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231.
Cáceres TP Megharaj M Naidu R 《Journal of environmental science and health. Part. B》2008,43(7):605-610
Fenamiphos (0-ethyl-0(3-methyl-4-methylthiophenyl)-isopropylamido-phosphate) is a widely used nematicide and insecticide in bowling greens and agriculture, but information on its sorption including its metabolites is limited. Hence, the sorption of fenamiphos (nematicide) and its major degradation products fenamiphos sulfoxide (FSO) and fenamiphos sulfone (FSO2) were determined in thirteen contrasting soils collected from Australia and Ecuador. The sorption coefficients (Kd) exhibited a wide range of variation from 2.48 to 14.94 L/Kg for fenamiphos; from 0 to 7.42 L/Kg for FSO and from 0 to 9.49 L/Kg for FSO2. The sorption affinity of the three compounds for all soils tested was as follows: fenamiphos > fenamiphos sulfone > fenamiphos sulfoxide. The results showed that the sorption of fenamiphos and its metabolites in some soils is very low, and in one case is nonexistant for the metabolites. This is of particular concern as due to its low sorption coefficient, the compound could easily migrate and contaminate water bodies. Fenamiphos and its oxidation products have been reported to be highly toxic to aquatic invertebrates and therefore, the information generated in this study assumes great importance in the risk assessment of fenamiphos and its metabolites in the environment. 相似文献
232.
Ureña-Amate MD Socías-Viciana MM González-Pradas E Cantos-Molina A Villafranca-Sánchez M López-Teruel C 《Journal of environmental science and health. Part. B》2008,43(2):141-150
The adsorption of chloridazon (5-amine-4-chloro-2-phenylpyridazin-3(2H)-one) on kerolite samples heated at 110 degrees C (K-110), 200 degrees C (K-200), 400 degrees C (K-400), 600 degrees C (K-600) and acid-treated with H(2)SO(4) solutions of two different concentrations (0.25 and 0.5 M) (K-0.25 and K-0.5, respectively) from pure water at 25 degrees C has been studied by using batch and column experiments. The adsorption experimental data points were fitted to the Freundlich equation in order to calculate the adsorption capacities (K(f)) of the samples; K(f) values ranged from 184.7 mg kg(-1) (K-0.5) up to 2253 mg kg(-1) (K-600). This indicated that the heat treatment given to the kerolite greatly increases its adsorption capacity for the herbicide whereas the acid treatment produces a clear decrease in the amount of chloridazon adsorbed. The removal efficiency (R) was also calculated; R values ranging from 52.8% (K-0.5) up to 88.3% (K-600). Thus, the results showed that the 600 degrees C heat-treated kerolite was more effective in relation to adsorption of chloridazon and it might be reasonably used in removing this herbicide from water. 相似文献
233.
Kinetic extractions to assess mobilization of Zn, Pb, Cu, and Cd in a metal-contaminated soil: EDTA vs. citrate 总被引:4,自引:0,他引:4
Labanowski J Monna F Bermond A Cambier P Fernandez C Lamy I van Oort F 《Environmental pollution (Barking, Essex : 1987)》2008,152(3):693-701
Kinetic EDTA and citrate extractions were used to mimic metal mobilization in a soil contaminated by metallurgical fallout. Modeling of metal removal rates vs. time distinguished two metal pools: readily labile (QM1) and less labile (QM2). In citrate extractions, total extractability (QM1+QM2) of Zn and Cd was proportionally higher than for Pb and Cu. Proportions of Pb and Cu extracted with EDTA were three times higher than when using citrate. We observed similar QM1/QM2 ratios for Zn and Cu regardless of the extractant, suggesting comparable binding energies to soil constituents. However, for Pb and Cd, more heterogeneous binding energies were hypothesized to explain different kinetic extraction behaviors. Proportions of citrate-labile metals were found consistent with their short-term, in-situ mobility assessed in the studied soil, i.e., metal amount released in the soil solution or extracted by cultivated plants. Kinetic EDTA extractions were hypothesized to be more predictive for long-term metal migration with depth. 相似文献
234.
