Emissions from oil and gas operations in the United States and their air quality implications

The energy supply infrastructure in the United States has been changing dramatically over the past decade. Increased production of oil and natural gas, particularly from shale resources using horizontal drilling and hydraulic fracturing, made the United States the world’s largest producer of oil and natural gas in 2014. This review examines air quality impacts, specifically, changes in greenhouse gas, criteria air pollutant, and air toxics emissions from oil and gas production activities that are a result of these changes in energy supplies and use. National emission inventories indicate that volatile organic compound (VOC) and nitrogen oxide (NO_x) emissions from oil and gas supply chains in the United States have been increasing significantly, whereas emission inventories for greenhouse gases have seen slight declines over the past decade. These emission inventories are based on counts of equipment and operational activities (activity factors), multiplied by average emission factors, and therefore are subject to uncertainties in these factors. Although uncertainties associated with activity data and missing emission source types can be significant, multiple recent measurement studies indicate that the greatest uncertainties are associated with emission factors. In many source categories, small groups of devices or sites, referred to as super-emitters, contribute a large fraction of emissions. When super-emitters are accounted for, multiple measurement approaches, at multiple scales, produce similar results for estimated emissions. Challenges moving forward include identifying super-emitters and reducing their emission magnitudes. Work done to date suggests that both equipment malfunction and operational practices can be important. Finally, although most of this review focuses on emissions from energy supply infrastructures, the regional air quality implications of some coupled energy production and use scenarios are examined. These case studies suggest that both energy production and use should be considered in assessing air quality implications of changes in energy infrastructures, and that impacts are likely to vary among regions.

Implications: The energy supply infrastructure in the United States has been changing dramatically over the past decade, leading to changes in emissions from oil and natural gas supply chain sources. In many source categories along these supply chains, small groups of devices or sites, referred to as super-emitters, contribute a large fraction of emissions. Effective emission reductions will require technologies for both identifying super-emitters and reducing their emission magnitudes.     

Impact of emissions from natural gas production facilities on ambient air quality in the Barnett Shale area: A pilot study

Rapid and extensive development of shale gas resources in the Barnett Shale region of Texas in recent years has created concerns about potential environmental impacts on water and air quality. The purpose of this study was to provide a better understanding of the potential contributions of emissions from gas production operations to population exposure to air toxics in the Barnett Shale region. This goal was approached using a combination of chemical characterization of the volatile organic compound (VOC) emissions from active wells, saturation monitoring for gaseous and particulate pollutants in a residential community located near active gas/oil extraction and processing facilities, source apportionment of VOCs measured in the community using the Chemical Mass Balance (CMB) receptor model, and direct measurements of the pollutant gradient downwind of a gas well with high VOC emissions. Overall, the study results indicate that air quality impacts due to individual gas wells and compressor stations are not likely to be discernible beyond a distance of approximately 100 m in the downwind direction. However, source apportionment results indicate a significant contribution to regional VOCs from gas production sources, particularly for lower-molecular-weight alkanes (<C6). Although measured ambient VOC concentrations were well below health-based safe exposure levels, the existence of urban-level mean concentrations of benzene and other mobile source air toxics combined with soot to total carbon ratios that were high for an area with little residential or commercial development may be indicative of the impact of increased heavy-duty vehicle traffic related to gas production

ImplicationsRapid and extensive development of shale gas resources in recent years has created concerns about potential environmental impacts on water and air quality. This study focused on directly measuring the ambient air pollutant levels occurring at residential properties located near natural gas extraction and processing facilities, and estimating the relative contributions from gas production and motor vehicle emissions to ambient VOC concentrations. Although only a small-scale case study, the results may be useful for guidance in planning future ambient air quality studies and human exposure estimates in areas of intensive shale gas production.     

