Life cycle modelling of environmental impacts of application of processed organic municipal solid waste on agricultural land (EASEWASTE).

A model capable of quantifying the potential environmental impacts of agricultural application of composted or anaerobically digested source-separated organic municipal solid waste (MSW) is presented. In addition to the direct impacts, the model accounts for savings by avoiding the production and use of commercial fertilizers. The model is part of a larger model, Environmental Assessment of Solid Waste Systems and Technology (EASEWASTE), developed as a decision-support model, focusing on assessment of alternative waste management options. The environmental impacts of the land application of processed organic waste are quantified by emission coefficients referring to the composition of the processed waste and related to specific crop rotation as well as soil type. The model contains several default parameters based on literature data, field experiments and modelling by the agro-ecosystem model, Daisy. All data can be modified by the user allowing application of the model to other situations. A case study including four scenarios was performed to illustrate the use of the model. One tonne of nitrogen in composted and anaerobically digested MSW was applied as fertilizer to loamy and sandy soil at a plant farm in western Denmark. Application of the processed organic waste mainly affected the environmental impact categories global warming (0.4-0.7 PE), acidification (-0.06 (saving)-1.6 PE), nutrient enrichment (-1.0 (saving)-3.1 PE), and toxicity. The main contributors to these categories were nitrous oxide formation (global warming), ammonia volatilization (acidification and nutrient enrichment), nitrate losses (nutrient enrichment and groundwater contamination), and heavy metal input to soil (toxicity potentials). The local agricultural conditions as well as the composition of the processed MSW showed large influence on the environmental impacts. A range of benefits, mainly related to improved soil quality from long-term application of the processed organic waste, could not be generally quantified with respect to the chosen life cycle assessment impact categories and were therefore not included in the model. These effects should be considered in conjunction with the results of the life cycle assessment.     

Leaching and crop uptake of nitrogen and phosphorus from pig slurry as affected by different application rates

The influence of increasing pig slurry applications on leaching and crop uptake of N and P by cereals was evaluated in a 3-yr study of lysimeters filled with a sandy soil. The slurry was applied at N rates of 50 (S50), 100 (S100), 150 (S150), and 200 (S200) kg ha(-1) during 2 of the 3 yr. The P rates applied with slurry were: 40 (S50), 80 (S100), 120 (S150), and 160 (S200) kg ha(-1) yr(-1). Simultaneously, NH4NO3 and Ca(H2PO4)2 were applied at rates of 100 kg N ha(-1) and 50 kg P ha(-1), respectively, to additional lysimeters (F100), while others were left unfertilized (F0). During the 3-yr period, the leaching load of total N tended to increase with increasing slurry application to, on average, 139 kg ha(-1) at the highest application rate (S200). The corresponding N leaching loads (kg ha(-1)) in the other treatments were: 75 (F0), 103 (F100), 93 (S50), 120 (S100), and 128 (S150). The loads of slurry-derived N in the S100, S150, and S200 treatments were significantly larger (P < 0.05) than those of fertilizer-derived N. In contrast, P leaching tended to decrease with increasing input of slurry, and it was lower in all treatments that received P at or above 50 kg P ha(-1) yr(-1) with slurry or fertilizer than in the unfertilized treatment. The crop use efficiency of added N and P was clearly higher when NH4NO3 and Ca(H2PO4)2 were used rather than slurry (60 vs. 35% for N, 38 vs. 6-9% for P), irrespective of slurry application rate. Therefore, from both a production and water quality point of view, inorganic fertilizers seem to have environmental benefits over pig slurry when used on sandy soils.     

Can Repeated Fertilizer Applications to Young Norway Spruce Enhance Avian Diversity in Intensively Managed Forests?

Repeated fertilization of forests to increase biomass production is an environmentally controversial proposal, the effects of which we assessed on breeding birds in stands of young Norway spruce (Picea abies), in an intensively managed forest area in southern Sweden. Our results show that fertilized stands had 38% more species and 21% more individuals than unfertilized stands. Compared with stands under traditional management, the further intensification of forestry by repeated applications of fertilizers thus seemed to enhance species richness and abundance of forest birds. We cannot conclude at this stage whether the response in the bird community was caused by changes in food resources or increased structural complexity in the forest canopy due to the skid roads used for the application of the fertilizers. Future studies should focus on structural and compositional effects of fertilization processes during the entire rotation period and at assessing its effects in a landscape context.     

Analysis of safety functions and barriers in accidents

A new method for accident investigations is presented. It is based on the concept of safety function, which is defined as a technical or organisational function, a human action or a combination of these, that can reduce the probability and/or consequences of accidents and other unwanted events in a system. An analysis starts with the identification of safety functions related to the event. These are structured; an assessment is then made of whether they worked or not, and finally safety improvements are proposed.The method has been applied to five different incidents, coming from different types of work sites, such as electrical power distribution, a railway, and hospitals. For each case, around 40 safety functions were identified, of which less than half had worked. It was found that technical, organisational and human safety features existed side-by-side. The method supports a consistent analysis of a variety of safety features, and can integrate them into a common format.Each system contained formal and informal elements in parallel, often overlapping. This can be seen as safety redundancy, which makes the safety system less vulnerable to change that supports the preservation of safety. It might be more adequate to describe this as a safety web rather than a distinct set of barriers, and there is also an analogy with the concept of safety resilience.     

