叶酸、L-苯丙氨酸、维生素E废水治理方案研究

根据叶酸、L-苯丙氨酸、维生素E废水水质酸度高、色度深、盐度高、有机物含量高、可生化降解性差的特点,选择了"化学中和十兼氧/好氧PACT生化处理工艺".运行结果表明,经该工艺处理后,废水中的COD、BOD5、色度、PH等指标均能达标排放.     

Relationships between ecological variables and four organochlorine pollutants in an artic glaucous gull (Larus hyperboreus) population

The Arctic has become a sink for organochlorine contaminants (OCs) from lower latitudes, and relatively high levels have been found in different biota. Recent studies of the glaucous gull, Larus hyperboreus, a top predator in the arctic food web, have documented that high blood residues of various OCs are related to lower reproductive performance and reduced adult survival. Here we provide additional evidence that OCs are having ecological effects in the glaucous gull population at Bear Island in the Norwegian Arctic, and compare the effects of the four major OCs found in the glaucous gulls: HCB, oxychlordane, DDE and PCBs, which made up >95% of measured OCs. Firstly; it has previously been shown that gulls with high levels of PCBs in their blood spent more time away from the nest site during incubation than gulls with low levels. Here we reanalyzed the data and found that PCBs (P<0.02) and oxychlordane (P<0.05) were positive and significantly related to time away from the nest site, while DDE and HCB were not related to this trait. Secondly, among females which bred in an area where fish dominated the diet, and thus had high flight costs during feeding, early chick growth was negatively related to maternal levels of all four OCs, especially HCB and DDE (P<0.01). On the contrary, among females breeding in an area where the diet was dominated by eggs and young from nearby seabird colonies, and thus feeding costs were low, there were no effects of OC levels on early chick growth. This indicates that additional stress may be fundamental in causing reproductive effects of OCs in this population. Finally, during three breeding seasons we examined the probability of adults returning to the breeding grounds in the subsequent season, as a function of blood concentration of the four OCs. Overall, return rate from one year to the next was negatively related to blood residues of oxychlordane (P=0.02), but not significantly related to the other three compounds. Further support for the importance of oxychlordane was that a 60% drop in the blood levels between 1997 and 2000 led to a significant increase in return rate between these two years.     

Deposition to forests in Europe: most important factors influencing dry deposition and models used for generalisation

Dry deposition of gases and particles to forests is influenced by factors influencing the turbulent transport, such as wind speed, tree height, canopy closure, LAI, etc. as well as by factors influencing surface condition, such as precipitation, relative humidity, global radiation, etc. In this paper, an overview of these factors is given and it is shown which are the most important determining temporal and spatial variation of dry deposition of sodium and sulphur. Furthermore, it is evaluated how well current deposition models are able to describe the temporal and spatial variation in dry deposition. It is concluded that the temporal variation is not modelled well enough, because of limited surface-wetness exchange parameterisations. The influence of forest characteristics are modelled reasonably well, provided enough data describing the forests and the spatial variation in concentration is available. For Europe these data are not available. The means to decrease the atmospheric deposition through forest management is discussed.     

Removal of selected natural and synthetic estrogenic compounds in a Canadian full-scale municipal wastewater treatment plant.

The effect of a full-scale municipal wastewater treatment plant (WWTP) and each of the treatment units within the stream on the removal of endocrine-disrupting compounds was evaluated by tracking 17-beta-estradiol (E2), estrone (E1), and 17-alpha-ethinylestradiol (EE2). The overall performance of the WWTP compared well with other plants, as 90.5% removal of E1+E2 and 74.9% removal of EE2 were observed. A larger fraction of EE2 entered the plant in particulate form than E1 and E2, while a lower fraction of EE2 left the plant in particulate form than soluble form. The activated sludge units reduced the concentration of E1+E2 and EE2 in the liquid phase by 88.2% and 44.6%, respectively. The UV treatment process did not reduce the amount of estrogens. The aqueous phase of the tertiary lagoon solids contained higher levels of estrogens compared with the lagoon influent.     

Investigation of interactions between surface water and petroleum-type pollutants

