Motor-vehicle boarding and alighting injury--how large a problem?

The Journal of Safety Research has partnered with the National Center for Injury Prevention and Control at the Centers for Disease Control and Prevention (CDC) in Atlanta, Georgia, USA, to briefly report on some of the latest findings in the research community. This report is the fifth in a series of CDC articles.     

Characterization and modeling of nutrient-deficient tomato-processing wastewater treatment using an anaerobic/aerobic system

Tomato-processing wastewaters are typical of slowly biodegradable high strength wastewaters generated from the food canning industry. Three different samples of influent and three samples of anaerobic effluents corresponding to the three influents collected from an on-site pilot-scale anaerobic/aerobic system were characterized using respirometric methods. Respirometric studies demonstrated that the pretreatment in the anaerobic reactor of the pilot-scale system increased the readily biodegradable fraction from an average of 40% of the SCOD in the influent to 50% of the SCOD in the anaerobic effluent, improved kinetics from an average micro(max) of 1.5d(-1) in the influent to 3.5d(-1) in the anaerobic effluent, and eliminated nutrient deficiency. Furthermore, the system was calibrated and simulated by application of wastewater characterization and biokinetic data derived form respirometric tests of influent and anaerobic effluent in Activated Sludge Model no.1 (ASM1).     

Prediction models for the flash point of pure components

The flash point for a liquid is defined as the lowest temperature at which its vapor forms a spontaneously ignitable mixture when brought in contact with air. Having a good estimation of the flash point temperature at normal conditions is relevant because it is one of the main properties used to characterize fire and explosion hazards for liquids. Most of predictive correlations in the literature include a physical effect by including the normal boiling temperature in their formulation. To achieve combustion, sufficient evaporation is required and then a part of the liberated energy from the combustion is used to support the evaporation. Thus the evaporation energy and a chemical effect given by the heat of reaction are incorporated in this work. It is firstly verified that the relation between the flash point temperature and the normal boiling temperature tends to be a constant. Thus a heuristic approach based on 611 chemical species of diverse families indicates that this relation is around 0.75. The dispersion of the error has been reduced by using two proposed correlations where both physical and chemical properties are included in the model. In particular, the second equation is based on the group contributions method, which has been developed for alkanes. This method is in fact a combination of the group contributions method and the first model to overcome the difficulties in predicting isomeric differences.     

Removal of arsenate from water by adsorbents: a comparative case study

Laboratory and field filtration experiments were conducted to study the effectiveness of As(V) removal for five types of adsorbent media. The media included activated alumina (AA), modified activated alumina (MAA), granular ferric hydroxide (GFH), granular ferric oxide (GFO), and granular titanium dioxide (TiO?). In laboratory batch and column experiments, the synthetic challenge water was used to evaluate the effectiveness for five adsorbents. The results of the batch experiments showed that the As(V) adsorption decreased as follows at pH 6.5: TiO? > GFO > GFH > MAA > AA. At pH 8.5, however, As(V) removal decreased in the following order: GFO = TiO? > GFH > MAA > AA. In column experiments, at pH 6.5, the adsorbed As(V) for adsorbents followed the order: TiO? > GFO > GFH, whereas at pH 8.5 the order became: GFO = TiO? > GFH when the challenge water containing 50 μg/L of As(V) was used. Field filtration experiments were carried out in parallel at a wellhead in New Jersey. Before the effluent arsenic concentration increased to 10 μg/L, approximately 58,000 and 41,500 bed volumes of groundwater containing an average of 47 μg/L of As(V) were treated by the filter system packed with GFO and TiO?, respectively. The As(V) adsorption decreased in the following sequence: GFO > TiO? > GFH > MAA > AA. Filtration results demonstrated that GFO and TiO? adsorbents could be used as media in small community filtration systems for As(V) removal.     

Effect of biochar on fate and transport of manure-borne estrogens in sandy soil

The feasibility of using two types of biochars to reduce steroid hormone pollution from poultry and swine manure application on agricultural land was evaluated.The sorption affinity and desorption resistance of softwood and hardwood biochars were also determined for two estrogen hormones,17β-estradiol(E2) and its primary metabolite estrone(E1).The softwood and hardwood biochars demonstrated high retention capacity for both estrogens.The effective distribution coefficient(K_d~(eff)) of soil-softwood-derived biochar(SBS_(450)) was significantly higher than soil-hardwood-derived biochar(SBH750),indicating the stronger sorption affinity of SBS450 for estrogens.To validate the laboratory results,a field lysimeter experiment was conducted to study the fate and transport of E2 and E1 in soil and leachate in the presence of 1% softwood-biochar(BS450) in topsoil and to compare it with soil without any amendments.The spatio-temporal distribution of both estrogens was monitored at four depths over a 46-day period.The lysimeters,in which the surface layer of soil was amended with biochar,retained significantly higher concentrations of both estrogen hormones.Although they leached through the soil and were detected in leachates,collected at 1.0 m depth,the concentrations were significantly lower in the leachate collected from biochar-amended lysimeters.The result confirmed the efficacy of biochar amendment as a remediation technique to alleviate the manure-borne hormonal pollution of groundwater.     

Pyrethrins and piperonyl butoxide residues on potato leaves and in soil under field conditions.

