Gaseous mercury fluxes from the forest floor of the Adirondacks

The flux of gaseous elemental mercury (Hg⁰) from the forest floor of the Adirondack Mountains in New York (USA) was measured numerous times throughout 2005 and 2006 using a polycarbonate dynamic flux chamber (DFC). The Hg flux ranged between −2.5 and 27.2 ng m⁻² h⁻¹ and was positively correlated with temperature and solar radiation. The measured Hg emission flux was highest in spring, and summer, and lowest in winter. During leaf-off periods, the Hg emission flux was highly dependent on solar radiation and less dependent on temperature. During leaf-on periods, the Hg emission flux was fairly constant because the forest canopy was shading the forest floor. Two empirical models were developed to estimate yearly Hg⁰ emissions, one for the leaf-off period and one for the leaf-on period. Using the U.S. EPA's CASTNET meteorological data, the cumulative estimated emission flux was approx. 7.0 μg Hg⁰ m⁻² year⁻¹.     

Development of combined plant of biogas and bio solid-refuse-fuel from swine manure slurry

Journal of Material Cycles and Waste Management - An environment-friendly treatment of organic waste like swine manure and food waste is considered to be big challenge, because the residue of...     

Excellent dye degradation performance of FeSiBP amorphous alloys by Fenton-like process

Amorphous alloys are being newly applied in wastewater treatment because of their unique atomic packing structure. They possess excellent degradation efficiency, stability and reusability. In this work, Fe₈₀Si₁₀B₁₀ and Fe₈₃Si₅B₈P₄ amorphous ribbons exhibited advanced catalytic performance for the degradation of Methyl Blue (MB) and Rhodamine B (RhB) dyes, and the color removal reach nearly 100% within 11 min for both the dyes. Compared with the Fe₈₀Si₁₀B₁₀ amorphous ribbon, the Fe₈₃Si₅B₈P₄ ribbon showed higher degradation efficiency due to its lower reaction activation energy, higher electron transfer ability and higher Fe content, and the formation of the galvanic cell between the strong Fe–P bonds and the weak Fe–B bonds. It also exhibited high stability and reusability. The degradation efficiency was improved when the appropriate concentration of H₂O₂ is added. As regards the pH, high degradation efficiency was observed in acidic MB solution, but it decreased as the pH increased up to pH 7. The application of the electro–Fenton–like process is discussed, which can effectively improve the degradation performance in a nearly natural solution. This study presents a high efficiency low-cost catalyst for synthetic dye degradation and expands the functional applications of Fe-based amorphous alloys.     

Distinct effects of intrinsic motivation and extrinsic rewards on radical and incremental creativity: The moderating role of goal orientations

Previous studies have investigated the role of intrinsic motivation and extrinsic rewards in enhancing employee creativity. However, the possibility that these motivational factors affect the creativity of different types remains largely unexplored, particularly in the organizational settings. Moreover, the potential that personality traits may moderate the function of these motivational factors toward creativity is another underresearched area. By drawing on the person–situation interaction perspective, we propose that both intrinsic motivation and extrinsic rewards predict creativity but of different types. Thus, we diverge from the view that creativity is a uniform criterion domain by adopting the distinction between radical and incremental creativity. Our empirical analysis of 220 independent employee–supervisor dyads confirmed that intrinsic motivation and extrinsic rewards predict radical and incremental creativity, respectively. Moreover, the effects of intrinsic motivation on radical and incremental creativity are more positive for employees with higher learning goal orientation. By contrast, the effect of extrinsic rewards on incremental creativity is more positive for employees with higher performance goal orientation. This study offers elaborate and nuanced perspectives and insights into the role of different motivational processes in the development of different types of creativity.     

Decomposition of greenhouse gases by plasma

The topic of decomposition and reduction of greenhouse gases is becoming an important issue in tackling the global warming effect since several years ago. Several technologies, including plasma-utilized process, were proposed to improve the treatment ability for the destruction of green house gases usually emitted by industrial activities. In this review paper, the application of plasma to reduce the emission of greenhouse gases was briefly summarized.     

Reducing ammonia emissions and volatile fatty acids in poultry litter with liquid aluminum chloride

This study was a pen trial in which the effects of adding different rates of liquid aluminum chloride (AlCl₃) on litter pH, total volatile fatty acids (VFAs), and ammonia (NH₃) fluxes was evaluated. Liquid AlCl₃ treatments used in this study were sprayed on the rice hull surface at rates of 100 g, 200 g, and 300 g liquid AlCl₃/kg rice hulls; untreated rice hulls served as controls. Litter pH, total VFAs, and NH₃ fluxes were all lowered (P< 0.05) by all of the liquid AlCl₃ treatments compared with controls during certain times of the 5 week study. However, there were no significant differences among treatments on litter pH at the end of the study (from 3 to 5 weeks) or NH₃ fluxes at beginning of the study (0 to 3 weeks). Total VFAs were reduced 16 %, 29 %, and 53 % by 100 g liquid AlCl₃/kg rice hulls, 200 g liquid AlCl₃/kg rice hulls, and 300 g liquid AlCl₃/kg rice hulls, respectively. Liquid AlCl₃additions reduced NH₃ fluxes by 35 %, 57 % and 67 %, respectively, at the low, medium and high rates. In summary, these results indicate that adding liquid aluminum chloride to rice hulls would be a useful tool in reducing the negative environmental impact of poultry litter. It should be noted that the decreased VFA production and NH₃ volatilization was chiefly associated with reduction in litter pH.     

