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83.
好氧颗粒污泥自生动态膜生物反应器处理碱减量印染废水 总被引:1,自引:0,他引:1
自生动态膜生物反应器(SFDMBR)接种颗粒污泥启动,研究溶解氧浓度和水力停留时间对该反应器处理碱减量印染废水的影响。自生动态膜生物反应器形成稳定的动态膜后,出水浊度小于10 NTU,系统对浊度的去除率在90%以上,溶解氧和水力停留时间对反应器出水浊度基本无影响。系统对废水色度的去除率随着溶解氧浓度的提高和水力停留时间的延长而增加,但是系统对色度的去除效率一般不超过40%。溶解氧浓度由0.3 mg/L逐渐增大至2.4 mg/L,COD的去除率由40%提升至80%,而当溶解氧浓度大于1.0 mg/L后,UV254的去除率达到95%。水力停留时间在8~48 h时,COD去除效率由65%逐渐上升至85%左右;水力停留时间在8~32 h,UV254去除效率为68%~93%,超过32 h后水力停留时间对UV254去除效率的影响已不明显。 相似文献
84.
大坝通过坝身泄流时,巨大的洪水卷吸空气中的大量气体直泻到下游河床,造成下游河道特别是近坝区域气体含量过饱和,给下游水生生物带来不利影响,其中鱼类气泡病就是水体气体过饱和造成的典型病症。为探明大坝泄流对坝下河道溶解氧饱和度的影响,以三峡 葛洲坝区域坝下近坝区定点区域的溶解氧实测资料为基础,建立溶解氧饱和度的BP网络预测模型,对大坝不同运行工况进行下游溶解氧饱和度的预测仿真计算,并将仿真预测值与实测及数值模拟结果进行比较分析。结果得出BP网络模型能很好地逼近坝下近坝区指定区域的溶解氧饱和度,可根据大坝运行工况对下游水体溶解氧饱和度进行快速预测,为有效控制坝下水体溶解氧饱和度提供借鉴 相似文献
85.
Gottschalk F Ort C Scholz RW Nowack B 《Environmental pollution (Barking, Essex : 1987)》2011,159(12):3439-3445
Probabilistic material flow analysis and graph theory were combined to calculate predicted environmental concentrations (PECs) of engineered nanomaterials (ENMs) in Swiss rivers: 543 river sections were used to assess the geographical variability of nano-TiO2, nano-ZnO and nano-Ag, and flow measurements over a 20-year period at 21 locations served to evaluate temporal variation. A conservative scenario assuming no ENM removal and an optimistic scenario covering complete ENM transformation/deposition were considered. ENM concentrations varied by a factor 5 due to uncertain ENM emissions (15%-85% quantiles of ENM emissions) and up to a factor of 10 due to temporal river flow variations (15%-85% quantiles of flow). The results indicate highly variable local PECs and a location- and time-dependent risk evaluation. Nano-TiO2 median PECs ranged from 11 to 1′623 ng L−1 (conservative scenario) and from 2 to 1′618 ng L−1 (optimistic scenario). The equivalent values for nano-ZnO and nano-Ag were by factors of 14 and 240 smaller. 相似文献
86.
In the new European Pesticide Regulation (EC) No. 1107/2009, the harmonisation of approaches for estimation of the environmental exposure of pesticides is considered a major goal. Several member states currently require their own models for the calculation of predicted environmental concentrations (PEC) in surface water. The variety of methods makes risk evaluations rather time-consuming for both notifiers and evaluating authorities. In the present study we compare surface water concentrations of 19 compounds using EU and country-specific models and risk assessment approaches to evaluate to which extent the resulting estimated exposure concentrations differ. Our results show that EU and country specific approaches and the resulting surface water concentrations differ considerably regarding basic model assumptions and assessment methods. The results indicate that the aimed harmonisation of risk assessment approaches within the EU will be difficult based on current models. New scenarios may help to achieve a harmonisation taking country-specific features into account. 相似文献
87.
Tracing the sources of refractory dissolved organic matter in a large artificial lake using multiple analytical tools 总被引:2,自引:0,他引:2
Structural and chemical characteristics of refractory dissolved organic matter (RDOM) from seven different sources (algae, leaf litter, reed, compost, field soil, paddy water, treated sewage) were examined using multiple analytical tools, and they were compared with those of RDOM in a large artificial lake (Lake Paldang, Korea). Treated sewage, paddy water, and field soil were distinguished from the other sources investigated by their relatively low specific UV absorbance (SUVA) values and more pronounced fulvic-like versus humic-like fluorescence of the RDOM samples. Microbial derived RDOM from algae and treated sewage showed relatively low apparent molecular weight and a higher fraction of hydrophilic bases relative to the total hydrophilic fraction. For the biopolymer types, the presence of polyhydroxy aromatics with the high abundance of proteins was observed only for vascular plant-based RDOM (i.e., leaf litter and reed). Molecular weight values exhibited positive correlations with the SUVA and the hydrophobic content among the different RDOM, suggesting that hydrophobic and condensed aromatic structures may be the main components of high molecular weight RDOM. Principal component analysis revealed that approximately 77% of the variance in the RDOM characteristics might be explained by the source difference (i.e., terrestrial and microbial derived) and a tendency of further microbial transformation. Combined results demonstrated that the properties of the lake RDOM were largely affected by the upstream sources of field soil, paddy water, and treated sewage, which are characterized by low molecular weight UV-absorbing and non-aromatic structures with relatively high resistance to further degradation. 相似文献
88.
Biofilm responses to marine fish farm wastes 总被引:1,自引:0,他引:1
Sanz-Lázaro C Navarrete-Mier F Marín A 《Environmental pollution (Barking, Essex : 1987)》2011,159(3):825-832
The changes in the biofilm community due to organic matter enrichment, eutrophication and metal contamination derived from fish farming were studied. The biofilm biomass, polysaccharide content, trophic niche and element accumulation were quantified along an environmental gradient of fish farm wastes in two seasons. Biofilm structure and trophic diversity was influenced by seasonality as well as by the fish farm waste load. Fish farming enhanced the accumulation of organic carbon, nutrients, selenium and metals by the biofilm community. The accumulation pattern of these elements was similar regardless of the structure and trophic niche of the community. This suggests that the biofilm communities can be considered a reliable tool for assessing dissolved aquaculture wastes. Due to the ubiquity of biofilms and its wide range of consumers, its role as a sink of dissolved wastes may have important implications for the transfer of aquaculture wastes to higher trophic levels in coastal systems. 相似文献
89.
研究了混凝一气浮工艺对不同分子量区间三卤甲烷生成势(trihalomethanes formation potential,THMFP)的去除效果及絮体形态对THMFP去除效果的影响。结果表明,混凝一气浮工艺以去除大分子量区间THMFP为主,对小分子量区间THMFP的去除效果较差。UV254值与THMFP值的线性相关系数为0.9449,UV254值可以较好地反映THMFP的含量。絮体的分形维数为1.17~1.2时,孔隙率较大,可增加絮体对THMFP的活性吸附空间,且絮体相对密度较小,可增强同向絮凝作用,增加絮体和THMFP的接触概率,有利于气浮对THMFP的去除。 相似文献
90.