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81.
Cadmium in blood of Tunisian men and risk of bladder cancer: interactions with arsenic exposure and smoking 总被引:1,自引:0,他引:1
Molka Feki-Tounsi Pablo Olmedo Fernando Gil Rim Khlifi Mohamed-Nabil Mhiri Ahmed Rebai Amel Hamza-Chaffai 《Environmental science and pollution research international》2013,20(10):7204-7213
Prior investigations identified an association between low-level blood arsenic (As) and bladder cancer risk among Tunisian men but questions remain regarding confounding by cadmium (Cd), a well-established bladder carcinogen. A case–control study of Tunisian men was re-examined to assess the levels of cadmium in blood and reparse the association between the simultaneous exposure to these metals and bladder cancer risk. Levels of blood Cd were significantly twice higher among cases than in controls (P?<?0.05) and were positively correlated with smoking and age. Additionally, analysis of metal levels among non-smokers according to the region of residence showed very high blood Cd and As levels for the coastal regions of Sfax and central Tunisia. After controlling for potential confounders, for low blood As levels (<0.67 μg/L), the OR for blood Cd was 4.10 (95 % CI 1.64–10.81), while for higher levels (>0.67 μg/L), it was reduced to 2.10 (CI, 1.06–4.17). Adjustment for Cd exposure did not alter the risk associated to As exposure. This study is the first to report the relationship between Cd exposure and risk of bladder cancer occurrence in interaction with smoking and As exposure. Smoking is shown to be the main exposure source to Cd in the Tunisian population but also environmental pollution seems to be responsible of Cd exposure among non-smokers. Exposure assessment studies encompassing a wider population are needed. 相似文献
82.
In this paper, Loofa egyptiaca (LE), an agricultural plant cultivated in Egypt, was used to prepare low-cost activated carbon (LEC1 and LEC2) adsorbents. The adsorbents (LE, LEC1 and LEC2) were evaluated for their ability to remove direct blue 106 dye from aqueous solutions. Batch mode experiments were conducted using various parameters such as pH, contact time, dye concentration and adsorbent concentration. The surface chemistry of LE, LEC1 and LEC2 was analyzed by scanning electron microscopy (SEM). The experimental data were examined using Langmuir, Freundlich, Temkin and Harkins–Jura isotherms. The results showed that the adsorption of direct blue 106 was maximal at the lowest value of pH (pH = 2). Removal efficiency was increased with an increase in dye concentration and a decrease in amount of adsorbent. Maximum adsorption capacity was found to be 57.14, 63.3 and 73.53 mg/g for LE, LEC1 and LEC2 respectively. Kinetics were also investigated using pseudo-first-order, pseudo-second-order and intra-particle diffusion models. The experimental data fitted very well with the pseudo-first-order and pseudo-second-order kinetic models. The results indicate that LE, LEC1 and LEC2 could be employed as adsorbents for the removal of direct blue dye from aqueous solutions. 相似文献
83.
Heavy metal contamination from mining sites in South Morocco: Monitoring metal content and toxicity of soil runoff and groundwater 总被引:5,自引:0,他引:5
El Khalil H El Hamiani O Bitton G Ouazzani N Boularbah A 《Environmental monitoring and assessment》2008,136(1-3):147-160
The aim of the present work is the assessment of metal toxicity in runoff, in their contaminated soils and in the groundwater
sampled from two mining areas in the region of Marrakech using a microbial bioassay MetPLATE™. This bioassay is based on the
specific inhibition of the β-galactosidase enzyme of a mutant strain of Escherichia coli, by the metallic pollutants. The stream waters from all sampling stations in the two mines were all very toxic and displayed
percent enzyme inhibition exceeding 87% except SWA4 and SWB1 stations in mine C. Their high concentrations of copper (Cu) and zinc (Zn) confirm the acute toxicity shown by MetPLATE.