The influence of cosolvent and heat on the solubility and reactivity of organophosphorous pesticide DNAPL alkaline hydrolysis

The presented research concerned the compatibility of cosolvents with in situ alkaline hydrolysis (ISAH) for treatment of organophosphorous (OPP) pesticide contaminated sites. In addition, the influence of moderate temperature heat increments was studied as a possible enhancement method. A complex dense non-aqueous phase liquid (DNAPL) of primarily parathion (~50 %) and methyl parathion (~15 %) obtained from the Danish Groyne 42 site was used as a contaminant source, and ethanol and propan-2-ol (0, 25, and 50 v/v%) was used as cosolvents in tap water and 0.34 M NaOH. Both cosolvents showed OPP solubility enhancement at 50 v/v% cosolvent content, with slightly higher OPP concentrations reached with propan-2-ol. Data on hydrolysis products did not show a clear trend with respect to alkaline hydrolysis reactivity in the presence of cosolvents. Results indicated that the hydrolysis rate of methyl-parathion (MP3) decreased with addition of cosolvent, whereas the hydrolysis rate of ethyl-parathion (EP3) remained constant, and overall indications were that the hydrolysis reactions were limited by the rate of hydrolysis rather than NAPL dissolution. In addition to cosolvents, the influence of low-temperature heating on ISAH was studied. Increasing reaction temperature from 10 to 30 °C provided an average rate of hydrolysis enhancement by a factor of 1.4–4.8 dependent on the base of calculation. When combining 50 v/v% cosolvent addition and heating to 30 °C, EP3 solubility was significantly enhanced and results for O,O-diethyl-thiophosphoric acid (EP2 acid) showed a significant enhancement of hydrolysis as well. However, this could not be supported by para-nitrophenol (PNP) data indicating the instability of this product in the presence of cosolvent.

     

Fire Tests on E-vehicle Battery Cells and Packs

Objective: The purpose of this study was to investigate the effects of abuse conditions, including realistic crash scenarios, on Li ion battery systems in E-vehicles in order to develop safe practices and priorities when responding to accidents involving E-vehicles.

Method: External fire tests using a single burning item equipment were performed on commercial Li ion battery cells and battery packs for electric vehicle (E-vehicle) application. The 2 most common battery cell technologies were tested: Lithium iron phosphate (LFP) and mixed transition metal oxide (lithium nickel manganese cobalt oxide, NMC) cathodes against graphite anodes, respectively. The cell types investigated were “pouch” cells, with similar physical dimensions, but the NMC cells have double the electric capacity of the LFP cells due to the higher energy density of the NMC chemistry, 7 and 14 Ah, respectively.

Heat release rate (HRR) data and concentrations of toxic gases were acquired by oxygen consumption calorimetry and Fourier transform infrared spectroscopy (FTIR), respectively.

Results: The test results indicate that the state of charge (SOC) affects the HRR as well as the amount of toxic hydrogen fluoride (HF) gas formed during combustion. A larger number of cells increases the amount of HF formed per cell. There are significant differences in response to the fire exposure between the NMC and LFP cells in this study. The LFP cells generate a lot more HF per cell, but the overall reactivity of the NMC cells is higher. However, the total energy released by both batteries during combustion was independent of SOC, which indicates that the electric energy content of the test object contributes to the activation energy of the thermal and heat release process, whereas the chemical energy stored in the materials is the main source of thermal energy in the batteries.

Conclusions: The results imply that it is difficult to draw conclusions about higher order system behavior with respect to HF emissions based on data from tests on single cells or small assemblies of cells. This applies to energy release rates as well. The present data show that mass and shielding effects between cells in multicell assemblies affect the propagation of a thermal event.     

Dissolution of a CO2 lake, modeled by using an advanced vertical turbulence mixing scheme

The dissolution of CO₂ from a CO₂ lake with and without a hydrate layer, located at a flat bottom at 3000 m depth has been modeled using the MIT General Circulation Model coupled with the General Ocean Turbulence Model (GOTM). The vertical turbulent mixing scheme takes into account density effects and should give more realistic results for the CO₂ plume than previously used constant eddy diffusivity models. The introduction of a third direction gives qualitatively different results for the spreading of the CO₂ plume than previous 2D results. The dissolution rate and near field dissolved CO₂ concentrations approach a steady state for a given far field ocean current within less than a day. The dissolution rate is highly dependent on the velocity of the ambient current and is reduced with 1.6 when a hydrate layer is introduced.