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Black carbon (BC), characterized by high microporosity and high specific surface area (SSA), has been demonstrated to have substantial contributions to the sorption of hydrophobic organic chemicals in soils and sediments. Other naturally occurring organic matters provide soft and penetrable sorption domains while may cling to BC and affect its original surface properties. In this work, we studied the sorption sites of a Yangtze River sediment sample with organic carbon (OC) content of 3.3 % and the preheated sediment (combusted at 375 °C) with reduced OC content (defined as BC) of 0.4 % by gas and pyrene sorption. The SSA and microporosity of the pristine and preheated sediments were characterized by N2 and CO2 adsorption. The results suggest that the adsorption of N2 was hindered by amorphous organic carbon (AOC) in the pristine sediment but CO2 was not. Instead, the uptake of CO2 was higher in the presence of AOC, likely due to the partition of CO2 molecules into the organic matter. The pyrene adsorptions to BC in pristine and preheated sediments show a similar adsorption capacity at high concentration, suggesting that AOC of ca. 2.9 % in the pristine sediment does not reduce the accessibility to the sorption sites on BC for pyrene.  相似文献   
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Burning of western low sulfur coal, to reduce sulfur oxide emissions, has resulted in decreased electrostatic precipi-tator collection efficiencies. In an effort to restore pre-cipitator performance a flue gas conditioning program was established by the company. This paper is a brief history of Commonwealth Edison Company’s experience with sulfur trioxide as a flue gas conditioning agent. Testing at State Line Station has proven that sulfur trioxide conditioning can effectively be used to improve precipitator performance when burning low sulfur coals. Although the first phase of the conditioning program is not completed, information has been gained which is being used as a basis in design and evaluation of future systems.  相似文献   
46.
In the run-up for amending the Austrian landfill ordinance, parameters were developed to assess the stability/reactivity of mechanically–biologically pretreated residual wastes. The Landfill Ordinance 2008 regulates limit values for Respiration Activity (=“Atmungsaktivität”) RA4 (AT4) < 7 mgO2 * (g dry matter (DM))?1, Gas Generation Sum GS21 < 20 Nl * kg DM?1 and alternatively Gas Evolution (=“Gasbildung”) GB21 < 20 Nl * kg DM?1. Methods for analysing these parameters were established by the Austrian Standards Institute (2004). As laboratory practice shows, these methods also are used for the assessment of other wastes (sewage sludge, commercial waste, material from abandoned sites, biowaste compost). For measurement of respiration activity in Austria mainly two methods are used: the Sapromat®-method and the OxiTop®-method. Whether respectively to what extent these two methods give same results, is discussed in this paper.Since 2009 at ABF-BOKU 169 respiration activity tests of samples taken from different stages of MBT – as well as biowaste composting processes, materials from landfills as well as abandoned sites and residues from anaerobic treatment plants were analysed parallel by Sapromat® and OxiTop®. The results manifest very strong correlation between the Sapromat® and OxiTop® method. The correlation coefficient is 0.993. As a very clear tendency OxiTop® gives lower amounts than Sapromat®. In average the lower values of OxiTop® are around 88%.  相似文献   
47.
Biomechanical model of the P-type ion pumps of the cell   总被引:1,自引:0,他引:1  
The mechanisms of the Na/K pump and of the primary Ca pumps of the cell have not yet been clarified. A biomechanical model of these so-called p-type ion pumps is proposed here. It is based on the assumption that the Na + and Ca 2+ ions are occluded by a contracting protein chain cooperating with the ATPase section of the pump. After transfer of the chain into the region of high Na + or Ca 2+ concentration, the ions are released through stretching of the chain by the ATPase. In the backward transfer of the chain, a retrograde transport of Na + ions is prevented through occlusion of K + ions by another region of the same chain. In the case of Ca 2+ ions, a similar effect is expected from hydrated Mg 2+ ions. The two sections of the chain discriminate between the electrical field strength at the surface and the polarizability of the ions. The most likely mechanism for the transfer of the ion-binding chain is considered to involve a thermally induced transition of a pump dimer between two almost equivalent stable orientations in the membrane.  相似文献   
48.
