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141.
Use of USLE/GIS Methodology for Predicting Soil Loss in a Semiarid Agricultural Watershed 总被引:1,自引:0,他引:1
The Universal Soil Loss Equation (USLE) is an erosion model to estimate average soil loss that would generally result from
splash, sheet, and rill erosion from agricultural plots. Recently, use of USLE has been extended as a useful tool predicting
soil losses and planning control practices in agricultural watersheds by the effective integration of the GIS-based procedures
to estimate the factor values in a grid cell basis. This study was performed in the Kazan Watershed located in the central
Anatolia, Turkey, to predict soil erosion risk by the USLE/GIS methodology for planning conservation measures in the site.
Rain erosivity (R), soil erodibility (K), and cover management factor (C) values of the model were calculated from erosivity
map, soil map, and land use map of Turkey, respectively. R values were site-specifically corrected using DEM and climatic
data. The topographical and hydrological effects on the soil loss were characterized by LS factor evaluated by the flow accumulation
tool using DEM and watershed delineation techniques. From resulting soil loss map of the watershed, the magnitude of the soil
erosion was estimated in terms of the different soil units and land uses and the most erosion-prone areas where irreversible
soil losses occurred were reasonably located in the Kazan watershed. This could be very useful for deciding restoration practices
to control the soil erosion of the sites to be severely influenced. 相似文献
142.
143.
144.
离子化有机污染物在沉积物和水相间的平衡分配计算 总被引:4,自引:0,他引:4
本文从热力学平衡原理出发,推导出离子化有机污染物在沉积物/水相间分配系数的理论计算模型,并以苯酚,邻氯酚,2,4-二氯酚、五氯酚和苯胺的吸附实验数据为例,计算了它们在中性分子和带电荷的离子形态下的分配系数Kd和Kdi。以及总体分配系数Kdo研究结果表明,离子化有机污染物在沉积物和分配行为不仅与该化学物的pKa和存在形态有关。而且还取决于环境介质的pH。 相似文献
145.
本文采用摇瓶法测定了14各甲酰苯胺类化合物的溶解度及正辛醇/水分配系数,二者之间具有较好的相关性,应用线性溶剂化相关方法获得的相关方程,能更好地预测测苯甲酰苯胺类化合物的的水溶解度和正辛醇/水分配系数。 相似文献
146.
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
147.
Pb/Zn冶炼废渣中重金属的生物浸出-盐浸处理 总被引:3,自引:0,他引:3
利用中温嗜热菌对某铅锌冶炼废渣进行生物浸出盐浸处理研究,并根据国家固体废物浸出毒性方法(HJ/T299-2007)对盐浸后余渣进行毒性分析。研究结果表明,在pH 1.5、温度65℃、矿浆浓度5%的优化条件下生物浸出3 d后,废渣中Cu、In、Ga和Zn的浸出率分别达到了91.5%、91.8%、84.9%和93.4%;盐浸生物浸出渣,其浸出液中Ag、Pb浓度分别为7.6和247.5 mg/L,可从废渣中有效回收Cu、In、Ga、Zn、Ag和Pb。生物浸出盐浸处理后余渣约为原渣量的70%;毒性分析浸出液中重金属元素Ag、As、Cd、Cu、Pb和Zn浓度分别为2~3.5、2~3、0.3~0.5、30~50、2~4、20~60 mg/L,低于国家危险废物鉴别标准(GB5085.3-2007)。根据试验结果,提出了针对冶炼废渣资源化、减量化、无害化的生物浸出盐浸联用工艺。 相似文献
148.
Chun Wai Lee Dennis G. Tabor Kenneth A. Cowen 《Journal of Material Cycles and Waste Management》2008,10(1):38-45
The performance of four dioxin emission monitors, including two long-term sampling devices, the Dioxin-MonitoringSystem (DMS)
and AMESA (the adsorption method for sampling dioxins and furans), and two semireal-time continuous monitors, the resonance
ionization with multimirror photon accumulation time-of-flight mass spectrometer (RIMMPA-TOFMS) and the jet resonance-enhanced
multiphoton ionization (jet-REMPI) system were tested. A package boiler burning a simulated chlorinated hazardous waste was
used for a total of nine tests. Reference samples were collected during each test and analyzed for polychlorinated dibenzodioxins
and dibenzofurans (PCDDs/Fs) using gas chromatography mass spectrometry. The PCDD/F concentrations of the reference samples
measured by EPA Method 23 ranged from 0.9 to 6.0 ng toxic equivalence (TEQ)/dry standard cubic meter. The relative accuracies
achieved by DMS, AMESA, and jet-REMPI varied from 22.6% to 78.2%, with 100% data completeness. The RIMMPA-TOFMS produced no
quantifiable results due to various difficulties associated with the instrument during the testing. The two long-term samplers
were easy to install and operate and provided a cumulative, averaged emission for the sampling period. The operations of the
two semi-real-time continuous monitors were relatively complex, but one of them provided on-site, real-time data for PCDD/F
emissions from measurement of a TEQ correlative indicator compound. This article summarizes results from the individual Environmental
Technology Verification reports for the four dioxin monitors.
This work was presented, in part, at the Fourth International Conference on Combustion, Incineration/Pyrolysis and Emission
Control (i-CIPEC) 相似文献
149.
150.