Estimate Emission Rates Research Articles

Variability in Spatially and Temporally Resolved Emissions and Hydrocarbon Source Fingerprints for Oil and Gas Sources in Shale Gas Production Regions.

A gridded inventory for emissions of methane, ethane, propane, and butanes from oil and gas sources in the Barnett Shale production region has been developed. This inventory extends previous spatially resolved inventories of emissions by characterizing the overall variability in emission magnitudes and the composition of emissions at an hourly time resolution. The inventory is divided into continuous and intermittent emission sources. Sources are defined as continuous if hourly averaged emissions are greater than zero in every hour; otherwise, they are classified as intermittent. In the Barnett Shale, intermittent sources accounted for 14-30% of the mean emissions for methane and 10-34% for ethane, leading to spatial and temporal variability in the location of hourly emissions. The combined variability due to intermittent sources and variability in emission factors can lead to wide confidence intervals in the magnitude and composition of time and location-specific emission inventories; therefore, including temporal and spatial variability in emission inventories is important when reconciling inventories and observations. Comparisons of individual aircraft measurement flights conducted in the Barnett Shale region versus the estimated emission rates for each flight from the emission inventory indicate agreement within the expected variability of the emission inventory for all flights for methane and for all but one flight for ethane.

Methane emissions from a Californian landfill, determined from airborne remote sensing and in situ measurements

Abstract. Fugitive emissions from waste disposal sites are important anthropogenic sources of the greenhouse gas methane (CH4). As a result of the growing world population and the recognition of the need to control greenhouse gas emissions, this anthropogenic source of CH4 has received much recent attention. However, the accurate assessment of the CH4 emissions from landfills by modeling and existing measurement techniques is challenging. This is because of inaccurate knowledge of the model parameters and the extent of and limited accessibility to landfill sites. This results in a large uncertainty in our knowledge of the emissions of CH4 from landfills and waste management. In this study, we present results derived from data collected during the research campaign COMEX (CO2 and MEthane eXperiment) in late summer 2014 in the Los Angeles (LA) Basin. One objective of COMEX, which comprised aircraft observations of methane by the remote sensing Methane Airborne MAPper (MAMAP) instrument and a Picarro greenhouse gas in situ analyzer, was the quantitative investigation of CH4 emissions. Enhanced CH4 concentrations or CH4 plumes were detected downwind of landfills by remote sensing aircraft surveys. Subsequent to each remote sensing survey, the detected plume was sampled within the atmospheric boundary layer by in situ measurements of atmospheric parameters such as wind information and dry gas mixing ratios of CH4 and carbon dioxide (CO2) from the same aircraft. This was undertaken to facilitate the independent estimation of the surface fluxes for the validation of the remote sensing estimates. During the COMEX campaign, four landfills in the LA Basin were surveyed. One landfill repeatedly showed a clear emission plume. This landfill, the Olinda Alpha Landfill, was investigated on 4 days during the last week of August and first days of September 2014. Emissions were estimated for all days using a mass balance approach. The derived emissions vary between 11.6 and 17.8 kt CH4 yr−1 with related uncertainties in the range of 14 to 45 %. The comparison of the remote sensing and in situ based CH4 emission rate estimates reveals good agreement within the error bars with an average of the absolute differences of around 2.4 kt CH4 yr−1 (±2. 8 kt CH4 yr−1). The US Environmental Protection Agency (EPA) reported inventory value is 11.5 kt CH4 yr−1 for 2014, on average 2.8 kt CH4 yr−1 (±1. 6 kt CH4 yr−1) lower than our estimates acquired in the afternoon in late summer 2014. This difference may in part be explained by a possible leak located on the southwestern slope of the landfill, which we identified in the observations of the Airborne Visible/Infrared Imaging Spectrometer – Next Generation (AVIRIS-NG) instrument, flown contemporaneously aboard a second aircraft on 1 day.

