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1.
The distribution and seasonal variations of petroleum residues in the Shatt al-Arab water column have been determined spectrofluorometrically. Their concentrations were found to vary between 1.7 to 35.4 μg L?1 Kuwait crude oil equivalents. The results suggested that petroleum hydrocarbons present in this river originated from diverse sources. Hydrocarbon amounts tend to be highest in winter (averaged 17.4 μg L?1) and lowest in summer (averaged 3.1 μg L?1).  相似文献   

2.
The solubilities and diffusion coefficients of crude oils having API° ranging from 11 to 28 have been measured in distilled and saline water of 44 g L?1 NaCl at temperatures 25, 35, and 45 °C. A linear relationship was observed between the maximum oil solubilities in distilled water and those in saline water for all the crudes over the range of temperature studied. The Setschenow salting-out parameter was found to be 0.125 independent of temperature and API°. Such a parameter is valuable in estimating the crude oil solubilities in waters of different salinity. An analytical solution for unsteady-state diffusion was done using Fourier series. A linear relationship was found between the diffusion coefficients of oils in distilled water and those in saline water. Observed data for diffusion coefficients of the oils have been correlated in terms of API°, temperature and ionic strength with an average absolute deviation of 2%.  相似文献   

3.
Cell wall material was extracted by five different methods from an oenological strain of Saccharomyces cerevisiae. Enzyme preparations containing beta-glucanase activity (Zymolyase, Glucanex, and Finizym 250L) allowed a better extraction yield compared to that of dithiothreitol (DTT) and EDTA. The yeast extracts were only soluble in part in wine. The wine-soluble fraction (WSF) of the five extracts, differing in both protein and sugar contents, when added in increasing amounts to white wine differently affected protein haze formation, as determined by the heat test, giving dose/response curves of different shapes. The curves obtained with the WSF derived from DDT and Zymolyase extracts showed a plateau value corresponding to 90% and 80% of wine haze reduction, respectively. In contrast, addition of the WSF derived from the other extracts resulted in increased turbidity with respect to the original wine. The mannoproteins (MP), isolated from each yeast extract by Concanavalin-A chromatography, gave dose/response curves showing shapes more similar among them than those obtained with the whole WSFs. The best wine stabilization was obtained with the MP of the DTT and Zymolyase extracts. The supernatants obtained after heating the MP of the different extracts were also tested. The stabilizing effect of the heat-stable MP (HSMP) was always larger than that of the corresponding total (un-heated) MP. The HSMP obtained starting from the DTT and Zymolyase extracts showed the best haze-protecting effect, which was, however, lower than that obtained with their corresponding WSF. This result suggests that wine protein stabilization by compounds of the yeast cell wall could be related, in addition to the action of the MP, also to the presence of other substances of different nature.  相似文献   

4.
Acute toxicity screening tests were conducted with water soluble fractions (WSFs) of a solvent refined coal (SRC-II) liquid from a pilot plant and three reference organisms: the cladoceran Daphnia magna, the fathead (FH) minnow Pimephales promelas, and larvae of the midge fly Chironomus tentans. Stock WSFs typically contained 900 to 1100 mg l?1 total carbon (TC) and 700 to 800 mg l?1 total dye complexable phenolics, with lower concentrations of aromatic and saturate hydrocarbons and N compounds. Under standard test conditions (temperature 20 °C, pH 7.3 to 8.2 and hardness 65 to 80 mg l?1 CaCO3), mean LC50 values in mg l? TC were 3.3 for daphnia, 11.l for FH minnow, and 13.7 for midge larvae. Acute toxicity was also examined under other water quality conditions (temperature 10 or 25 °C, pH 6.0 or 6.5, and hardness ? 180 to 220 mg 1?1 CaCO3). The coal liquid was less toxic to daphnids at 10 °C than at 20 or 25 °C, but response of other organisms at different temperatures varied. The pH of the liquid had little effect on toxicity values. All organisms were less susceptible in hard water. Chemical compositions of stock WSFs were similar, suggesting that temperature, pH, and hardness had little effect on solubility of major synfucl components. Dilution indexes for stock WSFs were higher than for petroleum oils, and reflect the greater solubility of chemicals from the liquified coal in freshwater.  相似文献   

