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191.
Phthalic acid esters (PAE) are commonly found in the sludge generated in the wastewater treatment plants. Anaerobic digestion followed by land application is a common treatment and disposal practice of sludge. To date, many studies exist on the anaerobic biodegradation rates of PAE, especially of the easily biodegradable ones, whereas the higher molecular weight PAE have reported to be non-biodegradable under methanogenic conditions. Furthermore, there is no information on the effect of the PAE on the performance of the anaerobic digesters treating sludge. In this study, the anaerobic biodegradation of di-n-butyl phthalate (DBP), di-ethyl phthalate (DEP) and di-ethylhexyl phthalate (DEHP) was investigated and their relative rates of anaerobic degradation were calculated. Also, the biological removal of PAE during the anaerobic digestion of sludge in bench-scale digesters was investigated using DBP and DEHP as model compounds of one biodegradable and one recalcitrant PAE respectively. The degradation of all the PAE tested in this study (DEP, DBP and DEHP) is adequately described by first-order kinetics. Batch and continuous experiments showed that DEP and DBP present in sludge are rapidly degraded under mesophilic anaerobic conditions (a first-order kinetic constant of 8.04 x 10(-2) and 13.69 x 10(-2)-4.35 day(-1) respectively) while DEHP is degraded at a rate between one to two orders of magnitude lower (0.35 x 10(-2)-3.59 x 10(-2) day(-1)). It is of high significance that experiments with anaerobic sludge of different origin (US and Europe) showed that degradation of DEHP occurs under methanogenic conditions. Accumulation of high levels of DEHP (more than 60 mg/l) in the anaerobic digester has a negative effect on DBP and DEHP removal rates as well as on the biogas production.  相似文献   
192.
Reza J  Trejo A  Vera-Avila LE 《Chemosphere》2002,47(9):933-945
An improved dynamic coupled column liquid chromatographic (DCCLC) technique for determining water solubility data of hydrophobic compounds is presented. The technique is based on pumping water through a thermostated generator column in order to generate emulsion-free, saturated aqueous solutions of the compound under study. Through a switching valve system the solute in the aqueous solution is extracted and concentrated by an on-line solid-phase extraction process and subsequently eluted and analyzed by high performance liquid chromatography (fluorescence detection coupled to photodiode array detection). The improvements carried out to the original DCCLC technique have given rise to savings in time for the experimental work and increased sensitivity during the detection and quantification stage. Applicability of the method for studying highly hydrophobic substances is demonstrated by determining water solubility of anthracene and pyrene in the temperature range of 8.9-49.9 and 8.5-32.2 degrees C, respectively. The measured water solubilities are in good agreement with the best available literature data. The method has also been applied to the determination of water solubility of m-terphenyl, 9, 10-dihydrophenanthrene and guaiazulene, in the temperature range of 4.8-49.9, 4.8-25.0, and 4.5-29.9 degrees C, respectively. The uncertainty in the Sw values determined in this work ranged from 0.7% to 4.6%. The experimental water solubility data, as a function of temperature, are fitted to the equation In Sw = A + B/T; where Sw and T are given in mole fraction and Kelvin, respectively.  相似文献   
193.
Using industrial by-products (IBPs) in conjunction with buffer strips provides a potentially new strategy for enhancing soluble phosphorus (P) removal from agricultural runoff. Here, we investigate the feasibility of this approach by assessing the P sorption properties of IBPs at different solution-IBPs contact time (1–120 min) and solution pH (3, 5.5, 7.5), as well as possible adverse environmental effects including P desorption or heavy metal mobilisation from IBPs. Batch experiments were carried out on two widely available IBPs in the UK that demonstrated high P sorption capacity but different physicochemical characteristics, specifically ochre and Aluminium (Al) based water treatment residuals (Al-WTR). A series of kinetic sorption–desorption experiments alongside kinetic modelling were used to understand the rate and the mechanisms of P removal across a range of reaction times. The results of the kinetic experiments indicated that P was initially sorbed rapidly to both ochre and Al-WTR, followed by a second phase characterised by a slower sorption rate. The excellent fits of kinetic sorption data to a pseudo-second order model for both materials suggested surface chemisorption as the rate-controlling mechanism. Neither ochre nor Al-WTR released substantial quantities of either P or heavy metals into solution, suggesting that they could be applied to buffer strip soils at recommended rates (≤30 g kg?1 soil) without adverse environmental impact. Although the rate of P sorption by freshly-generated Al-WTR applied to buffer strips reduced following air-drying, this would not limit its practical application to buffer strips in the field if adequate contact time with runoff was provided.  相似文献   
194.
195.

Introduction  

It is predicted that demand for electricity in Islamic Republic of Iran will continue to increase dramatically in the future due to the rapid pace of economic development leading to construction of new power plants. At the present time, most of electricity is generated by burning fossil fuels which result in emission of great deal of pollutants and greenhouse gases (GHG) such as SO2, NOx, and CO2. The power industry is the largest contributor to these emissions. Due to minimal emission of GHG by renewable and nuclear power plants, they are most suitable replacements for the fossil-fueled power plants. However, the nuclear power plants are more suitable than renewable power plants in providing baseload electricity. The Bushehr Nuclear Power Plant, the only nuclear power plant of Iran, is expected to start operation in 2010. This paper attempts to interpret the role of Bushehr nuclear power plant (BNPP) in CO2 emission trend of power plant sector in Iran.  相似文献   
196.
