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.     

Sorption of radiolabelled glyphosate on biochar aged in contrasting soils

Glyphosate mobility from terrestrial to aquatic environments has raised concerns about it. Utilizing soil’s inherent properties along with sorption properties of aged biochar, we hypothesized that selective application of biochar would be more effective in economic terms for glyphosate sorption on contrasting soils. To test this hypothesis, batch experiments and liquid scintillation counting for ¹⁴ Okada, E.; Costa, J. L.; Bedmar, F. Adsorption and mobility of glyphosate in different soils under no-till and conventional tillage. Geoderma 2016, 263, 78–85.[Crossref], [Web of Science ®] , [Google Scholar]C labeled glyphosate were used. The sorption behavior of glyphosate was examined in four contrasting Australian soil types (Oxisol, Vertisol, Entisol, and Inceptisol) amended with aged biochar to determine glyphosate concentrations by measuring ¹⁴ Okada, E.; Costa, J. L.; Bedmar, F. Adsorption and mobility of glyphosate in different soils under no-till and conventional tillage. Geoderma 2016, 263, 78–85.[Crossref], [Web of Science ®] , [Google Scholar]C activity using liquid scintillation counting. Freundlich parameters were calculated for soil-soil/biochar combinations. The pattern of glyphosate sorption was Oxisol?>?Vertisol?>?Entisol?>?Inceptisol. Oxisol adsorbed approximately five times more glyphosate compared with Inceptisol. Oxisol soil system adsorbed maximum amount of glyphosate principally due to the presence of iron-aluminum oxides exhibiting variable charges which got increased due to the presence of aged biochar. Considering all the soil/soil-biochar systems, Inceptisol soil system showed the least adsorption of glyphosate. A significant contribution of char was observed only in the Entisol soil system and the finding is valuable as char can be applied in Entisol soil systems to control glyphosate mobility.     

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.     

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.     

Design and Verification of a Programmable Gas Dispensing System for Exposing Plants to Dynamic Concentrations of Air Pollutants

Abstract

Landfills represent a source of distributed emissions source over an irregular and heterogeneous surface. In the method termed “Other Test Method-10” (OTM-10), the U.S. Environmental Protection Agency (EPA) has proposed a method to quantify emissions from such sources by the use of vertical radial plume mapping (VRPM) techniques combined with measurement of wind speed to determine the average emission flux per unit area per time from nonpoint sources. In such application, the VRPM is used as a tool to estimate the mass of the gas of interest crossing a vertical plane. This estimation is done by fitting the field-measured concentration spatial data to a Gaussian or some other distribution to define a plume crossing the vertical plane. When this technique is applied to landfill surfaces, the VRPM plane may be within the emitting source area itself. The objective of this study was to investigate uncertainties associated with using OTM-10 for landfills. The spatial variability of emission in the emitting domain can lead to uncertainties of –34 to 190% in the measured flux value when idealistic scenarios were simulated. The level of uncertainty might be higher when the number and locations of emitting sources are not known (typical field conditions). The level of uncertainty can be reduced by improving the layout of the VRPM plane in the field in accordance with an initial survey of the emission patterns. The change in wind direction during an OTM-10 testing setup can introduce an uncertainty of 20% of the measured flux value. This study also provides estimates of the area contributing to flux (ACF) to be used in conjunction with OTM-10 procedures. The estimate of ACF is a function of the atmospheric stability class and has an uncertainty of 10–30%.     

The influence of hydroxyl volatile organic compounds on the oxidation of aqueous sulfur dioxide by oxygen

