Real-time measurement of outdoor tobacco smoke particles

The current lack of empirical data on outdoor tobacco smoke (OTS) levels impedes OTS exposure and risk assessments. We sought to measure peak and time-averaged OTS concentrations in common outdoor settings near smokers and to explore the determinants of time-varying OTS levels, including the effects of source proximity and wind. Using five types of real-time airborne particle monitoring devices, we obtained more than 8000 min worth of continuous monitoring data, during which there were measurable OTS levels. Measurement intervals ranged from 2 sec to 1 min for the different instruments. We monitored OTS levels during 15 on-site visits to 10 outdoor public places where active cigar and cigarette smokers were present, including parks, sidewalk cafés, and restaurant and pub patios. For three of the visits and during 4 additional days of monitoring outdoors and indoors at a private residence, we controlled smoking activity at precise distances from monitored positions. The overall average OTS respirable particle concentration for the surveys of public places during smoking was approximately 30 microg m(-3). OTS exhibited sharp spikes in particle mass concentration during smoking that sometimes exceeded 1000 microg m(-3) at distances within 0.5 m of the source. Some average concentrations over the duration of a cigarette and within 0.5 m exceeded 200 microg m(-3), with some average downwind levels exceeding 500 microg m(-3). OTS levels in a constant upwind direction from an active cigarette source were nearly zero. OTS levels also approached zero at distances greater than approximately 2 m from a single cigarette. During periods of active smoking, peak and average OTS levels near smokers rivaled indoor tobacco smoke concentrations. However, OTS levels dropped almost instantly after smoking activity ceased. Based on our results, it is possible for OTS to present a nuisance or hazard under certain conditions of wind and smoker proximity.     

Effect of decabromodiphenyl ether and antimony trioxide on controlled pyrolysis of high-impact polystyrene mixed with polyolefins

The controlled pyrolysis of polyethylene/polypropylene/polystyrene mixed with brominated high-impact polystyrene containing decabromodiphenyl ether as a brominated flame-retardant with antimony trioxide as a synergist was performed. The effect of decabromodiphenyl ether and antimony trioxide on the formation of its congeners and their effect on distribution of pyrolysis products were investigated. The controlled pyrolysis significantly affected the decomposition behavior and the formation of products. Analysis with gas chromatograph with electron capture detector confirmed that the bromine content was rich in step 1 (oil 1) liquid products leaving less bromine content in the step 2 (oil 2) liquid products. In the presence of antimony containing samples, the major portion of bromine was observed in the form of antimony bromide and no flame-retardant species were found in oil 1. In the presence of synergist, the step 1 and step 2 oils contain both light and heavy compounds. In the absence of synergist, the heavy compounds in step 1 oil and light compounds in step 2 oils were observed. The presence of antimony bromide was confirmed in the step 1 oils but not in step 2 oils.     

Economies of scale in global iron-making

In this paper, we investigate the presence of economies of scale in the global iron-making industry for integrated steel plants, iron making being the first stage in the steel-making process. Iron making depends on basic commodities, such as iron ore, coke and various forms of energy, required in the operation of the blast furnace, which can be classified as essential inputs and used in fixed proportions to produce iron. A generalized Leontief cost function is estimated using panel data for 69 integrated plants, such a specification being appropriate for technologies with essential inputs that are used in fixed proportions in production. A significant scale effect is observed due to the existence of fixed costs and a linear dependence of the cost function on production. Under a simple linear cost function, a rough estimate of the breakeven scale of plant, where costs equal revenue, is 4.5 Mt per year. Competitiveness, as measured by the ratio of plant average cost per tonne to best practice cost per tonne, can be shown to be positively related to the scale of production as well as the cost of essential inputs. Therefore, low-cost producers are also often producers with low raw material costs and production levels below the estimated breakeven scale of operation. Labor costs, although significant, are comparatively less important as a driver towards low costs.     

Biodegradability of Poly (lactic acid), Preparation and Characterization of PLA/Gum Arabic Blends

In this study, the biodegradation of PLA films using microorganisms from Lake Bogoria (Kenya) were investigated. The biodegradation tests done using certain strains of thermophilic bacteria showed faster biodegradation rates and demonstrated temperature dependency. The biodegradation of the PLA films was studied using Gel Permeation Chromatography (GPC) and light microscopy. The biodegradation of PLA was demonstrated by decrease in molecular weight. The preparation and characterization of PLA/Gum Arabic blends were also investigated using DSC, TGA, TMA and NMR. In summary, the results obtained in this research show that PLA films undergo fast biodegradation using thermophiles isolated from Lake Bogoria. The PLA/GA blends studies show it is possible to prepare films of varying hydrophobic–hydrophilic properties for various applications.     

LEAP2000:可持续能源分析的工具

LEAP是由斯德哥尔摩环境研究所(SEI)波士顿中心领导的一项合作项目,旨在为一体化的能源环境分析建立一套新的分析软件和数据库.LEAP2000项目的产品应尽早获得以广为传播.     

