted to establish the analytical and sampling variability associated with each device. All six devices were then used to collect ground water samples in water table (unconfined), semi-confined aquifer, and confined aquifer monitoring wells. Results were evaluated against a set of criteria that included intrasampling device variability (precision), volatile organic concentration (accuracy), sampling and analytical logistics, and cost. The study showed that, by using careful and reproducible procedures, overall sampling variability is low regardless of sampling device.

  1. SPECIATION OF TRACE ORGANIC LIGANDS AND INORGANIC AND ORGANOMETALLIC COMPOUNDS IN OIL SHALE PROCESS WATERS

    E-Print Network [OSTI]

    Fish, Richard H.

    2013-01-01T23:59:59.000Z

    organoarsenic compounds in oi.l shale process waters using aPresented at the 13th Oil Shale Symposium, Golden, CO, April~1ETALLIC COMPOUNDS IN OIL SHALE PROCESS WATERS Richard H.

  2. SPECIATION OF TRACE ORGANIC LIGANDS AND INORGANIC AND ORGANOMETALLIC COMPOUNDS IN OIL SHALE PROCESS WATERS

    E-Print Network [OSTI]

    Fish, Richard H.

    2013-01-01T23:59:59.000Z

    Presented at the 13th Oil Shale Symposium, Golden, CO, April~1ETALLIC COMPOUNDS IN OIL SHALE PROCESS WATERS Richard H.compounds in the seven oil shale process waters. These

  3. Petroporphyrins The most abundant and problematic metal compounds in crude oil exist as organic complexes of vanadium

    E-Print Network [OSTI]

    McQuade, D. Tyler

    Petroporphyrins ­The most abundant and problematic metal compounds in crude oil exist as organic of porphyrins is critical for developing petroleum upgrading processes, as well as linking crude oil to source routine analytical techniques due to the increased complexity associated with heavy crudes. Atmospheric

  4. An Exploratory Investigation of Polar Organic Compounds in Waters from a LeadZinc Mine and Mill Complex

    E-Print Network [OSTI]

    in southern Missouri. Lead­zinc mining and mineral extraction in the New Lead Belt generate large possible organic compounds coming from the milling process. Water samples contained rela- tively high, implying a lack of naturally occurring aquatic humic or fulvic acids. Samples were extracted by three

  5. Response threshold levels of selected organic compounds for rainbow trout (Oncorhynchus mykiss)

    SciTech Connect (OSTI)

    Kaiser, K.L.E.; McKinnon, M.B. [National Water Research Inst., Burlington, Ontario (Canada); Stendahl, D.H.; Pett, W.B. [Regional Municipality of Waterloo, Kitchener, Ontario (Canada)

    1995-12-01T23:59:59.000Z

    The responses of 27 organic compounds, mainly chloromethanes, -ethanes, -ethenes, and -phenols, were investigated by exposing rainbow trout fingerlings to low microgram-per-liter concentrations in a darkened flow-through system for up to 1 h. Responses by the fish were followed continuously by observing ventilation rates (frequency and amplitude), swimming patterns, and general activity using the low-voltage electric fields generated by the fishes` activity. The lowest level of response was found for trichloroethylene at 5 {micro}g/L. Dichloromethane, 1,1- and 1,2-dichloroethane, 1,1,1- and 1,1,2-trichloroethane, cis-1,2-dichloroethylene, 1,3-dichloropropene, and allyl acetate were responded to at concentrations of 10 {micro}g/L, carbon tetrachloride at 15 {micro}g/L, and 4-chlorophenol and 2,4-dichlorophenol at levels of 30 {micro}g/L. Unsubstituted phenol was not responded to at levels of up to 50 {micro}g/L.

  6. Source profiles for nonmethane organic compounds in the atmosphere of Cairo, Egypt.

    SciTech Connect (OSTI)

    Doskey, P. V.; Fukui, Y.; Sultan, M.; Maghraby, A. A.; Taher, A.; Environmental Research; Cairo Univ.

    1999-07-01T23:59:59.000Z

    Profiles of the sources of nonmethane organic compounds (NMOCs) were developed for emissions from vehicles, petroleum fuels (gasoline, liquefied petroleum gas (LPG), and natural gas), a petroleum refinery, a smelter, and a cast iron factory in Cairo, Egypt. More than 100 hydrocarbons and oxygenated hydrocarbons were tentatively identified and quantified. Gasoline-vapor and whole-gasoline profiles could be distinguished from the other profiles by high concentrations of the C{sub 5} and C{sub 6} saturated hydrocarbons. The vehicle emission profile was similar to the whole-gasoline profile, with the exception of the unsaturated and aromatic hydrocarbons, which were present at higher concentrations in the vehicle emission profile. High levels of the C{sub 2}-C{sub 4} saturated hydrocarbons, particularly n-butane, were characteristic features of the petroleum refinery emissions. The smelter and cast iron factory emissions were similar to the refinery emissions; however, the levels of benzene and toluene were greater in the former two sources. The LPG and natural gas emissions contained high concentrations of n-butane and ethane, respectively. The NMOC source profiles for Cairo were distinctly different from profiles for U.S. sources, indicating that NMOC source profiles are sensitive to the particular composition of petroleum fuels that are used in a location.

  7. Evaluation of a gas chromatograph with a novel surface acoustic wave detector (SAW GC) for screening of volatile organic compounds in Hanford waste tank samples

    SciTech Connect (OSTI)

    Lockrem, L.L.

    1998-01-12T23:59:59.000Z

    A novel instrument, a gas chromatograph with a Surface Acoustic Wave Detector (SAW GC), was evaluated for the screening of organic compounds in Hanford tank headspace vapors. Calibration data were developed for the most common organic compounds, and the accuracy and precision were measured with a certified standard. The instrument was tested with headspace samples collected from seven Hanford waste tanks.

  8. E-Print Network 3.0 - aromatic organic compounds Sample Search...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    aromatic compounds. 500 265 500 265 500 265 WAVELENGTH (nm) ARABIAN CRUDE LUBRICATING OIL... . 271 12;Although the spectra only give a qualitative analysis of the major types...

  9. Atmospheric outflow of anthropogenic semivolatile organic compounds from East Asia in Spring 2004

    SciTech Connect (OSTI)

    Toby Primbs; Staci Simonich; David Schmedding; Glenn Wilson; Dan Jaffe; Akinori Takami; Shungo Kato; Shiro Hatakeyama; Yoshizumi Kajii [Oregon State University, Corvallis, OR (United States). Departments of Chemistry and Environmental and Molecular Toxicology

    2007-05-15T23:59:59.000Z

    To estimate the emissions of anthropogenic semivolatile organic compounds (SOCs) from East Asia and to identify unique SOC molecular markers in Asian air masses, high-volume air samples were collected on the island of Okinawa, Japan between 22 March and 2 May 2004. Contributions from different source regions (China, Japan, the Koreas, Russia, and ocean/local) were estimated by use of source region impact factors (SRIFs). Elevated concentrations of hexachlorobenzene (HCB), hexachlorcyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), and particulate-phase polycyclic aromatic hydrocarbons (PAHs) were attributed to air masses from China. A large proportion of the variation in the current-use pesticides, gas-phase PAHs, and polychlorinated biphenyl (PCB) concentrations was explained by meteorology. Chlordanes showed a technical mixture profile and similar concentrations regardless of source region. {alpha}/{gamma} HCH and trans/cis chlordane ratios did not vary significantly with different source regions and had regional averages of 2.5 {+-} 1.0 and 1.2 {+-} 0.3, respectively. Particulate-phase PAH concentrations were significantly correlated (p value {lt} 0.05) with other incomplete combustion byproduct concentrations, including elemental mercury (Hg{sup 0}), CO, NOx{asterisk}, black carbon, submicrometer aerosols, and SO{sub 2}. By use of measured PAH, CO, and black carbon concentrations and estimated CO and black carbon emission inventories, the emission of six carcinogenic particulate-phase PAHs was estimated to be 1518-4179 metric tons/year for Asia and 778-1728 metric tons/year for China, respectively. These results confirm that East Asian outflow contains significant emissions of carcinogenic particulate-phase PAHs. 39 refs., 3 figs.

  10. Cellular uptake of lipoproteins and persistent organic compounds-An update and new data

    SciTech Connect (OSTI)

    Hjelmborg, Philip Sebastian [Department of Environmental and Occupational medicine, Unit of Cellular and Molecular Toxicology, Institute of Public Health, University of Aarhus, Aarhus, Vennelyst Boulevard 6, Bygn 1260, 8000 Aarhus C, DK (Denmark); Andreassen, Thomas Kjaergaard [Institute of Medical Biochemistry, University of Aarhus, Aarhus (Denmark); Bonefeld-Jorgensen, Eva Cecilie [Department of Environmental and Occupational medicine, Unit of Cellular and Molecular Toxicology, Institute of Public Health, University of Aarhus, Aarhus, Vennelyst Boulevard 6, Bygn 1260, 8000 Aarhus C, DK (Denmark)], E-mail: ebj@mil.au.dk

    2008-10-15T23:59:59.000Z

    There are a number of interactions related to the transport of lipophilic xenobiotic compounds in the blood stream of mammals. This paper will focus on the interactions between lipoproteins and persistent organic pollutants (POPs) and how these particles are taken up by cells. A number of POPs including the pesticide p,p'-dichlorodiphenyltrichloroethane (DDT), and especially its metabolite p,p'-dichlorodiphenyldichloroethene (DDE), interacts with nuclear hormone receptors causing these to malfunction, which in turn results in a range of deleterious health effects in humans. The aim of the present study was to determine the role of lipoprotein receptors in mouse embryonic fibroblast (MEF) cells in conjunction with uptake of DDT-lipoprotein complexes from supplemented media in vitro. Uptake of DDT by MEF cells was investigated using MEF1 cells carrying the receptors low-density lipoprotein receptor-related protein (LRP) and low-density lipoprotein receptor (LDLR) present and MEF4 cells with no LRP and LDLR expression. Cells were incubated together with the complex of low-density lipoproteins (LDL) and [{sup 14}C]DDT. The receptor function was further evaluated by adding the 40 kDa receptor-associated protein (RAP) which blocks receptor activity. The results showed that [{sup 14}C]DDT uptake was decreasing when the LDL concentration was increasing. There was no strong evidence for a receptor-mediated uptake of the [{sup 14}C]DDT-lipoprotein complex. To conclude, DDT travels in the blood stream and can cross cell membranes while being transported as a DDT-lipoprotein complex. The lipoproteins do not need receptors to cross cell membranes since passive diffusion constitutes a major passageway.

  11. Chemiresistor microsensors for in-situ monitoring of volatile organic compounds : final LDRD report.

    SciTech Connect (OSTI)

    Thomas, Michael Loren; Hughes, Robert Clark; Kooser, Ara S.; McGrath, Lucas K.; Ho, Clifford Kuofei; Wright, Jerome L.; Davis, Chad Edward

    2003-09-01T23:59:59.000Z

    This report provides a summary of the three-year LDRD (Laboratory Directed Research and Development) project aimed at developing microchemical sensors for continuous, in-situ monitoring of volatile organic compounds. A chemiresistor sensor array was integrated with a unique, waterproof housing that allows the sensors to be operated in a variety of media including air, soil, and water. Numerous tests were performed to evaluate and improve the sensitivity, stability, and discriminatory capabilities of the chemiresistors. Field tests were conducted in California, Nevada, and New Mexico to further test and develop the sensors in actual environments within integrated monitoring systems. The field tests addressed issues regarding data acquisition, telemetry, power requirements, data processing, and other engineering requirements. Significant advances were made in the areas of polymer optimization, packaging, data analysis, discrimination, design, and information dissemination (e.g., real-time web posting of data; see www.sandia.gov/sensor). This project has stimulated significant interest among commercial and academic institutions. A CRADA (Cooperative Research and Development Agreement) was initiated in FY03 to investigate manufacturing methods, and a Work for Others contract was established between Sandia and Edwards Air Force Base for FY02-FY04. Funding was also obtained from DOE as part of their Advanced Monitoring Systems Initiative program from FY01 to FY03, and a DOE EMSP contract was awarded jointly to Sandia and INEEL for FY04-FY06. Contracts were also established for collaborative research with Brigham Young University to further evaluate, understand, and improve the performance of the chemiresistor sensors.

  12. The effect of mean cell residence time on the adsorbability of dissolved organic compounds found in petrochemical wastewaters

    E-Print Network [OSTI]

    Johnson, Timothy Loring

    1979-01-01T23:59:59.000Z

    , each with a different mean cell residence time, biologically treated the waste- water. Follow1ng biolog1cal treatment, the wastewater was subjected to activated carbon adsorption treatment. The Freundlich isotherm, non-adsorbable organic compound... residence time on adsorbability is the same for petrochemical wastewater as it is for municipal wastewater. The purpose of this thesis is to determine if the mean cell residence time in a biological treatment process can af'feet the ad- sorbability...

  13. VOC Destruction by Catalytic Combustion Microturbine

    SciTech Connect (OSTI)

    Tom Barton

    2009-03-10T23:59:59.000Z

    This project concerned the application of a catalytic combustion system that has been married to a micro-turbine device. The catalytic combustion system decomposes the VOC's and transmits these gases to the gas turbine. The turbine has been altered to operate on very low-level BTU fuels equivalent to 1.5% methane in air. The performance of the micro-turbine for VOC elimination has some flexibility with respect to operating conditions, and the system is adaptable to multiple industrial applications. The VOC source that was been chosen for examination was the emissions from coal upgrading operations. The overall goal of the project was to examine the effectiveness of a catalytic combustion based system for elimination of VOCs while simultaneously producing electrical power for local consumption. Project specific objectives included assessment of the feasibility for using a Flex-Microturbine that generates power from natural gas while it consumes VOCs generated from site operations; development of an engineering plan for installation of the Flex-Microturbine system; operation of the micro-turbine through various changes in site and operation conditions; measurement of the VOC destruction quantitatively; and determination of the required improvements for further studies. The micro-turbine with the catalytic bed worked effectively to produce power on levels of fuel much lower than the original turbine design. The ability of the device to add or subtract supplemental fuel to augment the amount of VOC's in the inlet air flow made the device an effective replacement for a traditional flare. Concerns about particulates in the inlet flow and the presence of high sulfur concentrations with the VOC mixtures was identified as a drawback with the current catalytic design. A new microturbine design was developed based on this research that incorporates a thermal oxidizer in place of the catalytic bed for applications where particulates or contamination would limit the lifetime of the catalytic bed.

  14. An Assessment of the Stability and the Potential for In-Situ Synthesis of Regulated Organic Compounds in High Level Radioactive Waste Stored at Hanford, Richland, Washington

    SciTech Connect (OSTI)

    Wiemers, K.D.; Babad, H.; Hallen, R.T.; Jackson, L.P.; Lerchen, M.E.

    1999-01-04T23:59:59.000Z

    The stability assessment examined 269 non-detected regulated compounds, first seeking literature references of the stability of the compounds, then evaluating each compound based upon the presence of functional groups using professional judgment. Compounds that could potentially survive for significant periods in the tanks (>1 year) were designated as stable. Most of the functional groups associated with the regulated organic compounds were considered unstable under tank waste conditions. The general exceptions with respect to functional group stability are some simple substituted aromatic and polycyclic aromatic compounds that resist oxidation and the multiple substituted aliphatic and aromatic halides that hydrolyze or dehydrohalogenate slowly under tank waste conditions. One-hundred and eighty-one (181) regulated, organic compounds were determined as likely unstable in the tank waste environment.

  15. Isotopic constraints on the sources and associations of organic compounds in marine sediments

    E-Print Network [OSTI]

    White, Helen K

    2006-01-01T23:59:59.000Z

    To provide a new perspective on the fate of both natural organic matter and hydrophobic organic contaminants (HOCs) in marine sediments, we have investigated the relationship between radiocarbon (14C) age and the different ...

  16. Carbon isotope ratios of organic compound fractions in oceanic suspended particles

    E-Print Network [OSTI]

    Hwang, Jeomshik; Druffel, Ellen R. M

    2006-01-01T23:59:59.000Z

    Radiocarbon evidence of fossil-carbon cycling in sediments1968), Metabolic fractionation of carbon isotopes in marineof particulate organic carbon using bomb 14 C, Nature,

  17. Flux Measurements of Volatile Organic Compounds from an Urban Tower Platform in Houston, Texas: Trends and Tracers

    E-Print Network [OSTI]

    Hale, Martin C

    2014-05-08T23:59:59.000Z

    , and xylenes (BTEX) from winter 2009 compared to spring 2013. Median concentrations over the four-year period fell between 20 to 34 percent, comparable to long-term VOC reduction trends observed in other major metropolitan areas. Emissions of these species fell...

  18. Extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters by supercritical carbon dioxide

    SciTech Connect (OSTI)

    Schilling, J.B.

    1997-09-01T23:59:59.000Z

    Supercritical fluid extraction (SFE) using unmodified carbon dioxide has been explored as an alternative method for the extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters. HEPA filters provide the final stage of containment on many exhaust systems in US Department of Energy (DOE) facilities by preventing the escape of chemical and radioactive materials entrained in the exhausted air. The efficiency of the filters is tested by the manufacturer and DOE using dioctylphthalate (DOP), a substance regulated by the US Environmental Protection Agency under the Resource Conservation and Recovery Act. Therefore, the filters must be analyzed for semivolatile organics before disposal. Ninety-eight acid, base, and neutral semivolatile organics were spiked onto blank HEPA material and extracted using SFE, Soxhlet, automated Soxhlet, and sonication techniques. The SFE conditions were optimized using a Dionex SFE-703 instrument. Average recoveries for the 98 semivolatile compounds are 82.7% for Soxhlet, 74.0% for sonication, 70.2% for SFE, and 62.9% for Soxtec. Supercritical fluid extraction reduces the extraction solvent volume to 10--15 mL, a factor of 20--30 less than Soxhlet and more than 5 times less than Soxtec and sonication. Extraction times of 30--45 min are used compared to 16--18 h for Soxhlet extraction.

  19. "The disintegration of organic compounds by microorganisms is accompanied by the liberation of

    E-Print Network [OSTI]

    Lovley, Derek

    comple- ment of enzymes necessary to completely oxidize organic fuels to carbon dioxide is not yet they are `carbon-neutral'; the oxidation of the organic matter only releases recently fixed carbon back and sediments. The ubiquitous and innocuous properties of fuels for microbial fuel cells alleviates the need

  20. Radionuclides, Trace Metals, and Organic Compounds in Shells of Native Freshwater Mussels Along the Hanford Reach of the Columbia River: 6000 Years Before Present to Current Times

    SciTech Connect (OSTI)

    B. L. Tiller; T. E. Marceau

    2006-01-25T23:59:59.000Z

    This report documents concentrations of radionuclides, trace metals, and semivolatile organic compounds measured in shell samples of the western pearl shell mussel collected along the Hanford Reach of the Columbia River.

  1. Elemental ratio measurements of organic compounds using aerosol mass spectrometry: characterization, improved calibration, and implications

    E-Print Network [OSTI]

    Canagaratna, M. R.

    Elemental compositions of organic aerosol (OA) particles provide useful constraints on OA sources, chemical evolution, and effects. The Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS) is ...

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

    SciTech Connect (OSTI)

    NONE

    1996-08-01T23:59:59.000Z

    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.

  3. Brayton Cycle Heat Pump for VOC Control

    E-Print Network [OSTI]

    Kovach, J. L.

    The first full size continuous operation Brayton Cycle Heat Pump (1)(2)(3) application for VOC recovery occurred in 1988. The mixed solvent recovery system was designed and supplied by NUCON for the 3M facility in Weatherford, OK (4). This first...

  4. A novel Whole Air Sample Profiler (WASP) for the quantification of volatile organic compounds in the boundary layer

    SciTech Connect (OSTI)

    Mak, J. E.; Su, L.; Guenther, Alex B.; Karl, Thomas G.

    2013-10-16T23:59:59.000Z

    The emission and fate of reactive VOCs is of inherent interest to those studying chemical biosphere-atmosphere interactions. In-canopy VOC observations are obtainable using tower-based samplers, but the lack of suitable sampling systems for the full boundary 5 layer has limited the data characterizing the vertical structure of such gases above the canopy height and still in the boundary layer. This is the important region where many reactive VOCs are oxidized or otherwise removed. Here we describe an airborne sampling system designed to collect a vertical profile of air into a 3/800 OD tube 150m in length. The inlet ram air pressure is used to flow sampled air through the 10 tube, which results in a varying flow rate based on aircraft speed and altitude. Since aircraft velocity decreases during ascent, it is necessary to account for the variable flow rate into the tube. This is accomplished using a reference gas that is pulsed into the air stream so that the precise altitude of the collected air can be reconstructed post-collection. The pulsed injections are also used to determine any significant effect 15 from diffusion/mixing within the sampling tube, either during collection or subsequent extraction for gas analysis. This system has been successfully deployed, and we show some measured vertical profiles of isoprene and its oxidation products methacrolein and methyl vinyl ketone from a mixed canopy near Columbia, Missouri.

  5. The removal kinetics of industrial organic compounds in natural and synthetic systems

    E-Print Network [OSTI]

    Petrasek, Albert Charles

    1970-01-01T23:59:59.000Z

    on the value of the 1ndependent variable, and those data in which the dependent variable 1s a function of the 1ndependent variable. This program has wide appl1cation whenever data analysis is necessary, and the volume dictates more rapid', processing.... Lineprinter 'listing of dissolved oxygen unit rate curve parameters. 131 xii LI. ST OF TABLES (CONTINUED) Table Ul-10. Computer listing of NLSS values computed from the approximation function. UI-ll. List of computed total organic carbon concentrations...

  6. Polybenzimidazole compounds

    DOE Patents [OSTI]

    Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Wertsching, Alan K. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Luther, Thomas A. (Idaho Falls, ID); Jones, Michael G. (Pocatello, ID)

    2010-08-10T23:59:59.000Z

    A PBI compound that includes imidazole nitrogens, at least a portion of which are substituted with an organic-inorganic hybrid moiety. At least 85% of the imidazole nitrogens may be substituted. The organic-inorganic hybrid moiety may be an organosilane moiety, for example, (R)Me.sub.2SiCH.sub.2--, where R is selected from among methyl, phenyl, vinyl, and allyl. The PBI compound may exhibit similar thermal properties in comparison to the unsubstituted PBI. The PBI compound may exhibit a solubility in an organic solvent greater than the solubility of the unsubstituted PBI. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may occur at about room temperature and/or at about atmospheric pressure. Substituting may use at least five equivalents in relation to the imidazole nitrogens to be substituted or, preferably, about fifteen equivalents.

  7. Effects of solar radiation on manganese oxide reactions with selected organic compounds

    SciTech Connect (OSTI)

    Bertino, D.J.; Zepp, R.G. (Environmental Protection Agency, Athens, GA (United States))

    1991-07-01T23:59:59.000Z

    The effects of sunlight on aqueous redox reactions between manganese oxides (MnO{sub x}) and selected organic substances are reported. No sunlight-induced rate enhancement was observed for the MnO{sub x} oxidation of substituted phenols, anisole, o-dichlorobenzene, or p-chloroaniline. On the other hand, solar radiation did accelerate the reduction of manganese oxides by dissolved organic matter (DOM) from aquatic environments. The photoreduction of MnO{sub x} by DOM was little affected by molecular oxygen in air-saturated water (250 {mu}M), but was inhibited by 2,6-dichloroindophenol (0.5-6 {mu}M), and excellent electron acceptor. MnO{sub x} reduction also was photosensitized by anthraquinone-2-sulfonate. These results indicate that the photoreduction probably involves electron transfer from excited states of sorbed DOM to the oxide surface. Wavelength studies indicated that ultraviolet-B radiation (280-320 nm) plays an important role in this photoreduction.

  8. Polyphenoloxidases immobilized in organic gels: Properties and applications in the detoxification of aromatic compounds

    SciTech Connect (OSTI)

    Crecchio, C.; Ruggiero, P.; Pizzigallo, M.D.R. [Univ. di Bari (Italy). Ist. di Chimica Agraria

    1995-12-20T23:59:59.000Z

    Gelatine gels originate from water in oil microemulsions in which the ternary system consists of isooctane/sulfosuccinic acid bis [2-ethyl hexyl] ester/water; the solubilization of gelatin in the water pool of these microemulsions transforms them into viscous gels in which it is possible to cosolubilize various reactive molecules. These gels were used to immobilize two phenoloxidases, a laccase from Trametes versicolor and a tyrosinase from mushroom. The best balance between gel retention and catalytic activity was reached at a gelatine concentration of 2.5% (w/v) in the case of tyrosinase, while laccase immobilization was independent of gelatine concentration. Both enzymes kept the same optimum pH as the corresponding soluble controls, while a partial loss of activity was observed when they were immobilized. Immobilized enzymes showed an increased stability when incubated for several days at 4 C with a very low release from the gels in the incubation solutions. The immobilization of tyrosinase and of laccase enhanced stability to thermal inactivation. Furthermore, gel-entrapped tyrosinase was almost completely preserved from proteolysis: more than 80% of the activity was maintained, while only 25% of the soluble control activity was detected after the same proteolytic treatments. A column packed with gel-immobilized tyrosinase was used to demonstrate that enzymes immobilized with this technique may be reused several times in the same reaction without loosing their efficiency. Finally, gel-entrapped tyrosinase and laccase were capable of removing naturally occurring and xenobiotic aromatic compounds from aqueous suspensions with different degrees of efficiency.

  9. Emissions of volatile organic compounds from stationary combustion sources: Numerical modeling capabilities

    SciTech Connect (OSTI)

    Seebold, J.G. [Chevron Research and Technology Co., Richmond, CA (United States); Kee, R.J.; Lutz, A.J. [Sandia National Labs., Albuquerque, NM (United States); Pitz, W.J.; Westbrook, C.K. [Lawrence Livermore National Lab., CA (United States); Senkan, S. [California Univ., Los Angeles, CA (United States)

    1992-09-01T23:59:59.000Z

    A collaborative research program initiated to study the emissions of a wide variety of chemical species from stationary combustion systems. These product species have been included in the Clean Air act legislation and their emissions must be rigidly controlled, but there is a need for much better understanding of the physical and chemical mechanisms that produce and consume them. We are using numerical modeling study the chemical reactions and fluid mechanical factors that occur in industrial processes: we are examining systems including premixed and diffusion flames, stirred reactors and plug flow reactors in these modeling studies to establish the major factors leading to emissions of these chemicals. In addition, we are applying advanced laser diagnostic techniques to validate the model predictions and to study the possibilities of developing sophisticated sensors to detect emissions of undesirable species in real time. This paper will discuss the organization of this collaborative effort and its results to date.

  10. Identification of organic compounds contained in the bitumen of Chattanooga oil shale

    SciTech Connect (OSTI)

    Mc Gowan, C.W.; Greenwell, B.E.; Markuszewski, R.; Richard, J.J.; Sepaniak, M.J.

    1986-09-01T23:59:59.000Z

    The bitumen of Chattanooga Oil Shale has been extracted with benzene. The benzene-soluble material was separated into acid base and neutral fractions with ion exchange chromatography. This separation scheme has been used extensively to separate the organic material in Green River Oil Shale. The acid fraction was esterified with BF/sub 3//MeOH. A large portion of the acid fraction was not esterified and this material was considered to be phenolic. The bases were separated into two fractions using alumina. The esters, the two base fractions and the total neutral fraction were analyzed using gas chromatography coupled to mass spectrometry. Two series constituting the methyl esters of normal and isoprenoid acids were identified. Several homologous series were indicated in the base fraction. The major components in the neutral fractions were two series constituting normal and isoprenoid alkanes. The analysis scheme apparently does a good job of separating and identifying aliphatic materials.

  11. Single-reactor process for producing liquid-phase organic compounds from biomass

    DOE Patents [OSTI]

    Dumesic, James A. (Verona, WI); Simonetti, Dante A. (Middleton, WI); Kunkes, Edward L. (Madison, WI)

    2011-12-13T23:59:59.000Z

    Disclosed is a method for preparing liquid fuel and chemical intermediates from biomass-derived oxygenated hydrocarbons. The method includes the steps of reacting in a single reactor an aqueous solution of a biomass-derived, water-soluble oxygenated hydrocarbon reactant, in the presence of a catalyst comprising a metal selected from the group consisting of Cr, Mn, Fe, Co, Ni, Cu, Mo, Tc, Ru, Rh, Pd, Ag, W, Re, Os, Ir, Pt, and Au, at a temperature, and a pressure, and for a time sufficient to yield a self-separating, three-phase product stream comprising a vapor phase, an organic phase containing linear and/or cyclic mono-oxygenated hydrocarbons, and an aqueous phase.

  12. Photocatalytic and chemical oxidation of organic compounds in supercritical carbon dioxide. Progress report for FY97

    SciTech Connect (OSTI)

    Blake, D.M.; Bryant, D.L.; Reinsch, V.

    1997-09-30T23:59:59.000Z

    'The background for the project is briefly reviewed and the work done during the nine months since funding was received is documented. Work began in January, 1997. A post doctoral fellow joined the team in April. The major activities completed this fiscal year were: staffing the project, design of the experimental system, procurement of components, assembly of the system. preparation of the Safe Operating Procedure and ES and H compliance, pressure testing, establishing data collection and storage methodology, and catalyst preparation. Objective The objective of the project is to develop new chemistry for the removal of organic contaminants from supercritical carbon dioxide. This has application in processes used for continuous cleaning and extraction of parts and waste materials. A secondary objective is to increase the fundamental understanding of photocatalytic chemistry. Cleaning and extraction using supercritical carbon dioxide (scCO{sub 2}) can be applied to the solution of a wide range of environmental and pollution prevention problems in the DOE complex. Work is being done that explores scCO{sub 2} in applications ranging from cleaning contaminated soil to cleaning components constructed from plutonium. The rationale for use of scCO{sub 2} are based on the benign nature, availability and low cost, attractive solvent properties, and energy efficient separation of the extracted solute from the solvent by moderate temperature or pressure changes. To date, R and D has focussed on the methods and applications of the extraction steps of the process. Little has been done that addresses methods to polish the scCO{sub 2} for recycle in the cleaning or extraction operations. In many applications it will be desirable to reduce the level of contamination from that which would occur at steady state operation of a process. This proposal addresses chemistry to achieve that. This would be an alternative to removing a fraction of the contaminated scCO{sub 2} for disposal and using makeup scCO{sub 2}. A chemical polishing operation can reduce the release of CO{sub 2} from the process. It can also reduce the consumption of reagents that may be used in the process to enhance extraction and cleaning. A polishing operation will also reduce or avoid formation of an additional waste stream. Photocatalytic and other photochemical oxidation chemistry have not been investigated in scCO{sub 2}. The large base of information for these reactions in water, organic solvents, or air suggest that the chemistry will work in carbon dioxide. There are compelling reasons to believe that the properties of scCO{sub 2} should increase the performance of photocatalytic chemistry over that found in more conventional fluid phases.'

