Robust Energy Portfolios Under Climate Policy and Socioeconomic Uncertainty

Concerning the stabilization of greenhouse gases, the UNFCCC prescribes measures to anticipate, prevent, or minimize the causes of climate change and mitigate their adverse effects. Such measures should be cost-effective and scientific uncertainty should not be used as a reason for postponing them. However, in the light of uncertainty about climate sensitivity and other underlying parameters, it is difficult to assess the importance of different technologies in achieving robust long-term climate risk mitigation. One example currently debated in this context is biomass energy, which can be used to produce both carbon-neutral energy carriers, e.g., electricity, and at the same time offer a permanent CO₂ sink by capturing carbon from the biomass at the conversion facility and permanently storing it. We use the GGI Scenario Database IIASA [3] as a point of departure for deriving optimal technology portfolios across different socioeconomic scenarios for a range of stabilization targets, focusing, in particular, on new, low-emission scenarios. More precisely, the dynamics underlying technology adoption and operational decisions are analyzed in a real options model, the output of which then informs the portfolio optimization. In this way, we determine the importance of different energy technologies in meeting specific stabilization targets under different circumstances (i.e., under different socioeconomic scenarios), providing valuable insight to policymakers about the incentive mechanisms needed to achieve robust long-term climate risk mitigation.     

Statistical evaluation of photon count rate data for nanoscale particle measurement in wastewaters

The dynamic light scattering (DLS) technique can detect the concentration and size distribution of nanoscale particles in aqueous solutions by analyzing photon interactions. This study evaluated the applicability of using photon count rate data from DLS analyses for measuring levels of biogenic and manufactured nanoscale particles in wastewater. Statistical evaluations were performed using secondary wastewater effluent and a Malvern Zetasizer. Dynamic light scattering analyses were performed equally by two analysts over a period of two days using five dilutions and twelve replicates for each dilution. Linearity evaluation using the sixty sample analysis yielded a regression coefficient R(2) = 0.959. The accuracy analysis for various dilutions indicated a recovery of 100 ± 6%. Precision analyses indicated low variance coefficients for the impact of analysts, days, and within sample error. The variation by analysts was apparent only in the most diluted sample (intermediate precision ~12%), where the photon count rate was close to the instrument detection limit. The variation for different days was apparent in the two most concentrated samples, which indicated that wastewater samples must be analyzed for nanoscale particle measurement within the same day of collection. Upon addition of 10 mg l(-1) of nanosilica to wastewater effluent samples, the measured photon count rates were within 5% of the estimated values. The results indicated that photon count rate data can effectively complement various techniques currently available to detect nanoscale particles in wastewaters.     

Phosphorus recovery from wastewater--expert survey on present use and future potential

Today, a variety of different approaches to the recovery of phosphorus from wastewater, sludge, and sludge ash exist. These approaches differ basically by the origin of the used matter (wastewater, sludge liquor, fermented or nonfermented sludge ash) and the process (precipitation, wet-chemical extraction, and thermal treatment). To rate them according to their characteristics, the latter were phrased as hypotheses and subjected to an international expert survey. The survey showed that phosphorus recovery is expected to become an established process over the next 20 years in industrialized countries for economic reasons. A decisive aspect in this regard will be the quality of the produced fertilizer. Simple technologies such as the recovery from sludge liquor seem to be preferred. If sludge is incinerated, phosphorus recycling from ash then becomes more interesting and has to be considered. Phosphorus recovery and source-separating sanitation technologies are more appropriate for industrialized countries than for developing countries. Because the growing awareness of environmental issues will prevent sludge from being used agriculturally in an increasing number of countries in the next decade, the market potential for nutrient recovery technologies will increase in the immediate future.     

Organochlorine pesticides and polychlorinated biphenyls in air and soil across Azerbaijan

