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Sample records for fr04jn10p national emission

  1. Air Emission Inventory for the Idaho National Engineering and Environmental Laboratory - Calendar Year 1998 Emissions Report

    SciTech Connect

    S. K. Zohner

    1999-10-01

    This report presents the 1998 calendar year update of the Air Emission Inventory for the Idaho National Engineering and Environmental Laboratory (INEEL). The INEEL Air Emission Inventory documents sources and emissions of nonradionuclide pollutants from operations at the INEEL. The report describes the emission inventory process and all of the sources at the INEEL, and provides nonradiological emissions estimates for stationary sources.

  2. Air emission inventory for the Idaho National Engineering Laboratory: 1994 emissions report

    SciTech Connect

    1995-07-01

    This report Presents the 1994 update of the Air Emission inventory for the Idaho National Engineering Laboratory (INEL). The INEL Air Emission Inventory documents sources and emissions of non-radionuclide pollutants from operations at the INEL. The report describes the emission inventory process and all of the sources at the INEL, and provides non-radionuclide emissions estimates for stationary sources.

  3. Air Emission Inventory for the Idaho National Engineering and Environmental Laboratory - Calendar Year 1999 Emission Report

    SciTech Connect

    Zohner, S.K.

    2000-05-30

    This report presents the 1999 calendar year update of the Air Emission Inventory for the Idaho National Engineering and Environmental Laboratory (INEEL). The INEEL Air Emission Inventory documents sources and emissions of nonradionuclide pollutants from operations at the INEEL. The report describes the emission inventory process and all of the sources at the INEEL, and provides nonradionuclide emissions estimates for stationary sources.

  4. Air emissions inventory for the Idaho National Engineering Laboratory -- 1995 emissions report

    SciTech Connect

    1996-06-01

    This report presents the 1995 update of the Air Emission Inventory for the Idaho National Engineering Laboratory (INEL). The INEL Air Emission Inventory documents sources and emissions of non-radionuclide pollutants from operations at the INEL. The report describes the emission inventory process and all of the sources at the INEL, and provides non-radionuclide emissions estimates for stationary sources. The air contaminants reported include nitrogen oxides, sulfur oxides, carbon monoxide, volatile organic compounds, particulates, and hazardous air pollutants (HAPs).

  5. Air Emission Inventory for the Idaho National Engineering Laboratory, 1993 emissions report

    SciTech Connect

    Not Available

    1994-06-01

    This report presents the 1993 update of the Air Emission Inventory for the Idaho National Engineering Laboratory (INEL). The purpose of the Air Emission Inventory is to commence the preparation of the permit to operate application for the INEL, as required by the recently promulgated Title V regulations of the Clean Air Act. The report describes the emission inventory process and all of the sources at the INEL and provides emissions estimates for both mobile and stationary sources.

  6. National annual dioxin emissions estimate for hazardous waste incinerators

    SciTech Connect

    Cudahy, J.J.; Rigo, H.G.

    1997-12-31

    On April 19, 1996, the EPA proposed Maximum Achievable Control [MACT] Standards for Hazardous Waste Combustors. In that preamble, the EPA stated that annual estimated emissions of dioxins from the nation`s hazardous waste incinerators [HWIs] expressed as an equivalent amount of 2,3,7,8 TCDD (international toxic equivalents) are 77 grams. Commentors on EPA dioxin emission estimates from medical waste incinerators and cement kilns found them significantly overestimated. This paper presents an independent dioxin emissions estimate that takes advantage of correcting the errors in EPA`s HWI emissions database, an updated inventory of HWIs in the United States and statistical imputation techniques that maximum the information extractable from the limited dioxin emissions data for HWIs. Actual HWI dioxin emissions are probably between a quarter and half the HWC preamble estimate.

  7. Snowmobile contributions to mobile source emissions in Yellowstone National Park.

    PubMed

    Bishop, G A; Morris, J A; Stedman, D H

    2001-07-15

    Increases in the number of winter visitors to Yellowstone National Park during the past decade have raised concerns over the environmental impacts of snowmobiling in the park. During the 1998-99 season, more than 62,000 snowmobile and 1300 snow coach trips entered the park. Using the University of Denver's vehicle exhaust remote-sensing equipment, 1385 measurements of carbon monoxide (CO) and hydrocarbon (HC) emissions were collected from in-use snowmobiles at the west and south entrances to the park. Overall means of 392 +/- 4 g CO and 237 +/- 1 g HC were observed per kilogram of fuel consumed. In addition, using an ultraviolet monochromator, 460 measurements of toluene emissions were collected with a mean of 39 +/- 1 g toluene/kg of fuel. Using these data, a mobile source emissions inventory based on fuel use for Yellowstone National Park shows that snowmobiles account for 27% of the annual emissions of carbon monoxide and 77% of annual emissions of hydrocarbons using an equivalent best estimate for the summer mobile source emissions. Use of oxygenated fuels in snowmobiles was found to reduce CO emissions by 13.2 +/- 6.5% without an observed effect on HC emissions. Liquid-cooled sleds were found to have HC emissions 9.5 +/- 2.2% higher than those from fan-cooled sleds because of the increased intake and exhaust port sizes required in the larger liquid-cooled engines, which increases blowby in the 2-stroke engines.

  8. National Emission Standards for Hazardous Air Pollutants submittal -- 1997

    SciTech Connect

    Townsend, Y.E.; Black, S.C.

    1998-06-01

    Each potential source of Nevada Test Site (NTS) emissions was characterized by one of the following methods: (1) monitoring methods and procedures previously developed at the NTS; (2) a yearly radionuclide inventory of the source, assuming that volatile radionuclide are released to the environment; (3) the measurement of tritiated water (as HTO or T{sub 2}O) concentration in liquid effluents discharged to containment ponds and assuming all the effluent evaporates over the course of the year to become an air emission; or (4) using a combination of environmental measurements and CAP88-PC to calculate emissions. The emissions for National Emission Standards for Hazardous Air Pollutants (NESHAPs) reporting are listed. They are very conservative and are used in Section 3 to calculate the EDE to the maximally exposed individual offsite. Offsite environmental surveillance data, where available, are used to confirm that calculated emissions are, indeed, conservative.

  9. 77 FR 16508 - National Emission Standards for Hazardous Air Pollutant Emissions: Group IV Polymers and Resins...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-21

    ..., was published on January 9, 2012 (77 FR 1268). EPA has established the public docket for the proposed...: Group IV Polymers and Resins; Pesticide Active Ingredient Production; and Polyether Polyols Production... pollutants: National Emission Standards for Hazardous Air Pollutant Emissions: Group IV Polymers and...

  10. National annual dioxin emissions estimate for hazardous waste incinerators

    PubMed

    Cudahy; Rigo

    1998-11-01

    Reducing emissions of polychlorinated dibenzo-p-dioxins and dibenzofurans, commonly known as dioxins, is a high priority for environmental regulatory bodies throughout much of the world. In the United States, Section 112 (c)(6) of the Clean Air Act (CAA) requires the Environmental Protection Agency (EPA) to identify and control emissions from sources that are responsible for at least 90% of the overall emissions of seven targeted hazardous air pollutants, including dioxins. On April 19, 1996, the EPA proposed Maximum Achievable Control Technology (MACT) Standards for Hazardous Waste Combustors (HWCs). In that preamble, the EPA estimated annual dioxin emissions from the nation's hazardous waste incinerators (HWIs) to be 79 grams expressed as 2,3,7,8 tetrachloro dibenzo-p-dioxins (TCDD) international toxic equivalents (ITEQs). However, early EPA dioxin emission estimates from medical waste incinerators and cement kilns were significantly overestimated; so, the following independent national dioxin emissions estimate for HWIs was prepared. This estimate corrects the errors in the EPA's HWI emissions database, uses an updated inventory of HWIs in the United States, and applies statistical imputation techniques that take maximum advantage of the limited dioxin emissions data for HWIs.

  11. National Emission Standards for Hazardous Air Pollutants submittal -- 1994

    SciTech Connect

    Townsend, Y.E.; Black, S.C.

    1995-06-01

    This report focuses on air quality at the Nevada Test Site (NTS) for 1994. A general description of the effluent sources are presented. Each potential source of NTS emissions was characterized by one of the following: (1) by monitoring methods and procedures previously developed at NTS; (2) by a yearly radionuclide inventory of the source, assuming that volatile radionuclides are released to the environment; (3) by the measurement of tritiated water concentration in liquid effluents discharged to containment ponds and assuming all the effluent evaporates over the course of the year to become an air emission; or (4) by using a combination of environmental measurements and CAP88-PC to calculate emissions. Appendices A through J describe the methods used to determine the emissions from the sources. These National Emission Standards for Hazardous Air Pollutants (NESHAP) emissions are very conservative, are used to calculate the effective dose equivalent to the Maximally Exposed Individual offsite, and exceed, in some cases, those reported in DOE`s Effluent Information System (EIS). The NESHAP`s worst-case emissions that exceed the EIS reported emissions are noted. Offsite environmental surveillance data are used to confirm that calculated emissions are, indeed, conservative.

  12. Air Emission Inventory for the Idaho National Engineering Laboratory: 1992 emissions report

    SciTech Connect

    Stirrup, T.S.

    1993-06-01

    This report presents the 1992 Air Emission Inventory for the Idaho National Engineering Laboratory. Originally, this report was in response to the Environmental Oversight and Monitoring Agreement in 1989 between the State of Idaho and the Department of Energy Idaho Field Office, and a request from the Idaho Air Quality Bureau. The current purpose of the Air Emission Inventory is to provide the basis for the preparation of the INEL Permit-to-Operate (PTO) an Air Emission Source Application, as required by the recently promulgated Title V regulations of the Clean Air Act. This report includes emissions calculations from 1989 to 1992. The Air Emission Inventory System, an ORACLE-based database system, maintains the emissions inventory.

  13. New national emission inventory for navigation in Denmark

    NASA Astrophysics Data System (ADS)

    Winther, Morten

    This article explains the new emission inventory for navigation in Denmark, covering national sea transport, fisheries and international sea transport. For national sea transport, the new Danish inventory distinguishes between regional ferries, local ferries and other national sea transport. Detailed traffic and technical data lie behind the fleet activity-based fuel consumption and emission calculations for regional ferries. For local ferries and other national sea transport, the new inventory is partly fleet activity based; fuel consumption estimates are calculated for single years, and full fuel consumption coverage is established in a time series by means of appropriate assumptions. For fisheries and international sea transport, the new inventory remains fuel based, using fuel sales data from the Danish Energy Authority (DEA). The new Danish inventory uses specific fuel consumption (sfc) and NO x emission factors as a function of engine type and production year. These factors, which are used directly for regional ferries and, for the remaining navigation categories, are derived by means of appropriate assumptions, serve as a major inventory improvement, necessary for making proper emission trend assessments. International sea transport is the most important fuel consumption and emission source for navigation, and the contributions are large even compared with the overall Danish totals. If the contributions from international sea transport were included in the Danish all-sector totals, the extra contributions in 2005 from fuel consumption (and CO 2), NO x and SO 2 would be 5%, 34% and 167%, respectively. The 1990-2005 changes in fuel consumption as well as NO x and SO 2 emissions for national sea transport (-45, -45, -81), fisheries (-18, 6, -18) and international sea transport (-14, 1, -14) reflect changes in fleet activity/fuel consumption and emission factors. The 2006-2020 emission forecasts demonstrate a need for stricter fuel quality and NO x emission

  14. 1999 INEEL National Emission Standards for Hazardous Air Pollutants - Radionuclides

    SciTech Connect

    J. W. Tkachyk

    2000-06-01

    Under Section 61.94 of Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, ''National Emission Standards for Emission of Radionuclides Other Than Radon From Department of Energy Facilities,'' each Department of Energy (DOE) facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at the Idaho National Engineering and Environmental Laboratory (INEEL) for calendar year (CY) 1999. The Idaho Operations Office of the DOE is the primary contract concerning compliance with the National Emission Standards for Hazardous Air Pollutants (NESHAPs) at the INEEL. For CY 1999, airborne radionuclide emissions from the INEEL operations were calculated to result in a maximum individual dose to a member of the public of 7.92E-03 mrem (7.92E-08 Sievert). This effective dose equivalent (EDE) is well below the 40 CFR 61, Subpart H, regulatory standard of 10 mrem per year (1.0E-04 Sievert per year).

  15. 1998 INEEL National Emission Standard for Hazardous Air Pollutants - Radionuclides

    SciTech Connect

    J. W. Tkachyk

    1999-06-01

    Under Section 61.94 of Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, ''National Emission Standards for Emission of Radionuclides Other Than Radon From Department of Energy Facilities,'' each Department of Energy (DOE) facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at the Idaho National Engineering and Environmental Laboratory (INEEL) for calendar year (CY) 1998. The Idaho Operations Office of the DOE is the primary contract concerning compliance with the National Emission Standards for Hazardous Air Pollutants (NESHAPs) at the INEEL. For CY 1998, airborne radionuclide emissions from the INEEL operations were calculated to result in a maximum individual dose to a member of the public of 7.92E-03 mrem (7.92E-08 Sievert). This effective dose equivalent (EDE) is well below the 40 CFR 61, Subpart H, regulatory standard of 10 mrem per year (1.0E-04 Sievert per year).

  16. Air toxic emissions from snowmobiles in Yellowstone National Park.

    PubMed

    Zhou, Yong; Shively, David; Mao, Huiting; Russo, Rachel S; Pape, Bruce; Mower, Richard N; Talbot, Robert; Sive, Barkley C

    2010-01-01

    A study on emissions associated with oversnow travel in Yellowstone National Park (YNP) was conducted for the time period of February 13-16, 2002 and February 12-16, 2003. Whole air and exhaust samples were characterized for 85 volatile organic compounds using gas chromatography. The toxics including benzene, toluene, ethylbenzene, xylenes (p-, m-, and o-xylene), and n-hexane, which are major components of two-stroke engine exhaust, show large enhancements during sampling periods resulting from increased snowmobile traffic. Evaluation of the photochemical history of air masses sampled in YNP revealed that emissions of these air toxics were (i) recent, (ii) persistent throughout the region, and (iii) consistent with the two-stroke engine exhaust sample fingerprints. The annual fluxes were estimated to be 0.35, 1.12, 0.24, 1.45, and 0.36 Gg yr(-1) for benzene, toluene, ethylbenzene, xylenes, and n-hexane, respectively, from snowmobile usage in YNP. These results are comparable to the flux estimates of 0.23, 0.77, 0.17, and 0.70 Gg yr(-1) for benzene, toluene, ethylbenzene, and xylenes, respectively, that were derived on the basis of (i) actual snowmobile counts in the Park and (ii) our ambient measurements conducted in 2003. Extrapolating these results, annual emissions from snowmobiles in the U.S. appear to be significantly higher than the values from the EPA National Emissions Inventory (1999). Snowmobile emissions represent a significant fraction ( approximately 14-21%) of air toxics with respect to EPA estimates of emissions by nonroad vehicles. Further investigation is warranted to more rigorously quantify the difference between our estimates and emission inventories.

  17. Estimation method for national methane emission from solid waste landfills

    NASA Astrophysics Data System (ADS)

    Kumar, Sunil; Gaikwad, S. A.; Shekdar, A. V.; Kshirsagar, P. S.; Singh, R. N.

    In keeping with the global efforts on inventorisation of methane emission, municipal solid waste (MSW) landfills are recognised as one of the major sources of anthropogenic emissions generated from human activities. In India, most of the solid wastes are disposed of by landfilling in low-lying areas located in and around the urban centres resulting in generation of large quantities of biogas containing a sizeable proportion of methane. After a critical review of literature on the methodology for estimation of methane emissions, the default methodology has been used in estimation following the IPCC guidelines 1996. However, as the default methodology assumes that all potential methane is emitted in the year of waste deposition, a triangular model for biogas from landfill has been proposed and the results are compared. The methodology proposed for methane emissions from landfills based on a triangular model is more realistic and can very well be used in estimation on global basis. Methane emissions from MSW landfills for the year AD 1980-1999 have been estimated which could be used in computing national inventories of methane emission.

  18. 75 FR 80219 - National Emission Standards for Shipbuilding and Ship Repair (Surface Coating); National Emission...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-21

    ... X Nitrous Oxide NRC National Research Council NTTAA National Technology Transfer and Advancement Act...-Product Recovery Plants (Benzene NESHAP) (54 FR 38044, September 14, 1989). The first step in this process... is no higher than approximately 1-in-10 thousand, that risk level is considered acceptable.'' 54...

  19. 77 FR 16547 - Radionuclide National Emission Standards for Hazardous Air Pollutants; Notice of Construction...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-21

    ... for Radon Emissions from Underground Uranium Mines (Subpart B) and 40 CFR part 61, subpart W, National Emission Standards for Radon Emissions from Operating Mill Tailings (Subpart W). EPA Region 8 issued...

  20. 76 FR 12863 - National Emission Standards for Hazardous Air Pollutants for Reciprocating Internal Combustion...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-09

    ... that provided national emission standards for hazardous air pollutants for existing stationary spark... Docket Center (6102T), National Emission Standards for Hazardous Air Pollutant for Stationary... Standards for Hazardous Air Pollutant for Stationary Reciprocating Internal Combustion Engines...

  1. 76 FR 35806 - Amendments to National Emission Standards for Hazardous Air Pollutants for Area Sources: Plating...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-06-20

    ... AGENCY 40 CFR Part 63 RIN 2060-AM37 Amendments to National Emission Standards for Hazardous Air...: Proposed rule. SUMMARY: On June 12, 2008, EPA issued national emission standards for control of hazardous... Air Act (CAA). In today's action, EPA is proposing to amend the national emission standards...

  2. 77 FR 8575 - National Emissions Standards for Hazardous Air Pollutants: Secondary Aluminum Production

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-14

    ... February 14, 2012 Part V Environmental Protection Agency 40 CFR Part 63 National Emissions Standards for... 63 RIN 2060-AQ40 National Emissions Standards for Hazardous Air Pollutants: Secondary Aluminum... proposing amendments to the national emissions standards for hazardous air pollutants for Secondary...

  3. National Emission Standards for Hazardous Air Pollutants—Calendar Year 2010 INL Report for Radionuclides (2011)

    SciTech Connect

    Mark Verdoorn; Tom Haney

    2011-06-01

    This report documents the calendar Year 2010 radionuclide air emissions and resulting effective dose equivalent to the maximally exposed individual member of the public from operations at the Department of Energy's Idaho National Laboratory Site. This report was prepared in accordance with the Code of Federal Regulations, Title 40, 'Protection of the Environment,' Part 61, 'National Emission Standards for Hazardous Air Pollutants,' Subpart H, 'National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.'

  4. 76 FR 42052 - National Emission Standards for Hazardous Air Pollutants From Petroleum Refineries

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-18

    ... AGENCY 40 CFR Parts 9 and 63 RIN 2060-AO55 National Emission Standards for Hazardous Air Pollutants From... portions of the final rule amending the National Emission Standards for Hazardous Air Pollutants From...) establishes a two-stage regulatory process to address emissions of hazardous air pollutants (HAP)...

  5. Ammonia emission factors for the NAPAP (National Acid Precipitation Assessment Program) emission inventory. Final report, January 1985-December 1986

    SciTech Connect

    Misenheimer, D.C.; Warn, T.E.; Zelmanowitz, S.

    1987-01-01

    The report provides information on certain sources of ammonia emissions to the atmosphere for use in the National Acid Precipitation Assessment Program (NAPAP) emission inventories. Major anthropogenic sources of ammonia emissions to the atmosphere are identified, and emission factors for these sources are presented based on a review of the most recent data available. The emission factors developed are used to estimate nationwide emissions for base year 1980 and are compared to ammonia emission factors used in other emission inventories. Major anthropogenic source categories covered are cropland spreading of livestock wastes, beef cattle feedlots, fertilizer manufacture and use, fuel combustion, ammonia synthesis, petroleum refineries, and coke manufacture. Approximately 840,000 tons of ammonia is estimated to have been emitted in the U.S. in 1980; over 64% of which is estimated to have been from livestock wastes.

  6. National Emission Standards for Hazardous Air Pollutants - Radionuclide Emissions, Calendar Year 2010

    SciTech Connect

    NSTec Ecological and Environmental Monitoring

    2011-06-30

    The U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office operates the Nevada National Security Site (NNSS, formerly the Nevada Test Site) and North Las Vegas Facility (NLVF). From 1951 through 1992, the NNSS was the continental testing location for U.S. nuclear weapons. The release of radionuclides from NNSS activities has been monitored since the initiation of atmospheric testing. Limitation to underground detonations after 1962 greatly reduced radiation exposure to the public surrounding the NNSS. After nuclear testing ended in 1992, NNSS radiation monitoring focused on detecting airborne radionuclides from historically contaminated soils. These radionuclides are derived from re-suspension of soil (primarily by wind) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of tritium are also emitted to air at the NLVF, an NNSS support complex in North Las Vegas. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) (CFR, 2010a) limits the release of radioactivity from a U.S. Department of Energy (DOE) facility to that which would cause 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This limit does not include radiation unrelated to NNSS activities. Unrelated doses could come from naturally occurring radioactive elements, from sources such as medically or commercially used radionuclides, or from sources outside of the United States, such as those from the damaged Fukushima nuclear power plant in Japan. Because this report is intended to discuss radioactive air emissions during calendar year 2010, data on radionuclides in air from the 2011 Fukushima nuclear power plant releases are not presented but will be included in the report for calendar year 2011. The NNSS demonstrates compliance with the NESHAP

  7. National Emission Standards for Hazardous Air Pollutants Submittal - 1995

    SciTech Connect

    Black, S.C.; Townsend, Y.E.

    1996-06-01

    This report contains National Emission Standards for Hazardous Air Pollutants at the Nevada Test Site (NTS). It provides lists of figures and tables related to the NTS and includes a Site Description. The Source Description includes current and previous activities conducted on the NTS. The Site has been the primary location for testing of nuclear explosives in the Continental U.S. since 1951. Historical testing has included (1) atmospheric testing in the 1950`s and early 1960s, (2) earth-cratering experiments, and (3) open-air nuclear reactor and rocket engine testing. At the North Las Vegas Facility, operated for DOE/NV by EG&G Energy Measurements, there was an Unusual Occurrence that led to an insignificant potential exposure to an offsite person. The incident involved the release of tritiated water (HTO), and a description of the incident and the method of calculating the effective dose equivalent for offsite exposure are described. The Source Description further describes Ground Seepage of Noble Gases, Radioactive Waste Management Sites, and Plutonium Contaminated Surface Areas.

  8. National Emission Standards for Hazardous Air Pollutants Calendar Year 2005

    SciTech Connect

    Bechtel Nevada

    2006-06-01

    The Nevada Test Site (NTS) is operated by the U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office (NNSA/NSO). From 1951 through 1992, the NTS was operated as the nation’s site for nuclear weapons testing. The release of man-made radionuclides from the NTS as a result of testing activities has been monitored since the first decade of atmospheric testing. After 1962, when nuclear tests were conducted only underground, the radiation exposure to the public surrounding the NTS was greatly reduced. After the 1992 moratorium on nuclear testing, radiation monitoring on the NTS focused on detecting airborne radionuclides that are resuspended into the air (e.g., by winds, dust-devils) along with historically-contaminated soils on the NTS. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (40 Code of Federal Regulations 61 Subpart H) limits the release of radioactivity from a U. S. Department of Energy (DOE) facility (e.g., the NTS) to 10 millirem per year (mrem/yr) effective dose equivalent (EDE) to any member of the public. This is the dose limit established for someone living off of the NTS for inhaling radioactive particles that may be carried by wind off of the NTS. This limit assumes that members of the public surrounding the NTS may also inhale “background levels” or radioactive particles unrelated to NTS activities that come from naturally-occurring elements in the environment (e.g., radon gas from the earth or natural building materials) or from other man-made sources (e.g., cigarette smoke). The U. S. Environmental Protection Agency (EPA) requires DOE facilities (e.g., the NTS) to demonstrate compliance with the NESHAP dose limit by annually estimating the dose to a hypothetical member of the public, referred to as the maximally exposed individual (MEI), or the member of the public who resides within an 80-kilometer (50-mile

  9. National Emission Standards for Hazardous Air Pollutants—Calendar Year 2011 INL Report for Radionuclides (2012)

    SciTech Connect

    Mark Verdoorn; Tom Haney

    2012-06-01

    This report documents the calendar year 2011 radionuclide air emissions and resulting effective dose equivalent to the maximally exposed individual member of the public from operations at the Department of Energy's Idaho National Laboratory Site. This report was prepared in accordance with the Code of Federal Regulations, Title 40, 'Protection of the Environment,' Part 61, 'National Emission Standards for Hazardous Air Pollutants,' Subpart H, 'National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.' The effective dose equivalent to the maximally exposed individual member of the public was 4.58E-02 mrem per year, 0.46 percent of the 10 mrem standard.

  10. National Emission Standards for Hazardous Air Pollutants. Calendar Year 2012 INL Report for Radionuclides (2013)

    SciTech Connect

    Verdoorn, Mark; Haney, Tom

    2013-06-01

    This report documents the calendar year 2011 radionuclide air emissions and resulting effective dose equivalent to the maximally exposed individual member of the public from operations at the Department of Energy’s Idaho National Laboratory Site. This report was prepared in accordance with the Code of Federal Regulations, Title 40, ''Protection of the Environment,'' Part 61, ''National Emission Standards for Hazardous Air Pollutants,'' Subpart H, ''National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.'' The effective dose equivalent to the maximally exposed individual member of the public was 4.58E-02 mrem per year, 0.46 percent of the 10 mrem standard.

  11. National Emission Standards for Hazardous Air Pollutants. Calendar Year 2013 INL Report for Radionuclides [2014

    SciTech Connect

    Verdoorn, Mark; Haney, Tom

    2014-06-01

    This report documents the calendar year 2013 radionuclide air emissions and resulting effective dose equivalent to the maximally exposed individual member of the public from operations at the Department of Energy’s Idaho National Laboratory Site. This report was prepared in accordance with the Code of Federal Regulations, Title 40, ''Protection of the Environment,'' Part 61, ''National Emission Standards for Hazardous Air Pollutants,'' Subpart H, ''National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.'' The effective dose equivalent to the maximally exposed individual member of the public was 3.02 E-02 mrem per year, 0.30 percent of the 10 mrem standard.

  12. 76 FR 14839 - Delegation of National Emission Standards for Hazardous Air Pollutants for Source Categories...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-18

    ... AGENCY 40 CFR Part 63 Delegation of National Emission Standards for Hazardous Air Pollutants for Source... County Air Pollution Control District AGENCY: Environmental Protection Agency (EPA). ACTION: Proposed... national emission standards for hazardous air pollutants (NESHAP) to the Maricopa County Air...

  13. 77 FR 41146 - Delegation of National Emission Standards for Hazardous Air Pollutants for Source Categories...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-07-12

    ... AGENCY 40 CFR Part 63 Delegation of National Emission Standards for Hazardous Air Pollutants for Source.... SUMMARY: Pursuant to section 112(l) of the Clean Air Act as amended in 1990, EPA is proposing to grant delegation of specific national emission standards for hazardous air pollutants (NESHAP) to the Gila...

  14. 75 FR 8888 - Delegation of National Emission Standards for Hazardous Air Pollutants for Source Categories...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-02-26

    ... AGENCY 40 CFR Part 63 Delegation of National Emission Standards for Hazardous Air Pollutants for Source...). ACTION: Proposed rule. SUMMARY: Pursuant to section 112(l) of the 1990 Clean Air Act, EPA granted delegation of specific national emission standards for hazardous air pollutants (NESHAP) to the...

  15. 77 FR 11476 - Delegation of National Emission Standards for Hazardous Air Pollutants for Source Categories; Nevada

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-27

    ... section 112(l) of the 1990 Clean Air Act, EPA granted ] delegation of specific national emission standards... From the Federal Register Online via the Government Publishing Office ENVIRONMENTAL PROTECTION AGENCY 40 CFR Part 63 Delegation of National Emission Standards for Hazardous Air Pollutants for...

  16. 76 FR 81327 - National Emission Standards for Hazardous Air Pollutants From the Pulp and Paper Industry

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-27

    ... Hazardous Air Pollutants From the Pulp and Paper Industry; Proposed Rule #0;#0;Federal Register / Vol. 76... Part 63 RIN 2060-AQ41 National Emission Standards for Hazardous Air Pollutants From the Pulp and Paper... proposing amendments to the national emission standards for hazardous air pollutants for the pulp and...

  17. 76 FR 80531 - National Emission Standards for Hazardous Air Pollutants for Area Sources: Industrial, Commercial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-23

    ... category (see 40 CFR 63.7491(j), and 76 FR 15665 (March 21, 2011)), and is now proposing to do the same in... December 23, 2011 Part III Environmental Protection Agency 40 CFR Part 63 National Emission Standards for...; ] ENVIRONMENTAL PROTECTION AGENCY 40 CFR Part 63 RIN 2060-AR14 National Emission Standards for Hazardous...

  18. 78 FR 27375 - Standards of Performance for New Stationary Sources, National Emission Standards for Hazardous...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-05-10

    ... AGENCY Standards of Performance for New Stationary Sources, National Emission Standards for Hazardous Air...); the National Emission Standards for Hazardous Air Pollutants (NESHAP); and/ or the Stratospheric Ozone...) of the Clean Air Act (CAA) contain no specific regulatory provision providing that sources...

  19. 78 FR 25242 - Delegation of New Source Performance Standards and National Emission Standards for Hazardous Air...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-30

    ... AGENCY 40 CFR Parts 60 and 61 Delegation of New Source Performance Standards and National Emission... Source Performance Standards (NSPS) and National Emission Standards for Hazardous Air Pollutants (NESHAP... identity or contact information unless you provide it in the body of your comment. If you send...

  20. National Emission Standards for Hazardous Air Pollutants - Radionuclide Emissions Calendar Year 2012

    SciTech Connect

    Warren, R.

    2013-06-10

    The U.S. Department of Energy, National Nuclear Security Administration Nevada Field Office (NNSA/NFO) operates the Nevada National Security Site (NNSS) and North Las Vegas Facility (NLVF). From 1951 through 1992, the NNSS was the continental testing location for U.S. nuclear weapons. The release of radionuclides from NNSS activities has been monitored since the initiation of atmospheric testing. Limitation to underground detonations after 1962 greatly reduced radiation exposure to the public surrounding the NNSS. After nuclear testing ended in 1992, NNSS radiation monitoring focused on detecting airborne radionuclides from historically contaminated soils. These radionuclides are derived from re-suspension of soil (primarily by wind) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of legacy-related tritium are also emitted to air at the NLVF, an NNSS support complex in North Las Vegas. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) (CFR 2010a) limits the release of radioactivity from a U.S. Department of Energy (DOE) facility to that which would cause 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This limit does not include radiation unrelated to NNSS activities. Unrelated doses could come from naturally occurring radioactive elements, from sources such as medically or commercially used radionuclides, or from sources outside of the United States, such as the damaged Fukushima nuclear power plant in Japan in 2011. NNSA/NFO demonstrates compliance with the NESHAP limit by using environmental measurements of radionuclide air concentrations at critical receptor locations on the NNSS (U.S. Environmental Protection Agency [EPA] and DOE 1995). This method was approved by the EPA for use on the NNSS in 2001 (EPA 2001a) and has

  1. National Emission Standards for Hazardous Air Pollutants - Radionuclide Emissions, Calendar Year 2011

    SciTech Connect

    NSTec Ecological and Environmental Monitoring

    2012-06-19

    The U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office operates the Nevada National Security Site (NNSS) and North Las Vegas Facility (NLVF). From 1951 through 1992, the NNSS was the continental testing location for U.S. nuclear weapons. The release of radionuclides from NNSS activities has been monitored since the initiation of atmospheric testing. Limitation to underground detonations after 1962 greatly reduced radiation exposure to the public surrounding the NNSS. After nuclear testing ended in 1992, NNSS radiation monitoring focused on detecting airborne radionuclides from historically contaminated soils. These radionuclides are derived from re-suspension of soil (primarily by wind) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of legacy-related tritium are also emitted to air at the NLVF, an NNSS support complex in North Las Vegas. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) limits the release of radioactivity from a U.S. Department of Energy (DOE) facility to that which would cause 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This limit does not include radiation unrelated to NNSS activities. Unrelated doses could come from naturally occurring radioactive elements, from sources such as medically or commercially used radionuclides, or from sources outside of the United States, such as the damaged Fukushima nuclear power plant in Japan. Radionuclides from the Fukushima nuclear power plant were detected at the NNSS in March 2011 and are discussed further in Section III. The NNSS demonstrates compliance with the NESHAP limit by using environmental measurements of radionuclide air concentrations at critical receptor locations. This method was approved by the EPA for use on the

  2. National Emission Standards for Hazardous Air Pollutants - Radionuclide Emissions Calendar Year 2013

    SciTech Connect

    Warren, R.

    2014-06-04

    The U.S. Department of Energy, National Nuclear Security Administration Nevada Field Office (NNSA/NFO) operates the Nevada National Security Site (NNSS) and North Las Vegas Facility (NLVF). From 1951 through 1992, the NNSS was the continental testing location for U.S. nuclear weapons. The release of radionuclides from NNSS activities has been monitored since the initiation of atmospheric testing. Limitations to underground detonations after 1962 greatly reduced radiation exposure to the public surrounding the NNSS. After nuclear testing ended in 1992, NNSS radiation monitoring focused on detecting airborne radionuclides from historically contaminated soils. These radionuclides are derived from re-suspension of soil (primarily by wind) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of legacy-related tritium are also emitted to air at the NLVF, an NNSS support complex in North Las Vegas. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) (CFR 2010a) limits the release of radioactivity from a U.S. Department of Energy (DOE) facility to that which would cause 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This limit does not include radiation unrelated to NNSS activities. Unrelated doses could come from naturally occurring radioactive elements, from sources such as medically or commercially used radionuclides, or from sources outside of the United States, such as the damaged Fukushima nuclear power plant in Japan in 2011. NNSA/NFO demonstrates compliance with the NESHAP limit by using environmental measurements of radionuclide air concentrations at critical receptor locations on the NNSS (U.S. Environmental Protection Agency [EPA] and DOE 1995). This method was approved by the EPA for use on the NNSS in 2001 (EPA 2001a) and has

  3. Disproportionality in Power Plants' Carbon Emissions: A Cross-National Study.

    PubMed

    Jorgenson, Andrew; Longhofer, Wesley; Grant, Don

    2016-07-01

    Past research on the disproportionality of pollution suggests a small subset of a sector's facilities often produces the lion's share of toxic emissions. Here we extend this idea to the world's electricity sectors by calculating national-level disproportionality Gini coefficients for plant-level carbon emissions in 161 nations based on data from 19,941 fossil-fuel burning power plants. We also evaluate if disproportionalities in plant-level emissions are associated with increased national carbon emissions from fossil-fuel based electricity production, while accounting for other well-established human drivers of greenhouse gas emissions. Results suggest that one potential pathway to decreasing nations' greenhouse gas emissions could involve reducing disproportionality among fossil-fuel power plants by targeting those plants in the upper end of the distribution that burn fuels more inefficiently to produce electricity.

  4. Disproportionality in Power Plants' Carbon Emissions: A Cross-National Study.

    PubMed

    Jorgenson, Andrew; Longhofer, Wesley; Grant, Don

    2016-01-01

    Past research on the disproportionality of pollution suggests a small subset of a sector's facilities often produces the lion's share of toxic emissions. Here we extend this idea to the world's electricity sectors by calculating national-level disproportionality Gini coefficients for plant-level carbon emissions in 161 nations based on data from 19,941 fossil-fuel burning power plants. We also evaluate if disproportionalities in plant-level emissions are associated with increased national carbon emissions from fossil-fuel based electricity production, while accounting for other well-established human drivers of greenhouse gas emissions. Results suggest that one potential pathway to decreasing nations' greenhouse gas emissions could involve reducing disproportionality among fossil-fuel power plants by targeting those plants in the upper end of the distribution that burn fuels more inefficiently to produce electricity. PMID:27363677

  5. National Emission Standards for Hazardous Air Pollutants - Radionuclide Emissions Calendar Year 2009

    SciTech Connect

    NSTec Ecological and Environmental Monitoring

    2010-06-11

    The U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office operates the Nevada Test Site (NTS) and North Las Vegas Facility (NLVF). From 1951 through 1992, the NTS was the continental testing location for U.S. nuclear weapons. The release of radionuclides from NTS activities has been monitored since the initiation of atmospheric testing. Limitation to underground detonations after 1962 greatly reduced radiation exposure to the public surrounding the NTS. After nuclear testing ended in 1992, NTS radiation monitoring focused on detecting airborne radionuclides from historically contaminated soils. These radionuclides are derived from re-suspension of soil (primarily by wind) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of tritium were also emitted to air at the NLVF, an NTS support complex in North Las Vegas. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) limits the release of radioactivity from a U.S. Department of Energy facility to 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This limit does not include radiation not related to NTS activities. Unrelated doses could come from naturally occurring radioactive elements or from sources such as medically or commercially used radionuclides. The NTS demonstrates compliance with the NESHAP limit by using environmental measurements of radionuclide air concentrations at critical receptor locations. This method was approved by the U.S. Environmental Protection Agency for use on the NTS in 2001 and has been the sole method used since 2005. Six locations on the NTS have been established to act as critical receptor locations to demonstrate compliance with the NESHAP limit. These locations are actually pseudo-critical receptor stations, because no

  6. Disproportionality in Power Plants’ Carbon Emissions: A Cross-National Study

    NASA Astrophysics Data System (ADS)

    Jorgenson, Andrew; Longhofer, Wesley; Grant, Don

    2016-07-01

    Past research on the disproportionality of pollution suggests a small subset of a sector’s facilities often produces the lion’s share of toxic emissions. Here we extend this idea to the world’s electricity sectors by calculating national-level disproportionality Gini coefficients for plant-level carbon emissions in 161 nations based on data from 19,941 fossil-fuel burning power plants. We also evaluate if disproportionalities in plant-level emissions are associated with increased national carbon emissions from fossil-fuel based electricity production, while accounting for other well-established human drivers of greenhouse gas emissions. Results suggest that one potential pathway to decreasing nations’ greenhouse gas emissions could involve reducing disproportionality among fossil-fuel power plants by targeting those plants in the upper end of the distribution that burn fuels more inefficiently to produce electricity.

  7. Disproportionality in Power Plants’ Carbon Emissions: A Cross-National Study

    PubMed Central

    Jorgenson, Andrew; Longhofer, Wesley; Grant, Don

    2016-01-01

    Past research on the disproportionality of pollution suggests a small subset of a sector’s facilities often produces the lion’s share of toxic emissions. Here we extend this idea to the world’s electricity sectors by calculating national-level disproportionality Gini coefficients for plant-level carbon emissions in 161 nations based on data from 19,941 fossil-fuel burning power plants. We also evaluate if disproportionalities in plant-level emissions are associated with increased national carbon emissions from fossil-fuel based electricity production, while accounting for other well-established human drivers of greenhouse gas emissions. Results suggest that one potential pathway to decreasing nations’ greenhouse gas emissions could involve reducing disproportionality among fossil-fuel power plants by targeting those plants in the upper end of the distribution that burn fuels more inefficiently to produce electricity. PMID:27363677

  8. Pacific Northwest National Laboratory Facility Radionuclide Emission Points and Sampling Systems

    SciTech Connect

    Barfuss, Brad C.; Barnett, J. Matthew; Ballinger, Marcel Y.

    2009-04-08

    Battelle—Pacific Northwest Division operates numerous research and development laboratories in Richland, Washington, including those associated with the Pacific Northwest National Laboratory (PNNL) on the Department of Energy’s Hanford Site that have the potential for radionuclide air emissions. The National Emission Standard for Hazardous Air Pollutants (NESHAP 40 CFR 61, Subparts H and I) requires an assessment of all effluent release points that have the potential for radionuclide emissions. Potential emissions are assessed annually. Sampling, monitoring, and other regulatory compliance requirements are designated based upon the potential-to-emit dose criteria found in the regulations. The purpose of this document is to describe the facility radionuclide air emission sampling program and provide current and historical facility emission point system performance, operation, and design information. A description of the buildings, exhaust points, control technologies, and sample extraction details is provided for each registered or deregistered facility emission point. Additionally, applicable stack sampler configuration drawings, figures, and photographs are provided.

  9. Pacific Northwest National Laboratory Campus Radionuclide Air Emissions Report for Calendar Year 2013

    SciTech Connect

    Snyder, Sandra F.; Barnett, J. Matthew; Bisping, Lynn E.

    2014-06-01

    This report documents radionuclide air emissions that result in the highest effective dose equivalent (EDE) to a member of the public, referred to as the maximally exposed individual (MEI). The report has been prepared in compliance with the Code of Federal Regulations (CFR), Title 40, Protection of the Environment, Part 61, National Emission Standards for Hazardous Air Pollutants (NESHAP), Subpart H, National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities and Washington Administrative Code (WAC) Chapter 246-247, Radiation Protection Air Emissions. The dose to the PNNL Site MEI due to routine major and minor point source emissions in 2013 from PNNL Site sources is 2E-05 mrem (2E-07 mSv) EDE. The dose from fugitive emissions (i.e., unmonitored sources) is 2E-6 mrem (2E-8 mSv) EDE. The dose from radon emissions is 1E-11 mrem (1E-13 mSv) EDE. No nonroutine emissions occurred in 2013. The total radiological dose for 2013 to the MEI from all PNNL Site radionuclide emissions, including fugitive emissions and radon, is 2E-5 mrem (2E-7 mSv) EDE, or 100,000 times smaller than the federal and state standard of 10 mrem/yr, to which the PNNL Site is in compliance

  10. Pacific Northwest National Laboratory Site Radionuclide Air Emissions Report for Calendar Year 2012

    SciTech Connect

    Snyder, Sandra F.; Barnett, J. Matthew; Bisping, Lynn E.

    2013-06-06

    This report documents radionuclide air emissions that result in the highest effective dose equivalent (EDE) to a member of the public, referred to as the maximally exposed individual (MEI). The report has been prepared in compliance with the Code of Federal Regulations (CFR), Title 40, Protection of the Environment, Part 61, National Emission Standards for Hazardous Air Pollutants (NESHAP), Subpart H, National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities and Washington Administrative Code (WAC) Chapter 246-247, Radiation Protection Air Emissions. The dose to the PNNL Site MEI due to routine major and minor point source emissions in 2012 from PNNL Site sources is 9E-06 mrem (9E-08 mSv) EDE. The dose from fugitive emissions (i.e., unmonitored sources) is 1E-7 mrem (1E-9 mSv) EDE. The dose from radon emissions is 2E-6 mrem (2E-08 mSv) EDE. No nonroutine emissions occurred in 2012. The total radiological dose for 2012 to the MEI from all PNNL Site radionuclide emissions, including fugitive emissions and radon, is 1E-5 mrem (1E-7 mSv) EDE, or 100,000 times smaller than the federal and state standard of 10 mrem/yr, to which the PNNL Site is in compliance.

  11. 77 FR 75739 - National Emission Standards for Hazardous Air Pollutants for Chemical Manufacturing Area Sources

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-12-21

    ... Control Technology HAP Hazardous Air Pollutants HON National Emission Standards for Organic Hazardous Air Pollutants From the Synthetic Organic Chemical Manufacturing Industry ICR Information Collection Request lb... Hazardous Air Pollutants: Miscellaneous Organic Chemical Manufacturing MSDS Material Safety Data...

  12. 75 FR 10184 - National Emission Standards for Hazardous Air Pollutants: Area Source Standards for Paints and...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-05

    ..., and binders into paints and other coatings, such as stains, varnishes, lacquers, enamels, shellacs... Standards for Paints and Allied Products Manufacturing-- Technical Amendment AGENCY: Environmental...; National Emission Standards for Hazardous Air Pollutants: Paints and Allied Products Manufacturing...

  13. National emission standards for hazardous air pollutants submittal -- 1996

    SciTech Connect

    Townsend, Y.E.; Black, S.C.

    1997-06-01

    The Nevada Test Site (NTS) is operated by the US Department of Energy, Nevada Operations Office (DOE/NV) as the site for nuclear weapons testing. Monitoring and evaluation of the various activities conducted onsite indicate that the potential sources of offsite radiation exposure in 1996 were releases from the following: evaporation of tritiated water from containment ponds that receive drainage from E tunnel and from wells used for site characterization studies; onsite radioanalytical laboratories; the Area 5 RWMS facility; and diffuse sources of tritium and resuspension of plutonium. Section 1 describes these sources on the NTS. Section 2 tabulates the air emissions data for the NTS. These data are used to calculate the effective dose equivalents to offsite residents. Appendices describe the methods used to determine the emissions from the sources listed.

  14. Pacific Northwest National Laboratory Facility Radionuclide Emissions Units and Sampling Systems

    SciTech Connect

    Barnett, J. Matthew; Brown, Jason H.; Walker, Brian A.

    2012-04-01

    Battelle–Pacific Northwest Division operates numerous research and development (R&D) laboratories in Richland, WA, including those associated with Pacific Northwest National Laboratory (PNNL) on the U.S. Department of Energy (DOE)’s Hanford Site and PNNL Site that have the potential for radionuclide air emissions. The National Emission Standard for Hazardous Air Pollutants (NESHAP 40 CFR 61, Subparts H and I) requires an assessment of all emission units that have the potential for radionuclide air emissions. Potential emissions are assessed annually by PNNL staff members. Sampling, monitoring, and other regulatory compliance requirements are designated based upon the potential-to-emit dose criteria found in the regulations. The purpose of this document is to describe the facility radionuclide air emission sampling program and provide current and historical facility emission unit system performance, operation, and design information. For sampled systems, a description of the buildings, exhaust units, control technologies, and sample extraction details is provided for each registered emission unit. Additionally, applicable stack sampler configuration drawings, figures, and photographs are provided. Deregistered emission unit details are provided as necessary for up to 5 years post closure.

  15. 1997 Idaho National Engineering and Environmental Laboratory (INEEL) National Emission Standards for Hazardous Air Pollutants (NESHAPs) -- Radionuclides annual report

    SciTech Connect

    1998-06-01

    Under Section 61.94 of Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities, each Department of Energy (DOE) facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at the Idaho National Engineering and Environmental Laboratory (INEEL) for calendar year (CY) 1997. Section 1 of this report provides an overview of the INEEL facilities and a brief description of the radioactive materials and processes at the facilities. Section 2 identifies radioactive air effluent release points and diffuse sources at the INEEL and actual releases during 1997. Section 2 also describes the effluent control systems for each potential release point. Section 3 provides the methodology and EDE calculations for 1997 INEEL radioactive emissions.

  16. Pacific Northwest National Laboratory Potential Impact Categories for Radiological Air Emission Monitoring

    SciTech Connect

    Ballinger, Marcel Y.; Gervais, Todd L.; Barnett, J. Matthew

    2012-06-05

    In 2002, the EPA amended 40 CFR 61 Subpart H and 40 CFR 61 Appendix B Method 114 to include requirements from ANSI/HPS N13.1-1999 Sampling and Monitoring Releases of Airborne Radioactive Substances from the Stack and Ducts of Nuclear Facilities for major emission points. Additionally, the WDOH amended the Washington Administrative Code (WAC) 246-247 Radiation protection-air emissions to include ANSI/HPS N13.1-1999 requirements for major and minor emission points when new permitting actions are approved. A result of the amended regulations is the requirement to prepare a written technical basis for the radiological air emission sampling and monitoring program. A key component of the technical basis is the Potential Impact Category (PIC) assigned to an emission point. This paper discusses the PIC assignments for the Pacific Northwest National Laboratory (PNNL) Integrated Laboratory emission units; this revision includes five PIC categories.

  17. National Emission Standards for Hazardous Air Pollutants Calendar Year 2006

    SciTech Connect

    NSTec Environmental Technical Services

    2007-06-01

    The Nevada Test Site (NTS) is operated by the U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office (NNSA/NSO). From 1951 through 1992, the NTS was operated as the nation's site for nuclear weapons testing. The release of man-made radionuclides from the NTS as a result of testing activities has been monitored since the first decade of atmospheric testing. After 1962, when nuclear tests were conducted only underground, the radiation exposure to the public surrounding the NTS was greatly reduced. After the 1992 moratorium on nuclear testing, radiation monitoring on the NTS focused on detecting airborne radionuclides which come from historically-contaminated soils resuspended into the air (e.g., by winds) and tritium-contaminated soil moisture emitted to the air from soils through evapotranspiration.

  18. Pacific Northwest National Laboratory Site Radionuclide Air Emissions Report for Calendar Year 2011

    SciTech Connect

    Snyder, Sandra F.; Barnett, J. Matthew; Bisping, Lynn E.

    2012-06-12

    This report documents radionuclide air emissions that result in the highest effective dose equivalent (EDE) to a member of the public, referred to as the maximally exposed individual (MEI). The report has been prepared in compliance with the Code of Federal Regulations (CFR), Title 40, Protection of the Environment, Part 61, National Emission Standards for Hazardous Air Pollutants (NESHAP), Subpart H, National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities and Washington Administrative Code (WAC) Chapter 246-247, Radiation ProtectionAir Emissions. The EDE to the PNNL Site MEI due to routine emissions in 2011 from PNNL Site sources was 1.7E 05 mrem (1.7E-7 mSv) EDE. No nonroutine emissions occurred in 2011. The total radiological dose for 2011 to the MEI from all PNNL Site radionuclide emissions was more than 10,000 times smaller than the federal and state standard of 10 mrem/yr, to which the PNNL Site is in compliance.

  19. 76 FR 22565 - National Emission Standards for Hazardous Air Pollutant Emissions: Group I Polymers and Resins...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-04-21

    ... Document. On October 21, 2010 (75 FR 65068), EPA proposed revisions to six NESHAP that regulate 16... Emissions: Group I Polymers and Resins were promulgated on September 5, 1996 (62 FR 46925), and codified at... Rubber Production; Butyl Rubber Production; and Polysulfide Rubber Production. See 73 FR 76220,...

  20. 1996 Idaho National Engineering and Environmental Laboratory (INEEL) National Emissions Standards for Hazardous Air Pollutants (NESHAPs) -- Radionuclides. Annual report

    SciTech Connect

    1997-06-01

    Under Section 61.94 of Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, ``National Emission Standards for Emissions of Radionuclides Other Than Radon From Department of Energy Facilities,`` each Department of Energy (DOE) facility must submit an annual report documenting compliance. This report addresses the Section 61.94 reporting requirements for operations at the Idaho National Engineering and Environmental Laboratory (INEEL) for calendar year (CY) 1996. The Idaho Operations Office of the DOE is the primary contact concerning compliance with the National Emission Standards for Hazardous Air Pollutants (NESHAPs) at the INEEL. For calendar year 1996, airborne radionuclide emissions from the INEEL operations were calculated to result in a maximum individual dose to a member of the public of 3.14E-02 mrem (3.14E-07 Sievert). This effective dose equivalent (EDE) is well below the 40 CFR 61, Subpart H, regulatory standard of 10 mrem per year (1.0E-04 Sievert per year).

  1. Towards national-scale greenhouse gas emissions evaluation with robust uncertainty estimates

    NASA Astrophysics Data System (ADS)

    Rigby, Matthew; Swallow, Ben; Lunt, Mark; Manning, Alistair; Ganesan, Anita; Stavert, Ann; Stanley, Kieran; O'Doherty, Simon

    2016-04-01

    Through the Deriving Emissions related to Climate Change (DECC) network and the Greenhouse gAs Uk and Global Emissions (GAUGE) programme, the UK's greenhouse gases are now monitored by instruments mounted on telecommunications towers and churches, on a ferry that performs regular transects of the North Sea, on-board a research aircraft and from space. When combined with information from high-resolution chemical transport models such as the Met Office Numerical Atmospheric dispersion Modelling Environment (NAME), these measurements are allowing us to evaluate emissions more accurately than has previously been possible. However, it has long been appreciated that current methods for quantifying fluxes using atmospheric data suffer from uncertainties, primarily relating to the chemical transport model, that have been largely ignored to date. Here, we use novel model reduction techniques for quantifying the influence of a set of potential systematic model errors on the outcome of a national-scale inversion. This new technique has been incorporated into a hierarchical Bayesian framework, which can be shown to reduce the influence of subjective choices on the outcome of inverse modelling studies. Using estimates of the UK's methane emissions derived from DECC and GAUGE tall-tower measurements as a case study, we will show that such model systematic errors have the potential to significantly increase the uncertainty on national-scale emissions estimates. Therefore, we conclude that these factors must be incorporated in national emissions evaluation efforts, if they are to be credible.

  2. National Emission Standards for Hazardous Air Pollutants, June 2005

    SciTech Connect

    Robert F. Grossman

    2005-06-01

    sections present a general description of the present sources on the NTS and at the North Las Vegas Facility (NLVF). At the NLVF, parts of Building A-1 were contaminated with tritium by a previous contractor in 1995. The incident involved the release of tritium as HTO. This unusual occurrence led to a very small potential exposure to an offsite person. The HTO emission has continued at lower levels (probably re-emanation from building materials), even after cleanup activities in November and December 1997. A description of the incident and the potential effective dose equivalent (EDE) for offsite exposure are set forth in Appendix A.

  3. National Emission Standards for Hazardous Air Pollutants Submittal - 1998

    SciTech Connect

    Stuart Black; Yvonne Townsend

    1999-06-01

    The Nevada Test Site (NTS) is operated by the U.S. Department of Energy Nevada Operations Office (DOE/NV) as the site for nuclear weapons testing, now limited to readiness activities and experiments in support of the national Stockpile Stewardship Management Program. It is located in Nye County, Nevada, with the southeast corner about 105 km (65 mi) northwest of Las Vegas, Nevada. The NTS covers about 3,500 km2 (1,350 mi2), an area larger than Rhode Island. Its size is about 46 to 56 km (28 to 35 mi) east to west and from 64 to 88 km (40 to 55 mi)north to south. The NTS is surrounded, except on the south side, by public exclusion areas (Nellis Air Force Range) that provide another 24 to 104 km (15 to 65 mi) between the NTS and public lands. The NTS is characterized by desert valley and Great Basin mountain topography, with a climate, flora, and fauna typical of the southwest deserts. Surface waters are scarce on the NTS and there is great depth to slow-moving groundwater.

