Prospects in straw disintegration for biogas production

The pretreatment methods for enhancing biogas production from oat straw under study include hot maceration, steam explosion, and pressure shockwaves. The micropore area (9, 55, and 64 m² g^-1) inhibitor formations (0, 15, and 0 mL L^-1) as well as the overall methane yields (67, 179, and 255 CH₄ VS t^-1) were robustly analyzed. It was confirmed that the operating conditions of the steam explosion must be precisely tailored to the substrate. Furthermore, it was beneficial to prepend the hot maceration before the steam explosion and the pressure shockwaves. The second alternative may give increased methane yields (246 in comparison to 273 CH₄ VS t^-1); however, the application of pressure shockwaves still faces limitations for deployment on a commercial scale.     

Einschätzung der Konzentrationsprofile polyzyklischer aromatischer Kohlenwasserstoffe (PAK) in Böden des Biosphärenreservates Spreewald

To work out background values, the information of concentration profiles of PAHs in soils of uncontaminated territories is indispensable. This investigation shows PAH concentrations of different soil samples like agricultural soils, grassland, forest and litter from the biosphere reserve in Spreewald, Germany. The mean values of the soil samples are about 460 μg Σ-PAK/kg d.m. A top value of 7.2 mg Σ-PAK/kg d.m. shows a sample of a flooded grassland area. The relation of the concentrations in the litter, forest, grassland and agricultural soil samples is about 5∶3∶2∶1. Compared to the other samples, the litter samples contain a higher amount of low molecular PAHs. Increasing distance to the former power plants Lübbenau and Vetschau (brown coal) lead to decreasing PAH contents in the soil samples of forests from 2190.9 after 4 km to 294.8 Σ-PAK/kg d.m. after 16 km. In comparison to results obtained in Nordrhein-Westfalen and Bayern, the PAH measurements indicate Spreewald to be an uncontaminated and rural area.     

Determination of Hg and diet identification in otter (Lontra longicaudis) feces

An analytical procedure for the determination of Hg in otter (Lontra longicaudis) feces was developed, to separate fish scales for the identification of the animal diet. Samples were washed with ultra-pure water and the suspension was sampled and transferred for digestion. The solubilization was performed with nitric-perchloric acid mixture, and detection carried out by the atomic fluorescence spectrometry (AFS). The quality of the analytical procedure was assessed by analyzing in-house standard solutions and certified reference materials. Total Hg concentrations were in the range of 7.6-156 ng g(-1) (July 2004), 25.6-277 ng g(-1) (January 2005) and 14.6-744 ng g(-1) (May 2005) that is approximately the same order of magnitude for all samples collected in two reservoirs at the Tiete River, Brazil. Although Hg concentrations varied with sampling periods and diet, high levels were correlated to the percentage of carnivorous fish scales present in the otter feces.     

Anaerobic biodegradation of high strength 2-chlorophenol-containing synthetic wastewater in a fixed bed reactor

In this study the continuous treatment of 2-chlorophenol (2-CP) containing synthetic wastewater at increasing concentrations up to 2600 mg L-1 in an anaerobic fixed bed reactor was achieved. As a source of microorganisms municipal sewage sludge was acclimatised to maximally 50 mg L-1 2-CP by 3 successive feedings within 1.5 months. Then, an anaerobic fixed bed reactor was inoculated with this sludge and was operated for 318 d, during which the 2-CP influent concentration was stepwise increased from 50 to 2600 mg L-1 within 265 d. At a hydraulic retention time (HRT) of 2.2 d the 2-CP loading rate was 2 g L-1 d-1 and the average 2-CP removal rate was 0.87 g L-1 d-1, accounting for 73% removal. This is the highest 2-CP removal rate ever reported. The negative effect of a 2-CP loading rate of 1.36 g L-1 d-1 on 2-CP removal was reversible within 2 wk when lower loading conditions (e.g. 0.76 g 2-CP L-1 d-1) were re-established. The median chloride ion release per unit 2-CP degraded was 0.24, which was reasonably close to the theoretically expected value of 0.28. In a batch assay, carried out with relatively clear reactor effluent, the highest removal rate of 2-CP was 175 mg L-1 d-1. At the time of reactor termination on day 318, the 2-CP removal rate by the biofilm in the reactor was 0.61 g L-1 d-1, corresponding to a HRT of 3.4 d and a 2-CP loading rate of 0.76 g L-1 d-1. At these very stable conditions removal of COD was 84% and of 2-CP 81%     