The pH of stream waters from mine B and C varied between 2.1 and 6.2 and was probably responsible for metal mobilization,
suggesting a problem of acid mine drainage in these mining areas. The bioassay MetPLATE™ was also applied to mine tailings
and to soils contaminated by the acidic waters. The results show that the high toxicity of these soils and tailings was mainly
due to the relatively concentration of soluble Zn and Cu. The use of MetPLATE™ in groundwater toxicity testing shows that,
most of the samples exhibited low metal toxicity (2.7–45.5% inhibition) except GW3 of the mine B (95.3% inhibition during
the wet season and 82.9% inhibition during the dry season). This high toxicity is attributed to the higher than usual concentrations
of Cu (189 μg Cu l−1) and Zn (1505 μg Zn l−1). These results show the potential risk of the contamination of different ecosystems situated to the vicinity of these two
metalliferous sites. The general trend observed was an increase in metal toxicity measured by the MetPLATE with increasing
total and mobile metal concentrations in the studied matrices. Therefore, the MetPLATE bioassay is a reliable and fast bioassay
to estimate the metals toxicity in the aquatic and solids samples. 相似文献
84.
85.
Mass transfer and reaction kinetics of raw Nile water ozonation are examined. The contact system is a perfectly mixed reactor, and ozone is bubbled through a glass diffuser at different supply rates. The ozone residual is detected for different reaction time intervals. A simple mathematical model is proposed to describe the mechanism of the ozone reactions in the reactor. The proposed model quite accurately describes the mass transfer behaviour in the reactor and determines the ozone dissociation rate constant, together with the effect of the chemical reaction on the ozone transfer. A linear relationship is observed between the ozone feed rate and the ozone residual. First order reaction kinetics describes fairly well the autodecomposition and the global reaction rates of ozone in raw water. The mass transfer coefficient is about 0.18 min−1. The dissociation and the reaction rate constants are evaluated to be 0.33 mg L−1 and 0.19 mg L−1min−1. 相似文献
86.
The Distribution and Sources of Polycyclic Aromatic Hydrocarbons in Surface Sediments Along the Egyptian Mediterranean Coast 总被引:2,自引:0,他引:2
El Nemr A Said TO Khaled A El-Sikaily A Abd-Allah AM 《Environmental monitoring and assessment》2007,124(1-3):343-359
Coastal marine sediment samples were collected from 31 sampling stations along the Egyptian Mediterranean Sea coast. All sediment
samples were analyzed to determine aliphatic and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC)
contents and grain size analysis. Total concentrations of 16 EPA-PAHs in the sediments were varied from 88 to 6338 ng g−1 with an average value of 154 ng g−1 (dry weight). However, the concentrations of total aliphatic were varied from 1.3 to 69.9 ng g−1 with an average value of 15.6 ng g−1 (dry weight). The highest contents of PAHs were found in the Eastern harbor (6338 ng g−1), Manzala (5206 ng g−1) and El-Jamil East (4895 ng g−1) locations. Good correlations observed between a certain numbers of PAH concentrations allowed to identify its origin. The
average total organic carbon (TOC) percent was varied from 0.91 to 4.54%. Higher concentration of total pyrolytic hydrocarbons
(∑COMB) than total fossil hydrocarbons (∑PHE) declared that atmospheric fall-out is the significant source of PAHs to marine
sediments of the Egyptian Mediterranean coast. The selected marked compounds, a principal component analysis (PCA) and special
PAHs compound ratios (phenanthrene/anthracene vs fluoranthene/pyrene; ∑COMB/∑EPA-PAHs) suggest the pyrogenic origins, especially
traffic exhausts, are the dominant sources of PAHs in most locations. Interferences of rather petrogenic and pyrolytic PAH
contaminations were noticed in the harbors due to petroleum products deliveries and fuel combustion emissions from the ships
staying alongside the quays. 相似文献
87.
