共查询到20条相似文献，搜索用时 31 毫秒
1.
H. Hellmann 《洁净——土壤、空气、水》1995,23(3):121-130
Fine Resolution of UV Spectra by Differentiation of 1st and 2nd Order in Hydrocarbon Analysis Basic UV spectra (0th order) in unpolar solvents such as cyclohexane are useful — though with some reservations — in characterizing mineral oils occuring in pure form and aromatic fractions in environmental samples separated by chromatographic techniques. The common standard raffinates, biogenic hydrocarbons or other mixes of hydrocarbons including polycyclic aromatics can be approximately identified. The spectra of 1st and 2nd order improve the reliability of the results and permit above all to detect polycondensated aromatics even in traces. Finally, partial spectra of 1st and 2nd order in the wavelength ranges 205…240, 220…260, and 260…320 nm allow because of their very specific structures a simple and fast practically definite assignment to the above-mentioned groups of aromatics. Analogously, substituted aromatics in detergents and other technical products have already been identified. The method is suitable as a fast preliminary test, at least. 相似文献
2.
Craig L. Patterson Fernando Cadena Rajib Sinha Dzung Kim Ngo‐Kidd Abbas Ghassemi E. Radha Krishnan 《Ground Water Monitoring & Remediation》2013,33(2):44-52
Methyl‐tertiary butyl ether (MTBE) is often found in groundwater as a result of gasoline spills and leaking underground storage tanks. An extrapolation of occurrence data in 2008 estimated at least one detection of MTBE in approximately 165 small and large public water systems serving 896,000 people nationally (United States Environmental Protection Agency [U.S. EPA] 2008). The objective of this collaborative field study was to evaluate a small groundwater treatment system to determine the effectiveness of ultraviolet (UV)/ozone treatment in removing MTBE from contaminated drinking water wells. A pilot‐scale advanced oxidation process (AOP) system was tested to evaluate the oxidation efficiency of MTBE and intermediates under field conditions. This system used ozone as an oxidizer in the presence of UV light at hydraulic retention times varying from 1 to 3 min. MTBE removal efficiencies approaching 97% were possible with this system, even with low retention times. The intermediate t‐butyl alcohol (TBA) was removed to a lesser extent (71%) under the same test conditions. The main intermediate formed in the oxidation process of the contaminated groundwater in these studies was acetone. The concentrations of the other anticipated intermediates t‐butyl formate (TBF), isopropyl alcohol (IPA), methyl acetate (MAc), and possible co‐occurring aromatics (BTEX) in the effluent were negligible. 相似文献
3.
Hsu YY Hsiung TL Paul Wang H Fukushima Y Wei YL Chang JE 《Marine pollution bulletin》2008,57(6-12):873-876
The nitrogen-doped TiO(2) nanotube (N-TNT) thin films were synthesized using ZnO nanorods as the template and doped with urea at 623K. Under ultraviolet (UV) and visible light irradiation, the efficiencies for photocatalytic degradation of methylene blue is as high as 30%. About 10% of toluene (representing aromatics in the spill oils) in sea water can be photocatalytically degraded under visible light radiation for 120 min. The aliphatic model compound (1-hexadecene) has, on the contrary, a less efficiency (8%) on the N-TNT photocatalyst. On the average, under visible light radiation, the effectnesses of the N-TNT for photocatalytic degradation of model compounds in the spill oils in sea water are 0.38 mg toluene/gN-TNTh and 0.25 mg 1-hexadecene/gN-TNTh. It is expected that spill oils in the harbors or seashores can be adsorbed and photocatalytically degraded on the N-TNT thin films that are coated onto levee at the sea water surface level. 相似文献
4.
K.-M. Wollin 《洁净——土壤、空气、水》1987,15(5):459-469
Artificial nitrate solutions and a large number of membranefiltered nitrate-containing water samples from Mecklenburgian lakes and rivers were investigated in the spectral range of 200… 260 nm with a dual beam spectrophotometer. By the formation of derivative spectra there are achieved a higher spectral resolution and the elimination of undesired disturbing effects since first- and higher-order derivatives are formed. As it is known, the direct spectrophotometric nitrate determination is influenced by organic substances and some inorganic ions of natural waters. As a result, the UV derivative spectroscopy of 2nd order is recommended as a suitable technique of nitrate analysis for surface waters with a high degree of accuracy and precision – detailed reports on investigations being given. Compared with the equivalent salicylate method, however, the expenditure of the UV derivative spectroscopy described is considerably lower. 相似文献
5.
