A new approach to characterize emission contributions from area sources during optical remote sensing technique testing

In the method termed “Other Test Method-10,” the U.S. Environmental Protection Agency has proposed a method to quantify emissions from nonpoint sources by the use of vertical radial plume mapping (VRPM) technique. The surface area of the emitting source and the degree to which the different zones of the emitting source are contributing to the VRPM computed emissions are often unknown. The objective of this study was to investigate and present an approach to quantify the unknown emitting surface area that is contributing to VRPM measured emissions. Currently a preexisting model known as the “multiple linear regression model,” which is described in Thoma et al. (2009 Thoma, E.R., Green, R., Hater, G., Goldsmith, C., Swan, N., Chase, M. and Hashmonay, R. 2010. Development of EPA OTM-10 for landfill applications. J. Environ. Eng., 136: 769–776. [Crossref], [Web of Science ®] , [Google Scholar]), is used for quantifying the unknown surface area.

The method investigated and presented in this paper utilized tracer tests to collect data and develop a model much like that described in Thoma et al. (2009 Thoma, E.R., Green, R., Hater, G., Goldsmith, C., Swan, N., Chase, M. and Hashmonay, R. 2010. Development of EPA OTM-10 for landfill applications. J. Environ. Eng., 136: 769–776. [Crossref], [Web of Science ®] , [Google Scholar]). However, unlike the study used for development of the multiple linear regression model, this study is considered a very limited study due to the low number of pollutant releases performed (seven total releases). It was found through this limited study that the location of an emitting source impacts VRPM computed emissions exponentially, rather than linearly (i.e., the impact that an emitting source has on VRPM measurements decreases exponentially with increasing distances between the emitting source and the VRPM plane). The data from the field tracer tests were used to suggest a multiple exponential regression model. The findings of this study, however, are based on a very small number of tracer tests. More tracer tests performed during all types of climatic conditions, terrain conditions, and different emissions geometries are still needed to better understand the variation of capture efficiency with emitting source location. This study provides a step toward such an objective.

Implications The findings of this study will aid in the advancement of the VRPM technique. In particular, the contribution of this study is to propose a slight improvement in how the area contributing to flux is determined during VRPM campaigns. This will reduce some of the technique's inherent uncertainties when it is employed to estimate emissions from an area source under nonideal conditions.     

Fine Particle Removal Performance of a Two-Stage Wet Electrostatic Precipitator Using a Nonmetallic Pre-Charger

ABSTRACT

A novel two-stage wet electrostatic precipitator (ESP) has been developed using a carbon brush pre-charger and collection plates with a thin water film. The electrical and particle collection performance was evaluated for submicrometer particles smaller than 0.01～0.5 μm in diameter by varying the voltages applied to the pre-charger and collection plates as well as the polarity of the voltage. The collection efficiency was compared with that calculated by the theoretical models. The long-term performances of the ESP with and without water films were also compared in tests using Japanese Industrial Standards dust. The experimental results show that the carbon brush pre-charger of the two-stage wet ESP had approximately 10% particle capture, while producing ozone concentrations of less than 30 ppb. The produced amounts of ozone are significantly lower than the current limits set by international agencies. The ESP also achieved a high collection rate performance, averaging 90% for ultrafine particles, as based on the particle number concentration at an average velocity of 1 m/sec corresponding to a residence time of 0.17 sec. Higher particle collection efficiency for the ESP can be achieved by increasing the voltages applied to the pre-charger and the collection plates. The decreased collection efficiency that occurred during dust loading without water films was completely avoided by forming a thin water film on the collection plates at a water flow rate of 6.5 L/min/m2 Zukeran, A., Ikeda, Y., Ehara, Y., Matsuyama, M., Ito, T., Takahashi, T., Kawakami, H. and Takamatsu, T. 1999. Two-Stage-Type Electrostatic Precipitator Re-entrainment Phenomena under Diesel Flue Gases. IEEE. Trans. Ind. Appl, 35: 346–351. [Crossref], [Web of Science ®] , [Google Scholar].

IMPLICATIONS Current two-stage electrostatic precipitators (ESPs) have several technical problems such as a drop in collection efficiencies by small-particle re-entrainment during rapping and corrosion of metallic electrodes of the ESPs by corrosive gases. This paper evaluates a novel two-stage ESP that uses a nonmetallic pre-charger and water film collection plates to avoid the above mentioned problems of other ESPs. This ESP can be used not only for industrial applications but also for residential purposes because it has a high removal performance for fine particles with low ozone generation and maintains its efficiency due to the continuous cleaning of the collection plates with water film.     

Formation and growth of indoor air aerosol particles as a result of d-limonene oxidation

Oxidation of d-limonene, which is a common monoterpene, can lead to new aerosol particle formation in indoor environments. Thus, products containing d-limonene, such as citrus fruits, air refresheners, household cleaning agents, and waxes, can act as indoor air aerosol particle sources. We released d-limonene into the room air by peeling oranges and measured the concentration of aerosol particles of three different size ranges. In addition, we measured the concentration of d-limonene, the oxidant, and the concentration of ozone, the oxidizing gas. Based on the measurements we calculated the growth rate of the small aerosol particles, which were 3–10 nm in diameter, to be about , and the losses of the aerosol particles that were due to the coagulation and condensation processes. From these, we further approximated the concentration of the condensable vapour and its source rate and then calculated the formation rate of the small aerosol particles. For the final result, we calculated the nucleation rate and the maximum number of molecules in a critical cluster. The nucleation rate was in the order of and the number of molecules in a critical-sized cluster became 1.2. The results were in agreement with the activation theory.     