  4. National Emission Standards for Hazardous Air Pollutants Calendar Year 1999

    SciTech Connect

    R. F. Grossman

    2000-06-01

    The Nevada Test Site (NTS) is operated by the US Department of Energy's Nevada Operations Office (DOE/NV) as the site for nuclear weapons testing, now limited to readiness activities and experiments in support of the national Stockpile Stewardship Management Program. It is located in Nye County, Nevada, with the southeast corner about 105 km (65 mi) northwest of Las Vegas, Nevada. The NTS covers about 3,561 km{sup 2} (1,375 mi{sup 2}), an area larger than Rhode Island. Its size is about 46 to 56 km (28 to 35 mi) east to west and from 64 to 88 km (40 to 55 mi) north to south. The NTS is surrounded, except on the south side, by public exclusion areas (Nellis Air Force Range [NAFR]) that provide another 24 to 104 km (15 to 65 mi) between the NTS and public lands. The NTS is characterized by desert valley and Great Basin mountain topography, with a climate, flora, and fauna typical of the southwest deserts. Population density within 150 km (93 mi) of the NTS is only about 0.2 persons per square kilometer, excluding the Las Vegas area. Restricted access, low population density in the surrounding area, and extended wind transport times are advantageous factors for the activities conducted at the NTS. Surface waters are scarce on the NTS and there is great depth to slow-moving groundwater.

  5. Emissions Inventory Report Summary for Los Alamos National Laboratory for Calendar Year 2006

    SciTech Connect

    Ecology and Air Quality Group

    2007-09-28

    Los Alamos National Laboratory (LANL) is subject to annual emissions reporting requirements for regulated air pollutants under Title 20 of the New Mexico Administrative Code, Chapter 2, Part 73 (20.2.73 NMAC), Notice of Intent and Emissions Inventory Requirements. The applicability of the requirements is based on the Laboratory's potential to emit 100 tons per year of suspended particulate matter, nitrogen oxides, carbon monoxide, sulfur oxides, or volatile organic compounds. Additionally, on April 30, 2004, LANL was issued a Title V Operating Permit from the New Mexico Environment Department, Air Quality Bureau, under 20.2.70 NMAC. Modification Number 1 to this Title V Operating Permit was issued on June 15, 2006 (Permit No P-100M1) and includes emission limits and operating limits for all regulated sources of air pollution at LANL. The Title V Operating Permit also requires semi-annual emissions reporting for all sources included in the permit. This report summarizes both the annual emissions inventory reporting and the semi-annual emissions reporting for LANL for calendar year 2006. LANL's 2006 emissions are well below the emission limits in the Title V Operating Permit.

  6. Emissions Inventory Report Summary for Los Alamos National Laboratory for Calendar Year 2004

    SciTech Connect

    M. Stockton

    2005-10-01

    Los Alamos National Laboratory (LANL) is subject to annual emissions reporting requirements for regulated air pollutants under Title 20 of the New Mexico Administrative Code, Chapter 2, Part 73 (20.2.73 NMAC), ''Notice of Intent and Emissions Inventory Requirements''. The applicability of the requirements is based on the Laboratory's potential to emit 100 tons per year of suspended particulate matter, nitrogen oxides, carbon monoxide, sulfur oxides, or volatile organic compounds. Additionally, on April 30, 2004, LANL was issued a Title V Operating Permit from the New Mexico Environment Department, Air Quality Bureau, under 20.2.70 NMAC. This Title V Operating Permit (Permit No. P-100) includes emission limits and operating limits for all regulated sources of air pollution at LANL. The Title V Operating Permit also requires semi-annual emissions reporting for all sources included in the permit. This report summarizes both the annual emissions inventory reporting and the semi-annual emissions reporting for LANL for calendar year 2004. LANL's 2004 emissions are well below the emission limits in the Title V Operating Permit.

  7. Emissions Inventory Report Summary for Los Alamos National Laboratory for Calendar Year 2009

    SciTech Connect

    Environmental Stewardship Group

    2010-10-01

    Los Alamos National Laboratory (LANL) is subject to annual emissions reporting requirements for regulated air pollutants under Title 20 of the New Mexico Administrative Code, Chapter 2, Part 73 (20.2.73 NMAC), Notice of Intent and Emissions Inventory Requirements. The applicability of the requirements is based on the Laboratory's potential to emit 100 tons per year of suspended particulate matter, nitrogen oxides, carbon monoxide, sulfur oxides, or volatile organic compounds. Additionally, on April 30, 2004, LANL was issued a Title V Operating Permit from the New Mexico Environment Department/Air Quality Bureau, under 20.2.70 NMAC. This permit was modified and reissued on July 16, 2007. This Title V Operating Permit (Permit No. P-100M2) includes emission limits and operating limits for all regulated sources of air pollution at LANL. The Title V Operating Permit also requires semiannual emissions reporting for all sources included in the permit. This report summarizes both the annual emissions inventory reporting and the semiannual emissions reporting for LANL for calendar year 2009. LANL's 2009 emissions are well below the emission limits in the Title V Operating Permit.

  8. Emissions inventory report summary for Los Alamos National Laboratory for calendar year 2008

    SciTech Connect

    Ecology and Air Quality Group

    2009-10-01

    Los Alamos National Laboratory (LANL) is subject to annual emissions reporting requirements for regulated air pollutants under Title 20 of the New Mexico Administrative Code, Chapter 2, Part 73 (20.2.73 NMAC), Notice of Intent and Emissions Inventory Requirements. The applicability of the requirements is based on the Laboratory’s potential to emit 100 tons per year of suspended particulate matter, nitrogen oxides, carbon monoxide, sulfur oxides, or volatile organic compounds. Additionally, on April 30, 2004, LANL was issued a Title V Operating Permit from the New Mexico Environment Department/Air Quality Bureau, under 20.2.70 NMAC. This permit was modified and reissued on July 16, 2007. This Title V Operating Permit (Permit No. P-100M2) includes emission limits and operating limits for all regulated sources of air pollution at LANL. The Title V Operating Permit also requires semiannual emissions reporting for all sources included in the permit. This report summarizes both the annual emissions inventory reporting and the semiannual emissions reporting for LANL for calendar year 2008. LANL’s 2008 emissions are well below the emission limits in the Title V Operating Permit.

  9. National Emission Standards for Hazardous Air Pollutants Calendar Year 2001

    SciTech Connect

    Y. E. Townsend

    2002-06-01

    The Nevada Test Site (NTS) is operated by the U.S. Department of Energy (DOE), National Nuclear Security Administration Nevada Operations Office (NNSA/NV) as the site for nuclear weapons testing, now limited to readiness activities, experiments in support of the national Stockpile Stewardship Program, and the activities listed below. Located in Nye County, Nevada, the site's southeast corner is about 88 km (55 mi) northwest of the major population center, Las Vegas, Nevada. The NTS covers about 3,561 km2 (1,375 mi2), an area larger than Rhode Island. Its size is 46 to 56 km (28 to 35 mi) east to west and from 64 to 88 km (40 to 55 mi) north to south. The NTS is surrounded, except on the south side, by public exclusion areas (Nellis Air Force Range [NAFR]) that provide another 24 to 104 km (15 to 65 mi) between the NTS and public lands (Figure 1.0). The NTS is characterized by desert valley and Great Basin mountain topography, with a climate, flora, and fauna typical of the southwest deserts. Population density within 150 km (93 mi) of the NTS is only about 0.2 persons per square kilometer, excluding the Las Vegas area. Restricted access, low population density in the surrounding area, and extended wind transport times are advantageous factors for the activities conducted at the NTS. Surface waters are scarce on the NTS, and slow-moving groundwater is present hundreds to thousands of feet below the land surface. The sources of radionuclides include current and previous activities conducted on the NTS (Figure 2.0). The NTS was the primary location for testing of nuclear explosives in the Continental U.S. between 1951 and 1992. Historical testing above or at ground surface has included (1) atmospheric testing in the 1950s and early 1960s, (2) earth-cratering experiments, and (3) open-air nuclear reactor and rocket engine testing. Since the mid-1950s, testing of nuclear explosive devices has occurred underground in drilled vertical holes or in mined tunnels (DOE 1996a

  10. 75 FR 51569 - National Emission Standards for Hazardous Air Pollutants for Reciprocating Internal Combustion...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-08-20

    ...: Background Information Document. On March 5, 2009 (71 FR 9698), EPA proposed national emission standards for... sources on June 15, 2004 (69 FR 33474). EPA promulgated NESHAP for new and reconstructed stationary RICE... on January 18, 2008 (73 FR 3568). On March 3, 2010, EPA promulgated NESHAP for existing...

  11. 75 FR 28227 - National Emission Standards for Hazardous Air Pollutants: Gold Mine Ore Processing and Production...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-05-20

    ..., 2010, when EPA published the proposed rule (75 FR 22470). Several parties requested that EPA extend the... provided in the SUPPLEMENTARY INFORMATION section of the April 28, 2010 (75 FR 22470) Federal Register... AGENCY 40 CFR Parts 9 and 63 RIN 2060-AP48 National Emission Standards for Hazardous Air Pollutants:...

  12. 75 FR 9647 - National Emission Standards for Hazardous Air Pollutants for Reciprocating Internal Combustion...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-03-03

    ... . SUPPLEMENTARY INFORMATION: Background Information Document. On March 5, 2009 (71 FR 9698), EPA proposed national..., and reconstructed stationary RICE greater than 500 HP located at major sources on June 15, 2004 (69 FR... than or equal to 500 HP that are located at major sources of HAP emissions on January 18, 2008 (73...

  13. 77 FR 555 - National Emissions Standards for Hazardous Air Pollutants From Secondary Lead Smelting

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-01-05

    ... (62 FR 32216). The standards are codified at 40 CFR part 63, subpart X. The secondary lead smelting... January 5, 2012 Part II Environmental Protection Agency 40 CFR Part 63 National Emissions Standards for... / Thursday, January 5, 2012 / Rules and Regulations#0;#0; ] ENVIRONMENTAL PROTECTION AGENCY 40 CFR Part...

  14. 76 FR 74708 - National Emission Standards for Hazardous Air Pollutants for Source Categories

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-01

    ... AGENCY 40 CFR Part 63 National Emission Standards for Hazardous Air Pollutants for Source Categories CFR Correction In Title 40 of the Code of Federal Regulations, Part 63 (Sec. Sec. 63.600 to 63.1199), revised as of July 1, 2011, on page 602, Sec. 63.1196 is reinstated to read as follows: Sec. 63.1196...

  15. 76 FR 57913 - Amendments to National Emission Standards for Hazardous Air Pollutants for Area Sources: Plating...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-09-19

    ... Air Pollutants for Area Sources: Plating and Polishing'' which was published on June 20, 2011 (76 FR... AGENCY 40 CFR Part 63 RIN 2060-AQ74 Amendments to National Emission Standards for Hazardous Air... standards for hazardous air pollutants (NESHAP) for the plating and polishing area source category...

  16. 76 FR 38591 - National Emission Standards for Hazardous Air Pollutants: Secondary Lead Smelting; Extension of...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-07-01

    ... the National Emissions Standards for Hazardous Air Pollutants for Secondary Lead Smelting (76 FR 29032... Standards for Hazardous Air Pollutants: Secondary Lead Smelting, was published May 19, 2011 (76 FR 29032... current rule. DATES: Comments on the proposed rule published May 19, 2011 (76 FR 29032) must be...

  17. 76 FR 2832 - National Emission Standards for Hazardous Air Pollutants From the Portland Cement Manufacturing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-18

    ... amendments? On September 9, 2010 (75 FR 54970), EPA issued final amendments to National Emission Standards... production if significant adverse comments are filed. II. What are the changes to the final rules (75 FR... FR at 54993), and never discussed or otherwise suggested (in either the proposed or final rule)...

  18. 76 FR 13514 - National Emission Standards for Hazardous Air Pollutants for Chemical Manufacturing Area Sources

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-14

    ...). \\1\\ Chemical Manufacturing Process Unit. On February 12, 2010, the American Chemistry Council and the Society of Chemical Manufacturers and Affiliates (collectively referred to as ``Petitioners'') sought... AGENCY 40 CFR Part 63 RIN 2060-AQ89 National Emission Standards for Hazardous Air Pollutants for...

  19. 77 FR 65135 - National Emission Standards for Hazardous Air Pollutants for Chemical Manufacturing Area Sources

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-25

    ... Society of Chemical Manufacturers and Affiliates (collectively referred to as ``Petitioners'') sought... responsibilities between the federal government and Indian tribes, as specified by Executive Order 13175 (65 FR... AGENCY 40 CFR Part 63 RIN 2060-AQ89 National Emission Standards for Hazardous Air Pollutants for...

  20. The effect of lactation length on greenhouse gas emissions from the national dairy herd.

    PubMed

    Wall, E; Coffey, M P; Pollott, G E

    2012-11-01

    Many governments have signed up to greenhouse gas emission (GHGE) reduction programmes under their national climate change obligations. Recently, it has been suggested that the use of extended lactations in dairy herds could result in reduced GHGE. Dairy GHGE were modelled on a national basis and the model was used to compare emissions from lactations of three different lengths (305, 370 and 440 days), and a current 'base' scenario on the basis of maintaining current milk production levels. In addition to comparing GHGE from the average 'National Herd' under these scenarios, results were used to investigate how accounting for lactations of different lengths might alter the estimation of emissions calculated from the National Inventory methodology currently recommended by Intergovernmental Panel on Climate Change. Data for the three lactation length scenarios were derived from nationally recorded dairy performance information and used in the GHGE model. Long lactations required fewer milking cows and replacements to maintain current milk yield levels than short ones, but GHGEs were found to rise from 1214 t of CO2 equivalent (CE)/farm per year for lactations of 305 days to 1371 t CE/farm per year for 440-day lactations. This apparent anomaly can be explained by the less efficient milk production (kg milk produced per kg cow weight) found in later lactation, a more pronounced effect in longer lactations. The sensitivity of the model to changes in replacement rate, persistency and level of milk yield was investigated. Changes in the replacement rate from 25% to 20% and in persistency by −10% to +20% resulted in very small changes in GHGE. Differences in GHGE due to the level of milk yield were much more dramatic with animals in the top 10% for yield, producing about 25% less GHGE/year than the average animal. National Inventory results were investigated using a more realistic spread of lactation lengths than recommended for such calculations using emissions

  1. Atmosphere-derived National Emissions of Ozone Depleting Substances and Substitutes for the United States

    NASA Astrophysics Data System (ADS)

    Hu, L.; Montzka, S. A.; Miller, J. B.; Andrews, A. E.; Miller, B. R.; Lehman, S.; Godwin, D.; Thoning, K. W.; Sweeney, C.; Chen, H.; Fischer, M. L.; Biraud, S.; Torn, M. S.; Mountain, M. E.; Nehrkorn, T.; Eluszkiewicz, J.; Saikawa, E.; Hall, B. D.; Elkins, J. W.; Tans, P. P.

    2014-12-01

    Chlorofluorocarbons (CFCs), halons, carbon tetrachloride (CCl4), and methyl chloroform (CH3CCl3) are strong ozone-depleting substances (ODSs). Their production and consumption have been controlled by the Montreal Protocol since 1989 in developed countries and 1999 in developing countries. Although global atmospheric burdens of some of these gases have been declining for the last decade, their emissions continue due to releases from their existing reservoirs. Hydrochlorofluorocarbons (HCFCs) are transitional substitutes for CFCs; because they also deplete stratospheric ozone, they are also controlled by the Montreal Protocol. Hydrofluorocarbons (HFCs) are replacements for CFCs and HCFCs. Due to incomplete understanding of the reservoir size and emission rates for ODSs and their substitutes, uncertainty of their national emissions from inventory-based "bottom-up" estimates is undetermined. In this study, we use our atmospheric observations from multiple surface sites and aircraft profiles across the continental US from 2008 to 2012, along with data from remote sites over the Pacific basin, to derive national emissions of ODSs and their substitutes using inverse modeling. The performance of our modeling framework and the sensitivity of derived emissions to prior fluxes and model-data mismatch errors were investigated by conducting a suite of synthetic-data experiments. Sensitivity of derived fluxes to boundary values and transport was explored in real-data inversions. Our preliminary results suggest that (1) US emissions of HCFC-22 and HCFC-142b are currently declining at faster rates than those reported by US EPA; (2) our emission estimate of HFC-134a, the most abundant HFCs in the atmosphere, is consistent with the estimate reported by US EPA, whereas our estimates for some currently minor HFCs (i.e. HFC-125 and HFC-143a) show no significant emission trends during 2008 - 2012, which is inconsistent with a 70 - 120 % increase over this period reported by US EPA; and

  2. Agricultural soil greenhouse gas emissions: a review of national inventory methods.

    PubMed

    Lokupitiya, Erandathie; Paustian, Keith

    2006-01-01

    Parties to the United Nations Framework Convention on Climate Change (UNFCCC) are required to submit national greenhouse gas (GHG) inventories, together with information on methods used in estimating their emissions. Currently agricultural activities contribute a significant portion (approximately 20%) of global anthropogenic GHG emissions, and agricultural soils have been identified as one of the main GHG source categories within the agricultural sector. However, compared to many other GHG sources, inventory methods for soils are relatively more complex and have been implemented only to varying degrees among member countries. This review summarizes and evaluates the methods used by Annex 1 countries in estimating CO2 and N2O emissions in agricultural soils. While most countries utilize the Intergovernmental Panel on Climate Change (IPCC) default methodology, several Annex 1 countries are developing more advanced methods that are tailored for specific country circumstances. Based on the latest national inventory reporting, about 56% of the Annex 1 countries use IPCC Tier 1 methods, about 26% use Tier 2 methods, and about 18% do not estimate or report N2O emissions from agricultural soils. More than 65% of the countries do not report CO2 emissions from the cultivation of mineral soils, organic soils, or liming, and only a handful of countries have used country-specific, Tier 3 methods. Tier 3 methods usually involve process-based models and detailed, geographically specific activity data. Such methods can provide more robust, accurate estimates of emissions and removals but require greater diligence in documentation, transparency, and uncertainty assessment to ensure comparability between countries. Availability of detailed, spatially explicit activity data is a major constraint to implementing higher tiered methods in many countries.

  3. DAYCENT national-scale simulations of nitrous oxide emissions from cropped soils in the United States.

    PubMed

    Del Grosso, S J; Parton, W J; Mosier, A R; Walsh, M K; Ojima, D S; Thornton, P E

    2006-01-01

    Until recently, Intergovernmental Panel on Climate Change (IPCC) emission factor methodology, based on simple empirical relationships, has been used to estimate carbon (C) and nitrogen (N) fluxes for regional and national inventories. However, the 2005 USEPA greenhouse gas inventory includes estimates of N2O emissions from cultivated soils derived from simulations using DAYCENT, a process-based biogeochemical model. DAYCENT simulated major U.S. crops at county-level resolution and IPCC emission factor methodology was used to estimate emissions for the approximately 14% of cropped land not simulated by DAYCENT. The methodology used to combine DAYCENT simulations and IPCC methodology to estimate direct and indirect N2O emissions is described in detail. Nitrous oxide emissions from simulations of presettlement native vegetation were subtracted from cropped soil N2O to isolate anthropogenic emissions. Meteorological data required to drive DAYCENT were acquired from DAYMET, an algorithm that uses weather station data and accounts for topography to predict daily temperature and precipitation at 1-km2 resolution. Soils data were acquired from the State Soil Geographic Database (STATSGO). Weather data and dominant soil texture class that lie closest to the geographical center of the largest cluster of cropped land in each county were used to drive DAYCENT. Land management information was implemented at the agricultural-economic region level, as defined by the Agricultural Sector Model. Maps of model-simulated county-level crop yields were compared with yields estimated by the USDA for quality control. Combining results from DAYCENT simulations of major crops and IPCC methodology for remaining cropland yielded estimates of approximately 109 and approximately 70 Tg CO2 equivalents for direct and indirect, respectively, mean annual anthropogenic N2O emissions for 1990-2003.

  4. Characterization of road freight transportation and its impact on the national emission inventory in China

    NASA Astrophysics Data System (ADS)

    Yang, X. F.; Liu, H.; Man, H. Y.; He, K. B.

    2014-06-01

    monitoring data on different roads. Depending on the results in this research, the largest differences among the emission factors (in g km-1) on different roads exceed 70 and 50% for NOx and PM2.5, respectively. The differences were caused by different driving conditions that we monitored via GPS. The estimated NOx and PM2.5 emissions from diesel freight trucks in China were 5.0 (4.8-7.2) million t and 0.20 (0.17-0.22) million t, respectively, via the REIB approach in 2011. Another implication of this research is that different road infrastructure would have different impacts for NOx and PM2.5 emissions. A region with more inter-city freeways or national roads tends to have more NOx emissions, while urban streets play a more important role in primary PM2.5 emissions from freight trucks. Compared with former studies, which allocate emissions according to local truck registration number and neglect inter-region long distance transport trips, the REIB approach has advantages regarding the allocation of diesel truck emissions into the provinces. Furthermore, the different driving conditions on the different roads types are no longer overlooked with this approach.

  5. Inventory of Carbon Dioxide (CO2) Emissions at Pacific Northwest National Laboratory

    SciTech Connect

    Judd, Kathleen S.; Kora, Angela R.; Shankle, Steve A.; Fowler, Kimberly M.

    2009-06-29

    The Carbon Management Strategic Initiative (CMSI) is a lab-wide initiative to position the Pacific Northwest National Laboratory (PNNL) as a leader in science, technology and policy analysis required to understand, mitigate and adapt to global climate change as a nation. As part of an effort to walk the talk in the field of carbon management, PNNL conducted its first carbon dioxide (CO2) emissions inventory for the 2007 calendar year. The goal of this preliminary inventory is to provide PNNL staff and management with a sense for the relative impact different activities at PNNL have on the lab’s total carbon footprint.

  6. Statistical exploration of the effects of copper smelter emissions on visibility in southwestern National parks

    SciTech Connect

    Williams, M.D.; Nochumson, D.H.

    1984-01-01

    The copper strike in the summer of 1980 provided an opportunity to assess impacts of copper smelter emissions of the Southwest. Differences in sulfur composition between the summers of 1979 and of 1980 were significant at all of the Arizona NASN stations examined. The 1980 period showed decreased sulfate throughout most of the state with the largest changes near smelters. Outside of Arizona the aerosol sampling during 1979 was much less comprehensive with data for only three stations of interest available. Neither Zion nor Canyonlands showed significant differences and Mesa Verde showed an increase of sulfate rather than a decrease during the strike period. Visibility data in the parklands showed significant improvements in regions immediately east and northeast of the smelters - areas such as Bandelier National Monument, White Sands National Monument, Mesa Verde National Park, Chaco Culture National Historical Park, and Navajo National Monument. Park areas north to northwest of the smelters either showed no significant differences in visibility or reported decreased visibilities. Big Bend far to the southeast also reported decreased visibility during the strike. Examination of aerosol composition data near smelter sites suggested that high levels of copper, lead, and arsenic might be associated with high levels of sulfate. It appears that the smelter emissions (1) increase sulfates over much of Arizona, (2) affect long term visibility in northeastern Arizona and New Mexico, and (3) produce short term elevated sulfate and reduced visibilities in the southwestern park areas during periods when the winds are appropriate to carry the emissions towards the park areas. 6 references, 1 figure, 11 tables.

  7. Assessment of Unabated Facility Emission Potentials for Evaluating Airborne Radionuclide Monitoring Requirements at Pacific Northwest National Laboratory - 2007

    SciTech Connect

    Ballinger, Marcel Y.; Barfuss, Brad C.; Gervais, Todd L.

    2008-01-01

    Assessments were performed to evaluate compliance with the airborne radionuclide emission monitoring requirements in the National Emission Standards for Hazardous Air Pollutants (NESHAP – U.S. Code of Federal Regulations, Title 40, Part 61, Subpart H) and Washington Administrative Code (WAC) 246-247: Radiation Protection – Air Emissions. In these NESHAP assessments, potential unabated offsite doses were evaluated for emission locations at buildings that are part of the consolidated laboratory campus of the Pacific Northwest National Laboratory. This report describes the inventory-based methods and provides the results for the NESHAP assessment performed in 2007.

  8. Assessment of Unabated Facility Emission Potentials for Evaluating Airborne Radionuclide Monitoring Requirements at Pacific Northwest National Laboratory - 2010

    SciTech Connect

    Ballinger, Marcel Y.; Gervais, Todd L.; Barnett, J. Matthew

    2011-05-13

    Assessments were performed to evaluate compliance with the airborne radionuclide emission monitoring requirements in the National Emission Standards for Hazardous Air Pollutants ([NESHAP]; U.S. Code of Federal Regulations, Title 40, Part 61, Subpart H) and Washington Administrative Code 246-247: Radiation Protection - Air Emissions. In these NESHAP assessments, potential unabated off-site doses were evaluated for emission locations at buildings that are part of the consolidated laboratory campus of the Pacific Northwest National Laboratory. This report describes the inventory-based methods and provides the results for the NESHAP assessment performed in 2010.

  9. Assessment of Unabated Facility Emission Potentials for Evaluating Airborne Radionuclide Monitoring Requirements at Pacific Northwest National Laboratory - 2003

    SciTech Connect

    Ballinger, Marcel Y.; Sula, Monte J.; Gervais, Todd L.; Edwards, Daniel L.

    2003-12-05

    Assessments were performed to evaluate compliance with the airborne radionuclide emission monitoring requirements in the National Emission Standards for Hazardous Air Pollutants (NESHAP - U.S. Code of Federal Regulations, Title 40, Part 61, Subpart H) and Washington Administrative Code (WAC) 246-247: Radiation Protection - Air Emissions. In these assessments, potential unabated offsite doses were evaluated for emission locations at facilities owned by the U.S. Department of Energy and operated by Pacific Northwest National Laboratory (PNNL) on the Hanford Site. This report describes the inventory-based methods and provides the results for the assessment performed in 2003.

  10. Assessment of Unabated Facility Emission Potentials for Evaluating Airborne Radionuclide Monitoring Requirements at Pacific Northwest National Laboratory - 2001

    SciTech Connect

    Ballinger, Marcel Y.; Sula, Monte J.; Gervais, Todd L.; Shields, Keith D.; Edwards, Daniel R.

    2001-09-28

    Assessments were performed to evaluate compliance with the airborne radionuclide emission monitoring requirements in the National Emission Standards for Hazardous Air Pollutants (NESHAP - U.S. Code of Federal Regulations, Title 40 Part 61, Subpart H) and Washington Administrative Code (WAC) 246-247: Radiation Protection - Air Emissions. In these assessments, potential unabated offsite doses were evaluated for emission locations at facilities owned by the U.S. Department of Energy and operated by Pacific Northwest National Laboratory (PNNL) on the Hanford Site. This report describes the inventory-based methods, and provides the results, for the assessment performed in 2001.

  11. Basis to demonstrate compliance with the National Emission Standards for Hazardous Air Pollutants for the Stand-off Experiments Range

    SciTech Connect

    Michael Sandvig

    2011-01-01

    The purpose of this report is to provide the basis and the documentation to demonstrate general compliance with the National Emission Standard for Hazardous Air Pollutants (NESHAPS) 40 CFR 61 Subpart H, “National Emission Standards for Emissions of Radionuclides Other Than Radon from Department of Energy Facilities,” (the Standard) for outdoor linear accelerator operations at the Idaho National Laboratory (INL) Stand-off Experiments Range (SOX). The intent of this report is to inform and gain acceptance of this methodology from the governmental bodies regulating the INL.

  12. Characterization of road freight transportation and its impact on the national emission inventory in China

    NASA Astrophysics Data System (ADS)

    Yang, X. F.; Liu, H.; Man, H. Y.; He, K. B.

    2015-02-01

    Diesel trucks are major contributors of nitrogen oxides (NOx) and primary particulate matter smaller than 2.5 μm (PM2.5) in the transportation sector. However, there are more obstacles to existing estimations of diesel-truck emissions compared with those of cars. The obstacles include both inappropriate methodology and missing basic data in China. According to our research, a large number of trucks are conducting long-distance intercity or interprovincial transportation. Thus, the method used by most existing inventories, based on local registration number, is inappropriate. A road emission intensity-based (REIB) approach is introduced in this research instead of registration-population-based approach. To provide efficient data for the REIB approach, 1060 questionnaire responses and approximately 1.7 million valid seconds of onboard GPS monitoring data were collected in China. The estimated NOx and PM2.5 emissions from diesel freight trucks in China were 5.0 (4.8-7.2) million tonnes and 0.20 (0.17-0.22) million tonnes, respectively, in 2011. The province-based emission inventory is also established using the REIB approach. It was found that the driving conditions on different types of road have significant impacts on the emission levels of freight trucks. The largest differences among the emission factors (in g km-1) on different roads exceed 70 and 50% for NOx and PM2.5, respectively. A region with more intercity freeways or national roads tends to have more NOx emissions, while urban streets play a more important role in primary PM2.5 emissions from freight trucks. Compared with the inventory of the Ministry of Environment Protection, which allocates emissions according to local truck registration number and neglects interregional long-distance transport trips, the differences for NOx and PM2.5 are +28 and -57%, respectively. The REIB approach matches better with traffic statistical data on a provincial level. Furthermore, the different driving conditions on the

  13. Evaluation of national emissions inventories of anthropogenic air pollutants for Brunei Darussalam

    NASA Astrophysics Data System (ADS)

    Dotse, Sam-Quarcoo; Dagar, Lalit; Petra, Mohammad Iskandar; De Silva, Liyanage C.

    2016-05-01

    Haze and other air pollution related problems are getting more significant in Brunei Darussalam but till date there is absence of comprehensive national emission inventory for Brunei Darussalam. Although there are few regional and global inventories available for Brunei Darussalam, large variations in the emission estimates exist in these datasets. Therefore, there is an important need for an updated inventory, based on data available from government and other sources. This study presents a sector-wise anthropogenic emission estimates and trends (2001-2012) for the pollutants CO2, CH4, N2O, NOX, NMVOC, CO, SOX, and PM10. The results suggest no significant contributions from residential sector (<1%) whilst road transport is the main contributor for most of the pollutants. CO2 is largely emitted by power plants (∼72% in 2001 and∼ 62% in 2012) and the main source of CH4 is Solid waste disposal and wastewater handling (∼92%). There were also significant contributions from industrial processes and solvent use to NMVOC and PM10 emissions (∼74% and ∼45% respectively).

  14. "The Incorporation of National Emission Inventories into Version 2 of the Hemispheric Transport of Air Pollutants Inventory"

    EPA Science Inventory

    EPA’s National Emission Inventory has been incorporated into the Emission Database for Global Atmospheric Research-Hemispheric Transport of Air Pollutants (EDGAR-HTAP) version 2. This work involves the creation of a detailed mapping of EPA Source Classification Codes (SCC) to the...

  15. Electron Bernstein wave emission based diagnostic on National Spherical Torus Experiment (invited).

    PubMed

    Diem, S J; Taylor, G; Caughman, J B; Efthimion, P; Kugel, H; LeBlanc, B P; Preinhaelter, J; Sabbagh, S A; Urban, J; Wilgen, J

    2008-10-01

    National Spherical Torus Experiment (NSTX) is a spherical tokamak (ST) that operates with n(e) up to 10(20) m(-3) and B(T) less than 0.6 T, cutting off low harmonic electron cyclotron (EC) emission widely used for T(e) measurements on conventional aspect ratio tokamaks. The electron Bernstein wave (EBW) can propagate in ST plasmas and is emitted at EC harmonics. These properties suggest thermal EBW emission (EBE) may be used for local T(e) measurements in the ST. Practically, a robust T(e)(R,t) EBE diagnostic requires EBW transmission efficiencies of >90% for a wide range of plasma conditions. EBW emission and coupling physics were studied on NSTX with an obliquely viewing EBW to O-mode (B-X-O) diagnostic with two remotely steered antennas, coupled to absolutely calibrated radiometers. While T(e)(R,t) measurements with EBW emission on NSTX were possible, they were challenged by several issues. Rapid fluctuations in edge n(e) scale length resulted in >20% changes in the low harmonic B-X-O transmission efficiency. Also, B-X-O transmission efficiency during H modes was observed to decay by a factor of 5-10 to less than a few percent. The B-X-O transmission behavior during H modes was reproduced by EBE simulations that predict that EBW collisional damping can significantly reduce emission when T(e)<30 eV inside the B-X-O mode conversion (MC) layer. Initial edge lithium conditioning experiments during H modes have shown that evaporated lithium can increase T(e) inside the B-X-O MC layer, significantly increasing B-X-O transmission.

  16. Assessing Satellite-Based Fire Data for use in the National Emissions Inventory

    NASA Technical Reports Server (NTRS)

    Soja, Amber J.; Al-Saadi, Jassim; Giglio, Louis; Randall, Dave; Kittaka, Chieko; Pouliot, George; Kordzi, Joseph J.; Raffuse, Sean; Pace, Thompson G.; Pierce, Thomas E.; Moore, Tom; Biswadev, Roy; Pierce, R. Bradley; Szykman, James J.

    2009-01-01

    Biomass burning is significant to emission estimates because: (1) it can be a major contributor of particulate matter and other pollutants; (2) it is one of the most poorly documented of all sources; (3) it can adversely affect human health; and (4) it has been identified as a significant contributor to climate change through feedbacks with the radiation budget. Additionally, biomass burning can be a significant contributor to a regions inability to achieve the National Ambient Air Quality Standards for PM 2.5 and ozone, particularly on the top 20% worst air quality days. The United States does not have a standard methodology to track fire occurrence or area burned, which are essential components to estimating fire emissions. Satellite imagery is available almost instantaneously and has great potential to enhance emission estimates and their timeliness. This investigation compares satellite-derived fire data to ground-based data to assign statistical error and helps provide confidence in these data. The largest fires are identified by all satellites and their spatial domain is accurately sensed. MODIS provides enhanced spatial and temporal information, and GOES ABBA data are able to capture more small agricultural fires. A methodology is presented that combines these satellite data in Near-Real-Time to produce a product that captures 81 to 92% of the total area burned by wildfire, prescribed, agricultural and rangeland burning. Each satellite possesses distinct temporal and spatial capabilities that permit the detection of unique fires that could be omitted if using data from only one satellite.

  17. U.S. onroad transportation CO2 emissions analysis comparing highly resolved CO2 emissions and a national average approach : mitigation options and uncertainty reductions

    NASA Astrophysics Data System (ADS)

    Mendoza, D. L.; Gurney, K. R.

    2011-12-01

    The transportation sector is the second largest CO2 emitting economic sector in the United States, accounting for 32.3% of the total U.S. emissions in 2002. Within the transportation sector, the largest component (80%) is made up of onroad emissions. In order to accurately quantify future emissions and evaluate emissions regulation strategies, analysis must account for spatially-explicit fleet distribution, driving patterns, and mitigation strategies. Studies to date, however, have either focused on one of these three components, have been only completed at the national scale, or have not explicitly represented CO2 emissions instead relying on the use of vehicle miles traveled (VMT) as an emissions proxy. We compare a high resolution onroad emissions data product (Vulcan) to a national averaging of the Vulcan result. This comparison is performed in four groupings: light duty (LD) and heavy duty (HD) vehicle classes, and rural and urban road classes. Two different bias metrics are studied: 1) the state-specific, group-specific bias and 2) the same bias when weighted by the state share of the national group-specific emissions. In the first metric, we find a spread of positive and negative biases for the LD and HD vehicle groupings and these biases are driven by states having a greater/lesser proportion of LD/HD vehicles within their total state fleet than found from a national average. The standard deviation of these biases is 2.01% and 0.75% for the LD and HD groupings, respectively. These biases correlate with the road type present in a state, so that biases found in the urban and LD groups are both positive or both negative, with a similar relationship found between biases of the rural and HD groups. Additionally, the road group bias is driven by the distribution of VMT on individual road classes within the road groupings. When normalized by national totals, the state-level group-specific biases reflect states with large amounts of onroad travel that deviate

  18. Comparison of emissions estimates derived from atmospheric measurements with national estimates of HFCs, PFCs and SF6.

    PubMed

    Harnisch, Jochen; Höhne, Niklas

    2002-01-01

    This paper assesses the feasibility of using atmospheric measurement of fluorinated greenhouse gases (HFCs, PFCs and SF6) for the review and verification of greenhouse gas inventories provided by national governments. For this purpose, available data were compiled. It was found that atmospheric measurements of these gases are available and provide an indication of global annual emissions with sufficient certainty to reach the following conclusions: Within the uncertainty of the method, it was found that emissions of HFC-23, a by-product of HCFC-22 production, as obtained from atmospheric measurements did not decrease as fast, as the countries have reported. In contrast, SF6 concentrations in the atmosphere suggest higher emissions than reported by countries. Regional emission estimates from atmospheric measurements are still in a more pioneering state and cannot be compared to national estimates. Intensified efforts to measure HFCs, PFCs and SF6 in the atmosphere are recommended. PMID:12391806

  19. Assessment of Unabated Facility Emission Potentials for Evaluating Airborne Radionuclide Monitoring Requirements at Pacific Northwest National Laboratory - 1999

    SciTech Connect

    DL Edwards; KD Shields; MJ Sula; MY Ballinger

    1999-09-28

    Assessments were performed to evaluate compliance with the airborne radionuclide emission monitoring requirements in the National Emission Standards for Hazardous Air Pollutants (NESHAP--US Code of Federal Regulations, Title 40 Part 61, Subpart H). In these assessments, potential unabated offsite doses were evaluated for emission locations at facilities owned by the US Department of Energy and operated by Pacific Northwest National Laboratory (Pacific Northwest) on the Hanford Site. Two of the facilities evaluated, 325 Building Radiochemical Processing Laboratory, and 331 Building Life Sciences Laboratory met state and federal criteria for continuous sampling of airborne radionuclide emissions. One other building, the 3720 Environmental Sciences Laboratory, was recognized as being in transition with the potential for meeting the continuous sampling criteria.

  20. National emission standards for hazardous air pollutants--EPA. Final rule.

    PubMed

    1991-04-24

    Today EPA is staying the effectiveness of subpart I of 40 CFR part 61, the National Emission Standards for Hazardous Air Pollutants for Radionuclide Emissions (54 FR 51654, December 15, 1989) as applied to facilities licensed by the Nuclear Regulatory Commission or an Agreement State ("NRC-licensed facilities"), other than nuclear power reactors, until November 15, 1992. The purpose or this rule is to afford EPA the time required to make an initial determination pursuant to section 112(d)(9) of the 1990 Clean Air Amendments before subpart I becomes effective for such facilities. EPA intends to propose a rule pursuant to section 112(d)(9) to rescind subpart I for nuclear power reactors, and to take final action no later than June 30, 1991, concerning a separate proposal to stay the effectiveness of subpart I for nuclear power reactors during the pendency of the rulemaking on recission. This rule staying subpart I for NRC-licensed facilities other than nuclear power reactors, and the Agency's final action on its proposal to stay subpart I for nuclear power reactors, will completely supplant all stays previously entered for such facilities during the Agency's reconsideration of subpart I under Clean Air Act section 307(d)(7)(B).

  1. Integrated evaluation of cost, emissions, and resource potential for algal biofuels at the national scale.

    PubMed

    Davis, Ryan E; Fishman, Daniel B; Frank, Edward D; Johnson, Michael C; Jones, Susanne B; Kinchin, Christopher M; Skaggs, Richard L; Venteris, Erik R; Wigmosta, Mark S

    2014-05-20

    Costs, emissions, and resource availability were modeled for the production of 5 billion gallons yr(-1) (5 BGY) of renewable diesel in the United States from Chlorella biomass by hydrothermal liquefaction (HTL). The HTL model utilized data from a continuous 1-L reactor including catalytic hydrothermal gasification of the aqueous phase, and catalytic hydrotreatment of the HTL oil. A biophysical algae growth model coupled with weather and pond simulations predicted biomass productivity from experimental growth parameters, allowing site-by-site and temporal prediction of biomass production. The 5 BGY scale required geographically and climatically distributed sites. Even though screening down to 5 BGY significantly reduced spatial and temporal variability, site-to-site, season-to-season, and interannual variations in productivity affected economic and environmental performance. Performance metrics based on annual average or peak productivity were inadequate; temporally and spatially explicit computations allowed more rigorous analysis of these dynamic systems. For example, 3-season operation with a winter shutdown was favored to avoid high greenhouse gas emissions, but economic performance was harmed by underutilized equipment during slow-growth periods. Thus, analysis of algal biofuel pathways must combine spatiotemporal resource assessment, economic analysis, and environmental analysis integrated over many sites when assessing national scale performance.

  2. Integrated Evaluation of Cost, Emissions, and Resource Potential for Algal Biofuels at the National Scale

    SciTech Connect

    Davis, Ryan; Fishman, Daniel; Frank, Edward D.; Johnson, Michael C.; Jones, Susanne B.; Kinchin, Christopher; Skaggs, Richard; Venteris, Erik R.; Wigmosta, Mark S.

    2014-04-21

    Costs, emissions, and resource availability were modeled for the production of 5 billion gallons yr-1 (5 BGY) of renewable diesel in the United States from Chlorella biomass by hydrothermal liquefaction (HTL). The HTL model utilized data from a continuous 1-L reactor including catalytic hydrothermal gasification of the aqueous phase, and catalytic hydrotreatment of the HTL oil. A biophysical algae growth model coupled with weather and pond simulations predicted biomass productivity from experimental growth parameters, allowing site-by-site and temporal prediction of biomass production. The 5 BGY scale required geographically and climatically distributed sites. Even though screening down to 5 BGY significantly reduced spatial and temporal variability, site-to-site, season-to-season, and inter-annual variations in productivity affected economic and environmental performance. Performance metrics based on annual average or peak productivity were inadequate; temporally and spatially explicit computations allowed more rigorous analysis of these dynamic systems. For example, 3-season operation with a winter shutdown was favored to avoid high greenhouse gas emissions, and economic performance was harmed by underutilized equipment during slow-growth periods. Thus, analysis of algal biofuel pathways must combine spatiotemporal resource assessment, economic analysis, and environmental analysis integrated over many sites when assessing national scale performance.

  3. Advancing reference emission levels in subnational and national REDD+ initiatives: a CLASlite approach

    PubMed Central

    2015-01-01

    Conservation and monitoring of tropical forests requires accurate information on their extent and change dynamics. Cloud cover, sensor errors and technical barriers associated with satellite remote sensing data continue to prevent many national and sub-national REDD+ initiatives from developing their reference deforestation and forest degradation emission levels. Here we present a framework for large-scale historical forest cover change analysis using free multispectral satellite imagery in an extremely cloudy tropical forest region. The CLASlite approach provided highly automated mapping of tropical forest cover, deforestation and degradation from Landsat satellite imagery. Critically, the fractional cover of forest photosynthetic vegetation, non-photosynthetic vegetation, and bare substrates calculated by CLASlite provided scene-invariant quantities for forest cover, allowing for systematic mosaicking of incomplete satellite data coverage. A synthesized satellite-based data set of forest cover was thereby created, reducing image incompleteness caused by clouds, shadows or sensor errors. This approach can readily be implemented by single operators with highly constrained budgets. We test this framework on tropical forests of the Colombian Pacific Coast (Chocó) – one of the cloudiest regions on Earth, with successful comparison to the Colombian government’s deforestation map and a global deforestation map. PMID:25678933

  4. Atmosphere-based nation-wide emission estimates of hydrofluorocarbons and hydrochlorofluorocarbons from the U.S

    NASA Astrophysics Data System (ADS)

    Hu, L.; Montzka, S. A.; Miller, J. B.; Andrews, A. E.; Miller, B. R.; Thoning, K. W.; Sweeney, C.; Chen, H.; Bruhwiler, L.; Masarie, K.; Miller, S. M.; Fischer, M. L.; Saikawa, E.; Elkins, J. W.; Tans, P. P.

    2013-12-01

    Limiting the warming influence induced by greenhouse gases (GHGs) ultimately requires reductions in emissions. To evaluate emission magnitudes and their changes over time, we recommend verifying self-reported emission inventories with independent, atmosphere-based, 'top-down' estimates. Hydrochlorofluorocarbons (HCFCs) and hydrofluorocarbons (HFCs) are potent GHGs with global warming potentials up to thousands of times larger than CO2 over a 100-year time horizon. Reductions in HCFC production and consumption were required by the Montreal Protocol in developed countries beginning in 2004. However, it is uncertain whether emissions of these gases are declining within the US because emissions are not linearly related to production or consumption due to the existence of substantial 'banks' (stores of in-use chemicals that have not yet escaped to the atmosphere). HFCs are replacements for CFCs and HCFCs. Without regulation, CO2 equivalent emissions of HFCs could become substantial in the future relative to CO2. In this study, we estimated emissions of HCFC-22 and HFC-134a within the US from 2008 - 2012 using a Bayesian approach of a regional inverse model with atmospheric observations from 8 tall-tower sites, 5 surface flask sites and 19 aircraft sites. We used a maximum likelihood estimation to estimate model-data mismatch errors, prior flux uncertainty, and temporal and spatial correlations in flux deviations between prior and posterior fluxes. We optimized our model design and tested our model performance by conducting synthetic data experiments. With this optimized design and boundary mixing ratios calculated with three different approaches, we derived national emissions of HCFC-22 and HFC-134a. This study provides the first multi-year atmosphere-based national emission estimates of HCFC-22 and HFC-134a, derived from multiple sites distributed across the US.

  5. RADIOLOGICAL EMISSIONS AND ENVIRONMENTAL MONITORING FOR BROOKHAV EN NATIONAL LABORATORY, 1947 - 1961.

    SciTech Connect

    MEINHOLD,C.B.; MEINHOLD,A.F.

    2001-05-30

    Brookhaven National Laboratory (BNL) has monitored its releases to the environment since its inception in 1947. From 1962 to 1966 and from 1971 to the present, annual reports,were published that recorded the emissions and releases to the environment from Laboratory operations. In 1998, a report was written to summarize the environmental data for the years 1967 to 1970. One of the purposes of the current report is to complete BNL's environmental history by covering the period from 1948 through 1961. The activities in 1947 were primarily organizational and there is no information on the use of radiation at the Laboratory before 1948. An additional objective of this report is to provide environmental data to the Agency for Toxic Substances and Disease Registry (ATSDR). The report does not provide an estimate of the doses associated with BNL operations. The report is comprised of two parts. The first part is a summary of emissions, releases, and environmental monitoring information including a discussion of the uncertainties in these data. Part two contains the detailed information on the approach taken to estimate the releases from the fuel cartridge failures at the Brookhaven Graphite Research Reactor (BGRR). A series of appendices present more detailed information on these events in tabular form. The approach in this report is to be reasonable, conservative, (pessimistic), and transparent in estimating releases from fuel cartridge ruptures. Clearly, reactor stack monitoring records and more extensive records would have greatly improved this effort, but in accordance with Atomic Energy Commission (AEC) Appendix 0230 Annex C-9, many of the detailed records from this time were not retained.

  6. 23 CFR Appendix A to Part 772 - National Reference Energy Mean Emission Levels as a Function of Speed

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 23 Highways 1 2010-04-01 2010-04-01 false National Reference Energy Mean Emission Levels as a Function of Speed A Appendix A to Part 772 Highways FEDERAL HIGHWAY ADMINISTRATION, DEPARTMENT OF... Function of Speed EC14OC91.013...

  7. TRACKING THE EMISSION OF CARBON DIOXIDE BY NATION, SECTOR, AND FUEL TYPE: A TRACE GAS ACCOUNTING SYSTEM (TGAS)

    EPA Science Inventory

    The paper describes a new way to estimate an efficient econometric model of global emissions of carbon dioxide (CO2) by nation, sector, and fuel type. Equations for fuel intensity are estimated for coal, oil, natural gas, electricity, and heat for six sectors: agricultural, indus...

  8. The incorporation of the US national emission inventory into version 2 of the Hemispheric Transport of air Pollutants inventory

    EPA Science Inventory

    EPA's 2008 national emission inventory has been incorporated into version 2 of the Hemispheric Transport of Air Pollutants Inventory. This work involves the creation of a detailed mapping of EPA Source Classification Codes (SCC) to the International Nomenclature for Reporting Sy...

  9. Mitigation of agriculture emissions in the tropics: comparing forest land-sparing options at the national level

    NASA Astrophysics Data System (ADS)

    Carter, S.; Herold, M.; Rufino, M. C.; Neumann, K.; Kooistra, L.; Verchot, L.

    2015-04-01

    Emissions from agriculture-driven deforestation are of global concern, but forest land-sparing interventions such as agricultural intensification and utilization of available land offer opportunities for mitigation. In many tropical countries, where agriculture is the major driver of deforestation, interventions in the agriculture sector can reduce deforestation emissions as well as reducing emissions in the agriculture sector. Our study uses a novel approach to quantify agriculture-driven deforestation and associated emissions in the tropics. Emissions from agriculture-driven deforestation in the tropics between 2000 and 2010 are 4.3 Gt CO2 eq yr-1 (97 countries). We investigate the national potential to mitigate these emissions through forest land-sparing interventions, which can potentially be implemented under REDD+. We consider intensification, and utilization of available non-forested land as forest land-sparing opportunities since they avoid the expansion of agriculture into forested land. In addition, we assess the potential to reduce agriculture emissions on existing agriculture land, interventions that fall under climate-smart agriculture (CSA). The use of a systematic framework demonstrates the selection of mitigation interventions by considering sequentially the level of emissions, mitigation potential of various interventions, enabling environment and associated risks to livelihoods at the national level. Our results show that considering only countries with high emissions from agriculture-driven deforestation, where there is a potential for forest-sparing interventions, and where there is a good enabling environment (e.g. effective governance or engagement in REDD+), the potential to mitigate is 1.3 Gt CO2 eq yr-1 (20 countries of 78 with sufficient data). For countries where we identify agriculture emissions as priority for mitigation, up to 1 Gt CO2 eq yr-1 could be reduced from the agriculture sector including livestock. Risks to livelihoods from

  10. Global EDGAR greenhouse gas emissions and national emissions reporting under the UN Climate Convention: availability, structure, definitions and role of uncertainties

    NASA Astrophysics Data System (ADS)

    Olivier, J. G.; Monni, S.; van Aardenne, J.; Doering, U. M.; Janssens-Maenhout, G.; Peters, J. A.; Pagliari, V.

    2010-12-01

    JRC and PBL have compiled a comprehensive EDGAR v4 dataset for the ‘six’ greenhouse gases included in the Kyoto Protocol (CO2, CH4, N2O, HFCs, PFCs and SF6), which were constructed using consistently the 2006 IPCC methodology and combining activity data (international statistics) from publicly available sources and for the first time - to the extent possible - emission factors as recommended by the IPCC 2006 guidelines for GHG emission inventories. This dataset, that covers all countries, provides independent estimates for all anthropogenic sources from 1970 onwards that are consistent over time and comparable between countries. By using high resolution global grid maps per source category, we also compiled datasets with annual emissions on a 0.1x0.1 degree grid, as input for atmospheric models. Of the 220 UN nations only 43 industrialised countries (‘Annex I’) annually report their national GHG emissions in large detail from 1990 up to (presently) 2008, while most developing countries (‘non-Annex I’) for the UN Climate Convention (UNFCCC) and the Kyoto Protocol only report a summary table with emissions for one or more years (many only for 1994). All emissions in EDGAR 4 are detailed at country level using the same standard IPCC inventory source categories as used by industrialised countries in their report to the Climate Convention. Thus we provide full and up-to-date inventories per country, also for developing countries that go beyond the mostly very aggregated UNFCCC reports of the developing countries. Moreover, the time series back in time to 1970 provides for the UNFCCC trends a historic perspective. As part of our objective to contribute to more reliable inventories by providing a reference emissions database for emission scenarios, inventory comparisons and for atmospheric modellers, we strive to transparently document all data sources used and assumptions made where data was missing, in particular for assumptions made on the shares of

  11. Applications of advanced kinetic collisional radiative modeling and Bremsstrahlung emission to quantitative impurity analysis on the National Spherical Torus Experiment

    NASA Astrophysics Data System (ADS)

    Muñoz Burgos, J. M.; Tritz, K.; Stutman, D.; Bell, R. E.; LeBlanc, B. P.; Sabbagh, S. A.

    2015-12-01

    An advanced kinetic collisional radiative model is used to predict beam into plasma charge-exchange visible and extreme UV (XUV ∽ 50 -700 Å ) light emission to quantify impurity density profiles on NSTX. This kinetic model is first benchmarked by predicting line-of-sight integrated emission for the visible λ = 5292.0 Å line of carbon (C VI n = 8 → 7), and comparing these predictions to absolute calibrated measurements from the active CHarge-Exchange Recombination Spectroscopy diagnostic (CHERS) on NSTX. Once benchmarked, the model is used to predict charge-exchange emission for the 182.1 Å line of carbon (C VI n = 3 → 2) that is used to scale Bremsstrahlung continuum emission in the UV/XUV region. The scaled Bremsstrahlung emission is used as a base to estimate an absolute intensity calibration curve of a XUV Transmission Grating-based Imaging Spectrometer (TGIS) diagnostic installed on the National Spherical Torus Experiment (NSTX and upgrade NSTX-U). The TGIS diagnostic operates in the wavelength region ∽ 50 -700 Å , and it is used to measure impurity spectra from charge-exchange emission. Impurity densities are estimated by fitting synthetic emission from the kinetic charge-exchange model to TGIS spectral measurements.

  12. 76 FR 15266 - National Emission Standards for Hazardous Air Pollutants; Notice of Reconsideration

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-21

    ... standards of performance for new Commercial and ] Industrial Solid Waste Incineration Units and emission guidelines for existing Commercial and Industrial Solid Waste Incineration Units published as final rules... Sources and Emission Guidelines for Existing Sources: Commercial and Industrial Solid Waste...

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

    SciTech Connect

    Dibley, V. R., LLNL

    1998-02-01

    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.