5.
Effects of water-soluble-fractions (WSFs) from No. 2 Fuel Oil on growth and reproduction in a laboratory strain of Neanthes arenaceodentata were studied in experiments simulating conditions of acute and chronic sublethal exposure. Effects were defined relative to concentrations of diaromatic hydrocarbons (naphthalenes) and total dissolved hydrocarbons. Hatching of metatrochophore larvae was inversely related to WSF concentration and to the length of time larvae were exposed prior to hatching. Growth of larvae into juveniles was unaffected by low concentrations. Inhibition of larval growth by higher WSF concentrations was reversible upon return of larvae to hydrocarbon-free sea water. Growth of juveniles into adult polychaetes was inversely related to concentration. Rate of development to the feeding juvenile stage was not affected by WSF in three successive generations of continuously exposed polychaetes. Oocyte maturation rates in the four WSF concentrations (2.5, 5, 10, 2507o) increased with each successive generation. All concentrations suppressed fecundity in each generation. Survival to the 32-segment juvenile stage (brood mortality) was inversely related to concentration in first generation animals. Brood mortality in all WSF concentrations decreased with successive generations thereafter. Levels of naphthalenes in worms declined with each generation. Naphthalenes concentrations in third generation animals was very similar to those of exposure media.  相似文献   

6.
The effectiveness sewage sludge pellet fertilizer (SPF) as a nutrient source for containerized poinsettia (Euphorbia pulcherrima Willd. ex Klotz) was determined by comparing the growth and nutrient element content of ‘Eckespoint Celebrate 2’ plants grown with SPF in the growth medium versus plants fertilized with conventional water‐soluble fertilizer (WSF). Plants were grown in 1.6‐L pots of soilless growth medium with SPF incorporated at planting at the rates of 1.0, 1.5, 2.0, 2.5, or 3.0 gm nitrogen (N) pot‐1. Sludge pellet fertilizer plants received either no WSF or a dilute solution of 2ON‐4.3P‐16.6 potassium (K) (50 mg N L‐1) twice a week. Control plants had no SPF and were fertilized with WSF at 250 mg N L‐1 twice a week. At the end of the experiment plant growth measurements were made, leaves were analyzed for their nutrient element content, and growth medium was analyzed for pH and electrical conductivity (EC). Plants grown with SPF, with or without dilute WSF, were of commercially acceptable quality, but were somewhat smaller than the control plants. Plants growing with SPF alone and no WSF developed a chlorosis suggestive of N deficiency which was largely prevented by the application of WSF. Foliar analysis revealed that N in the leaves of plants receiving SPF alone was at the critical level for deficiency established for poinsettia. In treatments where dilute WSF was applied, the N content of the leaves was within the normal range. The foliar levels of all other nutrients fell within the normal ranges established for poinsettia in all SPF treatments. In addition to N deficiency, high growth medium EC at planting and low EC by the end of the experiment might also explain the inhibition of growth with SPF versus the WSF control. Results of this study suggest that poinsettia can be successfully grown using SPF as the sole source of nutrition, however the best growth is possible only when a dilute solution of N‐containing WSF is applied on a regular basis.  相似文献   

7.
Ninety-one ground water samples (predominantly from springs) in two mineralized areas of the Ouachita Mountains in west-central Arkansas, were analyzed for Fe, Mn, Zn, Cu, Co, Ni, Pb, Hg, Sb, Sr, Ba, Ca, and Li. These areas contain Mn, barite, strontianite, cinnabar, stibnite and scattered Pb-Zn mineralization, Cumulative frequency curves were used to determine the threshold and anomalous concentrations for each element in the two areas. These values were, in general, higher in the ground water from the more mineralized area for several of the base metals, but most notably for Mn and Fe, the principal metals in the Mn oxide minerals. The United States Environmental Protection Agency (EPA, 1976) criteria for Fe (300 μg L ?1) and Mn (50 μg L?1) in drinking water were exceeded, respectively, in 34% and 30% of the springs in Area I, and 13% and 23% in Area II. One spring exceeded the EPA Hg criterion (2 μg L?1) and 3 springs exceeded the 50 μg L?1 criterion for Pb. In spite of the large number of anomalous Ba concentrations, the highest concentration of Ba was 930 μg L?1 (EPA criterion 1000 μg L ?1).  相似文献   