Cluster analysis and quality assessment of logged water at an irrigation project, eastern Saudi Arabia 总被引:8,自引:2,他引:6
A multivariate statistical technique, cluster analysis, was used to assess the logged surface water quality at an irrigation project at Al-Fadhley, Eastern Province, Saudi Arabia. The principal idea behind using the technique was to utilize all available hydrochemical variables in the quality assessment including trace elements and other ions which are not considered in conventional techniques for water quality assessments like Stiff and Piper diagrams. Furthermore, the area belongs to an irrigation project where water contamination associated with the use of fertilizers, insecticides and pesticides is expected. This quality assessment study was carried out on a total of 34 surface/logged water samples. To gain a greater insight in terms of the seasonal variation of water quality, 17 samples were collected from both summer and winter seasons. The collected samples were analyzed for a total of 23 water quality parameters including pH, TDS, conductivity, alkalinity, sulfate, chloride, bicarbonate, nitrate, phosphate, bromide, fluoride, calcium, magnesium, sodium, potassium, arsenic, boron, copper, cobalt, iron, lithium, manganese, molybdenum, nickel, selenium, mercury and zinc. Cluster analysis in both Q and R modes was used. Q-mode analysis resulted in three distinct water types for both the summer and winter seasons. Q-mode analysis also showed the spatial as well as temporal variation in water quality. R-mode cluster analysis led to the conclusion that there are two major sources of contamination for the surface/shallow groundwater in the area: fertilizers, micronutrients, pesticides, and insecticides used in agricultural activities, and non-point natural sources. 相似文献
88.
Alireza A. Shamshirsaz Kelsey A. Stewart Hadi Erfani Ahmed A. Nassr Nathan C. Sundgren Amy R. Mehollin-Ray Shaine A. Morris Jimmy Espinoza Magdalena Sanz Cortes Christopher Cassady Timothy C. Lee Eumenia C. Castro Olutoyin A. Olutoye Deepak K. Mehta Darrell Cass Oluyinka O. Olutoye Michael A. Belfort 《黑龙江环境通报》2019,39(4):287-292
89.
Harrelkas F Paulo A Alves MM El Khadir L Zahraa O Pons MN van der Zee FP 《Chemosphere》2008,72(11):1816-1822
A photocatalytic process based on immobilized titanium dioxide was used to treat crude solutions of azo, anthraquinone and phthalocyanine textile dyes. In addition, the process was applied to the treat autoxidized chemically reduced azo dyes, i.e. representatives of recalcitrant dye residues after biological sequential anaerobic-aerobic treatment. Photocatalysis was able to remove more than 90% color from crude as well as autoxidized chemically reduced dye solutions. UV-absorbance and COD were also removed but to a lower extent (50% in average). The end products of photocatalytic treatment were not toxic toward methanogenic bacteria. The results demonstrate that photocatalysis can be used as a pre- or post-treatment method to biological anaerobic treatment of dye-containing textile wastewater. 相似文献
90.
Dissolution of raw phosphate (apatite) in sea water of the Gulf of Aqaba was investigated through lab incubation experiments. Three types from three different sources (Al-Hasa, Al-Abyad and Esh-Shydiya) have been used for these experiments. Impact of quantity, grain size, and source (type) of raw phosphate on dissolution rate were studied. Statistical analysis shows significant differences between the results obtained from comparing each two weights; as weight of apatite increased, dissolved inorganic phosphate-phosphorus (DIP) and fluoride in sea water solution increased. The differences between the dissolution rates of raw phosphate from the three sites were not significant while the differences between the different grain size fractions were significant. Dissolution rates were inversely related to particle size. Using a worst-case scenario, a conservative estimate of the maximum increase in DIP in seawater of the Gulf of Aqaba due to the apatite particles lost to the sea during ship loading resulted in DIP concentrations of 0.03 μM per year. As the residence time of the water in the Gulf of Aqaba is about one year, the DIP concentration will not increase by more than 0.03 μM under the estimated annual quantity of exported phosphate. Fluoride will not increase by more than 0.03 mg/l under the same conditions. 相似文献