A method is described for the determination of fifteen active ingredients of plant protecting products in ground-, raw, and drinking water. After extraction and enrichment of the pesticides from the water sample with solid-phase extraction, the extract is fractionated on silica-coated TLC plates, first in a so-called screening gradient by AMD (automated multiple development). The detection of the pesticides is performed by UV multidetection. Positive results from the first separation are confirmed by a second separation on silica in an AMD gradient of distinctly different selectivity, compared to the first separation. Following this strategy, it is possible to distinguish nearly all nonvolatile, from water extractable, active ingredients of plant protecting products in the market. UV spectra are taken for further confirmation of positive results. In most cases, this is possible even at the limit of determination. All chromatograms and spectra shown are raw data, resulting from the confirmatory test DIN 38407 part 11, in the laboratory of one participant*). The method is standardized in the meantime as DIN V 38407-11. 相似文献
6.
Ying-Ya Hsu Tung-Li Hsiung H. Paul Wang Yasuhiro Fukushima Yu-Ling Wei Juu-En Chang 《Marine pollution bulletin》2008,57(6-12):873
The nitrogen-doped TiO2 nanotube (N-TNT) thin films were synthesized using ZnO nanorods as the template and doped with urea at 623 K. Under ultraviolet (UV) and visible light irradiation, the efficiencies for photocatalytic degradation of methylene blue is as high as 30%. About 10% of toluene (representing aromatics in the spill oils) in sea water can be photocatalytically degraded under visible light radiation for 120 min. The aliphatic model compound (1-hexadecene) has, on the contrary, a less efficiency (8%) on the N-TNT photocatalyst. On the average, under visible light radiation, the effectnesses of the N-TNT for photocatalytic degradation of model compounds in the spill oils in sea water are 0.38 mg toluene/gN-TNT h and 0.25 mg 1-hexadecene/gN-TNT h. It is expected that spill oils in the harbors or seashores can be adsorbed and photocatalytically degraded on the N-TNT thin films that are coated onto levee at the sea water surface level. 相似文献
7.
Monitoring and evaluation of groundwater quality in drinking water protectorates is of particular interest if the uncontrolled entry of pollutants, for example by infiltrating river water, cannot be excluded. A fluorescence spectroscopic method is presented as possible alternative to the conventional expensive hydrochemical investigations. This method uses the information yielded by synchronous fluorescence spectra. After a Fourier transformation of the original spectra and a following discriminant analysis, the samples can be classified in different groups corresponding to the different types of groundwater. The method was tested in the drinking water protectorate of a waterworks of a German metropolis (Halle, Sachsen-Anhalt). We found a prediction rate of about 90% in the investigated case. 相似文献
8.
In presence of disinfectants, PAH are remobilized from the coal tar lining of water distribution mains. Reactions of the PAH with chlorine and chlorine dioxide can lead to chlorinated PAH that might show higher mutagenic effects than the parent PAH. The application of the solid-phase microextraction as a sampling preparation method in combination with a gas chromatographic mass spectrometric device is a reliable and useful method to achieve detection limits in the lower nanogramme-per-liter level for PAH and chlorinated PAH. Thus, the reactions of four PAH (anthracene, fluoranthene, fluorene, and phenanthrene) with chlorine and chlorine dioxide under conditions prevalent in drinking water distribution systems could be investigated. In batch experiments with demineralized and drinking water at pH 7, the concentrations of fluoranthene, fluorene, and phenanthrene remained constant, whereas anthracene reacted quantitatively with both disinfectants. In these reactions, no chlorinated products could be detected, only mono-hydroxyanthracene and anthraquinone were formed. A reaction mechanism for both reaction products is proposed. The results suggest that oxidation is the major pathway of the reaction of PAH with disinfectants in the systems under investigation. 相似文献
9.
