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Biomedical subjects

M Bahadir

Publications and source records attributed to M Bahadir.

17 recordsLinked to original sources

A microscale device for measuring emissions from materials for indoor use.

Emission test chambers or cells are used to determine organic vapour emissions from construction products under controlled conditions. Polymeric car trim component emissions are typically evaluated using direct thermal desorption/extraction. The Microchamber/Thermal Extractor (mu-CTE, Markes International) was developed to provide both a complementary tool for rapid screening of volatile organic compound (VOC) emissions--suitable for industrial quality control--and a means for thermal extraction of larger, more representative samples of car trim components. To determine the degree of correlation between conventional emission test methods and the microchamber, experiments were carried out under different conditions of temperature, air change rate and sample conditioning time. Good quantitative and qualitative correlation was obtained for measurements at ambient temperature. Moreover, it was shown that ambient-temperature emissions data collected using the mu-CTE as rapidly as possible--i.e. with minimal or no sample conditioning time--nevertheless provided a reliable guide as to how well that material would perform in subsequent 3-day chamber tests of VOC emissions. The parameters found to have the greatest influence on data correlation for experiments carried out at elevated temperatures were the sample mass (for bulk emissions testing) and the conditioning time. The results also showed that, within the constraints of inherent sample homogeneity, the mu-CTE gave reproducible emissions data, despite its small sample size/capacity relative to that of conventional chambers. Preliminary results of modelling the air flow within a microchamber using computational fluid dynamics showed a high degree of turbulent flow and two potential areas of still air which could cause sink effects. However, the experimental data reported here and in previous studies showed enhanced recovery of semivolatile components from the mu-CTE relative to a recovery from a 1 m(3) conventional chamber. This indicates that if these areas of relatively still air are present within the microchamber, they do not appear to be significant in practice.

Journal Article↗

Assessment of the environmental impact of landfill sites with open combustion located in arid regions by combined chemical and ecotoxicological studies.

Two different waste disposal sites in Jordan were investigated in order to determine the environmental situation in context with waste disposal techniques. One landfill, located at Marka/Amman, had been closed about 25 years ago and covered with soil. Here, the waste had been actively open combusted and openings in the cover, still emitting smoke, indicated that waste was still smoldering inside the landfill's body. The second disposal site close to Ekeeder/Irbid is still operated. On this ground, the solid waste is not intentionally burned, although spontaneous fires frequently come up. Samples of waste, soil, and entrained dust were collected and analyzed. From the solid samples, respectively, their eluates, sum parameters, ecotoxicological effects as well as contents of elements/heavy metals and organic pollutants (PAH, PCDD/F) were determined. In general, the Ekeeder-samples were low-contaminated. The investigation of the Marka-samples showed higher contamination of the site's center, clearly being influenced by combustion processes. A significant contamination of the landfill's vicinity by its emissions could not be derived from the analytical data. Ecotoxicological investigations, applying a bio-test battery, revealed correlations with the sum parameters but not with the trace pollutants. Thus, the Marka-samples with the highest measured values of sum parameters caused adverse effects on three different test species, whereas other samples from Marka and Ekeeder had small or no effects. The results of these investigations depict the influence of different disposal techniques on the contamination situation of a landfill and they shall contribute to assess the conditions of other disposal sites in (semi)arid regions.

Benzofurans↗

Isomer specific synthesis using the Suzuki-coupling. Polychlorinated terphenyls as standards for environmental analysis.

Defined polychlorinated terphenyl (PCT) single congeners as reference standards are the prerequisite for the development of analytical methods for their determination and quantification in the environment. The selective synthesis of PCTs for environmental analytical purposes by application of the Suzuki-coupling reaction is described. Under easily modified standard reaction conditions of this coupling process the PCTs can be obtained by reaction of benzeneboronic acids with dibromobenzenes mostly in good yields, as described by the synthesis of following PCT congeners: p-PCT (3,3("),5,5(")-tetrachloro-, 2,2("),4,4(")-tetrachloro-, 2('),3,3("),5,5(")-pentachloro-); m-PCT (3,3("),5,5(")-tetrachloro-) and o-PCT (3,3("),5,5(")-tetrachloro-). The terphenyl congeners were characterized by NMR (1H, 13C)- and FT-IR-spectroscopy. Their purity was checked by GC/MS analysis. The experimental and quantum-chemically calculated FT-IR-spectra were compared and it was shown, that the determination of the chlorine substitution pattern in the terphenyl congeners by their typical absorption spectra is possible.