  13. Estimated monthly emissions of sulfur dioxide, oxides of nitrogen, and volatile organic compounds for the 48 contiguous states, 1985-1986: Volume 2, Sectoral emissions by month for states

    SciTech Connect (OSTI)

    Kohout, E.J.; Knudson, D.A.; Saricks, C.L.; Miller, D.J.

    1987-11-01T23:59:59.000Z

    A listing by source of sulfur dioxide, nitrogen oxides and volatile organic compounds emitted in 48 states of the US is provided. (CBS)

  14. Analysis of C1, C2, and C10 through C33 particle-phase and semi-volatile organic compound emissions from heavy-duty diesel engines

    E-Print Network [OSTI]

    Wu, Mingshen

    from heavy-duty diesel engines Z. Gerald Liu a,*, Devin R. Berg a , Victoria N. Vasys a , Melissa E 18 November 2009 Keywords: Organic compound emissions Particulate matter emissions Heavy-duty diesel engines Aftertreatment technology Diesel particulate filter Chemical speciation a b s t r a c t To meet

  15. The conversion of solar energy to the chemical energy of organic compounds is a complex process that includes electron transport and

    E-Print Network [OSTI]

    Ehleringer, Jim

    The conversion of solar energy to the chemical energy of organic compounds is a complex process energy or photon units. Irradiance is the amount of energy that falls on a flat sensor of known area per and energy units for sunlight can be intercon- verted relatively easily, provided that the wavelength

  16. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    fuel combustion, especially coal and residential oil, andthe oil sands (r 2 combustion tracersand combustion sources on ethene and other alkenes at the oil

  17. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    Oil sands comprise 30% of the world’s oil reserves andthe crude oil reserves in Canada’s oil sands deposits are30% of total world oil reserves (Alboudwarej et al. , 2006)

  18. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    West, C. : Highlighting heavy oil, Oilfield Rev. , 34–53,and enhancement of Mo-heavy oil interaction, Fuel, 83,sticky extra-heavy crude oil that is “unconventional”,

  19. Boreal forest fire emissions in fresh Canadian smoke plumes: C1-C10 volatile organic compounds (VOCs), CO2, CO, NO2, NO, HCN and CH3CN

    E-Print Network [OSTI]

    2011-01-01T23:59:59.000Z

    propene, acetone, benzene, propane and ?-pinene (Table 1).cyanide Acetonitrile Ethane Propane i-Butane n-Butane i-= Ethane Ethane Ethane Ethane Propane Propane Propane ARCTAS

  20. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    K. : Atmospheric chemistry of gasoline-related emissions:chemistry. Methyl tert-butyl ether is a solvent and gasoline

  1. Boreal forest fire emissions in fresh Canadian smoke plumes: C1-C10 volatile organic compounds (VOCs), CO2, CO, NO2, NO, HCN and CH3CN

    E-Print Network [OSTI]

    2011-01-01T23:59:59.000Z

    and Fehsenfeld, F. C. : Emission sources and ocean uptake ofand No- vakov, T. : Emissions of trace gases and particlesGroot, W. J. : Future emissions from Canadian boreal forest

  2. Characterization of trace gases measured over Alberta oil sands mining operations: 76 speciated C2-C10 volatile organic compounds (VOCs), CO2, CH4, CO, NO, NO2, NOy, O3 and SO2

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    over Alberta oil sands mining operations Soc. , 81(7), 1537–over Alberta oil sands mining operations: 76 speciated C 2 –over Alberta oil sands mining operations Burstyn, I. ,

  3. HYDROGEN AND VOC RETENTION IN WASTE BOXES

    SciTech Connect (OSTI)

    PACE ME; MARUSICH RM

    2008-11-21T23:59:59.000Z

    The Hanford Waste Management Project Master Documented Safety Analysis (MDSA) (HNF-14741, 2003) identifies derived safety controls to prevent or mitigate the risks of a single-container deflagration during operations requiring moving, venting or opening transuranic (TRU)-waste containers. The issue is whether these safety controls are necessary for operations involving TRU-waste boxes that are being retrieved from burial at the Hanford Site. This paper investigates the potential for a deflagration hazard within these boxes and whether safety controls identified for drum deflagration hazards should be applied to operations involving these boxes. The study evaluates the accumulation of hydrogen and VOCs within the waste box and the transport of these gases and vapors out of the waste box. To perform the analysis, there were numerous and major assumptions made regarding the generation rate and the transport pathway dimensions and their number. Since there is little actual data with regards to these assumptions, analyses of three potential configurations were performed to obtain some indication of the bounds of the issue (the concentration of hydrogen or flammable VOCs within a waste box). A brief description of each of the three cases along with the results of the analysis is summarized.

  4. Zevenhoven & Kilpinen VOCs, PAHs, soot, tar, CO 17.6.2001 6-1 Chapter 6 VOCs, PAHs,

    E-Print Network [OSTI]

    Laughlin, Robert B.

    Zevenhoven & Kilpinen VOCs, PAHs, soot, tar, CO 17.6.2001 6-1 Chapter 6 VOCs, PAHs, soot, tar, CO 6 or global environment. These effects can be very diverse: water and soil acidification, human health and phenol, polycyclic aromatic hydrocarbons (PAHs) like naphtalene and anthracene (see Table 6.7), pyridines

  5. HELSINKI UNIVERSITY OF TECHNOLOGY ENE-47.153 VOCsVOCs,, PAHsPAHs, soot, tar, CO, soot, tar, CO

    E-Print Network [OSTI]

    Zevenhoven, Ron

    of tar (from biomass gasificationbiomass gasification)) ·· COCO see: www.hut.fi/~see: www-level ozone in Europeand ground-level ozone in Europe VOC emissions (VOC emissions (inclincl. methane). methane) in Europe, 1994 (tonnes)in Europe, 1994 (tonnes) Ground-level ozone in Europe,Ground-level ozone

  6. Organics in soils and groundwater at non-arid sites (A-1) integrated demonstration

    SciTech Connect (OSTI)

    Steele, J.L.; Kaback, D.S.; Looney, B.B.

    1994-06-01T23:59:59.000Z

    One of the most common environmental problems in the United States is soils and groundwater contaminated with volatile chemical solvents classified as Volatile Organic Compounds (VOCs), which were used as degreasers and cleaning agents. Leakage of solvents (trichloroethylene and tetrachloroethylene) from an underground process sewer line has contaminated soils and underlying groundwaters at SRS. This site was chosen for DOE-OTD`s integrated demonstration program to demonstrate innovative technologies for cleanup of soils and groundwater contaminated with VOCs. The Savannah River Site was especially well suited as the test bed for this integrated demonstration project due to the presence of a pre-existing line source of soil and groundwater-based contamination, on-going environmental remediation efforts at the site, and full cooperation from the concerned environmental regulatory agencies. The Integrated Demonstration (ID) at the Savannah River Site has demonstrated systems of technologies and evaluated them with respect to performance, safety and cost effectiveness.

  7. French permanent survey on indoor air quality--microenvironmental concentrations of volatile organic compounds in 90 French dwellings

    E-Print Network [OSTI]

    Boyer, Edmond

    conducted in France on indoor pollution. The survey's design (sampling, analytical methods, questionnaire, temperature, humidity) and questionnaires on building characteristics, occupants' description and time (30 compounds including formaldehyde, acetaldehyde, BTEX) were measured by passive samplers, during 7

  8. VOC treatment provided after 20-year legal battle

    SciTech Connect (OSTI)

    Platt, F.N. Jr. (Killam Associates, Inc., Randolph, NJ (United States))

    1993-12-01T23:59:59.000Z

    This article examines the treatment of a Superfund site, the Runyon Watershed just outside of Perth Amboy, New Jersey, for volatile organic compounds. The beginning of treatment was the result of a 20-year legal battle begun in 1971 and resolved after the city's consulting engineering firm designed and implemented a specialized approach to identify and develop key critical issues.

  9. Identification and separation of the organic compounds in coal-gasification condensate waters. [5,5 dimethyl hydantoin, dihydroxy benzenes, acetonitrile

    SciTech Connect (OSTI)

    Mohr, D.H. Jr.; King, C.J.

    1983-08-01T23:59:59.000Z

    A substantial fraction of the organic solutes in condensate waters from low-temperature coal-gasification processes are not identified by commonly employed analytical techniques, have low distriution coefficients (K/sub C/) into diisopropyl ether (DIPE) or methyl isobutyl ketone (MIBK), and are resistant to biological oxidation. These compounds represent an important wastewater-treatment problem. Analytical techniques were developed to detect these polar compounds, and the liquid-liquid phase equilibria were measured with several solvents. A high-performance liquid - chromatography (HPLC) technique was employed to analyze four condensate-water samples from a slagging fixed-bed gasifier. A novel sample-preparation technique, consisting of an azeotropic distillation with isopropanol, allowed identification of compounds in the HPLC eluant by combined gas chromatography and mass spectrometry. 5,5-dimethyl hydantoin and related compounds were identified in condensate waters for the first time, and they account for 1 to 6% of the chemical oxygen demand (COD). Dimethyl hydatoin has a K/sub D/ of 2.6 into tributyl phosphate (TBP) and much lower K/sub D/ values into six other solvents. It is also resistant to biological oxidation. Phenols (59 to 76% of the COD), dihydroxy benzenes (0.02 to 9.5% of the COD), and methanol, acetonitrile, and acetone (15% of the COD in one sample) were also detected. Extraction with MIBK removed about 90% of the COD. MIBK has much higher K/sub D/ values than DIPE for dihydroxy benzenes. Chemical reactions occurred during storage of condensate-water samples. The reaction products had low K/sub D/ values into MIBK. About 10% of the COD had a K/sub D/ of nearly zero into MIBK. These compounds were not extracted by MIBK over a wide range of pH. 73 references, 6 figures, 35 tables.

  10. Control of the accumulation of non-process elements and organic compounds in pulp mills with bleach filtrate reuse. Quarterly report 3, January--March, 1997

    SciTech Connect (OSTI)

    Frederick, W.J.; Laver, M.L.; Rorrer, G.L.

    1997-05-01T23:59:59.000Z

    Progress during this quarter is described on four tasks. The first task involves the recovery of organic matter from bleach effluents and black liquors, separation of carbohydrates and lignin degradation products, analysis of functional groups, and characterization of carbohydrate polymers. Progress in the second task was made in the selection of model compounds. Several subtasks are complete in Task 3, but the paper summarizes progress made in the determination of the residual hemicellulose content in the pulp samples. Finally, results are given for the measurement of metal adsorption isotherms on wood pulp. Goals for the next quarter are listed.

  11. Electron transport in naphthylamine-based organic compounds S. C. Tse, K. C. Kwok, and S. K. Soa

    E-Print Network [OSTI]

    So, Shu K.

    are organic light-emitting diodes OLEDs , thin-film transistors, solar cells, and photodetectors.1­4 Among them, OLED is now a leading contender in ultrathin, flexible, flat panel display technology. A simple

  12. Associations of indoor carbon dioxide concentrations, VOCS, environmental susceptibilities with mucous membrane and lower respiratory sick building syndrome symptoms in the BASE study: Analyses of the 100 building dataset

    SciTech Connect (OSTI)

    Apte, M.G.; Erdmann, C.A.

    2002-10-01T23:59:59.000Z

    Using the 100 office-building Building Assessment Survey and Evaluation (BASE) Study dataset, we performed multivariate logistic regression analyses to quantify the associations between indoor minus outdoor CO{sub 2} (dCO{sub 2}) concentrations and mucous membrane (MM) and lower respiratory system (Lresp) Sick Building Syndrome (SBS) symptoms, adjusting for age, sex, smoking status, presence of carpet in workspace, thermal exposure, relative humidity, and a marker for entrained automobile exhaust. Using principal components analysis we identified a number of possible sources of 73 measured volatile organic compounds in the office buildings, and assessed the impact of these VOCs on the probability of presenting the SBS symptoms. Additionally we included analysis adjusting for the risks for predisposition of having SBS symptoms associated with the allergic, asthmatic, and environmentally sensitive subpopulations within the office buildings. Adjusted odds ratios (ORs) for statistically significant, dose-dependant associations (p<0.05) for dry eyes, sore throat, nose/sinus congestion, and wheeze symptoms with 100-ppm increases in dCO{sub 2} ranged from 1.1 to 1.2. These results suggest that increases in the ventilation rates per person among typical office buildings will, on average significantly reduce the prevalence of several SBS symptoms, up to 80%, even when these buildings meet the existing ASHRAE ventilation standards for office buildings. VOC sources were observed to play an role in direct association with mucous membrane and lower respiratory irritation, and possibly to be indirectly involved in indoor chemical reactions with ozone that produce irritating compounds associated with SBS symptoms. O-xylene, possibly emitted from furniture coatings was associated with shortness of breath (OR at the maximum concentration = 8, p < 0.05). The environmental sensitivities of a large subset of the office building population add to the overall risk of SBS symptoms (ORs ranging from 2 to above 11) within the buildings.

  13. Environmental effects of dredging. The k{sub oc} of nonpolar organic compounds in sediment. Technical notes

    SciTech Connect (OSTI)

    Brannon, J.M.; Pennington, J.C.; Hayes, C.; McFarland, V.

    1992-12-01T23:59:59.000Z

    This technical note describes testing conducted to determine the partitioning of contaminants between sediment organic carbon and sediment interstitial water, assess the effects of sediment organic carbon upon K(oc) of selected PCBs and fluoranthene, and investigate the effect of time of contact between contaminants and sediment upon the value of K(oc). The U.S. Environmental Protection Agency is authorized to develop and implement sediment quality criteria (SQC) under section 304(a) of the Clean Water Act. SQC, when promulgated, will profoundly affect U.S. Army Corps of Engineers (USACE) dredging and disposal operations. Aquatic disposal of dredged material and selection of aquatic disposal sites will be based on SQC. Most SQC approaches currently under development involve a determination of the relationship between contaminant concentrations in sediment and biological effects on organisms exposed to the contaminated sediment. The USACE is presently investigating the link between contaminant levels in sediment and sediment geochemistry, as well as contaminant levels and effects in aquatic organisms.

  14. Abstract ID: P2-66 Hydrogen production during the irradiation of gaseous organic compounds: advantage of an

    E-Print Network [OSTI]

    Boyer, Edmond

    of propane, the radiolytic yield value of hydrogen G(H2) is equal to 3.7 for total doses in the range of 0, hydrogen production, propane radiolysis. Corresponding author: C. Pichon Institut de Physique Nucléaire de be explained by the instability of some organics materials under vacuum. In order to analyse samples in air

  15. Recent VOC Control Test Data for a Reactive VOC Converter- Scrubber System for Non-Thermal Control of VOCs 

    E-Print Network [OSTI]

    McGinness, M.

    2003-01-01T23:59:59.000Z

    of real estate. Non-thermal VOHAP (Volatile Organic Hazardous Air Pollutant) emission control devices require additional maintenance. They also require the replacement of costly consumables such as activated carbon or they use large amounts of energy...

  16. Carbon tetrachloride contamination, 200 West Area, Hanford Site: Arid Site Integrated Demonstration for remediation of volatile organic compounds

    SciTech Connect (OSTI)

    Last, G.V. (Pacific Northwest Lab., Richland, WA (United States)); Rohay, V.J. (Westinghouse Hanford Co., Richland, WA (United States))

    1991-05-06T23:59:59.000Z

    The Arid State Integrated Demonstration is a US Department of Energy (DOE) program targeted at the acquisition, development, demonstration, and deployment of technologies for evaluation and cleanup of volatile organic and associated contaminants in soils and ground waters. Several DOE laboratories, universities, and industry will participate in the program. Candidate technologies will be demonstrated in the areas of site characterization; performance prediction, monitoring, and evaluations; contaminant extraction and ex situ treatment; in situ remediations; and site closure and monitoring. The performance of these demonstrated technologies will be compared to baseline technologies and documented to promote the transfer of new technologies to industry for use at DOE facilities. The initial host site is the Hanford Site's 200 West Area. The location of the demonstration contains primarily carbon tetrachloride (CCl{sub 4}), chloroform, and a variety of associated mixed waste contaminants. Chemical processes used to recover and purify plutonium at Hanford's plutonium finishing plant (Z Plant) resulted in the production of actinide-bearing waste liquid. Both aqueous and organic liquid wastes were generated, and were routinely discharged to subsurface disposal facilities. The primary radionuclide in the waste streams was plutonium, and the primary organic was CCl{sub 4}. This paper contains brief descriptions of the principal CCl{sub 4} waste disposal facilities in Hanford's 200 West Area, associated hydrogeology, existing information on the extent of soil and ground-water contamination, and a conceptual outline of suspected subsurface CCl{sub 4} distributions.

  17. Carbon tetrachloride contamination, 200 West Area, Hanford Site: Arid Site Integrated Demonstration for remediation of volatile organic compounds

    SciTech Connect (OSTI)

    Last, G.V. [Pacific Northwest Lab., Richland, WA (United States); Rohay, V.J. [Westinghouse Hanford Co., Richland, WA (United States)

    1991-05-06T23:59:59.000Z

    The Arid State Integrated Demonstration is a US Department of Energy (DOE) program targeted at the acquisition, development, demonstration, and deployment of technologies for evaluation and cleanup of volatile organic and associated contaminants in soils and ground waters. Several DOE laboratories, universities, and industry will participate in the program. Candidate technologies will be demonstrated in the areas of site characterization; performance prediction, monitoring, and evaluations; contaminant extraction and ex situ treatment; in situ remediations; and site closure and monitoring. The performance of these demonstrated technologies will be compared to baseline technologies and documented to promote the transfer of new technologies to industry for use at DOE facilities. The initial host site is the Hanford Site`s 200 West Area. The location of the demonstration contains primarily carbon tetrachloride (CCl{sub 4}), chloroform, and a variety of associated mixed waste contaminants. Chemical processes used to recover and purify plutonium at Hanford`s plutonium finishing plant (Z Plant) resulted in the production of actinide-bearing waste liquid. Both aqueous and organic liquid wastes were generated, and were routinely discharged to subsurface disposal facilities. The primary radionuclide in the waste streams was plutonium, and the primary organic was CCl{sub 4}. This paper contains brief descriptions of the principal CCl{sub 4} waste disposal facilities in Hanford`s 200 West Area, associated hydrogeology, existing information on the extent of soil and ground-water contamination, and a conceptual outline of suspected subsurface CCl{sub 4} distributions.

  18. Low VOC drying of lumber and wood panel products. Progress report No. 8

    SciTech Connect (OSTI)

    Su, W.; Yan, H.; Hooda, U.; Wild, M.P.; Banerjee, S. [Inst. of Paper Science and Technology, Atlanta, GA (United States)] [Inst. of Paper Science and Technology, Atlanta, GA (United States); Shmulsky, R.; Thompson, A.; Ingram, L.; Conners, T. [Mississippi State Univ., MS (United States)] [Mississippi State Univ., MS (United States)

    1998-07-01T23:59:59.000Z

    This study was initiated by an Institute of Paper Science and Technology finding that heating softwood in a low-headspace environment removed much of the VOCs without removing the water. This offered the possibility of removing VOCs from wet wood, capturing them as a product, and then drying the VOC-depleted wood conventionally with little or no VOC controls. Two means of low-headspace heating were explored: steam and radiofrequency (RF). It was found in the previous year, that while both steam and RF were able to drive out VOCs, steam was impracticably slow for lumber. Hence the effect of RF or microwave on wood was the principal focus of the work reported here. Finally, in order to understand the mechanism of VOC release, the transport of the VOCs in wood was studied, together with the seasonal effects that influence VOC concentration in trees.

  19. JV Task 86 - Identifying the Source of Benzene in Indoor Air Using Different Compound Classes from TO-15 Data

    SciTech Connect (OSTI)

    Steven B. Hawthorne

    2007-04-15T23:59:59.000Z

    Volatile organic compound (VOC) data that had already been collected using EPA method TO-15 at four different sites under regulatory scrutiny (a school, strip mall, apartment complex, and business/residential neighborhood) were evaluated to determine whether the source of indoor air benzene was outdoor air or vapor intrusion from contaminated soil. Both the use of tracer organics characteristic of different sources and principal component statistical analysis demonstrated that the source of indoor air at virtually all indoor sampling locations was a result of outdoor air, and not contaminated soil in and near the indoor air-sampling locations. These results show that proposed remediation activities to remove benzene-contaminated soil are highly unlikely to reduce indoor air benzene concentrations. A manuscript describing these results is presently being prepared for submission to a peer-reviewed journal.

  20. Development and validation of a cleanup method for hydrocarbon containing samples for the analysis of semivolatile organic compounds

    SciTech Connect (OSTI)

    Hoppe, E.W.; Stromatt, R.W.; Campbell, J.A.; Steele, M.J.; Jones, J.E.

    1992-04-01T23:59:59.000Z

    Samples obtained from the Hanford single shell tanks (SSTs) are contaminated with normal paraffin hydrocarbon (NPH) as hydrostatic fluid from the sampling process or can be native to the tank waste. The contamination is usually high enough that a dilution of up to several orders of magnitude may be required before the sample can be analyzed by the conventional gas chromatography/mass spectrometry methodology. This can prevent detection and measurement of organic constituents that are present at lower concentration levels. To eliminate or minimize the problem, a sample cleanup method has been developed and validated and is presented in this document.

  1. An In-Situ Ion Mobility Spectrometer Sensor System for Detecting Gaseous VOCs in Unsaturated Soils

    E-Print Network [OSTI]

    Baker, R. Jacob

    An In-Situ Ion Mobility Spectrometer Sensor System for Detecting Gaseous VOCs in Unsaturated Soils and will be ultimately equipped with water content, temperature, and pressure sensors. The proposed system is designed knowledge, an in-situ IMS for detection of subsurface gaseous VOCs has not been previously developed. VOCs

  2. ACCEPTED BY WATER ENVIRONMENT RESEARCH ODOR AND VOC REMOVAL FROM WASTEWATER TREATMENT PLANT

    E-Print Network [OSTI]

    ACCEPTED BY WATER ENVIRONMENT RESEARCH _______ ODOR AND VOC REMOVAL FROM WASTEWATER TREATMENT PLANT of biofilters for sequential removal of H2S and VOCs from wastewater treatment plant waste air. The biofilter of VOCs. In Europe, biological treatment in biofilters has rapidly been gaining ground as a relatively

  3. VOC Emission Control with the Brayton Cycle Pilot Plant Operations

    E-Print Network [OSTI]

    Enneking, J. C.

    A mobile pilot plant capable of removing VOC emissions from exhaust air streams was cooperatively funded by SCE, EPRI, 3M, and NUCON. Valuable information about the process and the recovery operation has been gained by performing tests at a number...

  4. VOC Emission Control with the Brayton Cycle Pilot Plant Operations 

    E-Print Network [OSTI]

    Enneking, J. C.

    1992-01-01T23:59:59.000Z

    A mobile pilot plant capable of removing VOC emissions from exhaust air streams was cooperatively funded by SCE, EPRI, 3M, and NUCON. Valuable information about the process and the recovery operation has been gained by performing tests at a number...

  5. Comparative evaluation of several small mammal species as monitors of heavy metals, radionuclides, and selected organic compounds in the environment

    SciTech Connect (OSTI)

    Talmage, S.S. (Tennessee Univ., Knoxville, TN (USA) Oak Ridge National Lab., TN (USA)); Walton, B.T. (Oak Ridge National Lab., TN (USA))

    1990-08-01T23:59:59.000Z

    The primary purpose of this study was to evaluate which small mammal species are the best monitors of specific environmental contaminants. The evaluation is based on the published literature and on an analysis of small mammals trapped at several sites on the Oak Ridge National Laboratory (ORNL) Reservation in Oak Ridge, Tennessee. Studies on the uptake of heavy metals, radionuclides, and organic chemicals are reviewed in Chapter II to evaluate several small mammal species for their capacity to serve as sentinels for the presence, accumulation, and effects of various contaminants. Where several species were present at a site, a comparative evaluation was made and species are ranked for their capacity to serve as monitors of specific contaminants. Food chain accumulation and food habits of the species are used to establish a relationship with suitability as a biomonitor. Tissue-specific concentration factors were noted in order to establish target tissues. Life histories, habitat, and food habits are reviewed in order to make generalizations concerning the ability of similar taxa to serve as biomonitor. Finally, the usefulness of several small mammal species as monitors of three contaminants -- benzo(a)pyrene, mercury, and strontium-90 -- present on or near the ORNL facilities was investigated. 133 refs., 5 figs., 20 tabs.

  6. Process for preparing a deuterated or tritiated compound

    DOE Patents [OSTI]

    Klei, Steven R.; Bergman, Robert C.

    2006-06-06T23:59:59.000Z

    A process for labeling organic compounds with deuterium and tritium is described using specific catalysts.

  7. Process for preparing a deuterated or tritiated compound

    DOE Patents [OSTI]

    Bergman, Robert C.; Klei, Steven R.

    2006-05-16T23:59:59.000Z

    A process for labeling organic compounds with deuterium and tritium is described using specific catalysts.

  8. Process for preparing a deuterated or tritiated compound

    DOE Patents [OSTI]

    Bergman, Robert C.; Klei, Steven R.

    2004-09-21T23:59:59.000Z

    A process for labeling organic compounds with deuterium and tritium is described using specific catalysts.

  9. Laboratory Studies of Processing of Carbonaceous Aerosols by Atmospheric Oxidants/Hygroscopicity and CCN Activity of Secondary & Processed Primary Organic Aerosols

    SciTech Connect (OSTI)

    Ziemann, P.J.; Arey, J.; Atkinson, R.; Kreidenweis, S.M.; Petters, M.D.

    2012-06-13T23:59:59.000Z

    The atmosphere is composed of a complex mixture of gases and suspended microscopic aerosol particles. The ability of these particles to take up water (hygroscopicity) and to act as nuclei for cloud droplet formation significantly impacts aerosol light scattering and absorption, and cloud formation, thereby influencing air quality, visibility, and climate in important ways. A substantial, yet poorly characterized component of the atmospheric aerosol is organic matter. Its major sources are direct emissions from combustion processes, which are referred to as primary organic aerosol (POA), or in situ processes in which volatile organic compounds (VOCs) are oxidized in the atmosphere to low volatility reaction products that subsequent condense to form particles that are referred to as secondary organic aerosol (SOA). POA and VOCs are emitted to the atmosphere from both anthropogenic and natural (biogenic) sources. The overall goal of this experimental research project was to conduct laboratory studies under simulated atmospheric conditions to investigate the effects of the chemical composition of organic aerosol particles on their hygroscopicity and cloud condensation nucleation (CCN) activity, in order to develop quantitative relationships that could be used to more accurately incorporate aerosol-cloud interactions into regional and global atmospheric models. More specifically, the project aimed to determine the products, mechanisms, and rates of chemical reactions involved in the processing of organic aerosol particles by atmospheric oxidants and to investigate the relationships between the chemical composition of organic particles (as represented by molecule sizes and the specific functional groups that are present) and the hygroscopicity and CCN activity of oxidized POA and SOA formed from the oxidation of the major classes of anthropogenic and biogenic VOCs that are emitted to the atmosphere, as well as model hydrocarbons. The general approach for this project was to carry out reactions of representative anthropogenic and biogenic VOCs and organic particles with ozone (O3), and hydroxyl (OH), nitrate (NO3), and chlorine (Cl) radicals, which are the major atmospheric oxidants, under simulated atmospheric conditions in large-volume environmental chambers. A combination of on-line and off-line analytical techniques were used to monitor the chemical and physical properties of the particles including their hygroscopicity and CCN activity. The results of the studies were used to (1) improve scientific understanding of the relationships between the chemical composition of organic particles and their hygroscopicity and CCN activity, (2) develop an improved molecular level theoretical framework for describing these relationships, and (3) establish a large database that is being used to develop parameterizations relating organic aerosol chemical properties and SOA sources to particle hygroscopicity and CCN activity for use in regional and global atmospheric air quality and climate models.

  10. ARM - Measurement - Volatile organic compounds

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625govInstrumentstdmadap Documentation TDMADAP : XDCnarrowbandheat flux ARM DatagovMeasurementsVisibility ARM

  11. Flexible CHP System with Low NOx, CO and VOC Emissions - Fact...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Sheet, 2014 Flexible CHP System with Low NOx, CO and VOC Emissions - Fact Sheet, 2014 The Gas Technology Institute, in collaboration with Cannon Boiler Works, Integrated CHP...

  12. Health and Safety Guide for Home Performance Contractors

    E-Print Network [OSTI]

    Stratton, Chris

    2014-01-01T23:59:59.000Z

    Organic Compounds (VOCs) Water heater repair/replacementfireplaces Pipe insulation Water heater insulation Asbestosboilers woodstoves water heaters ranges clothes dryers

  13. Microsoft Word - DOE EA 1606 FONSI_Dec2011.doc

    Office of Environmental Management (EM)

    aircraft, portable generators, and portable pumps. Emissions will include volatile organic compounds (VOCs), carbon monoxide, nitrogen oxides, sulfur dioxide, and...

  14. Paso del Norte ozone study VOC measurements, 1996

    SciTech Connect (OSTI)

    Seila, R.L.; Main, H.; Arriaga, J.L.; Martinez, G.V.; Ramadan, A.B.

    1999-01-01T23:59:59.000Z

    The results of VOC determinations of ambient air samples collected at surface air quality monitoring sites and near sources of interest on the US and Mexican side of the border during six weeks of the 1996 Paso del Norte Ozone Study are reported. Carbonyl samples were collected on DNPH impregnated cartridges at three surface sites and analyzed by HPLC to quantify 13, C-1 to C-8 species. Whole air samples were collected in electro-polished stainless steel canisters which were returned to laboratory for determination of C-2 to C-10+ hydrocarbons by cryogenic preconcentration capillary gas chromatography with flame ionization detection (gc-fid). Several sources were sampled: rush hour traffic, propane-powered bus exhaust, automobile paint shop emissions, propane fuel, petroleum refinery, and industrial manufacturing site. Spatial and temporal characteristics of VOC species concentrations and compositions are presented. Overall surface TNMOC values ranged from 0.1 to 3.4 ppmC with the highest concentrations recorded in the morning at three vehicle-dominated sites, two in Cuidad Juarez and one in downtown El Paso. Toluene in El Paso samples and propane, which is used as a cooking and transportation fuel in Cuidad Juarez, were the most abundant hydrocarbons.

