Synthetischer Crandallit

Crandallite (Ca,Sr) Al₃ (PO₄)₂ (OH)₅ · H₂O crystallizes in the alunitecrystal lattice. Because of its open structure, the cations Ca²⁺, Sr²⁺, and Al³⁺ can be replaced by various elements depending on their diadochial properties; the element entering into the crystal network thus becomes immobilized. Artificial amorphous crandallite has been shown to eliminate the heavy metal ions: Pb²⁺>>Cu²⁺>Hg²⁺>>Cd²⁺ from contamined water in the presence of lateritic phosphates. Pb²⁺ could be removed nearly quantitatively in all cases.     

Ozonation of hydrolyzed azo dye reactive yellow 84 (CI).

The combination of chemical and biological water treatment processes is a promising technique to reduce recalcitrant wastewater loads. The key to the efficiency of such a system is a better understanding of the mechanisms involved during the degradation processes. Ozonation has been applied to many fields in water and wastewater treatment. Especially for textile mill effluents ozonation can achieve high color removal, enhance biodegradability, destroy phenols and reduce the chemical oxygen demand (COD). However, little is known about the reaction intermediates and products formed during ozonation. This work deals with the degradation of hydrolyzed Reactive Yellow 84 (Color Index), a widely used azo dye in textile finishing processes with two monochlorotriazine anchor groups. Ozonation of the hydrolyzed dye in ultra pure water was performed in a laboratory scale cylindric batch reactor. Decolorization, determined by measuring the light absorbance at the maximum wavelength in the visible range (400 nm), was almost complete after 60 and 90 min with an ozone concentration of 18.5 and 9.1 mg/l, respectively. The TOC/TOC0 ratio after ozonation was about 30%, the COD was diminished to 50% of the initial value. The BOD5/COD ratio increased from 0.01 to about 0.8. Oxidation and cleavage of the azo group yield nitrate. Cleavage of the sulfonic acid groups of aromatic rings caused increases in the amount of sulfate. Formic acid and oxalic acid were identified as main oxidation products by high performance ion chromatography (HPIC). The concentrations of these major products were monitored at defined time intervals during ozonation.     

Absch?tzung der Quecksilberexposition

Zusammenfassung  Ein quecksilberkontaminierter Altstandort dient als Beispiel für eine umweltmedizinische Beurteilung der Belastung der im Umfeld wohnenden Personen durch Quecksilberimmissionen. Dabei wird die innere Exposition für sieben verschiedene Altersgruppen bezüglich der KontaktmedienBoden, Luft undNahrungsmittel anhand von konventionell festgelegten Szenarien abgesch?tzt und ein Vergleich mit den epidemiologischen Ergebnissen eines Humanmonitorings angestrebt. Die standortspezifisch und pfadspezifisch durchgeführte Expositionsabsch?tzung stützt sich auf cine Vielzahl von unterschiedlichen Probenehmern sowie auf über mehrere Jahre durchgeführte Konzentrationsmessungen in den aufnahmerelevanten Kompartimenten. Sowohl die Berechnungen als auch die epidemiologischen Untersuchungen zeigen eine leichte Erh?hung der Quecksilberexposition, gemessen an strengen Richtwerten.      

Investigation on the influence of methanol on adsorption and leaching of pesticides with soil column liquid chromatography

The effect of methanol of low concentration on adsorption and leaching of atrazine and tebuconazole was studied in this paper. The adsorption coefficients and the retardation factors (R^m) of pesticides on EUROSOIL 3# log-linearly decreased as volumetric fraction of methanol (f^c) was increased in the binary solvent mixtures of methanol and water. These data are consistent with solvophobic theory formerly outlined for describing the adsorption and transport of hydrophobic organic chemicals from mixed solvents. Nevertheless, the adsorption of these pesticides in soil–water system slightly increased when the soil was pre-washed with methanol in comparison with that pre-washed with water (pure water system). Furthermore, their adsorption coefficients were still higher in binary solvent systems with methanol of very low concentrations, i.e. f^c<0.03 for atrazine and f^c<0.01 for tebuconazole, than those in pure water system. The adsorption coefficients (logK^w) of atrazine and tebuconazole predicted by solvophobic theory were 0.5792 and 1.6525, respectively, and their experimental logK^w were 0.3701 and 1.6275 in pure water system. Obviously, the predicted logK^w of the two pesticides was higher than the experimental log K^w in pure water system. The predicted K^w and the retardation factor (R^w) in pure water system by solvophobic theory are thus possibly inaccurate.     