Determination of organic compounds in indoor air with potential reference to air quality

Concentrations of 15 volatile organic compounds have been investigated in the air of two schoolrooms. The chemical analysis included enrichment on porous polymer beads, heat desorption and gas Chromatographic separation on a capillary column connected to either a flame ionization detector or a mass spectrometer. Samples were collected from the indoor air both in the presence and in the absence of the pupils (boys and girls, age 16–19) as well as from the ambient outdoor air. The qualitative composition of indoor and outdoor air was found to be about the same : aliphatic and aromatic hydrocarbons predominate, though indoors the number of compounds detected is larger and the concentrations are higher. Both the number and the concentration increase in the presence of humans. The mean concentrations of acetone and the sum of the concentrations of C₂-alkylbenzenes were 7.7 and 8.2 μg m⁻³ respectively in an unoccupied room and increased to 19.8 and 12.1 μg m⁻³ respectively in an occupied room.     

An exploratory study of air emissions associated with shale gas development and production in the Barnett Shale

Information regarding air emissions from shale gas extraction and production is critically important given production is occurring in highly urbanized areas across the United States. Objectives of this exploratory study were to collect ambient air samples in residential areas within 61 m (200 feet) of shale gas extraction/production and determine whether a “fingerprint” of chemicals can be associated with shale gas activity. Statistical analyses correlating fingerprint chemicals with methane, equipment, and processes of extraction/production were performed. Ambient air sampling in residential areas of shale gas extraction and production was conducted at six counties in the Dallas/Fort Worth (DFW) Metroplex from 2008 to 2010. The 39 locations tested were identified by clients that requested monitoring. Seven sites were sampled on 2 days (typically months later in another season), and two sites were sampled on 3 days, resulting in 50 sets of monitoring data. Twenty-four-hour passive samples were collected using summa canisters. Gas chromatography/mass spectrometer analysis was used to identify organic compounds present. Methane was present in concentrations above laboratory detection limits in 49 out of 50 sampling data sets. Most of the areas investigated had atmospheric methane concentrations considerably higher than reported urban background concentrations (1.8–2.0 ppm_v). Other chemical constituents were found to be correlated with presence of methane. A principal components analysis (PCA) identified multivariate patterns of concentrations that potentially constitute signatures of emissions from different phases of operation at natural gas sites. The first factor identified through the PCA proved most informative. Extreme negative values were strongly and statistically associated with the presence of compressors at sample sites. The seven chemicals strongly associated with this factor (o-xylene, ethylbenzene, 1,2,4-trimethylbenzene, m- and p-xylene, 1,3,5-trimethylbenzene, toluene, and benzene) thus constitute a potential fingerprint of emissions associated with compression.

Implications: Information regarding air emissions from shale gas development and production is critically important given production is now occurring in highly urbanized areas across the United States. Methane, the primary shale gas constituent, contributes substantially to climate change; other natural gas constituents are known to have adverse health effects. This study goes beyond previous Barnett Shale field studies by encompassing a wider variety of production equipment (wells, tanks, compressors, and separators) and a wider geographical region. The principal components analysis, unique to this study, provides valuable information regarding the ability to anticipate associated shale gas chemical constituents.     

Updated methods for assessing the impacts of nearby gas drilling and production on neighborhood air quality and human health

An explosive growth in natural gas production within the last decade has fueled concern over the public health impacts of air pollutant emissions from oil and gas sites in the Barnett and Eagle Ford shale regions of Texas. Commonly acknowledged sources of uncertainty are the lack of sustained monitoring of ambient concentrations of pollutants associated with gas mining, poor quantification of their emissions, and inability to correlate health symptoms with specific emission events. These uncertainties are best addressed not by conventional monitoring and modeling technology, but by increasingly available advanced techniques for real-time mobile monitoring, microscale modeling and source attribution, and real-time broadcasting of air quality and human health data over the World Wide Web. The combination of contemporary scientific and social media approaches can be used to develop a strategy to detect and quantify emission events from oil and gas facilities, alert nearby residents of these events, and collect associated human health data, all in real time or near-real time. The various technical elements of this strategy are demonstrated based on the results of past, current, and planned future monitoring studies in the Barnett and Eagle Ford shale regions.