Environmental Monitoring↗

Influence of heavy metals on the formation and the distribution behavior of PAH and PCDD/F during simulated fires.

Combustion experiments were performed with an artificial fire load (polystyrene and quartz powder) in a laboratory scale incinerator in the presence of gaseous HCl to simulate accidental fire conditions. The aim of this investigation was to trace back the alterations of the formation and the distribution behavior of PAH and PCDD/PCDF to the presence of CuO or a mixture of metal oxides (CdO, CuO, Fe(2)O(3), PbO, MoO(3), ZnO). The total amount of the 16 PAH target compounds was reduced by the factor of 5-9 when the mixture of metal oxides was present rather than merely CuO. PAH patterns as well as their distribution behavior were significantly influenced by these oxides. In general, transportation inside the installation was enhanced for most of the 16 analyzed PAH. Only fluorene and dibenzo[a,h]anthracene were transported to a smaller extent. In contrast to PAH, total concentrations of PCDD were increased by factor 9 and of PCDF by factor 10, respectively, when CuO was present. Adding the mixture of metal oxides resulted in an increase of PCDD by factor 14 and of PCDF by factor 7. CuO and the mixture of metal oxides had a different influence on the PCDD/F homologue patterns. For instance, the HxCDF to OCDF ratio after incineration without any metal oxide was 1 to 6, whereas addition of CuO or the mixture of the metal oxides shifted the HxCDF to OCDF ratios towards 1 to 40 or 1 to 17, respectively. Combustion along with CuO increased transportation of higher chlorinated PCDF congeners, whereas the mixture of the metal oxides caused a strong decrease of PCDF distribution throughout the system.

Fires↗

Formation of PBDD/F from flame-retarded plastic materials under thermal stress.

Thermal treatment of plastics flame retarded with brominated compounds often lead to the formation of PBDD/F, especially if polybrominated diphenyl ethers are used. By the presence of antimony(III) oxide, water and some other metals, the amounts of PBDD/F increase. Even during the production and recycling processes of plastics, PBDD/F can be found in considerable amounts. By the use of flame retardants, which are not direct precursors of PBDD/F, the amounts can significantly be decreased. An incomplete and uncontrolled incineration, occurring in fire accidents in private residences, can form high amounts of PBDD/F, which can endanger the environment and persons in contact with fire residues. Complete and controlled incineration of bromine-containing compounds as usually conducted in municipal waste incinerators, however, show no raised risk. An overview about the formation of PBDD/F primarily during combustion and also during production and recycling processes of flame-retarded plastic materials is given in this paper.

Benzofurans↗

Thermal formation of PBDD/F from tetrabromobisphenol A--a comparison of polymer linked TBBP A with its additive incorporation in thermoplastics.