In order to examine the condition of biota in Atlantic coast estuaries, "Contaminant Exposure and Effects—Terrestrial Vertebrates" database (CEE-TV) has been compiled through computerized search of published literature, review of existing databases, and solicitation of unpublished reports from conservation agencies, private groups, and universities. Summary information has been entered into the database, including species, collection date (1965–present), site coordinates, estuary name, hydrologic unit code, sample matrix, contaminant concentrations, biomarker and bioindicator responses, and reference source, utilizing a 98-field character and numeric format. Currently, the CEE-TV database contains 3699 geo-referenced records representing 190 vertebrate species and >140,000 individuals residing in estuaries from Maine through Florida. This relational database can be directly queried or imported into a Geographic Information System to examine spatial patterns, identify data gaps and areas of concern, generate hypotheses, and focus ecotoxicological field assessments. Information on birds made up the vast majority (83%) of the database, with only a modicum of data on amphibians (<0.1%). Of the >75,000 chemical compounds in commerce, only 118 commonly measured environmental contaminants were quantified in tissues of terrestrial vertebrates. There were no CEE-TV data records in 15 of the 67 estuaries located along the Atlantic coast and Florida Gulf coast. The CEE-TV database has a number of potential applications including focusing biomonitoring efforts to generate critically needed ecotoxicological data in the numerous "gaps" along the coast, reducing uncertainty about contaminant risk, identifying areas for mitigation, restoration or special management, and ranking ecological conditions of estuaries.  相似文献   
49.
For enhanced phytoextraction, mobilization of heavy metals (HMs) from the soil solid phase to soil pore water is an important process. A pot incubation experiment mimicking field conditions was conducted to investigate the performance of three soil additives in mobilizing HMs from contaminated paddy soil (Gleyi-Stagnic Anthrosol): the [S, S]-isomer of ethylenediamine disuccinate (EDDS) with application rates of 2.3, 4.3, and 11.8 mmol kg−1 of soil, ethylenediamine tetraacetate (EDTA; 1.4, 3.8, and 7.5 mmol kg−1), and elemental sulfur (100, 200, and 400 mmol kg−1). Temporal changes in soil pore water HM and dissolved organic carbon concentrations and pH were monitored for a period of 119 days. EDDS was the most effective additive in mobilizing soil Cu. However, EDDS was only effective during the first 24 to 52 days, and was readily biodegraded with a half-life of 4.1 to 8.7 days. The effectiveness of EDDS decreased at the highest application rate, most probably as a result of depletion of the readily desorbable Cu pool in soil. EDTA increased the concentrations of Cu, Pb, Zn, and Cd in the soil pore water, and remained effective during the whole incubation period due to its persistence. The highest rate of sulfur application led to a decrease in pH to around 4. This increased the pore water HM concentrations, especially those of Zn and Cd. Concentrations of HMs in the soil pore water can be regulated to a large extent by choosing the proper application rate of EDDS, EDTA, or sulfur. Hence, a preliminary work such as our pot experiment in combination with further plant experiments (not included in this study) will provide a good tool to evaluate the applicability of different soil additives for enhanced phytoextraction of a specific soil.  相似文献   
50.
Phosphorus (P) losses from agricultural soils have caused surface water quality impairment in many regions of the world, including The Netherlands. Due to the large amounts of P accumulated in Dutch soils, the generic fertilizer and manure policy will not be sufficient to reach in time the surface water quality standards of the European Water Framework Directive. Additional measures must be considered to further reduce P enrichment of surface waters. One option is to immobilize P in soils or manure or to trap P when it moves through the landscape by using reactive materials with a large capacity to retain P. We characterized and tested two byproducts of the process of purification of deep groundwater for drinking water that could be used as reactive materials: iron sludge and iron-coated sand. Both materials contain low amounts of inorganic contaminants, which also have a low (bio)availability, and bound a large amount of P. We could describe sorption of P to the iron sludge in batch experiments well with the kinetic Freundlich equation (Q = × t (m) × C(n)). Kinetics had a large influence on P sorption in batch and column experiments and should be taken into account when iron-containing materials are tested for their capability to immobilize or trap P. A negative aspect of the iron sludge is its low hydraulic conductivity; even when mixed with pure sand to a mixture containing 20% sludge, the conductivity was very low, and only 10% sludge may be needed before application is possible in filters or barriers for removing P from groundwater. Due to its much higher hydraulic conductivity, iron-coated sand has greater potential for use under field conditions. Immobilizing P could be an option for using iron sludge as a reactive material.  相似文献   
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