8.
Background, Aim and Scope  Unresolved complex mixtures (UCM) of hydrocarbons, containing many thousands of compounds which cannot be resolved by conventional gas chromatography (GC), are common contaminants of sediments but little is known of their potential to affect sediment-dwelling organisms. Evidence exists for reduced health status in mussels, arising from aqueous exposure to aromatic UCM components acting through a narcotic mode of action. However, UCM contaminants in sediments may not be sufficiently bioavailable to elicit toxic effects. The aim of our study was therefore to measure the sublethal effects of chronic exposure to model UCM-dominated oils at environmentally realistic concentrations and compare this to effects produced by a UCM containing weathered crude oil. A further aim was to determine which, if any, fractions of the oils were responsible for any observed toxicity. Materials and Methods  Whole oils were spiked into estuarine sediment to give nominal concentrations of 500 μg g−1 dry weight. Juveniles of the estuarine amphipod Corophium volutator were exposed to the contaminated sediment for 35 days and their survival, growth rate and reproductive success quantified. Using an effect-directed fractionation approach, the oils were fractionated into aliphatic and two aromatic fractions by open column chromatography and their toxicity assessed by further chronic exposures using juvenile C. volutator. Results  The growth rates of amphipods were reduced following exposure to the oils although this was only statistically significant for the weathered oil; reproductive success was reduced by all oil exposures. Sediment spiked with UCM fractions also caused reduced growth and reproduction but no particular fraction was found to be responsible for the observed toxicity. Survivorship was not affected by any oil or fraction. Discussion  The study showed that chronic exposure to sediments contaminated by UCM-dominated oils could have population level effects on amphipods. The observed effects could not be explained by hydrocarbons resolved by conventional GC and effects were similar for both UCM-dominated and weathered oils. All of the fractions appeared to contribute to the observed effects; this is in contrast to previous research which had shown that an aliphatic UCM did not cause adverse effects in mussels. Conclusions  To our knowledge, this is the first study to demonstrate population-level effects arising from exposure to sediments contaminated by realistic environmental concentrations of UCM hydrocarbons. The results are consistent with many compounds, at very low individual concentrations, contributing towards the overall observed toxicity. Recommendations  Risk assessments of contaminated sediments should take into account the contribution towards the potential for toxic effects from UCM hydrocarbons. Studies into sediment contamination should report both aliphatic and aromatic UCM concentrations to aid risk assessments. ESS-Submission Editor: Henner Hollert (hollert@uni-heidelberg.de) This paper has been developed from a presentation at SETAC Europe 16th Annual Meeting 2006 held at the The Hague, The Netherlands.  相似文献   

9.
The stability of the antioxidant fraction in edible vegetable oils has been evaluated during a simulated deep frying process at 180 °C. Four edible oils (i.e., extra-virgin olive oil with a 400 μg/mL overall content in naturally existing phenols; high-oleic sunflower oil without natural content of these compounds but enriched either with hydrophilic antioxidants isolated from olive pomace or with an oxidation inhibitor, dimethylsiloxane; and sunflower oil without enrichment) were subjected to deep heating consisting of 20 cycles at 180 °C for 5 min each. An oil aliquot was sampled after each heating cycle to study the influence of heating on the antioxidant fraction composed of hydrophilic and lipophilic antioxidants such as phenols and tocopherols, respectively. The decomposition curves for each group of compounds caused by the influence of deep heating were studied to compare their resistance to oxidation. Thus, the suitability of olive pomace as raw material to obtain these compounds offers an excellent alternative to the use of olive-tree materials different from leaves. The enrichment of refined edible oils with natural antioxidants from olive pomace is a sustainable strategy to take benefits from this residue.  相似文献   