  15. Paso del Norte ozone study VOC measurements, 1996

    SciTech Connect (OSTI)

    Seila, R.L.; Main, H.; Arriaga, J.L.; Martinez, G.V.; Ramadan, A.B.

    1999-11-01T23:59:59.000Z

    The results of VOC determinations of ambient air samples collected at surface air quality monitoring sites and near sources of interest on the US and Mexican side of the border during six weeks of the 1996 Paso del Norte Ozone Study are reported. Carbonyl samples were collected on DNPH impregnated cartridges at three surface sites and analyzed by HPLC to quantify 13, C-1 to C-8 species. Whole air samples were collected in electro-polished stainless steel canisters which were returned to laboratory for determination of C-2 to C-10+ hydrocarbons by cryogenic preconcentration capillary gas chromatography with flame ionization detection (gc-fid). Several sources were sampled: rush hour traffic, propane-powered bus exhaust, automobile paint shop emissions, propane fuel, petroleum refinery, and industrial manufacturing site. Spatial and temporal characteristics of VOC species concentrations and compositions are presented. Overall surface TNMOC values ranged from 0.1 to 3.4 ppmC with the highest concentrations recorded in the morning at three vehicle-dominated sites, two in Cuidad Juarez and one in downtown El Paso. Toluene in El Paso samples and propane, which is used as a cooking and transportation fuel in Cuidad Juarez, were the most abundant hydrocarbons.

  16. ALDEHYDE AND OTHER VOLATILE ORGANIC CHEMICAL EMISSIONS IN FOUR FEMA TEMPORARY HOUSING UNITS ? FINAL REPORT

    SciTech Connect (OSTI)

    Salazar, Olivia; Maddalena, Randy L.; Russell, Marion; Sullivan, Douglas P.; Apte, Michael G.

    2008-05-04T23:59:59.000Z

    Four unoccupied FEMA temporary housing units (THUs) were studied to assess their indoor emissions of volatile organic compounds including formaldehyde. Measurement of whole-THU VOC and aldehyde emission factors (mu g h-1 per m2 of floor area) for each of the four THUs were made at FEMA's Purvis MS staging yard using a mass balance approach. Measurements were made in the morning, and again in the afternoon in each THU. Steady-state indoor formaldehyde concentrations ranged from 378 mu g m-3 (0.31ppm) to 632 mu g m-3 (0.52 ppm) in the AM, and from 433 mu g m-3 (0.35 ppm) to 926 mu g m-3 (0.78 ppm) in the PM. THU air exchange rates ranged from 0.15 h-1 to 0.39 h-1. A total of 45 small (approximately 0.025 m2) samples of surface material, 16 types, were collected directly from the four THUs and shipped to Lawrence Berkeley Laboratory. The material samples were analyzed for VOC and aldehyde emissions in small stainless steel chambers using a standard, accurate mass balance method. Quantification of VOCs was done via gas chromatography -- mass spectrometry and low molecular weight aldehydes via high performance liquid chromatography. Material specific emission factors (mu g h-1 per m2 of material) were quantified. Approximately 80 unique VOCs were tentatively identified in the THU field samples, of which forty-five were quantified either because of their toxicological significance or because their concentrations were high. Whole-trailer and material specific emission factors were calculated for 33 compounds. The THU emission factors and those from their component materials were compared against those measured from other types of housing and the materials used in their construction. Whole THU emission factors for most VOCs were typically similar to those from comparative housing. The three exceptions were exceptionally large emissions of formaldehyde and TMPD-DIB (a common plasticizer in vinyl products), and somewhat elevated for phenol. Of these three compounds, formaldehyde was the only one with toxicological significance at the observed concentrations. Whole THU formaldehyde emissions ranged from 173 to 266 mu g m-2 h 1 in the morning and 257 to 347 mu g m-2 h-1 in the afternoon. Median formaldehyde emissions in previously studied site-built and manufactured homes were 31 and 45 mu g m-2 h-1, respectively. Only one of the composite wood materials that was tested appeared to exceed the HUD formaldehyde emission standard (430 mu g/m2 h-1 for particleboard and 130 mu g/m2 h-1 for plywood). The high loading factor (material surface area divided by THU volume) of composite wood products in the THUs and the low fresh air exchange relative to the material surface area may be responsible for the excessive concentrations observed for some of the VOCs and formaldehyde.

  17. Surface acoustic wave sensing of VOCs in harsh chemical environments

    SciTech Connect (OSTI)

    Pfeifer, K.B.; Martin, S.J.; Ricco, A.J.

    1993-06-01T23:59:59.000Z

    The measurement of VOC concentrations in harsh chemical and physical environments is a formidable task. A surface acoustic wave (SAW) sensor has been designed for this purpose and its construction and testing are described in this paper. Included is a detailed description of the design elements specific to operation in 300{degree}C steam and HCl environments including temperature control, gas handling, and signal processing component descriptions. In addition, laboratory temperature stability was studied and a minimum detection limit was defined for operation in industrial environments. Finally, a description of field tests performed on steam reforming equipment at Synthetica Technologies Inc. of Richmond, CA is given including a report on destruction efficiency of CCl{sub 4} in the Synthetica moving bed evaporator. Design improvements based on the field tests are proposed.

  18. 1996 Paso del Norte ozone study VOC measurements

    SciTech Connect (OSTI)

    Seila, R.L.; Main, H.; Arriaga, J.L.; Martinez, G.; Ramadan, A.B.

    1999-07-01T23:59:59.000Z

    Ambient air VOC samples were collected at surface air quality monitoring sites, near sources of interest, and aloft on the US and Mexican side of the border during a six week period of the 1996 Paso del Norte Ozone Study. On nine intensive operations (IOP) days, when high ozone concentrations were forecast, five 2-hr samples were collected at five IOP sites, three on the US side and two on the Mexican side. Six special survey sites on the US side and two on the Mexican side were sampled to characterize up-wind, down-wind and other emissions. In Ciudad Juarez, rush hour traffic, propane-powered bus exhaust, automobile paint shop emissions, propane and butane fuels, and an industrial manufacturing site were sampled. Carbonyl samples were collected at three surface sites. Carbonyl and canister grab samples were also collected during aircraft and hot air balloon flights. Most of the hydrocarbon samples were collected in electro-polished stainless steel canisters which were returned to laboratories for determination of C-2 to C-10+ hydrocarbons by cryogenic preconcentration GC-FID. The carbonyl samples were collected on DNPH impregnated C-18 Sep-Pak cartridges and analyzed by HPLC to quantify 13, C-1 to C-8 species. This paper presents the spatial and temporal characteristics of VOC species concentrations and compositions to examine the differences and similarities of the various locations and time periods. Overall surface TNMOC values ranged from 0.1 to 3.4 ppmC with the highest concentrations being recorded in the morning at three vehicle-dominated sites, two in Ciudad Juarez and one in downtown El Paso. Toluene in El Paso samples and propane, which is used as a cooking and transportation fuel in Ciudad Juarez, were the most abundant hydrocarbons. The most abundant carbonyls were acetaldehyde and acetone.

  19. Polybenzimidazole compounds

    DOE Patents [OSTI]

    Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Jones, Michael G. (Chubbuck, ID); Wertsching, Alan K. (Idaho Falls, ID); Luther, Thomas A. (Idaho Falls, ID); Trowbridge, Tammy L. (Idaho Falls, ID)

    2011-11-22T23:59:59.000Z

    A PBI compound includes imidazole nitrogens at least a portion of which are substituted with a moiety containing a carbonyl group, the substituted imidazole nitrogens being bonded to carbon of the carbonyl group. At least 85% of the nitrogens may be substituted. The carbonyl-containing moiety may include RCO--, where R is alkoxy or haloalkyl. The PBI compound may exhibit a first temperature marking an onset of weight loss corresponding to reversion of the substituted PBI that is less than a second temperature marking an onset of decomposition of an otherwise identical PBI compound without the substituted moiety. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may use more than 5 equivalents in relation to the imidazole nitrogens to be substituted.

  20. Detection of Volatile Organics Using a Surface Acoustic Wave Array System

    SciTech Connect (OSTI)

    ANDERSON, LAWRENCE F.; BARTHOLOMEW, JOHN W.; CERNOSEK, RICHARD W.; COLBURN, CHRISTOPHER W.; CROOKS, R.M.; MARTINEZ, R.F.; OSBOURN, GORDON C.; RICCO, A.J.; STATON, ALAN W.; YELTON, WILLIAM G.

    1999-10-14T23:59:59.000Z

    A chemical sensing system based on arrays of surface acoustic wave (SAW) delay lines has been developed for identification and quantification of volatile organic compounds (VOCs). The individual SAW chemical sensors consist of interdigital transducers patterned on the surface of an ST-cut quartz substrate to launch and detect the acoustic waves and a thin film coating in the SAW propagation path to perturb the acoustic wave velocity and attenuation during analyte sorption. A diverse set of material coatings gives the sensor arrays a degree of chemical sensitivity and selectivity. Materials examined for sensor application include the alkanethiol-based self-assembled monolayer, plasma-processed films, custom-synthesized conventional polymers, dendrimeric polymers, molecular recognition materials, electroplated metal thin films, and porous metal oxides. All of these materials target a specific chemical fi.mctionality and the enhancement of accessible film surface area. Since no one coating provides absolute analyte specificity, the array responses are further analyzed using a visual-empirical region-of-influence (VERI) pattern recognition algorithm. The chemical sensing system consists of a seven-element SAW array with accompanying drive and control electronics, sensor signal acquisition electronics, environmental vapor sampling hardware, and a notebook computer. Based on data gathered for individual sensor responses, greater than 93%-accurate identification can be achieved for any single analyte from a group of 17 VOCs and water.

  1. Energy efficient indoor VOC air cleaning with activated carbon fiber (ACF) filters Meera A. Sidheswaran a

    E-Print Network [OSTI]

    to reduce the energy required for heating and cooling of ventilation air by 35% to almost 50%. Ó 2011 Keywords: Activated carbon fiberVolatile organic compoundIndoor pollutantEnergy efficient ventilation a b allow reduced rates and energy consumption for outdoor air ventilation. We evaluated the use of ACF

  2. Apparatus for sensing volatile organic chemicals in fluids

    DOE Patents [OSTI]

    Hughes, Robert C.; Manginell, Ronald P.; Jenkins, Mark W.; Kottenstette, Richard; Patel, Sanjay V.

    2005-06-07T23:59:59.000Z

    A chemical-sensing apparatus is formed from the combination of a chemical preconcentrator which sorbs and concentrates particular volatile organic chemicals (VOCs) and one or more chemiresistors that sense the VOCs after the preconcentrator has been triggered to release them in concentrated form. Use of the preconcentrator and chemiresistor(s) in combination allows the VOCs to be detected at lower concentration than would be possible using the chemiresistor(s) alone and further allows measurements to be made in a variety of fluids, including liquids (e.g. groundwater). Additionally, the apparatus provides a new mode of operation for sensing VOCs based on the measurement of decay time constants, and a method for background correction to improve measurement precision.

  3. Modeling indoor exposures to VOCs and SVOCs as ventilation rates vary

    E-Print Network [OSTI]

    Parthasarathy, Srinandini

    2013-01-01T23:59:59.000Z

    J. 2008. Analysis of ventilation data from the United StatesASHRAE Standard 62.1-2010, Ventilation for Acceptable Indoorto VOCs and   SVOCs as ventilation rates vary   Srinandini 

  4. The Chicago VOC trading system : the consequences of market design for performance

    E-Print Network [OSTI]

    Kosobud, Richard F.

    2004-01-01T23:59:59.000Z

    The Chicago cap-and-trade approach to regulating stationary source VOC emissions in the Chicago ozone non-attainment area is a pioneering program that could set a precedent for other urban areas troubled by high ozone ...

  5. Semiconducting compounds and devices incorporating same

    SciTech Connect (OSTI)

    Marks, Tobin J; Facchetti, Antonio; Boudreault, Pierre-Luc; Miyauchi, Hiroyuki

    2014-06-17T23:59:59.000Z

    Disclosed are molecular and polymeric compounds having desirable properties as semiconducting materials. Such compounds can exhibit desirable electronic properties and possess processing advantages including solution-processability and/or good stability. Organic transistor and photovoltaic devices incorporating the present compounds as the active layer exhibit good device performance.

  6. Emission and Chemistry of Organic Carbon in the Gas and Aerosol Phase at a Sub-Urban Site Near Mexico City in March 2006 During the MILAGRO Study

    SciTech Connect (OSTI)

    de Gouw, Joost A.; Welsh-Bon, Daniel; Warneke, Carsten; Kuster, W. C.; Alexander, M. L.; Baker, Angela K.; Beyersdorf, Andreas J.; Blake, D. R.; Canagaratna, Manjula R.; Celada, A. T.; Huey, L. G.; Junkermann, W.; Onasch, Timothy B.; Salcido, A.; Sjostedt, S. J.; Sullivan, Amy; Tanner, David J.; Vargas-Ortiz, Leroy; Weber, R. J.; Worsnop, Douglas R.; Yu, Xiao-Ying; Zaveri, Rahul A.

    2009-05-28T23:59:59.000Z

    Volatile organic compounds (VOCs) and carbonaceous aerosol were measured at a sub-urban site near Mexico City in March of 2006 during the MILAGRO study (Megacity Initiative: Local and Global Research Objectives). Diurnal variations of hydrocarbons, elemental carbon (EC) and hydrocarbon-like organic aerosol (HOA) were dominated by a high peak in the early morning when local emissions accumulated in a shallow boundary layer, and a minimum in the afternoon when the emissions were diluted in a significantly expanded boundary layer and, in case of the reactive gases, removed by OH. In comparison, diurnal variations of species with secondary sources such as the aldehydes, ketones, oxygenated organic aerosol (OOA) and water-soluble organic carbon (WSOC) stayed relatively high in the afternoon indicating strong photochemical formation. Emission ratios of many hydrocarbon species relative to CO were higher in Mexico City than in the U.S., but we found similar emission ratios for most oxygenated VOCs and organic aerosol. Secondary formation of acetone may be more efficient in Mexico City than in the U.S., due to higher emissions of alkane precursors from the use of liquefied petroleum gas. Secondary formation of organic aerosol was similar between Mexico City and the U.S. Combining the data for all measured gas and aerosol species, we describe the budget of total observed organic carbon (TOOC), and find that the enhancement ratio of TOOC relative to CO is conserved between the early morning and mid afternoon despite large compositional changes. Finally, the influence of biomass burning is investigated using the measurements of acetonitrile, which was found to correlate with levoglucosan in the particle phase. Diurnal variations of acetonitrile indicate a contribution from local burning sources. Scatter plots of acetonitrile versus CO suggest that the contribution of biomass burning to the enhancement of most gas and aerosol species was not dominant and perhaps not dissimilar from observations in the U.S.

  7. The influences of various factors on the adsorption-desorption behaviors of hydrophobic organic compounds in sediments of Lake Charles, LA

    SciTech Connect (OSTI)

    Wei Chen; Kan, A.T.; Tomson, M.B. [Rice Univ., Houston, TX (United States)

    1996-10-01T23:59:59.000Z

    Both the adsorption and the desorption processes play important roles in the transport and fate of organic contaminants in water-sediments and groundwater systems. The adsorption-desorption processes are shown to be influenced by a number of factors, including sediments organic carbon content, contaminant aqueous solubility, aqueous-phase concentration as well as some natural environmental factors such as pH, pE, ionic strength and temperature. External mechanical forces, such as sediment perturbation, and repeated dredging will also have finite effect on the microscopic interparticle forces that control bonds between large and small grain particles. The objective of this research is to study the influences of various environmental effects on the equilibrium or non-equilibrium desorption behavior of nonpolar organic pollutants in historically contaminated natural sediments of Lake Charles, LA. Differences of desorption behavior between freshly and historically contaminated sediments will be compared in order to evaluated the desorption mechanism. The influences of particle size, mineral composition, organic matter concentration, and aqueous phase matrix composition on desorption behaviour will also be evaluated.

  8. TMVOC, simulator for multiple volatile organic chemicals

    SciTech Connect (OSTI)

    Pruess, Karsten; Battistelli, Alfredo

    2003-03-25T23:59:59.000Z

    TMVOC is a numerical simulator for three-phase non-isothermal flow of water, soil gas, and a multicomponent mixture of volatile organic chemicals (VOCs) in multidimensional heterogeneous porous media. It is an extension of the TOUGH2 general-purpose simulation program developed at the Lawrence Berkeley National Laboratory. TMVOC is designed for applications to contamination problems that involve hydrocarbon fuel or organic solvent spills in saturated and unsaturated zones. It can model contaminant behavior under ''natural'' environmental conditions, as well as for engineered systems, such as soil vapor extraction, groundwater pumping, or steam-assisted source remediation. TMVOC is upwards compatible with T2VOC (Falta et al., 1995) and can be initialized from T2VOC-style initial conditions. The main enhancements in TMVOC relative to T2VOC are as follows: a multicomponent mixture of volatile organic chemicals can be modeled; any and all combinations of the three phases water-oil-gas are treated; several non-condensible gases may be present; diffusion is treated in all phases in a manner that is fully coupled with phase partitioning. This paper gives a brief summary of the methodology used in TMVOC as well as highlighting some implementation issues. Simulation of a NAPL spill and subsequent remediation is discussed for a 2-D vertical section of a saturated-unsaturated flow problem.

  9. Alternative current conduction mechanisms of organic-inorganic compound [N(CH{sub 3}){sub 3}H]{sub 2}ZnCl{sub 4}

    SciTech Connect (OSTI)

    Ben Bechir, M., E-mail: mohamedbenbechir@hotmail.fr; Karoui, K.; Guidara, K.; Ben Rhaiem, A. [Laboratory of Condensed Matter, Faculty of Sciences, University of Sfax, BP1171, 3018 Sfax (Tunisia); Tabellout, M. [LUNAM Université, Université du Maine, CNRS UMR 6283, Institut des Molécules et Matériaux du Mans (IMMM), Avenue Olivier Messiaen, F-72085, Le Mans Cedex 09 (France)

    2014-04-21T23:59:59.000Z

    [N(CH{sub 3}){sub 3}H]{sub 2}ZnCl{sub 4} has been studied by X-ray powder diffraction patterns, differential scanning calorimetry (DSC), and impedance spectroscopy. The [N(CH{sub 3}){sub 3}H]{sub 2}ZnCl{sub 4} hybrid compound is crystallized at room temperature (T ? 300?K) in the orthorhombic system with Pnma space group. Five phase transitions (T{sub 1}?=?255?K, T{sub 2}?=?282?K, T{sub 3}?=?302?K, T{sub 4}?=?320?K, and T{sub 5}?=?346?K) have been proved by DSC measurements. The electrical technique was measured in the 10{sup ?1}-10{sup 7}?Hz frequency range and 233–363?K temperature interval. The frequency dependence of alternative current (AC) conductivity is interpreted in terms of Jonscher's law. The AC electrical conduction in [N(CH{sub 3}){sub 3}H]{sub 2}ZnCl{sub 4} is analyzed by different processes, which can be attributed to several models: the correlated barrier hopping model in phase I, the overlapping large polaron tunneling model in phase II, the quantum mechanical tunneling model in phase IV, and the non-overlapping small polaron tunneling model in phases III, V, and VI. The conduction mechanism is studied with the help of Elliot's theory, and the Elliot's parameters are determined.

  10. Alternative current conduction mechanisms of organic-inorganic compound [N(CH{sub 3}){sub 3}H]{sub 2}CuCl{sub 4}

    SciTech Connect (OSTI)

    Ben Bechir, M., E-mail: mohamedbenbechir@hotmail.fr; Karoui, K.; Guidara, K.; Ben Rhaiem, A. [Laboratory of Condensed Matter, Faculty of Sciences, University of Sfax, BP1171, 3018 Sfax (Tunisia); Tabellout, M. [LUNAM Université, Université du Maine, CNRS UMR 6283, Institut des Molécules et Matériaux du Mans (IMMM), Avenue Olivier Messiaen, F-72085 Le Mans Cedex 09 (France)

    2014-05-28T23:59:59.000Z

    The [N(CH{sub 3}){sub 3}H]{sub 2}CuCl{sub 4} single crystal has been analyzed by X-ray powder diffraction patterns, differential scanning calorimetry (DSC), and electrical impedance spectroscopy. [N(CH{sub 3}){sub 3}H]{sub 2}CuCl{sub 4} crystallizes at room temperature in the monoclinic system with P2{sub 1}/{sub C} space group. Three phase transitions at T{sub 1}?=?226?K, T{sub 2}?=?264?K, and T{sub 3}?=?297?K have been evidenced by DSC measurements. The electrical technique was measured in the 10{sup ?1}–10{sup 7}?Hz frequency range and 203–313?K temperature intervals. The frequency dependence of alternative current (AC) conductivity is interpreted in terms of Jonscher's law (developed). The AC electrical conduction in [N(CH{sub 3}){sub 3}H]{sub 2}CuCl{sub 4} compound is studied by two processes which can be attributed to a hopping transport mechanism: the correlated barrier hopping model in phases I, II, and III, the non-overlapping small polaron tunneling model in phase IV. The conduction mechanism is interpreted with the help of Elliot's theory, and the Elliot's parameters are found.

  11. Oxidized organic functional groups in aerosol particles from forest emissions measured at mid-mountain and high- elevation mountain sites in Whistler, BC

    E-Print Network [OSTI]

    Schwartz, Rachel E.

    2010-01-01T23:59:59.000Z

    FTIR) and X-ray fluorescence (XRF) techniques for organicPTR-MS SOA SP2 STXM-NEXAFS VOC XRF Aerosol Mass SpectrometerPTR-MS), X-ray fluorescence (XRF), single particle soot

  12. Bismaleimide compounds

    DOE Patents [OSTI]

    Adams, J.E.; Jamieson, D.R.

    1986-01-14T23:59:59.000Z

    Bismaleimides of the formula shown in the diagram wherein R[sub 1] and R[sub 2] each independently is H, C[sub 1-4]-alkyl, C[sub 1-4]-alkoxy, Cl or Br, or R[sub 1] and R[sub 2] together form a fused 6-membered hydrocarbon aromatic ring, with the proviso that R[sub 1] and R[sub 2] are not t-butyl or t-butoxy; X is O, S or Se; n is 1--3; and the alkylene bridging group, optionally, is substituted by 1--3 methyl groups or by fluorine, form polybismaleimide resins which have valuable physical properties. Uniquely, these compounds permit extended cure times, i.e., they remain fluid for a time sufficient to permit the formation of a homogeneous melt prior to curing.

  13. Bismaleimide compounds

    DOE Patents [OSTI]

    Adams, Johnnie E. (Grandview, MO); Jamieson, Donald R. (Merriam, KS)

    1986-01-14T23:59:59.000Z

    Bismaleimides of the formula ##STR1## wherein R.sub.1 and R.sub.2 each independently is H, C.sub.1-4 -alkyl, C.sub.1-4 -alkoxy, C1 or Br, or R.sub.1 and R.sub.2 together form a fused 6-membered hydrocarbon aromatic ring, with the proviso that R.sub.1 and R.sub.2 are not t-butyl or t-butoxy; X is O, S or Se; n is 1-3; and the alkylene bridging group, optionally, is substituted by 1-3 methyl groups or by fluorine, form polybismaleimide resins which have valuable physical properties. Uniquely, these compounds permit extended cure times, i.e., they remain fluid for a time sufficient to permit the formation of a homogeneous melt prior to curing.

  14. Method for lowering the VOCS emitted during drying of wood products

    DOE Patents [OSTI]

    Banerjee, Sujit (1832 Jacksons Creek Point, Marietta, GA 30068); Boerner, James Robert (154 Junedale Rd., Cincinnati, OH 45218); Su, Wei (2262 Orleans Ave., Marietta, GA 30062)

    2000-01-01T23:59:59.000Z

    The present invention is directed to a method for removal of VOCs from wood products prior to drying the wood products. The method of the invention includes the steps of providing a chamber having an opening for receiving wood and loading the chamber with green wood. The wood is loaded to an extent sufficient to provide a limited headspace in the chamber. The chamber is then closed and the wood is heated in the chamber for a time and at a temperature sufficient to saturate the headspace with moisture and to substantially transfer VOCs from the wood product to the moisture in the headspace.

  15. Water-soluble organometallic compounds. 3. Kinetic investigations of dissociative phosphine substitution processes involving water-soluble group 6 metal derivatives in miscible aqueous/organic media

    SciTech Connect (OSTI)

    Darensbourg, D.J.; Bischoff, C.J. (Texas A M Univ., College Station (United States))

    1993-01-06T23:59:59.000Z

    Mechanistic aspects of ligand substitution reactions of group 6 metal carbonyl derivatives containing the trisulfonated phosphine P(m-C[sub 6]H[sub 4]SO[sub 3]Na)[sub 3] (hereafter referred to as TPPTS) in pure water and water/THF media have been investigated by examination of the reactions of these derivatives with carbon monoxide as an incoming ligand. The reactions, which were carried out under 500 psi of CO in the temperature range 110-160[degrees]C, were monitored in situ by infrared spectroscopy employing a cylindrical internal reflectance reactor. Kinetic measurements show the reactions are first-order in metal complex concentration and independent of CO pressure at high CO pressures, and the rates are retarded by added TPPTS. The activation parameters for TPPTS dissociation from M(CO)[sub 5]TPPTS derivatives (M = Mo, W), e.g., in 1:1 THF/H[sub 2]O, [Delta]H[double dagger] = 28.8 [plus minus] 1.4 kcal/mol and [Delta]S[double dagger] = [minus]4.2 [plus minus] 3.5 eu and [Delta]H[double dagger] = 31.8 [plus minus] 1.5 kcal/mol and [Delta]S[double dagger] = [minus]0.73 [plus minus] 3.6 eu, respectively were shown to be quite similar to those determined for the analogous processes involving the nonsulfonated PPh[sub 3] ligand in the same solvent systems. In addition only small solvent effects were noted in going from aqueous to organic solvents for these dissociative processes. For the cis-Mo(CO)[sub 4][TPPTS][sub 2] derivative, in which the sodium ions are encapsulated by a cryptand, kryptofix-221, a steric acceleration of TPPTS dissociation is noted relative to its PPh[sub 3] analog. 27 refs., 5 figs., 6 tabs.

  16. Services Initiatives | Department of Energy

    Energy Savers [EERE]

    and is very low in Volatile Organic Compounds (VOCs) which evaporate little and cause no air pollution, whereas petroleum-based inks are high in VOCs and cause air pollution when...

  17. Characterizing the formation of secondary organic aerosols

    SciTech Connect (OSTI)

    Lunden, Melissa; Black, Douglas; Brown, Nancy

    2004-02-01T23:59:59.000Z

    Organic aerosol is an important fraction of the fine particulate matter present in the atmosphere. This organic aerosol comes from a variety of sources; primary organic aerosol emitted directly from combustion process, and secondary aerosol formed in the atmosphere from condensable vapors. This secondary organic aerosol (SOA) can result from both anthropogenic and biogenic sources. In rural areas of the United States, organic aerosols can be a significant part of the aerosol load in the atmosphere. However, the extent to which gas-phase biogenic emissions contribute to this organic load is poorly understood. Such an understanding is crucial to properly apportion the effect of anthropogenic emissions in these rural areas that are sometimes dominated by biogenic sources. To help gain insight on the effect of biogenic emissions on particle concentrations in rural areas, we have been conducting a field measurement program at the University of California Blodgett Forest Research Facility. The field location includes has been used to acquire an extensive suite of measurements resulting in a rich data set, containing a combination of aerosol, organic, and nitrogenous species concentration and meteorological data with a long time record. The field location was established in 1997 by Allen Goldstein, a professor in the Department of Environmental Science, Policy and Management at the University of California at Berkeley to study interactions between the biosphere and the atmosphere. The Goldstein group focuses on measurements of concentrations and whole ecosystem biosphere-atmosphere fluxes for volatile organic compounds (VOC's), oxygenated volatile organic compounds (OVOC's), ozone, carbon dioxide, water vapor, and energy. Another important collaborator at the Blodgett field location is Ronald Cohen, a professor in the Chemistry Department at the University of California at Berkeley. At the Blodgett field location, his group his group performs measurements of the concentrations of important gas phase nitrogen compounds. Experiments have been ongoing at the Blodgett field site since the fall of 2000, and have included portions of the summer and fall of 2001, 2002, and 2003. Analysis of both the gas and particle phase data from the year 2000 show that the particle loading at the site correlates with both biogenic precursors emitted in the forest and anthropogenic precursors advected to the site from Sacramento and the Central Valley of California. Thus the particles at the site are affected by biogenic processing of anthropogenic emissions. Size distribution measurements show that the aerosol at the site has a geometric median diameter of approximately 100 nm. On many days, in the early afternoon, growth of nuclei mode particles (<20 nm) is also observed. These growth events tend to occur on days with lower average temperatures, but are observed throughout the summer. Analysis of the size resolved data for these growth events, combined with typical measured terpene emissions, show that the particle mass measured in these nuclei mode particles could come from oxidation products of biogenic emissions, and can serve as a significant route for SOA partitioning into the particle phase. During periods of each year, the effect of emissions for forest fires can be detected at the Blodgett field location. During the summer of 2002 emissions from the Biscuit fire, a large fire located in Southwest Oregon, was detected in the aerosol data. The results show that increases in particle scattering can be directly related to increased black carbon concentration and an appearance of a larger mode in the aerosol size distribution. These results show that emissions from fires can have significant impact on visibility over large distances. The results also reinforce the view that forest fires can be a significant source of black carbon in the atmosphere, which has important climate and visibility. Continuing work with the 2002 data set, particularly the combination of the aerosol and gas phase data, will continue to provide important information o

  18. Ambient air measurements related to traffic : volution of VOCs over three years

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    hours. The major VOC are : benzène and toluène, MTBE, 1,3-butadiene, formaldehyde, phénol, naphtalene, but will not be discussed hère. Aromatic hydrocarbons and MTBE are sampled b

  19. Photoconductive Decay Lifetime and Suns-Voc Diagnostics of Efficient Heterojunction Solar Cells: Preprint

    SciTech Connect (OSTI)

    Page, M. R.; Iwaniczko, E.; Xu, Y.; Roybal L.; Bauer, R.; Yan, H.-C.; Wang, Q.; Meier, D. L.

