Elimination des Zytostatikums Ifosfamid während der simulierten Zersetzung von Hausmüll im Labormaßstab

Drugs are emitted into the environment by hospitals, private households, veterinary and human practices. Remnants of these products are primarily disposed of in landfill sites. At the present, there is no information available about the behaviour of pharmaceutical drugs, like their anaerobic biodegradation or adsorption, in sanitary landfills. Some of these drugs, e.g. antineoplastic substances such as ifosfamide, are supposed to be cancerogenic, mutagenic, fetotoxic or embryotoxic. Therefore, we investigated the behaviour of ifosfamide during waste decomposition in a laboratory-scale lysimeter. Up to 50% of the ifosfamide was eliminated under methanogenic conditions; but the mechanism applying for the elimination remains unclear. As far as present day knowledge is concerned, the risk for the environment through the emission of emitting ifosfamide from sanitary landfills should be negligible.     

Use of fungi for the bioconversion of rice straw into cellulase enzyme

Cellulase production was carried out by solid state bioconversion (SSB) method using rice straw, a lignocellulosic material and agricultural waste, as the substrate of three Trichoderma spp. and Phanerochaete chrysosporium in lab-scale experiments. The results were compared to select the best fungi among them for the production of cellulase. Phanerochaete chrysosporium was found to be the best among these species of fungi, which produced the highest cellulase enzyme of 1.43 IU/mL of filter paper activity (FPase) and 2.40 IU/mL of carboxymethylcellulose activity (CMCase). The "glucosamine" and "reducing sugar" parameters were observed to evaluate the growth and substrate utilization in the experiments. In the case of Phanerochaete Chrysosporium, the highest glucosamine concentration was 1.60 g/L and a high concentration of the release of reducing sugar was measured as 2.58 g/L obtained on the 4th day of fermentation. The pH values were also recorded. The range of the pH was about 5.15 to 5.56 in the case of Phanerochaete Chrysosporium.     

Trends and problems of solid waste management in developing countries: a case study in seven Palestinian districts

There is a great interest in solving problems related to municipal solid waste (MSW) management in the Palestinian territory. However, few studies have been done to assess the extent of these problems and suggest the best alternative solutions. This study aims at assessing MSW conditions in the seven major districts in northern West Bank, Palestinian territory. The study focuses on comparing several MSW management elements (such as collection, budget, and disposal) in municipalities, village councils, and refugee camps in the studied districts and the problems faced by these institutions in handling the waste. It also provides information on MSW collection service availability and waste disposal practices in the districts studied. It was found that, although MSW collection service was available for 98% of the residents in the areas surveyed, no proper treatment or landfill procedure was followed for the collected waste in most of these areas. Instead, waste burning in open dumpsites was the most common practice. Moreover, due to inefficient collection of waste disposal fees from the residents, municipalities were forced to sometimes cut the collection service and reduce its labor force, especially in villages. The budget for MSW management was between 2% and 8% of the total budget of the municipalities studied, indicating a low priority for this issue.     

Effect of vehicle exhaust on the quantity of polycyclic aromatic hydrocarbons (PAHs) in soil

PAHs are formed during the incomplete combustion of organic substances containing carbon and hydrogen and are one of the first atmospheric pollutants identified as carcinogens. Most of the PAH environmental burden is found in the soil (95%). Soil samples collected from different roadsides were analyzed for seven polycyclic aromatic hydrocarbons (PAHs). The quantitative and qualitative analysis was carried out by UV Spectrophotometer. The individual PAH value ranged from 0.1 to 18.0 mg/kg. Phenenthrene and Pyrene were found to be the most abundant compounds. Vehicle emissions are the principal source of PAH in the Roadside soils. The highest concentration was found at site S2 (Hasthtnagri Roadside) which shows the highest traffic density.     

Trace metal contents in chewing gums and candies marketed in Turkey

Cu, Ni, Pb, Fe, Mn, Cr and Cd contents were determined in 17 different brands of chewing gum and candy samples available in local markets of Kayseri, Turkey. Concentration of selected trace metals were estimated using flame atomic absorption spectrometer after dry and wet digestion methods. Out of 17 brands of chewing gums and candies analysed, four were cocoa based, two were sugar based and other were of fruit based. Copper level ranged from 0.219 to 2.455 microg/g with an average of 1.390 microg/g. Nickel ranged from 0.120 to 2.588 microg/g with an average of 0.846 microg/g. Lead level ranged from 0.031 to 2.46 microg/g with an average of 0.746 microg/g. Iron level ranged from 3.963 to 9.863 microg/g with an average of 6.618 microg/g. Manganese level ranged from 1.872 to 5.067 microg/g with an average of 3.196 microg/g. Chromium ranged from 0.740 to 6.265 microg/g with an average of 2.473 microg/g and cadmium level ranged from 0.027 to 0.825 microg/g with an average of 0.296 microg/g. Cocoa based samples were found to have higher contents of the analysed metals than sugar and fruit based samples.     

Reuse of municipal effluent with drip irrigation and evaluation the effect on soil properties in a semi-arid area

Irrigation with municipal effluent was evaluated during 25 months in Southern Iran from 2003 to 2005 in which 14 tree species were irrigated with effluent and borehole water at an annual supply rate of 3,940 and 5,395 m(3) ha(-1), respectively. To mitigate the environmental effects, a drip irrigation system was designed and the amount of applied water based on pan evaporation was measured by flow meters and soil properties were monitored. The statistical results showed that the applied effluent had no adverse effect on soil properties. The soil salinity was reduced from 8.2, 6.8 and 7.0 dSm(-1) to 1.07, 1.12 and 3.5 dSm(-1 )in the soil layers 0-30, 30-60 and 60-90 cm, respectively. The SAR decreased significantly, while soil pH increased by 0.8 and 0.6 units in the layers 0-30 and 30-60 cm. A total application of 9,335 m(3)ha(-1 )of effluent with a nitrogen and phosphorus concentration of 7.9 and 10.3 mg l(-1), added 73 and 101 kg ha(-1) of nitrogen and phosphorus to the soil. Organic carbon also increased significantly. Twenty-five months irrigation with effluent caused a slight increase in soil bulk density and a slight decrease in mean permeability. Because of an efficient filtration and high discharge rate of bubblers (drippers), no considerable sign of clogging was observed.     