Concentrations of selected organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) are reported in air and surface soil in an extensive spatial survey across Azerbaijan, a country bordering the Caspian Sea with a history of OCP production and extensive use. Polyurethane foam disc passive air samplers (PAS) were deployed during October-November 2008 with soil samples collected in July 2009. Levels of Σ(7)PCB in ambient air were generally low (mean of 0.046 ng m(-3), n?=?13) and comparable to concentrations reported in countries within Eastern Europe and similar to or lower than concentrations reported in urban air in the UK and other western countries. Surprisingly, PCB concentrations in rural/background soil fell below the method detection limits at most sites, although concentrations were 0.209 and 0.071 ng Σ(7)PCB g(-1) dry weight (dw) for two urban sites, again comparable to PCB levels measured at background sites in Europe. Levels of α-HCH, β-HCH, γ-HCH and p,p'-DDT/E were elevated in ambient air across Azerbaijan in comparison to PAS-derived concentrations reported elsewhere, with concentrations of α-HCH in air ranging from 0.085 to 2.699 ng m(-3) and p,p'-DDE, 0.037-2.290 ng m(-3). High concentrations of OCPs occurred at several of the urban sites and at sites in proximity to old pesticide storage facilities with concentrations in soil >0.1 μg g(-1) dw for p,p'-DDE and p,p'-DDT at several sites. The ratio of p,p'-DDT/p,p'-DDE was close to unity in the soil at these sites, but elsewhere, the ratio was <1, indicating a weathered DDT pattern, which was also reflected in the air at all sites. A fugacity approach revealed the strong likelihood of net soil-to-air transfer at the majority of sites for all OCPs. The calculated annual fluxes or loading to the atmosphere from a rural/agricultural area (representing land as vineyards and cotton cultivation) were estimated to be on the order of ≈10-100 kg year(-1) for the HCH isomers (including the β -isomer) and p,p'-DDE. The high levels of OCPs in soils, particularly in the vicinity of obsolete-pesticide storage facilities and at select urban sites are of concern and warrant regular monitoring activities and the development of containment or mitigation strategies.     

Selective Lead(II) Adsorption and Flocculation Characteristics of the Grafted Sodium Alginate: A Comparative Study

Synthesis of sodium alginate-g-poly(acrylamide-co-N-methylacrylamide) [S-III], sodium alginate-g-poly(N-methylacrylamide-co-N,N-dimethylacrylamide) [S-II], sodium alginate-g-poly(acrylamide-co-N,N-dimethylacrylamide) [S-I]. Sodium alginate-g-poly(N,N-dimethylacrylamide) [SAG-g-PDMA] and sodium alginate-g-poly(acrylamide) [SAG-g-PAM] were prepared by solution polymerization technique using potassium peroxydisulfate as the initiator at 70?°C in water medium. The graft copolymers were characterized by FTIR and NMR (¹H and ¹³C) spectroscopy, SEM and XRD studies. All the five graft copolymers were used to remove Pb(II) ions from the aqueous solution and also in flocculation studies of kaolin clay (1.0 wt%), silica (1.0 wt%) and iron ore slime (0.25 wt%) suspensions. A comparative studies of all the five graft copolymers were also made in both the two cases. The Pb(II) ion removal capacity of all the graft copolymers follows the order S-III?>?SAG-g-PAM?>?S-II?>?SAG-g-PDMA?>?S-I. But the flocculation performance of the graft copolymers follows the order S-II?>?S-I?>?S-III?>?SAG-g-PDMA?>?SAG-g-PAM. S-III was also used for the competitive metal ion removal with Hg(II), Cd(II), Cu(II) and Zn(II). Pb(II) adsorption of S-III (the best Pb(II) ion adsorber) follows pseudo second order rate equation and Langmuir adsorption isotherm.     

Thermo- and fluid-dynamical modelling of two-phase multi-component carbon dioxide mixtures

A method for calculating the transport and depressurization of a two-phase multi-component CO₂ mixture is presented. The thermodynamical and transport properties for a CO₂–CH₄ mixture are calculated using the Soave–Redlich–Kwong equation of state (SRK). The fluid flow is described by a drift-flux model, which is solved using the multi-stage (MUSTA) centred scheme. Numerical results are shown, illustrating the effect of mixture composition and the feasibility of the approach.     

Alkyl nitrate photochemistry during the tropospheric organic chemistry experiment

Alkyl nitrates (C₁–C₅) were measured at two sites (near urban and rural) in southeast England during the Tropospheric Organic Chemistry Experiment (TORCH). Methyl nitrate was the dominant species during both campaigns accounting for on average about one third of the total measured alkyl nitrates. High mixing ratios (>50 pptv) and variability of methyl nitrate were observed at the near urban site (TORCH1) that were not seen at the rural site (TORCH2) and which could not be explained by local photochemical production or direct emissions. The diurnal variation of methyl nitrate during TORCH1 showed a morning maximum that would be consistent with nighttime chemistry followed by transport to the surface by boundary layer dynamics. Similarly, elevated morning mixing ratios were also observed during TORCH2 although the magnitudes were much smaller. As a result, methyl nitrate could represent a tracer for nighttime chemistry seen at the ground the following day. At both campaigns, the dominant source of short chain alkyl nitrates and carbonyl precursor radicals (≤C₄) were from decomposition of larger compounds. The magnitude of the source increased with decreasing carbon number consistent with increasing total precursor abundance. Non-photochemical emissions of acetaldehyde and acetone could not be accounted for by automobile exhaust emissions alone and indicated that other direct sources are likely important in this environment.     