    2008-05-01T23:59:59.000Z

    We report results of minority carrier lifetime measurements for double-sided p-type Si heterojunction devices and compare Suns-Voc results to Light I-V measurements on 1 cm2 solar cell devices measured on an AM1.5 calibrated XT-10 solar simulator.

  20. Amorphous Molecular Organic Solids for Gas Adsorption. | EMSL

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Molecular Organic Solids for Gas Adsorption. Amorphous Molecular Organic Solids for Gas Adsorption. Abstract: We show that molecular organic compounds with large accessible...

  1. Ex 7.6(a) The vapor pressure of benzene is 400 Torr at 60.6C, but it fell to 386 Torr when 19.0 g of an involatile organic compound was dissolved in 500 g of benzene. Calculate the

    E-Print Network [OSTI]

    Findley, Gary L.

    Ex 7.6(a) The vapor pressure of benzene is 400 Torr at 60.6°C, but it fell to 386 Torr when 19.0 g of an involatile organic compound was dissolved in 500 g of benzene. Calculate the molar mass of the involatile

  2. Volatile Organic Compound Detection Using Nanostructured Copolymers

    E-Print Network [OSTI]

    Weiss, Lee E.

    conductivity of these copolymers increased or decreased depending upon the polymer composition and the specific,3-6 conductive poly- mers (CPs),7-12 and carbon black-polymer composites.13,14 Metal oxide materials Carbon black-polymer composites have also attracted a lot of research interest as a promising sensing

  3. Hydrophobic VOC absorption in two-phase partitioning bioreactors; influence of silicone oil volume fraction on absorber diameter.

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    1 Hydrophobic VOC absorption in two-phase partitioning bioreactors; influence of silicone oil of a mixture of an aqueous phase and a NAPL, before being introduced into a two-phase partitioning bioreactor

  4. Reliable fieldable VOC analysis with an automated microprocessor controlled two stage sample processor

    SciTech Connect (OSTI)

    Overton, E.B.; Stewart, M.; Carney, K.R.; D`Harmasena, H. [Louisiana State Univ., Baton Rouge, LA (United States). Inst. for Environmental Studies

    1995-12-31T23:59:59.000Z

    High quality field analysis of VOCs from a variety of sample types has many environmental applications. In order to achieve desired data quality from field analysis, the entire analytical sequence, from collection of samples through instrumental analysis and data interpretation, must be controlled and have documented precision. To this end, the authors have developed a Sample Processing Device for use with fieldable VOC analyses. The unit is microprocessor controlled, small, rugged, and uses less than 25 watts of power at 12 VDC. It is ideally suited for use with microchip GC analyzers but will work with a variety of other field analytical devices. In addition to processing a variety of sample types, the unit allows control of water interference in the analytical sequence. Since the functions of the sample processing device are microprocessor controlled, the sample analysis procedures have the precision and reliability of automated, methods driven analytical techniques.

  5. A Case for Safer Building Materials: Lifecycle Concerns, Data Gaps, and

    E-Print Network [OSTI]

    Lee, Seung-Wuk

    ;Conventional Building Materials · Wood · Stone · Cement · Metal · Glass · Straw · Ceramics #12;Synthetic;Volatile organic compounds (VOCs) · Aliphatic hydrocarbons, aromatic hydrocarbons, halogenated hydrocarbons

  6. Process for reducing aromatic compounds in ethylenediamine with calcium

    DOE Patents [OSTI]

    Benkeser, R.A.; Laugal, J.A.; Rappa, A.

    1985-08-06T23:59:59.000Z

    Olefins are produced by containing an organic compound having at least one benzene ring with ethylenediamine and calcium metal, the calcium metal being used in large excess or alternatively in conjunction with an inert abrasive particulate substance. Substantially all of the organic compounds are converted to corresponding cyclic olefins, largely mono-olefins.

  7. Process for reducing aromatic compounds in ethylenediamine with calcium

    DOE Patents [OSTI]

    Benkeser, Robert A. (West Lafayette, IN); Laugal, James A. (Lostant, IL); Rappa, Angela (Baltimore, MD)

    1985-01-01T23:59:59.000Z

    Olefins are produced by containing an organic compound having at least one benzene ring with ethylenediamine and calcium metal, the calcium metal being used in large excess or alternatively in conjunction with an inert abrasive particulate substance. Substantially all of the organic compounds are converted to corresponding cyclic olefins, largely mono-olefins.

  8. Volatile organic chemical emissions from carpets. Final report

    SciTech Connect (OSTI)

    Hodgson, A.T.; Wooley, J.D.; Daisey, J.M.

    1992-04-01T23:59:59.000Z

    The primary objective of this research, was to measure the emission rates of selected individual VOC, including low molecular-weight aldehydes, released by samples of four new carpets that are typical of the major types of carpets used in residences, schools and offices. The carpet samples were collected directly from the manufacturers` mills and packaged to preserve their chemical integrity. The measurements of the concentrations and emission rates of these compounds were made under simulated indoor conditions in a 20-M{sup 3} environmental chamber designed specifically for investigations of VOC. The measurements were conducted over a period of one week following the installation of the carpet samples in the chamber. Duplicate experiments were conducted for one carpet. In addition, the concentrations and emission rates of VOC resulting from the installation of a new carpet in a residence were measured over a period of seven weeks. The stabilities of the week-long ventilation rates and temperatures were one percent relative standard deviation. The four carpets emitted a variety of VOC, 40 of which were positively identified. Eight of these were considered to be dominant. They were (in order of chromatographic retention time) formaldehyde, vinyl acetate, 2,2,4-trimethylpentane (isooctane), 1,2-propanediol (propylene glycol), styrene, 2-ethyl-l-hexanol, 4-phenylcyclohexene (4-PCH), and 2,6 di-tert-butyl-4-methylphenol (BHT). With the exception of formaldehyde, only limited data are available on the toxicity and irritancy of these compounds at low concentrations. Therefore, it is difficult to determine at this time the potential magnitude of the health and comfort effects that may occur among the population from exposures to emissions from new carpets. The concentrations and emission rates of most compounds decreased rapidly over the first 12 h of the experiments.

  9. Mixed crystal organic scintillators

    DOE Patents [OSTI]

    Zaitseva, Natalia P; Carman, M Leslie; Glenn, Andrew M; Hamel, Sebastien; Hatarik, Robert; Payne, Stephen A; Stoeffl, Wolfgang

    2014-09-16T23:59:59.000Z

    A mixed organic crystal according to one embodiment includes a single mixed crystal having two compounds with different bandgap energies, the organic crystal having a physical property of exhibiting a signal response signature for neutrons from a radioactive source, wherein the signal response signature does not include a significantly-delayed luminescence characteristic of neutrons interacting with the organic crystal relative to a luminescence characteristic of gamma rays interacting with the organic crystal. According to one embodiment, an organic crystal includes bibenzyl and stilbene or a stilbene derivative, the organic crystal having a physical property of exhibiting a signal response signature for neutrons from a radioactive source.

  10. Elements & Compounds Atoms (Elements)

    E-Print Network [OSTI]

    Frey, Terry

    #12;Elements & Compounds #12;Atoms (Elements) Molecules (Compounds) Cells Elements & Compounds #12 #12;First shell Second shell Third shell Hydrogen 1H Lithium 3Li Sodium 11Na Beryllium 4Be Magnesium energy Higher energy (a) A ball bouncing down a flight of stairs provides an analogy for energy levels

  11. Pilot-scale study of the solar detoxification of VOC-contaminated groundwater

    SciTech Connect (OSTI)

    Mehos, M.; Turchi, C. [National Renewable Energy Lab., Golden, CO (United States)] [National Renewable Energy Lab., Golden, CO (United States); Pacheco, J. [Sandia National Labs., Albuquerque, NM (United States)] [Sandia National Labs., Albuquerque, NM (United States); Boegel, A.J.; Merrill, T.; Stanley, R. [Lawrence Livermore National Lab., CA (United States)] [Lawrence Livermore National Lab., CA (United States)

    1992-08-01T23:59:59.000Z

    The Solar Detoxification Field Experiment was designed to investigate the photocatalytic decomposition of organic contaminants in groundwater at a Superfund site at Lawrence Livermore National Laboratory (LLNL). The process uses ultraviolet (UV) energy, available in sunlight, in conjunction with the photocatalyst, titanium dioxide, to decompose organic chemicals into nontoxic compounds. The field experiment was developed by three federal laboratories: the National Renewable Energy Laboratory (NREL), Sandia National Laboratory (SNLA), and LLNL. The US Department of Energy funded the experiment. The objectives of the pilot-scale study included the advancement of the solar technology into a nonlaboratory waste-remediation environment the compilation of test data to help guide laboratory research and future demonstrations and the development of safe operational procedures. Results of the pilot study are discussed, emphasizing the effect of several process variables on the system performance. These variables include alkalinity, catalyst loading, flow velocity through the reactor, and incident solar UV radiation. The performance of the solar detoxification process are discussed as it relates to concentrating and nonconcentrating collectors.

  12. Brookhaven National Laboratory - OU I/IV VOC | Department of Energy

    Office of Environmental Management (EM)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625 1,006 492 742 33 111 1,613PortsmouthBartlesville Energy ResearchAchievingHydraulic Institute StandardsHFBRI/IV VOC

  13. Mapping isoprene emissions over North America using formaldehyde column observations from space

    E-Print Network [OSTI]

    Chance, Kelly

    Mapping isoprene emissions over North America using formaldehyde column observations from space. [1] We present a methodology for deriving emissions of volatile organic compounds (VOC) using space to local VOC emissions, with a spatial smearing that increases with the VOC lifetime. Isoprene

  14. Electric Turbo Compounding Technology Update

    Broader source: Energy.gov (indexed) [DOE]

    Turbo Compounding Technology Update Electric Turbo Compounding Technology Update 15 August, 2007 Carl Vuk 15 August, 2007 Carl Vuk Electric Turbo Compounding Highlights Electric...

  15. Low VOC drying of lumber and wood panel products. Progress report number 9

    SciTech Connect (OSTI)

    Hooda, U.; Banerjee, S. [Inst. of Paper Science and Technology, Atlanta, GA (United States); Ingram, L.; Conners, T. [Mississippi State Univ., MS (United States)

    1998-10-01T23:59:59.000Z

    This project is based on the finding that brief microwave or RF-treatment of wood under low-headspace conditions leads to the release of VOCs. On occasion the authors have found that prolonged irradiation increases turpentine yield much more than anticipated from a simple mass balance; i.e., more pinene appeared to be released than was present in the wood in the first place. If taken at face value, this suggests that brief low-headspace irradiation removes VOCs, while prolonged exposure creates it. While seemingly improbable, this could follow if dielectric heating exposed regions of wood that were otherwise inaccessible to the solvent used for extraction (unlikely), or if the irradiation induced depolymerization of terpene dimers or higher polymers. In this report the authors attempt to identify the conditions that lead to this apparent enhancement of terpene yield, by constructing relationships between yield and irradiation parameters. The tentative conclusions are that this enhancement only occurs with relatively wet heartwood, and only under prolonged irradiation. An additional conclusion is that continuing analyses of twelve trees in the MSU forest confirm that the absence of a significant seasonal influence on turpentine content. An apparatus for permeability testing has been constructed, and work is underway.

  16. XAFS Model Compound Library

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Newville, Matthew

    The XAFS Model Compound Library contains XAFS data on model compounds. The term "model" compounds refers to compounds of homogeneous and well-known crystallographic or molecular structure. Each data file in this library has an associated atoms.inp file that can be converted to a feff.inp file using the program ATOMS. (See the related Searchable Atoms.inp Archive at http://cars9.uchicago.edu/~newville/adb/) This Library exists because XAFS data on model compounds is useful for several reasons, including comparing to unknown data for "fingerprinting" and testing calculations and analysis methods. The collection here is currently limited, but is growing. The focus to date has been on inorganic compounds and minerals of interest to the geochemical community. [Copied, with editing, from http://cars9.uchicago.edu/~newville/ModelLib/

  17. Preparation of uranium compounds

    DOE Patents [OSTI]

    Kiplinger, Jaqueline L; Montreal, Marisa J; Thomson, Robert K; Cantat, Thibault; Travia, Nicholas E

    2013-02-19T23:59:59.000Z

    UI.sub.3(1,4-dioxane).sub.1.5 and UI.sub.4(1,4-dioxane).sub.2, were synthesized in high yield by reacting turnings of elemental uranium with iodine dissolved in 1,4-dioxane under mild conditions. These molecular compounds of uranium are thermally stable and excellent precursor materials for synthesizing other molecular compounds of uranium including alkoxide, amide, organometallic, and halide compounds.

  18. Partially fluorinated ionic compounds

    DOE Patents [OSTI]

    Han, legal representative, Amy Qi (Hockessin, DE); Yang, Zhen-Yu (Hockessin, DE)

    2008-11-25T23:59:59.000Z

    Partially fluorinated ionic compounds are prepared. They are useful in the preparation of partially fluorinated dienes, in which the repeat units are cycloaliphatic.

  19. Persistent Organic By Steven Jackson

    E-Print Network [OSTI]

    Toohey, Darin W.

    Persistent Organic Pollutants By Steven Jackson #12;What are POP's? · POP's are organic compounds, rivers and surface ocean water. · Bio accumulation- POPs work their way through the food chain by accumulating in the body fat of living organisms and becoming more concentrated as they move from one creature

  20. Source Contributions to VOC's to Ozone Formation in Southeast Texas Using a Source-oriented Air Quality Model 

    E-Print Network [OSTI]

    Krishnan, Anupama

    2011-08-08T23:59:59.000Z

    Houston-Galveston-Brazoria area is in severe non-attainment status for ozone compliance. Source-oriented mechanistic modeling was used to determine the major sources of VOCs that contributes to ozone formation during the Texas Air Quality Study (Tex...

  1. WAT ENVIRON RESEARCH (in press, final version may have small changes) ODOR AND VOC TREATMENT BY BIOTRICKLING FILTERS: PILOT SCALE

    E-Print Network [OSTI]

    of the reactor was continuously monitored over a period of 10 months. At an average empty bed gas residence time odorous waste gases. The waste gas from the Headworks at HTP (100,000 cfm) contains 10-50 ppm H2S generate VOCs, which are subsequently emitted into the atmosphere (Witherspoon et al., 1995). Other

  2. Source Contributions to VOC's to Ozone Formation in Southeast Texas Using a Source-oriented Air Quality Model

    E-Print Network [OSTI]

    Krishnan, Anupama

    2011-08-08T23:59:59.000Z

    Houston-Galveston-Brazoria area is in severe non-attainment status for ozone compliance. Source-oriented mechanistic modeling was used to determine the major sources of VOCs that contributes to ozone formation during the Texas Air Quality Study (Tex...

  3. Low-Temperature, Vacuum-Aided Thermal Desorption Studies on a Simulated Organic Sludge Waste

    SciTech Connect (OSTI)

    R. K. Farnsworth; D. R. Peterman; Gary L. Anderson; T. G. Garn

    2002-12-01T23:59:59.000Z

    This report describes an initial set of small scale lab tests conducted on surrogate waste materials to investigate mass release behavior of volatile organics (VOC’s) from a solidified liquid organic sludge matrix under vacuumaided, low-temperature thermal desorption conditions. Low temperature thermal desorption is being considered as a potential processing technology alternative to incineration, to remove gas generation limitations affecting the transportation of transuranic (TRU) contaminated organic sludge wastes to a designated off-site repository (i.e., the Waste Isolation Pilot Plant). The lab-scale tests provide initial exploratory level information on temperature profiles and rates of volatile organic desorption for a range of initial VOC/oil liquid mixture concentrations in a calcium silicate matrix, under low temperature heating and vacuum boundary conditions that are representative of potentially desirable “in-drum desorption” conditions. The results of these tests indicate that reduced operating pressures have a potential for significantly enhancing the rate of thermal desorption experienced from a liquid organic/oil solidified “sludge” waste. Furthermore, the results indicate that in-drum thermal desorption can be performed on organic sludge wastes, at reduced pressures, while maintaining an operating temperature sufficiently low to prevent destruction of the waste drum packaging materials (confinement) surrounding the waste. The results also indicate that VOC release behavior/rates in the vacuum thermal desorption process cannot be represented by a simple liquid-liquid mass-diffusion model, since overall mass release rates observed are generally two orders of magnitude greater than predicted by simple liquid-liquid mass diffusion. This is partially attributed to the effects of the transient temperature profiles within the sludge during heat up; however, the primary cause is thought to be micro boiling of the volatile organics within the simulated sludge. Micro boiling of VOC’s would be expected to occur in localized volumes within the organic sludge where temperatures exceed the volatile organic saturation temperature sufficiently to form vapor bubbles. Further model based evaluations reflecting the transient temperatures, local boiling, and subsequent vapor in liquid/sludge transport conditions are needed, with supporting controlled testing of the vacuum-aided thermal desorption process at small and full-scale conditions in order to fully develop this process.

  4. Modeling kinetic partitioning of secondary organic aerosol and size distribution dynamics: representing effects of volatility, phase state, and particle-phase reaction

    SciTech Connect (OSTI)

    Zaveri, Rahul A.; Easter, Richard C.; Shilling, John E.; Seinfeld, J. H.

    2014-05-27T23:59:59.000Z

    Evidence is mounting that the majority of the climatically active aerosols are produced through the growth of smaller particles via secondary organic aerosol (SOA) formation from gas-to-particle conversion of anthropogenic and biogenic volatile organic compounds (VOCs). The timescale of SOA partitioning and the associated size distribution dynamics are expected to depend on the gas-phase oxidation of the precursor VOCs and their products, volatility of these organic solutes, composition and phase state of the pre-existing particles, and diffusivity and reactivity of the solute within the particle phase. This paper describes a new framework for modeling kinetic gas-particle partitioning of SOA, with an analytical treatment for the diffusion-reaction process within the particle phase. The formulation is amenable for eventual use in regional and global climate models, although it currently awaits implementation of the actual particle-phase reactions that are important for SOA formation. In the present work, the model is applied to investigate the competitive growth dynamics of the Aitken and accumulation mode particles while the Kelvin effect and coagulation are neglected for simplicity. The timescale of SOA partitioning and evolution of number and composition size distributions are evaluated for a range of solute volatilities (C*), particle-phase bulk diffusivities (Db), and particle-phase reactivity, as exemplified by a pseudo-first-order rate constant (kc). Results show that irreversible condensation of non-volatile organic vapors (equivalent to ) produces significant narrowing of the size distribution. At the other extreme, non-reactive partitioning of semi-volatile organic vapors is volume-controlled in which the final (equilibrium) size distribution simply shifts to the right on the diameter axis while its shape remains unchanged. However, appreciable narrowing of the size distribution may occur when the pre-existing particles are highly viscous semi-solids such that small particles reach quasi-equilibrium much faster than the large ones. In the case of reactive partitioning (finite ), the size distribution experiences permanent narrowing, which is especially pronounced for Db < 10-13 cm2 s-1 and kc > 0.01 s-1. As a result, both number and composition size distributions are needed to effectively constrain and evaluate the next generation of SOA models that treat phase state thermodynamics, particle-phase diffusion and particle-phase chemical reactions.

  5. Heart testing compound

    DOE Patents [OSTI]

    Knapp, F.F. Jr.; Goodman, M.M.

    1983-06-29T23:59:59.000Z

    The compound 15-(p-(/sup 125/I)-iodophenyl)-6-tellurapentadecanoic acid is disclosed as a myocardial imaging agent having rapid and pronounced uptake, prolonged myocardial retention, and low in vivo deiodination.

  6. Heart testing compound

    DOE Patents [OSTI]

    Knapp, Jr., Furn F. (Oak Ridge, TN); Goodman, Mark M. (Knoxville, TN)

    1985-01-01T23:59:59.000Z

    The compound 15-(p-[.sup.125 I]-iodophenyl)-6-tellurapentadecanoic acid is disclosed as a myocardial imaging agent having rapid and pronounced uptake, prolonged myocardial retention, and low in vivo deiodination.

  7. Microoptical compound lens

    DOE Patents [OSTI]

    Sweatt, William C. (Albuquerque, NM); Gill, David D. (Albuquerque, NM)

    2007-10-23T23:59:59.000Z

    An apposition microoptical compound lens comprises a plurality of lenslets arrayed around a segment of a hollow, three-dimensional optical shell. The lenslets collect light from an object and focus the light rays onto the concentric, curved front surface of a coherent fiber bundle. The fiber bundle transports the light rays to a planar detector, forming a plurality of sub-images that can be reconstructed as a full image. The microoptical compound lens can have a small size (millimeters), wide field of view (up to 180.degree.), and adequate resolution for object recognition and tracking.

  8. Reactive codoping of GaAlInP compound semiconductors

    DOE Patents [OSTI]

    Hanna, Mark Cooper (Boulder, CO); Reedy, Robert (Golden, CO)

    2008-02-12T23:59:59.000Z

    A GaAlInP compound semiconductor and a method of producing a GaAlInP compound semiconductor are provided. The apparatus and method comprises a GaAs crystal substrate in a metal organic vapor deposition reactor. Al, Ga, In vapors are prepared by thermally decomposing organometallic compounds. P vapors are prepared by thermally decomposing phospine gas, group II vapors are prepared by thermally decomposing an organometallic group IIA or IIB compound. Group VIB vapors are prepared by thermally decomposing a gaseous compound of group VIB. The Al, Ga, In, P, group II, and group VIB vapors grow a GaAlInP crystal doped with group IIA or IIB and group VIB elements on the substrate wherein the group IIA or IIB and a group VIB vapors produced a codoped GaAlInP compound semiconductor with a group IIA or IIB element serving as a p-type dopant having low group II atomic diffusion.

  9. Design of Semiconductor-Based Back Reflectors for High Voc Monolithic Multijunction Solar Cells: Preprint

    SciTech Connect (OSTI)

    Garcia, I.; Geisz, J.; Steiner, M.; Olson, J.; Friedman, D.; Kurtz, S.

    2012-06-01T23:59:59.000Z

    State-of-the-art multijunction cell designs have the potential for significant improvement before going to higher number of junctions. For example, the Voc can be substantially increased if the photon recycling taking place in the junctions is enhanced. This has already been demonstrated (by Alta Devices) for a GaAs single-junction cell. For this, the loss of re-emitted photons by absorption in the underlying layers or substrate must be minimized. Selective back surface reflectors are needed for this purpose. In this work, different architectures of semiconductor distributed Bragg reflectors (DBR) are assessed as the appropriate choice for application in monolithic multijunction solar cells. Since the photon re-emission in the photon recycling process is spatially isotropic, the effect of the incident angle on the reflectance spectrum is of central importance. In addition, the DBR structure must be designed taking into account its integration into the monolithic multijunction solar cells, concerning series resistance, growth economics, and other issues. We analyze the tradeoffs in DBR design complexity with all these requirements to determine if such a reflector is suitable to improve multijunction solar cells.

  10. Aminopropyl thiophene compounds

    DOE Patents [OSTI]

    Goodman, Mark M. (Knoxville, TN); Knapp, Jr., Furn F. (Oak Ridge, TN)

    1990-01-01T23:59:59.000Z

    Radiopharmaceuticals useful in brain imaging comprising radiohalogenated thienylethylamine derivatives. The compounds are 5-halo-thiophene-2-isopropyl amines able to cross the blood-brain barrier and be retained for a sufficient length of time to allow the evaluation of regional blood flow by radioimaging of the brain.

  11. Control of the accumulation of non-process elements and organic compounds in pulp mills with bleach filtrate reuse. Milestones and progress, Quarter 9 (July 1--September 30, 1998)

    SciTech Connect (OSTI)

    Frederick, W.J.; Laver, M.L.; Rorrer, G.L.; Rudie, A.W.; Schmidl, W.

    1998-12-31T23:59:59.000Z

    The two approach changes that were discussed and recommended in the Quarter 8 (April 1--June 30, 1998) progress report have been implemented in the current project plan. The OLI software has been used to develop a preliminary process model for predicting the distribution of NPE`s in a two stage brownstock washer, and the OLI database has been upgraded to include improved chemical equilibrium data for metal-organic interactions. This exercise served as a tool to evaluate the data and methods developed in this study, and to demonstrate its utility to industry. The Weyerhaeuser-NAELS software has also been applied to predicting inorganic solubility behavior. Task C-1.2, Estimation of unavailable thermodynamic parameters (scheduled completion date: 12/97), has been combined with Task D-2.1, Evaluation of the estimation procedure (scheduled completion date: 3/99) with a new scheduled completion date of 8/99. A model for the adsorption of metal ions on wood pulp fibers will include transport effects as well as adsorption equilibrium, and will be combined with a brownstock washer model to evaluate its predictive capability in comparison with mill data, and to demonstrate the applicability of the results obtained in this project. Three tasks are behind schedule: Task A-2.3, Measurement of stability constants for wood organics with metal ions (scheduled completion date: 6/98), Task B-2.1, Measure metal adsorption isotherms on wood pulp (scheduled completion date: 9/97), and Task B-2.3, Measure metal ion adsorption kinetics for strongly adsorbing metal species (scheduled completion date: 3/98). The reasons and expected completion dates are discussed in the Performance Variances and Open Items section. All other tasks are either completed, on, or ahead of schedule.

  12. Global Emissions of Terpenoid VOCs from Terrestrial Vegetation in the Last Millennium

    SciTech Connect (OSTI)

    Acosta Navarro, J. C.; Smolander, S.; Struthers, H.; Zorita, E.; Ekman, A. M.; Kaplan, J. O.; Guenther, Alex B.; Arneth, A.; Riipinen, I.

    2014-06-16T23:59:59.000Z

    We investigated the millennial variability of global BVOC emissions by using two independent numerical models: The Model of Emissions of Gases and Aerosols from Nature (MEGAN), for isoprene, monoterpene and sesquiterpene and Lund-Potsdam-Jena General Ecosystem Simulator (LPJ8 GUESS), for isoprene and monoterpenes. We found the millennial trends of global isoprene emissions to be mostly affected by land cover and atmospheric carbon dioxide changes, whereas monoterpene and sesquiterpene emission were dominated by temperature change. Isoprene emissions declined substantially in regions with large and rapid land cover change. In addition, isoprene emission sensitivity to drought proved to have signicant short term global effects. By the end of the past millennium MEGAN isoprene emissions were 634 TgC yr-1 (13% and 19% less than during during 1750-1850 and 1000- 15 1200, respectively) and LPJ-GUESS emissions were 323 TgC yr-1 (15% and 20% less than during 1750-1850 and 1000-1200, respectively). Monoterpene emissions were 89 TgC yr-1 (10% and 6% higher than during 1750-1850 and 1000-1200, respectively) in MEGAN, and 24 TgC yr-1 (2% higher and 5% 19 20 less than during 1750-1850 and 1000-1200, respectively) in LPJ-GUESS. MEGAN sesquiterpene emissions were 36 TgC yr-1 (10% and 4% higher than during1750-1850 and 1000-1200, respectively). Although both models capture similar We investigated the millennial variability of global BVOC emissions by using two independent numerical models: The Model of Emissions of Gases and Aerosols from Nature (MEGAN), for isoprene, monoterpene and sesquiterpene and Lund-Potsdam-Jena General Ecosystem Simulator (LPJ8GUESS), for isoprene and monoterpenes. We found the millennial trends ofglobal isoprene emissions to be mostly a*ected by land cover and atmospheric carbon dioxide changes, whereas monoterpene and sesquiterpene emission were dominated by temperature change. Isoprene emissions declined substantially in regions with large and rapid land cover change. In addition, isoprene emission sensitivity to drought proved to have signifcant short term global effects. By the end of the past millennium MEGAN isoprene emissions were 634 TgC yr-1 (13% and 19% less than during during 1750-1850 and 1000- 1200, respectively) and LPJ-GUESS emissions were 323 TgC yr-1 (15% and 16 17 20% less than during 1750-1850 and 1000-1200, respectively). Monoterpene emissions were 89 TgC yr-1 (10% and 6% higher than during 1750-1850 and 18 1000-1200, respectively) in MEGAN, and 24 TgC yr-1 (2% higher and 5% less than during 1750-1850 and 1000-1200, respectively) in LPJ-GUESS. MEGAN sesquiterpene emissions were 36 TgC yr-1 (10% and 4% higher than during1750-1850 and 1000-1200, respectively). Although both models capture similar emission trends, the magnitude of the emissions are different. This highlights the importance of building better constraints on VOC emissions from terrestrial vegetation.emission trends, the magnitude of the emissions are different. This highlights the importance of building better constraints on VOC emissions from terrestrial vegetation.

  13. Control of the accumulation of non-process elements and organic compounds in pulp mills with bleach filtrate reuse. Milestones and progress, Quarter 8 (April 1--June 30, 1998)

    SciTech Connect (OSTI)

    Frederick, W.J.; Laver, M.L.; Rorrer, G.L.; Rudie, A.W.; Schmidl, W.

    1998-08-01T23:59:59.000Z

    Overall, this project is on schedule and proceeding as planned. Two approach changes are recommended. One is to rely on commercially developed software, in particular that developed by OLI Systems, Inc., and now being expanded in a collaborative effort between OLI Systems, Inc. and IPST to provide a simulation package for the pulp and paper industry and to integrate it with existing process simulation tools used by that industry. The second is the development of a detailed brownstock/bleached fiber washer model as a tool to evaluate the data and methods developed in this study, and to demonstrate its utility to industry. Both of these are discussed in more detail in the Approach Changes section of this report. Two tasks are behind schedule. They are Task A-2.3, Measurement of stability constants for wood organics with metal ions (scheduled completion date: 6/98), and Task C-1.2, Estimation of unavailable thermodynamic parameters (scheduled completion date: 12/97). The reasons and expected completion dates for these tasks are discussed in the Performance Variances and Open Items section of this report. All other tasks are either completed, or on or ahead of schedule.

  14. Complex Compound Chemical Heat Pumps 

    E-Print Network [OSTI]

    Rockenfeller, U.; Langeliers, J.; Horn, G.

    1987-01-01T23:59:59.000Z

    Complex-compound solid-vapor fluid pairs can be used in heat of reaction heat pumps for temperature amplifier (TA) as well as heat amplifier (HA) cycle configurations. This report describes the conceptual hardware design for complex compound...