Thomas Heberer Dirk Feldmann Kirsten Reddersen Hans‐Juergen Altmann Thomas Zimmermann 《洁净——土壤、空气、水》2002,30(1):24-33
In military out of area missions of the Bundeswehr, it can be necessary to produce drinking water even from highly polluted surface waters containing a variety of organic, inorganic, and microbiological contaminants. Thus, mobile drinking water purification systems must be able to remove such contaminants as far as possible to meet the requirements of the German and European drinking water regulation/directive. Presently, two novel drinking water purification units applying membrane filtration undergo intensive long‐term trials carried out by the Bundeswehr. If these trials positively proof the functionality of these units and their ability to remove all possible contaminants they shall substitute so far available devices which use large amounts of chemicals and charcoal filtration for water purification.In the course of a research project, the functionality of the new devices and their efficacy to remove high amounts of algae, microbes, and organic and inorganic pollutants are additionally tested in “worst‐case” field studies. In September 2000, the first mobile drinking water purification unit was tested at the Teltowkanal in Berlin, Germany.This canal was chosen because it carries high burdens of municipal sewage effluents. The results from the fatigue test confirmed the ability of the water purification unit to reduce the concentrations of all contaminants meeting the maximum tolerance levels set by the German/European drinking water regulation.The pre‐filtration device was very effective in removing algae and solid particles to protect the membranes from clogging and to enable an almost maintenance‐free operation. Residues of pharmaceuticals and some other organic contaminants have almost totally been removed from the surface water where they were detected at individual concentrations up to the μg/L‐level. 相似文献
10.
Vera Pavlova Pavel Babica Detelina Todorova Zlatka Bratanova Blahoslav Mar&#x;lek 《洁净——土壤、空气、水》2006,34(5):437-441
This paper presents the results from analyses of water samples from 15 Bulgarian reservoirs and lakes for detection of microcystins presence by high‐performance liquid chromatography (HPLC) coupled to a ultraviolet (UV) and photo diode array (PDA) detector. In 3 of the studied drinking water reservoirs cyanobacterial blooms were not detected. Cyanobacterial blooms were observed in 6 of 12 investigated water bodies used for fishing and water sports. Microcystis was the dominant cyanobacterial genus. The concentration of total microcystins in the biomasses ranged from 8 to 1070 μg g–1 (d.w.). Microcystin‐LR and microcystin‐RR were the predominant microcystins, followed by microcystin‐YR. Presence of dissolved microcystins was obtained in one water sample with concentration of total microcystins 1.64 μg L–1. Presence of microcystin‐LF and ‐LW or unknown peaks possessing characteristic microcystin‐like UV‐spectra were not detected. Those first results for occurrence of microcystins in some Bulgarian reservoirs and lakes are a contribution to the knowledge on their distribution. 相似文献
11.
Bacterial growth measurements in treated waters from different origins. Measuring growth curves of bacteria in a drinking water gives information on the regrowth potential of the water in the pipe system. The method which was developed by Werner was used for analyzing drinking waters from different origins. As a negative control high purity water and as positive control acetate were used. It is proposed to use acetate-C-equivalents for quantification because the biodegradable part of total dissolved organic carbon (DOC) is mostly below 0,1 mg/1 in treated waters. The analyses of treated surface waters showed results from 40–80 μg/1 acetate-C-equivalents, whereas in treated waters from ground water and bankfiltrates the concentration of easily biodegradable organic carbon was between 10 and 20 μg/1 acetate-C-equivalents. This is in the region of high purity water, where in average 9 μg/1 acetate-C-equivalents are detected, which therefore is the detection limit of the method. These waters normally do not show any regrowth problems. 相似文献
12.
Results of Investigations of Substances Deriving from Detergents in Eastern German Rivers Based on detergent related parameters like surfactants, phosphate, and boron as well as general pollution parameters like TOC, DOC, COD and O2, a differentiated picture of the loading situation of the most important rivers in Eastern Germany is drawn. In comparison with investigations previously carried out in the GDR, the development of the surface water pollution will be demonstrated, and it can be shown that a significant improvement of the water quality has taken place. Comparisons between the loads of the river Rhine and those found in East German rivers show clear differences that are obviously due to different populations in the river catchment areas as well as to different hydrographical conditions. Increased surfactant and boron concentrations can be found especially in smaller Eastern German rivers with relatively great catchment areas. The introduction of phosphate replacements in detergents in 1990 led to a drastic reduction of the phosphate concentrations in most Eastern German rivers. 相似文献
13.
In a survey in Greece from 1987 to 2000 hepatotoxic cyanobacterial blooms were observed in 9 out of 33 freshwaters. Microcystins (MCYSTs) were detected by HPLC in 7 of these lakes, and the total MCYST concentration per scum dry weight ranged from 50.3 to 1638 ± 464 μg g—1. Cyanobacterial genera (Microcystis, Anabaena, Anabaenopsis, Aphanizomenon, Cylindrospermopsis) with known toxin producing taxa were present in 31 freshwaters. From our data and a review of the literature, it would appear that Mediterranean countries are more likely 1) to have toxic cyanobacterial blooms consisting of Microcystis spp. and 2) to have higher intracellular MCYST concentrations. A case study in Lake Kastoria is used to highlight seasonal patterns of cyanobacterial and MCYST‐LR occurrence and to assess cyanotoxin risk. Cyanobacterial biovolume was high (> 11 μL L—1) throughout the year and was in excess of Guidance Level 2 (10 μL L—1) proposed by WHO for recreational waters and Alert Level 2 for drinking water. Further, surface water samples from April to November exceeded Guidance Level 3, with the potential for acute cyanobacterial poisoning. Intracellular MCYST‐LR concentrations (max 3186 μg L—1) exceeded the WHO guideline for drinking water (1 μg L—1) from September to November with a high risk of adverse health effects. Preliminary evidence indicates that in 3 lakes microcystins are accumulated in some aquatic organisms. Generally, a high risk level can be deduced from the data for the Mediterranean region. 相似文献
14.