Hernández-Allica J Becerril JM Garbisu C 《Environmental pollution (Barking, Essex : 1987)》2008,152(1):32-40
A hydroponic screening method was used to identify high biomass crop plants with the ability to accumulate metals. Highest values of shoot accumulation were found in maize cv. Ranchero, rapeseed cv. Karat, and cardoon cv. Peralta for Pb (18 753 mg kg(-1)), Zn (10 916 mg kg(-1)), and Cd (242 mg kg(-1)), respectively. Subsequently, we tested the potential of these three cultivars for the phytoextraction of a metal spiked compost, finding out that, in cardoon and maize plants, increasing Zn and Cd concentrations led to lower values of root and shoot DW. By contrast, rapeseed shoot growth was not significantly affected by Cd concentration. Finally, a metal polluted soil was used to check these cultivars' phytoextraction capacity. Although the soil was phytotoxic enough to prevent the growth of cardoon and rapeseed plants, maize plants phytoextracted 3.7 mg Zn pot(-1). We concluded that the phytoextraction performance of cultivars varies depending on the screening method used. 相似文献
235.
In field arsenic removal from natural water by zero-valent iron assisted by solar radiation 总被引:1,自引:0,他引:1
Cornejo L Lienqueo H Arenas M Acarapi J Contreras D Yáñez J Mansilla HD 《Environmental pollution (Barking, Essex : 1987)》2008,156(3):827-831
An in situ arsenic removal method applicable to highly contaminated water is presented. The method is based in the use of steel wool, lemon juice and solar radiation. The method was evaluated using water from the Camarones River, Atacama Desert in northern Chile, in which the arsenic concentration ranges between 1000 and 1300 μg L−1. Response surface method analysis was used to optimize the amount of zero-valent iron (steel wool) and the citrate concentration (lemon juice) to be used. The optimal conditions when using solar radiation to remove arsenic from natural water from the Camarones river are: 1.3 g L−1 of steel wool and one drop (ca. 0.04 mL) of lemon juice. Under these conditions, removal percentages are higher than 99.5% and the final arsenic concentration is below 10 μg L−1. This highly effective arsenic removal method is easy to use and inexpensive to implement. 相似文献
236.
Alletto L Benoit P Bergheaud V Coquet Y 《Environmental pollution (Barking, Essex : 1987)》2008,156(3):678-688
Laboratory studies were conducted to evaluate the effects of temperature and water pressure head on the degradation of the diketonitrile metabolite (DKN) of isoxaflutole during 84 d in samples collected in a loamy soil under conventional (CT) and conservation (MT) tillage systems. Soil temperature was the major factor controlling DKN degradation in the two tillage systems. The shortest half-lives (T1/2) were measured in the seedbed samples under MT at 25 °C and −33 cm water pressure head. We found that mouldboard ploughing under CT was responsible for the spatial variability of herbicide degradation properties, whereas under MT herbicide degradation was associated to the vertical distribution of organic matter. 相似文献
237.
Pambrun V Marquot A Racault Y 《Environmental science and pollution research international》2008,15(7):592-599
Background, aims, and scope Sometimes, urban wastewaters convey a more or less significant part of toxic products from industries or the craft industry.
Nitrifying activity can be affected by these substances, implying higher ammonia concentrations in the outlet effluent and
contributing to toxicity for the aquatic environment. Moreover, the more stringently treated wastewater standards now require
a reliable treatment for nitrogen. One of the key issues is the identification of the inhibition behavior of nitrifying bacteria
facing a toxic substance. This new understanding could then finally be integrated into models in order to represent and to
optimize wastewater treatment plants (WWTP) operation in cases involving ‘toxic scenarios’.
Materials and methods The toxic substances studied in this work, cadmium and 3.5-dichlorophenol (3.5-DCP), are representative of chemical substances
commonly found in municipal sewage and industrial effluents and symbolize two different contaminant groups. The effects of
Cd and 3.5-DCP on nitrification kinetics have been investigated using respirometry techniques.
