Effect of biomass burning and regional background aerosols on CCN activity derived from airborne in-situ measurements

Airborne in-situ measurements were analyzed to investigate the effects of biomass burning and regional background aerosols on cloud condensation nuclei (CCN) activity in the Pacific Dust Experiment (PACDEX) during April and May 2007. Airmass trajectories with both horizontal and vertical motions were provided to identify the aerosol sources. In the biomass burning cases, the elevated aerosol layers were clearly observed at dry conditions because of the convection of airmass in the source region. The relative aging of aerosols was supported by the ratios of BC to particles with size ranging from 0.1 to 1.0 μm (N_0.1–1.0) and BC to carbon monoxide. Compared to aerosols in the precedent plume of biomass burning, aged particles in the latter plume were more activated to CCN at 0.4% (CCN_0.4%) than 0.1% supersaturation (CCN_0.1%) due to aerosols chemical modification during the aging process. On the other hand, significant difference of CCN_0.4% and CCN_0.1% at regional background aerosols over the Pacific Ocean was due to the activated particles below 1 μm in diameter. Although higher concentrations of aged particles were observed over the eastern Pacific Ocean, activated aerosols to cloud droplet was comparatively similar in the western Pacific Ocean because of the similar concentrations of N_0.1–1.0 in both cases.     

Volatile Organic Compounds in Ambient Air at Four Residential Locations in Seoul, Korea

To investigate the environmental behavior of volatile organic compounds (VOCs) in urban areas, their concentrations were measured at four urban monitoring sites (namely, N, S, E, and W) in Seoul, Korea (February to December 2009). A total of 27 compounds were quantified that consist of four chemical groups: aromatic (AR), halogenated aromatic, halogenated paraffin, and halogenated olefin. Results were evaluated by focusing on these four functional groups just mentioned and their summation term as total VOC (TVOC) along with several individual species (mainly AR species, that is, benzene, toluene, ethylbenzene, and xylene). The highest concentration of chemical groups was found from AR (71.1±42.1?ppbC), while that for individual species confirmed the dominance of toluene (7.48±3.88?ppb). The analysis of spatial distribution indicated that high TVOC levels were recorded at sites N and W, while it was not so significant such as S and E in terms of TVOC budget. Seasonal variation of these VOCs was characterized by the peak values in December to reflect the combined effects of pronounced source activities and meteorological conditions. Analysis of spatial variations in VOC levels between the four urban sites indicated that their distributions are tightly affected by local source processes in each area.     

Examination of Critical Factors Related to Summer Chlorophyll a Concentration in the Sueo Dam Reservoir, Republic of Korea

This study examined critical factors related to the short-term variation of algae growth in reservoirs during the summer. To this end, statistical tests were carried out at a small dam reservoir to determine how chemical factors (e.g., nutrient concentrations) and physical factors (e.g., theoretical and relative residence times, temperature) influenced the chlorophyll a (Chl-a) concentration. Statistical tests revealed that, although phosphorus (P) concentration was significant for Chl-a, residence time had much stronger relationship to Chl-a concentration than chemical factors. In addition, the study verified that relative residence time (RRT) best explained the relation of water status to algae growth. RRT was found to be useful in identifying water status related to the summer algae bloom. Finally, this study raised the possibility of inhibiting summer algae growth by operating dam reservoirs moderately. These findings need to be seriously considered when reservoir operators establish effective strategies for water quality management in summer.     

Application of phosphate-solubilizing bacteria for enhancing bioavailability and phytoextraction of cadmium (Cd) from polluted soil

In this study, phosphate-solubilizing bacteria (PSB), Bacillus megaterium, were used to enhance Cd bioavailability and phytoextractability of Cd from contaminated soils. This strain showed a potential for directly solubilizing phosphorous from soils more than 10 folds greater than the control without inoculation. The results of pot experiments revealed that inoculation with B. megaterium significantly increased the extent of Cd accumulation in Brassica juncea and Abutilon theophrasti by two folds relative to the uninoculated control. The maximum Cd concentrations due to inoculation were 1.6 and 1.8 mg Cd g⁻¹ plant for B. juncea and A. theophrasti after 10 wk, respectively. The total biomass of A. theophrasti was not significantly promoted by the inoculation treatment, yet the total biomass of B. juncea increased from 0.087 to 0.448 g. It is also worth to mention that B. juncea predominantly accumulates Cd in its stems (39%) whereas A. theophrasti accumulates it in its leaves (68%) after 10 wk. The change of the Cd speciation indicated that inoculation of B. megaterium as PSB increased the bioavailabilty of Cd and consequently enhanced its uptake by plants. The present study may provide a new insight for improving phytoremediation using PSB in the Cd-contaminated soils.     