  14. Nevada Test Site National Emission Standards for Hazardous Air Pollutants Calendar Year 2008

    SciTech Connect

    Ronald Warren and Robert F. Grossman

    2009-06-30

    The Nevada Test Site (NTS) is operated by the U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office. From 1951 through 1992, the NTS was the continental testing location for U.S. nuclear weapons. The release of radionuclides from NTS activities has been monitored since the initiation of atmospheric testing. Limitation to under-ground detonations after 1962 greatly reduced radiation exposure to the public surrounding the NTS. After nuclear testing ended in 1992, NTS radiation monitoring focused on detecting airborne radionuclides from historically contaminated soils. These radionuclides are derived from re-suspension of soil (primarily by winds) and emission of tritium-contaminated soil moisture through evapotranspiration. Low amounts of tritium were also emitted to air at the North Las Vegas Facility (NLVF), an NTS support complex in the city of North Las Vegas. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) (CFR, 2008a) limits the release of radioactivity from a U.S. Department of Energy facility (e.g., the NTS) to 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This limit does not include radiation not related to NTS activities. Unrelated doses could come from naturally occurring radioactive elements or from other man-made sources such as medical treatments. The NTS demonstrates compliance with the NESHAP limit by using environmental measurements of radionuclide air concentrations at critical receptor locations. This method was approved by the U.S. Environmental Protection Agency for use on the NTS in 2001 and has been the sole method used since 2005. Six locations on the NTS have been established to act as critical receptor locations to demonstrate compliance with the NESHAP limit. These locations are actually pseudo

  15. Producing remote sensing-based emission estimates of prescribed burning in the contiguous United States for the U.S. Environmental Protection Agency 2011 National Emissions Inventory

    NASA Astrophysics Data System (ADS)

    McCarty, J. L.; Pouliot, G. A.; Soja, A. J.; Miller, M. E.; Rao, T.

    2013-12-01

    Prescribed fires in agricultural landscapes generally produce smaller burned areas than wildland fires but are important contributors to emissions impacting air quality and human health. Currently, there are a variety of available satellite-based estimates of crop residue burning, including the NOAA/NESDIS Hazard Mapping System (HMS) the Satellite Mapping Automated Reanalysis Tool for Fire Incident Reconciliation (SMARTFIRE 2), the Moderate Resolution Imaging Spectroradiometer (MODIS) Official Burned Area Product (MCD45A1)), the MODIS Direct Broadcast Burned Area Product (MCD64A1) the MODIS Active Fire Product (MCD14ML), and a regionally-tuned 8-day cropland differenced Normalized Burn Ratio product for the contiguous U.S. The purpose of this NASA-funded research was to refine the regionally-tuned product utilizing higher spatial resolution crop type data from the USDA NASS Cropland Data Layer and burned area training data from field work and high resolution commercial satellite data to improve the U.S. Environmental Protection Agency's (EPA) National Emissions Inventory (NEI). The final product delivered to the EPA included a detailed database of 25 different atmospheric emissions at the county level, emission distributions by crop type and seasonality, and GIS data. The resulting emission databases were shared with the U.S. EPA and regional offices, the National Wildfire Coordinating Group (NWGC) Smoke Committee, and all 48 states in the contiguous U.S., with detailed error estimations for Wyoming and Indiana and detailed analyses of results for Florida, Minnesota, North Dakota, Oklahoma, and Oregon. This work also provided opportunities in discovering the different needs of federal and state partners, including the various geospatial abilities and platforms across the many users and how to incorporate expert air quality, policy, and land management knowledge into quantitative earth observation-based estimations of prescribed fire emissions. Finally, this work

  16. Mitigation of agricultural emissions in the tropics: comparing forest land-sparing options at the national level

    NASA Astrophysics Data System (ADS)

    Carter, S.; Herold, M.; Rufino, M. C.; Neumann, K.; Kooistra, L.; Verchot, L.

    2015-08-01

    Emissions from agriculture-driven deforestation are of global concern, but forest land-sparing interventions such as agricultural intensification and utilization of available non-forest land offer opportunities for mitigation. In many tropical countries, where agriculture is the major driver of deforestation, interventions in the agriculture sector could reduce deforestation emissions as well as reduce emissions in the agriculture sector. Our study uses a novel approach to quantify agriculture-driven deforestation and associated emissions in the tropics between 2000 and 2010. Emissions from agriculture-driven deforestation in the tropics (97 countries) are 4.3 GtCO2e yr-1. We investigate the national potential to mitigate these emissions through forest land-sparing interventions, which can potentially be implemented under REDD+. We consider intensification and utilization of available non-forested land as forest land-sparing opportunities since they avoid the expansion of agriculture into forested land. In addition, we assess the potential to reduce agricultural emissions on existing agriculture land. The use of a systematic framework demonstrates the selection of mitigation interventions by considering sequentially the level of emissions, mitigation potential of various interventions, enabling environment and associated risks to livelihoods at the national level. Our results show that considering only countries with high emissions from agriculture-driven deforestation, with potential for forest-sparing interventions and a good enabling environment (e.g. effective governance or engagement in REDD+), there is a potential to mitigate 1.3 GtCO2e yr-1 (20 countries of 78 with sufficient data). For countries where we identify agricultural emissions as a priority for mitigation, up to 1 GtCO2e yr-1 could be reduced from the agriculture sector including livestock. Risks to livelihoods from implementing interventions based on national level data call for detailed

  17. Nevada Test Site National Emission Standards for Hazardous Air Pollutants Calendar Year 2007

    SciTech Connect

    Robert Grossman; Ronald Warren

    2008-06-01

    The Nevada Test Site (NTS) is operated by the U.S. Department of Energy, National Nuclear Security Administration Nevada Site Office. From 1951 through 1992, the NTS was operated as the nation's site for nuclear weapons testing. The release of man-made radionuclides from the NTS as a result of testing activities has been monitored since the first decade of atmospheric testing. After 1962, when nuclear tests were conducted only underground, the radiation exposure to the public surrounding the NTS was greatly reduced. After the 1992 moratorium on nuclear testing, radiation monitoring on the NTS focused on detecting airborne radionuclides which come from historically contaminated soils resuspended into the air (e.g., by winds) and tritium-contaminated soil moisture emitted to the air from soils through evapotranspiration. To protect the public from harmful levels of man-made radiation, the Clean Air Act, National Emission Standards for Hazardous Air Pollutants (NESHAP) (Title 40 Code of Federal Regulations [CFR] Part 61 Subpart H) limits the release of radioactivity from a U.S. Department of Energy facility (e.g., the NTS) to 10 millirem per year (mrem/yr) effective dose equivalent to any member of the public. This is the dose limit established for someone living off of the NTS from radionuclides emitted to air from the NTS. This limit does not include the radiation doses that members of the public may receive through the intake of radioactive particles unrelated to NTS activities, such as those that come from naturally occurring elements in the environment (e.g., naturally occurring radionuclides in soil or radon gas from the earth or natural building materials), or from other man-made sources (e.g., medical treatments). The NTS demonstrates compliance using environmental measurements of radionuclide air concentrations at critical receptor locations. This method was approved by the U.S. Environmental Protection Agency for use on the NTS in 2001 and has been the sole

  18. Development of a national estimate of methane emissions from United States natural gas gathering facilities and processing plants

    NASA Astrophysics Data System (ADS)

    Marchese, A. J.; Robinson, A. L.; Zimmerle, D.; Vaughn, T. L.; Martinez, D. M.; Williams, L.; Mitchell, A.; Subramanian, R.; Roscioli, J. R.; Herndon, S. C.

    2015-12-01

    New facility-level methane emissions measurements obtained from 114 natural gas gathering facilities and 16 processing plants in 13 U.S. states were combined with facility counts obtained from state and national databases in a Monte Carlo simulation to estimate methane emissions from U.S. natural gas gathering and processing operations. Total annual methane emissions of 2,421 (+245/-237) Gg were estimated for all U.S. gathering and processing operations, representing a methane loss rate of 0.47% (±0.05%) when normalized by 2012 CH4 production. The largest source of emissions from gathering and processing operations were attributed to normal operation of gathering facilities (1,697 +189/-185 Gg). The methane emissions from processing plants (506 +55/-52 Gg) was 40% lower than the 2014 EPA Greenhouse Gas Inventory (GHGI) estimate but a factor of three higher than that reported under the EPA Greenhouse Gas Reporting Program. Since gathering operations are currently embedded within the production segment of the EPA GHGI, field observations equipment counts at gathering facilities were used to estimate the fraction of the methane emissions in the EPA production inventory to assign to gathering facilities. Based on this analysis, the study results suggest that methane emissions from gathering facilities could be as high as eight times that of the EPA GHGI estimate. Because methane emissions from most gathering facilities are not reported under the current rule and not all source categories are reported for processing plants, the total CH4 emissions from gathering and processing reported under the EPA GHGRP (180 Gg) represents only 14% of that tabulated in the EPA GHGI and 7% of that predicted from this study.

  19. Quantifying methane and nitrous oxide emissions from the UK and Ireland using a national-scale monitoring network

    NASA Astrophysics Data System (ADS)

    Ganesan, A. L.; Manning, A. J.; Grant, A.; Young, D.; Oram, D. E.; Sturges, W. T.; Moncrieff, J. B.; O'Doherty, S.

    2015-06-01

    The UK is one of several countries around the world that has enacted legislation to reduce its greenhouse gas emissions. In this study, we present top-down emissions of methane (CH4) and nitrous oxide (N2O) for the UK and Ireland over the period August~2012 to August~2014. These emissions were inferred using measurements from a network of four sites around the two countries. We used a hierarchical Bayesian inverse framework to infer fluxes as well as a set of covariance parameters that describe uncertainties in the system. We inferred average UK total emissions of 2.09 (1.65-2.67) Tg yr-1 CH4 and 0.101 (0.068-0.150) Tg yr-1 N2O and found our derived UK estimates to be generally lower than the a priori emissions, which consisted primarily of anthropogenic sources and with a smaller contribution from natural sources. We used sectoral distributions from the UK National Atmospheric Emissions Inventory (NAEI) to determine whether these discrepancies can be attributed to specific source sectors. Because of the distinct distributions of the two dominant CH4 emissions sectors in the UK, agriculture and waste, we found that the inventory may be overestimated in agricultural CH4 emissions. We found that annual mean N2O emissions were consistent with both the prior and the anthropogenic inventory but we derived a significant seasonal cycle in emissions. This seasonality is likely due to seasonality in fertilizer application and in environmental drivers such as temperature and rainfall, which are not reflected in the annual resolution inventory. Through the hierarchical Bayesian inverse framework, we quantified uncertainty covariance parameters and emphasized their importance for high-resolution emissions estimation. We inferred average model errors of approximately 20 and 0.4 ppb and correlation timescales of 1.0 (0.72-1.43) and 2.6 (1.9-3.9) days for CH4 and N2O, respectively. These errors are a combination of transport model errors as well as errors due to unresolved

  20. Long-term trends in nitrogen oxide emissions from motor vehicles at national, state, and air basin scales

    NASA Astrophysics Data System (ADS)

    McDonald, Brian C.; Dallmann, Timothy R.; Martin, Elliot W.; Harley, Robert A.

    2011-11-01

    A fuel-based approach is used to estimate nitrogen oxides (NOx = NO + NO2) emissions from gasoline- and diesel-powered motor vehicles. Estimates are made at the national level for the period 1990-2010. Vehicle emissions are also estimated at the state level for California, and for the South Coast (Los Angeles) and San Joaquin Valley air basins. Fuel-based emission estimates are compared with predictions from widely used emission inventory models. Changes in diesel NOxemissions vary over time: increasing between 1990 and 1997, stable between 1997 and 2007, and decreasing since 2007. In contrast, gasoline engine-related NOxemissions have decreased steadily, by ˜65% overall between 1990 and 2010, except in the San Joaquin Valley, where reductions were not as large due to faster population growth. In the San Joaquin Valley, diesel engines were the dominant on-road NOxsource in all years considered (reaching ˜70% in 2010). In the urbanized South Coast air basin, gasoline engine emissions dominated in the past and have been comparable to on-road diesel sources since 2007 (down from ˜75% in 1990). Other major anthropogenic sources of NOxare added to compare emission trends with trends in surface pollutant observations and satellite-derived data. When all major anthropogenic NOx sources are included, the overall emission trend is downward in all cases (-45% to -60%). Future reductions in motor vehicle NOxwill depend on the effectiveness of new exhaust after-treatment controls on heavy-duty trucks, as well as further improvements todurabilityof emission control systems on light-duty vehicles.

  1. Long-term trends in nitrogen oxide emissions from motor vehicles at national, state, and air basin scales

    NASA Astrophysics Data System (ADS)

    McDonald, Brian C.; Dallmann, Timothy R.; Martin, Elliot W.; Harley, Robert A.

    2012-09-01

    A fuel-based approach is used to estimate nitrogen oxides (NOx = NO + NO2) emissions from gasoline- and diesel-powered motor vehicles. Estimates are made at the national level for the period 1990-2010. Vehicle emissions are also estimated at the state level for California, and for the South Coast (Los Angeles) and San Joaquin Valley air basins. Fuel-based emission estimates are compared with predictions from widely used emission inventory models. Changes in diesel NOxemissions vary over time: increasing between 1990 and 1997, stable between 1997 and 2007, and decreasing since 2007. In contrast, gasoline engine-related NOxemissions have decreased steadily, by ˜65% overall between 1990 and 2010, except in the San Joaquin Valley, where reductions were not as large due to faster population growth. In the San Joaquin Valley, diesel engines were the dominant on-road NOxsource in all years considered (reaching ˜70% in 2010). In the urbanized South Coast air basin, gasoline engine emissions dominated in the past and have been comparable to on-road diesel sources since 2007 (down from ˜75% in 1990). Other major anthropogenic sources of NOxare added to compare emission trends with trends in surface pollutant observations and satellite-derived data. When all major anthropogenic NOx sources are included, the overall emission trend is downward in all cases (-45% to -60%). Future reductions in motor vehicle NOxwill depend on the effectiveness of new exhaust after-treatment controls on heavy-duty trucks, as well as further improvements todurabilityof emission control systems on light-duty vehicles.

  2. Estimation of the carbon monoxide emissions due to Sandia National Laboratories commuter and on-base traffic for conformity determination

    SciTech Connect

    McClellan, Y.; Royer, R.

    1996-09-01

    This report describes the analysis and conclusion of an investigation of the carbon monoxide emissions resulting from Sandia National Laboratories and Department of Energy (DOE) commuter and on-base traffic for the Clean Air Act (CAA) Conformity Determination. Albuquerque/Bernalillo County was classified as a nonattainment area by the Environmental Protection Agency. Nonattainment area is an area which is shown by monitored data or which is calculated by air quality modeling to exceed any National Ambient Air Quality Standard (NAAQS) for the pollutant. Albuquerque/Bernalillo County exceeds the NAAQS for carbon monoxide and ozone. The Conformity Determination was needed to complete the CAA Title V Permitting process for SNL and the DOE. The analysis used the EPA approved MOBILE5a Carbon Monoxide (CO) emissions modeling program. This analysis will provide a baseline for mobile sources to allow Sandia to estimate any future activity and how that activity will impact CO emissions. The General Conformity Rule (AQCR 43) requires that operations which will increase CO emissions in nonattaimnent or maintenance areas such as Bernalillo County undergo conformity analyses to determine whether or not they will impact ambient air quality in the area.

  3. Verification of national halogenated greenhouse gas emissions in Europe using top-down estimates inferred from ambient air measurements

    NASA Astrophysics Data System (ADS)

    Brunner, D.; Keller, C. A.; Vollmer, M. K.; Reimann, S.; O'Doherty, S.

    2010-12-01

    To check for compliance with the reduction targets defined under the Kyoto protocol, each country has to report its greenhouse gas emissions to the UNFCCC (United Nations Framework Convention on Climate Change). These emissions are calculated using a bottom-up approach, by combining categories of com-pound use with specific activity functions and using import/export statistics. The uncertainties of these estimates are not well defined, thereby making an independent validation of the reported emissions highly desirable. In this study, a novel Kalman filter inversion technique was implemented to estimate European emissions of halogenated greenhouse gases including hydrofluorocarbons (HFC), perfluorocarbons (PFC) and SF6. The inversion is based on high-frequency measurements at two European background sites (Jungfraujoch and Mace Head) coupled to backward simulations from the Lagrangian particle dispersion model FLEXPART. The sequential nature of the inversion approach allows tracing slow seasonal and interannual emission changes. Furthermore, by including the estimation of a smoothly varying concentration background into the inversion, potential inconsistencies introduced by independent background subtraction methods are avoided. Further advantages are the applicability to a potentially large number of receptor (measurement) locations and the quantification of uncertainties along with absolute emissions. Annual emissions were estimated for the years 2006 to 2009 on a country-by-country basis and compared with numbers reported to the UNFCCC. Good agreement was found for HFC-134a and HFC-125, which are ubiquitously used for refrigeration and air conditioning. Much higher emissions than reported, however, were estimated for HFC-23, a potent greenhouse gas with a 100-yr global warming potential of 14’800. HFC-23 is an unintentional by-product of HCFC-22 manufacture and our source attribution reveals significant contributions from HCFC-22 production plants in Italy

  4. 77 FR 60341 - National Emission Standards for Hazardous Air Pollutants for Reciprocating Internal Combustion...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-10-03

    ... Source Performance Standards for Stationary Internal Combustion Engines'' (77 FR 33812). The June 7, 2012... Reciprocating Internal Combustion Engines; New Source Performance Standards for Stationary Internal Combustion... Emission Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal......

  5. 77 FR 36248 - National Uniform Emission Standards for Storage Vessel and Transfer Operations, Equipment Leaks...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-06-18

    ... Uniform Emission Standards General Provisions, was published on March 26, 2012 (77 FR 17898). The EPA has... for this extension from the American Petroleum Institute (API) and the American Chemistry Council...

  6. Development of an air emissions inventory for Oak Ridge National Laboratory

    SciTech Connect

    Skipper, D.D.

    1996-08-01

    Accurate air emissions inventory is important in an effective Clean Air Act (CAA) compliance program; without it, a facility may have difficulty proving compliance with regulations or permit conditions. An emissions inventory can also serve for evaluating the applicability of new regulations (eg, Title V of CAA) and in complying with them. Therefore it is important for the inventory to be well-planned and comprehensive. Preparation of an emissions inventory for a large R&D facility such as ORNL can be a challenging task. ORNL, a government facility managed by Lockheed Martin Energy Research Corp. for US DOE, consists of more than 300 buildings on about 1,500 acres. It has several thousand diverse emission sources, including small laboratory hoods, several wastewater treatment facilities, and a steam plant. This paper describes the development of ORNL`s emissions inventory with emphasis on setting goals and identifying the scope of the inventory, identifying the emission points, developing/implementing the inventory methodology, compiling data, and evaluating the results.

  7. Estimating national landfill methane emissions: an application of the 2006 Intergovernmental Panel on Climate Change Waste Model in Panama.

    PubMed

    Weitz, Melissa; Coburn, Jeffrey B; Salinas, Edgar

    2008-05-01

    This paper estimates national methane emissions from solid waste disposal sites in Panama over the time period 1990-2020 using both the 2006 Intergovernmental Panel on Climate Change (IPCC) Waste Model spreadsheet and the default emissions estimate approach presented in the 1996 IPCC Good Practice Guidelines. The IPCC Waste Model has the ability to calculate emissions from a variety of solid waste disposal site types, taking into account country- or region-specific waste composition and climate information, and can be used with a limited amount of data. Countries with detailed data can also run the model with country-specific values. The paper discusses methane emissions from solid waste disposal; explains the differences between the two methodologies in terms of data needs, assumptions, and results; describes solid waste disposal circumstances in Panama; and presents the results of this analysis. It also demonstrates the Waste Model's ability to incorporate landfill gas recovery data and to make projections. The former default method methane emissions estimates are 25 Gg in 1994, and range from 23.1 Gg in 1990 to a projected 37.5 Gg in 2020. The Waste Model estimates are 26.7 Gg in 1994, ranging from 24.6 Gg in 1990 to 41.6 Gg in 2020. Emissions estimates for Panama produced by the new model were, on average, 8% higher than estimates produced by the former default methodology. The increased estimate can be attributed to the inclusion of all solid waste disposal in Panama (as opposed to only disposal in managed landfills), but the increase was offset somewhat by the different default factors and regional waste values between the 1996 and 2006 IPCC guidelines, and the use of the first-order decay model with a time delay for waste degradation in the IPCC Waste Model. PMID:18512440

  8. Estimating national landfill methane emissions: an application of the 2006 Intergovernmental Panel on Climate Change Waste Model in Panama.

    PubMed

    Weitz, Melissa; Coburn, Jeffrey B; Salinas, Edgar

    2008-05-01

    This paper estimates national methane emissions from solid waste disposal sites in Panama over the time period 1990-2020 using both the 2006 Intergovernmental Panel on Climate Change (IPCC) Waste Model spreadsheet and the default emissions estimate approach presented in the 1996 IPCC Good Practice Guidelines. The IPCC Waste Model has the ability to calculate emissions from a variety of solid waste disposal site types, taking into account country- or region-specific waste composition and climate information, and can be used with a limited amount of data. Countries with detailed data can also run the model with country-specific values. The paper discusses methane emissions from solid waste disposal; explains the differences between the two methodologies in terms of data needs, assumptions, and results; describes solid waste disposal circumstances in Panama; and presents the results of this analysis. It also demonstrates the Waste Model's ability to incorporate landfill gas recovery data and to make projections. The former default method methane emissions estimates are 25 Gg in 1994, and range from 23.1 Gg in 1990 to a projected 37.5 Gg in 2020. The Waste Model estimates are 26.7 Gg in 1994, ranging from 24.6 Gg in 1990 to 41.6 Gg in 2020. Emissions estimates for Panama produced by the new model were, on average, 8% higher than estimates produced by the former default methodology. The increased estimate can be attributed to the inclusion of all solid waste disposal in Panama (as opposed to only disposal in managed landfills), but the increase was offset somewhat by the different default factors and regional waste values between the 1996 and 2006 IPCC guidelines, and the use of the first-order decay model with a time delay for waste degradation in the IPCC Waste Model.

  9. MercNet: A national monitoring network to assess responses to changing mercury emissions in the United States

    USGS Publications Warehouse

    Schmeltz, D.; Evers, D.C.; Driscoll, C.T.; Artz, R.; Cohen, M.; Gay, D.; Haeuber, R.; Krabbenhoft, D.P.; Mason, R.; Morris, K.; Wiener, J.G.

    2011-01-01

    A partnership of federal and state agencies, tribes, industry, and scientists from academic research and environmental organizations is establishing a national, policy-relevant mercury monitoring network, called MercNet, to address key questions concerning changes in anthropogenic mercury emissions and deposition, associated linkages to ecosystem effects, and recovery from mercury contamination. This network would quantify mercury in the atmosphere, land, water, and biota in terrestrial, freshwater, and coastal ecosystems to provide a national scientific capability for evaluating the benefits and effectiveness of emission controls. Program development began with two workshops, convened to establish network goals, to select key indicators for monitoring, to propose a geographic network of monitoring sites, and to design a monitoring plan. MercNet relies strongly on multi-institutional partnerships to secure the capabilities and comprehensive data that are needed to develop, calibrate, and refine predictive mercury models and to guide effective management. Ongoing collaborative efforts include the: (1) development of regional multi-media databases on mercury in the Laurentian Great Lakes, northeastern United States, and eastern Canada; (2) syntheses and reporting of these data for the scientific and policy communities; and (3) evaluation of potential monitoring sites. The MercNet approach could be applied to the development of other monitoring programs, such as emerging efforts to monitor and assess global mercury emission controls. ?? 2011 Springer Science+Business Media, LLC (outside the USA).

  10. National Acid Precipitation Assessment Program (NAPAP) Interim Assessment: the causes and effects of acidic deposition. Volume 2. Emissions and control

    SciTech Connect

    Not Available

    1987-01-01

    This volume on Emissions and Controls is the second in a four-volume set which comprises the NAPAP Interim Assessment. It contains three chapters, (1) Historical Emissions, (2) Emission Control Technologies, and (3) Future Emissions. Volume III, Atmospheric Processes and Deposition, contains chapters on (4) Atmospheric Processes, and (5) Acidic Deposition and Air Quality. The last volume, entitled, Effects of Acidic Deposition, covers (6) Agricultural Crops, (7) Forests, (8) Aquatics Systems, (9) 'Materials, and (10) Human Health and Visibility. Each of these chapters describes the National Program's research orientation and major conclusions within each of the ten primary areas of substantive concern. In order to learn how these first-order conclusions relate to the issue of acidic deposition in an overall, or synoptic, sense, the reader is directed to Volume I, Executive Summary, where the conclusions from each of the ten chapters are distilled in a manner that will allow interested parties to quickly reference the status of a variety of factors that pertain to the scientific understanding of acidic deposition.

  11. Determining national greenhouse gas emissions from waste-to-energy using the Balance Method.

    PubMed

    Schwarzböck, Therese; Rechberger, Helmut; Cencic, Oliver; Fellner, Johann

    2016-03-01

    Different directives of the European Union require operators of waste-to-energy (WTE) plants to report the amount of electricity that is produced from biomass in the waste feed, as well as the amount of fossil CO2 emissions generated by the combustion of fossil waste materials. This paper describes the application of the Balance Method for determining the overall amount of fossil and thus climate relevant CO2 emissions from waste incineration in Austria. The results of 10 Austrian WTE plants (annual waste throughput of around 2,300 kt) demonstrate large seasonal variations in the specific fossil CO2 emissions of the plants as well as large differences between the facilities (annual means range from 32±2 to 51±3 kg CO(2,foss)/GJ heating value). An overall amount of around 924 kt/yr of fossil CO2 for all 10 WTE plants is determined. In comparison biogenic (climate neutral) CO2 emissions amount to 1,187 kt/yr, which corresponds to 56% of the total CO2 emissions from waste incineration. The total energy input via waste feed to the 10 facilities is about 22,500 TJ/yr, of which around 48% can be assigned to biogenic and thus renewable sources.

  12. NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS (NESHAP) SUBPART H RADIONUCLIDES POTENTIAL TO EMIT CALCULATIONS

    SciTech Connect

    EARLEY JN

    2008-07-23

    This document provides an update of the status of stacks on the Hanford Site and the potential radionuclide emissions, i.e., emissions that could occur with no control devices in place. This review shows the calculations that determined whether the total effective dose equivalent (TEDE) received by the maximum public receptor as a result of potential emissions from any one of these stacks would exceed 0.1 millirem/year. Such stacks require continuous monitoring of the effluent, or other monitoring, to meet the requirements of Washington Administrative code (WAC) 246-247-035(1)(a)(ii) and WAC 246-247-075(1), -(2), and -(6). This revised update reviews the potential-to-emit (PTE) calculations of 31 stacks for Fluor Hanford, Inc. Of those 31 stacks, 11 have the potential to cause a TEDE greater than 0.1 mrem/year.

  13. Hanford Site radionuclide national emission standards for hazardous air pollutants registered stack source assessment

    SciTech Connect

    Davis, W.E.; Barnett, J.M.

    1994-07-01

    On February 3, 1993, the US Department of Energy, Richland Operations Office received a Compliance Order and Information Request from the Director of the Air and Toxics Division of the US Environmental Protection Agency,, Region 10. The Compliance Order requires the Richland Operations Office to evaluate all radionuclide emission points at the Hanford Site . The evaluation also determined if the effective dose equivalent from any of these stack emissions exceeded 0.1 mrem/yr, which will require the stack to have continuous monitoring. The result of this assessment identified a total of 16 stacks as having potential emissions that,would cause an effective dose equivalent greater than 0.1 mrem/yr.

  14. Effects of the updated national emission regulation in China on circulating fluidized bed boilers and the solutions to meet them.

    PubMed

    Li, Jingji; Yang, Hairui; Wu, Yuxin; Lv, Junfu; Yue, Guangxi

    2013-06-18

    The advantage of circulating fluidized bed (CFB) boilers in China is their ability to utilize low rank coal with low cost emission control. However, the new National Emission Regulation (NER) issued in early 2012 brings much more stringent challenges on the CFB industries, which also causes much attention from other countries. Based on the principle of a CFB boiler and previous operating experience, it is possible for the CFB boilers to meet the new NER and maintain the advantage of low cost emission control, while, more influences should be considered in their design and operation. To meet the requirement of the new NER, the fly ash collector should adopt a bag house or combination of electrostatic precipitator and bag filter to ensure dust emissions of less than 30 mg · Nm(-3). For SO2 emission control, the bed temperature should be strictly lower than 900 °C to maintain high reactivity and pores. The limestone particle size distribution should be ranged within a special scope to optimize the residence time and gas-solid reaction. At the same time, the injecting point should be optimized to ensure fast contact of lime with oxygen. In such conditions, the desulfurization efficiency could be increased more than 90%. For lower sulfur content fuels (<1.5%, referred value based on the heating value of standard coal of China), increasing Ca/S enough could decrease SO2 emissions lower than that of the new NER, 100 mg · Nm(-3). For fuels with sulfur content higher than 1.5%, some simplified systems for flue gas desulfurization, such as flash dryer absorber (FDA), are needed. And the NOx emissions of a CFB can be controlled to less than 100 mg · Nm(-3) without any equipment at a bed temperature lower than 900 °C for fuels with low volatiles content (<12%), while for fuels with high volatiles, selective non-catalytic reduction (SNCR) should be considered. Due to the unique temperature in CFB as well as the circulating ash, the efficiency of SNCR could reach as high as

  15. Comparing two national datasets of CO2 Emissions for U.S. Powerplants

    NASA Astrophysics Data System (ADS)

    Huang, J.; Gurney, K. R.

    2011-12-01

    Fossil fuel CO2 emissions from powerplants account for about 40% of total U.S. fossil fuel CO2 emissions. The Energy Information Administration (EIA) Data and Clean Air Markets Data (CAMD) are two major primary power-plant CO2 emission datasets. EIA calculates CO2 emission by multiplying the heat input with CO2 emission factors. The CAMD dataset, by contrast, includes a mixture of measurement/calculation methods. The different measurement/calculation approaches in the two datasets generates differences at each emitting facility. The relative population difference over the last ten years between CAMD and EIA is 0.24% for all of the matched plants, 0.51% for NCHP (non-combined heat/power facilities), and -5.47% for CHP (combined heat/power facilities). Exploring the difference at the plant level (using 2007 as an example), we find that for both NCHP and CHP, the absolute emission differences are dominated by the very large powerplants. However, when these differences are represented as a percent of powerplant size, the small powerplants have proportionally larger biases (Fig 1). The hourly CAMD data and monthly EIA data also allows us to explore the elements that cause the emissions bias. From the CAMD data, we find that multiple measurement/calculation methods are employed during the year, which falls into six flagged categories. With about 1000 matched power plants between the two datasets, we can build a regression model to explore the relationships between the emissions differences and the measurement/calculation flag. Again taking 2007 as an example year, we find that if the CAMD data is "measured", it will be 0.6% lower than EIA data; if the CAMD data is "substituted", it will be 21.9% higher; if the data is "undetermined", it will be 2.5% higher. Because EIA provides the monthly heat input data by plant and fuel type, we can also build the regression model as a function of fuel type. We find that the burning of bituminous coal results in the CAMD data emitting

  16. Assessing Satellite-based Fire Data for use in the National Emissions Inventory

    EPA Science Inventory

    Biomass burning is significant to emission estimated because: (1) it can be a major contributor of particulate matter and other pollutants; (2) it is one of the most poorly documented of all sources; (3) it can adversely affect human health; and (4) it has been identified as a si...

  17. 75 FR 32005 - National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-04

    ... section 112(c)(6) due to emissions of polycyclic organic matter (POM) and mercury (63 FR 17838, 17848... vacated the Commercial and Industrial Solid Waste Incineration (CISWI) Definitions Rule, 70 FR 55568... Advance Notice of Proposed Rulemaking (74 FR 41, January 2, 2009) soliciting comment on whether...

  18. 75 FR 32682 - National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-06-09

    ... the deadline for written comments on the proposed rules (75 FR 32006 (major source boilers), 75 FR 31896 (area source boilers), 75 FR 31938 (CISWI), and 75 FR 31844 (waste definition)) to August 3, 2010... New Stationary Sources and Emission Guidelines for Existing Sources: Commercial and Industrial...

  19. Building capacity for national carbon measurements for reducing emissions from deforestation and forest degradation

    NASA Astrophysics Data System (ADS)

    Goetz, S. J.; Laporte, N.; Horning, N.; Pelletier, J.; Jantz, P.; Ndunda, P.

    2014-12-01

    Many tropical countries are now working on developing their strategies for reducing emissions from deforestation and forest degradation, including activities that result in conservation or enhancement of forest carbon stocks and sustainable management of forests to effectively decrease atmospheric carbon emissions (i.e. REDD+). A new international REDD+ agreement is at the heart of recent negotiations of the parties to the UN Framework Convention on Climate Change (UNFCCC). REDD+ mechanisms could provide an opportunity to not only diminish an important source of emissions, but also to promote large-scale conservation of tropical forests and establish incentives and opportunities to alleviate poverty. Most tropical countries still lack basic information for developing and implementing their forest carbon stock assessments, including the extent of forest area and the rate at which forests are being cleared and/or degraded, and the carbon amounts associated with these losses. These same countries also need support to conduct integrated assessments of the most promising approaches for reducing emissions, and in identifying those policy options that hold the greatest potential while minimizing potential negative impacts of REDD+ policies. The WHRC SERVIR project in East Africa is helping to provide these data sets to countries via best practice tools and methods to support cost effective forest carbon monitoring solutions and more informed decision making processes under REDD+. We will present the results of our capacity building activites in the region and planned future efforts being coordinated with the NASA-SERVIR Hub in Kenya to support to REDD+ decision support.

  20. 76 FR 28318 - National Emission Standards for Hazardous Air Pollutants From the Portland Cement Manufacturing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-17

    ... emission limits applicable to the Portland cement industry. See 75 FR 54970 (Sept. 9, 2010). The rule... Clean Air Act, 75 FR 49556, 49561 (Aug. 13, 2010). This interpretation is appropriate in light of the... see 75 FR 49556, 49560-49563 (August 13, 2010) and 76 FR 4780, 4786-4788 (January 26, 2011). II....

  1. 75 FR 54969 - National Emission Standards for Hazardous Air Pollutants From the Portland Cement Manufacturing...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-09

    ... requirements through the Integrated Urban Air Toxics Strategy (64 FR 38715, July 19, 1999).\\2\\ \\1\\ An area... Industry (64 FR 31898, June 14, 1999) included emission limits based on performance of MACT for the control... of CAA section 112(c)(6), we set MACT standards for these pollutants. 63 FR 17838, 17848, April...

  2. 76 FR 15607 - National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-03-21

    ... pursuant to CAA section 112(c)(6) due to emissions of POM and Hg (63 FR 17838, 17848, April 10, 1998). In... Commercial and Industrial Solid Waste Incineration (CISWI) Definitions Rule, 70 FR 55568 (September 22, 2005... rule. See 75 FR 32009. CAA section 129 covers any facility that combusts any solid waste; CAA...

  3. 78 FR 6673 - National Emission Standards for Hazardous Air Pollutants for Reciprocating Internal Combustion...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-30

    ....melanie@epa.gov . SUPPLEMENTARY INFORMATION: Background Information Document. On June 7, 2012 (77 FR 33812... emissions in 2004 (69 FR 33473). The EPA addressed new stationary RICE less than or equal to 500 HP located at major sources and new stationary RICE located at area sources in 2008 (73 FR 3568). Most...

  4. 76 FR 80261 - National Emission Standards for Hazardous Air Pollutants: Area Source Standards for Prepared...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-12-23

    ... published on January 5, 2010, (75 FR 522) if adverse comments are received on this direct final rule. If we.... V. What amendments are being made to this rule? On January 5, 2010 (75 FR 522), the EPA promulgated... Air Pollutant (HAP) emissions control (75 FR 533). We added the 95-percent design...

  5. Investigation of EBW thermal emission and mode-conversion physics in the national spherical torus experiment

    NASA Astrophysics Data System (ADS)

    Diem, Stephanie Josephine

    2008-10-01

    NSTX is a spherical tokamak (ST) that operates with ne up to 1020 m-3 and BT less than 0.6 T, cutting off low harmonic electron cyclotron (EC) waves widely used for electron temperature measurements and EC heating and current drive in conventional aspect ratio tokamaks. The electron Bernstein wave (EBW) can propagate in ST plasmas and is readily absorbed and emitted at EC harmonics. Additionally, EBWs do not experience a density dependent cutoff. As such, EBWs may enable local electron temperature measurements and provide local electron heating and current drive. EBWs cannot propagate in vacuum but can couple to electromagnetic waves, so for these applications efficient coupling between the EBWs and electromagnetic waves outside the plasma is needed. In this thesis, EBW emission via the oblique double mode conversion process to the X- and O-modes (B-X-O) is measured with two remotely steered antennas located outside of the vacuum vessel. These emission measurements have been used to determine the EBW transmission efficiency for a wide range of plasma conditions. The antennas collect fundamental (8-18 GHz), second and third (18-40 GHz) harmonic emission. The remote steering capability allowed detailed measurements (as a function of toroidal and poloidal pointing angle) of the B-X-O transmission window. Peak L-mode B-X-O transmission efficiencies of 90% and 35% for fundamental and second harmonic emission, respectively, were measured. The measured and theoretical optimal pointing angles agreed within 5° of the simulated values. Evidence of strong EBW collisional damping near the fundamental and second harmonic B-X-O conversion region was observed in H-mode discharges, reducing the B-X-O transmission efficiency to nearly 0% in some cases. Edge conditioning, via Li evaporation, successfully reduced this EBW damping and increased transmission efficiencies to 50-60%, agreeing with EBW emission (EBE) simulations. These results provide experimental evidence supporting B

  6. National Emission Standard for Hazardous Air Pollutants compliance verification plan for the K-1435 Toxic Substances Control Act Incinerator

    SciTech Connect

    Ambrose, M.L.

    1986-07-28

    This documentation was prepared for submittal to the Environmental Protection Agency (EPA) in order to meet the requirements of the National Emissions Standards for Hazardous Air Pollutants (NESHAP). This document will emphasize the control of radioactive emissions from the K-1435 Toxic Substances Control Act (TSCA) Incinerator. The TSCA Incinerator is a dual purpose solid/liquid incinerator that is under construction at the Oak Ridge Gaseous Diffusion Plant to destroy radioactively contaminated polychlorinated biphenyls (PCBs) and other hazardous organic wastes in compliance with the TSCA and the Resource Conservation and Recovery Act (RCRA). These wastes are generated at the facilities managed by the Department of Energy, Oak Ridge Operations (DOE-ORO). Destruction of the PCBs and the hazardous organic wastes will be accomplished in a rotary kiln incinerator with an afterburner. The incinerator will thermally destroy the organic constituents of the liquids, solids, and sludges to produce an organically inert ash. In addition to the incinerator, an extensive off-gas treatment facility is being constructed to remove particulate and acidic gas air emissions.

  7. Estimates of global, regional, and national annual CO{sub 2} emissions from fossil-fuel burning, hydraulic cement production, and gas flaring: 1950--1992

    SciTech Connect

    Boden, T.A.; Marland, G.; Andres, R.J.

    1995-12-01

    This document describes the compilation, content, and format of the most comprehensive C0{sub 2}-emissions database currently available. The database includes global, regional, and national annual estimates of C0{sub 2} emissions resulting from fossil-fuel burning, cement manufacturing, and gas flaring in oil fields for 1950--92 as well as the energy production, consumption, and trade data used for these estimates. The methods of Marland and Rotty (1983) are used to calculate these emission estimates. For the first time, the methods and data used to calculate CO, emissions from gas flaring are presented. This C0{sub 2}-emissions database is useful for carbon-cycle research, provides estimates of the rate at which fossil-fuel combustion has released C0{sub 2} to the atmosphere, and offers baseline estimates for those countries compiling 1990 C0{sub 2}-emissions inventories.

  8. The Relationship between National-Level Carbon Dioxide Emissions and Population Size: An Assessment of Regional and Temporal Variation, 1960–2005

    PubMed Central

    Jorgenson, Andrew K.; Clark, Brett

    2013-01-01

    This study examines the regional and temporal differences in the statistical relationship between national-level carbon dioxide emissions and national-level population size. The authors analyze panel data from 1960 to 2005 for a diverse sample of nations, and employ descriptive statistics and rigorous panel regression modeling techniques. Initial descriptive analyses indicate that all regions experienced overall increases in carbon emissions and population size during the 45-year period of investigation, but with notable differences. For carbon emissions, the sample of countries in Asia experienced the largest percent increase, followed by countries in Latin America, Africa, and lastly the sample of relatively affluent countries in Europe, North America, and Oceania combined. For population size, the sample of countries in Africa experienced the largest percent increase, followed countries in Latin America, Asia, and the combined sample of countries in Europe, North America, and Oceania. Findings for two-way fixed effects panel regression elasticity models of national-level carbon emissions indicate that the estimated elasticity coefficient for population size is much smaller for nations in Africa than for nations in other regions of the world. Regarding potential temporal changes, from 1960 to 2005 the estimated elasticity coefficient for population size decreased by 25% for the sample of Africa countries, 14% for the sample of Asia countries, 6.5% for the sample of Latin America countries, but remained the same in size for the sample of countries in Europe, North America, and Oceania. Overall, while population size continues to be the primary driver of total national-level anthropogenic carbon dioxide emissions, the findings for this study highlight the need for future research and policies to recognize that the actual impacts of population size on national-level carbon emissions differ across both time and region. PMID:23437323

  9. Volatile emissions and gas geochemistry of Hot Spring Basin, Yellowstone National Park, USA

    USGS Publications Warehouse

    Werner, C.; Hurwitz, S.; Evans, William C.; Lowenstern, J. B.; Bergfeld, D.; Heasler, H.; Jaworowski, C.; Hunt, A.

    2008-01-01

    We characterize and quantify volatile emissions at Hot Spring Basin (HSB), a large acid-sulfate region that lies just outside the northeastern edge of the 640??ka Yellowstone Caldera. Relative to other thermal areas in Yellowstone, HSB gases are rich in He and H2, and mildly enriched in CH4 and H2S. Gas compositions are consistent with boiling directly off a deep geothermal liquid at depth as it migrates toward the surface. This fluid, and the gases evolved from it, carries geochemical signatures of magmatic volatiles and water-rock reactions with multiple crustal sources, including limestones or quartz-rich sediments with low K/U (or 40*Ar/4*He). Variations in gas chemistry across the region reflect reservoir heterogeneity and variable degrees of boiling. Gas-geothermometer temperatures approach 300????C and suggest that the reservoir feeding HSB is one of the hottest at Yellowstone. Diffuse CO2 flux in the western basin of HSB, as measured by accumulation-chamber methods, is similar in magnitude to other acid-sulfate areas of Yellowstone and is well correlated to shallow soil temperatures. The extrapolation of diffuse CO2 fluxes across all the thermal/altered area suggests that 410 ?? 140??t d- 1 CO2 are emitted at HSB (vent emissions not included). Diffuse fluxes of H2S were measured in Yellowstone for the first time and likely exceed 2.4??t d- 1 at HSB. Comparing estimates of the total estimated diffuse H2S emission to the amount of sulfur as SO42- in streams indicates ~ 50% of the original H2S in the gas emission is lost into shallow groundwater, precipitated as native sulfur, or vented through fumaroles. We estimate the heat output of HSB as ~ 140-370??MW using CO2 as a tracer for steam condensate, but not including the contribution from fumaroles and hydrothermal vents. Overall, the diffuse heat and volatile fluxes of HSB are as great as some active volcanoes, but they are a small fraction (1-3% for CO2, 2-8% for heat) of that estimated for the entire

  10. 78 FR 25185 - Delegation of New Source Performance Standards and National Emission Standards for Hazardous Air...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-30

    ... January 14, 2002 (67 FR 1676). As additional assurance of national consistency, state and local agencies... review by the Office of Management and Budget under Executive Order 12866 (58 FR 51735, October 4, 1993... implications as specified in Executive Order 13132 (64 FR 43255, August 10, 1999); is not an...

  11. Assessing N emissions in surface water at the national level: comparison of country-wide vs. regionalized models.

    PubMed

    Dupas, Rémi; Curie, Florence; Gascuel-Odoux, Chantal; Moatar, Florentina; Delmas, Magalie; Parnaudeau, Virginie; Durand, Patrick

    2013-01-15

    Many countries are developing models to estimate N emissions in rivers as part of national-scale water quality assessments. Generally, models are applied with national databases, while at the regional scale, more detailed databases are sometimes available. This paper discusses pros and cons of developing regionalized models versus applying countrywide models. A case study is used to support the discussion. The model used, called Nutting-N (NUTrient Transfer modelING-Nitrogen), relies on a statistical approach linking nitrogen sources and watershed land and river characteristics and aims to evaluate the risk of water bodies failing to reach quality objectives defined by national and federal policies. After calibration and evaluation at the national scale (France), the predictive quality of the model was compared with two regionalized models in a crystalline massif (Brittany, western France, 27,000 km(2)) and in a sedimentary basin (Seine, Paris basin, 78,000 km(2)), where detailed regional databases are available. The national-scale model provided robust predictions in most conditions encountered in France (efficiency=0.69). Terrestrial retention was related mainly to specific runoff, and its median value was estimated at 49% of the N surplus, whereas median river retention represented 18% of incoming N discharge. Regionalizing the model generally improved goodness-of-fit, as the root mean squared error was reduced by 6-24%. However, precision of parameter estimates degraded when too few monitoring basins were available or when variability in land and river characteristics was too low in the calibration dataset. Hence, regional-scale models should be advocated only after the trade-off between improvement of fit and degradation of parameter estimates is examined. PMID:23183226

  12. 78 FR 24073 - Reconsideration of Certain New Source Issues: National Emission Standards for Hazardous Air...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-04-24

    ... AGENCY 40 CFR Parts 60 and 63 RIN 2060-AR62 Reconsideration of Certain New Source Issues: National... examine the applicability criteria in 40 CFR 60.40, 60.40Da, or 60.40c or in 40 CFR 63.9982. If you have... or 40 CFR 63.13 (General Provisions). B. How do I obtain a copy of this document? In addition...

  13. Tank exhaust comparison with 40 CFR 61.93, Subpart H, and other referenced guidelines for Tank Farms National Emission Standards for Hazardous Air Pollutant (NESHAP) designated stacks

    SciTech Connect

    Bachand, D.D.; Crummel, G.M.

    1994-07-01

    The US Environmental Protection Agency (EPA) promulgated National Emission Standards other than Radon from US Department of Energy (DOE) Facilities (40 CFR 61, Subpart H) on December 15, 1989. The regulations specify procedures, equipment, and test methods that.are to be used to measure radionuclide emissions from exhaust stacks that are designated as National Emission Standards for Hazardous Air Pollutant (NESHAP) stacks. Designated NESHAP stacks are those that have the potential to cause any member of the public to receive an effective dose equivalent (EDE) greater than or equal to 0.1 mrem/year, assuming all emission controls were removed. Tank Farms currently has 33 exhaust stacks, 15 of which are designated NESHAP stacks. This document assesses the compliance status of the monitoring and sampling systems for the designated NESHAP stacks.

  14. Assessment of Microphysical Models in the National Combustion Code (NCC) for Aircraft Particulate Emissions: Particle Loss in Sampling Lines

    NASA Technical Reports Server (NTRS)

    Wey, Thomas; Liu, Nan-Suey

    2008-01-01

    This paper at first describes the fluid network approach recently implemented into the National Combustion Code (NCC) for the simulation of transport of aerosols (volatile particles and soot) in the particulate sampling systems. This network-based approach complements the other two approaches already in the NCC, namely, the lower-order temporal approach and the CFD-based approach. The accuracy and the computational costs of these three approaches are then investigated in terms of their application to the prediction of particle losses through sample transmission and distribution lines. Their predictive capabilities are assessed by comparing the computed results with the experimental data. The present work will help establish standard methodologies for measuring the size and concentration of particles in high-temperature, high-velocity jet engine exhaust. Furthermore, the present work also represents the first step of a long term effort of validating physics-based tools for the prediction of aircraft particulate emissions.

  15. Modeling the effects of changes in new source review on national SO{sub 2} and NOx emissions from electricity-generating units

    SciTech Connect

    David A. Evans; Benjamin F. Hobbs; Craig Oren; Karen L. Palmer

    2008-01-15

    The Clean Air Act establishes New Source Review (NSR) programs that apply to construction or modification of major stationary sources. In 2002 and 2003, EPA revised its rules to narrow NSR's coverage of renovations. Congress mandated a National Research Council study of the revisions' impacts. In that study, we used an electricity-sector model to explore possible effects of the equipment replacement provision (ERP), the principal NSR change directed at power plants. We find that, assuming implementation of the Clean Air Interstate Rule (CAIR), tight enforcement of the prerevision NSR rules would likely lead to no or limited decreases in national emissions compared to policies such as ERP. However, emissions might shift forward in time because the previous NSR rules would depress allowance prices, discouraging banking and encouraging allowance use. Only under the most aggressive prerevision NSR enforcement scenario, in which essentially all coal capacity is compelled to retrofit controls by 2020, do NOx emissions fall below ERP levels. Even then, total 2007-2020 SO{sub 2} emissions are unaffected. Further decreases in national emissions could be accomplished more cheaply by tighter emissions caps than through NSR because caps provide incentives for efficient operating strategies, such as fuel switching, as well as retrofits. 23 refs., 2 figs., 1 tab.

  16. National emission standards for hazardous air pollutants application for approval to stabilize the 105N Basin

    SciTech Connect

    Not Available

    1994-05-01

    The 105N Basin (basin) Stabilization will place the basin in a radiologically and environmentally safe condition so that it can be decommissioned at a later date. The basin stabilization objectives are to inspect for Special Nuclear Material (SNM) (i.e., fuel assemblies and fuel pieces), remove the water from the basin and associated pits, and stabilize the basin surface. The stabilization will involve removal of basin hardware, removal of basin sediments, draining of basin water, and cleaning and stabilizing basin surfaces-to prevent resuspension of radioactive emissions to the air. These activities will be conducted in accordance with all applicable regulations. The basin is in the 105N Building, which is located in the 100N Area. The 100N Area is located in the Northern portion of the Hanford Site approximately 35 miles northwest of the city of Richland, Washington. The basin is a reinforced unlined concrete structure 150 feet long, 50 feet wide, and 24 feet deep. The basin is segregated into seven areas sharing a common pool of water; the Discharge/Viewing (``D``) Pit, the fuel segregation pit (including a water tunnel that connects the ``D`` pit and segregation pit), two storage basins designated as North Basin and South Basin, two cask load-out pits, and a fuel examination area. The North Basin floor is entirely covered and the South Basin is partly covered by a modular array of cubicles formed by boron concrete posts and boron concrete panels.

  17. Finisher hog production in the Southeastern United States: Ancillary measurements derived from the National Air Emissions Monitoring Study (NAEMS)

    NASA Astrophysics Data System (ADS)

    Robarge, W. P.; Lee, S.; Walker, J. T.

    2010-12-01

    Measurements of emissions of gases and fine particulate matter from swine animal feeding operations (AFOs) in the southeastern US have typically been confined to relatively short periods (days to several weeks) and have generally focused on waste lagoons. Access to swine animal housing units and other ancillary information has been limited. The National Air Emissions Monitoring Study (NAEMS) provided a unique opportunity to characterize emissions from swine housing units for an extended period of time (~ 2 years), and allowed access to ancillary measurements regarding nutrient flows (feed amounts and composition), manure dynamics, animal inventories, water usage and farm management. Presented here is a summary of the observations made for a NAEMS finisher site (NC3B) selected as being representative of swine production in the southeastern US. Finisher hogs are raised in rotations (~ 140 days) with a target market weight of 123 kg/hog. Among the population during a rotation (700-800 hogs/barn) the actual growth rate varies with a series of “grade-outs” of market-weight hogs starting ~ 110 days from initial load-in. Derivation of the standing live-weight in the barns during a rotation therefore requires use of a growth model and summation over several different “populations” of hogs within a single barn. Up to 5 different feed formulations are fed during a rotation with %N content ranging from (3.4 to 2.2% N; total feed consumed 181,000 kg/barn). Across 4 complete rotations, N consumed was ~50 g N per hog/day. Of this amount, we estimate ~ 60% is excreted as fecal matter and urine. The TAN (NH3 + NH4+) content of the shallow pits is consistently higher (1880 ±390 mg TAN/L) than that found in the anaerobic lagoon (800 ±70 mg TAN/L), except immediately after recharge following pit-pull (pH of the two liquids was similar). The presence of a recalcitrant layer of sludge in the shallow pits (liquid height = 20 cm; sludge depth = 5-10 cm; TAN = 2500 mg N/L; total

  18. Estimating nitrate emissions to surface water at regional and national scale: comparison of models using detailed regional and national-wide databases (France)

    NASA Astrophysics Data System (ADS)

    Dupas, R.; Gascuel-Odoux, C.; Durand, P.; Parnaudeau, V.

    2012-04-01

    The European Union (EU) Water Framework Directive (WFD) requires River Basin District managers to carry out an analysis of nutrient pressures and impacts, in order to evaluate the risk of water bodies failing to reach "good ecological status" and to identify those catchments where prioritized nonpoint-source control measures should be implemented. A model has been developed to estimate nitrate nonpoint-source emissions to surface water, using readily available data in France. It was inspired from US model SPARROW (Smith al., 1997) and European model GREEN (Grizzetti et al., 2008), i.e. statistical approaches consisting of linking nitrogen sources and catchments' land and rivers characteristics. The N-nitrate load (L) at the outlet of a catchment is expressed as: L= R*(B*Lsgw+Ldgw+PS)-denitlake Where denitlake is a denitrification factor for lakes and reservoirs, Lsgw is the shallow groundwater discharge to streams (derived from the base flow index and N surplus in kgN.ha-1.yr-1), Ldgw is the deep groundwater discharge to streams (derived from total runoff, the base flow index and deep groundwater N concentration), PS is point sources from domestic and industrial origin (kgN.ha-1.yr-1) and R and B are the river system and basin reduction factor, respectively. Besides calibrating and evaluating the model at a national scale, its predictive quality was compared with those of regionalized models in Brittany (Western France) and in the Seine river basin (Paris basin), where detailed regional databases are available. The national-scale model proved to provide robust predictions in most conditions encountered in France, as it fitted observed N-nitrate load with an efficiency of 0.69. Regionalization of the model reduced the standard error in the prediction of N-nitrate loads by about 19 Hence, the development of regionalized models should be advocated only after the trade-off between improvement of fit and degradation of parameters' estimation has come under scrutiny.