10.
Some important edible oils (extra virgin olive oil, canola oil, and sunflower oil) were added to aqueous glucose-lysine or xylose-lysine model systems to investigate their effect on the formation of volatiles from the Maillard reaction (MR). The volatile compounds were extracted by a Likens-Nickerson apparatus and quantified. Pyrazines, Maillard reaction products with an important impact on food flavor, appeared to be particularly sensitive to the presence of the oils in both the xylose-lysine and glucose-lysine model systems. The unsubstituted pyrazine was formed more with olive oil, less with canola oil, and even less with sunflower oil, whereas 2-methylpyrazine, 2,5-methylpyrazine, and 2,3-dimethylpyrazine were formed less with olive oil, more with canola oil, and even more with sunflower. The oxidative states of the oils and their fatty acid fingerprints were determined: the results indicated that the relative amounts of the pyrazines are sensitive to the degree of unsaturation of the oil. The autoxidation of the volatile compounds generated from the MR, investigated by the addition of free radical modulators (antioxidants alpha-tocopherol, 2,6-di-tert-butyl-4-methylphenol, and rosemary extract; or pro-oxidant alpha,alpha'-azobis-isobutyronitrile, a free radical initiator), was limited in respect to aqueous model systems.  相似文献   

11.
N-alkanes were measured both in dissolved and particulate-adsorbed phases of water samples collected from five stations located along Shatt al-Arab River in Iraq. The aim of this study was to provide a background information on the presence, origin, and distribution of n-alkanes in the waters of Shatt al-Arab River. Total concentrations of n-alkanes were lower in the dissolved phase (29.37 (μg L?1) than in the particulate-adsorbed fraction (17.62 μg g?1 dw). Distribution of n-alkanes in both fractions is characterized by two distinct patterns. First, for C compounds numbered C14 to C22, the ‘odd’ numbered hydrocarbons were slightly more abundant with C17 being the most concentrated. The second is shown within n-alkanes greater than C22. In these the ‘odd’ numbered hydrocarbons show even greater predominance indicating that much of the n-alkanes in the waters of Shatt al-Arab, may have originated from aquatic biogenic sources; i.e., diatoms, algal forms, bacterial activities, and higher plants. The CPI values were found to be from 0.99 to 1.98 in the dissolved fraction and from 0.70 to 2.10 in the particulate fraction. Petroleum hydrocarbon inputs and urban related oil discharges (anthropogenic pollution) may also have contributed to the input of n-alkanes in Shatt al-Arab, particularly near the city of Basrah (St. IV). Total concentrations at station IV were much higher (8.40 μg L?1 and 5.80 μg g?1) than that for the most upstream station, # I, (3.20 μg L?1 and 1.48 μg g?1) and decreased again further downstream at station V (7.10 μg L?1 and 4.32 μg g?1). The CPI values were around 1.0 in station IV. In a conclusion, results obtained in this study indicate that the n-alkanes in the waters of Shatt al-Arab River are of aquatic biogenic and anthropogenic (petroleum related) origins.  相似文献   

12.
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13.
In order to elucidate the details of both the distribution and fate of organotin compounds (OTs) in the costal ecosystem, the concentrations of butyltin compounds (BTs) and phenyltin compounds (PTs) were determined in seawater, sediment and blue mussels Mytilus galloprovincialis collected in Maizuru Bay, Japan. The concentrations of tributyltin (TBT) in seawater, sediments and mussels ranged from 3.9 to 27 ng l?1, from 1.2 to 19 ng g?1 dry wt and from 0.77 to 11 ng g?1 wet wt, respectively. Although the levels of TBT in seawater, sediments and mussels from Maizuru Bay were lower than those reported previously at other sites in Japan, the levels can still be toxic to susceptible organisms. Trace amounts of PTs were also found in seawater, sediment and mussel samples, indicating that there is a slight input of triphenyltin (TPT) into the seawater in the bay at present. The highest TBT concentration in seawater among all sites measured in the bay was found near a glass factory, and the lowest concentrations were observed at the center of the bay. The highest concentration of TBT in sediment was detected near a shipyard. In mussels, a high concentration of TBT was detected near a cement plant and timberyard. These results indicate that the major sources of contamination of OTs in the bay are considered to be from those facilities and ships. The proportion of TBT in seawater and mussels showed that, of total BTs, it was the predominant compound at most sites. These results suggested that there is a continuous input of TBT into the seawater and thereafter an accumulation of TBT in mussels due to their low metabolic capacity to degrade TBT. In sediment, the proportion of monobutyltin (MBT) was the highest of BTs at most sites. This could reflect a previous contamination by TBT used before the regulation of its usage in the bay.  相似文献   

