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排序方式: 共有809条查询结果,搜索用时 31 毫秒
31.
Zhenshu Wang Yunpeng Shi Xiaodi Wang Qi Zhang Shichao Qu 《International Journal of Green Energy》2016,13(12):1267-1280
The drying up of the fossil energy sources and the damage from unchecked carbon emissions demand the development of low carbon economy, which promotes the development of new energy sources, such as wind power and photovoltaic. However, the direct connections of wind/photovoltaic power into power grid bring great impacts on power systems, thus affecting the security and stability of power system operations, which challenges the power system dispatching. In despite of many methods for power system dispatch, lack of the models, for power system containing wind power and photovoltaic considering carbon trading and spare capacity variation (PSCWPCCTSCV), restricts the further optimal operations of power systems. This paper studies the economic dispatch modeling problem of power system containing wind power and photovoltaic, establishes the model of economic dispatch of PSCWPCCTSCV. On this basis, adaptive immune genetic algorithm is applied to conduct the economic operation optimization, which can provide the optimal carbon trading price and the optimal power distribution coefficient. Finally, simulations based on the newly proposed models are made to illustrate the economic dispatch of PSCWPCCTSCV. The results show that optimization with the proposed model can not only weaken the volatility of the new energy effectively, but also reduce carbon emissions and reduce power generation costs. 相似文献
32.
针对腈纶废水生化单元出水,对比研究了Al2(SO4)3和Fe2(SO4)3在不同絮凝剂投量和p H时的混凝处理效果,并利用紫外-可见分光光度法(UV-Vis)、三维荧光光谱(EEM)、凝胶渗透色谱(HPSEC)等对混凝特性进行了初步探讨。研究显示,2种混凝剂在投量为63.5 mg/L时可获得30%以上的COD去除率,且最佳p H为中性附近。当投量小于32 mg/L时,Al2(SO4)3较Fe2(SO4)3具有更高的COD去除率,进一步增大混凝剂的投量很难提高Al2(SO4)3对COD的去除率,而Fe2(SO4)3则在有限范围内能持续提高COD去除率。EEM光谱分析显示,与Al2(SO4)3相比,Fe2(SO4)3对有机物具有更广的处理范围和更好的去除效果。HPSEC分析表明,Fe2(SO4)3相对于Al2(SO4)3在去除重均分子量为2 776、1 856和1 325 Da的有机物组分方面具有优势。铁盐或铝盐混凝是深度净化腈纶废水生化单元出水的可行方案之一。 相似文献
33.
活性炭纤维催化臭氧化降解苯酚及其对炭表面性能的影响 总被引:2,自引:1,他引:1
研究了活性炭纤维(ACF)存在下苯酚的臭氧化降解,以及臭氧化过程对炭表面的影响.结果表明:ACF存在下的臭氧化能够显著提高苯酚的分解和矿化,ACF的用量为1 g时.反应10 min后苯酚和COD的去除率分别为96.8%和88.4%,而活性炭在同样条件下对苯酚和COD的去除率仅分别为68.0%和63.6%;臭氧化后的ACF表面含氧官能团、比表面积和总孔体积都发生了变化,内酯基减少,羧基、羟基和羰基增多,表面更亲水;比表面积增加且主要集中在微孔,而微孔体积的减少表明较小孔径的微孔数量显著增多,同时出现极少量中孔和大孔. 相似文献
34.
Qu Yang Luo Hongjie Gao Guolei Wang Yaowu Wu Linli Gao Yang Xing Yulong 《Journal of Material Cycles and Waste Management》2023,25(2):1130-1141
Journal of Material Cycles and Waste Management - Secondary aluminum dross (SAD) is classified as hazardous waste by many countries in the world because it contains a large number of toxic and... 相似文献
35.
Fang Shubo Cui Qu Dai Xiaoyan 《Environmental science and pollution research international》2020,27(9):8835-8845
Environmental Science and Pollution Research - This study proposed an in situ soil experimental system to quantify concentration and accumulation rates of polychlorinated biphenyl (PCB) congeners... 相似文献
36.
通过室内模拟实验,探讨了在非水相硝基苯污染含水层的条件下,其在含水层中的迁移及释放规律。迁移规律表明,非水相硝基苯并非在含水层中直接进行垂向迁移,而是一方面在自身重力作用下向含水层下部迁移,另一方面在地下水流的作用下随地下水同向运移,整体表现为随地下水流的侧向运移,并最终迁移至含水层底部。释放规律表明,非水相硝基苯在含水层迁移的过程中会向地下水大量释放,释放出的硝基苯在水流的作用下随地下水同向运移,污染源及迁移至含水层底部的非水相硝基苯均存在再次释放。 相似文献
37.