  19. Evaluation of on-road vehicle CO and NOx National Emission Inventories using an urban-scale source-oriented air quality model

    NASA Astrophysics Data System (ADS)

    Kota, Sri Harsha; Zhang, Hongliang; Chen, Gang; Schade, Gunnar W.; Ying, Qi

    2014-03-01

    The MOBILE6.2 model was replaced by the Motor Vehicle Emission Simulator (MOVES) in 2012 as an official tool recommended by the United States Environmental Protection Agency (US EPA) to predict vehicular pollutant emission factors. In this study, on-road vehicle emission inventories of CO and NOx for Southeast Texas generated by MOVES and MOBILE6.2 in two versions of the 2005 National Emission Inventory (NEI) were studied by comparing predicted CO and NOx using the EPA's Community Multiscale Air Quality (CMAQ) Model incorporated with a source-oriented gas phase chemical mechanism with measurements made at six urban and industrial sites in Southeast Texas. The source tracing technique allows direct determination of contributions of on-road vehicles to overall CO and NOx concentrations and identification of ambient concentration measurements which are mostly impacted by vehicle emissions. By grouping the fractional bias (FB) values of the hourly predictions based on vehicle contributions to total CO or NOx concentrations, clear trends in the FB were observed, indicating systematic biases in the emission inventory for these species. Data points dominated by vehicle emissions suggest that surface CO concentrations due to vehicle exhaust are significantly over-estimated by a factor of 2 using either MOVES or MOBILE6.2. NOx concentrations are overestimated by approximately 20-35% and 70% by using the MOBILE6.2 and MOVES emissions, respectively. Emission scaling runs show that a domain-wide reduction of MOBILE6.2 CO emissions by 60% and NOx emissions by 15-25% leads to better model performance of exhaust CO and NOx concentrations in the current study.

  20. Hydrogen Fuel Cell Vehicle Fuel Economy Testing at the U.S. EPA National Vehicle and Fuel Emissions Laboratory (SAE Paper 2004-01-2900)

    EPA Science Inventory

    The introduction of hydrogen fuel cell vehicles and their new technology has created the need for development of new fuel economy test procedures and safety procedures during testing. The United States Environmental Protection Agency-National Vehicle Fuels and Emissions Laborato...

  1. Global Warming and the Neglected Greenhouse Gas: A Cross-National Study of the Social Causes of Methane Emissions Intensity, 1995

    ERIC Educational Resources Information Center

    Jorgenson, Andrew

    2006-01-01

    The human dimensions of greenhouse gas emissions and global warming attract considerable attention in macrosociology. However, cross-national analyses generally neglect greenhouse gases other than carbon dioxide. The current study addresses this paucity through the testing of theoretically derived models for the social structural causes of the…

  2. Analysis of the uncertainty associated with national fossil fuel CO2 emissions datasets for use in the global Fossil Fuel Data Assimilation System (FFDAS) and carbon budgets

    NASA Astrophysics Data System (ADS)

    Song, Y.; Gurney, K. R.; Rayner, P. J.; Asefi-Najafabady, S.

    2012-12-01

    High resolution quantification of global fossil fuel CO2 emissions has become essential in research aimed at understanding the global carbon cycle and supporting the verification of international agreements on greenhouse gas emission reductions. The Fossil Fuel Data Assimilation System (FFDAS) was used to estimate global fossil fuel carbon emissions at 0.25 degree from 1992 to 2010. FFDAS quantifies CO2 emissions based on areal population density, per capita economic activity, energy intensity and carbon intensity. A critical constraint to this system is the estimation of national-scale fossil fuel CO2 emissions disaggregated into economic sectors. Furthermore, prior uncertainty estimation is an important aspect of the FFDAS. Objective techniques to quantify uncertainty for the national emissions are essential. There are several institutional datasets that quantify national carbon emissions, including British Petroleum (BP), the International Energy Agency (IEA), the Energy Information Administration (EIA), and the Carbon Dioxide Information and Analysis Center (CDIAC). These four datasets have been "harmonized" by Jordan Macknick for inter-comparison purposes (Macknick, Carbon Management, 2011). The harmonization attempted to generate consistency among the different institutional datasets via a variety of techniques such as reclassifying into consistent emitting categories, recalculating based on consistent emission factors, and converting into consistent units. These harmonized data form the basis of our uncertainty estimation. We summarized the maximum, minimum and mean national carbon emissions for all the datasets from 1992 to 2010. We calculated key statistics highlighting the remaining differences among the harmonized datasets. We combine the span (max - min) of datasets for each country and year with the standard deviation of the national spans over time. We utilize the economic sectoral definitions from IEA to disaggregate the national total emission into

  3. Comparison of beam emission spectroscopy and gas puff imaging edge fluctuation measurements in National Spherical Torus Experiment

    SciTech Connect

    Sechrest, Y.; Munsat, T.; Smith, D.; Stotler, D. P.; Zweben, S. J.

    2015-05-15

    In this study, the close physical proximity of the Gas Puff Imaging (GPI) and Beam Emission Spectroscopy (BES) diagnostics on the National Spherical torus Experiment (NSTX) is leveraged to directly compare fluctuation measurements, and to study the local effects of the GPI neutral deuterium puff during H-mode plasmas without large Edge Localized Modes. The GPI and BES views on NSTX provide partially overlapping coverage of the edge and scrape-off layer (SOL) regions above the outboard midplane. The separation in the toroidal direction is 16°, and field lines passing through diagnostic views are separated by ∼20 cm in the direction perpendicular to the magnetic field. Strong cross-correlation is observed, and strong cross-coherence is seen for frequencies between 5 and 15 kHz. Also, probability distribution functions of fluctuations measured ∼3 cm inside the separatrix exhibit only minor deviations from a normal distribution for both diagnostics, and good agreement between correlation length estimates, decorrelation times, and structure velocities is found at the ±40% level. While the two instruments agree closely in many respects, some discrepancies are observed. Most notably, GPI normalized fluctuation levels exceed BES fluctuations by a factor of ∼9. BES mean intensity is found to be sensitive to the GPI neutral gas puff, and BES normalized fluctuation levels for frequencies between 1 and 10 kHz are observed to increase during the GPI puff.

  4. Hydrogeological and geophysical investigations to evaluate groundwater influences on GHG emissions at the national research site Skogaryd

    NASA Astrophysics Data System (ADS)

    Banzhaf, Stefan; Klemedtsson, Leif; Sturkell, Erik; Nyström, Elin; Barthel, Roland

    2015-04-01

    The overall objective of the presented study is to explore the impact of groundwater fluctuations on greenhouse gas (GHG) emissions from peatlands and in particular from drained organic soils. The hypothesis is that drained organic soils react sensitively to changing water content, i.e. that frequent changes of groundwater level enhance the emissions of GHG from these soils and thus contribute significantly to global warming. The area under investigation is based at the Skogaryd Research Catchment (within Swedish Infrastructure for Ecosystem Sciences, SITES) in western Sweden (Meyer, et al., 2013), which was recently assigned the status of a national research site by the Swedish research council (www.vr.se). Skogaryd is a unique place in Sweden for doing research on organic soils as the area was simultaneously afforested in the 1960s and the drained fertile soils have a different land-use history. The ditching for drainage purposes throughout the entire area has had and still has a huge influence on groundwater level, which in turn is assumed to trigger GHG emissions from the organic soils at Skogaryd. To address the influence of groundwater dynamics on GHG emissions in this system, a characterisation of the subsurface using electrical resistivity and Ground Penetrating Radar (GPR) measurements was carried out. These geophysical measurements were combined with drilling along them to allow for ground truthing. An average peat thickness of around 3 m was estimated for the field site. Below the peat follows a fine sand layer, which reaches a maximum thickness of around 1.0 m right at the valley borders and thins out significantly towards the middle of the valley. Below the fine sand layer follows a layer of marine clay, which extends down to the bedrock at depths between 12 and 15 m below ground surface. The results show that the peat layer in Skogaryd forms an isolated hydraulic system without interaction with deeper or regional groundwater systems. The continuously

  5. Towards a measurement-based national verification system for GHG emissions: UK emission estimates of CO2 from the GAUGE experiment

    NASA Astrophysics Data System (ADS)

    Gonzi, Siegfried; Palmer, Paul; O'Doherty, Simon; Young, Dickon; Stanley, Kieran; Stavert, Ann; Grant, Aoife; Helfter, Carole; Mullinger, Neil; Nemitz, Eiko; Allen, Grant; Pitt, Joseph; Le Breton, Michael; Bösch, Hartmut; Sembhi, Harjinder; Sonderfeld, Hannah; Parker, Robert; Bauguitte, Stephane

    2016-04-01

    Robust quantification of emissions of greenhouse gases (GHG) is central to the success of ongoing international efforts to slow current emissions and mitigate future climate change. The Greenhouse gAs Uk and Global Emissions (GAUGE) project aims to quantify the magnitude and uncertainty of country-scale emissions of carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) using concentration measurements from a network of tall towers and mobile platforms (aircraft and ferry) distributed across the UK. The GAUGE measurement programme includes: (a) GHG measurements on a regular ferry route down the North Sea aimed at sampling UK outflow; (b) campaign deployment of the UK BAe-146 research aircraft to provide vertical profile measurements of GHG over and around the UK; (c) a high-density GHG measurement network over East Anglia that is primarily focused on the agricultural sector; and (d) regular measurements of CO2 and CH4 isotopologues used for GHG source attribution. We also use satellite observations from the Japanese Greenhouse gases Observing SATellite (GOSAT) to provide continental-scale constraints on GHG flux estimates. We present CO2 flux estimates for the UK inferred from GAUGE measurements using a nested, high-resolution (25 km) version of the GEOS-Chem global atmospheric chemistry and transport model and an ensemble Kalman filter. We will present our current best estimate for CO2 fluxes and a preliminary assessment of the efficacy of individual GAUGE data sources to spatially resolve CO2 flux estimates over the UK. We will also discuss how flux estimates inferred from the different models used within GAUGE can help to assess the role of transport model error and to determine an ensemble CO2 flux estimate for the UK.

  6. National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial, Commercial, and Institutional Boilers; Guidance for Calculating Emission Credits Resulting from Implementation of Energy Conservation Measures

    SciTech Connect

    Cox, Daryl; Papar, Riyaz; Wright, Dr. Anthony

    2012-07-01

    The purpose of this document is to provide guidance for developing a consistent approach to documenting efficiency credits generated from energy conservation measures in the Implementation Plan for boilers covered by the Boiler MACT rule (i.e., subpart DDDDD of CFR part 63). This document divides Boiler System conservation opportunities into four functional areas: 1) the boiler itself, 2) the condensate recovery system, 3) the distribution system, and 4) the end uses of the steam. This document provides technical information for documenting emissions credits proposed in the Implementation Plan for functional areas 2) though 4). This document does not include efficiency improvements related to the Boiler tune-ups.

  7. Influence of ship emissions on air quality and input of contaminants in southern Alaska National Parks and Wilderness Areas during the 2006 tourist season

    NASA Astrophysics Data System (ADS)

    Mölders, Nicole; Porter, Stacy E.; Cahill, Catherine F.; Grell, Georg A.

    2010-04-01

    The impact of ship emissions on air quality in Alaska National Parks and Wilderness Areas was investigated using the Weather Research and Forecasting model inline coupled with chemistry (WRF/Chem). The visibility and deposition of atmospheric contaminants was analyzed for the length of the 2006 tourist season. WRF/Chem reproduced the meteorological situation well. It seems to have captured the temporal behavior of aerosol concentrations when compared with the few data available. Air quality follows certain predetermined patterns associated with local meteorological conditions and ship emissions. Ship emissions have maximum impacts in Prince William Sound where topography and decaying lows trap pollutants. Along sea-lanes and adjacent coastal areas, NO x, SO 2, O 3, PAN, HNO 3, and PM 2.5 increase up to 650 pptv, 325 pptv, 900 pptv, 18 pptv, 10 pptv, and 100 ng m -3. Some of these increases are significant (95% confidence). Enhanced particulate matter concentrations from ship emissions reduce visibility up to 30% in Prince William Sound and 5-25% along sea-lanes.

  8. Particulate Emissions Control using Advanced Filter Systems: Final Report for Argonne National Laboratory, Corning Inc. and Hyundai Motor Company CRADA Project

    SciTech Connect

    Seong, Hee Je; Choi, Seungmok

    2015-10-09

    This is a 3-way CRADA project working together with Corning, Inc. and Hyundai Motor Co. (HMC). The project is to understand particulate emissions from gasoline direct-injection engines (GDI) and their physico-chemical properties. In addition, this project focuses on providing fundamental information about filtration and regeneration mechanisms occurring in gasoline particulate filter (GPF) systems. For the work, Corning provides most advanced filter substrates for GPF applications and HMC provides three-way catalyst (TWC) coating services of these filter by way of a catalyst coating company. Then, Argonne National Laboratory characterizes fundamental behaviors of filtration and regeneration processes as well as evaluated TWC functionality for the coated filters. To examine aging impacts on TWC and GPF performance, the research team evaluates gaseous and particulate emissions as well as back-pressure increase with ash loading by using an engine-oil injection system to accelerate ash loading in TWC-coated GPFs.

  9. How emissions, climate, and land use change will impact mid-century air quality over the United States: a focus on effects at national parks

    NASA Astrophysics Data System (ADS)

    Martin, M. Val; Heald, C. L.; Lamarque, J.-F.; Tilmes, S.; Emmons, L. K.; Schichtel, B. A.

    2015-03-01

    We use a global coupled chemistry-climate-land model (CESM) to assess the integrated effect of climate, emissions and land use changes on annual surface O3 and PM2.5 in the United States with a focus on national parks (NPs) and wilderness areas, using the RCP4.5 and RCP8.5 projections. We show that, when stringent domestic emission controls are applied, air quality is predicted to improve across the US, except surface O3 over the western and central US under RCP8.5 conditions, where rising background ozone counteracts domestic emission reductions. Under the RCP4.5 scenario, surface O3 is substantially reduced (about 5 ppb), with daily maximum 8 h averages below the primary US Environmental Protection Agency (EPA) National Ambient Air Quality Standards (NAAQS) of 75 ppb (and even 65 ppb) in all the NPs. PM2.5 is significantly reduced in both scenarios (4 μg m-3; ~50%), with levels below the annual US EPA NAAQS of 12 μg m-3 across all the NPs; visibility is also improved (10-15 dv; >75 km in visibility range), although some western US parks with Class I status (40-74 % of total sites in the US) are still above the 2050 planned target level to reach the goal of natural visibility conditions by 2064. We estimate that climate-driven increases in fire activity may dominate summertime PM2.5 over the western US, potentially offsetting the large PM2.5 reductions from domestic emission controls, and keeping visibility at present-day levels in many parks. Our study indicates that anthropogenic emission patterns will be important for air quality in 2050. However, climate and land use changes alone may lead to a substantial increase in surface O3 (2-3 ppb) with important consequences for O3 air quality and ecosystem degradation at the US NPs. Our study illustrates the need to consider the effects of changes in climate, vegetation, and fires in future air quality management and planning and emission policy making.

  10. Hanford Site radionuclide national emission standards for hazardous ari pollutants registered and and unregistered stack (powered exhaust) source assessment

    SciTech Connect

    Davis, W.E.

    1995-12-01

    On February 3, 1993, US DOE Richland Operations Office received a Compliance Order and Information Request from the Director of the Air and Toxics Div. of US EPA, Region X. The compliance order requires the Richland Operations Office to evaluate all radionuclide emission points at the Hanford site to determine which are subject to the continuous emission measurement requirements in Title 40, Code of Federal Regulations (CFR), Part 61, Subpart H, and to continuously measure radionuclide emissions in accordance with 40 CFR 61.93. The Information Request required The provision of a written compliance plan to meet the requirements of the compliance order. A compliance plan was submitted to EPA, Region X, on April 30, 1993. It set as one of the milestones, the complete assessment of the Hanford Site 84 stacks registered with the Washington State Department of Health, by December 17, 1993. This milestone was accomplished. The compliance plan also called for reaching a Federal Facility Compliance Agreement; this was reached on February 7, 1994, between DOE Richland Operations and EPA, Region X. The milestone to assess the unregistered stacks (powered exhaust) by August 31, 1994, was met. This update presents assessments for 72 registered and 22 unregistered stacks with potential emissions > 0.1 mrem/yr.

  11. 77 FR 9303 - National Emission Standards for Hazardous Air Pollutants From Coal- and Oil-Fired Electric...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-02-16

    ...). See 76 FR 25003-25005 for a fuller discussion of the health effects associated with these pollutants... generating units (76 FR 24976). After consideration of public comments, the EPA is finalizing these rules in... protects air quality and promotes public health by reducing emissions of the HAP listed in CAA section...

  12. Building capacity for national level carbon Measurement, Reporting, and Verification (MRV) systems for a ``Reduction of Emissions from Deforestation and Degradation'' (REDD)

    NASA Astrophysics Data System (ADS)

    Laporte, N.; Goetz, S. J.; Baccini, A.; Walker, W. S.; Ndunda, P.; Mekui, P.; Kellndorfer, J. M.; Knight, D.

    2010-12-01

    An international policy mechanism is under negotiation for compensating tropical nations that succeed in lowering their greenhouse gas emissions from tropical deforestation and forest degradation, responsible for approximately one-fifth of worldwide carbon emissions. One of the barriers to its success is the adoption of a unique MRV system and the participation of developing countries in carbon monitoring. A successful REDD policy must rely on a robust, scalable, cost effective method that will allow the Measurement Reporting and Verification from local to national scales, while also developing well-trained technical personnel to implement national REDD carbon monitoring systems. Participation of governments and forest stakeholders in forest and carbon monitoring methods at WHRC is achieved through ongoing technical workshops which include training of participants to collect field data to calibrate biomass models, and an annual Scholar’s Program where forest officers from the tropical regions of Latin America, Africa and Southeast Asia work with Woods Hole Research Center scientsts to improve skills in forest measurement and remote sensing monitoring techniques . Capacity building activities focus on technical aspects and approaches to forest-cover and carbon mapping and the use of satellite imagery together with ground-based measurement techniques in the development of forest cover and carbon-stock maps. After two years, the three-year project has involved more than 200 forest specialists from governments and NGOs in Bolivia, Cambodia, Colombia, the Democratic Republic of Congo, Gabon, Indonesia, Lao PDR, Kenya, Uganda, Vietnam and Zambia, among others with participation of ten scholars actively participating in the developement of National REDD plans for forest mapping and monitoring. Field Training Mbandaka- DR Congo 2010

  13. Emissions from Medium-Duty Conventional and Diesel-Electric Hybrid Vehicles; NREL (National Renewable Energy Laboratory)

    SciTech Connect

    Ragatz, A.; Duran, A.; Thornton, M.; Walkowicz, K.

    2014-04-02

    This presentation discusses the results of emissions testing for medium-duty conventional and diesel-electric hybrid vehicles. Testing was based on a field evaluation approach that utilized the Fleet DNA drive cycle database and NREL’s Renewable Fuels and Lubricants (ReFUEL) Laboratory chassis dynamometer. Vehicles tested included parcel delivery (Class 6 step vans), beverage delivery (Class 8 tractors), and parcel delivery (Class 7 box trucks) vehicles, all with intended service class medium/heavy heavy-duty diesel (MHDD).
    Results for fuel economy and tailpipe NOx emissions included: diesel hybrid electric vehicles showed an average fuel economy advantage on identified test cycles: Class 6 Step Vans: 26%; Class 7 Box Trucks: 24.7%; Class 8 Tractors: 17.3%. Vehicle miles traveled is an important factor in determining total petroleum and CO2 displacement. Higher NOx emissions were observed over some test cycles: highly drive cycle dependent; engine-out differences may result from different engine operating point; and selective catalyst reduction temperature may play a role, but does not explain the whole story.

  14. Emission assessment from full-scale co-combustion tests of binder- enhanced dRDF pellets and high sulfur coal at Argonne National Laboratory

    SciTech Connect

    Ohlsson, O.O.; Livengood, C.D. ); Daugherty, K.E. )

    1990-06-04

    Argonne National Laboratory (ANL) and University of North Texas (UNT) research teams collected over 800 emissions and ash samples during the combustion of over 650 tons of binder enhanced densified refuse-drived fuel (b-dRDF) pellets with high sulfur coal in a spreader-stoker boiler at ANL. This full-scale test burn was conducted to validate predictions from laboratory and pilot scale test results that indicated substantial reductions of SO{sub 2}, NO{sub x} and CO{sub 2} in the flue gas, and the reduction of heavy metals and organics in the ash residue, when combusting the b-dRDF pellets with coal. Effects of varying fuel composition on performance of the boiler's spray-dryer/fabric filter emissions control system was also evaluated. This paper describes the b-dRDF pellet/coal cofiring tests, the emission and ash samples that were taken, the analyses that were conducted on these samples, and the final test results. 5 refs., 1 fig., 1 tab.

  15. Air Emission Inventory for the INEEL -- 1999 Emission Report

    SciTech Connect

    Zohner, Steven K

    2000-05-01

    This report presents the 1999 calendar year update of the Air Emission Inventory for the Idaho National Engineering and Environmental Laboratory (INEEL). The INEEL Air Emission Inventory documents sources and emissions of nonradionuclide pollutants from operations at the INEEL. The report describes the emission inventory process and all of the sources at the INEEL, and provides nonradionuclide emissions estimates for stationary sources.

  16. 40 CFR 61.42 - Emission standard.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium Rocket Motor Firing § 61.42 Emission standard. (a) Emissions to the atmosphere from rocket-motor test sites shall...

  17. 40 CFR 61.42 - Emission standard.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium Rocket Motor Firing § 61.42 Emission standard. (a) Emissions to the atmosphere from rocket-motor test sites shall...

  18. 40 CFR 61.42 - Emission standard.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium Rocket Motor Firing § 61.42 Emission standard. (a) Emissions to the atmosphere from rocket-motor test sites shall...

  19. 40 CFR 61.42 - Emission standard.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium Rocket Motor Firing § 61.42 Emission standard. (a) Emissions to the atmosphere from rocket-motor test sites shall...

  20. 40 CFR 61.42 - Emission standard.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium Rocket Motor Firing § 61.42 Emission standard. (a) Emissions to the atmosphere from rocket-motor test sites shall...

  1. 23 CFR Appendix A to Part 772 - National Reference Energy Mean Emission Levels as a Function of Speed

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ..., 109 Stat. 568, 605; 49 CFR 1.48(b). § 772.1 Purpose. To provide procedures for noise studies and noise... Impact (FONSI), or the Record of Decision (ROD), as defined in 23 CFR part 771. Design year. The future...) of title 5, U.S.C. and part 51 of title 1, CFR, and are on file at the National Archives and...

  2. Reconciliation of Measured and TRANSP-calculated Neutron Emission Rates in the National Spherical Torus Experiment: Circa 2002-2005

    SciTech Connect

    S.S. Medley; D.S. Darrow; A.L. Roquemore

    2005-06-15

    A change in the response of the neutron detectors on the National Spherical Torus Experiment occurred between the 2002-2003 and 2004 experimental run periods. An analysis of this behavior by investigating the neutron diagnostic operating conditions and comparing measured and TRANSP-calculated neutron rates is presented. Also a revised procedure for cross calibration of the neutron scintillator detectors with the fission chamber detectors was implemented that delivers good agreement amongst the measured neutron rates for all neutron detectors and all run periods. For L-mode discharges, the measured and TRANSP-calculated neutron rates now match closely for all run years. For H-mode discharges over the entire 2002-2004 period, the 2FG scintillator and fission chamber measurements match each other but imply a neutron deficit of 11.5% relative to the TRANSP-calculated neutron. The results of this report impose a modification on all of the previously used calibration factors for the entire neutron detector suite over the 2002-2004 period. A tabular summary of the new calibration factors is provided including certified calibration factors for the 2005 run.

  3. Accumulation of dioxins and induction of cytochrome P450 1A4/1A5 enzyme activities in common cormorants from Lake Biwa, Japan: temporal trends and validation of national regulation on dioxins emission.

    PubMed

    Kubota, Akira; Watanabe, Michio X; Kim, Eun-Young; Yoneda, Kumiko; Tanabe, Shinsuke; Iwata, Hisato

    2012-09-01

    To validate the outcome of the national regulation on dioxins emission implemented in 1999, this study investigated temporal trends of chlorinated dioxins and related compounds (DRCs) in liver of common cormorants (Phalacrocorax carbo) collected from Lake Biwa, Japan between 2001 and 2008, as a part of the "Survey on the State of Dioxins Accumulation in Wildlife" conducted by the Ministry of the Environment, Japan. We also measured a biomarker of DRCs exposure, the cytochrome P450 1A (CYP1A)-dependent O-dealkylation activity of alkoxyresorufins (AROD), including methoxy-, ethoxy-, pentoxy- and benzyloxy-resorufins in the samples over 2001-2007. Neither TEQ nor AROD activity showed any clear declining trend over the time period, although the emission of DRCs during the corresponding period was estimated to be apparently decreasing. Our data indicate that the concentration of recalcitrant DRCs in the cormorant during 2001-2008 was scarcely affected by the national regulation on dioxins emission. PMID:22610036

  4. Technical and Non-Technical Measures for air pollution emission reduction: The integrated assessment of the regional Air Quality Management Plans through the Italian national model

    NASA Astrophysics Data System (ADS)

    D'Elia, I.; Bencardino, M.; Ciancarella, L.; Contaldi, M.; Vialetto, G.

    2009-12-01

    The Italian Air Quality legislation underwent sweeping changes with the implementation of the 1996 European Air Quality Framework Directive when the Italian administrative Regions were entrusted with air quality management tasks. The most recent Regional Air Quality Management Plans (AQMPs) highlighted the importance of Non-Technical Measures (NTMs), in addition to Technical Measures (TMs), in meeting environmental targets. The aim of the present work is to compile a list of all the TMs and NTMs taken into account in the Italian Regional AQMPs and to give in the target year, 2010, an estimation of SO 2, NO x and PM 10 emission reductions, of PM 10 concentration and of the health impact of PM 2.5 concentrations in terms of Life Expectancy Reduction. In order to do that, RAINS-Italy, as part of the National Integrated Modeling system for International Negotiation on atmospheric pollution (MINNI), has been applied. The management of TMs and NTMs inside RAINS have often obliged both the introduction of exogenous driving force scenarios and the control strategy modification. This has inspired a revision of the many NTM definitions and a clear choice of the definition adopted. It was finally highlighted that only few TMs and NTMs implemented in the AQMPs represent effective measures in reaching the environmental targets.

  5. Optical alignment techniques for line-imaging velocity interferometry and line-imaging self-emission of targets at the National Ignition Facility (NIF)

    SciTech Connect

    Malone, Robert; Celeste, John; Celliers, Peter; Frogget, Brent; Robert Guyton,,; Kaufman, Morris; Lee, Tony; MacGowan, Brian; Ng, Edmend; Reinbachs, Imants; Robinson, Ronald; Tunnell, Thomas; Watts, Phillip

    2007-08-01

    The National Ignition Facility (NIF) requires optical diagnostics for measuring shock velocities in shock physics experiments. The nature of the NIF facility requires the alignment of complex three-dimensional optical systems of very long distances. Access to the alignment mechanisms can be limited, and any alignment system must be operator friendly. The Velocity Interferometer System for Any Reflector (VISAR) measures shock velocities, shock breakout times, and emission of 1- to 5-mm targets at a location remote to the NIF target chamber. Three optical systems using the same vacuum chamber port each have a total track of 21 m. All optical lenses are on kinematic mounts or sliding rails, enabling pointing accuracy of the optical axis to be checked. Counter-propagating laser beams (orange and red) align these diagnostics to a listing of tolerances. Movable aperture cards, placed before and after lens groups, show the spread of alignment spots created by the orange and red alignment lasers. Optical elements include 1-in. to 15-in. diameter mirrors, lenses with up to 10.5-in. diameters, beamsplitters, etalons, dove prisms, filters, and pellicles. Alignment of more than 75 optical elements must be verified before each target shot. Archived images from eight alignment cameras prove proper alignment before each shot.

  6. Optical Alignment Techniques for Line-Imaging Velocity Interferometry and Line-Imaging Self-Emission of Targets at the National Ignition Facility (NIF)

    SciTech Connect

    Malone, R M; Celeste, J R; Celliers, P M; Frogget, B .; Guyton, R L; Kaufman, M I; Lee, T L; MacGowan, B J; Ng, E W; Reinbachs, I P; Robinson, R B; Tunnell, T W; Watts, P W

    2007-07-31

    The National Ignition Facility (NIF) requires optical diagnostics for measuring shock velocities in shock physics experiments. The nature of the NIF facility requires the alignment of complex three-dimensional optical systems of very long distances. Access to the alignment mechanisms can be limited, and any alignment system must be operator friendly. The Velocity Interferometer System for Any Reflector measures shock velocities, shock breakout times, and emission of 1- to 5-mm targets at a location remote to the NIF target chamber. Three optical systems using the same vacuum chamber port each have a total track of 21 meters. All optical lenses are on kinematic mounts or sliding rails, enabling pointing accuracy of the optical axis to be checked. Counter-propagating laser beams (orange and red) align these diagnostics to a listing of tolerances. Movable aperture cards, placed before and after lens groups, show the spread of alignment spots created by the orange and red alignment lasers. Optical elements include 1-in. to 15-in. diameter mirrors, lenses with up to 10.5-in. diameters, beamsplitters, etalons, dove prisms, filters, and pellicles. Alignment of more than 75 optical elements must be verified before each target shot. Archived images from eight alignment cameras prove proper alignment before each shot.

  7. Optical alignment techniques for line-imaging velocity interferometry and line-imaging self-emission of targets at the National Ignition Facility (NIF)

    NASA Astrophysics Data System (ADS)

    Malone, Robert M.; Celeste, John R.; Celliers, Peter M.; Frogget, Brent C.; Guyton, Robert L.; Kaufman, Morris I.; Lee, Tony L.; MacGowan, Brian J.; Ng, Edmund W.; Reinbachs, Imants P.; Robinson, Ronald B.; Tunnell, Thomas W.; Watts, Phillip W.

    2007-09-01

    The National Ignition Facility (NIF) requires optical diagnostics for measuring shock velocities in shock physics experiments. The nature of the NIF facility requires the alignment of complex three-dimensional optical systems of very long distances. Access to the alignment mechanisms can be limited, and any alignment system must be operator-friendly. The Velocity Interferometer System for Any Reflector (VISAR) measures shock velocities and shock breakout times of 1- to 5-mm targets at a location remote to the NIF target chamber. A third imaging system measures self-emission of the targets. These three optical systems using the same vacuum chamber port each have a total track of 21 m. All optical lenses are on kinematic mounts or sliding rails, enabling pointing accuracy of the optical axis to be systematically checked. Counter-propagating laser beams (orange and red) align these diagnostics to a listing of tolerances. Floating apertures, placed before and after lens groups, display misalignment by showing the spread of alignment spots created by the orange and red alignment lasers. Optical elements include 1-in. to 15-in. diameter mirrors, lenses with up to 10.5-in. diameters, beam splitters, etalons, dove prisms, filters, and pellicles. Alignment of more than 75 optical elements must be verified before each target shot. Archived images from eight alignment cameras prove proper alignment is achieved before each shot.

  8. Ozone and Volatile Organic Compound Distributions in Rocky Mountain National Park During FRAPPÉ: Impacts of Oil and Natural Gas Operations and Urban Emissions on Park Air Quality

    NASA Astrophysics Data System (ADS)

    Sive, B. C.; Zhou, Y.; Evanoski-Cole, A.; Benedict, K. B.; Prenni, A. J.; Thompson, T. M.; Day, D.; Fischer, E. V.; Callahan, S. L.; Cheatham, J.; Schichtel, B. A.; Apel, E. C.; Hornbrook, R. S.; Sullivan, A.; Vimont, J.; Collett, J. L., Jr.

    2015-12-01

    The Front Range Air Pollution and Photochemistry Éxperiment (FRAPPÉ) occurred during July and August 2014. This study focused on characterizing and understanding summertime air quality in the Northern Front Range Metropolitan Area (NFRMA), with an emphasis on ozone and its precursors. Exceedances of the National Ambient Air Quality Standard (NAAQS) for ozone occur regularly in the NFRMA during the summertime and impact air quality in Rocky Mountain National Park (ROMO). As part of FRAPPÉ, the National Park Service supplemented its long-term monitoring at its Longs Peak site (~9000 ft.) with enhanced trace gas and aerosol measurements; ozone and meteorological measurements were also deployed at a high altitude site off of Trail Ridge Road (~11,600 ft.). At Longs Peak, a suite of volatile organic compounds (VOCs), including nonmethane hydrocarbons, halocarbons, alkyl nitrates and oxygenated VOCs (OVOCs), were measured using a cryogen-free gas chromatographic system and a proton transfer reaction-mass spectrometer. Additionally, whole air samples were collected along a route from Fort Collins, CO up to Trail Ridge Road several times per week. The transect samples were typically collected during upslope events and aircraft deployment days to characterize air mass composition and to aid in linking the surface and airborne measurements. Ozone distributions from Trail Ridge Road and Longs Peak generally tracked well temporally, with the highest ozone levels measured at the high elevation site; maximum hourly values during FRAPPÉ were 82 ppb and 79 ppb, respectively. A mixed signature containing both urban and oil and gas emissions was regularly observed in air masses encountered in the park, with elevated ozone and VOC levels measured during upslope events. However, the highest levels of alkanes measured at Longs Peak were associated with oil and gas operations, based on the isopentane to n-pentane ratio. Transect samples and aircraft data collected during an upslope

  9. 40 CFR 61.163 - Emission monitoring.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... requirements and procedures contained in Performance Specification 1 of appendix B of 40 CFR part 60. (c...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic...

  10. 40 CFR 61.163 - Emission monitoring.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... requirements and procedures contained in Performance Specification 1 of appendix B of 40 CFR part 60. (c...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic...

  11. 40 CFR 61.163 - Emission monitoring.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... requirements and procedures contained in Performance Specification 1 of appendix B of 40 CFR part 60. (c...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic...

  12. 40 CFR 61.163 - Emission monitoring.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... requirements and procedures contained in Performance Specification 1 of appendix B of 40 CFR part 60. (c...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic...

  13. 40 CFR 61.163 - Emission monitoring.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... requirements and procedures contained in Performance Specification 1 of appendix B of 40 CFR part 60. (c...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic...

  14. 40 CFR 61.183 - Emission monitoring.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... CFR part 60. (2) Comply with the provisions of § 60.13(d) of 40 CFR part 60. (3) Except for system...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions From Arsenic Trioxide and Metallic Arsenic Production Facilities § 61.183 Emission monitoring....

  15. 40 CFR 61.183 - Emission monitoring.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... CFR part 60. (2) Comply with the provisions of § 60.13(d) of 40 CFR part 60. (3) Except for system...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions From Arsenic Trioxide and Metallic Arsenic Production Facilities § 61.183 Emission monitoring....

  16. 40 CFR 61.183 - Emission monitoring.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... CFR part 60. (2) Comply with the provisions of § 60.13(d) of 40 CFR part 60. (3) Except for system...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions From Arsenic Trioxide and Metallic Arsenic Production Facilities § 61.183 Emission monitoring....

  17. 40 CFR 61.183 - Emission monitoring.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... CFR part 60. (2) Comply with the provisions of § 60.13(d) of 40 CFR part 60. (3) Except for system...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions From Arsenic Trioxide and Metallic Arsenic Production Facilities § 61.183 Emission monitoring....

  18. 40 CFR 61.183 - Emission monitoring.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... CFR part 60. (2) Comply with the provisions of § 60.13(d) of 40 CFR part 60. (3) Except for system...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions From Arsenic Trioxide and Metallic Arsenic Production Facilities § 61.183 Emission monitoring....

  19. 40 CFR 61.68 - Emission monitoring.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 9 2013-07-01 2013-07-01 false Emission monitoring. 61.68 Section 61.68 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Vinyl Chloride § 61.68 Emission monitoring. (a) A vinyl...

  20. 40 CFR 61.271 - Emission standard.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... device requirements of 40 CFR 60.18. (3) The specifications and requirements listed in paragraphs (c)(1...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Benzene Emissions From Benzene Storage Vessels § 61.271 Emission standard. The owner or operator of each storage...

  1. 40 CFR 61.271 - Emission standard.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... device requirements of 40 CFR 60.18. (3) The specifications and requirements listed in paragraphs (c)(1...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Benzene Emissions From Benzene Storage Vessels § 61.271 Emission standard. The owner or operator of each storage...

  2. 40 CFR 61.271 - Emission standard.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... device requirements of 40 CFR 60.18. (3) The specifications and requirements listed in paragraphs (c)(1...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Benzene Emissions From Benzene Storage Vessels § 61.271 Emission standard. The owner or operator of each storage...

  3. 40 CFR 61.271 - Emission standard.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... device requirements of 40 CFR 60.18. (3) The specifications and requirements listed in paragraphs (c)(1...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Benzene Emissions From Benzene Storage Vessels § 61.271 Emission standard. The owner or operator of each storage...

  4. 40 CFR 61.271 - Emission standard.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... device requirements of 40 CFR 60.18. (3) The specifications and requirements listed in paragraphs (c)(1...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Benzene Emissions From Benzene Storage Vessels § 61.271 Emission standard. The owner or operator of each storage...

  5. 40 CFR 63.1652 - Emission standards.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 12 2011-07-01 2009-07-01 true Emission standards. 63.1652 Section 63...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards... Emission standards. (a) New and reconstructed submerged arc furnaces. No owner or operator shall cause...

  6. Emission Standards for Particulates

    ERIC Educational Resources Information Center

    Walsh, George W.

    1974-01-01

    Promulgation of standards of performance under Section 111 and national emission standards for hazardous pollutants under Section 112 of the Clean Air Act is the responsibility of the Emission Standards and Engineering Division of the Environmental Protection Agency. The problems encountered and the bases used are examined. (Author/BT)

  7. 40 CFR 61.52 - Emission standard.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Mercury § 61.52 Emission standard. (a) Emissions to the atmosphere from mercury ore processing facilities and mercury cell chlor-alkali plants shall not exceed 2.3 kg (5.1 lb) of mercury per 24-hour period. (b) Emissions to...

  8. 40 CFR 61.52 - Emission standard.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Mercury § 61.52 Emission standard. (a) Emissions to the atmosphere from mercury ore processing facilities and mercury cell chlor-alkali plants shall not exceed 2.3 kg (5.1 lb) of mercury per 24-hour period. (b) Emissions to...

  9. 40 CFR 61.52 - Emission standard.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Mercury § 61.52 Emission standard. (a) Emissions to the atmosphere from mercury ore processing facilities and mercury cell chlor-alkali plants shall not exceed 2.3 kg (5.1 lb) of mercury per 24-hour period. (b) Emissions to...

  10. 40 CFR 63.1403 - Emission standards.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... of 40 CFR part 63, subpart SS (national emission standards for closed vent systems, control devices, recovery devices). (b) Combined emission streams. When emissions of different kinds (e.g., emissions from... the emission streams would be required by this subpart to apply controls in the absence of...

  11. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  12. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  13. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  14. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  15. 40 CFR 61.162 - Emission limits.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Inorganic Arsenic Emissions... total arsenic emissions from the glass melting furnace shall be less than 2.5 Mg (2.7 ton) per year, or (2) Total arsenic emissions from the glass melting furnace shall be conveyed to a control device...

  16. 40 CFR 63.1403 - Emission standards.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... of 40 CFR part 63, subpart SS (national emission standards for closed vent systems, control devices, recovery devices). (b) Combined emission streams. When emissions of different kinds (e.g., emissions from... the emission streams would be required by this subpart to apply controls in the absence of...

  17. 40 CFR 61.52 - Emission standard.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Mercury § 61.52 Emission standard. (a) Emissions to the atmosphere from mercury ore processing facilities and mercury cell chlor-alkali plants shall not exceed 2.3 kg (5.1 lb) of mercury per 24-hour period. (b) Emissions to...

  18. DEVELOPMENT AND SELECTION OF AMMONIA EMISSION FACTORS FOR THE 1985 NAPAP EMISSIONS INVENTORY

    EPA Science Inventory

    The report, prepared for the National Acid Precipitation Assessment Program (NAPAP), identifies the most appropriate ammonia (NH3) emission factors available for inclusion in the 1985 NAPAP Emissions Inventory. H3 emission factors developed for several new NAPAP source categories...

  19. Air/Superfund national technical guidance study series, Volume 2. Estimation of baseline air emission at Superfund sites. Interim report(Final)

    SciTech Connect

    Not Available

    1989-01-01

    This volume is one in a series of manuals prepared for EPA to assist its Remedial Project Managers in the assessment of the air contaminant pathway and developing input data for risk assessment. The manual provides guidance on developing baseline-emission estimates from hazardous waste sites. Baseline-emission estimates (BEEs) are defined as emission rates estimated for a site in its undisturbed state. Specifically, the manual is intended to: Present a protocol for selecting the appropriate level of effort to characterize baseline air emissions; Assist site managers in designing an approach for BEEs; Describe useful technologies for developing site-specific baseline emission estimates (BEEs); Help site managers select the appropriate technologies for generating site-specific BEEs.

  20. California Natural Disasters - Using NASA Earth Observations to Assess Smoke Emissions, Fuel Loading, Moisture Content, and Vegetation Loss due to the 2009 Station Fire in the Angeles National Forest

    NASA Astrophysics Data System (ADS)

    Jones, M. L.; Reedy, J.; Moustafa, S.; Brundage, D.; Anderson, K.; Ferrare, R. A.; Swanson, A. J.; Yang, M. M.

    2010-12-01

    Wildfires are a normal occurrence in the state of California. Evidence of this can be seen in the Station Fire of 2009 (26 August - 16 October), a fire which destroyed over 154,000 acres of the Angeles National Forest and the combined summer fires of 2008 (22 May-29 August), which burned over 1,500,000 acres. In order to understand these fires it is important to consider several factors, including fire suppression, fuel loading, and the California climate. NDVI and NDMI maps for Angeles National forest were developed using Landsat 5 TM. The trend in live vegetation moisture content and vegetation condition for 2009 was found using these maps of Angeles National Forest. The NDMI maps were analyzed to understand changes in live vegetation moisture content that preceded the forest fires. Fuel for the Station fire was mapped using land classification through Landsat 5 TM and ASTER. This classification, along with moisture content levels, allowed for a method to map change in vegetation distribution, condition, and fuel load. The fuel load from these fires produces harmful emissions. These emissions contain large amounts of PM, including PM2.5, which are 2.5 micrometers in diameter and smaller (PM2.5). HYSPLIT trajectories were used to follow emissions from the 2008 summer fires to correlate with ARCTAS CARB data. HYSPLIT dispersion models were also used to show the deposition of particles in surrounding counties. Terra’s ASTER, MODIS, as well as data from EPA’s AirNow system, CARB AQMIS, and ARCTAS CARB flights were used to observe air quality factors such as PM2.5 levels, AOD, trace gases, and UV aerosol index. The results obtained from this study will demonstrate the feasibility of current and future NASA satellites to offer California policy makers assistance with more informed decision making.

  1. Modeling dry and wet deposition of sulfate, nitrate, and ammonium ions in Jiuzhaigou National Nature Reserve, China using a source-oriented CMAQ model: Part II. Emission sector and source region contributions.

    PubMed

    Qiao, Xue; Tang, Ya; Kota, Sri Harsha; Li, Jingyi; Wu, Li; Hu, Jianlin; Zhang, Hongliang; Ying, Qi

    2015-11-01

    A source-oriented Community Multiscale Air Quality (CMAQ) model driven by the meteorological fields generated by the Weather Research and Forecasting (WRF) model was used to study the dry and wet deposition of nitrate (NO3(-)), sulfate (SO4(2-)), and ammonium (NH4(+)) ions in the Jiuzhaigou National Nature Reserve (JNNR), China from June to August 2010 and to identify the contributions of different emission sectors and source regions that were responsible for the deposition fluxes. Contributions from power plants, industry, transportation, domestic, biogenic, windblown dust, open burning, fertilizer, and manure management sources to deposition fluxes in JNNR watershed and four EANET sites are determined. In JNNR, 96%, 82%, and 87% of the SO4(2-), NO3(-) and NH4(+) deposition fluxes are in the form of wet deposition of the corresponding aerosol species. Industry and power plants are the two major sources of SO4(2-) deposition flux, accounting for 86% of the total wet deposition of SO4(2-), and industry has a higher contribution (56%) than that of power plants (30%). Power plants and industry are also the top sources that are responsible for NO3(-) wet deposition, and contributions from power plants (30%) are generally higher than those from industries (21%). The major sources of NH4(+) wet deposition flux in JNNR are fertilizer (48%) and manure management (39%). Source-region apportionment confirms that SO2 and NOx emissions from local and two nearest counties do not have a significant impact on predicted wet deposition fluxes in JNNR, with contributions less than 10%. While local NH3 emissions account for a higher fraction of the NH4(+) deposition, approximately 70% of NH4(+) wet deposition in JNNR originated from other source regions. This study demonstrates that S and N deposition in JNNR is mostly from long-range transport rather than from local emissions, and to protect JNNR, regional emission reduction controls are needed. PMID:26050092

  2. Modeling dry and wet deposition of sulfate, nitrate, and ammonium ions in Jiuzhaigou National Nature Reserve, China using a source-oriented CMAQ model: Part II. Emission sector and source region contributions.

    PubMed

    Qiao, Xue; Tang, Ya; Kota, Sri Harsha; Li, Jingyi; Wu, Li; Hu, Jianlin; Zhang, Hongliang; Ying, Qi

    2015-11-01

    A source-oriented Community Multiscale Air Quality (CMAQ) model driven by the meteorological fields generated by the Weather Research and Forecasting (WRF) model was used to study the dry and wet deposition of nitrate (NO3(-)), sulfate (SO4(2-)), and ammonium (NH4(+)) ions in the Jiuzhaigou National Nature Reserve (JNNR), China from June to August 2010 and to identify the contributions of different emission sectors and source regions that were responsible for the deposition fluxes. Contributions from power plants, industry, transportation, domestic, biogenic, windblown dust, open burning, fertilizer, and manure management sources to deposition fluxes in JNNR watershed and four EANET sites are determined. In JNNR, 96%, 82%, and 87% of the SO4(2-), NO3(-) and NH4(+) deposition fluxes are in the form of wet deposition of the corresponding aerosol species. Industry and power plants are the two major sources of SO4(2-) deposition flux, accounting for 86% of the total wet deposition of SO4(2-), and industry has a higher contribution (56%) than that of power plants (30%). Power plants and industry are also the top sources that are responsible for NO3(-) wet deposition, and contributions from power plants (30%) are generally higher than those from industries (21%). The major sources of NH4(+) wet deposition flux in JNNR are fertilizer (48%) and manure management (39%). Source-region apportionment confirms that SO2 and NOx emissions from local and two nearest counties do not have a significant impact on predicted wet deposition fluxes in JNNR, with contributions less than 10%. While local NH3 emissions account for a higher fraction of the NH4(+) deposition, approximately 70% of NH4(+) wet deposition in JNNR originated from other source regions. This study demonstrates that S and N deposition in JNNR is mostly from long-range transport rather than from local emissions, and to protect JNNR, regional emission reduction controls are needed.

  3. THE 1985 NAPAP EMISSIONS INVENTORY: DEVELOPMENT OF TEMPORAL ALLOCATION FACTORS

    EPA Science Inventory

    The report documents the development and processing of temporal allocation factors for the 1985 National Acid Precipitation Assessment Program (NAPAP) emissions inventory (Version 2). The NAPAP emissions inventory represents the most comprehensive emissions data base available fo...

  4. 40 CFR 63.777 - Alternative means of emission limitation.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... equivalent to the reduction in HAP emissions from that source achieved under the applicable requirements in... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES... alternative achieves equivalent emission reductions....

  5. 40 CFR 63.1287 - Alternative means of emission limitation.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... equivalent to the reduction in HAP emissions from that source achieved under the applicable requirements in... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES... achieves equivalent emission reductions....

  6. 40 CFR 63.777 - Alternative means of emission limitation.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... equivalent to the reduction in HAP emissions from that source achieved under the applicable requirements in... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES... alternative achieves equivalent emission reductions....

  7. 40 CFR 63.777 - Alternative means of emission limitation.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... equivalent to the reduction in HAP emissions from that source achieved under the applicable requirements in... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES... alternative achieves equivalent emission reductions....

  8. Atmospheric mercury footprints of nations.

    PubMed

    Liang, Sai; Wang, Yafei; Cinnirella, Sergio; Pirrone, Nicola

    2015-03-17

    The Minamata Convention was established to protect humans and the natural environment from the adverse effects of mercury emissions. A cogent assessment of mercury emissions is required to help implement the Minamata Convention. Here, we use an environmentally extended multi-regional input-output model to calculate atmospheric mercury footprints of nations based on upstream production (meaning direct emissions from the production activities of a nation), downstream production (meaning both direct and indirect emissions caused by the production activities of a nation), and consumption (meaning both direct and indirect emissions caused by final consumption of goods and services in a nation). Results show that nations function differently within global supply chains. Developed nations usually have larger consumption-based emissions than up- and downstream production-based emissions. India, South Korea, and Taiwan have larger downstream production-based emissions than their upstream production- and consumption-based emissions. Developed nations (e.g., United States, Japan, and Germany) are in part responsible for mercury emissions of developing nations (e.g., China, India, and Indonesia). Our findings indicate that global mercury abatement should focus on multiple stages of global supply chains. We propose three initiatives for global mercury abatement, comprising the establishment of mercury control technologies of upstream producers, productivity improvement of downstream producers, and behavior optimization of final consumers.

  9. Atmospheric mercury footprints of nations.

    PubMed

    Liang, Sai; Wang, Yafei; Cinnirella, Sergio; Pirrone, Nicola

    2015-03-17

    The Minamata Convention was established to protect humans and the natural environment from the adverse effects of mercury emissions. A cogent assessment of mercury emissions is required to help implement the Minamata Convention. Here, we use an environmentally extended multi-regional input-output model to calculate atmospheric mercury footprints of nations based on upstream production (meaning direct emissions from the production activities of a nation), downstream production (meaning both direct and indirect emissions caused by the production activities of a nation), and consumption (meaning both direct and indirect emissions caused by final consumption of goods and services in a nation). Results show that nations function differently within global supply chains. Developed nations usually have larger consumption-based emissions than up- and downstream production-based emissions. India, South Korea, and Taiwan have larger downstream production-based emissions than their upstream production- and consumption-based emissions. Developed nations (e.g., United States, Japan, and Germany) are in part responsible for mercury emissions of developing nations (e.g., China, India, and Indonesia). Our findings indicate that global mercury abatement should focus on multiple stages of global supply chains. We propose three initiatives for global mercury abatement, comprising the establishment of mercury control technologies of upstream producers, productivity improvement of downstream producers, and behavior optimization of final consumers. PMID:25723898

  10. National Emission Standards for Hazardous Air Pollutants for Major Sources: Industrial, Commercial, and Institutional Boilers; Guidance for Calculating Efficiency Credits Resulting from Implementation of Energy Conservation Measures

    SciTech Connect

    Cox, Daryl; Papar, Riyaz; Wright, Dr. Anthony

    2013-02-01

    The purpose of this document is to provide guidance for developing a consistent approach to documenting efficiency credits generated from energy conservation measures in the Implementation Plan for boilers covered by the Boiler MACT rule (i.e., subpart DDDDD of CFR part 63). This document divides Boiler System conservation opportunities into four functional areas: 1) the boiler itself, 2) the condensate recovery system, 3) the distribution system, and 4) the end uses of the steam. This document provides technical information for documenting emissions credits proposed in the Implementation Plan for functional areas 2) though 4). This document does not include efficiency improvements related to the Boiler tune-ups.

  11. Comprehensive assessment of the specific compounds present in combustion processes. Volume 4. National estimates of emission of specific compounds from coal fired utility boiler plants. Final report

    SciTech Connect

    Lucas, R.M.; Kircher, G.W.

    1985-08-01

    Specimens were acquired from influents and effluents from seven coal-fired utility boilers. The specimens were chemically analyzed for toxic compounds in the polycyclic organic matter group. The specific target compounds were polychlorinated dibenzo(p)-dioxins (PCDDs), dibenzofurans (PCDFs), biphenyls (PCBs), selected polynuclear aromatic hydrocarbons (PAHs) and selected phthalates. Twelve PAH compounds and six phthalate compounds were included among the targetted compounds. Naphthalene was the most prevalent PAH compound detected. It was found in the flue gas emissions from all seven facilities. Other PAHs were also detected in the coal at all seven facilities but were only rarely detected in the other media. No PCDDs or PCDFs were detected in any of the acquired specimens. PCBs were only detected in one other media, the influent combustion air.

  12. Pacific Northwest National Laboratory Site Dose-per-Unit-Release Factors for Use in Calculating Radionuclide Air Emissions Potential-to-Emit Doses

    SciTech Connect

    Barnett, J. Matthew; Rhoads, Kathleen

    2009-06-11

    This report documents assumptions and inputs used to prepare the dose-per-unit-release factors for the Pacific Northwest National Laboratory (PNNL) Site (including the buildings that make up the Physical Sciences Facility [PSF] as well as the Environmental Molecular Sciences Laboratory [EMSL]) calculated using the EPA-approved Clean Air Act Assessment Package 1988–Personal Computer (CAP88-PC) Version 3 software package. The dose-per-unit-release factors are used to prepare dose estimates for a maximum public receptor (MPR) in support of Radioactive Air Pollutants Notice of Construction (NOC) applications for the PNNL Site.

  13. Pacific Northwest National Laboratory Site Dose-per-Unit-Release Factors for Use in Calculating Radionuclide Air Emissions Potential-to-Emit Doses

    SciTech Connect

    Barnett, J. Matthew; Rhoads, Kathleen

    2008-09-29

    This report documents assumptions and inputs used to prepare the dose-per-unit-release factors for the Pacific Northwest National Laboratory (PNNL) Site (including the buildings that make up the Physical Sciences Facility [PSF] as well as the Environmental Molecular Sciences Laboratory [EMSL]) calculated using the EPA-approved Clean Air Act Assessment Package 1988–Personal Computer (CAP88-PC) Version 3 software package. The dose-per-unit-release factors are used to prepare dose estimates for a maximum public receptor (MPR) in support of Radioactive Air Pollutants Notice of Construction (NOC) applications for the PNNL Site.

