Biodegradable Fraction (biodegradable + fraction)

Distribution by Scientific Domains


Selected Abstracts


Bioavailability and biodegradation of nonylphenol in sediment determined with chemical and bioanalysis,

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 4 2008
Jasperien de Weert
Abstract The surfactant nonylphenol (NP) is an endocrine-disrupting compound that is widely spread throughout the environment. Although environmental risk assessments are based on total NP concentrations, only the bioavailable fraction posses an environmental risk. The present study describes the bioavailability and biodegradability of NP over time in contaminated river sediment of a tributary of the Ebro River in Spain. The bioavailable fraction was collected with Tenax TA® beads, and biodegradation was determined in aerobic batch experiments. The presence of NP was analyzed chemically using gas chromatography-mass spectrometry and indirectly as estrogenic potency using an in vitro reporter gene assay (ER, - luc assay). Of the total extractable NP in the sediment, 95% ± 1.5% (mean ± standard error) desorbed quickly into the water phase. By aerobic biodegradation, the total extractable NP concentration and the estrogenic activity were reduced by 97% ± 0.5% and 94% ± 2%, respectively. The easily biodegradable fraction equals the potential bioavailable fraction. Only 43 to 86% of the estrogenic activity in the total extractable fraction, as detected in the ER, - luc assay, could be explained by the present NP concentration. This indicates that other estrogenic compounds were present and that their bioavailability and aerobic degradation were similar to that of NP. Therefore, we propose to use NP as an indicator compound to monitor estrogenicity of this Ebro River sediment. To what extent this conclusion holds for other river sediments depends on the composition of the contaminants and/or the nature of these sediments and requires further testing. [source]


Utilization of oligo- and polysaccharides at microgram-per-litre levels in freshwater by Flavobacterium johnsoniae

JOURNAL OF APPLIED MICROBIOLOGY, Issue 4 2010
E.L.W. Sack
Abstract Aims:, To obtain a bacterial strain that can be used to quantify biodegradable polysaccharides at concentrations of a few micrograms per litre in freshwater. Methods and Results:,Flavobacterium johnsoniae strain A3 was isolated from tap water supplemented with laminarin, pectin or amylopectin at 100 ,g C l,1 and river Rhine water. The organism utilized 14 of 23 oligo- and polysaccharides, and 1 of 9 monosaccharides, but none of the sugar acids, sugar alcohols, carboxylic acids or aromatic acids tested at 10 ,g C l,1. Amino acids promoted growth of strain A3, but not in coculture with assimilable organic carbon (AOC) test strain Pseudomonas fluorescens P17, which utilized these compounds more rapidly than strain A3. Compounds released by strain P17 and AOC test strain Spirillum sp. NOX grown on acetate promoted the growth of strain A3 at Nmax values of , 2 × 105 CFU ml,1 of strain P17 and , 5 × 105 CFU ml,1 of strain NOX. Significant growth of strain A3 was observed in surface water and in tap water in the presence of strain P17 (Nmax P17 < 2 × 105 CFU ml,1). Conclusions:, Strain A3 utilizes oligo- and polysaccharides at microgram-per-litre levels. In surface water and in tap water, the organism was able to utilize compounds that were not utilized by strain P17. These compounds may include oligo- and/or polysaccharides. Significance and Impact of the Study:, Phytoplanktonic and bacterial polysaccharides can constitute an important biodegradable fraction of natural organic matter in water and may promote growth of heterotrophic bacteria during water treatment and drinking water distribution. Strain A3 can be used to quantify a group of compounds that includes oligo- and polysaccharides at microgram-per-litre levels in freshwater. [source]


Biodegradability of slaughterhouse wastewater with high blood content under anaerobic and aerobic conditions

JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 4 2003
Rodrigo del Pozo
Abstract In this work, the biodegradability of wastewater from a slaughterhouse located in Ke,an, Turkey, was studied under aerobic and anaerobic conditions. A very high total COD content of 7230,mg,dm,3 was found, due to an inefficient blood recovery system. Low BOD5/COD ratio, high organic nitrogen and soluble COD contents, were in accordance with a high blood content. A respirometry test for COD fractionation showed a very low readily biodegradable fraction (SS) of 2%, a rapidly hydrolysable fraction (SH) of 51%, a slowly hydrolysable fraction (XS) of 33% and an inert fraction of 6%. Kinetic analysis revealed that hydrolysis rates were much slower than these of domestic sewage. The results underlined the need for an anaerobic stage prior to aerobic treatment. Tests with an anaerobic batch reactor indicated efficient COD degradation, up to around 80% removal. Further anaerobic degradation of the remaining COD was much slower and resulted in the build up of inert COD compounds generated as part of the metabolic activities in the anaerobic reactor. Accordingly, it is suggested that an appropriate combination of anaerobic and aerobic reactors would have to limit anaerobic degradation to around 80% of the tCOD and an effluent concentration above 1000,mg,dm,3, for the optimum operation of the following aerobic stage. © 2003 Society of Chemical Industry [source]


Intermediate accumulation and efficiency of anaerobic digestion treatment of surfactant (alcohol sulfate)-rich wastewater at increasing surfactant/biomass ratios

JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 9 2002
Heiko Feitkenhauer
Abstract Textile (eg cotton) finishing industry wastewater is characterised by high concentrations of surfactants (up to 2,g,dm,3) and of readily biodegradable biopolymers (COD 5,15,g,dm,3). The anionic surfactant decyl sulfate (DS) was chosen as model surfactant and soluble starch (size) as model compound for the readily biodegradable fraction of the wastewater. Twenty-two batch experiments with increasing DS/biomass ratio (and starch/biomass ratio) were started simultaneously. Biomass concentrations ranged from 50 to 15,000,mg,dm,3. Minor inhibition effects were found for the surfactant degradation itself at all DS/biomass ratios (maximum biodegradation rate 7.7,mgDS gbiomass,1h,1). The starch hydrolysis started without a lag-phase at DS/biomass ratios of up to 0.15,gDS gbiomass,1. The lag-phase was prolonged to about 100,h at a very high DS/biomass ratio (3,gDS gbiomass,1). The relative importance of the accumulated intermediates was dependent on the DS/biomass ratio. Above 0.3,gDS gbiomass,1 10% of the substrate organic carbon accumulated as ethanol, but no ethanol accumulation was observed at low DS/biomass ratios. Moderate DS/biomass ratios caused a considerable delay of the methanogenesis; high DS/biomass ratios prevented the methanogenesis almost completely. © 2002 Society of Chemical Industry [source]


Characterization and modelling of denim-processing wastewaters for activated sludge

JOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 9 2001
Derin Orhon
Abstract The study involved characterization of denim-processing wastewaters, mainly to generate the necessary experimental data for the modelling and evaluation of the activated sludge process. The striking feature of the wastewater quality was the excessive suspended solids content requiring effective removal before biological treatment. COD fractionation was, however, typical for a textile effluent in general, with a biodegradable fraction of 90%, a readily biodegradable COD ratio of 20%, a predominantly soluble slowly biodegradable fraction of 55,60% and negligible particulate inert COD. Hydrolysis was identified as the significant step in the biodegradation kinetics with rate coefficients quite specific to plant operation. Evaluation of the hydrolysis kinetics showed that the magnitude of the slowly biodegradable COD could be reduced with a higher hydraulic detention time, effectively improving the quality of the soluble effluent. © 2001 Society of Chemical Industry [source]