Quality Requirements for Fresh Waters: Water Quality Targets, Water Quality Objectives, and Chemical Water Quality Classification In the Federal Republic of Germany, water quality requirements for the protection of inland surface waters against hazardous substances are formulated on the basis of a quality targets derivation concept developed jointly by the Federal Government and the Federal States. The quality requirements were termed “water quality targets” in order to make it clear that the values derived are orientational values rather than legally binding limit values. The international comparison of quality requirements for surface waters shows that, on the whole, the national quality targets ensure a high level of protection. According to present scientific knowledge, impairments of uses, such as supply of drinking water, or risks to aquatic communities need not to be expected if the quality targets are complied with. A comparison of water quality data with the water quality targets makes it possible, on the one hand, to identify those substances whose inputs must be further reduced; on the other hand, it also shows that, for a number of substances, there is no need at present for concern over their adversely water quality. A further differentiation of the aquatic hazard potential of pollutants allows a water quality classification system to be developed on the basis of the quality targets derivation concept. The basic elements of this water quality classification system are presented, and its application is explained by way of examples. 相似文献
15.
《Marine pollution bulletin》2013,69(1-2):13-20
Many studies have investigated phototoxicity under controlled laboratory conditions, however, few have actually demonstrated it occurring in environmental samples. Here we report on the potential for UK marine coastal waters to demonstrate phototoxicity when tested using the oyster embryo (Crassostrea gigas) bioassay in the presence UV light. Subsurface water, sea surface microlayer samples and subsurface water samples that had been extracted through solid phase extraction (SPE) columns were analysed. Results demonstrated that the majority of samples failed to display any phototoxic potential. However, those collected from Belfast Lough did display an increase in toxicity when bioassays were performed in the presence of UV light when compared to identical samples assayed in the absence of UV light. Analysis of water samples at this location identified known phototoxic PAHs, pyrene and fluoranthene. These findings suggest the need to consider the potential UV light has when determining the toxicity of environmental samples. 相似文献
16.
M. Kruhm-Pimpl 《洁净——土壤、空气、水》1993,21(3):145-152
The results of a series of investigations are presented, performed by the governmental chemical laboratory Karlsruhe (CLUA) in order to determine pesticides in drinking water for purposes of food monitoring. 231 samples of 8 municipal water supplies (groundwater wells/no bank filtrate) and 34 private water supplies close to the bank of the river Rhine (groundwater wells/partly bank filtrate) were analysed. The sampling sites were located between Mannheim and Greffern, Germany. In 1986 high amounts of atrazine and simazine were determined in the drinking water wells of several private water supplies, especially at the sampling sites in the south. The likewise high chloride content of the samples was taken as a proof of bank filtrate contributing to the water. The decrease of atrazine load in the river water of the Rhine since 1987 has its parallel in the analytical results for the concerned drinking water wells. Obviously the pesticide contamination of water from bank filtrate pumping wells is mainly depending on the pesticide load of the river water. The application of fertilizers and pesticides in the fields seems not to be a significant source of the pesticide contamination of dringing waters derived from bank filtrate water. For reasons of public health a monitoring of pesticide content in bank filtrate pumping wells of private water supplies is recommended. 相似文献
17.
Aromatic sulfonates can be found in drinking water. Thus, they must have passed water treatment and survived ozonation. Degradation of aromatic sulfonates can be achieved by the UV/H2O2‐process. Since drinking water is often treated with chlorine as a disinfectant, the formation of disinfection by‐products has to be considered. Therefore, the production of AOX (on activated carbon adsorbable organic halogens) after chlorination of the sulfonates with and without preoxidation was investigated. Instead of the analysis of the individual degradation products, the determination of the sum parameter AOX was used as a fast screening method. The investigated sulfonates were: anthraquinone‐2‐sulfonate, naphthalene‐2‐sulfonate, 2‐aminonaphthalene‐1‐sulfonate, and 4,4′‐diaminostilbene‐2,2′‐disulfonate. All sulfonates containing amino groups showed high potentials of AOX formation. The preoxidation with ozone increased the potentials of AOX formation in general. Treating the sulfonates by using the UV/H2O2‐process, the formation potentials run to zero after going through a maximum value. 相似文献
18.