Implications: Resources should not be invested in expanding the conventional air quality monitoring network in the vicinity of oil and gas exploration and production sites. Rather, more contemporary monitoring and data analysis techniques should take the place of older methods to better protect the health of nearby residents and maintain the integrity of the surrounding environment.     

A laboratory study of sediment and contaminant release during gas ebullition

Significant quantities of gas are generated from labile organic matter in contaminated sediments. The implications for the gas generation and subsequent release of contaminants from sediments are unknown but may include enhanced direct transport such as pore water advection and diffusion. The behavior of gas in sediments and the resulting migration of a polyaromatic hydrocarbon, viz phenanthrene, were investigated in an experimental system with methane injection at the base of a sediment column. Hexane above the overlying water layer was used to trap any phenanthrene migrating out of the sediment layer. The rate of suspension of solid particulate matter from the sediment bed into the overlying water layer was also monitored. The experiments indicated that significant amounts of both solid particulate matter and contaminant can be released from a sediment bed by gas movement with the amount of release related to the volume of gas released. The effective mass transfer coefficient of gas bubble-facilitated contaminant release was estimated under field conditions, being around three orders of magnitude smaller than that of bioturbation. A thin sand-capping layer (2 cm) was found to dramatically reduce the amount of contaminant or particles released with the gas because it could prevent or at least reduce sediment suspension. Based on the experimental observations, gas bubble-facilitated contaminant transport pathways for both uncapped and capped systems were proposed. Sediment cores were sliced to obtain phenanthrene concentration. X-ray computed tomography (CT) was used to investigate the void space distribution in the sediment penetrated by gas bubbles. The results showed that gas bubble migration could redistribute the sediment void spaces and may facilitate pore water circulation in the sediment.     

A model study for ambient air quality analysis using routine meteorological observations

In the present study, more realistic and easily adaptable input parameters have been used with a view to investigating the long-range air quality analysis for the dispersion of air pollutants emitted from an area source with a multiple box model. The model formulation has been discussed at length for the ground level sources when convective conditions prevail. The routine meteorological observations have been used for the computation of sensible surface heat flux, friction velocity and mixing depth. A radiation model provides the estimates of the sensible surface heat flux. Based on the similarity theory, an iterative procedure has been adopted for the estimation of friction velocity which provides a coupling of radiation computation and the surface layer of the planetary boundary layer through surface heat flux expression. The important parameters—wind speed and eddy diffusivity profiles—have been derived and have been used to obtain the concentration patterns as hourly averages. The procedure could be easily adopted where observed meteorological parameters may be used for studying the dispersal of pollutants from the ground level sources.     

Scenarios of animal waste production and fertilizer use and associated ammonia emission for the developing countries

Livestock production and the use of synthetic fertilizer are responsible for about half of the global emission of NH₃. Depending on the animal category between 10 and 36% of the N in animal excreta is lost as NH₃. The current annual NH₃ emission in developing countries of 15 million ton N accounts for of the global emission from animal excreta. In addition, 7.2 million tons NH₃N of synthetic N fertilizers are lost as NH₃ in developing countries. This is 80% of the global NH₃ emission from synthetic fertilizer's use. Along with human population increase and economic growth, livestock production in developing countries may even increase by a factor of 3 between now and 2025. The net result of rapid increase of livestock production combined with higher efficiency is an increase in NH₃ emissions of only 60% from 15 to 24 million tons NH₃N between 1990 and 2025 in developing countries. Livestock production is an important consumer of feedstuffs, mainly cereals, thereby inducing additional demand for synthetic fertilizers. Despite the projected major increase of synthetic fertilizer use from 42 to 106 million ton N between 1990 and 2025, the NH₃ loss in developing countries may decrease if a shift towards other fertilizer types, that are less vulnerable to NH₃ volatilization, is realized. According to the scenario, the total emission of NH₃ associated with food production in developing countries will increase from 22 to 30 million ton N yr⁻¹ between 1990 and 2025. Although the NH₃ emission increases more slowly than food production, in particular, animal production may show geographic concentration in certain regions, which may lead to high local emission densities and associated environmental problems.     

