Simulation of Sulfate and Nitrate Chemistry in Power Plant Plumes

ABSTRACT

The rate of formation of secondary particulate matter (PM) in power plant plumes varies as the plume material mixes with the background air. Consequently, the rate of oxidation of sulfur dioxide (SO₂) and nitrogen dioxide (NO₂) to sulfate and nitric acid, respectively, can be very different in plumes and in the background air (i.e., air outside the plume). In addition, the formation of sulfate and nitric acid in a power plant plume is a strong function of the chemical composition of the background air and the prevailing meteorological conditions.

We describe the use of a reactive plume model, the Reactive and Optics Model of Emissions, to simulate sulfate and nitrate formation in a power plant plume for a variety of background conditions. We show that SO₂ and NO₂ oxidation rates are maximum in the background air for volatile organic compound (VOC)-limited airsheds but are maximum at some downwind distance in the plume when the background air is nitrogen oxide (NO_x)-limited. Our analysis also shows that it is essential to obtain measurements of background concentrations of ozone, aldehydes, peroxyacetyl nitrate, and other VOCs to properly describe plume chemistry.     

Big concerns with small projects: Evaluating the socio-ecological impacts of small hydropower projects in India

Although Small Hydropower Projects (SHPs) are encouraged as sources of clean and green energy, there is a paucity of research examining their socio-ecological impacts. We assessed the perceived socio-ecological impacts of 4 SHPs within the Western Ghats in India by conducting semi-structured interviews with local respondents. Primary interview data were sequentially validated with secondary data, and respondent perceptions were subsequently compared against the expected baseline of assured impacts. We evaluated the level of awareness about SHPs, their perceived socio-economic impacts, influence on resource access and impacts on human–elephant interactions. The general level of awareness about SHPs was low, and assurances of local electricity and employment generation remained largely unfulfilled. Additionally most respondents faced numerous unanticipated adverse impacts. We found a strong relationship between SHP construction and increasing levels of human–elephant conflict. Based on the disparity between assured and actual social impacts, we suggest that policies regarding SHPs be suitably revised.     

Agro-economic evaluation of water resource project--a modeling approach

Feasibility of an irrigation project is evaluated by two criteria viz., reservoir capacity to irrigate its command area and economic returns by incremental crop production versus capital investment for dam construction. The annual water requirement of different crops in the command area is estimated and compared with the availability of water from the dam for irrigation purpose. The annual crop water requirement is estimated as the sum of evapotranspiration for crops and transmission and other losses. Evapotranspiration is estimated by modified Penman formula. Economics of crop production is analyzed by first estimating the monetary value of existing crop production under current rain fed conditions and then estimating the incremental production of irrigated command area for the proposed crop pattern. The proposed cropping pattern is prepared so as to maximize the benefit of crop production and fodder requirement while maintaining a better crop rotation to improve and maintain physical, chemical, and biological conditions of the soil. The dam is to be used for irrigation and water supply only. Command area served by this reservoir will be 76,500 ha. The existing annual agricultural return is Rs. 2995.56 lakhs and with the proposed irrigation scheme, it is estimated as Rs. 1,77,91.90 lakhs. The incremental annual return would be Rs. 1,47,96.35 lakhs i.e., 642.68% increase in annual return.     

The effect of temperature on PAHs emission from incineration of acrylic waste

Incineration of acrylic waste solution in a lab scale quartz tube vertical incinerator showed the presence of 12–15 polycyclic aromatic hydrocarbons (PAHs) from a list of 16 priority pollutants at 700–1100^˚C after an interval of 50^˚C. The amount of total 16 PAHs at 900 and 1100^˚C was about 8.5 and 1.25 times higher than those at 700^˚C (739.48 μg g⁻¹) respectively. The amount of total probable (2A) and possible (2B) human carcinogenic PAHs was minimum at 700^˚C.     

Dust events and their influence on aerosol optical properties over Jaipur in Northwestern India

In this study, we systematically document the link between dust episodes and local scale regional aerosol optical properties over Jaipur located in the vicinity of Thar Desert in the northwestern state of Rajasthan. The seasonal variation of AOT_{500 nm} (aerosol optical thickness) shows high values (0.51?±?0.18) during pre-monsoon (dust dominant) season while low values (0.36?±?0.14) are exhibited during winter. The Ångström wavelength exponent has been found to exhibit low value (<0.25) indicating relative dominance of coarse-mode particles during pre-monsoon season. The AOT increased from 0.36 (April_mean) to 0.575 (May–June_mean). Consequently, volume concentration range increases from April through May–June followed by a sharp decline in July during the first active phase of the monsoon. Significantly high dust storms were observed over Jaipur as indicated by high values of single scattering albedo (SSA_{440 nm}?=?0.89, SSA_{675 nm}?=?0.95, SSA_{870 nm}?=?0.97, SSA_{1,020 nm}?=?0.976) than the previously reported values over IGP region sites. The larger SSA values (more scattering aerosol), especially at longer wavelengths, is due to the abundant dust loading, and is attributed to the measurement site’s proximity to the Thar Desert. The mean and standard deviation in SSA and asymmetry parameter during pre-monsoon season over Jaipur is 0.938?±?0.023 and 0.712?±?0.017 at 675 nm wavelength, respectively. Back-trajectory air mass simulations suggest Thar Desert in northwestern India as the primary source of high aerosols dust loading over Jaipur region as well as contribution by long-range transport from the Arabian Peninsula and Middle East gulf regions, during pre-monsoon season.     