Lightning NOx Emissions: Reconciling Measured and Modeled Estimates With Updated NOx Chemistry

AbstractLightning is one of the most important sources of upper tropospheric NOx; however, there is a large spread in estimates of the global emission rates (2–8 Tg N yr−1). We combine upper tropospheric in situ observations from the Deep Convective Clouds and Chemistry (DC3) experiment and global satellite‐retrieved NO2 tropospheric column densities to constrain mean lightning NOx (LNOx) emissions per flash. Insights from DC3 indicate that the NOx lifetime is ~3 h in the region of outflow of thunderstorms, mainly due to production of methyl peroxy nitrate and alkyl and multifunctional nitrates. The lifetime then increases farther downwind from the region of outflow. Reinterpreting previous analyses using the 3 h lifetime reduces the spread among various methods that have been used to calculate mean LNOx emissions per flash and indicates a global LNOx emission rate of ~9 Tg N yr−1, a flux larger than the high end of recent estimates.

Effects of an Experimental Water-level Drawdown on Methane Emissions from a Eutrophic Reservoir

Reservoirs are a globally significant source of methane (CH4) to the atmosphere. However, emission rate estimates may be biased low due to inadequate monitoring during brief periods of elevated emission rates (that is, hot moments). Here we investigate CH4 bubbling (that is, ebullition) during periods of falling water levels in a eutrophic reservoir in the Midwestern USA. We hypothesized that periods of water-level decline trigger the release of CH4-rich bubbles from the sediments and that these emissions constitute a substantial fraction of the annual CH4 flux. We explored this hypothesis by monitoring CH4 ebullition in a eutrophic reservoir over a 7-month period, which included an experimental water-level drawdown. We found that the ebullitive CH4 flux rate was among the highest ever reported for a reservoir (mean = 32.3 mg CH4 m−2 h−1). The already high ebullitive flux rates increased by factors of 1.4–77 across the nine monitoring sites during the 24-h experimental water-level drawdown, but these emissions constituted only 3% of the CH4 flux during the 7-month monitoring period due to the naturally high ebullitive CH4 flux rates that persist throughout the warm weather season. Although drawdown emissions were found to be a minor component of annual CH4 emissions in this reservoir, our findings demonstrate a link between water-level change and CH4 ebullition, suggesting that CH4 emissions may be mitigated through water-level management in some reservoirs.

Urban traffic and induced air quality modeling and simulation: Methodology and illustrative example

Modeling vehicular pollution in urban areas is essential in decision-making for urban planning and sustainable transport policies. Indeed, guaranteeing a breathable air quality in the acceptable levels specified by the World Health Organization (WHO) reinforces the road towards a sustainable urban development.In this work, we present the methodology and the different steps for the implementation of a sustainable transport decision tool permitting to perform a macroscopic simulation of road traffic using a first-order approach using the Cell Transmission Model (CTM) approach and a Dynamic Node Transmission Model (DNTM) approach for intersections; an estimation of the linear emission rates of the roads based on fleet statistics and the implementation of the simplified COPERT4 method; and finally the estimation of the near-instantaneous concentration of pollutants in urban areas. This tool is used to estimate the map of CO and NOx pollutants in the vicinity of a roundabout in the city of Sousse-Tunisia for the reference year 2015.

Influence of infrastructure on water quality and greenhouse gas dynamics in urban streams.