Die rolle der umweltprobenbank in der Umweltüberwachung am beispiel von chlorierten kohlenwasserstoffen in ausgewählten matrizes

For precautinary environmental protection the Environmental Specimen Bank (ESB) has been successfully established as a permanent environmental surveillance tool in Germany. The presented monitoring results on chlorinated hydrocarbons (CHC) show very clearly the effects of political decisions and can be used for the identification of pollutant sources. The CHC burden of breams (Abramis brama) from five German rivers (Elbe, Rhein, Saar, Mulde, Saale) gives an current overview of the pollution situation of different limnic ecosystems in Germany. A calculation model about the distribution of organic pollutants between different tissues offers the possibility to predict concentrations in liver and muscle of breams. Legislative emission restrictions have led to a significant decrease of dioxin levels in herring gull (Larus argentatus) eggs between 1988–1996.     

Gliding arc plasma processing for decomposition of chloroform

The decomposition of chloroform (CHCl₃) diluted in air was studied. The experiment was carried out by using a gliding arc plasma. Different values of initial concentrations of chloroform, total gas flow rates, and input power frequencies have been used to investigate this effects on the conversion reaction products both qualitatively and quantitatively. Experimental results indicate that the maximum conversion of chloroform was 97% at a total gas flow rate of 180?L?h^?1 containing 1% chloroform. Using air as carrier gas, decomposition of CHCl₃ produces CCl₄, CO₂, CO, and Cl₂ as the main products. Small amounts of HCl and COCl₂ are also detected. Liquid products were also produced.     

Treatment of Dichloromethane Using Gliding Arc Plasma

Decomposition of dichloromethane (CH₂Cl₂) using a gliding plasma was examined and reported in this paper. The effects of initial concentrations of CH₂Cl₂, total gas flow rates, and input frequency have been studied to evaluate the performance of gliding arc on CH₂Cl₂ decomposition. Using atmospheric pressure air as the carrier gas, experimental results indicate that the maximum conversion of CH₂Cl₂ was 95.1% at a total gas flow rate of 180 L/hr containing 1% by volume of CH₂Cl₂. The reaction occurred at an exothermic condition and gaseous products are dominated by CO, CHCl₃, and Cl₂. CO₂ and CCl₄ are also detected in the product stream in small amounts. The conversion of CH₂Cl₂ increases with the increasing applied voltage and decreasing total gas flow rate.     

Comparison of dioxin-like-response in vitro and chemical analysis of emissions and materials

Samples from industrial and domestic emissions and materials were investigated by using in vitro assays for dioxin-like-response (DLR) and chemical analysis. The results show a small part of persistent bioaccumulative toxicants (PBT) to be responsive in vitro. Clean-up procedures directed to persistence decrease the amount of inducing toxicants substantially. The comparison of biological in vitro (B) and chemical (A) analysis show ratios between B and A below 10 for DLR of persistent inductors. The consideration of PAH improved the knowledge about unknown less persistent agonists.     

Main products and kinetics of the thermal degradation of polyamides

The thermal degradation of the polyamides (PA) 6, 12, 66 and 612 was investigated by means of thermal analysis/mass spectrometry (TA-MS) and pyrolysis in a german standard oven. Sample masses were about 20 and 40 mg. The heating rates used in the dynamic studies were 1, 5 and 10 K min(-1). Both air and nitrogen atmospheres were utilized. The kinetic parameters were calculated from the TA-MS measurements and the main decomposition products were registered online. The evolved products from the pyrolysis oven were captured and analyzed off-line by GC/MS.