  15. Complex Compound Chemical Heat Pumps

    E-Print Network [OSTI]

    Rockenfeller, U.; Langeliers, J.; Horn, G.

    Complex-compound solid-vapor fluid pairs can be used in heat of reaction heat pumps for temperature amplifier (TA) as well as heat amplifier (HA) cycle configurations. This report describes the conceptual hardware design for complex compound...

  16. Partitioning of Volatile Organics in Diesel Particulate and Exhaust...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    in Diesel Particulate and Exhaust Evaluation of how sampling details affect the measurement of volatile organic compounds in diesel exhaust deer08strzelec.pdf More Documents...

  17. Titanium alkoxide compound

    DOE Patents [OSTI]

    Boyle, Timothy J. (Albuquerque, NM)

    2007-08-14T23:59:59.000Z

    A titanium alkoxide composition is provided, as represented by the chemical formula (OC.sub.6H.sub.5N).sub.2Ti(OC.sub.6H.sub.5NH.sub.2).sub.2. As prepared, the compound is a crystalline substance with a hexavalent titanium atom bonded to two OC.sub.6H.sub.5NH.sub.2 groups and two OC.sub.6H.sub.5N groups with a theoretical molecular weight of 480.38, comprising 60.01% C, 5.04% H and 11.66% N.

  18. Boronated porphyrin compounds

    DOE Patents [OSTI]

    Kahl, Stephen B. (Portola Valley, CA); Koo, Myoung-Seo (San Francisco, CA)

    1992-01-01T23:59:59.000Z

    A compound is described having the structure ##STR1## where R preferably is ##STR2## and most preferably R.sup.3 is a closo-carborane and R.sup.2 is --H, an alkyl or aryl having 1 to about 7 carbon atoms, This invention was made with Government support under NIH Grant No. CA-37961 awarded by the Department of Health and Human Services and under the Associated Universities Inc. Contract No. De-AC02-76CH00016 with the U.S. Department of Energy. The Government has rights in this invention.

  19. Boronated porphyrin compounds

    DOE Patents [OSTI]

    Kahl, S.B.; Koo, M.S.

    1992-09-22T23:59:59.000Z

    A compound is described having the structure ##STR1## where R preferably is ##STR2## and most preferably R.sup.3 is a closo-carborane and R.sup.2 is --H, an alkyl or aryl having 1 to about 7 carbon atoms, This invention was made with Government support under NIH Grant No. CA-37961 awarded by the Department of Health and Human Services and under the Associated Universities Inc. Contract No. De-AC02-76CH00016 with the U.S. Department of Energy. The Government has rights in this invention.

  20. CSTB / CTBA Wood Preservation -Cannes 2001 MEASUREMENT OF VOC EMISSIONS FROM CURATIVE TREATED WOOD

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    Committee for Standardization (CEN) and the International Organization for Standardization (ISO of International Organization for Standardization (ISO) has prepared the draft international standard ISO/DIS 16000 analytical methods are needed. The aim of this paper is to present the new standards prepared by the European

  1. Scanning Probe AFM Compound Microscope | EMSL

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Probe AFM Compound Microscope Scanning Probe AFM Compound Microscope The atomic force microscope (AFM) compound microscope is designed primarily for fluorescence imaging in the...

  2. Organic Separation Test Results

    SciTech Connect (OSTI)

    Russell, Renee L.; Rinehart, Donald E.; Peterson, Reid A.

    2014-09-22T23:59:59.000Z

    Separable organics have been defined as “those organic compounds of very limited solubility in the bulk waste and that can form a separate liquid phase or layer” (Smalley and Nguyen 2013), and result from three main solvent extraction processes: U Plant Uranium Recovery Process, B Plant Waste Fractionation Process, and Plutonium Uranium Extraction (PUREX) Process. The primary organic solvents associated with tank solids are TBP, D2EHPA, and NPH. There is concern that, while this organic material is bound to the sludge particles as it is stored in the tanks, waste feed delivery activities, specifically transfer pump and mixer pump operations, could cause the organics to form a separated layer in the tank farms feed tank. Therefore, Washington River Protection Solutions (WRPS) is experimentally evaluating the potential of organic solvents separating from the tank solids (sludge) during waste feed delivery activities, specifically the waste mixing and transfer processes. Given the Hanford Tank Waste Treatment and Immobilization Plant (WTP) waste acceptance criteria per the Waste Feed Acceptance Criteria document (24590-WTP-RPT-MGT-11-014) that there is to be “no visible layer” of separable organics in the waste feed, this would result in the batch being unacceptable to transfer to WTP. This study is of particular importance to WRPS because of these WTP requirements.

  3. Sandia National Laboratories: compound semiconductor

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    compound semiconductor Sandia and EMCORE: Solar Photovoltaics, Fiber Optics, MODE, and Energy Efficiency On March 29, 2013, in Concentrating Solar Power, Energy, Partnership,...

  4. A study of volatile compounds in the breath of children with type 1 diabetes

    E-Print Network [OSTI]

    Stevens, S; Wei, C; Greenwood, R; Hamilton-Shield, J; Costello, B de Lacy; Ratcliffe, N; Probert, C

    2013-01-01T23:59:59.000Z

    A pilot study of exhaled volatile compounds and their correlation with blood glucose levels in eight children with type 1 diabetes is reported. Five paired blood and breath samples were obtained from each child over a 6 hour period. The blood glucose concentration ranged from 41.4 to 435.6 mg/dL. Breath samples were collected in Tedlar bags and immediately evacuated through thermal desorption tubes packed with Carbopack B and C. The VOCs were later recovered by thermal desorption and analysed using gas chromatography mass spectrometry. The study identified 74 volatile compounds present in at least 10% of the patient samples. Of these 74 volatiles 36 were found in all patient samples tested. Further analysis of the 36 compounds found that none showed significant overall correlation with blood glucose levels. Isoprene showed a weak negative correlation with blood glucose levels. Acetone was found to have no correlation with blood glucose levels for the patients studied. Some patients showed significant individu...

  5. Hydrogenolysis of 6-carbon sugars and other organic compounds

    DOE Patents [OSTI]

    Werpy, Todd A.; Frye, Jr., John G.; Zacher, Alan H.; Miller, Dennis J.

    2005-01-11T23:59:59.000Z

    Methods for hydrogenolysis are described which use a Re-containing multimetallic catalyst for hydrogenolysis of both C--O and C--C bonds. Methods and compositions for reactions of hydrogen over a Re-containing catalyst with compositions containing a 6-carbon sugar, sugar alcohol, or glycerol are described. It has been surprisingly discovered that reaction with hydrogen over a Re-containing multimetallic catalyst resulted in superior conversion and selectivity to desired products such as propylene glycol.

  6. Three-Dimensional Simulation of Volatile Organic Compound Mass...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    simulations using data from the U.S. Department of Energy’s Hanford Site, where carbon tetrachloride is present in a low permeability zone about 30 m above the...

  7. Glossary of Volatile Organic Compounds Ethylbenzene Carbon tetrachloride

    E-Print Network [OSTI]

    ;Ethylbenzene Ethylbenzene is a colorless, flammable liquid found in natural products such as coal tar into the environment from burning oil, gas, and coal, and from discharges of ethylbenzene from factories. Ethylbenzene-made activities and natural processes. Benzene is widely used in the United States and ranks in the top 20

  8. Particulate Matter Sampling and Volatile Organic Compound Removal...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    being proposed to mitigate adverse human health and environmental impacts of internal combustion engines. With that in mind, it has been proposed that vehicular...

  9. Class 2 Permit Modification Request Revise Volatile Organic Compound...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    is provided in Figure N-1" Attachment N, Section N-4a(3) Replaced "Treated stainless steel" with "The" Deleted "is" Replaced "from the desired sample point to the sample...

  10. Control of spider mites on cotton by organic sulphur compounds

    E-Print Network [OSTI]

    King, Charles Edward

    1954-01-01T23:59:59.000Z

    Toxicity tests ............. .................. . 23 Ovicidal t e sts...................................... 25 Residual toxicity tests............................... 26 Calculation of dosage-mortality curves ......... ? ? ? ? ? 28 Results... and Discussions . . . . ........... . . . . . . . . . 38 Toxicity tests 1950-1951.............. ...............38 Toxicity tests 1951-1952 .............. ............... 51 Ovicidal tests ............ ......................... 52 Residual t e...

  11. Control of spider mites on cotton by organic sulphur compounds 

    E-Print Network [OSTI]

    King, Charles Edward

    1954-01-01T23:59:59.000Z

    Toxicity tests ............. .................. . 23 Ovicidal t e sts...................................... 25 Residual toxicity tests............................... 26 Calculation of dosage-mortality curves ......... ? ? ? ? ? 28 Results... and Discussions . . . . ........... . . . . . . . . . 38 Toxicity tests 1950-1951.............. ...............38 Toxicity tests 1951-1952 .............. ............... 51 Ovicidal tests ............ ......................... 52 Residual t e...

  12. Nanoparticle Formation of Organic Compounds With Retained Biological Activity

    E-Print Network [OSTI]

    Zare, Richard N.

    solvents and/ or higher temperatures.4 Owing to the high compres- sibility of SCFs, the physical properties to be formed as well as control of the size distribution.7 Moreover, SC-CO2 antisolvent precipitation is highly.58C and 75.8 bar). Supercritical carbon dioxide (SC-CO2) is also nonflammable and inexpensive.6

  13. anthropogenic organic compounds: Topics by E-print Network

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Agency inventory, and is consistent with field are poorly quantified in emission inventories, as shown by air quality studies in eastern Texas (Ryerson et al 2003, Parrish et...

  14. Hydrogen-Evolving Organic Compounds - Energy Innovation Portal

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOEThe Bonneville PowerCherries 82981-1cnHigh School footballHydrogen and Fuel CellFew-LayerGasStorageNRELEnergy

  15. Estimating monthly and state-level NO sub x , SO sub 2 , VOC and CO sub 2 emissions using the MSCET database

    SciTech Connect (OSTI)

    Cilek, C.M.; Kohout, E.

    1992-01-01T23:59:59.000Z

    This paper describes the Month and State Current Emission Trends (MSCET) database. It describes the methodology used to estimate NO{sub x}, SO{sub 2}, VOC, and CO{sub 2} emissions and the data sources used by the methodology. Selected emissions results from the database are presented. 2 refs., 6 figs.

  16. Estimating monthly and state-level NO{sub x}, SO{sub 2}, VOC and CO{sub 2} emissions using the MSCET database

    SciTech Connect (OSTI)

    Cilek, C.M.; Kohout, E.

    1992-07-01T23:59:59.000Z

    This paper describes the Month and State Current Emission Trends (MSCET) database. It describes the methodology used to estimate NO{sub x}, SO{sub 2}, VOC, and CO{sub 2} emissions and the data sources used by the methodology. Selected emissions results from the database are presented. 2 refs., 6 figs.

  17. Method for treatment of soils contaminated with organic pollutants

    DOE Patents [OSTI]

    Wickramanayake, Godage B. (Cranbury, NJ)

    1993-01-01T23:59:59.000Z

    A method for treating soil contaminated by organic compounds wherein an ozone containing gas is treated with acid to increase the stability of the ozone in the soil environment and the treated ozone applied to the contaminated soil to decompose the organic compounds. The soil may be treated in situ or may be removed for treatment and refilled.

  18. Effects of anthropogenic activities on the molecular composition of urban organic aerosols: an ultrahigh resolution mass spectrometry study

    E-Print Network [OSTI]

    Kourtchev, I.; O'Connor, I. P.; Giorio, C.; Fuller, S.; Kristenen, K.; Maenhaut, W.; Wenger, J. C.; Sodeau, J. R.; Glasius, M.; Kalberer, M.

    2014-02-23T23:59:59.000Z

    (secondary organic aerosol, SOA). Various sources contribute 56 to formation of PM and include anthropogenic sources such as use of diesel and petrol, 57 burning of fossil fuel and biomass. Biogenic sources include VOCs emitted by vegetation. 58 Urban... 279405). 417 418 References 419 Birch, M.E., Cary, R.A., 1996. Elemental carbon-based method for monitoring occupational 420 exposure to particulate diesel exhaust. Aerosol Science and Technology 25, 221–241. 421 Cecinato, A., Di Palo, V., Pomata, D...

  19. The design of new ligands and transition metal compounds for the oxidation of organic compounds

    E-Print Network [OSTI]

    Grill, Joseph Michael

    2009-06-02T23:59:59.000Z

    ........................................................................................... 108 APPENDIX B............................................................................................ 215 APPENDIX C............................................................................................ 225 VITA..., oxidation of manganese (III) to manganese (V) occurs, followed by addition of an olefin to form a C-O bond and a carbon radical. Collapse of the radical species t 12 then gives the epoxide (Scheme 1.8). 38 This mechanism allows for the possibility...

  20. Devices for collecting chemical compounds

    DOE Patents [OSTI]

    Scott, Jill R; Groenewold, Gary S

    2013-12-24T23:59:59.000Z

    A device for sampling chemical compounds from fixed surfaces and related methods are disclosed. The device may include a vacuum source, a chamber and a sorbent material. The device may utilize vacuum extraction to volatilize the chemical compounds from a fixed surface so that they may be sorbed by the sorbent material. The sorbent material may then be analyzed using conventional thermal desorption/gas chromatography/mass spectrometry (TD/GC/MS) instrumentation to determine presence of the chemical compounds. The methods may include detecting release and presence of one or more chemical compounds and determining the efficacy of decontamination. The device may be useful in collection and analysis of a variety of chemical compounds, such as residual chemical warfare agents, chemical attribution signatures and toxic industrial chemicals.

  1. Atmos. Chem. Phys., 14, 58715891, 2014 www.atmos-chem-phys.net/14/5871/2014/

    E-Print Network [OSTI]

    Pierce, Jeffrey

    inventories by measurements of ambient volatile organic compounds in Beijing, China M. Wang1, M. Shao1, W inventories to eval- uate the spatial distribution, species-specific emissions, and source structure of VOCs, whereas current emission inventories suggested that VOC emissions were concentrated in downtown areas. Com

  2. WearAir: Expressive T-shirts for Air Quality Sensing Sunyoung Kim and Eric Paulos

    E-Print Network [OSTI]

    Mankoff, Jennifer

    are less proactively concerned with air quality. AIR POLLUTANT: VOLATILE ORGANIC COMPOUNDS Different types of air pollutants contribute to air quality in different locations: Ozone, CO, NOx and VOCs are major contributors to outdoor air pollution; and particulate matters, VOCs, carbon monoxide and lead are common air

  3. Chemical Engineering Journal 87 (2002) 101110 Co-treatment of H2S and toluene in a biotrickling filter

    E-Print Network [OSTI]

    2002-01-01T23:59:59.000Z

    Chemical Engineering Journal 87 (2002) 101­110 Co-treatment of H2S and toluene in a biotrickling-gases contain H2S and a wide range of volatile organic compounds (VOCs). Since co-treatment of odors and VOCs in biotrickling filters is a relatively unexplored area, the simultaneous biotreatment of H2S and toluene (as

  4. Oxidation of propylene in the presence of catalysts containing copper compounds

    E-Print Network [OSTI]

    Woodham, John Frank

    1959-01-01T23:59:59.000Z

    : lo Homogeneity of catalyst mass. 2. Reproducibility of catalytic properties. 3. Negligible catalytic activity toward the formation of organic compounds other than carbonyl compounds. o h Minimum formation of compounds other than acrolein, carbon... hydrocarbons are available in the theses and dissertations of Sanderson (3F ) , Looney (26), Burns (6)P Dunlop (9)? Woodham (45), Perkins (30)j and Billingsley (4)0 In order to avoid repetition of the material covered in the exhaustive surveys presented...

  5. Understanding complex Earth systems: volatile metabolites as microbial ecosystem proxies and student conceptual model development of coastal eutrophication

    E-Print Network [OSTI]

    McNeal, Karen Sue

    2009-05-15T23:59:59.000Z

    research strands which contribute to the scientific and pedagogical understanding of complex Earth systems. In the first strand, a method that characterizes volatile organic compounds (VOCs) as ecological proxies of soil microbial ecosystems was validated...

  6. Draft Environmental Impact Statement for Construction and Operation...

    Office of Environmental Management (EM)

    U.S. Department of Agriculture USEC United States Enrichment Corporation USFWS U.S. Fish and Wildlife Service USGS U.S. Geological Survey VOC volatile organic compound WM PEIS...

  7. PROPOSED INSTALLATION AND OPERATION OF A

    Office of Environmental Management (EM)

    U.S. Department of Agriculture USEPA U.S. Environmental Protection Agency USFWS U.S. Fish and Wildlife Service VOC Volatile Organic Compound VPP Voluntary Protection Program...

  8. Vapor intrusion modeling : limitations, improvements, and value of information analyses

    E-Print Network [OSTI]

    Friscia, Jessica M. (Jessica Marie)

    2014-01-01T23:59:59.000Z

    Vapor intrusion is the migration of volatile organic compounds (VOCs) from a subsurface source into the indoor air of an overlying building. Vapor intrusion models, including the Johnson and Ettinger (J&E) model, can be ...

  9. A cost-effectiveness analysis of alternative ozone control strategies : flexible nitrogen oxide (NOx) abatement from power plants in the eastern United States

    E-Print Network [OSTI]

    Sun, Lin, S.M. Massachusetts Institute of Technology

    2009-01-01T23:59:59.000Z

    Ozone formation is a complex, non-linear process that depends on the atmospheric concentrations of its precursors, nitrogen oxide (NOx) and Volatile Organic Compounds (VOC), as well as on temperature and the available ...

  10. Evaluation of the pathways of tropospheric nitrophenol formation from benzene and phenol using a multiphase model 

    E-Print Network [OSTI]

    Heal, Mathew R; Harrison, Mark A J; Cape, Neil

    2005-01-01T23:59:59.000Z

    Phenols are a major class of volatile organic compounds (VOC) whose reaction within, and partitioning between, the gas and liquid phases affects their lifetime within the atmosphere, the local oxidising capacity, and the ...

  11. Laboratory simulation of subsurface airflow beneath a building

    E-Print Network [OSTI]

    Corsello, Joseph William

    2014-01-01T23:59:59.000Z

    Vapor intrusion is the vapor-phase migration of volatile organic compounds (VOCs) into buildings due to subsurface soil or groundwater contamination. Oxygen replenishment rates beneath a building are significant for ...

  12. Study of building material emissions and indoor air quality

    E-Print Network [OSTI]

    Yang, Xudong, 1966-

    1999-01-01T23:59:59.000Z

    Building materials and furnishings emit a wide variety of indoor pollutants, such as volatile organic compounds (VOCs). At present, no accurate models are available to characterize material emissions and sorption under ...

  13. Alternate Fuels: Is Your Waste Stream a Fuel Source? 

    E-Print Network [OSTI]

    Coerper, P.

    1992-01-01T23:59:59.000Z

    Before the year 2000, more than one quarter of U.S. businesses will be firing Alternate Fuels in their boiler systems. And, the trend toward using Process Gases, Flammable Liquids, and Volatile Organic Compounds (VOC's), to supplement fossil fuels...

  14. CX-011446: Categorical Exclusion Determination | Department of...

    Broader source: Energy.gov (indexed) [DOE]

    Modeling to Quantify Emissions of Methane and Volatile Organic Compounds (VOCs) from Shale Gas Operations CX(s) Applied: B3.1 Date: 11132013 Location(s): Pennsylvania...

  15. PDID: Pulsed-Discharge Ionization Detector A new detector for...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Administration under contract DE-AC04-94AL85000. SAND2015-1387C Sandia's Volatile Organic Compound (VOC) Biomarker Detection Technology 0.25" grid Photons emitted from a...

  16. Life-cycle assessment of computational logic produced from 1995 through 2010

    E-Print Network [OSTI]

    Boyd, Sarah; A. Horvath; Dornfeld, David

    2010-01-01T23:59:59.000Z

    in each fab model include a central acid scrubber, anammonia scrubber, a volatile organic compound (VOC) oxidizer99% ef?ciency in the fab scrubber and though liquid HCl is

  17. Physical and Chemical Characterization of Particulate and Gas phase Emissions from Biomass Burning

    E-Print Network [OSTI]

    Hosseini, Seyedehsan

    2012-01-01T23:59:59.000Z

    Base VOC Volatile Organic Compound XRF X-ray Fluorescence ?mFluorescence spectrometry (XRF) (Na through Pb), inorganicby X-ray fluorescence (XRF). The USFS samples were analyzed

  18. Nez Perce Tribe Formaldehyde Study 2011 Kayla Warden and Etta Axtell-Northwest Indian College

    E-Print Network [OSTI]

    Collins, Gary S.

    volatile organic compounds (VOC) were measured using a Proton Transfer Reaction Mass Spectrometer (PTR Acknowledgements: This research was funded by EPA/FaST DOE and NSF Research Experience for Undergraduates (REU). I

  19. Syntheses of Functionalized Benzylic Compounds: Development of Palladium-Catalyzed Decarboxylative Benzylation Reactions

    E-Print Network [OSTI]

    Torregrosa, Robert Ryan P.

    2012-08-31T23:59:59.000Z

    Carbon-carbon bond formation between the benzyl carbon and a functional group is important in organic synthesis because majority of the compounds in the chemical literature contain aromatic cores appended with different ...

  20. Possible explosive compounds in the Savannah River Site waste tank farm facilities

    SciTech Connect (OSTI)

    Hobbs, D.T.

    2000-04-13T23:59:59.000Z

    This report will be revised upon completion of current testing investigating the radiolytic stability of additional energetic materials and the analysis of tank farm samples for volatile and semi-volatile organic compounds.

  1. Polishing compound for plastic surfaces

    DOE Patents [OSTI]

    Stowell, M.S.

    1995-08-22T23:59:59.000Z

    A polishing compound for plastic surfaces is disclosed. The compound contains by weight approximately 4 to 17 parts at least one petroleum distillate lubricant, 1 to 6 parts mineral spirits, 2.5 to 15 parts abrasive particles, and 2.5 to 10 parts water. The abrasive is tripoli or a similar material that contains fine particles silica. Preferably, most of the abrasive particles are less than approximately 10 microns, more preferably less than approximately 5 microns in size. The compound is used on PLEXIGLAS{trademark}, LEXAN{trademark}, LUCITE{trademark}, polyvinyl chloride (PVC) and similar plastic materials whenever a smooth, clear polished surface is desired. 5 figs.

  2. Polishing compound for plastic surfaces

    DOE Patents [OSTI]

    Stowell, Michael S. (New Ellenton, SC)

    1995-01-01T23:59:59.000Z

    A polishing compound for plastic surfaces. The compound contains by weight approximately 4 to 17 parts at least one petroleum distillate lubricant, 1 to 6 parts mineral spirits, 2.5 to 15 parts abrasive particles, and 2.5 to 10 parts water. The abrasive is tripoli or a similar material that contains fine particles silica. Preferably, most of the abrasive particles are less than approximately 10 microns, more preferably less than approximately 5 microns in size. The compound is used on PLEXIGLAS.TM., LEXAN.TM., LUCITE.TM., polyvinyl chloride (PVC) and similar plastic materials whenever a smooth, clear polished surface is desired.

  3. Polishing compound for plastic surfaces

    DOE Patents [OSTI]

    Stowell, M.S.

    1993-01-01T23:59:59.000Z

    A polishing compound for plastic surfaces is disclosed. The compound contains by weight approximately 4 to 17 parts at least one petroleum distillate lubricant, 1 to 6 parts mineral spirits, 2.5 to 15 parts abrasive particles, and 2.5 to 10 parts water. The abrasive is tripoli or a similar material that contains colloidal silica. Preferably, most of the abrasive particles are less than approximately 10 microns, more preferably less than approximately 5 microns in size. The compound is used on PLEXIGLAS{sup TM}, LEXAN{sup TM}, LUCITE{sup TM}, polyvinyl chloride (PVC) and similar plastic materials whenever a smooth, clear polished surface is desired.

  4. COMBUSTION SOURCES OF NITROGEN COMPOUNDS

    E-Print Network [OSTI]

    Brown, Nancy J.

    2011-01-01T23:59:59.000Z

    Rasmussen, R.A. (1976). Combustion as a source of nitrousx control for stationary combustion sources. Prog. Energy,CA, March 3-4, 1977 COMBUSTION SOURCES OF NITROGEN COMPOUNDS

  5. Detection of chlorinated aromatic compounds

    DOE Patents [OSTI]

    Ekechukwu, A.A.

    1996-02-06T23:59:59.000Z

    A method for making a composition for measuring the concentration of chlorinated aromatic compounds in aqueous fluids, and an optical probe for use with the method are disclosed. The composition comprises a hydrophobic polymer matrix, preferably polyamide, with a fluorescent indicator uniformly dispersed therein. The indicator fluoresces in the presence of the chlorinated aromatic compounds with an intensity dependent on the concentration of these compounds in the fluid of interest, such as 8-amino-2-naphthalene sulfonate. The probe includes a hollow cylindrical housing that contains the composition in its distal end. The probe admits an aqueous fluid to the probe interior for exposure to the composition. An optical fiber transmits excitation light from a remote source to the composition while the indicator reacts with chlorinated aromatic compounds present in the fluid. The resulting fluorescence light signal is reflected to a second optical fiber that transmits the light to a spectrophotometer for analysis. 5 figs.

  6. Polishing compound for plastic surfaces

    DOE Patents [OSTI]

    Stowell, M.S.

    1991-01-01T23:59:59.000Z

    This invention is comprised of a polishing compound for plastic materials. The compound includes approximately by approximately by weight 25 to 80 parts at least one petroleum distillate lubricant, 1 to 12 parts mineral spirits, 50 to 155 parts abrasive paste, and 15 to 60 parts water. Preferably, the compound includes approximately 37 to 42 parts at least one petroleum distillate lubricant, up to 8 parts mineral spirits, 95 to 110 parts abrasive paste, and 50 to 55 parts water. The proportions of the ingredients are varied in accordance with the particular application. The compound is used on PLEXIGLAS{trademark}, LEXAN{trademark}, LUCITE{trademark}, polyvinyl chloride (PVC), and similar plastic materials whenever a smooth, clear polished surface is desired.

  7. Method for digesting a nitro-bearing explosive compound

    DOE Patents [OSTI]

    Shah, Manish M. (Richland, WA)

    2000-01-01T23:59:59.000Z

    The present invention is a process wherein superoxide radicals from superoxide salt are used to break down the explosive compounds. The process has an excellent reaction rate for degrading explosives, and operates at ambient temperature and atmospheric pressure in aqueous or non-aqueous conditions. Because the superoxide molecules are small, much smaller than an enzyme molecule for example, they can penetrate the microstructure of plastic explosives faster. The superoxide salt generates reactive hydroxyl radicals, which can destroy other organic contaminants, if necessary, along with digesting the explosive nitro-bearing compound.

  8. Aza compounds as anion receptors

    DOE Patents [OSTI]

    Lee, H.S.; Yang, X.Q.; McBreen, J.

    1998-01-06T23:59:59.000Z

    A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of Li{sup +} ion in alkali metal batteries. 3 figs.

  9. Process for production of a borohydride compound

    DOE Patents [OSTI]

    Chin, Arthur Achhing; Jain, Puja; Linehan, Suzanne; Lipiecki, Francis Joseph; Maroldo, Stephen Gerard; November, Samuel J; Yamamoto, John Hiroshi

    2013-02-19T23:59:59.000Z

    A process for production of a borohydride compound. The process comprises combining a compound comprising boron and oxygen with an adduct of alane.

  10. Method of digesting an explosive nitro compound

    DOE Patents [OSTI]

    Shah, Manish M. (Richland, WA)

    2000-01-01T23:59:59.000Z

    The present invention is a process wherein bleaching oxidants are used to digest explosive nitro compounds. The process has an excellent reaction rate for digesting explosives and operates under multivariate conditions. Reaction solutions may be aqueous, non-aqueous or a combination thereof, and can also be any pH, but preferably have a pH between 2 and 9. The temperature may be ambient as well as any temperature above which freezing of the solution would occur and below which any degradation of the bleaching oxidant would occur or below which any explosive reaction would be initiated. The pressure may be any pressure, but is preferably ambient or atmospheric, or a pressure above a vapor pressure of the aqueous solution to avoid boiling of the solution. Because the bleaching oxidant molecules are small, much smaller than an enzyme molecule for example, they can penetrate the microstructure of plastic explosives faster. The bleaching oxidants generate reactive hydroxyl radicals, which can destroy other organic contaminants, if necessary, along with digesting the explosive nitro compound.

  11. Polybenzimidazole compounds, polymeric media, and methods of post-polymerization modifications

    DOE Patents [OSTI]

    Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Wertsching, Alan K. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Luther, Thomas A. (Idaho Falls, ID); Jones, Michael G. (Pocatello, ID)

    2007-08-21T23:59:59.000Z

    A PBI compound includes imidazole nitrogens at least a portion of which are substituted with an organic-inorganic hybrid moiety. At least 85% of the imidazole nitrogens may be substituted. The organic-inorganic hybrid moiety may be an organosilane moiety, for example, (R)Me.sub.2SiCH.sub.2-- where R is selected from among methyl, phenyl, vinyl, and allyl. The PBI compound may exhibit similar thermal properties in comparison to the unsubstituted PBI. The PBI compound may exhibit a solubility in an organic solvent greater than the solubility of the unsubstituted PBI. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may occur at about room temperature and/or at about atmospheric pressure. Substituting may use at least 5 equivalents in relation to the imidazole nitrogens to be substituted or, preferably, about 15.

  12. Global data set of biogenic VOC emissions calculated by the MEGAN model over the last 30 years

    SciTech Connect (OSTI)

    Sindelarova, K.; Granier, Claire; Bouarar, I.; Guenther, Alex B.; Tilmes, S.; Stavrakou, T.; Muller, J. F.; Kuhn, U.; Stefani, P.; Knorr, W.

    2014-09-09T23:59:59.000Z

    The Model of Emissions of Gases and Aerosols from Nature (MEGANv2.1) together with the Modern-Era Retrospective Analysis for Research and Applications (MERRA) meteorological fields were used to create a global emission dataset of biogenic VOCs available on a monthly basis for the time period of 1980 - 2010. This dataset is called MEGAN-MACC. The model estimated mean annual total BVOC emission of 760 Tg(C) yr1 consisting of isoprene (70%), monoterpenes (11%), methanol (6%), acetone (3%), sesquiterpenes (2.5%) and other BVOC species each contributing less than 2 %. Several sensitivity model runs were performed to study the impact of different model input and model settings on isoprene estimates and resulted in differences of * 17% of the reference isoprene total. A greater impact was observed for sensitivity run applying parameterization of soil moisture deficit that led to a 50% reduction of isoprene emissions on a global scale, most significantly in specific regions of Africa, South America and Australia. MEGAN-MACC estimates are comparable to results of previous studies. More detailed comparison with other isoprene in ventories indicated significant spatial and temporal differences between the datasets especially for Australia, Southeast Asia and South America. MEGAN-MACC estimates of isoprene and*-pinene showed a reasonable agreement with surface flux measurements in the Amazon andthe model was able to capture the seasonal variation of emissions in this region.