Streams and rivers are significant sources of nitrous oxide (N2O), carbon dioxide (CO2), and methane (CH4) globally, and watershed management can alter greenhouse gas (GHG) emissions from streams. We hypothesized that urban infrastructure significantly alters downstream water quality and contributes to variability in GHG saturation and emissions. We measured gas saturation and estimated emission rates in headwaters of two urban stream networks (Red Run and Dead Run) of the Baltimore Ecosystem Study Long-Term Ecological Research project. We identified four combinations of stormwater and sanitary infrastructure present in these watersheds, including: (1) stream burial, (2) inline stormwater wetlands, (3) riparian/floodplain preservation, and (4) septic systems. We selected two first order catchments in each of these categories and measured GHG concentrations, emissions, and dissolved inorganic and organic carbon (DIC and DOC) and nutrient concentrations biweekly for 1 year. From a water quality perspective, the DOC : NO3 - ratio of streamwater was significantly different across infrastructure categories. Multiple linear regressions including DOC : NO3 - and other variables (dissolved oxygen, DO; total dissolved nitrogen, TDN; and temperature) explained much of the statistical variation in nitrous oxide (N2O, r2 = 0.78), carbon dioxide (CO2, r2 = 0.78) and methane (CH4, r 2 = 0.50) saturation in stream water. We measured N2O saturation ratios, which were among the highest reported in the literature for streams, ranging from 1.1 to 47 across all sites and dates. N2O saturation ratios were highest in streams draining watersheds with septic systems and strongly correlated with TDN. The CO2 saturation ratio was highly correlated with the N2O saturation ratio across all sites and dates, and the CO2 saturation ratio ranged from 1.1 to 73. CH4 was always supersaturated, with saturation ratios ranging from 3.0 to 2157. Longitudinal surveys extending form headwaters to third-order outlets of Red Run and Dead Run took place in spring and fall. Linear regressions of these data yielded significant negative relationships between each gas with increasing watershed size as well as consistent relationships between solutes (TDN or DOC, and DOC : TDN ratio) and gas saturation. Despite a decline in gas saturation between the headwaters and stream outlet, streams remained saturated with GHGs throughout the drainage network, suggesting that urban streams are continuous sources of CO2, CH4, and N2O. Our results suggest that infrastructure decisions can have significant effects on downstream water quality and greenhouse gases, and watershed management strategies may need to consider coupled impacts on urban water and air quality.

Allowed and unique first-forbidden stellar electron emission rates of neutron-rich copper isotopes

The allowed charge-changing transitions are the most common weak interaction processes of spin-isospin form that play a crucial role in several nuclear/astrophysical processes. The first-forbidden (FF) transition becomes important, in the circumstances where allowed Gamow-Teller (GT) transitions are unfavored, specifically for neutron-rich nuclei due to phase space considerations. In this paper deformed proton-neutron quasi-particle random phase approximation (pn-QRPA) model is applied, for the first time, for the estimation of allowed GT and unique first-forbidden (U1F) transitions ( $|\Delta J| = 2$ ) of neutron rich copper isotopes in mass range $72 \leq A \leq 82$ under stellar conditions. We compared our computed terrestrial $\beta$ -decay half-life values with previous calculations and experimental results. It was concluded that the pn-QRPA calculation is in good accordance with measured data. Our study suggests that the addition of rank (0 and 1) operators in FF transitions can further improve the comparison which remain unattended at this stage. The deformed pn-QRPA model was employed for the estimation of GT and U1F stellar electron emission ( $\beta^{-}$ -decay) rates over wide range of stellar temperature (0.01 GK–30 GK) and density ( $10\mbox{--}10^{11}\mbox{ g}/\mbox{cm}^{3}$ ) domains for astrophysical applications. Our study shows that, in high density and low temperature regions, the contribution of U1F rates to total electron emission rates of neutron-rich copper nuclei is negligible.

Estimating airborne particulate emissions using a finite-volume forward solver coupled with a Bayesian inversion approach

We propose a numerical algorithm for solving the atmospheric dispersion problem with elevated point sources and ground-level deposition. The problem is modelled by the 3D advection-diffusion equation with delta-distribution source terms, as well as height-dependent advection speed and diffusion coefficients. We construct a finite volume scheme using a splitting approach in which the Clawpack software package is used as the advection solver and an implicit time discretization is proposed for the diffusion terms. The algorithm is then applied to an actual industrial scenario involving emissions of airborne particulates from a zinc smelter using actual wind measurements. We also address various practical considerations such as choosing appropriate methods for regularizing noisy wind data and quantifying sensitivity of the model to parameter uncertainty. Afterwards, we use the algorithm within a Bayesian framework for estimating emission rates of zinc from multiple sources over the industrial site. We compare our finite volume solver with a Gaussian plume solver within the Bayesian framework and demonstrate that the finite volume solver results in tighter uncertainty bounds on the estimated emission rates.