14.
A simple and precise analytical method for the determination of hydroxy pentacyclic triterpene acids (HPTAs) in vegetable oils was developed. The acidic fraction was isolated by solid-phase extraction using bonded aminopropyl cartridges, and the extract was silylated and analyzed by gas chromatography. Repeatability and recovery of the method were determined. In virgin olive oils, similar amounts of oleanolic (3beta-hydroxyolean-12-en-28-oic) and maslinic (2alpha,3beta-dihydroxyolean-12-ene-28oic) acids and traces of ursolic (3beta-hydroxyurs-12-en-28-oic) acid were found. The main factor affecting HPTA concentration was the oil quality since that increases as the quality decreases, while olive variety, olive ripeness, and oil extraction system had less influence. In crude olive pomace oils, the concentrations were very much higher than in virgin olive oils. During refining processes, total or significant losses of HPTAs were observed. Esterified derivatives of HPTAs were not found.  相似文献   

15.
Solvents, greases, and rinse waters from routine vehicle maintenance contain heavy metals and volatile organic chemicals (VOCs). In Wisconsin, these fluids enter catch basins along with rinsing waters and are discharged to soil infiltration systems drainfields after mixing with domestic wastewaters in a septic tank. The purpose of this study was to monitor heavy metal and VOC removal and treatment in catch basins and septic tanks at four publicly-owned motor vehicle service stations (MVSS). Cadmium, chromium, and lead were found in catch basin wastewater, septic tank effluent, and septic tank sludge at concentrations ranging from 0.002–7.7 mg L?1. Lead was found in the highest concentration. The highest concentrations of metals were in septic tank sludge. Of the >50 VOCs scanned for in catch basin wastewater, septic tank effluent, and septic tank sludge samples, 29 were found in concentrations that exceeded analytical detection limits. Concentrations of detected VOCs ranged from 1.0–15,800 µg L?1 and the highest concentrations of VOCs were found in catch basin wastewater and septic tank sludge. Acetone, ethylbenzene, toluene, and xylenes were the most commonly found VOCs at all sampling locations. Thus, heavy metals and VOCs were not completely removed in catch basins and were discharged to septic tanks where removal occured possibly as these contaminants settled with solids in the sludge. The level of treatment was, however, inadequate and heavy metals and VOCs were discharged to drainfields.  相似文献   

16.
The objective of this study was to identify and quantify volatile organic compounds (VOCs) produced during composting of poultry litter. The VOCs produced from in-vessel composting with a controlled aeration system were tested using the F-ITR method by VOC analyzer. Alkanes and alkylated benzenes were emitted in the highest amounts from poultry litter, while aldehydes, terpenes, ketones were emitted in much lesser amounts. Studies showed that VOCs generation was the greatest early during the composting process and greatly reduced thereafter. Composting temperatures were found to affect VOCs. All VOCs were least with the high temperatures generated during composting.  相似文献   

