Spatial patterns in wet and dry deposition of atmospheric mercury and trace elements in central Illinois,USA

An intensive 1-month atmospheric sampling campaign was conducted concurrently at eight monitoring sites in central Illinois, USA, from June 9 to July 3, 2011 to assess spatial patterns in wet and dry deposition of mercury and other trace elements. Summed wet deposition of mercury ranged from 3.1 to 5.4 μg/m² across sites for the total study period, while summed dry deposition of reactive mercury (gaseous oxidized mercury plus particulate bound mercury) ranged from 0.7 to 1.6 μg/m², with no statistically significant differences found spatially between northern and southern sites. Ratios of summed wet to summed dry mercury deposition across sites ranged from 2.2 to 4.9 indicating that wet deposition of mercury was dominant during the study period. Volume-weighted mean mercury concentrations in precipitation were found to be significantly higher at northern sites, while precipitation depth was significantly higher at southern sites. These results showed that substantial amounts of mercury deposition, especially wet deposition, occurred during the study period relative to typical annual wet deposition levels. Summed wet deposition of anthropogenic trace elements was much higher, compared to summed dry deposition, for sulfur, selenium, and copper, while at some sites summed dry deposition dominated summed wet deposition for lead and zinc. This study highlights that while wet deposition of Hg was dominant during this spring/summer-season study, Hg dry deposition also contributed an important fraction and should be considered for implementation in future Hg deposition monitoring studies.     

Remedial Options for Leaking Underground Storage Tanks

Remedial options for leaking underground storage tanks were investigated in a joint project of the Electric Power Research Institute and the Underground Storage Tank Committee of the Utility Solid Waste Activities Group. Both existing and emerging technologies were examined. Thirteen remedial techniques were identified and initially characterized as in situ or non-in situ. In situ methods include volatilization, biodegradation, leaching and chemical reaction, vitrification, passive remediation, and isolation or containment. Non-in situ techniques include land treatment, thermal treatment, asphalt incorporation, solidification and stabilization, groundwater extraction and treatment, chemical extraction, and excavation. Soil and groundwater remediation problems have many site-specific considerations which must be considered in choosing an appropriate remedial option; these include cleanup goals, site and contaminant characteristics, cost, exposure pathways, and others. Appropriate remedial techniques are chosen by assessing technical, implementational, environmental and economic considerations of each available option to achieve the desired cleanup goal at the specified site.     

Industrial Pollution Prevention! A Critical Review

Abstract

Pyrolytic product distribution rates and pyrolysis behavior of tire-derived fuels (TDF) were investigated using thermogravimetric analyzer (TGA) techniques. A TGA was designed and built to investigate the behavior and products of pyrolysis of typical TDF specimens. The fundamental knowledge of TGA analysis and principal fuel analysis are applied in this study. Thermogravimetry of the degradation temperature of the TDF confirms the overall decomposition rate of the volatile products during the depolymerization reaction. The principal fuel analysis (proximate and ultimate analysis) of the pyrolytic char products show the correlation of volatilization into the gas and liquid phases and the existence of fixed carbon and other compounds that remain as a solid char. The kinetic parameters were calculated using least square with minimizing sum of error square technique. The results show that the average kinetic parameters of TDF are the activation energy, E = 1322 ± 244 kJ/mol, a pre-exponential constant of A = 2.06 ± 3.47 × 10¹⁰ min^?1, and a reaction order n = 1.62 ± 0.31. The model-predicted rate equations agree with the experimental data. The overall TDF weight conversion represents the carbon weight conversion in the sample.     

Airborne Emissions of Mercury from Municipal Solid Waste. II: Potential Losses of Airborne Mercury before Landfill