On the use of different spectral windows in DOAS evaluations: Effects on the estimation of SO2 emission rate and mixing ratios during strong emission of Popocatépetl volcano

Reported SO2 emission values at strongly degassing volcanoes might be underestimated. Scanning spectroscopic instruments are widely used at volcanoes to quantify SO2 emission rates and, occasionally, molar ratios between SO2 and other gases such as BrO. Frequently, Differential Optical Absorption Spectroscopy is applied to evaluate spectra in the ultraviolet range. If radiative transfer effects are not considered in the evaluations, the retrieved column densities may vary depending on which spectral window is used. We compare the use of different windows for data collected at Popocatépetl volcano during strong degassing periods, when high column densities lead to especially high dependence on the applied evaluation window. We propose the use of three different windows (310–322nm, 314.7–326.7nm and 322–334nm) and a simple algorithm to choose the most accurate column density from them. The SO2 evaluation using proper spectral windows would allow a more realistic estimation of the SO2 emission rates.

Simultaneous and multi-point measurement of ammonia emanating from human skin surface for the estimation of whole body dermal emission rate.

Ammonia is one of the members of odor gases and a possible source of odor in indoor environment. However, little has been known on the actual emission rate of ammonia from the human skin surface. Then, this study aimed to estimate the whole-body dermal emission rate of ammonia by simultaneous and multi-point measurement of emission fluxes of ammonia employing a passive flux sampler - ion chromatography system. Firstly, the emission fluxes of ammonia were non-invasively measured for ten volunteers at 13 sampling positions set in 13 anatomical regions classified by Kurazumi et al. The measured emission fluxes were then converted to partial emission rates using the surface body areas estimated by weights and heights of volunteers and partial rates of 13 body regions. Subsequent summation of the partial emission rates provided the whole body dermal emission rate of ammonia. The results ranged from 2.9 to 12mgh-1 with an average of 5.9±3.2mgh-1 per person for the ten healthy young volunteers. The values were much greater than those from human breath, and thus the dermal emission of ammonia was found more significant odor source than the breath exhalation in indoor environment.

Estimation of odor emission rate from swine nursery facilities using probability distribution

Estimation of odor emission rate from swine nursery facilities using probability distribution

Variations of Ammonia Emissions from Cattle Operations: Effects of Air Temperature and Dietary Crude Protein Content

<abstract> <b><sc>Abstract.</sc></b> The objective of this study was to conduct a systematic review of the published literature on ammonia (NH₃) emissions from beef feedlots and dairy barns using a meta-analytical approach in order to improve the estimation of emission rates, to understand the sources of variation, and to specifically quantify the effects of air temperature and dietary crude protein (CP) on NH₃ emissions. Emissions from lagoons or other manure storage facilities were not included. The review compiled results from 91 studies (published from 1997 to 2016) and from the five dairy sites in the National Air Emissions Monitoring Study (NAEMS). Based on the results, the average NH₃ emission rate was 105.9 g d^-1 animal^-1 for beef feedlots and 125.6 g d^-1 animal^-1 for open-lot dairy barns, which were much higher than the emission factors proposed by the U.S. Environmental Protection Agency. Expressing NH₃ emissions as the NH₃-N loss as a percentage of nitrogen (N) intake can address the effect of N feed intake, can reduce uncertainties in estimation of emissions, and can be used as a key parameter in establishing emission inventories and evaluating mitigation strategies. The average NH₃-N loss as a percentage of N intake was 53.1%, 15.6%, 8.7%, and 5.1% for beef feedlots, open-lot dairy barns, free-stall dairy barns, and tie-stall dairy barns, respectively. Results showed that the measured NH₃ emission rates could be affected by measurement method. The chamber method tends to underestimate, while the N balance method tends to overestimate. Proper adjustment and validation may be needed when using the tracer ratio method in free-stall/tie-stall barns in order to avoid potential overestimation. Regression models were developed to quantify the effects of air temperature and dietary CP on emissions from various types of cattle operations. The sensitivity of NH₃ emission rate to air temperature obtained for various operations was consistent (2.33, 2.39, and 2.66 g d^-1 animal^-1 per °C, respectively, for beef feedlots, open-lot dairy barns, and free-stall/tie-stall dairy barns with natural ventilation). Higher dietary CP resulted in significantly higher NH₃ emission rates and also corresponded with higher NH₃-N loss as a percentage of N intake for beef feedlots and free-stall/tie-stall dairy barns with natural ventilation. The sensitivity of emission rates to dietary CP obtained for various types of dairy cattle operations was consistent (9.91, 12.68, and 10.40 g d^-1 animal^-1 per 1% CP, respectively, for beef feedlots, open-lot dairy barns, and free-stall/tie-stall dairy barns with natural ventilation). The average NH₃ emission rate for barns with mechanical ventilation was less than half that for barns with natural ventilation. When developing mitigating strategies, managing N intake and improving feed efficiency seem to represent the greatest opportunities.