  13. Method of increasing biodegradation of sparingly soluble vapors

    DOE Patents [OSTI]

    Cherry, Robert S. (Idaho Falls, ID)

    2000-01-01T23:59:59.000Z

    A method for increasing biodegradation of sparingly soluble volatile organic compounds (VOCs) in a bioreactor is disclosed. The method comprises dissolving in the aqueous phase of the bioreactor a water soluble, nontoxic, non-biodegradable polymer having a molecular weight of at least 500 and operable for decreasing the distribution coefficient of the VOCs. Polyoxyalkylene alkanols are preferred polymers. A method of increasing the growth rate of VOC-degrading microorganisms in the bioreactor and a method of increasing the solubility of sparingly soluble VOCs in aqueous solution are also disclosed.

  14. New Air Cleaning Strategies for Reduced Commercial Building Ventilation Energy ? FY11 Final Report

    SciTech Connect (OSTI)

    Sidheswaran, Meera; Destaillats, Hugo; Cohn, Sebastian; Sullivan, Douglas P.; Fisk, William J.

    2011-10-31T23:59:59.000Z

    The research carried out in this project focuses on developing novel volatile organic compounds (VOCs) air cleaning technologies needed to enable energy-saving reductions in ventilation rates. we targeted a VOC air cleaning system that could enable a 50% reduction in ventilation rates. In a typical commercial HVAC system that provides a mixture of recirculated and outdoor air, a VOC air cleaner in the supply airstream must have a 15% to 20% VOC removal efficiency to counteract a 50% reduction in outdoor air supply.

  15. Leadership, Organizations

    E-Print Network [OSTI]

    Palmeri, Thomas

    Leadership, Policy & Organizations #12;2 At Peabody students have the opportunity to develop new College, in the Department of Leadership, Policy and Organizations (LPO). The faculty believes Patricia and Rodes Hart Chair, and Professor of Education Policy and Leadership, Ellen Goldring also serves

  16. Organic materials with nonlinear optical properties

    DOE Patents [OSTI]

    Stupp, S.I.; Son, S.; Lin, H.C.

    1995-05-02T23:59:59.000Z

    The present invention is directed to organic materials that have the ability to double or triple the frequency of light that is directed through the materials. Particularly, the present invention is directed to the compound 4-[4-(2R)-2-cyano-7-(4{prime}-pentyloxy-4-biphenylcarbonyloxy)phenylheptylidenephenylcarbonyloxy]benzaldehyde, which can double the frequency of light that is directed through the compound. The invention is also directed to the compound (12-hydroxy-5,7-dodecadiynyl)-4{prime}-[(4{prime}-pentyloxy-4-biphenyl)carbonyloxy]-4-biphenylcarboxylate, and its polymeric form. The polymeric form can triple the frequency of light directed through it. 4 figs.

  17. The temporal dynamics of terrestrial organic matter transfer to the oceans : initial assessment and application

    E-Print Network [OSTI]

    Drenzek, Nicholas J

    2007-01-01T23:59:59.000Z

    This thesis employs compound-specific stable carbon and radiocarbon isotopic analysis of organic biomarkers to (a) resolve petrogenic from pre-aged vascular plant organic carbon (OC) in continental margin sediments, (b) ...

  18. Prediction of crystal densities of organic explosives by group additivity

    SciTech Connect (OSTI)

    Stine, J R

    1981-08-01T23:59:59.000Z

    The molar volume of crystalline organic compound is assumed to be a linear combination of its constituent volumes. Compounds consisting only of the elements hydrogen, carbon, nitrogen, oxygen, and fluorine are considered. The constituent volumes are taken to be the volumes of atoms in particular bonding environments and are evaluated from a large set of crystallographic data. The predicted density has an expected error of about 3%. These results are applied to a large number of explosives compounds.

  19. Organic Superconductors

    SciTech Connect (OSTI)

    Charles Mielke

    2009-02-27T23:59:59.000Z

    Intense magnetic fields are an essential tool for understanding layered superconductors. Fundamental electronic properties of organic superconductors are revealed in intense (60 tesla) magnetic fields. Properties such as the topology of the Fermi surface and the nature of the superconducting order parameter are revealed. With modest maximum critical temperatures~13K the charge transfer salt organic superconductors prove to be incredibly valuable materials as their electronically clean nature and layered (highly anisotropic) structures yield insights to the high temperature superconductors. Observation of de Haas-van Alphen and Shubnikov-de Haas quantum oscillatory phenomena, magnetic field induced superconductivity and re-entrant superconductivity are some of the physical phenomena observed in the charge transfer organic superconductors. In this talk, I will discuss the nature of organic superconductors and give an overview of the generation of intense magnetic fields; from the 60 tesla millisecond duration to the extreme 1000 tesla microsecond pulsed magnetic fields.

  20. Process Development for High Voc CdTe Solar Cells: Phase I, Annual Technical Report, October 2005 - September 2006

    SciTech Connect (OSTI)

    Ferekides, C. S.; Morel, D. L.

    2007-04-01T23:59:59.000Z

    The focus of this project is the open-circuit voltage of the CdTe thin-film solar cell. CdTe continues to be one of the leading materials for large-scale cost-effective production of photovoltaics, but the efficiency of the CdTe solar cell has been stagnant for the last few years. At the manufacturing front, the CdTe technology is fast paced and moving forward with U.S.-based First Solar LLC leading the world in CdTe module production. To support the industry efforts and continue the advancement of this technology, it will be necessary to continue improvements in solar cell efficiency. A closer look at the state-of-the-art performance levels puts the three solar cell efficiency parameters of short-circuit current density (JSC), open-circuit voltage (VOC), and fill factor (FF) in the 24-26 mA/cm2, 844?850 mV, and 74%-76% ranges respectively. During the late 1090s, efforts to improve cell efficiency were primarily concerned with increasing JSC, simply by using thinner CdS window layers to enhance the blue response (<510 nm) of the CdTe cell. These efforts led to underscoring the important role 'buffers' (or high-resistivity transparent films) play in CdTe cells. The use of transparent bi-layers (low-p/high-p) as the front contact is becoming a 'standard' feature of the CdTe cell.

  1. Superconductivity in graphite intercalation compounds

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Smith, Robert P. [Univ. of Cambridge (United Kingdom); Dean, Mark P. M. [Brookhaven National Lab. (BNL), Upton, NY (United States); Weller, Thomas E. [Univ. College of London (United Kingdom); Howard, Christopher A. [Univ. College of London (United Kingdom); Rahnejat, Kaveh C. [Univ. College of London (United Kingdom); Saxena, Siddharth S. [Univ. of Cambridge (United Kingdom); Ellerby, Mark [Univ. College of London (United Kingdom)

    2015-07-01T23:59:59.000Z

    The field of superconductivity in the class of materials known as graphite intercalation compounds has a history dating back to the 1960s This paper recontextualizes the field in light of the discovery of superconductivity in CaC? and YbC? in 2005. In what follows, we outline the crystal structure and electronic structure of these and related compounds. We go on to experiments addressing the superconducting energy gap, lattice dynamics, pressure dependence, and how this relates to theoretical studies. The bulk of the evidence strongly supports a BCS superconducting state. However, important questions remain regarding which electronic states and phonon modes are most important for superconductivity and whether current theoretical techniques can fully describe the dependence of the superconducting transition temperature on pressure and chemical composition.

  2. Superconductivity in graphite intercalation compounds

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Smith, Robert P.; Dean, Mark P. M.; Weller, Thomas E.; Howard, Christopher A.; Rahnejat, Kaveh C.; Saxena, Siddharth S.; Ellerby, Mark

    2015-07-01T23:59:59.000Z

    The field of superconductivity in the class of materials known as graphite intercalation compounds has a history dating back to the 1960s This paper recontextualizes the field in light of the discovery of superconductivity in CaC? and YbC? in 2005. In what follows, we outline the crystal structure and electronic structure of these and related compounds. We go on to experiments addressing the superconducting energy gap, lattice dynamics, pressure dependence, and how this relates to theoretical studies. The bulk of the evidence strongly supports a BCS superconducting state. However, important questions remain regarding which electronic states and phonon modes aremore »most important for superconductivity and whether current theoretical techniques can fully describe the dependence of the superconducting transition temperature on pressure and chemical composition.« less

  3. Compound semiconductor optical waveguide switch

    DOE Patents [OSTI]

    Spahn, Olga B.; Sullivan, Charles T.; Garcia, Ernest J.

    2003-06-10T23:59:59.000Z

    An optical waveguide switch is disclosed which is formed from III-V compound semiconductors and which has a moveable optical waveguide with a cantilevered portion that can be bent laterally by an integral electrostatic actuator to route an optical signal (i.e. light) between the moveable optical waveguide and one of a plurality of fixed optical waveguides. A plurality of optical waveguide switches can be formed on a common substrate and interconnected to form an optical switching network.

  4. Muon-spin spectroscopy of the organometallic spin-1/2 kagome-lattice compound Cu(1,3-benzenedicarboxylate)

    E-Print Network [OSTI]

    Marcipar, Lital

    Using muon-spin resonance, we examine the organometallic hybrid compound Cu(1,3-benzenedicarboxylate) [Cu(1,3-bdc)], which has structurally perfect spin-1/2 copper kagome planes separated by pure organic linkers. This ...

  5. Method for removing sulfur compounds from C/sub 6/ and lower alkanes

    SciTech Connect (OSTI)

    Keyworth, D.A.

    1989-03-28T23:59:59.000Z

    A process is described for recovering a low sulfur content hydrocarbon fraction having a boiling point of n-hexane or less from a hydrocarbon stream containing hydrocarbons boiling at or below the boiling point of hexane and organic sulfur compounds comprising monosulfides boiling at or below the boiling point of n-hexane. It consists of contacting the hydrocarbon stream with a dilute aqueous solution of sodium hypochlorite for a time sufficient to convert a selected amount of monosulfide compounds present to compounds having boiling points above the boiling point of n-hexane, separating an aqueous phase and a hydrocarbon phase and fractionally distilling the hydrocarbon phase to recover a hydrocarbon fraction having a boiling point of n-hexane or less, and having a reduced amount of the organic sulfur compounds.

  6. Feedback Capacity of the Compound Channel

    E-Print Network [OSTI]

    Shrader, Brooke E.

    In this work, we find the capacity of a compound finite-state channel (FSC) with time-invariant deterministic feedback. We consider the use of fixed length block codes over the compound channel. Our achievability result ...

  7. Bibliography of work on the photocatalytic removal of hazardous compounds from water and air

    SciTech Connect (OSTI)

    Blake, D.M.

    1994-05-01T23:59:59.000Z

    This is a bibliography of information in the open literature on work that has been done to date on the photocatalytic oxidation of compounds, principally organic compounds. The goal of the listing is removing hazardous oompounds from water or air. It contains lists of substances and literature citations. The bibliography includes information obtained through the middle of 1993 and some selected references for the balance of that year.

  8. Red Balloon, Green Balloon, Sensors in the Sky Stacey Kuznetsov1

    E-Print Network [OSTI]

    Paulos, Eric

    color based on input from attached air quality sensors (exhaust, diesel, or volatile organic compounds). The balloons change color in response to one of exhaust gas, diesel, or VOC's (volatile organic compounds]. Diesel exhaust consists of fine particulate matter emitted by engines and industrial processes [44

  9. Equation calculates activated carbon's capacity for adsorbing pollutants

    SciTech Connect (OSTI)

    Yaws, C.L.; Bu, L.; Nijhawan, S. (Lamar Univ., Beaumont, TX (United States))

    1995-02-13T23:59:59.000Z

    Adsorption on activated carbon is an effective method for removing volatile organic compound (VOC) contaminants from gases. A new, simple equation has been developed for calculating activated carbon's adsorption capacity as a function of the VOC concentration in the gas. The correlation shows good agreement with experimental results. Results from the equation are applicable for conditions commonly encountered in air pollution control techniques (25 C, 1 atm). The only input parameters needed are VOC concentrations and a table of correlation coefficients for 292 C[sub 8]-C[sub 14] compounds. The table is suitable for rapid engineering usage with a personal computer or hand calculator.

  10. Thin films of mixed metal compounds

    DOE Patents [OSTI]

    Mickelsen, R.A.; Chen, W.S.

    1985-06-11T23:59:59.000Z

    Disclosed is a thin film heterojunction solar cell, said heterojunction comprising a p-type I-III-IV[sub 2] chalcopyrite substrate and an overlying layer of an n-type ternary mixed metal compound wherein said ternary mixed metal compound is applied to said substrate by introducing the vapor of a first metal compound to a vessel containing said substrate from a first vapor source while simultaneously introducing a vapor of a second metal compound from a second vapor source of said vessel, said first and second metals comprising the metal components of said mixed metal compound; independently controlling the vaporization rate of said first and second vapor sources; reducing the mean free path between vapor particles in said vessel, said gas being present in an amount sufficient to induce homogeneity of said vapor mixture; and depositing said mixed metal compound on said substrate in the form of a uniform composition polycrystalline mixed metal compound. 5 figs.

  11. Gas Separation Using Organic-Vapor-Resistent Membranes In Conjunctin With Organic-Vapor-Selective Membranes

    DOE Patents [OSTI]

    Baker, Richard W. (Palo Alto, CA); Pinnau, Ingo (Palo Alto, CA); He, Zhenjie (Fremont, CA); Da Costa, Andre R. (Menlo Park, CA); Daniels, Ramin (San Jose, CA); Amo, Karl D. (Mountain View, CA); Wijmans, Johannes G. (Menlo Park, CA)

    2003-06-03T23:59:59.000Z

    A process for treating a gas mixture containing at least an organic compound gas or vapor and a second gas, such as natural gas, refinery off-gas or air. The process uses two sequential membrane separation steps, one using membrane selective for the organic compound over the second gas, the other selective for the second gas over the organic vapor. The second-gas-selective membranes use a selective layer made from a polymer having repeating units of a fluorinated polymer, and demonstrate good resistance to plasticization by the organic components in the gas mixture under treatment, and good recovery after exposure to liquid aromatic hydrocarbons. The membrane steps can be combined in either order.

  12. Giant magnetoresistive cobalt oxide compounds

    DOE Patents [OSTI]

    Schultz, P.G.; Xiang, X.; Goldwasser, I.

    1998-07-07T23:59:59.000Z

    Methods and apparatus are disclosed for the preparation and use of a substrate having an array of diverse materials in predefined regions thereon. A substrate having an array of diverse materials thereon is generally prepared by delivering components of materials to predefined regions on a substrate, and simultaneously reacting the components to form at least two materials. Materials which can be prepared using the methods and apparatus of the present invention include, for example, covalent network solids, ionic solids and molecular solids. More particularly, materials which can be prepared using the methods and apparatus of the present invention include, for example, inorganic materials, intermetallic materials, metal alloys, ceramic materials, organic materials, organometallic materials, non-biological organic polymers, composite materials (e.g., inorganic composites, organic composites, or combinations thereof), etc. Once prepared, these materials can be screened for useful properties including, for example, electrical, thermal, mechanical, morphological, optical, magnetic, chemical, or other properties. Thus, the present invention provides methods for the parallel synthesis and analysis of novel materials having useful properties. 58 figs.

  13. Giant magnetoresistive cobalt oxide compounds

    DOE Patents [OSTI]

    Schultz, Peter G. (Oakland, CA); Xiang, Xiaodong (Alameda, CA); Goldwasser, Isy (Menlo Park, CA)

    1998-01-01T23:59:59.000Z

    Methods and apparatus for the preparation and use of a substrate having an array of diverse materials in predefined regions thereon. A substrate having an array of diverse materials thereon is generally prepared by delivering components of materials to predefined regions on a substrate, and simultaneously reacting the components to form at least two materials. Materials which can be prepared using the methods and apparatus of the present invention include, for example, covalent network solids, ionic solids and molecular solids. More particularly, materials which can be prepared using the methods and apparatus of the present invention include, for example, inorganic materials, intermetallic materials, metal alloys, ceramic materials, organic materials, organometallic materials, non-biological organic polymers, composite materials (e.g., inorganic composites, organic composites, or combinations thereof), etc. Once prepared, these materials can be screened for useful properties including, for example, electrical, thermal, mechanical, morphological, optical, magnetic, chemical, or other properties. Thus, the present invention provides methods for the parallel synthesis and analysis of novel materials having useful properties.

  14. Organizing Committee

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOE Office of Science (SC)IntegratedSpeeding access toTest andOptimize carbon AboutOrganizing Committee

  15. Oxygen stabilized zirconium vanadium intermetallic compound

    DOE Patents [OSTI]

    Mendelsohn, Marshall H. (Woodridge, IL); Gruen, Dieter M. (Downers Grove, IL)

    1982-01-01T23:59:59.000Z

    An oxygen stabilized intermetallic compound having the formula Zr.sub.x OV.sub.y where x=0.7 to 2.0 and y=0.18 to 0.33. The compound is capable of reversibly sorbing hydrogen at temperatures from -196.degree. C. to 450.degree. C. at pressures down to 10.sup.-6 Torr. The compound is also capable of selectively sorbing hydrogen from gaseous mixtures in the presence of CO and CO.sub.2.

  16. Gas and Particulate Sampling of Airborne Polycyclic Aromatic Compounds

    SciTech Connect (OSTI)

    Lane, D.A.; Gundel, L.A.

    1995-10-01T23:59:59.000Z

    The denuder surfaces of the gas and particle (GAP) sampler (developed at the Atmospheric Environment Service of Environment Canada) have been modified by coating with XAD-4 resin, using techniques developed at Lawrence Berkeley National Laboratory (LBNL) for the lower capacity integrated organic vapor/particle sampler (IOVPS). The resulting high capacity integrated organic gas and particle sampler (IOGAPS) has been operated in ambient air at 16.7 L min{sup -1} for a 24-hour period in Berkeley, California, USA. Simultaneous measurements were made at the same collection rate with a conventional sampler that used a filter followed by two sorbent beds. Gas and particle partition measurements were determined for 13 polycyclic aromatic hydrocarbons (PAH) ranging from 2-ring to 6-ring species. The IOGAPS indicated a higher particle fraction of these compounds than did the conventional sampler, suggesting that the conventional sampler suffered from 'blow-off' losses from the particles collected on the filter.

  17. From association to organization

    E-Print Network [OSTI]

    Mandler, George

    2011-01-01T23:59:59.000Z

    S.M. (1978). Organization theory and memory for prose: Aand summarize organization theory and relevant empiricalexplained in terms of organization theory. The hierarchical

  18. Organization Chart - Home

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    LSD Logo About Us People & Organization Research News & Events Safety Internal Resources Organization Chart Departments Scientific Staff Directory Committees Organization Chart...

  19. The Periodic Table as a Part of the Periodic Table of Chemical Compounds

    E-Print Network [OSTI]

    Labushev, Mikhail M

    2011-01-01T23:59:59.000Z

    The numbers of natural chemical elements, minerals, inorganic and organic chemical compounds are determined by 1, 2, 3 and 4-combinations of a set 95 and are respectively equal to 95, 4,465, 138,415 and 3,183,545. To explain these relations it is suggested the concept of information coefficient of proportionality as mathematical generalization of the proportionality coefficient for any set of positive numbers. It is suggested a hypothesis that the unimodal distributions of the sets of information coefficients of proportionality for atomic weights of chemical elements of minerals and chemical compounds correspond to unimodal distributions of the above sets for combination of 2, 3 and 4 atomic weights of 95 natural chemical elements. The expected values of symmetrized distributions of information coefficients of proportionality sets for atomic weights of minerals and chemical compounds are proposed to be used to define chemical compounds, like atomic weights define chemical elements. Variational series of the e...

  20. Organic solvent alteration of hydraulic properties of sedimentary rocks of low permeability: a review

    SciTech Connect (OSTI)

    Sklarew, D.S.

    1985-05-01T23:59:59.000Z

    A review of the current literature on hydrophysical interactions of organic solutes with sedimentary rocks of low permeability is presented. The motivation was the premise that low permeability rocks may act as secondary (aquifer) barriers for the containment of hazardous organic wastes, thus preventing these wastes from contaminating the groundwater. However, this premise may be incorrect if organic wastes can affect the hydraulic conductivity of these rocks. The results indicate that very little work has been done concerning interactions of organics with consolidated subsurface materials. Available information on three related topics was summarized: the effect of organic compounds on the hydrophysical properties of clays, case studies concerning the interactions of organic compounds with clays and sedimentary rocks, and the effect of shales on inorganic transport. These studies give an indication of some research areas that need to be explored with regard to the effect of organic compounds on the hydrophysical properties of sedimentary rocks; these research needs are briefly summarized. 42 refs.

  1. Identification of Sediment Organic Carbon Location and Association with Polycyclic Aromatic Hydrocarbons (PAHs) in Contaminated Sediment

    E-Print Network [OSTI]

    Identification of Sediment Organic Carbon Location and Association with Polycyclic Aromatic is known about the mechanisms of PAH and other hydrophobic organic compound sequestration and aging microspectroscopy at the NSLS beamline U10B and ALS beamline 1.4 were used to identify organic carbon location

  2. Partitioning Behavior of Organic Contaminants in Carbon Storage Environments: A Critical Review

    SciTech Connect (OSTI)

    Burant, Aniela; Lowry, Gregory V.; Karamalidis, Athanasios K.

    2013-01-01T23:59:59.000Z

    Carbon capture and storage is a promising strategy for mitigating the CO{sub 2} contribution to global climate change. The large scale implementation of the technology mandates better understanding of the risks associated with CO{sub 2} injection into geologic formations and the subsequent interactions with groundwater resources. The injected supercritical CO{sub 2} (sc-CO{sub 2}) is a nonpolar solvent that can potentially mobilize organic compounds that exist at residual saturation in the formation. Here, we review the partitioning behavior of selected organic compounds typically found in depleted oil reservoirs in the residual oil–brine–sc-CO{sub 2} system under carbon storage conditions. The solubility of pure phase organic compounds in sc-CO{sub 2} and partitioning of organic compounds between water and sc-CO{sub 2} follow trends predicted based on thermodynamics. Compounds with high volatility and low aqueous solubility have the highest potential to partition to sc-CO{sub 2}. The partitioning of low volatility compounds to sc-CO{sub 2} can be enhanced by co-solvency due to the presence of higher volatility compounds in the sc-CO{sub 2}. The effect of temperature, pressure, salinity, pH, and dissolution of water molecules into sc-CO{sub 2} on the partitioning behavior of organic compounds in the residual oil-brine-sc-CO{sub 2} system is discussed. Data gaps and research needs for models to predict the partitioning of organic compounds in brines and from complex mixtures of oils are presented. Models need to be able to better incorporate the effect of salinity and co-solvency, which will require more experimental data from key classes of organic compounds.

  3. Innovative technology summary report: in situ air stripping using horizontal wells

    SciTech Connect (OSTI)

    NONE

    1995-04-01T23:59:59.000Z

    In situ air stripping (ISAS) technology was developed to remediate soils and ground water contaminated with volatile organic compounds (VOCs) both above and below the water table. ISAS employs horizontal wells to inject (sparge) air into the ground water and vacuum extract VOCs from vadose zone soils. The innovation is creation of a system that combines two somewhat innovative technologies, air sparging and horizontal wells, with a baseline technology, soil vapor extraction, to produce a more efficient in situ remediation system.

  4. Organic materials for fusion-reactor applications

    SciTech Connect (OSTI)

    Hurley, G.F.; Coltman, R.R. Jr.

    1983-09-01T23:59:59.000Z

    Organic materials requirements for fusion-reactor magnets are described with reference to the temperature, radiation, and electrical and mechanical stress environment expected in these magnets. A review is presented of the response to gamma-ray and neutron irradiation at low temperatures of candidate organic materials; i.e. laminates, thin films, and potting compounds. Lifetime-limiting features of this response as well as needed testing under magnet operating conditions not yet adequately investigated are identified and recomendations for future work are made.

  5. Digital Construction Platform: A Compound Arm Approach

    E-Print Network [OSTI]

    Spielberg, Nathan A.

    2014-01-01T23:59:59.000Z

    We introduce a novel large-scale Digital Construction Platform (DCP) for on-site sensing, analysis, and fabrication. The DCP is an in-progress research project consisting of a compound robotic arm system comprised of a ...

  6. Production method for making rare earth compounds

    DOE Patents [OSTI]

    McCallum, R. William (Ames, IA); Ellis, Timothy W. (Ames, IA); Dennis, Kevin W. (Ames, IA); Hofer, Robert J. (Ames, IA); Branagan, Daniel J. (Ames, IA)

    1997-11-25T23:59:59.000Z

    A method of making a rare earth compound, such as a earth-transition metal permanent magnet compound, without the need for producing rare earth metal as a process step, comprises carbothermically reacting a rare earth oxide to form a rare earth carbide and heating the rare earth carbide, a compound-forming reactant (e.g. a transition metal and optional boron), and a carbide-forming element (e.g. a refractory metal) that forms a carbide that is more thermodynamically favorable than the rare earth carbide whereby the rare earth compound (e.g. Nd.sub.2 Fe.sub.14 B or LaNi.sub.5) and a carbide of the carbide-forming element are formed.

  7. Production method for making rare earth compounds

    DOE Patents [OSTI]

    McCallum, R.W.; Ellis, T.W.; Dennis, K.W.; Hofer, R.J.; Branagan, D.J.

    1997-11-25T23:59:59.000Z

    A method of making a rare earth compound, such as a earth-transition metal permanent magnet compound, without the need for producing rare earth metal as a process step, comprises carbothermically reacting a rare earth oxide to form a rare earth carbide and heating the rare earth carbide, a compound-forming reactant (e.g., a transition metal and optional boron), and a carbide-forming element (e.g., a refractory metal) that forms a carbide that is more thermodynamically favorable than the rare earth carbide whereby the rare earth compound (e.g., Nd{sub 2}Fe{sub 14}B or LaNi{sub 5}) and a carbide of the carbide-forming element are formed.

  8. Quarterly sampling of the wetlands along the old F-Area effluent ditch, Revision 1

    SciTech Connect (OSTI)

    Dixon, K.L.; cummins, C.L.

    1994-05-01T23:59:59.000Z

    In May 1994, well point water and bucket samples were collected for tritium and volatile organic compounds in the wetlands along the old F-Area effluent ditch south of 643-E (old burial ground). The well point samples were collected from seven locations and the bucket samples from four locations. Results support that T and VOCs originating from 643-E are outcropping in the wetlands near this ditch. Based on differences in tritium contents at each location, it was determined that the sampling devices intercepted different groundwater flow paths; however, when VOCs were normalized, based on differences in T, resulting well point and bucket VOCs were comparable in most cases.

  9. Cyclic membrane separation process

    DOE Patents [OSTI]

    Nemser, Stuart M.

    2005-05-03T23:59:59.000Z

    A cyclic process for controlling environmental emissions of volatile organic compounds (VOC) from vapor recovery in storage and dispensing operations of liquids maintains a vacuum in the storage tank ullage. In the first part of a two-part cyclic process ullage vapor is discharged through a vapor recovery system in which VOC are stripped from vented gas with a selectively gas permeable membrane. In the second part, the membrane is inoperative while gas pressure rises in the ullage. In one aspect of this invention, a vacuum is drawn in the membrane separation unit thus reducing overall VOC emissions.

  10. In situ bioremediation using horizontal wells

    SciTech Connect (OSTI)

    NONE

    1995-04-01T23:59:59.000Z

    In Situ Bioremediation (ISB), which is the term used in this report for Gaseous Nutrient Injection for In Situ Bioremediation, remediates soils and ground water contaminated with volatile organic compounds (VOCs) both above and below the water table. ISB involves injection of air and nutrients (sparging and biostimulation) into the ground water and vacuum extraction to remove .VOCs from the vadose zone concomitant with biodegradation of VOCs. The innovation is in the combination of 3 emerging technologies, air stripping, horizontal wells, and bioremediation via gaseous nutrient injection with a baseline technology, soil vapor extraction, to produce a more efficient in situ remediation system.

  11. Aza crown ether compounds as anion receptors

    DOE Patents [OSTI]

    Lee, H.S.; Yang, X.O.; McBreen, J.

    1998-08-04T23:59:59.000Z

    A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the new family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of LI{sup +} ion in alkali metal batteries. 3 figs.

  12. Apparatus for treatment of soils contaminated with organic pollutants

    DOE Patents [OSTI]

    Wickramanayake, Godage B. (Columbus, OH)

    1993-01-01T23:59:59.000Z

    An apparatus for treating soil contaminated by organic compounds wherein an ozone containing gas is treated with acid to increase the stability of the ozone in the soil environment and the treated ozone applied to the contaminated soil in a manner adapted to decompose the organic compounds; one embodiment of the apparatus comprises a means to supply ozone as a gas-ozone mixture, a stability means to treat ozone obtained from the supply and distribution means to apply the stabilized gas-ozone to soil. The soil may be treated in situ or may be removed for treatment and refilled.

  13. Polymers containing borane or carborane cage compounds and related applications

    SciTech Connect (OSTI)

    Bowen, III, Daniel E; Eastwood, Eric A

    2013-04-23T23:59:59.000Z

    Polymers comprising residues of cage compound monomers having at least one polyalkoxy silyl substituent are provided. The cage compound monomers are selected from borane cage compound monomers comprising at least 7 cage atoms and/or carborane cage compound monomers comprising 7 to 11 cage compound monomers. Such polymers can further comprise one or more reactive matrices and/or co-monomers covalently bound with the cage compound monomer residues. Articles of manufacture comprising such polymers are also disclosed.

  14. Targeting Organic Anion Transporting Polypeptides in Cancer to Improve Diagnostics and Therapy

    E-Print Network [OSTI]

    Hays, Amanda Lynne

    2012-08-12T23:59:59.000Z

    Organic Anion Transporting Polypeptides (OATPs) are multispecific transport proteins that mediate the uptake of numerous endogenous and exogenous compounds into cells. Recently, OATPs have been shown to have altered ...