For a long period, polybrominated flame retardants are under discussion because of the formation of polybrominated dibenzo-p-dioxins (PBDD)/dibenzofurans (PBDF) (PBDD/F) in case of thermal stress. Concerning polymer linked tetrabromobisphenol A (TBBP A), formation of PBDD/F was commonly presumed to be sterically hindered because of the covalent fixation into the polymer backbone. Combustion experiments with additively incorporated TBBP A compared with its polymer linkage revealed, that this assumption is incorrect and has to be revised. Under same conditions, similar PBDD/F concentrations in the range of 17.5-19.6 mg PBBD/F per kg TBBP A applied were analyzed. PBDD/F homologue distribution patterns were almost identical predominated by low brominated PBDF. These findings for PBDD/F formation have to be considered in future discussions regarding thermal stress caused by combustion or recycling processes, including other flame retardants bound in polymer matrix, e.g. polybrominated polystyrene (PS), or those with molecular structures showing less analogy to PBDD/F, like hexabromocyclododecane. The second aspect introduced, is the influence of different plastics on the formation rates of PBDD/F. In this context, combustion experiments were performed in an atmosphere consisting of synthetic air and HBr. PBDD/F concentrations were 8.47 mg/kg polyethylene, 1.67 mg/kg PS, 3.92 mg/kg phenolic resin and 18.1 mg/kg epoxy resin. Distribution patterns of PBDD/F homologues could partly be correlated with the occurrence of the precursors polybrominated benzenes and phenols.

Benzofurans↗

Distribution behavior of heavy metals investigated in a laboratory-scale incinerator.

The distribution behavior of Pb, Cd, Fe, Cu, Mo and Zn was determined in a laboratory-scale incinerator. Points of interest were the influence of the temperature and combustion atmosphere on the emission rates of those metals, orientating at frequent combustion conditions of accidental fires. The experiments were carried out at 600 degrees C and 800 degrees C in N2, air, N2 + HCl and air + HCl atmospheres. Furthermore, the influence of the matrix (quartz, polyethylene and cellulose powder) on the distribution behavior of the heavy metals was investigated as well. It was determined whether the distribution behavior of Cu, Pb and Cd were affected by the other heavy metals. In conclusion, it was found that in air and N2 atmosphere a temperature increase from 600 degrees C to 800 degrees C and the addition of the matrix had no effect on the evaporation rates of the heavy metals, except for Cd. Addition of gaseous HCl led to increased evaporation of the heavy metals. The increase of the evaporation rates during the experiments with matrix was higher for Fe, remained the same for Pb, Cd, Zn, and lower for Mo and Cu compared to the experiments without matrix.

Air Pollutants↗

Use of supercritical fluid extraction in the analysis of pesticides in soil.

The applicability of supercritical fluid extraction (SFE) in pesticide residue analysis in soil was investigated by analysing real soil samples from field experiments. Additionally, radiotracer batch experiments were performed to study the release of non-extractable residues. High repeatability, accuracy and high selectivity were the most important advantages of SFE in residue analysis. Extracts with low amounts of coextractants from the soil matrix were achieved, allowing extracts to be pooled and concentrated without further clean up steps. Thus, the limited volume of extraction thimbles of the SFE apparatus used could be compensated and insufficiently high limits of determination could be improved. Although the application of methanol-modified supercritical CO(2) was a time-saving extraction procedure which reduced solvent usage and solvent waste, SFE efficiency proved only competitive to conventional slurry and Soxhlet extraction. No exhaustive release of non-extractable residues was achieved in radiotracer batch experiments.

Carbamates↗

Surface contamination with PASH, PAH and PCDD/F after fire accidents in private residences.

Surface samples were taken from two private residences after real fire accidents. The goal was, to determine the surface contaminations with polycyclic aromatic sulfur heterocycles (PASH), as representatives of a substance class, not investigated in this context, by now, polycyclic aromatic hydrocarbons (PAH) and polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F). Analytical method for the determination of PASH was developed for the respective matrix. Concentrations measured ranged between 1.70 and 465 micrograms/m2 for PASH, 34.3 and 58,800 micrograms/m2 for PAH (EPA), and 4.15 and 1,300 ng/m2 for PCDD/F, as well. Obviously, PASH were formed during the fire accidents. Nevertheless, PAH were the most relevant pollutants after these small fires.

Benzofurans↗

On the degradability of tetrachloroethene in biologically treated wastes.

Investigation on the degradability of tetrachloroethene was performed using fresh and mechanically-biologically pretreated household waste. The corresponding metabolites were determined and the experimental conditions were characterized by the concentrations of methane, organic acids, sulfate and nitrate as well as by pH and redox potential. Furthermore, sorption studies on the substances in different wastes were carried out. With pretreated waste the degradation efficiency was much higher than with fresh waste. On the other hand, the fresh waste showed higher sorption capacity for the chlorinated compounds.