Lidar Method to Estimate Emission Rates from Extended Sources

AbstractPollutant emissions to the atmosphere commonly derive from nonpoint sources that are extended in space. Such sources may contain area, volume, line, or a combination of emission types. Currently, point measurements, often combined with models, are the primary means by which atmospheric emission rates are estimated from extended sources. Point measurement arrays often lack in spatial and temporal resolution and accuracy. In recent years, lidar has supplemented point measurements in agricultural research by sampling spatial ensembles nearly instantaneously. Here, a methodology using backscatter data from an elastic scanning lidar is presented to estimate emission rates from extended sources. To demonstrate the approach, a known amount of particulate matter was released upwind of a vegetative environmental buffer, a barrier designed to intercept emissions from animal production facilities. The emission rate was estimated downwind of the buffer, and the buffer capture efficiency (percentage of particles captured) was calculated. Efficiencies ranged from 21% to 74% and agree with the ranges previously published. A comprehensive uncertainty analysis of the lidar methodology was performed, revealing an uncertainty of 20% in the emission rate estimate; suggestions for significantly reducing this uncertainty in future studies are made. The methodology introduced here is demonstrated by estimating the efficiency of a vegetative buffer, but it can also be applied to any extended emission source for which point samples are inadequate, such as roads, animal feedlots, and cotton gin operations. It can also be applied to any pollutant for which a lidar system is configured, such as particulate matter, carbon dioxide, and ammonia.

Comparing facility-level methane emission rate estimates at natural gas gathering and boosting stations

Coordinated dual-tracer, aircraft-based, and direct component-level measurements were made at midstream natural gas gathering and boosting stations in the Fayetteville shale (Arkansas, USA). On-site component-level measurements were combined with engineering estimates to generate comprehensive facility-level methane emission rate estimates (“study on-site estimates (SOE)”) comparable to tracer and aircraft measurements. Combustion slip (unburned fuel entrained in compressor engine exhaust), which was calculated based on 111 recent measurements of representative compressor engines, accounts for an estimated 75% of cumulative SOEs at gathering stations included in comparisons. Measured methane emissions from regenerator vents on glycol dehydrator units were substantially larger than predicted by modelling software; the contribution of dehydrator regenerator vents to the cumulative SOE would increase from 1% to 10% if based on direct measurements. Concurrent measurements at 14 normally-operating facilities show relative agreement between tracer and SOE, but indicate that tracer measurements estimate lower emissions (regression of tracer to SOE = 0.91 (95% CI = 0.83–0.99), R2 = 0.89). Tracer and SOE 95% confidence intervals overlap at 11/14 facilities. Contemporaneous measurements at six facilities suggest that aircraft measurements estimate higher emissions than SOE. Aircraft and study on-site estimate 95% confidence intervals overlap at 3/6 facilities. The average facility level emission rate (FLER) estimated by tracer measurements in this study is 17–73% higher than a prior national study by Marchese et al.

Do convection-permitting models improve the representation of the impact of LUC?