Abstract

Waste distribution and compaction at the working face of municipal waste landfills releases mercury vapor (Hg⁰) to the atmosphere, as does the flaring of landfill gas. Waste storage and processing before its addition to the landfill also has the potential to release Hg⁰ to the air if it is initially present or formed by chemical reduction of Hg^II to Hg⁰ within collected waste. We measured the release of Hg vapor to the atmosphere during dumpster and transfer station activities and waste storage before landfilling at a municipal landfill operation in central Florida. We also quantified the potential contribution of specific Hg-bearing wastes, including mercury (Hg) thermometers and fluorescent bulbs, and searched for primary Hg sources in sorted wastes at three different landfills. Surprisingly large fluxes were estimated for Hg losses at transfer facilities (～100 mg/hr) and from dumpsters in the field (～30 mg/hr for 1,000 dumpsters), suggesting that Hg emissions occurring before landfilling may constitute a significant fraction of the total emission from the disposal/landfill cycle and a need for more measurements on these sources. Reducing conditions of landfill burial were obviously not needed to generate strong Hg⁰ signals, indicating that much of the Hg was already present in a metallic (Hg⁰) form. Attempts to identify specific Hg sources in excavated and sorted waste indicated few readily identifiable sources; because of effective mixing and diffusion of Hg⁰, the entire waste mass acts as a source. Broken fluorescent bulbs and thermometers in dumpsters emitted Hg⁰ at 10 to >100 μg/hr and continued to act as near constant sources for several days.     

Self‐protective reactions to peer abusive supervision: The moderating role of prevention focus and the mediating role of performance instrumentality

Across 3 studies, we apply a self‐protection perspective of observed mistreatment to examine a moderated mediation model on “when” and “why” third parties are motivated by peer abusive supervision. We hypothesize that prevention‐focused third parties will increase their performance effort as a response to peer abusive supervision, and this effect is mediated by performance instrumentality. In a field study of working adults (Study 1) and an experimental study that manipulated peer abusive supervision (Study 2), we found that peer abusive supervision interacted with third parties' prevention focus to predict their performance effort such that peer abuse was positively related to third parties' performance effort only for those high on prevention focus. Results were replicated in a second field study of working adults (Study 3). Further, we found support for the mediating effect of performance instrumentality. The theoretical and practical implications of our results are discussed.     

Waste rechargeable electric lamps: characterisation and recovery of lead from their lead-acid batteries

Electrical electronics constitute a significant quantity of municipal solid wastes which are discarded after use in open dumpsites especially in the developing countries. The aim of this study was to characterise the material and chemical components, evaluate current management practices and investigate recovery of lead from battery electrodes (BEs) of waste rechargeable electric lamps (RLs). Twenty-six waste RLs of different models were sampled in Nigeria and characterised. Their BEs were analysed for Pb, Cr, Mn, Cu, Zn, Ni and Fe after acid digestion. Questionnaires were distributed to unselected respondents to assess usage and disposal of the lamps. Reaction of citric acid solutions with Pb in the presence of H₂O₂ was used for the recovery of Pb. 69 % of the respondents disposed their waste RLs in open dumpsites. The mean ± SD concentrations of Pb, Cr, Mn, Cu, Zn, Ni and Fe in the BEs were 600 ± 0.2 g/kg, 65.4 ± 40 mg/kg, 5.05 ± 4.0 mg/kg, 6.81 ± 5.0 mg/kg, 5.98 ± 3.0 mg/kg, 50.0 ± 30 mg/kg and 40.2 ± 35 mg/kg, respectively. The results show that the batteries are lead-acid batteries which require management. At the optimal conditions of S/L = 0.14, temperature = 20 °C and leaching time = 5 h, about 95 % Pb was recovered in form of lead citrate from the battery. High recovery of Pb is possible with simple and environment-friendly reactions.     

Analysis of the effects of combustion emissions and Santa Ana winds on ambient ozone during the October 2007 southern California wildfires

Combustion emissions and strong Santa Ana winds had pronounced effects on patterns and levels of ambient ozone (O₃) in southern California during the extensive wildland fires of October 2007. These changes are described in detail for a rural receptor site, the Santa Margarita Ecological Reserve, located among large fires in San Diego and Orange counties. In addition, O₃ changes are also described for several other air quality monitoring sites in the general area of the fires. During the first phase of the fires, strong, dry and hot northeasterly Santa Ana winds brought into the area clean continental air masses, which resulted in minimal diurnal O₃ fluctuations and a 72-h average concentration of 36.8 ppb. During the second phase of the fires, without Santa Ana winds present and air filled with smoke, daytime O₃ concentrations steadily increased and reached 95.2 ppb while the lowest nighttime levels returned to ～0 ppb. During that period the 8-h daytime average O₃ concentration reached 78.3 ppb, which exceeded the federal standard of 75 ppb. After six days of fires, O₃ diurnal concentrations returned to pre-fire patterns and levels.