Solen Quéguiner Luc Musson Genon Yelva Roustan Philippe Ciffroy 《Atmospheric environment (Oxford, England : 1994)》2010,44(7):958-967
A modeling approach has been developed to estimate the contribution of atmospheric emissions to the contamination of leaf vegetables by persistent organic pollutants (POPs). It combines an Eulerian chemical transport model for atmospheric processes (Polair3D/Polyphemus) with a fate and transport model for soil and vegetation (Ourson). These two models were specifically adapted for POPs. Results are presented for benzo(a)pyrene (BaP). As expected no accumulation of BaP in leaf vegetables appears during the growth period for each harvest over the 10 years simulated. For BaP and leaf vegetables, this contamination depends primarily on direct atmospheric deposition without chemical transfer from the soil to the plant. These modeling results are compared to available data. 相似文献
38.
X.X. Zhang P.J. Shi L.Y. Liu Y. Tang H.W. Cao X.N. Zhang X. Hu L.L. Guo Y.L. Lue Z.Q. Qu Z.J. Jia Y.Y. Yang 《Atmospheric environment (Oxford, England : 1994)》2010,44(13):1641-1648
Based on environmental monitoring data in 93 major cities and meteorological records at 398 weather stations in China from 1981 to 2007, total suspended particle (TSP) concentration, the intensity of dustfall, and sand and dust storm frequency (Fd) were analysed. During the past 27 years, the annual average TSP concentration (CTSP) in 93 cities was 402 μg m?3. Annual average CTSP decreased from the north to the south and from inland to the coast areas with a peak value of 628.8 μg m?3 in Lanzhou. In the 1980s, 1990s and 2000s, annual average CTSP was 628.7, 319.2, and 250.1 μg m?3, respectively. Annual average intensity of dustfall (Id) was 240.5 t km?2 a?1, decreased from northern to southern China and from inland to the coast areas with the maximum value of 717.2 t km?2 a?1 in Baotou. In the 1980s, 1990s and 2000s, annual average Id was 334.8, 220.9, 146 t km?2 a?1 respectively. Annual average Id in the Loess Plateau region was commonly higher than 200 t km?2 a?1. The annual average Fd decreased from arid regions in northwestern China to humid areas in southeastern China with two sand and sand storm centers existing in Xinjiang Taklamakan Desert and western Inner Mongolia. The annual average Fd in the 1980s, 1990s, 2000s was 16, 8, 6 days respectively, decreased steadily from 18 days in 1981–5 days in 2007. Annual average Id had a positive linear relation to annual average CTSP (R2 = 0.96). Annual average Fd had a positive relation with annual average CTSP (R2 = 0.97) as well as annual average Id (R2 = 0.94). TSP was the chief pollutant influencing Air Pollution Index (API) in northern China in spring and winter seasons. Sand and dust storm might be a major factor affecting the temporal variability and spatial distribution of TSP and dustfall in China. 相似文献
39.
Quan Zhang Cui Wang Wanpeng Liu Jiapeng Qu Ming Liu Yanming Zhang Meirong Zhao 《Environmental science and pollution research international》2014,21(1):652-659
Quinestrol has shown potential for use in the fertility control of the plateau pika population of the Qinghai–Tibet Plateau. However, the environmental safety and fate of this compound are still obscure. Our study investigated degradation of quinestrol in a local soil and aquatic system for the first time. The results indicate that the degradation of quinestrol follows first-order kinetics in both soil and water, with a dissipation half-life of approximately 16.0 days in local soil. Microbial activity heavily influenced the degradation of quinestrol, with 41.2 % removal in non-sterile soil comparing to 4.8 % removal in sterile soil after incubation of 10 days. The half-lives in neutral water (pH 7.4) were 0.75 h when exposed to UV light (λ?=?365 nm) whereas they became 2.63 h when exposed to visible light (λ?>?400 nm). Acidic conditions facilitated quinestrol degradation in water with shorter half-lives of 1.04 and 1.47 h in pH 4.0 and pH 5.0 solutions, respectively. Moreover, both the soil and water treatment systems efficiently eliminated the estrogenic activity of quinestrol. Results presented herein clarify the complete degradation of quinestrol in a relatively short time. The ecological and environmental safety of this compound needs further investigation. 相似文献
40.