In this study we assess the added value of convection permitting scale (CPS) simulations in studies using regional climate models to quantify the bio-geophysical climate impact of land-use change (LUC). To accomplish this, a comprehensive model evaluation methodology is applied to both non-CPS and CPS simulations. The main characteristics of the evaluation methodology are (1) the use of paired eddy-covariance site observations (forest vs open land) and (2) a simultaneous evaluation of all surface energy budget components. Results show that although generally satisfactory, non-CPS simulations fall short of completely reproducing the observed LUC signal because of three key biases. CPS scale simulations succeed at significantly reducing two of these biases, namely, those in daytime shortwave radiation and daytime sensible heat flux. Also, CPS slightly reduces a third bias in nighttime incoming longwave radiation. The daytime improvements can be attributed partially to the switch from parameterized to explicit convection, the associated improvement in the simulation of afternoon convective clouds, and resulting surface energy budget and atmospheric feedbacks. Also responsible for the improvements during daytime is a better representation of surface heterogeneity and thus, surface roughness. Meanwhile, the modest nighttime longwave improvement can be attributed to increased vertical atmospheric resolution. However, the model still fails at reproducing the magnitude of the observed nighttime longwave difference. One possible explanation for this persistent bias is the nighttime radiative effect of biogenic volatile organic compound emissions over the forest site. A correlation between estimated emission rates and the observed nighttime longwave difference, as well as the persistence of the longwave bias provide support for this hypothesis. However, more research is needed to conclusively determine if the effect indeed exists.

Sequential multi-nuclide emission rate estimation method based on gamma dose rate measurement for nuclear emergency management

In case of a nuclear accident, the source term is typically not known but extremely important for the assessment of the consequences to the affected population. Therefore the assessment of the potential source term is of uppermost importance for emergency response. A fully sequential method, derived from a regularized weighted least square problem, is proposed to reconstruct the emission and composition of a multiple-nuclide release using gamma dose rate measurement. The a priori nuclide ratios are incorporated into the background error covariance (BEC) matrix, which is dynamically augmented and sequentially updated. The negative estimations in the mathematical algorithm are suppressed by utilizing artificial zero-observations (with large uncertainties) to simultaneously update the state vector and BEC. The method is evaluated by twin experiments based on the JRodos system. The results indicate that the new method successfully reconstructs the emission and its uncertainties. Accurate a priori ratio accelerates the analysis process, which obtains satisfactory results with only limited number of measurements, otherwise it needs more measurements to generate reasonable estimations. The suppression of negative estimation effectively improves the performance, especially for the situation with poor a priori information, where it is more prone to the generation of negative values.

The role of soil flux and soil gas monitoring in the characterisation of a CO2 surface leak: A case study in Qinghai, China

Following the drilling of a shallow natural CO2 reservoir at the Qinghai research site, west of Haidong, China, it was discovered that CO2 was continuously leaking from the wellbore due to well-failure. The site has become a useful research facility in China for studying CO2 leakage and monitoring technologies for application to geological storage sites of CO2. During an eight day period in 2014, soil gas and soil flux surveys were conducted to characterise the distribution, magnitude and likely source of the leaking CO2.Two different sampling patterns were utilised during soil flux surveys. A regular sampling grid was used to spatially map out the two high-flux zones which were located 20–50m away from the wellhead. An irregular sampling grid, with higher sampling density in the high-flux zones, allowed for more accurate mapping of the leak distribution and estimation of total field emission rate using cubic interpolation. The total CO2 emission rate for the site was estimated at 649-1015kgCO2/d and there appeared to be some degree of spatial correlation between observed CO2 fluxes and elevated surface H2O fluxes.Sixteen soil gas wells were installed across the field to test the real-time application of Romanak et al.’s (2012) process-based approach for soil gas measurements (using ratios of major soil gas components to identify the CO2 source) using a portable multi-gas analyser. Results clearly identified CO2 as being derived from one exogenous source, and are consistent with gas samples collected for laboratory analysis. Carbon-13 isotopes in the centre of each leak zone (−0.21‰ and −0.22‰) indicate the underlying CO2 is likely sourced from the thermal decomposition of marine carbonates.Surface soil mineralisation (predominantly calcite) can be used to infer prior distribution of the CO2 hotspots and as a consequence highlighted plume migration of 20m in 11 years. The broadening of the affected area beyond the wellbore at the Qinghai research site markedly increases the area that needs surveying at sufficient density to detect a leak. This challenges the role of soil gas and soil flux in a CCS monitoring and verification program for leak detection, suggesting that these techniques may be better applied for characterising the source and emission rate of a CO2 leak, respectively.