  14. India Co2 Emissions

    NASA Astrophysics Data System (ADS)

    Sharan, S.; Diffenbaugh, N. S.

    2010-12-01

    Is there a way to find a balance between improving living conditions for the people on the margins and also reducing emissions while limiting our negative impacts on the climate? This is a critical question today because there are many arguments between developed and developing countries about who is responsible for global warming. Developed countries believe that it is the poor countries because they are not educated enough to know about how they are affecting the climate. While the developing countries hold wealthy nations responsible because they are using the most resources. However it is important to acknowledge the fact that if there was no gap in between the developed and developing countries our emissions total would be much higher. This “gap” has been a natural controlling factor in climate change. This is why I wanted to see if I could plot what it would look like if a developing country such as India were to produce emissions that the US or Switzerland or Norway are producing as developed countries. India has a population total of 1.1 billion compared to the US with only 298 million, Switzerland with 7.5 million, and Norway with 4.6 million people. When the population is compared to the emissions output in metric tons, per capita, India produced the least emissions out of these countries, 1.4 tons per person while having the second largest population in the world, while the US produced 19 tons per capita, Switzerland produced 5.6 and Norway produced 8.7 tons per capita in 2006. The emissions rate is growing every year and increases widely and globally. If India was producing emissions that equal Norway, Switzerland and the US the total emissions it would be producing annually would be 9 billion for Norway, 6 billion for Switzerland and 20 billion emissions for the US, all in the year 2006 alone. This shows how the balance between countries with huge populations and very little emission output and average population and high emission out put has

  15. Development of national reference energy mean emission levels for the FHWA traffic noise model (FHWA TNM (trade name)), version 1.0. Final report, July 1993-November 1995

    SciTech Connect

    Fleming, G.G.; Rapoza, A.S.; Lee, C.S.Y.

    1995-11-01

    During the period, July 1993 through November 1995, the U.S. Department of Transportation , Research and Special Programs Administration, John A. Volpe National Transportation Systems Center (Volpe Center), Acoustics Facility. This report also presents the results of the study, including the measurement, data reduction and analysis procedures used to develop the Data Base. It discusses data for constant-flow and interrupted-flow roadway traffic, and data related to vehicle subsource heights. This report also presents the statistical methodology used to establish the Data Base for the FHWA TNM. Sound level regressions are presented as a function of several parameters, including vehicle speed, vehicle type, one-third octave-band frequency, roadway pavement type, roadway grade, traffic-flow condition and vehicle subsource height.

  16. 2009 LANL radionuclide air emissions report

    SciTech Connect

    Fuehne, David P.

    2010-06-01

    The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2009. This report meets the reporting requirements established in the regulations.

  17. 2008 LANL radionuclide air emissions report

    SciTech Connect

    Fuehne, David P.

    2009-06-01

    The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2008. This report meets the reporting requirements established in the regulations.

  18. 2010 LANL radionuclide air emissions report /

    SciTech Connect

    Fuehne, David P.

    2011-06-01

    The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2010. This report meets the reporting requirements established in the regulations.

  19. Simulation study of optimizing the 3-5 keV x-ray emission from pure Ar K-shell vs. Ag L-shell targets on the National Ignition Facility

    NASA Astrophysics Data System (ADS)

    Kemp, G. E.; Colvin, J. D.; Fournier, K. B.; Patel, M. V.; Scott, H. A.; Marinak, M.; Fisher, J. H.; Davis, J. F.

    2014-10-01

    High-flux x-ray sources are desirable for testing the radiation hardness of materials used in various civilian, space and military applications. For this study, there is an interest to design a source with primarily mid-energy (~ 3 keV) but limited soft (< 1 keV) x-ray contributions; we focus on optimizing the 3--5 keV non-LTE emission from targets consisting of pure Ar (K-shell) or Ag (L-shell) at sub-critical densities (~nc / 10) to ensure supersonic, volumetric laser heating with minimal losses to kinetic energy and thermal x rays. However, K and L-shell sources are expected to optimize at different temperatures and densities and it is a priori unclear under what target and laser conditions this will occur. Using HYDRA, a multi-dimensional, arbitrary Lagrangian-Eulerian, radiation-hydrodynamics code, we performed a simulation study by varying initial target density and laser parameters for each material as it would perform on the National Ignition Facility (NIF). We employ a model, benchmarked against Kr data collected on the NIF, that uses flux-limited Lee-More thermal conductivity and implicit Monte-Carlo photonics with non-LTE, detailed configuration accounting opacities from CRETIN. This work was performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract No. DE-AC52-07NA27344.

  20. 78 FR 34820 - Formaldehyde Emissions Standards for Composite Wood Products

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-06-10

    ...: Cindy Wheeler, National Program Chemicals Division, Office of Pollution Prevention and Toxics...-based resins (Ref. 3). Formaldehyde is an irritant and the National Toxicology Program recently... plywood and composite wood products (PCWP) National Emission Standards for Hazardous Air...

  1. 40 CFR 63.6603 - What emission limitations and operating limitations must I meet if I own or operate an existing...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) National Emissions Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal Combustion Engines Emission and Operating Limitations § 63.6603 What emission limitations and...

  2. 40 CFR 63.9634 - How do I demonstrate continuous compliance with the emission limitations that apply to me?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air... similar air pollution control device applied to each similar emission unit within a defined group...

  3. International Global Atmospheric Chemistry Programme global emissions inventory activity: Sulfur emissions from volcanoes, current status

    SciTech Connect

    Benkovitz, C.M.

    1995-07-01

    Sulfur emissions from volcanoes are located in areas of volcanic activity, are extremely variable in time, and can be released anywhere from ground level to the stratosphere. Previous estimates of global sulfur emissions from all sources by various authors have included estimates for emissions from volcanic activity. In general, these global estimates of sulfur emissions from volcanoes are given as global totals for an ``average`` year. A project has been initiated at Brookhaven National Laboratory to compile inventories of sulfur emissions from volcanoes. In order to complement the GEIA inventories of anthropogenic sulfur emissions, which represent conditions circa specific years, sulfur emissions from volcanoes are being estimated for the years 1985 and 1990.

  4. 40 CFR 63.1305 - Alternative means of emission limitation.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 11 2010-07-01 2010-07-01 true Alternative means of emission limitation. 63.1305 Section 63.1305 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous...

  5. 40 CFR 61.244 - Alternative means of emission limitation.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard...) Permission to use an alternative means of emission limitation under section 112(e)(3) of the Clean Air Act... 40 Protection of Environment 9 2012-07-01 2012-07-01 false Alternative means of...

  6. 40 CFR 61.244 - Alternative means of emission limitation.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard...) Permission to use an alternative means of emission limitation under section 112(e)(3) of the Clean Air Act... 40 Protection of Environment 9 2014-07-01 2014-07-01 false Alternative means of...

  7. 40 CFR 61.244 - Alternative means of emission limitation.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard...) Permission to use an alternative means of emission limitation under section 112(e)(3) of the Clean Air Act... 40 Protection of Environment 8 2011-07-01 2011-07-01 false Alternative means of...

  8. 40 CFR 61.244 - Alternative means of emission limitation.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard...) Permission to use an alternative means of emission limitation under section 112(e)(3) of the Clean Air Act... 40 Protection of Environment 8 2010-07-01 2010-07-01 false Alternative means of...

  9. 40 CFR Table 1 to Subpart Ssssss... - Emission Limits

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 14 2011-07-01 2011-07-01 false Emission Limits 1 Table 1 to Subpart... (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants for Glass Manufacturing Area Sources Pt. 63,...

  10. Monitoring the progress of emission inventories

    SciTech Connect

    Levy, J.A. Jr.; Solomon, D.; Husk, M.; Irving, B.; Kruger, D.; Levin. L.

    2006-12-15

    This issue of EM contains three articles which focus on the latest improvements on the emissions inventory process. The first, 'Building the national emissions inventory: challenges and plans for improvements' by Doug Solomon and Martin Husk (pages 8-11), looks at the US national emissions inventory. The next, 'Greenhouse gas inventories - a historical perspective and assessment of improvements since 1990' by Bill Irving and Dina Kruger (pages 12-19) assesses improvements in national and international greenhouse gas emissions inventories over the last 15 years. The third article, 'The global mercury emissions inventory' by Leonard Levin (pages 20-25) gives an overview of the challenges associated with conducting a worldwide inventory of mercury emissions.

  11. Odor and odorous chemical emissions from animal buildings: Part 3 - chemical emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This study was an add-on study to the National Air Emission Monitoring Study (NAEMS). The objective of this study was to measure odor emissions and corresponding concentrations and emissions of target odorous gases. Odor and odorous gas measurements at four NAEMS sites (dairy barns in Wisconsin-WI5B...

  12. Odor and odorous chemical emissions from animal buildings: Part 2. Odor emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This study was an add-on project to the National Air Emissions Monitoring Study (NAEMS) and focused on comprehensive measurement of odor emissions considering variations in seasons, animal types and olfactometry laboratories. Odor emissions from four of 14 NEAMS sites with nine barns/rooms (two dair...

  13. Odor and odorous chemical emissions from animal buildings: Part 2 - odor emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This study was an add-on project to the National Air Emissions Monitoring Study (NAEMS) and focused on comprehensive measurement of odor emissions. Odor emissions from two animal species (dairy and swine) from four sites with nine barns/rooms (two dairy barns in Wisconsin, two dairy barns and two sw...

  14. Odor and odorous chemical emissions from animal buildings: Part 3. Chemical emissions

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The objective of this study was to measure the long-term odor emissions and corresponding concentrations and emissions of 20 odorous volatile organic compounds (VOCs). This study was an add-on study to the National Air Emission Monitoring Study (NAEMS). Odor and odorous gas measurements at four NAEM...

  15. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; use of a modified ultrasonic nebulizer for the analysis of low ionic-strength water by inductively coupled optical emission spectrometry

    USGS Publications Warehouse

    Harris, Carl M.; Litteral, Charles J.; Damrau, Donna L.

    1997-01-01

    The U.S. Geological Survey National Water Quality Laboratory has developed a method for the determination of dissolved calcium, iron, magnesium, manganese, silica, and sodium using a modified ultrasonic nebulizer sample-introduction system to an inductively coupled plasma-optical emission spectrometer. The nebulizer's spray chamber has been modified to avoid carryover and memory effects common in some conventional ultrasonic designs. The modified ultrasonic nebulizer is equipped with a high-speed rinse cycle to remove previously analyzed samples from the spray chamber without excessive flush times. This new rinse cycle decreases sample washout times by reducing carryover and memory effects from salt or analytes in previously analyzed samples by as much as 45 percent. Plasma instability has been reduced by repositioning the argon carrier gas inlet on the spray chamber and by directly pumping waste from the chamber, instead of from open drain traps, thereby maintaining constant pressure to the plasma. The ultrasonic nebulizer improves signal intensities, which are 8 to 16 times greater than for a conventional cross-flow pneumatic nebulizer, without being sensitive to clogging from salt buildup as in cross-flow nebulizers. Detection limits for the ultrasonic nebulizer are 4 to 18 times less than detection limits achievable using a cross-flow pneumatic nebulizer, with equivalent sample analysis time.

  16. Seasonal variability in anthropogenic halocarbon emissions.

    PubMed

    Gentner, Drew R; Miller, Angela M; Goldstein, Allen H

    2010-07-15

    Ambient concentrations of eight predominantly anthropogenic halocarbons were measured via in situ gas chromatography in California's South Coast air basin for both summer and fall during the 2005 Study of Organic Aerosols at Riverside (SOAR). Ongoing emissions of the banned halocarbons methylchloroform and CFC-11 were observed in the South Coast air basin, whereas CFC-113 emissions have effectively ceased. We estimate anthropogenic emissions in the South Coast air basin for methylchloroform, CFC-11, HCFC-141b, chloroform, tetrachloroethene (PCE), trichloroethylene (TCE), and dichloromethane based on regressions of halocarbon to carbon monoxide mixing ratios and carbon monoxide emission inventories. We estimate per capita methylchloroform and chloroform emissions in the South Coast air basin for the year 2005 to be 6.6 +/- 0.4 g/(person.year) and 19 +/- 1 g/(person.year), respectively. We compare our results to national emission estimates calculated from previous work; for several compounds, emissions in the South Coast air basin are significantly lower than national per capita emissions. We observed strong seasonal differences in anthropogenic emissions of methylchloroform and chloroform; emissions were 4.5 and 2.5 times greater in summer than in fall, respectively. Possible seasonal sources include landfills and water chlorination. We conclude that seasonal variability in methylchloroform emissions has not been included in previous inventories and may cause errors in methylchloroform emission estimates after the year 2000 and seasonally resolved inversion calculations of hydroxyl radical abundance. PMID:20536226

  17. Implications of diesel emissions control failures to emission factors and road transport NOx evolution

    NASA Astrophysics Data System (ADS)

    Ntziachristos, Leonidas; Papadimitriou, Giannis; Ligterink, Norbert; Hausberger, Stefan

    2016-09-01

    Diesel NOx emissions have been at the forefront of research and regulation scrutiny as a result of failures of late vehicle technologies to deliver on-road emissions reductions. The current study aims at identifying the actual emissions levels of late light duty vehicle technologies, including Euro 5 and Euro 6 ones. Mean NOx emission factor levels used in the most popular EU vehicle emission models (COPERT, HBEFA and VERSIT+) are compared with latest emission information collected in the laboratory over real-world driving cycles and on the road using portable emissions measurement systems (PEMS). The comparison shows that Euro 5 passenger car (PC) emission factors well reflect on road levels and that recently revealed emissions control failures do not call for any significant corrections. However Euro 5 light commercial vehicles (LCVs) and Euro 6 PCs in the 2014-2016 period exhibit on road emission levels twice as high as used in current models. Moreover, measured levels vary a lot for Euro 6 vehicles. Scenarios for future evolution of Euro 6 emission factors, reflecting different degree of effectiveness of emissions control regulations, show that total NOx emissions from diesel Euro 6 PC and LCV may correspond from 49% up to 83% of total road transport emissions in 2050. Unless upcoming and long term regulations make sure that light duty diesel NOx emissions are effectively addressed, this will have significant implications in meeting future air quality and national emissions ceilings targets.

  18. Delineating outcomes of patients with diffuse large b cell lymphoma using the national comprehensive cancer network-international prognostic index and positron emission tomography-defined remission status; a population-based analysis.

    PubMed

    Bishton, Mark J; Hughes, Simon; Richardson, Faith; James, Eleanor; Bessell, Eric; Sovani, Vishakha; Ganatra, Rakesh; Haynes, Andrew P; McMillan, Andrew K; Fox, Christopher P

    2016-01-01

    The recently devised National Comprehensive Cancer Network International Prognostic Index (NCCN-IPI) appears superior to the revised IPI (R-IPI) in delineating outcome in diffuse large B-cell lymphoma. We examined the outcome of a population-based cohort of 223 consecutive patients treated with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisolone) or R-CHOP-like immuno-chemotherapy between January 2005 and December 2011 by both the NCCN-IPI and R-IPI, and further stratified outcome by the achievement of both computerized tomography (CT) and positron emission tomography (PET)-CT complete remission (CR), with the latter reassessed using blinded central review by an independent nuclear medicine and radiology specialist. The NCCN-IPI was superior to the R-IPI in identifying patients at very high risk of systemic and/or central nervous system relapse. Notably, both the NCCN-IPI and the R-IPI remained strongly predictive of relapse irrespective of CT or PET-defined remission status following R-CHOP. Patients with high-risk NCCN-IPI scores (≥6) have a dismal outcome following R-CHOP therapy regardless of PET-defined response to R-CHOP. Moreover, such patients appear refractory to salvage chemotherapy and thus require alternative therapeutic approaches, although age and performance status may, for many patients, preclude the safe delivery of a primary intensified regimen. By contrast, patients with NCCN-IPI 1-5 who achieve PET-CR following R-CHOP have excellent outcomes and may merit reduced follow up frequency. PMID:26577576

  19. Proposal of new expanded selection criteria using total tumor size and 18F-fluorodeoxyglucose - positron emission tomography/computed tomography for living donor liver transplantation in patients with hepatocellular carcinoma: The National Cancer Center Korea criteria

    PubMed Central

    Lee, Seung Duk; Lee, Bora; Kim, Seong Hoon; Joo, Jungnam; Kim, Seok-Ki; Kim, Young-Kyu; Park, Sang-Jae

    2016-01-01

    AIM: To expand the living donor liver transplantation (LT) pool of eligible patients with hepatocellular carcinoma (HCC) using new morphological and biological criteria. METHODS: Patients with HCC who underwent living donor LT (LDLT) from March 2005 to May 2013 at the National Cancer Center Korea (NCCK) were enrolled. We performed the 18F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT) before LDLT. Overall and disease-free survival analysis was done in patients to evaluate the usefulness of new NCCK criteria using PET/CT and total tumor size (10 cm). RESULTS: We enrolled a total of 280 patients who pathologically confirmed to have HCC and performed the PET/CT before transplantation. Among them, 164 (58.6%) patients fulfilled the NCCK criteria and 132 patients (47.1%) met the Milan criteria. Five-year overall and disease-free survival rates for patients who fulfilled the NCCK criteria showed 85.2% and 84.0%, respectively, and were significantly higher than those beyond the NCCK criteria (60.2% and 44.4%, respectively; P < 0.001). The correlation analysis between preoperative imaging tests and pathologic reports using Cohen’s Kappa demonstrated the better results in the NCCK criteria than those in the Milan criteria (0.850 vs 0.583). The comparison of disease-free analysis among the NCCK, Milan, and University of California, San Francisco (UCSF) criteria using the receiver operating characteristics curves revealed the similar area under the curve value criteria (NCCK vs Milan, P = 0.484; NCCK vs UCSF, P = 0.189 at 5-years). CONCLUSION: The NCCK criteria using hybrid concept of both morphological and biological parameters showed an excellent agreement between preoperative imaging and pathological results, and favorable survival outcomes. These new criteria might select the optimal patients with HCC waiting LDLT and expand the selection pool. PMID:27358787

  20. Emissions averaging top option for HON compliance

    SciTech Connect

    Kapoor, S. )

    1993-05-01

    In one of its first major rule-setting directives under the CAA Amendments, EPA recently proposed tough new emissions controls for nearly two-thirds of the commercial chemical substances produced by the synthetic organic chemical manufacturing industry (SOCMI). However, the Hazardous Organic National Emission Standards for Hazardous Air Pollutants (HON) also affects several non-SOCMI processes. The author discusses proposed compliance deadlines, emissions averaging, and basic operating and administrative requirements.

  1. 40 CFR 61.32 - Emission standard.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium § 61.32 Emission... shall not exceed 10 grams (0.022 lb) of beryllium over a 24-hour period, except as provided in paragraph... beryllium in the vicinity of the stationary source of 0.01 µg/m 3 (4.37×10−6 gr/ft 3), averaged over a...

  2. 40 CFR 61.32 - Emission standard.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium § 61.32 Emission... shall not exceed 10 grams (0.022 lb) of beryllium over a 24-hour period, except as provided in paragraph... beryllium in the vicinity of the stationary source of 0.01 µg/m 3 (4.37×10−6 gr/ft 3), averaged over a...

  3. 40 CFR 61.32 - Emission standard.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard for Beryllium § 61.32 Emission... shall not exceed 10 grams (0.022 lb) of beryllium over a 24-hour period, except as provided in paragraph... beryllium in the vicinity of the stationary source of 0.01 µg/m 3 (4.37×10−6 gr/ft 3), averaged over a...

  4. [Emission Factors of Vehicle Exhaust in Beijing].

    PubMed

    Fan, Shou-bin; Tian, Ling-di; Zhang, Dong-xu; Qu, Song

    2015-07-01

    Based on the investigation of basic data such as vehicle type composition, driving conditions, ambient temperature and oil quality, etc., emission factors of vehicle exhaust pollutants including carbon monoxide (CO), nitrogen oxides (NOx), hydrocarbons (HC) and particulate matter(PM) were calculated using COPERT IV model. Emission factors of typical gasoline passenger cars and diesel trucks were measured using on-board measurement system on actual road. The measured and modeled emission factors were compared and the results showed that: the measured emission factors of CO, NOx and HC were 0. 96, 0. 64 and 4. 89 times of the modeled data for passenger cars conforming to the national IV emission standard. For the light, medium and heavy diesel trucks conforming to the national III emission standard, the measured data of CO emission factors were 1.61, 1. 07 and 1.76 times of the modeled data, respectively, the measured data of NOx emission factors were 1. 04, 1. 21 and 1. 18 times of the modeled data, and the measured data of HC emission factors were 3. 75, 1. 84 and 1. 47 times of the modeled data, while the model data of PM emission factors were 1. 31, 3. 42 and 6. 42 times of the measured data, respectively. PMID:26489301

  5. [Emission Factors of Vehicle Exhaust in Beijing].

    PubMed

    Fan, Shou-bin; Tian, Ling-di; Zhang, Dong-xu; Qu, Song

    2015-07-01

    Based on the investigation of basic data such as vehicle type composition, driving conditions, ambient temperature and oil quality, etc., emission factors of vehicle exhaust pollutants including carbon monoxide (CO), nitrogen oxides (NOx), hydrocarbons (HC) and particulate matter(PM) were calculated using COPERT IV model. Emission factors of typical gasoline passenger cars and diesel trucks were measured using on-board measurement system on actual road. The measured and modeled emission factors were compared and the results showed that: the measured emission factors of CO, NOx and HC were 0. 96, 0. 64 and 4. 89 times of the modeled data for passenger cars conforming to the national IV emission standard. For the light, medium and heavy diesel trucks conforming to the national III emission standard, the measured data of CO emission factors were 1.61, 1. 07 and 1.76 times of the modeled data, respectively, the measured data of NOx emission factors were 1. 04, 1. 21 and 1. 18 times of the modeled data, and the measured data of HC emission factors were 3. 75, 1. 84 and 1. 47 times of the modeled data, while the model data of PM emission factors were 1. 31, 3. 42 and 6. 42 times of the measured data, respectively.

  6. 40 CFR Table 1 to Subpart Cccc of... - Emission Limitations

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...) National Emission Standards for Hazardous Air Pollutants: Manufacturing of Nutritional Yeast Pt. 63, Subpt... comply with the emission limitations in the following table: For each fed-batch fermenter producing yeast in the following fermentation stage . . . You must meet the following emission limitation . . ....

  7. 40 CFR Table 1 to Subpart Cccc of... - Emission Limitations

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...) National Emission Standards for Hazardous Air Pollutants: Manufacturing of Nutritional Yeast Pt. 63, Subpt... comply with the emission limitations in the following table: For each fed-batch fermenter producing yeast in the following fermentation stage . . . You must meet the following emission limitation . . ....

  8. 40 CFR Table 1 to Subpart Cccc of... - Emission Limitations

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...) National Emission Standards for Hazardous Air Pollutants: Manufacturing of Nutritional Yeast Pt. 63, Subpt... comply with the emission limitations in the following table: For each fed-batch fermenter producing yeast in the following fermentation stage . . . You must meet the following emission limitation . . ....

  9. 40 CFR Table 1 to Subpart Ssssss... - Emission Limits

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... glass produced; ORb. The 3-hour block average production-based metal HAP mass emission rate must not...) National Emission Standards for Hazardous Air Pollutants for Glass Manufacturing Area Sources Pt. 63, Subpt... must meet one of the following emission limits. . . 1. New or existing glass melting furnace...

  10. 40 CFR Table 1 to Subpart Ssssss... - Emission Limits

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... glass produced; ORb. The 3-hour block average production-based metal HAP mass emission rate must not...) National Emission Standards for Hazardous Air Pollutants for Glass Manufacturing Area Sources Pt. 63, Subpt... must meet one of the following emission limits. . . 1. New or existing glass melting furnace...

  11. 40 CFR Table 1 to Subpart Ssssss... - Emission Limits

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... glass produced; ORb. The 3-hour block average production-based metal HAP mass emission rate must not...) National Emission Standards for Hazardous Air Pollutants for Glass Manufacturing Area Sources Pt. 63, Subpt... must meet one of the following emission limits. . . 1. New or existing glass melting furnace...

  12. A new perspective: Measuring and modeling of landfill methane emissions

    SciTech Connect

    Bogner, J. |; Meadows, M.; Repa, E.

    1998-06-01

    Estimating landfill methane emissions at national and global levels is fraught with uncertainties. The goal for the near-term is to improve national and global estimates based on improved models, which more realistically simulate a growing database of field measurements. This would assist regulators and policy makers to more accurately evaluate landfill methane emissions and guide development of national mitigation strategies. This article provides an updated perspective on landfill methane emissions by: (1) discussing recent field measurements and research results; (2) proposing research still needed; and (3) suggesting improved modeling strategies (including regulatory approaches) to assess landfill methane emissions more accurately.

  13. SENSITIVITY ANALYSIS AND EVALUATION OF MICROFACO: A MICROSCALE MOTOR VEHICLE EMISSION FACTOR MODEL FOR CO EMISSIONS

    EPA Science Inventory

    The United States Environmental Protection Agency's National Exposure Research Laboratory has initiated a project to improve the methodology for modeling human exposure to motor vehicle emissions. The overall project goal is to develop improved methods for modeling the source t...

  14. 40 CFR 63.1451 - How do I demonstrate initial compliance with the emission limitations, work practice standards...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... CATEGORIES National Emission Standards for Hazardous Air Pollutants for Primary Copper Smelting Initial... matter emission limits. For each copper concentrate dryer, smelting furnace, slag cleaning vessel, and... acid particulate matter emissions limits. For each smelting furnace, slag cleaning vessel, and...

  15. 40 CFR 63.1451 - How do I demonstrate initial compliance with the emission limitations, work practice standards...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants for Primary Copper Smelting... particulate matter emission limits. For each copper concentrate dryer, smelting furnace, slag cleaning vessel... acid particulate matter emissions limits. For each smelting furnace, slag cleaning vessel, and...

  16. 40 CFR 63.1451 - How do I demonstrate initial compliance with the emission limitations, work practice standards...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants for Primary Copper Smelting... particulate matter emission limits. For each copper concentrate dryer, smelting furnace, slag cleaning vessel... acid particulate matter emissions limits. For each smelting furnace, slag cleaning vessel, and...

  17. 40 CFR 63.1583 - What are the emission points and control requirements for an industrial POTW treatment plant?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... control requirements for an industrial POTW treatment plant? 63.1583 Section 63.1583 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous...

  18. 40 CFR 63.1583 - What are the emission points and control requirements for an industrial POTW treatment plant?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... control requirements for an industrial POTW treatment plant? 63.1583 Section 63.1583 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous...

  19. 40 CFR 63.11955 - What are my initial and continuous compliance requirements for other emission sources?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air... gallons, whichever is larger, at standard temperature and pressure. (b) Before opening a...

  20. 40 CFR 63.11955 - What are my initial and continuous compliance requirements for other emission sources?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air... gallons, whichever is larger, at standard temperature and pressure. (b) Before opening a...

  1. 40 CFR 63.11955 - What are my initial and continuous compliance requirements for other emission sources?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air... gallons, whichever is larger, at standard temperature and pressure. (b) Before opening a...

  2. 40 CFR 63.6002 - How do I demonstrate initial compliance with the emission limits for puncture sealant application...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National... subpart. (b) You must submit the Notification of Compliance Status containing the results of the...

  3. Observational Evaluation of Mobile Source Emissions

    NASA Astrophysics Data System (ADS)

    Frost, G. J.; McKeen, S.; Trainer, M.; Aikin, K.; Peischl, J.; Ryerson, T.; Holloway, J.; Petron, G.; Tans, P.; Harley, R.

    2007-12-01

    Ambient ratios of NOx, CO, and CO2 sampled by aircraft in Houston and Dallas during the 2000 and 2006 Texas Air Quality Study (TexAQS) are compared with each other and with observations at a Houston highway tunnel. From these measurements we estimate 2000 and 2006 emissions for Houston and Dallas mobile sources. The observations demonstrate time-of-day variations in the relative contributions from gasoline and diesel combustion which are consistent with known traffic patterns. We incorporate CO2 emissions derived from the Federal Highway Administration's motor vehicle fuel use statistics into the EPA's National Emission Inventory (NEI), resulting in an emission data set for NOx, CO, and CO2 with 4-km spatial and hourly temporal resolution. Comparison of the emission ratios derived from the TexAQS observations with this inventory allows a direct evaluation of the NEI mobile source NOx and CO emissions.

  4. 76 FR 24476 - Agency Information Collection Activities; Proposed Collection; Comment Request; National Volatile...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-02

    ... Organic Compound Emission Standards for Aerosol Coatings AGENCY: Environmental Protection Agency (EPA... Manufacturing''. Title: National Volatile Organic Compound (VOC) Emission Standards for Aerosol Coatings (40 CFR... volatile organic compounds emissions from the use of consumer and commercial products. Pursuant to...

  5. Gaseous and particulate emissions from rural vehicles in China

    NASA Astrophysics Data System (ADS)

    Yao, Zhiliang; Huo, Hong; Zhang, Qiang; Streets, David G.; He, Kebin

    2011-06-01

    Rural vehicles (RVs) could contribute significantly to air pollutant emissions throughout Asia due to their considerable population, extensive usage, and high emission rates, but their emissions have not been measured before and have become a major concern for the accuracy of regional and global emission inventories. In this study, we measured CO, HC, NO x and PM emissions of RVs using a combined on-board emission measurement system on real roads in China. We also compared the emission levels of the twenty RVs to those of nineteen Euro II light-duty diesel trucks (LDDTs) that we measured for previous studies. The results show that one-cylinder RVs have lower distance-based emission factors compared to LDDTs because of their smaller weight and engine power, but they have significantly higher fuel-based PM emission factors than LDDTs. Four-cylinder RVs have equivalent emission levels to LDDTs. Based on the emission factors and the activity data obtained, we estimate that the total emissions of RVs in China in 2006 were 1049 Gg of CO, 332 Gg of HC, 933 Gg of NO x, and 54 Gg of PM, contributing over 40% to national on-road diesel CO, NO x, and PM emissions. As RVs are a significant contributor to national emissions, further research work is needed to improve the accuracy of inventories at all levels, and the government should strengthen the management of RVs to facilitate both policy making and research work.

  6. Aviation Particle Emissions Workshop

    NASA Technical Reports Server (NTRS)

    Wey, Chowen C. (Editor)

    2004-01-01

    The Aviation Particle Emissions Workshop was held on November 18 19, 2003, in Cleveland, Ohio. It was sponsored by the National Aeronautic and Space Administration (NASA) under the Vehicle Systems Program (VSP) and the Ultra- Efficient Engine Technology (UEET) Project. The objectives were to build a sound foundation for a comprehensive particulate research roadmap and to provide a forum for discussion among U.S. stakeholders and researchers. Presentations included perspectives from the Federal Aviation Administration, the U.S. Environmental Protection Agency, NASA, and United States airports. There were five interactive technical sessions: sampling methodology, measurement methodology, particle modeling, database, inventory and test venue, and air quality. Each group presented technical issues which generated excellent discussion. The five session leads collaborated with their members to present summaries and conclusions to each content area.

  7. Projection of hazardous air pollutant emissions to future years.

    PubMed

    Strum, Madeleine; Cook, Rich; Thurman, James; Ensley, Darrell; Pope, Anne; Palma, Ted; Mason, Richard; Michaels, Harvey; Shedd, Stephen

    2006-08-01

    Projecting a hazardous air pollutant (HAP) emission inventory to future years can provide valuable information for air quality management activities such as prediction of program successes and helping to assess future priorities. We have projected the 1999 National Emission Inventory for HAPs to numerous future years up to 2020 using the following tools and data: the Emissions Modeling System for Hazardous Air Pollutants (EMS-HAP), the National Mobile Inventory Model (NMIM), emission reduction information resulting from national standards and economic growth data. This paper discusses these projection tools, the underlying data, limitations and the results. The results presented include total HAP emissions (sum of pollutants) and toxicity-weighted HAP emissions for cancer and respiratory noncancer effects. Weighting emissions by toxicity does not consider fate, transport, or location and behavior of receptor populations and can only be used to estimate relative risks of direct emissions. We show these projections, along with historical emission trends. The data show that stationary source programs under Section 112 of the Clean Air Act Amendments of 1990 and mobile source programs which reduce hydrocarbon and particulate matter emissions, as well as toxic emission performance standards for reformulated gasoline, have contributed to and are expected to continue to contribute to large declines in air toxics emissions, in spite of economic and population growth. We have also analyzed the particular HAPs that dominate the source sectors to better understand the historical and future year trends and the differences across sectors.

  8. 40 CFR 63.4491 - What are my options for meeting the emission limits?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... emission limits? 63.4491 Section 63.4491 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants for Surface Coating of Plastic Parts...

  9. 40 CFR 63.4542 - How do I demonstrate continuous compliance with the emission limitations?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... compliance with the emission limitations? 63.4542 Section 63.4542 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants for Surface...

  10. 40 CFR 63.2983 - What emission limits must I meet?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ....2983 Section 63.2983 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants for Wet-Formed Fiberglass Mat Production Emission Limitations §...

  11. Feasibility of including fugitive PM-10 emissions estimates in the EPA emissions trends report

    SciTech Connect

    Barnard, W.; Carlson, P.

    1990-09-01

    The report describes the results of Part 2 of a two part study. Part 2 was to evaluate the feasibility of developing regional emission trends for PM-10. Part 1 was to evaluate the feasibility of developing VOC emission trends, on a regional and temporal basis. These studies are part of the effort underway to improve the national emission trends. Part 1 is presented in a separate report. The categories evaluated for the feasibility of developing regional emissions estimates were: unpaved roads, paved roads, wind erosion, agricultural tilling, construction activities, feedlots, burning, landfills, mining and quarrying unpaved parking lots, unpaved airstrips and storage piles.

  12. 2014 LANL Radionuclide Air Emissions Report

    SciTech Connect

    Fuehne, David Patrick

    2015-07-21

    This report describes the emissions of airborne radionuclides from operations at Los Alamos National Laboratory (LANL) for calendar year 2014, and the resulting off-site dose from these emissions. This document fulfills the requirements established by the National Emissions Standards for Hazardous Air Pollutants in 40 CFR 61, Subpart H – Emissions of Radionuclides other than Radon from Department of Energy Facilities, commonly referred to as the Radionuclide NESHAP or Rad-NESHAP. Compliance with this regulation and preparation of this document is the responsibility of LANL’s RadNESHAP compliance program, which is part of the Environmental Protection Division. The information in this report is required under the Clean Air Act and is being submitted to the U.S. Environmental Protection Agency (EPA) Region 6.

  13. Emissions trading - time to get serious

    SciTech Connect

    Vitelli, A.

    2007-11-15

    The Kyoto Protocol's five year compliance period begins in 2008. Industrialized nations around the world have pledged to cut carbon emissions, but the job seems to get harder, not easier, as 2008 approaches. Can market mechanisms make the crucial difference? The article discloses recent initiatives and developments worldwide. It concludes that it is clear that the market is maintaining its central role in fighting climate change and that bringing emissions trading to developing countries and to the US can only reinforce that role.

  14. 40 CFR 63.1113 - Procedures for approval of alternative means of emission limitation.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants for Source... of an affected source may request a determination of alternative means of emission limitation to the... limitation will achieve a reduction in HAP emissions at least equivalent to the reduction in emissions...

  15. Portable emission measurements of Yellowstone Park snowcoaches and snowmobiles.

    PubMed

    Bishop, Gary A; Stadtmuller, Ryan; Stedman, Donald H; Ray, John D

    2009-08-01

    As part of the National Park Service's Temporary Winter Use Plans Environmental Assessment, the University of Denver has been collecting in-use tailpipe emissions data from snowcoaches and snowmobiles in Yellowstone National Park. During the winter of 2006, using a portable emissions monitoring system, tailpipe data were collected from 10 snowcoaches and 2 four-stroke snowmobiles. These vehicles were operated over a standard route within the park, and the snowcoaches all carried identical passenger loads. These snowcoaches were newer in age with more advanced fuel management technology than those studied earlier, and average emissions were lower as a result (120, 1.7, and 11 g/mi for carbon monoxide [CO], hydrocarbons [HC], and oxides of nitrogen [NOx]). Large emissions variability was still observed despite using a standardized route and equal passenger loading. A comparison between five nearly identically equipped snowcoaches that had CO emissions ranging between 12 and 310 g/mi suggests that snow and road conditions are the most important factors behind the large emissions variability observed between modern snowcoaches: The first comprehensive emission measurements, using a portable emissions measurement system, on two snowmobiles showed that computer-controlled fuel management systems have increased fuel economy (>25 mpg) and are a major reason that emissions from these winter vehicles have dropped so dramatically. Using all of the tailpipe emissions data collected to date shows that the two primary winter vehicles in Yellowstone National Park are now very similar in their per-passenger emissions.

  16. US Department of Energy - Office of FreedomCar and Vehicle Technologies and US Centers for Disease Control and Prevention - National Institute for Occupational Safety and Health Inter-Agency Agreement Research on "The Analysis of Genotoxic Activities of Exhaust Emissions from Mobile Natural Gas, Diesel, and Spark-Ignition Engines"

    SciTech Connect

    William E. Wallace

    2006-09-30

    The US Department of Energy-Office of Heavy Vehicle Technologies (now the DOE-Office of FreedomCar and Vehicle Technologies) signed an Interagency Agreement (IAA) with National Institute for Occupational Safety and Health (NIOSH), No.01-15 DOE, 9/4/01, for 'The analysis of genotoxic activities of exhaust emissions from mobile natural gas, diesel, and spark-ignition engines'; subsequently modified on 3/27/02 (DOE IAG No.01-15-02M1); subsequently modified 9/02/03 (IAA Mod No. 01-15-03M1), as 'The analysis of genotoxic activities of exhaust emissions from mobile internal combustion engines: identification of engine design and operational parameters controlling exhaust genotoxicity'. The DOE Award/Contract number was DE-AI26-01CH11089. The IAA ended 9/30/06. This is the final summary technical report of National Institute for Occupational Safety and Health research performed with the US Department of Energy-Office of FreedomCar and Vehicle Technologies under that IAA: (A) NIOSH participation was requested by the DOE to provide in vitro genotoxicity assays of the organic solvent extracts of exhaust emissions from a suite of in-use diesel or spark-ignition vehicles; (B) research also was directed to develop and apply genotoxicity assays to the particulate phase of diesel exhaust, exploiting the NIOSH finding of genotoxicity expression by diesel exhaust particulate matter dispersed into the primary components of the surfactant coating the surface of the deep lung; (C) from the surfactant-dispersed DPM genotoxicity findings, the need for direct collection of DPM aerosols into surfactant for bioassay was recognized, and design and developmental testing of such samplers was initiated.

  17. AIR EMISSIONS FROM RESIDENTIAL HEATING: THE WOOD HEATING OPTION PUT INTO ENVIRONMENTAL PERSPECTIVE

    EPA Science Inventory

    The paper compares the national scale (rather than local) air quality impacts of the various residential space heating options. Specifically, it compares the relative contribution of the space heating options to fine particulate emissions, greenhouse gas emissions, and acid preci...

  18. Inventory of Alabama greenhouse gas emissions and sinks: 1990

    SciTech Connect

    Li, Chumeng; Herz, W.J.; Griffin, R.A.

    1996-12-31

    Greenhouse gas concentrations in the atmosphere have been increasing since the industrial revolution. Worldwide efforts are being made to study anthropogenic greenhouse gas emissions. This study quantified the anthropogenic greenhouse gas emissions in Alabama in 1990. Alabama anthropogenic greenhouse gas emissions and sinks from 13 sources were studied. 1990 Alabama total anthropogenic greenhouse gas emissions and sinks were estimated to be 153.42 and 21.66 million tons of carbon dioxide equivalent. As a result, the net total greenhouse gas emissions were estimated to be 131.76 million tons of carbon dioxide equivalent. Fossil fuel combustion is the major source of emissions, representing approximately 78 percent. Coal mining and landfills are other two significant emission sources, representing approximately 10 and 6 percent of the total emissions respectively. Forests in Alabama represent the major sink, offsetting approximately 14 percent of the total emissions. On a per capita basis, Alabama`s emission rate is 32.3 tons of carbon dioxide equivalent per capita in 1990, compared to the national per capita average of 23.4 tons of carbon dioxide equivalent. The high emission rate is attributed to higher emissions than the national average from fossil fuel combustion, from coal mining and landfills in Alabama.

  19. Acoustic emission descriptors

    NASA Astrophysics Data System (ADS)

    Witos, Franciszek; Malecki, Ignacy

    The authors present selected problems associated with acoustic emission interpreted as a physical phenomenon and as a measurement technique. The authors examine point sources of acoustic emission in isotropic, homogeneous linearly elastic media of different shapes. In the case of an unbounded medium the authors give the analytical form of the stress field and the wave shift field of the acoustic emission. In the case of a medium which is unbounded plate the authors give a form for the equations which is suitable for numerical calculation of the changes over time of selected acoustic emission values. For acoustic emission as a measurement technique, the authors represent the output signal as the resultant of a mechanical input value which describes the source, the transient function of the medium, and the transient function of specific components of the measurement loop. As an effect of this notation, the authors introduce the distinction between an acoustic measurement signal and an acoustic measurement impulse. The authors define the basic parameters of an arbitrary impulse. The authors extensively discuss the signal functions of acoustic emission impulses and acoustic emission signals defined in this article as acoustic emission descriptors (or signal functions of acoustic emission impulses) and advanced acoustic emission descriptors (which are either descriptors associated with acoustic emission applications or the signal functions of acoustic emission signals). The article also contains the results of experimental research on three different problems in which acoustic emission descriptors associated with acoustic emission pulses, acoustic emission applications, and acoustic emission signals are used. These problems are respectively: a problem of the amplitude-load characteristics of acoustic emission pulses in carbon samples subjected to compound uniaxial compression, the use of acoustic emission to predict the durability characteristics of conveyor belts, and

  20. Radionuclide air emissions report for the Hanford site, Calendar year 1994

    SciTech Connect

    Gleckler, B.P.; Diediker, L.P.; Jette, S.J.; Rhoads, K.; Soldat, S.K.

    1995-06-01

    This report documents radionuclide air emissions from the Hanford Site in 1994, and the resulting effective dose equivalent to the maximally exposed member of the public, referred to as the ``MEI.`` The report has been prepared and will be submitted in accordance with reporting requirements in the Code of Federal Regulations, title 40, Protection of the Environment, Part 61, ``National Emissions Standards for Hazardous Air Pollutants,`` Subpart H, ``National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.``

  1. Radionuclide air emissions report for the Hanford Site, calendar year 1992

    SciTech Connect

    Diediker, L.P.; Johnson, A.R.; Rhoads, K.; Klages, D.L.; Soldat, J.K.; Rokkan, D.J.

    1993-06-01

    This report documents radionuclide air emissions from the Hanford Site in 1992 and the resulting effective dose equivalent to an member of the public. The report has been prepared and will be submitted in accordance with reporting requirements in the Code of Federal Regulations, Title 40, Protection of the Environment, Part 61, ``National Emissions Standards for Hazardous Air Pollutants,`` Subpart H, ``National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.``

  2. Ammonia emissions in Europe, part II: How ammonia emission abatement strategies affect secondary aerosols

    NASA Astrophysics Data System (ADS)

    Backes, Anna M.; Aulinger, Armin; Bieser, Johannes; Matthias, Volker; Quante, Markus

    2016-02-01

    In central Europe, ammonium sulphate and ammonium nitrate make up a large fraction of fine particles which pose a threat to human health. Most studies on air pollution through particulate matter investigate the influence of emission reductions of sulphur- and nitrogen oxides on aerosol concentration. Here, we focus on the influence of ammonia (NH3) emissions. Emission scenarios have been created on the basis of the improved ammonia emission parameterization implemented in the SMOKE for Europe and CMAQ model systems described in part I of this study. This includes emissions based on future European legislation (the National Emission Ceilings) as well as a dynamic evaluation of the influence of different agricultural sectors (e.g. animal husbandry) on particle formation. The study compares the concentrations of NH3, NH4+, NO3 -, sulphur compounds and the total concentration of particles in winter and summer for a political-, technical- and behavioural scenario. It was found that a reduction of ammonia emissions by 50% lead to a 24% reduction of the total PM2.5 concentrations in northwest Europe. The observed reduction was mainly driven by reduced formation of ammonium nitrate. Moreover, emission reductions during winter had a larger impact than during the rest of the year. This leads to the conclusion that a reduction of the ammonia emissions from the agricultural sector related to animal husbandry could be more efficient than the reduction from other sectors due to its larger share in winter ammonia emissions.

  3. Pathways of human development and carbon emissions embodied in trade

    NASA Astrophysics Data System (ADS)

    Steinberger, Julia K.; Timmons Roberts, J.; Peters, Glen P.; Baiocchi, Giovanni

    2012-02-01

    It has long been assumed that human development depends on economic growth, that national economic expansion in turn requires greater energy use and, therefore, increased greenhouse-gas emissions. These interdependences are the topic of current research. Scarcely explored, however, is the impact of international trade: although some nations develop socio-economically and import high-embodied-carbon products, it is likely that carbon-exporting countries gain significantly fewer benefits. Here, we use new consumption-based measures of national carbon emissions to explore how the relationship between human development and carbon changes when we adjust national emission rates for trade. Without such adjustment of emissions, some nations seem to be getting far better development `bang' for the carbon `buck' than others, who are showing scant gains for disproportionate shares of global emissions. Adjusting for the transfer of emissions through trade explains many of these outliers, but shows that further socio-economic benefits are accruing to carbon-importing rather than carbon-exporting countries. We also find that high life expectancies are compatible with low carbon emissions but high incomes are not. Finally, we see that, despite strong international trends, there is no deterministic industrial development trajectory: there is great diversity in pathways, and national histories do not necessarily follow the global trends.

  4. Quantifying aluminum and semiconductor industry perfluorocarbon emissions from atmospheric measurements

    NASA Astrophysics Data System (ADS)

    Kim, Jooil; Fraser, Paul J.; Li, Shanlan; Mühle, Jens; Ganesan, Anita L.; Krummel, Paul B.; Steele, L. Paul; Park, Sunyoung; Kim, Seung-Kyu; Park, Mi-Kyung; Arnold, Tim; Harth, Christina M.; Salameh, Peter K.; Prinn, Ronald G.; Weiss, Ray F.; Kim, Kyung-Ryul

    2014-07-01

    The potent anthropogenic perfluorocarbon greenhouse gases tetrafluoromethane (CF4) and hexafluoroethane (C2F6) are emitted to the atmosphere mainly by the aluminum and semiconductor industries. Global emissions of these perfluorocarbons (PFCs) calculated from atmospheric measurements are significantly greater than expected from reported national and industry-based emission inventories. In this study, in situ measurements of the two PFCs in the Advanced Global Atmospheric Gases Experiment network are used to show that their emission ratio varies according to the relative regional presence of these two industries, providing an industry-specific emission "signature" to apportion the observed emissions. Our results suggest that underestimated emissions from the global semiconductor industry during 1990-2010, as well as from China's aluminum industry after 2002, account for the observed differences between emissions based on atmospheric measurements and on inventories. These differences are significant despite the large uncertainties in emissions based on the methodologies used by these industries.

  5. 40 CFR 63.6601 - What emission limitations must I meet if I own or operate a new or reconstructed 4SLB stationary...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (CONTINUED) National Emissions Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal Combustion Engines Emission and Operating Limitations § 63.6601 What emission limitations must I meet if...

  6. 40 CFR 63.6601 - What emission limitations must I meet if I own or operate a new or reconstructed 4SLB stationary...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) National Emissions Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal Combustion Engines Emission and Operating Limitations § 63.6601 What emission limitations must I meet if...

  7. 40 CFR 63.6601 - What emission limitations must I meet if I own or operate a new or reconstructed 4SLB stationary...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) National Emissions Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal Combustion Engines Emission and Operating Limitations § 63.6601 What emission limitations must I meet if...

  8. 40 CFR 63.6601 - What emission limitations must I meet if I own or operate a new or reconstructed 4SLB stationary...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... (CONTINUED) National Emissions Standards for Hazardous Air Pollutants for Stationary Reciprocating Internal Combustion Engines Emission and Operating Limitations § 63.6601 What emission limitations must I meet if...

  9. Carbon dioxide emissions from international air freight

    NASA Astrophysics Data System (ADS)

    Howitt, Oliver J. A.; Carruthers, Michael A.; Smith, Inga J.; Rodger, Craig J.

    2011-12-01

    Greenhouse gas emissions from international air transport were excluded from reduction targets under the Kyoto Protocol, partly because of difficulties with quantifying and apportioning such emissions. Although there has been a great deal of recent research into calculating emissions from aeroplane operations globally, publicly available emissions factors for air freight emissions are scarce. This paper presents a methodology to calculate the amount of fuel burnt and the resulting CO 2 emissions from New Zealand's internationally air freighted imports and exports in 2007. This methodology could be applied to other nations and/or regions. Using data on fuel uplift, air freight and air craft movements, and assumptions on mean passenger loadings and the mass of passengers and air freight, CO 2 emissions factors of 0.82 kg CO 2 per t-km and 0.69 kg CO 2 per t-km for short-haul and long-haul journeys, respectively, were calculated. The total amount of fuel consumed for the international air transport of New Zealand's imports and exports was calculated to be 0.21 Mt and 0.17 Mt respectively, with corresponding CO 2 emissions of 0.67 Mt and 0.53 Mt.

  10. Tropospheric Emission Spectrometer and Airborne Emission Spectrometer

    NASA Technical Reports Server (NTRS)

    Glavich, T.; Beer, R.

    1996-01-01

    The Tropospheric Emission Spectrometer (TES) is an instrument being developed for the NASA Earth Observing System Chemistry Platform. TES will measure the distribution of ozone and its precursors in the lower atmosphere. The Airborne Emission Spectrometer (AES) is an aircraft precursor to TES. Applicable descriptions are given of instrument design, technology challenges, implementation and operations for both.

  11. Culinary nationalism.

    PubMed

    Ferguson, Priscilla Parkhurst

    2010-01-01

    Culinary consciousness raisers, cooking texts often serve as vehicles of national identification. From Pampille (Marthe Allard Daudet) and her cookbook, Les Bons Plats de France, in 1913 to the international culinary competitions of today such as the Bocuse d'or, culinary distinction promotes national interests. In contrast to the strident nationalism of the early twentieth century, culinary nationalism today operates in an increasingly globalized world. National culinary distinction defines the nation and sells its products in a highly competitive international arena. A recent culinary text, the South Korean film Le Grand Chef [Sik Gaek ] (2007), illustrates the phenomenon, subsuming national culinary promotion in a mega culinary competition, all in the service of Korean culinary achievement. PMID:21539054

  12. Culinary nationalism.

    PubMed

    Ferguson, Priscilla Parkhurst

    2010-01-01

    Culinary consciousness raisers, cooking texts often serve as vehicles of national identification. From Pampille (Marthe Allard Daudet) and her cookbook, Les Bons Plats de France, in 1913 to the international culinary competitions of today such as the Bocuse d'or, culinary distinction promotes national interests. In contrast to the strident nationalism of the early twentieth century, culinary nationalism today operates in an increasingly globalized world. National culinary distinction defines the nation and sells its products in a highly competitive international arena. A recent culinary text, the South Korean film Le Grand Chef [Sik Gaek ] (2007), illustrates the phenomenon, subsuming national culinary promotion in a mega culinary competition, all in the service of Korean culinary achievement.

  13. NARSTO EMISSION INVENTORY ASSESSMENT

    EPA Science Inventory

    The NARSTO Ozone and Particulate Matter Assessments emphasized that emission inventories are critical to the success of air quality management programs and that emissions inventories in Canada, Mexico, and the United States need improvement to meet expectations for quality, timel...

  14. Control of Emissions

    NASA Technical Reports Server (NTRS)

    Parrish, Clyde F. (Inventor); Chung, Landy (Inventor)

    2013-01-01

    Methods and apparatus utilizing chlorine dioxide and hydrogen peroxide are useful to reduce NOx emissions, as well as SOx and mercury (or other heavy metal) emissions, from combustion flue gas streams.

  15. ORNL Fuels, Engines, and Emissions Research Center (FEERC)

    ScienceCinema

    None

    2016-07-12

    This video highlights the Vehicle Research Laboratory's capabilities at the Fuels, Engines, and Emissions Research Center (FEERC). FEERC is a Department of Energy user facility located at the Oak Ridge National Laboratory.

  16. ORNL Fuels, Engines, and Emissions Research Center (FEERC)

    SciTech Connect

    2013-04-12

    This video highlights the Vehicle Research Laboratory's capabilities at the Fuels, Engines, and Emissions Research Center (FEERC). FEERC is a Department of Energy user facility located at the Oak Ridge National Laboratory.

  17. THE 1985 NAPAP EMISSIONS INVENTORY: DEVELOPMENT OF SPECIES ALLOCATION FACTORS

    EPA Science Inventory

    The report describes the methodologies and data bases used to develop species allocation factors and data processing software used to develop the 1985 National Acid Precipitation Assessment Program (NAPAP) Modelers' Emissions Inventory (Version 2). Species allocation factors were...

  18. Methods of analysis by the U.S. Geological Survey National Water Quality Laboratory; determination of dissolved aluminum and boron in water by inductively coupled plasma-atomic emission spectrometry

    USGS Publications Warehouse

    Struzeski, T.M.; DeGiacomo, W.J.; Zayhowski, E.J.

    1996-01-01

    Inductively coupled plasma-atomic emission spectrometry is a sensitive, rapid, and accurate method for determining the dissolved concentration of aluminum and boron in water samples. The method detection limits are 5 micrograms per liter for aluminum and 4 micrograms per liter for boron. For aluminum, low-level (about 30 micrograms per liter) short-term precision (single-operator, seven days) is about 5 percent relative standard deviation and the low-level long-term precision (single-operator, nine months) is about 8 percent relative standard deviation. For boron, the low-level short-term precision is about 4 percent relative standard deviation, and the low-level long-term precision is about 5 percent relative standard deviation. Spike recoveries for aluminum ranged from 86 to 100 percent, and recoveries for boron ranged from 92 to 109 percent.