Weekly periodicities of meteorological variables and their possible association with aerosols in Korea

The weekly periodicities in meteorological variables and its association with aerosols in Korea are investigated using long-term surface measurements of meteorology (1975–2005) and aerosols (1999–2005). Through an analysis of the annual (and/or seasonal) values averaged over 10 stations, we identified distinct weekly periodicities in the daily minimum temperature (T_min), diurnal temperature range (DTR), cloud fraction, and solar insolation, although they have different characteristics from each other. The weekly association among variables is discussed in this study. Positive anomalies of the cloud fraction and T_min and negative anomalies of solar insolation and DTR are seen for the second half of the week and the reverse for the first half of the week, i.e., more cloudiness and less insolation for Wednesday?Thursday and less cloudiness and more insolation for Monday?Tuesday. Furthermore, seasonal dependence of weekly anomalies shows that the weekly periodicities are enhanced especially in autumn, more than 2–3 times as great as those of the annual mean. The weekly cycles in such variables are most likely driven by changes in cloud fraction, possibly through aerosol–cloud interactions induced by aerosol variations between working weekdays and Sunday, which are clearly identified in PM10 weekly cycles. This study also suggests that the weekly periodicities in meteorological variables are possibly associated with long-range transport of weekly periodicities, as well as aerosol–cloud-precipitation interactions over the region.     

A combined approach for the evaluation of a volatile organic compound emissions inventory

Emissions inventories significantly affect photochemical air quality model performance and the development of effective control strategies. However, there have been very few studies to evaluate their accuracy. Here, to evaluate a volatile organic compound (VOC) emissions inventory, we implemented a combined approach: comparing the ratios of carbon bond (CB)-IV VOC groups to nitrogen oxides (NOx) or carbon monoxide (CO) using an emission preprocessing model, comparing the ratios of VOC source contributions from a source apportionment technique to NOx or CO, and comparing ratios of CB-IV VOC groups to NOx or CO and the absolute concentrations of CB-IV VOC groups using an air quality model, with the corresponding ratios and concentrations observed at three sites (Maryland, Washington, DC, and New Jersey). The comparisons of the ethene/NOx ratio, the xylene group (XYL)/NOx ratio, and ethene and XYL concentrations between estimates and measurements showed some differences, depending on the comparison approach, at the Maryland and Washington, DC sites. On the other hand, consistent results at the New Jersey site were observed, implying a possible overestimation of vehicle exhaust. However, in the case of the toluene group (TOL), which is emitted mainly from surface coating and printing sources in the solvent utilization category, the ratios of TOL/ NOx or CO, as well as the absolute concentrations revealed an overestimate of these solvent sources by a factor of 1.5 to 3 at all three sites. In addition, the overestimate of these solvent sources agreed with the comparisons of surface coating and printing source contributions relative to NOx from a source apportionment technique to the corresponding value of estimates at the Maryland site. Other studies have also suggested an overestimate of solvent sources, implying a possibility of inaccurate emission factors in estimating VOC emissions from surface coating and printing sources. We tested the impact of these overestimates with a chemical transport model and found little change in ozone but substantial changes in calculated secondary organic aerosol concentrations.     

Transport characteristics of gas phase ozone in unsaturated porous media for in-situ chemical oxidation

Encapsulation technology is being investigated as a method for controlling pH in situ at contaminated groundwater sites where pH may limit remediation of organic contaminants. This study examined the effectiveness of using KH2PO4 buffer encapsulated in a pH-sensitive coating to neutralize pH in laboratory sand columns (1.5-1) under a simulated groundwater flow rate and characterized the pattern of capsule release in the flow-through system. Denitrification was used in the columns to increase the pH of the pore water. Each of three columns was equipped with three miniature mesh wells to allow contact of the buffer with column pore water, but capsules (15 g) were inserted into only one column (amended). The two other columns served as amendment (no buffer) and abiotic (no denitrification) controls. Oxidation-reduction potential, dissolved organic and inorganic carbon, NH4+, NO3- +NO2-, PO(4)3-, and pH were measured in the influent, two side ports, and effluent of the columns over time. Near complete conversion of 80 mg N/1 of nitrate and 152 mg/l of ethanol per day resulted in a mean pH increase from 6.2 to 8.2 in the amendment control column. The amended column maintained the target pH of 7.0 +/- 0.2 for 4 weeks until the capsules began to be depleted, after which time the pH slowly started to increase. The capsules exhibited pulses of buffer release, and were effectively dissolved after 7.5 weeks of operation. Base-neutralizing capacity contributed by the encapsulated buffer over the entire study period, calculated as cation equivalents, was 120 mM compared to 8 mM without buffer. This study demonstrates the potential for this technology to mediate pH changes and provides the framework for future studies in the laboratory and in the field, in which pH is controlled in order to enhance organic contaminant remediation by pH-sensitive systems.