A highly sensitive and specific enzyme immunoassay (EIA) is described for the detection of the atrazine metabolite hydroxyatrazine. Polyclonal antibodies were raised in rabbits by immunization with a hapten-bovine serum albumin (BSA) conjugate containing 8 hapten residues per molecule of BSA. An EIA with a horseradish peroxidase (HRP) hapten tracer was optimized in microtitre plates. A concentration of 50% B/B0 was found at 0.10 μg/L for hydroxyatrazine. A limit of determination for hydroxyatrazine was reached at approximately 0.01 μg/L, i.e. well below the maximum concentration permitted by the EU guidelines for drinking water and the drinking water ordinance of the FRG. The assay did not require concentration or clean-up steps for drinking water or ground water samples. Validation experiments confirmed a good accuracy and precision. Hydroxyatrazine is reported to be the main atrazine metabolite found in soil samples. As organic solvents are usually employed for soil extraction, the influence of methanol as representative organic solvent on the assay was examined. Up to a concentration of 5% (v/v) methanol, the organic solvent did not affect the assay. 相似文献
19.
The present study aims to investigate physico‐chemical and bacterial characteristics of Nasser Lake water and houses drinking water, as well as fish cultures and its wastewater, in three villages west of Lake Nasser, Egypt. Fifteen representative water samples (Nasser Lake, different drinking water, fish cultures, and wastewater sources) were collected from three villages (Garf Hussein, Bashaier, and Kalabsha) in the west of Lake Nasser. Physico‐chemical, total viable counts, and bacterial qualification of water were achieved. The obtained results indicated that the produced water, supposed to be for domestic use in the three villages, contained all the tested organisms. The investigated water samples of the lake and drinking water in the selected three villages are supposed to be chemically safe according to World Health Organization and to Egyptian standards for drinking water. Water pollution index (WPI) was used in this study and the result concluded that for irrigation canals from the lake to the agriculture site, fish cultures (both concrete and earth pond systems), and drainage canal of fish ponds need to be treated before it is discharged to the lake. It is better to reuse it after treatment for agricultural purposes or recycled it to the fish cultures. 相似文献
20.
Juan Pesántez Christian Birkel Giovanny M. Mosquera Pablo Peña Viviana Arízaga-Idrovo Emma Mora William H. McDowell Patricio Crespo 《水文研究》2021,35(9):e14357
Monitoring the temporal variation of solute concentrations in streams at high temporal frequency can play an important role in understanding the hydrological and biogeochemical behaviour of catchments. UV–visible spectrometry is a relatively inexpensive and easily used tool to infer those concentrations in streams at high temporal resolution. However, it is not yet clear which solutes can be modelled with such an in-situ sensor. Here, we installed a UV–visible spectrometer probe (200–750 nm) in a high-altitude tropical Páramo stream to record the wavelength absorbance at a 5-min temporal resolution. For calibration, we simultaneously sampled stream water at a 4-h frequency from February 2018 to March 2019 for subsequent laboratory analysis. Absorbance spectra and laboratory-determined solute concentrations were used to identify the best calibration method and to determine which solute concentrations can be effectively inferred using in situ spectrometry through the evaluation of six calibration methods of different mathematical complexity. Based on the Nash – Sutcliffe efficiency (NSE) and Akaike information criterion metrics, our results suggest that multivariate methods always outperformed simpler strategies to infer solute concentrations. Eleven out of 21 studied solutes (Al, DOC, Ca, Cu, K, Mg, N, Na, Rb, Si and Sr) were successfully calibrated (NSE >0.50) and could be inferred using UV–visible spectrometry even with a reduced daily sampling frequency. It is worth noting that most calibrated solutes were correlated with wavelengths (WLs) in the low range of the spectra (i.e., UV range) and showed relatively good correlation with DOC. The latter suggests that estimation of metal concentrations could be possible in other streams with a high organic load (e.g., peat dominated catchments). In situ operation of spectrometers to monitor water quality parameters at high temporal frequency (sub-hourly) can enhance the protection of human water supplies and aquatic ecosystems as well as providing information for assessing catchment hydrological functioning. 相似文献