Biodegradation, Environmental↗

Sorption behavior of prochloraz in different soils.

The sorption behavior of the imidazole fungicide prochloraz [PCZ; N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide] was studied in batch experiments with different soils. The soil organic matter content was found to control the amount sorbed by different soils. K(d) values ranged from 56 +/- 0 to 552 +/- 10 (mean = 221 +/- 5) and K(OC) values from 7273 +/- 0 to 16250 +/- 1300 (mean = 11829 +/- 303). As calculated from a linear regression of K(d) versus %OC, K(OC) was 12900 +/- 1300. Additionally, the pH value of the soil had considerable influence on the sorption of the weakly basic PCZ (pK(a) = 3.8), giving rise to stronger sorption at lower pH. K(d) values determined on pH-modified soils confirmed the pH dependency. Sorption isotherms on two soils were recorded, initial concentrations ranging from 0.09 to 5.71 mg L(-)(1). The Freundlich isotherm was fitted to the values measured. The Freundlich exponents calculated were significantly smaller than unity, indicating nonlinear sorption. Sorption experiments with two metabolites of PCZ (PCZ-formylurea and PCZ-urea) revealed K(d) values one-fourth to one-third those for PCZ on two soils.

Adsorption↗

Dependence of genotoxicity of benzo[a]pyrene suspensions in Mutatox test on dissolved concentration and S9 addition.

The Mutatox test is a novel genotoxicity test measuring the ability of a test chemical to restore the luminescent state in dark mutants of Vibrio fischeri. Chemicals can be tested with or without rat hepatic S9 enzymes for metabolic activity, so that promutagenic agents can be detected as well. In the Microbics Mutatox Manual (1993, Microbics Corp., Carlsbad, CA), benzo[a]pyrene is recommended as positive control for S9 medium at a nominal concentration of 10 mg/liter with 2% DMSO as carrier solvent. The concentration of benzo[a]pyrene dissolved in this test suspension without addition of S9 was determined by GC-MS. It was significantly lower than the nominal concentration and did not reveal a genotoxic effect in the Mutatox test with S9. The analytical concentration of benzo[a]pyrene in the supernatant of the test suspension in S9 medium was significantly higher and induced the luminescence of bacteria. Therefore, S9 microsomes seem, apart from metabolizing benzo[a]pyrene to its genotoxic epoxide, to increase transfer of benzo[a]pyrene into V. fischeri in such a way that the genotoxic effect is produced. This suggests that sparingly soluble compounds might have different ecotoxicological effects as suspensions than as solutions. Therefore, the possible uptake of suspended particles by organisms without being completely dissolved before should be considered in ecotoxicological tests.

Animals↗

Comparison of acute toxicity and genotoxic concentrations of single compounds and waste elutriates using the Microtox/Mutatox test system.

The Mutatox test has been developed by Microbics Corp., U.S.A., in addition to the widely used acute toxicity test Microtox. The Mutatox test indicates the presence of any material in a test sample that causes genetic damage to dark variants of the luminescent bacteria Vibrio fischeri. As the Microtox test is less time-consuming and more cost-effective than the Mutatox test, the possibility of using the EC50 measured by Microtox for range-finding of genotoxic concentrations for the Mutatox test was examined. Both tests were applied on single compounds and several waste elutriates. The genotoxic potential of two PAH metabolites--1-hydroxypyrene and 9-fluorenone-1-carboxylic acid--was detected. According to the present results the highest concentration of a sample in the Mutatox test should in general exceed the EC50 by about 5-10 times. Elutriates were submitted to analyses of TOC, heavy metals, phenols, and PAH; additionally GC/MS screening analyses were carried out. In most cases correlations of ecotoxicological effects with single contaminants were not possible, but it can be assumed that these effects were produced by the interaction of inorganic and organic compounds present in the elutriates.

