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Activated carbons (ACs) were developed from bio-waste materials like rice husk and peanut shell (PS) by various physicochemical activation methods. PS char digested in nitric acid followed by treatment at 673 K resulted in high surface area up to ~585 m2/g. The novelty of the present study is the identification of oxygen functional groups formed on the surface of activated carbons by infrared and X-ray photoelectron spectroscopy and quantification by using temperature programmed decomposition (TPD). Typical TPD data indicated that each activation method may lead to varying amounts of acidic and basic functional groups on the surface of the adsorbent, which may be a crucial factor in determining the adsorption capacity. It was shown that ACs developed during the present study are good adsorbents, especially for the removal of a model textile dye methylene blue (MB) from aqueous solution. As MB is a basic dye, H2O2-treated rice husk showed the best adsorption capacity, which is in agreement with the acidic groups present on the surface. Removal of the dye followed Langmuir isotherm model, whereas MB adsorption on ACs followed pseudo-second-order kinetics.  相似文献   
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The concentrations of chromium, iron, copper, nickel, lead, vanadium, and zinc in fish were determined to assess the impact of petroleum-refining activities and the 1991 Gulf War. Twenty-eight species of fish from the Kuwait coast were collected 50 m apart. Sample solutions prepared were analyzed using the atomic absorption spectrophotometry technique. Results show that fish samples contain 6.2 to 6.8 μg/g Cr, 4.2 to 96.2 μg/g Cu, 18.8 to 126.4 μg/g Fe, 0.5 to 20.4 μg/g Ni, 0.2 to 14.6 μg/g Pb, 0.02 to 15.6 μg/g V, and 7.6 to 81.3 μg/g Zn. Copper, nickel, and zinc in Station I, covering the Kuwait City area, were often greatly in excess of those present in Station II, covering the Al-Ahmadi area, while chromium, iron, lead, and vanadium were greater in Station II. Significant correlations were observed between some trace metals in fishes, indicating their common association.  相似文献   
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Azo dyes are among the oldest man-made chemicals and they are still widely used in the textile, printing and the food industries.About 10% - 15% of the total dyes used in the industry is released into the environment during the manufacturing and usage. Some dyes and some of their N-substituted aromatic bio-transformation products are toxic and/or carcinogenic and therefore these dyes are considered to beenvironmental pollutants and health hazards. These azo dyes are degraded by physico-chemical and biological methods. Of these, biological methods are considered to be the most economical and efficient. In this work, attempts were made to degrade these dyes aerobically. Theorganisms which were efficient in degrading the following azo dyes-Red RB, Remazol Red, Remazol Blue, Remazol Violet, Remazol Yellow,Golden Yellow, Remazol Orange, Remazol Black- were isolated from three different sources viz., wastewater treatment plant, paper milleffluent treatment plant and tannery was tewater treatment plant. The efficiency of azo dye degradation by mixed cultures from each source wasanalyzed. It was found that mixed cultures from tannery treatment plant worked efficiently in decolorizing Remazol Red, Remazol Orange,Remazol Blue and Remazol Violet, while mixed cultures from the paper mill effluent worked efficiently in decolorizing Red RB, Golden Yellow and Remazol Yellow. The mixed cultures from wastewater treatment plant efficiently decolorized Remazol Black.  相似文献   
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A facile and novel method has been developed for the determination of cadmium, chromium, copper, lead, and zinc from various water samples using FAAS. In the present investigation, a syringe was loaded with sorbent (rice bran) for the separation and enrichment of cadmium, chromium, copper, lead, and zinc, prior to their analysis by flame atomic absorption spectrometry which was described to substitute the batch and column techniques. The syringe was loaded with 2.0 g of sorbent in order to retain the analyte elements. Six milliliter of sample solution (pH 8.0 ± 0.2) was drawn into the syringe in 15 s and discharged over a period of 15 s. Then, 2.0 M HCl eluent was drawn into the syringe and ejected back to desorb the analyte elements. At the optimum conditions, the percentage recoveries of Cd, Cr, Cu, Pb, and Zn was in the range of 95.5–99.4% with SD of 0.10%. The elements could be concentrated by drawing and discharging several portions of sample successively. The detailed study of various interferences made the confirmation of the method highly selective. The risk of contamination is less than that with the column technique. The method was successfully applied for the determination of Cd, Cr, Cu, Pb, and Zn in spiked and natural water samples. The results obtained are in good agreement with the reported methods at the 95% confidence level.  相似文献   