  15. Characterising an Extractive Electrospray Ionisation (EESI) source for the online mass spectrometry analysis of organic aerosols

    E-Print Network [OSTI]

    Gallimore, Peter J.; Kalberer, Markus

    2013-05-28T23:59:59.000Z

    Organic compounds comprise a major fraction of tropospheric aerosol and understanding their chemical complexity is a key factor for determining their climate and health effects. We present and characterise here a new online technique...

  16. Variations in organic aerosol optical and hygroscopic properties upon heterogeneous OH oxidation

    E-Print Network [OSTI]

    Cappa, Christopher D.

    Measurements of the evolution of organic aerosol extinction cross sections (?[subscript ext]) and subsaturated hygroscopicity upon heterogeneous OH oxidation are reported for two model compounds, squalane (a C30 saturated ...

  17. Microsoft Word - NRAP_TRS_III_Mobilization_and_Transport_of_Organic...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mobilization and Transport of Organic Compounds from Geologic Carbon Sequestration Reservoirs 21 May 2015 Office of Fossil Energy NRAP-TRS-III-002-2015 Disclaimer This report was...

  18. Sediment-Water Partition Coefficients of Hydrophobic Persistent Organic Pollutants (POPs)

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    Sediment-Water Partition Coefficients of Hydrophobic Persistent Organic Pollutants (POPs aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs) were determined in sediments from five of performance reference compounds (PRCs). Marked differ- ences in freely dissolved PAH and PCB concentrations

  19. Chemical characterization of dissolved organic matter (DOM) in seawater : structure, cycling, and the role of biology

    E-Print Network [OSTI]

    Quan, Tracy M. (Tracy Michelle), 1977-

    2005-01-01T23:59:59.000Z

    The goal of this thesis is to investigate three different areas relating to the characterization of dissolved organic matter (DOM): further determination of the chemical compounds present in high molecular weight DOM ...

  20. Compound and Elemental Analysis At Clear Lake Area (Thompson...

    Open Energy Info (EERE)

    Compound and Elemental Analysis At Clear Lake Area (Thompson, Et Al., 1992) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Compound and...

  1. Novel Compounds for Enhancing Electrolyte Stability and Safety...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Compounds for Enhancing Electrolyte Stability and Safety of Lithium-ion Cells Novel Compounds for Enhancing Electrolyte Stability and Safety of Lithium-ion Cells 2010 DOE Vehicle...

  2. Compound and Elemental Analysis At Newberry Caldera Area (Goles...

    Open Energy Info (EERE)

    Compound and Elemental Analysis At Newberry Caldera Area (Goles & Lambert, 1990) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Compound and...

  3. Figure S1. Relative contribution to total OH reactivity (a), of observed VOCs to calculated OH reactivity (b) and alkyl nitrate production (c,d) in the afternoon (12pm

    E-Print Network [OSTI]

    Meskhidze, Nicholas

    production from aromatic VOCs is highly uncertain, and the result is thus bracketed by lower and upper extremes for aromatic branching ratios (see text). #12;2 Table S1. Speciated ANs precursors observed.07E-13(2) 0.00037 0.084 Propane 5. 7 0.036 1.07E-12(1) 0.0055 0.29 Propene 0.42 0.015 2.66E-11(3) 0

  4. Synchrotron based mass spectrometry to investigate the molecular properties of mineral-organic associations

    SciTech Connect (OSTI)

    Liu, Suet Yi; Kleber, Markus; Takahashi, Lynelle K.; Nico, Peter; Keiluweit, Marco; Ahmed, Musahid

    2013-04-01T23:59:59.000Z

    Soil organic matter (OM) is important because its decay drives life processes in the biosphere. Analysis of organic compounds in geological systems is difficult because of their intimate association with mineral surfaces. To date there is no procedure capable of quantitatively separating organic from mineral phases without creating artifacts or mass loss. Therefore, analytical techniques that can (a) generate information about both organic and mineral phases simultaneously and (b) allow the examination of predetermined high-interest regions of the sample as opposed to conventional bulk analytical techniques are valuable. Laser Desorption Synchrotron Postionization (synchrotron-LDPI) mass spectrometry is introduced as a novel analytical tool to characterize the molecular properties of organic compounds in mineral-organic samples from terrestrial systems, and it is demonstrated that when combined with Secondary Ion Mass Spectrometry (SIMS), can provide complementary information on mineral composition. Mass spectrometry along a decomposition gradient in density fractions, verifies the consistency of our results with bulk analytical techniques. We further demonstrate that by changing laser and photoionization energies, variations in molecular stability of organic compounds associated with mineral surfaces can be determined. The combination of synchrotron-LDPI and SIMS shows that the energetic conditions involved in desorption and ionization of organic matter may be a greater determinant of mass spectral signatures than the inherent molecular structure of the organic compounds investigated. The latter has implications for molecular models of natural organic matter that are based on mass spectrometric information.

  5. he Sun Rises From the Village (Gne Kyden

    E-Print Network [OSTI]

    Gürel, Levent

    the volatile organic compounds (VOCs) that come out of bacterial activities at an early stage, well before food University's umbrella organization for student volunteer activity. The goal of The Sun Rises From the Village than a human nose can, the food can be consumed or discarded well before it becomes a danger to health

  6. Process for production of a borohydride compound

    DOE Patents [OSTI]

    Allen, Nathan Tait; Butterick, III, Robert; Chin, Arthur Achhing; Millar, Dean Michael; Molzahn, David Craig

    2014-08-19T23:59:59.000Z

    A process for production of a borohydride compound M(BH.sub.4).sub.y. The process has three steps. The first step combines a compound of formula (R.sup.1O).sub.yM with aluminum, hydrogen and a metallic catalyst containing at least one metal selected from the group consisting of titanium, zirconium, hafnium, niobium, vanadium, tantalum and iron to produce a compound of formula M(AlH.sub.3OR.sup.1).sub.y, wherein R.sup.1 is phenyl or phenyl substituted by at least one alkyl or alkoxy group; M is an alkali metal, Be or Mg; and y is one or two; wherein the catalyst is present at a level of at least 200 ppm based on weight of aluminum. The second step combines the compound of formula M(AlH.sub.3OR.sup.1).sub.y with a borate, boroxine or borazine compound to produce M(BH.sub.4).sub.y and a byproduct mixture containing alkali metal and aluminum aryloxides. The third step separates M(BH.sub.4).sub.y from the byproduct mixture.

  7. Effect of Hydrophobic Primary Organic Aerosols on Secondary Organic...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Hydrophobic Primary Organic Aerosols on Secondary Organic Aerosol Formation from Ozonolysis of ?-Pinene. Effect of Hydrophobic Primary Organic Aerosols on Secondary Organic...

  8. Measuring Spatial Variability of Vapor Flux to Characterize Vadose-zone VOC Sources: Flow-cell Experiments

    SciTech Connect (OSTI)

    Mainhagu, Jon; Morrison, C.; Truex, Michael J.; Oostrom, Martinus; Brusseau, Mark

    2014-10-20T23:59:59.000Z

    A method termed vapor-phase tomography has recently been proposed to characterize the distribution of volatile organic contaminant mass in vadose-zone source areas, and to measure associated three-dimensional distributions of local contaminant mass discharge. The method is based on measuring the spatial variability of vapor flux, and thus inherent to its effectiveness is the premise that the magnitudes and temporal variability of vapor concentrations measured at different monitoring points within the interrogated area will be a function of the geospatial positions of the points relative to the source location. A series of flow-cell experiments was conducted to evaluate this premise. A well-defined source zone was created by injection and extraction of a non-reactive gas (SF6). Spatial and temporal concentration distributions obtained from the tests were compared to simulations produced with a mathematical model describing advective and diffusive transport. Tests were conducted to characterize both areal and vertical components of the application. Decreases in concentration over time were observed for monitoring points located on the opposite side of the source zone from the local–extraction point, whereas increases were observed for monitoring points located between the local–extraction point and the source zone. The results illustrate that comparison of temporal concentration profiles obtained at various monitoring points gives a general indication of the source location with respect to the extraction and monitoring points.

  9. Process for producing phenolic compounds from lignins

    DOE Patents [OSTI]

    Agblevor, F.A.

    1998-09-15T23:59:59.000Z

    A process is described for the production of low molecular weight phenolic compounds from lignins through the pyrolysis of the lignins in the presence of a strong base. In a preferred embodiment, potassium hydroxide is present in an amount of from about 0.1% to about 5% by weight, the pyrolysis temperature is from about 400 C to about 600 C at atmospheric pressure, and the time period for substantial completion of the reaction is from about 1--3 minutes. Examples of low molecular weight phenolic compounds produced include methoxyphenols, non-methoxylated phenols, and mixtures thereof. 16 figs.

  10. Dry etching method for compound semiconductors

    DOE Patents [OSTI]

    Shul, R.J.; Constantine, C.

    1997-04-29T23:59:59.000Z

    A dry etching method is disclosed. According to the present invention, a gaseous plasma comprising, at least in part, boron trichloride, methane, and hydrogen may be used for dry etching of a compound semiconductor material containing layers including aluminum, or indium, or both. Material layers of a compound semiconductor alloy such as AlGaInP or the like may be anisotropically etched for forming electronic devices including field-effect transistors and heterojunction bipolar transistors and for forming photonic devices including vertical-cavity surface-emitting lasers, edge-emitting lasers, and reflectance modulators. 1 fig.

  11. Inelastic neutron scattering in valence fluctuation compounds

    SciTech Connect (OSTI)

    Jon M Lawrence

    2011-02-15T23:59:59.000Z

    The valence fluctuation compounds are rare earth intermetallics where hybridization of the nearly-localized 4f electrons with the conduction electrons leads to incorporation of the 4f's into the itinerant states. This hybridization slows down the conduction electrons and hence gives them a heavy effective mass, justifying application of the term 'heavy Fermion' (HF) to these materials. During the project period, we grew large single crystals of several such compounds and measured their properties using both standard thermodynamic probes and state-of-the-art inelastic neutron scattering. We obtained three main results. For the intermediate valence compounds CePd{sub 3} and YbAl{sub 3}, we showed that the scattering of neutrons by the fluctuations of the 4f magnetic moment does not have the momentum dependence expected for the itinerant heavy mass state; rather, the scattering is more typical of a localized spin fluctuation. We believe that incoherent scattering localizes the excitation. For the heavy Fermion compound Ce(Ni{sub 0.935}Pd{sub 0.065}){sub 2}Ge{sub 2}, which sits at a T = 0 critical point for transformation into an antiferromagnetic (AF) phase, we showed that the scattering from the AF fluctuations does not exhibit any of the divergences that are expected at a phase transition. We speculate that alloy disorder profoundly suppresses the growth of the fluctuating AF regions, leading to short range clusters rather than regions of infinite size. Finally, we explored the applicability of key concepts used to describe the behavior of rare earth heavy Fermions to uranium based HF compounds where the 5f electrons are itinerant as opposed to localized. We found that scaling laws relating the spin fluctuation energy measured in neutron scattering to the low temperature specific heat and susceptibility are valid for the uranium compounds, once corrections are made for AF fluctuations; however, the degeneracy of the high temperature moment is smaller than expected for rare-earth-like Hund's rule behavior, essentially because the orbital moment is suppressed for itinerant 5f electrons. We also found that the standard local-moment-based theory of the temperature dependence of the specific heat, susceptibility and neutron scattering fails badly for URu{sub 2}Zn{sub 20} and UCo{sub 2}Zn{sub 20}, even though the theory is phenomenally successful for the closely related rare earth compound YbFe{sub 2}Zn{sub 20}. Both these results highlight the distinction between the itineracy of the 5f's and the localization of the 4f's. It is our hope that these results are sufficiently significant as to stimulate deeper investigation of these compounds.

  12. Dry etching method for compound semiconductors

    DOE Patents [OSTI]

    Shul, Randy J. (Albuquerque, NM); Constantine, Christopher (Safety Harbor, FL)

    1997-01-01T23:59:59.000Z

    A dry etching method. According to the present invention, a gaseous plasma comprising, at least in part, boron trichloride, methane, and hydrogen may be used for dry etching of a compound semiconductor material containing layers including aluminum, or indium, or both. Material layers of a compound semiconductor alloy such as AlGaInP or the like may be anisotropically etched for forming electronic devices including field-effect transistors and heterojunction bipolar transistors and for forming photonic devices including vertical-cavity surface-emitting lasers, edge-emitting lasers, and reflectance modulators.

  13. Beta cell device using icosahedral boride compounds

    DOE Patents [OSTI]

    Aselage, Terrence L. (62 Avenida Del Sol, Cedar Crest, NM 87008); Emin, David (1502 Harvard Ct., NE., Albuquerque, NM 87106-3712)

    2002-01-01T23:59:59.000Z

    A beta cell for converting beta-particle energies into electrical energy having a semiconductor junction that incorporates an icosahedral boride compound selected from B.sub.12 As.sub.2, B.sub.12 P.sub.2, elemental boron having an .alpha.-rhombohedral structure, elemental boron having a .beta.-rhombohedral structure, and boron carbides of the chemical formula B.sub.12-x C.sub.3-x, where 0.15compound self-heals, resisting degradation from radiation damage.

  14. Experimental investigation of single carbon compounds under hydrothermal conditions

    E-Print Network [OSTI]

    Rhoads, James

    reactant during the abiotic synthesis of reduced carbon compounds via Fischer­Tropsch-type processes

  15. Compositions containing borane or carborane cage compounds and related applications

    DOE Patents [OSTI]

    Bowen, III, Daniel E; Eastwood, Eric A

    2014-11-11T23:59:59.000Z

    Compositions comprising a polymer-containing matrix and a filler comprising a cage compound selected from borane cage compounds, carborane cage compounds, metal complexes thereof, residues thereof, mixtures thereof, and/or agglomerations thereof, where the cage compound is not covalently bound to the matrix polymer. Methods of making and applications for using such compositions are also disclosed.

  16. Compositions containing borane or carborane cage compounds and related applications

    DOE Patents [OSTI]

    Bowen, III, Daniel E; Eastwood, Eric A

    2013-05-28T23:59:59.000Z

    Compositions comprising a polymer-containing matrix and a filler comprising a cage compound selected from borane cage compounds, carborane cage compounds, metal complexes thereof, residues thereof, mixtures thereof, and/or agglomerations thereof, where the cage compound is not covalently bound to the matrix polymer. Methods of making and applications for using such compositions are also disclosed.

  17. Organic Photovoltaics Philip Schulz

    E-Print Network [OSTI]

    Firestone, Jeremy

    Field Effect Transistors Organic Light Emitting Diodes Organic Solar Cells .OFET, OTFT .RF-ID tag 1977 ­ Conductivity in polymers 1986 ­ First heterojunction OPV 1987 ­ First organic light emitting diode (OLED) 1993 ­ First OPV from solution processing 2001 ­ First certified organic solar cell with 2

  18. Departmental Organization and Management

    Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

    1993-06-10T23:59:59.000Z

    Effective immediately, the Departmental organization structure reflected in the chart at Attachment 1 has been approved.

  19. HYDROGEN LOCAL VIBRATIONAL MODES IN COMPOUND SEMICONDUCTORS

    E-Print Network [OSTI]

    McCluskey, Matthew

    HYDROGEN LOCAL VIBRATIONAL MODES IN COMPOUND SEMICONDUCTORS M.D. MCCLUSKEY* University) spectroscopy of hydrogen and deuterium in GaP, AlSb, ZnSe, and GaN has provided important information about the structures of dopant- hydrogen complexes and their interaction with the host lattice. In GaN:Mg, for example

  20. Quaternary Ammonium Compounds as Water Channel Blockers

    E-Print Network [OSTI]

    de Groot, Bert

    /AQP2/AQP4, whereas the water permeability of AQP3 and AQP5, which lack a corresponding TyrQuaternary Ammonium Compounds as Water Channel Blockers SPECIFICITY, POTENCY, AND SITE OF ACTION, West Mains Road, EH9 3JJ Scotland, United Kingdom Excessive water uptake through Aquaporins (AQP) can

  1. Stable surface passivation process for compound semiconductors

    DOE Patents [OSTI]

    Ashby, Carol I. H. (Edgewood, NM)

    2001-01-01T23:59:59.000Z

    A passivation process for a previously sulfided, selenided or tellurated III-V compound semiconductor surface. The concentration of undesired mid-gap surface states on a compound semiconductor surface is reduced by the formation of a near-monolayer of metal-(sulfur and/or selenium and/or tellurium)-semiconductor that is effective for long term passivation of the underlying semiconductor surface. Starting with the III-V compound semiconductor surface, any oxidation present thereon is substantially removed and the surface is then treated with sulfur, selenium or tellurium to form a near-monolayer of chalcogen-semiconductor of the surface in an oxygen-free atmosphere. This chalcogenated surface is then contacted with a solution of a metal that will form a low solubility chalcogenide to form a near-monolayer of metal-chalcogen-semiconductor. The resulting passivating layer provides long term protection for the underlying surface at or above the level achieved by a freshly chalcogenated compound semiconductor surface in an oxygen free atmosphere.

  2. Superconductivity in iron compounds G. R. Stewart

    E-Print Network [OSTI]

    Wu, Zhigang

    of the superconductivity in this new class of compounds. These iron pnictide and chalcogenide (FePn/Ch) superconductors-phonon coupled ``conventional'' superconductors. Clearly, superconductivity and magnetism or magnetic of magnetism and superconductivity in FePn/Ch superconductors 1606 D. Tc and TS=TSDW versus pressure 1607 1

  3. Organe und Gremien Organe der Stiftung

    E-Print Network [OSTI]

    , Batavia IL (USA) Prof. Dr. F. Krausz BESSY GmbH, Berlin Prof. Dr. B. Naroska Universität Hamburg Prof. Dr. F. Pauss European Organization for Particle Physics CERN, Geneva (CH) Dr. N. Roe Lawrence Berkeley Organization for Particle Physics CERN, Geneva (CH) Dr. A. Wrulich Paul Scherrer Institut, Villigen (CH) 14 #12

  4. Organe und Gremien Organe der Stiftung

    E-Print Network [OSTI]

    Medizinische Forschung, Heidelberg Prof. Dr. E. Jaeschke BESSY GmbH, Berlin Prof. Dr. W. Jentschke Institut für Experimentalphysik, Universität Hamburg (Ehrenmitglied) Dr. K.-H. Kissler European Organization for Particle Physics Organization for Particle Physics CERN, Geneva (CH) Prof. Dr. W. Sandner Max-Born-Institut, Berlin Dr. M

  5. Organe und Gremien Organe der Stiftung

    E-Print Network [OSTI]

    Kassel Prof. Dr. S. Großmann Fachbereich Physik, Universität Marburg Prof. Dr. E. Jaeschke BESSY Gmb Organization for Particle Physics CERN, Genf (CH) Prof. Dr. V. Metag Gesellschaft für Schwerionenforschung GSI, Darmstadt Dr. D. Möhl European Organization for Particle Physics CERN, Genf (CH) Prof. Dr. J. Stachel

  6. Organe und Gremien Organe der Stiftung

    E-Print Network [OSTI]

    BESSY GmbH, Berlin Prof. Dr. W. Jentschke II. Institut für Experimentalphysik, Universität Hamburg (Ehrenmitglied) Dr. K.-H. Kissler European Organization for Particle Physics CERN, Geneva (CH) Prof. Dr. K. Königsmann Albert-Ludwigs-Universität Freiburg Dr. J. May European Organization for Particle Physics CERN

  7. Metal-Organic Frameworks for Highly Selective Separations

    SciTech Connect (OSTI)

    Omar M. Yaghi

    2009-09-28T23:59:59.000Z

    This grant was focused on the study of metal-organic frameworks with these specific objectives. (1) To examine the use of MOFs with well-defined open metal sites for binding of gases and small organics. (2) To develop a strategy for producing MOFs that combine large pore size with high surface area for their use in gas adsorption and separation of polycyclic organic compounds. (3) To functionalize MOFs for the storage of inert gases such as methane. A brief outline of our progress towards these objectives is presented here as it forms part of the basis for the ideas to be developed under the present proposal.

  8. Complexant stability investigation. Task 2. Organic complexants

    SciTech Connect (OSTI)

    Martin, E.C.

    1985-06-01T23:59:59.000Z

    The safety of high-level defense waste operations has always been given highest priority at the Hanford site. This document is part of the continued effort to appraise and reevaluate the safety of the waste stored in underground tanks on the Hanford Reservation. Hanford high-level defense waste consists mainly of moist, inorganic salts, NaNO/sub 3/, NaAl(OH)/sub 4/, Na/sub 2/CO/sub 3/, and other sodium salts. However, in addition to these salts, quantities of organic compounds constitute a significant portion of the waste. The potential reaction of the organic compounds with inorganic salts to form explosive substances is examined and found to be nonexistent or negligible. The concept that the waste mixture might react exothermically is found to be untenable under the present storage conditions. The phenomenon of slurry growth in double-shell waste storage tanks is expected to cause no increase in exothermic reaction potential within the waste. The results of this study indicate that the presence of organic material in the high-level defense waste does not constitute undue hazard under the present storage conditions.

  9. Direct synthesis of catalyzed hydride compounds

    DOE Patents [OSTI]

    Gross, Karl J.; Majzoub, Eric

    2004-09-21T23:59:59.000Z

    A method is disclosed for directly preparing alkali metal aluminum hydrides such as NaAlH.sub.4 and Na.sub.3 AlH.sub.6 from either the alkali metal or its hydride, and aluminum. The hydride thus prepared is doped with a small portion of a transition metal catalyst compound, such as TiCl.sub.3, TiF.sub.3, or a mixture of these materials, in order to render them reversibly hydridable. The process provides for mechanically mixing the dry reagents under an inert atmosphere followed by charging the mixed materials with high pressure hydrogen while heating the mixture to about 125.degree. C. The method is relatively simple and inexpensive and provides reversible hydride compounds which are free of the usual contamination introduced by prior art wet chemical methods.

  10. Organic photovoltaics and concentrators

    E-Print Network [OSTI]

    Mapel, Jonathan King

    2008-01-01T23:59:59.000Z

    The separation of light harvesting and charge generation offers several advantages in the design of organic photovoltaics and organic solar concentrators for the ultimate end goal of achieving a lower cost solar electric ...

  11. Organizing and Personalizing Intelligence

    E-Print Network [OSTI]

    Tan, Ah-Hwee

    Vista). More sophis- ticated ones, such as Northern Light, BullsEye and Copernic go a step further organize

  12. Hydromechanical transmission with compound planetary assembly

    DOE Patents [OSTI]

    Orshansky, Jr., deceased, Elias (late of San Francisco, CA); Weseloh, William E. (San Diego, CA)

    1980-01-01T23:59:59.000Z

    A power transmission having three distinct ranges: (1) hydrostatic, (2) simple power-split hydromechanical, and (3) compound power-split hydromechanical. A single compound planetary assembly has two sun gears, two ring gears, and a single carrier with two sets of elongated planet gears. The two sun gears may be identical in size, and the two ring gears may be identical in size. A speed-varying module in driving relationship to the first sun gear is clutchable, in turn, to (1) the input shaft and (2) the second sun gear. The speed-varying means may comprise a pair of hydraulic units hydraulically interconnected so that one serves as a pump while the other serves as a motor and vice versa, one of the units having a variable stroke and being the one clutchable to either the input shaft or to the second sun gear. The other unit, which may have a fixed stroke, is connected in driving relation to the first sun gear. A brake grounds the carrier in the first range and in reverse and causes drive to be delivered to the output shaft through the first ring gear in a hydrostatic mode, the first ring gear being rigidly connected to the output shaft. The input shaft is also clutchable to the second ring gear of the compound planetary assembly.

  13. Organic photosensitive devices

    DOE Patents [OSTI]

    Rand, Barry P; Forrest, Stephen R

    2013-11-26T23:59:59.000Z

    The present invention generally relates to organic photosensitive optoelectronic devices. More specifically, it is directed to organic photosensitive optoelectronic devices having a photoactive organic region containing encapsulated nanoparticles that exhibit plasmon resonances. An enhancement of the incident optical field is achieved via surface plasmon polariton resonances. This enhancement increases the absorption of incident light, leading to a more efficient device.

  14. CCPPolicyBriefing Organization

    E-Print Network [OSTI]

    Feigon, Brooke

    . METHODOLOGY · The author incorporates the economic theory of organizations into the framework of public law to establish the theory of cartel organization, and calls for further studies to disclose the sophisticatedCCPPolicyBriefing September 2008 Cartel Organization and Antitrust Enforcement W: www

  15. Isoreticular metal-organic frameworks, process for forming the same, and systematic design of pore size and functionality therein, with application for gas storage

    DOE Patents [OSTI]

    Yaghi, Omar M.; Eddaoudi, Mohamed; Li, Hailian; Kim, Jaheon; Rosi, Nathaniel

    2005-08-16T23:59:59.000Z

    An isoreticular metal-organic framework (IRMOF) and method for systematically forming the same. The method comprises the steps of dissolving at least one source of metal cations and at least one organic linking compound in a solvent to form a solution; and crystallizing the solution under predetermined conditions to form a predetermined IRMOF. At least one of functionality, dimension, pore size and free volume of the IRMOF is substantially determined by the organic linking compound.

  16. Water quality studies in Kranji Catchment, Singapore : use of organic tracer and PEDs for identifying potential sewage sources

    E-Print Network [OSTI]

    Mendez Sagel, Adriana (Adriana Raquel)

    2010-01-01T23:59:59.000Z

    The objective of this study was to identify organic compounds that could serve as indicators of potential human fecal contamination sources to the Kranji Reservoir in Singapore that could be used as confirmation indicators ...

  17. Intercalation compounds and electrodes for batteries

    DOE Patents [OSTI]

    Chiang, Yet-Ming; Sadoway, Donald R.; Jang, Young-Il; Huang, Biyan

    2004-09-07T23:59:59.000Z

    This invention concerns intercalation compounds and in particular lithium intercalation compounds which have improved properties for use in batteries. Compositions of the invention include particulate metal oxide material having particles of multicomponent metal oxide, each including an oxide core of at least first and second metals in a first ratio, and each including a surface coating of metal oxide or hydroxide that does not include the first and second metals in the first ratio formed by segregation of at least one of the first and second metals from the core. The core may preferably comprise Li.sub.x M.sub.y N.sub.z O.sub.2 wherein M and N are metal atom or main group elements, x, y and z are numbers from about 0 to about 1 and y and z are such that a formal charge on M.sub.y N.sub.z portion of the compound is (4-x), and having a charging voltage of at least about 2.5V. The invention may also be characterized as a multicomponent oxide microstructure usable as a lithium intercalation material including a multiphase oxide core and a surface layer of one material, which is a component of the multiphase oxide core, that protects the underlying intercalation material from chemical dissolution or reaction. In a particular preferred example the multicomponent oxide may be an aluminum-doped lithium manganese oxide composition. Such aluminum-doped lithium manganese oxide compositions, having an orthorhombic structure, also form a part of the invention. In addition, the invention includes articles, particularly electrodes, for batteries formed from the compositions of the invention, and batteries including such electrodes. The invention further relates to a composite intercalation material comprising at least two compounds in which at least one compound has an orthorhombic structure Li.sub.x Al.sub.y Mn.sub.1-y O.sub.2, where y is nonzero, or a mixture of orthorhombic and monoclinic Li.sub.x Al.sub.y Mn.sub.1-y O.sub.2.

  18. Hydroxyalkyl phosphine compounds for use as diagnostic and therapeutic pharmaceuticals

    DOE Patents [OSTI]

    Katti, Kattesh V. (Columbia, MO); Singh, Prahlad R. (Columbia, MO); Reddy, V. Sreenivasa (Columbia, MO); Katti, Kavita K. (Columbia, MO); Volkert, Wynn A. (Columbia, MO); Ketring, Alan R. (Columbia, MO)

    1999-01-01T23:59:59.000Z

    A compound and method of making a compound for use as a diagnostic or therapeutic pharmaceutical comprises a functionalized hydroxyalkyl phosphine ligand and a metal combined with the ligand.

  19. Expanded Use of Bicyclic Guanidinate Ligands in Dimetal Paddlewheel Compounds

    E-Print Network [OSTI]

    Young, Mark D.

    2010-01-16T23:59:59.000Z

    ^6+ compounds, both of which are examined structurally and electrochemically. [Os2(hpp)4]^+ is examined to improve upon earlier studies, yielding a model of the g-tensor components with respect to the compound structure. An additional project included...

  20. Surface passivation process of compound semiconductor material using UV photosulfidation

    DOE Patents [OSTI]

    Ashby, Carol I. H. (Edgewood, NM)

    1995-01-01T23:59:59.000Z

    A method for passivating compound semiconductor surfaces by photolytically disrupting molecular sulfur vapor with ultraviolet radiation to form reactive sulfur which then reacts with and passivates the surface of compound semiconductors.

  1. Hydroxyalkyl phosphine compounds for use as diagnostic and therapeutic pharmaceuticals

    DOE Patents [OSTI]

    Katti, K.V.; Singh, P.R.; Reddy, V.S.; Katti, K.K.; Volkert, W.A.; Ketring, A.R.

    1999-03-02T23:59:59.000Z

    This research discloses a compound and method of making a compound for use as a diagnostic or therapeutic pharmaceutical comprises a functionalized hydroxyalkyl phosphine ligand and a metal combined with the ligand. 16 figs.

  2. Differential heterotrophic utilization of organic compounds by diatoms and bacteria under light and dark conditions

    E-Print Network [OSTI]

    Kelly, John J.

    competition by niche separation. Eight light- and dark-grown diatom taxa and five bacterial species were-grown counterparts, indicating that the transport systems for these molecules may be light activated. Therefore for survival, or when substrates are plentiful. A principal components analysis indicated discernible

  3. Carbon isotope ratios of organic compound fractions in oceanic suspended particles

    E-Print Network [OSTI]

    Hwang, Jeomshik; Druffel, Ellen R. M

    2006-01-01T23:59:59.000Z

    in the northeast Pacific Ocean, J. Geophys. Res. , 101,slope to the abyssal NE Pacific Ocean, Deep Sea Res. , Partwaters of the equatorial Pacific Ocean, Deep Sea Res. , Part

  4. Atmospheric Environment 33 (1999) 783--795 The solvent-extractable organic compounds in the Indonesia

    E-Print Network [OSTI]

    Zheng, Mei

    in the Indonesia biomass burning aerosols -- characterization studies M. Fang *, M. Zheng , F. Wang , K.L. To , A-of-control biomass burning for agricultural purposes in Indonesia started in June 1997, has become a severe Elsevier Science Ltd. All rights reserved. Keywords: Indonesia forest fire; Malaysia; Biomass burning

  5. Emissions of volatile organic compounds inferred from airborne flux measurements over a megacity

    E-Print Network [OSTI]

    Karl, T.; Apel, E.; Hodzic, A.; Riemer, D. D; Blake, D. R; Wiedinmyer, C.