Results IC50 values determination gives concentrations of 3.1 mg/L for 3.5-DCP and 45.8 mg/L for Cd at 21 ± 1°C. The variation to
low temperature seems to have no real effect on IC50 for DCP, but induces a decrease of cadmium IC50 to 27.5 mg/L at 14°C.
Finally, specific respirometric tests have been carried out in order to determine the potential effect of these toxic substances
on the nitrifying decay rate b
a
. No significant effect has been noticed for Cd, whereas the presence of 3.5-DCP (at IC50 concentration) induced a dramatic
increase of b
a
at 20°C. The same behavior has been confirmed by experiments performed in winter periods with a sludge temperature around
12°C.
Discussion The target substances have different modes of action on activity and mortality, notably due to the abilities of the contaminant
to be precipitated, accumulated, or even to be progressively degraded. Studies realized at low temperature confirmed this
assumption, and put in evidence the effect of temperature on toxic substances capable of being biosorbed. However, the change
in the sludge sample characteristics can be pointed out as a problem in the investigation of the temperature effect on nitrification
inhibition, as biosorption, bioaccumulation, and predation are directly linked to the sludge characteristics (VSS concentration,
temperature) and the plant operating conditions (loading rates, sludge age, etc.).
Conclusions This work brings new understandings concerning the action mode of these specific contaminants on nitrifying bacteria and,
in particular, on the role of temperature. The experiments lead to the determination of the IC50 values for both toxic substances
on biological nitrification. The inhibition mechanisms of Cd and 3.5-DCP on nitrifying activity have been simply represented
by a non-competitive inhibition model.
Recommendations and perspectives Other experiments carried out in a continuous lab-scale pilot plant should be done with a proper control of the operating
conditions and of the sludge characteristics in order to better understand the mechanisms of nitrification inhibition for
each contaminant. Finally, these first results show that toxic substances can have an effect on the growth rate but also on
the decay rate, depending on the characteristics of the toxic substance and the sludge. This eventual double effect would
imply different strategies of WWTP operation according to the behavior of the contaminant on the bacteria. 相似文献
238.
Levels of perfluorochemicals in water samples from Catalonia,Spain: is drinking water a significant contribution to human exposure? 总被引:2,自引:0,他引:2
Ericson I Nadal M van Bavel B Lindström G Domingo JL 《Environmental science and pollution research international》2008,15(7):614-619
Background, aim, and scope In recent years, due to a high persistence, biomagnification in food webs, presence in remote regions, and potential toxicity,
perfluorochemicals (PFCs) have generated a considerable interest. The present study was aimed to determine the levels of perfluorooctane
sulfonate (PFOS), perfluorooctanoic acid (PFOA), and other PFCs in drinking water (tap and bottled) and river water samples
from Tarragona Province (Catalonia, Spain).
Materials and methods Municipal drinking (tap) water samples were collected from the four most populated towns in the Tarragona Province, whereas
samples of bottled waters were purchased from supermarkets. River water samples were collected from the Ebro (two samples),
Cortiella, and Francolí Rivers. After pretreatment, PFC analyses were performed by HPLC-MS. Quantification was done using
the internal standard method, with recoveries between 68% and 118%.
Results In tap water, PFOS and PFOA levels ranged between 0.39 and 0.87 ng/L (0.78 and 1.74 pmol/L) and between 0.32 and 6.28 ng/L
(0.77 and 15.2 pmol/L), respectively. PFHpA, PFHxS, and PFNA were also other detected PFCs. PFC levels were notably lower
in bottled water, where PFOS could not be detected in any sample. Moreover, PFHpA, PFHxS, PFOA, PFNA, PFOS, PFOSA, and PFDA
could be detected in the river water samples. PFOS and PFOA concentrations were between <0.24 and 5.88 ng/L (<0.48 and 11.8 pmol/L)
and between <0.22 and 24.9 ng/L (<0.53 and 60.1 pmol/L), respectively.
Discussion Assuming a human water consumption of 2 L per day, the daily intake of PFOS and PFOA by the population of the area under evaluation
was calculated (0.78–1.74 and 12.6 ng, respectively). It was found that drinking water might be a source of exposure to PFCs
as important as the dietary intake of these pollutants.