Residues of pyrethrin-I (Py-I) and pyrethrin-II (Py-II), the major insecticidal components of the pyrethrum daisy (Tanacetum cinerariifolium) as well as residues of piperonyl butoxide (PBO, a pyrethrum synergist) were determined in soil and on potato foliage grown under field conditions. A pyrethrum formulation (Multi-Purpose Insecticide) containing the three active ingredients was sprayed twice at the rate of 6 lbs of formulated product.acre(-1) ( 5.4 and 27.2 g A.I. of pyrethrin and PBO, respectively) on potato foliage during the growing season. In soil, three management practices (yard waste compost, grass filter strips, and a no mulch treatment) were used to study the impact of surface soil characteristics on the amount of pyrethrins (Pys) and PBO retained in soil. Soil samples and potato leaves were collected at different time intervals after spraying. Samples were purified and concentrated using solid-phase extraction columns containing C18-Octadecyl bonded silica. Residues were quantified by high-performance liquid chromatograph equipped with a UV detector. The first spray resulted in mean initial deposits of 0.18, 0.40, and 0.99 microg.g(-1) potato leaves for Py-I, Py-II, and PBO, respectively. Residues in soil were higher in compost treatments compared to no mulch treatments.     

Lichens reveal air PAH fractionation in the Himalaya

This paper shows that gas/particulate phase partitioning of polycyclic aromatic hydrocarbons (PAHs) can be monitored using lichens. Anthropogenic sources are responsible for the release of PAHs, which are bioaccumulated in plants at various spatial scales based on their physicochemical properties. Atmospheric PAHs are distributed both in the gaseous and particulate states. Here, a lichen species, Dermatocarpon vellereum Zschacke, has been collected at different altitudes in and around the Rudraprayag valley, located in Central Himalayan region of India, in order to study the spatial distribution of PAHs in the valley. Results show that PAH concentration ranged from 0.136 to 4.96 μg g^?1. Findings reveal that the bioaccumulation of 2- and 3-ringed PAHs was higher in high-altitude samples, whereas bioaccumulation of fluoranthene, a 4-ringed PAH, showed higher concentration in samples from localities away from town centre. 5- and 6-ring PAHs were then confined to the lower altitude at the base of the valley, thus justifying their particulate-bound nature. This is the first report showing the utility of lichen to biomonitor PAHs in the Himalayan ecosystem.     

Lichens to distinguish urban from industrial PAHs

This paper shows that lichens can be used as biomonitors to distinguish urban from industrial polycyclic aromatic hydrocarbons (PAHs). PAHs are atmospheric pollutants originating mainly from incomplete combustion of fuels in vehicles and industry. The occurrence of PAHs in air is a serious health issue in urban areas and industrial areas because some PAHs are carcinogenic. Biomonitoring PAHs with lichens is generally applied for quantification of PAHs. However, the precise sources of PAHs are not well known. Here we use lichen to trace the source of PAHs. PAHs were analyzed in Pyxine subcinerea Stirton, a lichen species collected from twelve sites which vary from urban and industrial to periurban forest area of Haridwar, in the foothills of the Indian Himalayas. Total PAH concentration ranged between 1.25 and 187.3 μg g⁻¹. Results indicate a clear distinction between urban and industrial PAHs profile, using principal component analysis. Lichen sampled from industrial sites exhibited higher concentrations of two-, five-, and six-ringed PAHs, up to 60% of total PAHs, while samples from urban sites were dominated by four-ringed PAHs, predominantly fluoranthene and acenaphthylene. Molecular ratios indicate that combustion was the dominant source of origin of PAHs in industrial area, while urban sites showed mixed origin of PAHs, both pyro- and petrogenic.     

Economics and GHG emission reduction of a PLA bio-refinery system—Combining bottom-up analysis with price elasticity effects

This paper analyses energy savings, GHG emission reductions and costs of bio-refinery systems for polylactic acid (PLA) production. The systems comprise ‘multi-functional’ uses of biomass resources, i.e. use of agricultural residues for energy consumption, use of by-products, and recycling and waste-to-energy recovery of materials. We evaluate the performance of these systems per kg of bio-based polymer produced and per ha of biomass production. The evaluation is done using data of Poland assuming that biomass and PLA production is embedded in a European energy and material market. First, the performance of different bio-refinery systems is investigated by means of a bottom-up chain analysis. Second, an analysis is applied that derives market prices of products and land depending on the own-price elasticity of demand. Thus, the costs of bio-refinery systems depending on the demand of land and material are determined. It is found that all PLA bio-refinery systems considered lead to net savings of non-renewable energy consumption of 70–220 GJ/(ha yr) and net GHG emission reductions of 3–17 Mg CO_2eq/(ha yr). Most of these PLA bio-refinery systems lead to net costs for the overall system of up to 4600 €/(ha yr). PLA production from short rotation wood leads to net benefits of about 1100 €/(ha yr) if a high amount of a high value product, i.e. fibres, is produced. Multi-functionality is necessary to ensure the viability of PLA bio-refinery systems from biomass with regard to energy savings and GHG emission reduction. However, the multi-functional use of biomass does not contribute much to overall incomes. Multifunctional biomass use – especially the use of biomass residues for energy consumption – contributes significantly to savings of non-renewable energy sources. Own-price elasticity of the demand for materials influences the overall costs of the bio-refinery system strongly. The own-price elasticity of land demand markets could become important if bio-refineries are introduced on a large scale.