    2009-01-01T23:59:59.000Z

    methyl-tertiary-butyl- ether (MTBE) and the biomass burningfrom all source categories. MTBE is a gasoline additive andwith the fuel tracer MTBE (e.g. 0.82 for MTBE/benzene).

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

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    Methanol Ethanol Acetone MEK MTBE CO Methane UCI UCI TOGA/methyl tertiary butyl ether (MTBE), and toluene all ratioedthe observed decay. For MTBE, also a species that is not

  7. QUANTIFYING NON-POINT SOURCES OF VOLATILE ORGANIC COMPOUNDS IN STORMWATER FROM A PARKING LOT

    E-Print Network [OSTI]

    -butyl ether (MTBE) on urban particles indicates a site- specific interaction between MTBE and a particulate is a possible source only for the gasoline oxygenate methyl tert-butyl ether (MTBE). Lopes and Bender (1998

  8. High-precision optical measurements of 13 isotope ratios in organic compounds at

    E-Print Network [OSTI]

    Zare, Richard N.

    range with an average precision of 0.95 and 0.67 for ethane and propane, respec- tively. The calibrated accuracy for methane, ethane, and propane is within 3 of the values determined using isotope ratio mass place in chemistry, especially in geochemistry, for determining reaction mechanisms and pro- viding

  9. SPECIATION OF TRACE ORGANIC LIGANDS AND INORGANIC AND ORGANOMETALLIC COMPOUNDS IN OIL SHALE PROCESS WATERS

    E-Print Network [OSTI]

    Fish, Richard H.

    2013-01-01T23:59:59.000Z

    1979). retort water, boiler blowdown, and heater- treaterGeokinetics Retort Water Occidental Heater-Treater :ss.ssa) situ Occidental Heater-Treater Water Retort 6 modified

  10. Factors Affecting Indoor Air Concentrations of Volatile Organic Compounds at a Site of Subsurface Gasoline Contamination

    E-Print Network [OSTI]

    Fischer, M.L.

    2011-01-01T23:59:59.000Z

    OF SUBSURFACE GASOLINE CONTAMINATION Marc L. Fischer, AbraOF SUBSURFACE GASOLINE CONTAMINATION Marc L. Fischer, Abrareporting indoor air contamination (6,7). Estimation of

  11. Methyl halide and biogenic volatile organic compound fluxes from perennial bioenergy crops and annual arable crops 

    E-Print Network [OSTI]

    Morrison, Eilidh Christina

    2013-11-28T23:59:59.000Z

    The depletion of fossil fuel resources, pollution concerns and the challenge of energy security are driving the search for renewable energy sources. The use of lignocellulosic plant biomass as an energy source is increasing ...

  12. Observations of nonmethane organic compounds during ARCTAS - Part 1: Biomass burning emissions and plume enhancements

    E-Print Network [OSTI]

    2011-01-01T23:59:59.000Z

    burning in Siberia and Kazakhstan as an important source forgrassland fires in Kazakhstan (Warneke et al. , 2009) duringfires from East Asia/Kazakhstan. Likewise there was no sta-

  13. Hybrid membranes and their use in volatile organic compound/air separations

    E-Print Network [OSTI]

    Krohn, John Eric

    2001-01-01T23:59:59.000Z

    of membrane. This housing is equipped with a gasket seal between the high and low pressure sides ol tbe membrane. While the feed/retentate side of the membrane is held at 20-30 in HtO above atmospheric pressure, the permeate side is held at approximately...

  14. Measurements and receptor modeling of volatile organic compounds in Southeastern Mexico City, 2000 2007

    E-Print Network [OSTI]

    Meskhidze, Nicholas

    to account for non-vehicular emissions entering the tunnel from outside. The time for each sample was 2 hours Traffic count Total: 673 vehicles per hour Gasoline vehicle (car, pickup): 91% Diesel vehicle (truck / bus (truck / bus): 11% motor bike: 3% Figure 2. Fotos from inside the Subterránea (left and middle panel

  15. A study of the tropospheric oxidation of volatile organic compounds using chemical ionization mass spectrometry

    E-Print Network [OSTI]

    Broekhuizen, Keith Edward, 1974-

    2002-01-01T23:59:59.000Z

    The mechanisms and kinetics of reactions important to the troposphere have been investigated using a high pressure, turbulent, discharge-flow technique coupled to a chemical ionization mass spectrometer. The ability to ...

  16. Source characteristics of volatile organic compounds during high ozone episodes in Hong Kong, Southern China

    E-Print Network [OSTI]

    Zhang, J.; Wang, T.; Chameides, W. L; Cardelino, C.; Blake, D. R; Streets, D. G

    2008-01-01T23:59:59.000Z

    related to industrial/petrochemical activities. This in turnrelated to industrial/petrochemical activities. However,were likely related to petrochemical/industrial, waterfront,

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

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    and dispersion of a Mexico City pollution out- flow eventon air pollution in the Mexico City Metropolitan Area,pollution transport during the MILAGRO-2006 campaign: a case study of a major Mexico

  18. Toxic Volatile Organic Compounds in Environmental Tobacco Smoke: Emission Factors for Modeling Exposures of California Populations

    E-Print Network [OSTI]

    Daisey, J.M.; Mahanama, K.R.R.; Hodgson, A.T.

    1994-01-01T23:59:59.000Z

    acrylate Ethy lbenzene 3-Methyl- 1-butanol Pyridine Pyrroleethyl acrylate, 3-methyl-1-butanol, N-nitrosodiethylamineEthylbenzene Formaldehyde 3-Methyl-1-butanol Phenol Styrene

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

    E-Print Network [OSTI]

    2010-01-01T23:59:59.000Z

    C-130 T0 T1 G1 Ethane Propane i-Butane n-Butane i-Pentane n-ppbv) Ethane Ethene Ethyne Propane Propene i-Butane n-Butanee.g. , ethane, ethene, propane, propane, methanol, ethanol,

  20. Occurrence of priority and emerging organic compounds in fishes from the Rhone River , P. Labadie2**

    E-Print Network [OSTI]

    ) and hexachloro-butadiene (HCBD). About 50 fish samples (individual specimens or pooled fishes) were collected is confirmed. In contrast, the pertinence of a priority status for HCBD, which was never quantified in our

  1. Remedial extraction and catalytic hydrodehalogenation for treatment of soils contaminated by halogenated hydrophobic organic compounds

    E-Print Network [OSTI]

    Wee, Hun Young

    2009-05-15T23:59:59.000Z

    for the extraction of 1,2,4,5-tetrachlorobenzne (TeCB) or pentachlorophenol (PCP) from contaminated soil. Palladium-catalyzed hydrodehalogenation (HDH) was applied for destroying TeCB or PCP in mixtures of water and ethanol in a batch mode. The experimental results...

  2. Atmospheric Aerosols Aging Involving Organic Compounds and Impacts on Particle Properties

    E-Print Network [OSTI]

    Qiu, Chong

    2013-02-01T23:59:59.000Z

    through sandstorm.2 Examples of anthropogenic sources are vehicle exhaust, plant emission, and construction sites. Some aerosols may have both biogenic and anthropogenic sources. For example, soot aerosols, also known as black carbon, can be produced... with an initial size of 150 nm increases slightly faster than those of soot with the initial size of 80 or 100 nm. Table 1. Properties of Fresh Soot Particles. Dp, nm mp, 10 ?16 g Dve, nm Npp a 82.4 1.47 54.1 20 101 2.34 63.2 32 155 7.77 94.3 105 a...

  3. In-situ remediation system for volatile organic compounds with deep recharge mechanism

    DOE Patents [OSTI]

    Jackson, Jr., Dennis G. (Augusta, GA); Looney, Brian B. (Aiken, SC); Nichols, Ralph L. (Augusta, SC); Phifer, Mark A. (Augusta, SC)

    2001-01-01T23:59:59.000Z

    A method and apparatus for the treatment and remediation of a contaminated aquifer in the presence of an uncontaminated aquifer at a different hydraulic potential. The apparatus consists of a wellbore inserted through a first aquifer and into a second aquifer, an inner cylinder within the wellbore is supported and sealed to the wellbore to prevent communication between the two aquifers. Air injection is used to sparge the liquid having the higher static water level and, to airlift it to a height whereby it spills into the inner cylinder. The second treatment area provides treatment in the form of aeration or treatment with a material. Vapor stripped in sparging is vented to the atmosphere. Treated water is returned to the aquifer having the lower hydraulic potential.

  4. Simple general limiting law for the overall decay of organic compounds with global pollution potential

    SciTech Connect (OSTI)

    Mueller-Herold, U. [Swiss Federal Inst. of Technology, Zuerich (Switzerland)] [Swiss Federal Inst. of Technology, Zuerich (Switzerland)

    1996-02-01T23:59:59.000Z

    It is rigorously shown that the effective decay rate in the environment of a chemical is between the minimum decay rate in one of its possible compartments and an upper value, which is the weighted-average decay rates in all compartments. The weights are the compartments` volumes and the equilibrium concentrations that would have occurred in the compartment due to transport alone, with no degradation. This upper value is approached, in the sense of a general limiting law, if degradation is much slower than transport. This limiting law, together with an estimate for the spatial range of a persistent chemical, could serve as a minimal base for exposure-based assessment of environmental risk. As a first illustration, the result is applied to DDT and hexachloroethane. A broader group of chemicals will be discussed elsewhere. 20 refs., 3 figs., 2 tabs.

  5. Annual research plan, 1983-84. [Organic compounds derived from fossil substances

    SciTech Connect (OSTI)

    None

    1984-05-01T23:59:59.000Z

    The National Institute for Petroleum and Energy Research (NIPER) resulted from efforts by the Department of Energy (DOE) to ensure the continuity of the unique energy research capabilities that had been developed at the Bartlesville Energy Technology Center (BETC) over the past 65 years. This was accomplished by a Cooperative Agreement between DOE and IIT Research Institute (IITRI). The agreement to operate NIPER for the five fiscal years 1984-88 became effective October 1, 1983. The NIPER Annual Research Plan for 1983-84 consists of eight projects in the Base Program and 13 projects in the Optional Program. A sampling of potential Work for Others projects is also presented. The Base Program consists of five EOR and three Fundamental Petroleum Chemistry projects. The Optional Program has three EOR projects, one Unconventional Gas Recovery project, five APT projects, and four Advanced Utilization Research projects.

  6. Removal of volatile organic compounds from polluted air in a reverse flow reactor: An experimental study

    SciTech Connect (OSTI)

    Beld, B. van de; Borman, R.A.; Derkx, O.R.; Woezik, B.A.A. van; Westerterp, K.R. (Univ. of Twente, Enschede (Netherlands). Dept. of Chemical Engineering)

    1994-12-01T23:59:59.000Z

    An experimental study of the reverse flow reactor for the purification of contaminated air has been carried out. An experimental reactor with an inner diameter of 0.145 m has been constructed. It almost completely reached the goal of an adiabatically operating system. The influence of several operating parameters such as gas velocity, cycle period, chemical character, and concentration of the pollutants and reactor pressure are discussed. The reactor could be operated autothermally provided that the inlet concentrations were sufficiently high. If a mixture of contaminants is fed to the reactor, it might be necessary to increase the total hydrocarbon concentration to assure an autothermal process. Increasing the reactor pressure will hardly change the axial temperature profiles, if the mass flux is kept constant. Increasing the mass flow rate will lead to a higher plateau temperature. Not only the reactor behavior at fixed operating conditions, but also the response of the reactor toward variations in inlet conditions is reported.

  7. Impact of California Reformulated Gasoline on Motor Vehicle Emissions. 2. Volatile Organic Compound Speciation and Reactivity

    E-Print Network [OSTI]

    Kirchstetter, Thomas; Singer, Brett; Harley, Robert

    1999-01-01T23:59:59.000Z

    diurnal, hot-soak, and running loss emissions lie somewherea contribution from running loss evaporative emissions. Asof diurnal, hot-soak, and running loss evaporative emissions

  8. Temperature dependence of volatile organic compound evaporative emissions from motor vehicles

    E-Print Network [OSTI]

    Silver, Whendee

    emissions associated with venting of fuel tank vapors as temperature increases during the day, running loss

  9. A study of the Reaction Between Antimony (III) Bromide and Organic Amine Hydrobromide Compounds

    E-Print Network [OSTI]

    Yeakley, Richard Lee

    1960-01-01T23:59:59.000Z

    is deeply appreciated. In addition, I wish to thank the other members of my committee. A special word of appreciation is due the Dow Chemical Company for allowing me to do this work. ABLE OP SON~EN S I?RODU'(~'PION EXPEHINEN:. 'AL PBOOETJTJPZ...-C+He)&NH&)SbBr+, and ((CHs)sNH&)sSbsBrr~ from the reaction of ant;imony( II) brom' de and the correspond- . ng amine hvdrabrom"des. Dragules . u and Florea (10) used the react' on of acridine in excess hydrobr. omic acid t;a develop a sens' t've spot. test; for antimony...

  10. Flux Measurements of Volatile Organic Compounds from an Urban Tower Platform

    E-Print Network [OSTI]

    Park, Chang Hyoun

    2011-08-08T23:59:59.000Z

    11. INTRODUCTION Air quality studies overwhelmingly focus on the concentration of US Environmental Protection Agency (EPA) criteria air pollutants using monitoring and numerical modeling. While the latter uses surface fluxes from emission... chemistry and public health. Urban air pollution sources are related to a multitude of land-uses and human-made structures, which, together with natural and introduced vegetation, make up the urban fabric. To measure pollutant flux over urban terrain, a...

  11. Emissions of volatile organic compounds inferred from airborne flux measurements over a megacity

    E-Print Network [OSTI]

    Karl, T.; Apel, E.; Hodzic, A.; Riemer, D. D; Blake, D. R; Wiedinmyer, C.

    2009-01-01T23:59:59.000Z

    P. R. , and Hao, W. M. : Emissions from forest fires nearM. O. and Merlet, P. : Emission of trace gases and aerosolsW. : Automo- bile Emissions of Acetonitrile: Assessment of

  12. Investigation of Nitro-Organic Compounds in Diesel Engine Exhaust: Final Report, February 2007 - April 2008

    SciTech Connect (OSTI)

    Dane, J.; Voorhees, K. J.

    2010-06-01T23:59:59.000Z

    The National Renewable Energy Laboratory upgraded its ReFUEL engine and vehicle testing facility to speciate unregulated gas-phase emissions. To complement this capability, the laboratory contracted with the Colorado School of Mines (CSM) to study the effects of soy biodiesel fuel and a diesel particle filter (DPF) on emissions of polycyclic aromatic hydrocarbons (PAH) and nitro-polycyclic aromatic hydrocarbons (NPAH). CSM developed procedures to sample diesel particulate matter (PM) emissions from raw and diluted exhaust, with and without a DPF. They also developed improved procedures for extracting PAH and NPAH from the PM and quantifying them with a gas chromatograph-electron monochromator mass spectrometer. The study found the DPF generally reduced PAH emissions by 1 to 3 orders of magnitude. PAH conversion was lowest for B100, suggesting that PAHs were forming in the DPF. Orders of magnitude reductions were also found for NPAH emissions exiting the DPF.

  13. New electrolyte systems for capillary zone electrophoresis of metal cations and non-ionic organic compounds

    SciTech Connect (OSTI)

    Shi, Y.

    1995-06-19T23:59:59.000Z

    Excellent separations of metal ions can be obtained very quickly by capillary electrophoresis provided a weak complexing reagent is incorporated into the electrolyte to alter the effective mobilities of the sample ions. Indirect photometric detection is possible by also adding a UV-sensitive ion to the electrolyte. Separations are described using phthalate, tartrate, lactate or hydroxyisobutyrate as the complexing reagent. A separation of twenty-seven metal ions was achieved in only 6 min using a lactate system. A mechanism for the separation of lanthanides is proposed for the hydroxyisobutyrate system.

  14. Detecting Volatile Organic Compounds from Orbit J. J. Harrison & P. F. Bernath

    E-Print Network [OSTI]

    ethane retrievals are currently being optimised by updating and improving the microwindow set. Propane cross sections have also been determined from spectra recorded at the MSF. Propane 215 K Propane Q

  15. Class 2 Permit Modification Request Revise Volatile Organic Compound Monitoring Procedures

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645 3,625govInstrumentstdmadapInactiveVisiting the TWPSuccessAlamosCharacterization2 Permit Modification Request Revise

  16. Microsoft Word - NRAP_TRS_III_Mobilization_and_Transport_of_Organic_Compound_final.20150515.docx

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative1 First Use of Energy for All Purposes (Fuel and Nonfuel), 2002; Level: National5Sales for4,645U.S. DOEThe Bonneville PowerCherries 82981-1cnHighandSWPA / SPRA / USACE LMI-EFRCAddendum 1April 1, 2011

  17. In Vitro Genotoxicity of Particulate and Semi-Volatile Organic Compound

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels DataDepartment of Energy Your Density Isn't YourTransport(Fact Sheet),EnergyImprovement of the LostDepartment ofParticulate andExhaust

  18. Method for conversion of .beta.-hydroxy carbonyl compounds

    DOE Patents [OSTI]

    Lilga, Michael A. (Richland, WA); White, James F. (Richland, WA); Holladay, Johnathan E. (Kennewick, WA); Zacher, Alan H. (Kennewick, WA); Muzatko, Danielle S. (Kennewick, WA); Orth, Rick J. (Kennewick, WA)

    2010-03-30T23:59:59.000Z

    A process is disclosed for conversion of salts of .beta.-hydroxy carbonyl compounds forming useful conversion products including, e.g., .alpha.,.beta.-unsaturated carbonyl compounds and/or salts of .alpha.,.beta.-unsaturated carbonyl compounds. Conversion products find use, e.g., as feedstock and/or end-use chemicals.

  19. HOT NEW SPIN-1/2 PERFECT KAGOM COMPOUND

    E-Print Network [OSTI]

    Keren, Amit

    to 3.5K. At even lower temperature the low frequency peak vanishes. L. Marcipar et al. PRB 80 132402 L. Marcipar et al. PRB 80 132402 (2009) Does this compound behave as expected from a kagome. Marcipar et al. PRB 80 132402 (2009) Does this compound behave as expected from a kagome compound: Does

  20. Synthesis, structure and magnetic properties of lanthanide cluster compounds

    E-Print Network [OSTI]

    Sweet, Lucas Edward

    2009-05-15T23:59:59.000Z

    This dissertation focuses on the exploratory synthesis of compounds that contain R6ZI12 (R= Ce, Gd, Er; Z=Mn, Fe, Co, C2) clusters with the goal of finding magnetically interesting compounds. Several new compounds were made via high temperature...

  1. From Population to Organization Thinking

    E-Print Network [OSTI]

    Lane, David; Maxfield, Robert; Read, Dwight W; van der Leeuw, Sander E

    2009-01-01T23:59:59.000Z

    Herbert Simon developed a theory of organization for complexin need of a theory of organization. As we have alreadya deeper theory of organization: complex networks,

  2. Glassy dynamics distinguishes chromosome organization across organisms

    E-Print Network [OSTI]

    Hongsuk Kang; Young-Gui Yoon; D. Thirumalai; Changbong Hyeon

    2015-06-03T23:59:59.000Z

    Recent experiments showing scaling of the intrachromosomal contact probability, $P(s)\\sim s^{-1}$ with the genomic distance $s$, are interpreted to mean a self-similar fractal-like chromosome organization. However, scaling of $P(s)$ varies across organisms, requiring an explanation. We illustrate that dynamical arrest in a highly confined space as a discriminating marker for genome organization, by modeling chromosome inside a nucleus as a self-avoiding homopolymer confined to a sphere of varying sizes. Brownian dynamics simulations show that the chain dynamics slows down as the polymer volume fraction ($\\phi$) inside the confinement approaches a critical value $\\phi_c$. Using finite size scaling analysis, we determine $\\phi_c^{\\infty}\\approx 0.44$ for a sufficiently long polymer ($N\\gg 1$). Our study shows that the onset of glassy dynamics is the reason for the formation of segregated organization in human chromosomes ($N\\approx 3\\times 10^9$, $\\phi\\gtrsim\\phi_c^{\\infty}$), whereas chromosomes of budding yeast ($N\\approx 1.2\\times 10^7$, $\\phi<\\phi_c^{\\infty}$) are equilibrated with no clear signature of such organization.

  3. Sociology: Computational Organization Theory Sociology: Computational Organization Theory

    E-Print Network [OSTI]

    Sadeh, Norman M.

    Sociology: Computational Organization Theory Sociology: Computational Organization Theory Kathleen; organization theory; organizational learning; social networks; expert systems Citation: Kathleen Carley, 1994, "Sociology: Computational Organization Theory." Social Science Computer Review, 12(4): 611-624. #12;Sociology

  4. Theory of Organic Magnetoresistance in Disordered Organic Semiconductors

    E-Print Network [OSTI]

    Flatte, Michael E.

    Theory of Organic Magnetoresistance in Disordered Organic Semiconductors Nicholas J. Harmon semiconductors, disordered semiconductors, organic magnetoresistance, percolation theory, spin transport organic semiconductors. The theory proposed here maps the complex phenomena of spin-dependent hopping onto

  5. Natural attenuation: Chlorinated and recalcitrant compounds

    SciTech Connect (OSTI)

    NONE

    1998-12-31T23:59:59.000Z

    Natural, or intrinsic, attenuation is an increasingly important component of site closure strategy. At first maligned as a do-nothing alternative, natural attenuation is now being recognized as a legitimate approach that can supplement and sometimes even supplant more costly approaches. Having gained more widespread acceptance as an option at hydrocarbon-contaminated sites, natural attenuation is now beginning to emerge as an option for sites contaminated with chlorinated solvents and other recalcitrant compounds such as MTBE. This book brings together the latest research and field applications, with chapters covering field characterization and monitoring, transformation processes, natural attenuation of MTBE, and a number of natural attenuation case studies.

  6. Compound droplet manipulations on fiber arrays

    E-Print Network [OSTI]

    Weyer, Floriane; Dreesen, Laurent; Vandewalle, Nicolas

    2015-01-01T23:59:59.000Z

    Recent works demonstrated that fiber arrays may constitue the basis of an open digital microfluidics. Various processes, such as droplet motion, fragmentation, trapping, release, mixing and encapsulation, may be achieved on fiber arrays. However, handling a large number of tiny droplets resulting from the mixing of several liquid components is still a challenge for developing microreactors, smart sensors or microemulsifying drugs. Here, we show that the manipulation of tiny droplets onto fiber networks allows for creating compound droplets with a high complexity level. Moreover, this cost-effective and flexible method may also be implemented with optical fibers in order to develop fluorescence-based biosensor.

  7. Ternary compound electrode for lithium cells

    DOE Patents [OSTI]

    Raistrick, I.D.; Godshall, N.A.; Huggins, R.A.

    1980-07-30T23:59:59.000Z

    Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and of light weight. One type of lithium-based cell utilizes a molten salt electrolyte and normally is operated in the temperature range of about 350 to 500/sup 0/C. Such high temperature operation accelerates corrosion problems. The present invention provides an electrochemical cell in which lithium is the electroactive species. The cell has a positive electrode which includes a ternary compound generally represented as Li-M-O, wherein M is a transition metal. Corrosion of the inventive cell is considerably reduced.

  8. Ternary compound electrode for lithium cells

    DOE Patents [OSTI]

    Raistrick, Ian D. (Menlo Park, CA); Godshall, Ned A. (Stanford, CA); Huggins, Robert A. (Stanford, CA)

    1982-01-01T23:59:59.000Z

    Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and of light weight. One type of lithium-based cell utilizes a molten salt electrolyte and normally is operated in the temperature range of about 350.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems. The present invention provides an electrochemical cell in which lithium is the electroactive species. The cell has a positive electrode which includes a ternary compound generally represented as Li-M-O, wherein M is a transition metal. Corrosion of the inventive cell is considerably reduced.

  9. Compound and Elemental Analysis | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page onYou are now leaving Energy.gov You are now leaving Energy.gov You are beingZealand JumpConceptual Model, clickInformationNew| Open Energy Information Goff & Janik,Compound

  10. Evaluation of Ultra-Violet Photocatalytic Oxidation for Indoor AirApplications

    SciTech Connect (OSTI)

    Hodgson, A.T.; Sullivan, D.P.; Fisk, W.J.

    2006-02-01T23:59:59.000Z

    Acceptable indoor air quality in office buildings may be achieved with less energy by combining effective air cleaning systems for volatile organic compounds (VOCs) with particle filtration then by relying solely on ventilation. For such applications, ultraviolet photocatalytic oxidation (UVPCO) systems are being developed for VOC destruction. An experimental evaluation of a UVPCO system is reported. The evaluation was unique in that it employed complex mixtures of VOCs commonly found in office buildings at realistically low concentrations. VOC conversion efficiencies varied over a broad range, usually exceeded 20%, and were as high as {approx}80%. Conversion efficiency generally diminished with increased air flow rate. Significant amounts of formaldehyde and acetaldehyde were produced due to incomplete mineralization. The results indicate that formaldehyde and acetaldehyde production rates may need to be reduced before such UVPCO systems can be deployed safely in occupied buildings.

  11. In situ bioremediation using horizontal wells. Innovative technology summary report

    SciTech Connect (OSTI)

    NONE

    1995-04-01T23:59:59.000Z

    In Situ Bioremediation (ISB) is the term used in this report for Gaseous Nutrient Injection for In Situ Bioremediation. This process (ISB) involves injection of air and nutrients (sparging and biostimulation) into the ground water and vacuum extraction to remove Volatile Organic Compounds (VOCs) from the vadose zone concomitant with biodegradation of the VOCs. This process is effective for remediation of soils and ground water contaminated with VOCs both above and below the water table. A full-scale demonstration of ISB was conducted as part of the Savannah River Integrated Demonstration: VOCs in Soils and Ground Water at Nonarid Sites. This demonstration was performed at the Savannah River Site from February 1992 to April 1993.

  12. Materials Chemistry and Performance of Silicone-Based Replicating Compounds.

    SciTech Connect (OSTI)

    Brumbach, Michael T.; Mirabal, Alex James; Kalan, Michael; Trujillo, Ana B; Hale, Kevin

    2014-11-01T23:59:59.000Z

    Replicating compounds are used to cast reproductions of surface features on a variety of materials. Replicas allow for quantitative measurements and recordkeeping on parts that may otherwise be difficult to measure or maintain. In this study, the chemistry and replicating capability of several replicating compounds was investigated. Additionally, the residue remaining on material surfaces upon removal of replicas was quantified. Cleaning practices were tested for several different replicating compounds. For all replicating compounds investigated, a thin silicone residue was left by the replica. For some compounds, additional inorganic species could be identified in the residue. Simple solvent cleaning could remove some residue.

  13. Feasibility of Organizations -A Refinement of Chemical Organization Theory

    E-Print Network [OSTI]

    Hinze, Thomas

    Feasibility of Organizations - A Refinement of Chemical Organization Theory with Application to P a theorem providing a criteria for an unfeasible organization. This is a refinement of organization theory organization. Key words: reaction networks, constructive dynamical systems, chem- ical organization theory

  14. Uncertainty in the future distribution of tropospheric ozone over West Africa due to variability in anthropogenic emissions estimates between

    E-Print Network [OSTI]

    Haak, Hein

    over the next few decades due to rising population and more energy intensive lifestyles. Here we activities such as transport, energy production, bio-fuel use, industrial processes and biomass burning (BB Organic Compounds (VOCs) have recently been measured in the lower troposphere (LT) near Lagos, Nigeria (6

  15. Woodland Route 72 Dump EPA ID#: NJD980505879

    E-Print Network [OSTI]

    -volatiles, heavy metals, and pesticides. The ground surface at two areas on the site had elevated levels of gamma, and harvesting of cedar and pine for wood products. Residents rely on ground water for drinking, household use. Threat and Contaminants Ground water is contaminated with volatile organic compounds (VOCs), semi

  16. Woodland Route 532 Dump EPA ID#: NJD980505887

    E-Print Network [OSTI]

    and Contaminants Ground water and surface soils were contaminated with volatile organic compounds (VOCs), semi-volatiles, heavy metals, and pesticides. Goodwater Run contained elevated levels of zinc and lead. Subsurface soils a study of soil and ground water pollution at the site in 1989. In 1990, EPA and NJDEP selected

  17. Mass-Transit Options Around Brandeis University

    E-Print Network [OSTI]

    Fraden, Seth

    ://www.publictransportation.org/facts/ EPANational Vehicle and Fuel Emissions Laboratory http (CO), 90% less volatile organic compounds (VOCs), and about half as much carbon dioxide (CO2 emissions represent 82% of total US human-made greenhouse emissions · Vehicle emissions fromthe combustion

  18. *Corresponding author. Tel.: #1-510-643-2451; fax: #1-510-643-5098.

    E-Print Network [OSTI]

    Goldstein, Allen

    contributions to acetone mixing ratios in a rural environment Allen H. Goldstein*, Gunnar W. Schade Ecosystem correlated with acetone mixing ratios (r"0.80), suggesting that the quantity of biogenic and anthropogenic of biogenically and anthropogenically emitted volatile organic compounds (VOCs), and biomass burning

  19. A backward-time stochastic Lagrangian air quality model Deyong Wen a,*, John C. Lin a

    E-Print Network [OSTI]

    Mlllet, Dylan B.

    that simulated O3 concentrations usually agree well with observations across sites in rural areas, small towns). Biomass burning from land use change has been accelerating (Setzer et al., 1994), releasing large quantities of NOx (NO þ NO2) and volatile organic compounds (VOC) to the atmosphere (Chatfield and Delany

  20. Zevenhoven & Kilpinen PREFACE / INTRODUCTION 13.4.2002 1-1 Chapter 1 Preface /

    E-Print Network [OSTI]

    Laughlin, Robert B.

    .2 Objectives and scope Textbooks on this subject are, in general, limited to what can be called "conventional" flue gas cleaning for conventional pulverised coal combustion processes, i.e. wet flue gas and furanes; and volatile organic compounds (VOCs) and polycyclic aromatic hydrocarbons (PAHs). Also