Although the effect of volatile organic compounds (VOCs) on the oxidation of dissolved sulfur dioxide by oxygen has been the subject of many investigations, this is the first study which examines the effect of a large number of precisely 16 hydroxy compounds. The kinetics both in the absence and the presence of VOCs was defined by rate laws (A and B): A $$ \hbox{-} \mathrm{d}\left[\mathrm{S}\left(\mathrm{IV}\right)\right]/\mathrm{dt}={R}_o={k}_o\left[\mathrm{S}\left(\mathrm{IV}\right)\right] $$ B $$ \hbox{-} \mathrm{d}\left[\mathrm{S}\left(\mathrm{IV}\right)\right]/\mathrm{dt}={R}_i={k}_i\left[\mathrm{S}\left(\mathrm{IV}\right)\right] $$ where R _o and k _o are the initial rate and first-order rate constant, respectively, in the absence of VOCs, R _i , and k _i are the initial rate and the first-order rate constant, respectively, in the presence of VOCs, and [S(IV)] is the concentration of dissolved sulfur dioxide, sulfur(IV). The nature of the dependence of k _i on the concentration of inhibitor, [Inh], was defined by Eq. (C). C $$ {k}_i={k}_0/\left(1+B\left[\mathrm{Inh}\right]\right) $$ where B is an empirical inhibition parameter. The values of B have been determined from the plots of 1/k _i versus [Inh]. Among aliphatic and aromatic hydroxy compounds studied, t-butyl alcohol and pinacol were without any inhibition effect due to the absence of secondary or tertiary hydrogen. The values of inhibition parameter, B, were related to k _inh , the rate constant for the reaction of SO₄ ^? radical with the inhibitor, by Eq. (D). D $$ B=\left(9\pm 2\right)\times 1{0}^{-4}\times {k}_{inh} $$ Equation (D) may be used to calculate the values of either of B or k _inh provided that the other is known. The extent of inhibition depends on the value of the composite term, B[Inh]. However, in accordance with Eq. (C), the extent of inhibition would be sizeable and measurable when B[Inh]?>?0.1 and oxidation of S(IV) would be almost completely stopped when B[Inh]?≥?10. B[Inh] value can be used as a guide whether the reaction step: SO₄ ^??+?organics? \( \overset{k_{inh}}{\to } \) ?SO₄ ^2??+?non-chain products: should be included in the multiphase models or not.     

Characterization of PM10 atmospheric aerosol at urban and urban background sites in Fuzhou city, China

Background

PM₁₀ aerosol samples were simultaneously collected at two urban and one urban background sites in Fuzhou city during two sampling campaigns in summer and winter. PM₁₀ mass concentrations and chemical compositions were determined.

Methods

Water-soluble inorganic ions (Cl^?, NO ₃ ^? , SO ₄ ^2? , NH ₄ ⁺ , K⁺, Na⁺, Ca²⁺, and Mg²⁺), carbonaceous species (elemental carbon and organic carbon), and elements (Al, Si, Mg, K, Ca, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, As, Se, Br, and Pb) were detected using ion chromatography, thermal/optical reflectance, and proton-induced X-ray emission methods, respectively.

Results

PM₁₀ mass concentrations, as well as most of the chemical components, were significantly increased from urban background to urban sites, which were due to enhanced anthropogenic activities in urban areas. Elements, carbonaceous species, and most of the ions were more uniformly distributed at different types of sites in winter, whereas secondary ion SO ₄ ^2? , NO ₃ ^? , and NH ₄ ⁺ showed more evident urban-background contrast in this season. The chemical mass closure indicated that mineral dust, organic matters, and sulfate were the most abundant components in PM₁₀. The sum of individually measured components accounted for 86.9?C97.7% of the total measured PM₁₀ concentration, and the discrepancy was larger in urban area than in urban background area.

Conclusion

According to the principal component analysis?Cmultivariate linear regression model, mineral dust, secondary inorganic ions, sea salt, and motor vehicle were mainly responsible for the PM₁₀ particles in Fuzhou atmosphere, and contributed 19.9%, 53.3%, 21.3%, and 5.5% of PM₁₀, respectively.     

Effect of alginate on the aggregation kinetics of copper oxide nanoparticles (CuO NPs): bridging interaction and hetero-aggregation induced by Ca<Superscript>2+</Superscript>

The stability of CuO nanoparticles (NPs) is expected to play a key role in the environmental risk assessment of nanotoxicity in aquatic systems. In this study, the effect of alginate (model polysaccharides) on the stability of CuO NPs in various environmentally relevant ionic strength conditions was investigated by using time-resolved dynamic light scattering. Significant aggregation of CuO NPs was observed in the presence of both monovalent and divalent cations. The critical coagulation concentrations (CCC) were 54.5 and 2.9 mM for NaNO₃ and Ca(NO₃)₂, respectively. The presence of alginate slowed nano-CuO aggregation rates over the entire NaNO₃ concentration range due to the combined electrostatic and steric effect. High concentrations of Ca²⁺ (>6 mM) resulted in stronger adsorption of alginate onto CuO NPs; however, enhanced aggregation of CuO NPs occurred simultaneously under the same conditions. Spectroscopic analysis revealed that the bridging interaction of alginate with Ca²⁺ might be an important mechanism for the enhanced aggregation. Furthermore, significant coagulation of the alginate molecules was observed in solutions of high Ca²⁺ concentrations, indicating a hetero-aggregation mechanism between the alginate-covered CuO NPs and the unabsorbed alginate. These results suggested a different aggregation mechanism of NPs might co-exist in aqueous systems enriched with natural organic matter, which should be taken into consideration in future studies.

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Graphical abstract Hetero-aggregation mechanism of CuO nanoparticles and alginate under high concentration of Ca²⁺