Metallic components of traffic-induced urban aerosol, their spatial variation, and source apportionment

This study proposes a practical method to estimate elemental composition and distribution in order to attribute source and quantify impacts of aerosol particles at an urban region in Kolkata, India. Twelve-hour total particulates were collected in winter (2005–2006) and analyzed by energy-dispersive X-ray fluorescence technique to determine multi-elemental composition, especially trace metals. The aerosols consist of various elements including K, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, and Pb which exhibit significant concentration at various sites (p?<?0.05). The concentration of different metallic elements were found in the order of Zn ?> ?Pb ?> ?Ni ?> ?Cu ?> ?Cr ?>? Co. Statistical multivariate analysis and correlation matrix analyses were performed for factor identification and consequent source apportionment. Contour profiles demonstrate spatial variation of elemental compositions indicating possible source contribution along with meteorological influences. Spatial differences were clearly most significant for Zn, Ni, Pb, and Cu reflecting the importance of anthropogenic inputs, primarily from automobile sources.     

A Multivariate Time Series Approach to Study the Interdependence among O3, NO x , and VOCs in Ambient Urban Atmosphere

A multivariate time series approach vector autoregression (VAR) along with impulse response function and variance decomposition technique has been employed to look into the interrelationship among O₃, NO, NO₂, and volatile organic compounds (VOCs, namely, benzene, ethylbenzene, toluene, and xylene in the present study) using 3 months long continuous time series data of 1 h average concentration of these pollutants at one of the traffic sites in Delhi, India. It is found that the VAR of order 2 (i.e., past two lagged values of 1 h interval) is sufficient to represent the observed time series at the station studied. The impulse response function and variance decomposition analysis indicate that O₃ concentration shows an immediate rise and persists for a longer duration (typically 8–10 h) once the impulse of NO₂, benzene, ethylbenzene, or xylene is given in the ambient environment. However, in case of toluene, the reverse effect has been observed. Since O₃ forms in the troposphere due to photolysis of NO₂, it is not surprising that its impulse triggers O₃ formation in the ambient environment. However, in case of VOCs, this has been attributed to their tendency to show higher inclination toward intermediary reactions leading to the formation of O₃ rather than their (VOCs) reaction with O₃. Among VOCs, only toluene has been observed to show higher inclination toward its reaction with O₃. Apart from this, variance decomposition technique also reveals that the relation of NO with NO₂ is more important than the relation of NO with O₃ creating a conducive atmosphere for O₃ formation in the present scenario. Thus, the multivariate time series approach provides significant insight about the role played by the dominant individual VOCs and NO _x in influencing the O₃ concentration in ambient urban atmosphere whereas a photochemical modeling approach gives an overall view of NO _x and VOCs behavior with respect to O₃ by using the O₃ isopleth technique.     

Physicochemical and toxicological characteristics of urban aerosols during a recent Indonesian biomass burning episode

Air particulate matter (PM) samples were collected in Singapore from 21 to 29 October 2010. During this time period, a severe regional smoke haze episode lasted for a few days (21–23 October). Physicochemical and toxicological characteristics of both haze and non-haze aerosols were evaluated. The average mass concentration of PM_2.5 (PM with aerodynamic diameter of ≤2.5 μm) increased by a factor of 4 during the smoke haze period (107.2 μg/m³) as compared to that during the non-smoke haze period (27.0 μg/m³). The PM_2.5 samples were analyzed for 16 priority polycyclic aromatic hydrocarbons (PAHs) listed by the United States Environmental Protection Agency and 10 transition metals. Out of the seven PAHs known as potential or suspected carcinogens, five were found in significantly higher levels in smoke haze aerosols as compared to those in the background air. Metal concentrations were also found to be higher in haze aerosols. Additionally, the toxicological profile of the PM_2.5 samples was evaluated using a human epithelial lung cell line (A549). Cell viability and death counts were measured after a direct exposure of PM_2.5 samples to A459 cells for a period of 48 h. The percentage of metabolically active cells decreased significantly following a direct exposure to PM samples collected during the haze period. To provide further insights into the toxicological characteristics of the aerosol particles, glutathione levels, as an indirect measure of oxidative stress and caspase-3/7 levels as a measure of apoptotic death, were also evaluated.     

A combined model–observation approach to estimate historic gridded fields of PM2.5 mass and species concentrations

This paper introduces a methodology for estimating gridded fields of total and speciated fine particulate matter (PM_2.5) concentrations for time periods and regions not covered by observational data. The methodology is based on performing long-term regional scale meteorological and air quality simulations and then integrating these simulations with available observational data. To illustrate this methodology, we present an application in which year-round simulations with a meteorological model (the National Center for Atmospheric Research/Penn State Mesoscale Model, hereafter referred to as MM5) and a photochemical air quality model (the Community Multiscale Air Quality Model, hereafter referred to as CMAQ) have been performed over the northeastern United States for 1988–2005. Model evaluation results for total PM_2.5 mass and individual species for the time period from 2000 to 2005 show that model performance varies by species, season, and location. Therefore, an approach is developed to adjust CMAQ output with factors based on these three variables. The adjusted model values for total PM_2.5 mass for 2000–2005 are compared against independent measurements not utilized for the adjustment approach. This comparison reveals that the adjusted model values have a lower root mean square error (RMSE) and higher correlation coefficients than the original model values. Furthermore, the PM_2.5 estimates from these adjusted model values are compared against an alternate method for estimating historic PM_2.5 values that is based on PM_2.5/PM₁₀ ratios calculated at co-located monitors. Results reveal that both methods yield estimates of historic PM_2.5 mass that are broadly consistent; however, the adjusted CMAQ values provide greater spatial coverage and information for PM_2.5 species in addition to total PM_2.5 mass. Finally, strengths and limitations of the proposed approach are discussed in the context of potential uses of this method.