Recovering valuable metals from recycled photovoltaic modules

Recovering valuable metals such as Si, Ag, Cu, and Al has become a pressing issue as end-of-life photovoltaic modules need to be recycled in the near future to meet legislative requirements in most countries. Of major interest is the recovery and recycling of high-purity silicon (>99.9%) for the production of wafers and semiconductors. The value of Si in crystalline-type photovoltaic modules is estimated to be ?$95/kW at the 2012 metal price. At the current installed capacity of 30 GW/yr, the metal value in the PV modules represents valuable resources that should be recovered in the future. The recycling of end-of-life photovoltaic modules would supply >88,000 and 207,000 tpa Si by 2040 and 2050, respectively. This represents more than 50% of the required Si for module fabrication. Experimental testwork on crystalline Si modules could recover a >99.98%-grade Si product by HNO₃/NaOH leaching to remove Al, Ag, and Ti and other metal ions from the doped Si. A further pyrometallurgical smelting at 1520ºC using CaO–CaF₂–SiO₂ slag mixture to scavenge the residual metals after acid leaching could finally produce >99.998%-grade Si. A process based on HNO₃/NaOH leaching and subsequent smelting is proposed for recycling Si from rejected or recycled photovoltaic modules.

Implications:The photovoltaic industry is considering options of recycling PV modules to recover metals such as Si, Ag, Cu, Al, and others used in the manufacturing of the PV cells. This is to retain its “green” image and to comply with current legislations in several countries. An evaluation of potential resources made available from PV wastes and the technologies used for processing these materials is therefore of significant importance to the industry. Of interest are the costs of processing and the potential revenues gained from recycling, which should determine the viability of economic recycling of PV modules in the future.     

Developing and evaluating techniques for localizing pollutant emission sources with open-path Fourier transform infrared measurements and wind data

This paper presents the simulation and field evaluation results of two approaches to localize pollutant emission sources with open-path Fourier transform infrared (OP-FTIR) spectroscopy. The first approach combined the plume's peak location information reconstructed from the Smooth Basis Function Minimization (SBFM) algorithm and the wind direction data to calculate source projection lines. In the second approach, the plume's peak location was determined with the Monte Carlo methodology by randomly sampling within the beam segment having the largest path-integrated concentration. We first conducted a series of simulation studies to investigate the sensitivity of using different basis functions in the SBFM algorithm. It was found that fitting with the beta and Weibull basis functions generally gave better estimates of the peak locations than with the normal basis function when the plumes were mainly within the OP-FTIR's monitoring line. However, for plumes that were symmetric to the peak position or spread over the OP-FTIR, fitting with the normal basis function gave better performance. In the field experiment, two tracer gases were released simultaneously from two locations and the OP-FTIR collected data downwind from the sources with a maximum beam path length of 97 m. For the first approach, the release locations were within the 0.25- to 0.5-probability area only after the uncertainty of the peak locations was included in the calculation process. The second approach was easy to implement and still performed as satisfactorily as the first approach. The distances from the sources to the best-fit lines (i.e., the regression lines) of the estimated locations were smaller than 10 m.     

Investigation of heavy metal accumulation in Polygonum thunbergii for phytoextraction

In this study, cadmium (II), lead (II), copper (II) and zinc (II) were determined in Polygonum thunbergii and soil from the Mankyung River watershed, Korea. Soil samples contained detectable lead (<17.5 g g(-1)), copper (<8.4 g g(-1)) and zinc (<24.5 g g(-1)), whereas cadmium was undetectable. Whole plants of P. thunbergii contained detectable lead (<320.8 g g(-1)), copper (<863.2 g g(-1)) and zinc (<2427.3 g g(-1)), whereas cadmium was detectable only in the stem (<7.4 g g(-1)) and root (<10.1 g g(-1)). Whole plant concentrations were very different for each metal, particularly in the case of zinc. The mean content of heavy metal in the whole plants increased in the order of cadmium (8.5 g g(-1))相似文献   

Characterization and reactivity of natural manganese ore catalysts in the selective catalytic oxidation of ammonia to nitrogen

Natural manganese ore (NMO) catalysts were characterized and tested in the selective catalytic oxidation of ammonia to nitrogen oxides under dilute conditions. Also, the oxidation of ammonia (NH(3)) was carried out using pure MnO(2), Mn(2)O(3) for comparing with the activity. It is found that the activity of NMO was similar to that of MnO(2) at low temperature below 150 degrees C but above this temperature, the activity of these catalysts showed the difference. In the course of NH(3) oxidation, N(2), NO, N(2)O and H(2)O were produced. But the quantity of NO(2) produced in this experiment was negligible. At temperature below 250 degrees C, selectivity into N(2) from NH(3) oxidation was in the order, NMO > MnO(2) > Mn(2)O(3). This is the reverse of activity of these manganese oxides. Also the characterization of NH(3) oxidation was proposed and supported by the effect of space velocity, inlet O(2) and NH(3) concentration. The increase of space velocity remarkably influenced not only the conversion but also selectivity into N(2). The higher the reaction temperature was, the higher the effect of inlet O(2) and NH(3) concentration on the reaction rate was. By introducing NO during NH(3) oxidation reaction, the possibility of NMO as selective catalytic reduction catalyst at low temperature was studied and showed positive results.