Conclusions The contribution of drinking water (tap and bottled) to the human daily intake of various PFCs has been compared for the first
time with data from dietary intake of these PFCs. It was noted that in certain cases, drinking water can be a source of exposure
to PFCs as important as the dietary intake of these pollutants although the current concentrations were similar or lower than
those reported in the literature for surface water samples from a number of regions and countries.
Recommendations and perspectives Further studies should be carried out in order to increase the knowledge of the role of drinking water in human exposure to
PFCs. 相似文献
239.
Preparation of a porous clay heterostructure and study of its adsorption capacity of phenol and chlorinated phenols from aqueous solutions. 总被引:1,自引:0,他引:1
Sofía Arellano-Cárdenas Tzayhrí Gallardo-Velázquez Guillermo Osorio-Revilla Ma del Socorro López-Cortez 《Water environment research》2008,80(1):60-67
A porous clay heterostructure (PCH) from a Mexican clay was prepared and characterized, and its aqueous phenol and dichlorophenols (DCPs) adsorption capacities were studied using a batch equilibrium technique. The PCH displayed a surface area of 305.5 m2/g, 37.2 A average porous diameter, and a basal space of 23.2 A. The adsorption capacity shown by the PCH for both phenol and DCPs from water (14.5 mg/g for phenol; 48.7 mg/g for 3,4-DCP; and 45.5 mg/g for 2,5-DCP) suggests that the PCH has both hydrophobic and hydrophilic characteristics, as a result of the presence of silanol and siloxane groups formed during the pillaring and calcination of the PCH. The values of maximal adsorption capacity for dichlorophenols were higher than those reported for aluminum pillared clays and some inorgano-organo clays and comparable with some ionic exchange resins. 相似文献
240.
de Souza Pereira M Heitmann D Reifenhäuser W Meire RO Santos LS Torres JP Malm O Körner W 《Chemosphere》2007,67(9):1736-1745
Monitoring of immission of persistent organic pollutants in the industrialized area of Volta Redonda (V.R.) and in the National Park of Itatiaia (PNI) in southeast Brazil was performed using an endemic bromeliad species as biomonitor and measuring bulk deposition rates of polychlorinated biphenyls (PCB) and polycyclic aromatic hydrocarbons (PAH). For the sum of PCB, overall deposition rates were between 17 and 314 ng/(m2 day) in winter and between 43 and 81 ng/(m2 day) in summer, respectively. Deposition rates of dioxin-like PCBs ranged from 0.14 to 2.8 pg WHO-TEQ/(m2 day) in winter and from 0.90 to 4.3 pg WHO-TEQ/(m2 day) in summer. PCB deposition rates (total PCB and WHO-TEQ) were in the same range in winter in V.R. and PNI. In summer, contamination levels in V.R. were 6-10-folds higher than in PNI. PCB concentrations in biomonitor samples from V.R. and PNI were in the same range in summer and in winter. Concentrations of total PCB ranged from 14 to 95 microg/kg dry matter (d.m.) in winter and from 18 to 27 microg/kg d.m. in summer, respectively. The TEQ values were between 1.7 and 4.1 ng WHO-TEQ/kg d.m. in winter and between 1.9 and 2.9 ng WHO-TEQ/kg d.m. in summer. PCB concentrations of di-ortho PCB but not of non-ortho PCB were a factor of 2-4 lower in summer in both areas. PCB congener profiles resembled those from technical formulations. The profiles shifted to the higher chlorinated congeners in summer, probable due to revolatilisation of the lighter components at higher temperatures. PCB profiles in biomonitor resembled those from deposition samples and the shift to the heavier congeners in summer was even more pronounced. PAH deposition rates were in a similar range in both areas (131-2415 ng/(m2 day)). PAH levels in biomonitor samples from V.R. were about one order of magnitude higher than in samples from PNI indicating the impact of local sources. PAH profiles revealed stationary thermal processes as main source of contamination in V.R. whereas in PNI, biomass burning seems to be the main contamination source. 相似文献