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Soil nitrifiers have been showing an important role in assessing environmental pollution as sensitive biomarkers. In this study, the abundance and diversity of ammonia-oxidizing archaea (AOA) and ammonia-oxidizing bacteria (AOB) were investigated in long-term industrial waste effluent (IWE) polluted soils. Three different IWE polluted soils characterized as uncontaminated (R1), moderately contaminated (R2), and highly contaminated (R3) were collected in triplicate along Mahi River basin, Gujarat, Western India. Quantitative numbers of ammonia monooxygenase α-subunit (amoA) genes as well as 16S rRNA genes indicated apparent deleterious effect of IWE on abundance of soil AOA, AOB, bacteria, and archaeal populations. Relatively, AOB was more abundant than AOA in the highly contaminated soil R3, while predominance of AOA was noticed in uncontaminated (R1) and moderately contaminated (R2) soils. Soil potential nitrification rate (PNR) significantly (P?<?0.05) decreased in polluted soils R2 and R3. Reduced diversity accompanied by apparent community shifts of both AOB and AOA populations was detected in R2 and R3 soils. AOB were dominated with Nitrosospira-like sequences, whereas AOA were dominated by Thaumarchaeal “group 1.1b (Nitrososphaera clusters).” We suggest that the significant reduction in abundance and diversity AOA and AOB could serve as relevant bioindicators for soil quality monitoring of polluted sites. These results could be further useful for better understanding of AOB and AOA communities in polluted soils.  相似文献   
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Sediment samples were collected during the research vessel Umitaka-Maru cruises in the Gulf region from 15–16 December 1993 and 15–27 December 1994, from 19 and 24 locations, respectively. These samples were subjected to trace metal analysis to determine the 1991 Gulf War oil spill environmental impact in the area. The samples investigated are texturally classified into two main sediment classes: sand and mud. The total concentrations of lead, nickel, and vanadium found in the sediments from individual stations were investigated. The differences in trace metal concentrations reflect the variation in the overall composition of their host sediments. To better appraise the trace element composition of their host sediments and to determine the factors governing the trace metal distribution, the data were sub-divided into five groups among 1993 collections and seven groups during 1994. The concentration ranges of all three metals, lead (0.2–4.85), nickel (4.90–86.00), and vanadium (2.00–38.00) varied in different stations among the groups. The partitioning of trace elements between the detrial and non-detrital fractions of the sediments shows that: 1) The high concentrations of elements in mud is coupled with the increase in the detrital fraction; 2) In muddy sand sediments, nickel is bonded to the structural lattice of detrital minerals, whereas vanadium and lead held in the environmentally mobile fraction; and, 3) In sandy mud sediments, Ni is found in the detrital fraction, whereas V to slightly less extent and Pb show their non-detrital nature. The data were compared with unpolluted sediments throughout the ROPME Sea and worldwide, so the effect of anthropogenic enrichment upon the absolute concentration of the elements is minimal.  相似文献   
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The metal levels of arsenic, chromium, copper, lead, magnesium, manganese, selenium, vanadium, and zinc concentrations were determined in various body organs, viz., hepatopancreas, gills, gonad, gastric stomach, and muscle of the blue crab, Portunus pelagicus (Crustacea: Decapoda) to assess the bioaccumulation of metals associated with petroleum input a decade after the 1991 Gulf War oil spillage. Sample solutions prepared were analyzed using an atomic absorption spectrophotometry. High concentrations of Zn and Cu in the muscle and hepatopancreas tissues were a strong indicative of high exposure of P. pelagicus to these metals. However, muscle tissue had been found to accumulate the highest values for all metal speciations analyzed. Copper, zinc, and chromium in samples collected from Station II covering the Kuwait City area were often in excess of those present in Station I and III. Arsenic, lead, magnesium, manganese, selenium, and vanadium were greater in individuals obtained from Station I. A significant correlation was found to exist between Se and V in crab muscle with a surge in Se metal concentration, which was found to be inversely proportional to that of V metal concentration irrespective of the sex of the crab. The difference in patterns of metal occurrence and the significant increase in the Cu and Zn concentrations in various organs of the crab were largely associated with the 1991 Gulf War oil spill. Such results could be used as a baseline for the monitoring of the level of metals in marine organisms of future studies.  相似文献   
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In this study, advanced oxidation process utilizing Fenton's reaction was investigated for the decolorization and degradation of two commercial dyes viz., Red M5B, Blue MR and H-acid, a dye intermediate used in chemical industries for the synthesis of direct, reactive and azo dyes. Effect of Fe2 +, H2O2, pH, and contact time on the degradation of the dyes was studied. Maximum color and COD removal was obtained for Red MSB, H-acid and Blue MR at 10-25 mg/l of Fe2+ dose and 400-500 mg/l of H2O2 dose at pH 3.0. The initial oxidation reaction was found to fit into first order rate kinetics and the rate of oxidation of H-acid was higher than the other dyes. Release of chloride and sulfate from the Fenton's treated Red M5B dye and sulfate from H-acid and Blue MR indicates that the dye degradation proceeds through cleavage of the substituent group.  相似文献   
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