  19. National Intelligence and National Prosperity

    ERIC Educational Resources Information Center

    Hunt, Earl; Wittmann, Werner

    2008-01-01

    What is the relation between the cognitive competence of a national population that nation's economic prosperity? Lynn and Vanhanen [Lynn, R. & Vanhanen, T. (2002). "IQ and the wealth of nations." Westport, CT: Praeger.] presented data pointing to an exceptionally strong relationship between IQ scores and Gross Domestic Product per capita (GDP/c).…

  20. Acoustic emission frequency discrimination

    NASA Technical Reports Server (NTRS)

    Sugg, Frank E. (Inventor); Graham, Lloyd J. (Inventor)

    1988-01-01

    In acoustic emission nondestructive testing, broadband frequency noise is distinguished from narrow banded acoustic emission signals, since the latter are valid events indicative of structural flaws in the material being examined. This is accomplished by separating out those signals which contain frequency components both within and beyond (either above or below) the range of valid acoustic emission events. Application to acoustic emission monitoring during nondestructive bond verification and proof loading of undensified tiles on the Space Shuttle Orbiter is considered.

  1. DEVELOPMENT OF A MICROSCALE EMISSION FACTOR MODEL FOR PARTICULATE MATTER (MICROFACPM) FOR PREDICTING REAL-TIME MOTOR VEHICLE EMISSIONS

    EPA Science Inventory

    The United States Environmental Protection Agency's National Exposure Research Laboratory has initiated a project to improve the methodology for modeling human exposure to motor vehicle emissions. The overall project goal is to develop improved methods for modeling the source t...

  2. DEVELOPMENT OF A MICROSCALE EMISSION FACTOR MODEL FOR CO (MICROFACCO) FOR PREDICTING REAL-TIME VEHICLE EMISSIONS

    EPA Science Inventory

    The United States Environmental Protection Agency's National Exposure Research Laboratory has initiated a project to improve the methodology for modeling human exposure to motor vehicle emissions. The overall project goal is to develop improved methods for modeling the source t...

  3. DEVELOPMENT OF A MICROSCALE EMISSION FACTOR MODEL FOR PARTICULATE MATTER (MICROFACPM) FOR PREDICTING REAL-TIME MOTOR VEHICLE EMISSIONS

    EPA Science Inventory

    The United States Environmental Protection Agency's National Exposure Research Laboratory is pursuing a project to improve the methodology for modeling human exposure to motor vehicle emissions. The overall project is to develop improved methods for modeling the source through...

  4. Life Cycle Greenhouse Gas Emissions from Solar Photovoltaics (Fact Sheet)

    SciTech Connect

    Not Available

    2012-11-01

    The National Renewable Energy Laboratory (NREL) recently led the Life Cycle Assessment (LCA) Harmonization Project, a study that helps to clarify inconsistent and conflicting life cycle GHG emission estimates in the published literature and provide more precise estimates of life cycle GHG emissions from PV systems.

  5. 40 CFR Table 1 to Subpart Ssssss... - Emission Limits

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... SSSSSS of Part 63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS...) National Emission Standards for Hazardous Air Pollutants for Glass Manufacturing Area Sources Pt. 63, Subpt. SSSSSS, Table 1 Table 1 to Subpart SSSSSS of Part 63—Emission Limits As required in § 63.11451, you...

  6. Developing NASA's VIIRS LST and Emissivity EDRs using a physics based Temperature Emissivity Separation (TES) algorithm

    NASA Astrophysics Data System (ADS)

    Islam, T.; Hulley, G. C.; Malakar, N.; Hook, S. J.

    2015-12-01

    Land Surface Temperature and Emissivity (LST&E) data are acknowledged as critical Environmental Data Records (EDRs) by the NASA Earth Science Division. The current operational LST EDR for the recently launched Suomi National Polar-orbiting Partnership's (NPP) Visible Infrared Imaging Radiometer Suite (VIIRS) payload utilizes a split-window algorithm that relies on previously-generated fixed emissivity dependent coefficients and does not produce a dynamically varying and multi-spectral land surface emissivity product. Furthermore, this algorithm deviates from its MODIS counterpart (MOD11) resulting in a discontinuity in the MODIS/VIIRS LST time series. This study presents an alternative physics based algorithm for generation of the NASA VIIRS LST&E EDR in order to provide continuity with its MODIS counterpart algorithm (MOD21). The algorithm, known as temperature emissivity separation (TES) algorithm, uses a fast radiative transfer model - Radiative Transfer for (A)TOVS (RTTOV) in combination with an emissivity calibration model to isolate the surface radiance contribution retrieving temperature and emissivity. Further, a new water-vapor scaling (WVS) method is developed and implemented to improve the atmospheric correction process within the TES system. An independent assessment of the VIIRS LST&E outputs is performed against in situ LST measurements and laboratory measured emissivity spectra samples over dedicated validation sites in the Southwest USA. Emissivity retrievals are also validated with the latest ASTER Global Emissivity Database Version 4 (GEDv4). An overview and current status of the algorithm as well as the validation results will be discussed.

  7. Natural VOC emissions from forests in Poland

    NASA Astrophysics Data System (ADS)

    Isidorov, V.; Jaroszynska, J.; Sacharewicz, T.; Piroznikow, E.

    On the basis of the last inventory of forests and climatic conditions in Poland, a national evaluation of the emissions of reactive volatile organic compounds (VOCs) was carried out. Calculations took into account the composition and age structure of forests as well as the temperature dependencies of VOC emission rate for the main European forest-forming tree species. In the case of isoprene, the dependence on illumination level and day length was also taken into account. Estimations were made for all 49 administrative regions of Poland. Depending on weather conditions in different years, the total VOC emission of Polish forests can be in the range 186-763 kt yr -1. For instance, for a moderately warm year, 1992, it was estimated at 440.6 kt, which represents 25% of the total VOC emissions in Poland.

  8. Anthropogenic emissions of methane in the United States

    PubMed Central

    Miller, Scot M.; Wofsy, Steven C.; Michalak, Anna M.; Kort, Eric A.; Andrews, Arlyn E.; Biraud, Sebastien C.; Dlugokencky, Edward J.; Eluszkiewicz, Janusz; Fischer, Marc L.; Janssens-Maenhout, Greet; Miller, Ben R.; Miller, John B.; Montzka, Stephen A.; Nehrkorn, Thomas; Sweeney, Colm

    2013-01-01

    This study quantitatively estimates the spatial distribution of anthropogenic methane sources in the United States by combining comprehensive atmospheric methane observations, extensive spatial datasets, and a high-resolution atmospheric transport model. Results show that current inventories from the US Environmental Protection Agency (EPA) and the Emissions Database for Global Atmospheric Research underestimate methane emissions nationally by a factor of ∼1.5 and ∼1.7, respectively. Our study indicates that emissions due to ruminants and manure are up to twice the magnitude of existing inventories. In addition, the discrepancy in methane source estimates is particularly pronounced in the south-central United States, where we find total emissions are ∼2.7 times greater than in most inventories and account for 24 ± 3% of national emissions. The spatial patterns of our emission fluxes and observed methane–propane correlations indicate that fossil fuel extraction and refining are major contributors (45 ± 13%) in the south-central United States. This result suggests that regional methane emissions due to fossil fuel extraction and processing could be 4.9 ± 2.6 times larger than in EDGAR, the most comprehensive global methane inventory. These results cast doubt on the US EPA’s recent decision to downscale its estimate of national natural gas emissions by 25–30%. Overall, we conclude that methane emissions associated with both the animal husbandry and fossil fuel industries have larger greenhouse gas impacts than indicated by existing inventories. PMID:24277804

  9. Anthropogenic emissions of methane in the United States.

    PubMed

    Miller, Scot M; Wofsy, Steven C; Michalak, Anna M; Kort, Eric A; Andrews, Arlyn E; Biraud, Sebastien C; Dlugokencky, Edward J; Eluszkiewicz, Janusz; Fischer, Marc L; Janssens-Maenhout, Greet; Miller, Ben R; Miller, John B; Montzka, Stephen A; Nehrkorn, Thomas; Sweeney, Colm

    2013-12-10

    This study quantitatively estimates the spatial distribution of anthropogenic methane sources in the United States by combining comprehensive atmospheric methane observations, extensive spatial datasets, and a high-resolution atmospheric transport model. Results show that current inventories from the US Environmental Protection Agency (EPA) and the Emissions Database for Global Atmospheric Research underestimate methane emissions nationally by a factor of ∼1.5 and ∼1.7, respectively. Our study indicates that emissions due to ruminants and manure are up to twice the magnitude of existing inventories. In addition, the discrepancy in methane source estimates is particularly pronounced in the south-central United States, where we find total emissions are ∼2.7 times greater than in most inventories and account for 24 ± 3% of national emissions. The spatial patterns of our emission fluxes and observed methane-propane correlations indicate that fossil fuel extraction and refining are major contributors (45 ± 13%) in the south-central United States. This result suggests that regional methane emissions due to fossil fuel extraction and processing could be 4.9 ± 2.6 times larger than in EDGAR, the most comprehensive global methane inventory. These results cast doubt on the US EPA's recent decision to downscale its estimate of national natural gas emissions by 25-30%. Overall, we conclude that methane emissions associated with both the animal husbandry and fossil fuel industries have larger greenhouse gas impacts than indicated by existing inventories.

  10. Revising China's energy consumption and carbon emissions

    NASA Astrophysics Data System (ADS)

    Liu, Z.

    2015-12-01

    China is the world's largest carbon emitter and takes the lion's share of new increased emission since 2000, China's carbon emissions and mitigation efforts have received global attentions (Liu et al., Nature 500, 143-145)1. Yet China's emission estimates have been approved to be greatly uncertain (Guan et al., Nature Climate Change 2, 672-675)2. Accurate estimation becomes even crucial as China has recently pledged to reach a carbon emission peak by 2030, but no quantitative target has been given, nor is it even possible to assess without a reasonable baseline. Here we produced new estimates of Chinese carbon emissions for 1950-2012 based on a new investigation in energy consumption activities and emission factors using extensively surveyed and experimental data from 4243 mines and 602 coal samples. We reported that the total energy consumption is 10% higher than the nationally published value. The investigated emission factors used in China are significantly (40%) different from the IPCC default values which were used in drawing up several previous emission inventories. The final calculated total carbon emissions from China are 10% different than the amount reported by international data sets. The new estimate provides a revision of 4% of global emissions, which could have important implications for global carbon budgets and burden-sharing of climate change mitigation. 1 Liu, Z. et al. A low-carbon road map for China. Nature 500, 143-145 (2013). 2 Guan, D., Liu, Z., Geng, Y., Lindner, S. & Hubacek, K. The gigatonne gap in China's carbon dioxide inventories. Nature Climate Change, 672-675 (2012).

  11. Characterization of emissions from commercial aircraft engines during the Aircraft Particle Emissions eXperiment (APEX) 1 to 3

    EPA Science Inventory

    The fine particulate matter emissions from aircraft operations at large airports located in areas of the U. S. designated as non-attainment for the National Ambient Air Quality Standard for PM-2.5 are of major environmental concern. PM emissions data for commercial aircraft engin...

  12. Galactic Diffuse Emissions

    SciTech Connect

    Digel, Seth W.; /SLAC

    2007-10-25

    Interactions of cosmic rays with interstellar nucleons and photons make the Milky Way a bright, diffuse source of high-energy {gamma}-rays. Observationally, the results from EGRET, COMPTEL, and OSSE have now been extended to higher energies by ground-based experiments, with detections of diffuse emission in the Galactic center reported by H.E.S.S. in the range above 100 GeV and of diffuse emission in Cygnus by MILAGRO in the TeV range. In the range above 100 keV, INTEGRAL SPI has found that diffuse emission remains after point sources are accounted for. I will summarize current knowledge of diffuse {gamma}-ray emission from the Milky Way and review some open issues related to the diffuse emission -- some old, like the distribution of cosmic-ray sources and the origin of the 'excess' of GeV emission observed by EGRET, and some recently recognized, like the amount and distribution of molecular hydrogen not traced by CO emission -- and anticipate some of the advances that will be possible with the Large Area Telescope on GLAST. We plan to develop an accurate physical model for the diffuse emission, which will be useful for detecting and accurately characterizing emission from Galactic point sources as well as any Galactic diffuse emission from exotic processes, and for studying the unresolved extragalactic emission.

  13. Cermet Filters for Diesel Engine Emissions Reduction

    SciTech Connect

    Kong, Peter Chuen Sun

    2001-08-01

    Pollution from diesel engines is a significant part of our nation's air-quality problem. Even under the more stringent standards for heavy-duty engines set to take effect in 2004, these engines will continue to emit large amounts of nitrogen oxides and particulate matter, both of which affect public health. To address this problem, the Idaho National Engineering and Environmental Laboratory (INEEL) invented a self-cleaning, high temperature, cermet filter that reduces heavy-duty diesel engine emissions. The main advantage of the INEEL cermet filter, compared to current technology, is its ability to destroy carbon particles and NOx in diesel engine exhaust. As a result, this technology is expected to improve our nation's environmental quality by meeting the need for heavy-duty diesel engine emissions control. This paper describes the cermet filter technology and the initial research and development effort.

  14. Decimetric radio dot emissions

    NASA Astrophysics Data System (ADS)

    Mészárosová, H.; Karlický, M.; Sawant, H. S.; Fernandes, F. C. R.; Cecatto, J. R.; de Andrade, M. C.

    2008-11-01

    Context: We study a rare type of solar radio bursts called decimetric dot emissions. Aims: In the period 1999-2001, 20 events of decimetric dot emissions observed by the Brazilian Solar Spectroscope (BSS) in the frequency range 950-2640 MHz are investigated statistically and compared with radio fine structures of zebras and fibers. Methods: For the study of the spectral characteristics of the dot emissions we use specially developed Interactive Data Language (IDL) software called BSSView and basic statistical methods. Results: We have found that the dm dot emissions, contrary to the fine structures of the type IV bursts (i.e. zebras, fibers, lace bursts, spikes), are not superimposed on any background burst emission. In the radio spectrum, in most cases the dot emissions form chains that appear to be arranged in zebra patterns or fibers. Because some zebras and fibers, especially those observed with high time and high spectral resolutions, also show emission dots (but superimposed on the background burst emission), we compared the spectral parameters of the dot emissions with the dots being the fine structure of zebras and fibers. For both these dots, similar spectral characteristics were found. Some similarities of the dot emissions can be found also with the lace bursts and spikes. For some events the dot emissions show structural evolution from patterns resembling fibers to patterns resembling zebras and vice versa, or they evolve into fully chaotic patterns. Conclusions: For the first time, we present decimetric dot emissions that appear to be arranged in zebra patterns or fibers. We propose that these emissions are generated by the plasma emission mechanism at the locations in the solar atmosphere where the double resonance condition is fulfilled.

  15. Methods of Analysis by the U.S. Geological Survey National Water Quality Laboratory - Determination of Elements in Whole-Water Digests Using Inductively Coupled Plasma-Optical Emission Spectrometry and Inductively Coupled Plasma-Mass Spectrometry

    USGS Publications Warehouse

    Garbarino, John R.; Struzeski, Tedmund M.

    1998-01-01

    Inductively coupled plasma-optical emission spectrometry (ICP-OES) and inductively coupled plasma-mass spectrometry (ICP-MS) can be used to determine 26 elements in whole-water digests. Both methods have distinct advantages and disadvantages--ICP-OES is capable of analyzing samples with higher elemental concentrations without dilution, however, ICP-MS is more sensitive and capable of determining much lower elemental concentrations. Both techniques gave accurate results for spike recoveries, digested standard reference-water samples, and whole-water digests. Average spike recoveries in whole-water digests were 100 plus/minus 10 percent, although recoveries for digests with high dissolved-solid concentrations were lower for selected elements by ICP-MS. Results for standard reference-water samples were generally within 1 standard deviation of hte most probable values. Statistical analysis of the results from 43 whole-water digest indicated that there was no significant difference among ICP-OES, ICP-MS, and former official methods of analysis for 24 of the 26 elements evaluated.

  16. Silicon oxynitride: A field emission suppression coating

    NASA Astrophysics Data System (ADS)

    Theodore, Nimel D.

    We have studied coatings deposited using our inductively-coupled RF plasma ion implantation and desposition system to suppress field emission from large, 3-D electrode structures used in high voltage applications, like those used by Thomas Jefferson National Accelerator Facility in their DC-field photoelectron gun. Currently time and labor-intensive hand-polishing procedures are used to minimize field emission from these structures. Previous work had shown that the field emission from polished stainless steel (27 muA of field-emitted current at 15 MV/m) could be drastically reduced with simultaneous deposition of sputtered silicon dioxide during nitrogen implantation (167 pA of field-emitted current at 30 MV/m). We have determined that this unique implantation and deposition procedure produces high-purity silicon oxynitride films that can suppress field emission from stainless steel regardless of their initial surface polish. However, when this implantation procedure was applied to large, 3-D substrates, arcs occurred, damaging the coating and causing unreliable and unrepeatable field emission suppression. We have developed a novel reactive sputtering procedure to deposit high-purity silicon oxynitride coatings without nitrogen ion implantation. We can control the stoichometry and deposition rate of these coatings by adjusting the nitrogen pressure and incident RF-power. Using profilometry, Auger electron spectroscopy, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, Rutherford backscattering spectrometry, elastic recoil detection analysis, and current-voltage measurements, we have determined that the elemental composition, chemical bonding, density, and electrical properties of the reactively-sputtered silicon oxynitride coatings are similar to those produced by nitrogen implantation during silicon dioxide deposition. Furthermore, high voltage tests determined that both coatings similarly suppress field emission from 6" diameter, polished

  17. Low Emissions Aftertreatment and Diesel Emissions Reduction

    SciTech Connect

    2005-05-27

    Detroit Diesel Corporation (DDC) has successfully completed a five-year Low Emissions Aftertreatment and Diesel Emissions Reduction (LEADER) program under a DOE project entitled: ''Research and Development for Compression-Ignition Direct-Injection Engines (CIDI) and Aftertreatment Sub-Systems''. The objectives of the LEADER Program were to: Demonstrate technologies that will achieve future federal Tier 2 emissions targets; and Demonstrate production-viable technical targets for engine out emissions, efficiency, power density, noise, durability, production cost, aftertreatment volume and weight. These objectives were successfully met during the course of the LEADER program The most noteworthy achievements in this program are listed below: (1) Demonstrated Tier 2 Bin 3 emissions target over the FTP75 cycle on a PNGV-mule Neon passenger car, utilizing a CSF + SCR system These aggressive emissions were obtained with no ammonia (NH{sub 3}) slip and a combined fuel economy of 63 miles per gallon, integrating FTP75 and highway fuel economy transient cycle test results. Demonstrated feasibility to achieve Tier 2 Bin 8 emissions levels without active NOx aftertreatment. (2) Demonstrated Tier 2 Bin 3 emissions target over the FTP75 cycle on a light-duty truck utilizing a CSF + SCR system, synergizing efforts with the DOE-DDC DELTA program. This aggressive reduction in tailpipe out emissions was achieved with no ammonia slip and a 41% fuel economy improvement, compared to the equivalent gasoline engine-equipped vehicle. (3) Demonstrated Tier 2 near-Bin 9 emissions compliance on a light-duty truck, without active NOx aftertreatment devices, in synergy with the DOE-DDC DELTA program. (4) Developed and applied advanced combustion technologies such as ''CLEAN Combustion{copyright}'', which yields simultaneous reduction in engine out NOx and PM emissions while also improving engine and aftertreatment integration by providing favorable exhaust species and temperature

  18. The Wildland Fire Emission Inventory: emission estimates and an evaluation of uncertainty

    NASA Astrophysics Data System (ADS)

    Urbanski, S. P.; Hao, W. M.; Nordgren, B.

    2011-08-01

    We present the Wildland Fire Emission Inventory (WFEI), a high resolution model for non-agricultural open biomass burning (hereafter referred to as wildland fires) in the contiguous United States (CONUS). WFEI was used to estimate emissions of CO and PM2.5 for the western United States from 2003-2008. The estimated annual CO emitted ranged from 436 Gg yr-1 in 2004 to 3107 Gg yr-1 in 2007. The extremes in estimated annual PM2.5 emitted were 65 Gg yr-1 in 2004 and 454 Gg yr-1 in 2007. Annual wildland fire emissions were significant compared to other emission sources in the western United States as estimated in a national emission inventory. In the peak fire year of 2007, fire emissions were ~20 % of total CO emissions and ~39 % of total PM2.5 emissions. During the months with the greatest fire activity, wildland fires accounted for the majority of CO and PM2.5 emitted across the study region. The uncertainty in the inventory estimates of CO and PM2.5 emissions (ECO and EPM2.5, respectively) have been quantified across spatial and temporal scales relevant to regional and global modeling applications. The uncertainty in annual, domain wide emissions was 28 % to 51 % for CO and 40 % to 65 % for PM2.5. Sensitivity of the uncertainty in ECO and EPM2.5 to the emission model components depended on scale. At scales relevant to regional modeling applications (Δx = 10 km, Δt = 1 day) WFEI estimates 50 % of total ECO with an uncertainty <133 % and half of total EPM2.5 with an uncertainty <146 %. The uncertainty in ECO and EPM2.5 is significantly reduced at the scale of global modeling applications (Δx = 100 km, Δt = 30 day). Fifty percent of total emissions are estimated with an uncertainty <50 % for CO and <64 % for PM2.5. Uncertainty in the burned area drives the emission uncertainties at regional scales. At global scales the uncertainty in ECO is most sensitive to uncertainties in the fuel load consumed while the uncertainty in the emission factor for PM2.5 drives the

  19. The effects of energy paths and emission controls and standards on future trends in China's emissions of primary air pollutants

    NASA Astrophysics Data System (ADS)

    Zhao, Y.; Zhang, J.; Nielsen, C. P.

    2014-09-01

    To examine the efficacy of China's actions to control atmospheric pollution, three levels of growth of energy consumption and three levels of implementation of emission controls are estimated, generating a total of nine combined activity-emission control scenarios that are then used to estimate trends of national emissions of primary air pollutants through 2030. The emission control strategies are expected to have more effects than the energy paths on the future emission trends for all the concerned pollutants. As recently promulgated national action plans of air pollution prevention and control (NAPAPPC) are implemented, China's anthropogenic pollutant emissions should decline. For example, the emissions of SO2, NOx, total suspended particles (TSP), PM10, and PM2.5 are estimated to decline 7, 20, 41, 34, and 31% from 2010 to 2030, respectively, in the "best guess" scenario that includes national commitment of energy saving policy and implementation of NAPAPPC. Should the issued/proposed emission standards be fully achieved, a less likely scenario, annual emissions would be further reduced, ranging from 17 (for primary PM2.5) to 29% (for NOx) declines in 2015, and the analogue numbers would be 12 and 24% in 2030. The uncertainties of emission projections result mainly from the uncertain operational conditions of swiftly proliferating air pollutant control devices and lack of detailed information about emission control plans by region. The predicted emission trends by sector and chemical species raise concerns about current pollution control strategies: the potential for emissions abatement in key sectors may be declining due to the near saturation of emission control devices use; risks of ecosystem acidification could rise because emissions of alkaline base cations may be declining faster than those of SO2; and radiative forcing could rise because emissions of positive-forcing carbonaceous aerosols may decline more slowly than those of SO2 emissions and thereby

  20. The effects of energy paths and emission controls and standards on future trends in China's emissions of primary air pollutants

    NASA Astrophysics Data System (ADS)

    Zhao, Y.; Zhang, J.; Nielsen, C. P.

    2014-03-01

    To examine the efficacy of China's actions to control atmospheric pollution, three levels of growth of energy consumption and three levels of implementation of emission controls are estimated, generating a total of nine combined activity-emission control scenarios that are then used to estimate trends of national emissions of primary air pollutants through 2030. The emission control strategies are expected to have more effects than the energy paths on the future emission trends for all the concerned pollutants. As recently promulgated national action plans of air pollution prevention and control (NAPAPPC) are implemented, China's anthropogenic pollutant emissions should decline. For example, the emissions of SO2, NOx, total primary particulate matter (PM), PM10, and PM2.5 are estimated to decline 7%, 20%, 41%, 34%, and 31% from 2010 to 2030, respectively, in the "best guess" scenario that includes national commitment of energy saving policy and partial implementation of NAPAPPC. Should the issued/proposed emission standards be fully achieved, a less likely scenario, annual emissions would be further reduced, ranging from 17% (for primary PM2.5) to 29% (for NOx) declines in 2015, and the analogue numbers would be 12% and 24% in 2030. The uncertainties of emission projections result mainly from the uncertain operational conditions of swiftly proliferating air pollutant control devices and lack of detailed information about emission control plans by region. The predicted emission trends by sector and chemical species raise concerns about current pollution control strategies: the potential for emissions abatement in key sectors may be declining due to the near saturation of emission control devices use; risks of ecosystem acidification could rise because emissions of alkaline base cations may be declining faster than those of SO2; and radiative forcing could rise because emissions of positive-forcing carbonaceous aerosols may decline more slowly than those of SO2

  1. Mapping man-made CO2 emissions using satellite-observed nighttime lights

    NASA Astrophysics Data System (ADS)

    Oda, T.; Maksyutov, S. S.; Andres, R. J.; Elvidge, C.; Baugh, K.; Hsu, F. C.; Roman, M. O.

    2015-12-01

    The Open-Data Inventory for Anthropogenic Carbon dioxide (ODIAC) is a global high spatial resolution (1x1km) emission dataset for CO2 emissions from fossil fuel combustion. The original version of ODIAC was developed at the Japanese Greenhouse Gas Observing Satellite (GOSAT) project to prescribe their inverse model. ODIAC first introduced the combined use of satellite-observed nighttime light data and individual power plant emission/geolocation information to estimate the spatial extent of fossil fuel CO2. The ODIAC emission data has been widely used by the international carbon cycle research community and appeared in a number of publications in the literature. Since its original publication in 2011, we have made numerous modifications to the ODIAC emission model and the emission data have been updated on annual basis. We are switching from BP statistical data based emission estimates to estimates made by Carbon Dioxide Information Analysis Center (CDIAC) at Oak Ridge National Laboratory. In recent versions of ODIAC data, the emission seasonality has been adopted from the CDIAC monthly emission dataset. The emissions from international bunkers, which are not included in the CDIAC gridded emission data, are estimated using the UN Energy Database and included with the spatial distributions. In the next version of ODIAC emission model, we will explore the use of satellite data collected by the NASA's Suomi National Polar-orbiting Partnership (NPP) satellite. We will estimate emission spatial distributions using global 500x500m nighttime lights data created from VIIRS data. We will also utilize a combustion detection algorithm Nightfire developed at NOAA National Geophysical Data Center to map gas flaring emissions. We also plan to expand our two emission sector emission distributing approach (power plant emission and non-point source emissions) by introducing a transportation emission sector which should improve emission distributions in urban and rural areas.

  2. The National Environmental Respiratory Center (NERC) experiment in multi-pollutant air quality health research: III. Components of diesel and gasoline engine exhausts, hardwood smoke and simulated downwind coal emissions driving non-cancer biological responses in rodents.

    PubMed

    Mauderly, Joe L; Seilkop, Steven K

    2014-09-01

    An approach to identify causal components of complex air pollution mixtures was explored. Rats and mice were exposed by inhalation 6 h daily for 1 week or 6 months to dilutions of simulated downwind coal emissions, diesel and gasoline exhausts and wood smoke. Organ weights, hematology, serum chemistry, bronchoalveolar lavage, central vascular and respiratory allergic responses were measured. Multiple additive regression tree (MART) analysis of the combined database ranked 45 exposure (predictor) variables for importance to models best fitting 47 significant responses. Single-predictor concentration-response data were examined for evidence of single response functions across all exposure groups. Replication of the responses by the combined influences of the two most important predictors was tested. Statistical power was limited by inclusion of only four mixtures, albeit in multiple concentrations each and with particles removed for some groups. Results gave suggestive or strong evidence of causation of 19 of the 47 responses. The top two predictors of the 19 responses included only 12 organic and 6 inorganic species or classes. An increase in red blood cell count of rats by ammonia and pro-atherosclerotic vascular responses of mice by inorganic gases yielded the strongest evidence for causation and the best opportunity for confirmation. The former was a novel finding; the latter was consistent with other results. The results demonstrated the plausibility of identifying putative causal components of highly complex mixtures, given a database in which the ratios of the components are varied sufficiently and exposures and response measurements are conducted using a consistent protocol. PMID:25162720

  3. The National Environmental Respiratory Center (NERC) experiment in multi-pollutant air quality health research: II. Comparison of responses to diesel and gasoline engine exhausts, hardwood smoke and simulated downwind coal emissions.

    PubMed

    Mauderly, J L; Barrett, E G; Day, K C; Gigliotti, A P; McDonald, J D; Harrod, K S; Lund, A K; Reed, M D; Seagrave, J C; Campen, M J; Seilkop, S K

    2014-09-01

    The NERC Program conducted identically designed exposure-response studies of the respiratory and cardiovascular responses of rodents exposed by inhalation for up to 6 months to diesel and gasoline exhausts (DE, GE), wood smoke (WS) and simulated downwind coal emissions (CE). Concentrations of the four combustion-derived mixtures ranged from near upper bound plausible to common occupational and environmental hotspot levels. An "exposure effect" statistic was created to compare the strengths of exposure-response relationships and adjustments were made to minimize false positives among the large number of comparisons. All four exposures caused statistically significant effects. No exposure caused overt illness, neutrophilic lung inflammation, increased circulating micronuclei or histopathology of major organs visible by light microscopy. DE and GE caused the greatest lung cytotoxicity. WS elicited the most responses in lung lavage fluid. All exposures reduced oxidant production by unstimulated alveolar macrophages, but only GE suppressed stimulated macrophages. Only DE retarded clearance of bacteria from the lung. DE before antigen challenge suppressed responses of allergic mice. CE tended to amplify allergic responses regardless of exposure order. GE and DE induced oxidant stress and pro-atherosclerotic responses in aorta; WS and CE had no such effects. No overall ranking of toxicity was plausible. The ranking of exposures by number of significant responses varied among the response models, with each of the four causing the most responses for at least one model. Each exposure could also be deemed most or least toxic depending on the exposure metric used for comparison. The database is available for additional analyses. PMID:25162719

  4. The National Environmental Respiratory Center (NERC) experiment in multi-pollutant air quality health research: II. Comparison of responses to diesel and gasoline engine exhausts, hardwood smoke and simulated downwind coal emissions.

    PubMed

    Mauderly, J L; Barrett, E G; Day, K C; Gigliotti, A P; McDonald, J D; Harrod, K S; Lund, A K; Reed, M D; Seagrave, J C; Campen, M J; Seilkop, S K

    2014-09-01

    The NERC Program conducted identically designed exposure-response studies of the respiratory and cardiovascular responses of rodents exposed by inhalation for up to 6 months to diesel and gasoline exhausts (DE, GE), wood smoke (WS) and simulated downwind coal emissions (CE). Concentrations of the four combustion-derived mixtures ranged from near upper bound plausible to common occupational and environmental hotspot levels. An "exposure effect" statistic was created to compare the strengths of exposure-response relationships and adjustments were made to minimize false positives among the large number of comparisons. All four exposures caused statistically significant effects. No exposure caused overt illness, neutrophilic lung inflammation, increased circulating micronuclei or histopathology of major organs visible by light microscopy. DE and GE caused the greatest lung cytotoxicity. WS elicited the most responses in lung lavage fluid. All exposures reduced oxidant production by unstimulated alveolar macrophages, but only GE suppressed stimulated macrophages. Only DE retarded clearance of bacteria from the lung. DE before antigen challenge suppressed responses of allergic mice. CE tended to amplify allergic responses regardless of exposure order. GE and DE induced oxidant stress and pro-atherosclerotic responses in aorta; WS and CE had no such effects. No overall ranking of toxicity was plausible. The ranking of exposures by number of significant responses varied among the response models, with each of the four causing the most responses for at least one model. Each exposure could also be deemed most or least toxic depending on the exposure metric used for comparison. The database is available for additional analyses.

  5. The National Environmental Respiratory Center (NERC) experiment in multi-pollutant air quality health research: III. Components of diesel and gasoline engine exhausts, hardwood smoke and simulated downwind coal emissions driving non-cancer biological responses in rodents.

    PubMed

    Mauderly, Joe L; Seilkop, Steven K

    2014-09-01

    An approach to identify causal components of complex air pollution mixtures was explored. Rats and mice were exposed by inhalation 6 h daily for 1 week or 6 months to dilutions of simulated downwind coal emissions, diesel and gasoline exhausts and wood smoke. Organ weights, hematology, serum chemistry, bronchoalveolar lavage, central vascular and respiratory allergic responses were measured. Multiple additive regression tree (MART) analysis of the combined database ranked 45 exposure (predictor) variables for importance to models best fitting 47 significant responses. Single-predictor concentration-response data were examined for evidence of single response functions across all exposure groups. Replication of the responses by the combined influences of the two most important predictors was tested. Statistical power was limited by inclusion of only four mixtures, albeit in multiple concentrations each and with particles removed for some groups. Results gave suggestive or strong evidence of causation of 19 of the 47 responses. The top two predictors of the 19 responses included only 12 organic and 6 inorganic species or classes. An increase in red blood cell count of rats by ammonia and pro-atherosclerotic vascular responses of mice by inorganic gases yielded the strongest evidence for causation and the best opportunity for confirmation. The former was a novel finding; the latter was consistent with other results. The results demonstrated the plausibility of identifying putative causal components of highly complex mixtures, given a database in which the ratios of the components are varied sufficiently and exposures and response measurements are conducted using a consistent protocol.

  6. Developing a "Research Test Bed" to introduce innovative Emission Testing Technology to improve New Zealand's Vehicle Emission Standards

    NASA Astrophysics Data System (ADS)

    Cox, Stephen J.

    2012-05-01

    Vehicle exhaust emissions arise from the combustion of the fuel and air mixture in the engine. Exhaust emission gases generally include carbon monoxide (CO), oxides of nitrogen (NOx), hydrocarbons (HC), particulates, and the greenhouse gas carbon dioxide (CO2). In New Zealand improvements have occurred in emissions standards over the past 20 years however significant health related issues are now being discovered in Auckland as a direct effect of high vehicle emission levels. Pollution in New Zealand, especially via vehicle emissions are an increasing concern and threatens New Zealand's "clean and green" image. Unitec Institute of Technology proposes establishing a Vehicle Emissions Testing Facility, and with an understanding with Auckland University, National Institute of Water & Atmosphere Research Ltd (NIWA) this research group can work collaboratively on vehicle emissions testing. New Zealand research providers would support an application in the UK led by the University of Huddersfield to a range of European Union Structural Funds. New Zealand has an ideal "vehicle emissions research environment" supported by significant expertise in vehicle emission control technology and associated protocols at the University of Auckland, and the effects of high vehicle emissions on health at the National Institutes of Water and Atmosphere (NIWA).

  7. EDITORIAL: Tropical deforestation and greenhouse gas emissions

    NASA Astrophysics Data System (ADS)

    Gibbs, Holly K.; Herold, Martin

    2007-10-01

    Carbon emissions from tropical deforestation have long been recognized as a key component of the global carbon budget, and more recently of our global climate system. Tropical forest clearing accounts for roughly 20% of anthropogenic carbon emissions and destroys globally significant carbon sinks (IPCC 2007). Global climate policy initiatives are now being proposed to address these emissions and to more actively include developing countries in greenhouse gas mitigation (e.g. Santilli et al 2005, Gullison et al 2007). In 2005, at the Conference of the Parties (COP) in Montreal, the United Nations Framework Convention on Climate Change (UNFCCC) launched a new initiative to assess the scientific and technical methods and issues for developing policy approaches and incentives to reduce emissions from deforestation and degradation (REDD) in developing countries (Gullison et al 2007). Over the last two years the methods and tools needed to estimate reductions in greenhouse gas emissions from deforestation have quickly evolved, as the scientific community responded to the UNFCCC policy needs. This focus issue highlights those advancements, covering some of the most important technical issues for measuring and monitoring emissions from deforestation and forest degradation and emphasizing immediately available methods and data, as well as future challenges. Elements for effective long-term implementation of a REDD mechanism related to both environmental and political concerns are discussed in Mollicone et al. Herold and Johns synthesize viewpoints of national parties to the UNFCCC on REDD and expand upon key issues for linking policy requirements and forest monitoring capabilities. In response to these expressed policy needs, they discuss a remote-sensing-based observation framework to start REDD implementation activities and build historical deforestation databases on the national level. Achard et al offer an assessment of remote sensing measurements across the world

  8. Characterization of emissions from burning incense.

    PubMed

    Jetter, James J; Guo, Zhishi; McBrian, Jenia A; Flynn, Michael R

    2002-08-01

    The primary objective of this study was to improve the characterization of particulate matter emissions from burning incense. Emissions of particulate matter were measured for 23 different types of incense using a cyclone/filter method. Emission rates for PM2.5 (particulate matter less than 2.5 microm in aerodynamic diameter) ranged from 7 to 202 mg/h, and PM2.5 emission factors ranged from 5 to 56 mg/g of incense burned. Emission rates were also determined using an electrical low pressure impactor (ELPI) and a small electrostatic precipitator (ESP), and emission rates were compared to those determined using the cyclone/filter method. Emission rates determined by the ELPI method were consistently lower than those determined by the cyclone/filter method, and a linear regression correlation was found between emission rates determined by the two methods. Emission rates determined by the ESP method were consistently higher than those determined by the cyclone/filter method, indicating that the ESP may be a more effective method for measuring semivolatile particle emissions. A linear regression correlation was also found between emission rates determined by the ESP and cyclone/filter methods. Particle size distributions were measured with the ELPI, and distributions were found to be similar for most types of incense that were tested. Size distributions by mass typically ranged from approximately 0.06 to 2.5 microm in aerodynamic diameter, with peak values between 0.26 and 0.65 microm. Results indicated that burning incense emits fine particulate matter in large quantities compared to other indoor sources. An indoor air quality model showed that indoor concentrations of PM25 can far exceed the outdoor concentrations specified by the US EPA's National Ambient Air Quality Standards (NAAQS), so incense smoke can pose a health risk to people due to inhalation exposure of particulate matter. Emissions of carbon monoxide (CO), nitric oxide (NO), and sulfur dioxide (SO2) were

  9. Methane emissions from MBT landfills

    SciTech Connect

    Heyer, K.-U. Hupe, K.; Stegmann, R.

    2013-09-15

    ) model of the IPCC Guidelines for National Greenhouse Gas Inventories, 2006, was used to estimate the methane emissions from MBT landfills. Due to the calculation made by the authors emissions in the range of 60,000–135,000 t CO{sub 2-eq.}/a for all German MBT landfills can be expected. This wide range shows the uncertainties when the here used procedure and the limited available data are applied. It is therefore necessary to generate more data in the future in order to calculate more precise methane emission rates from MBT landfills. This is important for the overall calculation of the climate gas production in Germany which is required once a year by the German Government.

  10. Global Seabird Ammonia Emissions

    NASA Astrophysics Data System (ADS)

    Riddick, S. N.; Blackall, T. D.; Dragosits, U.; Daunt, F. H.; Braban, C. F.; Tang, Y. S.; Trathan, P.; Wanless, S.; Sutton, M. A.

    2010-12-01

    Seabird colonies represent a major source of atmospheric ammonia (NH3) in remote coastal and marine systems in temperate, tropical and polar regions. Previous studies have shown that NH3 emissions from Scottish seabird colonies were substantial - of similar magnitude to the most intensive agricultural point source emissions. The UK data were used to model global seabird NH3 emissions and suggested that penguins are a major source of emissions on and around the Antarctic continent. The largest seabird colonies are in the order of millions of seabirds. Due to the isolation of these colonies from anthropogenic nitrogen sources, they may play a major role in the nitrogen cycle within these ecosystems. A global seabird database was constructed and used in conjunction with a species-specific seabird bioenergetics model to map the locations of NH3 emissions from seabird colonies. The accuracy of the modelled emissions was validated with field data of NH3 emissions measured at key seabird colonies in different climatic regions of the world: temperate (Isle of May, Scotland), tropical (Ascension Island) and polar (Signy Island, South Georgia). The field data indicated good agreement between modelled and measured NH3 emissions. The measured NH3 emissions also showed the variability of emission with climate. Climate dependence of seabird NH3 emissions may have further implications under a changing global climate. Seabird colonies represent NH3 emission ‘hotspots’, often far from anthropogenic sources, and are likely to be the major source of nitrogen input to these remote coastal ecosystems. The direct manuring by seabirds at colony locations may strongly influence species richness and biodiversity. The subsequent volatilisation and deposition of NH3 increases the spatial extent of seabird influence on nitrogen cycling in their local ecosystem. As many seabird populations are fluctuating due to changing food supply, climate change or anthropogenic pressures, these factors

  11. ARS NP212 Climate change, soils and emissions program update

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The Agricultural Research Service National Program 212 (Climate Change, Soils, and Emissions) has a significant component focused on air quality studies. Presented here for the Agricultural Air Quality Task Force is an update on the status of ARS programs with focus on air quality. National Program ...

  12. Toluene emissions from plants

    NASA Astrophysics Data System (ADS)

    Heiden, A. C.; Kobel, K.; Komenda, M.; Koppmann, R.; Shao, M.; Wildt, J.

    The emission of toluene from different plants was observed in continuously stirred tank reactors and in field measurements. For plants growing without stress, emission rates were low and ranged from the detection limit up to 2·10-16 mol·cm-2·s-1. Under conditions of stress, the emission rates exceeded 10-14 mol·cm-2·s-1. Exposure of sunflower (Helianthus annuus L. cv. Gigantheus) to 13CO2 resulted in 13C-labeling of the emitted toluene on a time scale of hours. Although no biochemical pathway for the production of toluene is known, these results indicate that toluene is synthesized by the plants. The emission rates of toluene from sunflower are dependent on nutrient supply and wounding. Since α-pinene emission rates are also influenced by these factors, toluene and α-pinene emissions show a high correlation. During pathogen attack on Scots pines (Pinus sylvestris L.) significant toluene emissions were observed. In this case emissions of toluene and α-pinene also show a good correlation. Toluene emissions were also found in field experiments with pines using branch enclosures.

  13. Field emission chemical sensor

    DOEpatents

    Panitz, J.A.

    1983-11-22

    A field emission chemical sensor for specific detection of a chemical entity in a sample includes a closed chamber enclosing two field emission electrode sets, each field emission electrode set comprising (a) an electron emitter electrode from which field emission electrons can be emitted when an effective voltage is connected to the electrode set; and (b) a collector electrode which will capture said electrons emitted from said emitter electrode. One of the electrode sets is passive to the chemical entity and the other is active thereto and has an active emitter electrode which will bind the chemical entity when contacted therewith.

  14. REFINING FIRE EMISSIONS FOR AIR QUALITY MODELING WITH REMOTELY-SENSED FIRE COUNTS: A WILDFIRE CASE STUDY

    EPA Science Inventory

    This paper examines the use of Moderate Resolution Imaging Spectroradiometer (MODIS) observed active fire data (pixel counts) to refine the National Emissions Inventory (NEI) fire emission estimates for major wildfire events. This study was motivated by the extremely limited info...

  15. 40 CFR 63.8190 - What emission limitations must I meet?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Mercury Emissions From Mercury Cell... this section that applies to you. (1) New or reconstructed mercury cell chlor-alkali production facility. Emissions of mercury are prohibited from a new or reconstructed mercury cell...

  16. 40 CFR 63.8190 - What emission limitations must I meet?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Mercury Emissions From Mercury Cell... this section that applies to you. (1) New or reconstructed mercury cell chlor-alkali production facility. Emissions of mercury are prohibited from a new or reconstructed mercury cell...

  17. 40 CFR 63.8190 - What emission limitations must I meet?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Mercury Emissions From Mercury Cell... this section that applies to you. (1) New or reconstructed mercury cell chlor-alkali production facility. Emissions of mercury are prohibited from a new or reconstructed mercury cell...

  18. 40 CFR 63.4890 - What emission limits must I meet?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...) National Emission Standards for Hazardous Air Pollutants: Surface Coating of Metal Furniture Emission... alternative new source emission limit for specific metal furniture components or type of components for which... information demonstrating why no organic HAP-free coating technology can be used on the metal...

  19. 40 CFR 51.1008 - Emission inventory requirements for the PM2.5 NAAQS.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Provisions for Implementation of PM2.5 National Ambient Air Quality Standards § 51.1008 Emission inventory requirements for the PM2.5 NAAQS. (a) For purposes of meeting the emission inventory requirements of section... 40 Protection of Environment 2 2012-07-01 2012-07-01 false Emission inventory requirements for...

  20. 40 CFR 51.915 - What emissions inventory requirements apply under the 8-hour NAAQS?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... PLANS Provisions for Implementation of 8-hour Ozone National Ambient Air Quality Standard § 51.915 What... emissions inventory requirement in section 172(c)(3) of the Act shall apply, and an emission inventory SIP... emissions inventories for these areas, the ozone-relevant data element requirements under 40 CFR part...

  1. 40 CFR Table 3 to Subpart Jj of... - Summary of Emission Limits

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES... 3 Table 3 to Subpart JJ of Part 63—Summary of Emission Limits Emission point Existing source New source Finishing Operations: (a) Achieve a weighted average VHAP content across all coatings (maximum...

  2. A synthesis of carbon dioxide emissions from fossil-fuel combustion

    SciTech Connect

    Andres, Robert Joseph; Boden, Thomas A; Breon, F.-M.; Erickson, D; Gregg, J. S.; Jacobson, Andrew; Marland, Gregg; Miller, J.; Oda, T; Raupach, Michael; Rayner, P; Treanton, K.

    2012-01-01

    This synthesis discusses the emissions of carbon dioxide from fossil-fuel combustion and cement production. While much is known about these emissions, there is still much that is unknown about the details surrounding these emissions. This synthesis explores 5 our knowledge of these emissions in terms of why there is concern about them; how they are calculated; the major global efforts on inventorying them; their global, regional, and national totals at different spatial and temporal scales; how they are distributed on global grids (i.e. maps); how they are transported in models; and the uncertainties associated with these different aspects of the emissions. The magnitude of emissions 10 from the combustion of fossil fuels has been almost continuously increasing with time since fossil fuels were first used by humans. Despite events in some nations specifically designed to reduce emissions, or which have had emissions reduction as a byproduct of other events, global total emissions continue their general increase with time. Global total fossil-fuel carbon dioxide emissions are known to within 10% uncertainty (95% 15 confidence interval). Uncertainty on individual national total fossil-fuel carbon dioxide emissions range from a few percent to more than 50 %. The information discussed in this manuscript synthesizes global, regional and national fossil-fuel carbon dioxide emissions, their distributions, their transport, and the associated uncertainties.

  3. Odor and odorous chemical emissions from animal buildings: Part 6.Odor activity value

    Technology Transfer Automated Retrieval System (TEKTRAN)

    There is a growing concern with air and odor emissions from agricultural facilities. A supplementary research project was conducted to complement the U.S. National Air Emissions Monitoring Study (NAEMS). The overall goal of the project was to establish odor and chemical emission factors for animal...

  4. 40 CFR 63.1016 - Alternative means of emission limitation: Enclosed-vented process units.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 10 2011-07-01 2011-07-01 false Alternative means of emission... POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Equipment Leaks-Control Level 1 § 63.1016 Alternative means of emission limitation: Enclosed-vented process units. (a) Use of...

  5. 40 CFR 63.4552 - How do I demonstrate continuous compliance with the emission limitations?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... of Plastic Parts and Products Compliance Requirements for the Emission Rate Without Add-on Controls... compliance with the emission limitations? 63.4552 Section 63.4552 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS...

  6. 40 CFR 63.4563 - How do I demonstrate continuous compliance with the emission limitations?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... of Plastic Parts and Products Compliance Requirements for the Emission Rate with Add-on Controls... compliance with the emission limitations? 63.4563 Section 63.4563 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS...

  7. 40 CFR 63.8190 - What emission limitations must I meet?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Mercury Emissions From Mercury Cell... this section that applies to you. (1) New or reconstructed mercury cell chlor-alkali production facility. Emissions of mercury are prohibited from a new or reconstructed mercury cell...

  8. National contributions to observed global warming

    NASA Astrophysics Data System (ADS)

    Damon Matthews, H.; Graham, Tanya L.; Keverian, Serge; Lamontagne, Cassandra; Seto, Donny; Smith, Trevor J.

    2014-01-01

    There is considerable interest in identifying national contributions to global warming as a way of allocating historical responsibility for observed climate change. This task is made difficult by uncertainty associated with national estimates of historical emissions, as well as by difficulty in estimating the climate response to emissions of gases with widely varying atmospheric lifetimes. Here, we present a new estimate of national contributions to observed climate warming, including CO2 emissions from fossil fuels and land-use change, as well as methane, nitrous oxide and sulfate aerosol emissions While some countries’ warming contributions are reasonably well defined by fossil fuel CO2 emissions, many countries have dominant contributions from land-use CO2 and non-CO2 greenhouse gas emissions, emphasizing the importance of both deforestation and agriculture as components of a country’s contribution to climate warming. Furthermore, because of their short atmospheric lifetime, recent sulfate aerosol emissions have a large impact on a country’s current climate contribution We show also that there are vast disparities in both total and per-capita climate contributions among countries, and that across most developed countries, per-capita contributions are not currently consistent with attempts to restrict global temperature change to less than 2 °C above pre-industrial temperatures.

  9. Decadal emission estimates of carbon dioxide, sulfur dioxide, and nitric oxide emissions from coal burning in electric power generation plants in India.

    PubMed

    Mittal, Moti L; Sharma, Chhemendra; Singh, Richa

    2014-10-01

    This study aims to estimate the emissions of carbon dioxide (CO₂), sulfur dioxide (SO₂), and nitric oxide (NO) for coal combustion in thermal power plants in India using plant-specific emission factors during the period of 2001/02 to 2009/10. The mass emission factors have been theoretically calculated using the basic principles of combustion under representative prevailing operating conditions in the plants and fuel composition. The results show that from 2001/02 to 2009/10 period, total CO₂ emissions have increased from 324 to 499 Mt/year; SO₂ emissions have increased from 2,519 to 3,840 kt/year; and NO emissions have increased from 948 to 1,539 kt/year from the Indian coal-fired power plants. National average emissions per unit of electricity from the power plants do not show a noticeable improvement during this period. Emission efficiencies for new plants that use improved technology are found to be better than those of old plants. As per these estimates, the national average of CO₂ emissions per unit of electricity varies between 0.91 and 0.95 kg/kWh while SO₂ and NO emissions vary in the range of 6.9 to 7.3 and 2.8 to 2.9 g/kWh, respectively. Yamunagar plant in Haryana state showed the highest emission efficiencies with CO₂ emissions as 0.58 kg/kWh, SO₂ emissions as 3.87 g/kWh, and NO emissions as 1.78 g/kWh, while the Faridabad plant has the lowest emission efficiencies with CO₂ emissions as 1.5 kg/kWh, SO₂ emissions as 10.56 g/kWh, and NO emissions as 4.85 g/kWh. Emission values at other plants vary between the values of these two plants.

  10. National Anthem

    NASA Technical Reports Server (NTRS)

    1991-01-01

    A montage of video clips over the years, footage shows the spacecrews, launch, and landing for different orbiters and missions. Clips include the Endeavour and Atlantis Orbiters and are shown to the music of the American National Anthem.

  11. 40 CFR 63.4151 - How do I demonstrate initial compliance with the emission limitations?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants: Surface Coating of... period according to the requirements in § 63.4141(b). (c) Determine the density of each...

  12. 40 CFR 63.4151 - How do I demonstrate initial compliance with the emission limitations?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants... period according to the requirements in § 63.4141(b). (c) Determine the density of each...

  13. 40 CFR 63.177 - Alternative means of emission limitation: General.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Organic Hazardous Air Pollutants for Equipment Leaks § 63.177... 40 Protection of Environment 9 2010-07-01 2010-07-01 false Alternative means of...

  14. 40 CFR 63.177 - Alternative means of emission limitation: General.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Organic Hazardous Air Pollutants for Equipment Leaks § 63.177... 40 Protection of Environment 10 2014-07-01 2014-07-01 false Alternative means of...

  15. 40 CFR 63.177 - Alternative means of emission limitation: General.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Organic Hazardous Air Pollutants for Equipment Leaks § 63.177... 40 Protection of Environment 9 2011-07-01 2011-07-01 false Alternative means of...

  16. Documentation for Emissions of Greenhouse Gases in the United States 2008

    EIA Publications

    2011-01-01

    The Energy Policy Act of 1992 required the U.S. Energy Information Administration (EIA) to prepare an inventory of aggregate U.S. national emissions of greenhouse gases for the period 1987-1990, with annual updates thereafter. This report documents the methodology for the seventeenth annual inventory, covering national emissions over the period 1990-2008.

  17. 40 CFR 61.62 - Emission standard for ethylene dichloride plants.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission... dichloride purification. The concentration of vinyl chloride in each exhaust gas stream from any equipment used in ethylene dichloride purification is not to exceed 10 ppm (average for 3-hour period), except...

  18. 40 CFR 61.62 - Emission standard for ethylene dichloride plants.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ...) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission... dichloride purification. The concentration of vinyl chloride in each exhaust gas stream from any equipment used in ethylene dichloride purification is not to exceed 10 ppm (average for 3-hour period), except...

  19. 40 CFR 61.63 - Emission standard for vinyl chloride plants.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... plants. 61.63 Section 61.63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard... formation and purification: The concentration of vinyl chloride in each exhaust gas stream from...

  20. 40 CFR 61.63 - Emission standard for vinyl chloride plants.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... plants. 61.63 Section 61.63 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS National Emission Standard... formation and purification: The concentration of vinyl chloride in each exhaust gas stream from...

  1. 40 CFR 63.178 - Alternative means of emission limitation: Batch processes.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Organic Hazardous Air Pollutants for Equipment Leaks § 63.178... of this section provide the options of pressure testing or monitoring the equipment for leaks....

  2. 40 CFR 63.2850 - How do I comply with the hazardous air pollutant emission standards?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 12 2011-07-01 2009-07-01 true How do I comply with the hazardous air pollutant emission standards? 63.2850 Section 63.2850 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National...