As a large and diverse group of secondary metabolites, phenolic compounds are one of the most common chemical pollutants present in water resources. these compounds can have toxic effects on ecosystems and humans. Therefore, their removal from water sources appears to be of great importance. In this study, a magnetic graphene oxide (MGO) photocatalyst was synthesized and used to remove phenol from water. The fabricated GO magnetic nanocomposites were determined by SEM and FTIR techniques. Afterward, these nanoparticles were used to remove phenol from aquatic media considering different operational parameters, including pH of the solution, initial concentration of phenol, contact time, and adsorbent dosage. The results showed that the magnetized GO nanoparticles could remove 90.83% of phenol molecules under the optimal conditions of solution pH = 3.0, initial phenol concentration of 20 mg/L, adsorbent concentration of 300 mg/L, and contact time of 120 min. additionally have compared the results of UV, Fe3O4/GO, and Fe3O4/GO/UV on the removal of phenol under optimum conditions. Accordingly, the phenol removal efficiencies for UV alone, Fe3O4/GO, and Fe3O4/GO/UV were obtained at 4.5, 65.73, and 90.83%, respectively. Based on the findings, the prepared magnetic GO nanoparticles have extended capabilities such as easy and rapid separation from sample and high potential in removing phenolic compounds, so, it can be introduced as an appropriate adsorbent for removal of this pollutant from water and wastewater.  相似文献   
197.
Heterogeneous catalysts are used for control of environmental pollution. Heterogeneous catalysts are easily separated from the reaction mixture, thus allowing their recovery and re-use. There is a need for catalysts that are efficient under mild conditions. Here, we show that silica-supported antimony(III) chloride (SbCl3/SiO2) acts as a highly efficient heterogeneous Lewis acid catalyst for the Paal–Knorr pyrrole synthesis at room temperature. We found that condensation of hexane-2,5-dione with aromatic and aliphatic primary amines in hexane using SbCl3/SiO2 with 7.6 wt% SbCl3 was the best reaction condition. The silica support facilitated the workup of the reaction mixture and provided a reusable catalyst at least for 7 runs without significant loss in activity. Indeed, the yield was 98% for the first run and 84% for the 7th run. We conclude that low catalyst loading, operational simplicity, practicability and applicability to various substrates make this reaction an interesting alternative to previously applied procedures. From the environmental standpoint, this eco-friendly catalyst is stable, highly active, easy to prepare and handle.  相似文献   
198.
This investigation discloses a greener reaction to prepare pyrrole derivatives. Metal-free catalysts are greener alternatives to existing metal catalysts in synthetic organic chemistry. Indeed, transition metals are often costly and toxic. They may be found as traces in health reaction products such as pharmaceuticals. Alternatively small organic molecules termed “organocatalysts” allow the synthesis of valuable products without traces of toxic metals. Here, we show for the first time the use of vitamin B1 as new organocatalyst for the Paal–Knorr pyrrole synthesis under ambient conditions. Reaction conditions were optimized for the reaction of hexane-2,5-dione with 4-methoxyaniline. Ethanol was the most effective solvent. The conversion was quantitative using vitamin B1, by comparison with a low yield of 30?% without catalysis. The best conditions were performed in ethanol with 5?mol % of vitamin B1 during 1?h. This reaction was tested using various aromatic amines. To conclude the use of vitamin B1 for the Paal–Knorr pyrrole, cyclocondensation has mild reaction conditions, is simple to perform, and gives moderate to excellent yields. It is therefore a promising reaction for the preparation of various pyrrole derivatives.  相似文献   
199.
Plants are unique sources of useful metabolites. Plant essential oils display a wide range of antimicrobial effects against various pathogens. Here, we studied the essential oil from the seeds of Carum copticum. We monitored aflatoxin by high-performance liquid chromatography. Results show that Carum copticum essential oil inhibits Asergillus parasiticus growth and prevents aflatoxin production. The half-maximal inhibitory concentration (IC50) is 127.5 μg mL?1 for aflatoxin B1 and 23.22 μg mL?1 for aflatoxin G1. Our findings show that Carum copticum essential oil is a potential candidate for the protection of foodstuff and feeds from toxigenic fungus growth and their subsequent aflatoxin contamination.  相似文献   
200.
The concentrations of four metals (Cd, Ni, Pb, and Cr) were determined in the muscles, gills, and livers of two edible fish species (Liza klunzingeri and Sillago sihama) caught from the Hara biosphere of Southern Iran. In both fish species, metal concentrations and bioaccumulation factors were in the sequence liver?>?gill?>?muscle. Bioaccumulation factors were found to be highest in S. sihama. The metal concentrations were descending in the order of Ni?>?Cr?>?Pb?>?Cd, except for muscle samples from S. sihama showing an inversion of Pb and Cr. There is a significant negative correlation between the concentrations of the metals in each tissue with length, weight, and age, except for muscle in L. klunzingeri. Some metal levels in the muscle exceeded the limits recommended by FAO, WHO, and FEPA.  相似文献   
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