Analysis of mobile source air toxics (MSATs)—Near-road VOC and carbonyl concentrations

Exposures to mobile source air toxics (MSATs) have been associated with numerous adverse health effects. While thousands of air toxic compounds are emitted from mobile sources, members of a subset of compounds are considered high priority due to their significant contribution to cancer and noncancer health risks and the contribution of mobile sources to total exposure as evaluated by the U.S. Environmental Protection Agency (EPA) National-Scale Air Toxics Assessments (NATA). These pollutants include benzene, 1,3-butadiene, ethylbenzene, acrolein, acetaldehyde, formaldehyde, naphthalene, polycyclic organic matter, and diesel particulate matter/organic gases. This study provided year-long trends of benzene, 1,3-butadiene, acrolein, acetaldehyde, and formaldehyde in Las Vegas, NV. Results indicated that MSAT concentrations often did not exhibit trends typical of other primary emitted pollutants in this study. Instead, other mobile sources beyond the highway of interest contributed to the measured values, including a major arterial road, a large commercial airport, and a nearby parking lot. The data were compared with relevant census-tract NATA estimates, with estimated ambient 1,3-butadiene concentrations similar to the measured values. Measured benzene values were much lower relative to the NATA total ambient benzene concentrations. Measured acrolein values were much higher relative to the NATA total acrolein concentrations. Measured acetaldehyde and formaldehyde values were also higher relative to the NATA total acetaldehyde and formaldehyde concentrations for all wind conditions and downwind conditions. Some possible explanations for these differences include nearby sources influencing the measured values; meteorological influences that may not be well captured by the NATA modeling regime; chemical reactivity of measured compounds; and additional explanatory variables may be needed for certain urban areas in order to accurately disaggregate anthropogenic air toxics emissions.

Implications: Comparison of air toxics concentrations measured at four long-term near-road sites in Las Vegas, NV, show generally good agreement with the EPA 2005 U.S. Environmental Protection Agency. 2005. National Air Toxics Assessments (NATA)(accessed December 7, 2012) http://www.epa.gov/ttn/atw/natamain/index.html (http://www.epa.gov/ttn/atw/natamain/index.html)  [Google Scholar] NATA total ambient concentrations. Measured concentrations did not compare as well with EPA 2005 U.S. Environmental Protection Agency. 2005. National Air Toxics Assessments (NATA)(accessed December 7, 2012) http://www.epa.gov/ttn/atw/natamain/index.html (http://www.epa.gov/ttn/atw/natamain/index.html)  [Google Scholar] NATA for the on-road mobile portion of the ambient concentrations. This highlights the complexity of air toxic emission sources and impacts in urban areas, especially around large highway facilities; NATA's inability to capture local-scale meteorology and fine-scale ambient gradients; and that additional explanatory variables may be needed for certain urban areas in order to accurately disaggregate anthropogenic air toxics emissions.     

A field trial of nutrient stimulation of methanotrophs to reduce greenhouse gas emissions from landfill cover soils

Landfills are among the major sources of anthropogenic methane (CH₄) estimated to reach 40?×?10⁹kg per year worldwide by 2015 (IPCC, 2007 IPCC. 2007. Intergovernmental Panel on Climate Change, Synthesis Report on Contributions of Work Groups 1, 2, and 3 to the Fourth Assessment Report Core Writing Team, Edited by: Pauchar, R.K. and Reisinger, A. Geneva, Switzerland: IPCC.  [Google Scholar]). A 2½-year field experiment was conducted at a closed landfill in western Michigan where methanotrophs, methane-consuming bacteria, were stimulated by nutrient addition to the soil without significantly increasing biogenic nitrous oxide (N₂O) production. The effects of the nitrogen amendments (KNO₃ and NH₄Cl), phenylacetylene (a selective inhibitor of nitrifying bacteria that contribute to N₂O production), and a canopy (to reduce direct water infiltration) on the vertical soil gas profiles of CH₄, CO₂, and O₂ were measured in the top meter of the soil. Methane and nitrous oxide fluxes were calculated from the corresponding soil gas concentration gradients with respect to depth and a Millington–Quirk diffusivity coefficient in soil derived empirically from soil porosity, water content, and diffusivity coefficients in air from the literature. Methane flux estimates were as high as 218.4 g m^?2 day^?1 in the fall and 12.8 g/m^?2 day^?1 in the summer. During the spring and summer, CH₄ fluxes were reduced by more than half by adding KNO₃ and NH₄Cl into the soil as compared to control plots, while N₂O fluxes increased substantially. The concurrent addition of phenylacetylene to the amendment decreased peak N₂O production by half and the rate of peak methane oxidation by about one-third. The seasonal average methane and N₂O flux data were extrapolated to estimate the reduction of CH₄ and N₂O fluxes into the atmosphere by nitrogen and inhibitor addition to the cover soils. The results suggest that such additions coupled with soil moisture management may provide a potential strategy to significantly reduce greenhouse gas emissions from landfills.

Implications The results of a 2½-year study of effects of nutrient stimulation on methane oxidation in landfill cover soils demonstrates that nutrient addition does decrease methane emissions. The work further underscores the control which soil moisture exerts on methane oxidation. Water management is critical to the success of methane oxidation strategies.