Application of nanoclay for preconcentration of ultra trace amounts of palladium in environmental samples prior to its determination by ETAAS

In the present work, a batch preconcentration technique using nanoclay with 5-(4-dimethylaminobenzylidene)rhodanine coupled with electrothermal atomic absorption spectrometry was developed for the separation and determination of trace amounts of palladium. In this method, the sample solution was stirred with nanoclay as an adsorbent. Then, adsorbed palladium was subsequently eluted with HCl in acetone (1.5 mol L^?1) and, finally, this eluate was injected to electrothermal atomic absorption spectrometry. Under the optimum conditions, the limit of detection and linear dynamic range were found to be 2.6 and 10.0–133 ng L^?1 (in original solution), respectively. Furthermore, the enrichment factor and relative standard deviation of seven replicate determinations were 148 and ±5.1 %, respectively. This suggested method is simple, selective and sensitive and can be applied to the extraction and determination of palladium in water, tea leaves, synthetic sample and certified reference material with satisfactory results.     

A comparison of radiometric correction techniques in the evaluation of the relationship between LST and NDVI in Landsat imagery

Atmospheric corrections for multi-temporal optical satellite images are necessary, especially in change detection analyses, such as normalized difference vegetation index (NDVI) rationing. Abrupt change detection analysis using remote-sensing techniques requires radiometric congruity and atmospheric correction to monitor terrestrial surfaces over time. Two atmospheric correction methods were used for this study: relative radiometric normalization and the simplified method for atmospheric correction (SMAC) in the solar spectrum. A multi-temporal data set consisting of two sets of Landsat images from the period between 1991 and 2002 of Penang Island, Malaysia, was used to compare NDVI maps, which were generated using the proposed atmospheric correction methods. Land surface temperature (LST) was retrieved using ATCOR3_T in PCI Geomatica 10.1 image processing software. Linear regression analysis was utilized to analyze the relationship between NDVI and LST. This study reveals that both of the proposed atmospheric correction methods yielded high accuracy through examination of the linear correlation coefficients. To check for the accuracy of the equation obtained through linear regression analysis for every single satellite image, 20 points were randomly chosen. The results showed that the SMAC method yielded a constant value (in terms of error) to predict the NDVI value from linear regression analysis-derived equation. The errors (average) from both proposed atmospheric correction methods were less than 10%.     

Simultaneous derivatization and extraction of nitrophenols in soil and rain samples using modified hollow-fiber liquid-phase microextraction followed by gas chromatography–mass spectrometry

A simple and sensitive method based on a modified hollow-fiber liquid-phase microextraction followed by gas chromatography–mass spectrometry has been successfully developed for the extraction and simultaneous derivatization of some nitrophenols (NPs) in soil and rain samples. Microwave-assisted solvent extraction was used for the extraction of NPs from the soil, while the rain sample was directly applied to the previously mentioned method. Briefly, in this method, the analytes were extracted from aqueous samples into a thin layer of organic solvent (dodecane?+?10 % tri-n-octylphosphine oxide) sustained in the pores of a porous hollow fiber. Then, they were back-extracted using a small volume of organic acceptor solution (25 μl; 10 mg/L N-methyl-N-(trimethylsilyl)trifluoroacetamide, as derivatization reagent, in acetonitrile) that was located inside the lumen of the hollow fiber. Under the optimized extraction conditions, enrichment factors of 255 to 280 and limits of detection of 0.1 to 0.2 μg/L (S/N?=?3) with dynamic linear ranges of 1–100 μg/L were obtained for the analytes. The accuracy of the approach was tested by the relative recovery experiments on spiked samples, with results ranging from 93 to 113 %. The method was shown to be rapid, cost-effective, and potentially interesting for screening purposes.     

2-Nitroso-1-naphthol as a selective reagent for preconcentration of cobalt by vortex assisted combined with solidification of organic droplet and its determination by flame atomic absorption spectrometry

Highly rapid and selective vortex-assisted liquid–liquid microextraction based on solidification of organic drop has been used for determination of cobalt ion. 2-Nitroso-1-naphthol (2N1N) was used as a selective complexing agent to form stable cobalt–2N1N complex which can be extracted with 1-undecanol at a short time by the assistance of vortex agitator system followed by its determination using flame atomic absorption spectrometry. In vortex assisted, vigorous vortex stream as well as the vibrant effect of vortex system cause very fine droplets of extraction solvent to be produced and extraction occurred at a short time. Some parameters influencing the extraction process such as pH of samples, concentration of 2-nitroso-1-naphthol, extraction solvent volume, extraction time, ionic strength and surfactant addition, as well as interferences were evaluated in detail and optimum conditions were selected. At the optimum conditions, the calibration curve was linear in the range of 15 to 400 μg L^?1 of cobalt ions. The relative standard deviation based on ten replicate analysis of sample solution containing 50 μg L^?1 of cobalt was 3.4 %. The detection limit (calculated as the concentration equivalent to three times of the standard deviation of the blank divided by the slope of the calibration curve after preconcentration) was 5.4 μg L^?1. The accuracy of the proposed method was successfully evaluated by the analysis of certified reference materials. This selective and highly rapid method was used for determination of cobalt ions in different water samples.