Refining fire emissions for air quality modeling with remotely sensed fire counts: A wildfire case study

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 information available for many years of the United States Environmental Protection Agency (US EPA) NEI about the specific location and timing of major fire events. The MODIS fire data provide twice-daily snapshots of the locations and breadth of fires, which can be helpful for identifying major wildfires that typically persist for a minimum of several days. A major wildfire in Mallory Swamp, FL, is used here as a case study to test a reallocation approach for temporally and spatially distributing the state-level fire emissions based on the MODIS fire data. Community Multiscale Air Quality (CMAQ) model simulations using these reallocated emissions are then compared with another simulation based on the original NEI fire emissions. We compare total carbon (TC) predictions from these CMAQ simulations against observations from the Inter-agency Monitoring of Protected Visual Environments (IMPROVE) surface network. Comparisons at three IMPROVE sites demonstrate substantial improvements in the temporal variability and overall correlation for TC predictions when the MODIS fire data is used to refine the fire emission estimates. These results suggest that if limited information is available about the spatial and temporal extent of a major wildfire fire, remotely sensed fire data can be a useful surrogate for developing the fire emissions estimates for air quality modeling purposes.     

A nomographic technique for estimation of air quality in urban areas

Nomograms based on the ATDL model to calculate the concentration of pollutants in an urban area in a simple manner are presented. Their use for estimation of permissible emission rates in various grids of an urban region is also elucidated.     

A novel bioscrubber for the treatment of high loads of ammonia from polluted gas

Environmental Science and Pollution Research - This work presents a novel bioscrubber configuration for the treatment of high ammonia loads at short contact times. The biological reactor was...     

MM5 simulations for air quality modeling: An application to a coastal area with complex terrain

A series of modifications were implemented in MM5 simulation in order to account for wind along the Santa Clarita valley, a north–south running valley located in the north of Los Angeles. Due to high range mountains in the north and the east of the Los Angeles Air Basin, sea breeze entering Los Angeles exits into two directions. One branch moves toward the eastern part of the basin and the other to the north toward the Santa Clarita valley. However, the northward flow has not been examined thoroughly nor simulated successfully in the previous studies. In the present study, we proposed four modifications to trigger the flow separation. They were (1) increasing drag over the ocean, (2) increasing soil moisture content, (3) selective observational nudging, and (4) one-way nesting for the innermost domain. The Control run overpredicted near-surface wind speed over the ocean and sensible heat flux, in an urbanized area, which justifies the above 1st and 2nd modification. The Modified run provided an improvement in near-surface temperature, sensible heat flux and wind fields including southeasterly flow along the Santa Clarita valley. The improved MM5 wind field triggered a transport to the Santa Clarita valley generating a plume elongated from an urban center to the north, which did not exist in MM5 Control run. In all, the modified MM5 fields yielded better agreement in both CO and O₃ simulations especially in the Santa Clarita area.     

Validation and application of an analytical method for determining pesticides in the gas phase of ambient air

A method for determining atmospheric concentrations of eight pesticides applied to corn and soybean crops in Mato Grosso state, Brazil is presented. The method involved a XAD-2 resin cartridge coupled to a low volume air pump at 2 L min?1 over 8 hours. Pesticides were recovered from the resin using sonication with n-hexane:ethyl acetate and determined by GC-MS. Good accuracy (76-128%) and precision (CV < 20%) were obtained for atrazine, chlorpyrifos, alpha- and beta-endosulfan, endosulfan sulfate, flutriafol, malathion, metolachlor and permethrin. Method detection ranged from 9.0 to 17.9 ng m?3. This method was applied to 61 gas phase samples collected between December 2008 and June 2009. Atrazine and endosulfan were detected both in urban and rural areas indicating the importance of atmospheric dispersion of pesticides in tropical areas. The simple and efficient extraction method and sampling system employed was considered suitable for identifying pesticides in areas of intense agricultural production.     