17.
The water chemistry of 21 outlet brooks in undisturbed, forested catchments (0.074–38 km2) in Finland was monitored during three years (1997–1999) in order to estimate the background levels and leaching of total organic carbon (TOC), iron, nitrogen and phosphorus, and examine the relationships between catchment characteristics and brook water quality in pristine forested areas. The studied catchments are located throughout Finland except the northernmost parts of the country. The concentrations of TOC were relatively high, on average 20 mg L-1. Annual leaching of TOC ranged from 3000 to 10 000 kg km-2. The average total nitrogen concentration and annual leaching were 430 μg L-1 and 140 kg km-2, respectively. The average total phosphorus concentration and annual leaching were 15 μg L-1 and 5.4 kg km-2, respectively. On a national level temperature and discharge conditions were the most important variables for predicting total phosphorus, total nitrogen and TOC concentrations. Both total nitrogen and total phosphorus concentrationsdisplayed positive correlation with temperature, and thus the concentrations were higher in the south than in the north. Nitrogen was mainly organic and showed strong correlation with TOC. On the catchment level, both TOC and total nitrogen concentrations and export had a strongpositive correlation with the abundance of Norway spruce (Piceaabies Karsten) and a strong negative correlation with the abundance of Scots pine (Pinus sylvestris L.). Nitrate concentrations and leaching were related to average site type. The more fertile the average site type was in the catchment, the higher the nitrate concentrations and export were.  相似文献   

18.
Taking Cd as an example we introduce a procedure to estimate tolerable total content of heavy metals in soils with regard to a specific ground water quality criterion. Furthermore, we present a piston‐flow approach to estimate breakthrough times of a sorptive solute to the ground water. Both procedures are applied to the sandy soils in the 4300 ha wastewater irrigation area Braunschweig, Germany. Applicability of these procedures is tested by numerical simulations. The calculated breakthrough times of Cd for an input concentration of 3 μg L−1 and a mean water flux density of 570 mm yr−1 varies, as a function of depth of water table and sorption characteristics, between 10 and 805 years (mean = 141 years). The deviation between the piston‐flow approach and the numerical simulation is on the average 1.6%. We determined a mean tolerable total Cd content of 0.61 mg kg−1 with regard to a ground water quality criterion of 3 μg L−1. The limit of the German sewage sludge regulation (AbfKlärV, 1992) of 1 mg Cd kg−1 exceeds the calculated tolerable total content in 90% of the investigated Ap horizons. Moreover, the results of the numerical simulations show that the limit of 1 mg Cd kg−1 would lead to a concentration in seepage water significantly above 8 μg Cd L−1. We conclude that in the sandy soils of the wastewater irrigation area the current limit of 1 mg Cd kg−1 is not sufficient to keep the Cd concentration in seepage water below 3 μg L−1 and, thus, to ensure ground water protection in the long run.  相似文献   

19.
Sequential extraction processing (SEP) is a new approach to fractionating dried, flaked corn using 95% ethanol. In the original process, corn oil was extracted at 76°C in a countercurrent mode while simultaneously dehydrating the ethanol. This resulted in 20% of the protein (predominantly zein) coextracting with the oil. The process was modified to reduce the amount of coextracted protein. One modification (mSEP1) was to use a blend of 30% hexane and 70% ethanol at 56°C. A second modification (mSEP2) used a longer extraction column (L/D ratio 15) to replace the column with L/D 2 used in the original SEP system. To determine the effect of the modifications on oil quality, the quality of the crude corn oils produced from the modified SEP processes were compared with the quality of oil from the original SEP. To evaluate the quality of the three crude oils produced by SEP with the process typically used in industry, they were compared with the quality of laboratory hexane‐extracted corn oil. The results of the three SEP oils exhibited larger concentrations of fatty acids, phospholipids, and carotenoids, smaller concentrations of triacylglycerols, and darker red color than the hexane‐extracted oil. The oils from the two modified SEP processes contained smaller concentrations of free fatty acids and phospholipids and larger concentrations of triacylglycerols and carotenoids than the original SEP oil. In spite of the improvements to the oil through process modifications, the mSEP1 and mSEP2 oils exhibit greater refining losses than hexane‐extracted oil.  相似文献   

20.
The background levels of residual oils in the Western North Atlantic off the east coast of Nova Scotia decreased from approximately 6 to about 2 μgl?1 during May 1970 to January 1971 following a major spill of Bunker C fuel oil from the tanker ARROW which was wrecked in Chedabucto Bay, Nova Scotia on February 4, 1970.  相似文献   

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