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51.
污泥中重金属的形态及在小麦幼苗中的富集   总被引:13,自引:2,他引:11  
采用BCR连续提取法研究了污泥中Cd、Pb和Zn的化学形态分布,并通过室内土培实验研究了其在小麦幼苗中的富集效应。研究结果表明,Pb和Cd在污泥中主要以残渣态存在,相对比较稳定;Zn则主要以可交换态和可还原态存在,具有较强的潜在生物有效性。污泥中3种金属的潜在生物有效性由强到弱的顺序为:Zn>Cd>Pb。比较污泥中的Zn、Pb、Cd在小麦根和叶中的富集系数(EC),可发现3种金属在根中的富集系数均大于其在叶中的富集系数,说明小麦根部对这3种金属的富集能力大于其茎叶部分。3种金属在小麦中富集能力的强弱顺序在茎叶中为Zn>Cd>Pb,此结果与金属形态分析的结果相吻合。  相似文献   
52.
填埋垃圾腐殖质组成在填埋场稳定度表征中的应用   总被引:3,自引:0,他引:3  
通过对上海老港生活垃圾填埋场1991-2004年封场单元填埋垃圾腐殖质组成的分析,考察了填埋垃圾中腐殖质组成随填埋龄的变化规律.研究结果表明,填埋垃圾腐殖质的总可提取率和胡敏酸(HA)与富里酸(FA)比值(HA/FA)分别随填埋龄呈线性下降和上升趋势.因此,填埋垃圾总可提取率和HA/FA可用来有效表征填埋场和填埋垃圾稳定度.  相似文献   
53.
采用连通法,针对甲烷复杂反应机理,成功地进行了不同水平的机理简化研究。通过建立组分依赖关系的正规化Jacobian矩阵,精确地查明了燃烧组分之间的耦合关系,分别构造出仅包含重要化学路径的两个动力学简化模型,获得的简化机理分别包含227和138个反应,分别涉及39和26种组分。通过对层流预混火焰结构的模拟,所得简化机理和原详细反应动力学机理关于火焰结构的计算吻合很好,计算结果显示,两个简化机理具有较高的模拟精度。  相似文献   
54.
The maximum specific methanogenic activity (SMA) of a sludge originating from a brewery wastewater treatment plant on the degradation of glucose was investigated at various levels of sulfate on a specific loading basis. Batch experiments were conducted in serum bottles at pH 7 and 35℃. A comparison of the values indicates that the SMA of this mixed culture was increased and reached its highest level of 0.128 g CH4 gas COD/(g VSS.d) when biomass was in contact with sulfate at a ratio of 1:0.114 by weight.  相似文献   
55.
Three different sizes of hog farms were selected to analyze the carbon emissions reduction and the cost–benefit of three methane digester systems. The sizes of the digesters are 2,200, 2,200 and 800 m3, respectively. The sales of slaughter hogs from them are 50,000, 35,000 and 10,000 head, respectively. The carbon emissions reductions were 5,237, 4,017, and 1,334 tons, respectively. The results show that while the methane digester systems have a significant effect on carbon emissions reduction, it is difficult to operate the systems sustainably. If the carbon emissions reduction can be traded at high enough prices in the carbon offset markets, then the systems will be profitable and sustainable. Newly established China's domestic carbon offset market could provide this possibility, but more government support is needed. In addition, this study shows that scale economies make the digester adoption relatively more profitable for larger farms than smaller ones.  相似文献   
56.