Fresh Water↗

Pentafluorobenzylation of the fungicide metabolite fenpropimorphic acid for GC/MS investigations of soil samples.

For the determination of fenpropimorphic acid in soil samples, a derivatization step with pentafluorobenzylbromide has been established in order to perform GC/MS with negative chemical ionization. In spite of forming the electrophilic pentafluorobenzyl ester, only the fenpropimophic acid anion was detected. Additional derivatization reactions with diazomethane and 2,2,2-trichloroethanol showed that the formation of this acid anion was depending on the leaving group. In comparison with the determination of the methyl ester with GC/MS and electron impact ionization, the detection limit was however improved from 10 microg/kg to 2 microg/kg dry soil and the analytical quality was ensured due to higher stability of the pentafluorobenzyl ester standards.

Journal Article↗

Dioxins and furans in the Jordanian environment. Part 2: Levels of PCDD and PCDF in human milk samples from Jordan.

Thirty individual human milk samples were gathered from five main towns in Jordan. They were mixed to six pooled samples and analyzed for PCDD and PCDF. All examined samples were contaminated with 1,2,3,4,6,7,8-HeptaCDD (3.2-96.0 ng/kg fat) and OctaCDD (29.0-147 ng/kg fat). The calculated TEQ (BGA)-values range between 0.26 and 60.32 ng TEQ/kg fat, which are all above the calculated tolerable concentration of 0.19 ng TEQ/kg milk fat.

Adult↗

A comparative study on pesticide formulations for application in running waters.

Release rates into water of monolinuron, desmetryne, and carbofuran from three different types of formulations have been studied to control aquatic weeds in running waters. The migration of active ingredients (AI) from conventional wettable powder formulations was complete within 1 day, while the migration from ethylene-vinyl acetate copolymeric matrix (EVA) lasted significantly longer due to low diffusion coefficients of monomeric pesticides in polymeric matrices Do = 10(-8)-10(-12) (cm2 X sec-1). The herbicidal action could be extrapolated up to several years. Release duration of AI from calcium alginate beads lasted 2 weeks. Herbicidal effectiveness of terbutryne-EVA formulation has been investigated in a laboratory-scale simulated flow system device with duckweed plants (Lemna minor) as test organism. Growth inhibition of duckweed could be achieved at approx 20 ppb terbutryne in steady state.

Absorption↗

Organochlorine compounds in a Brazilian watershed with sugarcane and intense sediment redistribution.

Until 1985 persistent organochlorine compounds such as aldrin [(1alpha,4alpha,4abeta,5alpha,8alpha,8abeta)-1,2,3,4,10,10-hexachloro-1,4,4a,5,8,8a-hexahydro-1,4:5,8-dimethanonaphthalene] and heptachlor (1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro-4,7-methano-1H-indene) were recommended and used as insecticides on a large scale in sugarcane (Saccharum officinarum L.) cropping in Brazil. The environmental impact of these applications was not investigated in the past neither prior to nor after their restriction of use in Brazil. In a case study conducted during 1999, organochlorine insecticides were investigated in soils, colluviums, submerged sediments, and organisms in a watershed located in a traditional sugarcane-growing region in the southeastern region of Brazil. The results indicated that past applications of organochlorine insecticides (prior to 1985) do not represent an environmental threat at the present time. Most insecticides applied in the past were not detected or were present only in amounts that were below the detection limit. The organochlorine compounds lindane [(1alpha,2alpha,3beta, 4alpha,5alpha,6beta)-1,2,3,4,5,6-hexachlorocyclohexane] and heptachlor that remained on the market after 1985 for purposes other than for soil application were still detectable in significant amounts in soils, sediments, and soil organisms (heptachlor in form of the epoxide metabolites). This may suggest that these residues were originated from applications after 1985. These compounds showed a capacity for accumulation in sediments and soil organisms. The enrichment ratio from soils to sediments was 2 to 3 times and from soils to organisms up to 20 times.

Agriculture↗