Application of an Environmental Decision Support System to a Water Quality Trading Program Affected by Surface Water Diversions

Environmental decision support systems (EDSSs) are an emerging tool used to integrate the evaluation of highly complex and interrelated physicochemical, biological, hydrological, social, and economic aspects of environmental problems. An EDSS approach is developed to address hot-spot concerns for a water quality trading program intended to implement the total maximum daily load (TMDL) for phosphorus in the Non-Tidal Passaic River Basin of New Jersey. Twenty-two wastewater treatment plants (WWTPs) spread throughout the watershed are considered the major sources of phosphorus loading to the river system. Periodic surface water diversions to a major reservoir from the confluence of two key tributaries alter the natural hydrology of the watershed and must be considered in the development of a trading framework that ensures protection of water quality. An EDSS is applied that enables the selection of a water quality trading framework that protects the watershed from phosphorus-induced hot spots. The EDSS employs Simon’s (1960) three stages of the decision-making process: intelligence, design, and choice. The identification of two potential hot spots and three diversion scenarios enables the delineation of three management areas for buying and selling of phosphorus credits among WWTPs. The result shows that the most conservative option entails consideration of two possible diversion scenarios, and trading between management areas is restricted accordingly. The method described here is believed to be the first application of an EDSS to a water quality trading program that explicitly accounts for surface water diversions.     

Organic pollutants in compost and digestate. Part 2. Polychlorinated dibenzo-p-dioxins, and -furans, dioxin-like polychlorinated biphenyls, brominated flame retardants, perfluorinated alkyl substances, pesticides, and other compounds

Compost and digestate are important recycling fertilizers and have beneficial effects on soil parameters. However, they can contain significant amounts of organic pollutants. Here, the first comprehensive data set on dibenzo-p-dioxins and -furans (PCDD/F), dioxin-like polychlorinated biphenyls (DL-PCB), brominated flame retardants, perfluorinated alkyl substances (PFAS), pesticides, phthalates, nonylphenol and chlorinated paraffins (CP) in source-separated compost and digestate from Switzerland is presented (n = 3-18). The median summation 17PCDD/F and summation 12DL-PCB concentrations were at 3.2 ng I-TEQ kg(-1)dry weight (dw) and 3.0 ng WHO-TEQ kg(-1)dw, respectively. Brominated diphenyl ether 209 (BDE 209) accounted for 72% of the total polyBDE content (10 microg kg(-1)dw). Hexabromocyclododecane (HBCD) and tetrabromobisphenol A (TBBPA) levels were at 100 and 0.51 microg kg(-1)dw, respectively. PFAS were identified for the first time in compost and digestate (median concentration 6.3 microg kg(-1)dw, summation 21compounds). Out of 269 pesticides analysed, 30 fungicides, 14 herbicides, eight insecticides and one acaricide were detected. Di-(2-ethylhexyl)phthalate (DEHP) median concentration accounted for 280 microg kg(-1)dw and nonylphenol was below the detection limit of 1 mg kg(-1)dw. The sum of short and medium chain CP was between 90 and 390 microg kg(-1)dw. The concentrations observed were at or above the levels found in background soils, which are the main recipient of compost and digestate. Where actually applied, compost can contribute considerably to the total input of organic pollutants to the soil. However, on a total Swiss agricultural area base, inputs seem to be limited.