Part V—sorption of pharmaceuticals and personal care products   总被引:5,自引:0,他引:5  
Background, aim, and scope  Pharmaceuticals and personal care products (PPCPs) including antibiotics, endocrine-disrupting chemicals, and veterinary pharmaceuticals are emerging pollutants, and their environmental risk was not emphasized until a decade ago. These compounds have been reported to cause adverse impacts on wildlife and human. However, compared to the studies on hydrophobic organic contaminants (HOCs) whose sorption characteristics is reviewed in Part IV of this review series, information on PPCPs is very limited. Thus, a summary of recent research progress on PPCP sorption in soils or sediments is necessary to clarify research requirements and directions. Main features  We reviewed the research progress on PPCP sorption in soils or sediments highlighting PPCP sorption different from that of HOCs. Special function of humic substances (HSs) on PPCP behavior is summarized according to several features of PPCP–soil or sediment interaction. In addition, we discussed the behavior of xenobiotic chemicals in a three-phase system (dissolved organic matter (DOM)–mineral–water). The complexity of three-phase systems was also discussed. Results  Nonideal sorption of PPCPs in soils or sediments is generally reported, and PPCP sorption behavior is relatively a more complicated process compared to HOC sorption, such as the contribution of inorganic fractions, fast degradation and metabolite sorption, and species-specific sorption mechanism. Thus, mechanistic studies are urgently needed for a better understanding of their environmental risk and for pollution control. Discussion  Recent research progress on nonideal sorption has not been incorporated into fate modeling of xenobiotic chemicals. A major reason is the complexity of the three-phase system. First of all, lack of knowledge in describing DOM fractionation after adsorption by mineral particles is one of the major restrictions for an accurate prediction of xenobiotic chemical behavior in the presence of DOM. Secondly, no explicit mathematical relationship between HS chemical–physical properties, and their sorption characteristics has been proposed. Last but not least, nonlinear interactions could exponentially increase the complexity and uncertainties of environmental fate models for xenobiotics. Discussion on proper simplification of fate modeling in the framework of nonlinear interactions is still unavailable. Conclusions  Although the methodologies and concepts for studying HOC environmental fate could be adopted for PPCP study, their differences should be highly understood. Prediction of PPCP environmental behavior needs to combine contributions from various fractions of soils or sediments and the sorption of their metabolites and different species. Recommendations and perspectives  More detailed studies on PPCP sorption in separated soil or sediment fractions are needed in order to propose a model predicting PPCP sorption in soils or sediments based on soil or sediment properties. The information on sorption of PPCP metabolites and species and the competition between them is still not enough to be incorporated into any predictive models.  相似文献   
57.
The methane concentration profile from -1.5m depth in soil to 32m height in air was measured in alpine steppe located in the permafrost area. Methane concentrations showed widely variations both in air and in soil during the study period. The mean concentrations in atmosphere were all higher than those in soil, and the highest methane concentration was found in air at the height of 16m with the lowest concentration occurring at the depth of 1.5m in soil. The variations of atmospheric methane concentrations did not show any clear pattern both temporally and spatially, although they exhibited a more steadystable state than those in soil. During the seasonal variations, the methane concentrations at different depths in soil were significantly correlated (R^2〉0.6) with each other comparing to the weak correlations (R^2〈0.2) between the atmospheric concentra- tions at different heights. Mean methane concentrations in soil significantly decreased with depth. This was the compositive influence of the decreasing production rates and the increasing methane oxidation rates, which was caused by the descent soil moisture with depth. Although the methane concentrations at all depths varied widely during the growing season, they showed very distinct temporal variations in the non-growing season. It was indicated from the literatures that methane oxidation rates were positively correlated with soil temperature. The higher methane concentrations in soil during the winter were determined by the lower methane oxidation rates with decreasing soil temperatures, whereas methane production rates had no reaction to the lower temperature. Relations between methane contribution and other environmental factors were not discussed in this paper for lacking of data, which impulse us to carry out further and more detailed studies in this unique area.  相似文献   
58.
The paper is devoted to the phenomenon of methanogenic activity of woody debris, i.e., methane production in the course of wood decomposition by fungi, which are not directly involved in methane synthesis but form an initial link in the trophic chain leading to methanogenic archaea. Expert evaluation of probable amounts of methane emission is made. The results show that woody debris is an important global source of this greenhouse gas.  相似文献   
59.
关于植物中氟化物测定结果的计算   总被引:1,自引:0,他引:1  
李运玲 《干旱环境监测》2001,15(3):189-190,F001
针对植物中氟化物测定时由于绘制校准曲线的标准溶液体积与分析样品的定容体积不一样而引出的结果计算时的某些问题,提出了正确的计算方法和建议。  相似文献   
60.
甲烷-煤尘复合火焰的传播与温度特征   总被引:2,自引:0,他引:2  
为了揭示甲烷-煤尘复合体系的燃烧特征,利用高速摄像机、超细热电偶、显微镜头等对管道内甲烷-煤尘复合火焰的传播过程及其温度特征进行了试验研究.结果表明,随着煤尘浓度的增加,甲烷-煤尘复合火焰的最高温度及传播速度呈现先增大后减小的趋势; 对于甲烷-煤尘复合火焰,粒径较大的煤尘在较小的浓度达到最高温度,而粒径较小的煤尘则需要在较大的浓度达到最高温度.  相似文献   
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