Background, Aims and Scope In oil spill investigations, one of the most important steps is a proper choice of approaches that imply an investigation of samples taken from different sedimentary environments, samples of oil contaminants taken in different periods of time and samples taken at different distances from the oil spill. In all these cases, conclusion on the influence of the environment, microorganisms or migration on the oil contaminants' composition can be drawn from the comparison of chemical compositions of the investigated contaminants. However, in case of water contaminants, it is very important to define which part of organic matter has been analyzed. Namely, previous investigations showed that there were some differences in chemical composition of the same oil contaminant depending on the intensity of its contact with ground water. The aim of this work is to define more precisely the interactions between oil contaminant and water, i.e. the influence of the intensity of interaction between the oil contaminant and water on its chemical composition. The study was based on a comparison of four fractionated extracts of an oil pollutant, after they had been analyzed in details. Methods Oil polluted surface water (wastewater canal, Pančevo, Serbia) was investigated. The study was based on a comparison of four extracts of an oil contaminant: extract 1 (decanted part), and extracts 2, 3 and 4 (extracted by shaking for 1 minute, 5 minutes and 24 hours, respectively). The fractionated extracts were saponified with a solution of KOH in methanol, and neutralized with 10% hydrochloric acid. The products were dissolved in a mixture of dichloromethane and hexane, and individually fractionated by column chromatography on alumina and silica gel (saturated hydrocarbon, aromatic, alcohol and fatty acid fractions). n-Alkanes and isoprenoid aliphatic alkanes, polycyclic alkanes of sterane and triterpane types, alcohols and fatty acids were analyzed using gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). δ13CPDB values of individual n-alkanes in the aliphatic fractions were determined using gas chromatography-isotope ratio monitoring-mass spectrometry (GC-irmMS). Results and discussion. Extracts 1 and 2 are characterized by uniform distribution of n-alkanes, whereas extract 3 is characterized by an even-numbered members dominating the odd-ones, and extract 4 showed a bimodal distribution. Extract 1 is characterized by the least negative δ13CPDB values of C19-C26 n-alkanes. Sterane and triterpane analysis confirmed that all extracts originated from the same oil contaminant. n-Fatty acids, C19-C24, in all extracts are very low, being somewhat higher in extract 4. Even-numbered n-alcohols, C12–C16, were identified in the highest concentration in extract 3. It was assumed that algae were responsible for the composition of extract 3. Furthermore, a possible reason for higher concentrations of C19–C26 n-alkanes and C19–C24 fatty acids in extract 4 is the formation of inclusion compounds with colloidal micelles formed between the oil contaminant's NSO-compounds and water. Conclusion It was undoubtedly confirmed that there were specific differences in the compositions of the different extracts depending on the intensity of the interaction between the oil contaminant and the surface water. Recommendation and Outlook. When comparing the composition of oil contaminants from different water samples (regardless of the ultimate investigation goal) it is necessary to compare the extracts isolated under the same conditions, in other words, extracts that were in the same or very similar interaction with water.     

Estrogenic and esterase-inhibiting potency in rainwater in relation to pesticide concentrations,sampling season and location

In a year-round monitoring program (1998), pesticide composition and toxic potency of the mix of pollutants present in rainwater were measured. The goal of the study was to relate atmospheric deposition of toxic potency and pesticide composition to each other and to sampling period and local agricultural activity. Rainwater was collected in 26 consecutive periods of 14 days in a background location (BACK) and in two locations representative for different agricultural practices, i.e. intensive greenhouse horticulture (HORT) and flower bulb culture (BULB). Samples were chemically analyzed for carbamate (CARB), organophosphate (OP) and organochlorine (OC) pesticides and metabolites. Esterase inhibiting potency of rainwater extracts was measured in a specially developed bio-assay with honeybee esterases and was expressed as an equivalent concentration of the model inhibitor dichlorvos. Estrogenic potency of the extracts was measured in the ER-CALUX reporter gene assay and was expressed as an equivalent concentration of estradiol. Multivariate principal component analysis (PCA) techniques proved to be valuable tools to analyze the numerous pesticide concentrations in relation to toxic potency, sampling location, and sampling season. Pesticide composition in rainwater depended much more on sampling season than on sampling location, but differences between and were mainly attributed to local differences in agricultural practice. On average, the esterase inhibiting potency exceeded the maximum permissible concentration set for dichlorvos in The Netherlands, and was significantly higher in than in and . Esterase inhibition correlated significantly with OP and CARB concentrations, as expected given the working mechanism of these insecticides. The estrogenic potency incidentally exceeded NOEC levels reported for aquatic organisms and was highest in . Although estrogenic potency of rainwater correlated with OC concentrations, the ER-CALUX responses could not be attributed to any particular pesticides. Besides, the contribution of non-analyzed xeno-estrogens as alkylphenol(-ethoxylates) and bisphenol-A to the estrogenic potency of rainwater could not be excluded. Further research should focus on the chemical identification of estrogenic compounds in rainwater. In addition, more attention should be given to the ecological consequences of atmospheric deposition of individual pesticides and of total toxic potencies that regularly exceed environmental criteria for Dutch surface waters and/or toxic threshold values for aquatic organisms.     

Methane oxidation by Dutch grassland and peat soil microflora

The ability of Dutch grassland soil and Dutch peat soil for methane oxidation was investigated. The kinetics of methane oxidation by soil from different depths were determined in batch cultures incubated with 1; 10; 100; and 10,000 ppmv methane, respectively. All 4 applied concentrations of methane were degraded by both types of soil. Thereby, the highest oxidative activities were observed between 5 and 10 cm soil depth. Most importantly, these experiments demonstrated that this soil acts as a sink for methane even at concentrations well below 1 ppmv. Especially at higher methane concentrations (100 - 10,000 ppmv) much higher degradation rates were found in the peat soil. This also correlates with the higher methane production rates which had been observed in peat soil.