Volatile aldehydes in libraries and archives

Volatile aldehydes are produced during degradation of paper-based materials. This may result in their accumulation in archival and library repositories. However, no systematic study has been performed so far. In the frame of this study, passive sampling was carried out at ten locations in four libraries and archives. Despite the very variable sampling locations, no major differences were found, although air-filtered repositories were found to have lower concentrations while a non-ventilated newspaper repository exhibited the highest concentrations of volatile aldehydes (formaldehyde, acetaldehyde, furfural and hexanal). Five employees in one institution were also provided with personal passive samplers to investigate employees’ exposure to volatile aldehydes. All values were lower than the presently valid exposure limits.The concentration of volatile aldehydes, acetic acid, and volatile organic compounds (VOCs) in general was also compared with that of outdoor-generated pollutants. It was evident that inside the repository and particularly inside archival boxes, the concentration of VOCs and acetic acid was much higher than the concentration of outdoor-generated pollutants, which are otherwise more routinely studied in connection with heritage materials. This indicates that further work on the pro-degradative effect of VOCs on heritage materials is necessary and that monitoring of VOCs in heritage institutions should become more widespread.     

Polycyclic aromatic hydrocarbons in air on small spatial and temporal scales – I. Levels and variabilities

Polycyclic aromatic hydrocarbons (PAHs) were measured together with inorganic air pollutants at two urban sites and one rural background site in the Banja Luka area, Bosnia and Hercegovina, during 72 h in July 2008 using a high time resolution (5 samples per day) with the aim to study the spatial and temporal variabilities and to explore the significance of averaging effects inherent to 24 h-sampling. Measurement uncertainty was quantified on basis of three independent side-by-side samplers, deployed at one of the sites.PAH abundances in the urban and rural environments differed largely. Levels at the urban sites exceeded the levels at the rural site by >100%. The discrepancy was largely dominated by emission of 3–4 ring PAHs in the city, while 5–6 ring PAHs were more evenly distributed between city sites and the hill site. During the night a higher fraction of the semivolatile PAHs might have been stored in the soil or sorbed to surfaces. PAH patterns were undistinguishable across the three sites. However, concentrations of more particle-associated substances differed significantly between the urban sites than between one of the urban sites and the rural site (3σ uncertainty). Time-averaging (on a 24 h-basis) would have masked the significant inter-site differences of half of the substances which were found at different levels (on a 4 h-basis).     

Fish from industrially polluted freshwater as the main source of organochlorinated pollutants and increased frequency of thyroid disorders and dysglycemia

In a certain area of Michalovce district in East Slovakia, heavy industrial pollution by polychlorinated biphenyls (PCBs) developed in 1955-1984 and very high PCB levels in environmental and human samples are still persisting. Recently, a total of 2045 adults from this and the surrounding background pollution area have been examined using questionnaire data, thyroid volume by ultrasound (ThV), urinary iodine and serum levels of 15 PCB congeners, hexachlorobenzene (HCB), 2,2'-2-bis(4-chlorobiphenyl)-1,1-dichloroethylene (DDE), 2,2'-bis(4-chlorophenyl)-1,1,1-trichloroethane (DDT), alpha-, beta- and gamma-hexachlorocyclohexane (HCH), thyrotropin (TSH), free thyroxine (FT4), anti-thyroperoxidase antibodies (TPOab) and fasting glucose. As based on our previous findings of strikingly high level of PCBs in fish from high pollution area (e.g. mean level of 375430 ng/g lipid) and considerably lower, but still relatively high level in background pollution area (e.g. mean PCB level of 5150 ng/g), the information on the frequency of fish meals and approximate annual consumption of fish from local waters was obtained by questionnaires. The association of contaminated fish consumption with very high blood levels of PCBs, DDE and HCB and increased ThV as well as with increased frequency of positive TPOab, high values of FT4 and impaired fasting glucose (IFG) was found. These associations were also confirmed in 16 marital pairs from high pollution area with very high PCB level in both members associated with high fish consumption. It was concluded that, due to persistent heavy pollution of waters, soil and food chain namely by PCBs, but also by pesticides (e.g. DDE and HCB) resulting from their previous extensive use in agriculture, the fish from local waters still remains the most important source of these toxic pollutants which results in considerable adverse health effects.