Validation and application of an analytical method for determining pesticides in the gas phase of ambient air

A method for determining atmospheric concentrations of eight pesticides applied to corn and soybean crops in Mato Grosso state, Brazil is presented. The method involved a XAD-2 resin cartridge coupled to a low volume air pump at 2 L min^?1 over 8 hours. Pesticides were recovered from the resin using sonication with n-hexane:ethyl acetate and determined by GC-MS. Good accuracy (76–128%) and precision (CV < 20%) were obtained for atrazine, chlorpyrifos, alpha- and beta-endosulfan, endosulfan sulfate, flutriafol, malathion, metolachlor and permethrin. Method detection ranged from 9.0 to 17.9 ng m^?3. This method was applied to 61 gas phase samples collected between December 2008 and June 2009. Atrazine and endosulfan were detected both in urban and rural areas indicating the importance of atmospheric dispersion of pesticides in tropical areas. The simple and efficient extraction method and sampling system employed was considered suitable for identifying pesticides in areas of intense agricultural production.     

Winter air quality in a wood-burning community: A case study in Waterbury,Vermont

The recent upsurge in residential wood combustion has raised questions about potential adverse effects on ambient air quality and public health. Before policymakers can make informed and rational decisions about the need for government intervention, more information is needed concerning the nature and extent of the problem. This paper presents findings from the 1982 Harvard Wood-Burning Study in Waterbury, Vermont. Waterbury, a rural community of about 2000 people, was an ideal location for this investigation because: (1) half of the private residences are heated with wood fuel; (2) frequent winter temperature inversions promote pollution buildup in the valley; (3) there are no major industrial sources and (4) the Vermont Agency of Environmental Conservation has compiled a detailed wood-burning inventory. The ambient air monitoring study, from January to March 1982, emphasized measurements of total, inhalable and respirable particulate matter. Results indicate that 60–70% of the Waterbury aerosol was composed of particles less than 2.5 μm. A combination of indirect evidence suggests that wood burning was the major source of airborne particles in residential sections of the town. Dramatic diurnal variations in particulate concentrations were observed, with peak values at night exceeding afternoon levels by 5- to 10-fold. Both meteorology and emission patterns contributed to observed fluctuations.     

热水解超声组合预处理对污泥厌氧消化产气潜力的影响研究

针对城市污泥厌氧消化由于融胞困难所导致的消解速率低、产气量低等问题,采用热水解与超声组合的方法对污泥进行预处理,考察经预处理后污泥融胞效率的变化及对厌氧消化产气潜力的影响.结果显示,热水解与超声波组合工艺对污泥的破胞作用明显,在30 min热水解与0.53 W/mL超声声能密度组合工艺反应60 min条件下,相对于处理前污泥,预处理后污泥溶解性COD(SCOD)溶出率可提高41.6％,蛋白质增加值达282.7 mg/L,污泥厌氧消化的产气潜力显著增加;30 min热水解分别与0.53、0.33 W/mL超声声能密度组合工艺对污泥破胞效率的差异不大;随着超声时间的延长,在组合预处理工艺前20 min内SCOD的溶出速率较慢,20260 min时溶出速率逐渐提高.试验结果可为城市污泥厌氧消化预处理工艺的选择提供一定的理论依据.     

应用气箱脉冲袋除尘器净化铝电解含氟烟气的实践与研究

介绍了改进型气箱脉冲袋除尘器在铝电解烟气净化工程上的成功应用，实践结果表明，在保证净化效果的前提下，采用改进型气箱脉冲袋除尘器作为净化设备，可使其一次投资、能耗、年维修费与其他型式布袋除尘器相比均有所降低，为铝电解烟气净化工程扩大了除尘器的选择范围。