Influence of the fetch parameter on results from empirical correlations for estimating odorous emissions at passive liquid surfaces.

Passive liquid surfaces in wastewater treatment plants may be potential sources of odorous emissions. This study investigates the occurrence and significance of deviations that may originate from the use of the effective diameter as fetch parameter in the empirical correlations utilised by the WATER9 model to estimate odorous emissions at passive liquid surfaces. A sensitivity analysis was performed using benzene as a model compound and considering representative conditions of wind speed and wind alignment. The gas-film mass transfer coefficient (kG) was found relatively in sensitive to the choice of the fetch parameter, deviating less than 15% for aspect rations up to 15. The calculation of the liquid-film mass transfer coefficient (kL) was much more sensitive (positive extreme of 126.98% and negative extreme of -54.80%), partially because of the use of different equations for different fetch-to-depth ratios. For more volatile compounds, such as benzene, these discrepancies will be significantly manifested in the estimated emission rate. When appropriate, the use of the actual fetch instead of the effective diameter is recommended.

Use of CFD for static sampling hood design: An example for methane flux assessment on landfill surfaces

The work focuses on the principles for the design of a specific static hood and on the definition of an optimal sampling procedure for the assessment of landfill gas (LFG) surface emissions. This is carried out by means of computational fluid dynamics (CFD) simulations to investigate the fluid dynamics conditions of the hood. The study proves that understanding the fluid dynamic conditions is fundamental in order to understand the sampling results and correctly interpret the measured concentration values by relating them to a suitable LFG emission model, and therefore to estimate emission rates. For this reason, CFD is a useful tool for the design and evaluation of sampling systems, among others, to verify the fundamental hypotheses on which the mass balance for the sampling hood is defined. The procedure here discussed, which is specific for the case of the investigated landfill, can be generalized to be applied also to different scenarios, where hood sampling is involved.

VOCs emission rate estimate for complicated industrial area source using an inverse-dispersion calculation method: A case study on a petroleum refinery in Northern China

This study aimed to apply an inverse-dispersion calculation method (IDM) to estimate the emission rate of volatile organic compounds (VOCs) for the complicated industrial area sources, through a case study on a petroleum refinery in Northern China. The IDM was composed of on-site monitoring of ambient VOCs concentrations and meteorological parameters around the source, calculation of the relationship coefficient γ between the source's emission rate and the ambient VOCs concentration by the ISC3 model, and estimation of the actual VOCs emission rate from the source. Targeting the studied refinery, 10 tests and 8 tests were respectively conducted in March and in June of 2014. The monitoring showed large differences in VOCs concentrations between background and downwind receptors, reaching 59.7 ppbv in March and 248.6 ppbv in June, on average. The VOCs increases at receptors mainly consisted of ethane (3.1%–22.6%), propane (3.8%–11.3%), isobutane (8.5%–10.2%), n-butane (9.9%–13.2%), isopentane (6.1%–12.9%), n-pentane (5.1%–9.7%), propylene (6.1–11.1%) and 1-butylene (1.6%–5.4%). The chemical composition of the VOCs increases in this field monitoring was similar to that of VOCs emissions from China's refineries reported, which revealed that the ambient VOCs increases were predominantly contributed by this refinery. So, we used the ISC3 model to create the relationship coefficient γ for each receptor of each test. In result, the monthly VOCs emissions from this refinery were calculated to be 183.5 ± 89.0 ton in March and 538.3 ± 281.0 ton in June. The estimate in June was greatly higher than in March, chiefly because the higher environmental temperature in summer produced more VOCs emissions from evaporation and fugitive process of the refinery. Finally, the VOCs emission factors (g VOCs/kg crude oil refined) of 0.73 ± 0.34 (in March) and 2.15 ± 1.12 (in June) were deduced for this refinery, being in the same order with previous direct-measurement results (1.08–2.65 g VOCs/kg crude oil refined).An inverse-dispersion calculation method was applied to estimate VOCs emission rate for a petroleum refinery, being 183.5 ton/month (March) and 538.3 ton/month (June).