  3. 40 CFR 63.9000 - What emission limitations and work practice standards must I meet?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ..., and HCl transfer operations that are also subject to 40 CFR part 63, subpart EEE, National Emission Standards for Hazardous Air Pollutants for Hazardous Waste Combustors, or 40 CFR 266.107, subpart H, Burning... SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Hydrochloric...

  4. 40 CFR 63.9000 - What emission limitations and work practice standards must I meet?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ..., and HCl transfer operations that are also subject to 40 CFR part 63, subpart EEE, National Emission Standards for Hazardous Air Pollutants for Hazardous Waste Combustors, or 40 CFR 266.107, subpart H, Burning... SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Hydrochloric...

  5. 40 CFR 63.9000 - What emission limitations and work practice standards must I meet?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ..., and HCl transfer operations that are also subject to 40 CFR part 63, subpart EEE, National Emission Standards for Hazardous Air Pollutants for Hazardous Waste Combustors, or 40 CFR 266.107, subpart H, Burning... SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Hydrochloric...

  6. 40 CFR 63.9000 - What emission limitations and work practice standards must I meet?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ..., and HCl transfer operations that are also subject to 40 CFR part 63, subpart EEE, National Emission Standards for Hazardous Air Pollutants for Hazardous Waste Combustors, or 40 CFR 266.107, subpart H, Burning... SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Hydrochloric...

  7. 40 CFR 63.9000 - What emission limitations and work practice standards must I meet?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ..., and HCl transfer operations that are also subject to 40 CFR part 63, subpart EEE, National Emission Standards for Hazardous Air Pollutants for Hazardous Waste Combustors, or 40 CFR 266.107, subpart H, Burning... SOURCE CATEGORIES (CONTINUED) National Emission Standards for Hazardous Air Pollutants: Hydrochloric...

  8. [Unregulated emissions from the gasoline vehicle].

    PubMed

    You, Qiu-Wen; Ge, Ytun-Shan; You, Ke-Wei; Wang, Jun-Fang; He, Chao

    2009-02-15

    Based on the emission test cycle of China National Regulation Stage III, the aldehyde and alkone emissions and VOCs emissions of three typical gasoline cars were studied with HPLC and TD-GC/MS and the exhausted particulates number and mass concentration were researched using ELPI. The results indicate that the unregulated emissions of different cars is diverse changed, the brake specific emission of the carbonyls in three cars are 36.44, 16.71 and 10.43 mg/km respectively and TVOC are 155.39, 103.75 and 42.29 mg/km respectively. Formaldehyde, acetaldehyde, acrolein, acetone and cyclohexanone are the main compounds in gasoline cars exhaust, which accounted for 77.9%-89.7% of total carbonyl compounds. Aromatic hydrocarbons and alkane are the main part of VOCs, the detected number of which is occupied 31.6%-39.2% and 23.1%-27.9% of VOCs. Toluene, xylene and benzene have high concentration, which are occupied 16.68%, 16.87% and 5.23% of TVOC in average. Ultra-fine particles (< 100 nm) dominate the particulates emission. Exhausted particulate number of high speeds is higher than that of slow and medium speeds.

  9. The Global Emissions Inventory Activity (GEIA)

    NASA Astrophysics Data System (ADS)

    Middleton, P.; Guenther, A. B.; Granier, C.; Mieville, A.

    2010-12-01

    GEIA aims to bring together people, analyses, data, and tools to quantify the anthropogenic emissions and natural exchanges of trace gases and aerosols that drive earth system changes and to facilitate use of this information by the research, assessment and policy communities. This presentation provides an overview of the current activities of GEIA. The GEIA network currently includes over 1000 people around the globe, and the plan is to extend this network to different communities working on environmental changes issues. The GEIA Center (www.geiacenter.org) hosts a comprehensive set of emissions related information, and plans to maintain a new database of scientific papers as well as national and international reports dealing with emissions issues. Conclusions from the recent GEIA conference, held in October 2009, also are summarized. Given the differences often found among data sets, the formation of a GEIA working group composed of emission developers and modelers who will compare data sets and implications for modeling is discussed. It has been recognized that consistent information on emissions at the global and regional scale is required, as well as an accurate quantification of emissions in the different megacities of the world. In order to develop these perspectives, GEIA plans to begin strengthening links with different key regions through creation of regional centers in corporation with other entities and individuals working in these regions.

  10. Constraining CO emission estimates using atmospheric observations

    NASA Astrophysics Data System (ADS)

    Hooghiemstra, P. B.

    2012-06-01

    We apply a four-dimensional variational (4D-Var) data assimilation system to optimize carbon monoxide (CO) emissions and to reduce the uncertainty of emission estimates from individual sources using the chemistry transport model TM5. In the first study only a limited amount of surface network observations from the National Oceanic and Atmospheric Administration Earth System Research Laboratory (NOAA/ESRL) Global Monitoring Division (GMD) is used to test the 4D-Var system. Uncertainty reduction up to 60% in yearly emissions is observed over well-constrained regions and the inferred emissions compare well with recent studies for 2004. However, since the observations only constrain total CO emissions, the 4D-Var system has difficulties separating anthropogenic and biogenic sources in particular. The inferred emissions are validated with NOAA aircraft data over North America and the agreement is significantly improved from the prior to posterior simulation. Validation with the Measurements Of Pollution In The Troposphere (MOPITT) instrument shows a slight improved agreement over the well-constrained Northern Hemisphere and in the tropics (except for the African continent). However, the model simulation with posterior emissions underestimates MOPITT CO total columns on the remote Southern Hemisphere (SH) by about 10%. This is caused by a reduction in SH CO sources mainly due to surface stations on the high southern latitudes. In the second study, we compare two global inversions to estimate carbon monoxide (CO) emissions for 2004. Either surface flask observations from NOAA or CO total columns from the MOPITT instrument are assimilated in a 4D-Var framework. In the Southern Hemisphere (SH) three important findings are reported. First, due to their different vertical sensitivity, the stations-only inversion increases SH biomass burning emissions by 108 Tg CO/yr more than the MOPITT-only inversion. Conversely, the MOPITT-only inversion results in SH natural emissions

  11. National Biobanks

    PubMed Central

    Mitchell, Robert

    2010-01-01

    The development of genomics has dramatically expanded the scope of genetic research, and collections of genetic biosamples have proliferated in countries with active genomics research programs. In this essay, we consider a particular kind of collection, national biobanks. National biobanks are often presented by advocates as an economic “resource” that will be used by both basic researchers and academic biologists, as well as by pharmaceutical diagnostic and clinical genomics companies. Although national biobanks have been the subject of intense interest in recent social science literature, most prior work on this topic focuses either on bioethical issues related to biobanks, such as the question of informed consent, or on the possibilities for scientific citizenship that they make possible. We emphasize, by contrast, the economic aspect of biobanks, focusing specifically on the way in which national biobanks create biovalue. Our emphasis on the economic aspect of biobanks allows us to recognize the importance of what we call clinical labor—that is, the regularized, embodied work that members of the national population are expected to perform in their role as biobank participants—in the creation of biovalue through biobanks. Moreover, it allows us to understand how the technical way in which national biobanks link clinical labor to databases alters both medical and popular understandings of risk for common diseases and conditions. PMID:20526462

  12. Outsourcing CO2 Emissions

    NASA Astrophysics Data System (ADS)

    Davis, S. J.; Caldeira, K. G.

    2009-12-01

    CO2 emissions from the burning of fossil fuels are the primary cause of global warming. Much attention has been focused on the CO2 directly emitted by each country, but relatively little attention has been paid to the amount of emissions associated with consumption of goods and services in each country. This consumption-based emissions inventory differs from the production-based inventory because of imports and exports of goods and services that, either directly or indirectly, involved CO2 emissions. Using the latest available data and reasonable assumptions regarding trans-shipment of embodied carbon through third-party countries, we developed a global consumption-based CO2 emissions inventory and have calculated associated consumption-based energy and carbon intensities. We find that, in 2004, 24% of CO2 emissions are effectively outsourced to other countries, with much of the developed world outsourcing CO2 emissions to emerging markets, principally China. Some wealthy countries, including Switzerland and Sweden, outsource over half of their consumption-based emissions, with many northern Europeans outsourcing more than three tons of emissions per person per year. The United States is both a big importer and exporter of emissions embodied in trade, outsourcing >2.6 tons of CO2 per person and at the same time as >2.0 tons of CO2 per person are outsourced to the United States. These large flows indicate that CO2 emissions embodied in trade must be taken into consideration when considering responsibility for increasing atmospheric greenhouse gas concentrations.

  13. Evaluation of Mobile Source Emissions and Trends

    NASA Astrophysics Data System (ADS)

    Dallmann, Timothy Ryan

    Mobile sources contribute significantly to air pollution problems. Relevant pollutants include numerous gaseous and particle-phase species that can affect human health, ecosystems, and climate. Accurate inventories of emissions from these sources are needed to help understand possible adverse impacts, and to develop effective air quality management strategies. Unfortunately large uncertainties persist in the understanding of mobile source emissions, and how these emissions are changing over time. This dissertation aims to evaluate long-term trends in mobile source emissions in the United States, and to make detailed measurements of emissions from present-day fleets of on-road vehicles operating in California. Long-term trends in mobile source emissions of nitrogen oxides (NO x) and fine particulate matter (PM2.5) in the United States were investigated through development of a fuel-based emission inventory. Annual emissions from on- and off-road gasoline and diesel engines were quantified for the years 1996-2006. Diesel engines were found to be the dominant mobile source of NOx and PM2.5, and on-road diesel vehicles were identified as the single largest anthropogenic source of NOx emissions in the United States as of 2005. The importance of diesel engines as a source of exhaust particulate matter emissions has led to the recent introduction of advanced emission control technologies in the United States, such as diesel particle filters (DPF), which have been required since 2007 for all new on-road heavy-duty (HD) diesel engines. In addition to national requirements for the use of such control devices on new engines, California has mandated accelerated clean-up of statewide emissions from older in-use diesel engines. The plume capture method was further applied to measure emissions from a more diverse population of trucks observed at the Caldecott tunnel in summer 2010. Emissions from hundreds of individual trucks were measured, and emission factor distributions were

  14. Emission properties of explosive field emission cathodes

    SciTech Connect

    Roy, Amitava; Patel, Ankur; Menon, Rakhee; Sharma, Archana; Chakravarthy, D. P.; Patil, D. S.

    2011-10-15

    The research results of the explosive field emission cathode plasma expansion velocity and the initial emission area in the planar diode configuration with cathodes made of graphite, stainless steel, polymer velvet, carbon coated, and carbon fiber (needle type) cathodes are presented. The experiments have been performed at the electron accelerator LIA-200 (200 kV, 100 ns, and 4 kA). The diode voltage has been varied from 28-225 kV, whereas the current density has been varied from 86-928 A/cm{sup 2} with 100 ns pulse duration. The experimentally obtained electron beam diode perveance has been compared with the 1 dimensional Child-Langmuir- law. It was found that initially only a part of the cathode take part in the emission process. The plasma expands at 1.7-5.2 cm/{mu}s for 4 mm anode-cathode gap for various cathode materials. It was found that the plasma expansion velocity increases with the decrease in the cathode diameter. At the beginning of the accelerating pulse, the entire cathode area participates in the electron emission process only for the multiple needle type carbon fiber cathode.

  15. NARSTO EMISSION INVENTORY ASSESSMENT

    EPA Science Inventory

    The NARSTO Emission Inventory Committee has been pursuing enhancement of the emission inventory program for North American countries--Canada, Mexico, and the United States. With the completion of the NARSTO Ozone and Particulate Matter Assessments, it was recognized that emissio...

  16. Database of emission lines

    NASA Astrophysics Data System (ADS)

    Binette, L.; Ortiz, P.; Joguet, B.; Rola, C.

    1998-11-01

    A widely accessible data bank (available through Netscape) and consiting of all (or most) of the emission lines reported in the litterature is being built. It will comprise objects as diverse as HII regions, PN, AGN, HHO. One of its use will be to define/refine existing diagnostic emission line diagrams.

  17. Measurements of methane emissions at natural gas production sites in the United States

    PubMed Central

    Allen, David T.; Torres, Vincent M.; Thomas, James; Sullivan, David W.; Harrison, Matthew; Hendler, Al; Herndon, Scott C.; Kolb, Charles E.; Fraser, Matthew P.; Hill, A. Daniel; Lamb, Brian K.; Miskimins, Jennifer; Sawyer, Robert F.; Seinfeld, John H.

    2013-01-01

    Engineering estimates of methane emissions from natural gas production have led to varied projections of national emissions. This work reports direct measurements of methane emissions at 190 onshore natural gas sites in the United States (150 production sites, 27 well completion flowbacks, 9 well unloadings, and 4 workovers). For well completion flowbacks, which clear fractured wells of liquid to allow gas production, methane emissions ranged from 0.01 Mg to 17 Mg (mean = 1.7 Mg; 95% confidence bounds of 0.67–3.3 Mg), compared with an average of 81 Mg per event in the 2011 EPA national emission inventory from April 2013. Emission factors for pneumatic pumps and controllers as well as equipment leaks were both comparable to and higher than estimates in the national inventory. Overall, if emission factors from this work for completion flowbacks, equipment leaks, and pneumatic pumps and controllers are assumed to be representative of national populations and are used to estimate national emissions, total annual emissions from these source categories are calculated to be 957 Gg of methane (with sampling and measurement uncertainties estimated at ±200 Gg). The estimate for comparable source categories in the EPA national inventory is ∼1,200 Gg. Additional measurements of unloadings and workovers are needed to produce national emission estimates for these source categories. The 957 Gg in emissions for completion flowbacks, pneumatics, and equipment leaks, coupled with EPA national inventory estimates for other categories, leads to an estimated 2,300 Gg of methane emissions from natural gas production (0.42% of gross gas production). PMID:24043804

  18. Coal-fired power plant and its emission reduction in Indonesia

    SciTech Connect

    Kuntjoro, D.

    1994-12-31

    Power generation availability is one important key to the rapid growth of Indonesia`s industrial sector. To secure future national energy needs, coal-fired power generation has been set up as a primary energy source. There are environmental concerns related to the emission of gases, particulates, and ash resulting from coal combustion. This paper discusses emission controls from burning high calorie, low sulfur coal and the national strategy to reduce emissions.

  19. Measurements of methane emissions at natural gas production sites in the United States.

    PubMed

    Allen, David T; Torres, Vincent M; Thomas, James; Sullivan, David W; Harrison, Matthew; Hendler, Al; Herndon, Scott C; Kolb, Charles E; Fraser, Matthew P; Hill, A Daniel; Lamb, Brian K; Miskimins, Jennifer; Sawyer, Robert F; Seinfeld, John H

    2013-10-29

    Engineering estimates of methane emissions from natural gas production have led to varied projections of national emissions. This work reports direct measurements of methane emissions at 190 onshore natural gas sites in the United States (150 production sites, 27 well completion flowbacks, 9 well unloadings, and 4 workovers). For well completion flowbacks, which clear fractured wells of liquid to allow gas production, methane emissions ranged from 0.01 Mg to 17 Mg (mean = 1.7 Mg; 95% confidence bounds of 0.67-3.3 Mg), compared with an average of 81 Mg per event in the 2011 EPA national emission inventory from April 2013. Emission factors for pneumatic pumps and controllers as well as equipment leaks were both comparable to and higher than estimates in the national inventory. Overall, if emission factors from this work for completion flowbacks, equipment leaks, and pneumatic pumps and controllers are assumed to be representative of national populations and are used to estimate national emissions, total annual emissions from these source categories are calculated to be 957 Gg of methane (with sampling and measurement uncertainties estimated at ± 200 Gg). The estimate for comparable source categories in the EPA national inventory is ~1,200 Gg. Additional measurements of unloadings and workovers are needed to produce national emission estimates for these source categories. The 957 Gg in emissions for completion flowbacks, pneumatics, and equipment leaks, coupled with EPA national inventory estimates for other categories, leads to an estimated 2,300 Gg of methane emissions from natural gas production (0.42% of gross gas production).

  20. Black carbon and fine particle emissions in Finnish residential wood combustion: Emission projections, reduction measures and the impact of combustion practices

    NASA Astrophysics Data System (ADS)

    Savolahti, Mikko; Karvosenoja, Niko; Tissari, Jarkko; Kupiainen, Kaarle; Sippula, Olli; Jokiniemi, Jorma

    2016-09-01

    Residential wood combustion (RWC) is a major source of black carbon (BC) and PM2.5 emissions in Finland. Making a robust assessment of emissions on a national level is a challenge due to the varying heater technologies and the effect of users' combustion practices. In this paper we present an update of the emission calculation scheme for Finnish RWC, including technology-specific emission factors based on national measurements. Furthermore, we introduce a transparent method to assess the impact of poor combustion practices on emissions. Using a Finnish emission model, we assessed the emissions in 2000, 2010 and 2030, as well as the cost-efficiency of potential emission reduction measures. The results show that RWC is the biggest source of both PM2.5 and BC emissions in Finland, accounting for 37% and 55% of the total respective emissions. It will also remain the biggest source in the future, and it's role may become even more pronounced if wood consumption continues to increase. Sauna stoves cause the most emissions and also show the biggest potential for emission reductions. Informational campaigns targeted to improve heater users' combustion practices appear as a highly cost-efficient measure, although their impact on country-level emissions was estimated to be relatively limited.

  1. Observed Barium Emission Rates

    NASA Technical Reports Server (NTRS)

    Stenbaek-Nielsen, H. C.; Wescott, E. M.; Hallinan, T. J.

    1993-01-01

    The barium releases from the CRRES satellite have provided an opportunity for verifying theoretically calculated barium ion and neutral emission rates. Spectra of the five Caribbean releases in the summer of 1991 were taken with a spectrograph on board a U.S. Air Force jet aircraft. Because the line of sight release densities are not known, only relative rates could be obtained. The observed relative rates agree well with the theoretically calculated rates and, together with other observations, confirm the earlier detailed theoretical emission rates. The calculated emission rates can thus with good accuracy be used with photometric observations. It has been postulated that charge exchange between neutral barium and oxygen ions represents a significant source for ionization. If so. it should be associated with emissions at 4957.15 A and 5013.00 A, but these emissions were not detected.

  2. Graphene field emission devices

    SciTech Connect

    Kumar, S. Raghavan, S.; Duesberg, G. S.; Pratap, R.

    2014-09-08

    Graphene field emission devices are fabricated using a scalable process. The field enhancement factors, determined from the Fowler-Nordheim plots, are within few hundreds and match the theoretical predictions. The devices show high emission current density of ∼10 nA μm{sup −1} at modest voltages of tens of volts. The emission is stable with time and repeatable over long term, whereas the noise in the emission current is comparable to that from individual carbon nanotubes emitting under similar conditions. We demonstrate a power law dependence of emission current on pressure which can be utilized for sensing. The excellent characteristics and relative ease of making the devices promise their great potential for sensing and electronic applications.

  3. Historic patterns of CO{sub 2} emissions from fossil fuels: Implications for stabilization of emissions

    SciTech Connect

    Andres, R.J.; Marland, G.

    1994-10-01

    This paper examines the historical record of greenhouse gas emissions since 1950, reviews the prospects for emissions into the future, and projects what would be the short-term outcome if the stated targets of the FCCC were in fact achieved. The examination focuses on the most important of the greenhouse gases, CO{sub 2}. The extensive record of historic CO{sub 2} emissions is explored to ascertain if it is an adequate basis for useful extrapolation into the near future. Global carbon dioxide emissions from fossil fuel consumption have been documented. Emissions grew at 4.3% per year from 1950 until the time of the 1973 oil crisis. Another disruption in growth followed the oil price increases of 1979. Global total emissions have been increasing steadily since the 1982-1983 minimum and have grown by more than 20% since then. At present, emission Of CO{sub 2} from fossil fuel burning is dominated by a few countries: the U.S., the former Soviet Union, China, the developed countries of Europe and Japan. Only 20 countries emit 84% of emissions from all countries. However, rates of growth in many of the developed countries are now very low. In contrast, energy use has grown rapidly over the last 20 years in some of the large, developing economies. Emissions from fossil fuel consumption are now nearly 4 times those from land use change and are the primary cause of measured increases in the atmospheric concentration of CO{sub 2}. The increasing concentration of atmospheric CO{sub 2} has led to rising concern about the possibility of impending changes in the global climate system. In an effort to limit or mitigate potential negative effects of global climate change, 154 countries signed the United Nations Framework Convention on Climate Change (FCCC) in Rio de Janeiro in June, 1992. The FCCC asks all countries to conduct an inventory of their current greenhouse gas emissions setting non-binding targets.

  4. Historic Patterns of CO{sub 2} Emissions from Fossil Fuels: Implications for Stabilization of Emissions

    DOE R&D Accomplishments Database

    Andres, R. J.; Marland, G.

    1994-06-01

    This paper examines the historical record of greenhouse gas emissions since 1950, reviews the prospects for emissions into the future, and projects what would be the short-term outcome if the stated targets of the FCCC were in fact achieved. The examination focuses on the most important of the greenhouse gases, CO{sub 2}. The extensive record of historic CO{sub 2} emissions is explored to ascertain if it is an adequate basis for useful extrapolation into the near future. Global carbon dioxide emissions from fossil fuel consumption have been documented. Emissions grew at 4.3% per year from 1950 until the time of the 1973 oil crisis. Another disruption in growth followed the oil price increases of 1979. Global total emissions have been increasing steadily since the 1982-1983 minimum and have grown by more than 20% since then. At present, emission Of CO{sub 2} from fossil fuel burning is dominated by a few countries: the U.S., the former Soviet Union, China, the developed countries of Europe and Japan. Only 20 countries emit 84% of emissions from all countries. However, rates of growth in many of the developed countries are now very low. In contrast, energy use has grown rapidly over the last 20 years in some of the large, developing economies. Emissions from fossil fuel consumption are now nearly 4 times those from land use change and are the primary cause of measured increases in the atmospheric concentration of CO{sub 2}. The increasing concentration of atmospheric CO{sub 2} has led to rising concern about the possibility of impending changes in the global climate system. In an effort to limit or mitigate potential negative effects of global climate change, 154 countries signed the United Nations Framework Convention on Climate Change (FCCC) in Rio de Janeiro in June, 1992. The FCCC asks all countries to conduct an inventory of their current greenhouse gas emissions setting non-binding targets.

  5. 40 CFR 204.5-2 - National security exemptions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... PROGRAMS NOISE EMISSION STANDARDS FOR CONSTRUCTION EQUIPMENT General Provisions § 204.5-2 National security... for a national security exemption is required. (c) For purposes of section 11(d) of the Act, any... 40 Protection of Environment 25 2011-07-01 2011-07-01 false National security exemptions....

  6. Emissions from Biomass Burning in the Yucatan

    NASA Technical Reports Server (NTRS)

    Yokelson, R.; Crounse, J. D.; DeCarlo, P. F.; Karl, T.; Urbanski, S.; Atlas, E.; Campos, T.; Shinozuka, Y.; Kapustin, V.; Clarke, A. D.; Weinheimer, A.; Knapp, D. J.; Montzka, D. D.; Holloway, J.; Weibring, P.; Flocke, F.; Zheng, W.; Toohey, D.; Wennberg, P. O.; Wiedinmyer, C.; Mauldin, L.; Fried, A.; Richter, D.; Walega, J.; Jimenez, J. L.

    2009-01-01

    In March 2006 two instrumented aircraft made the first detailed field measurements of biomass burning (BB) emissions in the Northern Hemisphere tropics as part of the MILAGRO project. The aircraft were the National Center for Atmospheric Research C-130 and a University of Montana/US Forest Service Twin Otter. The initial emissions of up to 49 trace gas or particle species were measured from 20 deforestation and crop residue fires on the Yucatan peninsula. This included two trace gases useful as indicaters of BB (HCN and acetonitrile) and several rarely, or never before, measured species: OH, peroxyacetic acid, propanoic acid, hydrogen peroxide, methane sulfonic acid, and sulfuric acid. Crop residue fires emitted more organic acids and ammonia than deforestation fires, but the emissions from the main fire types were otherwise fairly similar. The Yucatan fires emitted unusually amounts of SO2 and particle chloride, likely due to a strong marine influence on the peninsula.

  7. 40 CFR 63.5996 - How do I demonstrate initial compliance with the emission limits for tire production affected...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emissions Standards for Hazardous Air... Status containing the results of the initial compliance demonstration according to the requirements...

  8. 40 CFR 63.5996 - How do I demonstrate initial compliance with the emission limits for tire production affected...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emissions Standards for... Compliance Status containing the results of the initial compliance demonstration according to...

  9. Fossil-Fuel C02 Emissions Database and Exploration System

    NASA Astrophysics Data System (ADS)

    Krassovski, M.; Boden, T.; Andres, R. J.; Blasing, T. J.

    2012-12-01

    The Carbon Dioxide Information Analysis Center (CDIAC) at Oak Ridge National Laboratory (ORNL) quantifies the release of carbon from fossil-fuel use and cement production at global, regional, and national spatial scales. The CDIAC emission time series estimates are based largely on annual energy statistics published at the national level by the United Nations (UN). CDIAC has developed a relational database to house collected data and information and a web-based interface to help users worldwide identify, explore and download desired emission data. The available information is divided in two major group: time series and gridded data. The time series data is offered for global, regional and national scales. Publications containing historical energy statistics make it possible to estimate fossil fuel CO2 emissions back to 1751. Etemad et al. (1991) published a summary compilation that tabulates coal, brown coal, peat, and crude oil production by nation and year. Footnotes in the Etemad et al.(1991) publication extend the energy statistics time series back to 1751. Summary compilations of fossil fuel trade were published by Mitchell (1983, 1992, 1993, 1995). Mitchell's work tabulates solid and liquid fuel imports and exports by nation and year. These pre-1950 production and trade data were digitized and CO2 emission calculations were made following the procedures discussed in Marland and Rotty (1984) and Boden et al. (1995). The gridded data presents annual and monthly estimates. Annual data presents a time series recording 1° latitude by 1° longitude CO2 emissions in units of million metric tons of carbon per year from anthropogenic sources for 1751-2008. The monthly, fossil-fuel CO2 emissions estimates from 1950-2008 provided in this database are derived from time series of global, regional, and national fossil-fuel CO2 emissions (Boden et al. 2011), the references therein, and the methodology described in Andres et al. (2011). The data accessible here take these

  10. Developments in glow discharge emission spectrometry

    NASA Astrophysics Data System (ADS)

    Ferreira, N. P.; Strauss, J. A.; Human, H. G. C.

    Developments in the field of glow discharge emission spectrometry at the National Physical Research Laboratory of the Council for Scientific and Industrial Research comprise measurement of fundamental plasma parameters, instrumental development and analytical applications. While reference is only made to published material, recent developments are described in more detail, e.g. the use of a fluorescent atomic vapour as spectral line isolator and the use of a microwave auxiliary discharge to augment excitation of sputtered material.

  11. Attributing Atmospheric Methane to Anthropogenic Emission Sources.

    PubMed

    Allen, David

    2016-07-19

    Methane is a greenhouse gas, and increases in atmospheric methane concentration over the past 250 years have driven increased radiative forcing of the atmosphere. Increases in atmospheric methane concentration since 1750 account for approximately 17% of increases in radiative forcing of the atmosphere, and that percentage increases by approximately a factor of 2 if the effects of the greenhouse gases produced by the atmospheric reactions of methane are included in the assessment. Because of the role of methane emissions in radiative forcing of the atmosphere, the identification and quantification of sources of methane emissions is receiving increased scientific attention. Methane emission sources include biogenic, geogenic, and anthropogenic sources; the largest anthropogenic sources are natural gas and petroleum systems, enteric fermentation (livestock), landfills, coal mining, and manure management. While these source categories are well-known, there is significant uncertainty in the relative magnitudes of methane emissions from the various source categories. Further, the overall magnitude of methane emissions from all anthropogenic sources is actively debated, with estimates based on source sampling extrapolated to regional or national scale ("bottom-up analyses") differing from estimates that infer emissions based on ambient data ("top-down analyses") by 50% or more. To address the important problem of attribution of methane to specific sources, a variety of new analytical methods are being employed, including high time resolution and highly sensitive measurements of methane, methane isotopes, and other chemical species frequently associated with methane emissions, such as ethane. This Account describes the use of some of these emerging measurements, in both top-down and bottom-up methane emission studies. In addition, this Account describes how data from these new analytical methods can be used in conjunction with chemical mass balance (CMB) methods for source

  12. Attributing Atmospheric Methane to Anthropogenic Emission Sources.

    PubMed

    Allen, David

    2016-07-19

    Methane is a greenhouse gas, and increases in atmospheric methane concentration over the past 250 years have driven increased radiative forcing of the atmosphere. Increases in atmospheric methane concentration since 1750 account for approximately 17% of increases in radiative forcing of the atmosphere, and that percentage increases by approximately a factor of 2 if the effects of the greenhouse gases produced by the atmospheric reactions of methane are included in the assessment. Because of the role of methane emissions in radiative forcing of the atmosphere, the identification and quantification of sources of methane emissions is receiving increased scientific attention. Methane emission sources include biogenic, geogenic, and anthropogenic sources; the largest anthropogenic sources are natural gas and petroleum systems, enteric fermentation (livestock), landfills, coal mining, and manure management. While these source categories are well-known, there is significant uncertainty in the relative magnitudes of methane emissions from the various source categories. Further, the overall magnitude of methane emissions from all anthropogenic sources is actively debated, with estimates based on source sampling extrapolated to regional or national scale ("bottom-up analyses") differing from estimates that infer emissions based on ambient data ("top-down analyses") by 50% or more. To address the important problem of attribution of methane to specific sources, a variety of new analytical methods are being employed, including high time resolution and highly sensitive measurements of methane, methane isotopes, and other chemical species frequently associated with methane emissions, such as ethane. This Account describes the use of some of these emerging measurements, in both top-down and bottom-up methane emission studies. In addition, this Account describes how data from these new analytical methods can be used in conjunction with chemical mass balance (CMB) methods for source

  13. Ship emissions and their externalities for Greece

    NASA Astrophysics Data System (ADS)

    Tzannatos, Ernestos

    2010-06-01

    The existing and emerging international and European policy framework for the reduction of ship exhaust emissions dictates the need to produce reliable national, regional and global inventories in order to monitor emission trends and consequently provide the necessary support for future policy making. Furthermore, the inventories of ship exhaust emissions constitute the basis upon which their external costs are estimated in an attempt to highlight the economic burden they impose upon the society and facilitate the cost-benefit analysis of the proposed emission abatement technologies, operational measures and market-based instruments prior to their implementation. The case of Greece is of particular interest mainly because the dense ship traffic within the Greek seas directly imposes the impact of its exhaust emission pollutants (NO x, SO 2 and PM) upon the highly populated, physically sensitive and culturally precious Greek coastline, as well as upon the land and seas of Greece in general, whereas the contribution of Greece in the global CO 2 inventory at a time of climatic change awareness cannot be ignored. In this context, this paper presents the contribution of Greece in ship exhaust emissions of CO 2, NO x, SO 2 and PM from domestic and international shipping over the last 25 years (1984-2008), utilizing the fuel-based (fuel sales) emission methodology. Furthermore, the ship exhaust emissions generated within the Greek seas and their externalities are estimated for the year 2008, through utilizing the fuel-based (fuel sales) approach for domestic shipping and the activity-based (ship traffic) approach for international shipping. On this basis, it was found that during the 1984 to 2008 period the fuel-based (fuel sales) ship emission inventory for Greece increased at an average annual rate of 2.85%. In 2008, the CO 2, NO x, SO 2 and PM emissions reached 12.9 million tons (of which 12.4 million tons of CO 2) and their externalities were found to be around 3

  14. Drivers of the growth in global greenhouse gas emissions.

    PubMed

    Arto, Iñaki; Dietzenbacher, Erik

    2014-05-20

    Greenhouse gas emissions increased by 8.9 Gigatons CO2 equivalent (Gt) in the period 1995-2008. A phenomenon that has received due attention is the upsurge of emission transfers via international trade. A question that has remained unanswered is whether trade changes have affected global emissions. For each of five factors (one of which is trade changes) in 40 countries we quantify its contribution to the growth in global emissions. We find that the changes in the levels of consumption per capita have led to an enormous growth in emissions (+14.0 Gt). This effect was partly offset by the changes in technology (-8.4 Gt). Smaller effects are found for population growth (+4.2 Gt) and changes in the composition of the consumption (-1.5 Gt). Changes in the trade structure had a very moderate effect on global emissions (+0.6 Gt). Looking at the geographical distribution, changes in the emerging economies (Brazil, Russia, India, Indonesia and China) have caused 44% of emission growth whereas the increase in their national emissions accounted for 59% of emission growth. This means that 15% (1.4 Gt) of all extra GHG emissions between 1995 and 2008 have been emitted in emerging countries but were caused by changes in other countries. PMID:24754816

  15. Drivers of the growth in global greenhouse gas emissions.

    PubMed

    Arto, Iñaki; Dietzenbacher, Erik

    2014-05-20

    Greenhouse gas emissions increased by 8.9 Gigatons CO2 equivalent (Gt) in the period 1995-2008. A phenomenon that has received due attention is the upsurge of emission transfers via international trade. A question that has remained unanswered is whether trade changes have affected global emissions. For each of five factors (one of which is trade changes) in 40 countries we quantify its contribution to the growth in global emissions. We find that the changes in the levels of consumption per capita have led to an enormous growth in emissions (+14.0 Gt). This effect was partly offset by the changes in technology (-8.4 Gt). Smaller effects are found for population growth (+4.2 Gt) and changes in the composition of the consumption (-1.5 Gt). Changes in the trade structure had a very moderate effect on global emissions (+0.6 Gt). Looking at the geographical distribution, changes in the emerging economies (Brazil, Russia, India, Indonesia and China) have caused 44% of emission growth whereas the increase in their national emissions accounted for 59% of emission growth. This means that 15% (1.4 Gt) of all extra GHG emissions between 1995 and 2008 have been emitted in emerging countries but were caused by changes in other countries.

  16. Advanced Emissions Control Development Program: Mercury Control

    SciTech Connect

    Evans, A.P.; Redinger, K.W.; Holmes, M.J.

    1997-07-01

    McDermott Technology, Inc. (a subsidiary of Babcock & Wilcox) is conducting the Advanced Emissions Control Development Project (AECDP) which is aimed at the development of practical, cost-effective strategies for reducing the emissions of hazardous air pollutants (HAPS) from coal-fired electric utility plants. The need for such controls may arise as the US Environmental Protection Agency (EPA) proceeds with implementation of requirements set forth in the Clean Air Act Amendments (CAAA`s) of 1990. Promulgation of air toxics emissions regulations for electric utility plants could dramatically impact utilities burning coal, their industrial and residential customers, and the coal industry. AECDP project work will supply the information needed by utilities to respond to potential HAPs regulations in a timely, cost-effective, enviromnentally-sound manner which supports the continued use of the Nation`s abundant reserves of coal, such as those in the State of Ohio. The development work is being carried out using the 10 MW Clean Environment Development Facility wherein air toxics emissions control strategies can be developed under controlled conditions. The specific objectives of the project are to (1) measure and understand production and partitioning of air toxics species for a variety of coals, (2) optimize the air toxics removal performance of conventional flue gas cleanup systems, (3) develop advanced air toxics emissions control concepts, (4) develop and validate air toxics emissions measurement and monitoring techniques, and (5) establish a comprehensive, self-consistent air toxics data library. This project is supported by the Department of Energy, the Ohio Coal Development Office within the Ohio Department of Development and Babcock & Wilcox. A comprehensive assessment of HAP emissions from coal-fired electric utility boilers sponsored by the Department of Energy and the Electric Power Research Institute concluded that with the exception of selenium and mercury

  17. NATCARB Interactive Maps and the National Carbon Explorer: a National Look at Carbon Sequestration

    DOE Data Explorer

    NATCARB is a national look at carbon sequestration. The NATCARB home page, National Carbon Explorer (http://www.natcarb.org/) provides access to information and interactive maps on a national scale about climate change, DOE's carbon sequestration program and its partnerships, CO2 emissions, and sinks. This portal provides access to interactive maps based on the Carbon Sequestration Atlas of the United States and Canada.

  18. Combustion and emissions technology

    NASA Technical Reports Server (NTRS)

    Grobman, J.; Anderson, D. N.; Diehl, L. A.; Niedzwiecki, R. W.

    1975-01-01

    Combustor development is discussed as it relates to emissions reduction. The nature of the aircraft pollution problem is examined along with the aircraft pollution standards that have been established by the Environmental Protection Agency. The effect of engine operating conditions on pollutant formation levels is shown, as well as how close present-day engines are to meeting the established standards. The magnitude of the emissions reductions required to meet these standards is indicated. The progress that has been made in evolving the needed emissions reduction technology is the main topic.

  19. Emission Abatement System

    DOEpatents

    Bromberg, Leslie; Cohn, Daniel R.; Rabinovich, Alexander

    2003-05-13

    Emission abatement system. The system includes a source of emissions and a catalyst for receiving the emissions. Suitable catalysts are absorber catalysts and selective catalytic reduction catalysts. A plasma fuel converter generates a reducing gas from a fuel source and is connected to deliver the reducing gas into contact with the absorber catalyst for regenerating the catalyst. A preferred reducing gas is a hydrogen rich gas and a preferred plasma fuel converter is a plasmatron. It is also preferred that the absorber catalyst be adapted for absorbing NO.sub.x.

  20. Emissivity of microstructured silicon.

    PubMed

    Maloney, Patrick G; Smith, Peter; King, Vernon; Billman, Curtis; Winkler, Mark; Mazur, Eric

    2010-03-01

    Infrared transmittance and hemispherical-directional reflectance data from 2.5 to 25 microm on microstructured silicon surfaces have been measured, and spectral emissivity has been calculated for this wavelength range. Hemispherical-total emissivity is calculated for the samples and found to be 0.84 before a measurement-induced annealing and 0.65 after the measurement for the sulfur-doped sample. Secondary samples lack a measurement-induced anneal, and reasons for this discrepancy are presented. Emissivity numbers are plotted and compared with a silicon substrate, and Aeroglaze Z306 black paint. Use of microstructured silicon as a blackbody or microbolometer surface is modeled and presented, respectively.

  1. MOVES2014: Evaporative Emissions Report

    EPA Science Inventory

    Vehicle evaporative emissions are now modeled in EPA’s MOVES according to physical processes, permeation, tank vapor venting, liquid leaks, and refueling emissions. With this update, the following improvements are being incorporated into MOVES evaporative emissions methodology, a...

  2. National Contests.

    ERIC Educational Resources Information Center

    Bamford, Paul J.; Vandenberg, Victoria

    1995-01-01

    "VICA Skills USA Championships" (Bamford) describes the competitions and events of the 1995 National Vocational Industrial Clubs of America Leadership and Skills Conference. "Student Robotics Contest" (Vandenberg) describes an annual competition that invites students to demonstrate their creativity and knowledge of robotics. (JOW)

  3. Nations Within.

    ERIC Educational Resources Information Center

    Sheets, Rosa Hernandez

    1998-01-01

    Karen Gayton Swisher (Sioux), chair of teacher education at Haskell Indian Nations University (Kansas), discusses the history of American Indian education, its effects on Indian families and cultures, overcoming stereotypes, how teachers can teach Indian children more effectively, the importance of Indian interpretations of Indian education and…

  4. Sequim Site Radionuclide Air Emissions Report for Calendar Year 2012

    SciTech Connect

    Snyder, Sandra F.; Barnett, J. Matthew; Gervais, Todd L.

    2013-04-01

    This report is prepared to document compliance with the Code of Federal Regulations (CFR), Title 40, Protection of the Environment, Part 61, National Emission Standards for Hazardous Air Pollutants (NESHAP), Subpart H, National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities and ashington Administrative Code (WAC) Chapter 246-247, Radiation Protection Air Emissions. This report meets the calendar year 2012 Sequim Site annual reporting requirement for its operations as a privately-owned facility as well as its federally-contracted status that began in October 2012. Compliance is indicated by comparing the estimated dose to the maximally exposed individual (MEI) with the 10 mrem/yr Environmental Protection Agency (EPA) standard. The MSL contains only sources classified as fugitive emissions. Despite the fact that the regulations are intended for application to point source emissions, fugitive emissions are included with regard to complying with the EPA standard. The dose to the Sequim Site MEI due to routine operations in 2012 was 9E-06 mrem (9E-08 mSv). No non-routine emissions occurred in 2012. The MSL is in compliance with the federal and state 10 mrem/yr standard.

  5. Reconciling reported and unreported HFC emissions with atmospheric observations

    PubMed Central

    Lunt, Mark F.; Rigby, Matthew; Ganesan, Anita L.; Manning, Alistair J.; Prinn, Ronald G.; O’Doherty, Simon; Mühle, Jens; Harth, Christina M.; Salameh, Peter K.; Arnold, Tim; Weiss, Ray F.; Saito, Takuya; Yokouchi, Yoko; Krummel, Paul B.; Steele, L. Paul; Fraser, Paul J.; Li, Shanlan; Park, Sunyoung; Reimann, Stefan; Vollmer, Martin K.; Lunder, Chris; Hermansen, Ove; Schmidbauer, Norbert; Maione, Michela; Arduini, Jgor; Young, Dickon; Simmonds, Peter G.

    2015-01-01

    We infer global and regional emissions of five of the most abundant hydrofluorocarbons (HFCs) using atmospheric measurements from the Advanced Global Atmospheric Gases Experiment and the National Institute for Environmental Studies, Japan, networks. We find that the total CO2-equivalent emissions of the five HFCs from countries that are required to provide detailed, annual reports to the United Nations Framework Convention on Climate Change (UNFCCC) increased from 198 (175–221) Tg-CO2-eq⋅y–1 in 2007 to 275 (246–304) Tg-CO2-eq⋅y–1 in 2012. These global warming potential-weighted aggregated emissions agree well with those reported to the UNFCCC throughout this period and indicate that the gap between reported emissions and global HFC emissions derived from atmospheric trends is almost entirely due to emissions from nonreporting countries. However, our measurement-based estimates of individual HFC species suggest that emissions, from reporting countries, of the most abundant HFC, HFC-134a, were only 79% (63–95%) of the UNFCCC inventory total, while other HFC emissions were significantly greater than the reported values. These results suggest that there are inaccuracies in the reporting methods for individual HFCs, which appear to cancel when aggregated together. PMID:25918401

  6. Reconciling reported and unreported HFC emissions with atmospheric observations.

    PubMed

    Lunt, Mark F; Rigby, Matthew; Ganesan, Anita L; Manning, Alistair J; Prinn, Ronald G; O'Doherty, Simon; Mühle, Jens; Harth, Christina M; Salameh, Peter K; Arnold, Tim; Weiss, Ray F; Saito, Takuya; Yokouchi, Yoko; Krummel, Paul B; Steele, L Paul; Fraser, Paul J; Li, Shanlan; Park, Sunyoung; Reimann, Stefan; Vollmer, Martin K; Lunder, Chris; Hermansen, Ove; Schmidbauer, Norbert; Maione, Michela; Arduini, Jgor; Young, Dickon; Simmonds, Peter G

    2015-05-12

    We infer global and regional emissions of five of the most abundant hydrofluorocarbons (HFCs) using atmospheric measurements from the Advanced Global Atmospheric Gases Experiment and the National Institute for Environmental Studies, Japan, networks. We find that the total CO2-equivalent emissions of the five HFCs from countries that are required to provide detailed, annual reports to the United Nations Framework Convention on Climate Change (UNFCCC) increased from 198 (175-221) Tg-CO2-eq ⋅ y(-1) in 2007 to 275 (246-304) Tg-CO2-eq ⋅ y(-1) in 2012. These global warming potential-weighted aggregated emissions agree well with those reported to the UNFCCC throughout this period and indicate that the gap between reported emissions and global HFC emissions derived from atmospheric trends is almost entirely due to emissions from nonreporting countries. However, our measurement-based estimates of individual HFC species suggest that emissions, from reporting countries, of the most abundant HFC, HFC-134a, were only 79% (63-95%) of the UNFCCC inventory total, while other HFC emissions were significantly greater than the reported values. These results suggest that there are inaccuracies in the reporting methods for individual HFCs, which appear to cancel when aggregated together.

  7. Reconciling reported and unreported HFC emissions with atmospheric observations.

    PubMed

    Lunt, Mark F; Rigby, Matthew; Ganesan, Anita L; Manning, Alistair J; Prinn, Ronald G; O'Doherty, Simon; Mühle, Jens; Harth, Christina M; Salameh, Peter K; Arnold, Tim; Weiss, Ray F; Saito, Takuya; Yokouchi, Yoko; Krummel, Paul B; Steele, L Paul; Fraser, Paul J; Li, Shanlan; Park, Sunyoung; Reimann, Stefan; Vollmer, Martin K; Lunder, Chris; Hermansen, Ove; Schmidbauer, Norbert; Maione, Michela; Arduini, Jgor; Young, Dickon; Simmonds, Peter G

    2015-05-12

    We infer global and regional emissions of five of the most abundant hydrofluorocarbons (HFCs) using atmospheric measurements from the Advanced Global Atmospheric Gases Experiment and the National Institute for Environmental Studies, Japan, networks. We find that the total CO2-equivalent emissions of the five HFCs from countries that are required to provide detailed, annual reports to the United Nations Framework Convention on Climate Change (UNFCCC) increased from 198 (175-221) Tg-CO2-eq ⋅ y(-1) in 2007 to 275 (246-304) Tg-CO2-eq ⋅ y(-1) in 2012. These global warming potential-weighted aggregated emissions agree well with those reported to the UNFCCC throughout this period and indicate that the gap between reported emissions and global HFC emissions derived from atmospheric trends is almost entirely due to emissions from nonreporting countries. However, our measurement-based estimates of individual HFC species suggest that emissions, from reporting countries, of the most abundant HFC, HFC-134a, were only 79% (63-95%) of the UNFCCC inventory total, while other HFC emissions were significantly greater than the reported values. These results suggest that there are inaccuracies in the reporting methods for individual HFCs, which appear to cancel when aggregated together. PMID:25918401

  8. Gaseous Emissions from Wastewater Facilities.

    PubMed

    Koh, Sock-Hoon; Shaw, Andrew R

    2016-10-01

    A review of the literature published in 2015 on topics relating to gaseous emissions from wastewater facilities is presented. This review is divided into the following sections: odorant emissions from wastewater treatment plants (WWTPs); greenhouse gas (GHG) emissions from WWTPs; gaseous emissions from wastewater collection systems; physiochemical odor/emissions control methods; biological odor/emissions control methods; odor characterization/monitoring; and odor impacts/ risk assessments. PMID:27620089

  9. Fossil-Fuel C02 Emissions Database and Exploration System

    NASA Astrophysics Data System (ADS)

    Krassovski, M.; Boden, T.

    2012-04-01

    Fossil-Fuel C02 Emissions Database and Exploration System Misha Krassovski and Tom Boden Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory The Carbon Dioxide Information Analysis Center (CDIAC) at Oak Ridge National Laboratory (ORNL) quantifies the release of carbon from fossil-fuel use and cement production each year at global, regional, and national spatial scales. These estimates are vital to climate change research given the strong evidence suggesting fossil-fuel emissions are responsible for unprecedented levels of carbon dioxide (CO2) in the atmosphere. The CDIAC fossil-fuel emissions time series are based largely on annual energy statistics published for all nations by the United Nations (UN). Publications containing historical energy statistics make it possible to estimate fossil-fuel CO2 emissions back to 1751 before the Industrial Revolution. From these core fossil-fuel CO2 emission time series, CDIAC has developed a number of additional data products to satisfy modeling needs and to address other questions aimed at improving our understanding of the global carbon cycle budget. For example, CDIAC also produces a time series of gridded fossil-fuel CO2 emission estimates and isotopic (e.g., C13) emissions estimates. The gridded data are generated using the methodology described in Andres et al. (2011) and provide monthly and annual estimates for 1751-2008 at 1° latitude by 1° longitude resolution. These gridded emission estimates are being used in the latest IPCC Scientific Assessment (AR4). Isotopic estimates are possible thanks to detailed information for individual nations regarding the carbon content of select fuels (e.g., the carbon signature of natural gas from Russia). CDIAC has recently developed a relational database to house these baseline emissions estimates and associated derived products and a web-based interface to help users worldwide query these data holdings. Users can identify, explore and download desired CDIAC

  10. Fugitive emissions monitoring trends

    SciTech Connect

    Brown, K.H.

    1997-02-01

    New Clean Air Act requirements are pushing facilities to reevaluate their monitoring programs. A description of the fugitive emission guidelines is included in this article, along with ideas about monitoring.

  11. Photon enhanced thermionic emission

    SciTech Connect

    Schwede, Jared; Melosh, Nicholas; Shen, Zhixun

    2014-10-07

    Photon Enhanced Thermionic Emission (PETE) is exploited to provide improved efficiency for radiant energy conversion. A hot (greater than 200.degree. C.) semiconductor cathode is illuminated such that it emits electrons. Because the cathode is hot, significantly more electrons are emitted than would be emitted from a room temperature (or colder) cathode under the same illumination conditions. As a result of this increased electron emission, the energy conversion efficiency can be significantly increased relative to a conventional photovoltaic device. In PETE, the cathode electrons can be (and typically are) thermalized with respect to the cathode. As a result, PETE does not rely on emission of non-thermalized electrons, and is significantly easier to implement than hot-carrier emission approaches.

  12. Aircraft Engine Emissions. [conference

    NASA Technical Reports Server (NTRS)

    1977-01-01

    A conference on a aircraft engine emissions was held to present the results of recent and current work. Such diverse areas as components, controls, energy efficient engine designs, and noise and pollution reduction are discussed.

  13. ROANOKE WOODSTOVE EMISSION TESTS

    EPA Science Inventory

    The report discusses a project, part of the Integrated Air Cancer Project Roanoke study, that characterizes and quantifies emissions generated by burning authentic Roanoke cordwood. The burning occurred in a controlled laboratory setting using two woodstoves, each operated at two...

  14. Galactic Diffuse Polarized Emission

    NASA Astrophysics Data System (ADS)

    Carretti, Ettore

    2011-12-01

    Diffuse polarized emission by synchrotron is a key tool to investigate magnetic fields in the Milky Way, particularly the ordered component of the large scale structure. Key observables are the synchrotron emission itself and the RM is by Faraday rotation. In this paper the main properties of the radio polarized diffuse emission and its use to investigate magnetic fields will be reviewed along with our current understanding of the galactic magnetic field and the data sets available. We will then focus on the future perspective discussing RM-synthesis - the new powerful instrument devised to unlock the information encoded in such an emission - and the surveys currently in progress like S-PASS and GMIMS.

  15. Potential options to reduce GHG emissions in Venezuela

    SciTech Connect

    Pereira, N.; Bonduki, Y.; Perdomo, M.

    1996-12-31

    The Government of Venezuela ratified the United Nations Framework Convention on Climate Change (UNFCCC) in December, 1994. The Convention requires all parties to develop and publish national inventories of anthropogenic greenhouse gas emissions (GHG) as well as national plans to reduce or control emissions, taking into account their common but differentiated responsibilities and their specific national and regional development priorities, objectives, and circumstances. Within this context, the Ministry of Environment and Renewable Natural Resources and the Ministry of Energy and Mines developed the `Venezuelan Case-Study to Address Climate Change`. The study was initiated in October 1993, with the financial and technical assistance of the Government of United States, through the U.S. Country Studies Program (USCSP), and the Global Environment Facility (GEF), through the United Nations Environment Programme (UNEP).

  16. Emissions from laboratory combustion of wildland fuels: emission factors and source profiles.

    PubMed

    Chen, L W Antony; Moosmüller, Hans; Arnott, W Patrick; Chow, Judith C; Watson, John G; Susott, Ronald A; Babbitt, Ronald E; Wold, Cyle E; Lincoln, Emily N; Hao, Wei Min

    2007-06-15

    Combustion of wildland fuels represents a major source of particulate matter (PM) and light-absorbing elemental carbon (EC) on a national and global scale, but the emission factors and source profiles have not been well characterized with respect to different fuels and combustion phases. These uncertainties limit the accuracy of current emission inventories, smoke forecasts, and source apportionments. This study investigates the evolution of gaseous and particulate emission and combustion efficiency by burning wildland fuels in a laboratory combustion facility. Emission factors for carbon dioxide (CO2), carbon monoxide (CO), total hydrocarbon (THC), nitrogen oxides (NO(x)), PM, light extinction and absorption cross sections, and spectral scattering cross sections specific to flaming and smoldering phases are reported. Emission factors are generally reproducible within +/- 20% during the flaming phase, which, despite its short duration, dominates the carbon emission (mostly in the form of CO2) and the production of light absorption and EC. Higher and more variable emission factors for CO, THC, and PM are found during the smoldering phase, especially for fuels containing substantial moisture. Organic carbon (OC) and EC mass account for a majority (i.e., > 60%) of PM mass; other important elements include potassium, chlorine, and sulfur. Thermal analysis separates the EC into subfractions based on analysis temperature demonstrating that high-temperature EC (EC2; at 700 degrees C) varies from 1% to 70% of PM among biomass burns, compared to 75% in kerosene soot. Despite this, the conversion factor between EC and light absorption emissions is rather consistent across fuels and burns, ranging from 7.8 to 9.6 m2/g EC. Findings from this study should be considered in the development of PM and EC emission inventories for visibility and radiative forcing assessments.

  17. Field emission electron source

    DOEpatents

    Zettl, Alexander Karlwalter; Cohen, Marvin Lou

    2000-01-01

    A novel field emitter material, field emission electron source, and commercially feasible fabrication method is described. The inventive field emission electron source produces reliable electron currents of up to 400 mA/cm.sup.2 at 200 volts. The emitter is robust and the current it produces is not sensitive to variability of vacuum or the distance between the emitter tip and the cathode. The novel emitter has a sharp turn-on near 100 volts.