The Bias of Complementarity Hotspots toward Marginal Populations

Abstract: It has been suggested that using complementarity to identify networks of important areas for conserving biodiversity may preferentially select areas within the margins of species ranges. We tested this idea by examining the location of complementarity hotspots in relation to two measures of range core-periphery. The first measures patterns of aggregation among records within each species' range to identify areas within the core (i.e., areas with aggregated distributions) and periphery (i.e., areas with scattered distributions) of the range. The second measures spatial turnover among species to identify areas with a high density of range edges. For three selected groups of terrestrial vertebrates in Europe—mammals, birds, and herptiles—areas chosen based on complementarity were located within the margins of species' ranges more often than expected by chance. This pattern was consistent for the two measures of core-periphery we used. The bias of complementarity hotspots toward marginal populations is especially important for species with restricted range sizes. If extinctions are determined mainly by demographic factors, then selecting areas at the peripheries of species' ranges might be a poor option. But if extinctions are determined mainly by extrinsic factors, then peripheral populations might be important to ensure the long-term persistence of species.     

Indices of Grassland Biodiversity in the Chihuahuan Desert Ecoregion Derived from Remote Sensing

Abstract: We used a relatively simple and direct remote-sensing approach to determine biodiversity values in arid ecosystems and thus identify potential conservation sites. We developed indices based on regression models between grass, shrub, litter, exposed-soil groundcover components, and Landsat thematic mapper satellite imagery reflectance values over a reference site in the northern Chihuahuan Desert in New Mexico. This site supports low-disturbance desert grasslands that have been excluded from livestock grazing for 55 years and moderate-disturbance grasslands that have been under a continuous grazing regime for over 100 years. Greater richness and abundance of noninvasive and nonruderal plant species were associated with the low-disturbance grasslands that had lower shrub abundance, increased litter and grass cover, and lower exposed soil. Using the thematic mapper indices, we computed an additive grassland biodiversity index such that, as exposed soil and shrub values go down, litter and grass values go up, as does the biodiversity index. When the biodiversity index was applied to the reference-site landscape, grasslands previously identified for their high conservation value were detected. As a further test, we applied the indices to a site in Chihuahua, Mexico, that supports similar grasslands but for which there are few other data on condition and conservation values. The soil, grass, and shrub indices were moderately effective in describing the range of variation at the Mexico site, but the litter equation was not. Still, higher biodiversity value in terms of nonruderal plant diversity tended to correspond to higher grass cover and lower soil exposure and a higher overall biodiversity index. Some localized calibration with geologic substrate may be required along with an assessment of the temporal constraints, but generally the index shows promise for quickly and efficiently detecting desert grasslands of high biodiversity conservation value.     

Estimating the aquatic emissions and fate of perfluorooctane sulfonate (PFOS) into the river Rhine

The sources, distribution, levels and sinks of perfluorooctane sulfonate (PFOS) estimated to be released from areas of high population density, have been explored using the river Rhine as a case study. A comparison between modelled and measured data is presented, along with analysis of the importance of PFOS sorption in riverine systems. PFOS releases into the Rhine were estimated to be 325-690 kg/yr based on per capita emission rates of 27-57 μg day(-1) from a population of 33 million living within a 50 km zone either side of the river. Sorption of PFOS to suspended particles and sediments may alter its fate in the aquatic environment. Therefore available measured and modelled partitioning data was assessed, and K(d) values (sorption coefficient) of 7.5 and 20 were selected. This resulted in sediment-water ratios of 23-76 : 1, which are similar to ratios reported in the literature, and resulted in modelled estimates that <20% of the total PFOS entering the Rhine binds to sediments or suspended particles. The calculated discharge from the Rhine to the North Sea based on measured data was 420-2200 kg/yr; our model predictions are in good agreement with these estimates. Emission trends were accurately predicted, suggesting population density can be effectively used as a surrogate for diffuse PFOS emissions from product use, while predicted concentrations were a factor of 2-4 below measured data showing the importance of other sources. Transfer of PFOS to sediment is estimated to be minimal, and consequently discharges to the North Sea are roughly equal to PFOS releases to river water.     

Factor analysis of H2S emission at a wastewater lift station: a case study

Odor and corrosion are common problems in domestic wastewater collection, transportation, pumping, and treatment processes. Based on the comparison among odorous compounds and onsite observations at a wastewater lift station, H₂S is more likely to have caused the odor and corrosion problems than methanethiol and other organic sulfides. The field data from both air and wastewater quality monitoring demonstrated that more H₂S (1 ppmv) was formed at a more negative redox potential, lower pH, and a higher temperature of wastewater. Since the lower detection level of most current analytical techniques is much greater than human’s smell and the reference concentration for adverse health effects, automatic monitoring on the threshold of H₂S formation provides a mechanism to trigger control techniques only when necessary for cost saving purposes. Based on Gibbs free energy, a more negative redox potential is required to form H₂S with an increase in pH and a decrease in temperature and SO ₄ ^2? concentration. However, pH effect is more significant than both temperature and SO ₄ ^2? concentration for H₂S formation. It is recommended that H₂S control techniques be started when the redox potential is below ?44 mV, the pH is lower than 5.6, and the temperature is higher than 11.5 °C to control H₂S below the reference concentration. Corroded concrete particles were examined by X-ray diffraction, which showed that the dominant crystal form was quartz.