  18. Historical evaluation of vehicle emission control in Guangzhou based on a multi-year emission inventory

    NASA Astrophysics Data System (ADS)

    Zhang, Shaojun; Wu, Ye; Liu, Huan; Wu, Xiaomeng; Zhou, Yu; Yao, Zhiliang; Fu, Lixin; He, Kebin; Hao, Jiming

    2013-09-01

    The Guangzhou government adopted many vehicle emission control policies and strategies during the five-year preparation (2005-2009) to host the 2010 Asian Games. This study established a multi-year emission inventory for vehicles in Guangzhou during 2005-2009 and estimated the uncertainty in total vehicle emissions by taking the assumed uncertainties in fleet-average emission factors and annual mileage into account. In 2009, the estimated total vehicle emissions in Guangzhou were 313 000 (242 000-387 000) tons of CO, 60 900 (54 000-70 200) tons of THC, 65 600 (56 800-74 100) tons of NOx and 2740 (2100-3400) tons of PM10. Vehicle emissions within the urban area of Guangzhou were estimated to be responsible for ˜40% of total gaseous pollutants and ˜25% of total PM10 in the entire city. Although vehicle use intensity increased rapidly in Guangzhou during 2005-2009, vehicle emissions were estimated to have been reduced by 12% for CO, 21% for THC and 20% for PM10 relative to those in 2005. NOx emissions were estimated to have remained almost constant during this period. Compared to the "without control" scenario, 19% (15%-23%) of CO, 20% (18%-23%) of THC, 9% (8%-10%) of NOx and 16% (12%-20%) of PM10 were estimated to have been mitigated from a combination of the implementation of Euro III standards for light-duty vehicles (LDVs) and heavy-duty diesel vehicles and improvement of fuel quality. This study also evaluated several enhanced vehicle emission control actions taken recently. For example, the enhanced I/M program for LDVs was estimated to reduce 11% (9%-14%) of CO, 9% (8%-10%) of THC and 2% (2%-3%) of NOx relative to total vehicle emissions in 2009. Total emission reductions by temporary traffic controls for the Asian Games were estimated equivalent to 9% (7%-11%) of CO, 9% (8%-10%) of THC, 5% (5%-6%) of NOx and 10% (8%-13%) of PM10 estimated total vehicle emissions in 2009. Those controls are essential to further vehicle emission mitigation in Guangzhou

  19. Estimated Carbon Dioxide Emissions in 2008: United States

    SciTech Connect

    Smith, C A; Simon, A J; Belles, R D

    2011-04-01

    Flow charts depicting carbon dioxide emissions in the United States have been constructed from publicly available data and estimates of state-level energy use patterns. Approximately 5,800 million metric tons of carbon dioxide were emitted throughout the United States for use in power production, residential, commercial, industrial, and transportation applications in 2008. Carbon dioxide is emitted from the use of three major energy resources: natural gas, coal, and petroleum. The flow patterns are represented in a compact 'visual atlas' of 52 state-level (all 50 states, the District of Columbia, and one national) carbon dioxide flow charts representing a comprehensive systems view of national CO{sub 2} emissions. Lawrence Livermore National Lab (LLNL) has published flow charts (also referred to as 'Sankey Diagrams') of important national commodities since the early 1970s. The most widely recognized of these charts is the U.S. energy flow chart (http://flowcharts.llnl.gov). LLNL has also published charts depicting carbon (or carbon dioxide potential) flow and water flow at the national level as well as energy, carbon, and water flows at the international, state, municipal, and organizational (i.e. United States Air Force) level. Flow charts are valuable as single-page references that contain quantitative data about resource, commodity, and byproduct flows in a graphical form that also convey structural information about the system that manages those flows. Data on carbon dioxide emissions from the energy sector are reported on a national level. Because carbon dioxide emissions are not reported for individual states, the carbon dioxide emissions are estimated using published energy use information. Data on energy use is compiled by the U.S. Department of Energy's Energy Information Administration (U.S. EIA) in the State Energy Data System (SEDS). SEDS is updated annually and reports data from 2 years prior to the year of the update. SEDS contains data on primary

  20. Simulations of NOx Emissions from Low Emissions Discrete Jet Injector Combustor Tests

    NASA Technical Reports Server (NTRS)

    Ajmani, Kumud; Breisacher, Kevin

    2014-01-01

    An experimental and computational study was conducted to evaluate the performance and emissions characteristics of a candidate Lean Direct Injection (LDI) combustor configuration with a mix of simplex and airblast injectors. The National Combustion Code (NCC) was used to predict the experimentally measured EINOx emissions for test conditions representing low power, medium power, and high-power engine cycle conditions. Of the six cases modeled with the NCC using a reduced-kinetics finite-rate mechanism and lagrangian spray modeling, reasonable predictions of combustor exit temperature and EINOx were obtained at two high-power cycle conditions.

  1. High-resolution mapping of motor vehicle carbon dioxide emissions

    NASA Astrophysics Data System (ADS)

    McDonald, Brian C.; McBride, Zoe C.; Martin, Elliot W.; Harley, Robert A.

    2014-05-01

    A fuel-based inventory for vehicle emissions is presented for carbon dioxide (CO2) and mapped at various spatial resolutions (10 km, 4 km, 1 km, and 500 m) using fuel sales and traffic count data. The mapping is done separately for gasoline-powered vehicles and heavy-duty diesel trucks. Emission estimates from this study are compared with the Emissions Database for Global Atmospheric Research (EDGAR) and VULCAN. All three inventories agree at the national level within 5%. EDGAR uses road density as a surrogate to apportion vehicle emissions, which leads to 20-80% overestimates of on-road CO2 emissions in the largest U.S. cities. High-resolution emission maps are presented for Los Angeles, New York City, San Francisco-San Jose, Houston, and Dallas-Fort Worth. Sharp emission gradients that exist near major highways are not apparent when emissions are mapped at 10 km resolution. High CO2 emission fluxes over highways become apparent at grid resolutions of 1 km and finer. Temporal variations in vehicle emissions are characterized using extensive day- and time-specific traffic count data and are described over diurnal, day of week, and seasonal time scales. Clear differences are observed when comparing light- and heavy-duty vehicle traffic patterns and comparing urban and rural areas. Decadal emission trends were analyzed from 2000 to 2007 when traffic volumes were increasing and a more recent period (2007-2010) when traffic volumes declined due to recession. We found large nonuniform changes in on-road CO2 emissions over a period of ~5 years, highlighting the importance of timely updates to motor vehicle emission inventories.

  2. Emission Characterization and Emission Inventories for the 21st Century

    EPA Science Inventory

    Emission inventories are the foundation of cost-effective air quality management strategies. A goal of the emissions community is to develop the ultimate emission inventory which would include all significant emissions from all sources, time periods and areas, with quantified un...

  3. Coordinating Low Emission Development in Columbia (Fact Sheet)

    SciTech Connect

    Watson, A.; Butheau, M.; Sandor, D.

    2013-11-01

    Colombia's economy has grown more than 4 percent per year for a decade, but climate change is posing new risks to sustaining that development. With the nation's coastal areas, mountain ranges, rain forests, plains, and river basins vulnerable to changing weather patterns and growing seasons, Colombia is building resilience to climate change while working to curb emissions and pursue new options for low emission development.

  4. NATIONAL-SCALE ASSESSMENT OF AIR TOXICS RISKS

    EPA Science Inventory

    The national-scale assessment of air toxics risks is a modeling assessment which combines emission inventory development, atmospheric fate and transport modeling, exposure modeling, and risk assessment to characterize the risk associated with inhaling air toxics from outdoor sour...

  5. On-road traffic emissions in a megacity

    NASA Astrophysics Data System (ADS)

    D'Angiola, Ariela; Dawidowski, Laura E.; Gómez, Darío R.; Osses, Mauricio

    2010-02-01

    A new annual bottom-up emission inventory of criteria pollutants and greenhouse gases from on-road mobile sources was developed for 2006 for the metropolitan area of Buenos Aires, Argentina, within a four-year regional project aimed at providing tools for chemical weather forecast in South America. Under the scarcity of local emission factors, we collected data from measuring campaigns performed in Argentina, Brazil, Chile and Colombia and compiled a data set of regional emission factors representative of Latin American fleets and driving conditions. The estimated emissions were validated with respect to downscaled national estimates and the EDGAR global emission database. Our results highlight the role of older technologies accounting in average for almost 80% of the emissions of all species. The area exhibits higher specific emissions than developed countries, with figures two times higher for criteria pollutants. We analyzed the effect on emissions of replacing gasoline by compressed natural gas, occurring in Argentina since 1995. We identified (i) a relationship between number of vehicles and a compound socioeconomic indicator, and (ii) time-lags in vehicle technologies between developed and developing countries, which can be respectively applied for spatial disaggregation and the development of projections for other Latin American cities. The results may also be employed to complement global emission inventories and by local policy makers as an environmental management tool.

  6. National estimates of residential firewood and air pollution emissions

    SciTech Connect

    Lipfert, F. W.; Dungan, J. L.

    1981-01-01

    Estimates are presented for the distribution and quantity of recent (1978-1979) use of residential firewood in the United States, based on a correlation of survey data from 64 New England counties. The available survey data from other states are in agreement with the relationship derived from New England; no constraints due to wood supply are apparent. This relationship indicates that the highest density of wood usage (Kg/ha) occurs in urban areas; thus exacerbation of urban air quality problems is a matter of some concern. The data presentation used here gives an upper limit to this density of firewood usage which will allow realistic estimates of air quality impact to be made.

  7. [Review of normal spectral emissivity standard reference materials].

    PubMed

    Yu, Kun; Liu, Yu-Fang; Zhao, Yue-Jin

    2012-11-01

    In order to improve the accuracy of spectral emissivity measurement, standard reference materials of spectral emissivity as the dissemination of quantity in spectral emissivity measurement are used for the calibration of spectral emissivity measurement apparatus. In the present paper, firstly the standard reference materials data proposed by the American National Institute of Standards and Technology are introduced, and some underlying standard reference materials suggested by some metering departments in Europe are analyzed in detail For the standard reference material Armco iron and SiC proposed by some researchers, the advantages and disadvantages were explored. Finally, the characteristics of standard reference materials are summarized, and the future development of spectral emissivity measurement standard is prospected.

  8. U.S. Government Supports Low Emission Economic Growth

    SciTech Connect

    2015-11-01

    Countries around the world face the challenge of maintaining long-term sustainable economic growth and development under the threat of climate change. By identifying and pursuing a sustainable development pathway now, they are better positioned to reach their economic growth goals while addressing climate change impacts and lowering greenhouse gas (GHG) emissions. Low emission development strategies - development plans that promote sustainable social and economic development while reducing long-term GHG emissions - provide a pathway to preparing for a global low emission future. Partner country governments are working with the U.S. government through the Enhancing Capacity for Low Emission Development Strategies (EC-LEDS) program to further their national development objectives.

  9. Emissions of greenhouse gases in the United States 1997

    SciTech Connect

    1998-10-01

    This is the sixth annual report on aggregate US national emissions of greenhouse gases. It covers emissions over the period 1990--1996, with preliminary estimates of emissions for 1997. Chapter one summarizes some background information about global climate change and the greenhouse effect. Important recent developments in global climate change activities are discussed, especially the third Conference of the Parties to the Framework Convention on Climate Change, which was held in December of 1997 in Kyoto, Japan. Chapters two through five cover emissions of carbon dioxide, methane, nitrous oxide, halocarbons and related gases, respectively. Chapter six describes potential sequestration and emissions of greenhouse gases as a result of land use changes. Six appendices are included in the report. 96 refs., 38 tabs.

  10. National Development Generates National Identities.

    PubMed

    Golob, Tea; Makarovič, Matej; Suklan, Jana

    2016-01-01

    The purpose of the article is to test the relationship between national identities and modernisation. We test the hypotheses that not all forms of identity are equally compatible with modernisation as measured by Human Development Index. The less developed societies are characterised by strong ascribed national identities based on birth, territory and religion, but also by strong voluntarist identities based on civic features selected and/or achieved by an individual. While the former decreases with further modernisation, the latter may either decrease or remain at high levels and coexist with instrumental supranational identifications, typical for the most developed countries. The results, which are also confirmed by multilevel regression models, thus demonstrate that increasing modernisation in terms of development contributes to the shifts from classical, especially ascribed, identities towards instrumental identifications. These findings are particularly relevant in the turbulent times increasingly dominated by the hardly predictable effects of the recent mass migrations. PMID:26841050

  11. National Development Generates National Identities

    PubMed Central

    2016-01-01

    The purpose of the article is to test the relationship between national identities and modernisation. We test the hypotheses that not all forms of identity are equally compatible with modernisation as measured by Human Development Index. The less developed societies are characterised by strong ascribed national identities based on birth, territory and religion, but also by strong voluntarist identities based on civic features selected and/or achieved by an individual. While the former decreases with further modernisation, the latter may either decrease or remain at high levels and coexist with instrumental supranational identifications, typical for the most developed countries. The results, which are also confirmed by multilevel regression models, thus demonstrate that increasing modernisation in terms of development contributes to the shifts from classical, especially ascribed, identities towards instrumental identifications. These findings are particularly relevant in the turbulent times increasingly dominated by the hardly predictable effects of the recent mass migrations. PMID:26841050

  12. Infrared emission from comets.

    PubMed

    Krishna-Swamy, K S; Sandford, S A; Allamandola, L J; Witteborn, F C; Bregman, J D

    1989-05-01

    A brief discussion of the infrared observations from 4 to 20 micrometers of seven comets is presented. The observed infrared emission from comets depends primarily on their heliocentric distance. A model based on grain populations composed of a mixture of silicate and amorphous carbon particles in the mass ratio of about 40 to 1, with a power-law size distribution similar to that inferred for comet Halley, is applied to the observations. The model provides a good match to the observed heliocentric variation of both the 10 micrometers feature and the overall thermal emission from comets West and Halley. Matches to the observations of comet IRAS-Araki-Alcock and the antitail of comet Kohoutek require slightly larger grains. While the model does not match the exact profile and position of the 3.4 micrometers feature discovered in comet Halley, it does produce a qualitative fit to the observed variation of the feature's strength as a function of heliocentric distance. The calculations predict that the continuum under the 3.4 micrometers feature is due primarily to thermal emission from the comet dust when the comet is close to the Sun and to scattered solar radiation at large heliocentric distances, as is observed. A brief discussion of the determination of cometary grain temperatures from the observed infrared emission is presented. It is found that the observed shape of the emission curve from about 4 to 8 micrometers provides the best spectral region for estimating the cometary grain temperature distribution.

  13. Estimating mobile source pollutant emission: Methodological comparison and planning implications.

    PubMed

    Kim, T J; Hoskote, N G

    1983-03-01

    In the United States, the Clean Air Act Amendments of 1977 require that all non-attainment metropolitan areas evaluate the potential of transportation controls in meeting 1982 National Ambient Air Quality Standards. Many of these controls are designed to impact on mobile source emissions by altering vehicular speed.The paper discusses differences in results obtained by two alternative methods for estimating the same area's mobile source emissions. The findings suggest that alternative zonal speed aggregation procedures can lead to widely diverging emission estimates. The paper further discusses the inherent assumptions in the aggregation procedures and the potential consequences of their uses in transportation planning for air quality controls.

  14. Climate Change Technology Scenarios: Energy, Emissions, and Economic Implications

    SciTech Connect

    Placet, Marylynn; Humphreys, Kenneth K.; Mahasenan, N Maha

    2004-08-15

    This report describes three advanced technology scenarios and various illustrative cases developed by staff of Pacific Northwest National Laboratory (PNNL) for the U.S. Climate Change Technology Program. These scenarios and illustrative cases explore the energy, emissions and economic implications of using advanced energy technologies and other climate change related technologies to reduce future emissions of greenhouse gases (GHGs). The cases were modeled using the Mini Climate Assessment Model (MiniCAM) developed by PNNL. The report describes the scenarios, the specifications for the cases, and the results. The report also provides background information on current emissions of GHGs and issues associated with stabilizing GHG concentrations.

  15. 36 CFR 13.1186 - What are the emission standards for vessels?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 36 Parks, Forests, and Public Property 1 2014-07-01 2014-07-01 false What are the emission standards for vessels? 13.1186 Section 13.1186 Parks, Forests, and Public Property NATIONAL PARK SERVICE, DEPARTMENT OF THE INTERIOR NATIONAL PARK SYSTEM UNITS IN ALASKA Special Regulations-Glacier Bay National...

  16. 36 CFR 13.1186 - What are the emission standards for vessels?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 36 Parks, Forests, and Public Property 1 2013-07-01 2013-07-01 false What are the emission standards for vessels? 13.1186 Section 13.1186 Parks, Forests, and Public Property NATIONAL PARK SERVICE, DEPARTMENT OF THE INTERIOR NATIONAL PARK SYSTEM UNITS IN ALASKA Special Regulations-Glacier Bay National...

  17. 36 CFR 13.1186 - What are the emission standards for vessels?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 36 Parks, Forests, and Public Property 1 2012-07-01 2012-07-01 false What are the emission standards for vessels? 13.1186 Section 13.1186 Parks, Forests, and Public Property NATIONAL PARK SERVICE, DEPARTMENT OF THE INTERIOR NATIONAL PARK SYSTEM UNITS IN ALASKA Special Regulations-Glacier Bay National...

  18. 36 CFR 13.1186 - What are the emission standards for vessels?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 36 Parks, Forests, and Public Property 1 2010-07-01 2010-07-01 false What are the emission standards for vessels? 13.1186 Section 13.1186 Parks, Forests, and Public Property NATIONAL PARK SERVICE, DEPARTMENT OF THE INTERIOR NATIONAL PARK SYSTEM UNITS IN ALASKA Special Regulations-Glacier Bay National...

  19. 36 CFR 13.1186 - What are the emission standards for vessels?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 36 Parks, Forests, and Public Property 1 2011-07-01 2011-07-01 false What are the emission standards for vessels? 13.1186 Section 13.1186 Parks, Forests, and Public Property NATIONAL PARK SERVICE, DEPARTMENT OF THE INTERIOR NATIONAL PARK SYSTEM UNITS IN ALASKA Special Regulations-Glacier Bay National...

  20. Radionuclide air emission report for the Hanford Site Calendar Year 1993

    SciTech Connect

    Diediker, L.P.; Curn, B.L.; Rhoads, K.; Damberg, E.G.; Soldat, J.K.; Jette, S.J.

    1994-08-01

    This report documents radionuclide air emissions from the Hanford Site in 1993 and the resulting effective dose equivalent to any member of the public. The report has been prepared and will be submitted in accordance with reporting requirements in the Code of Federal Regulations, Title 40, Protection of the Environment, Part 61, {open_quotes}National Emissions Standards for Hazardous Air Pollutants,{close_quotes} Subpart H, {open_quotes}National Emission Standards for Emissions of Radionuclides Other than Radon from Department of Energy Facilities.{close_quotes}

  1. DEVELOPMENT OF REAL-TIME SITE-SPECIFIC MICROSCALE EMISSION FACTOR MODEL FOR THE ASSESSMENT OF HUMAN EXPOSURE TO MOTOR VEHICLE EMISSIONS

    EPA Science Inventory

    The United States Environmental Protection Agency's (EPA) National Expsoure Research Laboratory (NERL) has initiated a project to improve the methodology for modeling urban-scale human exposure to mobile source emissions. The modeling project has started by considering the nee...

  2. U.S. DOE 2004 LANL Radionuclide Air Emissions

    SciTech Connect

    K.W. Jacobson

    2005-08-12

    Amendments to the Clean Air Act, which added radionuclides to the National Emissions Standards for Hazardous Air Pollutants (NESHAP), went into effect in 1990. Specifically, a subpart (H) of 40 CFR 61 established an annual limit on the impact to the public attributable to emissions of radionuclides from U.S. Department of Energy facilities, such as the Los Alamos National Laboratory (LANL). As part of the new NESHAP regulations, LANL must submit an annual report to the U.S. Environmental Protection Agency headquarters and the regional office in Dallas by June 30. This report includes results of monitoring at LANL and the dose calculations for the calendar year 2004.

  3. N2O and NO2 Emissions from Heavy-Duty Diesel Trucks with Advanced Emission Controls

    NASA Astrophysics Data System (ADS)

    Preble, C.; Harley, R.; Kirchstetter, T.

    2014-12-01

    Diesel engines are the largest source of nitrogen oxides (NOx) emissions nationally, and also a major contributor to the black carbon (BC) fraction of fine particulate matter (PM). Recently, diesel particle filter (DPF) and selective catalytic reduction (SCR) emission control systems that target exhaust PM and NOx have become standard equipment on new heavy-duty diesel trucks. However, the deliberate catalytic oxidation of engine-out nitric oxide (NO) to nitrogen dioxide (NO2) in continuously regenerating DPFs leads to increased tailpipe emission of NO2. This is of potential concern due to the toxicity of NO2 and the resulting increases in atmospheric formation of other air pollutants such as ozone, nitric acid, and fine PM. While use of SCR reduces emissions of both NO and NO2, it may lead to increased emissions of nitrous oxide (N2O), a potent greenhouse gas. Here we report results from on-road measurements of heavy-duty diesel truck emissions conducted at the Port of Oakland and the Caldecott Tunnel in the San Francisco Bay Area. Emission factors (g pollutant per kg of diesel) were linked via recorded license plates to individual truck attributes, including engine model year and installed emission control equipment. Between 2009 and 2013, the fraction of DPF-equipped trucks at the Port of Oakland increased from 2 to 99%, and median engine age decreased from 11 to 6 years. Over the same period, fleet-average emission factors for black carbon and NOx decreased by 76 ± 22% and 53 ± 8%, respectively. However, direct emissions of NO2 increased, and consequently the NO2/NOx emission ratio increased from 0.03 ± 0.02 to 0.18 ± 0.03. Older trucks retrofitted with DPFs emitted approximately 3.5 times more NO2 than newer trucks equipped with both DPF and SCR. Preliminary data from summer 2014 measurements at the Caldecott Tunnel suggest that some older trucks have negative emission factors for N2O, and that for newer trucks, N2O emission factors have changed sign and

  4. Progress in emission control technologies

    SciTech Connect

    1994-12-31

    Partial contents of this book include: Ozone precursor emissions from alternatively fueled vehicles; Cycle resolved measurements of diesel particulate by optical techniques; A lubricant formulation for lower unburnt hydrocarbon emissions; Chassis test cycles for assessing emissions from heavy duty trucks; A non-intrusive method of measuring PCV blowby constituents; Some problems in the improvement of measurement of transient emissions; and Oxidation catalyst systems for emission control of LPG-powered forklift trucks.

  5. Megacity and country emissions from combustion sources-Buenos Aires-Argentina

    NASA Astrophysics Data System (ADS)

    Dawidowski, L.; Gomez, D.; Matranga, M.; D'Angiola, A.; Oreggioni, G.

    2010-12-01

    Historic time series (1970-2006) emissions of greenhouse gases and air pollutants arising from stationary and mobile combustion sources were estimated at national level for Argentina and at regional level for the metropolitan area of Buenos Aires (MABA). All emissions were estimated using a bottom-up approach following the IPCC good practice guidance. For mobile sources, national emissions include all transport categories. Regional emissions account thus far only for on-road. For national emissions, methodologies and guidance by the IPCC were employed, applying the highest possible tier and using: i)country-specific emission factors for carbon and sulphur and technology-based information for other species, ii)activity data from energy balance series (1970-2007), and iii)complementary information concerning the non-energy use of fuels. Regional emissions in 2006 were estimated in-depth using a technology-based approach for the city of Buenos Aires (CBA) and the 24 neighboring districts composing the MABA. A regional emissions factors database was developed to better characterize Latin American fleets and driving conditions employing COPERT III-IV algorithms and emission factors measured in dynamometers and circulating vehicles in Argentina, Brazil, Chile and Colombia. Past emissions were back estimated from 2005 to 1970 using the best available information, which differs greatly among categories, spatial disaggregation and time periods. The time series of stationary and mobile combustion sources at the national and regional level allowed the identification of distinct patterns. National greenhouse gas emissions in 2006 amounted to ~ 150 million ton CO2-equivalent, 70% of which were contributed by stationary sources. On-road transport was the major contributor within mobile sources (28.1 %). The increasing emissions trends are dominated by on-road transport, agriculture and residential categories while the variability is largely associated with energy industries

  6. Oceanic emissions of ammonia

    NASA Astrophysics Data System (ADS)

    Paulot, F.; Jacob, D. J.; Johnson, M.; Bell, T. G.; Stock, C. A.; Doney, S. C.

    2013-12-01

    Half of natural ammonia (NH3) emissions is thought to originate from the oceans. Such large emissions have implications for the global budget of N and the acidity of marine aerosols. We develop two new inventories of oceanic NH3 emissions based on simulated monthly NH3 seawater concentrations from the GFDL-COBALT and the CESM-BEC ocean models. These new inventories explicitly account for the effect of temperature on the water-atmosphere exchange of NH3. We evaluate these inventory using cruise observations of gas-phase ammonia (AMT cruises) and ammonium (NOAA cruises) as well as seawater measurement of NHx. Implications of atmospheric NHx observations for the exchange of N between ocean and land and ocean N/P limitations are discussed.

  7. Automotive Emissions Control

    NASA Astrophysics Data System (ADS)

    Graham, George

    2002-03-01

    Serious efforts to control emissions from automobiles commenced more than thirty-five years ago, focusing initially on aspects of engine design and the combustion process. For the past quarter century, however, the major emphasis has been on treating the engine exhaust gas before it leaves the vehicle, in order to limit the release of toxic and other pollutants. The system that was eventually devised and is now used on most gasoline-burning automobiles combines sensing, electronic engine control, and catalysis to decrease the emission of certain pollutants by more than ninety percent. This presentation will describe how the system works and briefly touch upon some of the consequences of automotive emissions control.

  8. Global hexachlorobenzene emissions.

    PubMed

    Bailey, R E

    2001-04-01

    Information from a variety of sources has been assembled to give a global picture of hexachlorobenzene (HCB) emissions in the mid 1990s. No single overwhelming source of HCB was identified. The best estimates of global HCB emissions from different categories of sources are as follows: pesticides application - 6500 kg/yr; manufacturing - 9500 kg/yr; combustion - 7000 kg/yr, includes 500 kg from biomass burning. This adds up to total current HCB emissions of approximately 23,000 kg/yr with an estimated range 12,000-92,000 kg/yr. A substantial portion of HCB measured in the atmosphere is thought to come from volatilization of "old" HCB on the soil from past contamination along with unidentified sources. No information on potential sources in developing countries was available. PMID:11297396

  9. Emission control system

    NASA Technical Reports Server (NTRS)

    Parrish, Clyde F. (Inventor); Chung, J. Landy (Inventor)

    2009-01-01

    Methods and apparatus utilizing hydrogen peroxide are useful to reduce SOx and mercury (or other heavy metal) emissions from combustion flue gas streams. The methods and apparatus may further be modified to reduce NOx emissions. Continuous concentration of hydrogen peroxide to levels approaching or exceeding propellant-grade hydrogen peroxide facilitates increased system efficiency. In this manner, combustion flue gas streams can be treated for the removal of SOx and heavy metals, while isolating useful by-products streams of sulfuric acid as well as solids for the recovery of the heavy metals. Where removal of NOx emissions is included, nitric acid may also be isolated for use in fertilizer or other industrial applications.

  10. An overview of non-road equipment emissions in China

    NASA Astrophysics Data System (ADS)

    Wang, Fan; Li, Zhen; Zhang, Kaishan; Di, Baofeng; Hu, Baomei

    2016-05-01

    As the vehicle population has dramatically increased in China in the past two decades, vehicle emissions have become one of the major sources to air pollution across the entire country, especially for the metropolitan cities such as Beijing and Shanghai. Most of the non-road equipment are diesel-fueled and have been proved to be a key source for NOx and PM emissions, contributing significantly to the formation of haze/smog. Therefore, an accurate estimation of emission inventory from non-road equipment is essential for air quality improvement policy making, which mainly depends on the data availability of equipment population, activity, and emissions factor. Compared to on-road vehicles, less studies regarding emissions characterization have been conducted and investigated for non-road mobile sources in China. Thus, in order to identify the data gaps and future research needs, the objective of this study is to review the current status of research in non-road mobile emissions. Five types of non-road equipment were addressed in this study, including agricultural equipment, industrial equipment, river/ocean-going vessels, locomotives, and commercial airplanes, with a focus on the former two. The equipment are further classified mainly based on national standards and data availability to account for fuel type, job duties and others. This investigation has found that the research regarding emissions from non-road equipment is still at its early stage and there is a huge data gap for both activity and emissions factors. For most of the study, data used for emission inventory estimation were based on either literature with similar equipment or as-developed emissions models such as NONROAD or CORPERT. The representativeness of these data to the localities was not much discussed in those studies, which might have weakened the accuracy of the estimated emission inventory. For future study, real-world in-use measurements of activities and emissions for the non-road equipment

  11. 40 CFR 63.56 - Requirements for case-by-case determination of equivalent emission limitations after promulgation...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES Requirements for Control... promulgates a relevant emission standard under section 112(d) or (h) of the Act that is applicable to a source... determination of equivalent emission limitations after promulgation of subsequent MACT standard. 63.56...

  12. 40 CFR 63.56 - Requirements for case-by-case determination of equivalent emission limitations after promulgation...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES Requirements for Control... promulgates a relevant emission standard under section 112(d) or (h) of the Act that is applicable to a source... determination of equivalent emission limitations after promulgation of subsequent MACT standard. 63.56...

  13. 40 CFR 63.56 - Requirements for case-by-case determination of equivalent emission limitations after promulgation...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES Requirements for Control... promulgates a relevant emission standard under section 112(d) or (h) of the Act that is applicable to a source... determination of equivalent emission limitations after promulgation of subsequent MACT standard. 63.56...

  14. 40 CFR 63.56 - Requirements for case-by-case determination of equivalent emission limitations after promulgation...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ...) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES Requirements for Control... promulgates a relevant emission standard under section 112(d) or (h) of the Act that is applicable to a source... determination of equivalent emission limitations after promulgation of subsequent MACT standard. 63.56...

  15. 40 CFR 63.1037 - Alternative means of emission limitation: Enclosed-vented process units or affected facilities.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 10 2011-07-01 2011-07-01 false Alternative means of emission... FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES (CONTINUED) National Emission Standards for Equipment Leaks-Control Level 2 Standards § 63.1037 Alternative means of emission limitation:...

  16. Urea Fertilizer Decreases N2O Emissions Compared to Anhydrous Ammonia in Corn Cropping Systems in Minnesota

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Quantifying nitrous oxide (N2O) emissions from corn and soybean fields under different fertilizer regimes is essential to developing national inventories of greenhouse gas (GHG) emissions. The objective of this study was to compare N2O emissions in plots managed for more than 15 yr under continuous ...

  17. 77 FR 18297 - Air Traffic Noise, Fuel Burn, and Emissions Modeling Using the Aviation Environmental Design Tool...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-27

    ... Federal Aviation Administration Air Traffic Noise, Fuel Burn, and Emissions Modeling Using the Aviation... Aviation Environmental Design Tool version 2a (AEDT 2a) to analyze noise, fuel burn, and emissions for FAA... assess noise, fuel burn, and emissions impacts of such actions under the National Environmental...

  18. Potential environmental impacts of future halocarbon emissions

    SciTech Connect

    Holmes, K.J.; Ellis, J.H.

    1996-08-01

    An integrated analysis of future halocarbon emissions and their environmental impacts shows that strict global compliance is required if the Montreal Protocol is to accomplish the goal of eliminating the lower stratospheric ozone hole. This analysis is integrated in the sense that demographic, economic, and regulatory processes controlling future production were linked explicitly to the technological factors translating production into emissions and the environmental processes transforming emissions into environmental impacts. Given current models of halocarbon transformation and atmospheric response, this research suggests that if a small percentage of nations continues to expand production at modest rates, the ozone hole will not be eliminated. In addition, high growth rate assumptions for halocarbon production by noncompliance nations will result in significantly increased ozone depletion. This research also shows that the continued use of small amounts of ozone-depleting substances for essential uses and the failure to adequately replace all ozone-depleting substances can eliminate the possibility of returning the atmosphere to pre-ozone hole conditions. The global climate change potential of halocarbons is fairly small if growth rates for chlorofluorocarbon substitutes remain low. If growth rates return to precontrol levels, these substitutes could contribute significantly to global climate change. 41 refs., 3 figs., 3 tabs.

  19. The contribution of drained organic soils to the globally emitted greenhouse gases and emission hotspots

    NASA Astrophysics Data System (ADS)

    Barthelmes, Alexandra; Couwenberg, John; Joosten, Hans

    2016-04-01

    Key words: organic soils, peatlands, drainage, emissions, globally Peatlands cover only 3% of the global land surface. Some 15% of these peatlands have been drained for agriculture, forestry and grazing, which leads to the release of huge amounts of carbon. The '2013 Supplement to the 2006 IPCC Guidelines for National Greenhouse Gas Inventories: Wetlands' (IPCC 2014) offers up-to-date default emission factors for different land use types on organic soil and thus enables proper reporting. For this, realistic area data of drained organic soils are needed at a national scale. We analysed the drained organic soil areas and related emissions as reported to the UNFCCC in 2014 for several Nordic-Baltic countries . The analysis revealed that the areas often seem to be underestimated and that several countries use outdated emission factors. The re-assessment of the drained area and the application of the IPCC (2014) default emission factors resulted in 5-10 x higher emissions from drained organic soils for some countries. Out of 9 Nordic-Baltic countries only 1 country seems to have overestimated the drainage related organic soil emissions. If adopting the default emission factors from IPCC (2014) globally, the emissions from drained and degrading organic soils (~ 1,600 Mt CO2-eq.) amount to almost double the amount of CO2 emissions from aviation, even when emissions from peat fires are not included . By far the top single emitter of drained peatland related greenhouse gases is Indonesia, followed by the European Union and Russia. 25 countries are together responsible for 95% of global emissions from peatland drainage, excluding fires. Fires raise the importance of particularly Indonesia and Russian Federation. In 25 countries emissions from peatland degradation are over 50% of the emissions from fossil fuels and cement production combined, hence peatland emissions are of national significance.

  20. Historical variations of biogenic volatile organic compound emission inventories in China, 1981-2003

    NASA Astrophysics Data System (ADS)

    Li, L. Y.; Xie, S. D.

    2014-10-01

    To evaluate the variations in temporal and spatial distribution of biogenic volatile organic compound (BVOC) emissions in China, historical BVOC emission inventories at a spatial resolution of 36 km × 36 km for the period of 1981-2003 were developed firstly. Based on the time-varying statistical data and Vegetation Atlas of China (1:1,000,000), emissions of isoprene, 37 monoterpenes, 32 sesquiterpenes, and other volatile organic compounds (OVOCs) were estimated using MEGANv2.1 driven by WRF model. Results show China's BVOC emissions had increased by 28.01% at an annual average rate of 1.27% from 37.89 Tg in 1981 to 48.50 Tg in 2003. Emissions of isoprene, monoterpenes, sesquiterpenes, and OVOCs had increased by 41.60%, 34.78%, 41.05%, and 4.89%, respectively. With fixed meteorological variables, the estimated BVOC emissions would increase by 19.25%, resulting from the increasing of vegetation biomass during the last 23 years. On average, isoprene, monoterpenes, sesquiterpenes, and OVOCs were responsible for 52.40%, 12.73%, 2.58%, and 32.29% of the national BVOC emissions, respectively. β-pinene and α-pinene, farnesene and caryophyllene were the largest contributors to the total monoterpene and sesquiterpene emissions, respectively. The highest emissions were found over northeastern, southeastern, southwestern China, Qinling Mountain, and Hainan and Taiwan provinces. The regions with high emissions had been expanding over the years, especially in the Changbai Mountain, southern China, and southwestern forest regions. The lowest emissions in southern China occurred in 1984-1988. Almost all the provinces had experienced increasing emissions, but their contributions to the national emissions differed significantly over the past 23 years. Yunnan, Guangxi, Heilongjiang, Jiangxi, Fujian, Guangdong, and Sichuan provinces always dominated the national BVOC emissions, excluding in 1977-1981, when the three northeastern provinces had relatively lower emissions.

  1. Regulated and unregulated emissions from modern 2010 emissions-compliant heavy-duty on-highway diesel engines.

    PubMed

    Khalek, Imad A; Blanks, Matthew G; Merritt, Patrick M; Zielinska, Barbara

    2015-08-01

    The U.S. Environmental Protection Agency (EPA) established strict regulations for highway diesel engine exhaust emissions of particulate matter (PM) and nitrogen oxides (NOx) to aid in meeting the National Ambient Air Quality Standards. The emission standards were phased in with stringent standards for 2007 model year (MY) heavy-duty engines (HDEs), and even more stringent NOX standards for 2010 and later model years. The Health Effects Institute, in cooperation with the Coordinating Research Council, funded by government and the private sector, designed and conducted a research program, the Advanced Collaborative Emission Study (ACES), with multiple objectives, including detailed characterization of the emissions from both 2007- and 2010-compliant engines. The results from emission testing of 2007-compliant engines have already been reported in a previous publication. This paper reports the emissions testing results for three heavy-duty 2010-compliant engines intended for on-highway use. These engines were equipped with an exhaust diesel oxidation catalyst (DOC), high-efficiency catalyzed diesel particle filter (DPF), urea-based selective catalytic reduction catalyst (SCR), and ammonia slip catalyst (AMOX), and were fueled with ultra-low-sulfur diesel fuel (~6.5 ppm sulfur). Average regulated and unregulated emissions of more than 780 chemical species were characterized in engine exhaust under transient engine operation using the Federal Test Procedure cycle and a 16-hr duty cycle representing a wide dynamic range of real-world engine operation. The 2010 engines' regulated emissions of PM, NOX, nonmethane hydrocarbons, and carbon monoxide were all well below the EPA 2010 emission standards. Moreover, the unregulated emissions of polycyclic aromatic hydrocarbons (PAHs), nitroPAHs, hopanes and steranes, alcohols and organic acids, alkanes, carbonyls, dioxins and furans, inorganic ions, metals and elements, elemental carbon, and particle number were substantially (90

  2. Regulated and unregulated emissions from modern 2010 emissions-compliant heavy-duty on-highway diesel engines.

    PubMed

    Khalek, Imad A; Blanks, Matthew G; Merritt, Patrick M; Zielinska, Barbara

    2015-08-01

    The U.S. Environmental Protection Agency (EPA) established strict regulations for highway diesel engine exhaust emissions of particulate matter (PM) and nitrogen oxides (NOx) to aid in meeting the National Ambient Air Quality Standards. The emission standards were phased in with stringent standards for 2007 model year (MY) heavy-duty engines (HDEs), and even more stringent NOX standards for 2010 and later model years. The Health Effects Institute, in cooperation with the Coordinating Research Council, funded by government and the private sector, designed and conducted a research program, the Advanced Collaborative Emission Study (ACES), with multiple objectives, including detailed characterization of the emissions from both 2007- and 2010-compliant engines. The results from emission testing of 2007-compliant engines have already been reported in a previous publication. This paper reports the emissions testing results for three heavy-duty 2010-compliant engines intended for on-highway use. These engines were equipped with an exhaust diesel oxidation catalyst (DOC), high-efficiency catalyzed diesel particle filter (DPF), urea-based selective catalytic reduction catalyst (SCR), and ammonia slip catalyst (AMOX), and were fueled with ultra-low-sulfur diesel fuel (~6.5 ppm sulfur). Average regulated and unregulated emissions of more than 780 chemical species were characterized in engine exhaust under transient engine operation using the Federal Test Procedure cycle and a 16-hr duty cycle representing a wide dynamic range of real-world engine operation. The 2010 engines' regulated emissions of PM, NOX, nonmethane hydrocarbons, and carbon monoxide were all well below the EPA 2010 emission standards. Moreover, the unregulated emissions of polycyclic aromatic hydrocarbons (PAHs), nitroPAHs, hopanes and steranes, alcohols and organic acids, alkanes, carbonyls, dioxins and furans, inorganic ions, metals and elements, elemental carbon, and particle number were substantially (90

  3. 75 FR 81952 - Greenhouse Gas Emissions Standards and Fuel Efficiency Standards for Medium- and Heavy-Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-12-29

    ... Greenhouse Gas Emissions Standards and Fuel Efficiency Standards for Medium- and Heavy-Duty Engines and...-Duty National Program that will increase fuel efficiency and reduce greenhouse gas emissions for on... a comprehensive Heavy-Duty National Program that will increase fuel efficiency and reduce...

  4. 40 CFR 63.1453 - How do I demonstrate continuous compliance with the emission limitations, work practice standards...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... (CONTINUED) AIR PROGRAMS (CONTINUED) NATIONAL EMISSION STANDARDS FOR HAZARDOUS AIR POLLUTANTS FOR SOURCE CATEGORIES National Emission Standards for Hazardous Air Pollutants for Primary Copper Smelting Continuous...) Monitor the copper converter department capture system according to the requirements in § 63.1452(a)...

  5. 40 CFR 63.7920 - What emissions limitations and work practice standards must I meet for equipment leaks?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... applicable requirements under 40 CFR part 63, subpart TT—National Emission Standards for Equipment Leaks—Control Level 1; or (2) Control equipment leaks according to all applicable requirements under 40 CFR part 63, subpart UU—National Emission Standards for Equipment Leaks—Control Level 2. (c) If you use...

  6. 40 CFR 63.7920 - What emissions limitations and work practice standards must I meet for equipment leaks?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... applicable requirements under 40 CFR part 63, subpart TT—National Emission Standards for Equipment Leaks—Control Level 1; or (2) Control equipment leaks according to all applicable requirements under 40 CFR part 63, subpart UU—National Emission Standards for Equipment Leaks—Control Level 2. (c) If you use...

  7. 40 CFR 63.7920 - What emissions limitations and work practice standards must I meet for equipment leaks?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... applicable requirements under 40 CFR part 63, subpart TT—National Emission Standards for Equipment Leaks—Control Level 1; or (2) Control equipment leaks according to all applicable requirements under 40 CFR part 63, subpart UU—National Emission Standards for Equipment Leaks—Control Level 2. (c) If you use...

  8. 40 CFR 63.7920 - What emissions limitations and work practice standards must I meet for equipment leaks?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... applicable requirements under 40 CFR part 63, subpart TT—National Emission Standards for Equipment Leaks—Control Level 1; or (2) Control equipment leaks according to all applicable requirements under 40 CFR part 63, subpart UU—National Emission Standards for Equipment Leaks—Control Level 2. (c) If you use...

  9. 40 CFR 63.7920 - What emissions limitations and work practice standards must I meet for equipment leaks?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... applicable requirements under 40 CFR part 63, subpart TT—National Emission Standards for Equipment Leaks—Control Level 1; or (2) Control equipment leaks according to all applicable requirements under 40 CFR part 63, subpart UU—National Emission Standards for Equipment Leaks—Control Level 2. (c) If you use...

  10. Sharing global CO2 emission reductions among one billion high emitters.

    PubMed

    Chakravarty, Shoibal; Chikkatur, Ananth; de Coninck, Heleen; Pacala, Stephen; Socolow, Robert; Tavoni, Massimo

    2009-07-21

    We present a framework for allocating a global carbon reduction target among nations, in which the concept of "common but differentiated responsibilities" refers to the emissions of individuals instead of nations. We use the income distribution of a country to estimate how its fossil fuel CO(2) emissions are distributed among its citizens, from which we build up a global CO(2) distribution. We then propose a simple rule to derive a universal cap on global individual emissions and find corresponding limits on national aggregate emissions from this cap. All of the world's high CO(2)-emitting individuals are treated the same, regardless of where they live. Any future global emission goal (target and time frame) can be converted into national reduction targets, which are determined by "Business as Usual" projections of national carbon emissions and in-country income distributions. For example, reducing projected global emissions in 2030 by 13 GtCO(2) would require the engagement of 1.13 billion high emitters, roughly equally distributed in 4 regions: the U.S., the OECD minus the U.S., China, and the non-OECD minus China. We also modify our methodology to place a floor on emissions of the world's lowest CO(2) emitters and demonstrate that climate mitigation and alleviation of extreme poverty are largely decoupled.

  11. Emissions of greenhouse gases in the United States, 1987--1994

    SciTech Connect

    1995-09-25

    The Energy Information Administration (EIA) is required by the Energy Policy Act of 1992 to prepare a report on aggregate US national emissions of greenhouse gases for the period 1987--1992, with annual updates thereafter. This is the third annual update report,covering national emissions over the period 1987--1993, with preliminary estimates of US carbon dioxide and halocarbon emissions for 1994. Calculating national aggregate emissions(or ``national inventories``) of greenhouse gases is a recently developed form of intellectual endeavor. Greenhouse gas emissions are rarely measured directly or reported to statistical agencies. Thus, to prepare emissions inventories usually requires inferring emissions indirectly from information collected for other purposes. Both the available information and the inferences drawn may be of varying reliability. Chapter 1 of this report briefly recapitulates some background information about global climate change and the greenhouse effect and discusses important recent developments in global climate change activities. Chapters 2 through 6 cover emissions of carbon dioxide, methane, nitrous oxide, halocarbons, and criteria pollutants, respectively. Chapter 7 describes potential sequestration and emissions of greenhouse gases as a result of land use changes.

  12. Regional emissions of air pollutants in China.

    SciTech Connect

    Streets, D. G.

    1998-10-05

    As part of the China-MAP program, sponsored by the US National Aeronautics and Space Administration, regional inventories of air pollutants emitted in China are being characterized, in order that the atmospheric chemistry over China can be more fully understood and the resulting ambient concentrations in Chinese cities and the deposition levels to Chinese ecosystems be determined with better confidence. In addition, the contributions of greenhouse gases from China and of acidic aerosols that counteract global warming are being quantified. This paper presents preliminary estimates of the emissions of some of the major air pollutants in China: sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), carbon monoxide (CO), and black carbon (C). Emissions are estimated for each of the 27 regions of China included in the RAINS-Asia simulation model and are subsequently distributed to a 1{degree} x 1{degree} grid using appropriate disaggregation factors. Emissions from all sectors of the Chinese economy are considered, including the combustion of biofuels in rural homes. Emissions from larger power plants are calculated individually and allocated to the grid accordingly. Data for the period 1990-1995 are being developed, as well as projections for the future under alternative assumptions about economic growth and environmental control.

  13. Global Commercial Aviation Emissions Inventory for 2004

    NASA Astrophysics Data System (ADS)

    Wilkerson, J.; Balasubramanian, S.; Malwitz, A.; Wayson, R.; Fleming, G.; Jacobson, M. Z.; Naiman, A.; Lele, S.

    2008-12-01

    In 2004, the global commercial aircraft fleet included more than 13,000 aircraft flying over 30 billion km, burning more than 100 million tons of fuel. All this activity incurs substantial amounts of fossil-fuel combustion products at the cruise altitude within the upper troposphere and lower stratosphere that could potentially affect the atmospheric composition and climate. These emissions; such as CO, CO2, PM, NOx, SOx, are not distributed uniformly over the earth, so understanding the temporal and spatial distributions is an important component for modeling aviation climate impacts. Previous studies for specific years have shown that nearly all activity occurs in the northern hemisphere, and most is within mid-latitudes. Simply scaling older data by the annual global industry growth of 3-5 percent may provide emission trends which are not representative of geographically varying growth in aviation sector that has been noted over the past years. India, for example, increased its domestic aviation activity recently by 46 percent in one year. Therefore, it is important that aircraft emissions are best characterized and represented in the atmospheric models for impacts analysis. Data containing all global commercial flights for 2004 was computed using the Federal Aviation Administration's Aviation Environmental Design Tool (AEDT) and provided by the Volpe National Transportation Systems Center. The following is a summary of this data which illustrates the global aviation footprint for 2004, and provides temporal and three-dimensional spatial distribution statistics of several emissions constituents.

  14. A design for a relational database for the calculation and storage of greenhouse gas emissions.

    PubMed

    Newcomb, T M

    2001-10-01

    The Intergovernmental Panel on Climate Change (IPCC) has published guidelines for the development of national greenhouse gas-emissions inventories and recommendations for collecting data necessary to calculate greenhouse gas emissions. Many regional and local jurisdictions will be performing inventories of greenhouse gas emissions and estimating the benefits of mitigation strategies to reduce emissions. This article advocates the development of relational databases to calculate and store emissions estimates based on IPCC guidelines and quantities of precursors of greenhouse gases. Specific examples of tables and queries are used to illustrate calculation methods and formulae, the choice of database keys, and the choice of methods for joining tables to construct queries.

  15. Characterizing the emissivity of materials under dynamic compression (final report for LDRD project 79877).

    SciTech Connect

    Dolan, Daniel H.

    2007-10-01

    Temperature measurements are crucial to equation of state development, but difficult to perform reliably. In the case of infrared pyrometry, a large uncertainty comes from the fact that sample emissivity (the deviation from a blackbody) is unknown. In this project, a method for characterizing the emissivity of shocked materials was developed. By coupling infrared radiation from the National Synchrotron Light Source to a gas gun system, broad spectrum emissivity changes were studied to a peak stress of 8 GPa. Emissivity measurements were performed on standard metals (Al, Cr, Cu, and Pt) as well as a high emissivity coating developed at Sandia.

  16. Structuring economic incentives to reduce emissions from deforestation within Indonesia.

    PubMed

    Busch, Jonah; Lubowski, Ruben N; Godoy, Fabiano; Steininger, Marc; Yusuf, Arief A; Austin, Kemen; Hewson, Jenny; Juhn, Daniel; Farid, Muhammad; Boltz, Frederick

    2012-01-24

    We estimate and map the impacts that alternative national and subnational economic incentive structures for reducing emissions from deforestation (REDD+) in Indonesia would have had on greenhouse gas emissions and national and local revenue if they had been in place from 2000 to 2005. The impact of carbon payments on deforestation is calibrated econometrically from the pattern of observed deforestation and spatial variation in the benefits and costs of converting land to agriculture over that time period. We estimate that at an international carbon price of $10/tCO(2)e, a "mandatory incentive structure," such as a cap-and-trade or symmetric tax-and-subsidy program, would have reduced emissions by 163-247 MtCO(2)e/y (20-31% below the without-REDD+ reference scenario), while generating a programmatic budget surplus. In contrast, a "basic voluntary incentive structure" modeled after a standard payment-for-environmental-services program would have reduced emissions nationally by only 45-76 MtCO(2)e/y (6-9%), while generating a programmatic budget shortfall. By making four policy improvements--paying for net emission reductions at the scale of an entire district rather than site-by-site; paying for reductions relative to reference levels that match business-as-usual levels; sharing a portion of district-level revenues with the national government; and sharing a portion of the national government's responsibility for costs with districts--an "improved voluntary incentive structure" would have been nearly as effective as a mandatory incentive structure, reducing emissions by 136-207 MtCO(2)e/y (17-26%) and generating a programmatic budget surplus.

  17. Structuring economic incentives to reduce emissions from deforestation within Indonesia.

    PubMed

    Busch, Jonah; Lubowski, Ruben N; Godoy, Fabiano; Steininger, Marc; Yusuf, Arief A; Austin, Kemen; Hewson, Jenny; Juhn, Daniel; Farid, Muhammad; Boltz, Frederick

    2012-01-24

    We estimate and map the impacts that alternative national and subnational economic incentive structures for reducing emissions from deforestation (REDD+) in Indonesia would have had on greenhouse gas emissions and national and local revenue if they had been in place from 2000 to 2005. The impact of carbon payments on deforestation is calibrated econometrically from the pattern of observed deforestation and spatial variation in the benefits and costs of converting land to agriculture over that time period. We estimate that at an international carbon price of $10/tCO(2)e, a "mandatory incentive structure," such as a cap-and-trade or symmetric tax-and-subsidy program, would have reduced emissions by 163-247 MtCO(2)e/y (20-31% below the without-REDD+ reference scenario), while generating a programmatic budget surplus. In contrast, a "basic voluntary incentive structure" modeled after a standard payment-for-environmental-services program would have reduced emissions nationally by only 45-76 MtCO(2)e/y (6-9%), while generating a programmatic budget shortfall. By making four policy improvements--paying for net emission reductions at the scale of an entire district rather than site-by-site; paying for reductions relative to reference levels that match business-as-usual levels; sharing a portion of district-level revenues with the national government; and sharing a portion of the national government's responsibility for costs with districts--an "improved voluntary incentive structure" would have been nearly as effective as a mandatory incentive structure, reducing emissions by 136-207 MtCO(2)e/y (17-26%) and generating a programmatic budget surplus. PMID:22232665

  18. Structuring economic incentives to reduce emissions from deforestation within Indonesia

    PubMed Central

    Busch, Jonah; Lubowski, Ruben N.; Godoy, Fabiano; Steininger, Marc; Yusuf, Arief A.; Austin, Kemen; Hewson, Jenny; Juhn, Daniel; Farid, Muhammad; Boltz, Frederick

    2012-01-01

    We estimate and map the impacts that alternative national and subnational economic incentive structures for reducing emissions from deforestation (REDD+) in Indonesia would have had on greenhouse gas emissions and national and local revenue if they had been in place from 2000 to 2005. The impact of carbon payments on deforestation is calibrated econometrically from the pattern of observed deforestation and spatial variation in the benefits and costs of converting land to agriculture over that time period. We estimate that at an international carbon price of $10/tCO2e, a “mandatory incentive structure,” such as a cap-and-trade or symmetric tax-and-subsidy program, would have reduced emissions by 163–247 MtCO2e/y (20–31% below the without-REDD+ reference scenario), while generating a programmatic budget surplus. In contrast, a “basic voluntary incentive structure” modeled after a standard payment-for-environmental-services program would have reduced emissions nationally by only 45–76 MtCO2e/y (6–9%), while generating a programmatic budget shortfall. By making four policy improvements—paying for net emission reductions at the scale of an entire district rather than site-by-site; paying for reductions relative to reference levels that match business-as-usual levels; sharing a portion of district-level revenues with the national government; and sharing a portion of the national government's responsibility for costs with districts—an “improved voluntary incentive structure” would have been nearly as effective as a mandatory incentive structure, reducing emissions by 136–207 MtCO2e/y (17–26%) and generating a programmatic budget surplus. PMID:22232665

  19. 1992 Carbon emissions data

    SciTech Connect

    1995-12-31

    This article reports on the global total of carbon dioxide emissions from fossil-fuel burning and cement manufacture in 1992. The total estimate of 6097 million metric tons of carbon is essentially the same for 1990 and down slightly from 1991, but 7 of 9 geographical regions had increases.

  20. Coke oven emissions

    Integrated Risk Information System (IRIS)

    Coke oven emissions ; CASRN NA Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effects